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#
# Data type: Disease
# Data format: tsv
# README: 
# Source: Alliance of Genome Resources (Alliance)
# Source URL: http://alliancegenome.org/downloads
# Help Desk: help@alliancegenome.org
# Orthology Filter: Stringent
# Taxon IDs: NCBITaxon:10090
# Species: Mus musculus
# Alliance Database Version: 7.0.0
# Date file generated (UTC): 2024-02-27 10:49
#
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Taxon	SpeciesName	DBobjectType	DBObjectID	DBObjectSymbol	AssociationType	DOID	DOtermName	WithOrtholog	InferredFromID	InferredFromSymbol	ExperimentalCondition	Modifier	EvidenceCode	EvidenceCodeName	Reference	Date	Source
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8177042	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24595856	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:22596049	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:26718500	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24723555	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24437489	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:26441241	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:27479085	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12885755	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:16443782	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:7545550	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6NTac.BKS(D)-Lepr<sup>db</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12590922	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:15685168	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:3694548	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] BKS.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6991317	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:3655832	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] FVB.BKS-Lepr<sup>db</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12136396	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9970	obesity		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:16113078	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849178	Trp53<sup>tm1Elee</sup>/Trp53<sup>tm1Tyj</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S2/SvPas * 129S4/SvJae * FVB/N	is_model_of	DOID:3068	glioblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19477430	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910505	Tg(Myh6-Tnni3*L184)#Rste/0  [background:] B6.Cg-Tg(Myh6-Tnni3*L184)#Rste	is_model_of	DOID:0110313	hypertrophic cardiomyopathy 7						ECO:0000033	author statement supported by traceable reference	PMID:18096573	20170927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5754853	Dp(16Hspa13-App)2Yah/0  [background:] B6J.129P2-Dp(16Hspa13-App)2Yah	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25803843	20160329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755292	Pcare<sup>tm1Kpal</sup>/Pcare<sup>tm1Kpal</sup>  [background:] involves: C57BL/6J * C57BL/6NTac	is_model_of	DOID:0110364	retinitis pigmentosa 54						ECO:0000033	author statement supported by traceable reference	PMID:25616964	20160401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324029	Tg(Myh6-BAG3*P209L)#Mswi/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0080097	myofibrillar myopathy 6						ECO:0000033	author statement supported by traceable reference	PMID:27321750	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366720	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: C57BL/6 * C57BL/6J * Jcl:ICR	is_model_of	DOID:535	sleep disorder						ECO:0000033	author statement supported by traceable reference	PMID:17445238	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358249	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:21620777	20160126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358249	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22350410	20160126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175749	Ccw/Ccw<sup>+</sup>  [background:] involves: unpedigreed stock	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:8812411	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175749	Ccw/Ccw<sup>+</sup>  [background:] involves: unpedigreed stock	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:11062307	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638672	App<sup>tm2.1Tcs</sup>/App<sup>tm2.1Tcs</sup>  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24728269	20150608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6469361	Kbtbd13<sup>em1Coeo</sup>/Kbtbd13<sup>em1Coeo</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110935	nemaline myopathy 6						ECO:0000033	author statement supported by traceable reference	PMID:31671076	20201026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4442635	Pax2<sup>M1Bpb</sup>/Pax2<sup>M1Bpb</sup>  [background:] C57BL/6-Pax2<sup>M1Bpb</sup>	is_model_of	DOID:0090006	renal coloboma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20221250	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793784	Atp7a<sup>Mo-blo</sup>/Atp7a<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:1115218	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772457	Tg(CAG-SAC/EGFP)35Rang/0 Tg(TRAMP)8247Ng/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:17909035	20080229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849202	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/cNctr-Npc1<sup>m1N</sup>/J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22163015	20140905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849202	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/cNctr-Npc1<sup>m1N</sup>/J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:24391715	20140905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6681843	Myo9a<sup>em1Atuf</sup>/Myo9a<sup>+</sup>  [background:] C57BL/6J-Myo9a<sup>em1Atuf</sup>	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:33412162	20210408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693287	Zfp423<sup>nur12</sup>/Zfp423<sup>nur12</sup>  [background:] involves: BALB/c * C57BL/6 * C3H	is_model_of	DOID:2786	cerebellar disease						ECO:0000033	author statement supported by traceable reference	PMID:17151198	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295268	Cntnap2<sup>tm1Pele</sup>/Cntnap2<sup>tm1Pele</sup>  [background:] B6.129-Cntnap2<sup>tm1Pele</sup>	is_model_of	DOID:0090130	cortical dysplasia-focal epilepsy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21962519	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603339	Kit<sup>tm1Bpr</sup>/Kit<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:16061643	20051031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412015	Hbb<sup>d3th</sup>/Hbb<sup>d3th</sup> Tg(HBB-AR-HBA2,-HBB*)58Rub/0 Tg(LCR-HBA2,LCR-HBB)11Cos/0  [background:] involves: FVB/N * Swiss Webster	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:7662990	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7378837	Prmt1<sup>tm1Rchd</sup>/Prmt1<sup>tm1Rchd</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * CBA/J	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:29986157	20221107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563078	Tg(CAG-dsRed2/RNAi:Tardbp)6Zxu/0  [background:] involves: C57BL/6 * C57BL/6J * FVB/NJ * SJL	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:24616503	20140509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402055	Tg(CAG-DPP4)52Ctkt/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26446606	20200623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402055	Tg(CAG-DPP4)52Ctkt/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25589660	20200623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583539	Tg(ITGA2)1067Fmw/0 Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367994	Cngb3<sup>tm1Dgen</sup>/Cngb3<sup>tm1Dgen</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110008	achromatopsia 3						ECO:0000033	author statement supported by traceable reference	PMID:19767295	20151117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7314952	Sdhb<sup>tm1c(EUCOMM)Hmgu</sup>/Sdhb<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: C57BL/6J * C57BL/6N * CBA/J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:35472723	20220725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281484	Ighg1<sup>tm1(cre)Cgn</sup>/Ighg1<sup>+</sup> Myd88<sup>em1.1Rsky</sup>/Myd88<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac	is_model_of	DOID:7442	monoclonal gammopathy of uncertain significance						ECO:0000033	author statement supported by traceable reference	PMID:33343574	20220601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843172	Hbb<sup>tm1.1(HBG1,HBB*)Ryan</sup>/Hbb<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:19098001	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3761175	Tg(MMTV-neu/OT-I/OT-II)CBnel/? Tg(Trp53R172H)8512Jmr/?  [background:] involves: C57BL/6 * FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:17616705	20080617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324231	Atp7a<sup>Mo-ml</sup>/Y  [background:] involves: C3Hf/He	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:1819648	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324231	Atp7a<sup>Mo-ml</sup>/Y  [background:] involves: C3Hf/He	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	MGI:60964	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703555	Dlx5/Dlx6<sup>tm1Levi</sup>/Dlx5/Dlx6<sup>tm1Levi</sup>  [background:] Not Specified	is_model_of	DOID:0090021	split hand-foot malformation 1						ECO:0000033	author statement supported by traceable reference	PMID:12112878	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7264454	Large1<sup>m1Btlr</sup>/Large1<sup>m1Btlr</sup>  [background:] C57BL/6J-Large1<sup>m1Btlr</sup>	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175826	Dbh<sup>tm1Rpa</sup>/Dbh<sup>tm1Rpa</sup>  [background:] either: (involves: 129S7/SvEvBrd * 129/SvCpj) or (involves: 129S7/SvEvBrd * C57BL/6J)	is_model_of	DOID:0090145	dopamine beta-hydroxylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7715704	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176492	Gja8<sup>tm1Paul</sup>/Gja8<sup>tm1Paul</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110231	cataract 1 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:9813099	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5828153	Tg(Fabp4-ENPP1)#Naba/0  [background:] involves: C57BL/6J	is_model_of	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:21810932	20170310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655702	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] involves: C3H/He	is_model_of	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655702	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] involves: C3H/He	is_model_of	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:9931340	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620031	Clip2<sup>tm1.1Gal</sup>/Clip2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12195424	20060419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421780	Smim3<sup>tm1Anjm</sup>/Smim3<sup>+</sup> Cd74<sup>tm1Anjm</sup>/Cd74<sup>+</sup> Lmo2<sup>tm2(cre)Thr</sup>/Lmo2<sup>+</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>tm1Brd</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19966810	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721945	Evc<sup>tm1Jago</sup>/Evc<sup>tm1Jago</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:12714	Ellis-Van Creveld syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17660199	20070918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6305084	Tg(MECP2)1Hzo/0  [background:] FVB-Tg(MECP2)1Hzo/J	is_model_of	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000033	author statement supported by traceable reference	PMID:28743991	20190523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582953	Bicc1<sup>jcpk</sup>/Bicc1<sup>+</sup>  [background:] involves: 101 * C3H * T STOCK	is_model_of	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:7723240	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7328939	Bag5<sup>em1Asay</sup>/Bag5<sup>em1Asay</sup>  [background:] C57BL/6JJcl-Bag5<sup>em1Asay</sup>	is_model_of	DOID:0081162	dilated cardiomyopathy 2F						ECO:0000033	author statement supported by traceable reference	PMID:35044787	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5616148	Cplane2<sup>b2b2804Clo</sup>/Cplane2<sup>b2b2804Clo</sup>  [background:] C57BL/6J-Cplane2<sup>b2b2804Clo</sup>	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669721	Gjc2<sup>tm1(EGFP)Kwi</sup>/Gjc2<sup>tm1(EGFP)Kwi</sup> Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:0060787	hypomyelinating leukodystrophy 2						ECO:0000033	author statement supported by traceable reference	PMID:25524707	20151002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907609	Tg(MT2A-TGFBR2)4Rser/0  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:9334355	20170828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177044	Twist1<sup>Pde</sup>/Twist1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11350121	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661972	Ncf1<sup>m1J</sup>/Ncf1<sup>m1J</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J	is_model_of	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:10670582	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5550096	Marveld2<sup>tm1.1Sria</sup>/Marveld2<sup>tm1.1Sria</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110506	autosomal recessive nonsyndromic deafness 49						ECO:0000033	author statement supported by traceable reference	PMID:23979167	20140310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3578951	Irf8<sup>myls</sup>/Irf8<sup>myls</sup> Slc11a1<sup>r</sup>/Slc11a1<sup>r</sup>  [background:] BXH2/TyJ	is_model_of	DOID:0060761	familial chronic myelocytic leukemia-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15781580	20050607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6102908	Mecom<sup>Jbo</sup>/Mecom<sup>+</sup>  [background:] involves: BALB/c	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:20057387	20171218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6405398	Tardbp<sup>tm1.1Neas</sup>/Tardbp<sup>tm1.1Neas</sup>  [background:] B6(C3)-Tardbp<sup>tm1.1Neas</sup>	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:30625319	20200423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110172	Odad4<sup>em#Omra</sup>/Odad4<sup>em#Omra</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110620	primary ciliary dyskinesia 35						ECO:0000033	author statement supported by traceable reference	PMID:27486780	20180116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797588	Tg(Alb-TAg)1Gjh/0  [background:] C3.Cg-Tg(Alb-TAg)1Gjh	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16397233	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5924952	Rho<sup>Tvrm334</sup>/Rho<sup>+</sup>  [background:] B6.Cg-Rho<sup>Tvrm334</sup>/Pjn	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833108	Tg(SOD1*H46R*H48Q)58Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:12127151	20090223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6226089	Cacna1a<sup>tm1Lory</sup>/Cacna1a<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0050990	episodic ataxia type 2						ECO:0000033	author statement supported by traceable reference	PMID:28688851	20181106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621567	Erbb2<sup>tm1Cbm</sup>/Erbb2<sup>tm2Cbm</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12072561	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6715269	Pah<sup>em1Skym</sup>/Pah<sup>em1Skym</sup>  [background:] C57BL/6J-Pah<sup>em1Skym</sup>	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:33790381	20210611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6405042	Mc4r<sup>tm1Matsu</sup>/Mc4r<sup>tm1Matsu</sup>  [background:] C57BL/6J-Mc4r<sup>tm1Matsu</sup>	is_model_of	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000033	author statement supported by traceable reference	PMID:31990961	20200422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805518	Hps6<sup>ru-6J</sup>/Hps6<sup>ru-6J</sup>  [background:] involves: C3H/HeJ	is_model_of	DOID:0060544	Hermansky-Pudlak syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513306	Tcof1<sup>tm1Mjd</sup>/Tcof1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/1	is_model_of	DOID:2908	Treacher Collins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16938878	20190212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902325	Yy1<sup>tm2.1Yshi</sup>/Yy1<sup>tm2.1Yshi</sup> Tg(Nkx2-1-cre)2Sand/0  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:4769	pleuropulmonary blastoma						ECO:0000033	author statement supported by traceable reference	PMID:26329601	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028002	Pde6b<sup>atrd2</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6281659	Tg(Eif1a-LUM*L199P,-hrGFP)#Fzha/0  [background:] B6.Cg-Tg(Eif1a-LUM*L199P,-hrGFP)#Fzha	is_model_of	DOID:11830	myopia						ECO:0000033	author statement supported by traceable reference	PMID:27711221	20190308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198662	Gt(ROSA)26Sor<sup>tm1(CAG-MFN2*T105M)Dple</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	PMID:27907123	20180919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7464550	Got2<sup>em3Pcamp</sup>/Got2<sup>em3Pcamp</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:31422819	20230421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635158	Tg(HTT*)NXwy/0  [background:] involves: FVB/NJ	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25661181	20150508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722081	Cdh23<sup>v-5J</sup>/Cdh23<sup>v-5J</sup>  [background:] involves: SENCARA/PtJ	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6414964	Acvr1<sup>tm1Mak</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>/Gt(ROSA)26Sor<sup>+</sup> Olig2<sup>tm1.1(cre)Wdr</sup>/Olig2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:0060108	brain glioma						ECO:0000033	author statement supported by traceable reference	PMID:32142668	20200506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789948	Trim37<sup>Gt(RRO307)Byg</sup>/Trim37<sup>Gt(RRO307)Byg</sup>  [background:] B6J.129P2-Trim37<sup>Gt(RRO307)Byg</sup>	is_model_of	DOID:0050436	mulibrey nanism						ECO:0000033	author statement supported by traceable reference	PMID:27044324	20160826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311115	Sirt3<sup>tm1.1Fwa</sup>/Sirt3<sup>tm1.1Fwa</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21856199	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277819	Gt(ROSA)26Sor<sup>tm1(CAG-MYCN,-luc)Jhsc</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:2992	prostate neuroendocrine neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:34099734	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624987	Tg(Ckm-LPL)MRze/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:423	myopathy						ECO:0000033	author statement supported by traceable reference	PMID:7635990	20190806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3573788	Nbn<sup>tm1Nus</sup>/Nbn<sup>tm2Nus</sup> Tg(CD19-cre/ERT2)1Cgn/0  [background:] Not Specified	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15668392	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7256886	Fstl1<sup>tm1Ajn</sup>/Fstl1<sup>tm1Ajn</sup>  [background:] B6.Cg-Fstl1<sup>tm1Ajn</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:31834999	20220328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614947	Pstpip2<sup>cmo</sup>/Pstpip2<sup>cmo</sup>  [background:] C.Cg-Pstpip2<sup>cmo</sup>/J	is_model_of	DOID:0060645	chronic recurrent multifocal osteomyelitis						ECO:0000033	author statement supported by traceable reference	PMID:10678414	20230119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614947	Pstpip2<sup>cmo</sup>/Pstpip2<sup>cmo</sup>  [background:] C.Cg-Pstpip2<sup>cmo</sup>/J	is_model_of	DOID:0060645	chronic recurrent multifocal osteomyelitis						ECO:0000033	author statement supported by traceable reference	PMID:16122996	20230119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5912489	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-ERBB2*)5BKkw/0  [background:] involves: FVB/N	is_model_of	DOID:4829	adenosquamous lung carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19122144	20171106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452351	Tg(Myh6-STK4)28Jusa/0  [background:] involves: C57BL/6	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12750396	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5499738	Myh9<sup>tm7.1Rsad</sup>/Myh9<sup>+</sup>  [background:] involves: BALB/cJ	is_model_of	DOID:0060651	MYH-9 related disease						ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688354	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] D2.B10-Dmd<sup>mdx</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:20304955	20150925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278981	Tg(TBK1)#Andm/Tg(TBK1)#Andm  [background:] B6J.Cg-Tg(TBK1)#Andm	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:28025332	20190219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278003	Cacna1a<sup>tm3Hzo</sup>/Cacna1a<sup>tm3Hzo</sup>  [background:] B6.129S7-Cacna1a<sup>tm3Hzo</sup>/J	is_model_of	DOID:0050956	spinocerebellar ataxia type 6						ECO:0000033	author statement supported by traceable reference	PMID:26730403	20190213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843203	Men1<sup>tm1Ctre</sup>/Men1<sup>tm1Ctre</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:19208834	20090507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6726548	Macroh2a1<sup>tm1.1Oxbo</sup>/Macroh2a1<sup>tm1.1Oxbo</sup>  [background:] B6.Cg-Macroh2a1<sup>tm1.1Oxbo</sup>	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31439048	20210728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6825757	Abcc9<sup>em3Nich</sup>/Abcc9<sup>+</sup>  [background:] B6.Cg-Abcc9<sup>em3Nich</sup>	is_model_of	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000033	author statement supported by traceable reference	PMID:33529173	20211122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811798	Tg(IghMyc)22Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:3906410	20120912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811798	Tg(IghMyc)22Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22081075	20120912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688436	Clcn6<sup>tm1Tjj</sup>/Clcn6<sup>tm1Tjj</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:16950870	20061121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589107	Edn3<sup>ls</sup>/Edn3<sup>ls</sup>  [background:] involves: C57BL	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:5917257	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655482	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10381492	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655482	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10791995	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6389584	Frem2<sup>em1Hali</sup>/Frem2<sup>em2Hali</sup>  [background:] C57BL/6J-Frem2<sup>em1Hali</sup> Frem2<sup>em2Hali</sup>	is_model_of	DOID:0111717	isolated cryptophthalmia						ECO:0000033	author statement supported by traceable reference	PMID:30802441	20200526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6771478	Clp1<sup>em1Slac</sup>/Clp1<sup>em2Slac</sup>  [background:] C57BL/6J-Clp1<sup>em1Slac</sup>/Clp1<sup>em2Slac</sup>	is_model_of	DOID:0060279	pontocerebellar hypoplasia type 10						ECO:0000033	author statement supported by traceable reference	PMID:34548404	20211014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286087	Tg(GFAP-TAg121)1Tvd/0  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:12086874	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657002	Ahr<sup>tm1Yfk</sup>/Ahr<sup>tm1Yfk</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:9649	congenital nystagmus						ECO:0000033	author statement supported by traceable reference	PMID:23301081	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910392	Ppp1r13l<sup>tm1.1Xlu</sup>/Ppp1r13l<sup>tm1.1Xlu</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25691752	20170926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279070	Optn<sup>em1Hyua</sup>/Optn<sup>em1Hyua</sup>  [background:] C57BL/6J-Optn<sup>em1Hyua</sup>	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:33723228	20231003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279070	Optn<sup>em1Hyua</sup>/Optn<sup>em1Hyua</sup>  [background:] C57BL/6J-Optn<sup>em1Hyua</sup>	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:35436991	20231003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769342	Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:15545996	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882422	Tg(EmuSR-HDAC9)1468Kpet/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:27799148	20170406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301811	Fgfr1<sup>Eask</sup>/Fgfr1<sup>+</sup>  [background:] BALB/cByJ-Fgfr1<sup>Eask</sup>/GrsrJ	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661740	Celsr1<sup>Crsh</sup>/Celsr1<sup>+</sup> Vangl2<sup>Lp</sup>/Vangl2<sup>+</sup>  [background:] C3H.Cg-Vangl2<sup>Lp</sup> Celsr1<sup>Crsh</sup>	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:25128525	20150915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850388	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)1Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583532	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] D2J.B6(Cg)-Cys1<sup>cpk</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:4032601	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702557	Spry2<sup>tm1.1Mrt</sup>/Spry2<sup>tm1.1Mrt</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	PMID:34423857	20220705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943326	Tg(Lck-Tnfsf15,-EGFP)#Targ/0  [background:] involves: C57BL/6	is_model_of	DOID:0110896	inflammatory bowel disease 16						ECO:0000033	author statement supported by traceable reference	PMID:21264313	20110331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563662	Tg(KRT14-CASP1)1Miz/0  [background:] involves: C57BL/6	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:12151598	20140515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428882	Hspg2<sup>tm1Soni</sup>/Hspg2<sup>tm1Soni</sup>  [background:] involves: 129S/SvEv * DBA/2J	is_model_of	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:22449950	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766492	Tg(EmuSR-tTa)83Bop/Tg(EmuSR-tTa)83Bop Tg(tetO-NPM1/ALK,-luc)2Gde/0  [background:] involves: FVB/N	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:20223922	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697471	Crx<sup>tm1Clc</sup>/Crx<sup>tm1Clc</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110333	Leber congenital amaurosis 7						ECO:0000033	author statement supported by traceable reference	PMID:10581037	20110502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5707340	Slc3a1<sup>m1Crl</sup>/Slc3a1<sup>m1Crl</sup>  [background:] 129S2/SvPasCrl	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:25048459	20160205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042793	Shh<sup>tm1Chg</sup>/Shh<sup>tm1Chg</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110875	holoprosencephaly 3						ECO:0000033	author statement supported by traceable reference	PMID:15105374	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664791	Gja5<sup>tm1Paul</sup>/Gja5<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:12842919	20061030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905138	Tg(Myh6-Pln*)#Egk/0  [background:] Not Specified	is_model_of	DOID:0110439	dilated cardiomyopathy 1P						ECO:0000033	author statement supported by traceable reference	PMID:16432188	20170720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418371	Tg(Mt1-RET)304Ina/0  [background:] B6.C-Tg(Mt1-RET)304Ina	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:9778055	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5812300	Snap29<sup>tm1c(EUCOMM)Wtsi</sup>/Snap29<sup>tm1c(EUCOMM)Wtsi</sup> Tg(KRT14-cre)1Cgn/0  [background:] involves: C57BL/6 * C57BL/6N * DBA/2	is_model_of	DOID:0060337	CEDNIK syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26747696	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811261	Cdkn1b<sup>tm1Ako</sup>/Cdkn1b<sup>+</sup> Kit<sup>W-v</sup>/Kit<sup>W-v</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:27354067	20161207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5619302	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Postn-cre)1Sjc/0  [background:] involves: 129P2/OlaHsd * FVB/NTac	is_model_of	DOID:0111252	vestibular schwannomatosis						ECO:0000033	author statement supported by traceable reference	PMID:25113746	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3041531	Kcnj8<sup>tm1Sse</sup>/Kcnj8<sup>tm1Sse</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:3393	coronary artery disease						ECO:0000033	author statement supported by traceable reference	PMID:11984590	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304714	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:9007	sudden infant death syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22977222	20131101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6718507	Dzip1<sup>tm1Sasl</sup>/Dzip1<sup>tm1Sasl</sup> Nfatc1<sup>tm1.1(cre)Bz</sup>/Nfatc1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:988	mitral valve prolapse						ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514355	Fktn<sup>tm3.1Ttd</sup>/Fktn<sup>tm3.1Ttd</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6 * FVB	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:23562821	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719717	Atcay<sup>swd</sup>/Atcay<sup>swd</sup>  [background:] Not Specified	is_model_of	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906002	Gt(ROSA)26Sor<sup>tm1(CAG-Nr2f2)Tsa</sup>/Gt(ROSA)26Sor<sup>+</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:26356605	20170731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656637	Cebpb<sup>tm1Kish</sup>/Cebpb<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:2256	osteochondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:24885110	20221010	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428898	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22266220	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778897	Pnp<sup>e</sup>/Pnp<sup>e</sup>  [background:] involves: C3H/HeHa * C57BL/6J	is_model_of	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:2516826	20120928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722143	Tg(Thy1-APPLon)2Vln/0 Tg(Thy1-BACE1)16Vln/0  [background:] involves: C57BL/6 * DBA * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15509532	20070920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822351	Tg(RNU6-RNAi:Cldn16)551Dago/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060880	renal hypomagnesemia 3						ECO:0000033	author statement supported by traceable reference	PMID:17442678	20090107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702327	Ctsd<sup>tm1.1Thre</sup>/Ctsd<sup>tm1.1Thre</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * CBA * SJL	is_model_of	DOID:0110725	neuronal ceroid lipofuscinosis 10						ECO:0000033	author statement supported by traceable reference	PMID:26232697	20160111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581641	Tg(WapTAg)1Knw/0  [background:] C57BL/6J-Tg(WapTAg)1Knw/J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:9859214	20170623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5319225	Spink5<sup>m1Btlr</sup>/Spink5<sup>m1Btlr</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5319224	20120525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009554	Tg(Th-MYCN)41Waw/0 Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * BALB/c * C57BL/6J * FVB/N	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:9214616	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2429787	Hmox1<sup>tm1Poss</sup>/Hmox1<sup>tm1Poss</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2352	hemochromatosis						ECO:0000033	author statement supported by traceable reference	PMID:9380735	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7467130	Ctnna1<sup>em1Xjz</sup>/Ctnna1<sup>tm1Efu</sup> Gt(ROSA)26Sor<sup>tm14(CAG-tdTomato)Hze</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * C57BL/6J * C57BL/6NCrl * CBA	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6466733	Impg2<sup>em1Xjz</sup>/Impg2<sup>em1Xjz</sup>  [background:] C57BL/6J-Impg2<sup>em1Xjz</sup>	is_model_of	DOID:0110371	retinitis pigmentosa 56						ECO:0000033	author statement supported by traceable reference	PMID:32242237	20201013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663711	Bmpr1a<sup>tm1Bhr</sup>/Bmpr1a<sup>tm2.1Bhr</sup> Tg(GATA6-cre)#Jbeb/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16037571	20061016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188890	Itsn2<sup>tm1Kure</sup>/Itsn2<sup>tm1Kure</sup>  [background:] involves: C57BL/6	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29773874	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188648	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Hoxb7-cre)13Amc/0  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:21465620	20180716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429555	Ak8<sup>Gt(OST16378)Lex</sup>/Ak8<sup>Gt(OST16378)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524236	Tg(TG-BRAF*V600E)2Jaf/0  [background:] FVB/N-Tg(TG-BRAF*V600E)2Jaf	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15899815	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524236	Tg(TG-BRAF*V600E)2Jaf/0  [background:] FVB/N-Tg(TG-BRAF*V600E)2Jaf	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23372702	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677455	Sall1<sup>tm1Mrau</sup>/Sall1<sup>tm1Mrau</sup>  [background:] involves: 129X1/SvJ * ICR	is_model_of	DOID:0050887	Townes-Brocks syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12915476	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6828730	Zfp804a<sup>em1Yqd</sup>/Zfp804a<sup>em1Yqd</sup>  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:33303946	20211201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028851	Tg(aP2-SREBF1c)9884Reh/0  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:28490610	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759844	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] B6.129P2-Il10<sup>tm1Cgn</sup>/J	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:17574631	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759844	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] B6.129P2-Il10<sup>tm1Cgn</sup>/J	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:17617560	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810317	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129X1/SvJ * FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691547	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368188	Porcn<sup>tm1.2Lcm</sup>/Porcn<sup>tm1.2Lcm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3826852	Bsnd<sup>tm1Tjj</sup>/Bsnd<sup>tm1Tjj</sup> Tg(Sox10-cre)1Wdr/0  [background:] involves: 129/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110145	Bartter disease type 4a						ECO:0000033	author statement supported by traceable reference	PMID:18833191	20090119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6161223	Fgf9<sup>tm1Zgwg</sup>/Fgf9<sup>+</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0050794	multiple synostoses syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28169396	20180615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336110	Sdccag8<sup>em2Lji</sup>/Sdccag8<sup>em2Lji</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110138	Bardet-Biedl syndrome 16						ECO:0000033	author statement supported by traceable reference	PMID:35503560	20220914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907012	Tg(Myh6-cre)TG9Pjay/0  [background:] involves: FVB/N	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:16762803	20170815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356707	Myh6<sup>tm3.1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942363	Tg(Cma1-cre)ARoer/0 Tg(Kit*D814V)1Roer/0  [background:] involves: C57BL/6	is_model_of	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5463430	Tg(APPSWE)2576Kha/0 Tg(PSEN1)5Dbo/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23123627	20130212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6294720	Nkx2-5<sup>tm1.1Hkas</sup>/Nkx2-5<sup>+</sup>  [background:] 129S2.Cg-Nkx2-5<sup>tm1.1Hkas</sup>	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:26226998	20190429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6294720	Nkx2-5<sup>tm1.1Hkas</sup>/Nkx2-5<sup>+</sup>  [background:] 129S2.Cg-Nkx2-5<sup>tm1.1Hkas</sup>	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:25028484	20190429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6294294	Tg(Prnp-HTT*82Q)61Gschi/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15190011	20190424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587788	Ndst1<sup>tm1Hgx</sup>/Ndst1<sup>tm1Hgx</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12716	newborn respiratory distress syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10664446	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679475	Ptch1<sup>tm1Zim</sup>/Ptch1<sup>+</sup>  [background:] either: (involves: 129 * C57BL/6) or (involves: 129 * CD-1)	is_model_of	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9585239	20101104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532579	Clpp<sup>Gt(IST11134F10)Tigm</sup>/Clpp<sup>Gt(IST11134F10)Tigm</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0050857	Perrault syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23851121	20140129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3775240	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Tg(ACTA1-SMN)69Ahmb/Tg(ACTA1-SMN)69Ahmb Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:18178576	20080327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829465	Slc7a5<sup>tm1.1Daca</sup>/Slc7a5<sup>tm1.1Daca</sup> Tg(Tek-cre)12Flv/0  [background:] B6J.Cg-Slc7a5<sup>tm1.1Daca</sup> Tg(Tek-cre)12Flv	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27912058	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6163747	Gnat2<sup>m1Erica</sup>/Gnat2<sup>m1Erica</sup>  [background:] C.Cg-Gnat2<sup>m1Erica</sup>	is_model_of	DOID:0110010	achromatopsia 4						ECO:0000033	author statement supported by traceable reference	PMID:23580486	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811784	Pmm2<sup>tm1.1Jins</sup>/Pmm2<sup>tm2.1Jins</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000033	author statement supported by traceable reference	PMID:7884320	20161213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295452	Wasl<sup>tm1.1Ttha</sup>/Wasl<sup>tm1.1Ttha</sup> Tg(KRT14-cre)1Amc/0  [background:] involves: C57BL/6 * C57BL/6N * CBA	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:28779153	20190501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818886	Tg(Myh6-PRKAG2*T400N)1Feah/0  [background:] involves: FVB/N	is_model_of	DOID:0090101	lethal congenital glycogen storage disease of heart						ECO:0000033	author statement supported by traceable reference	PMID:20005292	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300566	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (FVB/NJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451350	Pax3<sup>Sp-d</sup>/Pax3<sup>+</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:14170406	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818341	Tdp1<sup>Gt(XD105)Byg</sup>/Tdp1<sup>Gt(XD105)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1						ECO:0000033	author statement supported by traceable reference	PMID:17914460	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648026	b2b3077Clo/b2b3077Clo  [background:] C57BL/6J-b2b3077Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767713	Serpini2<sup>pq</sup>/Serpini2<sup>pq</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16184191	20080117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565512	Flt3<sup>tm1.1Dosm</sup>/Flt3<sup>+</sup>  [background:] B6.129(C)-Flt3<sup>tm1.1Dosm</sup>	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24255108	20140529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586342	Csf2<sup>tm1Dran</sup>/Csf2<sup>tm1Dran</sup> Il3<sup>tm1Glli</sup>/Il3<sup>tm1Glli</sup>  [background:] B6.129S2-Csf2<sup>tm1Dran</sup> Il3<sup>tm1Glli</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12732663	20050831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367782	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>+</sup> Lrp6<sup>Gt(Ex187)Byg</sup>/Lrp6<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12712	nephronophthisis						ECO:0000033	author statement supported by traceable reference	PMID:19718039	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7355994	Far2<sup>em1Akih</sup>/Far2<sup>em1Akih</sup>  [background:] C57BL/6J-Far2<sup>em1Akih</sup>	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35238077	20221018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580091	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Mid1<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7434657	Cnga1<sup>m1Mhda</sup>/Cnga1<sup>m1Mhda</sup>  [background:] Not Specified	is_model_of	DOID:0110377	retinitis pigmentosa 49						ECO:0000033	author statement supported by traceable reference	PMID:36115851	20230215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315636	Zdhhc9<sup>tm1Lex</sup>/Y  [background:] B6.129S5-Zdhhc9<sup>tm1Lex</sup>	is_model_of	DOID:0060824	syndromic X-linked intellectual disability Raymond type						ECO:0000033	author statement supported by traceable reference	PMID:29944857	20190701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634093	Tg(Mbp-SNCA)29Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:16291942	20150429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6406385	Chn1<sup>tm1.1Ece</sup>/Chn1<sup>tm1.1Ece</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:12557	Duane retraction syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28346224	20200427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702324	Ctsd<sup>tm1.1Thre</sup>/Ctsd<sup>tm1.1Thre</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6N * SJL	is_model_of	DOID:0110725	neuronal ceroid lipofuscinosis 10						ECO:0000033	author statement supported by traceable reference	PMID:26232697	20160111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256838	Slc29a1<sup>tm1Msg</sup>/Slc29a1<sup>tm1Msg</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:6652	diffuse idiopathic skeletal hyperostosis						ECO:0000033	author statement supported by traceable reference	PMID:27237608	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819114	Tg(Umod*C147W)958Lura/0  [background:] involves: FVB	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:20472742	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055970	Nyx<sup>nob</sup>/Nyx<sup>nob</sup>  [background:] BALB/c-Nyx<sup>nob</sup>	is_model_of	DOID:0110870	congenital stationary night blindness 1A						ECO:0000033	author statement supported by traceable reference	PMID:9804152	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5704370	Dicer1<sup>tm1Tara</sup>/Dicer1<sup>tm1Tara</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Trp53<sup>tm2Tyj</sup>/Trp53<sup>+</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:25815421	20160122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188936	Tg(Myh6-Pkp2*/mRuby)5Rbrug/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110077	arrhythmogenic right ventricular dysplasia 9						ECO:0000033	author statement supported by traceable reference	PMID:27412010	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3806464	Robo1<sup>tm1Phr</sup>/Robo1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:15374951	20080917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430194	Tg(KRT5-Stat3*A661C*N663C)1Jdg/0  [background:] involves: FVB	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:15592573	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652543	Blnk<sup>tm1Pjln</sup>/Blnk<sup>tm1Pjln</sup> Btk<sup>tm1Wk</sup>/Btk<sup>tm1Wk</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:11449370	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5643944	Slc6a3<sup>tm1Rbl</sup>/Slc6a3<sup>tm1Rbl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:25331903	20150709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911896	Src<sup>inl</sup>/Src<sup>inl</sup>  [background:] involves: 129	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26464974	20171026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359828	Ush1c<sup>dfcr-4J</sup>/Ush1c<sup>dfcr-4J</sup>  [background:] 129P3/J-Ush1c<sup>dfcr-4J</sup>/J	is_model_of	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	MGI:6359814	20190913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154376	Kifbp<sup>em2Hmy</sup>/Kifbp<sup>em2Hmy</sup>  [background:] Not Specified	is_model_of	DOID:0060481	Goldberg-Shprintzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29192291	20180503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5771865	Apob<sup>tm2Sgy</sup>/Apob<sup>tm2Sgy</sup> Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Tg(Ins-Igf2)1Fbos/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:25231636	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437117	Megf8<sup>b2b1702.2Clo</sup>/Megf8<sup>b2b1702.2Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b1702.2Clo</sup>	is_model_of	DOID:0060234	Carpenter syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687246	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:15383546	20061110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055667	Dysf<sup>prmd</sup>/Dysf<sup>prmd</sup>  [background:] A/J	is_model_of	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:15254015	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5475286	Gclc<sup>tm1c(EUCOMM)Wtsi</sup>/Gclc<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Cryaa-cre)10Mlr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * FVB/N	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:23226398	20130425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796293	Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27274810	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640189	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] involves: C3H/HeDiSn	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:10859366	20080515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4999603	Fa2h<sup>tm1.1Hama</sup>/Fa2h<sup>tm1.1Hama</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110786	hereditary spastic paraplegia 35						ECO:0000033	author statement supported by traceable reference	PMID:21491498	20110523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304713	Egln1<sup>tm1Kael</sup>/Egln1<sup>tm1Kael</sup> Egln3<sup>tm1Vlcg</sup>/Egln3<sup>tm1Vlcg</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20733101	20170814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6113542	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-cre/ERT2)1Span/0  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:28360124	20180131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6113542	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-cre/ERT2)1Span/0  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:21228155	20180131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815300	Tg(Pax8-rtTA2S*M2)1Koes/0 Tg(tetO-MYC)36aBop/0  [background:] involves: C57BL/6 * DBA * FVB/N	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:18724376	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796777	Tg(Ins2-GLUD1*H454Y)2Csta/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:13317	hyperinsulinemic hypoglycemia						ECO:0000033	author statement supported by traceable reference	PMID:16574664	20161006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:18902556	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6729732	Awat2<sup>tm1.2Golc</sup>/Awat2<sup>tm1.2Golc</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32851726	20210809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766754	Del(11Mpo-Chad)18Brd/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000033	author statement supported by traceable reference	PMID:16489219	20210927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7492024	Ano5<sup>em2Huyi</sup>/Ano5<sup>em2Huyi</sup>  [background:] C57BL/6-Ano5<sup>em2Huyi</sup>	is_model_of	DOID:0111533	gnathodiaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:34841576	20230622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6317180	Thra<sup>em2Ffla</sup>/Thra<sup>+</sup>  [background:] C57BL/6-Thra<sup>em2Ffla</sup>	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29205102	20190711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5002697	Pdcd10<sup>tm1Wami</sup>/Pdcd10<sup>tm1Wami</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:0060671	cerebral cavernous malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:21321212	20180122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6195853	Arx<sup>tm1.1Ics</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N	is_model_of	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:29659809	20180829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432250	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-MYC)1Lach/0  [background:] involves: FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18356293	20170306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432250	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-MYC)1Lach/0  [background:] involves: FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11175856	20170306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911937	Tg(Ckm-Sgcg)4Mcn/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:11724	limb-girdle muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11287429	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437608	Ext1<sup>tm1.1Vcs</sup>/Ext1<sup>tm1.1Vcs</sup> Tg(Col2a1-rtTA,tetO-cre)22Pjro/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:206	hereditary multiple exostoses						ECO:0000033	author statement supported by traceable reference	PMID:20080592	20171214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275834	Pik3r1<sup>tm1.1Geno</sup>/Pik3r1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0111454	SHORT syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26974159	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690223	Serpine1<sup>tm1Mlg</sup>/Serpine1<sup>tm1Mlg</sup>  [background:] B6.129S2-Serpine1<sup>tm1Mlg</sup>/J	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:23919993	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4840095	Nf1<sup>tm1Par</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Elee</sup>/Trp53<sup>+</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * FVB/N	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:18451155	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175881	Fbxw4<sup>Dac</sup>/Fbxw4<sup>+</sup> mdac/mdac  [background:] involves: SM/Ckc	is_model_of	DOID:0090025	split hand-foot malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:8666395	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175881	Fbxw4<sup>Dac</sup>/Fbxw4<sup>+</sup> mdac/mdac  [background:] involves: SM/Ckc	is_model_of	DOID:0090025	split hand-foot malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:18392654	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5770790	Tg(CAG-TRIM29)ADims/0  [background:] FVB/NJ-Tg(CAG-TRIM29)ADims	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:26471361	20160523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687865	Uox<sup>tm1Bay</sup>/Uox<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:8290593	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5643856	Tg(Col1a1-tTA)139Niss/0 Tg(tetO-HTR4*D100A)2Niss/0  [background:] FVB/N-Tg(Col1a1-tTA)139Niss Tg(tetO-HTR4*D100A)2Niss	is_model_of	DOID:1858	McCune Albright syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24788917	20150708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7449243	Arl6<sup>tm2Vcs</sup>/Arl6<sup>tm2Vcs</sup>  [background:] B6.129-Arl6<sup>tm2Vcs</sup>	is_model_of	DOID:0110125	Bardet-Biedl syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:27170093	20230403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415731	Scn5a<sup>em1Coop</sup>/Scn5a<sup>+</sup>  [background:] involves: FVB/NJ	is_model_of	DOID:13884	sick sinus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30371314	20200511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812133	Dsg4<sup>hage</sup>/Dsg4<sup>hage</sup> Fas<sup>lpr</sup>/Fas<sup>lpr</sup> X/Yaa  [background:] EOD-Dsg4<sup>hage</sup>	is_model_of	DOID:0110703	hypotrichosis 6						ECO:0000033	author statement supported by traceable reference	PMID:18677469	20081027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515317	Sh2d1a<sup>tm1Lyin</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763438	Smarca4<sup>tm1Mag</sup>/Smarca4<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6J * CD-1	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423511	Mir140<sup>em1Tkob</sup>/Mir140<sup>+</sup>  [background:] C57BL/6-Mir140<sup>em1Tkob</sup>	is_model_of	DOID:2256	osteochondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30804514	20200520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196480	Rbp4<sup>tm1(RBP4)Zhel</sup>/Rbp4<sup>tm1(RBP4)Zhel</sup> Ttr<sup>tm2(TTR)Kymm</sup>/Ttr<sup>tm3(TTR*)Kymm</sup>  [background:] Not Specified	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:29330472	20180905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563098	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:24185277	20140509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043476	Htt<sup>tm2Detl</sup>/Htt<sup>tm2Detl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:17715336	20070828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697946	Tnnt1<sup>tm1.2Jin</sup>/Tnnt1<sup>tm1.2Jin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110936	nemaline myopathy 5A						ECO:0000033	author statement supported by traceable reference	PMID:24445317	20151203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6191698	Mpz<sup>tm3.1Wra</sup>/Mpz<sup>tm3.1Wra</sup>  [background:] FVB.129S2(Cg)-Mpz<sup>tm1.1Wra</sup>	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:22689911	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174925	Tgfb1<sup>tm1Doe</sup>/Tgfb1<sup>tm1Doe</sup>  [background:] involves: 129S2/SvPas * CF-1	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1436033	20050711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784505	Gusb<sup>mps</sup>/Gusb<sup>mps</sup>  [background:] B6.Cg-Gusb<sup>mps</sup>/BrkJ	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:2111021	20080509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578156	Idh2<sup>tm1Jwpk</sup>/Idh2<sup>tm1Jwpk</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0080005	bone remodeling disease						ECO:0000033	author statement supported by traceable reference	PMID:29527922	20220527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6489966	Ano5<sup>em1Huyi</sup>/Ano5<sup>em1Huyi</sup>  [background:] C57BL/6N-Ano5<sup>em1Huyi</sup>	is_model_of	DOID:0111533	gnathodiaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30712070	20210105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449062	C3<sup>tm1Pkna</sup>/C3<sup>tm1Pkna</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:8354	complement component 3 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9467654	20151118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3757568	Tg(HDexon1)62Gpb/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9267033	20071009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308946	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * CBA * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16585505	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6515623	Kmt2d<sup>Gt(RRT024)Byg</sup>/Kmt2d<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060473	Kabuki syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33431871	20210406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583541	Tg(ITGA2)1067Fmw/0 Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052930	Mbnl1<sup>tm1Sws</sup>/Mbnl1<sup>tm1Sws</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:450	myotonic disease						ECO:0000033	author statement supported by traceable reference	PMID:14671308	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603036	Tg(Prnp-SNCA*A53T)83Vle/Tg(Prnp-SNCA*A53T)83Vle  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12062037	20051027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652604	Snai2<sup>tm2Grid</sup>/Snai2<sup>tm2Grid</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:9258	Waardenburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12444107	20230703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca	is_model_of	DOID:12638	hypertrophic pyloric stenosis						ECO:0000033	author statement supported by traceable reference	PMID:15144277	20060726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487277	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>tm3Maag</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:22144569	20130526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358832	Mast1<sup>em1Dak</sup>/Mast1<sup>+</sup>  [background:] B6.Cg-Mast1<sup>em1Dak</sup>	is_model_of	DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations						ECO:0000033	author statement supported by traceable reference	PMID:30449657	20200518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4353802	Tg(Ckm-GSN*D187N)AJewe/0  [background:] C57BL/6J-Tg(Ckm-GSN*D187N)AJewe	is_model_of	DOID:0050637	Finnish type amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:19549824	20090819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6280694	Parl<sup>tm1Bdes</sup>/Parl<sup>tm1Bdes</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:30578322	20190228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4881338	Foxp3<sup>sf</sup>/Y  [background:] B6.Cg-Foxp3<sup>sf</sup>	is_model_of	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19661482	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908514	Tg(Myh6-Mybpc3*)24Rbns/0  [background:] Not Specified	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:10532952	20170907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5486680	Tg(Camk2a-DISC1)37Asaw/Tg(Camk2a-DISC1)37Asaw  [background:] C57BL/6-Tg(Camk2a-DISC1)37Asaw	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23314019	20130524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197905	Alms1<sup>m2Btlr</sup>/Alms1<sup>m2Btlr</sup>  [background:] C57BL/6J-Alms1<sup>m2Btlr</sup>	is_model_of	DOID:0050473	Alstrom syndrome						ECO:0000033	author statement supported by traceable reference	MGI:6197902	20180914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5573196	Tg(Thy1-Snca)1S13Putt/?  [background:] involves: C57BL/6	is_model_of	DOID:0060895	Parkinson's disease 4						ECO:0000033	author statement supported by traceable reference	PMID:21966373	20140718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618697	Tg(TcraAI4)1Dvs/0  [background:] NOD-Tg(TcraAI4)1Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604750	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(CAG-Bgeo,-tsA58T)T26Ichi/0 Tg(Pdx1-cre)6Tuv/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25042889	20141119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867689	Gba1<sup>tm1.1Pmis</sup>/Gba1<sup>tm1.2Pmis</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:20962279	20110113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906019	Tg(Myh6-Tpm1*E54K)30Dfw/0  [background:] involves: FVB/N	is_model_of	DOID:0110457	dilated cardiomyopathy 1Y						ECO:0000033	author statement supported by traceable reference	PMID:17556658	20170801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402903	None [background:] CC053/Unc	is_model_of	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28592648	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784778	Hras<sup>tm1Jaf</sup>/Hras<sup>tm1Jaf</sup> Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129S1/Sv * 129S6/SvEvTac * FVB/NCr	is_model_of	DOID:1781	thyroid cancer						ECO:0000033	author statement supported by traceable reference	PMID:26359368	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6694867	Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB	is_model_of	DOID:0110491	autosomal recessive nonsyndromic deafness 32						ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846168	Hba<sup>tm1(HBA)Tow</sup>/Hba<sup>tm1(HBA)Tow</sup> Hbb<sup>tm2(HBG1,HBD,HBB*)Ryan</sup>/Hbb<sup>tm3(HBG1,HBB)Tow</sup>  [background:] Not Specified	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:19258591	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554187	Drc1<sup>b2b2237Clo</sup>/Drc1<sup>b2b2237Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b2237Clo</sup>	is_model_of	DOID:0110596	primary ciliary dyskinesia 21						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6477390	Trp63<sup>tm3Aam</sup>/Trp63<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:23775923	20201203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6387275	Sqstm1<sup>tm1Keta</sup>/Sqstm1<sup>tm1Keta</sup>  [background:] involves: 129 * C57BL/6N	is_model_of	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:29555685	20200131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907041	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129/Sv * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19850880	20170816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174983	Pik3r1<sup>tm1Dfr</sup>/Pik3r1<sup>tm1Dfr</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:11062485	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174983	Pik3r1<sup>tm1Dfr</sup>/Pik3r1<sup>tm1Dfr</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:9888855	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275457	Mrgprd<sup>tm5Mjz</sup>/Mrgprd<sup>tm5Mjz</sup>  [background:] B6.129S1-Mrgprd<sup>tm5Mjz</sup>/Mmnc	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:30339496	20190131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776781	Del(MTmt-Tk-mt-Nd5)1Jiha  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:699	mitochondrial myopathy						ECO:0000033	author statement supported by traceable reference	PMID:16275929	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:10673499	20050926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177120	Msr1<sup>tm1Csk</sup>/Msr1<sup>tm1Csk</sup> Tg(APPV717F)109Ili/?  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2 * ICR	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10550330	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3760281	A<sup>y</sup>/a  [background:] involves: KK	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:5468422	20071105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4413583	Wt1<sup>tm1.1Lahe</sup>/Wt1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19797313	20091229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175185	Ntrk1<sup>tm1Bbd</sup>/Ntrk1<sup>tm1Bbd</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0050548	hereditary sensory neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:8145823	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798286	Del(5Letm1-D5Mit81)3Jcs/+  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11152656	20080722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694692	Pax2<sup>tm1Pgr</sup>/Pax2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090006	renal coloboma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8951055	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523972	Pax3<sup>Sp-1Wli</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6J * CBA/CaJ	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641920	Tg(MYOC*Y437H)#Sit/0  [background:] B6.FVB-Tg(MYOC*T437C)#Sit	is_model_of	DOID:1067	open-angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:18436825	20150625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294574	Tg(Fabp4-Il22)#Ychn/0  [background:] involves: ICR	is_model_of	DOID:3382	liposarcoma						ECO:0000033	author statement supported by traceable reference	PMID:21897855	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043693	Atp7b<sup>tm1Tcg</sup>/Atp7b<sup>tm1Tcg</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:10441329	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286582	Cacna1g<sup>tm1Hssh</sup>/Cacna1g<sup>tm1Hssh</sup> Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>tm1.1Geh</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J	is_model_of	DOID:4990	essential tremor						ECO:0000033	author statement supported by traceable reference	PMID:21621520	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5693162	Bmp1<sup>tm1.1Dgr</sup>/Bmp1<sup>tm1.1Dgr</sup> Tll1<sup>tm2.1Dgr</sup>/Tll1<sup>tm2.1Dgr</sup> Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/0  [background:] involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:24419319	20200625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804722	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1Plob</sup>  [background:] B6.129S1-Tpp1<sup>tm1Plob</sup>	is_model_of	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000033	author statement supported by traceable reference	PMID:18343701	20080908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902221	Braf<sup>tm1Tumg</sup>/Braf<sup>+</sup> Tg(CAG-cre)2Osb/0  [background:] involves: C57BL * C57BL/6J * DBA	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25035421	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6388457	Ngf<sup>tm1(NGF*)Cat</sup>/Ngf<sup>tm1(NGF*)Cat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0070145	hereditary sensory and autonomic neuropathy type 5						ECO:0000033	author statement supported by traceable reference	PMID:30612733	20200227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618527	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ	is_model_of	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:10862711	20060405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451201	Ltbp3<sup>tm1Bdvc</sup>/Ltbp3<sup>tm1Bdvc</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25669657	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6489606	Ppargc1a<sup>tm1Dpk</sup>/Ppargc1a<sup>tm1Dpk</sup>  [background:] B6.129X1-Ppargc1a<sup>tm1Dpk</sup>/J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:32439544	20210104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617307	Abcd1<sup>tm1Kds</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:15489218	20060322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6231210	Tg(H2-K-Hmga1)#Lmsr/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:363	uterine cancer						ECO:0000033	author statement supported by traceable reference	PMID:17483309	20181107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624680	Mecp2<sup>tm1Jae</sup>/Y Tg(Nes-cre)1Atp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242118	20060619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433295	b2b1519Clo/b2b1519Clo  [background:] C57BL/6J-b2b1519Clo	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6865686	Prkcg<sup>em1Jpka</sup>/Prkcg<sup>em1Jpka</sup>  [background:] FVB/N-Prkcg<sup>em1Jpka</sup>	is_model_of	DOID:0050964	spinocerebellar ataxia type 14						ECO:0000033	author statement supported by traceable reference	PMID:33478986	20220208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790498	Cdkn1a<sup>tm1Led</sup>/Cdkn1a<sup>tm1Led</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>tm1Mmt</sup> Tg(Upk2-cre)6Xrw/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:21368895	20160902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278939	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:0111227	chromosome 3-linked frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:27329763	20210201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789978	Lama2<sup>dy-6J</sup>/Lama2<sup>dy-6J</sup>  [background:] involves: C57BL/6JEi * DBA/2J	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	MGI:1342643	20080603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305730	Fgf23<sup>tm1.1Kew</sup>/Fgf23<sup>tm1.1Kew</sup>  [background:] B6.129-Fgf23<sup>tm1.1Kew</sup>	is_model_of	DOID:0050948	autosomal dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22006328	20120213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6502847	Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>/Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-A<sup>tm1Brd</sup> Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>/WtsiCnbc	is_model_of	DOID:906	peroxisomal disease						ECO:0000033	author statement supported by traceable reference	PMID:33244184	20210129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531186	Nod2<sup>tm1Mka</sup>/Nod2<sup>tm1Mka</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110892	inflammatory bowel disease 1						ECO:0000033	author statement supported by traceable reference	PMID:15692052	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5621173	Tg(SOD1*)D-14Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25305079	20150409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18439426	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:23977107	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603014	Myc<sup>tm1Lbox</sup>/Myc<sup>tm1Lbox</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:15687498	20051026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286061	Dis3l2<sup>em3Jtm</sup>/Dis3l2<sup>em3Jtm</sup>  [background:] C57BL/6J-Dis3l2<sup>em3Jtm</sup>	is_model_of	DOID:0060476	Perlman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29950491	20190404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575856	Srf<sup>tm1Zli</sup>/Srf<sup>tm1Zli</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129 * C57BL/6J * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:16260633	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5550547	Tg(NEFL-APP)#Nalb/0  [background:] involves: C57BL/6 * C3H	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20140314	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4415714	Fmr1<sup>tm1Rbd</sup>/Y  [background:] B6.129-Fmr1<sup>tm1Rbd</sup>	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20011099	20100112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784503	Pparg<sup>tm2(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317865	Tg(KRT5-rtTA)1Glk/0 Tg(tetO/CMV-Tslp)#Sfz/0  [background:] involves: C3H * C57BL/6 * FVB/N	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:16103410	20120509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850394	Nf2<sup>tm1Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)2Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706574	Ctnnb1<sup>tm1(Nfkbia)Rsu</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:11585809	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581030	Cdh23<sup>v-7J</sup>/Cdh23<sup>v-7J</sup>  [background:] CByJ(Cg)-Cdh23<sup>v-7J</sup>/GrsrJ	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663252	Ercc8<sup>tm1Jhjh</sup>/Ercc8<sup>tm1Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12509261	20151124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779417	Tg(Pmp22)My41Clh/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:12090404	20160629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6501732	Tg(Myh6-JUP*)1Dpju/0  [background:] FVB/N-Tg(Myh6-JUP*)1Dpju	is_model_of	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:27170944	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604814	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B10.D2/(58N)Sn	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7873879	20060417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850524	Sgcb<sup>tm1Oza</sup>/Sgcb<sup>tm1Oza</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E						ECO:0000033	author statement supported by traceable reference	PMID:10441321	20090716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779643	Braf<sup>tm1Cpri</sup>/Braf<sup>tm1Cpri</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129P2/OlaHsd * FVB/NCr	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21220306	20160701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175120	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae-Msx1<sup>tm1Rilm</sup>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J)	is_model_of	DOID:0050567	orofacial cleft						ECO:0000033	author statement supported by traceable reference	PMID:7914451	20060803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4354165	Srr<sup>rgsc1872</sup>/Srr<sup>rgsc1872</sup>  [background:] C57BL/6JJcl-Srr<sup>rgsc1872</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19483194	20090820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5898453	Apc<sup>tm2Rak</sup>/Apc<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pdx1-cre)6Tuv/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6J * FVB/N * SJL	is_model_of	DOID:7235	pancreatic mucinous cystadenoma						ECO:0000033	author statement supported by traceable reference	PMID:26411367	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6105949	Gns<sup>tm1e(EUCOMM)Hmgu</sup>/Gns<sup>tm1e(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-A<sup>tm1Brd</sup> Gns<sup>tm1e(EUCOMM)Hmgu</sup>	is_model_of	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:28334745	20171222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027496	Htr4<sup>tm1Comp</sup>/Htr4<sup>tm1Comp</sup>  [background:] 129/Sv-Htr4<sup>tm1Comp</sup>	is_model_of	DOID:8689	anorexia nervosa						ECO:0000033	author statement supported by traceable reference	PMID:17913892	20180515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817494	Tg(ACTA1-FRG1)highRotu/0  [background:] C57BL/6-Tg(ACTA1-FRG1)highRotu	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:16341202	20081124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467392	b2b1963Clo/b2b1963Clo  [background:] C57BL/6J-b2b1963Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617219	Ifih1<sup>Rgsc422</sup>/Ifih1<sup>+</sup>  [background:] D2JJcl.B6JJcl-Ifih1<sup>Rgsc422</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:24530055	20150302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672991	Kera<sup>tm1Cyl</sup>/Kera<sup>tm1Cyl</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060287	cornea plana						ECO:0000033	author statement supported by traceable reference	PMID:12665512	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6316332	Slc6a4<sup>tm2.1Rbl</sup>/Slc6a4<sup>tm2.1Rbl</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22431635	20190708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6316332	Slc6a4<sup>tm2.1Rbl</sup>/Slc6a4<sup>tm2.1Rbl</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27111230	20190708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818968	Tg(KRT5-AR)191Cct/0  [background:] involves: C57BL/6	is_model_of	DOID:0050801	androgenic alopecia						ECO:0000033	author statement supported by traceable reference	PMID:20233794	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6437929	Shank3<sup>tm2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6-Shank3<sup>tm2Cmpl</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27492494	20200707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589971	Foxp3<sup>sf</sup>/Y  [background:] involves: 101/H * C3H/HeH * STOCK MR	is_model_of	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:2320565	20051019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5573172	Tg(Cnp-SNCA)M2Vle/Tg(Cnp-SNCA)M2Vle  [background:] involves: C3H * C57BL/6	is_model_of	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:15797547	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7413047	Chd8<sup>tm1Kei</sup>/Chd8<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27602517	20221230	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684281	Dag1<sup>tm2Kcam</sup>/Dag1<sup>tm2Kcam</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:12140559	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636650	Tg(Lck-Tax)53Hall/0  [background:] involves: C57BL/6	is_model_of	DOID:5602	T-cell adult acute lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25035162	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636650	Tg(Lck-Tax)53Hall/0  [background:] involves: C57BL/6	is_model_of	DOID:5602	T-cell adult acute lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:16550188	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449895	Tg(SOD1*L126Z)#Deng/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16636275	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827766	Gt(ROSA)26Sor<sup>tm1(JAG1)Xin</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)20Fwan/?  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/NCrl	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:27345403	20170307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2674288	Akt1<sup>tm1Mbb</sup>/Akt1<sup>tm1Mbb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:14745448	20120726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6360454	Rab28<sup>tm1d(EUCOMM)Hmgu</sup>/Rab28<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N	is_model_of	DOID:0111024	cone-rod dystrophy 18						ECO:0000033	author statement supported by traceable reference	PMID:30228185	20190919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623749	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16394172	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623749	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12885755	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587815	Pah<sup>enu2</sup>/Pah<sup>enu2</sup>  [background:] involves: BTBR	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:9119379	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583553	Tg(ITGA5)0794Fmw/0 Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6199708	Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>/Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>	is_model_of	DOID:225	syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30082715	20180926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660888	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:0060867	macrocephaly-autism syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16675393	20150903	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028634	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm1Antc</sup>  [background:] 129-Nphs2<sup>tm1Antc</sup>	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14701729	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6492346	Prph2<sup>tm4.1Itl</sup>/Prph2<sup>tm4.1Itl</sup>  [background:] Not Specified	is_model_of	DOID:0060866	patterned macular dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:31914632	20210115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311937	Ift74<sup>b2b796Clo</sup>/Ift74<sup>b2b796Clo</sup>  [background:] C57BL/6J-Ift74<sup>b2b796Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307257	Brca1<sup>tm1Brn</sup>/Brca1<sup>tm1Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22172724	20120227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5693406	Mybpc3<sup>DBA/2J</sup>/Mybpc3<sup>DBA/2J</sup> Myh7<sup>DBA/2J</sup>/Myh7<sup>DBA/2J</sup>  [background:] DBA/2J	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:26241864	20170725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829879	Nfkbia<sup>tm1.1Pjc</sup>/Nfkbia<sup>tm1.1Pjc</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20696914	20100917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355902	Tg(GFAP-tTA)67Pop/0 Tg(tetO-Ifng)184Pop/0  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:15537876	20090903	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689511	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/NJ	is_model_of	DOID:13359	Ehlers-Danlos syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24443344	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677961	Slc7a11<sup>sut</sup>/Slc7a11<sup>sut</sup>  [background:] C3H/HeSnJ-Slc7a11<sup>sut</sup>/J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8699821	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438045	Vav2<sup>tm1Kdf</sup>/Vav2<sup>tm1Kdf</sup> Vav3<sup>tm1Swat</sup>/Vav3<sup>tm1Swat</sup>  [background:] B6.129S-Vav2<sup>tm1Kdf</sup> Vav3<sup>tm1Swat</sup>	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:20140222	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767418	Map3k14<sup>aly</sup>/Map3k14<sup>aly</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9010048	20091015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749256	Cep290<sup>Gt(CC0582)Wtsi</sup>/Cep290<sup>Gt(CC0582)Wtsi</sup>  [background:] 129P2/OlaHsd-Cep290<sup>Gt(CC0582)Wtsi</sup>	is_model_of	DOID:0111000	Joubert syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:24946806	20160505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749256	Cep290<sup>Gt(CC0582)Wtsi</sup>/Cep290<sup>Gt(CC0582)Wtsi</sup>  [background:] 129P2/OlaHsd-Cep290<sup>Gt(CC0582)Wtsi</sup>	is_model_of	DOID:0111000	Joubert syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:26301811	20160505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440902	Wnt7a<sup>px-J</sup>/Wnt7a<sup>px-J</sup>  [background:] C57BL/6J-Wnt7a<sup>px-J</sup>/GrsrJ	is_model_of	DOID:0090067	Fuhrmann syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5440718	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3612482	Fscn2<sup>tm2Sykk</sup>/Fscn2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110406	retinitis pigmentosa 30						ECO:0000033	author statement supported by traceable reference	PMID:16043865	20060210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814056	Tg(SOD1*G37R)106Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:7605627	20081106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574543	Dok1<sup>tm1Ppp</sup>/Dok1<sup>tm1Ppp</sup> Dok2<sup>tm1Ppp</sup>/Dok2<sup>tm1Ppp</sup>  [background:] 129S1/Sv-Dok1<sup>tm1Ppp</sup> Dok2<sup>tm1Ppp</sup>	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611295	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6317178	Thra<sup>em1Ffla</sup>/Thra<sup>+</sup>  [background:] C57BL/6-Thra<sup>em1Ffla</sup>	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29205102	20190711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5912341	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-Kras2)12Hev/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:3910	lung adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11751631	20171103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867520	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: BALB/cJ * C57BL/6 * C57BL/6J	is_model_of	DOID:3312	bipolar disorder						ECO:0000033	author statement supported by traceable reference	PMID:21123577	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638417	Foxo1<sup>tm1Rdp</sup>/Foxo1<sup>tm1Rdp</sup> Foxo3<sup>tm1Rdp</sup>/Foxo3<sup>tm1Rdp</sup> Foxo4<sup>tm1Rdp</sup>/Foxo4<sup>tm1Rdp</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA/J	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:25264246	20150605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6117171	None [background:] PWD/PhJ	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:25605412	20180807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3783296	Stat3<sup>tm1Flv</sup>/Stat3<sup>tm1Flv</sup> Tg(Tek-cre)12Flv/0  [background:] involves: 129 * C3H * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:12571365	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7545550	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6NTac.BKS(D)-Lepr<sup>db</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5771892	Notch1<sup>tm1Grid</sup>/Notch1<sup>+</sup> Notch3<sup>tm1Grid</sup>/Notch3<sup>tm1Grid</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:26563570	20160526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324956	Fech<sup>m1Pas</sup>/Fech<sup>tm1.1(FECH*)Emi</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6J	is_model_of	DOID:13270	erythropoietic protoporphyria						ECO:0000033	author statement supported by traceable reference	PMID:28093505	20190726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686810	Tg(Rho)1Wbae/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:8516292	20130619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616879	Aqp2<sup>F204V</sup>/Aqp2<sup>F204V</sup>  [background:] C57BL/6-Aqp2<sup>F204V</sup>	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:16121255	20060317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286082	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] (SJL/J x B6.129S2-Trp53<sup>tm1Tyj</sup> Nf1<sup>tm1Tyj</sup>/+ +)F1	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:10973261	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812399	Zeb1<sup>tm1Yhi</sup>/Zeb1<sup>tm1Yhi</sup>  [background:] either: (involves: 129 * C3H * C57BL/6) or (involves: 129 * C57BL/6 * ICR)	is_model_of	DOID:321	tropical spastic paraparesis						ECO:0000033	author statement supported by traceable reference	PMID:18467597	20081028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679324	Limk1<sup>tm1Zpj</sup>/Limk1<sup>tm1Zpj</sup>  [background:] involves: 129	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12123613	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110829	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>/Sclt1<sup>Tg(CAG-sb10)1Dla</sup>  [background:] FVB/N-Sclt1<sup>Tg(CAG-sb10)1Dla</sup>	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	PMID:28486600	20180118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850122	Smad9<sup>tm3Jfm</sup>/Smad9<sup>tm3Jfm</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:19419974	20090710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266814	Htt<sup>tm1Mem</sup>/Htt<sup>tm6Mem</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * Swiss Webster	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27623015	20220506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425229	Zbtb18<sup>tm1.1Nda</sup>/Zbtb18<sup>tm1.1Nda</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000033	author statement supported by traceable reference	PMID:22095278	20120620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7280905	Nphp1<sup>em1Lisu</sup>/Nphp1<sup>em1Lisu</sup>  [background:] C57BL/6J-Nphp1<sup>em1Lisu</sup>	is_model_of	DOID:0111112	nephronophthisis 1						ECO:0000033	author statement supported by traceable reference	PMID:34415307	20220526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529108	Mstn<sup>Cmpt</sup>/Mstn<sup>+</sup>  [background:] either: HCI or HCR	is_model_of	DOID:0111072	myostatin-related muscle hypertrophy						ECO:0000033	author statement supported by traceable reference	PMID:9335610	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5497990	T(7;18)50H/+  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1303278	20130729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157651	Notch2<sup>tm2.1Ecan</sup>/Notch2<sup>tm2.1Ecan</sup> Tg(BGLAP-cre)1Clem/0  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:2736	Hajdu-Cheney syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28592489	20180523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804125	Tg(Mafg-Nfe2l1)6Mym/0  [background:] involves: C57BL/6J * DBA/2	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25041126	20161019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4849441	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Gfap-cre)77.6Mvs/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6NHsd	is_model_of	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000033	author statement supported by traceable reference	PMID:19846776	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429501	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Ppargc1a)1Dpk/0  [background:] involves: FVB/N * FVB/NTac	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:14726475	20170830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6814676	Tg(Thy1-SNCA*)#Ztzh/0  [background:] involves: C57BL/6J	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:34744697	20211117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6406868	B3glct<sup>tm1.2Nari</sup>/B3glct<sup>tm1.2Nari</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J * DBA/2 * SJL	is_model_of	DOID:0080201	Peters plus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31600785	20200429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6199038	Grn<sup>tm1.1Hiok</sup>/Grn<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:29382817	20180921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662910	Lmna<sup>tm2Stw</sup>/Lmna<sup>tm2Stw</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:12748643	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361938	Il4ra<sup>tm2Tch</sup>/Il4ra<sup>tm2Tch</sup>  [background:] C.129X1-Il4ra<sup>tm2Tch</sup>	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:19770271	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7339183	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N * CBA	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34732824	20230815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6200350	Clcnkb<sup>tm1.1Doel</sup>/Clcnkb<sup>tm1.1Doel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:445	Bartter disease						ECO:0000033	author statement supported by traceable reference	PMID:27335120	20180928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6307806	Prss3b<sup>tm1.1Satom</sup>/Prss3b<sup>+</sup>  [background:] B6(FVB)-Prss3b<sup>tm1.1Satom</sup>	is_model_of	DOID:4989	pancreatitis						ECO:0000033	author statement supported by traceable reference	PMID:30487519	20190607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433489	Tmem67<sup>b2b1163.1Clo</sup>/Tmem67<sup>b2b1163.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1163.1Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312921	Cfc1<sup>b2b970Clo</sup>/Cfc1<sup>b2b970Clo</sup>  [background:] C57BL/6J-Cfc1<sup>b2b970Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669401	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6 * SJL	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:14690422	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159891	Slurp2<sup>tm1.1Sgy</sup>/Slurp2<sup>tm1.1Sgy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3390	palmoplantar keratosis						ECO:0000033	author statement supported by traceable reference	PMID:26967477	20180607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897864	Fan1<sup>tm1d(KOMP)Wtsi</sup>/Fan1<sup>tm1d(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0060911	karyomegalic interstitial nephritis						ECO:0000033	author statement supported by traceable reference	PMID:26980189	20170523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5547595	Dnaaf4<sup>tm1.2Jjlo</sup>/Dnaaf4<sup>tm1.2Jjlo</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0110615	primary ciliary dyskinesia 25						ECO:0000033	author statement supported by traceable reference	PMID:23872636	20140304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6694858	Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB	is_model_of	DOID:0110491	autosomal recessive nonsyndromic deafness 32						ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711319	Psap<sup>tm1Suz</sup>/Psap<sup>tm1Suz</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0111330	combined saposin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8776585	20200724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6199478	Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup> Lrp2<sup>tm1Tew</sup>/Lrp2<sup>tm1Tew</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:11829	degenerative myopia						ECO:0000033	author statement supported by traceable reference	PMID:26107939	20180925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6479897	Tcf4<sup>tm1a(EUCOMM)Wtsi</sup>/Tcf4<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29588831	20201217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903421	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-PyVT,-cre)1Mul/0  [background:] FVB/N-Tg(MMTV-rtTA)1Lach Tg(tetO-PyVT,-cre)#Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24457046	20170628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5560005	Tg(Myh6-PRKCE*A159E)344Robo/?  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22940544	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028382	Pde6b<sup>rd1-3H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711073	Rab27b<sup>tm1.2Seab</sup>/Rab27b<sup>tm1.2Seab</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:17384153	20070605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7258345	Mybpc1<sup>em1Lbmc</sup>/Mybpc1<sup>+</sup>  [background:] C57BL/6NTac-Mybpc1<sup>em1Lbmc</sup>/Lmcb	is_model_of	DOID:0081337	congenital myopathy						ECO:0000033	author statement supported by traceable reference	MGI:7256878	20230605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692743	Gfap<sup>tm3Mes</sup>/Gfap<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:17065456	20070108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324682	Tg(Thy1-APP*Swe*Ind)fAccu/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21143159	20190725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050655	Bamforth-Lazarus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697704	20050912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050655	Bamforth-Lazarus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15367491	20050912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400998	Nlgn1<sup>em1Taku</sup>/Nlgn1<sup>em1Taku</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28841651	20200323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3641169	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0111074	progressive familial heart block type IA						ECO:0000033	author statement supported by traceable reference	PMID:15809371	20060817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307894	Tnfsf11<sup>tles</sup>/Tnfsf11<sup>tles</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0110943	autosomal recessive osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:22068587	20160804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800927	Tg(HTT*97Q)IXwy/0  [background:] FVB-Tg(HTT*97Q)IXwy	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:18550760	20080811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7448597	Rr401<sup>em1Yushi</sup>/Rr401<sup>em1Yushi</sup>  [background:] Not Specified	is_model_of	DOID:5223	infertility						ECO:0000033	author statement supported by traceable reference	PMID:36613635	20230329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259432	Tg(Alb-SREBF1_ic)#Jkot/0  [background:] involves: C57BL/6	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:28490610	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473719	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-CTGF)#Swu/0  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:0050161	lower respiratory tract disease						ECO:0000033	author statement supported by traceable reference	PMID:19541844	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688834	Tg(Myh6-PRKAG2*R531G)22Dca/0  [background:] involves: C57BL/10 * CBA/Ca	is_model_of	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16339829	20061128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841583	Nr4a2<sup>tm1Tpe</sup>/Nr4a2<sup>+</sup>  [background:] B6.129P2-Nr4a2<sup>tm1Tpe</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17457314	20090428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4840094	Nf1<sup>tm1Par</sup>/Nf1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129S2/SvPas * 129S4/SvJae * 129X1/SvJ * FVB/N	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:18451155	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286560	Tg(Ckmm-Cav3)1Ysu/0  [background:] involves: C57BL/Slc * DBA/Slc	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:14645200	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655609	Atf2<sup>tm1Glm</sup>/Atf2<sup>tm1Glm</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:2256	osteochondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:8538792	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487914	Mip<sup>Cts</sup>/Mip<sup>+</sup>  [background:] involves: C57BL/6J * CTS/Shi	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:5487779	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7388558	Mettl23<sup>em2Itwa</sup>/Mettl23<sup>em2Itwa</sup>  [background:] C57BL/6J-Mettl23<sup>em2Itwa</sup>	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430325	b2b243Clo/b2b243Clo  [background:] C57BL/6J-b2b243Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311572	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup> Nat10<sup>tm1a(KOMP)Wtsi</sup>/Nat10<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6690664	Gck<sup>tm1Ydor</sup>/Gck<sup>+</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: C57BL/6 * C57BL/6J * DBA	is_model_of	DOID:0070216	familial hyperinsulinemic hypoglycemia 3						ECO:0000033	author statement supported by traceable reference	PMID:33558985	20210414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441085	Hdac4<sup>em1Hcu</sup>/Hdac4<sup>em1Hcu</sup>  [background:] involves: 129 * C57BL/6 * CBA	is_model_of	DOID:8670	eating disorder						ECO:0000033	author statement supported by traceable reference	PMID:32153359	20200710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6455517	Elmod3<sup>em1Jili</sup>/Elmod3<sup>em1Jili</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110533	autosomal recessive nonsyndromic deafness 88						ECO:0000033	author statement supported by traceable reference	PMID:31628468	20200916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404457	Pcca<sup>tm1Tmiy</sup>/Pcca<sup>tm1Tmiy</sup> Tg(CAG-PCCA*A138T,-EGFP)#Maba/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:14701	propionic acidemia						ECO:0000033	author statement supported by traceable reference	PMID:31678161	20200424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404457	Pcca<sup>tm1Tmiy</sup>/Pcca<sup>tm1Tmiy</sup> Tg(CAG-PCCA*A138T,-EGFP)#Maba/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:14701	propionic acidemia						ECO:0000033	author statement supported by traceable reference	PMID:23648696	20200424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6189180	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:29233179	20190403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822145	Dnah11<sup>avc4</sup>/Dnah11<sup>avc4</sup>  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6108884	Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup> Trmu<sup>tm1Tomik</sup>/Trmu<sup>tm1Tomik</sup>  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:409	liver disease						ECO:0000033	author statement supported by traceable reference	PMID:27689697	20180112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703807	Wwtr1<sup>tm1Whun</sup>/Wwtr1<sup>tm1Whun</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	is_model_of	DOID:12712	nephronophthisis						ECO:0000033	author statement supported by traceable reference	PMID:17251353	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559357	Tmem79<sup>ma</sup>/Tmem79<sup>ma</sup>  [background:] B6.CBACaGr-Tmem79<sup>ma</sup>/J	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24084074	20140418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5475008	Tg(Msr1-MMP9)#Apar/0  [background:] B6.Cg-Tg(Msr1-MMP9)#Apar	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:18408070	20130423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11802174	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20150727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359426	Atp6v1b2<sup>tm1Yoyu</sup>/Atp6v1b2<sup>tm1Yoyu</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31257146	20210120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512004	Ddb2<sup>tm1Pra</sup>/Ddb2<sup>tm1Pra</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110846	xeroderma pigmentosum group E						ECO:0000033	author statement supported by traceable reference	PMID:15558025	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618624	Eif2ak3<sup>tm1Drc</sup>/Eif2ak3<sup>tm1Drc</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0090060	Wolcott-Rallison syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11997520	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850478	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:4450	renal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19487675	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441532	Xbp1<sup>tm2Glm</sup>/Xbp1<sup>tm2Glm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18775308	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6470640	Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>/Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>  [background:] involves: 129/Sv * C57BL/6J	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:31765609	20221108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386447	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup> Xpa<sup>tm1Hvs</sup>/Xpa<sup>tm1Hvs</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110843	xeroderma pigmentosum group A						ECO:0000033	author statement supported by traceable reference	PMID:11950998	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7278827	Tg(Thy1-FUS*)1Dit/0  [background:] B6.Cg-Tg(Thy1-FUS*)1Dit	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:27368346	20220519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7278827	Tg(Thy1-FUS*)1Dit/0  [background:] B6.Cg-Tg(Thy1-FUS*)1Dit	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:28928015	20220519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423604	Lmna<sup>tm1Bliu</sup>/Lmna<sup>+</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:32128409	20200521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5823404	G6pc1<sup>tm1.1Ics</sup>/G6pc1<sup>tm1.1Ics</sup> Tg(Kap-icre)29066/2Sig/0  [background:] involves: 129S2/SvPas * C57BL/6J * SJL	is_model_of	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:24717294	20170207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797404	Igk<sup>tm1.1Cog</sup>/Igk<sup>tm1.1Cog</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:447	renal tubular transport disease						ECO:0000033	author statement supported by traceable reference	PMID:16543471	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790247	Fgfr1<sup>tm2.1Cxd</sup>/Fgfr1<sup>+</sup>  [background:] D2.129S6(Cg)-Fgfr1<sup>tm2.1Cxd</sup>	is_model_of	DOID:14705	Pfeiffer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21538817	20160831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7388554	Mettl23<sup>em1Itwa</sup>/Mettl23<sup>+</sup>  [background:] C57BL/6J-Mettl23<sup>em1Itwa</sup>	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5649319	Dnah5<sup>b2b3491Clo</sup>/Dnah5<sup>b2b3491Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b3491Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586712	Hpd<sup>hty</sup>/Hpd<sup>hty</sup>  [background:] ICRIII	is_model_of	DOID:0050727	tyrosinemia type III						ECO:0000033	author statement supported by traceable reference	MGI:62484	20050906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720701	Tg(Prnp-MAPT*P301L)JNPL3Hlmc/0  [background:] involves: C57BL/6 * DBA/2 * SJL * SW	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11520987	20070907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5787605	Aspa<sup>deaf14</sup>/Aspa<sup>deaf14</sup>  [background:] BALB/c-Aspa<sup>deaf14</sup>	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:24682784	20160801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582595	Ryr2<sup>tm2Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:22828895	20140915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052112	Tg(Mapt-MAPT*)#Hanr/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:680	tauopathy						ECO:0000033	author statement supported by traceable reference	PMID:18490011	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634332	Tg(Eno2-APP*Ind)#Kakiz/Tg(Eno2-APP*Ind)#Kakiz  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24489866	20150503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6810192	Ppara<sup>em1Tyrb</sup>/Ppara<sup>em1Tyrb</sup>  [background:] C57BL/6J-Ppara<sup>em1Tyrb</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:33279456	20211115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5426837	Tg(Myh6-BRUNOL4*)10Coop/0  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15988035	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827760	Tg(MMTV-Myc)141-3Led/0 Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Kras2)12Hev/0  [background:] involves: C57BL/6J * CD-1 * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18356293	20170306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311756	Rarres1<sup>tm1.2Mhl</sup>/Rarres1<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss	is_model_of	DOID:0050873	follicular lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707972	Disc1<sup>Rgsc1393</sup>/Disc1<sup>Rgsc1393</sup>  [background:] B6.Cg-Disc1<sup>Rgsc1393</sup>	is_model_of	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:17481393	20070514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324209	Atp7a<sup>Mo-blo</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:6685755	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711005	Gt(ROSA)26Sor<sup>tm2(SS18)Mrc</sup>/Gt(ROSA)26Sor<sup>tm2(SS18)Mrc</sup> Myf5<sup>tm1(cre)Mrc</sup>/Myf5<sup>tm1(cre)Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:5485	synovial sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:17418413	20091223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6150674	Del(7Chrna7-Fan1)3Arte/+  [background:] involves: C57BL/6J * C57BL/6NTac	is_model_of	DOID:0060394	chromosome 15q13.3 microdeletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24090792	20180412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603037	Tg(Prnp-SNCA*A53T)83Vle/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12062037	20051027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154645	Tg(Rho-GUCY2D*R838S)379Amd/0  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0111011	cone-rod dystrophy 6						ECO:0000033	author statement supported by traceable reference	PMID:27703005	20180504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620649	Ofd1<sup>tm2.1Bfra</sup>/Ofd1<sup>+</sup> Tg(CAG-cre)1Nagy/0  [background:] involves: 129S2/SvPas	is_model_of	DOID:0060316	orofaciodigital syndrome I						ECO:0000033	author statement supported by traceable reference	PMID:16311594	20060428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790180	Fgfr2<sup>tm2Cxd</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:21538817	20160830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5751716	Mecp2<sup>tm1.1Irsf</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25634563	20160310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162678	Atp1a3<sup>tm1Ute</sup>/Atp1a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050635	alternating hemiplegia of childhood						ECO:0000033	author statement supported by traceable reference	PMID:25523819	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620217	Tcra<sup>tm1Mom</sup>/Tcra<sup>tm1Mom</sup>  [background:] B6.129S2-Tcra<sup>tm1Mom</sup>	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18242214	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358603	Serpina1<sup>em#Chmu</sup>/Serpina1<sup>em#Chmu</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:29453277	20190906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663997	Kit<sup>tm2Bsm</sup>/Kit<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:12754375	20090630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367269	Rho<sup>R3</sup>/Rho<sup>+</sup>  [background:] C57BL/6J-Rho<sup>R3</sup>	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:19741247	20130619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029165	Smpd1<sup>tm1Wst</sup>/Smpd1<sup>tm1Wst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:7600574	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655821	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] 129X1.Cg-Cyp1b1<sup>tm1Gonz</sup>	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476672	Tg(Eno2-MFN2*R94Q)L51Ugfm/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	PMID:20418531	20130501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883306	Il2ra<sup>tm1Dw</sup>/Il2ra<sup>tm1Dw</sup>  [background:] B6.129S4-Il2ra<sup>tm1Dw</sup>/J	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17207605	20170417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910329	Mypn<sup>tm1.1Epu</sup>/Mypn<sup>+</sup>  [background:] either: (involves: 129S6/SvEv) or (involves: 129S6/SvEv * C57BL/6NCrl)	is_model_of	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25541130	20170926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509636	Ppil1<sup>em3Jgg</sup>/Ppil1<sup>em3Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em3Jgg</sup>	is_model_of	DOID:0112325	pontocerebellar hypoplasia type 14						ECO:0000033	author statement supported by traceable reference	PMID:33220177	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6459755	Tg(CAG-EPM2A*C266S)1Bmin/0  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:15102711	20201005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6459755	Tg(CAG-EPM2A*C266S)1Bmin/0  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:17118331	20201005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451081	Lipa<sup>tm1Ggb</sup>/Lipa<sup>tm1Ggb</sup>  [background:] involves: 129P2/OlaHsd * CF-1	is_model_of	DOID:0080217	lysosomal acid lipase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9700186	20190729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772447	mgb/mgb  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:24023768	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295756	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Rbl1<sup>tm1Tyj</sup>/Rbl1<sup>tm1Tyj</sup> Rbl2<sup>tm2.1Tyj</sup>/Rbl2<sup>tm2.1Tyj</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21875955	20111115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6113412	Pink1<sup>tm1.1Wrst</sup>/Pink1<sup>tm1.1Wrst</sup> Tg(Prnp-SNCA*A53T)AAub/?  [background:] involves: 129S2/SvPas * C57BL/6J * FVB/N	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:28360124	20180131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445935	Scn5a<sup>tm3(SCN5A*)Rdn</sup>/Scn5a<sup>tm3(SCN5A*)Rdn</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110433	dilated cardiomyopathy 1E						ECO:0000033	author statement supported by traceable reference	PMID:21824921	20170802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313541	b2b370Clo/b2b370Clo  [background:] C57BL/6J-b2b370Clo	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688197	Hcn1<sup>tm2Kndl</sup>/Hcn1<sup>tm2Kndl</sup>  [background:] involves: 129 * 129S/SvEv * C57BL/6J * C57BL/6N	is_model_of	DOID:13884	sick sinus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24218458	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820803	Ret<sup>tm2.1Heno</sup>/Ret<sup>tm2.1Heno</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:18414682	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7431290	Rr124128<sup>tm1.1Jfer</sup>/Rr124128<sup>tm1.1Jfer</sup> Tg(Pdx1-cre)6Tuv/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:36202974	20230203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525190	Tg(CAG-WRN*K577M)5025Wcl/0  [background:] involves: C3H * C57BL/6J	is_model_of	DOID:5688	Werner syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10628995	20081030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445215	Pkd1<sup>b2b1585Clo</sup>/Pkd1<sup>b2b1585Clo</sup>  [background:] C57BL/6J-Pkd1<sup>b2b1585Clo</sup>	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532293	Gtf2i<sup>tm1Vcam</sup>/Gtf2i<sup>tm1Vcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20403157	20140127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431571	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129 * FVB	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:19805914	20120816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841485	Ptprc<sup>tm1Weis</sup>/Ptprc<sup>tm1Weis</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11163182	20090428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177533	Cftr<sup>tm1Bay</sup>/Cftr<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7505691	20050809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513600	Mtmr2<sup>tm1.1Abol</sup>/Mtmr2<sup>tm1.1Abol</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0110191	Charcot-Marie-Tooth disease type 4B1						ECO:0000033	author statement supported by traceable reference	PMID:15557122	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638149	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16556734	20150603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5817425	Vipas39<sup>tm1c(KOMP)Mbp</sup>/Vipas39<sup>tm1c(KOMP)Mbp</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N	is_model_of	DOID:0050763	ARC syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27435297	20170112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680011	Stub1<sup>tm1Cpat</sup>/Stub1<sup>tm1Cpat</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0080029	autosomal recessive spinocerebellar ataxia 16						ECO:0000033	author statement supported by traceable reference	PMID:28593200	20180504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154152	Tg(EIIa-cre)C5379Lmgd/? Trip11<sup>tm1.2Psmi</sup>/Trip11<sup>tm1.2Psmi</sup>  [background:] involves: 129/Sv * C57BL/6 * FVB/N	is_model_of	DOID:0080054	achondrogenesis type IA						ECO:0000033	author statement supported by traceable reference	PMID:29180569	20180503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814903	Six3<sup>tm3Gco</sup>/Six3<sup>tm3Gco</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0110872	holoprosencephaly 2						ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430995	Pkhd1<sup>tm1Sswi</sup>/Pkhd1<sup>tm1Sswi</sup>  [background:] B6.Cg-Pkhd1<sup>tm1Sswi</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:18286309	20130917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6490343	Matr3<sup>em1Tcp</sup>/Matr3<sup>em1Tcp</sup>  [background:] C57BL/6J-Matr3<sup>em1Tcp</sup>	is_model_of	DOID:0060212	amyotrophic lateral sclerosis type 21						ECO:0000033	author statement supported by traceable reference	PMID:33082323	20210106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3775615	Fkbp8<sup>Gt(OST287985)Lex</sup>/Fkbp8<sup>Gt(OST287985)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0080016	spina bifida						ECO:0000033	author statement supported by traceable reference	PMID:18003640	20211231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812458	Gan<sup>tm1Jpj</sup>/Gan<sup>tm1Jpj</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0090068	giant axonal neuropathy 1						ECO:0000033	author statement supported by traceable reference	PMID:18680552	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:21049041	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:19364920	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634327	St14<sup>tm2Bug</sup>/St14<sup>tm3Bug</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24551030	20150503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6283591	Nf1<sup>Mhdadsk9</sup>/Nf1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:30571760	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7264693	Cant1<sup>tm1.2Aros</sup>/Cant1<sup>tm1.2Aros</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0060462	Desbuquois dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30439444	20220427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6194720	Ttr<sup>tm1.1Smoc</sup>/?  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:29360446	20180816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437465	Pign<sup>m1Nisw</sup>/Pign<sup>m1Nisw</sup>  [background:] involves: 129S1/SvImJ * C3H/HeJ * C57BL/6J	is_model_of	DOID:4621	holoprosencephaly						ECO:0000033	author statement supported by traceable reference	PMID:23213481	20190927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576258	B2m<sup>tm1Unc</sup>/B2m<sup>tm1Unc</sup> Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:9741021	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429796	Cst6<sup>ichq</sup>/Cst6<sup>+</sup>  [background:] involves: BALB/cJ	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:15044380	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429796	Cst6<sup>ichq</sup>/Cst6<sup>+</sup>  [background:] involves: BALB/cJ	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:9212754	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904828	Tg(Myh6-CACNA1C)M1Aschw/0  [background:] involves: FVB/N	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:11136699	20170717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3823250	Lama5<sup>tm3Jhm</sup>/Lama5<sup>tm3Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:16790509	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449123	Aprt<sup>tm1Dwm</sup>/Aprt<sup>tm1Dwm</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:0060350	adenine phosphoribosyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8864750	20120924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175743	Cat4<sup>Apcat1-2</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175743	Cat4<sup>Apcat1-2</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3773447	A<sup>y</sup>/A  [background:] involves: C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:18172198	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799369	Tg(Trp53R172H)8512Jmr/0  [background:] involves: FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:9519874	20211209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294956	Ctf1<sup>tm1Msd</sup>/Ctf1<sup>tm1Msd</sup>  [background:] B6.Cg-Ctf1<sup>tm1Msd</sup>	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:21803294	20111104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5142310	Kif3a<sup>tm1Gsn</sup>/Kif3a<sup>tm2Gsn</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR	is_model_of	DOID:0080322	polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:12672950	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5004709	Ptpn11<sup>tm4.2Bgn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N	is_model_of	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:21339643	20110608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286072	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129T2/SvEms * FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6491326	Rab32<sup>tm1b(KOMP)Wtsi</sup>/Rab32<sup>tm1b(KOMP)Wtsi</sup> Rab38<sup>tm1.1Ics</sup>/Rab38<sup>tm1.1Ics</sup>  [background:] involves: C57BL/6N * C57BL/6NTac	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31399401	20210111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7408196	Rbm24<sup>tm1.1Xixu</sup>/Rbm24<sup>tm1.1Xixu</sup> Tg(Myhc-cre)1Xya/0  [background:] involves: C57BL/6NTac	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:30267374	20221215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665402	Grip1<sup>eb</sup>/Grip1<sup>eb</sup>  [background:] involves: ATEB/Le * C57BL/6J	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450466	Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:8402910	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1912584	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11912185	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3775649	Hfe<sup>tm1.1Wsr</sup>/Hfe<sup>tm1.1Wsr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:17264297	20081230	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941336	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm2Tyj</sup>/Trp53<sup>+</sup> Tg(Pdx1-cre)6Tuv/0  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15894267	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J	is_model_of	DOID:0060825	Christianson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26515654	20181030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J	is_model_of	DOID:0060825	Christianson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29349289	20181030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J	is_model_of	DOID:0060825	Christianson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21964919	20181030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668608	Slc45a2<sup>uw-d</sup>/Slc45a2<sup>uw-d</sup>  [background:] involves: TF/Le	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703705	Del(16Dgcr2-Hira)1Rak/+  [background:] involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11239417	20070423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851906	Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup>/Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup> 7630403G23Rik<sup>Tg(Th-cre)1Tmd</sup>/7630403G23Rik<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:19630976	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693216	Acadm<sup>tm1Uab</sup>/Acadm<sup>tm1Uab</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16121256	20070111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580073	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:10591652	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574028	Clcn3<sup>tm1Suc</sup>/Clcn3<sup>tm1Suc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:12059962	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524086	Tg(MMTV-Myc*T58A)TA14Jrn/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7335182	Cdc42<sup>tm1.1Ayam</sup>/Cdc42<sup>tm1.1Ayam</sup> Tg(Mpz-cre)94Imeg/0  [background:] Not Specified	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:28326341	20220909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6270171	Tg(Camk2a-Polg*D181A)BTkato/0  [background:] C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	is_model_of	DOID:3324	mood disorder						ECO:0000033	author statement supported by traceable reference	PMID:16619054	20181231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6113543	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-icre)9190Gsc/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:21228155	20180131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713294	Gck<sup>tm2Mgn</sup>/Gck<sup>+</sup>  [background:] 129S6/SvEvTac-Gck<sup>tm2Mgn</sup>	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6512404	Pten<sup>tm1.2Mwst</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20194734	20210326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676371	Pitpna<sup>Gt(OST1152)Lex</sup>/Pitpna<sup>Gt(OST1152)Lex</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:0060357	chylomicron retention disease						ECO:0000033	author statement supported by traceable reference	PMID:12788952	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160485	Eif2b4<sup>tm1.1Vdk</sup>/Eif2b4<sup>tm1.1Vdk</sup> Eif2b5<sup>tm1.1Vdk</sup>/Eif2b5<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7523314	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>+</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>	is_model_of	DOID:2477	motor peripheral neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175787	Hps3<sup>coa-6J</sup>/Hps3<sup>coa-6J</sup>  [background:] C3H/HeJ-Hps3<sup>coa-6J</sup>/J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	MGI:1861465	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5556400	Tinf2<sup>tm2.2Tdl</sup>/Tinf2<sup>+</sup>  [background:] involves: BALB/cJ * C57BL/6	is_model_of	DOID:2729	dyskeratosis congenita						ECO:0000033	author statement supported by traceable reference	PMID:24449270	20140415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719120	Snrpn<sup>tm2Alb</sup>/Snrpn<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11431693	20070827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7265077	Myt1l<sup>em1Jdd</sup>/Myt1l<sup>+</sup>  [background:] C57BL/6-Myt1l<sup>em1Jdd</sup>/J	is_model_of	DOID:0070069	autosomal dominant intellectual developmental disorder 39						ECO:0000033	author statement supported by traceable reference	PMID:34614421	20220502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473965	Vwf<sup>tm1.1Vhf</sup>/Vwf<sup>tm1.1Vhf</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:12531	von Willebrand's disease						ECO:0000033	author statement supported by traceable reference	PMID:30565388	20201124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441186	Card14<sup>em2Tshu</sup>/Card14<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080475	psoriasis 2						ECO:0000033	author statement supported by traceable reference	PMID:29980436	20200713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613467	Pax6<sup>7Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0060673	Peters anomaly						ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653709	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-CDK5R1/GFP)337Lht/0  [background:] involves: C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22049418	20150506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028001	Pde6b<sup>atrd2</sup>/Pde6b<sup>atrd2</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580291	Lmbr1<sup>tm1Kng</sup>/Lmbr1<sup>tm1Kng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	is_model_of	DOID:0050603	acheiropody						ECO:0000033	author statement supported by traceable reference	PMID:11606546	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675470	Traf6<sup>tm1Jino</sup>/Traf6<sup>tm1Jino</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:12060722	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6285740	Dnaaf11<sup>tm1.2Hmd</sup>/Dnaaf11<sup>tm1.2Hmd</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl	is_model_of	DOID:0110608	primary ciliary dyskinesia 19						ECO:0000033	author statement supported by traceable reference	PMID:27353389	20190402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628757	Vegfa<sup>tm4Pec</sup>/Vegfa<sup>tm4Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12539040	20060711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4454331	Tg(Fabp4-LMNA*R482Q)11ACdl/0  [background:] FVB-Tg(Fabp4-LMNA*R482Q)11ACdl	is_model_of	DOID:0050440	familial partial lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19201734	20100608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441548	Tg(Ins2-Tag*,-flpe)#Gne/0  [background:] Not Specified	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20554752	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3848697	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>/Khdrbs2<sup>+</sup>  [background:] FVB-Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_model_of	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:19503083	20100222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6865691	Prkcg<sup>em1Jpka</sup>/Prkcg<sup>+</sup>  [background:] FVB/N-Prkcg<sup>em1Jpka</sup>	is_model_of	DOID:0050964	spinocerebellar ataxia type 14						ECO:0000033	author statement supported by traceable reference	PMID:33478986	20220208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653209	Zic2<sup>tm1Jaru</sup>/Zic2<sup>tm1Jaru</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110878	holoprosencephaly 5						ECO:0000033	author statement supported by traceable reference	PMID:10677508	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5485349	Syngap1<sup>tm1Rlh</sup>/Syngap1<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19145222	20130516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429556	Pomk<sup>Gt(OST243203)Lex</sup>/Pomk<sup>Gt(OST243203)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286096	Arid1b<sup>em1Iha</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Iha</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28867767	20190404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6101180	Nisch<sup>edsn</sup>/Nisch<sup>edsn</sup>  [background:] C3H.B6-Nisch<sup>edsn</sup>	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:28806779	20171218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286079	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] (C3H/HeJ x B6.129S2-Trp53<sup>tm1Tyj</sup> Nf1<sup>tm1Tyj</sup>/+ +)F1	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:10973261	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517484	Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup>  [background:] B6.1129-Syn2<sup>tm1Pggd</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6416492	Tg(FGFR3-G380R)7Aya/Tg(FGFR3-G380R)7Aya  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:10607835	20200514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415732	Scn5a<sup>em1Coop</sup>/Scn5a<sup>em1Coop</sup>  [background:] involves: C57BL/6NJ * FVB/NJ	is_model_of	DOID:13884	sick sinus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30371314	20200511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5049966	Tg(PDGF-S100B)36Cqin/0  [background:] C57BL/6-Tg(PDGF-S100B)36Cqin	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:21376255	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839539	Lpin1<sup>fld-2J</sup>/Lpin1<sup>fld-2J</sup>  [background:] C3H/HeJ-Lpin1<sup>fld-2J</sup>/J	is_model_of	DOID:811	lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11138012	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6759479	Cilk1<sup>tm1.1Zfu</sup>/Cilk1<sup>tm1.1Zfu</sup>  [background:] B6.Cg-Cilk1<sup>tm1.1Zfu</sup>	is_model_of	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29098359	20210917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6759479	Cilk1<sup>tm1.1Zfu</sup>/Cilk1<sup>tm1.1Zfu</sup>  [background:] B6.Cg-Cilk1<sup>tm1.1Zfu</sup>	is_model_of	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28380258	20210917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6285862	Ucp2<sup>tm1Lowl</sup>/Ucp2<sup>tm1Lowl</sup>  [background:] B6.129S4-Ucp2<sup>tm1Lowl</sup>	is_model_of	DOID:0050770	polycystic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:29154852	20190403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815114	Ccl2<sup>tm1Rol</sup>/Ccl2<sup>tm1Rol</sup>  [background:] B6.129S4-Ccl2<sup>tm1Rol</sup>	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:14566334	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361196	Tg(Krt19-Ptgs2,Krt19-Ptges)8Tko/0 Tg(Krt19-Wnt1)2Maos/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:17030179	20110411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610950	Eif4ebp2<sup>tm1Klan</sup>/Eif4ebp2<sup>tm1Klan</sup>  [background:] B6.129S4(C)-Eif4ebp2<sup>tm1Klan</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23172145	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4888960	Gria1<sup>tm1Rsp</sup>/Gria1<sup>tm1Rsp</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:5418	schizoaffective disorder						ECO:0000033	author statement supported by traceable reference	PMID:20699120	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583543	Tg(ITGA2)1070Fmw/0 Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555838	b2b2059Clo/b2b2059Clo  [background:] C57BL/6J-b2b2059Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459500	Gnasas1<sup>tm1.1Hju</sup>/Gnasas1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:4184	pseudohypoparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:20427744	20120727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6401826	Mafb<sup>em1Staka</sup>/Mafb<sup>em1Staka</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0111534	multicentric carpotarsal osteolysis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30369533	20200327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579982	Frem2<sup>Gt(KST252)Byg</sup>/Frem2<sup>my-Ucl</sup>  [background:] involves: 129P2/OlaHsd * CD-1 * NMRI	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15838507	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ	is_model_of	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6719082	Tjp1<sup>tm1.1Whun</sup>/Tjp1<sup>tm1.1Whun</sup> Tjp2<sup>tm2Whun</sup>/Tjp2<sup>tm2Whun</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * C57BL/6NTac * DBA/2	is_model_of	DOID:0070224	progressive familial intrahepatic cholestasis 4						ECO:0000033	author statement supported by traceable reference	PMID:33184034	20210706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603347	Casr<sup>Nuf</sup>/Casr<sup>Nuf</sup>  [background:] involves: 102/El * C3H/He	is_model_of	DOID:0090107	autosomal dominant hypocalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:15347804	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621470	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:2746	glycogen storage disease V						ECO:0000033	author statement supported by traceable reference	PMID:15328538	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278310	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-CHMP2B*)3Fbga/0  [background:] involves: C57BL/6	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:25401692	20190215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2182958	Gcdh<sup>tm1Dmk</sup>/Gcdh<sup>tm1Dmk</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0111254	glutaric acidemia I						ECO:0000033	author statement supported by traceable reference	PMID:11854167	20191122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6120521	Myo9a<sup>tm1.2Bah</sup>/Myo9a<sup>tm1.2Bah</sup>  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:14159	obstructive hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:19828736	20180309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197798	Gli2<sup>tm1(cre/ERT2)Tipe</sup>/Gli2<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:29999500	20180913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624988	Tg(Ckm-LPL)HRze/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:423	myopathy						ECO:0000033	author statement supported by traceable reference	PMID:7635990	20190806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3847290	Pds5a<sup>Gt(RRM243)Byg</sup>/Pds5a<sup>Gt(RRM243)Byg</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:11725	Cornelia de Lange syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19412548	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157072	None [background:] SAMP1/YitFcs	is_model_of	DOID:0060189	ileitis						ECO:0000033	author statement supported by traceable reference	PMID:12891551	20180518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759418	Cln3<sup>tm1Blda</sup>/Cln3<sup>tm1Blda</sup>  [background:] B6.129-Cln3<sup>tm1Blda</sup>	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:17855597	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509206	Tg(HBx)3Yu/0  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:10424292	20131002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841005	Ccr2<sup>tm1Mae</sup>/Ccr2<sup>tm1Mae</sup>  [background:] B6.129P2-Ccr2<sup>tm1Mae</sup>	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587028	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11239417	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3845014	Ptpn11<sup>tm6Bgn</sup>/Ptpn11<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:19179468	20090521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835361	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(NES-TVA)J12Ech/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:19805356	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7518590	Lmna<sup>em1Fenz</sup>/Lmna<sup>+</sup>  [background:] C57BL/6-Lmna<sup>em1Fenz</sup>	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:36583724	20230816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336692	Alx1<sup>em1Jian</sup>/Alx1<sup>em1Jian</sup>  [background:] C57BL/6N-Alx1<sup>em1Jian</sup>	is_model_of	DOID:0081047	frontonasal dysplasia 3						ECO:0000033	author statement supported by traceable reference	PMID:35127681	20220920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6431137	Rcbtb2<sup>tm1.1Xyw</sup>/Rcbtb2<sup>+</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:2570	malignant histiocytic disease						ECO:0000033	author statement supported by traceable reference	PMID:26291700	20200602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817230	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24735673	20190214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6151460	Golgb1<sup>em33Lanyu</sup>/Golgb1<sup>m1Lanyu</sup>  [background:] involves: A/J * FVB/NJ	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5751579	Nefl<sup>tm2.1Liem</sup>/Nefl<sup>+</sup>  [background:] B6.Cg-Nefl<sup>tm2.1Liem</sup>	is_model_of	DOID:0110165	Charcot-Marie-Tooth disease type 2E						ECO:0000033	author statement supported by traceable reference	PMID:25552649	20160310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448997	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup>  [background:] C.129S4-Fcgr2b<sup>tm1Ttk</sup>	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:17435165	20130312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295223	Dlg4<sup>tm2.1Grnt</sup>/Dlg4<sup>tm2.1Grnt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:20952458	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6477412	Cfap58<sup>em1Fzh</sup>/Cfap58<sup>em1Fzh</sup>  [background:] Not Specified	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:32791035	20201203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907286	Tg(Myh6-LMNA*E82K)35Lizh/0  [background:] involves: C57BL/6J	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:21151901	20170823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6438180	Dmd<sup>em4Eno</sup>/Y  [background:] C57BL/6-Dmd<sup>em4Eno</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:30854433	20200709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849882	Thrb<sup>tm6.1Few</sup>/Thrb<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19439650	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5142236	Tg(Pcp2-TBP*)69Hmhl/0  [background:] involves: FVB/N	is_model_of	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000033	author statement supported by traceable reference	PMID:21554323	20110906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818531	Coro1a<sup>ptcd</sup>/Coro1a<sup>ptcd</sup>  [background:] B6.CTS-Coro1a<sup>ptcd</sup>	is_model_of	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624521	Itgb1<sup>tm1Lscd</sup>/Itgb1<sup>tm1Ref</sup> Tg(PLAT-cre)116Sdu/0  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:16571628	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832643	Pomgnt1<sup>tm1Stk</sup>/Pomgnt1<sup>tm1Stk</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0050560	Walker-Warburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19114101	20090416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437999	Tg(Myl2-FGF19)1Dfre/?  [background:] involves: FVB	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:12057932	20121011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437999	Tg(Myl2-FGF19)1Dfre/?  [background:] involves: FVB	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22615798	20121011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7523309	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>em1Jmi</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>	is_model_of	DOID:870	neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196856	Gt(ROSA)26Sor<sup>tm1(OVAL/fla,GFP)Vnce</sup>/Gt(ROSA)26Sor<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:612	primary immunodeficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:29263322	20180906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175799	Cryaa<sup>tm1Wawr</sup>/Cryaa<sup>tm1Wawr</sup>  [background:] involves: 129/Sv * 129S4/SvJae	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:9023351	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821786	Pax6<sup>tm2Pgr</sup>/Pax6<sup>+</sup> Tg(Pax6-cre,GFP)1Pgr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB	is_model_of	DOID:1068	juvenile glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:20538882	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842843	Ush1c<sup>dfcr-3J</sup>/Ush1c<sup>dfcr-3J</sup>  [background:] STOCK Ush1c<sup>dfcr-3J</sup>/J	is_model_of	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	MGI:3842839	20090505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037642	Phex<sup>Hyp-Duk</sup>/Y  [background:] involves: BALB/cAnBomUrd	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811280	Pkd1<sup>tm3.1Jzh</sup>/Pkd1<sup>tm3.1Jzh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:18385665	20081020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507152	Tuba1a<sup>em2Rstot</sup>/Tuba1a<sup>em2Rstot</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:2490	congenital nervous system abnormality						ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6115249	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>/Y  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:0110415	retinitis pigmentosa 2						ECO:0000033	author statement supported by traceable reference	PMID:25422369	20180208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523996	Scn1a<sup>tm1Kea</sup>/Scn1a<sup>+</sup>  [background:] (C57BL/6J x 129S6/SvEvTac-Scn1a<sup>tm1Kea</sup>)F1	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24152123	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7316771	Sbf1<sup>em1Frobi</sup>/Sbf1<sup>em1Frobi</sup>  [background:] C57BL/6N-Sbf1<sup>em1Frobi</sup>	is_model_of	DOID:0110194	Charcot-Marie-Tooth disease type 4B3						ECO:0000033	author statement supported by traceable reference	PMID:34718573	20220729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590076	Nsdhl<sup>Str-1H</sup>/Nsdhl<sup>+</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:12305	Bloch-Sulzberger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11005611	20191224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614391	Arhgdia<sup>tm1Ytk</sup>/Arhgdia<sup>tm1Ytk</sup>  [background:] involves: 129S/SvEv * C57BL/6 * DBA	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10498891	20060302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896640	Ctsk<sup>tm1(cre)Ska</sup>/Ctsk<sup>+</sup> Plekhm1<sup>tm1.1Hzhao</sup>/Plekhm1<sup>tm1.1Hzhao</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:0110945	autosomal recessive osteopetrosis 6						ECO:0000033	author statement supported by traceable reference	PMID:27777970	20170712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2170703	None [background:] C3HeB/FeJ	is_model_of	DOID:2957	pulmonary tuberculosis						ECO:0000033	author statement supported by traceable reference	PMID:9949805	20180618	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836556	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup> Tg(MUC1)79.24Gend/0  [background:] B6.Cg-Kras<sup>tm4Tyj</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup> Tg(MUC1)79.24Gend	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26996122	20161007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6726370	Abcg2<sup>em1Omw</sup>/Abcg2<sup>em1Omw</sup>  [background:] C57BL/6J-Abcg2<sup>em1Omw</sup>	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:32488095	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5561310	Trappc10<sup>b2b2416Clo</sup>/Trappc10<sup>b2b2416Clo</sup>  [background:] Trappc10<sup>b2b2416Clo</sup>	is_model_of	DOID:0060341	agnathia-otocephaly complex						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811791	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6NCrl	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:18568033	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437766	Tg(Pkd1)26Mtru/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:20053665	20100323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5819194	Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>/Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	is_model_of	DOID:0050569	Seckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26158450	20170127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683230	Stat3<sup>tm1Flv</sup>/Stat3<sup>tm1Flv</sup> Tg(Tek-cre)1Xyfu/0  [background:] involves: C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:14623907	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4454427	Large1<sup>myd-3J</sup>/Large1<sup>myd-3J</sup>  [background:] STOCK Large1<sup>myd-3J</sup>/GrsrJ	is_model_of	DOID:0110637	muscular dystrophy-dystroglycanopathy type B6						ECO:0000033	author statement supported by traceable reference	MGI:4454310	20100609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659959	Wdr72<sup>tm1a(KOMP)Wtsi</sup>/Wdr72<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0110061	amelogenesis imperfecta hypomaturation type 2A3						ECO:0000033	author statement supported by traceable reference	PMID:25008349	20150826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819158	Immp2l<sup>Tg(HLA-A/H2-D)2Enge</sup>/0 Tg(Mt1-RET)304Ina/0  [background:] involves: BALB/c * C57BL/6 * CBA/Ca	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:18097012	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589925	Foxp3<sup>sf</sup>/Y  [background:] either: 129Rl.Cg-Foxp3<sup>sf</sup> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)	is_model_of	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11137992	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637429	Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:19734452	20150527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664093	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>tm2Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402523	Cmas<sup>tm1.1Bwei</sup>/Cmas<sup>tm1.1Bwei</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:31040189	20200402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6095197	Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup> Ptpn11<sup>tm6Bgn</sup>/Ptpn11<sup>+</sup>  [background:] B6.129S-Ptpn11<sup>tm6Bgn</sup> Emx1<sup>tm1(cre)Krj</sup>	is_model_of	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:28346493	20171206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5750217	Cntnap2<sup>tm2Pele</sup>/Cntnap2<sup>tm2Pele</sup>  [background:] B6.129(Cg)-Cntnap2<sup>tm2Pele</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26647347	20220526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6363217	Mrap<sup>tm1.2Geno</sup>/Mrap<sup>tm1.2Geno</sup>  [background:] involves: C57BL/6	is_model_of	DOID:9553	adrenal gland disease						ECO:0000033	author statement supported by traceable reference	PMID:29879378	20191010	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6316681	Nphs2<sup>tm2.1Antc</sup>/Nphs2<sup>tm3.1Antc</sup> Tg(CAG-cre/Esr1*)86Lbgn/0  [background:] involves: 129S2/SvPas * C57BL/6 * DBA	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29049388	20190709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569735	Tg(GFAP-SRC)1Aag/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:9160879	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711279	Gucy2e<sup>tm1Gar</sup>/Gucy2e<sup>tm1Gar</sup> Gucy2f<sup>tm1Wbae</sup>/Gucy2f<sup>tm1Wbae</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110078	Leber congenital amaurosis 1						ECO:0000033	author statement supported by traceable reference	PMID:17255100	20101110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689378	Cftr<sup>tm1Kth</sup>/Cftr<sup>tm1Kth</sup>  [background:] B6.129S7-Cftr<sup>tm1Kth</sup>	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:15246977	20061130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192530	None [background:] CC011/Unc	is_model_of	DOID:0060180	colitis						ECO:0000033	author statement supported by traceable reference	PMID:24487921	20180802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192451	Cftr<sup>em3Cwr</sup>/Cftr<sup>em3Cwr</sup>  [background:] C57BL/6J-Cftr<sup>em3Cwr</sup>/Cwr	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:29924856	20180801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665559	Ttpa<sup>tm1Hsz</sup>/Ttpa<sup>tm1Hsz</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0090028	familial isolated deficiency of vitamin E						ECO:0000033	author statement supported by traceable reference	PMID:11076932	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579980	Frem2<sup>my-Ucl</sup>/Frem2<sup>my-Ucl</sup>  [background:] involves: NMRI	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15838507	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5607258	Slc40a1<sup>tm1.1Mmfe</sup>/Slc40a1<sup>tm1.1Mmfe</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111028	hemochromatosis type 4						ECO:0000033	author statement supported by traceable reference	PMID:25100063	20141216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613373	Tor1a<sup>tm1Yql</sup>/Tor1a<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:16242683	20060222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815037	Ly6a<sup>tm1Pmf</sup>/Ly6a<sup>tm1Pmf</sup>  [background:] C.129P2-Ly6a<sup>tm1Pmf</sup>	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:12732718	20081114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5557980	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup> Nrl<sup>tm1Asw</sup>/Nrl<sup>tm1Asw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BXD24/TyJ * C57BL/6	is_model_of	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:21245082	20140410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654216	Maf<sup>Ofl</sup>/Maf<sup>+</sup>  [background:] either: 102/ElH or C3H/HeH	is_model_of	DOID:0110256	cataract 21 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:12620964	20091016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700375	Ikbkg<sup>tm1.1Mpa</sup>/Ikbkg<sup>tm1.1Mpa</sup> Tg(Alb1-cre)7Gsc/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:17292824	20150601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304399	Lim2<sup>Aca47</sup>/Lim2<sup>Aca47</sup>  [background:] C57BL/6J-Lim2<sup>Aca47</sup>	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:21617753	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6199144	Tg(BAC144D14)5D3Masu/0  [background:] B6.Cg-Tg(BAC144D14)5D3Masu	is_model_of	DOID:14681	Silver-Russell syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27798108	20180924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5606285	mt-Tk<sup>m1</sup>  [background:] involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:700	mitochondrial metabolism disease						ECO:0000033	author statement supported by traceable reference	PMID:24510903	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5306255	Bdnf<sup>tm3Jae</sup>/Bdnf<sup>tm3Jae</sup> Mecp2<sup>tm1.1Jae</sup>/Y Tg(Camk2a-cre)93Kln/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA/J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16446138	20120216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820807	Ret<sup>tm1Cos</sup>/Ret<sup>tm2(RET)Jmi</sup>  [background:] involves: 129S/Sv * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:18414682	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295127	Phf6<sup>em1Azbi</sup>/Y  [background:] B6.Cg-Phf6<sup>em1Azbi</sup>	is_model_of	DOID:0050681	Borjeson-Forssman-Lehmann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30403997	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175695	Alm/Alm<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7485960	Sbds<sup>em1(SBDS*)Dbau</sup>/Sbds<sup>em1(SBDS*)Dbau</sup>  [background:] C57BL/6J-Sbds<sup>em1(SBDS*)Dbau</sup>/Dbau	is_model_of	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000033	author statement supported by traceable reference	MGI:7485797	20230609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584136	Tg(TcraTcrbNY8.3)1Pesa/?  [background:] involves: C57BL/6 * NOD * SJL	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9362527	20050823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749228	Ryr1<sup>m1Nisw</sup>/Ryr1<sup>+</sup>  [background:] 129S1.B6-Ryr1<sup>m1Nisw</sup>	is_model_of	DOID:3529	congenital myopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:25564733	20160218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6390913	Col7a1<sup>em#Jtol</sup>/Col7a1<sup>em#Jtol</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/Ka * NOD	is_model_of	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:28892093	20200218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637428	Polg<sup>tm1Prol</sup>/Polg<sup>tm1Prol</sup>  [background:] B6J.129S7-Polg<sup>tm1Prol</sup>	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19734452	20150527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605005	Hydin<sup>hy3</sup>/Hydin<sup>hy3</sup>  [background:] involves: CBA	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:4784576	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655804	Mefv<sup>tm1Chae</sup>/Mefv<sup>tm1Chae</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	is_model_of	DOID:2987	familial mediterranean fever						ECO:0000033	author statement supported by traceable reference	PMID:12667444	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698561	Tuba1a<sup>Jna</sup>/Tuba1a<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:17218254	20070305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6279211	Krit1<sup>tm1Kwhi</sup>/Krit1<sup>tm1Kwhi</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl	is_model_of	DOID:0060669	cerebral cavernous malformation						ECO:0000033	author statement supported by traceable reference	PMID:27513872	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6279211	Krit1<sup>tm1Kwhi</sup>/Krit1<sup>tm1Kwhi</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl	is_model_of	DOID:0060669	cerebral cavernous malformation						ECO:0000033	author statement supported by traceable reference	PMID:27027284	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569826	Tg(AGER)#Eca/Tg(AGER)#Eca  [background:] C57BL/6J-Tg(AGER)#Eca	is_model_of	DOID:0050161	lower respiratory tract disease						ECO:0000033	author statement supported by traceable reference	PMID:23144333	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575650	Slc26a2<sup>tm1Aros</sup>/Slc26a2<sup>tm1Aros</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:14687	diastrophic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:15703192	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766076	Tg(Ela1-TAg)18Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1316086	20100816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037127	Scg5<sup>tm1Led</sup>/Scg5<sup>tm1Led</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * FVB) or (involves: 129S6/SvEvTac * C57BL/6)	is_model_of	DOID:3946	pituitary-dependent Cushing's disease						ECO:0000033	author statement supported by traceable reference	PMID:12021197	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763113	Tg(MMTV-LPAR3)#Gbm/Tg(MMTV-LPAR3)#Gbm  [background:] FVB/N-Tg(MMTV-LPAR3)#Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467323	Tg(Pcp2-ATXN2*127Q)#Plt/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0050955	spinocerebellar ataxia type 2						ECO:0000033	author statement supported by traceable reference	PMID:23087021	20130305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258418	Tg(KRT5-Terf2)POBlas/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050427	xeroderma pigmentosum						ECO:0000033	author statement supported by traceable reference	PMID:16142233	20181129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661079	Gdf5<sup>bp-J</sup>/Gdf5<sup>bp-J</sup> Gdf6<sup>tm1Kng</sup>/Gdf6<sup>tm1Kng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6J	is_model_of	DOID:0080052	acromesomelic dysplasia, Grebe type						ECO:0000033	author statement supported by traceable reference	PMID:12606286	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7493449	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: C57BL/6 * C57BL/6N * CBA	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28317875	20230627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287975	Atg5<sup>tm1Myok</sup>/Atg5<sup>tm1Myok</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7492422	Chd7<sup>tm2a(EUCOMM)Wtsi</sup>/Chd7<sup>+</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6N	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36232804	20230626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429557	Celsr2<sup>tm1Lex</sup>/Celsr2<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526103	Scnn1a<sup>tm1Rss</sup>/Scnn1a<sup>tm1Rss</sup> Tg(CMV-Scnn1a)1352Rss/0  [background:] involves: 129P2/OlaHsd * NMRI	is_model_of	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:9326675	20140103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3760091	Smad3<sup>tm1Cxd</sup>/Smad3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:11285272	20090225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784991	Lepr<sup>Db-Btlr</sup>/Lepr<sup>Db-Btlr</sup>  [background:] C57BL/6J-Lepr<sup>Db-Btlr</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:3778961	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606112	Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090031	D-bifunctional protein deficiency						ECO:0000033	author statement supported by traceable reference	PMID:10748062	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606112	Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090031	D-bifunctional protein deficiency						ECO:0000033	author statement supported by traceable reference	PMID:15769750	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662300	Adcy5<sup>tm1Yish</sup>/Adcy5<sup>tm1Yish</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:12665504	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818748	Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>tm1Brd</sup> Xrcc5<sup>tm1Dbr</sup>/Xrcc5<sup>tm1Dbr</sup>  [background:] involves: 129S7/SvEvBrd * C57BL	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16751807	20081209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4849989	Tg(KRT14-HPV16)wt1Dh/0  [background:] either: FVB.Cg-Tg(KRT14-HPV16)wt1Dh or (involves: C57BL/6 * DBA/2 * FVB/N)	is_model_of	DOID:3151	skin squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:8952526	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7495807	Mocos<sup>em2(IMPC)Ics</sup>/Mocos<sup>em2(IMPC)Ics</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0070453	xanthinuria type II						ECO:0000033	author statement supported by traceable reference	PMID:35372998	20230731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7286374	Specc1l<sup>em4Kumc</sup>/Specc1l<sup>+</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183668	Tg(NFH)120Jpj/0  [background:] Not Specified	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6888382	Tubb4a<sup>Jit</sup>/Tubb4a<sup>+</sup>  [background:] FVB.B6-Tubb4a<sup>Jit</sup>	is_model_of	DOID:0060798	hypomyelinating leukodystrophy 6						ECO:0000033	author statement supported by traceable reference	PMID:35171680	20220316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:1123	spondyloarthropathy						ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430345	Pcsk5<sup>b2b1549Clo</sup>/Pcsk5<sup>b2b1549Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b1549Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664861	B4galt1<sup>tm1Shur</sup>/B4galt1<sup>tm1Shur</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:28	endocrine system disease						ECO:0000033	author statement supported by traceable reference	PMID:9013935	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308721	Bgn<sup>tm1Mfy</sup>/Y Dcn<sup>tm1Ioz</sup>/Dcn<sup>tm1Ioz</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:0050802	Ehlers-Danlos syndrome spondylodysplastic type 2						ECO:0000033	author statement supported by traceable reference	PMID:12102052	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446326	Sbds<sup>tm2.1Jrom</sup>/Sbds<sup>tm3.1Jrom</sup> Ptf1a<sup>tm1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22510201	20121227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308722	Bgn<sup>tm1Mfy</sup>/Bgn<sup>tm1Mfy</sup> Dcn<sup>tm1Ioz</sup>/Dcn<sup>tm1Ioz</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:229	female reproductive system disease						ECO:0000033	author statement supported by traceable reference	PMID:21502335	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683647	Icos<sup>tm1Flv</sup>/Icos<sup>tm1Flv</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:12177	common variable immunodeficiency						ECO:0000033	author statement supported by traceable reference	PMID:11343121	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639603	Jund<sup>tm1Mya</sup>/Jund<sup>tm1Mya</sup> Tg(H2-K-Fosl1)1Wag/0  [background:] involves: 129S2/SvPas * C57BL/6 * CBA	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15655111	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5461561	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22652393	20130201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4887891	Tg(Plp)66Kan/Tg(Plp)66Kan  [background:] B6NCrl.Cg-Tg(Plp)66Kan	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:17133418	20110214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3026664	Vegfc<sup>tm1Ali</sup>/Vegfc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR	is_model_of	DOID:0050580	hereditary lymphedema						ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438262	Amelx<sup>Rgsc888</sup>/Amelx<sup>Rgsc888</sup>  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297594	Ccm2<sup>tm1.1Etl</sup>/Ccm2<sup>tm1Etl</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060670	cerebral cavernous malformation 2						ECO:0000033	author statement supported by traceable reference	PMID:21859843	20111208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476836	Pkd1<sup>tm1.1Pcha</sup>/Pkd1<sup>tm1.1Pcha</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23064367	20130502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941022	Tg(Col2a1*R789C)#Waho/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:11771668	20110315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624554	Mecp2<sup>tm1Hzo</sup>/Mecp2<sup>+</sup>  [background:] 129S7/SvEvBrd-Mecp2<sup>tm1Hzo</sup>	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12160743	20060616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694699	Pax2<sup>tm1Pgr</sup>/Pax2<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0090006	renal coloboma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15242798	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6783448	Scn2a<sup>em1Gsp</sup>/Scn2a<sup>+</sup>  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:34156984	20211029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181684	Crygs<sup>rncat</sup>/Crygs<sup>rncat</sup>  [background:] Kunming	is_model_of	DOID:0110240	cataract 20 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:12079281	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842800	Tg(RP23-65I14)2Jno/?  [background:] involves: FVB/N	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:19211869	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663447	Tg(Prnp-MAPT)43Vle/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:10595524	20120502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4849847	Myo3a<sup>tm1.1Mckg</sup>/Myo3a<sup>tm1.1Mckg</sup>  [background:] C57BL/6-Myo3a<sup>tm1.1Mckg</sup>	is_model_of	DOID:0110489	autosomal recessive nonsyndromic deafness 30						ECO:0000033	author statement supported by traceable reference	PMID:21165622	20101230	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441332	Tg(Igkv3-5*-MYC)24Plbe/0  [background:] C57BL/6J-Tg(Igkv3-5*-MYC)24Plbe/PlbeMmmh	is_model_of	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:18242516	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174785	Trp63<sup>tm1Fmc</sup>/Trp63<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:8534	gastroesophageal reflux disease						ECO:0000033	author statement supported by traceable reference	PMID:21703447	20111007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584463	Trp53<sup>tm2.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5510994	Tg(ACTB-Eif4e)#Ppp/?  [background:] B6.Cg-Tg(ACTB-Eif4e)#Ppp	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23263185	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800410	Tg(PDGFB-LRRK2*R1441C)31Hlw/0  [background:] FVB/N-Tg(PDGFB-LRRK2*R1441C)31Hlw	is_model_of	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:26363496	20161012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442586	Pax2<sup>1Neu</sup>/Pax2<sup>+</sup>  [background:] involves: 102 * CD-1	is_model_of	DOID:0090006	renal coloboma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17881463	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795669	Pkd1<sup>tm2Som</sup>/Pkd1<sup>tm2.1Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: C57BL/6 * ICR * SJL	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:18263604	20120718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7506311	G6pc1<sup>em1Jyc</sup>/G6pc1<sup>em1Jyc</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:33359667	20230711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276573	Tg(Mpz*S63C)33Mes/0  [background:] involves: FVB/N	is_model_of	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798606	Dmd<sup>mdx-3Cv</sup>/Y  [background:] involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:7843915	20090929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644816	Dkc1<sup>tm1.1Pjma</sup>/Y  [background:] B6.129X1(FVB)-Dkc1<sup>tm1.1Pjma</sup>	is_model_of	DOID:2729	dyskeratosis congenita						ECO:0000033	author statement supported by traceable reference	PMID:21241452	20150723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769776	Tg(Igh-Lmp2a)13FRdni/0  [background:] involves: C57BL/6 * CD-1 * SJL	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10430930	20080205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1	is_model_of	DOID:0090140	cortisone reductase deficiency 2						ECO:0000033	author statement supported by traceable reference	MGI:85353	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1	is_model_of	DOID:0090140	cortisone reductase deficiency 2						ECO:0000033	author statement supported by traceable reference	PMID:11546766	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1	is_model_of	DOID:0090140	cortisone reductase deficiency 2						ECO:0000033	author statement supported by traceable reference	PMID:9405715	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4882033	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Tyr-cre)1Lru/0  [background:] B6.Cg-Pten<sup>tm1Hwu</sup> Tg(Tyr-cre)1Lru	is_model_of	DOID:0080072	intestinal pseudo-obstruction						ECO:0000033	author statement supported by traceable reference	PMID:19884655	20200621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559052	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23906982	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559052	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:19956606	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559052	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:17676052	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6505558	Apc<sup>tm2Rak</sup>/Apc<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:30952657	20210209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3790760	Tg(H2-Ea-G6pc2)69Tkay/?  [background:] NOD-Tg(H2-Ea-G6pc2)69Tkay	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:17143333	20080609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797747	Xlch/Xlch<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110461	X-linked dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18424640	20080718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6194625	Tg(GFAP-ATXN7*92Q)2542Als/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837856	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Col1a1<sup>tm2(CAG-EGFR*)Char</sup>/Col1a1<sup>tm2(CAG-EGFR*)Char</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:19196966	20130322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6883630	Atf6<sup>tm1.1Rjk</sup>/Atf6<sup>tm1.1Rjk</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0110009	achromatopsia 7						ECO:0000033	author statement supported by traceable reference	PMID:26029869	20220225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188075	None [background:] FGS/Kist	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15965785	20180711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275192	Cngb3<sup>cpfl10</sup>/Cngb3<sup>cpfl10</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0110008	achromatopsia 3						ECO:0000033	author statement supported by traceable reference	PMID:30592498	20190130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619915	Nr4a2<sup>tm1Omc</sup>/Nr4a2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:15589522	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039274	Lrat<sup>tm1Kpal</sup>/Lrat<sup>tm1Kpal</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110188	Leber congenital amaurosis 14						ECO:0000033	author statement supported by traceable reference	PMID:18296659	20130814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5584182	Del(XArmcx5-Nxf3)3Jw/+  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:0060388	chromosomal deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24569167	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033364	Slc19a2<sup>tm1Gelb</sup>/Slc19a2<sup>tm1Gelb</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12393806	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175741	Pax6<sup>132-14Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412051	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz/0 Tg(Thy1-MAPT)183Gotz/0  [background:] B6.Cg-Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz Tg(Thy1-MAPT)183Gotz	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:19781645	20101130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6491217	Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>/Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] B6(FVB)-Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>	is_model_of	DOID:0080768	pyridoxine-dependent epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:32969477	20210111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582197	Col1a1<sup>tm3(CAG-IDH2*R140Q)Kkw</sup>/Col1a1<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N	is_model_of	DOID:0050575	D-2-hydroxyglutaric aciduria						ECO:0000033	author statement supported by traceable reference	PMID:24589777	20140911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433487	b2b1163Clo/b2b1163Clo  [background:] C57BL/6J-b2b1163Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300564	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (BALB/cByJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440827	Lamc2<sup>jeb</sup>/Lamc2<sup>jeb</sup>  [background:] 129X1/SvJ-Lamc2<sup>jeb</sup>	is_model_of	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:20336083	20100420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639713	Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16354928	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838320	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Fcr</sup> Tg(GFAP-cre)#Gtm/0  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:20600672	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588865	Relb<sup>tm1Brv</sup>/Relb<sup>tm1Brv</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: C57BL/6) or (involves: 129S2/SvPas * C57BL/6)	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:10940923	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3691279	Myh6<sup>tm1Ces</sup>/Myh6<sup>+</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618123	Dicer1<sup>tm1Snj</sup>/Dicer1<sup>tm1Snj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT5-cre/PGR)1Der/0  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6N * FVB/N * ICR	is_model_of	DOID:1749	squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24979267	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766122	Timo/Timo  [background:] either: B6.Cg-Timo or (involves: C57BL/6J * CBA/CaJ)	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:17652166	20080103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590141	Gck<sup>Rgsc552</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5588576	None [background:] NOD/ShiLtJ	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36674547	20230202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5588576	None [background:] NOD/ShiLtJ	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31479110	20230202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697288	Grhl3<sup>tm1Bogi</sup>/Grhl3<sup>tm1Bogi</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060239	Van der Woude syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24360809	20151125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6472965	Grhpr<sup>Gt(OST383093)Lex</sup>/Grhpr<sup>Gt(OST383093)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:0111671	primary hyperoxaluria type 2						ECO:0000033	author statement supported by traceable reference	PMID:31821850	20201118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7378415	Acad9<sup>tm1c(KOMP)Wtsi</sup>/Acad9<sup>tm1c(KOMP)Wtsi</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0112072	nuclear type mitochondrial complex I deficiency 20						ECO:0000033	author statement supported by traceable reference	PMID:34556413	20221102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623591	Tg(Igh-6/Igh-V281)3Jwt/0  [background:] NOD.B6-Tg(Igh-6/Igh-V281)3Jwt	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11698422	20060601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7529045	Cfap57<sup>em1Qsh</sup>/Cfap57<sup>em1Qsh</sup>  [background:] C57BL/6-Cfap57<sup>em1Qsh</sup>	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:36752199	20230920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789375	Alk<sup>tm1.1Ics</sup>/? Tg(Th-MYCN)41Waw/0  [background:] involves: 129S2/SvPas * 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29321660	20180904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789375	Alk<sup>tm1.1Ics</sup>/? Tg(Th-MYCN)41Waw/0  [background:] involves: 129S2/SvPas * 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24811913	20180904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425671	Alpl<sup>Mhdabap26</sup>/Alpl<sup>Mhdabap26</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap26</sup>	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435288	Galnt3<sup>tcal</sup>/Galnt3<sup>tcal</sup>  [background:] involves: C3H * C57BL/6J	is_model_of	DOID:0111063	hyperphosphatemic familial tumoral calcinosis						ECO:0000033	author statement supported by traceable reference	PMID:22912827	20121114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6438117	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>	is_model_of	DOID:0080354	Phelan-McDermid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911326	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793728	Atp7a<sup>Mo-blo</sup>/Y  [background:] Not Specified	is_model_of	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:1115218	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793728	Atp7a<sup>Mo-blo</sup>/Y  [background:] Not Specified	is_model_of	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:3385878	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491044	Tg(Prnp*P101L)2862Sbp/0  [background:] involves: FVB/N	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7495585	Ighmbp2<sup>em1Cx</sup>/Ighmbp2<sup>em1Cx</sup>  [background:] C57BL/6J-Ighmbp2<sup>em1Cx</sup>/Cx	is_model_of	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S						ECO:0000033	author statement supported by traceable reference	PMID:36413117	20230706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6281646	Fan1<sup>tm1a(KOMP)Wtsi</sup>/Fan1<sup>tm1a(KOMP)Wtsi</sup>  [background:] 129S1.B6-Fan1<sup>tm1a(KOMP)Wtsi</sup>	is_model_of	DOID:0060911	karyomegalic interstitial nephritis						ECO:0000033	author statement supported by traceable reference	PMID:27026368	20190307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5547758	Tg(Utg-TAg)7736Fjd/?  [background:] involves: FVB	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:9040936	20140304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619994	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:1929	supravalvular aortic stenosis						ECO:0000033	author statement supported by traceable reference	PMID:9819363	20060418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175706	Atm<sup>tm1Bal</sup>/Atm<sup>tm1Bal</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:8843193	20071017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175706	Atm<sup>tm1Bal</sup>/Atm<sup>tm1Bal</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:9356511	20071017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906294	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup> Pcdha9<sup>b2b635.1Clo</sup>	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507848	Dmd<sup>mdx</sup>/Y Tg(DMD*)#Spc/0  [background:] involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28505980	20210225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641752	Ltbp4<sup>Gt(E301B04)Wrst</sup>/Ltbp4<sup>Gt(E301B04)Wrst</sup>  [background:] B6N.129P2-Ltbp4<sup>Gt(E301B04)Wrst</sup>	is_model_of	DOID:3144	cutis laxa						ECO:0000033	author statement supported by traceable reference	PMID:25713297	20150625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763310	Tg(Fabp4-Phb*Y114F)#Smis/0  [background:] Not Specified	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:26751773	20160427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181627	Klf1<sup>tm1Sho</sup>/Klf1<sup>tm1Sho</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:7753195	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6095619	Kif20b<sup>magoo</sup>/Kif20b<sup>magoo</sup>  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:28359322	20171207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842959	Tg(KRT5-tTA)1216Glk/0 Tg(tetO-Tek)1Dmt/0  [background:] involves: CD-1 * FVB/N	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:19342373	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7564569	Tnfaip2<sup>tm1.1Ohno</sup>/Tnfaip2<sup>tm1.1Ohno</sup>  [background:] C.Cg-Tnfaip2<sup>tm1.1Ohno</sup>	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:33722931	20231211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846455	Dp(16Cbr1-Fam3b)1Rhr/0  [background:] involves: 129S6/SvEvTac * C3H/HeSnJ * C57BL/6Ei	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19420260	20090603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473224	Cfap276<sup>em2.1Fuxi</sup>/Cfap276<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050543	Charcot-Marie-Tooth disease intermediate type						ECO:0000033	author statement supported by traceable reference	PMID:32592472	20201119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909332	Tg(Myh6-Tnni3*R146G)121Rbns/0  [background:] Not Specified	is_model_of	DOID:0110313	hypertrophic cardiomyopathy 7						ECO:0000033	author statement supported by traceable reference	PMID:11055985	20170918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316002	Ezh2<sup>tm2Sho</sup>/Ezh2<sup>tm2Sho</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22431509	20120422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943177	Gt(ROSA)26Sor<sup>tm1(HBEGF)Awai</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Gh1-cre)bKnmn/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:0060870	isolated growth hormone deficiency						ECO:0000033	author statement supported by traceable reference	PMID:21283519	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829782	Tg(Prnp-MAPT*K274Q*K281Q)286Lgn/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27041503	20170329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140739	Ts(16C-tel)1Cje/0  [background:] involves: C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28069794	20180201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140739	Ts(16C-tel)1Cje/0  [background:] involves: C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19041304	20180201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421410	Snca<sup>tm1Nbm</sup>/Snca<sup>tm1Nbm</sup> Tg(SNCA*A30P)1Nbm/Tg(SNCA*A30P)1Nbm Tg(SNCA*A30P)2Nbm/Tg(SNCA*A30P)2Nbm  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:20106867	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6430623	Sh3rf2<sup>tm1Zhxu</sup>/Sh3rf2<sup>+</sup>  [background:] C57BL/6-Sh3rf2<sup>tm1Zhxu</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30540932	20200529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512998	Cd320<sup>Gt(CC0426)Wtsi</sup>/Cd320<sup>Gt(CC0426)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060741	methylmalonic acidemia due to transcobalamin receptor defect						ECO:0000033	author statement supported by traceable reference	PMID:23430977	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437110	b2b1291Clo/b2b1291Clo  [background:] C57BL/6J-b2b1291Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2667203	Fras1<sup>tm1Chpk</sup>/Fras1<sup>tm1Chpk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12766770	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296806	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Esr1)#Paf/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:15705859	20111129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308655	Samd9l<sup>tm1Homy</sup>/Samd9l<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24029230	20140701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367083	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Tg(APOC3)3707Bres/?  [background:] involves: 129S7/SvEvBrd * C57BL/6J * CBA/J	is_model_of	DOID:13809	familial combined hyperlipidemia						ECO:0000033	author statement supported by traceable reference	PMID:8994037	20091113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5553465	Tg(Prnp-APPSweArc)#Rmni/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:23840405	20140331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705321	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22350410	20160126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442379	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup> Tg(PRNP-APPSweInd)8Dwst/0  [background:] involves: BALB/c * C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22869680	20121120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910772	Tnnt2<sup>tm2.1Feah</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:27936050	20171002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400352	Dnase1<sup>tm2092.1Arte</sup>/Dnase1<sup>tm2092.1Arte</sup>  [background:] involves: C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:30758851	20200317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429854	b2b1528Clo/b2b1528Clo  [background:] C57BL/6J-b2b1528Clo	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5797380	Arsk<sup>tm1b(KOMP)Wtsi</sup>/Arsk<sup>tm1b(KOMP)Wtsi</sup>  [background:] B6N(Cg)-Arsk<sup>tm1b(KOMP)Wtsi</sup>/J	is_model_of	DOID:12798	mucopolysaccharidosis						ECO:0000033	author statement supported by traceable reference	PMID:32856704	20210405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6514899	Nexn<sup>tm1Chen</sup>/Nexn<sup>tm1Chen</sup> Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: MF1	is_model_of	DOID:0110424	dilated cardiomyopathy 1CC						ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6754175	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7491942	Nipbl<sup>Gt(RRS564)Byg</sup>/Nipbl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * CD-1	is_model_of	DOID:0080505	Cornelia de Lange syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:32800293	20230622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7309156	Zng1<sup>em2Skan</sup>/Zng1<sup>em2Skan</sup>  [background:] C57BL/6N-Zng1<sup>em2Skan</sup>	is_model_of	DOID:0080205	CAKUT						ECO:0000033	author statement supported by traceable reference	PMID:31862704	20220705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6231210	Tg(H2-K-Hmga1)#Lmsr/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15150086	20220608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432228	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5302204	Crbn<sup>tm1.2Jjh</sup>/Crbn<sup>tm1.2Jjh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000033	author statement supported by traceable reference	PMID:29459374	20190703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611210	App<sup>tm1.1Cep</sup>/App<sup>tm1.1Cep</sup> Psen1<sup>tm1Dgf</sup>/Psen1<sup>tm1Dgf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11959395	20060125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852759	Smpx<sup>em1Jgao</sup>/Smpx<sup>em1Jgao</sup>  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>	is_model_of	DOID:0111735	X-linked deafness 4						ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176568	Egfr<sup>wa2</sup>/Egfr<sup>wa2</sup>  [background:] STOCK Egfr<sup>wa2</sup>	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:10700187	20170724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689380	Cftr<sup>tm2Mrc</sup>/Cftr<sup>tm2Mrc</sup>  [background:] B6.129S6-Cftr<sup>tm2Mrc</sup>	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:15246977	20061130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818484	Tyrobp<sup>tm1.1Viv</sup>/Tyrobp<sup>tm1.1Viv</sup>  [background:] B6.129P2-Tyrobp<sup>tm1.1Viv</sup>	is_model_of	DOID:0090112	Nasu-Hakola disease						ECO:0000033	author statement supported by traceable reference	PMID:15632019	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461165	Tnfrsf1a<sup>tm1Rsie</sup>/Tnfrsf1a<sup>+</sup>  [background:] B6.Cg-Tnfrsf1a<sup>tm1Rsie</sup>	is_model_of	DOID:0090018	autosomal dominant familial periodic fever						ECO:0000033	author statement supported by traceable reference	PMID:20457915	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818740	Tg(Ins-Igf2)1Fbos/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110741	type 1 diabetes mellitus 2						ECO:0000033	author statement supported by traceable reference	PMID:10727441	20081208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176927	Crygc<sup>Chl3</sup>/Crygc<sup>Chl3</sup>  [background:] involves: 102/El * C3H/El	is_model_of	DOID:0110235	cataract 2 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11773036	20050923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007486	Acp3<sup>tm1Pivi</sup>/Acp3<sup>tm1Pivi</sup>  [background:] B6.Cg-Acp3<sup>tm1Pivi</sup>	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:24039861	20140424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140886	Cdh23<sup>Jera</sup>/Cdh23<sup>Jera</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110467	autosomal recessive nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175074	Irf8<sup>tm1Hor</sup>/Irf8<sup>tm1Hor</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	is_model_of	DOID:0060761	familial chronic myelocytic leukemia-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8861914	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028851	Tg(aP2-SREBF1c)9884Reh/0  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:9784493	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367101	Apobec1<sup>tm1Ddsn</sup>/Apobec1<sup>tm1Ddsn</sup> Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:9701246	20120221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029251	Tcof1<sup>tm1Mjd</sup>/Tcof1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:2908	Treacher Collins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10888597	20050913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450846	Tyrobp<sup>tm1Ttk</sup>/Tyrobp<sup>tm1Ttk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090112	Nasu-Hakola disease						ECO:0000033	author statement supported by traceable reference	PMID:12569157	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675319	Nbn<sup>tm1Xu</sup>/Nbn<sup>tm1Xu</sup>  [background:] Not Specified	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11889050	20060213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941746	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	is_model_of	DOID:2999	granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:18687666	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902457	Mapk1<sup>tm1Gela</sup>/Mapk1<sup>tm1Gela</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA/J	is_model_of	DOID:4258	Weissenbacher-Zweymuller syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26395480	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177312	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] STOCK Grhl3<sup>ct</sup>/J	is_model_of	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000033	author statement supported by traceable reference	MGI:48774	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831377	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] 129S6.129P2-Fgfr3<sup>tm1.1Aomw</sup>	is_model_of	DOID:0060703	Muenke Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196487	Tg(TTR-V30M)15Imeg/0  [background:] involves: C57BL/6	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:29330472	20180905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272036	Tnf<sup>Bpsm1</sup>/Tnf<sup>Bpsm1</sup>  [background:] involves: C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906382	rd21/rd21  [background:] Not Specified	is_model_of	DOID:8466	retinal degeneration						ECO:0000033	author statement supported by traceable reference	MGI:5906378	20170809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839558	Tg(FCGR2A)11Mkz/Tg(FCGR2A)11Mkz  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:16200626	20090410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906061	Tg(Myh7-Phc1)#Yota/0  [background:] involves: C57BL/6	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11950896	20170802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316720	Tg(ACTA1*D286G/EGFP)#Kjno/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:22174871	20120427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664551	Ncoa1<sup>tm1.1Hkaw</sup>/Ncoa1<sup>tm1.1Hkaw</sup>  [background:] B6.Cg-Ncoa1<sup>tm1.1Hkaw</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15312245	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6887846	Anapc7<sup>tm1.1Azbi</sup>/Anapc7<sup>tm1.1Azbi</sup>  [background:] B6.129S6(CBA)-Anapc7<sup>tm1.1Azbi</sup>	is_model_of	DOID:0050888	syndromic intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:34942119	20220310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0111013	cone-rod dystrophy 3						ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5587035	Ttc21b<sup>tm2c(KOMP)Wtsi</sup>/Ttc21b<sup>aln</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6N	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:24700869	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5470095	Psmc4<sup>tm1.1Ryot</sup>/Psmc4<sup>tm1.2Ryot</sup> Tg(SLC18A3-cre)KMisa/0  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:332	amyotrophic lateral sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23095749	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829790	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:24802098	20150331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815302	Tg(Th-SNCA)5Eric/Tg(Th-SNCA)5Eric  [background:] involves: C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:17537546	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6468250	Nexmif<sup>tm1(KOMP)Wtsi</sup>/Y  [background:] B6J.B6N-Nexmif<sup>tm1(KOMP)Wtsi</sup>	is_model_of	DOID:0112044	non-syndromic X-linked intellectual disability 98						ECO:0000033	author statement supported by traceable reference	PMID:31704787	20201022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6093713	Lifr<sup>tm1Imx</sup>/Lifr<sup>tm1Imx</sup>  [background:] B6;129S7-Lifr<sup>tm1Imx</sup>/J	is_model_of	DOID:0080205	CAKUT						ECO:0000033	author statement supported by traceable reference	PMID:28334964	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052308	Tg(HD82Gln)81Gschi/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21406230	20110805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696613	Atp7a<sup>Mo-dp</sup>/Atp7a<sup>+</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:25456742	20151118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583560	Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587029	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>tm1Bem</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636659	Apc<sup>Min</sup>/Apc<sup>+</sup> Msh2<sup>tm1Mak</sup>/Msh2<sup>tm1Mak</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:8674041	20150521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636659	Apc<sup>Min</sup>/Apc<sup>+</sup> Msh2<sup>tm1Mak</sup>/Msh2<sup>tm1Mak</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:23741483	20150521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513373	Plec<sup>tm2Gwi</sup>/Plec<sup>tm2Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9389647	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789376	Alk<sup>tm2.1Ics</sup>/? Tg(Th-MYCN)41Waw/0  [background:] involves: 129S2/SvPas * 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29321660	20180904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789376	Alk<sup>tm2.1Ics</sup>/? Tg(Th-MYCN)41Waw/0  [background:] involves: 129S2/SvPas * 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24811913	20180904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654500	Slc6a3<sup>tm1Mca</sup>/Slc6a3<sup>tm1Mca</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:9888856	20140116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6443692	Fras1<sup>rdf</sup>/Fras1<sup>rdf</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26813283	20221116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287871	Gprasp2<sup>tm1.1Jpe</sup>/Y  [background:] B6.129(FVB)-Gprasp2<sup>tm1.1Jpe</sup>	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:30926797	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844065	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:19340311	20090514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763734	Tg(Tyrp1-TAg)3434Bee/?  [background:] involves: BALB/c * C57BL/6J	is_model_of	DOID:4645	retinal cancer						ECO:0000033	author statement supported by traceable reference	PMID:11896616	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700822	Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup> Wrn<sup>tm1Lgu</sup>/Wrn<sup>tm1Lgu</sup>  [background:] involves: 129/Sv * BALB/c * C57BL/6 * SLJ	is_model_of	DOID:5688	Werner syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15235603	20070324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839946	En1<sup>tm1Gld</sup>/En1<sup>+</sup> En2<sup>tm1Alj</sup>/En2<sup>tm1Alj</sup>  [background:] involves: 129S/SvEv * 129S2/SvPas * C57BL/6 * Swiss Webster	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:17015829	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176960	Gck<sup>tm1Efr</sup>/Gck<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:7665557	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6105933	Mlc1<sup>tm1.1Vdk</sup>/Mlc1<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1						ECO:0000033	author statement supported by traceable reference	PMID:28695146	20190412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6105933	Mlc1<sup>tm1.1Vdk</sup>/Mlc1<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1						ECO:0000033	author statement supported by traceable reference	PMID:25382142	20190412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7261162	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:12270	coloboma						ECO:0000033	author statement supported by traceable reference	PMID:33075808	20220412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471480	Muc2<sup>eey</sup>/Muc2<sup>eey</sup>  [background:] C57BL/6-Muc2<sup>eey</sup>	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18318598	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5817744	Prkcq<sup>rpea1</sup>/Prkcq<sup>rpea1</sup>  [background:] B6.ABJ-Prkcq<sup>rpea1</sup>/BocJ	is_model_of	DOID:5327	retinal detachment						ECO:0000033	author statement supported by traceable reference	PMID:26978024	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509651	Krt13<sup>em1Hcha</sup>/Krt13<sup>em1Hcha</sup>  [background:] C57BL/6-Krt13<sup>em1Hcha</sup>	is_model_of	DOID:0050448	white sponge nevus						ECO:0000033	author statement supported by traceable reference	PMID:32758484	20210311	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491048	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp*P101L)2866Sbp/0  [background:] involves: 129S7/SvEvBrd * FVB/N	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177543	Cftr<sup>tm3Hgu</sup>/Cftr<sup>tm3Hgu</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:8605891	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046798	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5807347	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26670829	20161116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581451	Alg10b<sup>nse5</sup>/Alg10b<sup>nse5</sup>  [background:] 129S6.B6-Alg10b<sup>nse5</sup>	is_model_of	DOID:0050563	nonsyndromic deafness						ECO:0000033	author statement supported by traceable reference	PMID:24303013	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432115	Ryr2<sup>tm1.1Clhh</sup>/Ryr2<sup>tm1.1Clhh</sup>  [background:] 129S/SvEv-Ryr2<sup>tm1.1Clhh</sup>	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:18419777	20120823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304759	Col1a1<sup>tm2(tetO-RNAi:Rps19)Karl</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:21989989	20120202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425673	Alpl<sup>Mhdabap32</sup>/Alpl<sup>Mhdabap32</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap32</sup>	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774931	Atxn1<sup>tm1Hzo</sup>/Atxn1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:12086639	20080325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684391	Scgb1a1<sup>tm1Abm</sup>/Scgb1a1<sup>tm1Abm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:10470078	20190611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906020	Tg(Myh6-Tpm1*E54K)67Dfw/0  [background:] involves: FVB/N	is_model_of	DOID:0110457	dilated cardiomyopathy 1Y						ECO:0000033	author statement supported by traceable reference	PMID:17556658	20170801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473560	Eml1<sup>tm1.2Ics</sup>/Eml1<sup>tm1.2Ics</sup>  [background:] C57BL/6N-Eml1<sup>tm1.2Ics</sup>	is_model_of	DOID:0111169	subcortical band heterotopia						ECO:0000033	author statement supported by traceable reference	PMID:31173351	20201123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686996	Mitf<sup>Mi-H</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6401409	Asah1<sup>tm1.2Geno</sup>/Asah1<sup>tm1.2Geno</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050464	Farber lipogranulomatosis						ECO:0000033	author statement supported by traceable reference	PMID:29908121	20200325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583142	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583142	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8700894	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5615097	Trappc10<sup>b2b2613Clo</sup>/Trappc10<sup>b2b2613Clo</sup>  [background:] C57BL/6J-Trappc10<sup>b2b2613Clo</sup>	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175810	Cryge<sup>Aey1</sup>/Cryge<sup>+</sup>  [background:] C3HeB/FeJ-Cryge<sup>Aey1</sup>	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:10932192	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851211	Tg(Scn1a*)RH9Aesc/0  [background:] involves: FVB/NJ	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:19409490	20090724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418690	G6pc1<sup>tm2.2Jyc</sup>/G6pc1<sup>tm2.2Jyc</sup>  [background:] involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N	is_model_of	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:19548314	20100126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6718876	Nemf<sup>tvrm116</sup>/Nemf<sup>tvrm116</sup>  [background:] C57BL/6J-Nemf<sup>tvrm116</sup>/PjnCx	is_model_of	DOID:870	neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6836754	Aptx<sup>tm1Pmc</sup>/Aptx<sup>tm1Pmc</sup> Atm<sup>tm2.1Mfgc</sup>/Atm<sup>tm2.1Mfgc</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:34723800	20211221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6729288	Del(16Pi4ka-Hira)1Atai/+  [background:] C57BL/6N-Del(16Pi4ka-Hira)1Atai	is_model_of	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000033	author statement supported by traceable reference	PMID:32066675	20210806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902990	Adamtsl4<sup>tvrm267</sup>/Adamtsl4<sup>tvrm267</sup>  [background:] C57BL/6J-Adamtsl4<sup>tvrm267</sup>/Pjn	is_model_of	DOID:110	lens disease						ECO:0000033	author statement supported by traceable reference	PMID:26405179	20170620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286080	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] (CAST/EiJ x B6.129S2-Trp53<sup>tm1Tyj</sup> Nf1<sup>tm1Tyj</sup>/+ +)F1	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:10973261	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525209	Aipl1<sup>tm1Mad</sup>/Aipl1<sup>tm1Mad</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110332	Leber congenital amaurosis 4						ECO:0000033	author statement supported by traceable reference	PMID:15582159	20050531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907992	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6CrSlc * FVB	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:16959785	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507205	Phf6<sup>tm1.2Avo</sup>/Y  [background:] involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N	is_model_of	DOID:0050681	Borjeson-Forssman-Lehmann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32994169	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176483	Fgfr2<sup>tm2.3Dsn</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:14705	Pfeiffer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11274405	20080121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806507	Tg(SFTPC-SDC4/ROS1)141Tno/0  [background:] C57BL/6J-Tg(SFTPC-SDC4/ROS1)141Tno	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26964870	20161108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665401	Fmr1<sup>tm1Cgr</sup>/Fmr1<sup>tm1Cgr</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16055059	20070119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909891	Mybpc3<sup>tm2.1Lcrr</sup>/Mybpc3<sup>+</sup>  [background:] involves: 129S2/SvPasCrl * Black Swiss	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:22465693	20170919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814588	Tg(MT1A-Dyrk1a)9Xest/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18940310	20081111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581179	Lyst<sup>bg-J</sup>/Lyst<sup>bg-J</sup>  [background:] C57BL/6J-Lyst<sup>bg-J</sup>/J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7331344	Osbpl2<sup>em1Cya</sup>/Osbpl2<sup>em1Cya</sup>  [background:] C57BL/6-Osbpl2<sup>em1Cya</sup>	is_model_of	DOID:0110588	autosomal dominant nonsyndromic deafness 67						ECO:0000033	author statement supported by traceable reference	PMID:35041619	20220823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445971	b2b1432Clo/b2b1432Clo  [background:] C57BL/6J-b2b1432Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304801	Tg(Prnp-HTT*82Q)52Caro/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22219281	20120203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278554	C9orf72<sup>tm1.1Eggn</sup>/C9orf72<sup>tm1.1Eggn</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907140	Rnf170<sup>Gt(OST104375)Lex</sup>/Rnf170<sup>Gt(OST104375)Lex</sup>  [background:] B6.129S-Rnf170<sup>Gt(OST104375)Lex</sup>	is_model_of	DOID:0050951	hereditary ataxia						ECO:0000033	author statement supported by traceable reference	PMID:26433933	20170817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052366	Tg(JPH3*)CXwy/0  [background:] involves: FVB/N	is_model_of	DOID:0090104	Huntington's disease-like 2						ECO:0000033	author statement supported by traceable reference	PMID:21555070	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813925	Pts<sup>tm1Ich</sup>/Pts<sup>tm1Ich</sup> Tg(DBH-PTS)6Csic/0  [background:] B6.Cg-Pts<sup>tm1Ich</sup> Tg(DBH-PTS)6Csic	is_model_of	DOID:543	dystonia						ECO:0000033	author statement supported by traceable reference	PMID:16135092	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625848	Gdf1<sup>tm1Sjl</sup>/Gdf1<sup>tm1Sjl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060850	annular pancreas						ECO:0000033	author statement supported by traceable reference	PMID:10700179	20081215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606114	Ehhadh<sup>tm1Jkr</sup>/Ehhadh<sup>tm1Jkr</sup> Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0090031	D-bifunctional protein deficiency						ECO:0000033	author statement supported by traceable reference	PMID:15769750	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606114	Ehhadh<sup>tm1Jkr</sup>/Ehhadh<sup>tm1Jkr</sup> Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0090031	D-bifunctional protein deficiency						ECO:0000033	author statement supported by traceable reference	PMID:14500732	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7261196	Csf2ra<sup>em1Szut</sup>/Csf2ra<sup>em1Szut</sup>  [background:] C57BL/6-Csf2ra<sup>em1Szut</sup>	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:35043685	20220412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664355	Col3a1<sup>tm1Jae</sup>/Col3a1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:14756	vascular type Ehlers-Danlos syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9050868	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652736	Gpx1<sup>tm1Ysh</sup>/Gpx1<sup>tm1Ysh</sup> Gpx2<sup>tm2Coh</sup>/Gpx2<sup>tm2Coh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:11518697	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4887901	Tg(Plp)66Kan/0  [background:] B6NCrl.Cg-Tg(Plp)66Kan	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:17133418	20110214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300789	Pah<sup>enu2</sup>/Pah<sup>enu2</sup>  [background:] BTBR-Pah<sup>enu2</sup>/J	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:21640623	20120107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831004	Tg(Neurod2-Smo*A1)199Jols/Tg(Neurod2-Smo*A1)199Jols  [background:] C57BL/6-Tg(Neurod2-Smo*A1)199Jols	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22869526	20121228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6414873	Wnk4<sup>em1Cjc</sup>/Wnk4<sup>em1Cjc</sup>  [background:] Not Specified	is_model_of	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:30765526	20200505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903489	Tg(H2-Ea-HA)HACIIAjca/0 Tg(Tcra/Tcrb)1Vbo/0  [background:] C.Cg-Tg(H2-Ea-HA)HACIIAjca Tg(Tcra/Tcrb)1Vbo	is_model_of	DOID:848	arthritis						ECO:0000033	author statement supported by traceable reference	PMID:24591372	20170628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110583	Gucy2e<sup>tm1Gar</sup>/Gucy2e<sup>tm1Gar</sup> Nrl<sup>tm1Asw</sup>/Nrl<sup>tm1Asw</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110078	Leber congenital amaurosis 1						ECO:0000033	author statement supported by traceable reference	PMID:26247368	20180117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4431029	Prlr<sup>tm1Cnp</sup>/Prlr<sup>tm1Cnp</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd	is_model_of	DOID:0050547	familial medullary thyroid carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16166330	20100305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6317327	Pkd1<sup>tm2Som</sup>/Pkd1<sup>tm2Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJae * C57BL/6 * ICR	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430592	Tg(Pklr-Myc)73Ak/0  [background:] B6.Cg-Tg(Pklr-Myc)73Ak	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22251704	20120807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577766	Angptl6<sup>tm1Yo</sup>/Angptl6<sup>tm1Yo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15778720	20100603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6331093	Tg(Thy1-DCTN1*G71A)#Ytsu/0  [background:] involves: C57BL/6J	is_model_of	DOID:0060486	Perry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29154962	20190730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576657	Ptgs1<sup>tm1Fun</sup>/Ptgs1<sup>tm1Fun</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:15776109	20050512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified	is_model_of	DOID:0060856	right atrial isomerism						ECO:0000033	author statement supported by traceable reference	PMID:10574770	20060503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3848948	Lama2<sup>dy-8J</sup>/Lama2<sup>dy-8J</sup>  [background:] C57BL/6J-Lama2<sup>dy-8J</sup>/GrsrJ	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	MGI:3848945	20090626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432231	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:6032	juvenile type testicular granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6739868	Ppdpf<sup>tm1Nju</sup>/Ppdpf<sup>tm1Nju</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:34031390	20210816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707163	Abca3<sup>tm1Frm</sup>/Abca3<sup>tm1Frm</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:17142808	20070807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687954	Uox<sup>in</sup>/Uox<sup>in</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11474184	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4352675	Nfkb2<sup>tm2Brv</sup>/Nfkb2<sup>tm2Brv</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:12177	common variable immunodeficiency						ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7282305	Avpr2<sup>tm2.1Jwe</sup>/Y Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0081060	X-linked nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:19729836	20220606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473984	Dnah8<sup>em1Osb</sup>/Dnah8<sup>em1Osb</sup>  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0112164	spermatogenic failure 46						ECO:0000033	author statement supported by traceable reference	PMID:32619401	20210118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664350	Timp3<sup>tm1Web</sup>/Timp3<sup>tm1Web</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0090114	Sorsby's fundus dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:12147610	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843341	Braf<sup>tm1Cpri</sup>/Braf<sup>tm1Cpri</sup> Tg(Tyr-cre/ERT2)1Lru/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:19345328	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834745	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(tetO-BRAF*V600E)29Lc/0 Tg(Tyr-rtTA)37Lc/0  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:19079609	20090309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505671	Epg5<sup>tm1Ygz</sup>/Epg5<sup>tm1Ygz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:27715390	20200127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6715314	Shank3<sup>em1Hzo</sup>/Shank3<sup>em1Hzo</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30610205	20210614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834214	mt-Nd6<sup>m2Jiha</sup>  [background:] involves: C3H/An * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:3650	lactic acidosis						ECO:0000033	author statement supported by traceable reference	PMID:20674568	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5758892	Sco1<sup>tm1c(KOMP)Wtsi</sup>/Sco1<sup>tm1c(KOMP)Wtsi</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA	is_model_of	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:25683716	20160411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441509	Scamp5<sup>tm1Smoc</sup>/Scamp5<sup>tm1Smoc</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:32020363	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583552	Tg(ITGA5)0794Fmw/0 Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661970	Lrp6<sup>Cd</sup>/Lrp6<sup>Cd</sup>  [background:] A-Lrp6<sup>Cd</sup>	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:16126904	20130104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661970	Lrp6<sup>Cd</sup>/Lrp6<sup>Cd</sup>  [background:] A-Lrp6<sup>Cd</sup>	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:10545599	20130104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6389045	Ppargc1a<sup>tm1Brsp</sup>/Ppargc1a<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:29925537	20200207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558876	Tg(JAK2*V617F)FF1Rsko/0 Tg(Tek-cre)1Arnd/0  [background:] involves: C57BL/6 * CBA * DBA/2	is_model_of	DOID:1247	blood coagulation disease						ECO:0000033	author statement supported by traceable reference	PMID:24469804	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908275	Tg(Myh6*)1Lnwd/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10362699	20170906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428686	Tg(H2-K1-HLA-A*)28Mpla/0  [background:] B10.Cg-Tg(H2-K1-HLA-A*)28Mpla	is_model_of	DOID:0111079	birdshot chorioretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:11226280	20120723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925397	Cdc73<sup>tm1Btt</sup>/Cdc73<sup>tm1Btt</sup> Tg(PTH-cre)4167Slib/0  [background:] Not Specified	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904951	Tg(Myh6-Rab1a)lowGwd/0  [background:] involves: FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11739277	20170718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177047	Dmc1<sup>Mei11</sup>/Dmc1<sup>Mei11</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050457	Sertoli cell-only syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10700192	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438090	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/0 Usp9x<sup>tm1Tuv</sup>/Y  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22699621	20220511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192274	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Cd207<sup>tm2.1(cre)Bjec</sup>/Cd207<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:2571	Langerhans-cell histiocytosis						ECO:0000033	author statement supported by traceable reference	PMID:24638167	20180731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558879	Fbn1<sup>tm2.1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:24107997	20140414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429550	Kif27<sup>Gt(OST441915)Lex</sup>/Kif27<sup>Gt(OST441915)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6388425	Wdr62<sup>tm1.1Jfch</sup>/Wdr62<sup>tm1.1Jfch</sup>  [background:] involves: 129S1/SvImJ * C57BL/6N	is_model_of	DOID:0070293	primary autosomal recessive microcephaly 2 with or without cortical malformations						ECO:0000033	author statement supported by traceable reference	PMID:31197141	20200203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727060	Tsga8<sup>em1Ohbo</sup>/Y  [background:] C57BL/6-Tsga8<sup>em1Ohbo</sup>	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:33766931	20210729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295269	Spef2<sup>bgh</sup>/Spef2<sup>bgh</sup>  [background:] involves: C57BL/6J * C57BL/10J	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:21715716	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437115	Cep290<sup>b2b1454Clo</sup>/Cep290<sup>b2b1454Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1454Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7256634	Cacng8<sup>tm1Ran</sup>/Cacng8<sup>tm1Ran</sup>  [background:] C57BL/6-Cacng8<sup>tm1Ran</sup>	is_model_of	DOID:10939	antisocial personality disorder						ECO:0000033	author statement supported by traceable reference	PMID:34099816	20220324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727359	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>em1Alsh</sup>  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771372	Stat1<sup>tm1Rds</sup>/Stat1<sup>tm1Rds</sup>  [background:] 129S6/SvEv-Stat1<sup>tm1Rds</sup>/Tac	is_model_of	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20386712	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806468	X/Tg(Ela-KRAS*G12D)9Eps Tg(Mt1-TGFBR2*)AM3Epb/0  [background:] involves: C57BL/6 * FVB	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26980767	20161108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7511685	Chd4<sup>em1Flc</sup>/Chd4<sup>em1Flc</sup>  [background:] C57BL/6J-Chd4<sup>em1Flc</sup>	is_model_of	DOID:0060480	left ventricular noncompaction						ECO:0000033	author statement supported by traceable reference	PMID:37254794	20230804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428746	Tg(Wap-TAg)1Depp/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:0060074	ductal carcinoma in situ						ECO:0000033	author statement supported by traceable reference	PMID:10713686	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834683	Tg(SFTPC-EML4/ALK)502-4Hima/0  [background:] involves: C57BL/6J	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19064915	20090306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175204	Pax6<sup>Sey-Dey</sup>/Pax6<sup>+</sup>  [background:] C3H/HeJ-Pax6<sup>Sey-Dey</sup>	is_model_of	DOID:12271	aniridia						ECO:0000033	author statement supported by traceable reference	PMID:2173141	20071019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442145	Cep290<sup>b2b1752Clo</sup>/Cep290<sup>b2b1752Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1752Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883506	None [background:] YBR/EiJ	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:27483353	20180404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617399	Ciita<sup>tm1Ccum</sup>/Ciita<sup>tm1Ccum</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:5812	MHC class II deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8624807	20060323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7366893	Ndrg1<sup>em1Lxli</sup>/Ndrg1<sup>em1Lxli</sup>  [background:] C57BL/6N-Ndrg1<sup>em1Lxli</sup>	is_model_of	DOID:0110186	Charcot-Marie-Tooth disease type 4D						ECO:0000033	author statement supported by traceable reference	PMID:35708320	20221025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296508	Ppt1<sup>tm1Hof</sup>/Ppt1<sup>tm1Hof</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:22031903	20150701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661067	Reln<sup>rl</sup>/Reln<sup>+</sup>  [background:] B6C3Fe a/a-Reln<sup>rl</sup>/J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:11982630	20150908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5496284	Robo1<sup>b2b872Clo</sup>/Robo1<sup>b2b872Clo</sup>  [background:] C57BL/6J-Robo1<sup>b2b872Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6865772	Cfap69<sup>tm1b(KOMP)Wtsi</sup>/Cfap69<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0111929	spermatogenic failure 24						ECO:0000033	author statement supported by traceable reference	PMID:29606301	20220209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510439	Nbn<sup>tm1.1Md</sup>/Nbn<sup>tm1.1Md</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15333589	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838089	Ass1<sup>bar</sup>/Ass1<sup>bar</sup>  [background:] B6.BAR-Ass1<sup>bar</sup>	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2674328	Ar<sup>Tfm</sup>/Y  [background:] involves: STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2659009	Nr0b1<sup>tm1.1Lja</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0080156	X-linked adrenal hypoplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:11564714	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2659009	Nr0b1<sup>tm1.1Lja</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0080156	X-linked adrenal hypoplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:9843206	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5816495	Fgf10<sup>tm1Wss</sup>/Fgf10<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0050331	lacrimoauriculodentodigital syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:27590203	20170104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442123	Cntrl<sup>b2b1468.1Clo</sup>/Cntrl<sup>b2b1468.1Clo</sup>  [background:] C57BL/6J-Cntrl<sup>b2b1468.1Clo</sup>	is_model_of	DOID:12712	nephronophthisis						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655216	Tbx3<sup>tm1Pa</sup>/Tbx3<sup>tm1Pa</sup>  [background:] either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)	is_model_of	DOID:0060614	ulnar-mammary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12668638	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266256	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IGF1R)1Ramo/0  [background:] involves: 129 * C57BL/6 * FVB	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19568412	20220503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301598	Tg(H2-L-IL6)46Kish/Tg(H2-L-IL6)46Kish  [background:] C.B6-Tg(H2-L-IL6)46Kish	is_model_of	DOID:3721	plasmacytoma						ECO:0000033	author statement supported by traceable reference	PMID:11805288	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312334	Dnaaf4<sup>b2b811.1Clo</sup>/Dnaaf4<sup>b2b811.1Clo</sup>  [background:] C57BL/6J-Dnaaf4<sup>b2b811.1Clo</sup>	is_model_of	DOID:0060254	Robinow syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286081	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] (CBA/J x B6.129S2-Trp53<sup>tm1Tyj</sup> Nf1<sup>tm1Tyj</sup>/+ +)F1	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:10973261	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819280	Klf1<sup>Nan</sup>/Klf1<sup>+</sup>  [background:] either: B6.Cg-Klf1<sup>Nan</sup> or WB.Cg-Klf1<sup>Nan</sup>	is_model_of	DOID:12971	hereditary spherocytosis						ECO:0000033	author statement supported by traceable reference	PMID:19409822	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531409	Phox2a/Inppl1<sup>tm1Ssch</sup>/Phox2a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11343120	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811282	Pkd1<sup>tm3Jzh</sup>/Pkd1<sup>tm3Jzh</sup> Tg(Ggt1-cre)M3Egn/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:18385665	20081020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624726	Zeb2<sup>tm1.2Yhi</sup>/Zeb2<sup>tm1.2Yhi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:0060485	Mowat-Wilson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12522767	20060619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634271	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>tm1.1Sdie</sup>  [background:] B6.Cg-Cacna1f<sup>tm1.1Sdie</sup>/J	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7435433	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Slco1c1-icre/ERT2)1Mrks/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB	is_model_of	DOID:0060688	arteriovenous malformations of the brain						ECO:0000033	author statement supported by traceable reference	PMID:32552404	20230217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6263156	Phkb<sup>em1(IMPC)J</sup>/Phkb<sup>+</sup>  [background:] C57BL/6NJ-Phkb<sup>em1(IMPC)J</sup>/Mmjax	is_model_of	DOID:0111041	glycogen storage disease IXb						ECO:0000033	author statement supported by traceable reference	PMID:36077341	20221108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6758622	Tg(Umod*C217G)1Xrw/0  [background:] involves: FVB/N	is_model_of	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:29145399	20210910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576039	hpmd/hpmd  [background:] Not Specified	is_model_of	DOID:4258	Weissenbacher-Zweymuller syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11818962	20050526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175040	Gfra1<sup>tm1Jmi</sup>/Gfra1<sup>tm1Jmi</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:9728913	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942364	Tg(Cma1-cre)ARoer/0 Tg(Kit*D814V)3Roer/0  [background:] involves: C57BL/6	is_model_of	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6304487	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>tm1.1Jrpi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110319	hypertrophic cardiomyopathy 13						ECO:0000033	author statement supported by traceable reference	PMID:26304555	20190522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6304487	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>tm1.1Jrpi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110319	hypertrophic cardiomyopathy 13						ECO:0000033	author statement supported by traceable reference	PMID:28235781	20190522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6515750	Vcpip1<sup>em1Zlou</sup>/Vcpip1<sup>em1Zlou</sup>  [background:] C57BL/6NHsd-Vcpip1<sup>em1Zlou</sup>	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:32649882	20210407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6508539	Pank4<sup>em1Nju</sup>/Pank4<sup>em1Nju</sup>  [background:] Not Specified	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:30585370	20210303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907679	E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: FVB/N	is_model_of	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24565867	20170829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5302497	Tg(Mt1-IL6)28Gci/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:9120	amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:10233864	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ	is_model_of	DOID:1214	tympanosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27959908	20190917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868118	Myb<sup>boo</sup>/Myb<sup>boo</sup>  [background:] involves: C57BL/6	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:20610815	20110117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487550	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tgfbr1<sup>tm1.1Karl</sup>/Tgfbr1<sup>tm1.1Karl</sup> Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * CD-1 * FVB/N	is_model_of	DOID:6126	anal canal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24124460	20140812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5823026	Ido1<sup>tm1.1Mkks</sup>/Ido1<sup>tm1.1Mkks</sup>  [background:] B6.Cg-Ido1<sup>tm1.1Mkks</sup>	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:25602015	20170201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700786	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] B6.D2-Cacna1a<sup>tg</sup>/J	is_model_of	DOID:0050704	childhood electroclinical syndrome						ECO:0000033	author statement supported by traceable reference	PMID:572084	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581212	Atp8a2<sup>wl-vmd</sup>/Atp8a2<sup>wl-vmd</sup>  [background:] C3H/HeSnJ-Atp8a2<sup>wl-vmd</sup>/J	is_model_of	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634715	Emx1<sup>tm1(cre)Ito</sup>/Emx1<sup>+</sup> Tg(CAG-Mtor*)#Atai/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:24857653	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762186	Brca1<sup>tm1Brn</sup>/Brca1<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129P2/OlaHsd * BALB/cJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:17626182	20080624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259994	Col10a1<sup>tm2.1Rpbh</sup>/Col10a1<sup>+</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0080021	Schmid metaphyseal chondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30010889	20181213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284944	Tlr7<sup>em2Anu</sup>/Tlr7<sup>em2Anu</sup>  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703705	Del(16Dgcr2-Hira)1Rak/+  [background:] involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11239417	20070423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274313	Elp1<sup>tm1.1Gilas</sup>/Elp1<sup>tm1.1Gilas</sup> Tg(Dct-cre)1Apdn/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27997532	20190123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698627	Sall4<sup>tm1Brd</sup>/Sall4<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:17216607	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624038	Tg(INS-SOD2)3Pne/0  [background:] NOD.FVB-Tg(INS-SOD2)3Pne	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16731821	20060607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367270	Rho<sup>R3</sup>/Rho<sup>tm1Jlem</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:19741247	20130619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606731	Ctsc<sup>tm1Dgen</sup>/Ctsc<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6849724	Lss<sup>em1Zhaol</sup>/Lss<sup>em1Zhaol</sup>  [background:] C57BL/6J-Lss<sup>em1Zhaol</sup>	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:34926465	20220106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660929	Disc1<sup>tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho</sup>/Disc1<sup>del</sup>  [background:] 129S2/SvPasCrl-Disc1<sup>del</sup> Disc1<sup>tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:24908665	20150904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636486	Tg(Th-ALK*F1174L)2Loch/0 Tg(Th-MYCN)41Waw/0  [background:] involves: 129X1/SvJ * BALB/c * C57BL/6J * CBA	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22789543	20150519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721938	Tg(CMV-IghvaD11)DCat/0 Tg(CMV-IgkvaD11)ACat/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10841577	20140827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661986	Dkc1<sup>tm1Ppp</sup>/Y  [background:] involves: 129S1/Sv	is_model_of	DOID:2729	dyskeratosis congenita						ECO:0000033	author statement supported by traceable reference	PMID:12522253	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16921370	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693440	Tg(APPSwLon)96Btla/0  [background:] involves: 129S4/SvJae	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9285791	20070112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648122	Eml1<sup>heco</sup>/?  [background:] involves: CD-1	is_model_of	DOID:2490	congenital nervous system abnormality						ECO:0000033	author statement supported by traceable reference	PMID:24859200	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5463447	b2b1456Clo/b2b1456Clo  [background:] C57BL/6J-b2b1456Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056103	Timp3<sup>tm1Rkho</sup>/Timp3<sup>tm1Rkho</sup>  [background:] B6.129-Timp3<sup>tm1Rkho</sup>	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15262835	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6383402	Ift172<sup>tm1.1Rama</sup>/Ift172<sup>tm1.1Rama</sup> Tg(Rho-icre)1Ck/0  [background:] involves: 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:8466	retinal degeneration						ECO:0000033	author statement supported by traceable reference	PMID:29659833	20200106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196486	Rbp4<sup>tm1(RBP4)Zhel</sup>/Rbp4<sup>tm1(RBP4)Zhel</sup> Ttr<sup>tm2(TTR)Kymm</sup>/Ttr<sup>tm2(TTR)Kymm</sup>  [background:] B6.Cg-Ttr<sup>tm2(TTR)Kymm</sup> Rbp4<sup>tm1(RBP4)Zhel</sup>	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:29330472	20180905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6783439	Adamts10<sup>em1Jku</sup>/Adamts10<sup>em1Jku</sup>  [background:] C57BL/6J-Adamts10<sup>em1Jku</sup>	is_model_of	DOID:0050475	Weill-Marchesani syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34424262	20211029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5302203	Crbn<sup>tm1.1Jjh</sup>/Crbn<sup>tm1.1Jjh</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6	is_model_of	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000033	author statement supported by traceable reference	PMID:21995942	20190703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447490	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: C57BL/6J * CD-1	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22908258	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771729	Kit<sup>W</sup>/Kit<sup>W-v</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:2361	macrocytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910538	Tg(CMV-cat,-ROCK2*)3-1Koba/0 Tg(Tagln-cre)1Her/0  [background:] involves: C57BL/6 * C57BL/6JJcl * DBA/2 * SJL	is_model_of	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:26315406	20170928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942360	Tg(Kit*D814V)1Roer/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663620	Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110040	Alzheimer's disease 4						ECO:0000033	author statement supported by traceable reference	PMID:9354339	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583687	Gck<sup>tm1Tka</sup>/Gck<sup>+</sup> Irs1<sup>tm1Tka</sup>/Irs1<sup>tm1Tka</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * CBA * ICR	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9062343	20050816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295270	Spef2<sup>bgh</sup>/Spef2<sup>bgh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:21715716	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174979	Nos3<sup>tm1Plh</sup>/Nos3<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:10825	essential hypertension						ECO:0000033	author statement supported by traceable reference	PMID:7545787	20060410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5298094	Tg(CAG-cat,-Dcn*)#Debi/0 Tg(Kera-cre)KC4.3Wwk/0  [background:] involves: FVB/N	is_model_of	DOID:0060445	congenital stromal corneal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21893019	20111213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586967	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:6232310	20050908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:11802174	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176767	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:11297510	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762541	Des<sup>tm1.1Ccrs</sup>/Des<sup>+</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:25394388	20170823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795975	Rpl38<sup>Ts</sup>/Rpl38<sup>+</sup>  [background:] TSJ/Le	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:21062742	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789945	Chrnb2<sup>tm1.1Cont</sup>/Chrnb2<sup>tm1.1Cont</sup>  [background:] B6.129-Chrnb2<sup>tm1.1Cont</sup>	is_model_of	DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3						ECO:0000033	author statement supported by traceable reference	PMID:20603624	20160826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3521748	Hoxa13<sup>tm1Jwi</sup>/Hoxa13<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060739	hand-foot-genital syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15385446	20050701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107640	Mmachc<sup>Gt(AZ0348)Wtsi</sup>/Mmachc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC						ECO:0000033	author statement supported by traceable reference	PMID:24889031	20180104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174998	Psen1<sup>tm1Shn</sup>/Psen1<sup>tm1Shn</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9160754	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769260	Galnt1<sup>tm1.1Jxm</sup>/Galnt1<sup>tm1.1Jxm</sup>  [background:] B6NHsd.Cg-Galnt1<sup>tm1.1Jxm</sup>	is_model_of	DOID:4079	heart valve disease						ECO:0000033	author statement supported by traceable reference	PMID:25615642	20190715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580015	Axin2<sup>tm1Wbm</sup>/Axin2<sup>tm1Wbm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2340	craniosynostosis						ECO:0000033	author statement supported by traceable reference	PMID:15790973	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527432	Ccl2<sup>tm1Rol</sup>/Ccl2<sup>tm1Rol</sup> Cx3cr1<sup>tm1Litt</sup>/Cx3cr1<sup>tm1Litt</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:23637822	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6458735	Tg(Thy1/THY1)T6Gsv/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:14605274	20200930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6458735	Tg(Thy1/THY1)T6Gsv/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15034095	20200930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451166	Csnk2a2<sup>tm1Dcs</sup>/Csnk2a2<sup>tm1Dcs</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:10471512	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806875	Tg(Venus/SOX10*)55Kein/Tg(Venus/SOX10*)55Kein  [background:] involves: C3H/He * C57BL/6	is_model_of	DOID:0090111	PCWH syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25959061	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902157	Krt12<sup>tm1.1(KRT12*L132P)Arte</sup>/Krt12<sup>tm1.1(KRT12*L132P)Arte</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060451	Meesmann corneal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26758872	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7329919	Usp45<sup>em1Qzha</sup>/Usp45<sup>em1Qzha</sup>  [background:] C57BL/6J-Usp45<sup>em1Qzha</sup>	is_model_of	DOID:0081169	Leber congenital amaurosis 19						ECO:0000033	author statement supported by traceable reference	PMID:30573563	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6149568	Ano5<sup>tm1Lrk</sup>/Ano5<sup>tm1Lrk</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L						ECO:0000033	author statement supported by traceable reference	PMID:26911675	20180405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418448	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Pten<sup>tm1Rps</sup>/Pten<sup>tm1Rps</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] involves: 129/Sv * 129S1/Sv * C57BL/6J * FVB/N * SJL	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:20048081	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696621	Atp7a<sup>Mo-dp</sup>/Y  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:25456742	20151118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304716	Gt(ROSA)26Sor<sup>tm4(HIF2A*)Kael</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20733101	20170814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639133	H2-Ab1<sup>b-tm1Gru</sup>/H2-Ab1<sup>b-tm1Gru</sup> Tg(HLA-DQA1,HLA-DQB1)1Dv/0 Tg(HLA-DRB1)31Dmz/0 Tg(Ins2-CD80)3B7Flv/0  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/10SnJ * CBA * SJL	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11285306	20060727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6163475	Zmynd10<sup>tm1(KOMP)Wtsi</sup>/Zmynd10<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:0110597	primary ciliary dyskinesia 22						ECO:0000033	author statement supported by traceable reference	PMID:29601588	20180628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617944	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] B6;129-Ednrb<sup>tm1Ywa</sup>/J	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:24945437	20150309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622318	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060844	Norrie disease						ECO:0000033	author statement supported by traceable reference	PMID:15035989	20060515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897776	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NCr	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22514108	20170622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5614980	Dnah5<sup>b2b2570Clo</sup>/Dnah5<sup>b2b2570Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2570Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769337	Ahsp<sup>tm1.1Mjwe</sup>/Ahsp<sup>+</sup> Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:15545996	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804635	Rpsa<sup>tm1Ells</sup>/Rpsa<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	MGI:3804630	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689511	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/NJ	is_model_of	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:24443344	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905421	Egfr<sup>wa2</sup>/Egfr<sup>wa2</sup>  [background:] involves: C57BL/6	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:25997932	20170726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16697652	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10699173	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:7344126	20060731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:8055108	20060731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849173	Six1<sup>Cwe</sup>/Six1<sup>Cwe</sup>  [background:] C3HeB/FeJ-Six1<sup>Cwe</sup>	is_model_of	DOID:14702	branchiootorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19389353	20090629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175009	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/SvEv * MF1	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:7595168	20050711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175009	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/SvEv * MF1	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:8114940	20050711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789197	Lama2<sup>tm1Stk</sup>/Lama2<sup>tm1Stk</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:9326364	20110127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789197	Lama2<sup>tm1Stk</sup>/Lama2<sup>tm1Stk</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:21084425	20110127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276667	Tg(Mpz)88.1Mfel/0  [background:] FVB/N-Tg(Mpz)88.1Mfel	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:11086005	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278939	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:27329763	20190219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796628	Frem2<sup>ne</sup>/Frem2<sup>ne</sup>  [background:] STOCK Frem2<sup>ne</sup>/GrsrJ	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796628	Frem2<sup>ne</sup>/Frem2<sup>ne</sup>  [background:] STOCK Frem2<sup>ne</sup>/GrsrJ	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5428032	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814728	Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] C.129-Cx3cr1<sup>tm1Zm</sup>	is_model_of	DOID:0110024	age related macular degeneration 12						ECO:0000033	author statement supported by traceable reference	PMID:17909628	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2170195	Pitx2<sup>tm1Kki</sup>/Pitx2<sup>tm1Kki</sup>  [background:] involves: 129P2/OlaHsd * C57BL	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10572050	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603325	Spred2<sup>Gt(XB228)Byg</sup>/Spred2<sup>Gt(XB228)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:15946934	20051031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831340	Brca2<sup>tm1Brn</sup>/Brca2<sup>tm1Brn</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19164512	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157970	Tcf4<sup>em2Bdph</sup>/?  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29222403	20180524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574073	Cdkl5<sup>tm1.2Cogr</sup>/Cdkl5<sup>tm1.2Cogr</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	is_model_of	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:24838000	20201218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107229	Dzip1l<sup>warpy</sup>/Dzip1l<sup>warpy</sup>  [background:] involves: C57BL/6 * CD-1	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28530676	20180102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5585151	Agtr2<sup>tm1Tin</sup>/Y Efemp2<sup>tm1.1Hiya</sup>/Efemp2<sup>tm1.2Hiya</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:23636094	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5568994	Mecp2<sup>tm1.1Jtc</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24283265	20170308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714371	Erbb2<sup>tm8(Erbb2)Mul</sup>/Erbb2<sup>+</sup> Tg(MMTV-cre)7Mul/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:20961995	20110127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281829	Runx3<sup>tm3Yg</sup>/Runx3<sup>tm3Yg</sup> Tg(Pou4f1-cre/ERT2)2Jiz/0  [background:] involves: C57BL/6	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438241	Cul4b<sup>tm1Swl</sup>/Y Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] B6.Cg-Edil3<sup>Tg(Sox2-cre)1Amc</sup> Cul4b<sup>tm1Swl</sup>	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:22763239	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5704372	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Trp53<sup>tm2Tyj</sup>/Trp53<sup>+</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:25815421	20160122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822359	Dnm1<sup>Ftfl</sup>/Dnm1<sup>Ftfl</sup>  [background:] C57BL/6J-Dnm1<sup>Ftfl</sup>	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:20700442	20100910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431510	b2b904Clo/b2b904Clo  [background:] C57BL/6J-b2b904Clo	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634095	Tg(Mbp-SNCA)1Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:24310907	20150430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6378827	Adamtsl2<sup>tm1c(KOMP)Wtsi</sup>/Adamtsl2<sup>tm1c(KOMP)Wtsi</sup> Tg(Prrx1-cre)1Cjt/0  [background:] B6.Cg-Adamtsl2<sup>tm1c(KOMP)Wtsi</sup> Tg(Prrx1-cre)1Cjt	is_model_of	DOID:0111725	geleophysic dysplasia 1						ECO:0000033	author statement supported by traceable reference	PMID:30738849	20200518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818532	Coro1a<sup>koy</sup>/Coro1a<sup>koy</sup>  [background:] C57BL/6-Coro1a<sup>koy</sup>	is_model_of	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5795669	Dmd<sup>mdx</sup>/Y Utrn<sup>tm1Jrs</sup>/Utrn<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17889902	20160926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446903	Smurf2<sup>Gt(RRA098)Byg</sup>/Smurf2<sup>Gt(RRA098)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:28107482	20190709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5754489	Lmna<sup>tm11Lgf</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9164	achalasia						ECO:0000033	author statement supported by traceable reference	PMID:25652409	20160324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524136	Fat1<sup>tm1Fhel</sup>/Fat1<sup>tm1Fhel</sup> Pax3<sup>tm1(cre)Joe</sup>/Pax3<sup>+</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583906	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>	is_model_of	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9593767	20050819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177575	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * NOD	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:9391152	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574961	Mthfr<sup>tm1Rzn</sup>/Mthfr<sup>tm1Rzn</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:11181567	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615667	Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:11909969	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313813	Pcsk5<sup>b2b585Clo</sup>/Pcsk5<sup>b2b585Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b585Clo</sup>	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432013	Pitx3<sup>tm1.1Cai</sup>/Pitx3<sup>+</sup> Tg(tetO-SNCA*A53T)E2Cai/0  [background:] involves: 129 * C57BL/6J * FVB/N	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22764233	20171211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6431136	Rcbtb2<sup>tm1.1Xyw</sup>/Rcbtb2<sup>tm1.1Xyw</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:2570	malignant histiocytic disease						ECO:0000033	author statement supported by traceable reference	PMID:26291700	20200602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814328	Prkn<sup>tm1Ykt</sup>/Prkn<sup>tm1Ykt</sup> Tg(PDGFB-GPR37)20Ryot/0  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:18691389	20081110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834667	Tg(KRT5-tTA)1216Glk/0 Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer/0  [background:] involves: FVB/N	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:18334552	20090310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6095193	Tg(Prnp-TARDBP*Q331K)103Dwc/0  [background:] B6.Cg-Tg(Prnp-TARDBP*Q331K)103Dwc/J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:28334913	20171206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430992	Spart<sup>tm1.1Xen</sup>/Spart<sup>tm1.1Xen</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050886	Troyer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22619377	20120813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5298009	Selenon<sup>tm1.2Mred</sup>/Selenon<sup>tm1.2Mred</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0110633	rigid spine muscular dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:21858002	20111212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6467327	Nfix<sup>tm1.1Rmg</sup>/Nfix<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0112102	Sotos syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:30503862	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6492211	Lrrc7<sup>Tg(Myl2-TSPYL)1Sich</sup>/Lrrc7<sup>Tg(Myl2-TSPYL)1Sich</sup>  [background:] involves: FVB/N	is_model_of	DOID:0060037	developmental disorder of mental health						ECO:0000033	author statement supported by traceable reference	PMID:31582721	20210115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6491489	Frmd7<sup>tm1b(KOMP)Wtsi</sup>/Frmd7<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:0111790	congenital nystagmus 1						ECO:0000033	author statement supported by traceable reference	PMID:33007925	20210112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697681	Comt<sup>tm1Kara</sup>/Comt<sup>tm1Kara</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:18469803	20111003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829652	Flcn<sup>tm1Btt</sup>/Flcn<sup>tm1Btt</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * ICR	is_model_of	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18974783	20090130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559168	Tg(Myh6-Gnaq*Q209L)52Ejne/?  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:9811897	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836995	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp*D177N*M128V)A21Rchi/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CBA	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:19038218	20090325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438493	Tg(Thy1-TARDBP)6Singh/Tg(Thy1-TARDBP)6Singh  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:20133711	20100402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841180	Tg(Myh6-tTA)55Rbns/0 Tg(Myh6/tetO-PRKAG2*N488I)1Chib/0  [background:] Not Specified	is_model_of	DOID:0090101	lethal congenital glycogen storage disease of heart						ECO:0000033	author statement supported by traceable reference	PMID:18158359	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6317334	Pkd1<sup>tm1.1Pcha</sup>/Pkd1<sup>tm2Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * ICR	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821274	Phka1<sup>I/FnLn</sup>/Y  [background:] I/FnLn	is_model_of	DOID:0111040	glycogen storage disease IXd						ECO:0000033	author statement supported by traceable reference	PMID:7874115	20100913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5586979	Krt71<sup>Ca-19J</sup>/Krt71<sup>+</sup>  [background:] BALB/cJ-Krt71<sup>Ca-19J</sup>/GrsrJ	is_model_of	DOID:0110710	hypotrichosis 13						ECO:0000033	author statement supported by traceable reference	MGI:5586973	20141009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749252	Lamb3<sup>tm1.1Hosc</sup>/Lamb3<sup>tm1.1Hosc</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060737	junctional epidermolysis bullosa Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:25350318	20160218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431510	b2b904Clo/b2b904Clo  [background:] C57BL/6J-b2b904Clo	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7518241	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Neurod1-cre)RZ24Gsat/0  [background:] involves: C57BL/6J * C57BL/6N * FVB/NTac	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34732824	20230815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6220717	Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] B6.129-Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:29257745	20181102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355229	Apoe<sup>tm3(APOE*4)Mae</sup>/Apoe<sup>tm3(APOE*4)Mae</sup> Tg(APPSWE)2576Kha/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15772340	20090828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950564	Prpf3<sup>tm1.1Eap</sup>/Prpf3<sup>tm1.1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:0110356	retinitis pigmentosa 18						ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652395	Tg(Myh6-Ppara)404-3Dpk/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11781357	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7545539	Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>  [background:] STOCK Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/J	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:37158461	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702859	Psen1<sup>tm1Bdes</sup>/Psen1<sup>+</sup> Psen2<sup>tm1Bdes</sup>/Psen2<sup>tm1Bdes</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:15128703	20070413	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804451	Ednrb<sup>tm1.1Nrd</sup>/Ednrb<sup>tm1.1Nrd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:26240367	20161021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795387	Mcoln1<sup>tm1Sasl</sup>/Mcoln1<sup>tm1Sasl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:17924347	20210121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6268445	Tg(Tek-tTA)1Dmt/0 Tg(tetO-Tek)1Dmt/0  [background:] involves: CD-1	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:15743796	20181221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721894	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1.1Jme</sup> Tg(ACTA1-cre)79Jme/0  [background:] involves: 129 * C57BL/6J * SJL	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:11238465	20070917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316796	b2b913Clo/b2b913Clo  [background:] C57BL/6J-b2b913Clo	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624676	Mecp2<sup>tm1.1Jae</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22302819	20120603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618892	Fanca<sup>tm1Faw</sup>/Fanca<sup>tm1Faw</sup>  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:0111095	Fanconi anemia complementation group A						ECO:0000033	author statement supported by traceable reference	PMID:10915769	20060410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806094	Tg(Rho-Arl3*Q71L)#Visu/0  [background:] involves: 129 * FVB/N	is_model_of	DOID:0110415	retinitis pigmentosa 2						ECO:0000033	author statement supported by traceable reference	PMID:26936825	20161103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6386243	Fscn2<sup>em1Fhan</sup>/Fscn2<sup>em1Fhan</sup>  [background:] C57BL/6J-Fscn2<sup>em1Fhan</sup>	is_model_of	DOID:2742	auditory system disease						ECO:0000033	author statement supported by traceable reference	PMID:30082328	20200124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400710	Htt<sup>tm5Detl</sup>/Htt<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28927719	20200320	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197758	Pomt1<sup>tm1c(EUCOMM)Hmgu</sup>/Pomt1<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: C57BL/6N	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:29867208	20180912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911801	Cdk5rap2<sup>an</sup>/Cdk5rap2<sup>an</sup> Tyrp1<sup>B-lt</sup>/Tyrp1<sup>B-lt</sup>  [background:] WBB6F1	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:20460369	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5700212	Dysf<sup>im</sup>/Dysf<sup>im</sup> Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm2(FCMD)Ttd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL/J	is_model_of	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25198651	20151230	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588317	Bloc1s4<sup>cno</sup>/Bloc1s4<sup>cno</sup>  [background:] involves: C3H/HeJ	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12445206	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822142	Ift172<sup>avc1</sup>/Ift172<sup>avc1</sup>  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461160	Tnfrsf1a<sup>tm2.1Rsie</sup>/Tnfrsf1a<sup>+</sup>  [background:] B6.Cg-Tnfrsf1a<sup>tm2.1Rsie</sup>	is_model_of	DOID:0090018	autosomal dominant familial periodic fever						ECO:0000033	author statement supported by traceable reference	PMID:20457915	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4835032	Rai1<sup>tm1Jrl</sup>/Rai1<sup>+</sup>  [background:] B6.129S7-Rai1<sup>tm1Jrl</sup>/J	is_model_of	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20663924	20101014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682534	Slc6a9<sup>tm1Betz</sup>/Slc6a9<sup>tm1Betz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9268	glycine encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:14622582	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559461	Tg(KRT14-HPV8)9Vuc/0  [background:] FVB.Cg-Tg(KRT14-HPV8)9Vuc	is_model_of	DOID:4159	skin cancer						ECO:0000033	author statement supported by traceable reference	PMID:15735026	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565510	Flt3<sup>tm2.1Dosm</sup>/Flt3<sup>+</sup>  [background:] B6.129(C)-Flt3<sup>tm2.1Dosm</sup>	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24255108	20140529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655512	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10381492	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5640746	Jak2<sup>tm1.2Ble</sup>/Jak2<sup>+</sup> Picalm<sup>tm1.1Tmae</sup>/Picalm<sup>+</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/10 * CBA * SJL	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:25552701	20150616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7496108	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Slc1a3<sup>tm1(cre/ERT2)Mgoe</sup>/Slc1a3<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6N * SJL	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25183173	20230707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>	is_model_of	DOID:1935	Bardet-Biedl syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5642218	Bmp7<sup>tm1.1Dgra</sup>/Bmp7<sup>tm1.1Dgra</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * SJL/J	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:25889639	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907019	Pcdha9<sup>em1Clo</sup>/Pcdha9<sup>em1Clo</sup> Sap130<sup>em1Clo</sup>/Sap130<sup>em1Clo</sup>  [background:] C57BL/6J-Sap130<sup>em1Clo</sup> Pcdha9<sup>em1Clo</sup>/MurrJ	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040301	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm1Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:10555141	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402203	Tg(KRT18-DPP4)3Pbmj/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26486634	20200617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402203	Tg(KRT18-DPP4)3Pbmj/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29152574	20200617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5508218	Bmpr1a<sup>tm2.1Bhr</sup>/Bmpr1a<sup>tm2.1Bhr</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Krt14<sup>tm1.1(cre)Wbm</sup>/Krt14<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * 129X1/SvJ	is_model_of	DOID:0050904	salivary gland carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23736260	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7262692	Tg(KRT18*R89C)22Rgo/0  [background:] involves: FVB/N	is_model_of	DOID:2237	hepatitis						ECO:0000033	author statement supported by traceable reference	PMID:8522591	20220419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6101207	Ext1<sup>tm1.1Vcs</sup>/Ext1<sup>tm1.1Vcs</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:206	hereditary multiple exostoses						ECO:0000033	author statement supported by traceable reference	PMID:28445472	20171214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785829	Tg(Camk2a-ESR1/Disc1*)2698.1Sva/0  [background:] involves: C57BL/6 * C57BL/6NTac	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17984054	20120719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655823	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup> Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6.Cg-Tyr<sup>c-2J</sup> Cyp1b1<sup>tm1Gonz</sup>	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717687	Edar<sup>Tg(OVE1B)Ove</sup>/Edar<sup>Tg(OVE1B)Ove</sup>  [background:] involves: C3H * C57BL/6 * FVB/N	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10431242	20070809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7341464	Ftsj1<sup>tm1Tomik</sup>/Y  [background:] Not Specified	is_model_of	DOID:0112034	non-syndromic X-linked intellectual disability 9						ECO:0000033	author statement supported by traceable reference	PMID:33771871	20220928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027982	Slc4a1<sup>wan</sup>/Slc4a1<sup>wan</sup>  [background:] C3H/HeJ-Slc4a1<sup>wan</sup>/J	is_model_of	DOID:0110919	hereditary spherocytosis type 4						ECO:0000033	author statement supported by traceable reference	PMID:15070709	20100315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467971	Aldh2<sup>tm1a(EUCOMM)Wtsi</sup>/Aldh2<sup>tm1a(EUCOMM)Wtsi</sup> Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * C57BL/6N	is_model_of	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000033	author statement supported by traceable reference	PMID:21734703	20130326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7488670	Chd7<sup>Gt(XK403)Byg</sup>/Chd7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29168327	20230612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451066	Gusb<sup>tm3Sly</sup>/Gusb<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758089	Tg(Camk2a-DISC1)10Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)10Asaw	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23314019	20130524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758089	Tg(Camk2a-DISC1)10Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)10Asaw	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17675407	20130524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616169	Gan<sup>tm1Yany</sup>/Gan<sup>tm1Yany</sup>  [background:] Not Specified	is_model_of	DOID:0090068	giant axonal neuropathy 1						ECO:0000033	author statement supported by traceable reference	PMID:16303566	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616169	Gan<sup>tm1Yany</sup>/Gan<sup>tm1Yany</sup>  [background:] Not Specified	is_model_of	DOID:0090068	giant axonal neuropathy 1						ECO:0000033	author statement supported by traceable reference	PMID:16565160	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6431144	Myo6<sup>em1Bcgen</sup>/Myo6<sup>+</sup>  [background:] involves: C57BL/6J * CBA/CaJ	is_model_of	DOID:0110552	autosomal dominant nonsyndromic deafness 22						ECO:0000033	author statement supported by traceable reference	PMID:31103816	20200602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5461066	Epm2a<sup>Tg(TcraK,TcrbK)TG-BFlv</sup>/Epm2a<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * C57BR/cd * CBA/J	is_model_of	DOID:0060058	lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:16959610	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6433773	Ppp1r14c<sup>tm1Uhl</sup>/Ppp1r14c<sup>tm1Uhl</sup>  [background:] B6;129S6-Ppp1r14c<sup>tm1Uhl</sup>/J	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:27663205	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767853	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup> Xpa<sup>tm1Hvs</sup>/Xpa<sup>tm1Hvs</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17326724	20080118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429562	Hsf1<sup>tm1Ijb</sup>/Hsf1<sup>tm1Ijb</sup> Tg(TTR-V30M)15Imeg/0  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:18485534	20100310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623008	Cbs<sup>tm1Unc</sup>/Cbs<sup>+</sup>  [background:] B6.129P2-Cbs<sup>tm1Unc</sup>/J	is_model_of	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:25016930	20141013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188994	Fuca1<sup>tm1Tlub</sup>/Fuca1<sup>tm1Tlub</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:14500	fucosidosis						ECO:0000033	author statement supported by traceable reference	PMID:27491075	20180719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852756	Smpx<sup>em1Jgao</sup>/Y  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>	is_model_of	DOID:0111735	X-linked deafness 4						ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907236	Tg(Myh6-Htr2b)1Lum/0  [background:] involves: CD-1	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12810613	20170822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825357	Tcf3<sup>tm1(PBX1)Mlc</sup>/Tcf3<sup>+</sup> Cd79a<sup>tm1(cre)Reth</sup>/Cd79a<sup>+</sup>  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26301816	20170301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908182	Tg(Myh6-Mtpn)4Ssen/0  [background:] involves: FVB	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:14970239	20170905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778526	Dnah5<sup>hlb612</sup>/Dnah5<sup>hlb612</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	PMID:18037990	20081219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5912375	Kit<sup>W</sup>/Kit<sup>W</sup>  [background:] B6.Cg-Kit<sup>W</sup>/J	is_model_of	DOID:2361	macrocytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699323	Bckdk<sup>Gt(VICT48)710Lex</sup>/Bckdk<sup>Gt(VICT48)710Lex</sup>  [background:] B6.129S5/SvEvBrd-Bckdk<sup>Gt(VICT48)710Lex</sup>	is_model_of	DOID:0090126	branched-chain keto acid dehydrogenase kinase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:22956686	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5561311	b2b2140Clo/b2b2140Clo  [background:] C57BL/6J-b2b2140Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806789	Tg(Thy1-SNCA*E57K)16Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:24662516	20161110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830676	Scn1b<sup>tm1.1Bion</sup>/Scn1b<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:20628201	20100927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6468047	Vps13b<sup>tm1.2Ics</sup>/Vps13b<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0111590	Cohen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32915983	20201021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428846	Pals1<sup>tm1Caw</sup>/Pals1<sup>tm1Caw</sup> Tg(rx3-icre)1Mjam/0  [background:] Not Specified	is_model_of	DOID:14791	Leber congenital amaurosis						ECO:0000033	author statement supported by traceable reference	PMID:22398208	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5649319	Dnah5<sup>b2b3491Clo</sup>/Dnah5<sup>b2b3491Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b3491Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820822	Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro/0 Tg(Igh-V186.2-TCL1A)3Cro/0  [background:] involves: C3H * C57BL/6 * FVB/N	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20566844	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175909	Apc<sup>tm1Rak</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:8090754	20050601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6303809	Fkrp<sup>tm1Scbr</sup>/?  [background:] Not Specified	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:26306834	20190515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714196	Nfix<sup>tm1Aes</sup>/Nfix<sup>tm1Aes</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:13300	Scheuermann's disease						ECO:0000033	author statement supported by traceable reference	PMID:17353270	20070710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6711274	Nosip<sup>Gt(OST138992)Lex</sup>/Nosip<sup>Gt(OST138992)Lex</sup>  [background:] B6.129S5-Nosip<sup>Gt(OST138992)Lex</sup>	is_model_of	DOID:4621	holoprosencephaly						ECO:0000033	author statement supported by traceable reference	PMID:25546391	20210519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6725727	Galc<sup>m4Btlr</sup>/Galc<sup>m4Btlr</sup>  [background:] C57BL/6J-Galc<sup>m4Btlr</sup>	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629233	Tg(ITGAM-cre)2781Gkl/0 Tg(SOD1*G37R)1Dwc/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16741123	20060718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6388550	Tbr1<sup>tm1.1Csbd</sup>/Tbr1<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:31680851	20200204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628826	Dnmt3b<sup>tm7Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294346	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(CAG-EGFP,-PAX8/PPARG)1Rkoe/0 Tg(TPO-cre)1Shk/0  [background:] involves: 129S4/SvJae * FVB/NCr * FVB/NJ	is_model_of	DOID:3963	thyroid gland carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21952241	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278980	Tg(TBK1)#Andm/0  [background:] B6J.Cg-Tg(TBK1)#Andm	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:28025332	20190219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4365644	Sh3pxd2b<sup>nee</sup>/Sh3pxd2b<sup>nee</sup>  [background:] B10.Cg-H2<sup>h4</sup> Sh3pxd2b<sup>nee</sup>/GrsrJ	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:21282566	20190222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6257025	Tg(APPV717F)109Ili/0  [background:] B6.Cg-Tg(APPV717F)109Ili	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28806762	20181121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5584179	Del(XArmcx5-Nxf3)3Jw/Y  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:0060388	chromosomal deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24569167	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5912488	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-ERBB2*)26Kkw/0  [background:] involves: FVB/N	is_model_of	DOID:4829	adenosquamous lung carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19122144	20171106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5690061	Tg(LONP1-mt-ND4*,-mCherry*)#Jguy  [background:] B6(D2)-Tg(LONP1-mt-ND4*,-mCherry*)#Jguy	is_model_of	DOID:705	Leber hereditary optic neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:26438859	20151014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830521	Tg(Camk2a-Tardbp)#Ckjs/Tg(Camk2a-Tardbp)#Ckjs  [background:] FVB/N-Tg(Camk2a-Tardbp)#Ckjs	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:20660618	20100924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6407058	Fgfr2<sup>tm3.1Cxd</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:18242159	20200430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4456428	Apc<sup>tm1Rsmi</sup>/Apc<sup>+</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:20176656	20100625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6152756	Tfap2b<sup>tm1Rbu</sup>/Tfap2b<sup>tm2Will</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:13550	angle-closure glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:27483349	20180423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7495807	Mocos<sup>em2(IMPC)Ics</sup>/Mocos<sup>em2(IMPC)Ics</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0070314	obstructive nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:35372998	20230706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4455020	Mitf<sup>mi-ew</sup>/Mitf<sup>mi-ew</sup>  [background:] involves: C57BL/6Bn * NAW	is_model_of	DOID:4997	Camurati-Engelmann disease						ECO:0000033	author statement supported by traceable reference	PMID:11930005	20100615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007810	Gt(ROSA)26Sor<sup>tm3(NOTCH3*R1031C)Sat</sup>/Gt(ROSA)26Sor<sup>+</sup> Notch3<sup>Gt(PST033)Byg</sup>/Notch3<sup>Gt(PST033)Byg</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:21555590	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028389	Pde6b<sup>rd1-4H</sup>/Pde6b<sup>rd1-4H</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5823559	Sf3b1<sup>tm1.1Mdf</sup>/Sf3b1<sup>+</sup> Tet2<sup>tm1.1Iaai</sup>/Tet2<sup>tm1.1Iaai</sup> Tg(Mx1-cre)1Cgn/?  [background:] involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * CBA/J	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27622333	20170208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174990	Psen1<sup>tm1Bdes</sup>/Psen1<sup>tm1Bdes</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9450754	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6314154	Grn<sup>tm2.1Far</sup>/Grn<sup>tm2.1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:29511098	20190613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275138	Nf1<sup>tm1c(KOMP)Wtsi</sup>/Nf1<sup>tm1c(KOMP)Wtsi</sup> Tg(Dhh-cre)1Mejr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * FVB/N	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:27482814	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359477	Npc1<sup>tm1Tacf</sup>/Npc1<sup>tm1Tacf</sup>  [background:] B6(Cg)-Npc1<sup>tm1Tacf</sup>	is_model_of	DOID:0070113	Niemann-Pick disease type C1						ECO:0000033	author statement supported by traceable reference	PMID:28167839	20190911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7488220	St6galnac1<sup>em1Len</sup>/St6galnac1<sup>em1Len</sup>  [background:] Not Specified	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:35303419	20230608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509636	Ppil1<sup>em3Jgg</sup>/Ppil1<sup>em3Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em3Jgg</sup>	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:33220177	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695480	Agl<sup>tm1a(EUCOMM)Wtsi</sup>/Agl<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:2748	glycogen storage disease III						ECO:0000033	author statement supported by traceable reference	PMID:24613482	20151110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315869	Lztr1<sup>tm1a(EUCOMM)Wtsi</sup>/Lztr1<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0060588	Noonan syndrome 10						ECO:0000033	author statement supported by traceable reference	PMID:30442762	20190702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688660	Lrit3<sup>tm1Lex</sup>/Lrit3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0110864	congenital stationary night blindness 1F						ECO:0000033	author statement supported by traceable reference	PMID:24598786	20151001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654880	Aldh5a1<sup>tm1Kmg</sup>/Aldh5a1<sup>tm1Kmg</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:15262267	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767995	Lyn<sup>tm1Ard</sup>/Lyn<sup>tm1Ard</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:20512127	20100729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6330737	Tg(KRT14-VP16/NR1I2)13Sdub/?  [background:] involves: C57BL/6	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:28927887	20190729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677020	Glra1<sup>tm1Rah</sup>/Glra1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	PMID:12954867	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7569326	Dnaaf5<sup>em1Slb</sup>/Dnaaf5<sup>em1Slb</sup>  [background:] C57BL/6-Dnaaf5<sup>em1Slb</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:37104040	20231229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393415	Klhl3<sup>tm1.1Slin</sup>/Klhl3<sup>tm1.1Slin</sup>  [background:] Not Specified	is_model_of	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:30148674	20200306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6758644	Cerkl<sup>em1Gmar</sup>/Cerkl<sup>tm1.1Geno</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0110368	retinitis pigmentosa 26						ECO:0000033	author statement supported by traceable reference	PMID:32658961	20210910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648371	Sox10<sup>gt</sup>/Sox10<sup>gt</sup>  [background:] GT/Le	is_model_of	DOID:0090111	PCWH syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25399070	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5573199	Tg(Thy1-Snca)1S13Putt/0 Uchl1<sup>tm1Dgen</sup>/Uchl1<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22355774	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3806986	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17567478	20080922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613741	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10021468	20060301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>	is_model_of	DOID:0110596	primary ciliary dyskinesia 21						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6476981	Alk<sup>tm1.1(ALK*F1174L)Heno</sup>/Alk<sup>tm1.1(ALK*F1174L)Heno</sup> Tg(Mpz-cre)94Imeg/0 Tg(Th-MYCN)41Waw/0  [background:] involves: 129X1/SvJ * BALB/c * C57BL/6 * SJL	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:31218818	20201202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6403356	Egfr<sup>Mhdadsk5</sup>/Egfr<sup>+</sup>  [background:] involves: 129S1/SvImJ * C3HeB/FeJ	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:28404843	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295996	Gt(ROSA)26Sor<sup>tm9(CAG-tdTomato)Hze</sup>/Gt(ROSA)26Sor<sup>+</sup> Hmga2<sup>tm1.1Mmw</sup>/Hmga2<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/0 Trp53<sup>tm2Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28790031	20190506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908194	Tg(Myh6-POLG*Y955C)DWcc/0  [background:] Not Specified	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17310215	20170905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461790	Ttll1<sup>tm1Seto</sup>/Ttll1<sup>tm1Seto</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:20498047	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437710	X/Tg(SERPINC1-SV40)BPbr  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1660504	20121004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437710	X/Tg(SERPINC1-SV40)BPbr  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:12763373	20121004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576883	Bmal1<sup>tm2Bra</sup>/Bmal1<sup>tm2Bra</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * CBA * ICR	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:20562852	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830468	Ank2<sup>tm1Bnt</sup>/Ank2<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0050824	sinoatrial node disease						ECO:0000033	author statement supported by traceable reference	PMID:20525877	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313509	Cc2d2a<sup>b2b1035Clo</sup>/Cc2d2a<sup>b2b1035Clo</sup>  [background:] C57BL/6J-Cc2d2a<sup>b2b1035Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045547	Bbs4<sup>tm1Vcs</sup>/Bbs4<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:15173597	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797222	Vldlr<sup>tm1Her</sup>/Vldlr<sup>tm1Her</sup>  [background:] B6;129S7-Vldlr<sup>tm1Her</sup>/J	is_model_of	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:18172119	20080715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4410294	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup> Rdh8<sup>tm1Kpal</sup>/Rdh8<sup>tm1Kpal</sup>  [background:] involves: 129 * 129S4/SvJae	is_model_of	DOID:0110015	age related macular degeneration 2						ECO:0000033	author statement supported by traceable reference	PMID:19494204	20091210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308055	Tg(Prnp-TARDBP)3cPtrc/Tg(Prnp-TARDBP)3cPtrc  [background:] C57BL/6-Tg(Prnp-TARDBP)3cPtrc	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:20702714	20120229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141747	Tg(UPII-SV40T)29Xrw/0  [background:] involves: FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:10416618	20110902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719414	Txnip<sup>Hyplip1</sup>/Txnip<sup>Hyplip1</sup>  [background:] HcB19/Dem-Txnip<sup>Hyplip1</sup>	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517370	Brca1<sup>tm1Bhk</sup>/Brca1<sup>+</sup> Cdkn2c<sup>tm1Yxi</sup>/Cdkn2c<sup>tm1Yxi</sup>  [background:] C.129-Cdkn2c<sup>tm1Yxi</sup> Brca1<sup>tm1Bhk</sup>	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22777348	20131111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563692	Tg(SV40-KLK7)1010Teg/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:11874483	20140515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2667791	Mgat2<sup>tm1.1Jxm</sup>/Mgat2<sup>tm1.1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR	is_model_of	DOID:0070253	congenital disorder of glycosylation type IIa						ECO:0000033	author statement supported by traceable reference	PMID:11805078	20190516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569926	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>tm1Mms</sup> Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:11854455	20140627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6492344	Prph2<sup>tm4.1Itl</sup>/Prph2<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060866	patterned macular dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:31914632	20210115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638914	Efna2<sup>tm1Jgf</sup>/Efna2<sup>tm1Jgf</sup> Efna3<sup>tm1Rax</sup>/Efna3<sup>tm1Rax</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * Swiss Webster	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25281279	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925369	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129T2/SvEms * FVB/N	is_model_of	DOID:2513	basal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23404854	20171120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313503	Tg(CAG-Rpgr)mRDefWrght/0  [background:] C57BL/6-Tg(CAG-Rpgr)mRDefWrght	is_model_of	DOID:0110414	retinitis pigmentosa 3						ECO:0000033	author statement supported by traceable reference	PMID:21546531	20120330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318528	Jag1<sup>tm2Grid</sup>/Jag1<sup>tm2Grid</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22156581	20120517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6717173	Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup>/Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA	is_model_of	DOID:12236	primary biliary cholangitis						ECO:0000033	author statement supported by traceable reference	PMID:33513427	20210623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448162	Acadl<sup>tm1Uab</sup>/Acadl<sup>tm1Uab</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9861014	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400427	Dpp4<sup>em1Rba</sup>/Dpp4<sup>+</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27892925	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652059	Ldb3<sup>tm1Chen</sup>/Ldb3<sup>tm1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:0081337	congenital myopathy						ECO:0000033	author statement supported by traceable reference	PMID:11696561	20230605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4398737	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Rako</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:19497369	20111003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6280686	Parl<sup>tm1.1Bdes</sup>/Parl<sup>tm1.1Bdes</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:30578322	20190228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582637	E2f5<sup>tm1Dli</sup>/E2f5<sup>tm1Dli</sup>  [background:] either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:9553039	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6376646	Arl2bp<sup>em1Visu</sup>/Arl2bp<sup>em1Visu</sup>  [background:] involves: 129S2/SvPasCrl * C57BL/6J * FVB/N	is_model_of	DOID:0110419	retinitis pigmentosa with or without situs inversus						ECO:0000033	author statement supported by traceable reference	PMID:29718757	20191114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580534	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Tg(Tyr-cre)3Gfk/0  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:0050471	Carney complex						ECO:0000033	author statement supported by traceable reference	PMID:15930266	20050701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286592	Tg(SOD1*G127X)716Mrkl/Tg(SOD1*G127X)716Mrkl  [background:] B6JBom.Cg-Tg(SOD1*G127X)716Mrkl	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14534160	20110926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5302224	Lzts2<sup>tm1.1Zsu</sup>/Lzts2<sup>tm1.1Zsu</sup>  [background:] B6.Cg-Lzts2<sup>tm1.1Zsu</sup>	is_model_of	DOID:18	urinary system disease						ECO:0000033	author statement supported by traceable reference	PMID:21949185	20170619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4414647	Tspan12<sup>tm1Wye</sup>/Tspan12<sup>tm1Wye</sup>  [background:] either: B6.129S5-Tspan12<sup>tm1Wye</sup> or FVB.129S5-Tspan12<sup>tm1Wye</sup>	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:20159112	20120326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6150914	Rnf146<sup>tm1.1Rtpl</sup>/Rnf146<sup>tm1.1Rtpl</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: C57BL/6J * CD-1	is_model_of	DOID:2256	osteochondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:28581440	20221010	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4353803	Tg(Ckm-GSN*D187N)AJewe/Tg(Ckm-GSN*D187N)AJewe  [background:] C57BL/6J-Tg(Ckm-GSN*D187N)AJewe	is_model_of	DOID:0050637	Finnish type amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:19549824	20090819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274280	Tg(Krt14-Rac1*G12V)#Mrnk/0  [background:] involves: CBA/CaJ	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:27294528	20190122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6260058	Dhtkd1<sup>tm1Zgwg</sup>/Dhtkd1<sup>tm1Zgwg</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q						ECO:0000033	author statement supported by traceable reference	PMID:29661920	20181213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712759	Plod1<sup>tm1Soin</sup>/Plod1<sup>tm1Soin</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:13359	Ehlers-Danlos syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17197443	20121106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5795582	Psen1<sup>tm1Tak</sup>/Psen1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:16377636	20160926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432192	Tg(YAC128)55Hay/0  [background:] FVB/N-Tg(YAC128)55Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16230019	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7309153	Zng1<sup>em1Skan</sup>/Zng1<sup>em1Skan</sup>  [background:] C57BL/6N-Zng1<sup>em1Skan</sup>	is_model_of	DOID:0080205	CAKUT						ECO:0000033	author statement supported by traceable reference	PMID:31862704	20220705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684657	Psen1<sup>tm1Vln</sup>/Psen1<sup>tm1Vln</sup> Tg(Thy1-cre)1Vln/0  [background:] involves: FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11978821	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7261388	Tshz3<sup>tm2.1Lafa</sup>/Tshz3<sup>tm2.1Lafa</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:31060802	20220414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402832	Tg(CAG-ACE2)AC70Ctkt/0  [background:] either: (involves: BALB/c * C3H/HeJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6 * C57BL/6J)	is_model_of	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17108019	20200403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192108	Tg(Ela1-Tgfa)150Bri/0 Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11159909	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356705	Myh6<sup>tm2Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052328	Pdcd10<sup>tm1Kwhi</sup>/Pdcd10<sup>tm1.1Kwhi</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060671	cerebral cavernous malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:21490399	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296910	Cacna1c<sup>tm2Itl</sup>/Cacna1c<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac	is_model_of	DOID:0060173	Timothy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21878566	20111201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258951	Cfap44<sup>em1Fzh</sup>/Cfap44<sup>em1Fzh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0070166	spermatogenic failure 20						ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock	is_model_of	DOID:13628	favism						ECO:0000033	author statement supported by traceable reference	PMID:3377761	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock	is_model_of	DOID:13628	favism						ECO:0000033	author statement supported by traceable reference	PMID:12777375	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock	is_model_of	DOID:13628	favism						ECO:0000033	author statement supported by traceable reference	PMID:14751857	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794972	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:14507660	20080624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276046	Tg(Myh6-Camk2d_ic)LJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273518	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Gt(ROSA)26Sor<sup>tm4(ACTB-tdTomato,-EGFP)Luo</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Flt3-cre)#Ccb/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:28846072	20190115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2167526	None [background:] C3H/HeJ	is_model_of	DOID:986	alopecia areata						ECO:0000033	author statement supported by traceable reference	PMID:26960166	20180624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2167526	None [background:] C3H/HeJ	is_model_of	DOID:986	alopecia areata						ECO:0000033	author statement supported by traceable reference	PMID:8006447	20180624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295260	Muc5ac<sup>tm1.1Evns</sup>/Muc5ac<sup>tm1.1Evns</sup>  [background:] B6.129S1-Muc5ac<sup>tm1.1Evns</sup>	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23272068	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842612	Frem2<sup>my</sup>/Frem2<sup>my</sup>  [background:] MY/HuLeJ	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659973	Dph1<sup>tm1.1Cmch</sup>/Dph1<sup>tm1.1Cmch</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610379	Csf1<sup>op</sup>/Csf1<sup>op</sup>  [background:] B6C3Fe a/a-Csf1<sup>op</sup>/J	is_model_of	DOID:13533	osteopetrosis						ECO:0000033	author statement supported by traceable reference	PMID:1887865	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897837	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(TPO-cre)1Shk/0  [background:] 129.Cg-Tg(TPO-cre)1Shk Trp53<sup>tm1Brn</sup> Pten<sup>tm2.1Ppp</sup>	is_model_of	DOID:3963	thyroid gland carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22190384	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693680	Fbxo11<sup>Jf</sup>/Fbxo11<sup>Mutt</sup>  [background:] involves: BALB/c * C3H/HeN	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:17035249	20080721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471141	Pkd1<sup>tm1.1Fqi</sup>/Pkd1<sup>tm1.1Fqi</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23236168	20130401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5560742	Eml1<sup>heco</sup>/Eml1<sup>heco</sup>  [background:] involves: C57BL/6 * NOR	is_model_of	DOID:2490	congenital nervous system abnormality						ECO:0000033	author statement supported by traceable reference	PMID:18562329	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5642272	Bmp4<sup>tm4Blh</sup>/Bmp4<sup>tm4Blh</sup> Isl1<sup>tm1(cre)Sev</sup>/Isl1<sup>+</sup>  [background:] involves: 129 * 129S6/SvEvTac	is_model_of	DOID:0080015	physical disorder						ECO:0000033	author statement supported by traceable reference	PMID:23028455	20180605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558016	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Scarb1<sup>tm1Kri</sup>/Scarb1<sup>tm1Kri</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:3393	coronary artery disease						ECO:0000033	author statement supported by traceable reference	PMID:24082102	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3528946	Ap3d1<sup>mh</sup>/Ap3d1<sup>mh</sup>  [background:] B6.C3-Grxcr1<sup>pi</sup>	is_model_of	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:1912584	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850111	Otc<sup>spf</sup>/Y  [background:] Not Specified	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7707692	20090717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850111	Otc<sup>spf</sup>/Y  [background:] Not Specified	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:3981356	20090717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5754385	Psen1<sup>tm2Shn</sup>/Psen1<sup>tm4.1Shn</sup> Psen2<sup>tm1Haa</sup>/Psen2<sup>tm1Haa</sup> Tg(Camk2a-cre)1Shn/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25741723	20160324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3691620	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:12746448	20120221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177705	Gck<sup>tm1Tka</sup>/Gck<sup>tm1Tka</sup>  [background:] involves: 129X1/SvJ * ICR	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:8530440	20050816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176761	Casr<sup>tm1Ces</sup>/Casr<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:7493018	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5493228	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * SJL/J	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:22868293	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473225	Cfap276<sup>em2.1Fuxi</sup>/Cfap276<sup>em2.1Fuxi</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050543	Charcot-Marie-Tooth disease intermediate type						ECO:0000033	author statement supported by traceable reference	PMID:32592472	20201119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415340	Tg(FOXJ1-ACE2)1Rba/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:26976607	20200507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393411	Klhl3<sup>tm1.1Slin</sup>/Klhl3<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:30148674	20200306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580092	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Hccs<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590142	Gck<sup>Rgsc149</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198726	Phex<sup>Mhdabap024</sup>/Phex<sup>+</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:29735309	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640134	Glb1<sup>tm1Jmat</sup>/Glb1<sup>tm1Jmat</sup>  [background:] involves: C57BL/6 * CBA * ICR	is_model_of	DOID:3322	GM1 gangliosidosis						ECO:0000033	author statement supported by traceable reference	PMID:9071485	20060808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640134	Glb1<sup>tm1Jmat</sup>/Glb1<sup>tm1Jmat</sup>  [background:] involves: C57BL/6 * CBA * ICR	is_model_of	DOID:3322	GM1 gangliosidosis						ECO:0000033	author statement supported by traceable reference	PMID:9337086	20060808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295856	Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>/Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6-Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>	is_model_of	DOID:0111456	Kaufman oculocerebrofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30808755	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772367	A<sup>vy</sup>/a  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:17101998	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772367	A<sup>vy</sup>/a  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:14242032	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036124	Ar<sup>tm1.1Verh</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14745012	20081106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661963	Insl3<sup>tm1Par</sup>/Insl3<sup>tm1Par</sup>  [background:] involves: 129/Sv * CD-1	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:10391220	20050705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4439084	None [background:] (NZB/BlNJ x NZW/LacJ)F1/J	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:19414767	20100408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6476983	Alk<sup>tm1.1(ALK*F1174L)Heno</sup>/Alk<sup>+</sup> Tg(Mpz-cre)94Imeg/0 Tg(Th-MYCN)41Waw/0  [background:] involves: 129X1/SvJ * BALB/c * C57BL/6 * SJL	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:31218818	20201202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177905	Eng<sup>tm1Dyl</sup>/Eng<sup>tm1Dyl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:10348742	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576735	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] C.129S4-Sh2d1a<sup>tm1Cpt</sup>	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15774582	20050513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7569326	Dnaaf5<sup>em1Slb</sup>/Dnaaf5<sup>em1Slb</sup>  [background:] C57BL/6-Dnaaf5<sup>em1Slb</sup>	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:37104040	20231229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7437702	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em1Mdj</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>	is_model_of	DOID:1572	normal pressure hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441077	Hdac4<sup>em1Hcu</sup>/Hdac4<sup>+</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:8670	eating disorder						ECO:0000033	author statement supported by traceable reference	PMID:27884425	20200710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766754	Del(11Mpo-Chad)18Brd/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:16489219	20080108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392628	Hspb8<sup>tm1Vti</sup>/Hspb8<sup>tm1Vti</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl	is_model_of	DOID:0111208	obsolete distal hereditary motor neuronopathy type 2A						ECO:0000033	author statement supported by traceable reference	PMID:28780615	20200303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677273	Mest<sup>tm1Masu</sup>/Mest<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12242721	20181015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511746	Lepr<sup>tm1Chua</sup>/Lepr<sup>tm1Chua</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15389315	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6150918	Daam1<sup>tm1.1Tpy</sup>/Daam1<sup>tm1.1Tpy</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd	is_model_of	DOID:0060036	intrinsic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:26526197	20180417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911329	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618137	Snrpn<sup>tm1Kaj</sup>/Snrpn<sup>+</sup>  [background:] either: 129S1-Snrpn<sup>tm1Kaj</sup> or (involves: 129S1/Sv * C57BL/6J)	is_model_of	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16368707	20060329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6098756	Mecp2<sup>tm1Jae</sup>/Y Chat<sup>tm2(cre)Lowl</sup>/Chat<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175903	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] involves: AKR/J * C57BL/6J	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:1350108	20090601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415595	Scn5a<sup>tm1.1Iba</sup>/Scn5a<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110646	long QT syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:30144447	20200508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835028	H2<sup>u</sup>/H2<sup>u</sup> Tg(TCRA)B1Jg/? Tg(TCRB)C14Jg/?  [background:] involves: C57BL/6 * C57BL/10SnSg * DBA/2 * PL/J	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:7679952	20190528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4833684	Serpina6<sup>tm1.1Mmp</sup>/Serpina6<sup>tm1.1Mmp</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0090030	corticosteroid-binding globulin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:20022933	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4833684	Serpina6<sup>tm1.1Mmp</sup>/Serpina6<sup>tm1.1Mmp</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0090030	corticosteroid-binding globulin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:22930537	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909973	Tg(Myh6/tetO-Mybpc3*)#Rbns/0 Tg(Myh6-tTA)55Rbns/0  [background:] involves: FVB/N	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:23852539	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393881	Tmprss9<sup>tm1.3Hzo</sup>/Tmprss9<sup>tm1.3Hzo</sup>  [background:] involves: 129S1/Sv * C57BL/6J * C57BL/6NTac	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:31943016	20200311	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6117171	None [background:] PWD/PhJ	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25605412	20180807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6491490	Frmd7<sup>tm1b(KOMP)Wtsi</sup>/Y  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:0111790	congenital nystagmus 1						ECO:0000033	author statement supported by traceable reference	PMID:33007925	20210112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286248	Tg(Prnp-MAPT*P301S)50Hiw/0  [background:] B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	is_model_of	DOID:680	tauopathy						ECO:0000033	author statement supported by traceable reference	PMID:24406748	20190405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6194624	Tg(GFAP-ATXN7*92Q)2521Als/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)	is_model_of	DOID:0110915	childhood hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817493	Tg(ACTA1-FRG1)medRotu/0  [background:] C57BL/6-Tg(ACTA1-FRG1)medRotu	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:16341202	20081124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5708536	Enam<sup>tm1.1Jcch</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:24603688	20160216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7442184	Ccdc34<sup>em1Fzg</sup>/Ccdc34<sup>em1Fzg</sup>  [background:] C57BL/6-Ccdc34<sup>em1Fzg</sup>	is_model_of	DOID:0111910	spermatogenic failure						ECO:0000033	author statement supported by traceable reference	PMID:34348960	20230308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>	is_model_of	DOID:0060327	omphalocele						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575502	T(16;17)43H/0  [background:] involves: 101 * C3H * PWD/Ph	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18629032	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652375	Fxn<sup>tm1Mkn</sup>/Fxn<sup>tm1Pand</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25104852	20150316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3626292	Sgcb<sup>tm1Kcam</sup>/Sgcb<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E						ECO:0000033	author statement supported by traceable reference	PMID:10678176	20060706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266500	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:8466	retinal degeneration						ECO:0000033	author statement supported by traceable reference	PMID:33539865	20220504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838967	Oat<sup>rhg</sup>/Oat<sup>rhg</sup>  [background:] B6Ei;AKR-Oat<sup>rhg</sup>/J	is_model_of	DOID:1415	gyrate atrophy						ECO:0000033	author statement supported by traceable reference	PMID:25264521	20180626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442125	b2b1594Clo/b2b1594Clo  [background:] C57BL/6J-b2b1594Clo	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752313	Tbr1<sup>tm1Jlr</sup>/Tbr1<sup>+</sup>  [background:] B6.129X1-Tbr1<sup>tm1Jlr</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:24441682	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278552	C9orf72<sup>tm1Eggn</sup>/C9orf72<sup>tm1Eggn</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276042	Tg(Myh6-Camk2d_ic)MJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4840090	Nf1<sup>tm1Par</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * FVB/N	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:18451155	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438260	Amelx<sup>Rgsc888</sup>/Amelx<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054803	Aipl1<sup>tm1Tili</sup>/Aipl1<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110332	Leber congenital amaurosis 4						ECO:0000033	author statement supported by traceable reference	PMID:15365173	20050531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694491	Lrp6<sup>tm1Arma</sup>/Lrp6<sup>tm1Arma</sup>  [background:] C57BL/6-Lrp6<sup>tm1Arma</sup>	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:25917329	20151103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294359	Trib2<sup>Tg(Thy1-Trh/APP*)2.1Ingm</sup>/Trib2<sup>+</sup> Tg(Thy1-APP*)2.2Ingm/0  [background:] involves: C57BL/6 * DBA/1	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21900558	20111031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661820	Celsr1<sup>Scy</sup>/Celsr1<sup>+</sup> Scrib<sup>Crc</sup>/Scrib<sup>+</sup>  [background:] C3H.Cg-Scrib<sup>Crc</sup> Celsr1<sup>Scy</sup>	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:25128525	20150915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510652	Psen1<sup>tm1Lpr</sup>/Psen1<sup>tm1Lpr</sup> Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15466394	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663064	Mitf<sup>Mi-wh</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	MGI:2662103	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611042	Ldlrap1<sup>Gt(OST149604)Lex</sup>/Ldlrap1<sup>Gt(OST149604)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0090105	autosomal recessive hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:15472122	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110836	Tg(TTR)#Jbux/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:11310831	20180118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437605	Ext1<sup>tm1Vcs</sup>/Ext1<sup>tm1Vcs</sup> Tg(Col2a1-rtTA,tetO-cre)22Pjro/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:206	hereditary multiple exostoses						ECO:0000033	author statement supported by traceable reference	PMID:20080592	20171214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558108	Tg(CMV-SALL4_iB)#Chai/?  [background:] Not Specified	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16763212	20140411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575735	Smpd3<sup>tm1Wst</sup>/Smpd3<sup>tm1Wst</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:15764706	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653473	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(Mt1-Hgf)19Lmb/0  [background:] involves: 129/Sv * C57BL/6J * FVB/N * SJL	is_model_of	DOID:3247	rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:12368906	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056394	Tg(Prnp-ATN1)150Dbo/?  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000033	author statement supported by traceable reference	PMID:10677044	20110810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7435338	Lztfl1<sup>tm1.3Zpl</sup>/Lztfl1<sup>tm1.3Zpl</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N	is_model_of	DOID:0110139	Bardet-Biedl syndrome 17						ECO:0000033	author statement supported by traceable reference	PMID:30423168	20230217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429452	Fgfr4<sup>tm1Axul</sup>/Fgfr4<sup>tm1Axul</sup> Tg(WapTgfa)215Bri/0  [background:] B6.Cg-Fgfr4<sup>tm1Axul</sup> Tg(WapTgfa)215Bri	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:20068154	20100219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178291	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10192392	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790702	Glra1<sup>spd-ot9J</sup>/Glra1<sup>spd-ot9J</sup>  [background:] B6.Cg-Glra1<sup>spd-ot9J</sup>/GrsrJ	is_model_of	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	MGI:5790609	20160907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833377	Fras1<sup>tm1Chpk</sup>/Fras1<sup>tm1Chpk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15623520	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450976	Tg(Myh6-Tnf)1.6Amf/0  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15923312	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429499	Stat3<sup>tm1Dlv</sup>/Stat3<sup>tm1Dlv</sup> Tg(Csf1r-icre)1Jwp/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:20042677	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5550384	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24163243	20140312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7493591	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] 129S1.129S4(B6)-Chd7<sup>Gt(S20-7E1)Sor</sup>	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19279158	20230629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7493591	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] 129S1.129S4(B6)-Chd7<sup>Gt(S20-7E1)Sor</sup>	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21596839	20230629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000531	Id1<sup>tm1Zhu</sup>/Id1<sup>+</sup> Id3<sup>tm1Zhu</sup>/Id3<sup>tm1Zhu</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:34434211	20211007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6472964	Agxt<sup>tm1Ull</sup>/Agxt<sup>tm1Ull</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111670	primary hyperoxaluria type 1						ECO:0000033	author statement supported by traceable reference	PMID:31821850	20201118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834481	Tg(Ly6a-BCR/ABL1)IS1AIsg/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:19037256	20090305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300906	Gucy2c<sup>tm1Gar</sup>/Gucy2c<sup>tm1Gar</sup>  [background:] B6.129S6-Gucy2c<sup>tm1Gar</sup>	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21865642	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5506904	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr/0  [background:] FVB.Cg-Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23873941	20130918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653051	Ndn<sup>tm1Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * FVB	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10508517	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719416	Txnip<sup>Hyplip1</sup>/Txnip<sup>Hyplip1</sup>  [background:] involves: CAST/Ei * HcB19/Dem	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578132	Tg(Alb-PDGFC)#Jcam/0  [background:] involves: C57BL/6	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23929039	20140822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692534	Mc4r<sup>tm1Lowl</sup>/Mc4r<sup>tm1Lowl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:21906580	20111123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517439	Tg(CTSG-RARA/ZBTB16)#Sjch/0 Tg(CTSG-ZBTB16/RARA)#Sjch/0  [background:] Not Specified	is_model_of	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23382200	20131112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361326	Tbx22<sup>tm1.1Sta</sup>/Y  [background:] involves: 129/Sv * CD-1	is_model_of	DOID:0060613	X-linked cleft palate with or without ankyloglossia						ECO:0000033	author statement supported by traceable reference	PMID:19648291	20091013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7448446	Cfap61<sup>em1Yqt</sup>/Cfap61<sup>em1Yqt</sup>  [background:] C57BL/6-Cfap61<sup>em1Yqt</sup>	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:35387802	20230328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6101467	Fus<sup>tm1.1Emcf</sup>/Fus<sup>+</sup>  [background:] involves: C3H * C57BL/6J * C57BL/6N	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:29053787	20171215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038948	Rlbp1<sup>tm1Jsa</sup>/Rlbp1<sup>tm1Jsa</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0050683	Bothnia retinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11301032	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438702	Ank1<sup>MRI23420</sup>/Ank1<sup>MRI23420</sup>  [background:] SJL/J-Ank1<sup>MRI23420</sup>	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:22723917	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430234	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup> Tg(Prrx1-FUS/DDIT3)1Mete/0  [background:] involves: 129S2/SvPas * C57BL/6 * CBA	is_model_of	DOID:5363	myxoid liposarcoma						ECO:0000033	author statement supported by traceable reference	PMID:22293175	20120806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521547	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 Tg(tetO-RNAi:Trp53)ASlowe/0  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581037	Crb1<sup>rd8</sup>/Crb1<sup>rd8</sup>  [background:] STOCK Crb1<sup>rd8</sup>/J	is_model_of	DOID:0110079	Leber congenital amaurosis 8						ECO:0000033	author statement supported by traceable reference	PMID:20089206	20110520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6305814	H2<sup>u</sup>/H2<sup>u</sup> Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(Tcra19,Tcrb19)#Stl/0  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6 * PL/J) or (involves: 129S7/SvEvBrd * C57BL/6 * C57BL/10 * PL/J)	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:7520367	20190528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7435649	Dzip1<sup>em1Yxc</sup>/Dzip1<sup>em1Yxc</sup>  [background:] Not Specified	is_model_of	DOID:0112175	spermatogenic failure 47						ECO:0000033	author statement supported by traceable reference	PMID:32051257	20230220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908019	Del(7Chrna7-Fan1)1Mima/+  [background:] C57BL/6N-Del(7Chrna7-Fan1)1Mima	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26658876	20170901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907611	Tg(MT2A-TGFBR2)#Rser/0  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19933419	20170828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688001	Apob<sup>tm1Mae</sup>/Apob<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0111061	familial hypobetalipoproteinemia 2						ECO:0000033	author statement supported by traceable reference	PMID:10705993	20061117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688001	Apob<sup>tm1Mae</sup>/Apob<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0111061	familial hypobetalipoproteinemia 2						ECO:0000033	author statement supported by traceable reference	PMID:8921909	20061117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7517090	Rab33b<sup>em1Rmr</sup>/Rab33b<sup>em1Rmr</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0081271	Smith-McCort dysplasia 2						ECO:0000033	author statement supported by traceable reference	PMID:37359363	20230814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6403447	Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>/Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>  [background:] C57BL/6-Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30142928	20200409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5556112	Il6ra<sup>tm1.1(IL6R)Csk</sup>/Il6ra<sup>tm1.1(IL6R)Csk</sup> Tg(H2-L-IL6)40Csk/0  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0060704	lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23378927	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903891	Ildr1<sup>tm1.1Lwa</sup>/Ildr1<sup>tm1.1Lwa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110500	autosomal recessive nonsyndromic deafness 42						ECO:0000033	author statement supported by traceable reference	PMID:25819842	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695549	Abcd3<sup>tm1Safe</sup>/Abcd3<sup>tm1Safe</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0111066	congenital bile acid synthesis defect 5						ECO:0000033	author statement supported by traceable reference	PMID:25168382	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444635	Elp1<sup>tm1Id</sup>/Elp1<sup>tm1.1Id</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22922231	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315241	Irf6<sup>tm1Bcsl</sup>/Irf6<sup>tm1Bcsl</sup> Pitx2<sup>tm4(cre)Jfm</sup>/Pitx2<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:9296	cleft lip						ECO:0000033	author statement supported by traceable reference	PMID:27369589	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668613	Nr2e3<sup>rd7</sup>/Nr2e3<sup>rd7</sup>  [background:] Not Specified	is_model_of	DOID:0090059	enhanced S-cone syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10805811	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700786	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] B6.D2-Cacna1a<sup>tg</sup>/J	is_model_of	DOID:0050835	generalized dystonia						ECO:0000033	author statement supported by traceable reference	PMID:22850483	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445344	Flt3<sup>tm1Dgg</sup>/Flt3<sup>+</sup> Kmt2a<sup>tm1Clgr</sup>/Kmt2a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6J	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22674806	20121211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526050	Ccn6<sup>tm2Mawa</sup>/Ccn6<sup>tm2Mawa</sup>  [background:] 129S/SvEv-Ccn6<sup>tm2Mawa</sup>	is_model_of	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood						ECO:0000033	author statement supported by traceable reference	PMID:15601861	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6514900	Nexn<sup>tm1Chen</sup>/Nexn<sup>tm1Chen</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110424	dilated cardiomyopathy 1CC						ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6438116	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>tm3.2Cmpl</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5287852	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1Jme</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J * SJL	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:15076752	20111002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555838	b2b2059Clo/b2b2059Clo  [background:] C57BL/6J-b2b2059Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831430	Brca2<sup>tm1Brn</sup>/Brca2<sup>tm1Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11694875	20090212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429553	Ak7<sup>Gt(OST434404)Lex</sup>/Ak7<sup>Gt(OST434404)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911326	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907166	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup> Tg(Myh6-TNNI3*G203S)1Chs/0  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18362229	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566661	Tg(Pbsn-Tag)12T10Rjm/0  [background:] involves: CD-1	is_model_of	DOID:2526	prostate adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11280793	20180207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360917	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-PLAGL2)P3Ysy/0  [background:] involves: FVB/N	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:19574421	20091008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044561	Gck<sup>Gena348</sup>/Gck<sup>Gena348</sup>  [background:] involves: BALB/c * C3H/He	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15161764	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7431292	Rr124128<sup>tm1.2Jfer</sup>/Rr124128<sup>tm1.2Jfer</sup>  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:36202974	20230203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820806	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/Sv * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:18414682	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581611	Tg(Ins2-Fasl)24Ach/0  [background:] NOD-Tg(Ins2-Fasl)24Ach/J	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9094710	20061006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040304	Dnmt3a<sup>tm1Enl</sup>/Dnmt3a<sup>tm1Enl</sup> Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm1Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:10555141	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664346	Timp3<sup>tm1Web</sup>/Timp3<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0090114	Sorsby's fundus dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:12147610	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805043	a/a Hps6<sup>ru</sup>/Hps6<sup>ru</sup>  [background:] B6.Cg-Hps6<sup>ru</sup>	is_model_of	DOID:0060544	Hermansky-Pudlak syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3704912	Dbt<sup>tm1Geh</sup>/Dbt<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:9269	maple syrup urine disease						ECO:0000033	author statement supported by traceable reference	PMID:16579849	20070426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711939	Col17a1<sup>tm1Shzu</sup>/Col17a1<sup>tm1Shzu</sup>  [background:] B6.129S-Col17a1<sup>tm1Shzu</sup>	is_model_of	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:17322897	20090304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358609	Serpina1<sup>em2Chmu</sup>/Serpina1<sup>em2Chmu</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:29453277	20190906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662550	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:12091909	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437476	Cryaa<sup>tm1Ady</sup>/Cryaa<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:19619312	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664211	Phl1<sup>101/H</sup>/Phl1<sup>101/H</sup>  [background:] involves: 101/H * MAI/Pas	is_model_of	DOID:0110496	autosomal recessive nonsyndromic deafness 38						ECO:0000033	author statement supported by traceable reference	PMID:16897347	20061021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476929	Epcam<sup>Gt(RST412)Byg</sup>/Epcam<sup>Gt(RST412)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060776	congenital diarrhea 5 with tufting enteropathy						ECO:0000033	author statement supported by traceable reference	PMID:23209569	20130502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515356	Ccn6<sup>tm2Mawa</sup>/Ccn6<sup>tm2Mawa</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood						ECO:0000033	author statement supported by traceable reference	PMID:24040393	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790635	Pdgfrb<sup>tm1Msas</sup>/Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu/0  [background:] B6J.Cg-Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25803852	20160902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684461	Twist1<sup>Pas</sup>/Twist1<sup>+</sup>  [background:] involves: C57BL/6 * PDT/Pas	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14724733	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5492109	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:21478499	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784730	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>tm1.1Mag</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:1925	Coffin-Siris syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26806701	20171117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2429786	Hmox1<sup>tm1Mlee</sup>/Hmox1<sup>tm1Mlee</sup>  [background:] involves: 129S2/SvPas * BALB/c	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:19706490	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6717362	Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>/Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:32877400	20210625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20131014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6696394	Polr3h<sup>em2Cfe</sup>/Polr3h<sup>em2Cfe</sup>  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:5426	primary ovarian insufficiency						ECO:0000033	author statement supported by traceable reference	PMID:30830215	20210506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908988	Tg(Myh6-Tnnt2*R92W)1Jcf/0  [background:] B6.Cg-Tg(Myh6-Tnnt2*R92W)1Jcf	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:16326803	20170913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946226	Dag1<sup>tm2Kcam</sup>/Dag1<sup>tm2Kcam</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19797173	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903753	Map3k20<sup>em2Smun</sup>/Map3k20<sup>em2Smun</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl	is_model_of	DOID:0090020	split hand-foot malformation						ECO:0000033	author statement supported by traceable reference	PMID:26755636	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174947	Edn3<sup>tm1Ywa</sup>/Edn3<sup>tm1Ywa</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110954	Waardenburg syndrome type 4B						ECO:0000033	author statement supported by traceable reference	PMID:8001160	20100316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844656	Myf6<sup>tm1(cre)Mrc</sup>/Myf6<sup>+</sup> Pax3<sup>tm1Mrc</sup>/Pax3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:15489287	20090519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522660	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15082532	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836920	Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>/Igh-J<sup>+</sup>  [background:] B6.129P2-Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:19017966	20090324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5703659	Fmr1<sup>tm1Cgr</sup>/Y Tg(ACTB-Eif4e)#Ppp/0  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26306459	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696196	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] D2.NON(NZO)-Col4a4<sup>bwk</sup>/GrsrJ	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24522496	20151116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526972	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21822287	20140106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655702	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] involves: C3H/He	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446598	Acadvl<sup>tm1Uab</sup>/Acadvl<sup>tm1Uab</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:11590124	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590085	Fem1b<sup>tm1Jfma</sup>/Fem1b<sup>tm1Jfma</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16024793	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690017	Tg(Myh6-TNNI3*G203S)1Chs/0  [background:] Not Specified	is_model_of	DOID:0110313	hypertrophic cardiomyopathy 7						ECO:0000033	author statement supported by traceable reference	PMID:16950368	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461053	Abca12<sup>el12</sup>/Abca12<sup>el12</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:18802465	20100721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523888	Scn1a<sup>tm2.1Kzy</sup>/Scn1a<sup>+</sup> Tg(Pvalb-cre)1Tama/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23922229	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714838	Xylt2<sup>tm1Meh</sup>/Xylt2<sup>tm1Meh</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0080322	polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:17517600	20190924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6279179	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(PRNP)23454Sbp/0  [background:] involves: 129S7/SvEvBrd * FVB/N	is_model_of	DOID:5435	variant Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:27440899	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188511	None [background:] SAMP6/TaSlc	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:29618833	20180715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907647	Tg(HBx-HCV)C5Tto/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15618537	20170829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286094	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(GFAP-TAg121)1Tvd/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2 * FVB/N	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:15958561	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653351	Nr1h2<sup>tm1.1Gstr</sup>/Nr1h2<sup>tm1.1Gstr</sup> Nr1h3<sup>tm1.1Gstr</sup>/Nr1h3<sup>tm1.1Gstr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:3907	lung squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27335465	20190122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2388265	Adrb1<sup>tm1Bkk</sup>/Adrb1<sup>tm1Bkk</sup> Adrb2<sup>tm1Bkk</sup>/Adrb2<sup>tm1Bkk</sup> Adrb3<sup>tm1Lowl</sup>/Adrb3<sup>tm1Lowl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2 * FVB/N	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12161655	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110829	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>/Sclt1<sup>Tg(CAG-sb10)1Dla</sup>  [background:] FVB/N-Sclt1<sup>Tg(CAG-sb10)1Dla</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28486600	20180118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445374	Rc3h1<sup>san</sup>/Rc3h1<sup>+</sup>  [background:] involves: C57BL/6JSfdAnu	is_model_of	DOID:0050749	peripheral T-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22700722	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839497	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJae * ICR	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:18474617	20101123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>	is_model_of	DOID:3312	bipolar disorder						ECO:0000033	author statement supported by traceable reference	PMID:22025725	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>	is_model_of	DOID:3312	bipolar disorder						ECO:0000033	author statement supported by traceable reference	PMID:24342563	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4420394	Scn4a<sup>tm1Ljh</sup>/Scn4a<sup>tm1Ljh</sup>  [background:] B6.129S4-Scn4a<sup>tm1Ljh</sup>	is_model_of	DOID:14451	hyperkalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438223	Tg(ACTB-APP*V717F)1Colm/0  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20085783	20100330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16113078	20181012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538526	Mecp2<sup>tm3Meg</sup>/Y  [background:] B6.129-Mecp2<sup>tm3Meg</sup>	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23770587	20140205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3608495	Mybpc3<sup>tm1Lcrr</sup>/Mybpc3<sup>+</sup>  [background:] involves: 129S4/SvJae * Black Swiss	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:15249187	20051227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689381	Cftr<sup>tm3Mrc</sup>/Cftr<sup>tm3Mrc</sup>  [background:] B6.129S6-Cftr<sup>tm3Mrc</sup>	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:15246977	20061130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417904	Junb<sup>tm3Wag</sup>/Junb<sup>tm3Wag</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C3H * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:19918056	20100115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437568	Mid1<sup>tm1Mero</sup>/Y  [background:] B6.Cg-Mid1<sup>tm1Mero</sup>	is_model_of	DOID:0080697	Opitz GBBB syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20181585	20220608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5478500	Fas<sup>lpr</sup>/Fas<sup>lpr</sup> Tlr9<sup>tm1Aki</sup>/Tlr9<sup>tm1Aki</sup>  [background:] MRL.Cg-Tlr9<sup>tm1Aki</sup> Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:16973389	20130505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836556	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup> Tg(MUC1)79.24Gend/0  [background:] B6.Cg-Kras<sup>tm4Tyj</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup> Tg(MUC1)79.24Gend	is_model_of	DOID:657	adenoma						ECO:0000033	author statement supported by traceable reference	PMID:18713982	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275997	Ezh2<sup>em1Jbn</sup>/Ezh2<sup>em1Jbn</sup>  [background:] C57BL/6J-Ezh2<sup>em1Jbn</sup>	is_model_of	DOID:14731	Weaver syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29244146	20190205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429156	Tg(GFAP-HTT*160Q)1Xjl/0  [background:] either: (involves: FVB/NCrl) or (involves: C3H * C57BL/6 * FVB/NCrl)	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20018729	20100218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651508	Gba1<sup>tm1Rlp</sup>/Gba1<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:11994410	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487398	b2b1941Clo/b2b1941Clo  [background:] C57BL/6J-b2b1941Clo	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6101473	Fxn<sup>tm1.1Pand</sup>/Fxn<sup>tm1Mkn</sup>  [background:] B6.Cg-Fxn<sup>tm1.1Pand</sup> Fxn<sup>tm1Mkn</sup>/J	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:28444186	20171215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037638	Phex<sup>Hyp-2J</sup>/Y  [background:] C57BL/6-Phex<sup>Hyp-2J</sup>/J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5288598	Nrp1<sup>tm1.1Cruh</sup>/Nrp1<sup>tm1.1Cruh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:1727	retinal vein occlusion						ECO:0000033	author statement supported by traceable reference	PMID:21852397	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4455025	Rho<sup>Tvrm4</sup>/Rho<sup>+</sup>  [background:] B6.Cg-Rho<sup>Tvrm4</sup>/Pjn	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:20207741	20130619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661915	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:12376594	20050531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7314416	Ighmbp2<sup>em1Cll</sup>/Ighmbp2<sup>em1Cll</sup>  [background:] FVB/NJ-Ighmbp2<sup>em1Cll</sup>	is_model_of	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:34726235	20220720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431966	Tg(RIP1-Tag)2Dh/0  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:2986015	20120821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838157	Tg(COL1A1)73Prc/0  [background:] involves: FVB/N	is_model_of	DOID:0110334	osteogenesis imperfecta type 1						ECO:0000033	author statement supported by traceable reference	PMID:8432871	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652717	Trp53<sup>tm1Brd</sup>/Trp53<sup>tm1Brd</sup> Xrcc4<sup>tm2.1Fwa</sup>/Xrcc4<sup>tm2Fwa</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16670198	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696742	Tg(Prl-EGFR)#Sme/0  [background:] Not Specified	is_model_of	DOID:5394	prolactinoma						ECO:0000033	author statement supported by traceable reference	PMID:25375038	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276334	Tg(CAG-Ncoa6)87Hwl/0  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763530	Dgkd<sup>Gt(RRT600)Byg</sup>/Dgkd<sup>Gt(RRT600)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050561	Lennox-Gastaut syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17357084	20071210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710324	Cdkn2c<sup>tm1Bbd</sup>/Cdkn2c<sup>tm1Bbd</sup> Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16260494	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6505557	Apc<sup>tm2Rak</sup>/Apc<sup>+</sup> Kras<sup>tm1.1Khai</sup>/Kras<sup>+</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:30952657	20210209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7367115	Rpl5<sup>Skax23-Jus</sup>/Rpl5<sup>+</sup>  [background:] 129S6.B6-Rpl5<sup>Skax23-Jus</sup>	is_model_of	DOID:0111879	Diamond-Blackfan anemia 6						ECO:0000033	author statement supported by traceable reference	PMID:34464976	20221026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582680	Mafa<sup>tm1Staka</sup>/Mafa<sup>tm1Staka</sup>  [background:] involves: ICR	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15923615	20050729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839392	Tg(CAG-Has2)99Nita/0 Tg(MMTV-cre)4Mam/0 Tg(MMTVneu)202Mul/0  [background:] FVB.Cg-Tg(CAG-Has2)99Nita Tg(MMTV-cre)4Mam Tg(MMTVneu)202Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:20823158	20101123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700822	Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup> Wrn<sup>tm1Lgu</sup>/Wrn<sup>tm1Lgu</sup>  [background:] involves: 129/Sv * BALB/c * C57BL/6 * SLJ	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:24626990	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618124	Dicer1<sup>tm1Snj</sup>/Dicer1<sup>tm1Snj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup> Tg(KRT5-cre/PGR)1Der/0  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6N * FVB/N * ICR	is_model_of	DOID:2513	basal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24979267	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5583019	Apc<sup>tm1Rsmi</sup>/Apc<sup>tm1Rsmi</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:24474556	20140919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3847120	Lepr<sup>brta</sup>/Lepr<sup>brta</sup>  [background:] C57BL/6JSfdAnu-Lepr<sup>brta</sup>/Anu	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:3611487	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5756630	Minar2<sup>tm1b(KOMP)Wtsi</sup>/Minar2<sup>tm1b(KOMP)Wtsi</sup>  [background:] C57BL/6N-Minar2<sup>tm1b(KOMP)Wtsi</sup>/Wtsi	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:32954300	20210113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850052	Nlrp3<sup>tm2Hhf</sup>/Nlrp3<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/?  [background:] involves: 129/Sv * C57BL/6 * CBA	is_model_of	DOID:0090062	familial cold autoinflammatory syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19501000	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441464	Snx10<sup>em1Ael</sup>/Snx10<sup>em1Ael</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6JOlaHsd	is_model_of	DOID:0110940	autosomal recessive osteopetrosis 8						ECO:0000033	author statement supported by traceable reference	PMID:32278070	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6302764	Borcs7<sup>Q87X</sup>/Borcs7<sup>Q87X</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:2476	hereditary spastic paraplegia						ECO:0000033	author statement supported by traceable reference	PMID:30067980	20190513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559465	Tg(KRT14-HPV8)85Vuc/0  [background:] FVB.Cg-Tg(KRT14-HPV8)85Vuc	is_model_of	DOID:4159	skin cancer						ECO:0000033	author statement supported by traceable reference	PMID:15735026	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174761	Tcirg1<sup>oc</sup>/Tcirg1<sup>oc</sup>  [background:] B6C3Fe a/a-Tcirg1<sup>oc</sup>/J	is_model_of	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000033	author statement supported by traceable reference	PMID:10709991	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715723	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15231697	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358608	Serpina1<sup>em1Chmu</sup>/Serpina1<sup>em1Chmu</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:29453277	20190906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530658	Kiss1r<sup>tm1Coll</sup>/Kiss1r<sup>tm1Coll</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:14573733	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7467137	Lrp5<sup>em1Xjz</sup>/Lrp5<sup>em1Xjz</sup>  [background:] C57BL/6J-Lrp5<sup>em1Xjz</sup>	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7447442	Hpdl<sup>em1Jgg</sup>/Hpdl<sup>em1Jgg</sup>  [background:] C57BL/6-Hpdl<sup>em1Jgg</sup>	is_model_of	DOID:1289	neurodegenerative disease						ECO:0000033	author statement supported by traceable reference	PMID:33188300	20230327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524134	Fat1<sup>Gt(KST249)Byg</sup>/Fat1<sup>Gt(KST249)Byg</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4354208	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(Tyr-BRAF*V600E)476Fgh/0  [background:] involves: 129/Sv * C57BL/6J * CBA * SJL	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:19398955	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586968	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup> Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3H/He * C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:12777251	20050908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141744	Tg(UPII-SV40T)2Xrw/0  [background:] involves: FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:10416618	20110902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297860	A<sup>y</sup>/a Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * KK/TaJcl	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21779871	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428897	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22266220	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304474	Tg(RP11-209M4)AGglo/Tg(RP11-209M4)AGglo  [background:] FVB-Tg(RP11-209M4)4Gglo	is_model_of	DOID:0080036	SOST-related sclerosing bone dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:15965026	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675149	Gdnf<sup>tm1Rosl</sup>/Gdnf<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:12668632	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174933	Aqp3<sup>tm1Ask</sup>/Aqp3<sup>tm1Ask</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:10737773	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846169	Hba<sup>tm1(HBA)Tow</sup>/Hba<sup>tm1(HBA)Tow</sup> Hbb<sup>tm2(HBG1,HBD,HBB*)Ryan</sup>/Hbb<sup>tm2(HBG1,HBD,HBB*)Ryan</sup>  [background:] Not Specified	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:19258591	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583551	Tg(ITGA5)0794Fmw/0 Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421776	Cd74<sup>tm1Anjm</sup>/Cd74<sup>+</sup> Lmo2<sup>tm2(cre)Thr</sup>/Lmo2<sup>+</sup> Smim3<sup>tm1Anjm</sup>/Smim3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19966810	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431978	Pten<sup>tm1Rdp</sup>/Pten<sup>tm1Rdp</sup> Tert<sup>tm3Rdp</sup>/Tert<sup>tm3Rdp</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22341455	20120822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695040	Glra1<sup>spd</sup>/Glra1<sup>spd</sup>  [background:] involves: A/HeJ	is_model_of	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	PMID:8733750	20070130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313256	Nhlrc1<sup>tm1Bmin</sup>/Nhlrc1<sup>tm1Bmin</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:21077101	20190214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906239	Tg(Myh6-ACTC1*E361G)361.20Sbm/0  [background:] Not Specified	is_model_of	DOID:0110456	dilated cardiomyopathy 1R						ECO:0000033	author statement supported by traceable reference	PMID:20600154	20170807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715267	Gfra1<sup>tm1Jmi</sup>/Gfra1<sup>tm2Jmi</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129/Sv * C57BL/6 * CBA * SJL	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:17507417	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317649	Dnah11<sup>b2b1279Clo</sup>/Dnah11<sup>b2b1279Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1279Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702932	Slc6a3<sup>tm1(cre)Lrsn</sup>/Slc6a3<sup>+</sup> Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:17227870	20110624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7263380	Cftr<sup>tm1.1Sdw</sup>/Cftr<sup>tm1.1Sdw</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:35392567	20220425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029356	Slc6a6<sup>tm1Dhau</sup>/Slc6a6<sup>tm1Dhau</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:11772953	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177313	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] involves: STOCK Grhl3<sup>ct</sup> * M. m. molossinus	is_model_of	DOID:0110563	autosomal dominant nonsyndromic deafness 36						ECO:0000033	author statement supported by traceable reference	PMID:7719036	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665272	Frem1<sup>bat</sup>/Frem1<sup>bat</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6790245	Ank2<sup>tm1Bnt</sup>/Ank2<sup>tm1Bnt</sup>  [background:] B6.129-Ank2<sup>tm1Bnt</sup>/Bnt	is_model_of	DOID:12849	autistic disorder						ECO:0000033	author statement supported by traceable reference	PMID:31285321	20211102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6306133	Tbc1d24<sup>em2Tbf</sup>/Tbc1d24<sup>em2Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em2Tbf</sup>	is_model_of	DOID:0080449	developmental and epileptic encephalopathy 16						ECO:0000033	author statement supported by traceable reference	PMID:30602030	20190529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5924950	Rpgrip1<sup>tvrm111</sup>/Rpgrip1<sup>tvrm111</sup>  [background:] C57BL/6J-Rpgrip1<sup>tvrm111</sup>/Pjn	is_model_of	DOID:0110329	Leber congenital amaurosis 6						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3802920	Edn3<sup>tmgc48</sup>/Edn3<sup>+</sup>  [background:] C57BL/6-19<sup>PWK</sup>	is_model_of	DOID:0110954	Waardenburg syndrome type 4B						ECO:0000033	author statement supported by traceable reference	PMID:17516928	20100330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653823	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:10412977	20050513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790841	Il33<sup>tm1(KOMP)Vlcg</sup>/Il33<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Il33<sup>tm1(KOMP)Vlcg</sup>	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28675392	20190405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796114	Col8a2<sup>tm2.1Asj</sup>/Col8a2<sup>tm2.1Asj</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA	is_model_of	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:7698753	20160929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175707	Atm<sup>tm1Fwa</sup>/Atm<sup>tm1Fwa</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:10716718	20050603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655731	Casp8<sup>tm1Raz</sup>/Casp8<sup>tm1Raz</sup> Tg(Lck-cre)548Jxm/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:0110116	autoimmune lymphoproliferative syndrome type 2B						ECO:0000033	author statement supported by traceable reference	PMID:16157684	20060822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822144	avc3/avc3  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3773672	Ndn<sup>tm1.1Mus</sup>/Ndn<sup>+</sup>  [background:] B6.129S2-Ndn<sup>tm1.1Mus</sup>	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17116257	20080313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305096	Del(14Trim13-Rnaseh2b)6Rdf/+ Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22174151	20120207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7414333	Ubap1<sup>em1Yta</sup>/Ubap1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA/2	is_model_of	DOID:0112341	hereditary spastic paraplegia 80						ECO:0000033	author statement supported by traceable reference	PMID:35962060	20230106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276671	Tg(Mpz)88.4Mfel/0  [background:] FVB/N-Tg(Mpz)88.4Mfel	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:11086005	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668968	Foxj1<sup>tm1Bph</sup>/Foxj1<sup>tm1Bph</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:9739041	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000243	Boc<sup>tm1Rsk</sup>/Boc<sup>tm1Rsk</sup> Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * 129S6/SvEvTac	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21183473	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036833	Six3<sup>tm1Gco</sup>/Six3<sup>tm1Gco</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110872	holoprosencephaly 2						ECO:0000033	author statement supported by traceable reference	PMID:12569128	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6283403	Mypn<sup>tm1.1Epu</sup>/Mypn<sup>tm1.1Epu</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110933	nemaline myopathy 11						ECO:0000033	author statement supported by traceable reference	PMID:28017374	20190318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432179	Gt(ROSA)26Sor<sup>tm51(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936856	Tg(KRT5-rtTA)#Glk/0 Tg(tetO-S100a7a)#Yus/0  [background:] involves: FVB/N	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:21148126	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611467	Efs<sup>tm1Kale</sup>/Efs<sup>tm1Kale</sup>  [background:] either: (involves: 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J)	is_model_of	DOID:8778	Crohn's disease						ECO:0000033	author statement supported by traceable reference	PMID:16314525	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6890374	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>+</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3783593	Nlgn4l<sup>Gt(XST093)Byg</sup>/Nlgn4l<sup>Gt(XST093)Byg</sup>  [background:] B6.129P2-Nlgn4x<sup>Gt(XST093)Byg</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:18227507	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459447	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Rbl2<sup>tm2Tyj</sup>/Rbl2<sup>tm2Tyj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20406986	20100713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6151466	Golgb1<sup>em8Lanyu</sup>/Golgb1<sup>em8Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368626	Polg2<sup>M1Rvt</sup>/Polg2<sup>+</sup>  [background:] involves: BALB/c * C3H/HeH	is_model_of	DOID:12679	nephrocalcinosis						ECO:0000033	author statement supported by traceable reference	PMID:30395686	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838180	Plp1<sup>tm1Kan</sup>/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:11872612	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014832	Trp53<sup>tm1.2Awbr</sup>/Trp53<sup>tm1.2Awbr</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:21411755	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902497	B3gnt6<sup>tm1Lx</sup>/B3gnt6<sup>tm1Lx</sup> C1galt1<sup>tm1.1Rpmc</sup>/C1galt1<sup>tm1.1Rpmc</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:10021	duodenum cancer						ECO:0000033	author statement supported by traceable reference	PMID:7890183	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3691282	Myh6<sup>tm2Ces</sup>/Myh6<sup>+</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ	is_model_of	DOID:0110453	dilated cardiomyopathy 1EE						ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576784	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:20562852	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6209558	Spry2<sup>tm1.1Mrt</sup>/Spry2<sup>+</sup> Spry4<sup>tm1.2Mrt</sup>/Spry4<sup>tm1.2Mrt</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	PMID:34423857	20220705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784503	Pparg<sup>tm2(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6	is_model_of	DOID:0050440	familial partial lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276042	Tg(Myh6-Camk2d_ic)MJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883140	Tg(Myh6-Pln*R9C)#Ces/0  [background:] involves: FVB/N	is_model_of	DOID:0110439	dilated cardiomyopathy 1P						ECO:0000033	author statement supported by traceable reference	PMID:12610310	20170413	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047403	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110887	inflammatory bowel disease 12						ECO:0000033	author statement supported by traceable reference	PMID:8613481	20130417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047403	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110887	inflammatory bowel disease 12						ECO:0000033	author statement supported by traceable reference	PMID:7663509	20130417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6467272	Foxp3<sup>tm4(YFP/icre)Ayr</sup>/Foxp3<sup>tm4(YFP/icre)Ayr</sup> Ikzf4<sup>tm1Djr</sup>/Ikzf4<sup>tm1Djr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:640	encephalomyelitis						ECO:0000033	author statement supported by traceable reference	PMID:31296356	20201015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459096	Tg(Mbp-Pad2)28Fgm/0  [background:] involves: CD-1	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19093029	20100712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660492	Spata7<sup>tm1Mrd</sup>/Spata7<sup>tm1Mrd</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110331	Leber congenital amaurosis 3						ECO:0000033	author statement supported by traceable reference	PMID:25398945	20150831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699376	Ctnna1<sup>Tvrm5</sup>/Ctnna1<sup>Tvrm5</sup>  [background:] C57BL/6J-Ctnna1<sup>Tvrm5</sup>/Pjn	is_model_of	DOID:0060864	patterned macular dystrophy 2						ECO:0000033	author statement supported by traceable reference	PMID:26691986	20161209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610455	Ptch1<sup>tm1Kmmt</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12542834	20060118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6152755	Cabyr<sup>em1Osb</sup>/Cabyr<sup>em1Osb</sup>  [background:] involves: C57BL/6NJcl * DBA/2NJcl	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:27802166	20180423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055585	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15322545	20100603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907162	Tg(Myh6-NEBL*A592E)#Jato/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20951326	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052380	Tg(HTT*/EGFP)190Nn/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15836623	20110805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175746	Cat4<sup>Apcat1-4</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:1511869	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7507073	Cfi<sup>em1Jiwe</sup>/Cfi<sup>em1Jiwe</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:2921	glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:34149444	20230714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836158	Tg(MMTV-AURKA)#Cxd/? Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:16715125	20090317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7467113	Ctnna1<sup>tm1Efu</sup>/Ctnna1<sup>tm1Efu</sup> Gt(ROSA)26Sor<sup>tm14(CAG-tdTomato)Hze</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * C57BL/6NCrl * CBA	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6854714	Tmem53<sup>em1Ikeg</sup>/Tmem53<sup>em1Ikeg</sup>  [background:] Not Specified	is_model_of	DOID:0112340	craniotubular dysplasia Ikegawa type						ECO:0000033	author statement supported by traceable reference	PMID:33824347	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515421	Tg(Eno2-Bmp4)3Jake/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:15466378	20131029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569928	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>+</sup> Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:11854455	20140627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654386	Tg(Myh6-Gnaq)40Gwd/0  [background:] involves: FVB/N	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:9223325	20170830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943534	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6J * ICR	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:18497742	20110404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763109	Tg(MMTV-LPAR3)22Gbm/Tg(MMTV-LPAR3)22Gbm  [background:] FVB/N-Tg(MMTV-LPAR3)22Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5760132	Slc2a9<sup>tm1Khm</sup>/Slc2a9<sup>tm1Khm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:25100214	20210319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287976	Becn1<sup>tm1Ebr</sup>/Becn1<sup>tm1Ebr</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800676	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup> Il4ra<sup>tm1Sz</sup>/Il4ra<sup>+</sup>  [background:] involves: BALB/cJ * C57BL/6J * C57BL/10 * DBA/2	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:11168809	20080811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6251480	Pkd2<sup>tm1.1Gwu</sup>/Pkd2<sup>tm1.1Gwu</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28244683	20181114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042895	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>tm1Sjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:905	Zellweger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12024045	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3662691	F9<sup>tm1Dws</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:9354664	20061004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635880	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/0 Trp53<sup>tm1Gev</sup>/Trp53<sup>tm1Gev</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25878147	20150514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175730	Cat2<sup>no2</sup>/Cat2<sup>+</sup>  [background:] DBA/2-Cat2<sup>no2</sup>	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:2072972	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183898	Psap<sup>tm2Suz</sup>/Psap<sup>tm2Suz</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:11371512	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943327	Tg(Csf1r-Tnfsf15,-EGFP)#Targ/0  [background:] involves: C57BL/6	is_model_of	DOID:0110896	inflammatory bowel disease 16						ECO:0000033	author statement supported by traceable reference	PMID:21264313	20110331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432113	Gt(ROSA)26Sor<sup>tm1(DTA)Jpmb</sup>/Gt(ROSA)26Sor<sup>+</sup> Hcn4<sup>tm1(cre/ERT2)Anlu</sup>/Hcn4<sup>+</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:13884	sick sinus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21193513	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>	is_model_of	DOID:0060230	basal ganglia calcification						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834848	Atrx<sup>tm1Rjg</sup>/Y Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19088125	20090309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576603	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0090111	PCWH syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12616486	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581211	Ush1g<sup>js</sup>/Ush1g<sup>js</sup>  [background:] B6.A-Ush1g<sup>js</sup>/J	is_model_of	DOID:0110834	Usher syndrome type 1G						ECO:0000033	author statement supported by traceable reference	PMID:12588793	20120606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758726	Dp(11Cops3-Rnf112)1Jrl/0 Tyr<sup>c-Brd</sup>/Tyr<sup>c-Brd</sup>  [background:] B6Brd.Cg-Tyr<sup>c-Brd</sup> Dp(11Cops3-Rnf112)1Jrl	is_model_of	DOID:0060853	Potocki-Lupski syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18469339	20130103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032576	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14706336	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544476	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: C3H	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4840250	Cth<sup>tm1Iish</sup>/Cth<sup>tm1Iish</sup>  [background:] B6.129-Cth<sup>tm1Iish</sup>/Iish	is_model_of	DOID:0090142	cystathioninuria						ECO:0000033	author statement supported by traceable reference	PMID:20566639	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266840	Adgrg6<sup>tm1Arte</sup>/Adgrg6<sup>tm1Arte</sup> Tg(Scx-GFP/cre)1Stzr/0  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:34318745	20220506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318527	Tg(Tuba1-MAPT)14Vle/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:12165467	20120517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908862	Ssu2<sup>tm1.1Xmx</sup>/Ssu2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:701	dentin dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:27680507	20170913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314017	Dnah5<sup>b2b1154Clo</sup>/Dnah5<sup>b2b1154Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1154Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720804	Tg(Ckm-APPSw)A6Lfa/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:3429	inclusion body myositis						ECO:0000033	author statement supported by traceable reference	PMID:11972038	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662454	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Ren-cre)#Kwg/0  [background:] involves: 129 * 129P2/OlaHsd	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24292676	20150922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107698	Thap1<sup>tm1.2Meeh</sup>/Thap1<sup>+</sup>  [background:] involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6	is_model_of	DOID:0090039	torsion dystonia 6						ECO:0000033	author statement supported by traceable reference	PMID:26376866	20180105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574974	Cat4<sup>Apcat1-3</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5621021	Aipl1<sup>tm1Visu</sup>/Aipl1<sup>tm1Visu</sup> Tg(Crx-AIPL1*P351)#Visu/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:0050572	cone-rod dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25274777	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6093458	Fkrp<sup>tvrm53</sup>/Fkrp<sup>tvrm53</sup>  [background:] C57BL/6J-Fkrp<sup>tvrm53</sup>/Pjn	is_model_of	DOID:9884	muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5924963	Alms1<sup>tvrm102</sup>/Alms1<sup>tvrm102</sup>  [background:] C57BL/6J-Alms1<sup>tvrm102</sup>/Pjn	is_model_of	DOID:0050473	Alstrom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278119	Ryr2<sup>tm1Slh</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:27482086	20190214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442125	b2b1594Clo/b2b1594Clo  [background:] C57BL/6J-b2b1594Clo	is_model_of	DOID:11193	syndactyly						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6193916	Tg(Myh6-Prkaca)33Eno/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11717156	20180809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949888	Mecp2<sup>tm1Vnar</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20163734	20110512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559491	Slx1b<sup>tm1.1Jrou</sup>/Slx1b<sup>tm1.1Jrou</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090066	Fanconi-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24076219	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000248	Boc<sup>tm1Rsk</sup>/Boc<sup>tm1Rsk</sup> Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] B6.129-Boc<sup>tm1Rsk</sup> Cdon<sup>tm1Rsk</sup>	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21183473	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5645239	Dnah5<sup>b2b2451Clo</sup>/Dnah5<sup>b2b2451Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2451Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430322	b2b243.1Clo/b2b243.1Clo  [background:] C57BL/6J-b2b243.1Clo	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5298084	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * CD-1	is_model_of	DOID:1749	squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21502497	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5561115	b2b2736Clo/b2b2736Clo  [background:] C57BL/6J-b2b2736Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665288	Tg(Ins1-GAS)1Sbr/0  [background:] involves: FVB/NTac	is_model_of	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:10611152	20150403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588584	Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:9275211	20050929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177433	Hexa<sup>tm1Rlp</sup>/Hexa<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:3320	Tay-Sachs disease						ECO:0000033	author statement supported by traceable reference	PMID:7937929	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635492	H2<sup>dlAb1-Ea</sup>/H2<sup>dlAb1-Ea</sup> Tg(HLA-DRA,HLA-DRB5*0101)hiKito/0 Tg(TRATL3A6,TRBTL3A6)#Kito/0  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:22888134	20150512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587410	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:9660052	20080912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587410	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:9097952	20080912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571190	Gjb2<sup>tm1Ugds</sup>/Gjb2<sup>tm1Ugds</sup> Tg(Sox10-cre)1Wdr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000033	author statement supported by traceable reference	PMID:24333301	20140702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581014	Sox9<sup>tm1.1Gsr</sup>/Sox9<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:11857796	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2659147	Mocs1<sup>tm1Jre</sup>/Mocs1<sup>tm1Jre</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111164	molybdenum cofactor deficiency type A						ECO:0000033	author statement supported by traceable reference	PMID:12471057	20230619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6825756	Abcc9<sup>em3Nich</sup>/Abcc9<sup>em3Nich</sup>  [background:] B6.Cg-Abcc9<sup>em3Nich</sup>	is_model_of	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000033	author statement supported by traceable reference	PMID:33529173	20211122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440830	Slc17a5<sup>tm1Lex</sup>/Slc17a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:3659	sialuria						ECO:0000033	author statement supported by traceable reference	PMID:20007460	20100420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814722	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(KRT14-cre)1Ipc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18172296	20081112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432191	Tg(YAC72)2511Hay/Tg(YAC72)2511Hay  [background:] FVB/N-Tg(YAC72)2511Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16165367	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5546382	Tg(KRT14-Hmgn2)#Baam/0  [background:] Not Specified	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:23975681	20140227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6690506	Gcgr<sup>em2Smoc</sup>/Gcgr<sup>em2Smoc</sup>  [background:] C57BL/6J-Gcgr<sup>em2Smoc</sup>	is_model_of	DOID:0112306	Mahvash Disease						ECO:0000033	author statement supported by traceable reference	PMID:32677665	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3801488	Mecp2<sup>tm1Pplt</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18557922	20150610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813927	Pts<sup>tm1Ich</sup>/Pts<sup>tm1Ich</sup> Tg(DBH-PTS)6Csic/0  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:543	dystonia						ECO:0000033	author statement supported by traceable reference	PMID:18713855	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430345	Pcsk5<sup>b2b1549Clo</sup>/Pcsk5<sup>b2b1549Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b1549Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276568	Tg(Mpz*S63C)32Mes/0  [background:] involves: FVB/N	is_model_of	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669541	Serpini1<sup>tm1Dpw</sup>/Serpini1<sup>tm1Dpw</sup>  [background:] involves: 129/Sv * C57BL/6JBom	is_model_of	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000033	author statement supported by traceable reference	PMID:12837630	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590138	Gck<sup>Rgsc236</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583221	Fkbp4<sup>tm1Dvds</sup>/Fkbp4<sup>tm1Dvds</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15831525	20050809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473858	Rac2<sup>em1Shl</sup>/Rac2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0112061	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia						ECO:0000033	author statement supported by traceable reference	PMID:30723080	20210909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950027	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>/Dpcd/Poll<sup>Gt(OST280355)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:20080492	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5927436	Tg(H2-K-Fosl2,-EGFP)13Wag/0  [background:] B6.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:27864286	20171122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315197	Tg(Vav1-Asxl1*Y588X)#Fcy/0  [background:] C57BL/6-Tg(Vav1-Asxl1*Y588X)#Fcy	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29113963	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897214	Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0  [background:] involves: C57BL/6 * NMRI * SJL	is_model_of	DOID:0050471	Carney complex						ECO:0000033	author statement supported by traceable reference	PMID:15591278	20170511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831373	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] B6.129P2-Fgfr3<sup>tm1.1Aomw</sup>	is_model_of	DOID:0060703	Muenke Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273247	Ubiad1<sup>em1Wwk</sup>/Ubiad1<sup>+</sup>  [background:] C57BL/6N-Ubiad1<sup>em1Wwk</sup>	is_model_of	DOID:0060456	Schnyder corneal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:29977031	20190111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6303984	Piga<sup>tm1Tak</sup>/Piga<sup>tm1Tak</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:15304084	20190517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705137	Slc7a14<sup>em1Jqu</sup>/Slc7a14<sup>em1Jqu</sup>  [background:] C57BL/6-Slc7a14<sup>em1Jqu</sup>	is_model_of	DOID:10003	sensorineural hearing loss						ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584475	Ihh<sup>tm1Amc</sup>/Ihh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:10821773	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446589	Abcd1<sup>tm1Kds</sup>/Y  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9256488	20050823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613200	Txnip<sup>tm1Jjy</sup>/Txnip<sup>tm1Jjy</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:14525	Reye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16254043	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427014	Bscl2<sup>tm1.1Lchan</sup>/Bscl2<sup>tm1.1Lchan</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:24358199	20161206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356398	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.BKS(D)-Lepr<sup>db</sup>/JOrlRj	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:22118645	20190821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5508896	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup> Itga1<sup>tm1Gdnr</sup>/Itga1<sup>tm1Gdnr</sup>  [background:] C.Cg-Ins2<sup>Akita</sup> Itga1<sup>tm1Gdnr</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22297672	20130927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178286	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] DBA/2J	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10192392	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908397	Gabrb3<sup>tm2.1Uru</sup>/Gabrb3<sup>tm2.1Uru</sup>  [background:] B6J.129S6(Cg)-Gabrb3<sup>tm2.1Uru</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26627235	20170906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4353654	Nlgn3<sup>tm1Bros</sup>/Nlgn3<sup>tm1Bros</sup>  [background:] B6.Cg-Nlgn3<sup>tm1Bros</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:19243448	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692745	Gfap<sup>tm2Mes</sup>/Gfap<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:17065456	20070108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6231210	Tg(H2-K-Hmga1)#Lmsr/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060058	lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:15150086	20181107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042129	Lama3<sup>tm1Crt</sup>/Lama3<sup>tm1Crt</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:10366601	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175789	Coc/Coc<sup>+</sup>  [background:] involves: 101 * C3H * C57BL/6	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723301	Casq2<sup>tm1Jse</sup>/Casq2<sup>tm1Jse</sup>  [background:] involves: FVB/N	is_model_of	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000033	author statement supported by traceable reference	PMID:17607358	20090821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582673	Blm<sup>tm1Grdn</sup>/Blm<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12242442	20050729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722101	Tg(GSK3B*S9A)1Vln/0 Tg(Thy1-MAPT)1Vln/Tg(Thy1-MAPT)1Vln  [background:] involves: FVB	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11007782	20070920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839293	Atp8a2<sup>wl-3J</sup>/Atp8a2<sup>wl-3J</sup>  [background:] CBA/J-Atp8a2<sup>wl-3J</sup>/J	is_model_of	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197910	Alms1<sup>m3Btlr</sup>/Alms1<sup>m3Btlr</sup>  [background:] C57BL/6J-Alms1<sup>m3Btlr</sup>	is_model_of	DOID:0050473	Alstrom syndrome						ECO:0000033	author statement supported by traceable reference	MGI:6197907	20180914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160487	Eif2b4<sup>tm1.1Vdk</sup>/Eif2b4<sup>+</sup> Eif2b5<sup>tm1.1Vdk</sup>/Eif2b5<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675764	Drd2<sup>tm1Ebo</sup>/Drd2<sup>tm1Ebo</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:9717839	20171210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838317	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk/0  [background:] 129S1.Cg-Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20676139	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719118	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6J) or (involves: 129S1/SvImJ * 129S4/SvJae C57BL/6J)	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17701983	20070827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648021	Plxnd1<sup>b2b3150Clo</sup>/Plxnd1<sup>b2b3150Clo</sup>  [background:] C57BL/6J-Plxnd1<sup>b2b3150Clo</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6151463	Golgb1<sup>m1Lanyu</sup>/Golgb1<sup>m1Lanyu</sup>  [background:] A/J-Golgb1<sup>m1Lanyu</sup>	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366162	Ttc7<sup>fsn</sup>/Ttc7<sup>fsn</sup>  [background:] involves: A/J * BALB/cByJ	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8406628	20170928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906203	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB	is_model_of	DOID:0014667	disease of metabolism						ECO:0000033	author statement supported by traceable reference	PMID:19001090	20170803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687163	Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(TcraBDC12-4.1)10Jos/0 Tg(TcrbBDC12-4.1)82Gse/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16804066	20061109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799316	Ankrd26<sup>Gt(XK525)Byg</sup>/Ankrd26<sup>Gt(XK525)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:18162531	20100603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825026	Slc6a8<sup>tm1.2Lbar</sup>/Y  [background:] involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N	is_model_of	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:27466184	20170224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837857	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Col1a1<sup>tm1(CAG-EGFR)Char</sup>/Col1a1<sup>tm2(CAG-EGFR*)Char</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:19196966	20130322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581681	App<sup>tm1Ck</sup>/App<sup>tm1Ck</sup> Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup> Tg(MAPT)8cPdav/0  [background:] B6.Cg-Tg(MAPT)8cPdav Psen1<sup>tm1Mpm</sup> App<sup>tm1Ck</sup>	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24278307	20140904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5788563	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:27101989	20160812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033469	Hfe<sup>tm3Sly</sup>/Hfe<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14673107	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043397	Ndrg1<sup>tm1Myta</sup>/Ndrg1<sup>tm1Myta</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110186	Charcot-Marie-Tooth disease type 4D						ECO:0000033	author statement supported by traceable reference	PMID:15082788	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512988	Gt(ROSA)26Sor<sup>tm1(MAML1)Wsp</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-cre)1Jaw/0  [background:] involves: 129 * C57BL/6 * FVB	is_model_of	DOID:12895	keratoconjunctivitis sicca						ECO:0000033	author statement supported by traceable reference	PMID:23293291	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618231	Gck<sup>tm1Hrt</sup>/Gck<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:24447392	20190520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618231	Gck<sup>tm1Hrt</sup>/Gck<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15569412	20190520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569737	Tg(GFAP-SRC)2Aag/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:9160879	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451237	Arx<sup>tm1Kki</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:12379852	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605476	Tg(Scgb1a1-Scnn1b)6608Bouc/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:15077107	20051122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7329792	Hmgcs2<sup>em1(IMPC)Tcp</sup>/Hmgcs2<sup>+</sup>  [background:] C57BL/6NCrl-Hmgcs2<sup>em1(IMPC)Tcp</sup>	is_model_of	DOID:0081168	HMG-CoA synthase 2 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:35421611	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5546346	Pkd1<sup>tm1Som</sup>/Pkd1<sup>+</sup> Tg(Pkd1*)39Mtru/0  [background:] involves: 129/Sv * C57BL/6J * CBA/J * SJL	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23439951	20140227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6479882	Tcf4<sup>tm1Zhu</sup>/Tcf4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J	is_model_of	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27568567	20201217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583764	Shh<sup>Dsh</sup>/Shh<sup>+</sup>  [background:] B10Rl.Cg-Shh<sup>Dsh</sup>	is_model_of	DOID:0110964	brachydactyly type A1						ECO:0000033	author statement supported by traceable reference	PMID:15841179	20050818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5508557	Tg(Thy1-VCP*A232E)BMaki/0  [background:] involves: C57BL/6J	is_model_of	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:23747512	20130926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766125	Timo/Timo<sup>+</sup>  [background:] either: B6.Cg-Timo or (involves: C57BL/6J * CBA/CaJ)	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:17652166	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774114	Snord116<sup>tm1Uta</sup>/Snord116<sup>+</sup> Tg(Zp3-cre)93Knw/0  [background:] involves: C57BL/6J	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18320030	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581032	Clcn1<sup>adr-mto</sup>/Clcn1<sup>adr-mto</sup>  [background:] SWR/J-Clcn1<sup>adr-mto</sup>/J	is_model_of	DOID:2106	myotonia congenita						ECO:0000033	author statement supported by traceable reference	PMID:8119941	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5642052	Tg(Ly6a-GCSAM)102AIsg/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:9120	amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:23299888	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178677	Dll3<sup>tm1Rbe</sup>/Dll3<sup>tm1Rbe</sup>  [background:] involves: 129P2/Ola * C57BL/6	is_model_of	DOID:0050568	spondylocostal dysostosis						ECO:0000033	author statement supported by traceable reference	PMID:11923214	20070409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618597	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] B6.129P2-Nos3<sup>tm1Unc</sup>/J	is_model_of	DOID:13042	persistent fetal circulation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15016731	20060406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5615582	Pomgnt1<sup>tm1.1Cfg</sup>/Pomgnt1<sup>tm1.1Cfg</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:26306834	20190515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777759	Crygb<sup>S11R</sup>/Crygb<sup>S11R</sup>  [background:] A/J-Crygb<sup>S11R</sup>	is_model_of	DOID:0110236	cataract 39 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:18172107	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850627	Man2a1<sup>tm1Jxm</sup>/Man2a1<sup>tm1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:1338	congenital dyserythropoietic anemia						ECO:0000033	author statement supported by traceable reference	PMID:9230311	20100302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717255	Tg(Thy1-MAPT)22Schd/0  [background:] B6.Cg-Tg(Thy1-MAPT)22Schd	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16877359	20110502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7427405	Tnfrsf11a<sup>tm1.1Sral</sup>/Tnfrsf11a<sup>+</sup>  [background:] B6.129P2(Cg)-Tnfrsf11a<sup>tm1.1Sral</sup>	is_model_of	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:33724536	20230117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620988	Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] B6.129S4-Zmpste24<sup>tm1Sgy</sup>	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:16484451	20060503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358058	Tsc2<sup>tm2.2Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19357198	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688741	None [background:] TALLYHO/JngJ	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11414755	20141105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838391	Fancd2<sup>Gt(OST57859)Lex</sup>/Fancd2<sup>Gt(OST57859)Lex</sup> Usp1<sup>tm1.1Ada</sup>/Usp1<sup>tm1.1Ada</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000033	author statement supported by traceable reference	PMID:19217432	20110518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192376	Kdm6a<sup>tm1Cdcn</sup>/Kdm6a<sup>tm1Cdcn</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29479066	20180731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687322	Matn3<sup>tm1Brd</sup>/Matn3<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:16877353	20061113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196047	Tg(CAG-Alk*F1174L,-luc)60Jhsc/0 Tg(Dbh-icre)1Gsc/0 Tg(Th-MYCN)41Waw/0  [background:] involves: 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6J * FVB/N	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22764207	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6444680	Ikbkb<sup>em1Macc</sup>/Ikbkb<sup>em1Macc</sup>  [background:] involves: C57BL/6NCrl	is_model_of	DOID:0111960	immunodeficiency 15A						ECO:0000033	author statement supported by traceable reference	PMID:30337470	20210120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675764	Drd2<sup>tm1Ebo</sup>/Drd2<sup>tm1Ebo</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:7566118	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6112031	Vrk3<sup>Gt(YTA189)Byg</sup>/Vrk3<sup>Gt(YTA189)Byg</sup>  [background:] B6.129P2-Vrk3<sup>Gt(YTA189)Byg</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28899869	20180126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579768	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] B6.129S-Col4a1<sup>deltaex40</sup>	is_model_of	DOID:0090125	brain small vessel disease 1						ECO:0000033	author statement supported by traceable reference	PMID:16598045	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366351	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25153086	20151214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366351	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8033209	20151214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819227	Id4<sup>tm1Fsky</sup>/Id4<sup>tm1Fsky</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:20628571	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336829	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>/Ankrd11<sup>+</sup> E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N	is_model_of	DOID:14780	KBG syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33996804	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766445	Ank1<sup>nb</sup>/Ank1<sup>nb</sup>  [background:] involves: C57BL/6J * WB/Re	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:1832936	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4353816	Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup>/Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup> 7630403G23Rik<sup>Tg(Th-cre)1Tmd</sup>/7630403G23Rik<sup>+</sup>  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:19630976	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3050786	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup> Msx2<sup>tm1Rilm</sup>/Msx2<sup>tm1Rilm</sup>  [background:] involves: 129S4/SvJae * BALB/c * CD-1	is_model_of	DOID:0050591	tooth agenesis						ECO:0000033	author statement supported by traceable reference	PMID:10742104	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559468	Tg(KRT14-HPV8)#Vuc/0  [background:] involves: C57BL/6 * DBA * FVB/N	is_model_of	DOID:4159	skin cancer						ECO:0000033	author statement supported by traceable reference	PMID:15735026	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698063	Kcnj10<sup>tm1Lst</sup>/Kcnj10<sup>tm1Lst</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0060484	EAST syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19420365	20151204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648534	Gt(ROSA)26Sor<sup>tm1(rtTA,EGFP)Nagy</sup>/Gt(ROSA)26Sor<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup> Tg(tetO-Kras*G12D)#Rdp/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22541435	20150814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc	is_model_of	DOID:0110112	atrial heart septal defect 7						ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774687	Gabra1<sup>tm1.1Mjga</sup>/Gabra1<sup>+</sup>  [background:] B6J.Cg-Gabra1<sup>tm1.1Mjga</sup>	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:26054439	20160601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625687	Arl3<sup>Gt(OST263303)Lex</sup>/Arl3<sup>Gt(OST263303)Lex</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:16565502	20060627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174998	Psen1<sup>tm1Shn</sup>/Psen1<sup>tm1Shn</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:9160754	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576602	Mpz<sup>tm1Msch</sup>/Mpz<sup>tm1Msch</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:7581451	20050511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275604	Cic<sup>tm1c(KOMP)Wtsi</sup>/Cic<sup>tm1c(KOMP)Wtsi</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6N	is_model_of	DOID:150	disease of mental health						ECO:0000033	author statement supported by traceable reference	PMID:28288114	20190201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6156408	Klhl41<sup>tm1a(KOMP)Wtsi</sup>/Klhl41<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6-Klhl41<sup>tm1a(KOMP)Wtsi</sup>	is_model_of	DOID:3191	nemaline myopathy						ECO:0000033	author statement supported by traceable reference	PMID:28826497	20180515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758821	Piga<sup>tm1Tak</sup>/Y Tg(KRT5-cre)1Tak/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:15304084	20190517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451348	Slc12a6<sup>tm1Dlp</sup>/Slc12a6<sup>tm1Dlp</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:12368912	20180617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818928	Dnm1l<sup>Py</sup>/Dnm1l<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20585624	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356709	Myh6<sup>tm1.1Jpsc</sup>/Myh6<sup>tm2Jse</sup>  [background:] involves: 129	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440863	Apc<sup>Min</sup>/Apc<sup>+</sup> Rab25<sup>tm1Jrgo</sup>/Rab25<sup>tm1Jrgo</sup>  [background:] B6.Cg-Rab25<sup>tm1Jrgo</sup> Apc<sup>Min</sup>	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:20197623	20100421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295638	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6NCrlj * C57BL/10 * CBA/Ca * CBA/JNCrlj	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21339326	20111114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287978	Rubcn<sup>em1Dgre</sup>/Rubcn<sup>em1Dgre</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6202041	Slc3a1<sup>tm1Jat</sup>/Slc3a1<sup>tm1Jat</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:28165480	20181015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6202041	Slc3a1<sup>tm1Jat</sup>/Slc3a1<sup>tm1Jat</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:19484501	20181015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836579	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:19117991	20090320	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905766	Tg(Myh6-Rest*)474Ysai/0  [background:] involves: C57BL/6J	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:14633990	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622794	Adora2a<sup>tm1Jfc</sup>/Adora2a<sup>tm1Jfc</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:11830	myopia						ECO:0000033	author statement supported by traceable reference	PMID:20484596	20101006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432178	Gt(ROSA)26Sor<sup>tm50(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5490868	Rho<sup>tm4.1(RHO*/EGFP)Jhw</sup>/Rho<sup>+</sup>  [background:] B6.129S7-Rho<sup>tm4.1(RHO*/EGFP)Jhw</sup>	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:22110080	20130619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622118	Musk<sup>tm1Vwi</sup>/Musk<sup>tm1.1Vwi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * FVB	is_model_of	DOID:0110670	congenital myasthenic syndrome 9						ECO:0000033	author statement supported by traceable reference	PMID:16337809	20150511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140073	Tg(Amelx-Ambn)1Mlp/Tg(Amelx-Ambn)1Mlp  [background:] Not Specified	is_model_of	DOID:2187	amelogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:12657627	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622763	Prf1<sup>tm1Clrk</sup>/Prf1<sup>tm1Clrk</sup>  [background:] involves: 129S7/SvEvBrd * BALB/c * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10946317	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625957	Ids<sup>tm1Muen</sup>/Y  [background:] Not Specified	is_model_of	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:12572850	20060629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625957	Ids<sup>tm1Muen</sup>/Y  [background:] Not Specified	is_model_of	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:16505002	20060629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3828048	Npr2<sup>cn</sup>/Npr2<sup>cn</sup>  [background:] involves: AKR/J	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	MGI:75337	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5461653	Dp(7Herc2-Mkrn3)1Taku/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22916201	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258769	Adamts10<sup>em1Cbal</sup>/Adamts10<sup>em1Cbal</sup>  [background:] involves: C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:0050475	Weill-Marchesani syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30060141	20181203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687754	Btk<sup>xid</sup>/Btk<sup>xid</sup>  [background:] CBA/HN-Btk<sup>xid</sup>	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584436	Ins1<sup>tm1Jja</sup>/Ins1<sup>tm1Jja</sup> Ins2<sup>tm1Jja</sup>/Ins2<sup>tm1Jja</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:11272179	20120117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584436	Ins1<sup>tm1Jja</sup>/Ins1<sup>tm1Jja</sup> Ins2<sup>tm1Jja</sup>/Ins2<sup>tm1Jja</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:9144203	20120117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906193	Tg(Myh6-Tnni3*)1Ammu/0  [background:] involves: A/J * C57BL/6	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15863459	20170803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6283412	Nrg3<sup>tm1.1Plet</sup>/Nrg3<sup>tm1.1Plet</sup>  [background:] involves: C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:27606322	20190318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575502	T(16;17)43H/0  [background:] involves: 101 * C3H * PWD/Ph	is_model_of	DOID:0080014	chromosomal disease						ECO:0000033	author statement supported by traceable reference	PMID:15755806	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5468673	Trp63<sup>tm1Cmis</sup>/Trp63<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090119	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23108156	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774672	Tg(KRT14-Snai1)1Efu/0  [background:] involves: CD-1	is_model_of	DOID:4159	skin cancer						ECO:0000033	author statement supported by traceable reference	PMID:24162662	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044560	Gck<sup>Gena348</sup>/Gck<sup>+</sup>  [background:] involves: BALB/c * C3H/He	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15161764	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688300	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-PTPN11*E76K)#Jiwu/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24480804	20150925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7448597	Rr401<sup>em1Yushi</sup>/Rr401<sup>em1Yushi</sup>  [background:] Not Specified	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:36613635	20230329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188926	Opa1<sup>tm1.1Geno</sup>/Opa1<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:23250881	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6394002	Hmbs<sup>tm1.1Rjde</sup>/Hmbs<sup>tm1.1Rjde</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:30615115	20200312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0110977	brachydactyly type A1C						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400523	Cacna1g<sup>em1Ftan</sup>/Cacna1g<sup>em1Ftan</sup>  [background:] C57BL/6NCrSlc-Cacna1g<sup>em1Ftan</sup>	is_model_of	DOID:0111742	cerebellar ataxia type 42						ECO:0000033	author statement supported by traceable reference	PMID:31229688	20200702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774852	Tg(RHO-SCA7)R7EJman/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:11030754	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258254	Tg(KRT5-Terf2)PMBlas/Y  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050427	xeroderma pigmentosum						ECO:0000033	author statement supported by traceable reference	PMID:16142233	20181129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5788294	Ciita<sup>tm1Wrth</sup>/Ciita<sup>tm1Wrth</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:24038328	20160809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160731	Insr<sup>tm1Dac</sup>/Insr<sup>+</sup> Ppp2r2a<sup>igt10</sup>/Ppp2r2a<sup>+</sup>  [background:] involves: 129S4/SvJae * C3H/HeH * C57BL/6J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26868295	20180613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583952	Hmga1<sup>tm1Brun</sup>/Hmga1<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15924147	20050819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304472	Tg(RP11-209M4)AGglo/0  [background:] FVB-Tg(RP11-209M4)4Gglo	is_model_of	DOID:0080036	SOST-related sclerosing bone dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:15965026	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6331339	Tg(Nphs1-rtTA*3G)8Jhm/0 Tg(tetO-GFP,-APOL1*S342G*I384M)#Susz/0  [background:] involves: C57BL/6J * CBA/J * FVB/N	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28218918	20190731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7286352	Specc1l<sup>em3Kumc</sup>/Specc1l<sup>em3Kumc</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:0080698	Teebi hypertelorism syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3830477	Qrfpr<sup>tm1Lex</sup>/Qrfpr<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J	is_model_of	DOID:0080010	bone structure disease						ECO:0000033	author statement supported by traceable reference	PMID:16382160	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355230	Apoe<sup>tm3(APOE*4)Mae</sup>/Apoe<sup>tm3(APOE*4)Mae</sup> Tg(Thy1-APPSwDutIowa)BWevn/?  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18480287	20090828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7493334	Chd7<sup>Trooper</sup>/Chd7<sup>+</sup>  [background:] BALB/c-Chd7<sup>Trooper</sup>	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29615807	20230627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198300	Clcnkb<sup>em1Haca</sup>/Clcnkb<sup>em1Haca</sup>  [background:] C57BL/6-Clcnkb<sup>em1Haca</sup>	is_model_of	DOID:0110144	Bartter disease type 3						ECO:0000033	author statement supported by traceable reference	PMID:27421685	20180917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656223	Bey/Bey<sup>+</sup>  [background:] 129S/SvEv-Bey	is_model_of	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9626498	20050718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586812	Polh<sup>tm1Fmh</sup>/Polh<sup>tm1Fmh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110847	xeroderma pigmentosum variant type						ECO:0000033	author statement supported by traceable reference	PMID:15939880	20050907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038706	Ror2<sup>tm1Ymi</sup>/Ror2<sup>tm1Ymi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060764	autosomal recessive Robinow syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14745966	20060517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441471	Snx10<sup>em2Ael</sup>/Snx10<sup>em2Ael</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6JOlaHsd	is_model_of	DOID:0110940	autosomal recessive osteopetrosis 8						ECO:0000033	author statement supported by traceable reference	PMID:32278070	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662454	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Ren-cre)#Kwg/0  [background:] involves: 129 * 129P2/OlaHsd	is_model_of	DOID:657	adenoma						ECO:0000033	author statement supported by traceable reference	PMID:24292676	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287973	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574284	Csmd1<sup>tm1Lex</sup>/Csmd1<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6NTac	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:24244513	20140723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159252	Prl3c1<sup>tm1(KOMP)Vlcg</sup>/Prl3c1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac * CD-1	is_model_of	DOID:11613	hyperandrogenism						ECO:0000033	author statement supported by traceable reference	PMID:28576872	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6236251	Rbpj<sup>tm1Kyo</sup>/Rbpj<sup>+</sup>  [background:] involves: 129S2/SvPas * CD-1	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:21493891	20181108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769907	Col1a1<sup>Aga2</sup>/Col1a1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0110341	osteogenesis imperfecta type 2						ECO:0000033	author statement supported by traceable reference	PMID:18248096	20080229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587031	Hoxa13<sup>Hd</sup>/Hoxa13<sup>+</sup>  [background:] B6C3Fe-a/a Hoxa13<sup>Hd</sup> Mcoln3<sup>Va-J</sup>/J	is_model_of	DOID:0060739	hand-foot-genital syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10210434	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5572798	Tshr<sup>hyt-3J</sup>/Tshr<sup>hyt-3J</sup>  [background:] CXB10/HiAJ-Tshr<sup>hyt-3J</sup>/GrsrJ	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	MGI:5571363	20140714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181800	Scnn1b<sup>tm1Wsh</sup>/Scnn1b<sup>tm1Wsh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:9990092	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181997	Hfm/Hfm<sup>+</sup>  [background:] involves: SWV-Mbp<sup>shi</sup>	is_model_of	DOID:2907	Goldenhar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7531669	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6438117	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476847	Tg(TARDBP)#Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:21752789	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7464784	Atl1<sup>tm1.1Cbla</sup>/Atl1<sup>tm1.1Cbla</sup> Reep1<sup>Gt(OST398247)Tigm</sup>/Reep1<sup>Gt(OST398247)Tigm</sup>  [background:] B6.Cg-Reep1<sup>Gt(OST398247)Tigm</sup> Atl1<sup>tm1.1Cbla</sup>	is_model_of	DOID:2476	hereditary spastic paraplegia						ECO:0000033	author statement supported by traceable reference	PMID:35348668	20230421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277716	Slc7a14<sup>em1Jin</sup>/Slc7a14<sup>em1Jin</sup>  [background:] C57BL/6J-Slc7a14<sup>em1Jin</sup>	is_model_of	DOID:10003	sensorineural hearing loss						ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582929	Tg(HCRT-tTA)1Ahky/0 Tg(tetO-DTA)1Gfi/0  [background:] B6.Cg-Tg(HCRT-tTA)1Ahky Tg(tetO-DTA)1Gfi	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:24806676	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582929	Tg(HCRT-tTA)1Ahky/0 Tg(tetO-DTA)1Gfi/0  [background:] B6.Cg-Tg(HCRT-tTA)1Ahky Tg(tetO-DTA)1Gfi	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:24806675	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6515830	Ryr1<sup>tm3.1Alle</sup>/Ryr1<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:8545	malignant hyperthermia						ECO:0000033	author statement supported by traceable reference	PMID:30236258	20210407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942179	Tg(Ins2-Hnf1a)#Cbw/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:0111102	maturity-onset diabetes of the young type 3						ECO:0000033	author statement supported by traceable reference	PMID:11713231	20110328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160055	Ecel1<sup>tm1Hiki</sup>/Ecel1<sup>tm1Hiki</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:26951213	20180608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6383409	Lyst<sup>bg-18J</sup>/Lyst<sup>bg-18J</sup>  [background:] B6.Cg-Lyst<sup>bg-18J</sup>/Boc	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20200106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6378570	Rho<sup>tm1Jlem</sup>/Rho<sup>tm1Jlem</sup> Tg(RHO*P347S)A1Tili/0  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:22809998	20191126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5518826	Is(In8B2-8B3.1;6C1)1Tshir/0  [background:] involves: A/WySn * C57BL/10 * M. m. molossinus * NZB	is_model_of	DOID:0060429	chromosomal duplication syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23449628	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3820405	Sod1<sup>tm1Leb</sup>/Sod1<sup>tm1Leb</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25036096	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651379	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110910	leukocyte adhesion deficiency 1						ECO:0000033	author statement supported by traceable reference	PMID:8101543	20050808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044689	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup>  [background:] involves: 129X1/SvJ * Black Swiss	is_model_of	DOID:0050711	aceruloplasminemia						ECO:0000033	author statement supported by traceable reference	PMID:10485908	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044689	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup>  [background:] involves: 129X1/SvJ * Black Swiss	is_model_of	DOID:0050711	aceruloplasminemia						ECO:0000033	author statement supported by traceable reference	PMID:11461924	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425922	Casr<sup>BCH011</sup>/Casr<sup>BCH011</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH011</sup>	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6693692	Impg2<sup>em1Visu</sup>/Impg2<sup>em1Visu</sup>  [background:] involves: C57BL/6J * DBA/2	is_model_of	DOID:0050661	vitelliform macular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32265257	20210420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6268336	Gcdh<sup>tm1Dmk</sup>/Gcdh<sup>tm1Dmk</sup>  [background:] involves: 129S4/SvJae * C57BL/6N * FVB/N	is_model_of	DOID:0111254	glutaric acidemia I						ECO:0000033	author statement supported by traceable reference	PMID:28545977	20191122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258952	Cfap43<sup>em1Fzh</sup>/Cfap43<sup>em1Fzh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0070170	spermatogenic failure 19						ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722063	Tg(Thy1-APPSwDutIowa)BWevn/0  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14985348	20070919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003460	Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15972962	20110607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003460	Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6695982	Rab39b<sup>em1Jfch</sup>/Y  [background:] C57BL/6N-Rab39b<sup>em1Jfch</sup>	is_model_of	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:32115408	20210503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6470789	Foxf1<sup>em1Vvk</sup>/Foxf1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:13042	persistent fetal circulation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31199666	20201105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449546	F8<sup>tm2Kaz</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12134	factor VIII deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7647782	20200113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449421	Tg(SOD1*)DF7Yaw/0  [background:] C57BL/6-Tg(SOD1*)DF7Yaw	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:15857664	20130117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6510523	Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/Ndor1<sup>+</sup> Rpl11<sup>tm1.1Srn</sup>/Rpl11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1	is_model_of	DOID:0111878	Diamond-Blackfan anemia 7						ECO:0000033	author statement supported by traceable reference	PMID:26489471	20210316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446380	b2b1430Clo/b2b1430Clo  [background:] C57BL/6J-b2b1430Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510639	Ccdc85c<sup>hhy</sup>/Ccdc85c<sup>hhy</sup>  [background:] involves: BALB/cHeA * STS/A	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:15283996	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278016	Tg(Actb-Ptma)T12Clwu/0  [background:] involves: FVB/N	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:23695700	20190213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159890	Slurp2<sup>tm1Lex</sup>/Slurp2<sup>tm1Lex</sup>  [background:] involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:3390	palmoplantar keratosis						ECO:0000033	author statement supported by traceable reference	PMID:26967477	20180607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6099058	Tg(Th-SNCA*A30P*A53T)39Eric/0  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:15009131	20171211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276577	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup> Tg(Mpz*S63X)31Mes/0  [background:] involves: 129S7/SvEvBrd * FVB/N	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451017	Mtm1<sup>tm1.1Jman</sup>/Y  [background:] involves: 129T1/Sv * C57BL/6	is_model_of	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:12391329	20120227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258953	Cfap43<sup>em2Fzh</sup>/Cfap43<sup>em2Fzh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0070170	spermatogenic failure 19						ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6116285	Tg(Plp1-Eif2ak3*)18Pop/Tg(Plp1-Eif2ak3*)18Pop  [background:] C57BL/6J-Tg(Plp1-Eif2ak3*)18Pop	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:25186761	20180214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819765	Nfkbiz<sup>tm1Aki</sup>/Nfkbiz<sup>tm1Aki</sup>  [background:] C.129P2-Nfkbiz<sup>tm1Aki</sup>	is_model_of	DOID:0050426	Stevens-Johnson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18441309	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430413	Gt(ROSA)26Sor<sup>tm1(CAG-Kcnj11*,-GFP)Nich</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:19187772	20100302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433031	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] D2.129(Cg)-Gabra1<sup>tm1.1Geh</sup>	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:22812724	20120906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:17466543	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:14595440	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5632508	Tg(THY1-SNCA*A53T)M53Sud/0  [background:] B6.Cg-Tg(THY1-SNCA*A53T)M53Sud/J	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:24325796	20150424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5519974	Bscl2<sup>tm1Geno</sup>/Bscl2<sup>tm1Geno</sup>  [background:] B6.129P2-Bscl2<sup>tm1Geno</sup>	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:23680914	20131126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841175	Tg(Myh6-PRKAG2*N488I)4623Jse/0  [background:] involves: FVB	is_model_of	DOID:0110312	hypertrophic cardiomyopathy 6						ECO:0000033	author statement supported by traceable reference	PMID:12782567	20090424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527229	Mybpc3<sup>tm1Rmos</sup>/Mybpc3<sup>tm1Rmos</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6)	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:11909824	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711108	Tg(HLA-A/H2-D/B2M)1Dvs/0  [background:] NOD/ShiLtDvs-Tg(HLA-A/H2-D/B2M)1Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16493087	20070606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7520358	Tafazzin<sup>em1Xfa</sup>/Y Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: C57BL/6NCrl * MF1	is_model_of	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34129362	20230824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941487	Slitrk6<sup>tm1.1Jaru</sup>/Slitrk6<sup>tm1.1Jaru</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10003	sensorineural hearing loss						ECO:0000033	author statement supported by traceable reference	PMID:21298075	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702286	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] B6.C3-Ap3b1<sup>pe</sup>/J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429442	Ppp1r3c<sup>tm1Ars</sup>/Ppp1r3c<sup>+</sup>  [background:] B6.129-Ppp1r3c<sup>tm1Ars</sup>	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12727934	20100218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174763	Tcirg1<sup>tm1Ypl</sup>/Tcirg1<sup>tm1Ypl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000033	author statement supported by traceable reference	PMID:10581033	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284986	Tlr7<sup>em2Anu</sup>/Y  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6195067	Pml<sup>tm1.1Ews</sup>/Pml<sup>tm1.1Ews</sup> Tg(PML-RARA)556Kog/0  [background:] FVB.Cg-Pml<sup>tm1.1Ews</sup> Tg(PML-RARA)556Kog	is_model_of	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29191918	20180820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752196	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Wap-cre)11738Mam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25330770	20160316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588988	Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup> Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15601645	20051006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107228	Dzip1l<sup>warpy</sup>/Dzip1l<sup>warpy</sup>  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28530676	20180102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655553	Fah<sup>1R</sup>/Fah<sup>1R</sup>  [background:] involves: BALB/cRl * C3H/Rl * C57BL/10Rl	is_model_of	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:11209059	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435676	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJaeSor	is_model_of	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6760664	Syce1<sup>em1Rrca</sup>/Syce1<sup>em1Rrca</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0080869	primary ovarian insufficiency 12						ECO:0000033	author statement supported by traceable reference	PMID:32402064	20210920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307126	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>tm1Sjg</sup>  [background:] B6.129-Pex11b<sup>tm1Sjg</sup>	is_model_of	DOID:905	Zellweger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21954064	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904595	Trem2<sup>em2Bwef</sup>/Trem2<sup>em2Bwef</sup>  [background:] involves: C57BL/6J * DBA/2J * FVB/N	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:28559417	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949137	Hcrt<sup>tm1Ywa</sup>/Hcrt<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:12797957	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659880	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:3908	lung non-small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17676035	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620352	Rp2<sup>tm1.2Asw</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110415	retinitis pigmentosa 2						ECO:0000033	author statement supported by traceable reference	PMID:23745007	20150330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4882081	Tg(Gfap-TGFB1)64Lms/0 Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>/0  [background:] involves: BALB/c * C57BL/6 * DBA/2 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21088218	20110207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272035	Tnf<sup>Bpsm1</sup>/Tnf<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449964	Epb42<sup>tm1Llp</sup>/Epb42<sup>tm1Llp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10359562	20050622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162682	Umod<sup>em1Duf</sup>/Umod<sup>+</sup>  [background:] C57BL/6J-Umod<sup>em1Duf</sup>	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28990932	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689882	Tg(Alb1HBV)44Bri/0  [background:] C57BL/6J-Tg(Alb1HBV)44Bri/J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26035378	20151013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5293613	Gbe1<sup>tm1Hoa</sup>/Gbe1<sup>tm1Hoa</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:2750	glycogen storage disease IV						ECO:0000033	author statement supported by traceable reference	PMID:21856731	20111027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5501106	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup>  [background:] involves: 129	is_model_of	DOID:0060688	arteriovenous malformations of the brain						ECO:0000033	author statement supported by traceable reference	PMID:22571958	20130814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680797	Clcn7<sup>tm1Tjj</sup>/Clcn7<sup>tm1Tjj</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110944	autosomal recessive osteopetrosis 4						ECO:0000033	author statement supported by traceable reference	PMID:11207362	20120117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839332	Tg(CAG-RPS19*R62W)#Dmb/0 Tg(Prnp-GFP/cre)1Blw/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:20606162	20101122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604892	Tg(MMTV-Erbb2)17Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3768649	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(Tyr-NRAS*Q61K)1Bee/?  [background:] involves: 129/Sv * C57BL/6 * DBA/2 * SJL	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:15899789	20200710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670516	Ldlrap1<sup>tm1Her</sup>/Ldlrap1<sup>tm1Her</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0090105	autosomal recessive hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:12746448	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5608466	Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>/Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi	is_model_of	DOID:0111044	gray platelet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25258341	20150526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3765154	Kcnn2<sup>fri</sup>/Kcnn2<sup>fri</sup>  [background:] involves: C3H	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:11442353	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3807528	Flvcr1<sup>tm1.1Jlab</sup>/Flvcr1<sup>tm1.1Jlab</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:18258918	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909088	Tg(Myh7-Ptpn11*Q510E)#Krnz/0  [background:] FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22058153	20170914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438494	Tg(Thy1-TARDBP)4Singh/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:20133711	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522704	pta/pta  [background:] C57BL/6J-pta	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6479076	Col4a5<sup>em1Keha</sup>/Y  [background:] C57BL/6J-Col4a5<sup>em1Keha</sup>	is_model_of	DOID:0110034	X-linked Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30582011	20201214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6474227	Ids<sup>tm1Dkji</sup>/Y  [background:] involves: C57BL/6	is_model_of	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:20652491	20201130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5466160	Tg(APOE-FGF23*R176Q)#Ack/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15284207	20130225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440461	Cybb<sup>tm1Din</sup>/Y Tg(SOD1*G93A)<sup>dl</sup>1Gur/0  [background:] B6.Cg-Cybb<sup>tm1Din</sup> Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16877542	20100414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432254	Pgap1<sup>m1Nisw</sup>/Pgap1<sup>m1Nisw</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:4621	holoprosencephaly						ECO:0000033	author statement supported by traceable reference	PMID:23213481	20190927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053060	Trex1<sup>tm1Tld</sup>/Trex1<sup>tm1Tld</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18724932	20090702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616771	Chd7<sup>Whi</sup>/Chd7<sup>+</sup>  [background:] involves: C3HeB/FeJ	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16207732	20060317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943704	Fas<sup>lpr</sup>/Fas<sup>lpr</sup> Il27ra<sup>tm1Mak</sup>/Il27ra<sup>tm1Mak</sup>  [background:] MRL.Cg-Il27ra<sup>tm1Mak</sup> Fas<sup>lpr</sup>	is_model_of	DOID:10976	membranous glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:16301622	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5465103	Anks6<sup>b2b1801.1Clo</sup>/Anks6<sup>b2b1801.1Clo</sup>  [background:] C57BL/6J-Anks6<sup>b2b1801.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652689	Csf2<sup>tm1Ard</sup>/Csf2<sup>tm1Ard</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:8202532	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714749	Mstn<sup>tm1Sjl</sup>/Mstn<sup>tm1Sjl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0111072	myostatin-related muscle hypertrophy						ECO:0000033	author statement supported by traceable reference	PMID:9139826	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4849842	Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo/Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16046140	20101230	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812126	Slc35d1<sup>tm1Hko</sup>/Slc35d1<sup>tm1Hko</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050775	schneckenbecken dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:17952091	20081027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6389105	Rapsn<sup>em1Gan</sup>/Rapsn<sup>em1Gan</sup>  [background:] C57BL/6J-Rapsn<sup>em1Gan</sup>	is_model_of	DOID:0110675	congenital myasthenic syndrome 11						ECO:0000033	author statement supported by traceable reference	PMID:31549961	20200210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5562646	Slit3<sup>tm1.1Dor</sup>/Slit3<sup>tm1.1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:24355925	20140507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670851	Slc27a4<sup>tm1Wsr</sup>/Slc27a4<sup>tm1Wsr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060762	restrictive dermopathy						ECO:0000033	author statement supported by traceable reference	PMID:12821645	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563125	Clcn7<sup>tm1.1Mjec</sup>/Clcn7<sup>+</sup>  [background:] involves: 129 * 129S/SvEv * C57BL/6	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:24185277	20140509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587678	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] involves: STOCK t	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1912584	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192490	Stat2<sup>tm1.1(STAT2)Diam</sup>/Stat2<sup>tm1.1(STAT2)Diam</sup>  [background:] C57BL/6-Stat2<sup>tm1.1(STAT2)Diam</sup>	is_model_of	DOID:0060478	Zika fever						ECO:0000033	author statement supported by traceable reference	PMID:29746837	20230821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431138	Gt(ROSA)26Sor<sup>tm1(tTA,tetO-Mir155)Fjsl</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Nes-cre)1Wmz/0  [background:] involves: 129 * C57BL/6 * FVB/N * SJL/J	is_model_of	DOID:0060058	lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22685206	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287207	Arhgef10<sup>tm1.1Ssfg</sup>/Arhgef10<sup>tm1.1Ssfg</sup>  [background:] B6.129S1-Arhgef10<sup>tm1.1Ssfg</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:29456827	20190412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819951	Tg(Camk2a-tTA)1Mmay/? Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/?  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16020737	20100820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834589	Tg(ATN1*)Q129Stsu/0  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000033	author statement supported by traceable reference	PMID:19039037	20090305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277716	Slc7a14<sup>em1Jin</sup>/Slc7a14<sup>em1Jin</sup>  [background:] C57BL/6J-Slc7a14<sup>em1Jin</sup>	is_model_of	DOID:1432	blindness						ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415690	Flvcr2<sup>tm1.2Tda</sup>/Flvcr2<sup>tm1.2Tda</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32369453	20200511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624868	Cacna1a<sup>tg-rol</sup>/Cacna1a<sup>tg-rol</sup>  [background:] involves: C57BL/6 * SIII	is_model_of	DOID:0050214	Lambert-Eaton myasthenic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18653245	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617489	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>tm2Jzh</sup>  [background:] either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:11689485	20060324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386443	Ercc2<sup>tm1Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2960	photosensitive trichothiodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9651581	20050822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324372	Atp7a<sup>tm1.1Mjp</sup>/Y Mnx1<sup>tm4(cre)Tmj</sup>/Mnx1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0111196	X-linked distal spinal muscular atrophy 3						ECO:0000033	author statement supported by traceable reference	PMID:25639447	20191122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850822	Igh<sup>tm2.1(Tag)Rwhe</sup>/Igh<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:19332766	20160622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688562	Lrp4<sup>mdig-3J</sup>/Lrp4<sup>mdig-3J</sup>  [background:] B6.Cg-Lrp4<sup>mdig-3J</sup>/GrsrJ	is_model_of	DOID:0060757	sclerosteosis 2						ECO:0000033	author statement supported by traceable reference	MGI:5688518	20150930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5528706	Tg(Amh-SMAD2*)2Tkw/?  [background:] involves: CD-1	is_model_of	DOID:11427	endosalpingiosis						ECO:0000033	author statement supported by traceable reference	PMID:16141389	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800496	Ncstn<sup>tm1.1Sud</sup>/Ncstn<sup>tm1.1Sud</sup> Olig1<sup>tm1(cre)Rth</sup>/Olig1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:27008863	20161013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524023	Trp53<sup>tm1.1Tldo</sup>/Trp53<sup>tm1.1Tldo</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:2729	dyskeratosis congenita						ECO:0000033	author statement supported by traceable reference	PMID:23770245	20131220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576479	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6314145	Card14<sup>em9Lutzy</sup>/Card14<sup>+</sup>  [background:] C57BL/6J-Card14<sup>em9Lutzy</sup>/J	is_model_of	DOID:0080475	psoriasis 2						ECO:0000033	author statement supported by traceable reference	PMID:29689250	20190613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634972	Per1<sup>tm1Drw</sup>/Per1<sup>tm1Drw</sup>  [background:] B6.129-Per1<sup>tm1Drw</sup>/J	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:25673850	20150507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867886	Itm2b<sup>tm3.1Ldad</sup>/Itm2b<sup>tm3.1Ldad</sup>  [background:] B6.129-Itm2b<sup>tm3.1Ldad</sup>	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21048150	20110114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5289971	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA*A53T)33Vle/0  [background:] involves: C3H/HeH * C57BL/6	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:21734300	20111011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294956	Ctf1<sup>tm1Msd</sup>/Ctf1<sup>tm1Msd</sup>  [background:] B6.Cg-Ctf1<sup>tm1Msd</sup>	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21803294	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617140	Fmr1<sup>tm1Usdn</sup>/Fmr1<sup>tm1Usdn</sup>  [background:] B6.129S6(Cg)-Fmr1<sup>tm1Usdn</sup>	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22470123	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621956	Pdlim3<sup>tm1Krc</sup>/Pdlim3<sup>tm1Krc</sup>  [background:] either: (involves: 129S) or (involves: C57BL/6) or (involves: Black Swiss)	is_model_of	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11329061	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821786	Pax6<sup>tm2Pgr</sup>/Pax6<sup>+</sup> Tg(Pax6-cre,GFP)1Pgr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB	is_model_of	DOID:0060673	Peters anomaly						ECO:0000033	author statement supported by traceable reference	PMID:20538882	20100906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402445	Tg(CAG-DPP4)4Yuzh/0  [background:] C57BL/6-Tg(CAG-DPP4)4Yuzh	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26701103	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060857	septooptic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:9620767	20060403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060857	septooptic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10626545	20060403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032575	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/?  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14706336	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300565	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (C3H/HeJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586968	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup> Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3H/He * C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:12777251	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831374	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] B6.129P2-Fgfr3<sup>tm1.1Aomw</sup>	is_model_of	DOID:0060703	Muenke Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908349	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10362699	20170906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7531415	Nsf<sup>tm1Himat</sup>/Nsf<sup>+</sup>  [background:] C57BL/6N-Nsf<sup>tm1Himat</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:34745222	20230928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6394127	Shank3<sup>tm2.1Bux</sup>/Shank3<sup>tm2.1Bux</sup>  [background:] B6(Cg)-Shank3<sup>tm2.1Bux</sup>	is_model_of	DOID:0080354	Phelan-McDermid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30302388	20200313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903076	Nmnat1<sup>tvrm113</sup>/Nmnat1<sup>tvrm113</sup>  [background:] C57BL/6J-Nmnat1<sup>tvrm113</sup>/Pjn	is_model_of	DOID:8466	retinal degeneration						ECO:0000033	author statement supported by traceable reference	PMID:27207593	20170623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3779048	Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:15976027	20080428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311833	Megf8<sup>b2b288Clo</sup>/Megf8<sup>b2b288Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b288Clo</sup>	is_model_of	DOID:0060234	Carpenter syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843606	Bcl2l1<sup>tm1.1Mam</sup>/Bcl2l1<sup>tm1.1Mam</sup> Tg(RIP1-Tag)2Dh/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19209227	20090511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722899	Prss8<sup>tm1.1Hum</sup>/Prss8<sup>tm1.2Hum</sup> Tg(KRT14-cre)1Ipc/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:16061697	20070927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711224	Abca3<sup>tm1Nina</sup>/Abca3<sup>tm1Nina</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:17267394	20070807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680045	Slc12a6<sup>tm1Tjj</sup>/Slc12a6<sup>tm1Tjj</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:14532115	20180617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461233	Tg(Igh-V-CD40lg)#Tsub/0  [background:] involves: C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:15128830	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512005	Ddb2<sup>tm1Pra</sup>/Ddb2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110846	xeroderma pigmentosum group E						ECO:0000033	author statement supported by traceable reference	PMID:15558025	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575716	Sh2d1a<sup>tm1Lyin</sup>/Sh2d1a<sup>tm1Lyin</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313516	Tg(Myh6-Actc1*R312H)307Iko/?  [background:] involves: C57BL/6	is_model_of	DOID:0110456	dilated cardiomyopathy 1R						ECO:0000033	author statement supported by traceable reference	PMID:20713897	20120330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432226	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806601	Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>/Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6NTac-Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>/Ieg	is_model_of	DOID:0060230	basal ganglia calcification						ECO:0000033	author statement supported by traceable reference	PMID:23934451	20161110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776560	Col1a1<sup>m1Btlr</sup>/Col1a1<sup>m1Btlr</sup>  [background:] C57BL/6J-Col1a1<sup>m1Btlr</sup>	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:28916811	20190627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654555	Dvl2<sup>tm1Awb</sup>/Dvl2<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Dvl2<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Swiss)	is_model_of	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000033	author statement supported by traceable reference	PMID:14976138	20210927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896639	Plekhm1<sup>tm1.2Hzhao</sup>/Plekhm1<sup>tm1.2Hzhao</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0110945	autosomal recessive osteopetrosis 6						ECO:0000033	author statement supported by traceable reference	PMID:27777970	20170712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850181	Clrn1<sup>tm1.1Kuna</sup>/Clrn1<sup>tm1.1Kuna</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110841	Usher syndrome type 3A						ECO:0000033	author statement supported by traceable reference	PMID:19414487	20090713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925396	Cdc73<sup>tm1Btt</sup>/Cdc73<sup>+</sup> Tg(PTH-cre)4167Slib/0  [background:] Not Specified	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429551	Stk36<sup>tm1Lex</sup>/Stk36<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522006	Del(11Cops3-Gid4)2Jrl/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15459175	20050527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907446	Cap2<sup>tm1e(EUCOMM)Wtsi</sup>/Cap2<sup>tm1e(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Cap2<sup>tm1e(EUCOMM)Wtsi</sup>	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22945801	20170825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273511	Kras<sup>tm5Tyj</sup>/Kras<sup>+</sup> Pdx1<sup>tm1.1(flpo)Most</sup>/Pdx1<sup>+</sup> Trp53<sup>tm1.1Dgk</sup>/Trp53<sup>+</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * Black Swiss * C57BL/6	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28934293	20190115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4939026	Tg(Igh-Maf)68Staka/0  [background:] C57BL/6-Tg(Igh-Maf)68Staka	is_model_of	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:21224354	20110228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611315	Pde6a<sup>nmf282</sup>/Pde6a<sup>nmf282</sup>  [background:] A.B6 Tyr<sup>+</sup>-Pde6a<sup>nmf282</sup>/J	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:18849587	20090126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286689	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf  [background:] involves: C57BL/6 * CBA * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22049426	20190410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571287	Umod<sup>Urehd1</sup>/Umod<sup>Urehd1</sup>  [background:] involves: C3HeB/FeJ	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:23748428	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614443	Ccr1<sup>tm1Gao</sup>/Ccr1<sup>tm1Gao</sup>  [background:] B6.129S4-Ccr1<sup>tm1Gao</sup>	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286078	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] B6.129S2-Trp53<sup>tm1Tyj</sup> Nf1<sup>tm1Tyj</sup>/+ +	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:10973261	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555835	b2b2025Clo/b2b2025Clo  [background:] C57BL/6J-b2b2025Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651886	Nmf15/Nmf15<sup>+</sup>  [background:] C57BL/6J-Nmf15/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:2651853	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197269	Gt(ROSA)26Sor<sup>tm7(Pik3ca*,EGFP)Rsky</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] B6.Cg-Gt(ROSA)26Sor<sup>tm7(Pik3ca*,EGFP)Rsky</sup> Tg(CAG-cre/Esr1*)5Amc	is_model_of	DOID:0080351	CLOVES syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29899452	20181221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4415607	Tg(Prnp-ITM2B*)1Ruvi/?  [background:] B6.C3Fe-Tg(Prnp-ITM2B*)1Ruvi	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:18410407	20100112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624986	Tg(Ckm-LPL)LRze/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:423	myopathy						ECO:0000033	author statement supported by traceable reference	PMID:7635990	20190806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677316	Eya1<sup>tm1Rilm</sup>/Eya1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:14702	branchiootorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6468250	Nexmif<sup>tm1(KOMP)Wtsi</sup>/Y  [background:] B6J.B6N-Nexmif<sup>tm1(KOMP)Wtsi</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:31704787	20201022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5495915	Ddc<sup>tm1.1Nwlh</sup>/Ddc<sup>tm1.1Nwlh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0090123	aromatic L-amino acid decarboxylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:23275025	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275112	Pitx2<sup>egl1</sup>/Pitx2<sup>egl1</sup>  [background:] C57BL/6J-Pitx2<sup>egl1</sup>/Boc	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	MGI:6275025	20190129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276576	Tg(Mpz*S63X)31Mes/0  [background:] involves: FVB/N	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840691	Kit<sup>W-v</sup>/Kit<sup>W-v</sup>  [background:] C57BL/6J-Kit<sup>W-v</sup>/J	is_model_of	DOID:2361	macrocytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824306	Tg(PDGFB-SNCA/EGFP)78Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:15765523	20170216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763106	Tg(MMTV-LPAR2)#Gbm/Tg(MMTV-LPAR2)#Gbm  [background:] FVB/N-Tg(MMTV-LPAR2)#Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695554	Ildr1<sup>Gt(D178D03)Wrst</sup>/Ildr1<sup>Gt(D178D03)Wrst</sup>  [background:] involves: 129S2/SvPas * Swiss Webster	is_model_of	DOID:0110500	autosomal recessive nonsyndromic deafness 42						ECO:0000033	author statement supported by traceable reference	PMID:25217574	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620044	Ryr1<sup>tm1Slh</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:8545	malignant hyperthermia						ECO:0000033	author statement supported by traceable reference	PMID:16284304	20060419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6119480	Tubb5<sup>tm1.1Dak</sup>/Tubb5<sup>tm1.1Dak</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:26903504	20180305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5546609	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup>  [background:] B6.129-Cfh<sup>tm1Mbo</sup>	is_model_of	DOID:0110017	age related macular degeneration 4						ECO:0000033	author statement supported by traceable reference	PMID:23799019	20140228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906259	Tg(Myh6-Snai1)B10Jcc/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17512504	20170807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6163637	Dmd<sup>em1Eno</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:29187645	20180628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720946	Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16354928	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160427	Fat1<sup>tm1.1Nsib</sup>/Fat1<sup>tm1.1Nsib</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129/Sv * 129S4/SvJaeSor * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26905694	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5492338	Phex<sup>m1Jrt</sup>/Phex<sup>+</sup>  [background:] B6.129S1-Phex<sup>M1Jrt</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22573557	20130627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589409	Alms1<sup>Gt(XH152)Byg</sup>/Alms1<sup>Gt(XH152)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16000322	20100603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356437	Del(7Ipw-Snord116)1Jbro/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27672097	20180119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6114152	Cav3<sup>tm1Ncnp</sup>/Cav3<sup>tm1Ncnp</sup>  [background:] involves: 129S4/SvJae * C57BL/10	is_model_of	DOID:0060255	rippling muscle disease 2						ECO:0000033	author statement supported by traceable reference	PMID:19535499	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769338	Ahsp<sup>tm1.1Mjwe</sup>/Ahsp<sup>tm1.1Mjwe</sup> Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:15545996	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3830854	Tymp<sup>tm1Mihi</sup>/Tymp<sup>tm1Mihi</sup> Upp1<sup>tm1Gp</sup>/Upp1<sup>tm1Gp</sup>  [background:] involves: 129 * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0080119	mitochondrial DNA depletion syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19028666	20140813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681537	Fbln5<sup>tm1Krc</sup>/Fbln5<sup>tm1Krc</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:3144	cutis laxa						ECO:0000033	author statement supported by traceable reference	PMID:11805835	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587764	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15888477	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5614980	Dnah5<sup>b2b2570Clo</sup>/Dnah5<sup>b2b2570Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2570Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20190214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402641	Tg(Ace2-ACE2)1Cqin/0  [background:] involves: ICR	is_model_of	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17974127	20200402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699093	Htt<sup>tm1.1Tna</sup>/Htt<sup>tm1.1Tna</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11494364	20070307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850627	Man2a1<sup>tm1Jxm</sup>/Man2a1<sup>tm1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11158608	20100302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684282	Dag1<sup>tm1Kcam</sup>/Dag1<sup>tm2Kcam</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:12140559	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721424	Cdk5r1<sup>tm1Lht</sup>/Cdk5r1<sup>tm1Lht</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:20832057	20150225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618788	Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(TcraAI4)1Dvs/0 Tg(TcrbAI4)1Dvs/0  [background:] NOD.Cg-Rag1<sup>tm1Mom</sup> Tg(TcraAI4)1Dvs Tg(TcrbAI4)1Dvs/Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12498815	20060407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7541130	Wwox<sup>em1Mald</sup>/Wwox<sup>em1Mald</sup>  [background:] FVB/N-Wwox<sup>em1Mald</sup>	is_model_of	DOID:0080060	autosomal recessive spinocerebellar ataxia 12						ECO:0000033	author statement supported by traceable reference	PMID:36828035	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4462829	Whrn<sup>tm1Tili</sup>/Whrn<sup>tm1Tili</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110840	Usher syndrome type 2D						ECO:0000033	author statement supported by traceable reference	PMID:20502675	20100803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3806979	Phex<sup>Pug</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:17710565	20120620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284279	Chmp2b<sup>tm1.1Hiok</sup>/Chmp2b<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449898	Tg(SOD1)2Gur/0 Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16636275	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441555	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Lejo</sup>/Trp53<sup>tm1Lejo</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784504	Pparg<sup>tm3(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6	is_model_of	DOID:0050440	familial partial lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707539	Nppc<sup>lbab</sup>/Nppc<sup>lbab</sup>  [background:] B6.PL-Nppc<sup>lbab</sup>/GrsrJ	is_model_of	DOID:2256	osteochondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:22271248	20220512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676317	Ush1c<sup>dfcr-2J</sup>/Ush1c<sup>dfcr-2J</sup>  [background:] B6;129S4	is_model_of	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689499	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6163736	Kdm5c<sup>tm1.2Yshi</sup>/Y  [background:] involves: 129 * 129S1/SvImJ * C57BL/6J	is_model_of	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type						ECO:0000033	author statement supported by traceable reference	PMID:26804915	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7278772	Acvr1<sup>tm1Glh</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1.2(CAG-EGFP)Glh</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:29396429	20220517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850502	Tg(Lck-Tslp)1Chea/0  [background:] B6.Cg-Tg(Lck-Tslp)1Chea	is_model_of	DOID:2917	cryoglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:11733384	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423338	Prph2<sup>tm1.1Itl</sup>/Prph2<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060866	patterned macular dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:25001182	20200519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623679	Fkbp1b<sup>tm1Amks</sup>/Fkbp1b<sup>tm1Amks</sup>  [background:] DBA/1LacJ-Fkbp1b<sup>tm1Amks</sup>	is_model_of	DOID:0060674	catecholaminergic polymorphic ventricular tachycardia						ECO:0000033	author statement supported by traceable reference	PMID:12837242	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530641	Lcat<sup>tm1Nsa</sup>/Lcat<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:1391	Norum disease						ECO:0000033	author statement supported by traceable reference	PMID:9054454	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617447	Fah<sup>tm1Mgo</sup>/Fah<sup>tm1Mgo</sup>  [background:] involves: 129S7/SvEvBrd * PT	is_model_of	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:10518553	20060323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256787	Fgfr3<sup>tm1Dor</sup>/Fgfr3<sup>tm1Dor</sup>  [background:] C3.129S6(B6)-Fgfr3<sup>tm1Dor</sup>	is_model_of	DOID:0060249	scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:25852647	20181116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7484465	Gba1<sup>tm1.1Smoc</sup>/Gba1<sup>tm1.1Smoc</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:35711931	20230524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437109	Odad2<sup>b2b227.1Clo</sup>/Odad2<sup>b2b227.1Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b227.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844353	Arx<sup>tm1Gldn</sup>/Arx<sup>+</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:19439424	20090515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512667	Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>/Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23502960	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5818292	Gnas<sup>tm4Lsw</sup>/Gnas<sup>+</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0080053	Albright's hereditary osteodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26671181	20170119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5564953	Fras1<sup>bfb</sup>/Fras1<sup>bfb</sup>  [background:] involves: C57BL/6JAnu	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24143185	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6490510	Ppp3r1<sup>tm1.1Jhon</sup>/Ppp3r1<sup>tm1.1Jhon</sup>  [background:] involves: C57BL/6 * C57BL/6NTac	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:32882262	20210107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614209	Wfs1<sup>tm1Perm</sup>/Wfs1<sup>tm1Perm</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:16215705	20060301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4999987	Col1a1<sup>tm4(tetO-GFP/RNAi:Apc)Slowe</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1037	lymphoid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:21458673	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188933	Tg(Myh6-Pkp2*/mRuby)4Rbrug/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110077	arrhythmogenic right ventricular dysplasia 9						ECO:0000033	author statement supported by traceable reference	PMID:27412010	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6394025	Dmd<sup>em#Tve</sup>/Y  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31028078	20200312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308942	Sgce<sup>tm1Ygl</sup>/Sgce<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0090034	myoclonic dystonia 11						ECO:0000033	author statement supported by traceable reference	PMID:22040906	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512665	Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23502960	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843917	Nrp2<sup>tm1.2Mom</sup>/Nrp2<sup>tm1.2Mom</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/NJ	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:18657176	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425921	Casr<sup>BCH007</sup>/Casr<sup>BCH007</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH007</sup>	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902072	Slc9a6<sup>tm1Dgen</sup>/Slc9a6<sup>tm1Dgen</sup>  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J	is_model_of	DOID:0060825	Christianson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21964919	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762620	Tg(S100b-v-erbB)4496Waw/0 Trp53<sup>tm1Brd</sup>/Trp53<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * DBA/2J	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:18470539	20160419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7437706	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>+</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>	is_model_of	DOID:1572	normal pressure hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160757	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>/Y Cnp<sup>tm1(cre)Kan</sup>/Cnp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	is_model_of	DOID:0110773	hereditary spastic paraplegia 2						ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159288	Abca4<sup>tm1.1Rsmy</sup>/Abca4<sup>tm1.1Rsmy</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:29145636	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6476763	Cd2ap<sup>em1Irgu</sup>/Cd2ap<sup>em1Irgu</sup>  [background:] C57BL/6-Cd2ap<sup>em1Irgu</sup>	is_model_of	DOID:0112245	focal segmental glomerulosclerosis 3						ECO:0000033	author statement supported by traceable reference	PMID:30612599	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6343571	Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>/Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000033	author statement supported by traceable reference	PMID:30520996	20190815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459466	Lmna<sup>Dhe</sup>/Lmna<sup>+</sup>  [background:] B6(D2)-Lmna<sup>Dhe</sup>/TyGrsrJ	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:22819531	20180206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763917	Tg(HSA*LR)20bCath/?  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5619656	fm/fm  [background:] involves: CBA/H	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:970440	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3686897	Sirt6<sup>tm1Fwa</sup>/Sirt6<sup>tm1Fwa</sup>  [background:] involves: 129S6/SvEvTac * 129X1/SvJ	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:16439206	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558108	Tg(CMV-SALL4_iB)#Chai/?  [background:] Not Specified	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:16763212	20140411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838163	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:12468647	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432258	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-IGF1R)1Ramo/0  [background:] involves: FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:16953219	20120828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707523	Eda<sup>Ta-6J</sup>/Y  [background:] C57BL/6J A<sup>w-J</sup>-Eda<sup>Ta-6J</sup>/J	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:14506134	20070628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653483	Fgf23<sup>tm1Sliu</sup>/Fgf23<sup>tm1Sliu</sup> Phex<sup>Hyp</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:16449303	20060905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5609024	Fam161a<sup>Gt(462E7)Cmhd</sup>/Fam161a<sup>Gt(462E7)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110365	retinitis pigmentosa 28						ECO:0000033	author statement supported by traceable reference	PMID:24833722	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259805	Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>/Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:0050679	blue cone monochromacy						ECO:0000033	author statement supported by traceable reference	PMID:28751656	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507866	Igs2<sup>tm1(CAG-Met)Zsu</sup>/Igs2<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129 * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:30401749	20210225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287155	Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080322	polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28666097	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615049	Spta1<sup>ihj</sup>/Spta1<sup>ihj</sup>  [background:] involves: HRS/J * LAH	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:20056793	20101210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661329	Col1a1<sup>tm4(CAG-FGFR2_iIIIb*K660N)Kkw</sup>/Col1a1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25035393	20150909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544308	Snca<sup>tm1Rosl</sup>/Snca<sup>tm1Rosl</sup> Tg(SNCA)OVX37Rwm/0  [background:] B6.Cg-Tg(SNCA)OVX37Rwm Snca<sup>tm1Rosl</sup>	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:24082145	20140217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538583	Tg(MMTV-Erbb2)NK1Mul/0  [background:] FVB/N-Tg(MMTV-Erbb2)NK1Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11200779	20140205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814819	Ccl2<sup>tm1Rol</sup>/Ccl2<sup>tm1Rol</sup> Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] involves: 129 * 129S4/SvJae	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:17652758	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336146	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] CAST.Cg-Tg(APPswe,PSEN1dE9)85Dbo/How	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:31150388	20220915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6860681	Hcfc1<sup>em1Poche</sup>/Y  [background:] C57BL/6J-Hcfc1<sup>em1Poche</sup>	is_model_of	DOID:0111814	methylmalonic acidemia and homocysteinemia cblX type						ECO:0000033	author statement supported by traceable reference	PMID:35013307	20220131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:33257679	20210331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:33465158	20210331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32841215	20210331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	MGI:6467226	20210331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3807714	None [background:] A/J	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:17041219	20200602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6316069	Ankfy1<sup>Gt(RRE069)Byg</sup>/Ankfy1<sup>+</sup>  [background:] B6.129P2-Ankfy1<sup>Gt(RRE069)Byg</sup>	is_model_of	DOID:0050946	Charlevoix-Saguenay spastic ataxia						ECO:0000033	author statement supported by traceable reference	PMID:28588446	20190705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256808	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*)#Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:27251290	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256808	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*)#Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:20033049	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159715	Arid1b<sup>em1Hzhu</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Hzhu</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28695822	20180606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818534	Coro1a<sup>ptcd</sup>/Coro1a<sup>tm1Achn</sup>  [background:] B6.Cg-Coro1a<sup>ptcd</sup> Coro1a<sup>tm1Achn</sup>	is_model_of	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764704	Ripply2<sup>tm1Asas</sup>/Ripply2<sup>tm1Asas</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050568	spondylocostal dysostosis						ECO:0000033	author statement supported by traceable reference	PMID:17531978	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510670	Irs1<sup>tm1Jos</sup>/Irs1<sup>+</sup> Irs2<sup>tm2Mfw</sup>/Irs2<sup>tm2Mfw</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15467829	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4436912	Vhl<sup>tm1.1Wkr</sup>/Vhl<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:19252526	20100310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571628	Tg(APOB)1102Sgy/?  [background:] B6.Cg-Tg(APOB)1102Sgy	is_model_of	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:19450445	20140709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709555	H2<sup>q</sup>/? Ncf1<sup>m1J</sup>/Ncf1<sup>m1J</sup>  [background:] B6.Cg-Ncf1<sup>m1J</sup> H2<sup>q</sup>	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:15310853	20070521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763076	Tg(MMTV-ENPP2)20Gbm/0  [background:] FVB/N-Tg(MMTV-ENPP2)20Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7450790	Stim1<sup>tm1.1Pg</sup>/Stim1<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080089	tubular aggregate myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:31666234	20230404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680386	Gba1<sup>tm1Ggb</sup>/Gba1<sup>tm1Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839954	Drd3<sup>tm1Dac</sup>/Drd3<sup>tm1Dac</sup>  [background:] B6.129S4-Drd3<sup>tm1Dac</sup>/J	is_model_of	DOID:0050425	restless legs syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15601940	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5645239	Dnah5<sup>b2b2451Clo</sup>/Dnah5<sup>b2b2451Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2451Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177042	Twist1<sup>Pde</sup>/Twist1<sup>Pde</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11350121	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7329791	Hmgcs2<sup>em1(IMPC)Tcp</sup>/Hmgcs2<sup>em1(IMPC)Tcp</sup>  [background:] C57BL/6NCrl-Hmgcs2<sup>em1(IMPC)Tcp</sup>	is_model_of	DOID:0081168	HMG-CoA synthase 2 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:35421611	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665237	Frem1<sup>tm1Ksek</sup>/Frem1<sup>tm1Ksek</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587032	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] B6C3Fe-a/a Hoxa13<sup>Hd</sup> Mcoln3<sup>Va-J</sup>/J	is_model_of	DOID:0060739	hand-foot-genital syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10569982	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661730	Ace2<sup>tm1Pngr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:17499227	20171101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5556259	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Smad4<sup>tm2.1Cxd</sup>/Smad4<sup>tm2.1Cxd</sup> Tg(Krt1-15-cre/PGR*)22Cot/0  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL/J	is_model_of	DOID:1749	squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23999427	20170531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7442320	Kcnt1<sup>em1Pqt</sup>/Kcnt1<sup>em1Pqt</sup>  [background:] C57BL/6J-Kcnt1<sup>em1Pqt</sup>	is_model_of	DOID:0080439	developmental and epileptic encephalopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:36173683	20230308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7275232	Rbm20<sup>em1Hgra</sup>/Rbm20<sup>+</sup>  [background:] C57BL/6-Rbm20<sup>em1Hgra</sup>	is_model_of	DOID:0110447	dilated cardiomyopathy 1DD						ECO:0000033	author statement supported by traceable reference	PMID:35041844	20220509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4398718	Tg(Pcp2-SCA7)P7EJman/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:11030754	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000309	Sos1<sup>tm1.2Rak</sup>/Sos1<sup>tm1.2Rak</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:0060582	Noonan syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:21041952	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721431	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1.1Jme</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J * SJL	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:10749994	20070913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566830	Myo7a<sup>sh1-13J</sup>/Myo7a<sup>sh1-13J</sup>  [background:] C.Cg-Myo7a<sup>sh1-13J</sup>/GrsrJ	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259179	Tg(Eno2-Thrsp)#Cheo/0  [background:] C57BL/6-Tg(Eno2-Thrsp)#Cheo	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:30138648	20181205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510669	Irs2<sup>tm2Mfw</sup>/Irs2<sup>tm2Mfw</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15467829	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046805	Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup> Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm3Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474460	Tg(Tagln-SLC6A4)#Edd/?  [background:] Not Specified	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:16614302	20130417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7314277	Prdm16<sup>tm1.1Brsp</sup>/Prdm16<sup>tm1.1Brsp</sup> Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: 129 * C57BL/6J * MF1	is_model_of	DOID:0060480	left ventricular noncompaction						ECO:0000033	author statement supported by traceable reference	PMID:34915728	20220721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279194	Pcsk1<sup>em2Irli</sup>/Pcsk1<sup>em2Irli</sup>  [background:] C57BL/6J-Pcsk1<sup>em2Irli</sup>	is_model_of	DOID:28	endocrine system disease						ECO:0000033	author statement supported by traceable reference	PMID:35245347	20220520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897821	Tprn<sup>em1Pghu</sup>/Tprn<sup>em1Pghu</sup>  [background:] B6.Cg-Tprn<sup>em1Pghu</sup>	is_model_of	DOID:0110526	autosomal recessive nonsyndromic deafness 79						ECO:0000033	author statement supported by traceable reference	PMID:27693694	20170712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429560	Slc26a7<sup>tm1Sole</sup>/Slc26a7<sup>tm1Sole</sup>  [background:] involves: 129	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:30333321	20220614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431966	Tg(RIP1-Tag)2Dh/0  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:3892	insulinoma						ECO:0000033	author statement supported by traceable reference	PMID:22562956	20181120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162677	Slc19a3<sup>tm1Said</sup>/Slc19a3<sup>tm1Said</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050659	biotin-responsive basal ganglia disease						ECO:0000033	author statement supported by traceable reference	PMID:28665968	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427498	Gt(ROSA)26Sor<sup>tm1(CAG-Bmi1,-EGFP)Nki</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm1Mro</sup>/Pten<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22505453	20120711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308205	Gars1<sup>Nmf249</sup>/Gars1<sup>+</sup>  [background:] involves: C57BL/6J * CAST/Ei	is_model_of	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:22144914	20120302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559028	Slc6a1<sup>tm1Mlit</sup>/Slc6a1<sup>tm1Mlit</sup>  [background:] B6.129S1-Slc6a1<sup>tm1Mlit</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23922840	20140415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400524	Cacna1g<sup>em1Ftan</sup>/Cacna1g<sup>+</sup>  [background:] C57BL/6NCrSlc-Cacna1g<sup>em1Ftan</sup>	is_model_of	DOID:0111742	cerebellar ataxia type 42						ECO:0000033	author statement supported by traceable reference	PMID:31229688	20200702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432228	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:2999	granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6388458	Ngf<sup>tm1(NGF*)Cat</sup>/Ngf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0070145	hereditary sensory and autonomic neuropathy type 5						ECO:0000033	author statement supported by traceable reference	PMID:31685654	20200203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681522	Ar<sup>tm1Ska</sup>/Y Tg(CMV-cre)1Ipc/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12943692	20100603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279103	Crppa<sup>em2Mbp</sup>/Crppa<sup>em2Mbp</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] B6.Cg-Myf5<sup>tm3(cre)Sor</sup> Crppa<sup>em2Mbp</sup>	is_model_of	DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U						ECO:0000033	author statement supported by traceable reference	PMID:35422047	20220519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174703	Pkd2<sup>tm1Som</sup>/Pkd2<sup>tm1Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:9568711	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431492	Gpr179<sup>nob5</sup>/Gpr179<sup>nob5</sup>  [background:] involves: C3H	is_model_of	DOID:0110869	congenital stationary night blindness 1E						ECO:0000033	author statement supported by traceable reference	PMID:22325362	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505276	Serpinh1<sup>tm2Kzn</sup>/Serpinh1<sup>tm2Kzn</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0110346	osteogenesis imperfecta type 10						ECO:0000033	author statement supported by traceable reference	PMID:22492985	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356523	Hvf/Hvf<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:0060249	scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:30283900	20220518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5646380	Klhl3<sup>tm1.1Esoh</sup>/Klhl3<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:24821705	20180522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447165	Jag1<sup>tm1Frad</sup>/Jag1<sup>tm1Frad</sup> Tg(Tagln-cre)1Her/0  [background:] B6.Cg-Jag1<sup>tm1Frad</sup> Tg(Tagln-cre)1Her	is_model_of	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21062863	20121231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5787933	Emg1<sup>tm1.1Btr</sup>/Emg1<sup>tm1.1Btr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	is_model_of	DOID:0050684	Bowen-Conradi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25708872	20160804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764685	Phex<sup>Hyp</sup>/Phex<sup>+</sup>  [background:] B6.Cg-Phex<sup>Hyp</sup>/J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4365717	Tg(Vim*R113C)1Tmm/0  [background:] B6.CBA-Tg(Vim*R113C)1Tmm	is_model_of	DOID:0110248	cataract 30						ECO:0000033	author statement supported by traceable reference	PMID:18940912	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581492	Myoz2<sup>tm1Eno</sup>/Myoz2<sup>+</sup> Tg(Myh6-MYOZ2*I246M)#Ajm/0  [background:] involves: 129/Sv * FVB/N	is_model_of	DOID:0110322	hypertrophic cardiomyopathy 16						ECO:0000033	author statement supported by traceable reference	PMID:22987565	20140902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3790954	Stk11<sup>tm1Tpm</sup>/Stk11<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12218179	20080610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175151	Nkx3-1<sup>tm1Hha</sup>/Nkx3-1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:10906459	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6690813	Dysf<sup>tm1.1Mdcb</sup>/Dysf<sup>tm1.1Mdcb</sup>  [background:] B6.129P2(Cg)-Dysf<sup>tm1.1Mdcb</sup>	is_model_of	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:30292141	20210415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3696675	Elovl4<sup>tm1Rayy</sup>/Elovl4<sup>+</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:17003453	20070213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305097	Is(14)1Rdf/Is(14)1Rdf Is(14)5Rdf/Is(14)5Rdf Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22174151	20120207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056392	Tg(Prnp-ATN1)124Dbo/?  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000033	author statement supported by traceable reference	PMID:10677044	20110810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361717	Tg(Prnp-TARDBP*A315T)95Balo/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:19833869	20111207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698041	Htt<sup>tm5Mem</sup>/Htt<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10699173	20070227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681520	Ghr<sup>tm1Arge</sup>/Ghr<sup>tm1Arge</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:9521	Laron syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11133160	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6193898	Tg(Myh6-MYL2*D94A)1Dsc/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:29463717	20180808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17641777	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686745	Npc1<sup>nmf164</sup>/Npc1<sup>nmf164</sup>  [background:] C57BL/6J-Npc1<sup>nmf164</sup>/J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22048958	20120131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5460885	Hbb-b1<sup>Rbc13</sup>/Hbb-b1<sup>Rbc13</sup>  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:23040355	20130128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429501	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Ppargc1a)1Dpk/0  [background:] involves: FVB/N * FVB/NTac	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:14726475	20170830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583544	Tg(ITGA2)1070Fmw/0 Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6103876	Fancf<sup>tm1Nki</sup>/Fancf<sup>tm1Nki</sup>  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:5426	primary ovarian insufficiency						ECO:0000033	author statement supported by traceable reference	PMID:21915857	20171220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056475	Sqstm1<sup>tm1.1Sral</sup>/Sqstm1<sup>tm1.1Sral</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:21515589	20110811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623448	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] NOD.Cg-Ifng<sup>tm1Ts</sup> Prkdc<sup>scid</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11714835	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555841	Mmp21<sup>b2b2458Clo</sup>/Mmp21<sup>b2b2458Clo</sup>  [background:] C57BL/6J-Mmp21<sup>b2b2458Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590685	Gck<sup>tm1.2Mgn</sup>/Gck<sup>tm1.2Mgn</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777383	Pla2g6<sup>tm1Tsu</sup>/Pla2g6<sup>tm1Tsu</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:21813701	20110919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7485763	Adar<sup>em3Qwan</sup>/Adar<sup>em3Qwan</sup>  [background:] Not Specified	is_model_of	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34332594	20230530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7444296	Mlx<sup>tm1.2Rne</sup>/Mlx<sup>tm1.2Rne</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:34669700	20230315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175870	Eya1<sup>bor</sup>/Eya1<sup>bor</sup>  [background:] C3HeB/FeJ-Eya1<sup>bor</sup>	is_model_of	DOID:14702	branchiootorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10072433	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336761	Copa<sup>tm1.1Shum</sup>/Copa<sup>+</sup>  [background:] B6(CBA)-Copa<sup>tm1.1Shum</sup>	is_model_of	DOID:0081242	autoimmune interstitial lung, joint, and kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:32198142	20230113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838642	Sav1<sup>tm1.1Dupa</sup>/Sav1<sup>tm1.1Dupa</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL	is_model_of	DOID:5353	colonic disease						ECO:0000033	author statement supported by traceable reference	PMID:21041407	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617390	Pkd1<sup>tm2.1Ggg</sup>/Pkd1<sup>tm2.1Ggg</sup>  [background:] involves: 129S4/SvJae * Black Swiss * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:15579506	20060323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430591	Tcra-J<sup>tm1Tgi</sup>/Tcra-J<sup>tm1Tgi</sup> Tg(Pklr-Myc)73Ak/0  [background:] B6.Cg-Tcra-J<sup>tm1Tgi</sup> Tg(Pklr-Myc)73Ak	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22251704	20120807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852560	Tg(DBH-SNCA)#Dwei/0  [background:] C57BL/6N-Tg(DBH-SNCA)#Dwei	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:32868457	20220112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6161438	b2b3183Clo/b2b3183Clo  [background:] C57BL/6J-b2b3183Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20180618	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295210	Tg(Thy1-BSCL2*N88S)1Dit/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:231	motor neuron disease						ECO:0000033	author statement supported by traceable reference	PMID:21750110	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904009	Lrfn2<sup>tm1.1Jaru</sup>/Lrfn2<sup>tm1.1Jaru</sup>  [background:] B6J.129P2-Lrfn2<sup>tm1.1Jaru</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28604739	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5619354	Rhot1<sup>tm1.1Jmsu</sup>/Rhot1<sup>tm1.1Jmsu</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:231	motor neuron disease						ECO:0000033	author statement supported by traceable reference	PMID:25136135	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583956	Pthlh<sup>tm1Hmk</sup>/Pthlh<sup>tm1Hmk</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	is_model_of	DOID:0080053	Albright's hereditary osteodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:8314082	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779422	Gt(ROSA)26Sor<sup>tm1.1(rtTA2S*M2)Whsu</sup>/Gt(ROSA)26Sor<sup>+</sup> Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(tetO-cre)1Jaw/0  [background:] involves: 129 * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25194568	20160629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720731	Tg(Thy1-APP)3Somm/0  [background:] B6.Cg-Tg(Thy1-APP)3Somm	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12426044	20070907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425546	Phex<sup>Mhdabap012</sup>/Phex<sup>Mhdabap012</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap012</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588875	Gjb2<sup>tm1Ugds</sup>/Gjb2<sup>tm1Ugds</sup> Tg(Otog-cre)1Ugds/0  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000033	author statement supported by traceable reference	PMID:12121617	20051005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450130	Fancc<sup>tm1Mab</sup>/Fancc<sup>tm1Mab</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111087	Fanconi anemia complementation group C						ECO:0000033	author statement supported by traceable reference	PMID:8630504	20110518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175225	Otc<sup>spf</sup>/Otc<sup>spf</sup>  [background:] involves: CD-1	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1575747	20090716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461139	Tg(Tnf)6074Gkl/0 Tnfrsf1b<sup>tm1Mwm</sup>/Tnfrsf1b<sup>tm1Mwm</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * CBA	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:9736029	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629875	Gpc3<sup>tm1Arge</sup>/Y H19<sup>tm1Tilg</sup>/H19<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:11846487	20060724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677019	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/?  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:10655541	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174792	Ttpa<sup>tm1Far</sup>/Ttpa<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090028	familial isolated deficiency of vitamin E						ECO:0000033	author statement supported by traceable reference	PMID:11095717	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621814	E2f1<sup>tm1Meg</sup>/E2f1<sup>tm1Meg</sup>  [background:] NOD.Cg-E2f1<sup>tm1Meg</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15470032	20060509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174947	Edn3<sup>tm1Ywa</sup>/Edn3<sup>tm1Ywa</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:8001160	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6715340	Fmr1<sup>tm1.1Ics</sup>/Fmr1<sup>tm1.1Ics</sup>  [background:] C57BL/6-Fmr1<sup>tm1.1Ics</sup>	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33692361	20210614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043596	Ercc5<sup>tm2Shm</sup>/Ercc5<sup>tm2Shm</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0110849	xeroderma pigmentosum group G						ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5319308	Inpp5d<sup>tm1Rkh</sup>/Inpp5d<sup>tm1Rkh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:12161749	20120525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693292	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO/CMV-KRAS*G12C)9.1Msmi/0  [background:] involves: FVB/N	is_model_of	DOID:3683	lung benign neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:16051643	20171102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910547	Erg<sup>tm1.1Iwamo</sup>/Erg<sup>tm1.1Iwamo</sup> Tg(Gdf5-cre,-ALPP)1Kng/?  [background:] involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:26097038	20170928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6241434	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae	is_model_of	DOID:0080143	congenital fibrosis of the extraocular muscles						ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423341	Prph2<sup>tm1.1Itl</sup>/Prph2<sup>tm1.1Itl</sup>  [background:] Not Specified	is_model_of	DOID:0060866	patterned macular dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:25001182	20200519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789334	Tg(SFTPC-EGFR*L858R)4-3Kkiu/0  [background:] involves: C57BL/6Cr	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19690148	20160819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5319646	Tg(NPHS2-Trpc6*E896K)F75aWalz/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0111129	focal segmental glomerulosclerosis 2						ECO:0000033	author statement supported by traceable reference	PMID:20877463	20120530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800634	Tg(CAMalpha1b)7Wjk/?  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11454600	20170830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308379	Tg(RP3-340H11)29Kel/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:0060334	transient neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15286800	20120307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447049	Tg(BCL2/IGH)#Jcre/0 Tg(H2-K/Igh-Traf2*)#Ywc/0  [background:] involves: BALB/c * C57BL/6 * CBA/J * FVB/N * SJL/J * SWR/J	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15545599	20121227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000033	author statement supported by traceable reference	PMID:12142349	20210927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000033	author statement supported by traceable reference	PMID:12818570	20210927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908453	Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup> Gt(ROSA)26Sor<sup>tm2(CARD11*L225LI)Jrld</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:26668357	20170907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6505486	Atrip<sup>tm1.1Pof</sup>/Atrip<sup>tm1.1Pof</sup> Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050569	Seckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32994318	20210208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429423	Pitx3<sup>eyl</sup>/Pitx3<sup>eyl</sup>  [background:] involves: C3H/He * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:20033184	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844300	Ank1<sup>Rbc2</sup>/Ank1<sup>Rbc2</sup>  [background:] involves: 129S1/Sv * BALB/c	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19179303	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6306320	B4galt1<sup>tm1Yiw</sup>/B4galt1<sup>tm1Yiw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:17255313	20190530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517703	Tg(Pax6-TAg)1796Hur/0  [background:] involves: FVB	is_model_of	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22562503	20131115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6306137	Tg(Col2a1-cre/ERT2)1Dic/0 Tgfbr1<sup>tm1.1Karl</sup>/Tgfbr1<sup>tm1.1Karl</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:28716756	20190529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046807	Cdkn1a<sup>tm1(HBsAg)Xya</sup>/Cdkn1a<sup>tm1(HBsAg)Xya</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6343406	Gas2l2<sup>tm1c(KOMP)Wtsi</sup>/Gas2l2<sup>tm1c(KOMP)Wtsi</sup> Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/Foxj1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:30665704	20190814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5817772	Ednra<sup>m1Mhda</sup>/Ednra<sup>m1Mhda</sup>  [background:] C3HeB/FeJ-Ednra<sup>m1Mhda</sup>	is_model_of	DOID:0060365	mandibulofacial dysostosis with alopecia						ECO:0000033	author statement supported by traceable reference	PMID:27671791	20170116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665403	Grip1<sup>eb</sup>/Grip1<sup>eb</sup>  [background:] involves: hairless stock	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	MGI:61605	20110125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849179	Nf1<sup>tm1Fcr</sup>/Nf1<sup>tm1Fcr</sup> Trp53<sup>tm1Elee</sup>/Trp53<sup>tm1Elee</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S/SvEv * 129S4/SvJae * FVB/N	is_model_of	DOID:3068	glioblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19477430	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311612	Tardbp<sup>tm1.1Sobue</sup>/Tardbp<sup>tm1.1Sobue</sup> Tg(SLC18A3-cre)Misa/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NTac	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:23449777	20220712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905051	Tg(Myh6-Gnaq*Q209L)44Ejne/0  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11448136	20170719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6850159	Nemf<sup>em8Cx</sup>/Nemf<sup>em8Cx</sup>  [background:] C57BL/6J-Nemf<sup>em8Cx</sup>/Cx	is_model_of	DOID:440	neuromuscular disease						ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6474216	Pqbp1<sup>tm1.1Hiok</sup>/Y Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060179	Renpenning syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25070536	20201130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621007	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/Ola * C57BL/6	is_model_of	DOID:0050440	familial partial lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11923874	20060503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583697	Fgl2<sup>tm1Pam</sup>/Fgl2<sup>tm1Pam</sup>  [background:] B6.129X1-Fgl2<sup>tm1Pam</sup>	is_model_of	DOID:0040094	autoimmune glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:18097026	20220531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617198	Manba<sup>tm1Khf</sup>/Manba<sup>tm1Khf</sup>  [background:] B6.129-Manba<sup>tm1Khf</sup>	is_model_of	DOID:3633	beta-mannosidosis						ECO:0000033	author statement supported by traceable reference	PMID:16377659	20060321	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818648	Ndufs4<sup>tm1Rpa</sup>/Ndufs4<sup>tm1Rpa</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * SJL	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:20534480	20100809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6115250	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>/Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:0110415	retinitis pigmentosa 2						ECO:0000033	author statement supported by traceable reference	PMID:25422369	20180208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5691824	Tnfsf11<sup>gum</sup>/Tnfsf11<sup>gum</sup>  [background:] STOCK Tnfsf11<sup>gum</sup>/GrsrJ	is_model_of	DOID:0110943	autosomal recessive osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:26234751	20151020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819492	Tg(PMP22)C61Clh/0  [background:] B6.Cg-Tg(PMP22)C61Clh	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:20093502	20100817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6209392	Slc9a9<sup>tm1.1Yzj</sup>/Slc9a9<sup>tm1.1Yzj</sup>  [background:] Not Specified	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26755066	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839171	Tg(SOD1*G93A)1Gur/0  [background:] B6.Cg-Tg(SOD1*G93A)1Gur	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19699279	20101119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663064	Mitf<sup>Mi-wh</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784770	Hras<sup>tm1Jaf</sup>/Hras<sup>tm1Jaf</sup> Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * FVB/NCr	is_model_of	DOID:1781	thyroid cancer						ECO:0000033	author statement supported by traceable reference	PMID:26359368	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606861	Npm1<sup>tm1Ppp</sup>/Npm1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16007073	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159294	Abca4<sup>tm1Kpal</sup>/Abca4<sup>tm1Kpal</sup> Rdh8<sup>tm1Kpal</sup>/Rdh8<sup>tm1Kpal</sup>  [background:] involves: 129	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:24712709	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905569	Esrrb<sup>tm1.1Nat</sup>/Esrrb<sup>tm1.1Nat</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:28130335	20170726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272015	Tnni2<sup>tm1Sgao</sup>/Tnni2<sup>+</sup>  [background:] involves: 129 * ICR	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:25340332	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175768	Cdkn1c<sup>tm1Sje</sup>/Cdkn1c<sup>tm1Sje</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:5572	Beckwith-Wiedemann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9144284	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6	is_model_of	DOID:0111077	pyruvate kinase deficiency of red cells						ECO:0000033	author statement supported by traceable reference	PMID:14595440	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903761	Nmnat1<sup>imh</sup>/Nmnat1<sup>imh</sup>  [background:] B6J.C(C3H)-Nmnat1<sup>imh</sup>	is_model_of	DOID:0110005	Leber congenital amaurosis 9						ECO:0000033	author statement supported by traceable reference	PMID:27207593	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576479	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386979	Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8988167	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7469827	Tbl1xr1<sup>em2H</sup>/Tbl1xr1<sup>em2H</sup>  [background:] C57BL/6J-Tbl1xr1<sup>em2H</sup>	is_model_of	DOID:0081362	Pierpont syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35416977	20231020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5485198	Col1a1<sup>tm1(tetO-EWSR1/ATF1)Yasu</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:4233	clear cell sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23281395	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581421	Glb1<sup>tm1Adz</sup>/Glb1<sup>tm1Adz</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:3322	GM1 gangliosidosis						ECO:0000033	author statement supported by traceable reference	PMID:9063740	20050712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179045	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9990064	20050708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421775	Smim3<sup>tm1Anjm</sup>/Smim3<sup>+</sup> Cd74<sup>tm1Anjm</sup>/Cd74<sup>+</sup> Lmo2<sup>tm2(cre)Thr</sup>/Lmo2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19966810	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558898	Fah<sup>tm1Mgo</sup>/Fah<sup>tm1Mgo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL	is_model_of	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:7545495	20140414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4880670	Fbn1<sup>tm1Lper</sup>/Fbn1<sup>+</sup>  [background:] involves: 129/Sv * CD-1	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21152435	20110127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3034088	Vps33a<sup>bf</sup>/Vps33a<sup>bf</sup>  [background:] C57BL/6J-Vps33a<sup>bf</sup>	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9585243	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5504390	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:11714	gestational diabetes						ECO:0000033	author statement supported by traceable reference	PMID:22427375	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695524	Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup>  [background:] B6J.Cg-Terc<sup>tm1Rdp</sup>	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:24626990	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6488226	Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N	is_model_of	DOID:0050425	restless legs syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31715135	20201223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523236	Tg(Pcp2-ATXN3*69Q)bHirai/0  [background:] Not Specified	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:18344973	20131210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664560	Fech<sup>tm1Dab</sup>/Fech<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:13270	erythropoietic protoporphyria						ECO:0000033	author statement supported by traceable reference	PMID:12149233	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907012	Tg(Myh6-cre)TG9Pjay/0  [background:] involves: FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17202264	20170815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6502639	Prrt2<sup>tm1d(KOMP)Wtsi</sup>/Prrt2<sup>tm1d(KOMP)Wtsi</sup>  [background:] B6(Cg)-Prrt2<sup>tm1d(KOMP)Wtsi</sup>	is_model_of	DOID:0090053	episodic kinesigenic dyskinesia 1						ECO:0000033	author statement supported by traceable reference	PMID:32891704	20210128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6416345	Hgd<sup>tm1a(KOMP)Wtsi</sup>/Hgd<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:9270	alkaptonuria						ECO:0000033	author statement supported by traceable reference	PMID:31600782	20200513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524277	Tg(tetO-BRAF*V600E)26Jaf/0 Tg(TG-rtTA)30Jaf/0  [background:] involves: FVB/N	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22105174	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038216	Gck<sup>Rgsc341</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711694	Eda<sup>Ta</sup>/Y  [background:] involves: A * C57BL * CBA * RIII	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:2348861	20070629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5805456	Tg(CD2-Rorc)#Staka/0  [background:] involves: C57BL/6	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25411202	20161027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4947978	Npr2<sup>cn-3J</sup>/Npr2<sup>cn-3J</sup>  [background:] MRL/MpJ-Npr2<sup>cn-3J</sup>/GrsrJ	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	MGI:4947088	20110426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429549	Nme5<sup>tm1Lex</sup>/Nme5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174818	Tg(APPV717F)109Ili/0  [background:] Not Specified	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:7845465	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188076	None [background:] NC/Nga	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:9916733	20180711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3528185	Myo6<sup>sv</sup>/Myo6<sup>sv</sup>  [background:] involves: B10.HA/(33NX)Sn * C57BL/6J	is_model_of	DOID:0110495	autosomal recessive nonsyndromic deafness 37						ECO:0000033	author statement supported by traceable reference	PMID:7493015	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5803810	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO/Prnp-APP*Swe*Lon)9191Krz/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25946042	20161017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655192	Slc1a1<sup>tm1Wst</sup>/Slc1a1<sup>tm1Wst</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060650	dicarboxylic aminoaciduria						ECO:0000033	author statement supported by traceable reference	PMID:9233792	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7339154	Lamp2<sup>tm1.2Ces</sup>/Y  [background:] involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:0050437	Danon disease						ECO:0000033	author statement supported by traceable reference	PMID:34459252	20220923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6888378	Tubb4a<sup>Jit</sup>/Tubb4a<sup>Jit</sup>  [background:] FVB.B6-Tubb4a<sup>Jit</sup>	is_model_of	DOID:0060798	hypomyelinating leukodystrophy 6						ECO:0000033	author statement supported by traceable reference	PMID:35171680	20220316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836962	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup> Tg(Atoh1-GFP)1Jejo/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19185848	20090325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6457570	Cfap43<sup>em1Sono</sup>/Cfap43<sup>em1Sono</sup>  [background:] Not Specified	is_model_of	DOID:1572	normal pressure hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:31004071	20200925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775440	Gata4<sup>tm1.1Sad</sup>/Gata4<sup>tm1.2Sad</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:25807280	20160609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285873	Cplx2<sup>tm1Bros</sup>/Cplx2<sup>tm1Bros</sup>  [background:] B6NCrl.Cg-Cplx2<sup>tm1Bros</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:20412316	20110919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669229	Prox1<sup>tm1Gco</sup>/Prox1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16170315	20060127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7329779	Zfhx2<sup>tm3Ymri</sup>/Zfhx2<sup>tm3Ymri</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0081075	Marsili syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29253101	20220816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368183	Porcn<sup>tm1.1Lcm</sup>/Y Tg(rx3-icre)1Mjam/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3773052	Kit<sup>tm1Shta</sup>/Kit<sup>tm1Shta</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:18098338	20080306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358610	Serpina1<sup>em3Chmu</sup>/Serpina1<sup>em3Chmu</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:29453277	20190906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588316	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>/J	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7089489	20050923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449544	F8<sup>tm1Kaz</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12134	factor VIII deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7647782	20200113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6279212	Ccm2<sup>tm1Mlkn</sup>/Ccm2<sup>tm1Mlkn</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129	is_model_of	DOID:0060670	cerebral cavernous malformation 2						ECO:0000033	author statement supported by traceable reference	PMID:27513872	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582643	Eif2ak3<sup>tm1Dron</sup>/Eif2ak3<sup>tm1Dron</sup>  [background:] involves: 129S6/SvEvTac * Swiss Webster	is_model_of	DOID:0090060	Wolcott-Rallison syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11430819	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4947966	Csrp3<sup>tm1.1Rkn</sup>/Csrp3<sup>tm1.1Rkn</sup>  [background:] either: (involves: Black Swiss) or (involves: C57BL/6N)	is_model_of	DOID:0110318	hypertrophic cardiomyopathy 12						ECO:0000033	author statement supported by traceable reference	PMID:20044516	20110425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324047	Shank3<sup>tm2Gfng</sup>/Shank3<sup>+</sup>  [background:] B6.129-Shank3<sup>tm2Gfng</sup>/J	is_model_of	DOID:0080354	Phelan-McDermid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27189882	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675506	Dnase2b<sup>tm1Osa</sup>/Dnase2b<sup>tm1Osa</sup>  [background:] Not Specified	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:12944971	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355020	Atr<sup>tm1Ofc</sup>/Atr<sup>tm1Ofc</sup>  [background:] Not Specified	is_model_of	DOID:0050569	Seckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19620979	20090826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052367	Tg(JPH3-GFP,-JPH3*)GXwy/0  [background:] involves: FVB/N	is_model_of	DOID:0090104	Huntington's disease-like 2						ECO:0000033	author statement supported by traceable reference	PMID:21555070	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622096	Abcc9<sup>tm1Cfb</sup>/Abcc9<sup>tm1Cfb</sup>  [background:] Not Specified	is_model_of	DOID:3393	coronary artery disease						ECO:0000033	author statement supported by traceable reference	PMID:12122112	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762763	Kiss1r<sup>tm1Rla</sup>/Kiss1r<sup>tm1Rla</sup>  [background:] involves: 129S1/SvImJ	is_model_of	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:17595229	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198725	Phex<sup>Mhdabap024</sup>/Y  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:29735309	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571280	Umod<sup>Urehd1</sup>/Umod<sup>+</sup>  [background:] involves: C3HeB/FeJ	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:23748428	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661815	Scrib<sup>Crc</sup>/Scrib<sup>+</sup> Vangl2<sup>Lp</sup>/Vangl2<sup>+</sup>  [background:] C3H.Cg-Vangl2<sup>Lp</sup> Scrib<sup>Crc</sup>	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:25128525	20150915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819114	Tg(Umod*C147W)958Lura/0  [background:] involves: FVB	is_model_of	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:20472742	20100813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618527	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ	is_model_of	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000033	author statement supported by traceable reference	PMID:10862711	20060405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620189	b2b2696Clo/b2b2696Clo  [background:] C57BL/6J-b2b2696Clo	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7442509	Srgap1<sup>tm1a(KOMP)Wtsi</sup>/Srgap1<sup>tm1a(KOMP)Wtsi</sup> Six2<sup>tm1(tTA,tetO-EGFP/cre)Amc</sup>/Six2<sup>+</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6N	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:33514561	20230309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432229	Grm1<sup>Tg(p18A4.B)1352Szc</sup>/0  [background:] Not Specified	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:12704387	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311833	Megf8<sup>b2b288Clo</sup>/Megf8<sup>b2b288Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b288Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950566	Prpf8<sup>tm1.1Eap</sup>/Prpf8<sup>tm1.1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:0110403	retinitis pigmentosa 13						ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441339	Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:22490684	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198577	Dync1h1<sup>tm1.1Sjki</sup>/Dync1h1<sup>+</sup>  [background:] involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J	is_model_of	DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O						ECO:0000033	author statement supported by traceable reference	PMID:29379136	20180918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950073	Kcnq2<sup>Nmf134</sup>/Kcnq2<sup>+</sup> Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:21156207	20110514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7328859	Myt1l<sup>em1Mwer</sup>/Myt1l<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0070069	autosomal dominant intellectual developmental disorder 39						ECO:0000033	author statement supported by traceable reference	PMID:35538503	20220811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655811	Lepr<sup>tm1.2Chua</sup>/Lepr<sup>tm1.2Chua</sup>  [background:] involves: 129 * C57BL/6J * FVB/N	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15207242	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850085	Baz1b<sup>tm1Ska</sup>/Baz1b<sup>+</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19470456	20090710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909888	Mybpc3<sup>tm2.1Lcrr</sup>/Mybpc3<sup>tm2.1Lcrr</sup>  [background:] involves: 129S2/SvPasCrl * Black Swiss	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:22465693	20170919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581521	Casp1<sup>tm1Sesh</sup>/Casp1<sup>tm1Sesh</sup> Casp4<sup>del</sup>/Casp4<sup>del</sup>  [background:] NOD.129S2(B6)-Casp1<sup>tm1Sesh</sup> Casp4<sup>del</sup>/LtJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14693703	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575662	Asxl1<sup>tm1.1Iaai</sup>/Asxl1<sup>tm1.1Iaai</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24218140	20140731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5767290	Tg(Ckm-DNAJB6_ib*F93L)#Ccwe/0  [background:] B6.Cg-Tg(Ckm-DNAJB6_ib*F93L)#Ccwe	is_model_of	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26362252	20160513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521287	Tg(Thy1-MAPT)22Schd/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23247080	20131203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052728	Disp1<sup>icb</sup>/Disp1<sup>tm1Amc</sup> Shh<sup>tm1Amc</sup>/Shh<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110875	holoprosencephaly 3						ECO:0000033	author statement supported by traceable reference	PMID:15269168	20050711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6416491	Tg(FGFR3-G380R)7Aya/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:10607835	20200514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3775522	Flnb<sup>Gt(RRF239)Byg</sup>/Flnb<sup>Gt(RRF239)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090116	spondylocarpotarsal synostosis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17635842	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843462	Avp<sup>tm1Lja</sup>/Avp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12388	neurohypophyseal diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:14660745	20090508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906283	Tg(APCS-Ifng)5Imeg/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17556594	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5750066	Jakmip1<sup>tm1(KOMP)Vlcg</sup>/Jakmip1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26627310	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188637	Tpi1<sup>rbc19</sup>/Tpi1<sup>rbc19</sup>  [background:] SJL-Tpi1<sup>rbc19</sup>	is_model_of	DOID:0050884	triosephosphate isomerase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:29720471	20180716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6115481	Arpc4<sup>tm1c(EUCOMM)Wtsi</sup>/Arpc4<sup>tm1c(EUCOMM)Wtsi</sup> Krt14<sup>tm1(cre)Wbm</sup>/Krt14<sup>+</sup>  [background:] B6.Cg-Arpc4<sup>tm1c(EUCOMM)Wtsi</sup> Krt14<sup>tm1(cre)Wbm</sup>	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:29113991	20180209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312336	Dnah11<sup>b2b598Clo</sup>/Dnah11<sup>b2b598Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b598Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603147	Crygb<sup>Clapper</sup>/Crygb<sup>Clapper</sup>  [background:] C57BL/6J-Crygb<sup>Clapper</sup>	is_model_of	DOID:0110236	cataract 39 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:15878859	20130513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3662906	Ret<sup>tm1Kln</sup>/Ret<sup>tm1Kln</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:16600854	20110125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618862	Dock1<sup>b2b3190Clo</sup>/Dock1<sup>b2b3190Clo</sup>  [background:] C57BL/6J-Dock1<sup>b2b3190Clo</sup>	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198013	Ids<sup>tm1Muen</sup>/Y  [background:] involves: C57BL/6	is_model_of	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:17876721	20180914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008633	Gt(ROSA)26Sor<sup>tm2Thl</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tyr<sup>c-Brd</sup>/Tyr<sup>c-Brd</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6	is_model_of	DOID:0050804	glioblastoma proneural subtype						ECO:0000033	author statement supported by traceable reference	PMID:21625383	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850354	Hr<sup>rh-8J</sup>/Hr<sup>rh-8J</sup>  [background:] B10.D2/nSnJ-Hr<sup>rh-8J</sup>	is_model_of	DOID:0050634	alopecia universalis						ECO:0000033	author statement supported by traceable reference	PMID:9799606	20090714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6506871	Gabrg1<sup>em1Ktka</sup>/Gabrg1<sup>em1Ktka</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:12098	trigeminal neuralgia						ECO:0000033	author statement supported by traceable reference	PMID:33083721	20210217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604616	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] B6SJL-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24709310	20141117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6754173	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:18902556	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3760369	Prkdc<sup>scid</sup>/Prkdc<sup>scid</sup>  [background:] C.BKa-Prkdc<sup>scid</sup>	is_model_of	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:6823332	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762188	Brca1<sup>tm1Brn</sup>/Brca1<sup>tm1Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129P2/OlaHsd * BALB/cJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:17626182	20080624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437116	Psme4<sup>b2b1508Clo</sup>/Psme4<sup>b2b1508Clo</sup>  [background:] C57BL/6J-Psme4<sup>b2b1508Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432344	Tg(Ela1-Myc)158Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1986386	20120828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440340	Lgi1<sup>tm1.1Jkc</sup>/Lgi1<sup>tm1.1Jkc</sup> Tyr<sup>c-Brd</sup>/Tyr<sup>c-Brd</sup>  [background:] B6.Cg-Tyr<sup>c-Brd</sup> Lgi1<sup>tm1.1Jkc</sup>	is_model_of	DOID:0060748	familial temporal lobe epilepsy 1						ECO:0000033	author statement supported by traceable reference	PMID:20130004	20100414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851517	Nsd2<sup>tm1Ykan</sup>/Nsd2<sup>tm1Ykan</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19483677	20090729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7434319	Cdh2<sup>em1Obir</sup>/Cdh2<sup>em1Obir</sup>  [background:] C57BL/6JRcc-Cdh2<sup>em1Obir</sup>	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:34702855	20230214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7280898	Krt18<sup>tm1Tmm</sup>/Krt18<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000033	author statement supported by traceable reference	PMID:27689336	20220526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15685168	20181012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16113078	20181012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16443782	20181012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580003	Tg(Crh)227.1Pbl/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:1597149	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428841	Tg(Pklr-HRAS*G12V)21Ak/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:9398057	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5615576	Qsox1<sup>b2b2673Clo</sup>/Qsox1<sup>b2b2673Clo</sup>  [background:] C57BL/6J-Qsox1<sup>b2b2673Clo</sup>	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6401000	Dpp4<sup>tm1.1(DPP4)Pbmj</sup>/Dpp4<sup>tm1.1(DPP4)Pbmj</sup>  [background:] involves: C57BL/6 * C57BL/6NTac	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28348219	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046798	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5546408	Prnp<sup>tm3Lnq</sup>/Prnp<sup>tm3Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:23959875	20140227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589435	Chd7<sup>Whi</sup>/Chd7<sup>+</sup>  [background:] C3HeB/FeJ-Chd7<sup>Whi</sup>	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36232804	20230626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359427	Atp6v1b2<sup>tm1Yoyu</sup>/Atp6v1b2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31257146	20210120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259526	Clcn7<sup>tm1.1Mawa</sup>/Clcn7<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N * CD-1	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:28942122	20181207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6387277	Bcs1l<sup>tm1.1Levp</sup>/Bcs1l<sup>tm1.1Levp</sup>  [background:] B6.129-Bcs1l<sup>tm1.1Levp</sup>	is_model_of	DOID:0080111	mitochondrial complex III deficiency nuclear type 1						ECO:0000033	author statement supported by traceable reference	PMID:28424480	20200131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6357214	Mir199a-2<sup>tm1Kinn</sup>/Mir199a-2<sup>tm1Kinn</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26344767	20190827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665277	Frem1<sup>heb</sup>/Frem1<sup>heb</sup>  [background:] involves: AKR/J	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752239	Cdkn2a<sup>tm2.1Nesh</sup>/Cdkn2a<sup>tm2.1Nesh</sup> Nras<sup>tm1.1Nesh</sup>/Nras<sup>tm1.1Nesh</sup> Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] B6J.Cg-Tg(Tyr-cre/ERT2)13Bos Nras<sup>tm1.1Nesh</sup> Cdkn2a<sup>tm2.1Nesh</sup> Stk11<sup>tm1.1Rdp</sup>	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25252692	20190123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196105	F9<sup>em3Dlli</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:26964564	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906296	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup>	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315749	Wdr19<sup>twto</sup>/Wdr19<sup>twto</sup>  [background:] involves: FVB/NJ	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	PMID:22228095	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>	is_model_of	DOID:0080109	infantile myofibromatosis						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669775	Actn4<sup>tm1Mrpk</sup>/Actn4<sup>tm1Mrpk</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000033	author statement supported by traceable reference	PMID:12782671	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6189202	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] either: (involves: BALB/cA * C57BL/6NCrlj * CBA/JNCrlj) or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23389689	20180723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175077	Idc/Idc<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583556	Tg(ITGA5)0844Fmw/0 Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829009	Cavin1<sup>tm1Pfp</sup>/Cavin1<sup>tm1Pfp</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0111138	congenital generalized lipodystrophy type 4						ECO:0000033	author statement supported by traceable reference	PMID:19546242	20100614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624037	Tg(INS-MT2A,Tyr)1Pne/0  [background:] NOD.FVB-Tg(INS-MT2A,Tyr)1Pne	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16731821	20060607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615496	Cdkn1a<sup>tm1Led</sup>/Cdkn1a<sup>tm1Led</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272838	Pgrmc1<sup>em1Ejho</sup>/Pgrmc1<sup>em1Ejho</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:30356113	20190110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784771	Hras<sup>tm1Jaf</sup>/Hras<sup>tm1Jaf</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * FVB/NCr	is_model_of	DOID:1781	thyroid cancer						ECO:0000033	author statement supported by traceable reference	PMID:26359368	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316488	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Tg(Camk2a-cre)2834Lusc/0  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22411800	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590415	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] PL.129S7-Itgb2<sup>tm1Bay</sup> Itgb2<sup>tm2Bay</sup>	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652414	Fbn1<sup>tm3Rmz</sup>/Fbn1<sup>tm3Rmz</sup>  [background:] Not Specified	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16407178	20060822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7451325	Sox9<sup>tm1.2Ksec</sup>/Sox9<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6 * FVB/N	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:36343245	20230407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7264822	Dyrk1a<sup>em1Kzy</sup>/Dyrk1a<sup>+</sup>  [background:] C57BL/6J-Dyrk1a<sup>em1Kzy</sup>	is_model_of	DOID:0070037	autosomal dominant intellectual developmental disorder 7						ECO:0000033	author statement supported by traceable reference	PMID:29223763	20220428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810319	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Tlx3<sup>tm1(cre)Qima</sup>/Tlx3<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691547	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3852128	Ube3a<sup>tm1Jwf</sup>/Ube3a<sup>+</sup>  [background:] B6.129S4-Ube3a<sup>tm1Jwf</sup>	is_model_of	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11895368	20090806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183662	Tg(NFH)120Jpj/Tg(NFH)120Jpj  [background:] Not Specified	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3821616	A<sup>iy</sup>/A  [background:] C3H/HeJ-A<sup>iy</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:5798139	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622312	Il1r1<sup>tm1Roml</sup>/Il1r1<sup>tm1Roml</sup>  [background:] NOD.Cg-Il1r1<sup>tm1Roml</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14693705	20060531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7496091	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36288662	20230707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7327617	Insr<sup>tm1Khn</sup>/Insr<sup>tm1Khn</sup> Tg(Pdgfrb-cre)#Rha/0  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:8947	diabetic retinopathy						ECO:0000033	author statement supported by traceable reference	PMID:34460911	20220808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784729	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>+</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:1925	Coffin-Siris syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26806701	20171117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903776	Kl<sup>ecalc1</sup>/Kl<sup>ecalc1</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:0111063	hyperphosphatemic familial tumoral calcinosis						ECO:0000033	author statement supported by traceable reference	PMID:25860694	20170703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400425	Dpp4<sup>em1Rba</sup>/Dpp4<sup>em1Rba</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27892925	20200615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400425	Dpp4<sup>em1Rba</sup>/Dpp4<sup>em1Rba</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31339932	20200615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843114	Adarb1<sup>tm1.1Skwa</sup>/Adarb1<sup>tm1.1Skwa</sup> Tg(SLC18A3-cre)KMisa/0  [background:] involves: C57BL/6	is_model_of	DOID:332	amyotrophic lateral sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:20826656	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275035	None [background:] C57BL/6NNia	is_model_of	DOID:0040097	autoimmune vasculitis						ECO:0000033	author statement supported by traceable reference	PMID:8053123	20190129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3691281	Myh6<sup>tm2Ces</sup>/Myh6<sup>tm2Ces</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ	is_model_of	DOID:0110453	dilated cardiomyopathy 1EE						ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644303	Tg(SFTPC-Tnf)2Pva/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7542280	20150716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805035	Bard1<sup>tm2Thl</sup>/Bard1<sup>tm2Thl</sup> Brca1<sup>tm1Thl</sup>/Brca1<sup>tm1Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129/Sv * 129S1/Sv * C57BL/6J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007794	Kras<sup>tm5Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:21512139	20171108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7437965	E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup> Snrpb<sup>em1Lajm</sup>/Snrpb<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6J * CD1	is_model_of	DOID:0111248	cerebrocostomandibular syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35593225	20230224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792143	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/?  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23184605	20160914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604250	Pink1<sup>tm1Aub</sup>/Pink1<sup>tm1Aub</sup> Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub  [background:] involves: 129S/SvEv * FVB/N	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:25296918	20180131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774940	Exoc5<sup>tm1c(KOMP)Mbp</sup>/Exoc5<sup>tm1c(KOMP)Mbp</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * ICR	is_model_of	DOID:0070314	obstructive nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:27511831	20190705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774940	Exoc5<sup>tm1c(KOMP)Mbp</sup>/Exoc5<sup>tm1c(KOMP)Mbp</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * ICR	is_model_of	DOID:0070314	obstructive nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:26046524	20190705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5706792	Fhl1<sup>tm1.1Mihi</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J * C57BL/6NJ	is_model_of	DOID:0060253	scapuloperoneal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:25274776	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175797	Crkl<sup>tm1Imo</sup>/Crkl<sup>tm1Imo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242111	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428747	Tg(Wap-TAg)NP8Depp/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:0060074	ductal carcinoma in situ						ECO:0000033	author statement supported by traceable reference	PMID:10713686	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045186	Psen1<sup>tm1Jzt</sup>/Psen1<sup>tm1Jzt</sup> Psen2<sup>tm1Ber</sup>/Psen2<sup>tm1Ber</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110040	Alzheimer's disease 4						ECO:0000033	author statement supported by traceable reference	PMID:15148382	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622062	Tnf<sup>tm1Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692382	Dnase2a<sup>tm1Osa</sup>/Dnase2a<sup>tm2Osa</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:17066036	20070104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818370	Del(10Prmt2-Pdxk)4Yey/+  [background:] 129S/SvEv-Del(10Prmt2-Pdxk)129S/SvEv-Del(10Prmt2-Pdxk)4Yey	is_model_of	DOID:0060388	chromosomal deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20512340	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625063	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup> Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0  [background:] NOD.Cg-Il4<sup>tm1Cgn</sup> Tg(TcraBDC2.5,TcrbBDC2.5)1Doi	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9703318	20060622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6267296	Far2<sup>tm2b(KOMP)Wtsi</sup>/Far2<sup>tm2b(KOMP)Wtsi</sup>  [background:] B6N(Cg)-Far2<sup>tm2b(KOMP)Wtsi</sup>/2J	is_model_of	DOID:987	alopecia						ECO:0000033	author statement supported by traceable reference	PMID:30372477	20181219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624424	Gaa<sup>tm1.1Rabn</sup>/Gaa<sup>tm1.1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014041	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] Not Specified	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21203469	20110712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766068	Morc1<sup>Tg(Tyr)1Az</sup>/Morc1<sup>Tg(Tyr)1Az</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:26275923	20160502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664441	Blm<sup>tm1Ches</sup>/Blm<sup>tm4Ches</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16914751	20061024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6466735	Impg2<sup>em2Xjz</sup>/Impg2<sup>em2Xjz</sup>  [background:] C57BL/6J-Impg2<sup>em2Xjz</sup>	is_model_of	DOID:0110371	retinitis pigmentosa 56						ECO:0000033	author statement supported by traceable reference	PMID:32242237	20201013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10673499	20050926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789257	Madd<sup>tm1Bpra</sup>/Madd<sup>tm1Bpra</sup> Tg(Ins2-cre/ERT)1Dam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24379354	20160818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316792	b2b520Clo/b2b520Clo  [background:] C57BL/6J-b2b520Clo	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7263453	Tg(HIV)26Aln/0  [background:] involves: FVB/N	is_model_of	DOID:635	acquired immunodeficiency syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12861038	20220425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275610	Atxn1<sup>tm2Hzo</sup>/Atxn1<sup>tm2Hzo</sup> Atxn1l<sup>tm2Hzo</sup>/Atxn1l<sup>tm2Hzo</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd	is_model_of	DOID:150	disease of mental health						ECO:0000033	author statement supported by traceable reference	PMID:28288114	20190201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188004	Tg(RHO*P347S)A1Tili/0  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:29242588	20180711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513833	Gars1<sup>Nmf249</sup>/Gars1<sup>+</sup>  [background:] C57BL/6J-Gars1<sup>Nmf249</sup>/J	is_model_of	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:16982418	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5912041	Des<sup>tm1Cba</sup>/Des<sup>tm1Cba</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11827695	20171030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5557989	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup>  [background:] involves: BXD24/TyJ	is_model_of	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:17898177	20140410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2170796	Dbf/Dbf<sup>+</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:9062079	20110125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7314211	Col5a1<sup>em1Brle</sup>/Col5a1<sup>+</sup>  [background:] C57BL/6-Col5a1<sup>em1Brle</sup>	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:34740257	20220719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6403905	Stat1<sup>tm1Dlv</sup>/Stat1<sup>tm1Dlv</sup> Tg(ANPEP)861Mmul/Tg(ANPEP)861Mmul  [background:] involves: 129S/SvEv * ICR	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:15919828	20200414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4849542	Vcp<sup>tm1Itl</sup>/Vcp<sup>+</sup>  [background:] B6.129S-Vcp<sup>tm1Itl</sup>	is_model_of	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:19713307	20101229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902129	Braf<sup>tm1Mmcm</sup>/Braf<sup>+</sup> Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * FVB	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:19282848	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452388	Tg(CYP1A1-PPARD)#Jfoe/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:20300524	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693880	Tg(SOD1*G93A)1Gur/0  [background:] B6.Cg-Tg(SOD1*G93A)1Gur/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23608112	20150529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4458421	Tfr2<sup>tm1.1Anro</sup>/Tfr2<sup>tm1.1Anro</sup>  [background:] 129.Cg-Tfr2<sup>tm1.1Anro</sup>	is_model_of	DOID:0111030	hemochromatosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:20179178	20100709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624527	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:23748075	20140131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5553144	Col2a1<sup>M3J</sup>/Col2a1<sup>+</sup>  [background:] B6(Cg)-Col2a1<sup>M3J</sup>/GrsrJ	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7397263	Phox2b<sup>tm1Rth</sup>/Phox2b<sup>+</sup> Hprt1<sup>tm1(CAG-cre)Mnn</sup>/?  [background:] involves: 129 * 129S1/Sv * C57BL/6	is_model_of	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25975378	20221205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655437	Apoca/Apoca<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521544	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266266	Mecp2<sup>tm1Nlnd</sup>/Y  [background:] involves: 129 * CD-1	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867519	Tg(CAG-ELN*)60Zu/0  [background:] C57BL/6J-Tg(CAG-ELN*)60Zu	is_model_of	DOID:3144	cutis laxa						ECO:0000033	author statement supported by traceable reference	PMID:20600892	20110111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762938	Gt(ROSA)26Sor<sup>tm4(Ikbkb)Rsky</sup>/Gt(ROSA)26Sor<sup>+</sup> Ighg1<sup>tm1(cre)Cgn</sup>/Ighg1<sup>+</sup> Prdm1<sup>tm2Masu</sup>/Prdm1<sup>tm2Masu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:21156282	20160422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393655	Atp7a<sup>tm1.2Mlke</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:0111196	X-linked distal spinal muscular atrophy 3						ECO:0000033	author statement supported by traceable reference	PMID:27293072	20200310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313544	Lox<sup>b2b370.2Clo</sup>/Lox<sup>b2b370.2Clo</sup>  [background:] C57BL/6J-Lox<sup>b2b370.2Clo</sup>	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5502689	Tg(Tek-tTA)1Rwng/0 Tg(tetO-Notch4*)1Rwng/0  [background:] involves: FVB/N	is_model_of	DOID:0060688	arteriovenous malformations of the brain						ECO:0000033	author statement supported by traceable reference	PMID:18667694	20130827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5649287	Kras<sup>tm4.1Bbd</sup>/Kras<sup>tm4.1Bbd</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:0060581	Noonan syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:25359213	20150819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471581	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0 Tg(Tagln-cre)1Her/0  [background:] involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23152628	20130403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852761	Smpx<sup>em1Jgao</sup>/Smpx<sup>+</sup>  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>	is_model_of	DOID:0111735	X-linked deafness 4						ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052330	Ccm2<sup>tm1Kwhi</sup>/Ccm2<sup>tm1.1Kwhi</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060670	cerebral cavernous malformation 2						ECO:0000033	author statement supported by traceable reference	PMID:21490399	20160831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676319	Ush1c<sup>dfcr</sup>/Ush1c<sup>dfcr</sup>  [background:] involves: BALB/cByJ	is_model_of	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7464549	Got2<sup>em2Pcamp</sup>/Got2<sup>em2Pcamp</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:31422819	20230421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159715	Arid1b<sup>em1Hzhu</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Hzhu</sup>	is_model_of	DOID:0070042	Coffin-Siris syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:28695822	20180606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604113	Csf2rb<sup>tm1Mur</sup>/Csf2rb<sup>tm1Mur</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:8839836	20051110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4848186	Gjb6<sup>tm1.1Fama</sup>/Gjb6<sup>tm1.1Fama</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000033	author statement supported by traceable reference	PMID:20858605	20101221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628914	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm6Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:14645205	20061031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:17029828	20061031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583010	Mmp14<sup>tm1Hbh</sup>/Mmp14<sup>tm1Hbh</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:10520996	20050805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5293760	Npc1<sup>tm1Mbjg</sup>/Npc1<sup>tm1Mbjg</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:21896731	20111028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578560	Tg(TG-TPR/NTRK1)5215Rstn/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11126359	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052466	Ciita<sup>tm2Wrth</sup>/Ciita<sup>tm2Wrth</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5812	MHC class II deficiency						ECO:0000033	author statement supported by traceable reference	PMID:15322541	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587820	Ebp<sup>Td</sup>/Ebp<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060292	X-linked chondrodysplasia punctata 1						ECO:0000033	author statement supported by traceable reference	PMID:10391218	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175805	Cryga<sup>1Neu</sup>/Cryga<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:6877261	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660941	Fdxr<sup>m1J</sup>/Fdxr<sup>m1J</sup> Otop2<sup>m1J</sup>/Otop2<sup>m1J</sup>  [background:] B6;129S-Fdxr<sup>m1J</sup> Otop2<sup>m1J</sup>/GrsrJ	is_model_of	DOID:699	mitochondrial myopathy						ECO:0000033	author statement supported by traceable reference	PMID:29040572	20171128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5787929	Nf1<sup>tm1Fcr</sup>/Nf1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] B6.Cg-Tg(Mx1-cre)1Cgn Nf1<sup>tm1Fcr</sup> Pten<sup>tm1Hwu</sup>	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26764354	20160804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661118	Dysf<sup>tm1Kcam</sup>/Dysf<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:12736685	20090630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435675	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S/SvEv * FVB	is_model_of	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622117	Musk<sup>tm1Vwi</sup>/Musk<sup>tm1Vwi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * FVB	is_model_of	DOID:0110670	congenital myasthenic syndrome 9						ECO:0000033	author statement supported by traceable reference	PMID:16337809	20150511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849592	Gpc3<sup>Gt(Ex136)Byg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689377	Epha2<sup>Gt(KST085)Byg</sup>/Epha2<sup>Gt(KST085)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0110229	cataract 6 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:19649315	20130512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6790238	Ank2<sup>em1Bnt</sup>/Ank2<sup>em1Bnt</sup>  [background:] C57BL/6J-Ank2<sup>em1Bnt</sup>	is_model_of	DOID:12849	autistic disorder						ECO:0000033	author statement supported by traceable reference	PMID:31285321	20211102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476837	Pkd1<sup>tm1Shh</sup>/Pkd1<sup>tm1.1Pcha</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23064367	20180801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314999	Tmc1<sup>stitch</sup>/Tmc1<sup>stitch</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822781	Hesx1<sup>tm3Jpmb</sup>/Hesx1<sup>tm3Jpmb</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N	is_model_of	DOID:0060857	septooptic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19093031	20090113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7427684	Defb19<sup>em1Cya</sup>/Defb19<sup>em1Cya</sup>  [background:] C57BL/6-Defb19<sup>em1Cya</sup>	is_model_of	DOID:229	female reproductive system disease						ECO:0000033	author statement supported by traceable reference	PMID:36513070	20230120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6780172	Dnah10<sup>em1Yxc</sup>/Dnah10<sup>em1Yxc</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0111910	spermatogenic failure						ECO:0000033	author statement supported by traceable reference	PMID:34237282	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904628	Tg(Myh6-MYL2*R58Q)#Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:19150977	20170714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792147	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23858101	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312337	b2b635Clo/b2b635Clo  [background:] C57BL/6J-b2b635Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052112	Tg(Mapt-MAPT*)#Hanr/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18490011	20110804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3852634	Ptprf<sup>tm1Wjh</sup>/Ptprf<sup>tm1Wjh</sup> Ptprs<sup>tm1Mtr</sup>/Ptprs<sup>tm1Mtr</sup>  [background:] B6.Cg-Ptprf<sup>tm1Wjh</sup> Ptprs<sup>tm1Mtr</sup>	is_model_of	DOID:4258	Weissenbacher-Zweymuller syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23863482	20230309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038213	Gck<sup>Rgsc210</sup>/Gck<sup>Rgsc210</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6095155	Tg(tetO-TARDBP*A315T)13Lmit/0 Tg(Thy1-tTA)6Lmit/0  [background:] involves: C57BL/6	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:26437864	20171206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6095155	Tg(tetO-TARDBP*A315T)13Lmit/0 Tg(Thy1-tTA)6Lmit/0  [background:] involves: C57BL/6	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:28334913	20171206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296959	Aebp2<sup>Gt(BC0681)Wtsi</sup>/Aebp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9258	Waardenburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21949878	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574086	Kcna10<sup>tm1Lex</sup>/Kcna10<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6	is_model_of	DOID:3426	vestibular disease						ECO:0000033	author statement supported by traceable reference	PMID:23528307	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437295	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Smad1<sup>tm2Rob</sup>/Smad1<sup>tm2Rob</sup> Smad5<sup>tm1Huy</sup>/Smad5<sup>tm1Huy</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:19819941	20100316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6302764	Borcs7<sup>Q87X</sup>/Borcs7<sup>Q87X</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:2367	neuroaxonal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:30067980	20190513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581822	Tg(GFAP)10Mes/0  [background:] involves: FVB/N	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:9466565	20050718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429559	Fzd3<sup>tm1(FZD3)Lex</sup>/Fzd3<sup>tm1(FZD3)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664549	Pafah1b1<sup>tm1Or</sup>/Pafah1b1<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11344260	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6416112	Eif2b5<sup>tm1.1Sidr</sup>/Eif2b5<sup>tm1.1Sidr</sup>  [background:] B6(Cg)-Eif2b5<sup>tm1.1Sidr</sup>	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:30624206	20200512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275557	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-TGFA)22.1Kor/0  [background:] involves: 129 * C57BL/6 * FVB/NJ	is_model_of	DOID:3770	pulmonary fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:28130263	20190131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906349	Dicer1<sup>tm1Smr</sup>/Dicer1<sup>tm1Smr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S7/SvEvBrd * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18256189	20170809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640608	Tg(Myh6-Pfkfb3)7Pne/0  [background:] FVB-Tg(Myh6-Pfkfb3)7Pne	is_model_of	DOID:3978	extrinsic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15331593	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307125	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>+</sup>  [background:] B6.129-Pex11b<sup>tm1Sjg</sup>	is_model_of	DOID:905	Zellweger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21954064	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009546	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	is_model_of	DOID:0050868	hepatocellular adenoma						ECO:0000033	author statement supported by traceable reference	PMID:21575863	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033467	Hfe<sup>tm2Sly</sup>/Hfe<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14673107	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5812135	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27109181	20161215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6849976	Pla2g6<sup>tm1.1Hlw</sup>/Pla2g6<sup>tm1.1Hlw</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0060900	Parkinson's disease 14						ECO:0000033	author statement supported by traceable reference	PMID:30088174	20220107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829790	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20837017	20150624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578216	Scn8a<sup>em1Mm</sup>/Scn8a<sup>+</sup>  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:24288358	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906030	Tg(Myh6-Tpm1*D175N)#Dfw/0  [background:] Not Specified	is_model_of	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:10400910	20170801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433295	b2b1519Clo/b2b1519Clo  [background:] C57BL/6J-b2b1519Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604775	Pepd<sup>dal</sup>/Pepd<sup>dal</sup>  [background:] involves: C3H/HeJ * CBA/J	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:21472842	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175712	Atp7a<sup>Mo</sup>/Atp7a<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:13103353	20050926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576477	Dclre1c<sup>tm2Mcow</sup>/Dclre1c<sup>tm2Mcow</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation						ECO:0000033	author statement supported by traceable reference	PMID:15699179	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5614941	Ephb4<sup>b2b2412Clo</sup>/Ephb4<sup>b2b2412Clo</sup>  [background:] C57BL/6J-Ephb4<sup>b2b2412Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652214	Tg(Thy1-SNCA*A30P)18Pjk/Tg(Thy1-SNCA*A30P)18Pjk  [background:] involves: C57BL/6	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12438441	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423102	Muc4<sup>tm1Unc</sup>/Muc4<sup>tm1Unc</sup>  [background:] B6NTac.129(FVB)-Muc4<sup>tm1Unc</sup>/Rand	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	MGI:6416514	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686902	Mpl<sup>tm1Fjs</sup>/Mpl<sup>tm1Fjs</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0090118	congenital amegakaryocytic thrombocytopenia						ECO:0000033	author statement supported by traceable reference	PMID:10611229	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777758	Crygb<sup>S11R</sup>/Crygb<sup>+</sup>  [background:] A/J-Crygb<sup>S11R</sup>	is_model_of	DOID:0110236	cataract 39 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:18172107	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311880	Dync2h1<sup>b2b414Clo</sup>/Dync2h1<sup>b2b414Clo</sup>  [background:] C57BL/6J-Dync2h1<sup>b2b414Clo</sup>	is_model_of	DOID:0110087	asphyxiating thoracic dystrophy 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621814	E2f1<sup>tm1Meg</sup>/E2f1<sup>tm1Meg</sup>  [background:] NOD.Cg-E2f1<sup>tm1Meg</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15470032	20060509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5303093	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>+</sup> Tg(Mt1-RET)304Ina/0  [background:] involves: 129S7/SvEvBrd * BALB/c * C57BL/6	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:20048069	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583545	Tg(ITGA2)1075Fmw/0 Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868493	Gbe1<sup>m1Yty</sup>/Gbe1<sup>m1Yty</sup>  [background:] C3HeB/FeJ-Gbe1<sup>m1Yty</sup>	is_model_of	DOID:2750	glycogen storage disease IV						ECO:0000033	author statement supported by traceable reference	PMID:21075835	20110119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790964	Myo5b<sup>tm1.1Cle</sup>/Myo5b<sup>tm1.1Cle</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * DBA/2	is_model_of	DOID:0060775	microvillus inclusion disease						ECO:0000033	author statement supported by traceable reference	PMID:26392529	20160909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4458390	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J * SJL	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:20100831	20110514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6164161	Braf<sup>tm1Tumg</sup>/Braf<sup>+</sup> Tg(CAG-cre)2Osb/0  [background:] involves: C57BL * C57BL/6J * DBA * ICR	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26472072	20180704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451194	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup> Tg(Hexb-tTA2S,tetO-Hexb)#Tjsa/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:23028353	20130125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620189	b2b2696Clo/b2b2696Clo  [background:] C57BL/6J-b2b2696Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844276	Tg(PTH-CCND1)PC2Anar/0  [background:] FVB/N-Tg(PTH-CCND1)PC2Anar	is_model_of	DOID:11202	primary hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:11342573	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814729	Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110024	age related macular degeneration 12						ECO:0000033	author statement supported by traceable reference	PMID:17909628	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677761	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1.1Lss</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:14500363	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707539	Nppc<sup>lbab</sup>/Nppc<sup>lbab</sup>  [background:] B6.PL-Nppc<sup>lbab</sup>/GrsrJ	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:17439653	20220512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716631	Rpgrip1l<sup>tm1Urt</sup>/Rpgrip1l<sup>tm1Urt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17558409	20150903	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525001	Bbs4<sup>tm1Vcs</sup>/Bbs4<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:15539463	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527906	Ppt1<sup>tm1Aj</sup>/Ppt1<sup>tm1Aj</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:15649713	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5572817	Tg(ASL1/Cryaa-Ralbp1)24Yca/0  [background:] involves: C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:24188744	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7260233	Ryr1<sup>em1Tmur</sup>/Ryr1<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:8545	malignant hyperthermia						ECO:0000033	author statement supported by traceable reference	PMID:34257294	20220408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7467133	Ctnnb1<sup>em1V</sup>/Ctnnb1<sup>em1V</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659910	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(CAG-HPV16E6E7,-luc)#Mspi/0 Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1 * FVB/N * FVB/NJ	is_model_of	DOID:8618	oral cavity cancer						ECO:0000033	author statement supported by traceable reference	PMID:24525739	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423631	Stk39<sup>tm1Pawe</sup>/Stk39<sup>tm1Pawe</sup> Pvalb<sup>tm1(cre)Arbr</sup>/Pvalb<sup>+</sup>  [background:] B6.129-Stk39<sup>tm1Pawe</sup> Pvalb<sup>tm1(cre)Arbr</sup>	is_model_of	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:28442491	20200521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281134	Mbtps1<sup>tm1Jdh</sup>/Mbtps1<sup>tm1Jdh</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CD-1	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:29437042	20220527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0110965	brachydactyly type A2						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838087	Ass1<sup>bar</sup>/Ass1<sup>bar</sup>  [background:] FVB.BAR-Ass1<sup>bar</sup>	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679917	Foxj1<sup>tm1Slb</sup>/Foxj1<sup>tm1Slb</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:10873152	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806872	Tg(Venus/SOX10*)55Kein/0  [background:] involves: C3H/He * C57BL/6	is_model_of	DOID:0090111	PCWH syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25959061	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763087	Tg(MMTV-LPAR1)27Gbm/Tg(MMTV-LPAR1)27Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)27Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437582	plt/plt  [background:] either: B6.DDD-plt or C.DDD-plt	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16473829	20100319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7545546	Lepr<sup>db-Nokl</sup>/Lepr<sup>db-Nokl</sup>  [background:] C57BL/6N-Lepr<sup>db-Nokl</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286487	Pnpla1<sup>tm1a(KOMP)Wtsi</sup>/Pnpla1<sup>tm1a(KOMP)Wtsi</sup>  [background:] B6NTac;B6N-A<sup>tm1Brd</sup> Pnpla1<sup>tm1a(KOMP)Wtsi</sup>/Ics	is_model_of	DOID:0060719	autosomal recessive congenital ichthyosis 10						ECO:0000033	author statement supported by traceable reference	PMID:28369476	20190409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6508693	Hsd17b3<sup>tm1.2Mpo</sup>/Hsd17b3<sup>tm1.2Mpo</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl	is_model_of	DOID:0112248	17-beta hydroxysteroid dehydrogenase 3 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:32190925	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902766	Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>/Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N	is_model_of	DOID:0050888	syndromic intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:27939640	20170619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178293	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup> Tyrp1<sup>isa</sup>/Tyrp1<sup>isa</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10192392	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902132	Braf<sup>tm1Mmcm</sup>/Braf<sup>+</sup> Pten<sup>tm1Rdp</sup>/Pten<sup>tm1Rdp</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:19282848	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702613	Ccdc154<sup>ntl</sup>/Ccdc154<sup>ntl</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000033	author statement supported by traceable reference	PMID:20121924	20160113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5470154	Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>/Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:23267094	20130327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003459	Tg(Hmgcr-PSEN1*M146L)#Lpr/0 Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003459	Tg(Hmgcr-PSEN1*M146L)#Lpr/0 Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15972962	20110607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7517089	Fgfr3<sup>tm3.1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0080041	hypochondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:37345656	20230812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6514802	Prickle3<sup>em1Mxg</sup>/Y  [background:] C57BL/6JSlacc-Prickle3<sup>em1Mxg</sup>	is_model_of	DOID:0111754	Leber plus disease						ECO:0000033	author statement supported by traceable reference	PMID:32516135	20210402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430105	Tg(Rho-GUCA1A*Y99C)L53Amd/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0080314	cone-rod dystrophy 14						ECO:0000033	author statement supported by traceable reference	PMID:22042849	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361922	Tg(MMTV-Erbb2*,-cre)1Mul/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18273058	20101110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313499	Tg(CAG-Rpgr)mRDefWrght/0 Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110414	retinitis pigmentosa 3						ECO:0000033	author statement supported by traceable reference	PMID:21546531	20120330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6505560	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/0 Trp53<sup>tm3.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30952657	20210209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038416	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0111008	X-linked cone-rod dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:10725384	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836994	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp*D177N*M128V)A21Rchi/Tg(Prnp*D177N*M128V)A21Rchi  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CBA	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:19038218	20090325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3704913	Dbt<sup>tm1Geh</sup>/Dbt<sup>tm1Geh</sup> Tg(tetO-DBT)A1Geh/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB * NMRI	is_model_of	DOID:9269	maple syrup urine disease						ECO:0000033	author statement supported by traceable reference	PMID:16579849	20070426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6297005	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh  [background:] involves: FVB/N	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:27732085	20190509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583546	Tg(ITGA2)1075Fmw/0 Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471365	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Slc6a3<sup>tm1(cre)Xz</sup>/Slc6a3<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:23152632	20130402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584470	Trp53<sup>tm3.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7333170	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Kmt2d<sup>tm2.1Kaig</sup>/Kmt2d<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060473	Kabuki syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32541010	20220902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5922033	Aipl1<sup>tvrm127</sup>/Aipl1<sup>tvrm127</sup>  [background:] C57BL/6J-Aipl1<sup>tvrm127</sup>/Pjn	is_model_of	DOID:0110332	Leber congenital amaurosis 4						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6296606	Cdh1<sup>tm1Jjon</sup>/Cdh1<sup>tm1Jjon</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Wap-cre)51Nki/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:3457	invasive lobular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21282721	20190507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6164043	Tg(Vav1-STAT5B*N642H)726Biat/0  [background:] C57BL/6NCrl-Tg(Vav1-STAT5B*N642H)726Biat	is_model_of	DOID:1240	leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29200404	20180703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910007	Atp6v1b1<sup>vtx</sup>/Atp6v1b1<sup>vtx</sup>  [background:] MRL/MpJ-Atp6v1b1<sup>vtx</sup>/Kjn	is_model_of	DOID:0050332	enlarged vestibular aqueduct						ECO:0000033	author statement supported by traceable reference	PMID:28934385	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367783	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>tm1Jgg</sup> Tg(TCF/Lef1-lacZ)34Efu/0  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12712	nephronophthisis						ECO:0000033	author statement supported by traceable reference	PMID:19718039	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177287	Gpi1<sup>b-m1Neu</sup>/Gpi1<sup>b-m1Neu</sup>  [background:] C3.Cg-Gpi1<sup>b-m1Neu</sup>	is_model_of	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:8417789	20110309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452482	C1qa<sup>tm1Mjw</sup>/C1qa<sup>tm1Mjw</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:20375278	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672965	Pts<sup>tm1Thny</sup>/Pts<sup>tm1Thny</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0090106	BH4-deficient hyperphenylalaninemia A						ECO:0000033	author statement supported by traceable reference	PMID:12734191	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6468047	Vps13b<sup>tm1.2Ics</sup>/Vps13b<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:32915983	20201021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431005	Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>/Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>  [background:] FVB/N-Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:18776131	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	MGI:78359	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3790867	Lrp2<sup>tm1Her</sup>/Lrp2<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:1062	Fanconi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10514418	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720759	Snca<sup>tm1Rosl</sup>/Snca<sup>tm1Rosl</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:10707987	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367214	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup> Nos3<sup>tm1Plh</sup>/Nos3<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12788381	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7545275	Pdgfra<sup>tm2Sor</sup>/Pdgfra<sup>tm2Sor</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:4297	scimitar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20071345	20231102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902990	Adamtsl4<sup>tvrm267</sup>/Adamtsl4<sup>tvrm267</sup>  [background:] C57BL/6J-Adamtsl4<sup>tvrm267</sup>/Pjn	is_model_of	DOID:0111149	autosomal recessive isolated ectopia lentis 2						ECO:0000033	author statement supported by traceable reference	PMID:26405179	20180306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698101	Ppib<sup>Gt(RST139)Byg</sup>/Ppib<sup>Gt(RST139)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110349	osteogenesis imperfecta type 9						ECO:0000033	author statement supported by traceable reference	PMID:24968150	20151207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752905	Kif1a<sup>lgdg</sup>/Kif1a<sup>lgdg</sup>  [background:] C3.Cg-Kif1a<sup>lgdg</sup>/GrsrJ	is_model_of	DOID:0110781	hereditary spastic paraplegia 30						ECO:0000033	author statement supported by traceable reference	MGI:5752885	20160323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297714	Tg(Mt1-RET)304Ina/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:20048069	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196129	Gt(ROSA)26Sor<sup>tm1(CAG-MYCN,-luc)Jhsc</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Dbh-icre)1Gsc/0  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:25174395	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838535	Prom1<sup>tm1Pec</sup>/Prom1<sup>tm1Pec</sup>  [background:] B6.129-Prom1<sup>tm1Pec</sup>	is_model_of	DOID:0110376	retinitis pigmentosa 41						ECO:0000033	author statement supported by traceable reference	PMID:19228982	20090403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447549	Lep<sup>m1Btlr</sup>/Lep<sup>m1Btlr</sup>  [background:] C57BL/6J-Lep<sup>m1Btlr</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:5447547	20130104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402641	Tg(Ace2-ACE2)1Cqin/0  [background:] involves: ICR	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32444876	20200604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402641	Tg(Ace2-ACE2)1Cqin/0  [background:] involves: ICR	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32380511	20200604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392094	Fancd2<sup>em1Tzh</sup>/Fancd2<sup>em1Tzh</sup>  [background:] C57BL/6-Fancd2<sup>em1Tzh</sup>	is_model_of	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000033	author statement supported by traceable reference	PMID:31078270	20200226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196032	Arx<sup>tm4Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6NHsd	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:28602636	20180829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361030	Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0  [background:] C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath	is_model_of	DOID:0080047	pseudoachondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:19762713	20160810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361030	Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0  [background:] C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath	is_model_of	DOID:0080047	pseudoachondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:24194321	20160810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000253	Tg(Alb-TAg)#Arnd/0  [background:] C3Fe.Cg-Tg(Alb-TAg)#Arnd	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19428549	20110526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713117	Hspg2<sup>tm1.1Rdgr</sup>/Hspg2<sup>tm1.1Rdgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:17213231	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834579	Slitrk1<sup>tm1Jaru</sup>/Slitrk1<sup>tm1Jaru</sup>  [background:] B6.129P2-Slitrk1<sup>tm1Jaru</sup>	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18794888	20090305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651618	Itgb2<sup>tm2Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0110910	leukocyte adhesion deficiency 1						ECO:0000033	author statement supported by traceable reference	PMID:9653089	20050808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580093	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5501103	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:18296659	20130814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5290081	Ift172<sup>avc1</sup>/Ift172<sup>avc1</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	PMID:21653639	20111011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6316985	Sacs<sup>tm1(NCOM)Mfgc</sup>/Sacs<sup>tm1(NCOM)Mfgc</sup>  [background:] Not Specified	is_model_of	DOID:0050946	Charlevoix-Saguenay spastic ataxia						ECO:0000033	author statement supported by traceable reference	PMID:22307627	20190710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438241	Tg(HTT*)1Xwy/0  [background:] FVB-Tg(HTT*)1Xwy	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20064390	20100330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418655	Ccr5<sup>tm1Kuz</sup>/Ccr5<sup>tm1Kuz</sup>  [background:] B6.129P2-Ccr5<sup>tm1Kuz</sup>	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4939883	Pparg<sup>tm1.1Gonz</sup>/Pparg<sup>tm1.1Gonz</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:21135166	20110307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425923	Casr<sup>BCH013</sup>/Casr<sup>BCH013</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH013</sup>	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6389011	Kcnj8<sup>em1Nich</sup>/Kcnj8<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7388555	Mettl23<sup>em1Itwa</sup>/Mettl23<sup>em1Itwa</sup>  [background:] C57BL/6J-Mettl23<sup>em1Itwa</sup>	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905195	Lrrc10<sup>tm1Sgt</sup>/Lrrc10<sup>tm1Sgt</sup>  [background:] B6.129P2-Lrrc10<sup>tm1Sgt</sup>	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23236519	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177531	Cftr<sup>tm1Hgu</sup>/Cftr<sup>tm1Hgu</sup>  [background:] involves: 129P2/OlaHsd * MF1	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:1382232	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317909	Gng3<sup>tm1.1Rbs</sup>/Gng3<sup>tm1.1Rbs</sup> Gng7<sup>tm1Lex</sup>/Gng7<sup>tm1Lex</sup>  [background:] B6.Cg-Gng7<sup>tm1Lex</sup> Gng3<sup>tm1.1Rbs</sup>	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:22207761	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784489	Foxo1<sup>tm1Rdp</sup>/Foxo1<sup>tm1.1Rdp</sup> Foxo3<sup>tm1Rdp</sup>/Foxo3<sup>tm1.1Rdp</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:26061565	20160726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462253	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup> Traf3ip2<sup>tm1Sbn</sup>/Traf3ip2<sup>+</sup>  [background:] involves: 129 * 129S4/SvJae * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23123062	20130207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7489810	Smc3<sup>tm1.2Toshi</sup>/Smc3<sup>+</sup>  [background:] B6.Cg-Smc3<sup>tm1.2Toshi</sup>	is_model_of	DOID:0080507	Cornelia de Lange syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:28408410	20230615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6718876	Nemf<sup>tvrm116</sup>/Nemf<sup>tvrm116</sup>  [background:] C57BL/6J-Nemf<sup>tvrm116</sup>/PjnCx	is_model_of	DOID:440	neuromuscular disease						ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689926	Igh<sup>tm1.1(Igh564)Tik</sup>/Igh<sup>tm1.1(Igh564)Tik</sup> Igk<sup>tm1(Igk564)Tik</sup>/Igk<sup>tm1(Igk564)Tik</sup>  [background:] B6.129S4-Igk<sup>tm1(Igk564)Tik</sup> Igh<sup>tm1(Igh564)Tik</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:16973388	20061206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663064	Mitf<sup>Mi-wh</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450541	Acvr2a<sup>tm1Zuk</sup>/Acvr2a<sup>tm1Zuk</sup>  [background:] either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)	is_model_of	DOID:4258	Weissenbacher-Zweymuller syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7885474	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5805821	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] B6.129S1-Pten<sup>tm1Rps</sup>/Nci	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25561290	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040915	Abcg2<sup>tm1Ahs</sup>/Abcg2<sup>tm1Ahs</sup>  [background:] either: (involves: 129P2/OlaHsd * FVB) or (involves: FVB)	is_model_of	DOID:13270	erythropoietic protoporphyria						ECO:0000033	author statement supported by traceable reference	PMID:12429862	20050913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6825769	Npnt<sup>em1Zhwe</sup>/Npnt<sup>em1Zhwe</sup>  [background:] C57BL/6-Npnt<sup>em1Zhwe</sup>	is_model_of	DOID:0080200	bilateral renal aplasia						ECO:0000033	author statement supported by traceable reference	PMID:34049960	20211122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6721005	Wdr45<sup>em1Wrst</sup>/Wdr45<sup>em1Wrst</sup>  [background:] involves: C57BL/6N * FVB	is_model_of	DOID:0110739	neurodegeneration with brain iron accumulation 5						ECO:0000033	author statement supported by traceable reference	PMID:34043061	20210714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192375	Kdm6a<sup>tm1Cdcn</sup>/Y Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29479066	20180731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6370003	Phf8<sup>tm1.1Cdcn</sup>/Y  [background:] B6.129S6(Cg)-Phf8<sup>tm1.1Cdcn</sup>	is_model_of	DOID:0060812	syndromic X-linked intellectual disability Siderius type						ECO:0000033	author statement supported by traceable reference	PMID:29317619	20191107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908863	Ssu2<sup>tm1.1Xmx</sup>/Ssu2<sup>tm1.1Xmx</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:701	dentin dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:27680507	20170913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2172351	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm1Jfm</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:14623826	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2172351	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm1Jfm</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10499585	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727062	Tsga8<sup>em2Ohbo</sup>/Tsga8<sup>em2Ohbo</sup>  [background:] C57BL/6-Tsga8<sup>em2Ohbo</sup>	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:33766931	20210729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054170	Vip<sup>tm1Clw</sup>/Vip<sup>tm1Clw</sup>  [background:] involves: 129S/Sv * C57BL/6	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:17309917	20130417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259615	Lamp2<sup>tm1Psa</sup>/Lamp2<sup>tm1Psa</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050437	Danon disease						ECO:0000033	author statement supported by traceable reference	PMID:28526246	20181207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617495	Tg(Krt18-EGFP,-TAg121)36Ysng/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5619081	Dnai2<sup>b2b3405Clo</sup>/Dnai2<sup>b2b3405Clo</sup>  [background:] C57BL/6J-Dnai2<sup>b2b3405Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905397	None [background:] STR/Ort	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:8292560	20181002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905397	None [background:] STR/Ort	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:592018	20181002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905397	None [background:] STR/Ort	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:592015	20181002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159581	Map2k1<sup>tm2.1Chrn</sup>/Map2k1<sup>tm2.1Chrn</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29590634	20180605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571860	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>tm1.1Ady</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110250	cataract 16 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:23872361	20140710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430642	Arsg<sup>tm1Tdi</sup>/Arsg<sup>tm1Tdi</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:12798	mucopolysaccharidosis						ECO:0000033	author statement supported by traceable reference	PMID:22689975	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157954	Cfap418<sup>em3Jyang</sup>/Cfap418<sup>em3Jyang</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0111022	cone-rod dystrophy 16						ECO:0000033	author statement supported by traceable reference	PMID:29440555	20180524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6451664	Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>/Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0112247	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder						ECO:0000033	author statement supported by traceable reference	PMID:31440507	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160388	Dst<sup>dt-23Rbrc</sup>/Dst<sup>dt-23Rbrc</sup>  [background:] involves: C3H/HeN * C57BL/6	is_model_of	DOID:0070151	hereditary sensory and autonomic neuropathy type 6						ECO:0000033	author statement supported by traceable reference	PMID:27693510	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849439	Tg(Lck-Tal1)4709Led/0  [background:] FVB/N-Tg(Lck-Tal1)4709Led	is_model_of	DOID:1037	lymphoid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:8895560	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	MGI:78359	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896655	Brpf1<sup>tm1c(EUCOMM)Wtsi</sup>/Brpf1<sup>tm1c(EUCOMM)Wtsi</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N	is_model_of	DOID:0050888	syndromic intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:27939640	20170619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5293439	Mapk1<sup>tm1.2Kuta</sup>/Mapk1<sup>tm1.2Kuta</sup> Tg(Nes-cre)1Kag/0  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21849556	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841692	Tg(Igh-V186.2-TCL1A)3Cro/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:12011454	20090428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697079	Ercc8<sup>tm1Jhjh</sup>/Ercc8<sup>tm1Jhjh</sup>  [background:] B6J.129P2-Ercc8<sup>tm1Jhjh</sup>	is_model_of	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25762674	20151124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720086	Hba<sup>b3(th)</sup>/Hba<sup>+</sup>  [background:] either: (involves: 101 * SEC) or (involves: 101 * C57BL * SEC)	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:879556	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574074	Cdkl5<sup>tm1.2Cogr</sup>/Y  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	is_model_of	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:24838000	20201218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908893	Tg(Myh6-MYL2*E22K)4Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:16076902	20170912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675255	Ednrb<sup>WS4</sup>/Ednrb<sup>WS4</sup>  [background:] involves: BALB/c * MSM	is_model_of	DOID:0110953	Waardenburg syndrome type 4A						ECO:0000033	author statement supported by traceable reference	PMID:11773966	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711109	B2m<sup>tm1Unc</sup>/B2m<sup>tm1Unc</sup> Tg(HLA-A/H2-D/B2M)1Dvs/0  [background:] NOD.Cg-B2m<sup>tm1Unc</sup> Tg(HLA-A/H2-D/B2M)1Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16493087	20070606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521486	Tg(CAG-Bgeo,-tTA,-EGFP)2A11Kuw/0 Tg(Pdx1-cre)6Tuv/0 X/Tg(tetO-MYC)36Bop  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23467612	20131204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617497	Brca2<sup>tm1Brn</sup>/Brca2<sup>tm1Brn</sup> Tg(Krt18-EGFP,-TAg121)36Ysng/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm2Tyj</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752255	Eif2b5<sup>tm1Itl</sup>/Eif2b5<sup>tm1Itl</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:23056417	20160317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181486	Kcne1<sup>tm1Sfh</sup>/Kcne1<sup>tm1Sfh</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11223304	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181486	Kcne1<sup>tm1Sfh</sup>/Kcne1<sup>tm1Sfh</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11438691	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175223	Otc<sup>spf-ash</sup>/Y  [background:] Not Specified	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:3162766	20090717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437300	Hps5<sup>ru2</sup>/Hps5<sup>ru2</sup>  [background:] involves: C57BL	is_model_of	DOID:0060543	Hermansky-Pudlak syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:12548288	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509640	Ppil1<sup>em4Jgg</sup>/Ppil1<sup>em4Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em4Jgg</sup>	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:33220177	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6199482	Clrn1<sup>tm2.1Kuna</sup>/Clrn1<sup>tm2.1Kuna</sup> Tg(Atoh1-Clrn1)#Kuna/0  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0110828	Usher syndrome type 3						ECO:0000033	author statement supported by traceable reference	PMID:27110679	20180925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906447	Per2<sup>M1Btlr</sup>/Per2<sup>M1Btlr</sup>  [background:] C57BL/6J-Per2<sup>M1Btlr</sup>	is_model_of	DOID:0110011	advanced sleep phase syndrome 1						ECO:0000033	author statement supported by traceable reference	MGI:6197761	20180913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6376530	Cd79a<sup>tm1(cre)Reth</sup>/Cd79a<sup>+</sup> Inpp5d<sup>tm1Rav</sup>/Inpp5d<sup>tm1Rav</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:22078222	20191113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157967	Tcf4<sup>tm1Hmb</sup>/Tcf4<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/Tmem163<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29222403	20180524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582588	Tg(H2-K-IL6)2Srj/0  [background:] B6.Cg-Tg(H2-K-IL6)2Srj	is_model_of	DOID:934	viral infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:22490805	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543907	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Nkx3-1<sup>tm4(cre/ERT2)Mms</sup>/Nkx3-1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22836754	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653534	Dlx5/Dlx6<sup>tm1Levi</sup>/Dlx5/Dlx6<sup>tm1Levi</sup>  [background:] Not Specified	is_model_of	DOID:0090021	split hand-foot malformation 1						ECO:0000033	author statement supported by traceable reference	PMID:12112878	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5485414	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(Cnp-EGFR)10Nrat/0 Tg(Dhh-cre)1Mejr/0  [background:] involves: 129S1/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000033	author statement supported by traceable reference	PMID:23319880	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6478321	Prss8<sup>em1Bug</sup>/Prss8<sup>em1Bug</sup> Spint2<sup>Gt(KST272)Byg</sup>/Spint2<sup>Gt(KST272)Byg</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * NIH Black Swiss	is_model_of	DOID:0060781	congenital secretory sodium diarrhea 3						ECO:0000033	author statement supported by traceable reference	PMID:29617460	20201208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6297092	Mlxipl<sup>tm1Kuy</sup>/Mlxipl<sup>tm1Kuy</sup>  [background:] B6.129S6-Mlxipl<sup>tm1Kuy</sup>/J	is_model_of	DOID:9778	irritable bowel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29669261	20190510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157969	Tcf4<sup>em1Bdph</sup>/?  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29222403	20180524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850048	Nlrp3<sup>tm2Hhf</sup>/Nlrp3<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090062	familial cold autoinflammatory syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19501000	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000281	Tg(AR*100Q)#Als/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:21317158	20110527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6431340	Ace2<sup>em1(ACE2)Yowa</sup>/Ace2<sup>em1(ACE2)Yowa</sup>  [background:] C57BL/6-Ace2<sup>em1(ACE2)Yowa</sup>	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32485164	20200603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544602	Ptch1<sup>dl</sup>/Ptch1<sup>dl</sup>  [background:] involves: 129S1/SvImJ * C57BL/6J	is_model_of	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23897749	20140512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5788097	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Col2a1-cre/ERT2)1Dic/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:23873233	20220608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793864	Atp7a<sup>Mo-blo</sup>/Y  [background:] B6.Cg-Atp7a<sup>Mo-blo</sup>/J	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:8895222	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7378801	Vps35<sup>tm1.1Mjff</sup>/Vps35<sup>tm1.1Mjff</sup>  [background:] B6.Cg-Vps35<sup>tm1.1Mjff</sup>	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:33745227	20221107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706514	Tg(Ins2-Nos2)40Okam/0  [background:] involves: C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:8499320	20070501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359207	Arx<sup>tm4Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:22565167	20130716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392161	Iqsec2<sup>em1Csbg</sup>/Y  [background:] C57BL/6NHsd-Iqsec2<sup>em1Csbg</sup>	is_model_of	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:31439632	20200227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7435429	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S4/SvJae * FVB	is_model_of	DOID:0060688	arteriovenous malformations of the brain						ECO:0000033	author statement supported by traceable reference	PMID:32552404	20230217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792057	Cacna1a<sup>tg</sup>/Cacna1a<sup>tm2.1Maag</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * DBA/2J * FVB/N	is_model_of	DOID:0050835	generalized dystonia						ECO:0000033	author statement supported by traceable reference	PMID:22850483	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461058	Mog<sup>tm1Dpd</sup>/Mog<sup>tm1Dpd</sup> Tg(Tcra2D2,Tcrb2D2)1Kuch/0  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19483694	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677979	Slc3a1<sup>pbl</sup>/Slc3a1<sup>pbl</sup>  [background:] involves: C3HeB/FeJ * MRL/MpJ	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:12923163	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710235	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Mpz-cre)94Imeg/0  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661928	Pdgfrb<sup>redeye</sup>/Pdgfrb<sup>redeye</sup>  [background:] C3N.C-Pdgfrb<sup>redeye</sup>	is_model_of	DOID:8946	severe nonproliferative diabetic retinopathy						ECO:0000033	author statement supported by traceable reference	PMID:23633653	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3852102	Tg(PER2*S662G)867Ljp/0  [background:] involves: C57BL/6	is_model_of	DOID:0110011	advanced sleep phase syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:17218255	20090806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793729	Atp7a<sup>Mo-vbr</sup>/Y  [background:] Not Specified	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:10098864	20190723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721531	Tg(APPV717F)109Ili/Tg(APPV717F)109Ili  [background:] Not Specified	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12145324	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525153	Abca1<sup>tm1Blt</sup>/Abca1<sup>tm1Blt</sup>  [background:] C57BL/6-Abca1<sup>tm1Blt</sup>	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:15163665	20050513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3708350	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17334657	20070515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5485272	Tg(Myh6-tTA)6Smbf/0 Tg(tetO-Spp1)5Gad/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20200330	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837653	Tg(CSNK1D*,-EGFP)816Yfu/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110012	advanced sleep phase syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:15800623	20130513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715718	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15231697	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629084	Ctse<sup>tm1Kjy</sup>/Ctse<sup>tm1Kjy</sup>  [background:] involves: C57BL/6	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:14769879	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404946	Rs1<sup>tm2.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277815	Prmt5<sup>tm2c(EUCOMM)Wtsi</sup>/Prmt5<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Col2a1-cre)#Amc/0  [background:] involves: C57BL/6N	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:31848143	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688288	Apc<sup>M1Tno</sup>/Apc<sup>+</sup>  [background:] either: B6JJcl.B6(D2JJcl)-Apc<sup>M1Tno</sup> or (involves: C57BL/6 * C57BL/6JJcl * DBA/2JJcl)	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:23551873	20150924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6161224	Fgf9<sup>tm1Zgwg</sup>/Fgf9<sup>tm1Zgwg</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0050794	multiple synostoses syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28169396	20180615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797751	Kcnq2<sup>Nmf134</sup>/Kcnq2<sup>+</sup> Tg(Eno2-Scn2a1*)Q54Mm/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:16464983	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294945	Tg(CAG-NRIP1)51Row/0  [background:] involves: FVB/N	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20083575	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797627	Xlch/?  [background:] C57BL/6J-Xlch	is_model_of	DOID:0110461	X-linked dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18424640	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141091	Tg(NEFL*E397K)#Milg/0  [background:] Not Specified	is_model_of	DOID:0110165	Charcot-Marie-Tooth disease type 2E						ECO:0000033	author statement supported by traceable reference	PMID:21493625	20110826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2385750	Tg(APOB)11Rub/0 Tg(UcpDta)1Kz/0  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:8264795	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054645	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] C.129S2(B6)-Pdcd1<sup>tm1Hon</sup>	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11209085	20170802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140029	Tg(Thy1-GLRA1*R271Q)300Wha/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:9091	REM sleep behavior disorder						ECO:0000033	author statement supported by traceable reference	PMID:21562273	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710320	Cdkn2c<sup>tm1Bbd</sup>/Cdkn2c<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16260494	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3528185	Myo6<sup>sv</sup>/Myo6<sup>sv</sup>  [background:] involves: B10.HA/(33NX)Sn * C57BL/6J	is_model_of	DOID:0110552	autosomal dominant nonsyndromic deafness 22						ECO:0000033	author statement supported by traceable reference	PMID:7493015	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5760132	Slc2a9<sup>tm1Khm</sup>/Slc2a9<sup>tm1Khm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25100214	20210319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715869	Slc25a12<sup>Gt(OST123999)Lex</sup>/Slc25a12<sup>Gt(OST123999)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0080349	developmental and epileptic encephalopathy 39						ECO:0000033	author statement supported by traceable reference	PMID:28429368	20181221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4460825	Cdk5rap2<sup>an</sup>/Cdk5rap2<sup>an</sup>  [background:] B6.Cg-Cdk5rap2<sup>an</sup>	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:20460369	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825063	Tg(BAC144D14)5A2Masu/0  [background:] B6J.Cg-Tg(BAC144D14)5A2Masu	is_model_of	DOID:14681	Silver-Russell syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26963625	20170224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3528030	Cngb1<sup>tm1.1Biel</sup>/Cngb1<sup>tm1.1Biel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:15634774	20100720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838324	Ttn<sup>tm1.1Isrd</sup>/Ttn<sup>tm1.1Isrd</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J						ECO:0000033	author statement supported by traceable reference	PMID:20855473	20101115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318339	Dnah11<sup>b2b1203Clo</sup>/Dnah11<sup>b2b1203Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1203Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032571	Tg<sup>cog</sup>/Tg<sup>cog</sup>  [background:] involves: AKR/J * C57BL/6By	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:3803305	20100125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367213	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup> Nos3<sup>tm1Plh</sup>/Nos3<sup>tm1Plh</sup>  [background:] B6.129S4-Nos3<sup>tm1Plh</sup> Nos1<sup>tm1Plh</sup>	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12788381	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720014	Rpgr<sup>Rd9</sup>/Y  [background:] C57BL/6-Rpgr<sup>Rd9</sup>	is_model_of	DOID:0110414	retinitis pigmentosa 3						ECO:0000033	author statement supported by traceable reference	PMID:22563472	20170111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6850120	Clcn2<sup>em1Uis</sup>/Clcn2<sup>+</sup>  [background:] C57BL/6N-Clcn2<sup>em1Uis</sup>	is_model_of	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:31727896	20220110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7265160	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-IGF1R)1Ramo/0  [background:] involves: FVB	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19568412	20220503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6163608	Atp1a3<sup>tm1.1Tmklh</sup>/Atp1a3<sup>+</sup>  [background:] B6JRj.129S1-Atp1a3<sup>tm1.1Tmklh</sup>	is_model_of	DOID:0050635	alternating hemiplegia of childhood						ECO:0000033	author statement supported by traceable reference	PMID:27549929	20180628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442140	b2b1723Clo/b2b1723Clo  [background:] C57BL/6J-b2b1723Clo	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4456999	Fbxw4<sup>Dac-2J</sup>/Fbxw4<sup>+</sup> mdac/mdac  [background:] CBy.MRL-Fbxw4<sup>Dac-2J</sup>/J	is_model_of	DOID:0090025	split hand-foot malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:18392654	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437114	Dnah11<sup>b2b1289Clo</sup>/Dnah11<sup>b2b1289Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1289Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314411	Tg(MECP2)1Hzo/0  [background:] either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1	is_model_of	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000033	author statement supported by traceable reference	PMID:22231481	20120408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583562	Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617218	Ifih1<sup>Rgsc422</sup>/Ifih1<sup>Rgsc422</sup>  [background:] D2JJcl.B6JJcl-Ifih1<sup>Rgsc422</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:24530055	20150302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107901	Bag3<sup>tm1c(EUCOMM)Hmgu</sup>/Bag3<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Myhca-cre)1Abel/0  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0110448	dilated cardiomyopathy 1HH						ECO:0000033	author statement supported by traceable reference	PMID:28737513	20180109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665144	Xpc<sup>tm1Brd</sup>/Xpc<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL	is_model_of	DOID:0110844	xeroderma pigmentosum group C						ECO:0000033	author statement supported by traceable reference	PMID:7675084	20061030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698534	Syn1<sup>tm1Pggd</sup>/Syn1<sup>tm1Pggd</sup> Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup> Syn3<sup>tm1Pggd</sup>/Syn3<sup>tm1Pggd</sup>  [background:] involves: 129 * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:21621590	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703544	Del(6Dlx6-Dlx5)1Tlu/Del(6Dlx6-Dlx5)1Tlu  [background:] Not Specified	is_model_of	DOID:0090021	split hand-foot malformation 1						ECO:0000033	author statement supported by traceable reference	PMID:12000792	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676319	Ush1c<sup>dfcr</sup>/Ush1c<sup>dfcr</sup>  [background:] involves: BALB/cByJ	is_model_of	DOID:0110473	autosomal recessive nonsyndromic deafness 18A						ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688878	Itgb3<sup>tm1Hyn</sup>/Itgb3<sup>tm1.1Wlbcr</sup> Tg(Pf4-icre)Q3Rsko/0  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2219	Glanzmann's thrombasthenia						ECO:0000033	author statement supported by traceable reference	PMID:19933310	20151002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6155766	Cabp2<sup>tm1b(KOMP)Mbp</sup>/Cabp2<sup>tm1b(KOMP)Mbp</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0110537	autosomal recessive nonsyndromic deafness 93						ECO:0000033	author statement supported by traceable reference	PMID:28183797	20180511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908019	Del(7Chrna7-Fan1)1Mima/+  [background:] C57BL/6N-Del(7Chrna7-Fan1)1Mima	is_model_of	DOID:0060394	chromosome 15q13.3 microdeletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26658876	20170901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4354207	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(Tyr-BRAF*V600E)470Fgh/0  [background:] involves: 129/Sv * C57BL/6J * CBA * SJL	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:19398955	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6323255	Slc7a8<sup>tm1Geno</sup>/Slc7a8<sup>tm1Geno</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:10003	sensorineural hearing loss						ECO:0000033	author statement supported by traceable reference	PMID:29355479	20190716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576781	Arhgef2<sup>Gt(IST13976A8)Tigm</sup>/Arhgef2<sup>Gt(IST13976A8)Tigm</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0080312	neurodevelopmental disorder with midbrain and hindbrain malformations						ECO:0000033	author statement supported by traceable reference	PMID:28453519	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527794	Ncoa1<sup>tm1Bwo</sup>/Ncoa1<sup>tm1Bwo</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10202153	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6357191	Cep250<sup>tm1Jzb</sup>/Cep250<sup>tm1Jzb</sup>  [background:] involves: C57BL/6	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:30998843	20190827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6156835	Clrn1<sup>tm1.1Kuna</sup>/Clrn1<sup>tm1.1Kuna</sup> Tg(Atoh1-Clrn1)#Kuna/0  [background:] involves: C57BL/6J	is_model_of	DOID:0110828	Usher syndrome type 3						ECO:0000033	author statement supported by traceable reference	PMID:29044151	20180517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432231	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:2999	granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697875	Tg(Plp1-LMNB1)1108Qsp/0  [background:] involves: FVB/N	is_model_of	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26311780	20151203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687164	H2<sup>g7</sup>/H2<sup>g7</sup> Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(TcraBDC12-4.1)10Jos/0 Tg(TcrbBDC12-4.1)82Gse/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16804066	20061109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6771693	Nbn<sup>em7Jpt</sup>/Nbn<sup>tm2Zqw</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:31285322	20211015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7329778	Tg(Zfhx2*R1907K)#Jcox/0  [background:] involves: C57BL/6	is_model_of	DOID:0081075	Marsili syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29253101	20220816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758961	Nlgn3<sup>tm1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:17823315	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6189158	Camk2a<sup>tm1Sva</sup>/Camk2a<sup>+</sup>  [background:] B6.129P2-Camk2a<sup>tm1Sva</sup>/J	is_model_of	DOID:3312	bipolar disorder						ECO:0000033	author statement supported by traceable reference	PMID:27028761	20180723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911924	Tg(Myh6-Sgcd*S151A)5Mcn/0  [background:] involves: 129T2/SvEms * C57BL/6J	is_model_of	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000033	author statement supported by traceable reference	PMID:17164264	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258654	Vwf<sup>tm1.1Geno</sup>/Vwf<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060574	von Willebrand's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:27212476	20181203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717654	Agxt<sup>tm1Ull</sup>/Agxt<sup>tm1Ull</sup>  [background:] B6.129X1-Agxt<sup>tm1Ull</sup>	is_model_of	DOID:0111670	primary hyperoxaluria type 1						ECO:0000033	author statement supported by traceable reference	PMID:17110443	20201118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622060	Tnf<sup>tm2Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902076	Slc9a6<sup>tm1Dgen</sup>/Slc9a6<sup>+</sup>  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J	is_model_of	DOID:0060825	Christianson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26515654	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177534	Cftr<sup>tm2Cam</sup>/Cftr<sup>tm2Cam</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7545494	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285700	Espl1<sup>Gt(XL058)Byg</sup>/Espl1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] B6.129-Trp53<sup>tm1Tyj</sup> Espl1<sup>Gt(XL058)Byg</sup>	is_model_of	DOID:0060058	lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:21799785	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359195	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19535499	20180205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428893	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] BTBR.Cg-Lep<sup>ob</sup>/WiscJ	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16280642	20130926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811207	Hspg2<sup>tm1Soni</sup>/Hspg2<sup>tm1Soni</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:18647752	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2385971	Lat<sup>tm1.1Mal</sup>/Lat<sup>tm1.1Mal</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0080356	IgG4-related disease						ECO:0000033	author statement supported by traceable reference	PMID:29902238	20191122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583558	Tg(ITGA5)0858Fmw/0 Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5810684	Tg(Hsf4/EGFP)N7Spbh/0  [background:] C57BL/6-Tg(Hsf4/EGFP)N7Spbh	is_model_of	DOID:0110255	cataract 5 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:25168898	20161202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621460	Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:15798202	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621460	Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:16510575	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437111	Tmem67<sup>b2b1291.1Clo</sup>/Tmem67<sup>b2b1291.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1291.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7523309	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>em1Jmi</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>	is_model_of	DOID:332	amyotrophic lateral sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555837	Ccdc39<sup>b2b2025.1Clo</sup>/Ccdc39<sup>b2b2025.1Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b2025.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5819051	Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110931	nemaline myopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:26035871	20170125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669003	Eng<sup>tm1Mle</sup>/Eng<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:10562296	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177207	Fxn<sup>tm2Mkn</sup>/Fxn<sup>tm2.1Mkn</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:11175786	20060719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530365	Gpc3<sup>tm1Fil</sup>/Y  [background:] B6.Cg-Gpc3<sup>tm1Fil</sup>	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10402475	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054675	Papss2<sup>bm</sup>/Papss2<sup>bm</sup>  [background:] LDJ/Le	is_model_of	DOID:0050812	spondyloepimetaphyseal dysplasia, Pakistani type						ECO:0000033	author statement supported by traceable reference	PMID:5713631	20090819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569536	Tg(CMV-HTT*89Q)ATag/0  [background:] involves: FVB/N	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763920	Tg(HSA*LR)20aCath/?  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6711469	Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>/Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0112321	alacrima, achalasia, and impaired intellectual development syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33755596	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6388659	Pkhd1<sup>em1Mrug</sup>/Pkhd1<sup>em1Mrug</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0080212	polycystic kidney disease 4						ECO:0000033	author statement supported by traceable reference	PMID:30600684	20200205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275135	Nf1<sup>tm1.1Kest</sup>/Nf1<sup>tm1c(KOMP)Wtsi</sup> Tg(Dhh-cre)1Mejr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * C57BL/6NTac * FVB/N	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:27482814	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586618	Tg(Myh6-Tnf)1Brgi/?  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:9577949	20170830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581965	Ighm<sup>tm1Cgn</sup>/Ighm<sup>tm1Cgn</sup> Tg(Igh-VB1-8/Igh-6m)1Mjsk/?  [background:] NODCaj.Cg-Ighm<sup>tm1Cgn</sup> Tg(Igh-VB1-8/Igh-6m)1Mjsk/FswJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15448087	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6885740	Hsp90b1<sup>tm1Zhli</sup>/Hsp90b1<sup>tm1.1Zhli</sup> Tg(Ddx4-cre)1Dcas/0  [background:] involves: 129S/SvEv * FVB	is_model_of	DOID:0112312	male infertility due to globozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:21208614	20220302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574973	Gnrhr<sup>hh</sup>/Gnrhr<sup>hh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:15625238	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008609	Aspa<sup>tm1a(EUCOMM)Wtsi</sup>/Aspa<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:21625469	20170922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904949	Tg(Myh6-Rab1a)highGwd/0  [background:] involves: FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11739277	20170718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794288	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:15703401	20080818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794288	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:1303281	20080818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3696576	Tg(Prnp-App/APPswe)E1-2Dbo/0  [background:] B6.C3-Tg(Prnp-App/APPswe)E1-2Dbo	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12742740	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815198	Ar<sup>Tfm</sup>/Y Tg(TSPY)9Jshm/0  [background:] involves: NMRI * STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491050	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp*P101L)2866Sbp/Tg(Prnp*P101L)2866Sbp  [background:] involves: 129S7/SvEvBrd * FVB/N	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451170	Sox9<sup>tm2Crm</sup>/Sox9<sup>tm2Crm</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819168	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] C.129S6-Trp53bp2<sup>tm1Xlu</sup>	is_model_of	DOID:0060412	chromosome 1q41-q42 deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6269453	Npr3<sup>kylb</sup>/Npr3<sup>kylb</sup>  [background:] involves: BALB/c * C57BL/6J	is_model_of	DOID:0080001	bone disease						ECO:0000033	author statement supported by traceable reference	PMID:27959934	20181227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417896	Tg(Krt14-Fyn)AJsey/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:37	skin disease						ECO:0000033	author statement supported by traceable reference	PMID:17046829	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4436744	Npc1<sup>m1N</sup>/Npc1<sup>tm1.2Apl</sup>  [background:] B6.Cg-Npc1<sup>m1N</sup>/Npc1<sup>tm1.2Apl</sup>	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:20007718	20100310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440925	Wnt7a<sup>px-2J</sup>/Wnt7a<sup>px-2J</sup>  [background:] B6;C3Fe-Wnt7a<sup>px-2J</sup>/GrsrJ	is_model_of	DOID:0090067	Fuhrmann syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5440720	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177530	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:1380723	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047228	Vegfa<sup>tm1Pec</sup>/Vegfa<sup>tm1Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12539040	20060711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7262713	Tg(KRT18*R89C)50Rgo/0  [background:] involves: FVB/N	is_model_of	DOID:2237	hepatitis						ECO:0000033	author statement supported by traceable reference	PMID:8522591	20220419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6193978	Tg(Myh6-MYL2*K104E)2Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:24992035	20180809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278937	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:27329763	20190219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6108900	Tg(CAG-Calr)#Mlk/0 Tg(Myh6-cre/Esr1*)1Liao/0  [background:] involves: C57BL/6	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:27441395	20180112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177536	Cftr<sup>tm1Kth</sup>/Cftr<sup>tm1Kth</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7560099	20050809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428443	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:22265892	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366531	Tg(Camk2a-App*,-Apbb1)25Spim/0  [background:] C57BL/6-Tg(Camk2a-App*,-Apbb1)25Spim	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19837693	20091109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851518	Nsd2<sup>tm1Ykan</sup>/Nsd2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19483677	20090729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428907	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22266220	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445972	b2b1709Clo/b2b1709Clo  [background:] C57BL/6J-b2b1709Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491041	Mecp2<sup>tm1.1Bird</sup>/Y Tg(MECP2*G273X/GFP)AHzo/0  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23452848	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197473	Tg(APCS-Tnfsf11*)#aKhs/0  [background:] C57BL/6J-Tg(APCS-Tnfsf11*)#aKhs	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:12434161	20180911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4442633	Pax2<sup>M1Bpb</sup>/Pax2<sup>+</sup>  [background:] C57BL/6-Pax2<sup>M1Bpb</sup>	is_model_of	DOID:0090006	renal coloboma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20221250	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438021	Slc39a4<sup>tm2Gka</sup>/Slc39a4<sup>tm2Gka</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:0050605	acrodermatitis enteropathica						ECO:0000033	author statement supported by traceable reference	PMID:22737083	20121009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313520	b2b942Clo/b2b942Clo  [background:] C57BL/6J-b2b942Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840657	Scn8a<sup>8J</sup>/Scn8a<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:24657915	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840657	Scn8a<sup>8J</sup>/Scn8a<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:19254928	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5805976	Tg(Cd4-NPM/ALK)N1Ingh/0  [background:] either: (involves: BALB/c * Swiss Webster) or (involves: C57BL/6 * Swiss Webster)	is_model_of	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:12424201	20161102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6886231	P2rx2<sup>em1Xzl</sup>/P2rx2<sup>+</sup>  [background:] CBA/J-P2rx2<sup>em1Xzl</sup>	is_model_of	DOID:0110567	autosomal dominant nonsyndromic deafness 41						ECO:0000033	author statement supported by traceable reference	PMID:33791800	20220307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361710	Lepr<sup>db</sup>/Lepr<sup>db</sup> Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] BKS.Cg-Lepr<sup>db</sup> Nos3<sup>tm1Unc</sup>	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16971655	20150513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442707	Kit<sup>tm4.1Bsm</sup>/Kit<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N	is_model_of	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:22652566	20121126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7278773	Acvr1<sup>tm1Glh</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1.2(CAG-EGFP)Glh</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Pdgfra-cre)1Clc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * FVB/N	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:29396429	20220517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5708062	L2hgdh<sup>Gt(DC0625)Wtsi</sup>/L2hgdh<sup>Gt(DC0625)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050574	L-2-hydroxyglutaric aciduria						ECO:0000033	author statement supported by traceable reference	PMID:25763823	20160211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836620	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17237784	20101028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664613	Lrp5<sup>tm1Kry</sup>/Lrp5<sup>tm1Kry</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	is_model_of	DOID:0060849	osteoporosis-pseudoglioma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11956231	20061025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311574	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup> Nat10<sup>tm1a(KOMP)Wtsi</sup>/Nat10<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604390	Park7<sup>tm1Xz</sup>/Park7<sup>tm1Xz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:15799973	20051114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7280953	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:0060564	spinal disease						ECO:0000033	author statement supported by traceable reference	PMID:28523278	20220526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400995	Nlgn1<sup>em1Taku</sup>/Nlgn1<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28841651	20200323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368181	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>tm1.2Lcm</sup> Tg(Six3-cre)69Frty/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586619	Tg(Myh6-Tnf)2Brgi/?  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:9577949	20170830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679734	Kat6b<sup>Gt(pKC199)1Pgr</sup>/Kat6b<sup>Gt(pKC199)1Pgr</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:3490	Noonan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21804188	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815301	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Pax8-rtTA2S*M2)1Koes/0 Tg(tetO-cre)LC1Bjd/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:18724376	20110502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615357	Lrp5<sup>tm1Grw</sup>/Lrp5<sup>tm1Grw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060849	osteoporosis-pseudoglioma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664614	Lrp5<sup>tm1Kry</sup>/Lrp5<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	is_model_of	DOID:0060849	osteoporosis-pseudoglioma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11956231	20061025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664276	Gpr12<sup>tm1Dgen</sup>/Gpr12<sup>tm1Dgen</sup>  [background:] B6.129P2-Gpr12<sup>tm1Dgen</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16887097	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437437	Tg(Lrrk2*G2019S)2Yue/0  [background:] involves: C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:20130188	20100318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819716	Pkd1<sup>tm1Gztn</sup>/Pkd1<sup>tm1Gztn</sup> Gt(ROSA)26Sor<sup>tm9(cre/ESR1)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S/Sv * 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:20562878	20110502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839510	Erbb2<sup>tm8(Erbb2)Mul</sup>/Erbb2<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(MMTV-cre)7Mul/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18381417	20101123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949761	Shank3<sup>tm2Gfng</sup>/Shank3<sup>tm2Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21423165	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275998	Ezh2<sup>em1Jbn</sup>/Ezh2<sup>+</sup>  [background:] C57BL/6J-Ezh2<sup>em1Jbn</sup>	is_model_of	DOID:14731	Weaver syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29244146	20190205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6450805	Myocd<sup>tm1.1Msp</sup>/mgb  [background:] involves: 129/Sv * FVB/N	is_model_of	DOID:0112014	congenital megabladder						ECO:0000033	author statement supported by traceable reference	PMID:31513549	20211027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444191	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] C57BL/6J-Prss56<sup>glcr4</sup>	is_model_of	DOID:0060835	isolated microphthalmia 6						ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028691	Ercc4<sup>tm1Fwa</sup>/Ercc4<sup>tm1Fwa</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110848	xeroderma pigmentosum group F						ECO:0000033	author statement supported by traceable reference	PMID:14729965	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1936982	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836163	Prph2<sup>tm1Nmc</sup>/Prph2<sup>tm1Nmc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110383	retinitis pigmentosa 7						ECO:0000033	author statement supported by traceable reference	PMID:11978760	20090317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421409	Slc24a5<sup>tm1Lex</sup>/Slc24a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0050633	ocular albinism 1						ECO:0000033	author statement supported by traceable reference	PMID:18424845	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278015	Tg(Actb-Ptma)T12Clwu/Tg(Actb-Ptma)T12Clwu  [background:] involves: FVB/N	is_model_of	DOID:0080322	polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:15840017	20190213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653547	Tg(Mpz)80.2Wra/0  [background:] involves: FVB/N	is_model_of	DOID:870	neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:10704451	20190211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587763	Myo7a<sup>816SB</sup>/Myo7a<sup>816SB</sup>  [background:] involves: BALB/cRl * 47BS/Rl	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:9435277	20060307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429407	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: STOCK Mlph<sup>ln</sup> a Tgfa<sup>wa1</sup> Cdh23<sup>v</sup> Ednrb<sup>s</sup>	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24680679	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846575	T(7;18)50H/+  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1303278	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825038	Acvr1<sup>tm2.1Vlcg</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm3.1(cre/ERT2)Vlcg</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:26333933	20170224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622103	Fkbp1a<sup>tm1Zuk</sup>/Fkbp1a<sup>tm1Zuk</sup>  [background:] either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	is_model_of	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9461216	20060512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6195746	Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup>/Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * CD-1 * SJL	is_model_of	DOID:5602	T-cell adult acute lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25565005	20180827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009549	Tg(Th-MYCN)41Waw/0  [background:] involves: BALB/c * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:9214616	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843817	Il6st<sup>tm1Thir</sup>/Il6st<sup>tm1Thir</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:12370259	20090512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6446738	Hgf<sup>tm1.1Tbf</sup>/Hgf<sup>tm1.1Tbf</sup>  [background:] B6.Cg-Hgf<sup>tm1.1Tbf</sup>/Tbf	is_model_of	DOID:0110497	autosomal recessive nonsyndromic deafness 39						ECO:0000033	author statement supported by traceable reference	PMID:32152201	20200730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451081	Lipa<sup>tm1Ggb</sup>/Lipa<sup>tm1Ggb</sup>  [background:] involves: 129P2/OlaHsd * CF-1	is_model_of	DOID:14497	Wolman disease						ECO:0000033	author statement supported by traceable reference	PMID:9700186	20190729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789123	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>/J	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:6583703	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192643	Cib2<sup>tm1.1Aela</sup>/Cib2<sup>tm1.1Aela</sup>  [background:] involves: BALB/c * C57BL/6 * C57BL/6N	is_model_of	DOID:0110505	autosomal recessive nonsyndromic deafness 48						ECO:0000033	author statement supported by traceable reference	PMID:29084757	20180803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850440	Cdkn2a<sup>tm2Brn</sup>/Cdkn2a<sup>tm2Brn</sup> Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1790	malignant mesothelioma						ECO:0000033	author statement supported by traceable reference	PMID:18328429	20090716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276135	Tg(Myh6-Camk2d_ic)#Jhb/0  [background:] Not Specified	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:17124532	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710761	Tg(Prnp-ITM2B/APP695*40)1Emcg/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16039562	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587787	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm2Jfm</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:14623826	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6294052	Pak2<sup>Gt(OST104058)Lex</sup>/Pak2<sup>+</sup>  [background:] B6;129S5-Pak2<sup>Gt(OST104058)Lex</sup>/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30134165	20190423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287231	Hepacam<sup>tm1Vlcg</sup>/Hepacam<sup>tm1Vlcg</sup>  [background:] Not Specified	is_model_of	DOID:0080315	megalencephalic leukoencephalopathy with subcortical cysts						ECO:0000033	author statement supported by traceable reference	PMID:28695146	20190412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532830	Sidt2<sup>tm1.1Hzha</sup>/Sidt2<sup>tm1.1Hzha</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:27233614	20180921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7276257	Mbd2<sup>tm1Bh</sup>/Mbd2<sup>tm1Bh</sup>  [background:] NOD.129P2(B6)-Mbd2<sup>tm1Bh</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:34420035	20220512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300563	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (A/J x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817506	Lmna<sup>tm1Lgf</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:16862216	20081124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683844	Blm<sup>tm1Ches</sup>/Blm<sup>tm1Ches</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9808625	20050919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5561116	Cfc1<sup>b2b2736.1Clo</sup>/Cfc1<sup>b2b2736.1Clo</sup>  [background:] C57BL/6J-Cfc1<sup>b2b2736.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752237	Cdkn2a<sup>tm2.1Nesh</sup>/Cdkn2a<sup>tm2.1Nesh</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] B6J.Cg-Tg(Tyr-cre/ERT2)13Bos Cdkn2a<sup>tm2.1Nesh</sup> Kras<sup>tm4Tyj</sup>	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25252692	20190123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695051	Irf6<sup>Gt(OST398253)Lex</sup>/Irf6<sup>Gt(OST398253)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0060055	popliteal pterygium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17041601	20070130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943741	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: 129S7/SvEvBrd * BALB/c * C57BL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21159977	20110405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4881537	Htr1a<sup>tm1Rhn</sup>/Htr1a<sup>tm1Rhn</sup>  [background:] involves: 129S/SvEv * 129S1/Sv	is_model_of	DOID:2030	anxiety disorder						ECO:0000033	author statement supported by traceable reference	PMID:20152131	20110201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196323	Ret<sup>tm2.1Cos</sup>/? Tg(Th-MYCN)41Waw/0  [background:] involves: 129S1/Sv * BALB/c * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29321660	20180904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7511767	Aicda<sup>em1Jaych</sup>/Aicda<sup>em1Jaych</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060758	immunodeficiency with hyper-IgM type 2						ECO:0000033	author statement supported by traceable reference	PMID:33098766	20230726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6690862	Eml1<sup>tvrm360</sup>/Eml1<sup>tvrm360</sup>  [background:] C57BL/6J-Eml1<sup>tvrm360</sup>/Pjn	is_model_of	DOID:0111169	subcortical band heterotopia						ECO:0000033	author statement supported by traceable reference	PMID:32221352	20210418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029765	Fhit<sup>tm1Hbn</sup>/Fhit<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0050465	Muir-Torre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10758156	20050622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6193618	Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup>/Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup> Tg(Osr1-cre)4Mrt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:2526	prostate adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21795710	20180807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676370	Pitpna<sup>tm1Vab</sup>/Pitpna<sup>tm1Vab</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060357	chylomicron retention disease						ECO:0000033	author statement supported by traceable reference	PMID:12788952	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574544	Dok2<sup>tm1Ppp</sup>/Dok2<sup>tm1Ppp</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: 129S1/Sv	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611295	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154633	Nup35<sup>m1Apb</sup>/Nup35<sup>m1Apb</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0080072	intestinal pseudo-obstruction						ECO:0000033	author statement supported by traceable reference	PMID:27427419	20200621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6694869	Cdc14a<sup>em1Tbf</sup>/Cdc14a<sup>em1Tbf</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110491	autosomal recessive nonsyndromic deafness 32						ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266283	Mecp2<sup>tm1Nlnd</sup>/Mecp2<sup>+</sup>  [background:] involves: 129 * CD-1	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609494	Agfg1<sup>tm1Jvd</sup>/Agfg1<sup>tm1Jvd</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:15705627	20220127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6740192	Gabrg2<sup>tm1.2Rmac</sup>/Gabrg2<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:33582225	20210817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6467338	Clrn1<sup>tm1.1Ugpa</sup>/Clrn1<sup>tm1.1Ugpa</sup> Myo15a<sup>tm1.1(cre)Ugds</sup>/Myo15a<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6N	is_model_of	DOID:0110841	Usher syndrome type 3A						ECO:0000033	author statement supported by traceable reference	PMID:29985171	20201016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817461	Mecp2<sup>tm1Bird</sup>/Y  [background:] (129S6.129P2-Mecp2<sup>tm1Bird</sup> x C57BL/6)F1	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18321864	20081121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274727	Gucy2e<sup>cpfl9</sup>/Gucy2e<sup>cpfl9</sup>  [background:] B6;129P2-Gucy2e<sup>cpfl9</sup>/BocJ	is_model_of	DOID:0110078	Leber congenital amaurosis 1						ECO:0000033	author statement supported by traceable reference	MGI:6274742	20190125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603845	Ifngr2<sup>tm1Pbro</sup>/Ifngr2<sup>tm1Pbro</sup>  [background:] NOD.129S1-Ifngr2<sup>tm1Pbro</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11714835	20101101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476432	Plxnd1<sup>b2b1863Clo</sup>/Plxnd1<sup>b2b1863Clo</sup>  [background:] C57BL/6J-Plxnd1<sup>b2b1863Clo</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851250	Tg(Kera-PITX2*A)BHjal/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:15509533	20090727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4833820	Kcna1<sup>tm1Tem</sup>/Kcna1<sup>tm1Tem</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:20392939	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256973	Rhbdf2<sup>em2Mvw</sup>/Rhbdf2<sup>em2Mvw</sup>  [background:] C57BL/6J-Rhbdf2<sup>em2Mvw</sup>/Mvw	is_model_of	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28655741	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358603	Serpina1<sup>em#Chmu</sup>/Serpina1<sup>em#Chmu</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:29453277	20190906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274282	Tg(Krt14-Rac1*G12V)#Mrnk/0  [background:] either: B6.CBACa-Tg(Krt14-Rac1*G12V)#Mrnk or C.CBACa-Tg(Krt14-Rac1*G12V)#Mrnk	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:27294528	20190122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038236	nm3/nm3  [background:] involves: RIIIS/J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:14966677	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3035937	Grip1<sup>tm1Rha</sup>/Grip1<sup>tm1Rha</sup>  [background:] B6.129-Grip1<sup>tm1Rha</sup>	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14730302	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577022	None [background:] SAMP1	is_model_of	DOID:0110892	inflammatory bowel disease 1						ECO:0000033	author statement supported by traceable reference	PMID:15762871	20050516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680399	Gba1<sup>tm2Ggb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904828	Tg(Myh6-CACNA1C)M1Aschw/0  [background:] involves: FVB/N	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11136699	20170717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554187	Drc1<sup>b2b2237Clo</sup>/Drc1<sup>b2b2237Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b2237Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620105	Tg(Pbsn-MYC)6Key/?  [background:] involves: FVB	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:14522256	20060420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274702	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616711	Mdm4<sup>tm2Glo</sup>/Mdm4<sup>tm2.1Glo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17533180	20170817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797405	Igk<sup>tm1.1Cog</sup>/Igk<sup>tm1.2Cog</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:447	renal tubular transport disease						ECO:0000033	author statement supported by traceable reference	PMID:16543471	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040184	Ticam2<sup>tm1Aki</sup>/Ticam2<sup>tm1Aki</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:28592648	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452488	Tg(Prnp-ITM2B*)7Jckr/0  [background:] C57BL/6-Tg(Prnp-ITM2B*)7Jckr	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:20385796	20100520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3701944	Trp53inp1<sup>tm1Acar</sup>/Trp53inp1<sup>tm1Acar</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:25828351	20170411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2168108	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:62273	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690015	Tg(Myh6-TNNI3*G203S)4Chs/0  [background:] Not Specified	is_model_of	DOID:0110313	hypertrophic cardiomyopathy 7						ECO:0000033	author statement supported by traceable reference	PMID:16950368	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565220	Tg(Ins2-HBEGF)5Rin/?  [background:] C57BL/6-Tg(Ins2-HBEGF)5Rin	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23747725	20140523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273176	Mpz<sup>tm1.1Wra</sup>/Mpz<sup>+</sup>  [background:] FVB.129S2-Mpz<sup>tm1.1Wra</sup>	is_model_of	DOID:870	neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:30239779	20190111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654632	Erbb2<sup>tm1Klee</sup>/Erbb2<sup>tm1Klee</sup> Tg(Nes-cre)1Atp/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:12526770	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796685	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup> Tg(Mt1-CBS)25Waku/0  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6	is_model_of	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:19858416	20161006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665400	Fmr1<sup>tm1Cgr</sup>/Fmr1<sup>tm1Cgr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8033209	20070119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571189	Pex1<sup>tm1.1Sjms</sup>/Pex1<sup>tm1.1Sjms</sup>  [background:] involves: 129 * C57BL/6N	is_model_of	DOID:905	Zellweger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24503136	20140702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175832	Dsg3<sup>bal-Pas</sup>/Dsg3<sup>bal-Pas</sup>  [background:] 129S2.Cg-Dsg3<sup>bal-Pas</sup>	is_model_of	DOID:0060851	pemphigus vulgaris						ECO:0000033	author statement supported by traceable reference	MGI:1202169	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925342	Npc1<sup>m1N</sup>/Npc1<sup>tm1.1Apl</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] B6J.Cg-Npc1<sup>m1N</sup>/Npc1<sup>tm1.1Apl</sup> Tg(CAG-cre/Esr1*)5Amc	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:21856732	20171120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559208	Ap3d1<sup>mh-4J</sup>/Ap3d1<sup>mh-4J</sup>  [background:] involves: 129P2/OlaHsd * BALB/cByJ * C57BL/6J	is_model_of	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	MGI:5558048	20140416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5553465	Tg(Prnp-APPSweArc)#Rmni/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27836896	20190724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653631	Tnfrsf11b<sup>tm1Khs</sup>/Tnfrsf11b<sup>tm1Khs</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:9647741	20210421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6360946	Slc39a8<sup>tm1.2Mrl</sup>/Slc39a8<sup>tm1.2Mrl</sup>  [background:] B6(Cg)-Slc39a8<sup>tm1.2Mrl</sup>	is_model_of	DOID:0060480	left ventricular noncompaction						ECO:0000033	author statement supported by traceable reference	PMID:29337306	20190925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6098717	Crtc1<sup>Gt(XK522)Byg</sup>/Crtc1<sup>Gt(XK522)Byg</sup>  [background:] B6N.129P2-Crtc1<sup>Gt(XK522)Byg</sup>	is_model_of	DOID:1470	major depressive disorder						ECO:0000033	author statement supported by traceable reference	PMID:22592058	20171208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4999584	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J	is_model_of	DOID:0080093	myofibrillar myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:21445271	20110523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175152	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>tm1Mms</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:10215624	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777760	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:17712420	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778898	Pnp<sup>e</sup>/Pnp<sup>e</sup>  [background:] C57BL/6J-Pnp<sup>e</sup>	is_model_of	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908356	Tg(Myh6-EGFR*)9-12Iko/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22216087	20170906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727359	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>em1Alsh</sup>  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623263	Cln3<sup>tm1Mkat</sup>/Cln3<sup>tm1Mkat</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:10440905	20060525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284974	Tlr7<sup>em2Anu</sup>/Tlr7<sup>+</sup>  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5647920	Tg(Tff3-Tmem207)1Tamo/0  [background:] C57BL/6-Tg(Tff3-Tmem207)1Tamo	is_model_of	DOID:2433	epidermal appendage tumor						ECO:0000033	author statement supported by traceable reference	PMID:25305140	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583125	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] involves: KK	is_model_of	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157365	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1.1Mrb</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:27519416	20180521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527337	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>/Col1a1<sup>+</sup> Tg(Scgb1a1-rtTA)1Jaw/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:3908	lung non-small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20952506	20171106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037958	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:15003170	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842704	Ebf1<sup>tm1Rug</sup>/Ebf1<sup>tm1Rug</sup>  [background:] involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	is_model_of	DOID:811	lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19130908	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660941	Fdxr<sup>m1J</sup>/Fdxr<sup>m1J</sup> Otop2<sup>m1J</sup>/Otop2<sup>m1J</sup>  [background:] B6;129S-Fdxr<sup>m1J</sup> Otop2<sup>m1J</sup>/GrsrJ	is_model_of	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:29040572	20171128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009037	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:21562564	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ	is_model_of	DOID:0110153	Charcot-Marie-Tooth disease type 1E						ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581823	Tg(GFAP)7Mes/0  [background:] involves: FVB/N	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:9466565	20050718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702414	Apc<sup>tm2.1Cip</sup>/Apc<sup>+</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:26214133	20160111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183938	Gla<sup>tm1Kul</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:22574107	20121008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183938	Gla<sup>tm1Kul</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:9122231	20121008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429853	Akt2<sup>tm1Hem</sup>/Akt2<sup>tm1Hem</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:11612	polycystic ovary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22275470	20120802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905032	Col4a1<sup>tm1.1Ics</sup>/Col4a1<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:26260163	20170719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785077	Flnb<sup>Gt(XD076)Byg</sup>/Flnb<sup>Gt(XD076)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090116	spondylocarpotarsal synostosis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17606870	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571040	Del(7Coro1a-Spn)1Dolm/+  [background:] involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6N * CD-1	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:24794428	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609951	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Myl1<sup>tm1(cre)Sjb</sup>/Myl1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:699	mitochondrial myopathy						ECO:0000033	author statement supported by traceable reference	PMID:16103131	20060112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583125	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] involves: KK	is_model_of	DOID:0111114	nephronophthisis 3						ECO:0000033	author statement supported by traceable reference	PMID:12872122	20050808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4947945	Efemp2<sup>tm1.1Hiya</sup>/Efemp2<sup>tm1.2Hiya</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:23636094	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883020	Tg(PGK1-Gnas*R201C)60Pabi/0  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * FVB/N)	is_model_of	DOID:1858	McCune Albright syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24764158	20170413	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586912	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242110	20050908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719415	Txnip<sup>Hyplip1</sup>/Txnip<sup>+</sup>  [background:] involves: CAST/Ei * HcB19/Dem	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908182	Tg(Myh6-Mtpn)4Ssen/0  [background:] involves: FVB	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:14970239	20170905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5291505	Del(7Slx1b-Sept1)4Aam/+  [background:] involves: 129S7/SvEvBrd * C57BL/6N	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21969575	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476655	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] B6.C3Sn-Rab27a<sup>ash</sup>	is_model_of	DOID:0050120	hemophagocytic lymphohistiocytosis						ECO:0000033	author statement supported by traceable reference	PMID:23160464	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620804	Hey2<sup>tm1Kkb</sup>/Hey2<sup>tm1Kkb</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:23288164	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766814	Crebbp<sup>tm2Pkb</sup>/Crebbp<sup>tm2Pkb</sup>  [background:] (B6.129P2-Crebbp<sup>tm2Pkb</sup>/Pkb x 129S2.129P2(B6)-Crebbp<sup>tm2Pkb</sup>/Pkb)F1	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26730956	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609722	Slc17a5<sup>tm1Lex</sup>/Slc17a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:3211	lysosomal storage disease						ECO:0000033	author statement supported by traceable reference	MGI:3609573	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259768	Cacna1f<sup>nob9</sup>/Cacna1f<sup>nob9</sup>  [background:] B6(PWD)-Cacna1f<sup>nob9</sup>/BocJ	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:30445045	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655296	Lig4<sup>tm1Icrf</sup>/Lig4<sup>tm1Icrf</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19076778	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804216	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>tm1Brd</sup> Tg(Gfap-cre)2Brn/0  [background:] involves: 129 * 129S7/SvEvBrd * FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:10783170	20080903	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6783465	Washc4<sup>em1Ssod</sup>/Washc4<sup>em1Ssod</sup>  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33749590	20211029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575514	Tg(CAG-Diap3)924Lesp/0  [background:] FVB/NJ-Tg(CAG-Diap3)924Lesp	is_model_of	DOID:0060690	autosomal dominant auditory neuropathy 1						ECO:0000033	author statement supported by traceable reference	PMID:23441200	20140730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433489	Tmem67<sup>b2b1163.1Clo</sup>/Tmem67<sup>b2b1163.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1163.1Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6780173	Dnah10<sup>em2Yxc</sup>/Dnah10<sup>em2Yxc</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0111910	spermatogenic failure						ECO:0000033	author statement supported by traceable reference	PMID:34237282	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278261	Mafb<sup>tm1.2Good</sup>/Mafb<sup>tm1.2Good</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:12557	Duane retraction syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27181683	20190215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810322	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Tg(Atoh1-cre/Esr1*)14Fsh/0  [background:] involves: 129X1/SvJ * FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691547	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723302	Casq2<sup>tm2Jse</sup>/Casq2<sup>tm2Jse</sup>  [background:] Not Specified	is_model_of	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000033	author statement supported by traceable reference	PMID:17607358	20090821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042182	Amhr2<sup>tm1Bhr</sup>/Amhr2<sup>tm1Bhr</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050791	persistent Mullerian duct syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21490063	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449556	Cybb<sup>tm1Din</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:7719350	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402037	Gt(ROSA)26Sor<sup>tm1Sor</sup>/Gt(ROSA)26Sor<sup>tm1Sor</sup> Tg(NPHS2-rtTA2*M2)1Jbk/Tg(NPHS2-rtTA2*M2)1Jbk Tg(tetO-cre)LC1Bjd/Tg(tetO-cre)LC1Bjd  [background:] involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/N	is_model_of	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:31588799	20200329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698359	Tg(MMTV-DMTF1_i2)7Kai/0  [background:] FVB/NJ-Tg(MMTV-DMTF1_i2)7Kai	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25537728	20151208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304756	Col1a1<sup>tm1(tetO-RNAi:Rps19)Karl</sup>/Col1a1<sup>tm1(tetO-RNAi:Rps19)Karl</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:21989989	20120202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672886	Ctns<sup>tm1Antc</sup>/Ctns<sup>tm1Antc</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:1064	cystinosis						ECO:0000033	author statement supported by traceable reference	PMID:12370309	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6401817	Col6a1<sup>tm1Sngi</sup>/Col6a1<sup>tm1Sngi</sup>  [background:] B6.Cg-Col6a1<sup>tm1Sngi</sup>	is_model_of	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28043812	20200327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392034	Hnrnpf<sup>tm1Jsdc</sup>/Hnrnpf<sup>tm1Jsdc</sup> Pax8<sup>tm1.1(cre)Mbu</sup>/Pax8<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9432	renal glycosuria						ECO:0000033	author statement supported by traceable reference	PMID:31673025	20200226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515728	Tyk2<sup>tm1Shmd</sup>/Tyk2<sup>tm1Shmd</sup>  [background:] either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:23217260	20131030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797755	Szt1/Szt1<sup>+</sup> Tg(Eno2-Scn2a1*)Q54Mm/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:16464983	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054668	Eya1<sup>tm1Rilm</sup>/Eya1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:14702	branchiootorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437115	Cep290<sup>b2b1454Clo</sup>/Cep290<sup>b2b1454Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1454Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6690698	Dhcr7<sup>tm1.1Sbpa</sup>/Dhcr7<sup>tm1.1Sbpa</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] B6.Cg-Dhcr7<sup>tm1.1Sbpa</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>	is_model_of	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33410752	20210414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5632308	Nrxn2<sup>tm1Sud</sup>/Nrxn2<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J * C57BL/6NClr	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25423136	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771806	Rpe65<sup>tm1Lrcb</sup>/Rpe65<sup>tm1Lrcb</sup>  [background:] 129S6/SvEvTac-Rpe65<sup>tm1Lrcb</sup>	is_model_of	DOID:0110353	retinitis pigmentosa 20						ECO:0000033	author statement supported by traceable reference	PMID:17933883	20110509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617753	Tg(Camk2a-Bdnf)A9Stl/0  [background:] C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:24768643	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6294898	Nlgn2<sup>tm1.1Gchn</sup>/Nlgn2<sup>tm1.1Gchn</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:29859117	20190429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6378441	Col1a1<sup>tm1(tetO-URI1)Ndj</sup>/Col1a1<sup>+</sup> Tg(Cebpb-tTA)#Bjd/0  [background:] B6.Cg-Col1a1<sup>tm1(tetO-URI1)Ndj</sup> Tg(Cebpb-tTA)#Bjd	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25453901	20191125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842801	Tg(RP23-65I14)1Jno/?  [background:] involves: FVB	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:19211869	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5788426	Tg(TNFSF11)5519Edou/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:24127173	20160810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6343572	Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000033	author statement supported by traceable reference	PMID:30520996	20190815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590207	Col2a1<sup>tm1Prc</sup>/Col2a1<sup>tm1Prc</sup>  [background:] involves: 129	is_model_of	DOID:0080056	achondrogenesis type II						ECO:0000033	author statement supported by traceable reference	PMID:11680679	20070308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804449	Ercc1<sup>tm1Jhjh</sup>/Ercc1<sup>tm1Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:0060590	XFE progeroid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17183314	20080904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911874	Sgcd<sup>tm1Ojml</sup>/Sgcd<sup>+</sup>  [background:] B6.129-Sgcd<sup>tm1Ojml</sup>	is_model_of	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000033	author statement supported by traceable reference	PMID:23695275	20171026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522704	pta/pta  [background:] C57BL/6J-pta	is_model_of	DOID:0110106	atrial heart septal defect 1						ECO:0000033	author statement supported by traceable reference	PMID:15548583	20101008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617910	Sall4<sup>Gt(XE027)Byg</sup>/Sall4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss * C57BL/6	is_model_of	DOID:0060747	Duane-radial ray syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16380715	20060328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6103873	Tg(Myh6-CRYAB*R120G)7302Ijb/0  [background:] involves: C57BL/6	is_model_of	DOID:0080093	myofibrillar myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:17693254	20171220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432226	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:2999	granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531404	Phox2a/Inppl1<sup>tm1Ssch</sup>/Phox2a/Inppl1<sup>tm1Ssch</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11343120	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4365946	Ts(17<sup>16</sup>)65Dn/0  [background:] B6EiC3Sn.BLiA-Ts(17<sup>16</sup>)65Dn/DnJ	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19720087	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305095	Is(14)1Rdf Is(14)5Rdf/Del(14Trim13-Rnaseh2b)6Rdf Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22174151	20120207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441551	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Lejo</sup>/Trp53<sup>tm1Lejo</sup>  [background:] involves: 129	is_model_of	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5586971	Cd46<sup>tm1Atk</sup>/Cd46<sup>tm1Atk</sup>  [background:] B6.129-Cd46<sup>tm1Atk</sup>	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:27295359	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178344	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] Not Specified	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:16576828	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7523314	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>+</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>	is_model_of	DOID:332	amyotrophic lateral sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356633	Rit1<sup>tm1.1Tumg</sup>/Rit1<sup>+</sup>  [background:] B6.Cg-Rit1<sup>tm1.1Tumg</sup>	is_model_of	DOID:0060586	Noonan syndrome 8						ECO:0000033	author statement supported by traceable reference	PMID:30898653	20190822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587945	Gpr143<sup>tm1Inc</sup>/Y  [background:] either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)	is_model_of	DOID:0050633	ocular albinism 1						ECO:0000033	author statement supported by traceable reference	PMID:11092754	20050919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315995	Tg(Myh6-MYL3*E143K)2Dsc/0  [background:] Not Specified	is_model_of	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:28371863	20190704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621491	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>/J	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:6583703	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157968	Tcf4<sup>tm1Hmb</sup>/Tcf4<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29222403	20180524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510311	Tbx1<sup>tm1Dsr</sup>/Tbx1<sup>+</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6101187	Tg(C9orf72)500Lpwr/0  [background:] FVB/NJ-Tg(C9orf72)500Lpwr	is_model_of	DOID:0060213	frontotemporal dementia and/or amyotrophic lateral sclerosis-1						ECO:0000033	author statement supported by traceable reference	PMID:27112499	20171214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3847312	Spast<sup>M1Gri</sup>/Spast<sup>M1Gri</sup>  [background:] B6.C-Spast<sup>M1Gri</sup>	is_model_of	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000033	author statement supported by traceable reference	PMID:19453301	20090609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721541	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Clu<sup>tm1Jakh</sup>/Clu<sup>tm1Jakh</sup> Tg(APPV717F)109Ili/Tg(APPV717F)109Ili  [background:] involves: 129P2/OlaHsd * 129S2/SvPas	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14741101	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5649275	Gt(ROSA)26Sor<sup>tm5(ASPSCR1/TFE3)Mrc</sup>/Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:4239	alveolar soft part sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:25453902	20150819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308013	Tg(ED-L2-IL1RN/IL1B)#Tcw/?  [background:] B6.Cg-Tg(ED-L2-IL1RN/IL1B)#Tcw	is_model_of	DOID:9206	Barrett's esophagus						ECO:0000033	author statement supported by traceable reference	PMID:22264787	20120229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831003	Tg(Neurod2-Smo*A1)199Jols/0  [background:] C57BL/6-Tg(Neurod2-Smo*A1)199Jols	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:15520185	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3691280	Myh6<sup>tm1Ces</sup>/Myh6<sup>tm1Ces</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176762	Nf1<sup>tm1Cbr</sup>/Nf1<sup>tm1Cbr</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:11279521	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3807529	Flvcr1<sup>tm1Jlab</sup>/Flvcr1<sup>tm1Jlab</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:18258918	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324924	Camk2a<sup>em1Rjco</sup>/Camk2a<sup>em1Rjco</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28130356	20190726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722133	Gopc<sup>tm1.1Tno</sup>/Gopc<sup>tm1.1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14227	azoospermia						ECO:0000033	author statement supported by traceable reference	PMID:12149515	20070920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694657	Map6<sup>tm1Job</sup>/Map6<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23002183	20151104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5564982	Tg(KRT14-Il4)#Lsch/0  [background:] involves: BALB/cBy * C57BL/6	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:11676841	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6719084	Nemf<sup>pdft</sup>/Nemf<sup>pdft</sup>  [background:] B6(C3)-Nemf<sup>pdft</sup>/Cx	is_model_of	DOID:440	neuromuscular disease						ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444471	Uqcrfs1<sup>tm1Ctm</sup>/Uqcrfs1<sup>tm1Ctm</sup> Tg(Camk2a-cre)#Szi/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:700	mitochondrial metabolism disease						ECO:0000033	author statement supported by traceable reference	PMID:22914734	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639520	Tg(Myh6-Acsl1)O7Jesc/0  [background:] FVB/N-Tg(Myh6-Acsl1)O7Jesc	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11285300	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799519	Tg(K6ODCtr)55Tgo/0  [background:] C57BL/6-Tg(K6ODCtr)55Tgo/J	is_model_of	DOID:0060689	atrichia with papular lesions						ECO:0000033	author statement supported by traceable reference	PMID:10772389	20080731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821788	Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1						ECO:0000033	author statement supported by traceable reference	PMID:9169515	20100906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444514	Elp1<sup>tm1Id</sup>/Elp1<sup>tm1Id</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22922231	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836356	Urah<sup>plt2</sup>/Urah<sup>plt2</sup>  [background:] C57BL/6-Urah<sup>plt2</sup>	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:30383838	20220415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5560283	Ift140<sup>b2b1283Clo</sup>/Ift140<sup>b2b1283Clo</sup>  [background:] C57BL/6J-Ift140<sup>b2b1283Clo</sup>	is_model_of	DOID:0110097	short-rib thoracic dysplasia 9 with or without polydactyly						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684458	Twist1<sup>Pas</sup>/Twist1<sup>Pas</sup>  [background:] involves: C57BL/6 * PDT/Pas	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14724733	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618826	1700093K21Rik<sup>b2b3025Clo</sup>/1700093K21Rik<sup>b2b3025Clo</sup>  [background:] C57BL/6J-1700093K21Rik<sup>b2b3025Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505901	Rnf168<sup>Gt(405F11)Cmhd</sup>/Rnf168<sup>Gt(405F11)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0090113	RIDDLE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21552324	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2387326	Aifm1<sup>Hq</sup>/Y  [background:] B6CBACa A<sup>w-J</sup>/A-Aifm1<sup>Hq</sup>/J	is_model_of	DOID:0060536	mitochondrial complex I deficiency						ECO:0000033	author statement supported by traceable reference	PMID:18791645	20171031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3768653	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>+</sup> Tg(Tyr-NRAS*Q61K)1Bee/?  [background:] involves: 129/Sv * C57BL/6 * DBA/2 * SJL	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:15899789	20200710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577712	Myd88<sup>tm1Aki</sup>/Myd88<sup>tm1Aki</sup>  [background:] B6.129P2-Myd88<sup>tm1Aki</sup>	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603003	Gck<sup>tm1.1Mgn</sup>/Gck<sup>tm1.1Mgn</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278015	Tg(Actb-Ptma)T12Clwu/Tg(Actb-Ptma)T12Clwu  [background:] involves: FVB/N	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:23695700	20190213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6195005	Col17a1<sup>tm1.1(COL17A1)Zliu</sup>/Col17a1<sup>tm1.1(COL17A1)Zliu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:8506	bullous pemphigoid						ECO:0000033	author statement supported by traceable reference	PMID:18922680	20180820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775312	Cc2d2a<sup>tm1Asw</sup>/Cc2d2a<sup>tm1Asw</sup>  [background:] Not Specified	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24947469	20160608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7282200	Gas2<sup>tm1a(EUCOMM)Hmgu</sup>/Gas2<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Gas2<sup>tm1a(EUCOMM)Hmgu</sup>	is_model_of	DOID:10003	sensorineural hearing loss						ECO:0000033	author statement supported by traceable reference	PMID:33964205	20220606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623997	H2-Ab1<sup>b-tm1Gru</sup>/H2-Ab1<sup>b-tm1Gru</sup> Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell/Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell  [background:] NOD.Cg-H2-Ab1<sup>b-tm1Gru</sup> Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:14570980	20171026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6378447	Col1a1<sup>tm1(tetO-URI1)Ndj</sup>/Col1a1<sup>tm1(tetO-URI1)Ndj</sup> Tg(Cebpb-tTA)#Bjd/0  [background:] B6.Cg-Col1a1<sup>tm1(tetO-URI1)Ndj</sup> Tg(Cebpb-tTA)#Bjd	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25453901	20191125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819097	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup> Nodal<sup>tm1Rob</sup>/Nodal<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:4621	holoprosencephaly						ECO:0000033	author statement supported by traceable reference	PMID:20508035	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578522	Tg(TG-NRAS*Q61K)#Msnt/0  [background:] Not Specified	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16785999	20140826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588732	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] AK.B6(Cg)-Cln8<sup>mnd</sup>	is_model_of	DOID:0110723	neuronal ceroid lipofuscinosis 8						ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680393	Gba1<sup>tm2Ggb</sup>/Gba1<sup>tm2Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639130	H2-Ab1<sup>b-tm1Gru</sup>/H2-Ab1<sup>b-tm1Gru</sup> Tg(HLA-DRB1)31Dmz/0 Tg(Ins2-CD80)3B7Flv/0  [background:] involves: 129S2/SvPas * C57BL/6 * CBA * SJL	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11285306	20060727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657109	Mip<sup>Cat-Tohm</sup>/Mip<sup>Cat-Tohm</sup>  [background:] involves: DDI	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:12676560	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911876	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] B6.129-Sgcd<sup>tm1Mcn</sup>/J	is_model_of	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000033	author statement supported by traceable reference	PMID:23695275	20171026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559052	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:1907	malignant fibrous histiocytoma						ECO:0000033	author statement supported by traceable reference	PMID:19956606	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509439	Bmp7<sup>tm1.1Dgra</sup>/Bmp7<sup>tm1.1Dgra</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * CBA/J	is_model_of	DOID:0050848	obstructive sleep apnea						ECO:0000033	author statement supported by traceable reference	PMID:33431521	20210310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274721	Tg(Emu-TXLNA)1Amjr/0  [background:] B6.Cg-Tg(Emu-TXLNA)1Amjr	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19038581	20190125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175702	Apo/Apo<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677768	Vhl<sup>tm1.1Lss</sup>/Vhl<sup>+</sup>  [background:] involves: A/J	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:14500363	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678410	Runx2<sup>tm1Kish</sup>/Runx2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:20375239	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622101	Ldlr<sup>Hlb301</sup>/Ldlr<sup>Hlb301</sup>  [background:] C57BL/6J-Ldlr<sup>Hlb301</sup>/J	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	MGI:2656149	20120221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175802	Cryba1<sup>Po1</sup>/Cryba1<sup>+</sup>  [background:] C3HeB/FeJ-Cryba1<sup>Po1</sup>	is_model_of	DOID:0110258	cataract 10 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:10585769	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699203	Sall4<sup>tm1Ryn</sup>/Sall4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060747	Duane-radial ray syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16790473	20070308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259995	Col10a1<sup>tm2.1Rpbh</sup>/Col10a1<sup>tm2.1Rpbh</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0080021	Schmid metaphyseal chondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30010889	20181213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822915	Tg(Ly6a-SET/NUP214)2969Gcg/0  [background:] involves: FVB/NJ	is_model_of	DOID:12603	acute leukemia						ECO:0000033	author statement supported by traceable reference	PMID:17569777	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796531	Kcnk3<sup>tm1.1Daba</sup>/Kcnk3<sup>tm1.1Daba</sup> Kcnk9<sup>tm1.1Daba</sup>/Kcnk9<sup>tm1.1Daba</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:18250325	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719582	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12382103	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907042	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19850880	20170816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5922030	Aipl1<sup>tvrm119</sup>/Aipl1<sup>tvrm119</sup>  [background:] C57BL/6J-Aipl1<sup>tvrm119</sup>/Pjn	is_model_of	DOID:0110332	Leber congenital amaurosis 4						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698146	Bgn<sup>tm1Mfy</sup>/Y Fmod<sup>tm1Aol</sup>/Fmod<sup>tm1Aol</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:16006154	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698146	Bgn<sup>tm1Mfy</sup>/Y Fmod<sup>tm1Aol</sup>/Fmod<sup>tm1Aol</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:16612079	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4455028	Rho<sup>Tvrm1</sup>/Rho<sup>+</sup> Rpe65<sup>rd12</sup>/Rpe65<sup>rd12</sup>  [background:] B6.Cg-Rpe65<sup>rd12</sup> Rho<sup>Tvrm1</sup>	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:20207741	20100616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7380585	Slc7a7<sup>em1Lbu</sup>/Slc7a7<sup>em1Lbu</sup>  [background:] involves: 129/SvEv * C57BL/6	is_model_of	DOID:0060439	lysinuric protein intolerance						ECO:0000033	author statement supported by traceable reference	PMID:32504080	20221109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6514801	Prickle3<sup>em1Mxg</sup>/Prickle3<sup>em1Mxg</sup>  [background:] C57BL/6JSlacc-Prickle3<sup>em1Mxg</sup>	is_model_of	DOID:0111754	Leber plus disease						ECO:0000033	author statement supported by traceable reference	PMID:32516135	20210402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6506468	Gt(ROSA)26Sor<sup>tm1.1(Alb-PCSK9)Mby</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:30646909	20210216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611043	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:21690266	20111104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576038	hpld/hpld  [background:] Not Specified	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:11818962	20050912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516348	Hspd1<sup>Gt(OST171441)Lex</sup>/Hspd1<sup>+</sup>  [background:] B6.129S5-Hspd1<sup>Gt(OST171441)Lex</sup>	is_model_of	DOID:0110766	hereditary spastic paraplegia 13						ECO:0000033	author statement supported by traceable reference	PMID:23466696	20131106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5797530	Cibar1<sup>tm1b(KOMP)Wtsi</sup>/Cibar1<sup>tm1b(KOMP)Wtsi</sup>  [background:] C57BL/6N-Cibar1<sup>tm1b(KOMP)Wtsi</sup>/Wtsi	is_model_of	DOID:1148	polydactyly						ECO:0000033	author statement supported by traceable reference	PMID:30395363	20190523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6281662	Hdac3<sup>tm1.1Eno</sup>/Hdac3<sup>tm1.1Eno</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:289	endometriosis						ECO:0000033	author statement supported by traceable reference	PMID:30626716	20190308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5556062	Fkrp<sup>tm1Scbr</sup>/Fkrp<sup>tm1Scbr</sup> Sox1<sup>tm1(cre)Take</sup>/Sox1<sup>+</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:24234655	20140408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680504	Gba1<sup>tm3Ggb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910334	Tg(Myh6-LDB3*S196L)93Mva/0  [background:] involves: C57BL/6J	is_model_of	DOID:0110423	dilated cardiomyopathy 1C						ECO:0000033	author statement supported by traceable reference	PMID:20852297	20170926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305276	Col8a2<sup>tm1.1Asj</sup>/Col8a2<sup>tm1.1Asj</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA	is_model_of	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22002996	20120209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014212	Tg(Gfap-rtTA,tetO-MAOB,-lacZ)1Jkan/0  [background:] involves: C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:18286173	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6376303	Gna11<sup>em1Mman</sup>/Gna11<sup>+</sup>  [background:] C57BL/6NCrl-Gna11<sup>em1Mman</sup>	is_model_of	DOID:0090108	autosomal dominant hypocalcemia 2						ECO:0000033	author statement supported by traceable reference	PMID:28194446	20191112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175019	Tnfrsf1a<sup>tm1Imx</sup>/Tnfrsf1a<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0090018	autosomal dominant familial periodic fever						ECO:0000033	author statement supported by traceable reference	PMID:9551933	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6102946	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:24312398	20171219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583557	Tg(ITGA5)0858Fmw/0 Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604139	Smad4<sup>tm2.1Cxd</sup>/Smad4<sup>tm2.1Cxd</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * CD-1	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:24006258	20170531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648026	b2b3077Clo/b2b3077Clo  [background:] C57BL/6J-b2b3077Clo	is_model_of	DOID:0060254	Robinow syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589409	Alms1<sup>Gt(XH152)Byg</sup>/Alms1<sup>Gt(XH152)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050473	Alstrom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16000322	20051012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718515	Tg(APP)8.9Btla/Tg(APP)8.9Btla  [background:] involves: 129S2/SvPas	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15016076	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662570	Chat<sup>tm1Fhg</sup>/Chat<sup>tm1Fhg</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110671	congenital myasthenic syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:12533614	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5518769	Mybl2<sup>tm1.1Jof</sup>/Mybl2<sup>+</sup> Tg(Zp3-cre)3Mrt/0  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22910183	20131120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174802	Vhl<sup>tm1.1Jae</sup>/Vhl<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:11171994	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412016	Hbb<sup>d3th</sup>/Hbb<sup>+</sup> Tg(HBB-AR-HBA2,-HBB*)58Rub/0 Tg(LCR-HBA2,LCR-HBB)11Cos/0  [background:] involves: FVB/N * Swiss Webster	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:7662990	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5293614	Gbe1<sup>tm1.1Hoa</sup>/Gbe1<sup>tm1.1Hoa</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:2750	glycogen storage disease IV						ECO:0000033	author statement supported by traceable reference	PMID:21856731	20111027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5771805	Smarcb1<sup>tm2Sho</sup>/Smarcb1<sup>tm2Sho</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(GFAP-cre)#Gtm/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:3620	central nervous system cancer						ECO:0000033	author statement supported by traceable reference	PMID:26363008	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4420395	Scn4a<sup>tm1Ljh</sup>/Scn4a<sup>+</sup>  [background:] B6.129S4-Scn4a<sup>tm1Ljh</sup>	is_model_of	DOID:14451	hyperkalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7444385	Dnajb4<sup>em2Sngi</sup>/Dnajb4<sup>em2Sngi</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:36512060	20230315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7332935	Tg(KRT14-Shh)#Cobm/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19394325	20220830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451320	Aldh1a2<sup>tm1Dll</sup>/Aldh1a2<sup>tm1Ipc</sup>  [background:] involves: CD-1	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12563036	20060713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842820	H2<sup>b</sup>/H2<sup>g7</sup> Tg(TcraR28,TcrbR28)KRNDim/0  [background:] involves: C57BL/6 * NOD * SJL	is_model_of	DOID:61	mitral valve disease						ECO:0000033	author statement supported by traceable reference	PMID:29386201	20220603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6277933	Lama3<sup>tm1Arte</sup>/Lama3<sup>tm1Arte</sup> Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: C57BL/6 * CD-1	is_model_of	DOID:3209	junctional epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:27729280	20190212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6448986	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9279	hyperhomocysteinemia						ECO:0000033	author statement supported by traceable reference	PMID:15622513	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6314222	Atp1a2<sup>tm1.1Tmklh</sup>/Atp1a2<sup>+</sup>  [background:] B6.129S1(Cg)-Atp1a2<sup>tm1.1Tmklh</sup>	is_model_of	DOID:0111182	familial hemiplegic migraine 2						ECO:0000033	author statement supported by traceable reference	PMID:26911348	20210810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6514898	Nexn<sup>tm1.1Chen</sup>/Nexn<sup>tm1.1Chen</sup>  [background:] Not Specified	is_model_of	DOID:0110424	dilated cardiomyopathy 1CC						ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582253	Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] B6;129-Hbb-b1<sup>tm1Unc</sup> Hbb-b2<sup>tm1Unc</sup>/J	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:24880340	20140911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625870	Kcna1<sup>tm1Tem</sup>/Kcna1<sup>tm1Tem</sup>  [background:] C3Fe.129S7-Kcna1<sup>tm1Tem</sup>	is_model_of	DOID:3328	temporal lobe epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:24270080	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473901	Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050787	juvenile polyposis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22773757	20130411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6725725	Hes7<sup>M1Btlr</sup>/Hes7<sup>+</sup>  [background:] C57BL/6J-Hes7<sup>M1Btlr</sup>	is_model_of	DOID:0050568	spondylocostal dysostosis						ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6155603	Magt1<sup>Gt(IST13422E1)Tigm</sup>/Y  [background:] involves: C57BL/6N	is_model_of	DOID:612	primary immunodeficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:29581357	20180510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified	is_model_of	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000033	author statement supported by traceable reference	PMID:10574770	20210927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259566	Cdk4<sup>tm1.1Bbd</sup>/Cdk4<sup>tm1.1Bbd</sup> Tg(Mt1-Hgf)#Lmb/0  [background:] B6.Cg-Cdk4<sup>tm1.1Bbd</sup> Tg(Mt1-Hgf)#Lmb	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:16877364	20181207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868118	Myb<sup>boo</sup>/Myb<sup>boo</sup>  [background:] involves: C57BL/6	is_model_of	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:20610815	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448405	Tg(Col11a2-Npr2*)28Keoz/0  [background:] involves: C57BL/6	is_model_of	DOID:0080006	bone development disease						ECO:0000033	author statement supported by traceable reference	PMID:22870295	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174727	Hps5<sup>ru2-mr</sup>/Hps5<sup>ru2-mr</sup>  [background:] Not Specified	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584455	Gt(ROSA)26Sor<sup>tm1(HD*103Q)Xwy</sup>/? Tg(Nes-cre)1Kln/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15882643	20050826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623997	H2-Ab1<sup>b-tm1Gru</sup>/H2-Ab1<sup>b-tm1Gru</sup> Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell/Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell  [background:] NOD.Cg-H2-Ab1<sup>b-tm1Gru</sup> Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell	is_model_of	DOID:820	myocarditis						ECO:0000033	author statement supported by traceable reference	PMID:14570980	20170731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699094	Sh3bp2<sup>tm1Bjro</sup>/Sh3bp2<sup>tm1Bjro</sup>  [background:] involves: 129S4/SvJae * BALB/cJ * C57BL/6J	is_model_of	DOID:1856	cherubism						ECO:0000033	author statement supported by traceable reference	PMID:17218256	20070307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4457194	Slc12a1<sup>urehr3</sup>/Slc12a1<sup>urehr3</sup>  [background:] involves: C3HeB/FeJ	is_model_of	DOID:0110142	Bartter disease type 1						ECO:0000033	author statement supported by traceable reference	PMID:20219826	20100630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5704363	Dicer1<sup>tm1Tara</sup>/Dicer1<sup>tm1Tara</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22331912	20160122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638792	Tg(Ddx4-cre)1Dcas/0 Tg(EIF1AX-Lin28a)#Gqda/0  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1 * FVB/N	is_model_of	DOID:2154	nephroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24732380	20150609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175801	Cryba1<sup>Po1</sup>/Cryba1<sup>Po1</sup>  [background:] C3HeB/FeJ-Cryba1<sup>Po1</sup>	is_model_of	DOID:0110258	cataract 10 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:10585769	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5006981	Tg(Mov1/Tyr)OVE876BPay/Y  [background:] FVB/N-Tg(Mov1/Tyr)OVE876BPay	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21093492	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507888	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Igs2<sup>tm1(CAG-Met)Zsu</sup>/Igs2<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:31819003	20210225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5511052	Postn<sup>tm1Sjc</sup>/Postn<sup>tm1Sjc</sup>  [background:] B6.Cg-Postn<sup>tm1Sjc</sup>	is_model_of	DOID:0080010	bone structure disease						ECO:0000033	author statement supported by traceable reference	PMID:23505553	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507151	Tuba1a<sup>em1Rstot</sup>/Tuba1a<sup>em1Rstot</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:2490	congenital nervous system abnormality						ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276669	Tg(Mpz)88.2Mfel/0  [background:] FVB/N-Tg(Mpz)88.2Mfel	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:11086005	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718057	Dp(16Cbr1-Fam3b)1Rhr/0  [background:] B6.129S6-Dp(16Cbr1-Fam3b)1Rhr	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28069794	20180201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361456	Thbs1<sup>tm1Hyn</sup>/Thbs1<sup>tm1Hyn</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19700744	20091014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272874	Nmnat1<sup>tm1Ruch</sup>/Nmnat1<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6J * C57BL/6N	is_model_of	DOID:0110005	Leber congenital amaurosis 9						ECO:0000033	author statement supported by traceable reference	PMID:29674119	20190110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906294	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup> Pcdha9<sup>b2b635.1Clo</sup>	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578629	Tg(CMV-IgkvaD11)BCat/Tg(CMV-IgkvaD11)BCat  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20182028	20140828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799268	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] C3.MRL-Fas<sup>lpr</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1565490	20080729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905194	Tg(Myh6-Des*)641Rbns/0  [background:] involves: FVB/N	is_model_of	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:11352891	20170720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710359	Serpina6<sup>tm1Tew</sup>/Serpina6<sup>tm1Tew</sup>  [background:] involves: 129/SvEmcTer * C57BL/6N	is_model_of	DOID:0090030	corticosteroid-binding globulin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16980625	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5466506	Zdhhc13<sup>Gt(AC0492)Wtsi</sup>/Zdhhc13<sup>Gt(AC0492)Wtsi</sup>  [background:] FVB.129P2-Zdhhc13<sup>Gt(AC0492)Wtsi</sup>	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23077216	20130227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844061	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Gcg-cre)1Slib/0  [background:] either: (involves: 129X1/SvJ * A/J) or (involves: 129X1/SvJ * C57BL/6)	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:19340311	20090514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437872	Cyp2g1<sup>tm1(rtTA)Lane</sup>/Cyp2g1<sup>+</sup> Tg(SFTPC-rtTA,tetO-Tnf)320-1Gwho/0  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:0050127	sinusitis						ECO:0000033	author statement supported by traceable reference	PMID:20147558	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038416	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110414	retinitis pigmentosa 3						ECO:0000033	author statement supported by traceable reference	PMID:10725384	20090720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710341	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:21199796	20110306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273246	Ubiad1<sup>em1Wwk</sup>/Ubiad1<sup>em1Wwk</sup>  [background:] C57BL/6N-Ubiad1<sup>em1Wwk</sup>	is_model_of	DOID:0060456	Schnyder corneal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:29977031	20190111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907293	Tg(Myh6-Cryab*R120G)708Rbns/0  [background:] FVB/N-Tg(Myh6-Cryab*R120G)708Rbns	is_model_of	DOID:0080093	myofibrillar myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:11440982	20170823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6241552	Adam17<sup>tm1.2Bbl</sup>/Adam17<sup>tm1.2Bbl</sup> Sox9<sup>tm3(cre)Crm</sup>/Sox9<sup>+</sup>  [background:] B6.129(SJL)-Sox9<sup>tm3(cre)Crm</sup> Adam17<sup>tm1.2Bbl</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:25902485	20181112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6241436	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>tm1.1Ece</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:0080143	congenital fibrosis of the extraocular muscles						ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907999	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: FVB	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:21195081	20170901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836915	Sord<sup>C57BL/Lia</sup>/Sord<sup>C57BL/Lia</sup>  [background:] involves: C57BL/LiA	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:18760274	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759051	Matn3<sup>tm1Mbri</sup>/Matn3<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0070299	multiple epiphyseal dysplasia 5						ECO:0000033	author statement supported by traceable reference	PMID:17517694	20190807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588579	Hjv<sup>tm1Arbr</sup>/Hjv<sup>tm1Arbr</sup>  [background:] involves: 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:0111027	hemochromatosis type 2A						ECO:0000033	author statement supported by traceable reference	PMID:16075058	20050929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6416462	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:28230213	20200514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3662655	Ush1g<sup>js-2J</sup>/Ush1g<sup>js-2J</sup>  [background:] B6(Cg)-Ush1g<sup>js-2J</sup>/J	is_model_of	DOID:0110834	Usher syndrome type 1G						ECO:0000033	author statement supported by traceable reference	MGI:3662705	20120606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6195853	Arx<sup>tm1.1Ics</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:29659809	20180829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838963	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-DISC1*)1001Plet/0  [background:] involves: C57BL/6 * CBA * SJL	is_model_of	DOID:0070085	schizophrenia 9						ECO:0000033	author statement supported by traceable reference	PMID:17848917	20190410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811870	Omp<sup>tm1(tTA)Gogo</sup>/Omp<sup>+</sup> Tg(tetO-APPSwInd)Dbo/0  [background:] involves: 129 * C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23884929	20161214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507051	Hexb<sup>lysd</sup>/Hexb<sup>lysd</sup>  [background:] B6.Cg-Hexb<sup>lysd</sup>/J	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:31547903	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7564087	None [background:] SKG/Jcl	is_model_of	DOID:1123	spondyloarthropathy						ECO:0000033	author statement supported by traceable reference	PMID:37907743	20231206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6460345	Akt1<sup>tm1Mjl</sup>/Akt1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	is_model_of	DOID:13482	Proteus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31194862	20201008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6386243	Fscn2<sup>em1Fhan</sup>/Fscn2<sup>em1Fhan</sup>  [background:] C57BL/6J-Fscn2<sup>em1Fhan</sup>	is_model_of	DOID:8466	retinal degeneration						ECO:0000033	author statement supported by traceable reference	PMID:30082328	20200124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3803013	Mta2<sup>tm1.1Yzha</sup>/Mta2<sup>tm1.1Yzha</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:18353770	20080915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286393	Slc25a46<sup>atc</sup>/Slc25a46<sup>atc</sup>  [background:] B6.Cg-Slc25a46<sup>atc</sup>	is_model_of	DOID:0080068	Charcot-Marie-Tooth disease type 6						ECO:0000033	author statement supported by traceable reference	PMID:28376086	20190408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361591	Tg(ACTB-TNFRSF6B)754Jwu/?  [background:] B6.Cg-Tg(Actb-TNFRSF6B)754Jwu	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:17968950	20091016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154327	Scn1a<sup>tm1.1Kzy</sup>/Scn1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29329111	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695610	Satb2<sup>tm1(cre)Vit</sup>/Satb2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110213	isolated cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:16960803	20070205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767400	Tg(HCRT-MJD)1Stak/?  [background:] involves: C57BL/6 * DBA/1	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:11394998	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4354215	Casq2<sup>tm1.1Sgp</sup>/Casq2<sup>tm1.1Sgp</sup>  [background:] involves: 129X1/SvJ * C57BL/6NCrL	is_model_of	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000033	author statement supported by traceable reference	PMID:18583715	20090821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911349	Tg(Myh6-tTA)6Smbf/0 Tg(tetO-TPR/MET,-EGFP)12Tcre/0  [background:] FVB.Cg-Tg(Myh6-tTA)6Smbf Tg(tetO-TPR/MET,-EGFP)12Tcre	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:27298830	20171012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836175	Rho<sup>tm2(RHO/GFP)Jhw</sup>/Rho<sup>tm2(RHO/GFP)Jhw</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:16979686	20130619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836291	Lgmn<sup>tm1Ihn</sup>/Lgmn<sup>tm1Ihn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:75	lymphatic system disease						ECO:0000033	author statement supported by traceable reference	PMID:19106291	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432018	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup> Tg(Ly6e-MALT1)#Isg/0  [background:] involves: 129S2/SvPas * C57BL/6 * CBA	is_model_of	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22689981	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909329	Tg(Myh6-Tnni3*R146G)133Rbns/0  [background:] Not Specified	is_model_of	DOID:0110313	hypertrophic cardiomyopathy 7						ECO:0000033	author statement supported by traceable reference	PMID:11055985	20170918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6754175	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719611	Tg(Myh6-Tnnt2)191Lnwd/0  [background:] involves: C57BL/6	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:9637714	20100521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688418	Gba1<sup>tm1Karl</sup>/Gba1<sup>tm1.1Karl</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:16954197	20061121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838165	Tg(ATXN3*)67.2Cce/0 Tg(ATXN3*)84.2Cce/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:11978767	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705749	Tg(OPTN*E50K,-EGFP)1Mde/0  [background:] involves: C57BL/6 * C57BL/6N * SJL	is_model_of	DOID:1070	primary open angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:25818176	20160128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696777	Afg3l2<sup>Emv66</sup>/Afg3l2<sup>+</sup>  [background:] involves: MEV/2Ty	is_model_of	DOID:0050977	spinocerebellar ataxia type 28						ECO:0000033	author statement supported by traceable reference	PMID:19625515	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315197	Tg(Vav1-Asxl1*Y588X)#Fcy/0  [background:] C57BL/6-Tg(Vav1-Asxl1*Y588X)#Fcy	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29113963	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903775	Tg(H2-Ea-HA)HACIIAjca/0 Tg(TcraS106-1,TcrbS106-1)TS1SWAjca/0  [background:] C.Cg-Tg(H2-Ea-HA)HACIIAjca Tg(TcraS106-1,TcrbS106-1)TS1SWAjca	is_model_of	DOID:848	arthritis						ECO:0000033	author statement supported by traceable reference	PMID:24591372	20170703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586490	Slc2a4<sup>tm1Mch</sup>/Slc2a4<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * CD-1 * SJL	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9334720	20050901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313515	Mmp21<sup>b2b873Clo</sup>/Mmp21<sup>b2b873Clo</sup>  [background:] C57BL/6J-Mmp21<sup>b2b873Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664549	Pafah1b1<sup>tm1Or</sup>/Pafah1b1<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:11344260	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028000	Pde6b<sup>atrd1</sup>/Pde6b<sup>atrd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6438116	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>tm3.2Cmpl</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>	is_model_of	DOID:0080354	Phelan-McDermid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5645990	Cdk4<sup>tm1.1Bbd</sup>/Cdk4<sup>tm1.1Bbd</sup> Tg(Tyr-NRAS*Q61K)1Bee/0  [background:] FVB.Cg-Cdk4<sup>tm1.1Bbd</sup> Tg(Tyr-NRAS*Q61K)1Bee	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:20718941	20150804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712576	Umod<sup>urehr4</sup>/Umod<sup>urehr4</sup>  [background:] C3HeB/FeJ-Umod<sup>urehr4</sup>	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:19692485	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386344	Mfrp<sup>rd6</sup>/Mfrp<sup>rd6</sup>  [background:] B6.C3-Mfrp<sup>rd6</sup>	is_model_of	DOID:11105	fundus albipunctatus						ECO:0000033	author statement supported by traceable reference	PMID:10967077	20050510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336104	Sdccag8<sup>em1Lji</sup>/Sdccag8<sup>em1Lji</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110138	Bardet-Biedl syndrome 16						ECO:0000033	author statement supported by traceable reference	PMID:35503560	20220914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356528	Mitf<sup>Mi-Or</sup>/Mitf<sup>Mi-Or</sup>  [background:] involves: 101/Rl * C3H/Rl	is_model_of	DOID:13533	osteopetrosis						ECO:0000033	author statement supported by traceable reference	PMID:7495310	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906377	Ptger4<sup>tm1.1Matb</sup>/Ptger4<sup>tm1.1Matb</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20008274	20170809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044676	Gamt<sup>tm1Isb</sup>/Gamt<sup>tm1Isb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050799	guanidinoacetate methyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:15028668	20090512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579384	Fcer1g<sup>tm1Rav</sup>/Fcer1g<sup>tm1Rav</sup> Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:14722612	20050613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805043	a/a Hps6<sup>ru</sup>/Hps6<sup>ru</sup>  [background:] B6.Cg-Hps6<sup>ru</sup>	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663041	Tg(Ins2-Fas*I246N)1Ach/0 Tg(Ins2-Fasl)24Ach/0  [background:] NOD-Tg(Ins2-Fas*I246N)1Ach Tg(Ins2-Fasl)24Ach	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12525697	20061006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442137	b2b1714Clo/b2b1714Clo  [background:] C57BL/6J-b2b1714Clo	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR	is_model_of	DOID:1123	spondyloarthropathy						ECO:0000033	author statement supported by traceable reference	PMID:7344126	20060731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7260274	sar/sar  [background:] BTBR-sar	is_model_of	DOID:0112307	sarcosinemia						ECO:0000033	author statement supported by traceable reference	PMID:1372986	20220411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717461	Jag1<sup>Mhdahtu</sup>/Jag1<sup>+</sup>  [background:] C3HeB/FeJ-Jag1<sup>Mhdahtu</sup>	is_model_of	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11259677	20070807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6150431	Zfp106<sup>tm1b(KOMP)Wtsi</sup>/Zfp106<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:332	amyotrophic lateral sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:28072389	20180411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6721006	Wdr45<sup>em1Wrst</sup>/Y  [background:] involves: C57BL/6N * FVB	is_model_of	DOID:0110739	neurodegeneration with brain iron accumulation 5						ECO:0000033	author statement supported by traceable reference	PMID:34043061	20210714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301598	Tg(H2-L-IL6)46Kish/Tg(H2-L-IL6)46Kish  [background:] C.B6-Tg(H2-L-IL6)46Kish	is_model_of	DOID:9120	amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:19149411	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7495510	Slc12a3<sup>em3Gpt</sup>/Slc12a3<sup>em4Gpt</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36370249	20230704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192631	Tg(Erbb2*)#Maed/0 Tg(Foxa3-cre)1Khk/0  [background:] involves: C57BL/6 * C57BL/6J * DBA	is_model_of	DOID:0060072	benign neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:29670173	20180803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>	is_model_of	DOID:0110598	primary ciliary dyskinesia 14						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275174	Gt(ROSA)26Sor<sup>tm1(SPOP*F133V)Mrbn</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm2.1Ppp</sup>/Pten<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28292441	20190130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710237	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266261	Mecp2<sup>tm1Nlnd</sup>/Y  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648030	b2b3077.2Clo/b2b3077.2Clo  [background:] C57BL/6J-b2b3077.2Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771317	Tg(Thy1-MAPT*P301L)2Vln/Tg(Thy1-MAPT*P301L)2Vln  [background:] FVB/N-Tg(Thy1-MAPT*P301L)2Vln	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15509565	20080220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843211	Dclre1c<sup>tm1Jsek</sup>/Dclre1c<sup>tm1Jsek</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation						ECO:0000033	author statement supported by traceable reference	PMID:19349461	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615592	Muc2<sup>wnn</sup>/Muc2<sup>wnn</sup>  [background:] C57BL/6-Muc2<sup>wnn</sup>	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18318598	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579026	Mc4r<sup>tm1Dhu</sup>/Mc4r<sup>tm1Dhu</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:9019399	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6488227	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	is_model_of	DOID:0050425	restless legs syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32446853	20201223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6766538	Notch2<sup>tm1.1Hhtg</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:2736	Hajdu-Cheney syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28856714	20211012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162647	Slc19a3<sup>tm1.1Nwak</sup>/Slc19a3<sup>tm1.1Nwak</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050659	biotin-responsive basal ganglia disease						ECO:0000033	author statement supported by traceable reference	PMID:28665968	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574845	Dsp<sup>rul</sup>/Dsp<sup>rul</sup>  [background:] RB156Bnr/Ei-Dsp<sup>rul</sup>/GrsrJ	is_model_of	DOID:0090128	Carvajal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25659760	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7439142	Iigp1c<sup>M1Btlr</sup>/Iigp1c<sup>M1Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>M1Btlr</sup>	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359481	Npc1<sup>tm1Tacf</sup>/Npc1<sup>tm2Tacf</sup>  [background:] B6(Cg)-Npc1<sup>tm1Tacf</sup> Npc1<sup>tm2Tacf</sup>	is_model_of	DOID:0070113	Niemann-Pick disease type C1						ECO:0000033	author statement supported by traceable reference	PMID:28167839	20190911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4353223	Arx<sup>tm1.1Jno</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:19587282	20090817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911876	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] B6.129-Sgcd<sup>tm1Mcn</sup>/J	is_model_of	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:28797108	20220517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175114	Mip<sup>Hfi</sup>/Mip<sup>Hfi</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:62456	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6681929	Pmfbp1<sup>em#Jfw</sup>/Pmfbp1<sup>em#Jfw</sup>  [background:] Not Specified	is_model_of	DOID:0111922	spermatogenic failure 31						ECO:0000033	author statement supported by traceable reference	PMID:30298696	20210408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256432	Nlrp3<sup>tm1Bhk</sup>/Nlrp3<sup>tm1Bhk</sup>  [background:] B6.129S6-Nlrp3<sup>tm1Bhk</sup>/J	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:28939830	20190117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6376290	Gna11<sup>em1Mman</sup>/Gna11<sup>em1Mman</sup>  [background:] C57BL/6NCrl-Gna11<sup>em1Mman</sup>	is_model_of	DOID:0090108	autosomal dominant hypocalcemia 2						ECO:0000033	author statement supported by traceable reference	PMID:28194446	20191112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6370045	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] B6.129S7-Bbs4<sup>Gt1Nk</sup>	is_model_of	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:31479441	20191107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6099056	Tg(Th-SNCA)5Eric/0  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:15009131	20171211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4882107	Sost<sup>tm1(KOMP)Vlcg</sup>/Sost<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0080036	SOST-related sclerosing bone dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:22886088	20121119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907122	Prox1<sup>tm2Gco</sup>/Prox1<sup>tm2Gco</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:24938781	20170816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543899	Tgfbr2<sup>tm1.1Hcd</sup>/Tgfbr2<sup>+</sup>  [background:] 129S6(Cg)-Tgfbr2<sup>tm1.1Hcd</sup>	is_model_of	DOID:0050466	Loeys-Dietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24355923	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614637	Agrn<sup>nmf380</sup>/Agrn<sup>nmf380</sup>  [background:] C57BL/6J-Agrn<sup>nmf380</sup>/J	is_model_of	DOID:0110657	congenital myasthenic syndrome 8						ECO:0000033	author statement supported by traceable reference	PMID:21890498	20150511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641710	Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:13223	uterine fibroid						ECO:0000033	author statement supported by traceable reference	PMID:23820898	20150624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517709	Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Nkx2-1-cre)2Sand/0  [background:] B6.Cg-Pten<sup>tm1Hwu</sup> Tg(Nkx2-1-cre)2Sand	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22167068	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806128	Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>/Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * C57BL/6NTac	is_model_of	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:27491071	20161103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679085	Rabggta<sup>gm</sup>/Rabggta<sup>gm</sup>  [background:] C57BL/6J-Rabggta<sup>gm</sup>	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	MGI:61612	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679085	Rabggta<sup>gm</sup>/Rabggta<sup>gm</sup>  [background:] C57BL/6J-Rabggta<sup>gm</sup>	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8490171	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582492	E2f4<sup>tm1Lees</sup>/E2f4<sup>tm1Lees</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:10983976	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825466	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Nes-cre/ERT2,-ALPP)1Sbk/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:27815386	20170302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277684	Eef1a2<sup>em#Abb</sup>/Eef1a2<sup>+</sup>  [background:] C57BL/6JCrl-Eef1a2<sup>em#Abb</sup>	is_model_of	DOID:0070068	autosomal dominant intellectual developmental disorder 38						ECO:0000033	author statement supported by traceable reference	PMID:32160274	20220513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043597	Ercc5<sup>tm3Shm</sup>/Ercc5<sup>tm3Shm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110849	xeroderma pigmentosum group G						ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818175	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17881658	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755137	Dp(7Herc2-Mkrn3)1Taku/0  [background:] B6J.129S7-Dp(7Herc2-Mkrn3)1Taku	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25418414	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402419	Kcnh6<sup>em2Jkya</sup>/Kcnh6<sup>em2Jkya</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:4194	glucose metabolism disease						ECO:0000033	author statement supported by traceable reference	PMID:30590050	20200401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867887	Itm2b<sup>tm1.1Ldad</sup>/Itm2b<sup>tm1.1Ldad</sup>  [background:] involves: 129	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21048150	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6389016	Abcc9<sup>em1Nich</sup>/Abcc9<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6102909	Fbxo11<sup>Jf</sup>/Fbxo11<sup>+</sup>  [background:] involves: BALB/cAnNCrl	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:20057387	20171218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176416	Ppt2<sup>tm1Hof</sup>/Ppt2<sup>tm1Hof</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000033	author statement supported by traceable reference	PMID:11717424	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576171	Tg(Myh6-TNNT2*R141W)#Lian/0  [background:] involves: C57BL/6J	is_model_of	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:18606313	20140805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655554	Fah<sup>2R</sup>/Fah<sup>2R</sup>  [background:] involves: BALB/cRl	is_model_of	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:11209059	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295642	Gata1<sup>tm1Mym</sup>/Y Tg(Gata1*V205G)1Mym/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:1588	thrombocytopenia						ECO:0000033	author statement supported by traceable reference	PMID:14656885	20111114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752054	Tg(Prnp-rtTA2S*M2)#Rkhu/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0  [background:] involves: C57BL/6JRj	is_model_of	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26060190	20160316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693291	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO/CMV-KRAS*G12C)9.1Msmi/0  [background:] involves: FVB/N	is_model_of	DOID:3683	lung benign neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:16051643	20171102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904770	Mocs2<sup>tm1(KOMP)Vlcg</sup>/Mocs2<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0111163	molybdenum cofactor deficiency type B						ECO:0000033	author statement supported by traceable reference	PMID:27138983	20230619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835654	Elp1<sup>Gt(BGB184)Byg</sup>/Elp1<sup>Gt(BGB184)Byg</sup>  [background:] B6.129P2-<sup>Gt(BGB184)Byg</sup>	is_model_of	DOID:0050120	hemophagocytic lymphohistiocytosis						ECO:0000033	author statement supported by traceable reference	PMID:19015235	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814367	Apc<sup>Min</sup>/Apc<sup>+</sup> Brca2<sup>tm1Mbn</sup>/Brca2<sup>+</sup>  [background:] B6.Cg-Brca2<sup>tm1Mbn</sup> Apc<sup>Min</sup>	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11215675	20081111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448852	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-TARDBP)12Vle/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:21206091	20130114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800315	Irak3<sup>tm1Flv</sup>/Irak3<sup>tm1Flv</sup>  [background:] NOD.129S1(B6)-Irak3<sup>tm1Flv</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24696448	20161011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6694857	Cdc14a<sup>tm1a(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB	is_model_of	DOID:0110491	autosomal recessive nonsyndromic deafness 32						ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356551	Pfkm<sup>tm1Fbos</sup>/Pfkm<sup>tm1Fbos</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:11721	glycogen storage disease VII						ECO:0000033	author statement supported by traceable reference	PMID:19696889	20090911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4457377	Tcap<sup>tm1Mkc</sup>/Tcap<sup>tm1Mkc</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110281	autosomal recessive limb-girdle muscular dystrophy type 2G						ECO:0000033	author statement supported by traceable reference	PMID:20233748	20100701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009555	Tg(Th-MYCN)41Waw/0  [background:] involves: 129X1/SvJ * BALB/c * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:21559450	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662361	Slit3<sup>tm1.1Dor</sup>/Slit3<sup>tm1.1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:12702769	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4844190	Kras<sup>tm1Bbd</sup>/Kras<sup>tm2Bbd</sup> Polr2a<sup>tm1(cre/ERT2)Bbd</sup>/Polr2a<sup>tm1(cre/ERT2)Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:20609353	20130820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197218	Slc6a8<sup>tm1e(KOMP)Wtsi</sup>/Y  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:30013483	20180910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448462	Tg(NES/TK-PDGFB,-lacZ)310Kfn/0  [background:] B6.Cg-Tg(NES/TK-PDGFB,-lacZ)310Kfn	is_model_of	DOID:0060282	persistent hyperplastic primary vitreous						ECO:0000033	author statement supported by traceable reference	PMID:22880002	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852757	Smpx<sup>em2Jgao</sup>/Y  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>	is_model_of	DOID:0111735	X-linked deafness 4						ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7523313	Chat<sup>tm2(cre)Lowl</sup>/Chat<sup>+</sup> Stmn2<sup>em2Jmi</sup>/Stmn2<sup>em2Jmi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6N	is_model_of	DOID:2477	motor peripheral neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580069	Nf1<sup>tm1Fcr</sup>/Nf1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S/SvEv * 129S2/SvPas * C57BL/6	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:10591653	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174793	Tub<sup>tub</sup>/Tub<sup>tub</sup>  [background:] B6(AU)-Tub<sup>tub</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:8606774	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6754183	Elp2<sup>em2Bjw</sup>/Elp2<sup>em3Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767323	Tcra<sup>tm1Mom</sup>/Tcra<sup>tm1Mom</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:8104709	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509330	Hbb<sup>d3th</sup>/Hbb<sup>+</sup> Tg(LCR-HBA2,LCR-HBB*)1Cos/0  [background:] involves: C57BL/6J * CBA/J * DBA/2J	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:1915288	20131003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6241435	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>tm1.1Ece</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae	is_model_of	DOID:0080143	congenital fibrosis of the extraocular muscles						ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6887866	Litaf<sup>tm1.1Cwc</sup>/Litaf<sup>tm1.1Cwc</sup>  [background:] B6.Cg-Litaf<sup>tm1.1Cwc</sup>	is_model_of	DOID:0110151	Charcot-Marie-Tooth disease type 1C						ECO:0000033	author statement supported by traceable reference	PMID:23576546	20220310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6358593	Dlgap4<sup>Gt(XH723)Byg</sup>/Dlgap4<sup>Gt(XH723)Byg</sup>  [background:] B6.129P2-Dlgap4<sup>Gt(XH723)Byg</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30664629	20190906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009036	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129 * C57BL/6 * CBA * SJL	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:21562564	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576517	Tg(Wap-Hgf)402Mig/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:14627990	20140808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625276	Chkb<sup>rmd</sup>/Chkb<sup>rmd</sup>  [background:] involves: BALB/cByJ * C57BL/6J	is_model_of	DOID:0110632	megaconial type congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:16371353	20120130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764817	Tg(CAG-SNCA*)1.1Ccs/?  [background:] involves: C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:21212098	20110307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524271	Slc4a11<sup>tm1.1Jrcy</sup>/Slc4a11<sup>tm1.1Jrcy</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060649	congenital hereditary endothelial dystrophy of cornea						ECO:0000033	author statement supported by traceable reference	PMID:23942972	20150515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720082	Hba<sup>b2(th)</sup>/Hba<sup>+</sup>  [background:] SEC-Hba<sup>b2(th)</sup>	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:7450330	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361283	Tbx22<sup>tm1.1Sta</sup>/Tbx22<sup>tm1.1Sta</sup>  [background:] involves: 129 * CD-1	is_model_of	DOID:0060613	X-linked cleft palate with or without ankyloglossia						ECO:0000033	author statement supported by traceable reference	PMID:19648291	20091013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6466594	Pak3<sup>tm1.1Rpo</sup>/Y  [background:] B6.129S2(Cg)-Pak3<sup>tm1.1Rpo</sup>	is_model_of	DOID:0112051	non-syndromic X-linked intellectual disability 30						ECO:0000033	author statement supported by traceable reference	PMID:31943058	20201012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526018	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] C.129P2-Abcb4<sup>tm1Bor</sup>	is_model_of	DOID:13580	cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:23545228	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5051942	Apoa4<sup>tm1Bres</sup>/Apoa4<sup>tm1Bres</sup> Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/?  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21356380	20110802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655625	Tg(KRT14-Vegfa)3Dtm/0  [background:] FVB/N-Tg(KRT14-Vegfa)3Dtm	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:15100155	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160009	Ecel1<sup>em1Hiki</sup>/Ecel1<sup>em1Hiki</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:26951213	20180608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd	is_model_of	DOID:6255	growth hormone secreting pituitary adenoma						ECO:0000033	author statement supported by traceable reference	PMID:12819299	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714016	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Gfap-cre)1Sbk/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:936	brain disease						ECO:0000033	author statement supported by traceable reference	PMID:19470613	20171116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838166	Tg(ATXN3*)84.2Cce/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:11978767	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620112	Col1a1<sup>Mov13</sup>/Col1a1<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110334	osteogenesis imperfecta type 1						ECO:0000033	author statement supported by traceable reference	PMID:2402497	20060421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427085	Polb<sup>tm1.1Jbsw</sup>/Polb<sup>tm1.1Jbsw</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:24388753	20140715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447979	Hhat<sup>Tg(TFAP2A-cre)1Will</sup>/Hhat<sup>Tg(TFAP2A-cre)1Will</sup>  [background:] Not Specified	is_model_of	DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24784881	20160519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5502373	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Col1a1-cre)1Bek/0  [background:] involves: 129S4/SvJae * CD-1	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23029375	20130822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6360310	Elovl4<sup>tm1Wked</sup>/Elovl4<sup>tm1Wked</sup> Tg(IVL-Elovl4)#Wked/0 Tg(KRT14-Elovl4)#Mpag/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:3146	lipid metabolism disorder						ECO:0000033	author statement supported by traceable reference	PMID:29168048	20190919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604242	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Fgfr3*R248C/Fgfr1)#Dor/0  [background:] involves: 129 * C57BL/6 * FVB/N * FVB/NTac	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:24349409	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430325	b2b243Clo/b2b243Clo  [background:] C57BL/6J-b2b243Clo	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6505559	Kras<sup>tm1.1Khai</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/0 Trp53<sup>tm3.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30952657	20210209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838721	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>tm1.1Sdie</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24163243	20140312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273760	Tor1a<sup>tm1Calak</sup>/Tor1a<sup>tm1Calak</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0050836	focal dystonia						ECO:0000033	author statement supported by traceable reference	PMID:27168150	20190117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629753	Ar<sup>tm3(AR)Dmr</sup>/Y Tg(TRAMP)8247Ng/0  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:16601069	20060721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911329	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5013951	Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup> Inpp5d<sup>tm1Rav</sup>/Inpp5d<sup>tm1Rav</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:707	B-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:20956547	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580111	Pparg<sup>tm1Lja</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15716267	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652424	Galc<sup>tm1Wngr</sup>/Galc<sup>tm1Wngr</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:11461188	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6501995	Ifnar1<sup>tm1Agt</sup>/Ifnar1<sup>tm1Agt</sup> Tg(CD46)373Zbz/Tg(CD46)373Zbz  [background:] involves: 129S2/SvPas * C3H/He * C57BL/6	is_model_of	DOID:8622	measles						ECO:0000033	author statement supported by traceable reference	PMID:9696838	20210126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428692	Hprt1<sup>tm1(Nphs1-CMIP)Dsah</sup>/Hprt1<sup>+</sup>  [background:] B6.Cg-Hprt1<sup>tm1(Nphs1-CMIP)Dsah</sup>	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20484117	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295359	Gnao1<sup>tm2Rneu</sup>/Gnao1<sup>+</sup>  [background:] B6.129S1-Gnao1<sup>tm2Rneu</sup>	is_model_of	DOID:0080450	developmental and epileptic encephalopathy 17						ECO:0000033	author statement supported by traceable reference	PMID:30682176	20190502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276575	Tg(Mpz*S63X)30Mes/0  [background:] involves: FVB/N	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7286375	Specc1l<sup>em3Kumc</sup>/Specc1l<sup>+</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>	is_model_of	DOID:0050635	alternating hemiplegia of childhood						ECO:0000033	author statement supported by traceable reference	PMID:26463346	20180628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432033	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup> Tg(CAG-Cfh*)#Mcp/0  [background:] involves: 129/Sv * C57BL/6 * CBA	is_model_of	DOID:12554	hemolytic-uremic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17517971	20120823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451063	Gusb<sup>tm1Sly</sup>/Gusb<sup>tm1Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843698	Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-Chrnb2*V287L)H3Gica/0  [background:] involves: 129S7/SvEvBrd * FVB	is_model_of	DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3						ECO:0000033	author statement supported by traceable reference	PMID:19153075	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5586690	Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:24493795	20141007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603348	Casr<sup>Nuf</sup>/Casr<sup>+</sup>  [background:] either: (involves: 102/El * 102/H * C3H/He) or (involves: 102/El * C3H/He * C3H/HeH)	is_model_of	DOID:0090107	autosomal dominant hypocalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:15347804	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444222	Tg(ACTA1-TPM3*M9R)4Hrd/0  [background:] FVB/NJ-Tg(ACTA1-TPM3*M9R)4Hrd	is_model_of	DOID:0110926	nemaline myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:11157795	20121203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5002366	Id1<sup>tm1Zhu</sup>/Id1<sup>tm1Zhu</sup> Id3<sup>tm1Zhu</sup>/Id3<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:34434211	20211007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404636	Tardbp<sup>tm3.1Ckjs</sup>/Tardbp<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:31964415	20200420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696385	Tg(Cd74-Nlrc4*)1Kyas/0  [background:] involves: C57BL/6N	is_model_of	DOID:0090065	familial cold autoinflammatory syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:25385754	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198766	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(CAG-MYC,-GFP*)#Rugg/0 Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:29720449	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797716	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> Tg(Pax3-cre)1Joe/0  [background:] involves: 129/Sv * C57BL/6 * SJL	is_model_of	DOID:13832	patent ductus arteriosus						ECO:0000033	author statement supported by traceable reference	PMID:18188448	20170816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315641	Grm5<sup>tm1Rod</sup>/Grm5<sup>tm1Rod</sup>  [background:] B6.129-Grm5<sup>tm1Rod</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:30401923	20190701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655088	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup> Foxk1<sup>tm1Djg</sup>/Foxk1<sup>tm1Djg</sup>  [background:] involves: 129S4/SvJae * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:10792059	20060919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663255	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:19903857	20170406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6285755	Glul<sup>tm1.1Ncd</sup>/Glul<sup>tm1.1Ncd</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] B6.Cg-Glul<sup>tm1.1Ncd</sup> Emx1<sup>tm1(cre)Krj</sup>	is_model_of	DOID:3328	temporal lobe epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:30053506	20190402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7514498	Ank2<sup>em1Melr</sup>/Ank2<sup>em1Melr</sup>  [background:] B6.Cg-Ank2<sup>em1Melr</sup>	is_model_of	DOID:0111700	ankyrin-B-related cardiac arrhythmia						ECO:0000033	author statement supported by traceable reference	PMID:37182735	20230804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6883565	Setx<sup>tm1.1Als</sup>/Setx<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060196	amyotrophic lateral sclerosis type 4						ECO:0000033	author statement supported by traceable reference	PMID:29725819	20220225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6115021	Otud7a<sup>em1Cpsc</sup>/Otud7a<sup>em1Cpsc</sup>  [background:] C57BL/6J-Otud7a<sup>em1Cpsc</sup>	is_model_of	DOID:0060394	chromosome 15q13.3 microdeletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29395075	20180418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622305	Tg(Myh6-Tmod1)65Msus/Tg(Myh6-Tmod1)65Msus  [background:] FVB/N-Tg(Myh6-Tmod1)65Msus	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:10595939	20170724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523973	Pax3<sup>Sp-1Wli</sup>/Pax3<sup>Sp-1Wli</sup>  [background:] involves: C57BL/6J * CBA/CaJ	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652088	Acox1<sup>tm1Jkr</sup>/Acox1<sup>tm1Jkr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050797	peroxisomal acyl-CoA oxidase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8798738	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5426828	Tg(ACTA1-cre/ERT2)97.16Mtz/0 Tg(CAG-DMPK*)1323Coop/0  [background:] involves: FVB	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:18272483	20120703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819956	Tg(Ggamma-T)15Cps/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:9041192	20081215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444503	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IL1B)KBry/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0050161	lower respiratory tract disease						ECO:0000033	author statement supported by traceable reference	PMID:16888287	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421692	Del(11Nmur2-Sparc)2Anjm/+ Del(11Sparc-Gpx3)91Anjm/+  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19966810	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432224	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:2999	granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522483	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv * Black Swiss	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:10616210	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822323	Tg(S100b-v-erbB)4496Waw/0 Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * DBA/2J * FVB/N	is_model_of	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:12670909	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5585410	Ppt1<sup>tm1.1Dprc</sup>/Ppt1<sup>tm1.1Dprc</sup>  [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6	is_model_of	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25205113	20150521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849881	Thrb<sup>tm6.1Few</sup>/Thrb<sup>tm6.1Few</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19439650	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907161	Tg(Myh6-NEBL*G202R)#Jato/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20951326	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6515831	Ryr1<sup>tm3.1Alle</sup>/Ryr1<sup>tm3.1Alle</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:8545	malignant hyperthermia						ECO:0000033	author statement supported by traceable reference	PMID:30236258	20210407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402390	Kcnh6<sup>em1Jkya</sup>/Kcnh6<sup>em1Jkya</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:4194	glucose metabolism disease						ECO:0000033	author statement supported by traceable reference	PMID:30590050	20200401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672144	Slc4a1<sup>tm1Llp</sup>/Slc4a1<sup>tm1Llp</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:14219	renal tubular acidosis						ECO:0000033	author statement supported by traceable reference	PMID:17409310	20090514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451195	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup> Tg(SYN1-tTA2S,tetO-Hexb)#Tjsa/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:23028353	20130125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175788	Coc/Coc  [background:] involves: 101 * C3H * C57BL/6	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695037	Glrb<sup>spa</sup>/Glrb<sup>spa</sup>  [background:] Not Specified	is_model_of	DOID:0060697	hyperekplexia 2						ECO:0000033	author statement supported by traceable reference	PMID:8733750	20120514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581978	Chrm3<sup>tm1Mmt</sup>/Chrm3<sup>tm1Mmt</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10944224	20140525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6377057	Arl2bp<sup>em1Visu</sup>/Arl2bp<sup>em1Visu</sup>  [background:] involves: FVB/N	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:31425546	20191115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192275	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Tg(Itgax-cre)1-1Reiz/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:2571	Langerhans-cell histiocytosis						ECO:0000033	author statement supported by traceable reference	PMID:24638167	20180731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046097	Chat<sup>tm1.1Jrs</sup>/Chat<sup>tm1.1Jrs</sup>  [background:] Not Specified	is_model_of	DOID:0110671	congenital myasthenic syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:12441053	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2170004	Pitx2<sup>tm1Sac</sup>/Pitx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10498698	20051011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279300	Glyr1<sup>em1Dsr</sup>/Glyr1<sup>em1Dsr</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:35182466	20220523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638106	Cd3e<sup>tm1Mal</sup>/Cd3e<sup>tm1Mal</sup> Tg(Tcrb-TCF3/PBX1)23Gusa/0  [background:] involves: C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:12603	acute leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15655112	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682644	Slc4a7<sup>tm1Krtz</sup>/Slc4a7<sup>tm1Krtz</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0110839	Usher syndrome type 2C						ECO:0000033	author statement supported by traceable reference	PMID:12808454	20061219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6431858	Cfap69<sup>em1Fzh</sup>/Cfap69<sup>em1Fzh</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0111929	spermatogenic failure 24						ECO:0000033	author statement supported by traceable reference	PMID:30415212	20200911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157954	Cfap418<sup>em3Jyang</sup>/Cfap418<sup>em3Jyang</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:29440555	20180524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582638	m12Anu/m12Anu  [background:] Not Specified	is_model_of	DOID:0050563	nonsyndromic deafness						ECO:0000033	author statement supported by traceable reference	PMID:24086324	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582278	Tg(Cryaa-APEH)KKS4Kksha/0  [background:] FVB/N-Tg(Cryaa-APEH)KKS4Kksha	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:24554718	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925413	Trex1<sup>tm1Tld</sup>/Trex1<sup>tm1Tld</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050169	cutaneous lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:28351661	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461401	Dp(10Prmt2-Pdxk)2Yey/0 Dp(16Lipi-Zbtb21)1Yey/0 Dp(17Abcg1-Rrp1b)3Yey/0  [background:] B6.129S7-Dp(10Prmt2-Pdxk)2Yey Dp(16Lipi-Zbtb21)1Yey Dp(17Abcg1-Rrp1b)3Yey	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20442137	20100723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581028	Cdh23<sup>v-2J</sup>/Cdh23<sup>v-2J</sup>  [background:] B6(V)-Cdh23<sup>v-2J</sup>/J	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:11138008	20090504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4940051	Atp7a<sup>Mo-ms</sup>/Y  [background:] Not Specified	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:20831904	20110308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4443207	Ryr2<sup>tm1.1Maya</sup>/Ryr2<sup>+</sup>  [background:] C57BL/6J-Ryr2<sup>tm1.1Maya</sup>	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:20224043	20100512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569005	Gt(ROSA)26Sor<sup>tm1(rtTA,EGFP)Nagy</sup>/Gt(ROSA)26Sor<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup> Tg(tetO-Kras2)12Hev/0 Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22232209	20140620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7564407	Dram2<sup>em1Jean</sup>/Dram2<sup>em1Jean</sup>  [background:] C57BL/6J-Dram2<sup>em1Jean</sup>	is_model_of	DOID:0050572	cone-rod dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:37691820	20231208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841558	Tacr3<sup>tm1Jasi</sup>/Tacr3<sup>tm1Jasi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090071	hypogonadotropic hypogonadism 11 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:22253416	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829566	Kmt2d<sup>Gt(RRT024)Byg</sup>/Kmt2d<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0060473	Kabuki syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25273096	20170327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7278768	Sgca<sup>tm2Kcam</sup>/Sgca<sup>tm2Kcam</sup>  [background:] B6.129S6-Sgca<sup>tm2Kcam</sup>/J	is_model_of	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:28797108	20220517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196044	Tg(CAG-Alk*F1174L,-luc)60Jhsc/0 Tg(Dbh-icre)1Gsc/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22764207	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292226	Tmem67<sup>tm1Dgen</sup>/Tmem67<sup>tm1Dgen</sup>  [background:] B6.129P2-Tmem67<sup>tm1Dgen</sup>	is_model_of	DOID:0111001	Joubert syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:23283079	20131104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804180	Nr1d2<sup>tm1Dgen</sup>/Nr1d2<sup>tm1Dgen</sup>  [background:] B6;129P2-Nr1d2<sup>tm1Dgen</sup>/H	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:27058611	20161020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7495806	Ighmbp2<sup>em5Cx</sup>/Ighmbp2<sup>em5Cx</sup>  [background:] C57BL/6J-Ighmbp2<sup>em5Cx</sup>/Cx	is_model_of	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S						ECO:0000033	author statement supported by traceable reference	PMID:36413117	20230706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950028	Nme7<sup>Gt(OST31116)Lex</sup>/Nme7<sup>Gt(OST31116)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107910	Bag3<sup>tm1c(EUCOMM)Hmgu</sup>/Bag3<sup>tm1.1Chen</sup> Tg(Myhca-cre)1Abel/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N	is_model_of	DOID:0110448	dilated cardiomyopathy 1HH						ECO:0000033	author statement supported by traceable reference	PMID:28737513	20180109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3828991	Pde6a<sup>nmf363</sup>/Pde6a<sup>nmf363</sup>  [background:] C57BL/6J-Pde6a<sup>nmf363</sup>/J	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:18849587	20090126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6098753	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>+</sup>  [background:] B6.129P2(C)-Mecp2<sup>tm1.1Bird</sup>/J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843311	Prkcq<sup>tm1Litt</sup>/Prkcq<sup>tm1Litt</sup>  [background:] B6.129P2-Prkcq<sup>tm1Litt</sup>	is_model_of	DOID:5327	retinal detachment						ECO:0000033	author statement supported by traceable reference	PMID:26978024	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637560	Gadd45gip1<sup>tm2Kong</sup>/Gadd45gip1<sup>tm2Kong</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25660120	20150528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6257845	Tg(Alb-SND1)3aDsar/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28428278	20181126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5561553	Cplane2<sup>b2b2827Clo</sup>/Cplane2<sup>b2b2827Clo</sup>  [background:] C57BL/6J-Cplane2<sup>b2b2827Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6313621	Tg(Itgam-FCAR)83Rcmo/0  [background:] involves: C57BL/6 * NOD	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:10839814	20190611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581209	Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6(Cg)-Tyr<sup>c-2J</sup>/J	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6474170	Cln3<sup>em1Dprc</sup>/Cln3<sup>em1Dprc</sup>  [background:] C57BL/6-Cln3<sup>em1Dprc</sup>	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:32601357	20201130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581425	Tg(TG-TPR/NTRK1)#Rstn/0  [background:] involves: 129S4/SvJaeSor * C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:1781	thyroid cancer						ECO:0000033	author statement supported by traceable reference	PMID:19261681	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7532607	Tuft1<sup>tm1a(KOMP)Wtsi</sup>/Tuft1<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:3390	palmoplantar keratosis						ECO:0000033	author statement supported by traceable reference	PMID:37716648	20231003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7339041	Tfrc<sup>tm3.1Nca</sup>/Tfrc<sup>tm3.1Nca</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * CBA/J	is_model_of	DOID:4258	Weissenbacher-Zweymuller syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27362800	20220922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5807153	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/JRj	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:25621497	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580056	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:9054942	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281440	Ppp4c<sup>em1Qys</sup>/Ppp4c<sup>em1Qys</sup> Tg(Stra8-icre)1Reb/0  [background:] involves: 129S/SvEv * C57BL/6 * FVB/NJ	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:33543287	20220601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6156912	Marveld2<sup>tm1Sats</sup>/Marveld2<sup>tm1Sats</sup>  [background:] B6.Cg-Marveld2<sup>tm1Sats</sup>	is_model_of	DOID:0110506	autosomal recessive nonsyndromic deafness 49						ECO:0000033	author statement supported by traceable reference	PMID:26677943	20180517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908460	Tg(Myh6-Mybpc3*)32Rbns/0  [background:] Not Specified	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:9769321	20170914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908460	Tg(Myh6-Mybpc3*)32Rbns/0  [background:] Not Specified	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:11549344	20170914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175113	Mip<sup>Cat-Lop</sup>/Mip<sup>+</sup>  [background:] involves: STOCK Rb(6.15)1Ald	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:8563764	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849590	Gpc3<sup>tm1Snd</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7545554	Lepr<sup>db</sup>/Lepr<sup>db-Nokl</sup>  [background:] B6NTac.Cg-Lepr<sup>db</sup> Lepr<sup>db-Nokl</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175150	Nkx3-1<sup>tm1Hha</sup>/Nkx3-1<sup>tm1Hha</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:10906459	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2167526	None [background:] C3H/HeJ	is_model_of	DOID:0050701	electroclinical syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25010494	20180621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2167526	None [background:] C3H/HeJ	is_model_of	DOID:0050701	electroclinical syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15800200	20180621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316427	Kiss1r<sup>tm1.1Lex</sup>/Kiss1r<sup>tm1.1Lex</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:22067321	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6741540	Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>/Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6-Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>	is_model_of	DOID:0110127	Bardet-Biedl syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:33560420	20210820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427915	Tg(APPV717F)109Ili/0  [background:] involves: BALB/c * C57BL * C57BL/6NTac	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22623685	20120716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792693	Ptchd1<sup>tm2.2Gfng</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:27007844	20170712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175193	Nuca/Nuca<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431512	b2b904.2Clo/b2b904.2Clo  [background:] C57BL/6J-b2b904.2Clo	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6460379	Akt1<sup>tm1.1Mjl</sup>/Akt1<sup>+</sup>  [background:] chimera involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:13482	Proteus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31194862	20201008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425918	Casr<sup>BCH002</sup>/Casr<sup>BCH002</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH002</sup>	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429499	Stat3<sup>tm1Dlv</sup>/Stat3<sup>tm1Dlv</sup> Tg(Csf1r-icre)1Jwp/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:20042677	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797579	Hyal1<sup>tm1Stn</sup>/Hyal1<sup>tm1Stn</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050809	mucopolysaccharidosis IX						ECO:0000033	author statement supported by traceable reference	PMID:18344557	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851446	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-HTT*94Q,-lacZ)1Rhn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10778856	20090729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281832	Adar<sup>em1Stsn</sup>/Adar<sup>tm1Olds</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34343497	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819593	Tg(Thy1-APPDutch)#Jckr/0 Tg(Thy1-BACE1)54/4Ppa/0  [background:] involves: C57BL/6	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:17596707	20100818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676545	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup>  [background:] either: B6SJL.129-Chrd<sup>tm1Emdr</sup> or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12810603	20070104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3057279	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:15514019	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705821	Sdccag8<sup>Gt(OST40418)Lex</sup>/Sdccag8<sup>Gt(OST40418)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:12712	nephronophthisis						ECO:0000033	author statement supported by traceable reference	PMID:24722439	20220915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6444681	Ikbkb<sup>em1Macc</sup>/Ikbkb<sup>+</sup>  [background:] involves: C57BL/6NCrl	is_model_of	DOID:0111960	immunodeficiency 15A						ECO:0000033	author statement supported by traceable reference	PMID:30337470	20210120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447166	Jag1<sup>tm1Frad</sup>/Jag1<sup>tm1Frad</sup> Tg(Cdh5-cre)7Mlia/0  [background:] B6.Cg-Jag1<sup>tm1Frad</sup> Tg(Cdh5-cre)7Mlia	is_model_of	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23095891	20121231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789554	Tg(KRT19-TAg)7Eps/0  [background:] involves: FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:10980120	20160822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003275	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup> Tg(APPSwe,tauP301L)1Lfa/?  [background:] B6.Cg-Psen1<sup>tm1Mpm</sup> Tg(APPSwe,tauP301L)1Lfa	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21368062	20110606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697977	Evc2<sup>tm1.1Mis</sup>/Evc2<sup>tm1.1Mis</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:12714	Ellis-Van Creveld syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26219237	20151204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6477029	Rbm20<sup>em1Hide</sup>/Rbm20<sup>em1Hide</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110447	dilated cardiomyopathy 1DD						ECO:0000033	author statement supported by traceable reference	PMID:33110103	20201202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6400455	Dpp4<sup>tm1(DPP4)Vlcg</sup>/?  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26124093	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798179	Maoa<sup>K284stop</sup>/Y  [background:] 129S6/SvEvTac-Maoa<sup>K284stop</sup>	is_model_of	DOID:0060693	Brunner Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18418249	20080721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5560741	Eml1<sup>heco</sup>/Eml1<sup>heco</sup>  [background:] involves: NOR	is_model_of	DOID:2490	congenital nervous system abnormality						ECO:0000033	author statement supported by traceable reference	PMID:18562329	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904627	Tg(Myh6-MYL2*N47K)#Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:19150977	20170714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3641098	Cps1<sup>tm1Mw</sup>/Cps1<sup>tm1Mw</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:9280	carbamoyl phosphate synthetase I deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:9862865	20060817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578176	Tg(HBV-HCV)Kko/0  [background:] C57BL/6N-Tg(HBV-HCV)Kko	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11389061	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906908	Stat3<sup>tm1Vpo</sup>/Stat3<sup>tm1Vpo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:9997	peripartum cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17289576	20170814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665504	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] C57BL/6J-Apc<sup>Min</sup>	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:12941845	20140225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798788	Dmd<sup>mdx-5Cv</sup>/Dmd<sup>mdx-5Cv</sup>  [background:] B6Ros.Cg-Dmd<sup>mdx-5Cv</sup>/J	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:16857961	20120720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318976	Mapt<sup>tm1(Mecp2)Jae</sup>/Mapt<sup>tm1(Mecp2)Jae</sup>  [background:] B6.Cg-Mapt<sup>tm1(Mecp2)Jae</sup>	is_model_of	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000033	author statement supported by traceable reference	PMID:22378884	20120522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796753	Cnga3<sup>cpfl5</sup>/Cnga3<sup>cpfl5</sup>  [background:] B6.RHJ-Cnga3<sup>cpfl5</sup>/BocJ	is_model_of	DOID:0110007	achromatopsia 2						ECO:0000033	author statement supported by traceable reference	PMID:22509403	20161007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815328	Tns2<sup>nph</sup>/Tns2<sup>nph</sup>  [background:] involves: ICR	is_model_of	DOID:0060852	Pierson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16688531	20081119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532944	Flg<sup>ft</sup>/Flg<sup>ft</sup>  [background:] STOCK a/a Tmem79<sup>ma</sup> Flg<sup>ft</sup>/J	is_model_of	DOID:0110098	atopic dermatitis 2						ECO:0000033	author statement supported by traceable reference	PMID:23844115	20140131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7461096	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0 Tg(KRT14-cre)1Amc/0  [background:] involves: C57BL/6 * CBA * DBA/2	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:26116174	20230411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5619081	Dnai2<sup>b2b3405Clo</sup>/Dnai2<sup>b2b3405Clo</sup>  [background:] C57BL/6J-Dnai2<sup>b2b3405Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176891	Dmd<sup>mdx</sup>/Y Dtna<sup>tm1Jrs</sup>/Dtna<sup>tm1Jrs</sup> Utrn<sup>tm1Jrs</sup>/Utrn<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:10559919	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6386739	Spata7<sup>tm1Mrd</sup>/Spata7<sup>tm2Mrd</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110331	Leber congenital amaurosis 3						ECO:0000033	author statement supported by traceable reference	PMID:29100828	20200129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813539	Men1<sup>tm2.1Gfk</sup>/Men1<sup>+</sup>  [background:] involves: 129T2/SvEms * C57BL/6	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:17044021	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3521745	Hoxa13<sup>tm1Jwi</sup>/Hoxa13<sup>tm1Jwi</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060739	hand-foot-genital syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15385446	20050701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487831	Bub1b<sup>tm2.1Jvd</sup>/Bub1b<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0080141	mosaic variegated aneuploidy syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23300461	20130531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583554	Tg(ITGA5)0844Fmw/0 Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527796	Lmna<sup>tm1Gbon</sup>/Lmna<sup>tm1Gbon</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:22773734	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810648	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Fabp7-cre,-lacZ)3Gtm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:18614544	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5086005	Amer1<sup>tm1.2Nbar</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL	is_model_of	DOID:0060886	osteopathia striata with cranial sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21571217	20110815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522090	Nppc<sup>tm1Yog</sup>/Nppc<sup>tm1Yog</sup>  [background:] either: 129X1/SvJ or (involves: 129 * C57BL/6J)	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:11259675	20220512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6191699	Mpz<sup>tm3.1Wra</sup>/Mpz<sup>+</sup>  [background:] FVB.129S2(Cg)-Mpz<sup>tm3.1Wra</sup>	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:22689911	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6189553	Reep6<sup>em1Ruch</sup>/Reep6<sup>em1Ruch</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080350	retinitis pigmentosa 77						ECO:0000033	author statement supported by traceable reference	PMID:27889058	20181221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639713	Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:16354928	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033465	Hfe<sup>tm1Sly</sup>/Hfe<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14673107	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5584025	Mecp2<sup>tm1.1Dhy</sup>/Y  [background:] C57BL/6N-Mecp2<sup>tm1.1Dhy</sup>	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24352790	20140923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789685	Il10rb<sup>tm1Agt</sup>/Il10rb<sup>tm1Agt</sup> Tg(Cd4-TGFBR2)16Flv/?  [background:] involves: 129S2/SvPas * C3H * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18318596	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5616119	Bmp10<sup>b2b2711Clo</sup>/Bmp10<sup>b2b2711Clo</sup>  [background:] C57BL/6J-Bmp10<sup>b2b2711Clo</sup>	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431539	b2b1436Clo/b2b1436Clo  [background:] C57BL/6J-b2b1436Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5013916	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20807812	20110711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694692	Dmp1<sup>tm1Mis</sup>/Dmp1<sup>tm1Mis</sup>  [background:] involves: 129S7/SvEvBrd * CD-1	is_model_of	DOID:0050949	autosomal recessive hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:21542006	20151105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7316678	Serac1<sup>em1Bcgen</sup>/Serac1<sup>em1Bcgen</sup>  [background:] C57BL/6N-Serac1<sup>em1Bcgen</sup>	is_model_of	DOID:0110001	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35235340	20220728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590414	Itgb2<sup>tm2Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442379	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup> Tg(PRNP-APPSweInd)8Dwst/0  [background:] involves: BALB/c * C3H/HeJ * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22869680	20121120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587412	Cd36<sup>tm1Mfe</sup>/Cd36<sup>tm1Mfe</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0111046	platelet-type bleeding disorder 10						ECO:0000033	author statement supported by traceable reference	PMID:10383407	20050913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5503965	Mks1<sup>tm1a(EUCOMM)Wtsi</sup>/Mks1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23454480	20130903	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7444862	Lemd2<sup>em1Eno</sup>/Lemd2<sup>em1Eno</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:36377660	20230317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:12814946	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275175	Gt(ROSA)26Sor<sup>tm1(SPOP*F133V)Mrbn</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28292441	20190130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6405015	Tgfbi<sup>em1Yaou</sup>/Tgfbi<sup>em1Yaou</sup>  [background:] involves: C57BL/6NCr	is_model_of	DOID:2566	corneal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32029872	20200422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526986	Dnaaf2<sup>tm1.1Mkis</sup>/Dnaaf2<sup>tm1.1Mkis</sup>  [background:] involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:0110612	primary ciliary dyskinesia 10						ECO:0000033	author statement supported by traceable reference	PMID:23525783	20191107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524085	Tg(MMTV-Myc)WT21Jrn/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587647	Tg(Cyp19)C2-3Rrte/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:0090122	aromatase excess syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11358670	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529018	Dmd<sup>mdx-4Cv</sup>/Dmd<sup>mdx-4Cv</sup> Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup>  [background:] B6.Cg-Terc<sup>tm1Rdp</sup> Dmd<sup>mdx-4Cv</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23831727	20140116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175179	Ntf3<sup>tm1Par</sup>/Ntf3<sup>tm1Par</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:8841198	20060426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198715	Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc  [background:] Not Specified	is_model_of	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	PMID:17959936	20180919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617468	Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>/Mbd5<sup>+</sup>  [background:] B6.Cg-Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>	is_model_of	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000033	author statement supported by traceable reference	PMID:25001218	20150417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359828	Ush1c<sup>dfcr-4J</sup>/Ush1c<sup>dfcr-4J</sup>  [background:] 129P3/J-Ush1c<sup>dfcr-4J</sup>/J	is_model_of	DOID:0110473	autosomal recessive nonsyndromic deafness 18A						ECO:0000033	author statement supported by traceable reference	MGI:6359814	20190913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281485	Cd19<sup>tm1(cre/ERT2)Rsky</sup>/Cd19<sup>+</sup> Myd88<sup>em1.1Rsky</sup>/Myd88<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac	is_model_of	DOID:7442	monoclonal gammopathy of uncertain significance						ECO:0000033	author statement supported by traceable reference	PMID:33343574	20220601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7261455	Cxcr4<sup>tm2Yzo</sup>/Cxcr4<sup>tm2Yzo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:31071921	20220418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445936	Scn5a<sup>tm1(SCN5A)Rdn</sup>/Scn5a<sup>tm3(SCN5A*)Rdn</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110433	dilated cardiomyopathy 1E						ECO:0000033	author statement supported by traceable reference	PMID:21824921	20170802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6121112	Cdyl<sup>tm1.1Yuw</sup>/Cdyl<sup>tm1.1Yuw</sup> Emx1<sup>tm1(cre)Yql</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:28076783	20180313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712364	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] involves: 129S1/Sv * C57BL/6 * C57BLKS/J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:15728853	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7260343	Msh5<sup>em1Jzc</sup>/Msh5<sup>em1Jzc</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080870	primary ovarian insufficiency 13						ECO:0000033	author statement supported by traceable reference	PMID:28175301	20220411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256730	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27032374	20181116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512041	Gp1bb<sup>tm1Ware</sup>/Gp1bb<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:2217	Bernard-Soulier syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15213102	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946081	Fzd9<sup>tm1Uta</sup>/Fzd9<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21402791	20110411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5568131	Lrrk1<sup>tm1.1Smo</sup>/Lrrk1<sup>tm1.1Smo</sup>  [background:] involves: 129S/Sv	is_model_of	DOID:13533	osteopetrosis						ECO:0000033	author statement supported by traceable reference	PMID:23526378	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835117	Tg(WapTAg)3Knw/0  [background:] C57BL/6J-Tg(WapTAg)3Knw	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:9859214	20170623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177541	Cftr<sup>tm3Bay</sup>/Cftr<sup>tm3Bay</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7482032	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606583	Lrp5<sup>tm1Dgen</sup>/Lrp5<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276352	Ncoa6<sup>tm1Jkr</sup>/Ncoa6<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620827	Gja1<sup>M1Jrt</sup>/Gja1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:16155213	20060502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909304	Tg(Myh6-Tnni3*R193H)42Xhu/0  [background:] involves: C57BL/6	is_model_of	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17027633	20170918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516191	Slc6a2<sup>tm1.1Mkh</sup>/Slc6a2<sup>+</sup>  [background:] B6.129S6-Slc6a2<sup>tm1.1Mkh</sup>	is_model_of	DOID:10273	heart conduction disease						ECO:0000033	author statement supported by traceable reference	PMID:23580201	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815142	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>+</sup> X/Tg(Tyr-HRAS)60Lc  [background:] involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	is_model_of	DOID:6039	uveal melanoma						ECO:0000033	author statement supported by traceable reference	PMID:17987514	20081117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:19364920	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941348	Crebbp<sup>tm1.2Ltz</sup>/Crebbp<sup>tm1.2Ltz</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: 129P2/OlaHsd * BALB/c * C57BL * C57BL/6J	is_model_of	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21289174	20110317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790646	Gnptab<sup>nym</sup>/Gnptab<sup>nym</sup>  [background:] involves: BALB/cAnNHsd * C3H/HeNHsd	is_model_of	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000033	author statement supported by traceable reference	PMID:25107912	20160906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6477029	Rbm20<sup>em1Hide</sup>/Rbm20<sup>em1Hide</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060224	atrial fibrillation						ECO:0000033	author statement supported by traceable reference	PMID:33110103	20201202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512772	Ywhae<sup>tm1Awb</sup>/Ywhae<sup>tm1Awb</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060480	left ventricular noncompaction						ECO:0000033	author statement supported by traceable reference	PMID:23071090	20131016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5701349	Lmod3<sup>em1Eno</sup>/Lmod3<sup>em1Eno</sup>  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0110931	nemaline myopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:25774500	20160106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6317190	Tg(Prnp-MAPT*)2652Gds/0  [background:] B6.Cg-Tg(Prnp-MAPT*)2652Gds	is_model_of	DOID:680	tauopathy						ECO:0000033	author statement supported by traceable reference	PMID:26041339	20190711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637537	Trhr<sup>tm1Bau</sup>/Trhr<sup>tm1Bau</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:25490146	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367450	Ank1<sup>pale</sup>/Ank1<sup>pale</sup>  [background:] C57BL/6J-Ank1<sup>pale</sup>/GrsrJ	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843451	Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:5485	synovial sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:19351831	20091223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441517	Gt(ROSA)26Sor<sup>tm1.1(CAG-COX8A/Dendra2)Dcc</sup>/Gt(ROSA)26Sor<sup>+</sup> Mfn2<sup>tm3Dcc</sup>/Mfn2<sup>tm3Dcc</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>/Slc6a3<sup>+</sup>  [background:] involves: 129 * 129S6/SvEvTac * C57BL/6J * SJL/J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22859504	20121114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7408192	Ts(17<sup>16</sup>)65Dn/0  [background:] involves: BALB/c * C3H/He * C57BL/6JEiJ * DBA/2J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36374158	20221215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295223	Dlg4<sup>tm2.1Grnt</sup>/Dlg4<sup>tm2.1Grnt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20952458	20111108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462366	Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0  [background:] involves: FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22881289	20130208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5693947	Abcb1a<sup>tm1Bor</sup>/Abcb1a<sup>tm1Bor</sup>  [background:] FVB.129P2-Abcb1a<sup>tm1Bor</sup>/TacImx	is_model_of	DOID:0110893	inflammatory bowel disease 13						ECO:0000033	author statement supported by traceable reference	PMID:9820555	20151029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286097	Tg(GFAP-Hras1)2Agu/Tg(GFAP-Hras1)2Agu  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR	is_model_of	DOID:3069	malignant astrocytoma						ECO:0000033	author statement supported by traceable reference	PMID:11325859	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6268326	Dhtkd1<sup>em1Hpr</sup>/Dhtkd1<sup>em1Hpr</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0111453	2-aminoadipic 2-oxoadipic aciduria						ECO:0000033	author statement supported by traceable reference	PMID:28545977	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6360703	Odad3<sup>tm1b(EUCOMM)Hmgu</sup>/Odad3<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Odad3<sup>tm1b(EUCOMM)Hmgu</sup>/Cnrm	is_model_of	DOID:0110624	primary ciliary dyskinesia 30						ECO:0000033	author statement supported by traceable reference	PMID:31383820	20190924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614439	Kiss1r<sup>tm1Gstn</sup>/Kiss1r<sup>tm1Gstn</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:14652023	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312933	b2b997Clo/b2b997Clo  [background:] C57BL/6J-b2b997Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5500085	Cacna1a<sup>smrl</sup>/Cacna1a<sup>smrl</sup>  [background:] CXB10/HiAJ-Cacna1a<sup>smrl</sup>/GrsrJ	is_model_of	DOID:0050956	spinocerebellar ataxia type 6						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6226150	Lama2<sup>dy-Pas</sup>/Lama2<sup>dy-Pas</sup>  [background:] involves: non-inbred stock	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:12609503	20181106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430328	b2b1470Clo/b2b1470Clo  [background:] C57BL/6J-b2b1470Clo	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197548	Pnpla3<sup>tm2.1Hobb</sup>/Pnpla3<sup>tm2.1Hobb</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:24917523	20180911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6466741	Clcn7<sup>tm1.1Aros</sup>/Clcn7<sup>tm1.1Aros</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:30865697	20201013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6399965	Tg(K18-ACE2)2Prlmn/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17079315	20200318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6726265	Tcf20<sup>em1Jwji</sup>/Tcf20<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:32510763	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487398	b2b1941Clo/b2b1941Clo  [background:] C57BL/6J-b2b1941Clo	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6156953	Auts2<sup>tm1Mhos</sup>/Auts2<sup>+</sup>  [background:] C57BL/6N-Auts2<sup>tm1Mhos</sup>	is_model_of	DOID:0070056	autosomal dominant intellectual developmental disorder 26						ECO:0000033	author statement supported by traceable reference	PMID:26717414	20180518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7567701	Atp6v1b2<sup>em1Pcamp</sup>/Atp6v1b2<sup>em1Pcamp</sup>  [background:] C57BL/6N-Atp6v1b2<sup>em1Pcamp</sup>	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:37628590	20231220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629188	Akt2<sup>tm1.1Mbb</sup>/Akt2<sup>tm1.1Mbb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11387480	20060717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6508400	Spg21<sup>tm1Mchan</sup>/Spg21<sup>tm1Mchan</sup>  [background:] Not Specified	is_model_of	DOID:0060245	Mast syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20661613	20210302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6406756	B3glct<sup>tm1b(KOMP)Wtsi</sup>/B3glct<sup>tm1b(KOMP)Wtsi</sup>  [background:] B6(Cg)-B3glct<sup>tm1b(KOMP)Wtsi</sup>	is_model_of	DOID:0080201	Peters plus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31600785	20200429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752235	Cdkn2a<sup>tm2.1Nesh</sup>/Cdkn2a<sup>tm2.1Nesh</sup> Nras<sup>tm1.1Nesh</sup>/Nras<sup>tm1.1Nesh</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] B6J.Cg-Tg(Tyr-cre/ERT2)13Bos Nras<sup>tm1.1Nesh</sup> Cdkn2a<sup>tm2.1Nesh</sup>	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25252692	20190123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052308	Hr<sup>rhsl</sup>/Hr<sup>rhsl</sup>  [background:] involves: BALB/c	is_model_of	DOID:0050634	alopecia universalis						ECO:0000033	author statement supported by traceable reference	PMID:15955095	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583540	Tg(ITGA2)1067Fmw/0 Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404021	Fkrp<sup>tm1.1Pg</sup>/Fkrp<sup>tm1.1Pg</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:26574668	20200415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579981	Fras1<sup>bl</sup>/Fras1<sup>bl</sup> Frem2<sup>my-Ucl</sup>/Frem2<sup>my-Ucl</sup>  [background:] involves: 101/H * C3H/HeH * NMRI	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15838507	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181881	srt/srt  [background:] Not Specified	is_model_of	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11818962	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526428	Nfkbiz<sup>tm1Mamo</sup>/Nfkbiz<sup>tm1Mamo</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:15491998	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614635	Abca1<sup>tm2Jp</sup>/Abca1<sup>+</sup> Tg(APOA1)427Bres/?  [background:] involves: 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:16024913	20060306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846703	Tg(Slc6a3-PARK2*Q311X)AXwy/0  [background:] FVB/NJ-Tg(Slc6a3-PARK2*Q311X)AXwy	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:19228951	20100505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942362	Tg(Kit*D814V)3Roer/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6163706	Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] FVB/NJ-Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:29247744	20190226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818371	Del(17Abcg1-Rrp1b)5Yey/+  [background:] 129S.129S7-Del(17Abcg1-Rrp1b)5Yey	is_model_of	DOID:0050888	syndromic intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:20512340	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360989	Rag2<sup>tm1Fwa</sup>/Rag2<sup>tm1Fwa</sup> Tbx21<sup>tm1Glm</sup>/Tbx21<sup>tm1Glm</sup>  [background:] involves: 129S/SvEv * 129S6/SvEvTac	is_model_of	DOID:8577	ulcerative colitis						ECO:0000033	author statement supported by traceable reference	PMID:17923086	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639744	Fgfr3<sup>tm2Wei</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * MF1	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:10200283	20060803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784305	Dmd<sup>mdx</sup>/? Myod1<sup>tm1Jae</sup>/Myod1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9874799	20080508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677039	Col2a1<sup>tm1Prc</sup>/Col2a1<sup>tm1Prc</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:7590256	20051006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907465	Lpl<sup>tm1Bres</sup>/Lpl<sup>+</sup> Tg(Myh6-LPL*)357Ijg/0  [background:] involves: 129S4/SvJae	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12569168	20170825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5506798	Tg(MMTV-rtTA)1Lach/0 Tg(TetO-Erbb2)1Lach/0  [background:] involves: FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:12498714	20130918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462095	Notch3<sup>tm1.1Dwr</sup>/Notch3<sup>tm1.1Dwr</sup>  [background:] involves: 129S/SvEv * Swiss	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:21940951	20130206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814579	Kmt2a<sup>tm1Saam</sup>/Kmt2a<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:18977325	20100813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ	is_model_of	DOID:0050644	arterial calcification of infancy						ECO:0000033	author statement supported by traceable reference	PMID:23798568	20140124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514353	Fktn<sup>tm3.1Ttd</sup>/Fktn<sup>tm3.1Ttd</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:23562821	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6159294	Abca4<sup>tm1Kpal</sup>/Abca4<sup>tm1Kpal</sup> Rdh8<sup>tm1Kpal</sup>/Rdh8<sup>tm1Kpal</sup>  [background:] involves: 129	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:24712709	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311569	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6280332	Gt(ROSA)26Sor<sup>tm1(DUX4)Sqh</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(ACTA1-cre/Esr1*)2Kesr/0  [background:] involves: 129S6/SvEvTac * C3H * C57BL/6	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:30429376	20190226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513541	Slc12a3<sup>tm1Ges</sup>/Slc12a3<sup>tm1Ges</sup>  [background:] Not Specified	is_model_of	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9786924	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7545577	Dll4<sup>tm1Frad</sup>/Dll4<sup>+</sup> Isl1<sup>tm1(cre)Tmj</sup>/Isl1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060227	Adams-Oliver syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33899511	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6369967	Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>/Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>  [background:] B6N(Cg)-Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>/J	is_model_of	DOID:0110612	primary ciliary dyskinesia 10						ECO:0000033	author statement supported by traceable reference	PMID:31107948	20191107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296959	Aebp2<sup>Gt(BC0681)Wtsi</sup>/Aebp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:21949878	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140748	Tg(APPSWE)2576Kha/0 Tg(PDGFB-PSEN1M146L)2Jhd/0  [background:] involves: C57BL/6 * DBA/2 * SJL * SW	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19041304	20110823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623426	Ighm<sup>tm1Cgn</sup>/Ighm<sup>+</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:8920894	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6798143	Gnat2<sup>cpfl3-2J</sup>/Gnat2<sup>cpfl3-2J</sup>  [background:] B6.Cg-Gnat2<sup>cpfl3-2J</sup>/Boc	is_model_of	DOID:13911	achromatopsia						ECO:0000033	author statement supported by traceable reference	MGI:6798134	20211110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5306390	Eif2b5<sup>tm1Itl</sup>/Eif2b5<sup>tm1Itl</sup>  [background:] involves: 129S/SvEv * C57BL * Swiss Webster	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:20826436	20160317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5776354	Shank3<sup>tm5.1Gfng</sup>/Shank3<sup>tm5.1Gfng</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26886798	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368185	Porcn<sup>tm1.1Lcm</sup>/Y H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911801	Cdk5rap2<sup>an</sup>/Cdk5rap2<sup>an</sup> Tyrp1<sup>B-lt</sup>/Tyrp1<sup>B-lt</sup>  [background:] WBB6F1	is_model_of	DOID:5621	histiocytic and dendritic cell cancer						ECO:0000033	author statement supported by traceable reference	PMID:20460369	20171102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558028	Scn11a<sup>tm1.1Ikth</sup>/Scn11a<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:0050548	hereditary sensory neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:24036948	20140410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714868	Cdh23<sup>v-6J</sup>/Cdh23<sup>v-6J</sup>  [background:] B10.A-H2<sup>h4</sup>/(4R)SgDvEgJ-Cdh23<sup>v-6J</sup>/J	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:11138008	20090504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6458731	Ap5z1<sup>tm1(KOMP)Wtsi</sup>/Ap5z1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: 129 * C57BL/6N	is_model_of	DOID:0110800	hereditary spastic paraplegia 48						ECO:0000033	author statement supported by traceable reference	PMID:30930081	20200930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852762	Smpx<sup>em2Jgao</sup>/Smpx<sup>+</sup>  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>	is_model_of	DOID:0111735	X-linked deafness 4						ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563659	Sptlc2<sup>tm1Yhir</sup>/Sptlc2<sup>tm1Yhir</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:23633022	20140515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6472629	Mecp2<sup>em1Jlzn</sup>/Y  [background:] C57BL/6-Mecp2<sup>em1Jlzn</sup>	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32469049	20201116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4443124	Kif3a<sup>tm2Gsn</sup>/Kif3a<sup>tm2Gsn</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:1934	dysostosis						ECO:0000033	author statement supported by traceable reference	PMID:20106874	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907206	Ilk<sup>tm1Star</sup>/Ilk<sup>tm1Star</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:16951252	20170822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6158940	None [background:] NZC	is_model_of	DOID:11111	hydronephrosis						ECO:0000033	author statement supported by traceable reference	PMID:5139908	20180530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5805256	Yme1l1<sup>tm1Tlan</sup>/Yme1l1<sup>tm1Tlan</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: C57BL/6 * C57BL/6NCrl * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:26785494	20170929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5461579	Tg(Myh6-Erbb2)6Kaga/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22912742	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587801	Nsdhl<sup>Bpa-1H</sup>/Nsdhl<sup>+</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:0060292	X-linked chondrodysplasia punctata 1						ECO:0000033	author statement supported by traceable reference	PMID:6682087	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5490787	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Tg(SMN1-SMN2*)16Cll/0 Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23390132	20130618	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910007	Atp6v1b1<sup>vtx</sup>/Atp6v1b1<sup>vtx</sup>  [background:] MRL/MpJ-Atp6v1b1<sup>vtx</sup>/Kjn	is_model_of	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000033	author statement supported by traceable reference	PMID:28934385	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7547513	Slitrk2<sup>tm1.1Jwum</sup>/Y Tg(Nes-cre)1Atp/0  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:35840571	20231113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583542	Tg(ITGA2)1070Fmw/0 Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318772	Slc6a3<sup>tm1Hhg</sup>/Slc6a3<sup>tm1Hhg</sup>  [background:] B6.129X1-Slc6a3<sup>tm1Hhg</sup>	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:22034972	20120520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6294293	Tg(Prnp-HTT*82Q)8AGschi/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15190011	20190424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6474005	Gch1<sup>em1Ypt</sup>/Gch1<sup>em1Ypt</sup>  [background:] C57BL/6-Gch1<sup>em1Ypt</sup>	is_model_of	DOID:0112225	BH4-deficient hyperphenylalaninemia B						ECO:0000033	author statement supported by traceable reference	PMID:30742839	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7282037	Hsf2bp<sup>em2Amp</sup>/Hsf2bp<sup>em2Amp</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0112278	primary ovarian insufficiency 19						ECO:0000033	author statement supported by traceable reference	PMID:32845237	20220603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5492341	Phex<sup>m1Jrt</sup>/Y  [background:] B6.129S1-Phex<sup>M1Jrt</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22573557	20130627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4456370	Tg(KRT5-IKBKB)2Armz/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2723	dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20200541	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430346	Dnah5<sup>b2b1565Clo</sup>/Dnah5<sup>b2b1565Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1565Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776069	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S6/SvEvTac	is_model_of	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000033	author statement supported by traceable reference	PMID:18242513	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036453	Slc12a1<sup>tm1Tkh</sup>/Slc12a1<sup>tm1Tkh</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110142	Bartter disease type 1						ECO:0000033	author statement supported by traceable reference	PMID:10779555	20131223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526091	Tg(ACTB-KRAS*G12V,-luc)#Lche/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23536778	20140102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>	is_model_of	DOID:2226	myeloproliferative neoplasm						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903412	Cacna1a<sup>tm2.1Maag</sup>/Cacna1a<sup>tm2.1Maag</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050753	cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:21870131	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716639	Pink1<sup>tm1Shn</sup>/Pink1<sup>tm1Shn</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060369	Parkinson's disease 6						ECO:0000033	author statement supported by traceable reference	PMID:17563363	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174973	Neurod1<sup>tm1Mjts</sup>/Neurod1<sup>tm1Mjts</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0110746	type 1 diabetes mellitus 7						ECO:0000033	author statement supported by traceable reference	PMID:9308961	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007927	Mefv<sup>tm4.1(MEFV)Chae</sup>/Mefv<sup>tm4.1(MEFV)Chae</sup>  [background:] B6.129S6-Mefv<sup>tm4.1(MEFV)Chae</sup>	is_model_of	DOID:2987	familial mediterranean fever						ECO:0000033	author statement supported by traceable reference	PMID:21600797	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256982	Rhbdf2<sup>cub</sup>/Rhbdf2<sup>cub</sup>  [background:] MRL.Cg-Rhbdf2<sup>cub</sup>	is_model_of	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29116018	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799157	None [background:] C58/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:29885454	20181028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687954	Uox<sup>in</sup>/Uox<sup>in</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:11474184	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300824	Tg(Tnfsf13b)1Fma/Tg(Tnfsf13b)1Fma  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:21881212	20120109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473834	Tg(SFTPC-rtTA)2Jaw/0 Tg(tetO-CTGF)#Swu/0  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:0050161	lower respiratory tract disease						ECO:0000033	author statement supported by traceable reference	PMID:21239535	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5486338	Cybb<sup>tm1Din</sup>/Cybb<sup>tm1Din</sup>  [background:] B6.129S-Cybb<sup>tm1Din</sup>/J	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762988	Tg(MMTV-NCOA3)#Mybr/0  [background:] FVB/N-Tg(MMTV-NCOA3)#Mybr	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:15380517	20160422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000279	Tg(AR*100Q)C25Als/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:15003169	20110527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000244	Boc<sup>tm1Rsk</sup>/Boc<sup>+</sup> Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * 129S6/SvEvTac	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21183473	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183034	Csf3r<sup>tm1Eur</sup>/Csf3r<sup>tm1Eur</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:0090120	hereditary neutrophilia						ECO:0000033	author statement supported by traceable reference	PMID:9639496	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197063	Atp1a3<sup>tm1Mika</sup>/Atp1a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050635	alternating hemiplegia of childhood						ECO:0000033	author statement supported by traceable reference	PMID:30071271	20180907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052741	Pcca<sup>tm1Tmiy</sup>/Pcca<sup>tm1Tmiy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14701	propionic acidemia						ECO:0000033	author statement supported by traceable reference	PMID:11461925	20200414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829628	Runx2<sup>tm1Jals</sup>/Runx2<sup>tm1Jals</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19028669	20090130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6754173	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818533	Coro1a<sup>tm1Achn</sup>/Coro1a<sup>tm1Achn</sup>  [background:] B6.129X1-Coro1a<sup>tm1Achn</sup>	is_model_of	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776838	Pax1<sup>un</sup>/Pax1<sup>+</sup> Tcf3<sup>tm1Cmu</sup>/Tcf3<sup>tm1Cmu</sup>  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:16315099	20080410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438261	Amelx<sup>Rgsc888</sup>/Y  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797606	Lgr4<sup>Gt(LST020)Byg</sup>/Lgr4<sup>Gt(LST020)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:18424556	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473661	Gt(ROSA)26Sor<sup>tm1(CAG-SNCA)Tanj</sup>/Gt(ROSA)26Sor<sup>tm1(CAG-SNCA)Tanj</sup> Tg(Plp1-cre/ERT)3Pop/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl * DBA/2	is_model_of	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:30910745	20201124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6437232	Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>/Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>  [background:] B6N(Cg)-Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:31844321	20210427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5828862	Tg(Prnp-TARDBP)96Dwc/0 Tg(Prnp-TARDBP*Q331K)31Dwc/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:26108367	20170320	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700949	Tg(Myh6-CASQ2)1Mord/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:10428792	20170824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7264531	Pbx1<sup>em1Dunw</sup>/Pbx1<sup>em1Dunw</sup>  [background:] C57BL/6J-Pbx1<sup>em1Dunw</sup>	is_model_of	DOID:0112359	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay						ECO:0000033	author statement supported by traceable reference	PMID:31625560	20220502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693295	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:17021169	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7493642	Foxi3<sup>em1Ybz</sup>/Foxi3<sup>em1Ybz</sup>  [background:] C57BL/6-Foxi3<sup>em1Ybz</sup>	is_model_of	DOID:2907	Goldenhar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:37041148	20230628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558947	Tnf<sup>tm2.1Gkl</sup>/Tnf<sup>tm2.1Gkl</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129S/SvEv * FVB/N	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:23977323	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471464	B4gat1<sup>m1Ddg</sup>/B4gat1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C3H/He * C57BL/6 * C57BL/6NTac	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:23217742	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624674	Mecp2<sup>tm1.1Jae</sup>/Y  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242118	20060619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4443335	Best1<sup>tm1.1Amar</sup>/Best1<sup>tm1.1Amar</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:0050661	vitelliform macular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7262709	Tg(KRT18*R89C)30Rgo/0  [background:] involves: FVB/N	is_model_of	DOID:2237	hepatitis						ECO:0000033	author statement supported by traceable reference	PMID:8522591	20220419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446500	Tg(Fabp4-SREBF1)#Dajl/0  [background:] involves: FVB	is_model_of	DOID:811	lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22792234	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042302	Phc1<sup>tm1Os</sup>/Phc1<sup>tm1Os</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:9367423	20101001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825021	Slc6a8<sup>tm1.2Lbar</sup>/Y  [background:] involves: 129 * 129S1/Sv * C57BL/6N	is_model_of	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:25485098	20170224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836157	Tg(MMTV-AURKA)#Cxd/?  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:16715125	20090317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6719084	Nemf<sup>pdft</sup>/Nemf<sup>pdft</sup>  [background:] B6(C3)-Nemf<sup>pdft</sup>/Cx	is_model_of	DOID:870	neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575317	Efna5<sup>tm1Ddmo</sup>/Efna5<sup>tm1Ddmo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060668	anencephaly						ECO:0000033	author statement supported by traceable reference	PMID:11089974	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198752	Zfp462<sup>Tn(pb-Act-RFP)1.090115023-HRAZhu</sup>/Zfp462<sup>+</sup>  [background:] involves: FVB/N	is_model_of	DOID:14320	generalized anxiety disorder						ECO:0000033	author statement supported by traceable reference	PMID:27621227	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6693811	Dhdds<sup>tm1.1Sjpi</sup>/Dhdds<sup>tm1.1Sjpi</sup> Tg(BEST1-rtTA,tetO-cre)1Yzl/0  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0110352	retinitis pigmentosa 59						ECO:0000033	author statement supported by traceable reference	PMID:32245241	20210421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6111393	Tg(Ins2-IAPP)L13Gjsc/0  [background:] FVB/N-Tg(Ins2-IAPP)L13Gjsc	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:18633116	20180122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516012	b2b2153Clo/b2b2153Clo  [background:] C57BL/6J-b2b2153Clo	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110012	Atm<sup>tm1.1Mmpl</sup>/Atm<sup>tm1.1Mmpl</sup>  [background:] involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:26310626	20180115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6306309	Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup> Tg(HBB*)L2Pai/0  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:15780748	20190530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781017	Tg(Mup3-Plau)350-2Eps/?  [background:] C57BL/6-Tg(Mup3-Plau)350-2Eps	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:25132496	20160722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559229	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0 Tg(Thy1-MAPT*)30Schd/0  [background:] involves: C57BL/6 * C57BL/6J * CBA * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24076100	20140417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767200	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup> Heph<sup>sla</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:18326691	20130805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2667689	Noa/Noa<sup>+</sup>  [background:] NOA	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	MGI:1097454	20100208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523889	Scn1a<sup>tm2.1Kzy</sup>/Scn1a<sup>tm2.1Kzy</sup> Tg(Pvalb-cre)1Tama/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23922229	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368208	Brd4<sup>M1Rvt</sup>/Brd4<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH	is_model_of	DOID:12679	nephrocalcinosis						ECO:0000033	author statement supported by traceable reference	PMID:30830987	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936865	Dmd<sup>mdx</sup>/Y Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup>  [background:] involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21145579	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266284	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * CD-1	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638045	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Scrib<sup>tm1.1Phum</sup>/Scrib<sup>tm1.1Phum</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24276238	20150602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653234	Cryaa<sup>Aey7</sup>/Cryaa<sup>+</sup>  [background:] C3HeB/FeJ-Cryaa<sup>Aey7</sup>/Ieg	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11687536	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6359449	Coq8a<sup>tm1.1Ics</sup>/Coq8a<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N	is_model_of	DOID:0070241	primary coenzyme Q10 deficiency 4						ECO:0000033	author statement supported by traceable reference	PMID:27499294	20190911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040327	Ptch1<sup>tm1Zim</sup>/Ptch1<sup>+</sup>  [background:] involves: 129 * CD-1	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:12386820	20101104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5320445	Ush1g<sup>js-3J</sup>/Ush1g<sup>js-3J</sup>  [background:] B6.Cg-Ush1g<sup>js-3J</sup>/Kjn	is_model_of	DOID:0110834	Usher syndrome type 1G						ECO:0000033	author statement supported by traceable reference	MGI:5320439	20120606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6501768	Cpa1<sup>tm1.1Satom</sup>/Cpa1<sup>tm1.1Satom</sup>  [background:] involves: C57BL/6NCrl * FVB/N	is_model_of	DOID:4989	pancreatitis						ECO:0000033	author statement supported by traceable reference	PMID:30045879	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360302	Tg(Myh6-CREB1*S133A)1Jml/0  [background:] involves: CD-1	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:9616213	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487655	Abhd12<sup>tm1Crv</sup>/Abhd12<sup>tm1Crv</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080181	PHARC syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23297193	20130529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311758	Rarres1<sup>tm1d(KOMP)Wtsi</sup>/Rarres1<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0050873	follicular lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606783	Tg(Lim2*G15V)1Rlc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110263	cataract 19 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:10851259	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7439148	Iigp1c<sup>em1Btlr</sup>/Iigp1c<sup>em1Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>em1Btlr</sup>	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437108	b2b227.2Clo/b2b227.2Clo  [background:] C57BL/6J-b2b227.2Clo	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>	is_model_of	DOID:0080046	Stickler syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699178	Gba1<sup>tm1Clk</sup>/Gba1<sup>tm1.1Clk</sup> Tg(Tek-cre)12Flv/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J	is_model_of	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:17079175	20070308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749790	Tg(Camk2a-MAPT)601Ymot/0  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:21324362	20160223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467575	Cenpf<sup>tm1Dbdr</sup>/Cenpf<sup>tm1Dbdr</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: C57BL/6 * DBA/2 * ICR	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22563055	20170809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784537	Tg(Eno2tTA)5030Nes/0 Tg(tetO-NRG1_i4)6Ajla/0  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:27122041	20160726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574653	Msmb<sup>tm1Xuan</sup>/Msmb<sup>tm1Xuan</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:15674347	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449181	Ank1<sup>nb</sup>/Ank1<sup>nb</sup>  [background:] either: (involves: non-inbred stock) or (involves: C57BL/6) or (involves: WB/Re)	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:1716634	20050601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5466335	Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Chx10-EGFP/cre,-ALPP)2Clc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * SJL	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:23001562	20140917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836725	Efhc1<sup>tm1Kzy</sup>/Efhc1<sup>+</sup>  [background:] B6.129P2-Efhc1<sup>tm1Kzy</sup>	is_model_of	DOID:4890	juvenile myoclonic epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:19147686	20090323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905888	A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup> Tg(Myh6-2A)#Know/0  [background:] involves: BALB/c * C57BL/6 * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17190866	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524138	Fat1<sup>tm1.2Fhel</sup>/Fat1<sup>tm1.2Fhel</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J * SJL	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538529	Smarcb1<sup>tm1Sho</sup>/Smarcb1<sup>+</sup> Tg(LPV-TAg121)2Tvd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J	is_model_of	DOID:2626	choroid plexus papilloma						ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579385	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:14722612	20050613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177637	Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup> Tg(Myhca-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB	is_model_of	DOID:12934	Kearns-Sayre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10737799	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393314	Tfap2b<sup>em1Fenli</sup>/Tfap2b<sup>em1Fenli</sup>  [background:] involves: C57BL/6	is_model_of	DOID:13832	patent ductus arteriosus						ECO:0000033	author statement supported by traceable reference	PMID:29804851	20200305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278556	C9orf72<sup>em1Eggn</sup>/C9orf72<sup>em1Eggn</sup>  [background:] involves: C57BL/6	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583547	Tg(ITGA2)1075Fmw/0 Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446426	Dnah11<sup>b2b1775Clo</sup>/Dnah11<sup>b2b1775Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1775Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668968	Foxj1<sup>tm1Bph</sup>/Foxj1<sup>tm1Bph</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9739041	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177829	Itgb3<sup>tm1Hyn</sup>/Itgb3<sup>tm1Hyn</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0060691	platelet-type bleeding disorder 16						ECO:0000033	author statement supported by traceable reference	PMID:9916135	20070926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575760	Asxl1<sup>tm1.1Mjxu</sup>/Asxl1<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24255920	20140731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710236	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Pax3-cre)1Joe/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392266	Tulp3<sup>m1Kflj</sup>/Tulp3<sup>m1Kflj</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:0080322	polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:30799240	20200228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7331489	Sar1b<sup>em2Emle</sup>/Sar1b<sup>+</sup>  [background:] C57BL/6N-Sar1b<sup>em2Emle</sup>	is_model_of	DOID:0060357	chylomicron retention disease						ECO:0000033	author statement supported by traceable reference	PMID:33964306	20220824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686996	Mitf<sup>Mi-H</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6313628	Tg(MMTV-Scgb1a1)#Abm/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:10470078	20190611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160484	Eif2b5<sup>tm1.1Vdk</sup>/Eif2b5<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037157	Csrp3<sup>tm1Crni</sup>/Csrp3<sup>tm1Crni</sup>  [background:] Not Specified	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:11087268	20171222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450917	Phex<sup>Ska1</sup>/Y  [background:] C57BL/6-Phex<sup>Ska1</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:12414538	20100513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444033	Dcc<sup>Tg(H2-Kb-Jak2*V617F)1Shmd</sup>/Dcc<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:18033315	20121130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651807	Lpl<sup>tm1Bres</sup>/Lpl<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8675619	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5646375	b2b2966Clo/b2b2966Clo  [background:] C57BL/6J-b2b2966Clo	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629331	Postn<sup>tm1Sjc</sup>/Postn<sup>tm1Sjc</sup>  [background:] involves: C57BL/6	is_model_of	DOID:1474	aggressive periodontitis						ECO:0000033	author statement supported by traceable reference	PMID:16314533	20060718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655820	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] B6.Cg-Cyp1b1<sup>tm1Gonz</sup>	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659950	Braf<sup>tm1Wds</sup>/Braf<sup>tm1Wds</sup> Raf1<sup>tm2Bacc</sup>/Raf1<sup>tm2Bacc</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * CBA/J	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18952847	20150826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574541	Dok1<sup>tm1Ppp</sup>/Dok1<sup>tm1Ppp</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: 129S1/Sv	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611295	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776413	Eya4<sup>tm1Jse</sup>/Eya4<sup>tm1Jse</sup>  [background:] involves: 129S6/SvEvTac * CBA/J	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:18219393	20080624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524084	Tg(MMTV-Myc)WT13Jrn/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697204	Ppox<sup>tm1Had</sup>/Ppox<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:4346	variegate porphyria						ECO:0000033	author statement supported by traceable reference	PMID:11929050	20151125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6189180	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:29233179	20190403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029674	Foxl2<sup>tm1Tre</sup>/Foxl2<sup>tm1Tre</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss * CD-1	is_model_of	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14736745	20071022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6201596	Slc9a9<sup>tm2d(KOMP)Wtsi</sup>/Slc9a9<sup>tm2d(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N * SJL	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:29362376	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2671059	Igsf1<sup>tm1Zuk</sup>/Y  [background:] either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	is_model_of	DOID:0111140	IGSF1 deficiency syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23143598	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:16025116	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715141	Lmx1b<sup>tm4.1Rjo</sup>/Lmx1b<sup>tm4.1Rjo</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:9467	nail-patella syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17316599	20070718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6193917	Tg(Myh6-Prkaca)2Eno/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11717156	20180809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174910	Rag2<sup>tm1Fwa</sup>/Rag2<sup>tm1Fwa</sup>  [background:] involves: 129S/SvEv * MF1	is_model_of	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:1547487	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6450809	Myocd<sup>em1Blk</sup>/Myocd<sup>tm1.1Msp</sup>  [background:] involves: 129	is_model_of	DOID:0112014	congenital megabladder						ECO:0000033	author statement supported by traceable reference	PMID:31513549	20211027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663794	Gnrh1<sup>hpg</sup>/Gnrh1<sup>hpg</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:0090072	hypogonadotropic hypogonadism 12 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:198666	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813319	Tg(SOD1*G93A)<sup>dl</sup>1Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:9382875	20081030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5607167	Enpp1<sup>asj-2J</sup>/Enpp1<sup>asj-2J</sup>  [background:] BALB/cJ-Enpp1<sup>asj-2J</sup>/GrsrJ	is_model_of	DOID:0050644	arterial calcification of infancy						ECO:0000033	author statement supported by traceable reference	PMID:25479107	20141215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720087	Hba<sup>b3(th)</sup>/Hba<sup>+</sup>  [background:] involves: C57BL/6J * SEC	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:6950407	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412191	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:20159112	20120326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6201594	Slc9a9<sup>tm2c(KOMP)Wtsi</sup>/Slc9a9<sup>tm2c(KOMP)Wtsi</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6N * SJL	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:29362376	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693614	Gata3<sup>tm1Gsv</sup>/Gata3<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15207274	20070115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277820	Gt(ROSA)26Sor<sup>tm1(CAG-MYCN,-luc)Jhsc</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Rb1<sup>tm2Brn</sup>/Rb1<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129 * 129S1/Sv * 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:2992	prostate neuroendocrine neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:34099734	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655576	Ostm1<sup>gl</sup>/Ostm1<sup>gl</sup>  [background:] GL/Le Edar<sup>dl-J</sup> +/+ Ostm1<sup>gl</sup>/J	is_model_of	DOID:0110939	autosomal recessive osteopetrosis 5						ECO:0000033	author statement supported by traceable reference	PMID:1155801	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763425	Flt3<sup>tm1Dgg</sup>/Flt3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:17936561	20160111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392256	Hnf4a<sup>tm1Sad</sup>/Hnf4a<sup>tm1Sad</sup> Six2<sup>tm1(tTA,tetO-EGFP/cre)Amc</sup>/Six2<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:1062	Fanconi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30046000	20200228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698637	Abcg2<sup>tm1Ahs</sup>/Abcg2<sup>tm1Ahs</sup>  [background:] FVB.129P2-Abcg2<sup>tm1Ahs</sup>/Tac	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:22473008	20210319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832892	Tg(Thy1-MAPT*V337M)1Godt/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:17517691	20090223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622299	Tg(Myh6-Tmod1)65Msus/Tg(Myh6-Tmod1)65Msus  [background:] involves: FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:9421465	20170724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038220	Gck<sup>Rgsc475</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5776501	Tg(Plp)72Kan/Tg(Plp)72Kan  [background:] B6N.Cg-Tg(Plp)72Kan	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:20091761	20160621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829793	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S4/SvJae * FVB	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12163417	20100916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045985	Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup>  [background:] Not Specified	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:24009558	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766096	Tshr<sup>tm1Rmar</sup>/Tshr<sup>tm1Rmar</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:12432094	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6194786	Abcd1<sup>tm1Kan</sup>/Y Gt(ROSA)26Sor<sup>tm2.1(CAG-ELOVL1)Geno</sup>/Gt(ROSA)26Sor<sup>+</sup> Cnp<sup>tm1(cre)Kan</sup>/Cnp<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27124591	20180816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3662853	F9<sup>tm1Emg</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:9639513	20061005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514360	Col6a3<sup>tm1Chu</sup>/Col6a3<sup>tm1Chu</sup>  [background:] B6.129-Col6a3<sup>tm1Chu</sup>	is_model_of	DOID:0050557	congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23564457	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033418	Acvrl1<sup>tm1Enl</sup>/Acvrl1<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:12588795	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428435	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Cyp19a1<sup>tm1Esi</sup>/Cyp19a1<sup>tm1Esi</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22185842	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:1712	aortic valve stenosis						ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6118197	Apela<sup>tm1.2Brre</sup>/Apela<sup>tm1.2Brre</sup>  [background:] B6(Cg)-Apela<sup>tm1.2Brre</sup>	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:28663440	20180301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307127	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] 129S6/SvEvTac-Was<sup>tm1Sbs</sup>/J	is_model_of	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22079330	20120226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653142	Rhbdf2<sup>cub</sup>/Rhbdf2<sup>cub</sup>  [background:] B6.Cg-Rhbdf2<sup>cub</sup>	is_model_of	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29116018	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415340	Tg(FOXJ1-ACE2)1Rba/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26976607	20200507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5500934	Del(XNxf2-Nxf3)1Jw/+  [background:] involves: 129S4/SvJae * C57BL/6 * FVB	is_model_of	DOID:0060388	chromosomal deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24569167	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665480	Wrn<sup>tm1Led</sup>/Wrn<sup>tm1Led</sup>  [background:] B6.129S6(BKSW)-Wrn<sup>tm1Led</sup>	is_model_of	DOID:5688	Werner syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16330174	20061103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4847595	App<sup>tm1Ck</sup>/App<sup>tm1Ck</sup> Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22336193	20140904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906758	Nsmce2<sup>tm2.1Ofc</sup>/Nsmce2<sup>tm2.1Ofc</sup> Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/0  [background:] involves: 129S/SvEv * C57BL/6 * SJL	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26443207	20170811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196101	F9<sup>em1Dlli</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:26964564	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804217	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Gfap-cre)2Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:10783170	20080903	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295357	Gnao1<sup>em1Rneu</sup>/Gnao1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrl	is_model_of	DOID:0080450	developmental and epileptic encephalopathy 17						ECO:0000033	author statement supported by traceable reference	PMID:30682176	20190501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6197223	Tg(Cebpb-tTA)5Bjd/0 Tg(tetO-MYC,-OVAL)#Gtgm/0  [background:] B6J.Cg-Tg(Cebpb-tTA)5Bjd Tg(tetO-MYC,-OVAL)#Gtgm	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19105207	20180910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796169	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>+</sup> Tg(Col1a1-cre)1Kry/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:26659571	20160930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679598	Tg(MMTV-PyVT)634Mul/0  [background:] FVB/N-Tg(MMTV-PyVT)634Mul/Nci	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:1312220	20080617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6098754	Mecp2<sup>tm2Bird</sup>/Y  [background:] B6.129P2-Mecp2<sup>tm2Bird</sup>/J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318689	Chrnb2<sup>tm1Jpc</sup>/Chrnb2<sup>tm1Jpc</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:12876201	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314653	Grhpr<sup>Gt(OST383093)Lex</sup>/Grhpr<sup>Gt(OST383093)Lex</sup>  [background:] B6.129S5-Grhpr<sup>Gt(OST383093)Lex</sup>	is_model_of	DOID:0111671	primary hyperoxaluria type 2						ECO:0000033	author statement supported by traceable reference	PMID:22189945	20201118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286097	Tg(GFAP-Hras1)2Agu/Tg(GFAP-Hras1)2Agu  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:11325859	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4442335	Pten<sup>tm2.1Gle</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20194734	20100504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680512	Gba1<sup>tm4Ggb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417932	Slitrk6<sup>tm1.1Jaru</sup>/Slitrk6<sup>tm1.1Jaru</sup>  [background:] B6.129P2-Slitrk6<sup>tm1.1Jaru</sup>	is_model_of	DOID:0111628	high myopia-sensorineural deafness syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23543054	20221103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5823987	Tmco1<sup>em1Smoc</sup>/Tmco1<sup>em1Smoc</sup>  [background:] C57BL/6J-Tmco1<sup>em1Smoc</sup>	is_model_of	DOID:0081072	craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27212239	20220616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028887	Btk<sup>tm1Wk</sup>/Btk<sup>tm1Wk</sup> Tec<sup>tm1Welm</sup>/Tec<sup>tm1Welm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:11104803	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452344	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0110887	inflammatory bowel disease 12						ECO:0000033	author statement supported by traceable reference	PMID:15219458	20100519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905050	Tg(Myh6-Gnaq*Q209L)44Ejne/Tg(Myh6-Gnaq*Q209L)44Ejne  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11448136	20170719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716929	Kiss1<sup>tm1Coll</sup>/Kiss1<sup>tm1Coll</sup>  [background:] involves: 129S/SvEv * 129S6/SvEvTac	is_model_of	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:17563351	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670272	Ro60<sup>tm1Woln</sup>/Ro60<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583686	Gck<sup>tm1Tka</sup>/Gck<sup>+</sup>  [background:] involves: 129X1/SvJ * ICR	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:8530440	20050816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661390	Agl<sup>tm1Geno</sup>/Agl<sup>tm1Geno</sup>  [background:] C57BL/6J-Agl<sup>tm1Geno</sup>	is_model_of	DOID:2748	glycogen storage disease III						ECO:0000033	author statement supported by traceable reference	PMID:25092169	20150910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312335	b2b386Clo/b2b386Clo  [background:] C57BL/6J-b2b386Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3578115	Abca1<sup>tm1.1Jp</sup>/Abca1<sup>tm1.1Jp</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:15841208	20050526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176972	Nr3c1<sup>tm2Gsc</sup>/Nr3c1<sup>tm2Gsc</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL	is_model_of	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:10471508	20171210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527439	Nbeal2<sup>tm1Lex</sup>/Nbeal2<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:0111044	gray platelet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23863626	20140110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179030	Pten<sup>tm1Mak</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10910075	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583154	Enc/Enc<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538404	Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:23843985	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429215	Ulk4<sup>tm1Lex</sup>/Ulk4<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511747	Lepr<sup>tm1.1Chua</sup>/Lepr<sup>tm1.1Chua</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15389315	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718076	Tg(PDGFB-MAPT*V337M)1Atak/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11756496	20140313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5560505	Rfx3<sup>b2b1213Clo</sup>/Rfx3<sup>b2b1213Clo</sup>  [background:] C57BL/6J-Rfx3<sup>b2b1213Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461806	Fgfr2<sup>m1Sgg</sup>/Fgfr2<sup>m1Sgg</sup>  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20503384	20100726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904950	Tg(Myh6-Rab1a)medGwd/0  [background:] involves: FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11739277	20170718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606703	Chst3<sup>tm1Dgen</sup>/Chst3<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839655	Tg(Prnp-TARDBP)4Jlel/0  [background:] involves: C57BL/6 * CD-1 * SJL	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:20621187	20101130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842683	Gnmt<sup>tm1Ymac</sup>/Gnmt<sup>tm1Ymac</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19035462	20150807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6314805	Cfh<sup>tm1.1Song</sup>/Cfh<sup>tm1.1Song</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28057640	20190625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6852760	Smpx<sup>em2Jgao</sup>/Smpx<sup>em2Jgao</sup>  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>	is_model_of	DOID:0111735	X-linked deafness 4						ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836162	Prph2<sup>tm1Nmc</sup>/Prph2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110383	retinitis pigmentosa 7						ECO:0000033	author statement supported by traceable reference	PMID:11978760	20090317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5700318	Hps4<sup>le</sup>/Hps4<sup>le</sup> Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>/J	is_model_of	DOID:0060542	Hermansky-Pudlak syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:25477496	20151231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604280	En1<sup>tm2Alj</sup>/En1<sup>+</sup> Tg(Th-EGFP)6-7Okn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J * OF1	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:25281317	20141113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844352	Arx<sup>tm1Gldn</sup>/Y Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:19439424	20090515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157364	Mmut<sup>tm1.1Mrb</sup>/Mmut<sup>tm1.1Mrb</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:27519416	20180521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822319	Tg(S100b-v-erbB)4496Waw/0  [background:] involves: C57BL/6J * DBA/2J * FVB/N	is_model_of	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:12670909	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697474	Bin1<sup>tm1Gcp</sup>/Bin1<sup>tm2Gcp</sup> Tg(MMTV-Myc)141-3Led/0 Tg(Wap-cre)11738Mam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	MGI:3697335	20080612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624717	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>tm1.1Bird</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242117	20060619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039437	Sell<sup>tm1Flv</sup>/Sell<sup>+</sup>  [background:] NOD.Cg-Sell<sup>tm1Flv</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7378550	Setd1a<sup>em1Yzhg</sup>/Setd1a<sup>+</sup>  [background:] B6.Cg-Setd1a<sup>em1Yzhg</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:35245111	20221103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324051	Tg(CAG-Ptafr)1Tksh/0  [background:] B6;D2-Tg(CAG-Ptafr)1Tksh/TkshRbrc	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:9009274	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836241	Tg(Pbsn-TAg)15Tvd/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:16288012	20101025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6270159	Tg(Nell1)1Ting/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:2340	craniosynostosis						ECO:0000033	author statement supported by traceable reference	PMID:12235118	20181231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715602	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11069286	20070723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312936	Nhlrc1<sup>tm1.2Geno</sup>/Nhlrc1<sup>tm1.2Geno</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:22186026	20120327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3847120	Lepr<sup>brta</sup>/Lepr<sup>brta</sup>  [background:] C57BL/6JSfdAnu-Lepr<sup>brta</sup>/Anu	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	MGI:3611487	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813631	Tg(SV40-Igh-64C8)H3Hon/0 Tg(SV40-Igk4C8)L1Hon/0  [background:] involves: C57BL/6	is_model_of	DOID:718	autoimmune hemolytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:1730928	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6506379	Dnm2<sup>tm2.1Ics</sup>/Dnm2<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:423	myopathy						ECO:0000033	author statement supported by traceable reference	PMID:32129442	20210216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769910	Nos2<sup>tm1Lau</sup>/Nos2<sup>tm1Lau</sup> Tg(APPSWE)2576Kha/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16908860	20080206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052046	Tg(Myh7-Pln)2Egk/0  [background:] FVB/N-Tg(Myh7-Pln)2Egk	is_model_of	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:26035394	20180112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832989	Tg(CMV-TOR1A*)2Nush/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:15930383	20090223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445974	Odad3<sup>b2b1885Clo</sup>/Odad3<sup>b2b1885Clo</sup>  [background:] C57BL/6J-Odad3<sup>b2b1885Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688527	Aqp2<sup>tm1(AQP2)Suc</sup>/Aqp2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:16968783	20061122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5495922	Nbea<sup>Tg(GH1)240BNec</sup>/Nbea<sup>+</sup>  [background:] B6JRj.Cg-Nbea<sup>Tg(GH1)240BNec</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23153818	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5646171	Tg(Thy1-APPSw)10Jiri/0 Tg(Thy1-PSEN1*M146V)#Jiri/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25620700	20150807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178041	Smarcad1<sup>tm1Gos</sup>/Smarcad1<sup>tm1Gos</sup>  [background:] 129S2/SvPas-Smarcad1<sup>tm1Gos</sup>	is_model_of	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22912419	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849867	Glis3<sup>tm1Hiha</sup>/Glis3<sup>tm1Hiha</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:19481545	20090708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028000	Pde6b<sup>atrd1</sup>/Pde6b<sup>atrd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192446	Hprt1<sup>tm1(MAPT)Dph</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:680	tauopathy						ECO:0000033	author statement supported by traceable reference	PMID:27297240	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437062	Is(14)1Rdf Is(14)2Rdf/Del(14Trim13-Dleu2)4Rdf Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20060366	20100311	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418721	nad/nad  [background:] C(D2)-nad	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:16542671	20100201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307063	Tg(CTSG-NUMA1/RARA)#Skr/0  [background:] involves: C57BL/6	is_model_of	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:14737102	20120224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897011	Dmd<sup>tm1Kmf</sup>/Y  [background:] involves: C57BL/6	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26365037	20170510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281769	Satb1<sup>tm2Kos</sup>/Satb1<sup>tm2Kos</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * CBA/Ca	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29127143	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154156	Trip11<sup>tm1.1Psmi</sup>/Trip11<sup>tm1.2Psmi</sup> Gt(ROSA)26Sor<sup>tm4(ACTB-tdTomato,-EGFP)Luo</sup>/? Tg(Col2a1-cre)1Bhr/?  [background:] involves: 129/Sv * C57BL/6 * SJL/J	is_model_of	DOID:0080054	achondrogenesis type IA						ECO:0000033	author statement supported by traceable reference	PMID:29180569	20180503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176786	Brca1<sup>tm1Cxd</sup>/Brca1<sup>tm2Cxd</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	is_model_of	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10319859	20130408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445974	Odad3<sup>b2b1885Clo</sup>/Odad3<sup>b2b1885Clo</sup>  [background:] C57BL/6J-Odad3<sup>b2b1885Clo</sup>	is_model_of	DOID:0110624	primary ciliary dyskinesia 30						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358795	Nr1h3<sup>tm1Djm</sup>/Nr1h3<sup>tm1Djm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19325005	20100511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273993	Tg(RP11-578M14)5Mkru/0  [background:] involves: FVB/N	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29206867	20190121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618238	Sgce<sup>tm1Ygl</sup>/Sgce<sup>tm1Ygl</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6	is_model_of	DOID:0090034	myoclonic dystonia 11						ECO:0000033	author statement supported by traceable reference	PMID:16099459	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619238	Kcnab2<sup>tm1Kmc</sup>/Kcnab2<sup>tm1Kmc</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060410	chromosome 1p36 deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21209188	20110225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6885557	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>/Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup> E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N	is_model_of	DOID:14780	KBG syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33996804	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459095	Tg(Mbp-Pad2)28Fgm/Tg(Mbp-Pad2)28Fgm  [background:] involves: CD-1	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19093029	20100712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367786	Tg(PRNP-APPSweInd)19959Dwst/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21925470	20131101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7413042	Mirc30<sup>em1Hhzg</sup>/Mirc30<sup>em1Hhzg</sup> Tg(Vav1-cre)#Cgp/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6NRj	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:32705746	20221228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000258	Stx1a<sup>tm1Tfuj</sup>/Stx1a<sup>tm1Tfuj</sup>  [background:] B6.Cg-Stx1a<sup>tm1Tfuj</sup>	is_model_of	DOID:150	disease of mental health						ECO:0000033	author statement supported by traceable reference	PMID:20576034	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6377285	Adck2<sup>tm1(KOMP)Vlcg</sup>/Adck2<sup>+</sup>  [background:] C57BL/6-Adck2<sup>tm1(KOMP)Vlcg</sup>	is_model_of	DOID:699	mitochondrial myopathy						ECO:0000033	author statement supported by traceable reference	PMID:31480808	20191118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925391	Cdc73<sup>Gt(RRE190)Byg</sup>/Cdc73<sup>+</sup>  [background:] B6.129P2-Cdc73<sup>Gt(RRE190)Byg</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719706	Atcay<sup>ji-hes</sup>/Atcay<sup>ji-hes</sup>  [background:] C3H/HeJ-Atcay<sup>ji-hes</sup>	is_model_of	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6369622	Relt<sup>em1Jpsi</sup>/Relt<sup>em1Jpsi</sup>  [background:] C57BL/6-Relt<sup>em1Jpsi</sup>	is_model_of	DOID:0111722	amelogenesis imperfecta type 3C						ECO:0000033	author statement supported by traceable reference	PMID:30506946	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6113926	Sox17<sup>tm1Ysk</sup>/Sox17<sup>+</sup>  [background:] B6.129S1-Sox17<sup>tm1Ysk</sup>	is_model_of	DOID:13608	biliary atresia						ECO:0000033	author statement supported by traceable reference	PMID:28432216	20180202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6113926	Sox17<sup>tm1Ysk</sup>/Sox17<sup>+</sup>  [background:] B6.129S1-Sox17<sup>tm1Ysk</sup>	is_model_of	DOID:13608	biliary atresia						ECO:0000033	author statement supported by traceable reference	PMID:23293295	20180202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712780	Tpmt<sup>tm1Rlng</sup>/Tpmt<sup>tm1Rlng</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * NMRI	is_model_of	DOID:0080172	thiopurine S-methyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:17510427	20070626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474009	Cacna1s<sup>tm1.1Cann</sup>/Cacna1s<sup>tm1.1Cann</sup>  [background:] involves: 129	is_model_of	DOID:14452	hypokalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:7962166	20130411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360690	Tg(Eno2-ATN1)3Tx/Tg(Eno2-ATN1)3Tx  [background:] B6.Cg-Tg(Eno2-ATN1)3Tx	is_model_of	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000033	author statement supported by traceable reference	PMID:16407196	20091007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6511096	Agtrap<sup>tm1Tamk</sup>/Agtrap<sup>tm1Tamk</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0060158	acquired metabolic disease						ECO:0000033	author statement supported by traceable reference	PMID:23902639	20210318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6316981	Col13a1<sup>tm3.1Pih</sup>/Col13a1<sup>tm3.1Pih</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110673	congenital myasthenic syndrome 19						ECO:0000033	author statement supported by traceable reference	PMID:28369367	20190710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6151468	Golgb1<sup>em8Lanyu</sup>/Golgb1<sup>em33Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4420313	Gja1<sup>tm1Dlg</sup>/Gja1<sup>tm1Dlg</sup> Tg(GFAP-cre)1Kdmc/0  [background:] involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:17311295	20100201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174994	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:9883847	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157847	Slc12a6<sup>em1Dlp</sup>/Slc12a6<sup>em1Dlp</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:2477	motor peripheral neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:27485015	20180523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6360225	Mrtfb<sup>em1Dsr</sup>/Mrtfb<sup>+</sup> Myh7<sup>em1Dsr</sup>/Myh7<sup>+</sup> Nkx2-5<sup>em1Dsr</sup>/Nkx2-5<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060480	left ventricular noncompaction						ECO:0000033	author statement supported by traceable reference	PMID:31147515	20190918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7466182	Vps35<sup>tm1.1Hlw</sup>/Vps35<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0060897	Parkinson's disease 17						ECO:0000033	author statement supported by traceable reference	PMID:33257649	20230425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7280898	Krt18<sup>tm1Tmm</sup>/Krt18<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27689336	20220526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6729736	Awat2<sup>tm1.2Golc</sup>/Y  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32851726	20210809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511141	Trp63<sup>tm2Brd</sup>/Trp63<sup>tm2Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:10227293	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6513140	Gnao1<sup>em2Rneu</sup>/Gnao1<sup>+</sup>  [background:] C57BL/6J-Gnao1<sup>em2Rneu</sup>	is_model_of	DOID:0112276	neurodevelopmental disorder with involuntary movements						ECO:0000033	author statement supported by traceable reference	PMID:31907305	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6471172	Glra1<sup>m1Cpai</sup>/Glra1<sup>m1Cpai</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060695	hyperekplexia						ECO:0000033	author statement supported by traceable reference	PMID:28724750	20201111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569535	Tg(CMV-HTT*48Q)BTag/Tg(CMV-HTT*48Q)BTag  [background:] involves: FVB/N	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5633987	Tg(H-2K1-Lrp5/Fkbp1a,-luc*)#Dmps/0 Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0  [background:] involves: FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:24305876	20150429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461136	Tg(Tnf)6074Gkl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:9736029	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617909	Sall4<sup>Gt(XE027)Byg</sup>/Sall4<sup>+</sup>  [background:] B6;129P2-Sall4<sup>Gt(XE027)Byg</sup>	is_model_of	DOID:0060747	Duane-radial ray syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16380715	20060328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620093	Chm<sup>tm1.1Seab</sup>/Chm<sup>tm1.1Seab</sup> Tg(Six3-cre)69Frty/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:9821	choroideremia						ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911576	Col1a1<sup>tm2(tetO-GFP/RNAi:Smc1a)Iaai</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:2226	myeloproliferative neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:26438359	20171017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762762	Kiss1<sup>tm1Rla</sup>/Kiss1<sup>tm1Rla</sup>  [background:] involves: 129S1/SvImJ	is_model_of	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia						ECO:0000033	author statement supported by traceable reference	PMID:17595229	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7378853	Dnm2<sup>Rbc12</sup>/Dnm2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:11252	microcytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:28466468	20221107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822321	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>+</sup> Tg(S100b-v-erbB)4496Waw/0  [background:] involves: 129/Sv * C57BL/6J * DBA/2J * FVB/N * SJL	is_model_of	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:12670909	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5614325	Cavin1<sup>tm1Pfp</sup>/Cavin1<sup>tm1Pfp</sup>  [background:] B6.129S6-Cavin1<sup>tm1Pfp</sup>/J	is_model_of	DOID:6432	pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:24303100	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359205	Arx<sup>tm2Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:22565167	20130716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476832	Tg(TARDBP*A315T)#Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:21752789	20130502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3848946	Tg(Pcp2-FMR1*)1Dln/0  [background:] C57BL/6-Tg(Pcp2-Fmr1*)1Dln	is_model_of	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19377084	20090625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3775243	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Tg(SMN1*A2G)2023Ahmb/0 Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:18178576	20080327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790977	Gt(ROSA)26Sor<sup>tm1Sor</sup>/Gt(ROSA)26Sor<sup>tm1Sor</sup> Pten<sup>tm1Mro</sup>/Pten<sup>tm1Mro</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:26704996	20160909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174790	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:10096549	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843916	Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(ARR2/Pbsn-FGF8)3Prb/0 Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:16489020	20101212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2173367	Fgfr2<sup>tm1.1Dsn</sup>/Fgfr2<sup>tm1.1Dsn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10486	intestinal atresia						ECO:0000033	author statement supported by traceable reference	PMID:15234214	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516484	Tgif1<sup>tm1.1Caw</sup>/Tgif1<sup>tm1.1Caw</sup>  [background:] B6.129S-Tgif1<sup>tm1.1Caw</sup>	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:23459932	20131107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513191	Plec<sup>tm1Gwi</sup>/Plec<sup>tm1Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9389647	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7530054	Poc1b<sup>em1Xjzha</sup>/Poc1b<sup>em1Xjzha</sup>  [background:] C57BL/6J-Poc1b<sup>em1Xjzha</sup>	is_model_of	DOID:0070311	oligoasthenoteratozoospermia						ECO:0000033	author statement supported by traceable reference	PMID:37070736	20230925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6695122	Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>/Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:31844321	20210427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392248	Pygl<sup>tm1a(KOMP)Wtsi</sup>/Pygl<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Pygl<sup>tm1a(KOMP)Wtsi</sup>	is_model_of	DOID:2754	glycogen storage disease VI						ECO:0000033	author statement supported by traceable reference	PMID:31701076	20200228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175693	Acc/Acc<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368186	Porcn<sup>tm1.1Lcm</sup>/Y H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6295837	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Lhx2-cre)1Lcar/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:0060648	anterior segment dysgenesis						ECO:0000033	author statement supported by traceable reference	PMID:28250050	20190929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6110828	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(CAG-Bmp4,-EGFP)1Ypc/0  [background:] involves: C57BL/6J * CBA/J * CD-1	is_model_of	DOID:0080313	cleft palate-lateral synechia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24785830	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160486	Eif2b4<sup>tm1.1Vdk</sup>/Eif2b4<sup>tm1.1Vdk</sup> Eif2b5<sup>tm1.1Vdk</sup>/Eif2b5<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6151404	Col2a1<sup>Rgsc413</sup>/Col2a1<sup>Rgsc413</sup>  [background:] involves: C57BL/6JJcl * DBA/2JJcl	is_model_of	DOID:0080027	spondyloepimetaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:26545783	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709293	Nr2e3<sup>rd7</sup>/Nr2e3<sup>rd7</sup>  [background:] B6.Cg-Nr2e3<sup>rd7</sup>/J	is_model_of	DOID:0090059	enhanced S-cone syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16110338	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008634	Gt(ROSA)26Sor<sup>tm2Thl</sup>/Gt(ROSA)26Sor<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Trp53<sup>tm1Thl</sup>/Trp53<sup>tm1Thl</sup> Tyr<sup>c-Brd</sup>/Tyr<sup>c-Brd</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6	is_model_of	DOID:0050804	glioblastoma proneural subtype						ECO:0000033	author statement supported by traceable reference	PMID:21625383	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617392	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S4/SvJae * FVB	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:15579506	20060323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7336151	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] WSB.Cg-Tg(APPswe,PSEN1dE9)85Dbo/How	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:31150388	20220915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7547388	Rab39b<sup>tm1Pdad</sup>/Y  [background:] B6N.Cg-Rab39b<sup>tm1Pdad</sup>	is_model_of	DOID:0112059	non-syndromic X-linked intellectual disability 72						ECO:0000033	author statement supported by traceable reference	PMID:34761259	20231113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449959	Epb41<sup>tm1Cnby</sup>/Epb41<sup>tm1Cnby</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:2373	hereditary elliptocytosis						ECO:0000033	author statement supported by traceable reference	PMID:9927493	20080321	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950027	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>/Dpcd/Poll<sup>Gt(OST280355)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653135	Cdon<sup>tm2Rsk</sup>/Cdon<sup>tm2Rsk</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:12620190	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582926	Crb1<sup>tm1Wij</sup>/Crb1<sup>+</sup> Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Chx10-EGFP/cre,-ALPP)2Clc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL	is_model_of	DOID:0110079	Leber congenital amaurosis 8						ECO:0000033	author statement supported by traceable reference	PMID:24339791	20140918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842683	Gnmt<sup>tm1Ymac</sup>/Gnmt<sup>tm1Ymac</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0111037	glycine N-methyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:17937387	20090504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6890374	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>+</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>	is_model_of	DOID:0111448	progressive myoclonus epilepsy 1B						ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766730	Icam1<sup>tm1Bay</sup>/Icam1<sup>tm1Bay</sup>  [background:] B6.129S7-Icam1<sup>tm1Bay</sup>/J	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:12769195	20130314	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278262	Mafb<sup>tm1.2Good</sup>/Mafb<sup>+</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:12557	Duane retraction syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27181683	20190215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797650	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6 * CBA	is_model_of	DOID:13832	patent ductus arteriosus						ECO:0000033	author statement supported by traceable reference	PMID:18188448	20170816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7517091	Rab33b<sup>em1Rmr</sup>/Rab33b<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0081271	Smith-McCort dysplasia 2						ECO:0000033	author statement supported by traceable reference	PMID:37359363	20230814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6434270	Nr2f1<sup>tm1Mjts</sup>/Nr2f1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0112226	Bosch-Boonstra-Schaaf optic atrophy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31600777	20220113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5465102	b2b1801Clo/b2b1801Clo  [background:] C57BL/6J-b2b1801Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429856	Frem2<sup>b2b1562Clo</sup>/Frem2<sup>b2b1562Clo</sup>  [background:] C57BL/6J-Frem2<sup>b2b1562Clo</sup>	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442129	b2b1639Clo/b2b1639Clo  [background:] C57BL/6J-b2b1639Clo	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044831	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:15071184	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000121	Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>/Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:21499268	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029782	Acads<sup>del-J</sup>/Acads<sup>del-J</sup>  [background:] involves: BALB/cByJ	is_model_of	DOID:0080154	short chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:2712823	20050822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043197	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>tm1.1Kry</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15109498	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809239	Fas<sup>lpr</sup>/Fas<sup>lpr</sup> Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>/Igh-J<sup>+</sup>  [background:] MRL.Cg-Fas<sup>lpr</sup> Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12486097	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566910	Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:21303860	20140606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6195751	Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup>/Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup> Tg(Cd4-cre)1Cwi/0  [background:] involves: C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:5602	T-cell adult acute lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25565005	20180827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430752	Inpp5b<sup>tm1Nbm</sup>/Inpp5b<sup>tm1Nbm</sup> Ocrl<sup>tm1Nbm</sup>/Y Tg(INPP5B)CNbm/0  [background:] involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	is_model_of	DOID:0050699	Dent disease						ECO:0000033	author statement supported by traceable reference	PMID:21183592	20120809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583121	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] KK-Nphp3<sup>pcy</sup>	is_model_of	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:3712587	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722144	pma/pma  [background:] involves: CF-1	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:3948960	20110125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6438177	Dmd<sup>em4Eno</sup>/Dmd<sup>em4Eno</sup>  [background:] C57BL/6-Dmd<sup>em4Eno</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:30854433	20200709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279112	Mapk8<sup>tm1Rjd</sup>/Mapk8<sup>tm1Rjd</sup> Mapk9<sup>tm1Flv</sup>/Mapk9<sup>tm1Flv</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0060249	scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:30664861	20220519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727363	Trpm3<sup>tm1Lex</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6682030	Ryr2<sup>em1Swch</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	PMID:33536282	20210409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581542	Hexa<sup>tm1Cota</sup>/Hexa<sup>tm1Cota</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:3320	Tay-Sachs disease						ECO:0000033	author statement supported by traceable reference	PMID:8747922	20050713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509640	Ppil1<sup>em4Jgg</sup>/Ppil1<sup>em4Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em4Jgg</sup>	is_model_of	DOID:0112325	pontocerebellar hypoplasia type 14						ECO:0000033	author statement supported by traceable reference	PMID:33220177	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:3408670	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272038	Tnf<sup>Bpsm1</sup>/Tnf<sup>+</sup>  [background:] C.Cg-Tnf<sup>Bpsm1</sup>	is_model_of	DOID:4079	heart valve disease						ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294332	Col11a1<sup>cho</sup>/Col11a1<sup>+</sup>  [background:] involves: C57BL/6Fr	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:13130470	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5912300	Tg(Myh6-Tnni3*R193H)594Jmme/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22683325	20171102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192107	Tg(Ela1-Tgfa)150Bri/0 Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11159909	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617499	Brca1<sup>tm1Brn</sup>/Brca1<sup>tm1Brn</sup> Tg(Krt18-EGFP,-TAg121)36Ysng/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583559	Tg(ITGA5)0858Fmw/0 Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578332	Jun<sup>tm4Wag</sup>/Jun<sup>tm4Wag</sup> Junb<sup>tm3Wag</sup>/Junb<sup>tm3Wag</sup> Tg(Krt1-5-cre/ERT)1Ipc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:16163348	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3775225	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Tg(Prnp-SMN)92Ahmb/Tg(Prnp-SMN)92Ahmb Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:18178576	20080327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174870	Tg(Msx2)1Rem/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:2340	craniosynostosis						ECO:0000033	author statement supported by traceable reference	PMID:7597092	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5807153	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/JRj	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:22118645	20190821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574537	Dok1<sup>tm1Yyam</sup>/Dok1<sup>tm1Yyam</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: C57BL/6	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611294	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450723	Abca1<sup>tm1Jdm</sup>/Abca1<sup>tm1Jdm</sup>  [background:] DBA/1LacJ-Abca1<sup>tm1Jdm</sup>	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:10760292	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925277	Clcn2<sup>nmf289</sup>/Clcn2<sup>nmf289</sup>  [background:] CByJ.Cg-Clcn2<sup>nmf289</sup>/Pjn	is_model_of	DOID:10579	leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653050	Ndn<sup>tm1Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10508517	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834442	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-PIK3CA*H1047R)13Lca/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19029981	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559056	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:17676052	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430324	b2b243.2Clo/b2b243.2Clo  [background:] C57BL/6J-b2b243.2Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287981	Timd4<sup>tm1Kuch</sup>/Timd4<sup>tm1Kuch</sup>  [background:] involves: C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907999	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:21195081	20170901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624416	Psen1<sup>tm1Zhe</sup>/Psen1<sup>tm1Zhe</sup> Tg(APPSWE)2576Kha/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16597739	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000259	Stx1a<sup>tm1Tfuj</sup>/Stx1a<sup>+</sup>  [background:] B6.Cg-Stx1a<sup>tm1Tfuj</sup>	is_model_of	DOID:150	disease of mental health						ECO:0000033	author statement supported by traceable reference	PMID:20576034	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7310130	Aqp5<sup>em1Cya</sup>/Aqp5<sup>em1Cya</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33013441	20220706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5629822	Slurp1<sup>tm1Lex</sup>/Slurp1<sup>tm1Lex</sup>  [background:] Not Specified	is_model_of	DOID:0060862	mal de Meleda						ECO:0000033	author statement supported by traceable reference	PMID:24499735	20150415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431511	b2b904.1Clo/b2b904.1Clo  [background:] C57BL/6J-b2b904.1Clo	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6443613	Tg(Tk1-DPP4)27Ysj/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31838832	20200721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6277926	Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup>/Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * C57BL/6N * SJL/J	is_model_of	DOID:0110660	congenital myasthenic syndrome 12						ECO:0000033	author statement supported by traceable reference	PMID:29905857	20190212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393679	Ezh2<sup>tm1.1Nesh</sup>/Ezh2<sup>+</sup> Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:707	B-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:27135738	20200310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2166944	Gli3<sup>Xt-J</sup>/Gli3<sup>Xt-J</sup>  [background:] involves: C3H * CD-1	is_model_of	DOID:14761	Greig cephalopolysyndactyly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8387379	20060322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897625	Tg(TG-RET/NCOA4)3209Rstn/0  [background:] involves: C57BL/6	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:9850089	20170518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429705	Rag2<sup>tm1.1Cgn</sup>/Rag2<sup>tm1.1Cgn</sup> Tg(HLA-DR2)#Lfug/0 Tg(TCROb.1A12)#Lfug/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:10610182	20120731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833392	Tg(Thy1-SERPINI1*G392E)333Icka/0  [background:] involves: C57BL * CD-1 * DBA	is_model_of	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000033	author statement supported by traceable reference	PMID:18940798	20090224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286555	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup> Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] B6.Cg-Ins2<sup>Akita</sup> Ldlr<sup>tm1Her</sup>	is_model_of	DOID:11713	diabetic angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21606463	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804131	Stk39<sup>tm2.1Arte</sup>/Stk39<sup>tm2.1Arte</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25994507	20161020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6437930	Shank3<sup>tm2Cmpl</sup>/Shank3<sup>tm2Cmpl</sup>  [background:] B6.129S6-Shank3<sup>tm2Cmpl</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27492494	20200707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4462833	Ppib<sup>tm1.1Rjb</sup>/Ppib<sup>tm1.1Rjb</sup>  [background:] Not Specified	is_model_of	DOID:0110349	osteogenesis imperfecta type 9						ECO:0000033	author statement supported by traceable reference	PMID:19997487	20160815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009542	Tg(Rbp3-SV40)IT-2Jjw/?  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:8112979	20110701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6288687	Rad54l<sup>em1Murr</sup>/Rad54l<sup>+</sup>  [background:] C57BL/6N-Rad54l<sup>em1Murr</sup>/MurrJ	is_model_of	DOID:0060252	sclerocornea						ECO:0000033	author statement supported by traceable reference	MGI:5576271	20200108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7309963	Spry2<sup>tm1.1Mrt</sup>/Spry2<sup>tm1.1Mrt</sup> Spry4<sup>tm1.2Mrt</sup>/Spry4<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	PMID:34423857	20220705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6093470	Ccn6<sup>tm1.1Cgkl</sup>/Ccn6<sup>tm1.1Cgkl</sup> Tg(MMTV-cre)1Mam/0  [background:] FVB/N-Ccn6<sup>tm1.1Cgkl</sup> Tg(MMTV-cre)1Mam	is_model_of	DOID:4680	breast metaplastic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27819674	20171130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2180104	Nr5a1<sup>tm2Klp</sup>/Nr5a1<sup>tm2.1Klp</sup> Tg(Cga-cre)3Sac/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL	is_model_of	DOID:0090070	hypogonadotropic hypogonadism						ECO:0000033	author statement supported by traceable reference	PMID:11124111	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574638	Tg(Msmb-TAg)186-3Xuan/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:12424611	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308984	Asl<sup>tm1Brle</sup>/Asl<sup>tm1Brle</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:14755	argininosuccinic aciduria						ECO:0000033	author statement supported by traceable reference	PMID:22541557	20130912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587187	Hps4<sup>le</sup>/Hps4<sup>le</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>	is_model_of	DOID:0060542	Hermansky-Pudlak syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:11836498	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3573927	Htt<sup>tm1Detl</sup>/Htt<sup>tm1Detl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11152661	20090223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906283	Tg(APCS-Ifng)5Imeg/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2237	hepatitis						ECO:0000033	author statement supported by traceable reference	PMID:8290572	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868214	Prkaca<sup>tm1Gsm</sup>/Prkaca<sup>+</sup> Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0090029	CINCA Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20940146	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5632165	Tg(Col2a1-Fgfr3/GH)BDor/0  [background:] FVB/N-Tg(Col2a1-Fgfr3/GH)BDor	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:9811582	20150422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286056	Dis3l2<sup>em1Jtm</sup>/Dis3l2<sup>em1Jtm</sup>  [background:] C57BL/6J-Dis3l2<sup>em1Jtm</sup>	is_model_of	DOID:0060476	Perlman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29950491	20190404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655464	Tfr2<sup>tm1Slu</sup>/Tfr2<sup>tm1Slu</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111030	hemochromatosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:12134060	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437112	b2b1291.2Clo/b2b1291.2Clo  [background:] C57BL/6J-b2b1291.2Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804115	Tg(Mafg-Nfe2l1)1Mym/0  [background:] involves: C57BL/6J * DBA/2	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25041126	20161019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417941	Tg(KRT14-Fyn*)aJsey/0  [background:] involves: C57BL/6 * CBA * FVB/N	is_model_of	DOID:3151	skin squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19934324	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657020	Lox<sup>tm1Ikh</sup>/Lox<sup>tm1Ikh</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:12473682	20060706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7260147	Adcy3<sup>tm1Drs</sup>/Adcy3<sup>tm1Drs</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:1470	major depressive disorder						ECO:0000033	author statement supported by traceable reference	PMID:26868444	20220407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6257021	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28806762	20181121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047105	Nfkbiz<sup>tm1Aki</sup>/Nfkbiz<sup>tm1Aki</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050426	Stevens-Johnson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15671285	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582966	Krt17<sup>tm1Cou</sup>/Krt17<sup>tm1Cou</sup> Krt6a/Krt6b<sup>tm1Cou</sup>/Krt6a/Krt6b<sup>tm1Cou</sup> Krt6a/Krt6b<sup>tm1Cou</sup>/Krt6a/Krt6b<sup>tm1Cou</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050449	pachyonychia congenita						ECO:0000033	author statement supported by traceable reference	PMID:15601842	20050804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707432	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Rbl2<sup>tm2.1Tyj</sup>/Rbl2<sup>tm2.1Tyj</sup> Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:17235288	20080501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3514172	Abcg8<sup>tm1Elk</sup>/Abcg8<sup>tm1Elk</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0090019	sitosterolemia						ECO:0000033	author statement supported by traceable reference	PMID:15040800	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574062	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup> Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJae * BALB/c	is_model_of	DOID:1679	cystitis						ECO:0000033	author statement supported by traceable reference	PMID:22432050	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825356	Tcf3<sup>tm1(PBX1)Mlc</sup>/Tcf3<sup>+</sup> Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26301816	20170301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3608977	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:16794820	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830462	Htr2c<sup>tm1.1Eme</sup>/Y  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20394819	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160483	Eif2b4<sup>tm1.1Vdk</sup>/Eif2b4<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842939	Tg(Vav-BCL2)69Jad/0  [background:] involves: C57BL/6J	is_model_of	DOID:0050873	follicular lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:14630790	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583904	Ins2<sup>Akita</sup>/Ins2<sup>+</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:9133560	20050819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664214	Phl1<sup>101/H</sup>/Phl1<sup>101/H</sup>  [background:] involves: 101/H * MBT/Pas	is_model_of	DOID:0110496	autosomal recessive nonsyndromic deafness 38						ECO:0000033	author statement supported by traceable reference	PMID:16897347	20061021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007718	Col2a1<sup>Rgsc856</sup>/Col2a1<sup>Rgsc856</sup>  [background:] involves: C57BL/6JJcl * DBA/2JJcl	is_model_of	DOID:0080027	spondyloepimetaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:21538020	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6471957	Bbs2<sup>tm1.1Huss</sup>/Bbs2<sup>tm1.1Huss</sup>  [background:] involves: 129S6/SvEv * C57BL/6	is_model_of	DOID:0110124	Bardet-Biedl syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:32620959	20201113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188077	None [background:] RFM	is_model_of	DOID:8692	myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:1268835	20180711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300906	Gucy2c<sup>tm1Gar</sup>/Gucy2c<sup>tm1Gar</sup>  [background:] B6.129S6-Gucy2c<sup>tm1Gar</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:21865642	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950056	Pld4<sup>thss</sup>/Pld4<sup>thss</sup>  [background:] BALB/cJ-Pld4<sup>thss</sup>/GrsrJ	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:30679154	20190826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311117	b2b464Clo/b2b464Clo  [background:] C57BL/6J-b2b464Clo	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286497	Tg(Myoc*Y423H)#Sit/0  [background:] B6.FVB-Tg(Myoc*Y423H)#Sit	is_model_of	DOID:1067	open-angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:17108164	20190409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712071	Aqp2<sup>tm1(cre)Blyg</sup>/Aqp2<sup>tm1(cre)Blyg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:17229678	20070619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6466738	Bpnt2<sup>tm1.2Aros</sup>/Bpnt2<sup>tm1.2Aros</sup>  [background:] B6(SJL)-Bpnt2<sup>tm1.2Aros</sup>	is_model_of	DOID:0112224	chondrodysplasia with joint dislocations gPAPP type						ECO:0000033	author statement supported by traceable reference	PMID:30865697	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640358	Fgfr3<sup>tm5.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:11181569	20060810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523475	Tg(DMWD,DMPK*,SIX5)1177Ggo/Tg(DMWD,DMPK*,SIX5)1177Ggo  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:11726559	20131211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6402953	Enpp1<sup>ttw-Ham</sup>/Enpp1<sup>ttw-Ham</sup>  [background:] Jcl:ICR-Enpp1<sup>ttw-Ham</sup>	is_model_of	DOID:0060887	ossification of the posterior longitudinal ligament of spine						ECO:0000033	author statement supported by traceable reference	PMID:24770645	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6272014	Tnni2<sup>tm1Sgao</sup>/Tnni2<sup>tm1Sgao</sup>  [background:] involves: 129 * ICR	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:25340332	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6281675	Chd7<sup>Looper</sup>/Chd7<sup>+</sup>  [background:] BALB/c-Chd7<sup>Looper</sup>	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24840056	20190308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314998	Tmc1<sup>nice</sup>/Tmc1<sup>nice</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437271	Lig4<sup>tm2.1Fwa</sup>/Lig4<sup>tm2.1Fwa</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060021	DNA ligase IV deficiency						ECO:0000033	author statement supported by traceable reference	PMID:20133615	20100315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415340	Tg(FOXJ1-ACE2)1Rba/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32516571	20200608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673834	Hey2<sup>tm1Uts</sup>/Hey2<sup>tm1Uts</sup>  [background:] either: (involves: 129X1/SvJ) or (involves: C57BL/6)	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:12372254	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5647883	Lmx1a<sup>tm1Tpe</sup>/Lmx1a<sup>tm1Tpe</sup> Lmx1b<sup>tm1Zfc</sup>/Lmx1b<sup>tm1Zfc</sup> Slc6a3<sup>tm1(cre)Lrsn</sup>/Slc6a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:25915474	20150812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5642335	Atp13a2<sup>tm1.2Wtd</sup>/Atp13a2<sup>tm1.2Wtd</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25855184	20150702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033884	Loxl1<sup>tm1Tili</sup>/Loxl1<sup>tm1Tili</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:13641	exfoliation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24425853	20200506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6718510	Ift88<sup>tm1Bky</sup>/Ift88<sup>tm1Bky</sup> Nfatc1<sup>tm1.1(cre)Bz</sup>/Nfatc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:61	mitral valve disease						ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659969	Dph1<sup>tm2Bhr</sup>/Dph1<sup>tm2Bhr</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176879	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup> Utrn<sup>tm1Ked</sup>/Utrn<sup>tm1Ked</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9288751	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440449	Tg(CAG-VCP*R155H)55Jpat/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:20147319	20100414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4455033	Kmt2a<sup>tm2(MLLT3)Thr</sup>/Kmt2a<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:10393173	20100616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706545	Tg(Ins2-Nos2)40Okam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16936199	20070502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623481	Col1a1<sup>tm1Jcm</sup>/Col1a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1)	is_model_of	DOID:0110341	osteogenesis imperfecta type 2						ECO:0000033	author statement supported by traceable reference	PMID:10608859	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175141	Nf1<sup>tm1Fcr</sup>/Nf1<sup>tm1Fcr</sup>  [background:] either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:7926784	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:22820288	20130110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713118	Hspg2<sup>tm1Rdgr</sup>/Hspg2<sup>tm1Rdgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:17213231	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437114	Dnah11<sup>b2b1289Clo</sup>/Dnah11<sup>b2b1289Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1289Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838389	Usp1<sup>tm1.1Ada</sup>/Usp1<sup>tm1.1Ada</sup>  [background:] C57BL/6-Usp1<sup>tm1.1Ada</sup>	is_model_of	DOID:13636	Fanconi anemia						ECO:0000033	author statement supported by traceable reference	PMID:19217432	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6682080	Prkar1a<sup>tm1.1Geno</sup>/Prkar1a<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:14669	acrodysostosis						ECO:0000033	author statement supported by traceable reference	PMID:27589370	20210409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6360455	Rab28<sup>tm1d(EUCOMM)Wtsi</sup>/Rab28<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N	is_model_of	DOID:0111024	cone-rod dystrophy 18						ECO:0000033	author statement supported by traceable reference	PMID:30228185	20190919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617490	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:11689485	20060324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6111404	Tcte1<sup>tm1a(KOMP)Wtsi</sup>/Tcte1<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Tcte1<sup>tm1a(KOMP)Wtsi</sup>	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:28630322	20180123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432215	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup> Tg(MUC1)79.24Gend/0  [background:] B6.Cg-Il10<sup>tm1Cgn</sup> Tg(MUC1)79.24Gend	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:17617560	20120827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284278	Vcp<sup>tm1.1Hiok</sup>/Vcp<sup>+</sup>  [background:] B6(Cg)-Vcp<sup>tm1.1Hiok</sup>	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665793	Ar<sup>Tfm</sup>/Y  [background:] STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>/+ +	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:5452809	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397678	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7256635	Cacng8<sup>tm1Ran</sup>/Cacng8<sup>+</sup>  [background:] C57BL/6-Cacng8<sup>tm1Ran</sup>	is_model_of	DOID:10939	antisocial personality disorder						ECO:0000033	author statement supported by traceable reference	PMID:34099816	20220324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911481	Dspp<sup>tm1Kul</sup>/Dspp<sup>tm1Kul</sup>  [background:] B6;129-Dspp<sup>tm1Kul</sup>/Mmnc	is_model_of	DOID:3388	periodontal disease						ECO:0000033	author statement supported by traceable reference	PMID:22934831	20171013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366153	Tg(SFTPC-env)1Yhch/0  [background:] FVB/N-Tg(SFTPC-env)1Yhch	is_model_of	DOID:3910	lung adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28419107	20190115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6119481	Tubb5<sup>tm2.1Dak</sup>/Tubb5<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:26903504	20180305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5908986	Tg(Myh6-Tnnt2*R92L)1Jcf/0  [background:] B6.Cg-Tg(Myh6-Tnnt2*R92L)1Jcf	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:16326803	20170913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N	is_model_of	DOID:0050771	pheochromocytoma						ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5465105	Cox7a1<sup>tm1Hutt</sup>/Cox7a1<sup>tm1Hutt</sup>  [background:] B6.129-Cox7a1<sup>tm1Hutt</sup>	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22119795	20170809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587678	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] involves: STOCK t	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806540	Nrl<sup>tm1Asw</sup>/Nrl<sup>tm1Asw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0090059	enhanced S-cone syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21659555	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574667	Enam<sup>Rgsc521</sup>/Enam<sup>Rgsc521</sup>  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7286353	Specc1l<sup>em4Kumc</sup>/Specc1l<sup>em4Kumc</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:0080698	Teebi hypertelorism syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258657	Vwf<sup>tm1.1Geno</sup>/Vwf<sup>tm1.1Geno</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060574	von Willebrand's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:27212476	20181203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6198763	Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>/Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0050563	nonsyndromic deafness						ECO:0000033	author statement supported by traceable reference	PMID:29590114	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623394	Hnf1a<sup>tm1.1Ylee</sup>/Hnf1a<sup>tm1.1Ylee</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9566924	20060526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530366	Gpc3<sup>tm1Fil</sup>/Gpc3<sup>+</sup>  [background:] B6.Cg-Gpc3<sup>tm1Fil</sup>	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10402475	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720677	Tg(DMD-APP*)18Neve/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:8744400	20070906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694548	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] BKS.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22609345	20121001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818797	Pdgfra<sup>tm2Sor</sup>/Pdgfra<sup>tm2Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:17568391	20100810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7465150	mrs1/Y  [background:] B6.Cg-mrs1/BocJ	is_model_of	DOID:8465	retinoschisis						ECO:0000033	author statement supported by traceable reference	MGI:7464180	20230424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6726265	Tcf20<sup>em1Jwji</sup>/Tcf20<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0080354	Phelan-McDermid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32510763	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6151467	Golgb1<sup>em33Lanyu</sup>/Golgb1<sup>em33Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>	is_model_of	DOID:674	cleft palate						ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6189103	Chd8<sup>tm2.1Kei</sup>/Chd8<sup>+</sup>  [background:] B6J.129P2-Chd8<sup>tm2.1Kei</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27602517	20180720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580003	Tg(Crh)227.1Pbl/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:1597149	20171210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6456764	Sugct<sup>tm1.2Kald</sup>/Sugct<sup>tm1.2Kald</sup>  [background:] B6.Cg-Sugct<sup>tm1.2Kald</sup>	is_model_of	DOID:0112246	glutaric acidemia type 3						ECO:0000033	author statement supported by traceable reference	PMID:31722069	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6278937	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:0111227	chromosome 3-linked frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:27329763	20210201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305581	Hsf4<sup>ldis1</sup>/Hsf4<sup>ldis1</sup>  [background:] involves: C57BL/6 * CAST/EiJ * RIIIS/J	is_model_of	DOID:0110255	cataract 5 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:22162625	20120210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6416454	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>/Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>  [background:] involves: 129	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:28230213	20200514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6191758	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] B6.129S6-Trp53bp2<sup>tm1Xlu</sup>	is_model_of	DOID:0060412	chromosome 1q41-q42 deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412290	Gt(ROSA)26Sor<sup>tm7(CAG-mCherry,-EGFP/tetX)Dym</sup>/Gt(ROSA)26Sor<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/0 Tg(Fev-flpe)1Dym/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:9007	sudden infant death syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27053202	20161101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576740	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] involves: 129S4/SvJae * BALB/c	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11323694	20050513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6105947	Tg(Myh6-Gnaq*Q209L/Esr1*)7Rzl/0  [background:] involves: C57BL/6	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:16210321	20171222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565211	Col6a3<sup>tm2.1Chu</sup>/Col6a3<sup>+</sup>  [background:] B6.129(Cg)-Col6a3<sup>tm2.1Chu</sup>	is_model_of	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24563484	20140522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618597	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] B6.129P2-Nos3<sup>tm1Unc</sup>/J	is_model_of	DOID:62	aortic valve disease						ECO:0000033	author statement supported by traceable reference	PMID:10821808	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681434	Prkn<sup>tm1Shn</sup>/Prkn<sup>tm1Shn</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:12930822	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036853	Sim1<sup>tm1Fan</sup>/Sim1<sup>+</sup> Sim2<sup>tm1Fan</sup>/Sim2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12024028	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582615	Mkks<sup>tm1Vcs</sup>/Mkks<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	is_model_of	DOID:0110128	Bardet-Biedl syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:15772095	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311880	Dync2h1<sup>b2b414Clo</sup>/Dync2h1<sup>b2b414Clo</sup>  [background:] C57BL/6J-Dync2h1<sup>b2b414Clo</sup>	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796444	Vegfa<sup>tm2Pec</sup>/Vegfa<sup>tm2Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:11381259	20080709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450776	Mmp20<sup>tm1Jdb</sup>/Mmp20<sup>tm1Jdb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110060	amelogenesis imperfecta hypomaturation type 2A2						ECO:0000033	author statement supported by traceable reference	PMID:12393861	20090121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762187	Brca1<sup>tm1Brn</sup>/Brca1<sup>tm1Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129P2/OlaHsd * BALB/cJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:17626182	20080624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6383471	Rs1<sup>em1Fegu</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:29379415	20200106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813458	Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:24039817	20140424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651381	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8700894	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651381	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:14634077	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5817471	Rai1<sup>tm2.1Luo</sup>/Rai1<sup>tm2.1Luo</sup> Tg(Nes-cre)1Kln/?  [background:] either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)	is_model_of	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27693255	20170113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6501754	Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>/Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:33168096	20210317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578346	Rps6ka3<sup>tm1.1Kry</sup>/Y  [background:] involves: 129X1/SvJ	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578346	Rps6ka3<sup>tm1.1Kry</sup>/Y  [background:] involves: 129X1/SvJ	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24416220	20140822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578736	Crh<sup>m1H</sup>/Crh<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:24302625	20171210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7339281	Rreb1<sup>em1Rtpl</sup>/Rreb1<sup>+</sup>  [background:] C57BL/6J-Rreb1<sup>em1Rtpl</sup>	is_model_of	DOID:0080690	RASopathy						ECO:0000033	author statement supported by traceable reference	PMID:32938917	20220926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028381	Pde6b<sup>rd1-2H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629203	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0060412	chromosome 1q41-q42 deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446806	Bcs1l<sup>tm1.1Levp</sup>/Bcs1l<sup>tm1.1Levp</sup>  [background:] involves: 129 * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0111455	GRACILE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21274865	20200131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432176	Gt(ROSA)26Sor<sup>tm48(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448549	Tg(SOD1)2Gur/0 Tg(SOD1*G85R)#Roos/0  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19233858	20130110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693491	Tg(PSEN1H163R)G9Btla/0  [background:] involves: 129S4/SvJae	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:10412057	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008441	Tg(Fabp4-LMNA*R482Q)17CCdl/0  [background:] FVB/N-Tg(Fabp4-LMNA*R482Q)17CCdl	is_model_of	DOID:0050440	familial partial lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19201734	20110622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680904	Abcd1<sup>tm1Kds</sup>/Abcd1<sup>tm1Kds</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11875044	20050823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428333	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp*)#Rgab/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:22072968	20120719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618862	Dock1<sup>b2b3190Clo</sup>/Dock1<sup>b2b3190Clo</sup>  [background:] C57BL/6J-Dock1<sup>b2b3190Clo</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727361	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J * CBA	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296515	Sh2b3<sup>tm1Paw</sup>/Sh2b3<sup>tm1Paw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20458146	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829639	Gon4l<sup>justy</sup>/Gon4l<sup>justy</sup>  [background:] C3HeB/FeJ-Gon4l<sup>justy</sup>	is_model_of	DOID:8850	salivary gland cancer						ECO:0000033	author statement supported by traceable reference	PMID:23608756	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474983	Pikfyve<sup>tm2.1Tssk</sup>/Pikfyve<sup>tm2.1Tssk</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:8778	Crohn's disease						ECO:0000033	author statement supported by traceable reference	PMID:23322734	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487835	Mip<sup>Cts</sup>/Mip<sup>Cts</sup>  [background:] CTS/Shi	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:5487779	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5426794	A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup> Tg(CAG-DMPK*)1323Coop/0  [background:] involves: FVB	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:17823658	20120702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6860682	Thap11<sup>em1Poche</sup>/Thap11<sup>em1Poche</sup>  [background:] C57BL/6J-Thap11<sup>em1Poche</sup>	is_model_of	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC						ECO:0000033	author statement supported by traceable reference	PMID:35013307	20220131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793701	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] NOD.129S2(B6)-Aire<sup>tm1.1Doi</sup>/Doi	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764515	Gba1<sup>tm2Karl</sup>/Gba1<sup>tm2Karl</sup> Tg(KRT14-cre)8Brn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:0110958	Gaucher's disease type II						ECO:0000033	author statement supported by traceable reference	PMID:17954912	20071214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727110	Cfap47<sup>em1Fzh</sup>/Y  [background:] C57BL/6-Cfap47<sup>em1Fzh</sup>	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:33472045	20210729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046803	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm3Bld</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284791	Npsr1<sup>em1Yfu</sup>/Npsr1<sup>+</sup>  [background:] C57BL/6J-Npsr1<sup>em1Yfu</sup>	is_model_of	DOID:535	sleep disorder						ECO:0000033	author statement supported by traceable reference	PMID:31619542	20220610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7339120	Rr266<sup>em1Hino</sup>/Rr266<sup>em1Hino</sup> Rr268<sup>em1Hino</sup>/Rr268<sup>em1Hino</sup>  [background:] C57BL/6J-Rr266<sup>em1Hino</sup> Rr268<sup>em1Hino</sup>	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:34645928	20220923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6509037	Eps15<sup>tm1c(KOMP)Wtsi</sup>/Eps15<sup>tm1c(KOMP)Wtsi</sup> Eps15l1<sup>tm2.1Noff</sup>/Eps15l1<sup>tm2.1Noff</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * C57BL/6N * SJL	is_model_of	DOID:0050642	hypochromic microcytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:30692166	20210305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620503	Gnao1<sup>tm2.1Rneu</sup>/Gnao1<sup>+</sup>  [background:] B6.129S-Gnao1<sup>tm2.1Rneu</sup>	is_model_of	DOID:0080450	developmental and epileptic encephalopathy 17						ECO:0000033	author statement supported by traceable reference	PMID:24700286	20190501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669893	Pts<sup>tm1Ich</sup>/Pts<sup>tm1Ich</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0090106	BH4-deficient hyperphenylalaninemia A						ECO:0000033	author statement supported by traceable reference	PMID:11517215	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702873	Gt(ROSA)26Sor<sup>tm1(GNAQ*)Cvrk</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Mitf-cre)7114Gsb/0  [background:] C3FeJ.Cg-Gt(ROSA)26Sor<sup>tm1(GNAQ*)Cvkr</sup> Tg(Mitf-cre)7114Gsb/Cvrk	is_model_of	DOID:6039	uveal melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26113083	20160115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3848974	Tg(Prnp-FTL*)4Ruvi/Tg(Prnp-FTL*)4Ruvi  [background:] B6.C3Fe-Tg(Prnp-FTL*)4Ruvi	is_model_of	DOID:0110737	neurodegeneration with brain iron accumulation 3						ECO:0000033	author statement supported by traceable reference	PMID:18171923	20090626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543898	Tgfbr1<sup>tm1.1Hcd</sup>/Tgfbr1<sup>+</sup>  [background:] 129S6(Cg)-Tgfbr1<sup>tm1.1Hcd</sup>	is_model_of	DOID:0050466	Loeys-Dietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24355923	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563481	Bbip1<sup>tm1.1Gne</sup>/Bbip1<sup>tm1.1Gne</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6N	is_model_of	DOID:0110140	Bardet-Biedl syndrome 18						ECO:0000033	author statement supported by traceable reference	PMID:24316073	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028004	Pde6b<sup>atrd3</sup>/Pde6b<sup>atrd3</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6448988	Cbs<sup>tm1Unc</sup>/Cbs<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:9279	hyperhomocysteinemia						ECO:0000033	author statement supported by traceable reference	PMID:15622513	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432232	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:2999	granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784583	Cryaa<sup>tm1.1Ady</sup>/Cryaa<sup>tm1.1Ady</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:18056999	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055719	Brca2<sup>tm1Mhun</sup>/Brca2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:14981540	20060807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563097	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>tm1.1Teti</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:24185277	20140509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620953	Tg(Camk2a-Magi2)1Shlee/?  [background:] C57BL/6J-Tg(Camk2a-Magi2)1Shlee	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25653350	20150406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432232	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:6032	juvenile type testicular granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648028	Wnt5a<sup>b2b3077.1Clo</sup>/Wnt5a<sup>b2b3077.1Clo</sup>  [background:] C57BL/6J-Wnt5a<sup>b2b3077.1Clo</sup>	is_model_of	DOID:0060254	Robinow syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720080	Hba<sup>b2(th)</sup>/Hba<sup>+</sup>  [background:] involves: C57BL/6J * SEC	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:6950407	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5528689	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24239348	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6302788	Sting1<sup>em1Jmin</sup>/Sting1<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0111457	STING-associated vasculopathy with onset in infancy						ECO:0000033	author statement supported by traceable reference	PMID:28951494	20220209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423170	Gnpat<sup>tm1Just</sup>/Gnpat<sup>tm1Just</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	is_model_of	DOID:150	disease of mental health						ECO:0000033	author statement supported by traceable reference	PMID:31412538	20200518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176343	Pltp<sup>tm1Jia</sup>/Pltp<sup>tm1Jia</sup>  [background:] involves: C57BL/6	is_model_of	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21514421	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587431	Bmp5<sup>se</sup>/Bmp5<sup>se</sup>  [background:] Not Specified	is_model_of	DOID:0060306	Meier-Gorlin syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7710253	20180305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6101205	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Acan<sup>tm1(cre/ERT2)Crm</sup>/Acan<sup>+</sup>  [background:] involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6NCrl	is_model_of	DOID:206	hereditary multiple exostoses						ECO:0000033	author statement supported by traceable reference	PMID:28445472	20171214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3051529	Cyb5r4<sup>tm1Hfb</sup>/Cyb5r4<sup>tm1Hfb</sup>  [background:] involves: 129S4/SvJae * BALB/cAnN	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15247412	20060320	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6718509	Dzip1<sup>em1Sasl</sup>/Dzip1<sup>+</sup>  [background:] C57BL/6J-Dzip1<sup>em1Sasl</sup>	is_model_of	DOID:988	mitral valve prolapse						ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6469470	Sdr9c7<sup>em1Maak</sup>/Sdr9c7<sup>em1Maak</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0080257	autosomal recessive congenital ichthyosis 13						ECO:0000033	author statement supported by traceable reference	PMID:31671075	20201027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678506	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>/Nphs1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12039988	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763111	Tg(MMTV-LPAR3)3Gbm/Tg(MMTV-LPAR3)3Gbm  [background:] FVB/N-Tg(MMTV-LPAR3)3Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428426	Gtf2ird1<sup>tm1Hrd</sup>/Gtf2ird1<sup>tm1Hrd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22198572	20120720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706554	Tg(Ins2-Nos2)40Okam/0 Tg(Kdr-AGER)102Hyam/0  [background:] involves: C57BL/6J * CBA/J * CD-1 * DBA/2	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11457879	20070502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441373	Tg(Rho*G90D*A337V)202Sie/0  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:0110862	congenital stationary night blindness autosomal dominant 1						ECO:0000033	author statement supported by traceable reference	PMID:11466416	20121114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157629	Notch2<sup>tm2.2Ecan</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:2736	Hajdu-Cheney syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28592489	20180523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653844	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB/N)	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:7977654	20100329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404118	Lrp4<sup>tm1.1Pg</sup>/Lrp4<sup>tm1.1Pg</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0060757	sclerosteosis 2						ECO:0000033	author statement supported by traceable reference	PMID:28477420	20200415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652398	Tg(Myh6-Ppara)402-2Dpk/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:9351	diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11781357	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000246	Boc<sup>tm2Rsk</sup>/Boc<sup>+</sup> Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * 129S6/SvEvTac	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21183473	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767200	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup> Heph<sup>sla</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0050711	aceruloplasminemia						ECO:0000033	author statement supported by traceable reference	PMID:15365174	20080110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752257	Ctsd<sup>m1J</sup>/Ctsd<sup>m1J</sup>  [background:] C3HeB/FeJ-Ctsd<sup>m1J</sup>/GrsrJ	is_model_of	DOID:0110725	neuronal ceroid lipofuscinosis 10						ECO:0000033	author statement supported by traceable reference	MGI:5751705	20160317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579845	Tbx20<sup>tm1.1Rph</sup>/Tbx20<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15843414	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6476763	Cd2ap<sup>em1Irgu</sup>/Cd2ap<sup>em1Irgu</sup>  [background:] C57BL/6-Cd2ap<sup>em1Irgu</sup>	is_model_of	DOID:783	end stage renal disease						ECO:0000033	author statement supported by traceable reference	PMID:30612599	20201201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811541	Bmp4<sup>tm2Blh</sup>/Bmp4<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * C57BL/6J	is_model_of	DOID:18	urinary system disease						ECO:0000033	author statement supported by traceable reference	PMID:10749566	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634279	Cacna1f<sup>tm1.2Sdie</sup>/Y  [background:] B6.Cg-Cacna1f<sup>tm1.2Sdie</sup>/J	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304757	Col1a1<sup>tm1(tetO-RNAi:Rps19)Karl</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:21989989	20120202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804499	Tnnt2<sup>tm2Mmto</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:17556660	20080904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038120	Gata1<sup>tm1Mym</sup>/Gata1<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9657742	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821985	Sptbn2<sup>tm1Mjac</sup>/Sptbn2<sup>tm1Mjac</sup>  [background:] B6.129P2-Sptbn2<sup>tm1Mjac</sup>	is_model_of	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000033	author statement supported by traceable reference	PMID:20371805	20100908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505671	Epg5<sup>tm1Ygz</sup>/Epg5<sup>tm1Ygz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	is_model_of	DOID:332	amyotrophic lateral sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23479740	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4888122	Klf15<sup>tm1Jain</sup>/Klf15<sup>tm1Jain</sup>  [background:] B6.129X1-Klf15<sup>tm1Jain</sup>	is_model_of	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:20375365	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722144	pma/pma  [background:] involves: CF-1	is_model_of	DOID:0090124	neurogenic-type arthrogryposis multiplex congenita-2						ECO:0000033	author statement supported by traceable reference	PMID:3948960	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583561	Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7408193	Ts(17<sup>16</sup>)66Yah/0  [background:] involves: C3H/HeSnJ * C57BL/6JEiJ * DBA/2J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36374158	20221215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174783	Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7922305	20050712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056188	Tg(Myh6-Ppp3ca)37Eno/0  [background:] involves: FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:9568714	20170731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5086009	Amer1<sup>tm1.1Nbar</sup>/Y Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:0060886	osteopathia striata with cranial sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21571217	20110815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324047	Shank3<sup>tm2Gfng</sup>/Shank3<sup>+</sup>  [background:] B6.129-Shank3<sup>tm2Gfng</sup>/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27189882	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6378723	Rasa3<sup>scat</sup>/Rasa3<sup>scat</sup>  [background:] involves: BALB/cBy * BALB/cByJ	is_model_of	DOID:12449	aplastic anemia						ECO:0000033	author statement supported by traceable reference	PMID:29922180	20191202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576233	B2m<sup>tm1Jae</sup>/B2m<sup>tm1Jae</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:2352	hemochromatosis						ECO:0000033	author statement supported by traceable reference	PMID:8013958	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175796	Crebbp<sup>tm1Sis</sup>/Crebbp<sup>+</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9294190	20050923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318687	Tg(CMV-IGL@AL080)55Dcs/0  [background:] involves: FVB	is_model_of	DOID:9120	amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:21998211	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769904	Scn5a<sup>tm1Care</sup>/Scn5a<sup>+</sup>  [background:] FVB.129P2-Scn5a<sup>tm1Care</sup>/Care	is_model_of	DOID:0110646	long QT syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:17145985	20080206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2667777	Mgat2<sup>tm1.1Jxm</sup>/Mgat2<sup>tm1.1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0070253	congenital disorder of glycosylation type IIa						ECO:0000033	author statement supported by traceable reference	PMID:11805078	20190516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5439184	Traf3ip2<sup>tm1.1Lix</sup>/Traf3ip2<sup>tm1.1Lix</sup>  [background:] C.129-Traf3ip2<sup>tm1.1Lix</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18624351	20121024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5284901	Pdlim5<sup>tm1Chen</sup>/Pdlim5<sup>tm1Chen</sup> Tg(Tnnt2-cre)5Blh/?  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 * DBA/2	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20538684	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4849441	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Gfap-cre)77.6Mvs/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6NHsd	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:19846776	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711534	Elovl4<sup>tm1Wked</sup>/Elovl4<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:17356513	20070613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7437708	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em2Mdj</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em2Mdj</sup>	is_model_of	DOID:1572	normal pressure hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273835	Gyg1<sup>tm1a(KOMP)Wtsi</sup>/Gyg1<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0050579	glycogen storage disease XV						ECO:0000033	author statement supported by traceable reference	PMID:33219378	20220318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6488175	Kcnq2<sup>tm1.1Lvi</sup>/Kcnq2<sup>+</sup>  [background:] 129-Kcnq2<sup>tm1.1Lvi</sup>/Lvi	is_model_of	DOID:0080462	developmental and epileptic encephalopathy 7						ECO:0000033	author statement supported by traceable reference	PMID:32239694	20201222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404948	Rs1<sup>tm3.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6388658	Pkhd1<sup>em1Mrug</sup>/Pkhd1<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0080212	polycystic kidney disease 4						ECO:0000033	author statement supported by traceable reference	PMID:30600684	20200205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5770244	Brinp1<sup>tm1.1Pib</sup>/Brinp1<sup>tm1.1Pib</sup>  [background:] involves: BALB/cJ * C57BL/6	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:27042284	20160517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6200082	Patl2<sup>tm1b(EUCOMM)Hmgu</sup>/Patl2<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:1100	ovarian disease						ECO:0000033	author statement supported by traceable reference	PMID:29661911	20180927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684307	F13a1<sup>tm1Gdi</sup>/F13a1<sup>tm1Gdi</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:2211	factor XIII deficiency						ECO:0000033	author statement supported by traceable reference	PMID:12933578	20111107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603406	Tg(Ins2-TCF1*P291)2Kya/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0111102	maturity-onset diabetes of the young type 3						ECO:0000033	author statement supported by traceable reference	PMID:11756330	20051101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6389024	Abcc9<sup>em1Nich</sup>/Abcc9<sup>em1Nich</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530609	Dcn<sup>tm1Ioz</sup>/Dcn<sup>tm1Ioz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:13359	Ehlers-Danlos syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9024701	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6890373	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>em1Yzou</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188328	Abca12<sup>smsk</sup>/Abca12<sup>smsk</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:27551807	20180713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821394	Egr1<sup>tm1Jmi</sup>/Egr1<sup>tm1Jmi</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17420284	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175075	Irf8<sup>tm1Hor</sup>/Irf8<sup>+</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	is_model_of	DOID:0060761	familial chronic myelocytic leukemia-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8861914	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183678	Tg(NEFH)200Jpj/0  [background:] Not Specified	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6193619	Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Osr1-cre)4Mrt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:2526	prostate adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21795710	20180807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296512	Jup<sup>tm1.1Shou</sup>/Jup<sup>tm1.1Shou</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:21880664	20111123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6765943	Zfp469<sup>em1Chms</sup>/Zfp469<sup>em1Chms</sup>  [background:] C57BL/6J-Zfp469<sup>em1Chms</sup>	is_model_of	DOID:14775	brittle cornea syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:34368841	20211007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154375	Kifbp<sup>em1Hmy</sup>/Kifbp<sup>em1Hmy</sup>  [background:] Not Specified	is_model_of	DOID:0060481	Goldberg-Shprintzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29192291	20180503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5584173	Del(XNxf2-Nxf3)1Jw/Y  [background:] involves: 129S4/SvJae * C57BL/6 * FVB	is_model_of	DOID:0060388	chromosomal deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24569167	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775199	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Tg(Tal1-cre/ERT)1Jrg/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811553	Pus1<sup>tm1.1Mdf</sup>/Pus1<sup>tm1.1Mdf</sup>  [background:] B6.129S7(C)-Pus1<sup>tm1.1Mdf</sup>	is_model_of	DOID:0080099	myopathy, lactic acidosis, and sideroblastic anemia						ECO:0000033	author statement supported by traceable reference	PMID:27197761	20161209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3607781	Ndn<sup>tm1Ky</sup>/Ndn<sup>+</sup>  [background:] involves: C57BL/6 * CBA * ICR/Slc	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16049186	20051220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586594	Igh-J<sup>tm1Mcdl</sup>/Igh-J<sup>tm1Mcdl</sup> Igk-J<sup>tm1Mcdl</sup>/Igk-J<sup>tm1Mcdl</sup> Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(DO11.10)10Dlo/?  [background:] involves: 129S/Sv * BALB/c * C3H * C57BL/6	is_model_of	DOID:3261	hyper IgE recurrent infection syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11696599	20050901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2659043	Capn3<sup>tm1Jsb</sup>/Capn3<sup>tm1Jsb</sup>  [background:] either: 129/Sv-Capn3<sup>tm1Jsb</sup> or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A						ECO:0000033	author statement supported by traceable reference	PMID:11134085	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616877	gnd/gnd  [background:] C3H/HeJ-gnd	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:1634998	20060317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6364110	Pianp<sup>tm1d(KOMP)Wtsi</sup>/Pianp<sup>tm1d(KOMP)Wtsi</sup>  [background:] involves: BALB/cJ * C57BL/6N * SJL	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:31511635	20210817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491219	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23565506	20130621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628828	Dnmt3b<sup>tm6Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820830	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] KOR-Traf3ip2<sup>adjm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6725719	Clcn1<sup>m1Btlr</sup>/Clcn1<sup>m1Btlr</sup>  [background:] C57BL/6J-Clcn1<sup>m1Btlr</sup>	is_model_of	DOID:2106	myotonia congenita						ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392909	Scn11a<sup>em1Akoi</sup>/Scn11a<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0111731	familial episodic pain syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:27224030	20210120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6415627	Fgfr2<sup>tm3Cxd</sup>/Fgfr2<sup>+</sup> Tg(Col2a1-cre)1Xya/0  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:28123344	20200508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6324210	Atp7a<sup>Mo-blo</sup>/Atp7a<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:6685755	20190722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6274702	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579842	Jak3<sup>tm1Tks</sup>/Jak3<sup>tm1Tks</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:8777722	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720800	Col1a2<sup>oim</sup>/Col1a2<sup>+</sup>  [background:] B6C3Fe a/a-Col1a2<sup>oim</sup>/J	is_model_of	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:8968022	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5443996	Npr2<sup>pwe</sup>/Npr2<sup>pwe</sup>  [background:] involves: C3H/HeJ * C57BL/6 * NAW/WI	is_model_of	DOID:0080050	acromesomelic dysplasia, Maroteaux type						ECO:0000033	author statement supported by traceable reference	PMID:23065701	20121130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838758	Tg(Tagln-rtTA)E1Jwst/0 Tg(tetO-Bmpr2*R899X)#Jwst/0  [background:] involves: FVB/N	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:20562228	20101117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620089	Chm<sup>tm1.2Seab</sup>/Chm<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:9821	choroideremia						ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451311	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: 101 * C3H/He * CBA/Ca	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:9344762	20100907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441547	Tg(Ins2-Tag*,-flpe)#Gne/0  [background:] involves: C57BL/6J	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705127	Tg(Prnp-ATXN7*92Q)1963Als/0  [background:] B6J.Cg-Tg(Prnp-ATXN7*92Q)1963Als	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:25859008	20160125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5561312	b2b2459Clo/b2b2459Clo  [background:] C57BL/6J-b2b2459Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722393	Tg(APPSw)40Btla/Tg(APPSw)40Btla  [background:] B6.129-Tg(APPSw)40Btla	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14506131	20070924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6154646	Tg(Rho-GUCY2D*R838S)362Amd/0  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0111011	cone-rod dystrophy 6						ECO:0000033	author statement supported by traceable reference	PMID:27703005	20180504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579847	Nkx2-5<sup>tm4Rph</sup>/Nkx2-5<sup>+</sup> Tbx20<sup>tm1.1Rph</sup>/Tbx20<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0110106	atrial heart septal defect 1						ECO:0000033	author statement supported by traceable reference	PMID:15843414	20060517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618702	Prkdc<sup>scid</sup>/Prkdc<sup>scid</sup> Tg(TcraAI4)1Dvs/0 Tg(TcrbAI4)1Dvs/0  [background:] NOD.Cg-Prkdc<sup>scid</sup> Tg(TcraAI4)1Dvs Tg(TcrbAI4)1Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6883568	Tg(Prnp-SETX*R2136H)1920Als/0  [background:] involves: C57BL/6J	is_model_of	DOID:0060196	amyotrophic lateral sclerosis type 4						ECO:0000033	author statement supported by traceable reference	PMID:29725819	20220225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656035	Clec3b<sup>tm1Umw</sup>/Clec3b<sup>tm1Umw</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:13300	Scheuermann's disease						ECO:0000033	author statement supported by traceable reference	PMID:11604516	20090128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431967	Tg(RIR-Tag)87Dh/0  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:2986015	20120821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7331486	Sar1b<sup>em1Emle</sup>/Sar1b<sup>+</sup>  [background:] C57BL/6N-Sar1b<sup>em1Emle</sup>	is_model_of	DOID:0060357	chylomicron retention disease						ECO:0000033	author statement supported by traceable reference	PMID:33964306	20220824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430068	Tg(KRT5-TGFB1)F2020Xjw/0  [background:] involves: C57BL/6 * DBA/2 * ICR	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:15057277	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849593	Gpc3<sup>Gt(Ex136)Byg</sup>/Gpc3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897675	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Pten<sup>tm1.1Mwst</sup>/Pten<sup>tm1.1Mwst</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NCr	is_model_of	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22514108	20170622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5632120	Cacna2d2<sup>du-2J</sup>/Cacna2d2<sup>du-2J</sup>  [background:] involves: C57BL/6 * C57BLKS/J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:23732642	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6270171	Tg(Camk2a-Polg*D181A)BTkato/0  [background:] C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato	is_model_of	DOID:3312	bipolar disorder						ECO:0000033	author statement supported by traceable reference	PMID:16619054	20181231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311738	Rarres1<sup>tm1.2Mhl</sup>/Rarres1<sup>tm1.2Mhl</sup>  [background:] involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss	is_model_of	DOID:0050873	follicular lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2658856	Rpl24<sup>Bst</sup>/Rpl24<sup>+</sup>  [background:] involves: C57BLKS	is_model_of	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:8589526	20090814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941746	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ	is_model_of	DOID:5331	testicular granulosa cell tumor						ECO:0000033	author statement supported by traceable reference	PMID:19237610	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6771475	Clp1<sup>em1Slac</sup>/Clp1<sup>em1Slac</sup>  [background:] C57BL/6J-Clp1<sup>em1Slac</sup>/J	is_model_of	DOID:0060279	pontocerebellar hypoplasia type 10						ECO:0000033	author statement supported by traceable reference	PMID:34548404	20211014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162247	Spata16<sup>em2Osb</sup>/Spata16<sup>em2Osb</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:29065458	20180625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763924	Tg(HSA*LR)21Cath/?  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661074	Dsg4<sup>lah</sup>/Dsg4<sup>lah</sup>  [background:] LAH/Pas	is_model_of	DOID:0110703	hypotrichosis 6						ECO:0000033	author statement supported by traceable reference	PMID:8752833	20190422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc	is_model_of	DOID:0090002	Tietz syndrome						ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677961	Slc7a11<sup>sut</sup>/Slc7a11<sup>sut</sup>  [background:] C3H/HeSnJ-Slc7a11<sup>sut</sup>/J	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8699821	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430804	Adgrl3<sup>Gt(S17-5H1)Sor</sup>/Adgrl3<sup>Gt(S17-5H1)Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:27247960	20190718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721103	F12<sup>tm1Pbfd</sup>/F12<sup>tm1Pbfd</sup>  [background:] B6.Cg-F12<sup>tm1Pbfd</sup>	is_model_of	DOID:2231	factor XII deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16009717	20151122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5469979	Tg(Pnkd*A7V*A9V,-DsRed)704Ljp/0  [background:] B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)704Ljp	is_model_of	DOID:0090049	paroxysmal nonkinesigenic dyskinesia 1						ECO:0000033	author statement supported by traceable reference	PMID:22214848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2180789	Tbx21<sup>tm1Glm</sup>/Tbx21<sup>tm1Glm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:11786643	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617496	Brca1<sup>tm1Brn</sup>/Brca1<sup>tm1Brn</sup> Tg(Krt18-EGFP,-TAg121)36Ysng/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm2Tyj</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583555	Tg(ITGA5)0844Fmw/0 Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6704951	Mkrn3<sup>em1Rhu</sup>/Mkrn3<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0112309	central precocious puberty 2						ECO:0000033	author statement supported by traceable reference	PMID:34692086	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393320	Gars1<sup>em1Rwb</sup>/Gars1<sup>em2Rwb</sup>  [background:] involves: C57BL/6NJ * FVB/NJ	is_model_of	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:31557132	20200305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906919	Tg(Myh6-Rxra)41Pcn/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:10675365	20170814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818925	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Tg(SMN2)11Tro/0 Tg(SMN2)46Tro/0  [background:] B6.Cg-Tg(SMN2)11Tro Tg(SMN2)46Tro Smn1<sup>tm1Msd</sup>/J	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:20085811	20100811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7378413	Acad9<sup>tm1c(KOMP)Wtsi</sup>/Acad9<sup>tm1c(KOMP)Wtsi</sup> Tg(ACTA1-cre)79Jme/0  [background:] involves: C57BL/6J * C57BL/6N * FVB/N * SJL	is_model_of	DOID:0112072	nuclear type mitochondrial complex I deficiency 20						ECO:0000033	author statement supported by traceable reference	PMID:34556413	20221102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6478931	Bub1b<sup>tm1Jvd</sup>/Bub1b<sup>tm3.1Jvd</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0080141	mosaic variegated aneuploidy syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:31738183	20201210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775603	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-ERBB2)#Jjz/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26977878	20160610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423106	Kif3b<sup>tm1Noh</sup>/Kif3b<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:31746486	20200518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822320	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Tg(S100b-v-erbB)4496Waw/0  [background:] involves: 129/Sv * C57BL/6J * DBA/2J * FVB/N * SJL	is_model_of	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:12670909	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586914	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242110	20050908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175179	Ntf3<sup>tm1Par</sup>/Ntf3<sup>tm1Par</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110106	atrial heart septal defect 1						ECO:0000033	author statement supported by traceable reference	PMID:8841198	20060426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6488233	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1c(EUCOMM)Wtsi</sup> Emx1<sup>tm1(cre)Yql</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N	is_model_of	DOID:0050425	restless legs syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31715135	20201223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7520358	Tafazzin<sup>em1Xfa</sup>/Y Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: C57BL/6NCrl * MF1	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:34129362	20230824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5925411	Emp2<sup>tm1.1Tac</sup>/Emp2<sup>tm1.1Tac</sup> Tg(Zp3-cre)93Knw/0  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N	is_model_of	DOID:3891	placental insufficiency						ECO:0000033	author statement supported by traceable reference	PMID:28295343	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702658	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:15199412	20160113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624801	L1cam<sup>tm1Mtei</sup>/Y  [background:] either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)	is_model_of	DOID:0060246	MASA syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9354804	20081114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716303	Zic1<sup>tm1Jaru</sup>/Zic1<sup>+</sup>  [background:] B6.129S4-Zic1<sup>tm1Jaru</sup>	is_model_of	DOID:0050777	Joubert syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11699604	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6164125	Tafa3<sup>em1Hssh</sup>/Tafa3<sup>em1Hssh</sup>  [background:] C57BL/6NTac-Tafa3<sup>em1Hssh</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:29184127	20180704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301550	Scn4a<sup>tm1.1Cann</sup>/Scn4a<sup>tm1.1Cann</sup>  [background:] involves: 129	is_model_of	DOID:14452	hypokalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:21881211	20120116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7496044	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J * DBA/2J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21875659	20230707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609426	Chuk<sup>tm1Ver</sup>/Chuk<sup>tm1Ver</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0060647	fetal encasement syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7467143	Cdh5<sup>tm1Dvst</sup>/Cdh5<sup>tm1Dvst</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6478875	Ins2<sup>em#Arak</sup>/Ins2<sup>+</sup>  [background:] C.129-Rag2<sup>tm1Fwa</sup> Ins2<sup>em#Arak</sup> Jak3<sup>tm1Tks</sup>/Arak	is_model_of	DOID:11717	neonatal diabetes						ECO:0000033	author statement supported by traceable reference	PMID:32699230	20201210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318339	Dnah11<sup>b2b1203Clo</sup>/Dnah11<sup>b2b1203Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1203Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525012	Nppa<sup>tm1Unc</sup>/Nppa<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10763	hypertension						ECO:0000033	author statement supported by traceable reference	PMID:7839143	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676935	Thrb<sup>tm3Few</sup>/Thrb<sup>tm3Few</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12925699	20070611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513188	Hoxd13<sup>tm1Mrc</sup>/Hoxd13<sup>tm1Mrc</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060242	synpolydactyly						ECO:0000033	author statement supported by traceable reference	PMID:8620844	20050912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720002	Cacna1f<sup>nob2</sup>/Y  [background:] AXB6/PgnJ	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:16597347	20070830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4888399	Casp8<sup>tm1Hed</sup>/Casp8<sup>tm1Hed</sup> Tg(KRT14-cre)1Efu/0  [background:] Not Specified	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:21135236	20110217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820831	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] A.KOR-Traf3ip2<sup>adjm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637742	Tg(MMTV-Espl1)1Pati/0  [background:] involves: C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24276237	20150529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687165	H2<sup>g7</sup>/H2<sup>q</sup> Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(TcraBDC12-4.1)10Jos/0 Tg(TcrbBDC12-4.1)82Gse/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16804066	20061109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653045	Fgfr3<sup>tm1Led</sup>/Fgfr3<sup>tm1Led</sup> Fgfr4<sup>tm1Cxd</sup>/Fgfr4<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss	is_model_of	DOID:0050161	lower respiratory tract disease						ECO:0000033	author statement supported by traceable reference	PMID:9716527	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3852220	Gpd2<sup>tm1Tka</sup>/Gpd2<sup>tm1Tka</sup> Slc25a13<sup>tm1Lct</sup>/Slc25a13<sup>tm1Lct</sup>  [background:] B6.Cg-Gpd2<sup>tm1Tka</sup> Slc25a13<sup>tm1Lct</sup>	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:17591776	20090807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790976	Gt(ROSA)26Sor<sup>tm1Sor</sup>/Gt(ROSA)26Sor<sup>tm1Sor</sup> Pten<sup>tm1Mro</sup>/Pten<sup>tm1Mro</sup> Slc1a3<sup>tm1(cre/ERT2)Mgoe</sup>/Slc1a3<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * 129S4/SvJaeSor	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:26704996	20160909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5478556	G6pc1<sup>tm1.1Ics</sup>/G6pc1<sup>tm1.1Ics</sup> Alb<sup>tm1(cre/ERT2)Mtz</sup>/Alb<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:21109326	20130731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582996	Klc1<sup>tm1Gsn</sup>/Klc1<sup>+</sup> Tg(APP695)3Dbo/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15731448	20050804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774862	Tg(Thy1-MAPT*L266V*G272V)13Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:11870	Pick's disease						ECO:0000033	author statement supported by traceable reference	PMID:25803611	20160602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849839	Tg(Lck-Tnfsf14)24Yxf/?  [background:] C57BL/6-Tg(Lck-Tnfsf14)24Yxf	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:15067315	20190612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5645264	Zfp366<sup>b2b2834Clo</sup>/Zfp366<sup>b2b2834Clo</sup>  [background:] C57BL/6J-Zfp366<sup>b2b2834Clo</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7444383	Dnajb4<sup>em1Sngi</sup>/Dnajb4<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:36512060	20230315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654500	Slc6a3<sup>tm1Mca</sup>/Slc6a3<sup>tm1Mca</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:8628395	20081006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3686900	Slc12a5<sup>tm1Dlp</sup>/Slc12a5<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:12000122	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882410	Cdkn2a<sup>tm1Cjs</sup>/Cdkn2a<sup>tm1Cjs</sup> Tg(CKMM-tTA)A3Rhvh/0 Tg(tetO-Hgf,-EGFP)24Tcre/0  [background:] involves: 129X1/SvJ * FVB	is_model_of	DOID:3246	embryonal rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:26987019	20211215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818741	Tg(Ins-Igf2)1Fbos/0  [background:] involves: C57BL/6 * C57BLKs/J * SJL	is_model_of	DOID:0110741	type 1 diabetes mellitus 2						ECO:0000033	author statement supported by traceable reference	PMID:10727441	20081208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285207	Tg(Thy1-HSPB1*S135F)#Lvdb/0  [background:] involves: FVB/N	is_model_of	DOID:0110163	Charcot-Marie-Tooth disease axonal type 2F						ECO:0000033	author statement supported by traceable reference	PMID:21785432	20110913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7311570	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174765	Tcm/Tcm<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6754183	Elp2<sup>em2Bjw</sup>/Elp2<sup>em3Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679917	Foxj1<sup>tm1Slb</sup>/Foxj1<sup>tm1Slb</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0050144	Kartagener syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10873152	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623923	Del(16Es2el-Ufd1l)217Bld/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000033	author statement supported by traceable reference	PMID:10517636	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867912	Cnga3<sup>cpfl5</sup>/Cnga3<sup>cpfl5</sup>  [background:] involves: RHJ/LeJ	is_model_of	DOID:0110007	achromatopsia 2						ECO:0000033	author statement supported by traceable reference	PMID:22509403	20151122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276351	Ncoa6<sup>tm1Jkr</sup>/Ncoa6<sup>tm1Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6446736	Hgf<sup>tm1Tbf</sup>/Hgf<sup>tm1Tbf</sup>  [background:] B6.Cg-Hgf<sup>tm1Tbf</sup>/Tbf	is_model_of	DOID:0110497	autosomal recessive nonsyndromic deafness 39						ECO:0000033	author statement supported by traceable reference	PMID:32152201	20200730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450509	Adamts1<sup>tm1Hku</sup>/Adamts1<sup>tm1Hku</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:5200	urinary tract obstruction						ECO:0000033	author statement supported by traceable reference	PMID:10811842	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5629933	Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>/Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0110718	Warburg micro syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:24764192	20150416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713529	Gabrd<sup>tm1Geh</sup>/Gabrd<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9478	postpartum depression						ECO:0000033	author statement supported by traceable reference	PMID:18667149	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6199190	Reep1<sup>Gt(OST398247)Tigm</sup>/Reep1<sup>Gt(OST398247)Tigm</sup>  [background:] B6J.Cg-Reep1<sup>Gt(OST398247)Tigm</sup>	is_model_of	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000033	author statement supported by traceable reference	PMID:27638887	20180924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359630	Tg(Krt14-Angptl2)1Yo/0  [background:] C.Cg-Tg(Krt14-Angptl2)1Yo	is_model_of	DOID:10223	dermatomyositis						ECO:0000033	author statement supported by traceable reference	PMID:22281496	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5502430	Kras<sup>tm1Bbd</sup>/Kras<sup>tm1Bbd</sup> Tg(Cela1-tTA)#Eps/? Tg(tetO-cre)3Jig/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17349585	20130822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196031	Arx<sup>tm5Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6NHsd	is_model_of	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:28602636	20180829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620001	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] B6.129-Eln<sup>tm1Dyl</sup>	is_model_of	DOID:1929	supravalvular aortic stenosis						ECO:0000033	author statement supported by traceable reference	PMID:14597767	20060418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6140058	Lrch1<sup>em1Hwa</sup>/Lrch1<sup>em1Hwa</sup>  [background:] Not Specified	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:28028151	20180316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039435	Sell<sup>tm1Flv</sup>/Sell<sup>tm1Flv</sup>  [background:] NOD.Cg-Sell<sup>tm1Flv</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046835	Cdkn1a<sup>tm2(HBx)Xya</sup>/Cdkn1a<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174975	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12638	hypertrophic pyloric stenosis						ECO:0000033	author statement supported by traceable reference	PMID:7505721	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763097	Tg(MMTV-LPAR1)#Gbm/Tg(MMTV-LPAR1)#Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)#Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3057279	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:16027362	20060825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5583018	Tg(IVL-KLK5)#Hov/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24534191	20140919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2667200	Cited2<sup>tm1Ycy</sup>/Cited2<sup>tm1Ycy</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:12149478	20050912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505710	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] C3H/HeSn-Rab27a<sup>ash</sup>/J	is_model_of	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:12070017	20130912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620094	Chm<sup>tm1.1Seab</sup>/Y Tg(Six3-cre)69Frty/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:9821	choroideremia						ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700128	Alms1<sup>L2131X</sup>/Alms1<sup>L2131X</sup>  [background:] involves: C57BL/6 * NOD	is_model_of	DOID:0050473	Alstrom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17206865	20080111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7388557	Mettl23<sup>em2Itwa</sup>/Mettl23<sup>+</sup>  [background:] C57BL/6J-Mettl23<sup>em2Itwa</sup>	is_model_of	DOID:1686	glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5466156	Kxd1<sup>tm1Wli</sup>/Kxd1<sup>tm1Wli</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22554196	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665276	Frem1<sup>bfd</sup>/Frem1<sup>bfd</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392258	Tg(Thy1-APP*)2Tbay/0  [background:] C57BL/6J-Tg(Thy1-APP*)2Tbay	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23685882	20200228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584474	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6507156	Tuba1a<sup>em1Rstot</sup>/Tuba1a<sup>quas</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:2490	congenital nervous system abnormality						ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432017	Tg(Ly6e-MALT1)#Isg/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue						ECO:0000033	author statement supported by traceable reference	PMID:22689981	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430601	Ccr7<sup>tm1Rfor</sup>/Ccr7<sup>tm1Rfor</sup>  [background:] B6.129P2-Ccr7<sup>tm1Rfor</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16473829	20100319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188940	Tg(Myh6-Pkp2*/mRuby)4Rbrug/0 Tg(Myh6-Pkp2*/mRuby)5Rbrug/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110077	arrhythmogenic right ventricular dysplasia 9						ECO:0000033	author statement supported by traceable reference	PMID:27412010	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6501726	Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>/Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:0110081	arrhythmogenic right ventricular dysplasia 10						ECO:0000033	author statement supported by traceable reference	PMID:27170944	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850502	Tg(Lck-Tslp)1Chea/0  [background:] B6.Cg-Tg(Lck-Tslp)1Chea	is_model_of	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:11733384	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476437	b2b1929Clo/b2b1929Clo  [background:] C57BL/6J-b2b1929Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664131	Sycp3<sup>tm1Hoog</sup>/Sycp3<sup>tm1Hoog</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14227	azoospermia						ECO:0000033	author statement supported by traceable reference	PMID:10678170	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527317	Tg(MMTV-ERBB2)5Erick/?  [background:] FVB/N-Tg(MMTV-ERBB2)5Erick	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:15073130	20140108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297589	Tg(SOD1*H46R)#Maw/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:15899257	20111208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815543	In(15)4H/+  [background:] involves: C3H/HeH	is_model_of	DOID:0111060	Ambras type hypertrichosis universalis congenita						ECO:0000033	author statement supported by traceable reference	PMID:18713754	20081119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580090	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902139	mt-Nd6<sup>m1Jbst</sup> mt-Ta<sup>m1Jbst</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl	is_model_of	DOID:700	mitochondrial metabolism disease						ECO:0000033	author statement supported by traceable reference	PMID:27626666	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256757	Tg(Myh6-Tpm1*D230N)HJcf/0  [background:] B6.FVB-Tg(Myh6-Tpm1*D230N)HJcf	is_model_of	DOID:0110457	dilated cardiomyopathy 1Y						ECO:0000033	author statement supported by traceable reference	PMID:28600229	20181116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5810302	Ctsl<sup>tm1Cptr</sup>/Ctsl<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11972068	20170802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6201559	Klhl31<sup>em1Eno</sup>/Klhl31<sup>em1Eno</sup>  [background:] involves: C57BL/6	is_model_of	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:28872460	20181011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522005	Del(11Cops3-Rnf112)1Jrl/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12724422	20050527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397673	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045183	Psen1<sup>tm1Jzt</sup>/Psen1<sup>tm1Jzt</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11738035	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6275631	Mdga2<sup>Tg(Prnp-PFN1*G118V)838Kiaei</sup>/Mdga2<sup>+</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0060209	amyotrophic lateral sclerosis type 18						ECO:0000033	author statement supported by traceable reference	PMID:28040732	20190201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906203	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19001090	20170803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397675	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] B6.129-Kcnq3<sup>tm1.1Naas</sup>	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418449	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>tm1Mmt</sup> Pten<sup>tm1Rps</sup>/Pten<sup>tm1Rps</sup> Tg(Tyr-cre/ERT2)13Bos/0  [background:] involves: 129/Sv * C57BL/6J * FVB * SJL	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:20048081	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784866	Nupr1<sup>tm1Jlio</sup>/Nupr1<sup>tm1Jlio</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050457	Sertoli cell-only syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18495683	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697531	Auts2<sup>tm1.1Dare</sup>/Auts2<sup>tm1.1Dare</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000033	author statement supported by traceable reference	PMID:25519132	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033165	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] BKSChpLt.HRS-Cpe<sup>fat</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:2250094	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510313	Tbx1<sup>tm1.1Dsr</sup>/Tbx1<sup>+</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574621	Muc2<sup>tm1Avel</sup>/Muc2<sup>tm1Avel</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:24945909	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361120	Xpa<sup>tm1Tnka</sup>/Xpa<sup>tm1Tnka</sup> Tg(KRT14-Kitl)1Takk/?  [background:] involves: C57BL/6 * CBA * SJL	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:16117793	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301577	Cdkal1<sup>tm1.1Tomik</sup>/Cdkal1<sup>tm1.1Tomik</sup> Tg(Ins2-cre)25Mgn/0  [background:] B6.Cg-Cdkal1<sup>tm1.1Tomik</sup> Tg(Ins2-cre)25Mgn	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:21841312	20130415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603515	Ighmbp2<sup>nmd-2J</sup>/Ighmbp2<sup>nmd-2J</sup>  [background:] B6.BKS-Ighmbp2<sup>nmd-2J</sup>/J	is_model_of	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:15269181	20051103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3757750	Prkn<sup>tm1Roo</sup>/Prkn<sup>tm1Roo</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:17623040	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584030	Ap3b1<sup>pe-rim2</sup>/Ap3b1<sup>pe-rim2</sup>  [background:] involves: B10.A(R201) * C57BL/10Slc	is_model_of	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:9434937	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361117	Xpa<sup>tm1Tnka</sup>/Xpa<sup>tm1Tnka</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110843	xeroderma pigmentosum group A						ECO:0000033	author statement supported by traceable reference	PMID:8751968	20190819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606425	Cpt1a<sup>tm1Pwo</sup>/Cpt1a<sup>+</sup>  [background:] either: 129S6/SvEvTac-Cpt1a<sup>tm1Pwo</sup> or (involves: 129S6/SvEvTac * C57BL/6NTac)	is_model_of	DOID:0090129	carnitine palmitoyltransferase I deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16169268	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3779043	Lyst<sup>bg-2Btlr</sup>/Lyst<sup>bg-2Btlr</sup>  [background:] C57BL/6J-Lyst<sup>bg-2Btlr</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	MGI:3778946	20080428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7277808	Tlcd3b<sup>em1(IMPC)Bay</sup>/Tlcd3b<sup>em1(IMPC)Bay</sup>  [background:] C57BL/6NJ-Tlcd3b<sup>em1(IMPC)Bay</sup>/Mmnc	is_model_of	DOID:0050572	cone-rod dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33077892	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5319509	Tg(Myh6-MYPN*Y20C)#Jato/0  [background:] involves: C57BL/6J	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22286171	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505899	Rnf168<sup>Gt(156B6)Cmhd</sup>/Rnf168<sup>Gt(156B6)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0090113	RIDDLE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21552324	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841959	Cyp11b1<sup>tm1Chjk</sup>/Cyp11b1<sup>tm1Chjk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050811	congenital adrenal hyperplasia						ECO:0000033	author statement supported by traceable reference	PMID:19029289	20151122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7439145	Iigp1c<sup>M2Btlr</sup>/Iigp1c<sup>M2Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>M2Btlr</sup>	is_model_of	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936857	Pkhd1<sup>tm1Gwu</sup>/Pkhd1<sup>tm1Gwu</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:20875407	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819098	Nog<sup>tm1Amc</sup>/Nog<sup>tm1Amc</sup> Smad3<sup>tm1Xfw</sup>/Smad3<sup>+</sup>  [background:] involves: 129/Sv * 129S1/Sv	is_model_of	DOID:4621	holoprosencephaly						ECO:0000033	author statement supported by traceable reference	PMID:20508035	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7367456	Aldh3a2<sup>tm1a(EUCOMM)Wtsi</sup>/Aldh3a2<sup>tm1a(EUCOMM)Wtsi</sup> Aldh3b2<sup>em1Akih</sup>/Aldh3b2<sup>em1Akih</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:14501	Sjogren-Larsson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34370553	20221027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053798	Plscr3<sup>tm1Sims</sup>/Plscr3<sup>tm1Sims</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15328404	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432177	Gt(ROSA)26Sor<sup>tm49(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367266	Rpgrip1<sup>nmf247</sup>/Rpgrip1<sup>nmf247</sup>  [background:] C57BL/6J-Rpgrip1<sup>nmf247</sup>	is_model_of	DOID:0110329	Leber congenital amaurosis 6						ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588510	Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>/Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI	is_model_of	DOID:3490	Noonan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9753320	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811208	Hspg2<sup>tm1.1Soni</sup>/Hspg2<sup>tm1.1Soni</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:18647752	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3826270	Mdm1<sup>m1J</sup>/Mdm1<sup>m1J</sup>  [background:] Not Specified	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:18805803	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5615273	Foxh1<sup>b2b2662Clo</sup>/Foxh1<sup>b2b2662Clo</sup>  [background:] C57BL/6J-Foxh1<sup>b2b2662Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451172	Sox9<sup>tm2Crm</sup>/Sox9<sup>+</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J * SJL/J	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6157462	Klhl3<sup>tm2.1Esoh</sup>/Klhl3<sup>tm2.1Esoh</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:28052936	20180522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429725	Dp(16Cbr1-Fam3b)1Rhr/0  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22354171	20120801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833153	Brca2<sup>tm1Kamc</sup>/Brca2<sup>tm1Kamc</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:0111089	Fanconi anemia complementation group D1						ECO:0000033	author statement supported by traceable reference	PMID:16859999	20090224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609425	Chuk<sup>tm1Aki</sup>/Chuk<sup>tm1Aki</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060647	fetal encasement syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273512	Kras<sup>tm5Tyj</sup>/Kras<sup>+</sup> Pdx1<sup>tm1.1(flpo)Most</sup>/Pdx1<sup>+</sup> Trp53<sup>tm1.1Dgk</sup>/Trp53<sup>tm1.1Dgk</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * Black Swiss * C57BL/6	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28934293	20190115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:9697704	20050912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662254	Ddhd2<sup>tm1Crv</sup>/Ddhd2<sup>tm1Crv</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110806	hereditary spastic paraplegia 54						ECO:0000033	author statement supported by traceable reference	PMID:25267624	20150921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5320790	Jak2<sup>tm1Mohi</sup>/Jak2<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:22144185	20120608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7509544	Csrp3<sup>tm1.1Kage</sup>/Csrp3<sup>tm1.1Kage</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:30048712	20230719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652947	Bsn<sup>tm1Gund</sup>/Bsn<sup>tm1Gund</sup>  [background:] Not Specified	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:12628169	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5902495	B3gnt6<sup>tm1Lx</sup>/B3gnt6<sup>tm1Lx</sup> C1galt1<sup>tm1.1Rpmc</sup>/C1galt1<sup>tm1.1Rpmc</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129S1/Sv * C57BL/6J * SJL	is_model_of	DOID:10021	duodenum cancer						ECO:0000033	author statement supported by traceable reference	PMID:27229122	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829609	Trip11<sup>m1Mawa</sup>/Trip11<sup>m1Mawa</sup>  [background:] C57BL/6J-Trip11<sup>m1Mawa</sup>	is_model_of	DOID:0080054	achondrogenesis type IA						ECO:0000033	author statement supported by traceable reference	PMID:20089971	20100915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437109	Odad2<sup>b2b227.1Clo</sup>/Odad2<sup>b2b227.1Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b227.1Clo</sup>	is_model_of	DOID:0110609	primary ciliary dyskinesia 23						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6304488	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110319	hypertrophic cardiomyopathy 13						ECO:0000033	author statement supported by traceable reference	PMID:26304555	20190521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897563	Grm6<sup>nob8</sup>/Grm6<sup>nob8</sup>  [background:] CBA/CaJ	is_model_of	DOID:0110865	congenital stationary night blindness 1B						ECO:0000033	author statement supported by traceable reference	PMID:28490646	20170522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7261455	Cxcr4<sup>tm2Yzo</sup>/Cxcr4<sup>tm2Yzo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:31071921	20220418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662181	Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654501	Tg(MMTVneu)202Mul/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:12483526	20080617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559492	Slx4<sup>tm1.2Jrou</sup>/Slx4<sup>tm1.2Jrou</sup>  [background:] B6.129P2-Slx4<sup>tm1.2Jrou</sup>	is_model_of	DOID:0090066	Fanconi-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24076219	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623594	Tg(Igh-6/Igh-V125)2Jwt/0 Tg(Igk-C/Igk-V125)1Jwt/0  [background:] NOD.B6-Tg(Igh-6/Igh-V125)2Jwt Tg(Igk-C/Igk-V125)1Jwt	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11698422	20060601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438092	Btbd9<sup>Gt(RRE078)Byg</sup>/Btbd9<sup>Gt(RRE078)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050425	restless legs syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22678064	20121010	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056404	Shank3<sup>tm1Yhj</sup>/Shank3<sup>tm1Yhj</sup>  [background:] B6.129S7-Shank3<sup>tm1Yhj</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21558424	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6104247	Ryr2<sup>tm3.1Hhv</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:25775566	20171221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652414	Fbn1<sup>tm3Rmz</sup>/Fbn1<sup>tm3Rmz</sup>  [background:] Not Specified	is_model_of	DOID:114	heart disease						ECO:0000033	author statement supported by traceable reference	PMID:16407178	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941606	Tg(FCGR2A)11Mkz/0 Tg(PF4)#Zcy/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:11126	acquired thrombocytopenia						ECO:0000033	author statement supported by traceable reference	PMID:11588041	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6729187	Fgf13<sup>em1Xuzh</sup>/Y  [background:] involves: C57BL/6J	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:34184986	20210806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590487	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315439	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315439	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:22002997	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652362	App<sup>tm1.1Cep</sup>/App<sup>tm1.1Cep</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620190	b2b2696.1Clo/b2b2696.1Clo  [background:] C57BL/6J-b2b2696.1Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559577	Kmt2a<sup>tm1.1(Sh3gl1)Lcc</sup>/Kmt2a<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6	is_model_of	DOID:1240	leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24122813	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769904	Scn5a<sup>tm1Care</sup>/Scn5a<sup>+</sup>  [background:] FVB.129P2-Scn5a<sup>tm1Care</sup>/Care	is_model_of	DOID:0110218	Brugada syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:17145985	20080206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6393456	Spast<sup>tm1.1Evre</sup>/Spast<sup>tm1.1Evre</sup>  [background:] C57BL/6-Spast<sup>tm1.1Evre</sup>	is_model_of	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000033	author statement supported by traceable reference	PMID:27019090	20200306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425918	Casr<sup>BCH002</sup>/Casr<sup>BCH002</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH002</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588731	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] involves: B6.KB2 * C3H/HeJ	is_model_of	DOID:0110723	neuronal ceroid lipofuscinosis 8						ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651494	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:12576554	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6192743	Myo15a<sup>tm1.1Jebd</sup>/Myo15a<sup>tm1.1Jebd</sup>  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:0110488	autosomal recessive nonsyndromic deafness 3						ECO:0000033	author statement supported by traceable reference	PMID:26302205	20180806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397575	Col10a1<sup>tm1.1Rpbh</sup>/Col10a1<sup>tm1.1Rpbh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0080021	Schmid metaphyseal chondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19834559	20091201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7264676	Cant1<sup>tm1.1Aros</sup>/Cant1<sup>tm1.1Aros</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0060462	Desbuquois dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30439444	20220427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839106	Megf8<sup>hlb611</sup>/Megf8<sup>hlb611</sup>  [background:] involves: C57BL/6J * C3H/HeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:18043505	20231103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292535	Col2a1<sup>M2J</sup>/Col2a1<sup>+</sup>  [background:] B6;C3Fe-Col2a1<sup>M2J</sup>/GrsrJ	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308954	Cdkn2a<sup>tm2.1Rdp</sup>/Cdkn2a<sup>tm2.1Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * CBA * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16585505	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4837384	Myh6<sup>tm3.1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:20811150	20101103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813482	Tg(Ppp1r1b-HTT*)1Meeh/0  [background:] C57BL/6J-Tg(Ppp1r1b-HTT*)1Meeh	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:18632688	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6098752	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] B6.129P2(C)-Mecp2<sup>tm1.1Bird</sup>/J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941907	Pink1<sup>tm1Hbu</sup>/Pink1<sup>tm1Hbu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060369	Parkinson's disease 6						ECO:0000033	author statement supported by traceable reference	PMID:21249202	20150303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6187717	Tardbp<sup>em1Rhbr</sup>/Tardbp<sup>em1Rhbr</sup>  [background:] C57BL/6J-Tardbp<sup>em1Rhbr</sup>	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:29556029	20180709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566833	Tg(Pbsn-MYC)#Tt/?  [background:] involves: C57BL/6J	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22144662	20140605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836904	Ppp1r13l<sup>wa3-J</sup>/Ppp1r13l<sup>wa3-J</sup>  [background:] BALB/cJ-Ppp1r13l<sup>wa3-J</sup>/J	is_model_of	DOID:0050737	autosomal recessive disease						ECO:0000033	author statement supported by traceable reference	PMID:28069640	20190702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711004	Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>/Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup> Myf5<sup>tm1(cre)Mrc</sup>/Myf5<sup>tm1(cre)Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:5485	synovial sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:17418413	20091223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906253	Tg(Myh6-Snai1)B10Jcc/Tg(Myh6-Snai1)B10Jcc  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17512504	20170807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604219	Fmr1<sup>tm1.1Cidz</sup>/Fmr1<sup>tm1.1Cidz</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16055059	20070119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692774	Tbx5<sup>tm1Jse</sup>/Tbx5<sup>+</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16870172	20150821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417895	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:19893033	20100115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5910053	Tg(Myh6-TNNT2*I79N)8Jdp/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:23532597	20170922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941028	Tg(Mt1-GH1)#Jjk/0  [background:] C57BL/6J-Tg(Mt1-GH1)#Jjk	is_model_of	DOID:2449	acromegaly						ECO:0000033	author statement supported by traceable reference	PMID:19269870	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683994	Ada<sup>tm1Mw</sup>/Ada<sup>tm1Mw</sup> Tg(PLADA)4118Rkmb/0  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:5810	adenosine deaminase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9478961	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6111174	Pabpn1<sup>tm1.2Gpvl</sup>/Pabpn1<sup>+</sup>  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:11719	oculopharyngeal muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28575395	20180119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441982	Rr20<sup>tm1.1Vlcg</sup>/Rr20<sup>tm1.1Vlcg</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0080036	SOST-related sclerosing bone dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:22886088	20121119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301335	B9d1<sup>tm1a(EUCOMM)Wtsi</sup>/B9d1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * CD-1	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21763481	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622411	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] NOD.129P2-Il4<sup>tm1Cgn</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16413168	20060516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5911391	Ts(16C-tel)1Cje/0  [background:] B6.Cg-Ts(16C-tel)1Cje	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32843708	20210603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6343393	Ugt1<sup>tm1.1Afmu</sup>/Ugt1<sup>tm1.1Afmu</sup>  [background:] FVB.Cg-Ugt1<sup>tm1.1Afmu</sup>	is_model_of	DOID:2383	neonatal jaundice						ECO:0000033	author statement supported by traceable reference	PMID:25062689	20190814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758631	Gdf5<sup>Rgsc451</sup>/Gdf5<sup>Rgsc451</sup>  [background:] C57BL/6JJcl-Gdf5<sup>Rgsc451</sup>	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:17656374	20071018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6191762	Galt<sup>Gt(E285B04)Wrst</sup>/Galt<sup>Gt(E285B04)Wrst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9870	galactosemia						ECO:0000033	author statement supported by traceable reference	PMID:24549051	20180727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175097	Lamb2<sup>tm1Jrs</sup>/Lamb2<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:2527	nephrosis						ECO:0000033	author statement supported by traceable reference	PMID:7670489	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517789	Nlrp3<sup>tm3.1Hhf</sup>/Nlrp3<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0090029	CINCA Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22558291	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0090100	ocular albinism with sensorineural deafness						ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356966	Jak2<sup>tm1.1Ble</sup>/Jak2<sup>+</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca	is_model_of	DOID:2226	myeloproliferative neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:29202466	20190826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7449370	Gt(ROSA)26Sor<sup>tm1.1(CAG-ATP1A3*D591V,-EGFP)Bcgen</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050572	cone-rod dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32440726	20230403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175073	Iac/Iac<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4888512	Btd<sup>tm1Bwol</sup>/Btd<sup>tm1Bwol</sup>  [background:] B6.Cg-Btd<sup>tm1Bwol</sup>	is_model_of	DOID:856	biotinidase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:21051254	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5289775	Olig2<sup>tm1(cre)Tmj</sup>/Olig2<sup>+</sup> Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1Msd</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup>  [background:] involves: 129 * 129P2/OlaHsd * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:20826664	20111007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5903847	Kl<sup>ecalc2</sup>/Kl<sup>ecalc2</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:0111063	hyperphosphatemic familial tumoral calcinosis						ECO:0000033	author statement supported by traceable reference	PMID:25860694	20170703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5319645	Tg(NPHS2-Trpc6*P111Q)F615Walz/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0111129	focal segmental glomerulosclerosis 2						ECO:0000033	author statement supported by traceable reference	PMID:20877463	20120530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622318	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796167	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>+</sup> Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Col1a1-cre)1Kry/0  [background:] involves: 129 * 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:26659571	20160930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7275231	Rbm20<sup>em1Hgra</sup>/Rbm20<sup>em1Hgra</sup>  [background:] C57BL/6-Rbm20<sup>em1Hgra</sup>	is_model_of	DOID:0110447	dilated cardiomyopathy 1DD						ECO:0000033	author statement supported by traceable reference	PMID:35041844	20220509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6466719	Adamts17<sup>tm1.2Taks</sup>/Adamts17<sup>tm1.2Taks</sup>  [background:] involves: C57BL * C57BL/6 * DBA	is_model_of	DOID:0050475	Weill-Marchesani syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31201465	20201013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797753	Tg(Eno2-Scn2a1*)Q54Mm/0  [background:] B6.Cg-Tg(Eno2-Scn2a1*)Q54Mm	is_model_of	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:16464983	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6390207	Pex1<sup>tm1.1Hrw</sup>/Pex1<sup>tm1.1Hrw</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:905	Zellweger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31207289	20200217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583124	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] either: D2.KK-Nphp3<sup>pcy</sup> or (involves: DBA/2Fg * DBA/2J * KK)	is_model_of	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:1883968	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575737	Sipa1<sup>tm1Nm</sup>/Sipa1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:12892713	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6369630	Armc2<sup>em1Pfr</sup>/Armc2<sup>em1Pfr</sup>  [background:] Not Specified	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:30686508	20191105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697681	Comt<sup>tm1Kara</sup>/Comt<sup>tm1Kara</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:1561	cognitive disorder						ECO:0000033	author statement supported by traceable reference	PMID:9707588	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6276046	Tg(Myh6-Camk2d_ic)LJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842387	Atf2<sup>tm1Sis</sup>/Atf2<sup>tm1Sis</sup>  [background:] either: (involves: C57BL/6 * CBA) or (involves: BALB/c * C57BL/6 * CBA) or (involves: C57BL/6 * CBA * ICR)	is_model_of	DOID:11049	meconium aspiration syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10364225	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4881776	Triobp<sup>tm1Tbf</sup>/Triobp<sup>tm1Tbf</sup>  [background:] C57BL/6-Triobp<sup>tm1Tbf</sup>	is_model_of	DOID:0110486	autosomal recessive nonsyndromic deafness 28						ECO:0000033	author statement supported by traceable reference	PMID:20510926	20220308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5615273	Foxh1<sup>b2b2662Clo</sup>/Foxh1<sup>b2b2662Clo</sup>  [background:] C57BL/6J-Foxh1<sup>b2b2662Clo</sup>	is_model_of	DOID:0060341	agnathia-otocephaly complex						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281842	Adar<sup>em1Stsn</sup>/Adar<sup>tm1.1Phs</sup> Meox2<sup>tm1(cre)Sor</sup>/Meox2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34343497	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6491890	Coasy<sup>tm1.1Vtr</sup>/Coasy<sup>tm1.1Vtr</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129 * C57BL/6N * CBA	is_model_of	DOID:0110740	neurodegeneration with brain iron accumulation 6						ECO:0000033	author statement supported by traceable reference	PMID:33352696	20210114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5284841	Etv6<sup>tm1.1(RUNX1,hsb5)Lvdw</sup>/Etv6<sup>+</sup> TgTn(sb-T2/Onc)76Dla/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/N	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:21628403	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196045	Tg(CAG-Alk*F1174L,-luc)60Jhsc/0 Th<sup>tm1(cre)Te</sup>/Th<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22764207	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7550770	Hnrnpu<sup>em1Frk</sup>/Hnrnpu<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0080418	developmental and epileptic encephalopathy 54						ECO:0000033	author statement supported by traceable reference	PMID:37782669	20231122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6506273	Uox<sup>em1Cli</sup>/Uox<sup>em1Cli</sup>  [background:] C57BL/6J-Uox<sup>em1Cli</sup>	is_model_of	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:28729031	20210212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702021	Hamp<sup>tm1Svl</sup>/Hamp<sup>tm1Svl</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0111032	hemochromatosis type 2B						ECO:0000033	author statement supported by traceable reference	PMID:16574947	20100330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047839	Fmod<sup>tm1Aol</sup>/Fmod<sup>tm1Aol</sup> Lum<sup>tm1Chak</sup>/Lum<sup>tm1Chak</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:12089156	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7284280	Tardbp<sup>tm1.1Hiok</sup>/Tardbp<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5603215	Cdkn2a<sup>tm2Brn</sup>/Cdkn2a<sup>tm2Brn</sup> Tg(Tyr-cre/ERT,-Hras1*,-Trap1a)10BJvde/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:16540681	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c	is_model_of	DOID:0111013	cone-rod dystrophy 3						ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033464	Hfe<sup>tm1Sly</sup>/Hfe<sup>tm1Sly</sup>  [background:] Not Specified	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14673107	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805735	Tomt<sup>m1Btlr</sup>/Tomt<sup>m1Btlr</sup>  [background:] C57BL/6J-Tomt<sup>m1Btlr</sup>	is_model_of	DOID:0110515	autosomal recessive nonsyndromic deafness 63						ECO:0000033	author statement supported by traceable reference	PMID:18794526	20081003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4411994	Pde6c<sup>cpfl1</sup>/Pde6c<sup>cpfl1</sup>  [background:] B6.CXB1-Pde6c<sup>cpfl1</sup>	is_model_of	DOID:13911	achromatopsia						ECO:0000033	author statement supported by traceable reference	PMID:19887631	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174788	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:10491404	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843219	Tg(Thy1-APPSw)10Jiri/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14596862	20101208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360984	n-TUtca2<sup>tm1Dhat</sup>/n-TUtca2<sup>tm1Dhat</sup> Tg(Col2a1-cre)1Bhr/0  [background:] B6.Cg-n-TUtca2<sup>tm1Dhat</sup> Tg(Col2a1-cre)1Bhr	is_model_of	DOID:65	connective tissue disease						ECO:0000033	author statement supported by traceable reference	PMID:19696890	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661068	Dsg4<sup>lah-J</sup>/Dsg4<sup>lah-J</sup>  [background:] involves: DBA/1LacJ	is_model_of	DOID:0110703	hypotrichosis 6						ECO:0000033	author statement supported by traceable reference	PMID:10839719	20190422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6725721	Clcn1<sup>em1Btlr</sup>/Clcn1<sup>em1Btlr</sup>  [background:] C57BL/6J-Clcn1<sup>em1Btlr</sup>	is_model_of	DOID:2106	myotonia congenita						ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6160805	Cpox<sup>Rbc16</sup>/Cpox<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:13269	hereditary coproporphyria						ECO:0000033	author statement supported by traceable reference	PMID:28600349	20180613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6435210	Dpp4<sup>tm1(DPP4)Vlcg</sup>/?  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27795435	20200619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5616747	Mbnl1<sup>tm1Sws</sup>/Mbnl1<sup>tm1Sws</sup> Mbnl2<sup>tm1.1Sws</sup>/Mbnl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * C57BL	is_model_of	DOID:450	myotonic disease						ECO:0000033	author statement supported by traceable reference	PMID:24293317	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580057	Grin1<sup>tm1Stl</sup>/Grin1<sup>+</sup> Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:9054942	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6403118	Tg(DPP4)2Nnag/0  [background:] B6.Cg-Tg(DPP4)2Nnag	is_model_of	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30626685	20200407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661079	Gdf5<sup>bp-J</sup>/Gdf5<sup>bp-J</sup> Gdf6<sup>tm1Kng</sup>/Gdf6<sup>tm1Kng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6J	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:12606286	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:27959908	20190917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174791	Ttpa<sup>tm1Far</sup>/Ttpa<sup>tm1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090028	familial isolated deficiency of vitamin E						ECO:0000033	author statement supported by traceable reference	PMID:11095717	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711227	Slc35c1<sup>tm1Cknr</sup>/Slc35c1<sup>tm1Cknr</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0070255	congenital disorder of glycosylation type IIc						ECO:0000033	author statement supported by traceable reference	PMID:17276979	20190516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474304	Efnb3<sup>m1Btlr</sup>/Efnb3<sup>m1Btlr</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:480	movement disease						ECO:0000033	author statement supported by traceable reference	MGI:5474302	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905035	Col4a1<sup>tm1.1Ics</sup>/Col4a1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:26260163	20170719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5906504	Lmna<sup>tm2.1Gbon</sup>/Lmna<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:23575224	20170810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6279297	Grn<sup>tm1.1Aidi</sup>/Grn<sup>tm1.1Aidi</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:30271659	20190221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047099	Fanca<sup>tm1.1Wong</sup>/Fanca<sup>tm1.1Wong</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0111095	Fanconi anemia complementation group A						ECO:0000033	author statement supported by traceable reference	PMID:12913077	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5750141	Tg(MAPT*V337M)1Gds/0  [background:] B6J.Cg-Tg(MAPT*V337M)1Gds	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:25471585	20160225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513191	Plec<sup>tm1Gwi</sup>/Plec<sup>tm1Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060736	epidermolysis bullosa simplex Ogna type						ECO:0000033	author statement supported by traceable reference	PMID:9389647	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5904617	Casz1<sup>Gt(CJ0565)Wtsi</sup>/Casz1<sup>Gt(CJ0565)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060410	chromosome 1p36 deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25190801	20170714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635161	Tg(HTT*)LXwy/0  [background:] involves: FVB/NJ	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25661181	20150508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798606	Dmd<sup>mdx-3Cv</sup>/Y  [background:] involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus	is_model_of	DOID:9883	Becker muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:7843915	20090929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6451096	Cfap65<sup>em1Fzh</sup>/Cfap65<sup>em1Fzh</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0111918	spermatogenic failure 40						ECO:0000033	author statement supported by traceable reference	PMID:31501240	20200821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7491951	Hdac8<sup>tm1.2Eno</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0080509	Cornelia de Lange syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:32800293	20230622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446586	Abcd1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9418970	20050711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5522833	Tubb2b<sup>brdp</sup>/Tubb2b<sup>brdp</sup>  [background:] involves: A/J * FVB	is_model_of	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000033	author statement supported by traceable reference	PMID:23727838	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175809	Cryge<sup>Aey1</sup>/Cryge<sup>Aey1</sup>  [background:] C3HeB/FeJ-Cryge<sup>Aey1</sup>	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:10932192	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3578113	Abca1<sup>tm1Jp</sup>/Abca1<sup>tm1Jp</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * B6.Cg-Tg(Alb-cre)21Mgn/J	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:15841208	20050526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451173	Sox9<sup>tm2Crm</sup>/Sox9<sup>tm2Crm</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J * SJL/J	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432345	Tg(Ela1-Myc)159Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1986386	20120828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6342435	Cwc27<sup>em1Bay</sup>/Cwc27<sup>em1Bay</sup>  [background:] C57BL/6J-Cwc27<sup>em1Bay</sup>	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:28285769	20190807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575312	Nfe2l1<sup>tm1Jefc</sup>/Nfe2l1<sup>tm1Ywk</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15738389	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796298	Foxp3<sup>tm2.1(EGFP/cre)Shori</sup>/Y Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] involves: 129 * 129S2/SvPas * C57BL/6	is_model_of	DOID:4989	pancreatitis						ECO:0000033	author statement supported by traceable reference	PMID:27410049	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404227	Neb<sup>m1Anu</sup>/Neb<sup>m2Anu</sup>  [background:] C57BL/6J-Neb<sup>m1Anu</sup> Neb<sup>m2Anu</sup>	is_model_of	DOID:0110928	nemaline myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:32066503	20200416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639677	Gpr132<sup>tm1Witt</sup>/Gpr132<sup>tm1Witt</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:11371358	20060802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432230	Tg(Dct-Grm1)ESzc/0  [background:] involves: C57BL/6J	is_model_of	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:12704387	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588490	Gdnf<sup>tm1Lmgd</sup>/Gdnf<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * CD-1)	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:11774071	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7523000	Rtf1<sup>tm1c(KOMP)Wtsi</sup>/Rtf1<sup>tm1c(KOMP)Wtsi</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:37233188	20230831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762537	Des<sup>tm1.1Ccrs</sup>/Des<sup>tm1.1Ccrs</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:25394388	20170823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710355	Brca1<sup>tm1Aash</sup>/Brca1<sup>tm1Aash</sup> Tg(LGB-cre)74Acl/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:17212342	20080624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140029	Tg(Thy1-GLRA1*R271Q)300Wha/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	PMID:11923415	20110817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614342	Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?  [background:] FVB/N-Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:9528804	20101110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709758	Drd1<sup>tm2Jcd</sup>/Drd1<sup>+</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:17360497	20110805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587029	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>tm1Bem</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609192	Del(1)1Brk/Del(1)1Brk  [background:] involves: 129S6/SvEvTac * C57BL/6J * CBA/J	is_model_of	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:18039845	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623923	Del(16Es2el-Ufd1l)217Bld/+  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10517636	20060606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054644	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] B6.129S2-Pdcd1<sup>tm1Hon</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:10485649	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624975	X/Yaa  [background:] (NZW x BXSB)F1	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:6690614	20060621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946419	Aqp4<sup>tm1.1Lmno</sup>/Aqp4<sup>tm1.1Lmno</sup>  [background:] B6.Cg-Aqp4<sup>tm1.1Lmno</sup>	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:23277579	20131001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6390918	Chd8<sup>tm1.1Csbd</sup>/Chd8<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30104731	20200218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907886	Tg(Myh6-HBEGF)#Iko/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:15272002	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5605970	b2b386.1Clo/b2b386.1Clo  [background:] C57BL/6J-b2b386.1Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5751863	Tg(Hnrnpa2b1-rtTA2S*M2)9Jstr/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0  [background:] involves: C57BL/6JRj * FVB/N	is_model_of	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25486200	20160323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825359	Tcf3<sup>tm1(PBX1)Mlc</sup>/Tcf3<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * C57BL/6J * CBA/J	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26301816	20170301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702323	Msx1<sup>tm1Bero</sup>/Msx1<sup>tm1Bero</sup>  [background:] B6.129P2-Msx1<sup>tm1Bero</sup>	is_model_of	DOID:0050591	tooth agenesis						ECO:0000033	author statement supported by traceable reference	PMID:9256350	20110428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055584	Bbs1<sup>Gt1Nk</sup>/Bbs1<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15322545	20100603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603337	Kit<sup>tm1Bpr</sup>/Kit<sup>tm1Bpr</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:16061643	20051031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605029	Abcc6<sup>tm1Jfk</sup>/Abcc6<sup>tm1Jfk</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:16135817	20051118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522714	vsd/vsd  [background:] C57BL/6J-vsd	is_model_of	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692665	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] either: (involves: 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	is_model_of	DOID:0110519	autosomal recessive nonsyndromic deafness 68						ECO:0000033	author statement supported by traceable reference	PMID:26805784	20170406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834398	Syne1<sup>tm1.1Mcn</sup>/Syne1<sup>tm1.1Mcn</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL	is_model_of	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19008300	20100611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698752	Htt<sup>tm1.1Pfs</sup>/Htt<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10196365	20070305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177316	Tmc1<sup>Mhdabth</sup>/Tmc1<sup>+</sup>  [background:] C3HeB/FeJ-Tmc1<sup>Mhdabth</sup>/Ieg	is_model_of	DOID:0110563	autosomal dominant nonsyndromic deafness 36						ECO:0000033	author statement supported by traceable reference	MGI:2681078	20050622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6716878	Yap1<sup>tm1.1Hmc</sup>/Yap1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6 * C57BL/6NCrl	is_model_of	DOID:0050795	cone dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32801350	20210622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4881413	Ryr1<sup>tm1.1Dhm</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S2/SvPasCrl * 129S6/SvEvTac	is_model_of	DOID:3529	congenital myopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:19959667	20110131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569513	Msrb3<sup>tm1Hyk</sup>/Msrb3<sup>tm1Hyk</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110523	autosomal recessive nonsyndromic deafness 74						ECO:0000033	author statement supported by traceable reference	PMID:24191262	20140625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628916	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590146	Ncf1<sup>tm1Hbd</sup>/Ncf1<sup>tm1Hbd</sup>  [background:] involves: 129	is_model_of	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:11733538	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936861	Sptbn1<sup>tm1Mish</sup>/Sptbn1<sup>+</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:5572	Beckwith-Wiedemann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20739274	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7266813	Adgrg6<sup>tm1Arte</sup>/Adgrg6<sup>tm1Arte</sup> Tg(Col2a1-cre)#Amc/0  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:25954032	20220506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392615	Iqsec2<sup>em1Frk</sup>/Y  [background:] involves: C3HeB/FeJ * C57BL/6NJ	is_model_of	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:31978606	20200303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317004	Ccn6<sup>tm1(cre)Mawa</sup>/Ccn6<sup>tm1(cre)Mawa</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood						ECO:0000033	author statement supported by traceable reference	PMID:24040393	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794450	Tg(Pmp22)247Ueli/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:15755691	20080620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6331363	Tg(Nphs1-rtTA*3G)8Jhm/0 Tg(tetO-GFP,-APOL1*)#Susz/0  [background:] involves: C57BL/6J * CBA/J * FVB/N	is_model_of	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28218918	20190731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5905901	Tg(Myh6-tTA)6Smbf/0 Tg(tetORo1-lacZ)3Conk/0  [background:] FVB.Cg-Tg(Myh6-tTA)6Smbf Tg(tetORo1-lacZ)3Conk	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:10781088	20170731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695318	Dchs1<sup>tm1.2Irv</sup>/Dchs1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:988	mitral valve prolapse						ECO:0000033	author statement supported by traceable reference	PMID:26258302	20151110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2660653	Cav3<sup>tm1Mls</sup>/Cav3<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:0060255	rippling muscle disease 2						ECO:0000033	author statement supported by traceable reference	PMID:11259414	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5464285	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1Pai</sup> Tg(MUT)AHlps/0 Tg(MUT*R403X)#Hlps/0  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:23024777	20130215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036852	Sim1<sup>tm1Fan</sup>/Sim1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:11448938	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766287	Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>/Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>  [background:] B6.129P2-Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>	is_model_of	DOID:9268	glycine encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:25736695	20160503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702925	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:15207348	20070416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723060	P2ry12<sup>tm1Cjf</sup>/P2ry12<sup>tm1Cjf</sup>  [background:] involves: 129	is_model_of	DOID:0060692	platelet-type bleeding disorder 8						ECO:0000033	author statement supported by traceable reference	PMID:11413167	20151118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6444908	Tubb4a<sup>em1Avan</sup>/Tubb4a<sup>em1Avan</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060798	hypomyelinating leukodystrophy 6						ECO:0000033	author statement supported by traceable reference	PMID:32463361	20200727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6315197	Tg(Vav1-Asxl1*Y588X)#Fcy/0  [background:] C57BL/6-Tg(Vav1-Asxl1*Y588X)#Fcy	is_model_of	DOID:2226	myeloproliferative neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:29113963	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544331	Gnptab<sup>tm1Kkol</sup>/Gnptab<sup>tm1Kkol</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000033	author statement supported by traceable reference	PMID:24127423	20140217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175132	Myo15a<sup>sh2-2J</sup>/Myo15a<sup>sh2-2J</sup>  [background:] involves: STOCK Rb(16.17)7Bnr	is_model_of	DOID:0110488	autosomal recessive nonsyndromic deafness 3						ECO:0000033	author statement supported by traceable reference	MGI:2135933	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673459	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] B6.129S4-Fancd2<sup>tm1Hou</sup>	is_model_of	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000033	author statement supported by traceable reference	PMID:12893777	20110518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3807202	Add1<sup>tm1Llp</sup>/Add1<sup>tm1Llp</sup>  [background:] involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:18723693	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279301	Gata4<sup>tm1.1Sad</sup>/Gata4<sup>+</sup> Glyr1<sup>em1Dsr</sup>/Glyr1<sup>+</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:35182466	20220523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907886	Tg(Myh6-HBEGF)#Iko/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15272002	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517482	Syn1<sup>tm1Pggd</sup>/Syn1<sup>tm1Pggd</sup>  [background:] B6.129P2-Syn1<sup>tm1Pggd</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6501951	Col4a4<sup>m1H</sup>/Col4a4<sup>m1H</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31892712	20210126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3696575	Tg(APP695)3Dbo/0  [background:] B6.C3-Tg(APP695)3Dbo	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12742740	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425922	Casr<sup>BCH011</sup>/Casr<sup>BCH011</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH011</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6430624	Sh3rf2<sup>tm1Zhxu</sup>/Sh3rf2<sup>+</sup> Tg(Thy1-EGFP)MJrs/0  [background:] involves: C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30540932	20200529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162486	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>/Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>  [background:] B6.Cg-Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>	is_model_of	DOID:3614	Kallmann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29263200	20180626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604722	Dido1<sup>tm1Cmar</sup>/Dido1<sup>tm1Cmar</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:4972	myelodysplastic/myeloproliferative neoplasm						ECO:0000033	author statement supported by traceable reference	PMID:16127461	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007766	Cep290<sup>tm1.1Jgg</sup>/Cep290<sup>tm1.1Jgg</sup>  [background:] involves: 129	is_model_of	DOID:0111000	Joubert syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:21623382	20110616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712360	Scyl1<sup>mdf</sup>/Scyl1<sup>mdf</sup>  [background:] B6C3Fe a/a-Scyl1<sup>mdf</sup>/J	is_model_of	DOID:0050951	hereditary ataxia						ECO:0000033	author statement supported by traceable reference	PMID:17571074	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818603	Atg16l1<sup>Gt(BC0122)Wtsi</sup>/Atg16l1<sup>Gt(BC0122)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110885	inflammatory bowel disease 10						ECO:0000033	author statement supported by traceable reference	PMID:18849966	20081209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2172625	Dnah11<sup>iv</sup>/Dnah11<sup>iv</sup>  [background:] involves: C3H	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:48750	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5703970	Asb4<sup>tm1.2Cpat</sup>/Asb4<sup>tm1.2Cpat</sup>  [background:] involves: 129/SvEv	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:27821757	20170317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430751	Inpp5b<sup>tm1Nbm</sup>/Inpp5b<sup>tm1Nbm</sup> Ocrl<sup>tm1Nbm</sup>/Ocrl<sup>tm1Nbm</sup> Tg(INPP5B)CNbm/0  [background:] involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	is_model_of	DOID:1056	oculocerebrorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21183592	20120809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4889103	Edar<sup>dl-J</sup>/Edar<sup>dl-J</sup>  [background:] involves: FVB/N	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:9799834	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883506	None [background:] YBR/EiJ	is_model_of	DOID:240	iris disease						ECO:0000033	author statement supported by traceable reference	PMID:27483353	20180404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6729923	Atp1a2<sup>tm1.1Gica</sup>/Atp1a2<sup>+</sup>  [background:] B6.Cg-Atp1a2<sup>tm1.1Gica</sup>	is_model_of	DOID:0111182	familial hemiplegic migraine 2						ECO:0000033	author statement supported by traceable reference	PMID:21731499	20210810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6511077	Nexn<sup>em1Chen</sup>/Nexn<sup>em1Chen</sup>  [background:] C57BL/6J-Nexn<sup>em1Chen</sup>	is_model_of	DOID:0110424	dilated cardiomyopathy 1CC						ECO:0000033	author statement supported by traceable reference	PMID:32814711	20210318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4847969	Lrp2<sup>m267Asp</sup>/Lrp2<sup>m267Asp</sup>  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0090144	Donnai-Barrow syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20653565	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423510	Mir140<sup>em1Tkob</sup>/Mir140<sup>em1Tkob</sup>  [background:] C57BL/6-Mir140<sup>em1Tkob</sup>	is_model_of	DOID:2256	osteochondrodysplasia						ECO:0000033	author statement supported by traceable reference	PMID:30804514	20200520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7429209	Arb2a<sup>Tg(Tyr)TpNpin</sup>/Arb2a<sup>Tg(Tyr)TpNpin</sup>  [background:] involves: FVB/N	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29311329	20230130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664130	Pafah1b1<sup>tm2.2Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6356371	Jag1<sup>Ndr</sup>/Jag1<sup>Ndr</sup>  [background:] involves: C3HeB/FeJ * C57BL/6	is_model_of	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29162437	20190820	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039429	Sox10<sup>tm1Weg</sup>/Sox10<sup>tm1Weg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:3614	Kallmann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23643381	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844551	Tg(CAG-PKD2)#Hwl/?  [background:] involves: FVB/NJ	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:19098310	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7343893	Bcor<sup>tm1.1Vjba</sup>/Bcor<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/Tmem163<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6N * FVB/N	is_model_of	DOID:0111809	syndromic microphthalmia 2						ECO:0000033	author statement supported by traceable reference	PMID:32692983	20221006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621471	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6 * DBA	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:15798202	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438091	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/0 Usp9x<sup>tm1Tuv</sup>/Usp9x<sup>+</sup>  [background:] involves: 129S4/SvJae * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22699621	20220511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052222	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:9467	nail-patella syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15562281	20050722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6188005	Ntrk3<sup>tm1.1Tes</sup>/Ntrk3<sup>+</sup> Tg(RHO*P347S)A1Tili/0  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:29242588	20180711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5907165	Flnc<sup>tm1.1Rsdf</sup>/Flnc<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080096	myofibrillar myopathy 5						ECO:0000033	author statement supported by traceable reference	PMID:26472074	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3656023	Xirp1<sup>tm1Jl</sup>/Xirp1<sup>tm1Jl</sup>  [background:] involves: 129	is_model_of	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17766470	20170810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428021	Fam20c<sup>tm1.1Cqi</sup>/Fam20c<sup>tm1.1Cqi</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:22615579	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655503	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] Not Specified	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10791995	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619140	Gaa<sup>tm1Vdp</sup>/Gaa<sup>tm1Vdp</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	is_model_of	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:9384603	20060412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487546	Tg(Prnp*P101L)174Sbp/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1980379	20130529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6423629	Stk39<sup>tm1Pawe</sup>/Stk39<sup>tm1Pawe</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28442491	20200521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2387325	Aifm1<sup>Hq</sup>/Aifm1<sup>Hq</sup>  [background:] B6CBACa A<sup>w-J</sup>/A-Aifm1<sup>Hq</sup>/J	is_model_of	DOID:0060536	mitochondrial complex I deficiency						ECO:0000033	author statement supported by traceable reference	PMID:18791645	20171031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421411	Snca<sup>tm1Nbm</sup>/Snca<sup>tm1Nbm</sup> Tg(SNCA*A53T)1Nbm/Tg(SNCA*A53T)1Nbm Tg(SNCA*A53T)2Nbm/Tg(SNCA*A53T)2Nbm  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:20106867	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819121	Tg(Wnt1)1Hev/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:10713683	20100813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5519095	Rb1<sup>tm3Tyj</sup>/Rb1<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * CD-1 * FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:18559481	20131121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850821	Igh<sup>tm1.1(Tag)Rwhe</sup>/Igh<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:19332766	20160622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6473967	Vwf<sup>tm1.1Vhf</sup>/Vwf<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N	is_model_of	DOID:12531	von Willebrand's disease						ECO:0000033	author statement supported by traceable reference	PMID:30565388	20201124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6727361	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J * CBA	is_model_of	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6314698	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeH * C57BL/6JNju	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30740049	20190621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174725	Hps5<sup>ru2-hz</sup>/Hps5<sup>ru2-hz</sup>  [background:] involves: DBA/2J	is_model_of	DOID:0060543	Hermansky-Pudlak syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781308	Magel2<sup>tm1Stw</sup>/Magel2<sup>tm1Stw</sup>  [background:] C57BL/6-Magel2<sup>tm1Stw</sup>/J	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27436578	20160725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287871	Gprasp2<sup>tm1.1Jpe</sup>/Y  [background:] B6.129(FVB)-Gprasp2<sup>tm1.1Jpe</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30926797	20190418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575661	Asxl1<sup>tm1.1Iaai</sup>/Asxl1<sup>tm1.1Iaai</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S/SvEv * C57BL/6 * CBA	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24218140	20140731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008417	Mapt<sup>tm1(EGFP)Klt</sup>/Mapt<sup>tm1(EGFP)Klt</sup> Tg(MAPT)8cPdav/0  [background:] B6.Cg-Tg(MAPT)8cPdav Mapt<sup>tm1(EGFP)Klt</sup>/J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21573167	20110621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843460	Avp<sup>tm1Hari</sup>/Avp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:12388	neurohypophyseal diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:19297548	20090508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6695074	Dnah17<sup>em1Qsh</sup>/Dnah17<sup>em1Qsh</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:0111926	spermatogenic failure 39						ECO:0000033	author statement supported by traceable reference	PMID:31658987	20210427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286248	Tg(Prnp-MAPT*P301S)50Hiw/0  [background:] B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:24406748	20190405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525013	Nppa<sup>tm1Unc</sup>/Nppa<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:10763	hypertension						ECO:0000033	author statement supported by traceable reference	PMID:7839143	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429558	Mboat7<sup>tm1Lex</sup>/Mboat7<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287125	Tg(tetO-DISC1*)70Plet/0 Tg(Camk2a-tTA)1Mmay/0  [background:] involves: C57BL/6 * CBA * SJL	is_model_of	DOID:0070085	schizophrenia 9						ECO:0000033	author statement supported by traceable reference	PMID:17848917	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778632	Cdh23<sup>v</sup>/Cdh23<sup>v</sup>  [background:] involves: fancier's stocks	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4420974	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:14522255	20100205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832641	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm2(FCMD)Ttd</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19017726	20090220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677317	Pax2<sup>tm1Pgr</sup>/Pax2<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0090006	renal coloboma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8951055	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6782396	Cchcr1<sup>em1Aoka</sup>/Cchcr1<sup>em1Aoka</sup>  [background:] C57BL/6NJcl-Cchcr1<sup>em1Aoka</sup>	is_model_of	DOID:986	alopecia areata						ECO:0000033	author statement supported by traceable reference	PMID:32580135	20211027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5085920	Lrrtm1<sup>tm1.1Jaru</sup>/Lrrtm1<sup>tm1.1Jaru</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21818371	20110815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5426823	Krt16<sup>tm1(KOMP)Vlcg</sup>/Krt16<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Krt16<sup>tm1(KOMP)Vlcg</sup>	is_model_of	DOID:0050449	pachyonychia congenita						ECO:0000033	author statement supported by traceable reference	PMID:22336941	20140305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6162486	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>/Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>  [background:] B6.Cg-Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>	is_model_of	DOID:0060340	ciliopathy						ECO:0000033	author statement supported by traceable reference	PMID:29263200	20180626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622193	Ppp1r15a<sup>tm1.1Ajf</sup>/Ppp1r15a<sup>tm1.1Ajf</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:10241	thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:16478986	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4888959	Gria1<sup>tm1Rsp</sup>/Gria1<sup>tm1Rsp</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:5418	schizoaffective disorder						ECO:0000033	author statement supported by traceable reference	PMID:20699120	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6120564	Gt(ROSA)26Sor<sup>tm1.1(DUX4*)Plj</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(ACTA1-cre/Esr1*)2Kesr/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:29415061	20180309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7261449	Tg(Col2a1*G574S)1Waho/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0080044	hypochondrogenesis						ECO:0000033	author statement supported by traceable reference	PMID:9022054	20220415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441253	Col2a1<sup>Lpk</sup>/Col2a1<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:22028304	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605834	Tecta<sup>tm2Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0110544	autosomal dominant nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:15995703	20051129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5770121	Vps33b<sup>tm1.1Arte</sup>/Vps33b<sup>tm1.1Arte</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J	is_model_of	DOID:0050763	ARC syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25947942	20170112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3051589	Ghrh<sup>tm1Salv</sup>/Ghrh<sup>tm1Salv</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060873	isolated growth hormone deficiency type IA						ECO:0000033	author statement supported by traceable reference	PMID:15155578	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440978	Smn1<sup>tm5(Smn1/SMN2)Mrph</sup>/Smn1<sup>tm5(Smn1/SMN2)Mrph</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac	is_model_of	DOID:0050530	intermediate spinal muscular atrophy						ECO:0000033	author statement supported by traceable reference	PMID:22802075	20121108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009333	Clec16a<sup>curt</sup>/Clec16a<sup>curt</sup>  [background:] SWR/J-Clec16a<sup>curt</sup>/GrsrJ	is_model_of	DOID:1289	neurodegenerative disease						ECO:0000033	author statement supported by traceable reference	PMID:26987296	20191217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7536982	Best3<sup>tm1.1Zhoj</sup>/Best3<sup>tm1.1Zhoj</sup> Tg(Tagln-cre)1Her/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0080685	aortic dissection						ECO:0000033	author statement supported by traceable reference	PMID:37203562	20231005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7279138	Sf3b1<sup>tm1Hko</sup>/Sf3b1<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25481243	20220520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6715154	Trappc9<sup>em1Xyli</sup>/Trappc9<sup>em1Xyli</sup>  [background:] C57BL/6J-Trappc9<sup>em1Xyli</sup>	is_model_of	DOID:1059	intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:33208359	20210611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723222	Trps1<sup>tm1.1Shiv</sup>/Trps1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	is_model_of	DOID:14743	trichorhinophalangeal syndrome type I						ECO:0000033	author statement supported by traceable reference	PMID:12446778	20071002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762957	Ywhaz<sup>Gt(OST432062)Lex</sup>/Ywhaz<sup>Gt(OST432062)Lex</sup>  [background:] either: B6.129S5-Ywhaz<sup>Gt(OST432062)Lex</sup> or C.129S5-Ywhaz<sup>Gt(OST432062)Lex</sup> or (involves: 129S5/SvEvBrd * 129T2/SvEmsWehi))	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22124272	20160422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430604	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Nes-cre)Wme/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:20075061	20120808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522324	Apc<sup>tm2.1Cip</sup>/Apc<sup>tm2.1Cip</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15563600	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367868	Nipbl<sup>Gt(RRS564)Byg</sup>/Nipbl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * CD-1	is_model_of	DOID:0080505	Cornelia de Lange syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19763162	20230626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822317	Lepr<sup>tm1Yli</sup>/Lepr<sup>tm1Yli</sup>  [background:] B6.129-Lepr<sup>tm1Yli</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:19015522	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897798	Fan1<sup>tm1.1Jrou</sup>/Fan1<sup>tm1.1Jrou</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060911	karyomegalic interstitial nephritis						ECO:0000033	author statement supported by traceable reference	PMID:26980188	20170519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527337	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>/Col1a1<sup>+</sup> Tg(Scgb1a1-rtTA)1Jaw/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:20952506	20140109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758814	Comp<sup>tm1Mbri</sup>/Comp<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0080047	pseudoachondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:17588960	20071022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7281828	Runx3<sup>tm3Yg</sup>/Runx3<sup>tm3Yg</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060250	idiopathic scoliosis						ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6258771	Grin1<sup>tm1Bhk</sup>/Grin1<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22726567	20181203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107893	Copb2<sup>em1Rstot</sup>/Copb2<sup>em2Rstot</sup>  [background:] involves: C57BL/6 * C57BL/6J * CD-1 * DBA/2	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:29036432	20180109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844910	Ikbkg<sup>tm1Mpa</sup>/Ikbkg<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12305	Bloch-Sulzberger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10911992	20090520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653173	Hnf4a<sup>tm1.1Gonz</sup>/Hnf4a<sup>tm1.1Gonz</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA	is_model_of	DOID:0111099	maturity-onset diabetes of the young type 1						ECO:0000033	author statement supported by traceable reference	PMID:16377800	20060830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300942	Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup> Tg(KRT14-cre)52Smr/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * SJL/J	is_model_of	DOID:0110214	cleft soft palate						ECO:0000033	author statement supported by traceable reference	PMID:24496627	20140521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4850007	Tg(Igh-TCL1A)1Ypek/0  [background:] FVB/N-Tg(Igh-TCL1A)1Ypek	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20357824	20110103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6730293	Slc32a1<sup>tm2(cre)Lowl</sup>/Slc32a1<sup>tm2(cre)Lowl</sup>  [background:] either: B6J.129S6(FVB)-Slc32a1<sup>tm2(cre)Lowl</sup> or (involves: 129S6/SvEvTac * C57BL/6J * FVB/N)	is_model_of	DOID:3328	temporal lobe epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:32954490	20210812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6317329	Pkd2<sup>tm3Som</sup>/Pkd2<sup>tm3Som</sup> Tg(Pkhd1-cre)1Igr/0  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:28205547	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054527	Tg(DM15)26Bew/0  [background:] involves: FVB	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:15317754	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435568	Porcn<sup>tm1.1Vdv</sup>/Y Tg(KRT14-cre)1Efu/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624520	Dnah5<sup>Tg1Htz</sup>/Dnah5<sup>Tg1Htz</sup>  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	PMID:11912187	20060615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4456369	Tg(KRT5-IKBKB)1Armz/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2723	dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20200541	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584473	Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6500763	Slc26a4<sup>em1Jgao</sup>/Slc26a4<sup>em1Jgao</sup>  [background:] involves: CBA/CaJ	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31155292	20210118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6287156	Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>/Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0080322	polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:28666097	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5572808	Tshr<sup>hyt-3J</sup>/Tshr<sup>hyt-3J</sup>  [background:] CByJ;CXB10-Tshr<sup>hyt-3J</sup>/GrsrJ	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	MGI:5571363	20140714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174941	Cebpb<sup>tm1Vpo</sup>/Cebpb<sup>tm1Vpo</sup>  [background:] involves: 129S/SvEv * MF1	is_model_of	DOID:934	viral infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:7744000	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683609	Hba<sup>tm1Ney</sup>/Hba<sup>tm1Ney</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:12920035	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028730	Bcat2<sup>m1Ytc</sup>/Bcat2<sup>m1Ytc</sup>  [background:] C57BL/6J-Bcat2<sup>m1Ytc</sup>	is_model_of	DOID:9269	maple syrup urine disease						ECO:0000033	author statement supported by traceable reference	PMID:14755340	20050603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000245	Boc<sup>tm2Rsk</sup>/Boc<sup>tm2Rsk</sup> Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * 129S6/SvEvTac	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21183473	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6286233	Nkx2-5<sup>tm1.1Burg</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S2/SvPasCrl * 129X1/SvJ	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:28302382	20190405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909258	Tg(Myh6-MYL3*A57G)#Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110314	hypertrophic cardiomyopathy 8						ECO:0000033	author statement supported by traceable reference	PMID:23748425	20170915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717180	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup>  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL	is_model_of	DOID:0110184	Charcot-Marie-Tooth disease type 4J						ECO:0000033	author statement supported by traceable reference	PMID:17572665	20070806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6850159	Nemf<sup>em8Cx</sup>/Nemf<sup>em8Cx</sup>  [background:] C57BL/6J-Nemf<sup>em8Cx</sup>/Cx	is_model_of	DOID:870	neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6323048	Tg(HBB-Myc)#Cos/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:9422539	20190715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176444	Rxra<sup>tm1Rev</sup>/Rxra<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1682	congenital heart disease						ECO:0000033	author statement supported by traceable reference	PMID:8823298	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6273993	Tg(RP11-578M14)5Mkru/0  [background:] involves: FVB/N	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:29206867	20190121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6368182	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>tm1.2Lcm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7258133	Yars1<sup>tm1.1Rwb</sup>/Yars1<sup>tm1.1Rwb</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C						ECO:0000033	author statement supported by traceable reference	PMID:34516839	20220330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6502640	Prrt2<sup>tm1d(KOMP)Wtsi</sup>/Prrt2<sup>+</sup>  [background:] B6(Cg)-Prrt2<sup>tm1d(KOMP)Wtsi</sup>	is_model_of	DOID:0090053	episodic kinesigenic dyskinesia 1						ECO:0000033	author statement supported by traceable reference	PMID:32891704	20210128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6476699	Ids<sup>tm1Dkji</sup>/Y  [background:] involves: 129 * C57BL/6	is_model_of	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:22847837	20201201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428334	Tg(Prnp*)#Rgab/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:22072968	20120719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5909088	Tg(Myh7-Ptpn11*Q510E)#Krnz/0  [background:] FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz	is_model_of	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:25724491	20180126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5791061	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:26277094	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6107696	Thap1<sup>tm1.1Meeh</sup>/Thap1<sup>+</sup>  [background:] involves: 129S/SvEv * C3H * C57BL/6	is_model_of	DOID:0090039	torsion dystonia 6						ECO:0000033	author statement supported by traceable reference	PMID:26376866	20180105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720079	Hba<sup>b2(th)</sup>/Hba<sup>+</sup>  [background:] either: (involves: 101 * SEC) or (involves: 101 * C57BL * SEC)	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:879556	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587768	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C3H/HeNHsd * C57BL/6JOlaHsd	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15888477	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821001	Tacr1<sup>tm1Sph</sup>/Tacr1<sup>tm1Sph</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:9748515	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313510	Tg(CRYBB1-CRYGC*)#Jfhe/?  [background:] involves: FVB/N	is_model_of	DOID:0110235	cataract 2 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:21436266	20130429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259651	Pmfbp1<sup>em1Wli</sup>/Pmfbp1<sup>em1Wli</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:30032984	20181210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790680	Elp1<sup>tm1Id</sup>/Elp1<sup>tm1.1Id</sup> Tg(IKBKAP*)#Sasl/0  [background:] involves: 129S1/Sv * C57BL/6N	is_model_of	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26769677	20160907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662389	Del(5Gtf2i-Fkbp6)1Vcam/+  [background:] B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278)	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25027326	20150922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487550	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tgfbr1<sup>tm1.1Karl</sup>/Tgfbr1<sup>tm1.1Karl</sup> Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * CD-1 * FVB/N	is_model_of	DOID:5520	head and neck squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22859719	20130529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:9620767	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2384175	Trpv3<sup>Nh</sup>/Trpv3<sup>+</sup>  [background:] involves: DS	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:9250484	20060125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6441736	Dhtkd1<sup>tm1Mmgu</sup>/Dhtkd1<sup>tm1Mmgu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q						ECO:0000033	author statement supported by traceable reference	PMID:32169121	20200715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6414961	Acvr1<sup>tm1Mak</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>/Gt(ROSA)26Sor<sup>+</sup> H3c2<sup>tm1Mak</sup>/H3c2<sup>+</sup> Olig2<sup>tm1.1(cre)Wdr</sup>/Olig2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:0060108	brain glioma						ECO:0000033	author statement supported by traceable reference	PMID:32142668	20200506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662270	Slc27a4<sup>wrfr</sup>/Slc27a4<sup>wrfr</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0060762	restrictive dermopathy						ECO:0000033	author statement supported by traceable reference	PMID:12697906	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>	is_model_of	DOID:0080026	otospondylomegaepiphyseal dysplasia, autosomal recessive						ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793700	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] B6.129S2-Aire<sup>tm1.1Doi</sup>/Doi	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657302	Fras1<sup>bl</sup>/Fras1<sup>bl</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:0090001	Fraser syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12766769	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6403902	Stat1<sup>tm1Dlv</sup>/Stat1<sup>tm1Dlv</sup> Tg(ANPEP)270Mmul/Tg(ANPEP)270Mmul  [background:] involves: 129S/SvEv * ICR	is_model_of	DOID:0080599	Coronavirus infectious disease						ECO:0000033	author statement supported by traceable reference	PMID:15919828	20200414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6259595	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J	is_model_of	DOID:2513	basal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:10545995	20181207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6196139	Gt(ROSA)26Sor<sup>tm2(CAG-Lin28b,-luc)Jhsc</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Dbh-icre)1Gsc/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:23042116	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6187936	Ndufa1<sup>tm1.1Nay</sup>/Ndufa1<sup>tm1.1Nay</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac	is_model_of	DOID:0060536	mitochondrial complex I deficiency						ECO:0000033	author statement supported by traceable reference	PMID:28506826	20180712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:2662101	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175803	Crybb2<sup>Aey2</sup>/Crybb2<sup>+</sup>  [background:] C3HeB/FeJ-Crybb2<sup>Aey2</sup>	is_model_of	DOID:0110269	cataract 3 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11381063	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425919	Casr<sup>BCH003</sup>/Casr<sup>BCH003</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH003</sup>	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176707	Bcl2<sup>tm1Dlo</sup>/Bcl2<sup>tm1Dlo</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111142	oligomeganephronia						ECO:0000033	author statement supported by traceable reference	PMID:9794553	20180726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:7314827	Mdfic<sup>em#Nlh</sup>/Mdfic<sup>em#Nlh</sup>  [background:] C57BL/6J-Mdfic<sup>em#Nlh</sup>	is_model_of	DOID:0081030	central conducting lymphatic anomaly						ECO:0000033	author statement supported by traceable reference	PMID:35235341	20220722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663596	Epas1<sup>tm1Pec</sup>/Epas1<sup>tm1Pec</sup>  [background:] involves: 129/Sv * Swiss	is_model_of	DOID:12716	newborn respiratory distress syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12053176	20110217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175046	Grin1<sup>tm1Bhk</sup>/Grin1<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:10481908	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814998	Pde6g<sup>tm1Goff</sup>/Pde6g<sup>tm1Goff</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6 * MF1  * Swiss Webster) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * MF1 * Swiss Webster)	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:8638127	20081114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6187717	Tardbp<sup>em1Rhbr</sup>/Tardbp<sup>em1Rhbr</sup>  [background:] C57BL/6J-Tardbp<sup>em1Rhbr</sup>	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:29556029	20180709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6277930	S1pr2<sup>stdf</sup>/S1pr2<sup>stdf</sup>  [background:] involves: C57BL/6Brd * C57BL/6N	is_model_of	DOID:0110519	autosomal recessive nonsyndromic deafness 68						ECO:0000033	author statement supported by traceable reference	PMID:27383011	20190212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769345	Jak3<sup>tm1Ljb</sup>/Jak3<sup>tm1Ljb</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive						ECO:0000033	author statement supported by traceable reference	PMID:11034372	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5284902	Pdlim5<sup>tm1.1Chen</sup>/Pdlim5<sup>tm1.1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20538684	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6456066	Diaph3<sup>tm1.1Pji</sup>/Diaph3<sup>tm1.1Pji</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:1338	congenital dyserythropoietic anemia						ECO:0000033	author statement supported by traceable reference	PMID:26471482	20200918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628830	Dnmt3b<sup>tm6Enl</sup>/Dnmt3b<sup>tm6Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5629954	Bscl2<sup>tm1.1Gliu</sup>/Bscl2<sup>tm1.1Gliu</sup> Tg(Fabp4-cre)1Rev/0  [background:] involves: 129 * 129S4/SvJaeSor	is_model_of	DOID:12336	male infertility						ECO:0000033	author statement supported by traceable reference	PMID:24778225	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512040	Gp1bb<sup>tm1Ware</sup>/Gp1bb<sup>tm1Ware</sup>  [background:] Not Specified	is_model_of	DOID:2217	Bernard-Soulier syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15213102	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179512	Il2ra<sup>tm1Dw</sup>/Il2ra<sup>tm1Dw</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:7584142	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6164043	Tg(Vav1-STAT5B*N642H)726Biat/0  [background:] C57BL/6NCrl-Tg(Vav1-STAT5B*N642H)726Biat	is_model_of	DOID:0060058	lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:29200404	20180703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429555	Tg(Notch3*R169C)88Bbb/0  [background:] involves: FVB/N	is_model_of	DOID:2316	brain ischemia						ECO:0000033	author statement supported by traceable reference	PMID:20071773	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5469978	Tg(Pnkd*A7V*A9V,-DsRed)671Ljp/0  [background:] B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)671Ljp	is_model_of	DOID:0090049	paroxysmal nonkinesigenic dyskinesia 1						ECO:0000033	author statement supported by traceable reference	PMID:22214848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819421	T(9;17)138Ca/T(9;17)138Ca  [background:] Not Specified	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	MGI:4940633	20130103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6467541	Tg(SERPINA1-TAg)1812Jtsb/0  [background:] involves: C3H * C57BL/6 * ICR	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:2551499	20201019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6404937	Rs1<sup>tm1.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)	is_model_of	DOID:0110914	infantile hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008644	Tg(Plp1-SNCA)1Haa/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:15743798	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652741	Gpx1<sup>tm1Ysh</sup>/Gpx1<sup>+</sup> Gpx2<sup>tm2Coh</sup>/Gpx2<sup>tm2Coh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:11518697	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177295	Amelx<sup>tm1Kul</sup>/Amelx<sup>tm1Kul</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000033	author statement supported by traceable reference	PMID:11406633	20050601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056101	Timp3<sup>tm1Rkho</sup>/Timp3<sup>tm1Rkho</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:16037568	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606089	Slc19a2<sup>tm1Ejn</sup>/Slc19a2<sup>tm1Ejn</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac	is_model_of	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14567973	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6405401	Tardbp<sup>tm2.1Neas</sup>/Tardbp<sup>tm2.1Neas</sup>  [background:] B6(C3)-Tardbp<sup>tm2.1Neas</sup>	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:30625319	20200423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6256822	Col1a1<sup>tm1(CAG-EGFR*T790M*C797S*L858R)Mje</sup>/Col1a1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:27251290	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5519120	Del(16Dgcr2-Hira)3Aam/+  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:20360742	20131122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792659	Ifng<sup>tm1.1Hayg</sup>/Ifng<sup>tm1.1Hayg</sup>  [background:] Not Specified	is_model_of	DOID:12449	aplastic anemia						ECO:0000033	author statement supported by traceable reference	PMID:25342713	20160919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6405698	Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>/Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] B6J.Cg-Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:31824252	20200424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175153	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:10215624	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5570747	Tg(Slc1a2-tTA)#Waw/0 Tg(tetO-MYCN,-luc)#Waw/0  [background:] involves: FVB/NJ	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:20478998	20140701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576251	Nfil3<sup>tm1Pbro</sup>/Nfil3<sup>tm1Pbro</sup>  [background:] B6.129S6-Nfil3<sup>tm1Pbro</sup>	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:24442434	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538529	Smarcb1<sup>tm1Sho</sup>/Smarcb1<sup>+</sup> Tg(LPV-TAg121)2Tvd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J	is_model_of	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5608405	Aff3<sup>tm1a(EUCOMM)Wtsi</sup>/Aff3<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Aff3<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi	is_model_of	DOID:0112383	KINSSHIP syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33961779	20220613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:6392337	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>/Sdhc<sup>tm1c(EUCOMM)Wtsi</sup> Gt(ROSA)26Sor<sup>tm1.1(rtTA,tetO-cre)Bkmn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:31469588	20200302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175884	Fgf10<sup>tm1Ska</sup>/Fgf10<sup>tm1Ska</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10486	intestinal atresia						ECO:0000033	author statement supported by traceable reference	PMID:15234214	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056384	Ccdc39<sup>prh</sup>/Ccdc39<sup>prh</sup>  [background:] involves: A/J * FVB/N	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:29317443	20180222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771020	Efemp1<sup>tm1Lmar</sup>/Efemp1<sup>tm1Lmar</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17664227	20080215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:27270598	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:26608452	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:31317194	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:26398942	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:28610891	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:19151629	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV						ECO:0000033	author statement supported by traceable reference	PMID:32586947	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794204	Mcoln1<sup>tm1Sasl</sup>	is_implicated_in	DOID:0080490	mucolipidosis type IV		MGI:3795387	Mcoln1<sup>tm1Sasl</sup>/Mcoln1<sup>tm1Sasl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17924347	20210121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719077	Neu1<sup>a</sup>/Neu1<sup>a</sup>  [background:] SM/J	is_model_of	DOID:3343	glycoproteinosis						ECO:0000033	author statement supported by traceable reference	PMID:9425240	20070824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687203	Cdkn2a<sup>tm4Rdp</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30938713	20211119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687203	Cdkn2a<sup>tm4Rdp</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28685754	20211119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904804	Tg(Myh6-CACNA1C)M1Aschw	is_implicated_in	DOID:6000	congestive heart failure		MGI:5904828	Tg(Myh6-CACNA1C)M1Aschw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11136699	20170717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22422766	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26134627	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:36619669	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26911699	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22037760	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26758873	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27488123	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26621405	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:33382987	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26733414	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31127156	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25692239	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:20832308	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26030275	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24691550	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25557785	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26438828	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26276812	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25878277	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31060774	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26258776	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23656793	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22079083	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448989	Grm7<sup>Tg(SMN2)89Ahmb</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22763238	20230331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311110	F2rl1<sup>tm1Cgh</sup>/F2rl1<sup>tm1Cgh</sup> Spink5<sup>tm1Hov</sup>/Spink5<sup>tm1Hov</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20703245	20120319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16636275	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:18077368	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:15263088	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:8610185	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR	is_model_of	DOID:0060887	ossification of the posterior longitudinal ligament of spine						ECO:0000033	author statement supported by traceable reference	PMID:9359030	20060731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR	is_model_of	DOID:0060887	ossification of the posterior longitudinal ligament of spine						ECO:0000033	author statement supported by traceable reference	PMID:9662402	20060731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23577147	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25855725	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28300085	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24763051	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27197203	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27601049	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:30650356	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22006184	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050871	Tg(MMTV-Erbb2)NK1Mul	is_implicated_in	DOID:1612	breast cancer		MGI:5538583	Tg(MMTV-Erbb2)NK1Mul/0  [background:] FVB/N-Tg(MMTV-Erbb2)NK1Mul			ECO:0000033	author statement supported by traceable reference	PMID:11200779	20220401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838675	Tg(tetO-Bmpr2*R899X)#Jwst	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:4838758	Tg(Tagln-rtTA)E1Jwst/0 Tg(tetO-Bmpr2*R899X)#Jwst/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20562228	20130409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838675	Tg(tetO-Bmpr2*R899X)#Jwst	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20130409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565691	Tg(UBC-GFP/HTT*84Q)22Shya/0  [background:] involves: FVB	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22422149	20140530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932297	F9<sup>tm1Dws</sup>	is_implicated_in	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:25700434	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932297	F9<sup>tm1Dws</sup>	is_implicated_in	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:24425804	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932297	F9<sup>tm1Dws</sup>	is_implicated_in	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:31594977	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932297	F9<sup>tm1Dws</sup>	is_implicated_in	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:26443873	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932297	F9<sup>tm1Dws</sup>	is_implicated_in	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:27106122	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932297	F9<sup>tm1Dws</sup>	is_implicated_in	DOID:12259	hemophilia B		MGI:3662691	F9<sup>tm1Dws</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9354664	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818964	Tg(KRT5-AR)191Cct	is_implicated_in	DOID:0050801	androgenic alopecia		MGI:4818968	Tg(KRT5-AR)191Cct/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20233794	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449164	Myo7a<sup>sh1</sup>/Myo7a<sup>sh1</sup>  [background:] involves: BALB	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:4187938	20080121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449164	Myo7a<sup>sh1</sup>/Myo7a<sup>sh1</sup>  [background:] involves: BALB	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:63673	20080121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793766	Tg(Myh6*)1Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793766	Tg(Myh6*)1Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:5908275	Tg(Myh6*)1Lnwd/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10362699	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793766	Tg(Myh6*)1Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:5908349	Tg(Myh6*)1Lnwd/Tg(Myh6*)1Lnwd  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10362699	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:21047552	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5908182	Tg(Myh6-Mtpn)4Ssen/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:14970239	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19502558	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18037434	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15385543	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18620706	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20202977	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:20157292	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:24662047	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:28412297	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:28823869	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:24244862	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:25920768	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:3055667	Dysf<sup>prmd</sup>/Dysf<sup>prmd</sup>  [background:] A/J			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806870	Tg(Venus/SOX10*)55Kein	is_implicated_in	DOID:0090111	PCWH syndrome		MGI:5806875	Tg(Venus/SOX10*)55Kein/Tg(Venus/SOX10*)55Kein  [background:] involves: C3H/He * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25959061	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806870	Tg(Venus/SOX10*)55Kein	is_implicated_in	DOID:0090111	PCWH syndrome		MGI:5806872	Tg(Venus/SOX10*)55Kein/0  [background:] involves: C3H/He * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25959061	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908459	Tg(Myh6-Mybpc3*)32Rbns	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5908460	Tg(Myh6-Mybpc3*)32Rbns/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11549344	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908459	Tg(Myh6-Mybpc3*)32Rbns	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5908460	Tg(Myh6-Mybpc3*)32Rbns/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9769321	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908459	Tg(Myh6-Mybpc3*)32Rbns	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908459	Tg(Myh6-Mybpc3*)32Rbns	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:11549344	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444208	Tg(ACTA1-TPM3*M9R)4Hrd	is_implicated_in	DOID:0110926	nemaline myopathy 1		MGI:5444222	Tg(ACTA1-TPM3*M9R)4Hrd/0  [background:] FVB/NJ-Tg(ACTA1-TPM3*M9R)4Hrd			ECO:0000033	author statement supported by traceable reference	PMID:11157795	20121203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6810775	Tg(Thy1-SNCA*)#Ztzh	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:6814676	Tg(Thy1-SNCA*)#Ztzh/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34744697	20220523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6810775	Tg(Thy1-SNCA*)#Ztzh	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:35462005	20220523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603442	Fmr1<sup>tm1.1Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34714519	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603442	Fmr1<sup>tm1.1Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28082376	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603442	Fmr1<sup>tm1.1Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22522472	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603442	Fmr1<sup>tm1.1Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24811383	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603442	Fmr1<sup>tm1.1Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:3604219	Fmr1<sup>tm1.1Cidz</sup>/Fmr1<sup>tm1.1Cidz</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16055059	20230427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524146	Tg(MMTV-Myc*T58A)TA39Jrn/0  [background:] involves: FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30597232	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25799372	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30311654	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30596517	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27234656	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27143421	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31404586	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22581851	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20231476	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26086915	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33412244	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33341653	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30292394	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30936558	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27395445	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27407064	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27497681	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31308530	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34315531	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31146911	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24964199	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26776077	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26423933	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24960578	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30174598	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32485218	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25485684	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36135933	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25281826	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31303501	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30300917	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31818974	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29563870	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27030769	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31831179	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28319837	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33232936	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26780512	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28027926	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28011637	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27393253	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27207465	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34821024	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27103515	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27785573	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32950781	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30865678	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28598849	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28842416	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32070713	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26116027	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33221742	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26804996	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29844346	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32999398	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23512986	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31203190	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24792906	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26982728	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28577919	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23702344	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28683325	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27581687	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32514139	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30007162	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26779813	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32224066	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27516385	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32612165	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21788993	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27240542	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26827641	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28416393	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33336891	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31879131	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26865611	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32699218	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24569075	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26827653	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26609163	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26520465	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25174876	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26581893	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26549211	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33766652	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28360125	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20053373	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27091974	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32145065	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25617315	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35846991	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30851437	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31284126	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34099706	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30127003	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33623128	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28420695	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28750017	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31024293	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33190798	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31024073	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25500888	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27837675	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23863461	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26619807	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31585361	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35462302	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30797171	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26003667	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32320664	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26582899	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32884056	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28429406	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30687079	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18378045	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31252207	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29246925	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35013236	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24894464	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26928013	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23968591	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28398234	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33039900	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26578392	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28228716	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31481723	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31302265	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29038051	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36779013	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35806318	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30884411	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27641666	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27114526	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28108292	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29246793	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31213067	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32222058	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27903721	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33766653	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28351972	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33607163	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31520077	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29216449	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26230261	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17029828	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:6314698	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeH * C57BL/6JNju			ECO:0000033	author statement supported by traceable reference	PMID:30740049	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3665286	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:16899370	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5008418	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:21573167	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5701399	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] D2.Cg-Tg(APPswe,PSEN1dE9)85Dbo			ECO:0000033	author statement supported by traceable reference	PMID:25933409	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5008418	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:26780512	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5008418	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:20445063	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14645205	20231109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:7311569	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:7311570	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:33393189	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:29703891	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22030750	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21875900	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:31690656	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:33398110	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:30157432	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23690466	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295747	Lmna<sup>tm1.1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:5295754	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23690466	20220712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818943	Tg(CD2-Stat6*V625A*T626A)78Mhk/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20147633	20100811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510236	Clcn5<sup>tm1Gug</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050699	Dent disease						ECO:0000033	author statement supported by traceable reference	PMID:11115837	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661058	Gusb<sup>tm4Sly</sup>/Gusb<sup>tm4Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12700165	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119725	Tor1a<sup>tm1Calak</sup>	is_implicated_in	DOID:0050836	focal dystonia		MGI:6273760	Tor1a<sup>tm1Calak</sup>/Tor1a<sup>tm1Calak</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27168150	20190117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25728668	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27658617	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32332118	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32341542	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31992814	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31029017	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33540048	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36056186	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32963298	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30787942	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26314636	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28442538	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32810755	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24485508	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36075886	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32141089	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23605442	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30797170	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29793509	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31306446	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32424276	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29321225	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29273398	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33607163	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33254080	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33097708	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26884167	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:38012646	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26619118	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20619937	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26687814	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25697701	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34500034	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25637807	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26214837	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31156407	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26202697	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32879487	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30631278	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:37892143	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31213067	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31801888	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29501530	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24853300	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25766789	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32522622	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33362250	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29990310	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25361083	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31743728	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28284721	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24146979	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35236374	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31001105	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27288150	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30254165	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29129677	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24650793	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29444427	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24069328	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26686669	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24291517	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25078295	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31914599	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35033173	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27091843	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23499006	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29725016	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35516801	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22267726	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32599514	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35496999	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32999351	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29078331	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32479996	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32968166	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31349006	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32651420	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28361984	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35740989	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28119565	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26779813	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26142956	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26549211	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33830999	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33523861	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27091974	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33631273	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24360883	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32758917	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32619873	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25378159	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22223639	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3693295	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17021169	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5051941	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/?  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21356380	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5755045	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas  [background:] B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas			ECO:0000033	author statement supported by traceable reference	PMID:25697701	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5604616	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] B6SJL-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:24709310	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:6257021	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:28806762	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28059767	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:29228234	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26640144	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:31512783	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28515147	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:4358249	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21620777	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:4358249	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22350410	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:5827768	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)20Fwan/?  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27345403	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:4420974	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:14522255	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402051	Tg(CAG-DPP4)52Ctkt	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26184451	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402051	Tg(CAG-DPP4)52Ctkt	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6402055	Tg(CAG-DPP4)52Ctkt/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26446606	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402051	Tg(CAG-DPP4)52Ctkt	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30256968	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402051	Tg(CAG-DPP4)52Ctkt	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6402055	Tg(CAG-DPP4)52Ctkt/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25589660	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402051	Tg(CAG-DPP4)52Ctkt	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26446606	20200623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175836	Dysf<sup>im</sup>/Dysf<sup>im</sup>  [background:] involves: SJL	is_model_of	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:10508505	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5648248	Dnah5<sup>b2b3491Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5649319	Dnah5<sup>b2b3491Clo</sup>/Dnah5<sup>b2b3491Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b3491Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564782	Prdm16<sup>tm1.1Brsp</sup>	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:7314277	Prdm16<sup>tm1.1Brsp</sup>/Prdm16<sup>tm1.1Brsp</sup> Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: 129 * C57BL/6J * MF1			ECO:0000033	author statement supported by traceable reference	PMID:34915728	20220721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446162	b2b1941Clo	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5487398	b2b1941Clo/b2b1941Clo  [background:] C57BL/6J-b2b1941Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514344	Tg(CTSG-ZBTB16/RARA)#Ppp/0 Zbtb16<sup>tm1Ppp</sup>/Zbtb16<sup>tm1Ppp</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:11106752	20131024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522719	Tg(Upk2-HRAS*Q61L)5Xrw	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6512851	App<sup>em1Bdes</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33076948	20210329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6502853	Prickle3<sup>em1Mxg</sup>	is_implicated_in	DOID:0111754	Leber plus disease		MGI:6514801	Prickle3<sup>em1Mxg</sup>/Prickle3<sup>em1Mxg</sup>  [background:] C57BL/6JSlacc-Prickle3<sup>em1Mxg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32516135	20210402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6502853	Prickle3<sup>em1Mxg</sup>	is_implicated_in	DOID:0111754	Leber plus disease		MGI:6514802	Prickle3<sup>em1Mxg</sup>/Y  [background:] C57BL/6JSlacc-Prickle3<sup>em1Mxg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32516135	20210402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6274693	B3glct<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:0080201	Peters plus syndrome		MGI:6406756	B3glct<sup>tm1b(KOMP)Wtsi</sup>/B3glct<sup>tm1b(KOMP)Wtsi</sup>  [background:] B6(Cg)-B3glct<sup>tm1b(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31600785	20200429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653988	Ppp1r3a<sup>tm1Ptwc</sup>/Ppp1r3a<sup>tm1Ptwc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12606498	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27322773	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24163136	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22203986	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23145119	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24069165	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22750242	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29175489	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24023695	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26791230	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32360664	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27493188	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27158936	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23486940	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26416261	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31040321	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:33636390	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25252949	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26010802	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24474789	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24833719	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29789581	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24154542	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28186560	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:21372009	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27930290	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26853136	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25268710	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25283820	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25344630	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:33359475	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25820275	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32858144	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29154923	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26200799	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25085783	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22371592	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32032731	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25648889	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24667415	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26756888	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27114530	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:33436868	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23000617	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26362733	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23608112	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22390177	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26330466	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22871270	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28053031	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26320681	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22735487	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30295421	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28723387	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27083773	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25526593	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25684566	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26604138	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26502195	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29650983	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23836781	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:20732897	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:35523582	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23818595	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25914627	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31157617	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:34912047	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29486297	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:33174532	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25339858	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26210454	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22634363	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26067594	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23131553	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30674678	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26908600	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22558300	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22815892	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24945277	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22180738	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23466699	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23748038	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25753484	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29024785	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23029057	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23936040	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22431618	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26020962	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32719333	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28344074	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23139902	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32973290	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23043510	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31394426	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32973137	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29409912	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32750380	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22558322	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24381160	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25054289	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25892237	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24607225	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24040091	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:33557211	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:35021077	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26132656	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22521585	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28612258	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30038021	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28002846	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26221023	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29518482	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:32234507	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31540330	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25596588	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22621959	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16000321	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25377090	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22269142	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30134203	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29458840	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:34145375	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31061493	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22678056	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23825599	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23466698	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28864422	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27796305	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22438926	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24445319	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28666328	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31344397	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29524628	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:31575928	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8610185	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J			ECO:0000033	author statement supported by traceable reference	PMID:19187267	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16636275	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15263088	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J			ECO:0000033	author statement supported by traceable reference	PMID:25024188	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3688004	Tg(SOD1*G93A)1Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18077368	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3693880	Tg(SOD1*G93A)1Gur/0  [background:] B6.Cg-Tg(SOD1*G93A)1Gur/J			ECO:0000033	author statement supported by traceable reference	PMID:23608112	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J			ECO:0000033	author statement supported by traceable reference	PMID:12384220	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4829786	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur			ECO:0000033	author statement supported by traceable reference	PMID:19116365	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J			ECO:0000033	author statement supported by traceable reference	PMID:18997009	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183719	Tg(SOD1*G93A)1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4839171	Tg(SOD1*G93A)1Gur/0  [background:] B6.Cg-Tg(SOD1*G93A)1Gur			ECO:0000033	author statement supported by traceable reference	PMID:19699279	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857127	Apoa1<sup>tm1Unc</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20739292	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3612954	Pax9<sup>tm1Hpt</sup>/Pax9<sup>tm1Hpt</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050591	tooth agenesis						ECO:0000033	author statement supported by traceable reference	PMID:16236760	20060216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5519094	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * CD-1 * FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:33594717	20230529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5519094	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J * CD-1 * FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:18559481	20230529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175800	Cryaa<sup>tm1Wawr</sup>/Cryaa<sup>tm1Wawr</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:9023351	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867871	Itm2b<sup>tm3.1Ldad</sup>	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4867886	Itm2b<sup>tm3.1Ldad</sup>/Itm2b<sup>tm3.1Ldad</sup>  [background:] B6.129-Itm2b<sup>tm3.1Ldad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21048150	20120802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867871	Itm2b<sup>tm3.1Ldad</sup>	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:22514310	20120802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5700364	Tmem218<sup>Gt(OST40451)Lex</sup>/Tmem218<sup>Gt(OST40451)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0050576	Senior-Loken syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25161209	20160101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33482356	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31213067	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24055016	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29134514	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29691440	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33785038	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26446044	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23240999	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26003413	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28965984	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31004062	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22203986	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24069439	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22323736	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23555730	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24316473	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26010758	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23000537	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30311654	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31537873	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23910655	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27829153	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24746365	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33484828	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31951013	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24899720	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23922875	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26452999	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22608241	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34798897	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23049854	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31213631	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25698614	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23554921	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27798139	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24524966	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26305888	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25361083	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28186562	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24126163	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29097202	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28711595	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23506847	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24094580	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3029285	Tg(APPSWE)2576Kha/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22085694	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3710766	Tg(APPSWE)2576Kha/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17215356	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720700	Tg(APPSWE)2576Kha/0  [background:] involves: C57BL/6 * DBA/2 * SJL * SW			ECO:0000033	author statement supported by traceable reference	PMID:19041304	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385631	Tg(APPSWE)2576Kha	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3029285	Tg(APPSWE)2576Kha/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16236385	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5645358	Nras<sup>tm1.1Nesh</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:27236105	20190123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5903758	Nmnat1<sup>imh</sup>	is_implicated_in	DOID:0110005	Leber congenital amaurosis 9		MGI:5903761	Nmnat1<sup>imh</sup>/Nmnat1<sup>imh</sup>  [background:] B6J.C(C3H)-Nmnat1<sup>imh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27207593	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856798	A<sup>y</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24887517	20201102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856798	A<sup>y</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24339994	20201102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856798	A<sup>y</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25796170	20201102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856798	A<sup>y</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23583377	20201102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856798	A<sup>y</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:32999320	20201102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947239	Jup<sup>tm1.1Glr</sup>	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:22522917	20121016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947239	Jup<sup>tm1.1Glr</sup>	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12		MGI:4947241	Jup<sup>tm1.1Glr</sup>/Jup<sup>tm1.1Glr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21245375	20121016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806789	Tg(Thy1-SNCA*E57K)16Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:24662516	20161110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763922	Tg(HSA*LR)32bCath/?  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:17101178	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:15111796	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:23774686	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:15585404	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:12576554	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:16473336	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:22580166	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:23562162	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:15979918	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:16979922	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15979918	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12576554	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15111796	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5505265	Serpinh1<sup>tm2Kzn</sup>	is_implicated_in	DOID:0110346	osteogenesis imperfecta type 10		MGI:5505276	Serpinh1<sup>tm2Kzn</sup>/Serpinh1<sup>tm2Kzn</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22492985	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7449270	Stim1<sup>tm1.1Pg</sup>	is_implicated_in	DOID:0080089	tubular aggregate myopathy 1		MGI:7450790	Stim1<sup>tm1.1Pg</sup>/Stim1<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31666234	20230404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:24662047	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:25284161	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:31430305	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:25106553	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F		MGI:5911876	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] B6.129-Sgcd<sup>tm1Mcn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28797108	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F		MGI:3618527	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10862711	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619458	Tg(IGL-MYC)3Hm	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:24979794	20211005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619458	Tg(IGL-MYC)3Hm	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:24174629	20211005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619458	Tg(IGL-MYC)3Hm	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:26941288	20211005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619458	Tg(IGL-MYC)3Hm	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:26151313	20211005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619458	Tg(IGL-MYC)3Hm	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:34521752	20211005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619458	Tg(IGL-MYC)3Hm	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3619459	Tg(IGL-MYC)3Hm/0  [background:] C57BL/6N-Tg(IGL-MYC)3Hm/Nci			ECO:0000033	author statement supported by traceable reference	PMID:11034608	20211005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388423	Wdr62<sup>tm1.1Jfch</sup>	is_implicated_in	DOID:0070293	primary autosomal recessive microcephaly 2 with or without cortical malformations		MGI:6388425	Wdr62<sup>tm1.1Jfch</sup>/Wdr62<sup>tm1.1Jfch</sup>  [background:] involves: 129S1/SvImJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31197141	20200203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810779	Alms1<sup>tvrm102</sup>	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:5924963	Alms1<sup>tvrm102</sup>/Alms1<sup>tvrm102</sup>  [background:] C57BL/6J-Alms1<sup>tvrm102</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5423977	S1pr2<sup>stdf</sup>	is_implicated_in	DOID:0110519	autosomal recessive nonsyndromic deafness 68		MGI:6277930	S1pr2<sup>stdf</sup>/S1pr2<sup>stdf</sup>  [background:] involves: C57BL/6Brd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27383011	20190212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662066	Tg(VDR*L233S,luc)T807Pike/0 Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:25147982	20150917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6725085	Clcn1<sup>em1Btlr</sup>	is_implicated_in	DOID:2106	myotonia congenita		MGI:6725721	Clcn1<sup>em1Btlr</sup>/Clcn1<sup>em1Btlr</sup>  [background:] C57BL/6J-Clcn1<sup>em1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722079	Cdh23<sup>v-3J</sup>/Cdh23<sup>+</sup>  [background:] C57BL/6J-Cdh23<sup>v-3J</sup>	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29040313	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32616814	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26494287	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25614286	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15480770	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31123721	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12655582	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24531548	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24753820	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32987703	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27090893	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16380460	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22550139	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26798667	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26408953	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29246325	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15682009	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31043570	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18178469	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934906	Fbn1<sup>tm2Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3619460	Fbn1<sup>tm2Rmz</sup>/Fbn1<sup>tm2Rmz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10097121	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24752462	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31695761	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:15320950	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14690057	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:2385830	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:11152663	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385787	Slc26a4<sup>tm1Egr</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:17299139	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835761	Wfs1<sup>tm1Koks</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:31935437	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835761	Wfs1<sup>tm1Koks</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23914152	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835761	Wfs1<sup>tm1Koks</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23321269	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835761	Wfs1<sup>tm1Koks</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:21461749	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835761	Wfs1<sup>tm1Koks</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:5643859	Wfs1<sup>tm1Koks</sup>/Wfs1<sup>tm1Koks</sup>  [background:] 129S6/SvEvTac-Wfs1<sup>tm1Koks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21031341	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835761	Wfs1<sup>tm1Koks</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:5643859	Wfs1<sup>tm1Koks</sup>/Wfs1<sup>tm1Koks</sup>  [background:] 129S6/SvEvTac-Wfs1<sup>tm1Koks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24710642	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4453135	Cdh23<sup>12J</sup>	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:26748055	20160524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4453135	Cdh23<sup>12J</sup>	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12		MGI:5141009	Cdh23<sup>12J</sup>/Cdh23<sup>12J</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20644563	20160524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717572	Tg(Thy1-APPLon)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33848635	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717572	Tg(Thy1-APPLon)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25164658	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717572	Tg(Thy1-APPLon)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28711595	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717572	Tg(Thy1-APPLon)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3717577	Tg(Thy1-APPLon)2Vln/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15509532	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717572	Tg(Thy1-APPLon)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5003461	Tg(Thy1-APPLon)2Vln/0  [background:] involves: C57BL/6 * CBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14637096	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30126037	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25558816	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33482356	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35045281	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32858248	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26058840	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29669277	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23273572	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670768	Mapt<sup>tm1(EGFP)Klt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27856911	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763014	Acvr1<sup>tm2.1Vlcg</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:27881824	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763014	Acvr1<sup>tm2.1Vlcg</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:26896819	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763014	Acvr1<sup>tm2.1Vlcg</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:33705358	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763014	Acvr1<sup>tm2.1Vlcg</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5825038	Acvr1<sup>tm2.1Vlcg</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm3.1(cre/ERT2)Vlcg</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26333933	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763014	Acvr1<sup>tm2.1Vlcg</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5881966	Acvr1<sup>tm2.1Vlcg</sup>/Acvr1<sup>+</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: C57BL/6J * C57BL/6NTac * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:26896819	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618619	Pdgfrb<sup>b2b2903Clo</sup>	is_implicated_in	DOID:0060230	basal ganglia calcification		MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:20842126	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:20440271	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22869526	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:28031228	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24107773	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:20520772	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19351822	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19738049	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:32934143	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3831004	Tg(Neurod2-Smo*A1)199Jols/Tg(Neurod2-Smo*A1)199Jols  [background:] C57BL/6-Tg(Neurod2-Smo*A1)199Jols			ECO:0000033	author statement supported by traceable reference	PMID:22869526	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3831003	Tg(Neurod2-Smo*A1)199Jols/0  [background:] C57BL/6-Tg(Neurod2-Smo*A1)199Jols			ECO:0000033	author statement supported by traceable reference	PMID:15520185	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830738	Tg(Neurod2-Smo*A1)199Jols	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5791914	Tg(Neurod2-Smo*A1)199Jols/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25348795	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6201444	Slc9a9<sup>tm2d(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6201596	Slc9a9<sup>tm2d(KOMP)Wtsi</sup>/Slc9a9<sup>tm2d(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29362376	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4460999	Pign<sup>m1Nisw</sup>	is_implicated_in	DOID:4621	holoprosencephaly		MGI:5437465	Pign<sup>m1Nisw</sup>/Pign<sup>m1Nisw</sup>  [background:] involves: 129S1/SvImJ * C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23213481	20190927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22841817	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:25501597	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:26139610	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:24920619	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:32895435	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:31901258	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:27160072	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:27391551	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22039242	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388259	Pde6b<sup>rd10</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3581193	Pde6b<sup>rd10</sup>/Pde6b<sup>rd10</sup>  [background:] B6.CXB1-Pde6b<sup>rd10</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17267005	20201020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5500169	Wdr35<sup>yeti</sup>	is_implicated_in	DOID:0110090	short-rib thoracic dysplasia 7 with or without polydactyly		MGI:5501229	Wdr35<sup>yeti</sup>/Wdr35<sup>yeti</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21473986	20130815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:26452614	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:31472213	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:27466189	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:28369421	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:32032735	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:33621640	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2		MGI:5574073	Cdkl5<sup>tm1.2Cogr</sup>/Cdkl5<sup>tm1.2Cogr</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24838000	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2		MGI:5574074	Cdkl5<sup>tm1.2Cogr</sup>/Y  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24838000	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:26143616	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:29474534	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573238	Cdkl5<sup>tm1.2Cogr</sup>	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:24838000	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389055	Tg(Myh6-CASQ2)1Mord	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389055	Tg(Myh6-CASQ2)1Mord	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:30092100	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389055	Tg(Myh6-CASQ2)1Mord	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27992596	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389055	Tg(Myh6-CASQ2)1Mord	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3700949	Tg(Myh6-CASQ2)1Mord/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10428792	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655686	Kcna1<sup>tm1Jmay</sup>	is_implicated_in	DOID:0050989	episodic ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:28193892	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655686	Kcna1<sup>tm1Jmay</sup>	is_implicated_in	DOID:0050989	episodic ataxia type 1		MGI:2655695	Kcna1<sup>tm1Jmay</sup>/Kcna1<sup>+</sup>  [background:] B6.129S4-Kcna1<sup>tm1Jmay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12612586	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24367693	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27236019	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25966356	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26752648	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23916759	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25038828	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27179791	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26186895	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27493027	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26082469	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:36436748	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23295856	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:35053183	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24040016	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28934250	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33369245	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease		MGI:3757562	Tg(HDexon1)61Gpb/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9267033	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389466	Tg(HDexon1)61Gpb	is_implicated_in	DOID:12858	Huntington's disease		MGI:3757562	Tg(HDexon1)61Gpb/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22890713	20230331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430346	Dnah5<sup>b2b1565Clo</sup>/Dnah5<sup>b2b1565Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1565Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7264674	Cant1<sup>tm1.2Aros</sup>	is_implicated_in	DOID:0060462	Desbuquois dysplasia		MGI:7264693	Cant1<sup>tm1.2Aros</sup>/Cant1<sup>tm1.2Aros</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30439444	20220427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607257	Slc40a1<sup>tm1.1Mmfe</sup>	is_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:5607261	Slc40a1<sup>tm1.1Mmfe</sup>/Slc40a1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25100063	20141216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607257	Slc40a1<sup>tm1.1Mmfe</sup>	is_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:5607258	Slc40a1<sup>tm1.1Mmfe</sup>/Slc40a1<sup>tm1.1Mmfe</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25100063	20141216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767242	Tg(TcraR28,TcrbR28)KRNDim	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:23794629	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767242	Tg(TcraR28,TcrbR28)KRNDim	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:24489090	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767242	Tg(TcraR28,TcrbR28)KRNDim	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:31350760	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767242	Tg(TcraR28,TcrbR28)KRNDim	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:32973194	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767242	Tg(TcraR28,TcrbR28)KRNDim	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3842819	Tg(TcraR28,TcrbR28)KRNDim/0  [background:] involves: C57BL/6 * NOD * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8945509	20201022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698642	Zic3<sup>tm1Jwb</sup>/Y  [background:] either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	is_model_of	DOID:2907	Goldenhar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17127413	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27656887	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28530657	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23928995	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26249173	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28212608	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24038078	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27197172	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23825155	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23540692	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26738797	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23681607	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23720051	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27601049	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24638982	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28162974	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25164016	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25918249	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23520493	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23146906	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24015230	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27119753	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27038000	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22225988	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23695548	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27749822	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer		MGI:4361924	Tg(MMTV-PyVT)634Mul/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27264173	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679595	Tg(MMTV-PyVT)634Mul	is_implicated_in	DOID:1612	breast cancer		MGI:2679598	Tg(MMTV-PyVT)634Mul/0  [background:] FVB/N-Tg(MMTV-PyVT)634Mul/Nci			ECO:0000033	author statement supported by traceable reference	PMID:1312220	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661387	Agl<sup>tm1Geno</sup>	is_implicated_in	DOID:2748	glycogen storage disease III		MGI:5661390	Agl<sup>tm1Geno</sup>/Agl<sup>tm1Geno</sup>  [background:] C57BL/6J-Agl<sup>tm1Geno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25092169	20150910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26216548	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27061193	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27265504	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23076356	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16397221	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27742686	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24607504	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23042302	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27292635	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6294718	Nkx2-5<sup>tm1.1Hkas</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:6294720	Nkx2-5<sup>tm1.1Hkas</sup>/Nkx2-5<sup>+</sup>  [background:] 129S2.Cg-Nkx2-5<sup>tm1.1Hkas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26226998	20190429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6294718	Nkx2-5<sup>tm1.1Hkas</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:6294720	Nkx2-5<sup>tm1.1Hkas</sup>/Nkx2-5<sup>+</sup>  [background:] 129S2.Cg-Nkx2-5<sup>tm1.1Hkas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25028484	20190429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544446	Pde6b<sup>atrd1</sup>/Pde6b<sup>tm1Eye</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:23946405	20140218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037863	Fgf8<sup>tm1.3Mrt</sup>/Fgf8<sup>tm1.4Mrt</sup> Tg(Tbx1-cre)1Joe/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14975726	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5660490	Spata7<sup>tm1Mrd</sup>	is_implicated_in	DOID:0110331	Leber congenital amaurosis 3		MGI:5660492	Spata7<sup>tm1Mrd</sup>/Spata7<sup>tm1Mrd</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:25398945	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912484	Tg(tetO-ERBB2*)5BKkw	is_implicated_in	DOID:4829	adenosquamous lung carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912484	Tg(tetO-ERBB2*)5BKkw	is_implicated_in	DOID:4829	adenosquamous lung carcinoma		MGI:5912489	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-ERBB2*)5BKkw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19122144	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544911	Tg(HBVX*,-Myc)#Skp	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5544915	Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12519229	20140227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544911	Tg(HBVX*,-Myc)#Skp	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22889122	20140227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544911	Tg(HBVX*,-Myc)#Skp	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5544915	Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22889122	20140227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:27841758	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:27516389	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:18658088	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:28468800	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:32342224	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028000	Pde6b<sup>atrd1</sup>/Pde6b<sup>atrd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24411482	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22728099	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30215697	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28683325	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33753066	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30412792	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23954169	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24655393	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25122659	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25617315	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23520537	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30015035	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26365177	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29042514	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27586053	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28539885	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23029404	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24086624	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29215028	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22912745	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25673868	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31065079	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31103943	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27255814	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21235806	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25008180	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25309427	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23711927	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31842924	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22516463	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27509875	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31813629	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29213096	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26982728	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25541422	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22427376	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32417750	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31004063	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27460153	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25486177	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22796601	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23486975	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27896923	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23500896	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27460145	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26214837	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24842003	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23523959	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30397132	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32171592	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31213067	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35153718	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25896362	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32768866	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27103531	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29725016	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23312564	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23683389	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25552414	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22095718	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:37253603	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30594047	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32087004	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23555795	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32916195	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26876740	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26553823	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29331876	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24629673	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19664757	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23152608	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21738757	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25680266	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27189884	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22177720	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22870188	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27834631	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27425031	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27223629	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24630364	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672831	Tg(APPSwe,tauP301L)1Lfa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32619874	20230929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3757562	Tg(HDexon1)61Gpb/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22890713	20140220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3757562	Tg(HDexon1)61Gpb/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9267033	20140220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052540	Tg(APOA1)1Rub	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20847045	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705517	Gabra1<sup>tm1.1Mjga</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5774687	Gabra1<sup>tm1.1Mjga</sup>/Gabra1<sup>+</sup>  [background:] B6J.Cg-Gabra1<sup>tm1.1Mjga</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26054439	20160601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140838	Tg(Pcp2-cre)2Mpin/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.2Mjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21419848	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28159908	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26123488	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25878292	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32905841	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30311654	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28684271	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26192747	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31031598	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26196079	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32065917	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33287899	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27834631	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30007168	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23921129	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27570072	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26615780	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35675410	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28346227	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32848093	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26365177	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23748737	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24454724	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32682823	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26923399	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28533388	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23454197	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32371859	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27041503	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23467355	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30599271	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30791980	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31619689	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29167398	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23560052	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26784542	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24023774	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26086915	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057148	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3639711	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10818140	20231017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26604147	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25926782	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33010341	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26237041	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624554	Mecp2<sup>tm1Hzo</sup>/Mecp2<sup>+</sup>  [background:] 129S7/SvEvBrd-Mecp2<sup>tm1Hzo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12160743	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624551	Mecp2<sup>tm1Hzo</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12160743	20210517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183727	Mecp2<sup>tm1Hzo</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624553	Mecp2<sup>tm1Hzo</sup>/Y  [background:] 129S7/SvEvBrd-Mecp2<sup>tm1Hzo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12160743	20210517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579244	Polh<sup>tm1Crey</sup>/Polh<sup>tm1Crey</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110847	xeroderma pigmentosum variant type						ECO:0000033	author statement supported by traceable reference	PMID:15824086	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843437	Tg(Lck-Notch3)#Issc	is_implicated_in	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22120716	20121024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843437	Tg(Lck-Notch3)#Issc	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:4843447	Tg(Lck-Notch3)#Issc/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10880446	20121024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5310735	Mecp2<sup>tm1.1Joez</sup>/Y  [background:] B6.129-Mecp2<sup>tm1.1Joez</sup>	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22119903	20120315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942280	Tg(Prnp-SNCA*A53T)25Mkle	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5297859	Tg(Prnp-SNCA*A53T)25Mkle/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12084935	20111210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574016	Tg(SOD1*G37R)29Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26791230	20160329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574016	Tg(SOD1*G37R)29Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16000321	20160329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574016	Tg(SOD1*G37R)29Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3814057	Tg(SOD1*G37R)29Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12127151	20160329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574016	Tg(SOD1*G37R)29Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3814057	Tg(SOD1*G37R)29Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7605627	20160329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25873173	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:27775550	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23660685	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:28432220	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24994068	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26903243	20170921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771021	Efemp1<sup>tm1Lmar</sup>/Efemp1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17664227	20080215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716965	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm2Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22964582	20131018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833383	Tg(Thy1-MAPT*K369I)K3Gotz	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:32949670	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833383	Tg(Thy1-MAPT*K369I)K3Gotz	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:22920254	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833383	Tg(Thy1-MAPT*K369I)K3Gotz	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:36639708	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833383	Tg(Thy1-MAPT*K369I)K3Gotz	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:3833385	Tg(Thy1-MAPT*K369I)K3Gotz/0  [background:] B6.Cg-Tg(Thy1-MAPT*K369I)K3Gotz			ECO:0000033	author statement supported by traceable reference	PMID:18832465	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:24670412	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:34521872	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:24815352	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:29463793	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:26295839	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583531	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] C.B6(Cg)-Cys1<sup>cpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11004214	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583530	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] involves: C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8800407	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2175905	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7062441	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583529	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/JUnc			ECO:0000033	author statement supported by traceable reference	PMID:6624875	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2175905	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:3404974	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856831	Cys1<sup>cpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583532	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] D2J.B6(Cg)-Cys1<sup>cpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4032601	20211013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:33045060	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:22661702	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26023917	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:24620350	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:30796025	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:28097236	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26817955	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:24429338	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26690703	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26631480	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:27503873	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:32533970	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26265698	20210723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056733	Tg(HBA-HBBs)41Paz	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26286849	20210723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5553472	Tg(JAK2*V617F)FF1Rsko/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:18160670	20140329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931238	Brca1<sup>tm2Cxd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27322743	20171212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931238	Brca1<sup>tm2Cxd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11156526	20171212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931238	Brca1<sup>tm2Cxd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28649985	20171212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931238	Brca1<sup>tm2Cxd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25176624	20171212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931238	Brca1<sup>tm2Cxd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20171212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25557785	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26758873	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26621405	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:20832308	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22037760	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:36619669	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31060774	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:33382987	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24463453	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27488123	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26030275	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24691550	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22422766	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26733414	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22763238	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26911699	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31127156	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26258776	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25692239	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24191055	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26438828	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23656793	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24218366	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22079083	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26502195	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26134627	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25878277	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183946	Smn1<sup>tm1Msd</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26276812	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5489940	Phex<sup>m1Jrt</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5492341	Phex<sup>m1Jrt</sup>/Y  [background:] B6.129S1-Phex<sup>M1Jrt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22573557	20130627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5489940	Phex<sup>m1Jrt</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5492338	Phex<sup>m1Jrt</sup>/Phex<sup>+</sup>  [background:] B6.129S1-Phex<sup>M1Jrt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22573557	20130627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523956	Pax3<sup>Sp-1Wli</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:5523972	Pax3<sup>Sp-1Wli</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196138	Gt(ROSA)26Sor<sup>tm2(CAG-Lin28b,-luc)Jhsc</sup>	is_implicated_in	DOID:769	neuroblastoma		MGI:6196139	Gt(ROSA)26Sor<sup>tm2(CAG-Lin28b,-luc)Jhsc</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Dbh-icre)1Gsc/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23042116	20180831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:35021077	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23583105	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6324047	Shank3<sup>tm2Gfng</sup>/Shank3<sup>+</sup>  [background:] B6.129-Shank3<sup>tm2Gfng</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27189882	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27189882	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4949761	Shank3<sup>tm2Gfng</sup>/Shank3<sup>tm2Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21423165	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23142422	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30405356	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430994	Pkhd1<sup>tm1Sswi</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:23759744	20130917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430994	Pkhd1<sup>tm1Sswi</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:5430995	Pkhd1<sup>tm1Sswi</sup>/Pkhd1<sup>tm1Sswi</sup>  [background:] B6.Cg-Pkhd1<sup>tm1Sswi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18286309	20130917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440736	Ids<sup>tm1Eto</sup>/Ids<sup>tm1Eto</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:22704483	20121106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388725	Tg(Lck-Tnfsf4)1Nish	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20130423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388725	Tg(Lck-Tnfsf4)1Nish	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:2651594	Tg(Lck-Tnfsf4)1Nish/0  [background:] B6.Cg-Tg(Lck-Tnfsf4)1Nish			ECO:0000033	author statement supported by traceable reference	PMID:22171643	20130423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5532825	Sidt2<sup>tm1.1Hzha</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:5532830	Sidt2<sup>tm1.1Hzha</sup>/Sidt2<sup>tm1.1Hzha</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27233614	20180921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5004658	Ptpn11<sup>tm4.2Bgn</sup>	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines		MGI:5004709	Ptpn11<sup>tm4.2Bgn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21339643	20180126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5004658	Ptpn11<sup>tm4.2Bgn</sup>	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:28582432	20180126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5004658	Ptpn11<sup>tm4.2Bgn</sup>	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:24865967	20180126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5004658	Ptpn11<sup>tm4.2Bgn</sup>	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:27348588	20180126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523925	Tg(SFTPC-EZR/ROS1)AShiba	is_implicated_in	DOID:1324	lung cancer		MGI:5523927	Tg(SFTPC-EZR/ROS1)AShiba/0  [background:] C57BL/6-Tg(SFTPC-EZR/ROS1)AShiba			ECO:0000033	author statement supported by traceable reference	PMID:23418494	20131216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6456759	Sugct<sup>tm1.2Kald</sup>	is_implicated_in	DOID:0112246	glutaric acidemia type 3		MGI:6456764	Sugct<sup>tm1.2Kald</sup>/Sugct<sup>tm1.2Kald</sup>  [background:] B6.Cg-Sugct<sup>tm1.2Kald</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31722069	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582186	Rc3h1<sup>san</sup>/Rc3h1<sup>san</sup>  [background:] either: C57BL/6JSfdAnu-Rc3h1<sup>san</sup>/Anu or (involves: C57BL/6JSfdAnu * CBA/Ca)	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:15917799	20050721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306612	Trp53<sup>tm1.1Dgk</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306612	Trp53<sup>tm1.1Dgk</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175140	Ncf1<sup>tm1Shl</sup>/Ncf1<sup>tm1Shl</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:7650482	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:29979789	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:24290752	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:23769925	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:23843985	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:34175669	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:23382922	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:27798114	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22872701	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:28379564	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:24076310	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26467605	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26707209	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22493001	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:27687148	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:25319340	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:25522247	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:27083515	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26682800	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:25864931	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3044831	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15071184	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:4436745	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] B6.C-Npc1<sup>m1N</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20007718	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18160655	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3849202	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/cNctr-Npc1<sup>m1N</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24391715	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:23843985	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5305070	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/c-Npc1<sup>m1N</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21303697	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3849202	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/cNctr-Npc1<sup>m1N</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22163015	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:9950794	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:6257302	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:12528192	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857409	Npc1<sup>m1N</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5442413	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c * C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22869680	20211104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28472288	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24163134	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31013315	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33434240	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23426972	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25865621	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25112732	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21109597	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:30716510	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33979214	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25242522	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26744329	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:35865113	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26721686	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23823696	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28436144	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23471914	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27154199	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27466195	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23009292	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25710816	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26721683	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25260053	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25032964	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32070725	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26800321	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28453658	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25940966	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26301073	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28171583	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27106099	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31747313	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28481224	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26566673	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31017936	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24662047	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25921779	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33259860	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25121503	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32632164	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25298424	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33002037	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33617542	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25027324	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25054970	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33311457	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31310630	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24682306	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28463682	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22427904	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33362201	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25683516	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:30962487	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23911934	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25216637	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28315675	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31348492	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24812281	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26825125	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25859011	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24368419	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25504048	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24163132	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24070607	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33495503	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24015212	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26851247	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25607927	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27127236	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25935000	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33651713	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28970581	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:36099033	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31506484	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22766138	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26170062	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27015747	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24586653	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798607	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21893021	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3789123	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6583703	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3621491	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6583703	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5688354	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] D2.B10-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20304955	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798607	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19535499	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:4359195	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19535499	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856328	Dmd<sup>mdx</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5697652	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] D2.B10-Dmd<sup>mdx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26566673	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119463	Tubb5<sup>tm1.1Dak</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:6119480	Tubb5<sup>tm1.1Dak</sup>/Tubb5<sup>tm1.1Dak</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26903504	20180305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810318	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Olig2<sup>tm2(TVA,cre)Rth</sup>/Olig2<sup>+</sup>  [background:] involves: 129 * 129X1/SvJ	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691547	20110921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867659	Gba1<sup>tm1.1Pmis</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:24639522	20140519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867659	Gba1<sup>tm1.1Pmis</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:4867688	Gba1<sup>tm1.1Pmis</sup>/Gba1<sup>tm1.1Pmis</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20962279	20140519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867659	Gba1<sup>tm1.1Pmis</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:22665763	20140519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4844194	Cdk6<sup>tm1Bbd</sup>/Cdk6<sup>tm1Bbd</sup> Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Polr2a<sup>tm1(cre/ERT2)Bbd</sup>/Polr2a<sup>tm1(cre/ERT2)Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:20609353	20130820	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21336284	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22187438	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:19692612	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15843620	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:18809498	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20493905	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28123081	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:17947312	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16697652	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:18625748	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27561680	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27126634	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:18502655	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:19464370	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20152125	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:19845833	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:17613541	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26508634	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20097678	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:19228972	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:17394466	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:3613525	Tg(YAC128)53Hay/0  [background:] FVB/N-Tg(YAC128)53Hay			ECO:0000033	author statement supported by traceable reference	PMID:12812983	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:3613525	Tg(YAC128)53Hay/0  [background:] FVB/N-Tg(YAC128)53Hay			ECO:0000033	author statement supported by traceable reference	PMID:16697652	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613515	Tg(YAC128)53Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:3613525	Tg(YAC128)53Hay/0  [background:] FVB/N-Tg(YAC128)53Hay			ECO:0000033	author statement supported by traceable reference	PMID:16230019	20190808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6392156	Iqsec2<sup>em1Csbg</sup>	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:6392161	Iqsec2<sup>em1Csbg</sup>/Y  [background:] C57BL/6NHsd-Iqsec2<sup>em1Csbg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31439632	20200227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5660496	Tg(Myh6-Jup*)1Ajm	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12		MGI:5660497	Tg(Myh6-Jup*)1Ajm/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22021931	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5660496	Tg(Myh6-Jup*)1Ajm	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:24276085	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424979	Casr<sup>BCH002</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425918	Casr<sup>BCH002</sup>/Casr<sup>BCH002</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH002</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5883587	C9orf72<sup>tm1Eggn</sup>	is_implicated_in	DOID:417	autoimmune disease		MGI:6278552	C9orf72<sup>tm1Eggn</sup>/C9orf72<sup>tm1Eggn</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:2288383	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:9686356	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:1912099	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:7688531	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:9385451	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:8009964	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:8740228	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:7873696	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:2473662	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:7509170	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:8245411	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:8434133	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	MGI:63873	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:9358851	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:6324231	Atp7a<sup>Mo-ml</sup>/Y  [background:] involves: C3Hf/He			ECO:0000033	author statement supported by traceable reference	MGI:60964	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856466	Atp7a<sup>Mo-ml</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:6324231	Atp7a<sup>Mo-ml</sup>/Y  [background:] involves: C3Hf/He			ECO:0000033	author statement supported by traceable reference	PMID:1819648	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569734	Tg(TG-RET/NCOA4)3209Rstn	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5897625	Tg(TG-RET/NCOA4)3209Rstn/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9850089	20170518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6369620	Relt<sup>em1Jpsi</sup>	is_implicated_in	DOID:0111722	amelogenesis imperfecta type 3C		MGI:6369622	Relt<sup>em1Jpsi</sup>/Relt<sup>em1Jpsi</sup>  [background:] C57BL/6-Relt<sup>em1Jpsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30506946	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151181	Sgsh<sup>mps3a</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:23022219	20130408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151181	Sgsh<sup>mps3a</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:3037061	Sgsh<sup>mps3a</sup>/Sgsh<sup>mps3a</sup>  [background:] involves: 129X1/SvJ * CD-1 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10561464	20130408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806112	Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27001178	20161103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531157	Tg(tetO-MYC)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21996730	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531157	Tg(tetO-MYC)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28504653	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531157	Tg(tetO-MYC)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23770012	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531157	Tg(tetO-MYC)1Lach	is_implicated_in	DOID:1612	breast cancer		MGI:5432250	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-MYC)1Lach/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:18356293	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531157	Tg(tetO-MYC)1Lach	is_implicated_in	DOID:1612	breast cancer		MGI:5432250	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-MYC)1Lach/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:11175856	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:23468924	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:23255724	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:24825107	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:24593181	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:26139610	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22169101	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:23840814	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:25489083	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22967839	20170127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427936	Gata4<sup>tm1Grg</sup>/Gata4<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110107	atrial heart septal defect 2						ECO:0000033	author statement supported by traceable reference	PMID:22589735	20120716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25892230	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25911611	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22084065	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23644656	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22562956	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26785731	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26261055	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23540692	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21822305	20170321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5431966	Tg(RIP1-Tag)2Dh/0  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:2986015	20170321	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435559	Porcn<sup>tm1Vdv</sup>/Porcn<sup>+</sup>  [background:] chimera involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544915	Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp  [background:] Not Specified	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22889122	20140221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544915	Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp  [background:] Not Specified	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:12519229	20140221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430049	b2b243Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5430325	b2b243Clo/b2b243Clo  [background:] C57BL/6J-b2b243Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793780	Atp7a<sup>Mo-br</sup>/Y  [background:] involves: C57BL	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:4858102	20080620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942357	Tg(Kit*D814V)1Roer	is_implicated_in	DOID:350	mastocytosis		MGI:4942363	Tg(Cma1-cre)ARoer/0 Tg(Kit*D814V)1Roer/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21148330	20150309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942357	Tg(Kit*D814V)1Roer	is_implicated_in	DOID:350	mastocytosis		MGI:4942360	Tg(Kit*D814V)1Roer/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21148330	20150309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942357	Tg(Kit*D814V)1Roer	is_implicated_in	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:24788138	20150309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24141140	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24303840	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24097557	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:26365583	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:23505426	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:27035618	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:27496898	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:25642775	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:22679000	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:26823428	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24925982	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177529	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] B6.129P2-Cftr<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177529	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] B6.129P2-Cftr<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10570187	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856709	Cftr<sup>tm1Unc</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177530	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:1380723	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5902788	Nmnat1<sup>tvrm113</sup>	is_implicated_in	DOID:8466	retinal degeneration		MGI:5903076	Nmnat1<sup>tvrm113</sup>/Nmnat1<sup>tvrm113</sup>  [background:] C57BL/6J-Nmnat1<sup>tvrm113</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:27207593	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857091	Vps54<sup>wr</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27571131	20170420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857091	Vps54<sup>wr</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26349009	20170420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857091	Vps54<sup>wr</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5490471	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] involves: C57BL/6J * C57BL/Fa			ECO:0000033	author statement supported by traceable reference	PMID:20643756	20170420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857091	Vps54<sup>wr</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5490471	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] involves: C57BL/6J * C57BL/Fa			ECO:0000033	author statement supported by traceable reference	PMID:23539154	20170420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175115	Mip<sup>Hfi</sup>/Mip<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:62456	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5465569	Tg(APOE-FGF23*R176Q)#Ack	is_implicated_in	DOID:0050948	autosomal dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:26784541	20160524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5465569	Tg(APOE-FGF23*R176Q)#Ack	is_implicated_in	DOID:0050948	autosomal dominant hypophosphatemic rickets		MGI:5466160	Tg(APOE-FGF23*R176Q)#Ack/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15284207	20160524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5550573	Comp<sup>tm2.1Mbri</sup>/Comp<sup>tm2.1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0080047	pseudoachondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:22006726	20140314	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818653	Strc<sup>tm1Ugds</sup>/Strc<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J	is_model_of	DOID:0110471	autosomal recessive nonsyndromic deafness 16						ECO:0000033	author statement supported by traceable reference	PMID:18849963	20081209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640198	Fgfr3<sup>tm1.1Iwa</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	is_model_of	DOID:0050736	autosomal dominant disease						ECO:0000033	author statement supported by traceable reference	PMID:11406607	20170711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425315	Smarcal1<sup>tm1.1Cfbo</sup>/Smarcal1<sup>tm1.1Cfbo</sup>  [background:] either: B6.129-Smarcal1<sup>tm1.1Cfbo</sup> or (involves: 129 * C57BL/6)	is_model_of	DOID:0060490	Schimke immuno-osseous dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:22378147	20120620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176483	Fgfr2<sup>tm2.3Dsn</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:11274405	20080121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22323736	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31866158	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24075854	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29859094	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33556539	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24893973	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25443293	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27423698	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24291517	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33848635	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25852506	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24035915	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27020746	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29909177	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28711595	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5792143	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23184605	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765351	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5313530	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/0  [background:] C57BL/6-Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr			ECO:0000033	author statement supported by traceable reference	PMID:21228171	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424924	Alpl<sup>Mhdabap32</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425673	Alpl<sup>Mhdabap32</sup>/Alpl<sup>Mhdabap32</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap32</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285183	Gnas<sup>tm1Gwa</sup>/Gnas<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae	is_model_of	DOID:0080053	Albright's hereditary osteodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21747923	20110913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278014	Tg(Actb-Ptma)T12Clwu	is_implicated_in	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:26496995	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278014	Tg(Actb-Ptma)T12Clwu	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:6278016	Tg(Actb-Ptma)T12Clwu/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23695700	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278014	Tg(Actb-Ptma)T12Clwu	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:6278015	Tg(Actb-Ptma)T12Clwu/Tg(Actb-Ptma)T12Clwu  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23695700	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931238	Brca1<sup>tm2Cxd</sup>	is_implicated_in	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22915751	20130408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448550	Slc45a2<sup>uw-6J</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5450851	Slc45a2<sup>uw-6J</sup>/Slc45a2<sup>uw-6J</sup>  [background:] CAST/EiJ-Slc45a2<sup>uw-6J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5449587	20130123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5445964	Raf1<sup>tm2.1Ara</sup>	is_implicated_in	DOID:0060583	Noonan syndrome 5		MGI:5445966	Raf1<sup>tm2.1Ara</sup>/Raf1<sup>tm2.1Ara</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:22826437	20121214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424979	Casr<sup>BCH002</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425918	Casr<sup>BCH002</sup>/Casr<sup>BCH002</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH002</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438066	Ccdc39<sup>b2b1735Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621459	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm2Fdp</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16446309	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441310	Tg(Vav1-JAK2*V617F)AZjz	is_implicated_in	DOID:8997	polycythemia vera		MGI:5441312	Tg(Vav1-JAK2*V617F)AZjz/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18334677	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27292643	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25164016	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24107773	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22020329	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23770012	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23940356	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511875	Tg(MMTV-rtTA)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21996730	20170306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719290	Xpc<sup>tm1Ecf</sup>/Xpc<sup>tm1Ecf</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:16141330	20070827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22440813	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30480744	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24812425	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25536533	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25902541	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23349479	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22297672	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26122048	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24743240	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22427566	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:32913274	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23951058	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24491571	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23977269	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28017717	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28324005	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29654303	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24370601	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29420703	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:31506549	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25207540	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25789863	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29972779	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26683376	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24740573	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24458356	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5508894	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup>  [background:] C.B6N-Ins2<sup>Akita</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22297672	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849540	Vcp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:5500068	Vcp<sup>tm1Itl</sup>/Vcp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23029473	20170213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849540	Vcp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:25545721	20170213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849540	Vcp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:24158850	20170213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849540	Vcp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:4849542	Vcp<sup>tm1Itl</sup>/Vcp<sup>+</sup>  [background:] B6.129S-Vcp<sup>tm1Itl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19713307	20170213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849540	Vcp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:27106764	20170213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849540	Vcp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:26134519	20170213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:31337982	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28223216	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:37524876	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22596053	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:31611596	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26646098	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26230680	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23349481	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:33443065	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30865689	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27856609	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27227463	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29351404	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:31048370	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26384381	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27438594	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28583918	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29445185	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22922221	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25411784	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28072841	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28609678	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30420600	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24595856	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27193916	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22785174	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:31141724	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27699250	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24553436	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29474466	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29223734	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30339820	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23646149	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25377875	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23193188	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:37783236	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30359575	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:34179020	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23986522	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:32884086	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25633418	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26324181	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:33318569	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29444429	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29654303	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27350436	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:33148881	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22664955	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26193896	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27932386	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30104246	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26647385	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22086159	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23069626	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29018279	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3694548	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] BKS.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22609345	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:16113078	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:28359088	20190821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856009	Lepr<sup>db</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6356398	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.BKS(D)-Lepr<sup>db</sup>/JOrlRj			ECO:0000033	author statement supported by traceable reference	PMID:22118645	20190821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5310970	Tg(Thy1-TARDBP*)BOddo/0  [background:] C57BL/6-Tg(Thy1-TARDBP*)BOddo	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:22067910	20120316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603566	Man2b1<sup>tm1Psa</sup>/Man2b1<sup>tm1Psa</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:3413	alpha-mannosidosis						ECO:0000033	author statement supported by traceable reference	PMID:16014715	20051103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603566	Man2b1<sup>tm1Psa</sup>/Man2b1<sup>tm1Psa</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:3413	alpha-mannosidosis						ECO:0000033	author statement supported by traceable reference	PMID:10400983	20051103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175806	Crygb<sup>Nop</sup>/Crygb<sup>Nop</sup>  [background:] Not Specified	is_model_of	DOID:0110236	cataract 39 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:6479248	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430051	b2b243.2Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5430324	b2b243.2Clo/b2b243.2Clo  [background:] C57BL/6J-b2b243.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052365	Tg(JPH3-GFP,-JPH3*)GXwy	is_implicated_in	DOID:0090104	Huntington's disease-like 2		MGI:5052367	Tg(JPH3-GFP,-JPH3*)GXwy/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21555070	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429210	Celsr2<sup>tm1Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429557	Celsr2<sup>tm1Lex</sup>/Celsr2<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5662266	Tg(Cyp17a1-NGF)2456Oje	is_implicated_in	DOID:11612	polycystic ovary syndrome		MGI:5662267	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:25211588	20150922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:27493028	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:24150846	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:22736030	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:27147661	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:3614453	Ar<sup>tm4(AR)Dmr</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16981011	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:3614453	Ar<sup>tm4(AR)Dmr</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16400023	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360792	Tg(RBP3-ELOVL4*)2Kzh	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:29654292	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360792	Tg(RBP3-ELOVL4*)2Kzh	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:22427551	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360792	Tg(RBP3-ELOVL4*)2Kzh	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:24334447	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360792	Tg(RBP3-ELOVL4*)2Kzh	is_implicated_in	DOID:0050817	Stargardt disease		MGI:4360797	Tg(RBP3-ELOVL4*)2Kzh/0  [background:] C57BL/6-Tg(RBP3-ELOVL4*)2Kzh			ECO:0000033	author statement supported by traceable reference	PMID:15749821	20180705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417856	Slc6a4<sup>tm1(cre)Xz</sup>/Slc6a4<sup>tm1(cre)Xz</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:9007	sudden infant death syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19646988	20100114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810422	Rr320<sup>tm1.1Mkg</sup>/Rr320<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:10882079	20110524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5293612	Gbe1<sup>tm1.1Hoa</sup>	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:5293614	Gbe1<sup>tm1.1Hoa</sup>/Gbe1<sup>tm1.1Hoa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:21856731	20111027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158363	Zmpste24<sup>tm1Sgy</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:32196928	20200610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158363	Zmpste24<sup>tm1Sgy</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:30001457	20200610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158363	Zmpste24<sup>tm1Sgy</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20200610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158363	Zmpste24<sup>tm1Sgy</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:30216637	20200610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158363	Zmpste24<sup>tm1Sgy</sup>	is_implicated_in	DOID:3911	progeria		MGI:3620907	Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15608054	20200610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158363	Zmpste24<sup>tm1Sgy</sup>	is_implicated_in	DOID:3911	progeria		MGI:3620988	Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] B6.129S4-Zmpste24<sup>tm1Sgy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16484451	20200610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451067	Itga1<sup>tm1Gdnr</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22297672	20130927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697730	Slc26a3<sup>tm1Sole</sup>/Slc26a3<sup>tm1Sole</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0060296	congenital secretory chloride diarrhea 1						ECO:0000033	author statement supported by traceable reference	PMID:17001077	20070226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435287	Galnt3<sup>tcal</sup>	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:5435288	Galnt3<sup>tcal</sup>/Galnt3<sup>tcal</sup>  [background:] involves: C3H * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22912827	20121114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428462	Tg(Sox3)1Pqt/0 Tg(Sox3-EGFP)NrPqt/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10908	hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:22291885	20120720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857263	Trp53<sup>tm1Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16397221	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6272867	Nmnat1<sup>tm1Ruch</sup>	is_not_implicated_in	DOID:0110005	Leber congenital amaurosis 9		MGI:6272871	Nmnat1<sup>tm1Ruch</sup>/Nmnat1<sup>tm1Ruch</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:29674119	20190110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5006860	Tg(Mov1/Tyr)OVE876BPay	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5006985	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay  [background:] FVB/N-Tg(Mov1/Tyr)OVE876BPay			ECO:0000033	author statement supported by traceable reference	PMID:21093492	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5006860	Tg(Mov1/Tyr)OVE876BPay	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5006981	Tg(Mov1/Tyr)OVE876BPay/Y  [background:] FVB/N-Tg(Mov1/Tyr)OVE876BPay			ECO:0000033	author statement supported by traceable reference	PMID:21093492	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306369	Eif2b5<sup>tm1Itl</sup>	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000033	author statement supported by traceable reference	PMID:25920008	20160317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306369	Eif2b5<sup>tm1Itl</sup>	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:5752255	Eif2b5<sup>tm1Itl</sup>/Eif2b5<sup>tm1Itl</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:23056417	20160317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306369	Eif2b5<sup>tm1Itl</sup>	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:5306390	Eif2b5<sup>tm1Itl</sup>/Eif2b5<sup>tm1Itl</sup>  [background:] involves: 129S/SvEv * C57BL * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:20826436	20160317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758717	Gusb<sup>mps</sup>/Gusb<sup>mps</sup>  [background:] B6.C-H2-K<sup>bm1</sup>/ByBir-Gusb<sup>mps</sup>/J	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:2495302	20071019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837652	Tg(CSNK1D*,-EGFP)827Yfu/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110012	advanced sleep phase syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:15800623	20130513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437461	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:12839925	20101025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576483	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] B6.Cg-Aire<sup>tm1Mmat</sup>	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445419	Cftr<sup>tm1Eur</sup>/Cftr<sup>tm1Eur</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7556083	20121212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661116	Dysf<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:29175948	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661116	Dysf<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:2661118	Dysf<sup>tm1Kcam</sup>/Dysf<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12736685	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806239	Atm<sup>tm1.1Mmpl</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:6110012	Atm<sup>tm1.1Mmpl</sup>/Atm<sup>tm1.1Mmpl</sup>  [background:] involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26310626	20180115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834201	mt-Nd6<sup>m2Jiha</sup>	is_implicated_in	DOID:3650	lactic acidosis		MGI:4834214	mt-Nd6<sup>m2Jiha</sup>  [background:] involves: C3H/An * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20674568	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690367	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup> Ptch2<sup>tm1Pmc</sup>/Ptch2<sup>tm1Pmc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16849540	20110922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526413	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:28045930	20171113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526413	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3526657	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>/Ctsg<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12750176	20171113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526413	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3526657	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>/Ctsg<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14636558	20171113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906664	Nsmce2<sup>tm2.1Ofc</sup>	is_implicated_in	DOID:2717	Bloom syndrome		MGI:5906758	Nsmce2<sup>tm2.1Ofc</sup>/Nsmce2<sup>tm2.1Ofc</sup> Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/0  [background:] involves: 129S/SvEv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26443207	20170811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26392287	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26341908	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23667637	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28476636	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:16934409	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5435409	Tg(Thy1-SNCA)61Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12111846	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:27509067	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22356593	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22155155	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22815513	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:32502569	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:27126635	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26880341	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435401	Tg(Thy1-SNCA)61Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:31125602	20201222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174786	Trp73<sup>tm1Fmc</sup>/Trp73<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:10716451	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:25088199	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:24398427	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:23728346	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:35677533	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:23079657	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:26974160	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:23321674	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388478	Il6st<sup>tm1Ern</sup>	is_implicated_in	DOID:10534	stomach cancer		MGI:3837032	Il6st<sup>tm1Ern</sup>/Il6st<sup>tm1Ern</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14699500	20220801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814579	Kmt2a<sup>tm1Saam</sup>/Kmt2a<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:18977325	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5817900	Col5a2<sup>tm1.2Dgr</sup>	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:5817903	Col5a2<sup>tm1.2Dgr</sup>/Col5a2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25987251	20170117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559996	Tg(Myh6-PRKCE*A159E)344Robo	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15242976	20170815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559996	Tg(Myh6-PRKCE*A159E)344Robo	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:24713463	20170815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559996	Tg(Myh6-PRKCE*A159E)344Robo	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5560005	Tg(Myh6-PRKCE*A159E)344Robo/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22940544	20170815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559996	Tg(Myh6-PRKCE*A159E)344Robo	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17965277	20170815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559996	Tg(Myh6-PRKCE*A159E)344Robo	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:17503784	20170815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447489	Scn1a<sup>tm2.1Wac</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6274702	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559219	Slx4<sup>tm1.2Jrou</sup>	is_implicated_in	DOID:0090066	Fanconi-like syndrome		MGI:5559492	Slx4<sup>tm1.2Jrou</sup>/Slx4<sup>tm1.2Jrou</sup>  [background:] B6.129P2-Slx4<sup>tm1.2Jrou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24076219	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776498	Pkd1<sup>tm1Bdgz</sup>/Pkd1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:17928412	20110502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23327738	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30679017	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:35021077	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28607173	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28218269	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5316396	Fmr1<sup>tm1Cgr</sup>/Y  [background:] B6.129P2-Fmr1<sup>tm1Cgr</sup>/Nwu			ECO:0000033	author statement supported by traceable reference	PMID:21364941	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25524914	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25941406	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30044988	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:30290217	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24585709	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27213816	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22438574	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26997281	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24752583	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25685701	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26016715	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24781935	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29444429	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26068544	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5428893	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] BTBR.Cg-Lep<sup>ob</sup>/WiscJ			ECO:0000033	author statement supported by traceable reference	PMID:16280642	20190416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836620	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:21262837	20110409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6116703	Irf6<sup>tm1Bcsl</sup>	is_implicated_in	DOID:9296	cleft lip		MGI:6315241	Irf6<sup>tm1Bcsl</sup>/Irf6<sup>tm1Bcsl</sup> Pitx2<sup>tm4(cre)Jfm</sup>/Pitx2<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:27369589	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30981413	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23160469	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29078804	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23337808	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:5307127	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] 129S6/SvEvTac-Was<sup>tm1Sbs</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22079330	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:3525574	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9697838	20200805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417900	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup> Tg(KRT14-COL7A1*)1Shzu/0  [background:] involves: 129S1/Sv * C57BL/6 * DBA/2	is_model_of	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:19893033	20100115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714968	Spi1<sup>tm1.3Dgt</sup>/Spi1<sup>tm1.3Dgt</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15146183	20070717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6466717	Adamts17<sup>tm1.2Taks</sup>	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:6466719	Adamts17<sup>tm1.2Taks</sup>/Adamts17<sup>tm1.2Taks</sup>  [background:] involves: C57BL * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:31201465	20201013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287463	Bpnt2<sup>tm1.2Aros</sup>	is_implicated_in	DOID:0112224	chondrodysplasia with joint dislocations gPAPP type		MGI:6466738	Bpnt2<sup>tm1.2Aros</sup>/Bpnt2<sup>tm1.2Aros</sup>  [background:] B6(SJL)-Bpnt2<sup>tm1.2Aros</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30865697	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437102	Slit2<sup>b2b1200.1Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575895	Tg(Myh6-KCNQ1_i2)H05Desc/0  [background:] involves: FVB	is_model_of	DOID:0110644	long QT syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23542581	20140805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>	is_model_of	DOID:0050779	hydrolethalus syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430797	Pkd2<sup>tm3Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:6317329	Pkd2<sup>tm3Som</sup>/Pkd2<sup>tm3Som</sup> Tg(Pkhd1-cre)1Igr/0  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644283	Tg(Prnp-lacZ/ATXN10*)#Teas/0  [background:] involves: FVB/N	is_model_of	DOID:0050960	spinocerebellar ataxia type 10						ECO:0000033	author statement supported by traceable reference	PMID:22065565	20150715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:7390396	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:6194978	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:14173795	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:8934515	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:590190	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6726553	Tsga8<sup>em1Ohbo</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6727060	Tsga8<sup>em1Ohbo</sup>/Y  [background:] C57BL/6-Tsga8<sup>em1Ohbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33766931	20210729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158253	Atp7b<sup>tm1Tcg</sup>	is_implicated_in	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:31924743	20200605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158253	Atp7b<sup>tm1Tcg</sup>	is_implicated_in	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:22802922	20200605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158253	Atp7b<sup>tm1Tcg</sup>	is_implicated_in	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:22308360	20200605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158253	Atp7b<sup>tm1Tcg</sup>	is_implicated_in	DOID:893	Wilson disease		MGI:3043693	Atp7b<sup>tm1Tcg</sup>/Atp7b<sup>tm1Tcg</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:10441329	20200605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461321	Tg(CAG-Map3k7*K63W)1232Mds/0 Tg(Myh6-cre)2182Mds/0  [background:] involves: FVB/N	is_model_of	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17085580	20100723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432224	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843269	Tg(tetO-Gnas)1593Mpke	is_implicated_in	DOID:5419	schizophrenia		MGI:4843272	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Gnas)1593Mpke/0  [background:] B6.Cg-Tg(Camk2a-tTA)1Mmay Tg(tetO-Gnas)1593Mpke			ECO:0000033	author statement supported by traceable reference	PMID:19030002	20101209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6437927	Shank3<sup>tm2Cmpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6437929	Shank3<sup>tm2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6-Shank3<sup>tm2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27492494	20200708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6437927	Shank3<sup>tm2Cmpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6437930	Shank3<sup>tm2Cmpl</sup>/Shank3<sup>tm2Cmpl</sup>  [background:] B6.129S6-Shank3<sup>tm2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27492494	20200708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6437927	Shank3<sup>tm2Cmpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:32327468	20200708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446420	Tg(SOD1*G93A)2Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:8209258	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446420	Tg(SOD1*G93A)2Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:12802201	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446420	Tg(SOD1*G93A)2Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:7992831	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428441	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup> Il1r1<sup>tm1Imx</sup>/Il1r1<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * NOD	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20696775	20120720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:12674324	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:11416036	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:12205031	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:12689675	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:11415990	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6281438	Borcs7<sup>Q87X</sup>	is_implicated_in	DOID:2367	neuroaxonal dystrophy		MGI:6302764	Borcs7<sup>Q87X</sup>/Borcs7<sup>Q87X</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30067980	20190513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430344	Dnah5<sup>b2b1565Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5430346	Dnah5<sup>b2b1565Clo</sup>/Dnah5<sup>b2b1565Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1565Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3790955	Stk11<sup>tm1Tpm</sup>/Stk11<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CD-1	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15480979	20080610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039428	Sell<sup>tm1Flv</sup>/Sell<sup>tm1Flv</sup>  [background:] involves: C57BL/6 * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180080	Acadvl<sup>tm1Uab</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:24648546	20150112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180080	Acadvl<sup>tm1Uab</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:2446598	Acadvl<sup>tm1Uab</sup>/Acadvl<sup>tm1Uab</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11590124	20150112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857277	Ptprc<sup>tm1Holm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21273420	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847811	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_implicated_in	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:25301747	20160118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847811	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_implicated_in	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:26192625	20160118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847811	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_implicated_in	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:24427314	20160118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847811	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_implicated_in	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:24046356	20160118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847811	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_implicated_in	DOID:0060371	Parkinson's disease 8		MGI:3848697	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>/Khdrbs2<sup>+</sup>  [background:] FVB-Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19503083	20160118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847811	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>	is_implicated_in	DOID:0060371	Parkinson's disease 8		MGI:5471773	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>/Khdrbs2<sup>+</sup>  [background:] FVB/N-Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23936174	20160118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441312	Tg(Vav1-JAK2*V617F)AZjz/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:18334677	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717232	Tg(Thy1-MAPT)22Schd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32679397	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717232	Tg(Thy1-MAPT)22Schd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25443285	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717232	Tg(Thy1-MAPT)22Schd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24780254	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717232	Tg(Thy1-MAPT)22Schd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27497324	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717232	Tg(Thy1-MAPT)22Schd	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3717255	Tg(Thy1-MAPT)22Schd/0  [background:] B6.Cg-Tg(Thy1-MAPT)22Schd			ECO:0000033	author statement supported by traceable reference	PMID:16877359	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717232	Tg(Thy1-MAPT)22Schd	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5521287	Tg(Thy1-MAPT)22Schd/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:23247080	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5467732	Cacna1a<sup>tm2.1Kewa</sup>	is_implicated_in	DOID:0050956	spinocerebellar ataxia type 6						ECO:0000033	author statement supported by traceable reference	PMID:26034136	20151012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5467732	Cacna1a<sup>tm2.1Kewa</sup>	is_implicated_in	DOID:0050956	spinocerebellar ataxia type 6		MGI:5467734	Cacna1a<sup>tm2.1Kewa</sup>/Cacna1a<sup>tm2.1Kewa</sup>  [background:] B6.Cg-Cacna1a<sup>tm2.1Kewa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23054835	20151012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463119	Tg(Prnp-TARDBP*Q331K)103Dwc	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:32422502	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463119	Tg(Prnp-TARDBP*Q331K)103Dwc	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:29295857	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463119	Tg(Prnp-TARDBP*Q331K)103Dwc	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6095193	Tg(Prnp-TARDBP*Q331K)103Dwc/0  [background:] B6.Cg-Tg(Prnp-TARDBP*Q331K)103Dwc/J			ECO:0000033	author statement supported by traceable reference	PMID:28334913	20201217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412051	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz/0 Tg(Thy1-MAPT)183Gotz/0  [background:] B6.Cg-Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz Tg(Thy1-MAPT)183Gotz	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19781645	20091217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708167	Tg(tetO-APPSwInd)102Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33412147	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708167	Tg(tetO-APPSwInd)102Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21411653	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708167	Tg(tetO-APPSwInd)102Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24623762	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708167	Tg(tetO-APPSwInd)102Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30055413	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708167	Tg(tetO-APPSwInd)102Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22855807	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708167	Tg(tetO-APPSwInd)102Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3709182	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)102Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16279840	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803301	Tnnt2<sup>tm2Mmto</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:23539503	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803301	Tnnt2<sup>tm2Mmto</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:25000405	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803301	Tnnt2<sup>tm2Mmto</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:23383212	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803301	Tnnt2<sup>tm2Mmto</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:27106044	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803301	Tnnt2<sup>tm2Mmto</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:3804499	Tnnt2<sup>tm2Mmto</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17556660	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803301	Tnnt2<sup>tm2Mmto</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:3804498	Tnnt2<sup>tm2Mmto</sup>/Tnnt2<sup>tm2Mmto</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17556660	20170809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785610	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup> Tg(SMN2*delta7)4299Ahmb/Tg(SMN2*delta7)4299Ahmb  [background:] FVB.Cg-Grm7<sup>Tg(SMN2)89Ahmb</sup> Smn1<sup>tm1Msd</sup> Tg(SMN2*delta7)4299Ahmb/J	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:20693262	20101014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6140203	Ndufa1<sup>tm1.1Nay</sup>	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:6187936	Ndufa1<sup>tm1.1Nay</sup>/Ndufa1<sup>tm1.1Nay</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:28506826	20180712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181547	Tg(Col2a1-Fgfr3/GH)BDor	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:24048522	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181547	Tg(Col2a1-Fgfr3/GH)BDor	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:25456072	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181547	Tg(Col2a1-Fgfr3/GH)BDor	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:14702637	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181547	Tg(Col2a1-Fgfr3/GH)BDor	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:33952673	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181547	Tg(Col2a1-Fgfr3/GH)BDor	is_implicated_in	DOID:4480	achondroplasia		MGI:5632165	Tg(Col2a1-Fgfr3/GH)BDor/0  [background:] FVB/N-Tg(Col2a1-Fgfr3/GH)BDor			ECO:0000033	author statement supported by traceable reference	PMID:9811582	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:34526660	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25270258	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28825595	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:22494971	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:27717711	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28416491	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28199476	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28363996	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:29422500	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25540232	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:23886856	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:29383140	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:26223300	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28428272	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:26676750	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:33894331	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:23217706	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:29972790	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:26650508	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28619710	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28467911	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:34003774	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:24338666	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28416486	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:29339153	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:26246425	20220927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:2665504	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] C57BL/6J-Apc<sup>Min</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12941845	20220927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663104	C4b<sup>tm1Crr</sup>/C4b<sup>tm1Crr</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11067882	20061009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675620	Htt<sup>tm1Mfc</sup>/Htt<sup>tm1Mfc</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:12926013	20081212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675620	Htt<sup>tm1Mfc</sup>/Htt<sup>tm1Mfc</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:17239451	20081212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5766542	Slc24a1<sup>tm1Xen</sup>	is_implicated_in	DOID:0110868	congenital stationary night blindness 1D		MGI:5766543	Slc24a1<sup>tm1Xen</sup>/Slc24a1<sup>tm1Xen</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26246500	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180150	Akt1<sup>tm1Mbb</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21821099	20120726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180150	Akt1<sup>tm1Mbb</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:2674288	Akt1<sup>tm1Mbb</sup>/Akt1<sup>tm1Mbb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14745448	20120726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27856911	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30571684	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30508733	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	MGI:6512372	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33402227	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31160584	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33633159	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32707043	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29274751	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30784814	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32417748	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36001964	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33309748	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33607163	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637817	App<sup>tm3.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5638675	App<sup>tm3.1Tcs</sup>/App<sup>tm3.1Tcs</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24728269	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308396	Tg(Thy1-DCTN1*G59S)M2Pcw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25763819	20160211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308396	Tg(Thy1-DCTN1*G59S)M2Pcw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5707946	Tg(Thy1-DCTN1*G59S)M2Pcw/?  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18305234	20160211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4353222	Arx<sup>tm1.1Jno</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:24452264	20150430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4353222	Arx<sup>tm1.1Jno</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:22565167	20150430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4353222	Arx<sup>tm1.1Jno</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:4353223	Arx<sup>tm1.1Jno</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19587282	20150430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702862	Satb1<sup>tm2Kos</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:7281769	Satb1<sup>tm2Kos</sup>/Satb1<sup>tm2Kos</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:29127143	20220602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604147	Tg(PDGFB-MAPT*V337M)1Atak	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:26949217	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604147	Tg(PDGFB-MAPT*V337M)1Atak	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:3718076	Tg(PDGFB-MAPT*V337M)1Atak/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11756496	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175026	Foxe3<sup>dyl</sup>/Foxe3<sup>dyl</sup>  [background:] BALB/cLiA-Foxe3<sup>dyl</sup>	is_model_of	DOID:11367	congenital aphakia						ECO:0000033	author statement supported by traceable reference	PMID:11980846	20170130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175026	Foxe3<sup>dyl</sup>/Foxe3<sup>dyl</sup>  [background:] BALB/cLiA-Foxe3<sup>dyl</sup>	is_model_of	DOID:11367	congenital aphakia						ECO:0000033	author statement supported by traceable reference	PMID:10652278	20170130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629232	Isl1<sup>tm1(cre)Tmj</sup>/Isl1<sup>+</sup> Tg(SOD1*G37R)1Dwc/0  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16741123	20060718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6488232	Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:6488226	Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31715135	20201223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897214	Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0  [background:] involves: C57BL/6 * NMRI * SJL	is_model_of	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000033	author statement supported by traceable reference	PMID:15591278	20170511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:28412297	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:24662047	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:25920768	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055150	Dysf<sup>prmd</sup>	is_implicated_in	DOID:11720	distal myopathy		MGI:3055667	Dysf<sup>prmd</sup>/Dysf<sup>prmd</sup>  [background:] A/J			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4439300	Tg(CAG-lacZ,-SV40)#Bcv/0  [background:] involves: FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:20056833	20100412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039039	Tg(MMTV-Erbb2)10Pjo	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11156526	20160104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039039	Tg(MMTV-Erbb2)10Pjo	is_implicated_in	DOID:1612	breast cancer		MGI:5604880	Tg(MMTV-Erbb2)10Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:2567634	20160104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294340	Dnah5<sup>b2b002Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24629673	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22095718	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31213067	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21235806	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23029404	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27255814	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25486177	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21738757	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24842003	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27586053	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23520537	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22516463	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32768866	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23932880	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25673868	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31103943	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32171592	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22177720	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26876740	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22870188	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30594047	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27460153	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32619874	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22796601	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26982728	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30215697	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23152608	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23954169	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29042514	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25617315	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28539885	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35153718	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25309427	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24086624	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31813629	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23523959	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26455952	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25552414	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24655393	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23500896	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22728099	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30015035	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23555795	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30397132	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22427376	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27509875	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23711927	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26553823	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32916195	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31065079	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27223629	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22912745	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23486975	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27460145	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24630364	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:37253603	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28683325	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26365177	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27103531	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32417750	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36498839	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24278307	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23312564	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32087004	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23683389	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26039057	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25122659	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31842924	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25896362	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26214837	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33753066	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174994	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9883847	20230929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359790	Ttn<sup>tm1Brge</sup>	is_implicated_in	DOID:0110430	dilated cardiomyopathy 1G						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359790	Ttn<sup>tm1Brge</sup>	is_implicated_in	DOID:0110430	dilated cardiomyopathy 1G						ECO:0000033	author statement supported by traceable reference	PMID:25759365	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359790	Ttn<sup>tm1Brge</sup>	is_implicated_in	DOID:0110430	dilated cardiomyopathy 1G		MGI:4359814	Ttn<sup>tm1Brge</sup>/Ttn<sup>+</sup>  [background:] B6.Cg-Ttn<sup>tm1Brge</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19406126	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28232471	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23076356	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26996122	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26216548	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16397221	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25452273	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28442553	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26452271	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27941872	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23042302	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27893715	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28414315	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27742686	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27265504	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27061193	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26947075	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24607504	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:3032575	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/?  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14706336	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:3032576	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:14706336	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7439057	Iigp1c<sup>M1Btlr</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:7439142	Iigp1c<sup>M1Btlr</sup>/Iigp1c<sup>M1Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>M1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473223	Cfap276<sup>em2.1Fuxi</sup>	is_implicated_in	DOID:0050543	Charcot-Marie-Tooth disease intermediate type		MGI:6473225	Cfap276<sup>em2.1Fuxi</sup>/Cfap276<sup>em2.1Fuxi</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32592472	20201119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473223	Cfap276<sup>em2.1Fuxi</sup>	is_implicated_in	DOID:0050543	Charcot-Marie-Tooth disease intermediate type		MGI:6473224	Cfap276<sup>em2.1Fuxi</sup>/Cfap276<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32592472	20201119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24231356	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26203463	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21217767	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25134728	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:31036840	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:31063986	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27017930	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29104117	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23372043	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25748626	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23275441	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25682918	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:36650127	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33940179	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25144457	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27013675	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22848491	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26508634	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29066728	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25101683	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22698685	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24388981	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25646445	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25268775	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24336051	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29688337	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23209424	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29768217	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21926467	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28069792	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25986402	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22702510	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25662336	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26752648	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29895889	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25469887	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28263187	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:36574405	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22820300	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29289683	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23167744	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23586612	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25271153	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28007908	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:30797895	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23926255	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24955833	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22848498	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28694434	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25892655	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33370315	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28031289	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:30061661	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27561680	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33753290	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28578004	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22187438	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27131346	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29902468	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28550168	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24475300	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26123489	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease		MGI:3694681	Tg(HDexon1)62Gpb/0  [background:] B6CBA-Tg(HDexon1)62Gpb/1J			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease		MGI:3694681	Tg(HDexon1)62Gpb/0  [background:] B6CBA-Tg(HDexon1)62Gpb/1J			ECO:0000033	author statement supported by traceable reference	PMID:16697652	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease		MGI:3530234	Tg(HDexon1)62Gpb/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:8898202	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386951	Tg(HDexon1)62Gpb	is_implicated_in	DOID:12858	Huntington's disease		MGI:3757568	Tg(HDexon1)62Gpb/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9267033	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:24509080	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:28009297	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10074482	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3718111	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] 129S.129X1-Myh6<sup>tm1Jse</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16332958	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3531468	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15001446	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182704	Myh6<sup>tm1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3531468	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8614836	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24069439	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23468919	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24316473	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20813165	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34798897	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24623762	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22134919	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26010758	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33397961	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447326	Tg(PDGFB-PSEN1M146L)2Jhd	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856211	Cacna1a<sup>tg-rol</sup>	is_implicated_in	DOID:0050214	Lambert-Eaton myasthenic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18653245	20210329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856211	Cacna1a<sup>tg-rol</sup>	is_implicated_in	DOID:0050214	Lambert-Eaton myasthenic syndrome		MGI:3624868	Cacna1a<sup>tg-rol</sup>/Cacna1a<sup>tg-rol</sup>  [background:] involves: C57BL/6 * SIII			ECO:0000033	author statement supported by traceable reference	PMID:18653245	20210329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25801914	20160330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24569456	20160330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16720837	20160330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3035835	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14966562	20160330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14699048	20160330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583920	Polg<sup>tm1Prol</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25411424	20150527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583920	Polg<sup>tm1Prol</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5637428	Polg<sup>tm1Prol</sup>/Polg<sup>tm1Prol</sup>  [background:] B6J.129S7-Polg<sup>tm1Prol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19734452	20150527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712499	Tg(Prnp-ATXN7*92Q)6076Als/0  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:11580893	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712499	Tg(Prnp-ATXN7*92Q)6076Als/0  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:12077187	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712499	Tg(Prnp-ATXN7*92Q)6076Als/0  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389103	Rapsn<sup>em1Gan</sup>	is_implicated_in	DOID:0110675	congenital myasthenic syndrome 11		MGI:6389105	Rapsn<sup>em1Gan</sup>/Rapsn<sup>em1Gan</sup>  [background:] C57BL/6J-Rapsn<sup>em1Gan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31549961	20200210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7434652	Cnga1<sup>m1Mhda</sup>	is_implicated_in	DOID:0110377	retinitis pigmentosa 49		MGI:7434657	Cnga1<sup>m1Mhda</sup>/Cnga1<sup>m1Mhda</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:36115851	20230215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5287716	Trim32<sup>tm1Spc</sup>/Trim32<sup>tm1Spc</sup>  [background:] involves: 129S/SvEvBrd * BALB/cJ * C57BL/6J	is_model_of	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H						ECO:0000033	author statement supported by traceable reference	PMID:21775502	20110930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575736	Sipa1<sup>tm1Nm</sup>/Sipa1<sup>tm1Nm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:12892713	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056336	Shank3<sup>tm1Yhj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23583105	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056336	Shank3<sup>tm1Yhj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056336	Shank3<sup>tm1Yhj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056336	Shank3<sup>tm1Yhj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5056404	Shank3<sup>tm1Yhj</sup>/Shank3<sup>tm1Yhj</sup>  [background:] B6.129S7-Shank3<sup>tm1Yhj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21558424	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618818	Dnah5<sup>b2b2925Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044885	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup> Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:15071184	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388657	Pkhd1<sup>em1Mrug</sup>	is_implicated_in	DOID:0080212	polycystic kidney disease 4		MGI:6388659	Pkhd1<sup>em1Mrug</sup>/Pkhd1<sup>em1Mrug</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30600684	20200205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388657	Pkhd1<sup>em1Mrug</sup>	is_implicated_in	DOID:0080212	polycystic kidney disease 4		MGI:6388658	Pkhd1<sup>em1Mrug</sup>/Pkhd1<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30600684	20200205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6257762	Tlcd3b<sup>em1(IMPC)Bay</sup>	is_implicated_in	DOID:0050572	cone-rod dystrophy		MGI:7277808	Tlcd3b<sup>em1(IMPC)Bay</sup>/Tlcd3b<sup>em1(IMPC)Bay</sup>  [background:] C57BL/6NJ-Tlcd3b<sup>em1(IMPC)Bay</sup>/Mmnc			ECO:0000033	author statement supported by traceable reference	PMID:33077892	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176441	Vhl<sup>tm1Wml</sup>/Vhl<sup>tm1Wml</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:14604887	20160502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176441	Vhl<sup>tm1Wml</sup>/Vhl<sup>tm1Wml</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:9286594	20160502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:36256464	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26279302	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30938713	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28386018	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:31490946	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22052106	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28408354	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26929329	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26048156	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23275441	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29196686	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23372043	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25351248	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22187438	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25140802	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33636386	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23977241	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29462355	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26642438	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25505248	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease		MGI:2671158	Tg(HD82Gln)81Gschi/0  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9949199	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670626	Tg(HD82Gln)81Gschi	is_implicated_in	DOID:12858	Huntington's disease		MGI:5052308	Tg(HD82Gln)81Gschi/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21406230	20211230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607781	Gjb6<sup>tm2.2Kwi</sup>	is_implicated_in	DOID:14693	Clouston syndrome		MGI:5607782	Gjb6<sup>tm2.2Kwi</sup>/Gjb6<sup>tm2.2Kwi</sup>  [background:] involves: 129P2/OlaHsd * BALB/c * C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24685692	20150106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560902	Trappc10<sup>b2b2416Clo</sup>	is_implicated_in	DOID:0060341	agnathia-otocephaly complex		MGI:5561310	Trappc10<sup>b2b2416Clo</sup>/Trappc10<sup>b2b2416Clo</sup>  [background:] Trappc10<sup>b2b2416Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5883014	Tg(PGK1-Gnas*R201C)60Pabi	is_implicated_in	DOID:1858	McCune Albright syndrome		MGI:5883020	Tg(PGK1-Gnas*R201C)60Pabi/0  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:24764158	20170413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579140	Park7<sup>tm1Shn</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:26546471	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579140	Park7<sup>tm1Shn</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:21839811	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579140	Park7<sup>tm1Shn</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3579508	Park7<sup>tm1Shn</sup>/Park7<sup>tm1Shn</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15721235	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287305	Sting1<sup>em1Jmin</sup>	is_implicated_in	DOID:0111457	STING-associated vasculopathy with onset in infancy						ECO:0000033	author statement supported by traceable reference	PMID:33979608	20220209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287305	Sting1<sup>em1Jmin</sup>	is_implicated_in	DOID:0111457	STING-associated vasculopathy with onset in infancy		MGI:6302788	Sting1<sup>em1Jmin</sup>/Sting1<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28951494	20220209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5700053	Fxn<sup>tm1Mkn</sup>/Fxn<sup>tm1Mkn</sup> Tg(FXN)YG22Pook/0  [background:] involves: 129/Sv * C57BL/6 * CBA	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:16919418	20151228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003462	Tg(Hmgcr-PSEN1*M146L)#Lpr/0 Tg(Thy1-APPLon)2Vln/0  [background:] involves: C57BL/6 * CBA * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25979088	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28814546	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25713300	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26821816	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29742424	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29769330	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24351104	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24958891	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27670841	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33373327	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31291284	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35248529	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28687309	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22174313	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28334953	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32015540	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26214522	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29782864	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30038001	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28927958	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24958851	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35021077	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33383186	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26469053	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31229630	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624713	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20633611	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624718	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624713	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624717	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>tm1.1Bird</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3817230	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:24735673	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098752	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] B6.129P2(C)-Mecp2<sup>tm1.1Bird</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098753	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>+</sup>  [background:] B6.129P2(C)-Mecp2<sup>tm1.1Bird</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266284	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137311	Mecp2<sup>tm1.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5491051	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23452848	20230810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805721	Gp1bb<sup>tm2Frla</sup>/Gp1bb<sup>tm2Frla</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2217	Bernard-Soulier syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17095718	20111110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702658	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15199412	20160113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6368150	Porcn<sup>tm1.2Lcm</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368188	Porcn<sup>tm1.2Lcm</sup>/Porcn<sup>tm1.2Lcm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613697	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>tm1Rdd</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10021468	20060301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613697	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>tm1Rdd</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:8673132	20060301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4939781	Prkn<sup>tm1Ccs</sup>/Prkn<sup>tm1Ccs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:21212098	20110307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653129	Krt14<sup>tm1Der</sup>/Krt14<sup>tm1Der</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:4644	epidermolysis bullosa simplex						ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942359	Tg(Kit*D814V)3Roer	is_implicated_in	DOID:350	mastocytosis		MGI:4942362	Tg(Kit*D814V)3Roer/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942359	Tg(Kit*D814V)3Roer	is_implicated_in	DOID:350	mastocytosis		MGI:4942364	Tg(Cma1-cre)ARoer/0 Tg(Kit*D814V)3Roer/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438324	Pkhd1<sup>tm2Cjwa</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:5438332	Pkhd1<sup>tm2Cjwa</sup>/Pkhd1<sup>tm2Cjwa</sup>  [background:] either: B6.129(Cg)-Pkhd1<sup>tm2Cjwa</sup> or C.129(Cg)-Pkhd1<sup>tm2Cjwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22021705	20121012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055582	Enam<sup>Rgsc395</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:28334996	20171206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055582	Enam<sup>Rgsc395</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574665	Enam<sup>Rgsc395</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20171206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774418	Ankrd26<sup>Gt(XK525)Byg</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24633808	20160701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774418	Ankrd26<sup>Gt(XK525)Byg</sup>	is_implicated_in	DOID:9970	obesity		MGI:3799316	Ankrd26<sup>Gt(XK525)Byg</sup>/Ankrd26<sup>Gt(XK525)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18162531	20160701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7520216	Tafazzin<sup>em1Xfa</sup>	is_implicated_in	DOID:0050476	Barth syndrome		MGI:7520358	Tafazzin<sup>em1Xfa</sup>/Y Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: C57BL/6NCrl * MF1			ECO:0000033	author statement supported by traceable reference	PMID:34129362	20230824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5636724	Dok7<sup>tm2Yyam</sup>	is_implicated_in	DOID:0110668	congenital myasthenic syndrome 10		MGI:5636739	Dok7<sup>tm2Yyam</sup>/Dok7<sup>tm2Yyam</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25237101	20150521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851927	Hr<sup>Hp</sup>/Hr<sup>Hp</sup>  [background:] BALB/cJ-Hr<sup>Hp</sup>	is_model_of	DOID:0110701	hypotrichosis 4						ECO:0000033	author statement supported by traceable reference	PMID:19513791	20090804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618464	Sgcd<sup>tm1Kcam</sup>/Sgcd<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000033	author statement supported by traceable reference	PMID:10481911	20060404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:9382882	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:8706124	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:11454988	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:12594290	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:12213735	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:7670466	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473628	Coq9<sup>tm1.1Lcl</sup>	is_implicated_in	DOID:0050730	coenzyme Q10 deficiency disease		MGI:5473683	Coq9<sup>tm1.1Lcl</sup>/Coq9<sup>tm1.1Lcl</sup>  [background:] involves: C57BL/6 * C57BL/6NTac * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23255162	20130410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5466160	Tg(APOE-FGF23*R176Q)#Ack/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:0050948	autosomal dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15284207	20130225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462366	Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0  [background:] involves: FVB/N	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22881289	20130208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653681	Ripk4<sup>tm1Pmh</sup>/Ripk4<sup>tm1Pmh</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060055	popliteal pterygium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22197489	20130430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653681	Ripk4<sup>tm1Pmh</sup>/Ripk4<sup>tm1Pmh</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060055	popliteal pterygium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22197488	20130430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037643	Phex<sup>Hyp-Duk</sup>/Phex<sup>+</sup>  [background:] involves: BALB/cAnBomUrd	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317923	Pla2g6<sup>m1J</sup>/Pla2g6<sup>m1J</sup>  [background:] C3H/HeJ-Pla2g6<sup>m1J</sup>	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:22442204	20120516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052363	Tg(JPH3*)CXwy	is_implicated_in	DOID:0090104	Huntington's disease-like 2		MGI:5052366	Tg(JPH3*)CXwy/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21555070	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6201745	Pkd2<sup>tm1.1Gwu</sup>	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:6251480	Pkd2<sup>tm1.1Gwu</sup>/Pkd2<sup>tm1.1Gwu</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:28244683	20181114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23643146	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28484012	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24362760	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23260124	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22522613	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27069115	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28934252	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24599465	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33998138	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25731615	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28666707	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32522344	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27425031	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32678276	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30554086	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28262325	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25148207	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3663621	Tg(APP695)3Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14645205	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3696575	Tg(APP695)3Dbo/0  [background:] B6.C3-Tg(APP695)3Dbo			ECO:0000033	author statement supported by traceable reference	PMID:12742740	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31554841	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25561520	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33323119	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26601124	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23260144	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29339535	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25950728	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32036032	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33077777	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30242133	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24684608	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26182420	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23300470	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23396537	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25653361	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22796598	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21900387	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21856714	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30250263	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31882402	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34714519	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29038238	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22123412	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26968765	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23083736	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23250915	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22393900	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31350260	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27656021	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25859182	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25921541	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26888925	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29778627	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29040407	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25849048	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27294193	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28213518	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29114038	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33421563	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27653682	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25296296	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22750206	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27539535	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25921527	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24089476	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29096020	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27616423	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25153086	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18835858	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24046080	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33906942	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366351	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25153086	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366442	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8844056	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:2665400	Fmr1<sup>tm1Cgr</sup>/Fmr1<sup>tm1Cgr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8033209	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366351	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8033209	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366442	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:16055059	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857169	Fmr1<sup>tm1Cgr</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:2665401	Fmr1<sup>tm1Cgr</sup>/Fmr1<sup>tm1Cgr</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:16055059	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23220414	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26691352	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29883458	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24949563	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:5566682	Tg(YAC128)#Hay/0  [background:] FVB/N-Tg(YAC128)#Hay			ECO:0000033	author statement supported by traceable reference	PMID:15843620	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23786539	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25583186	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23160193	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23341618	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27033979	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29192125	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432149	Tg(YAC128)#Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28391013	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909317	Mpz<sup>tm3.1Wra</sup>	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6191699	Mpz<sup>tm3.1Wra</sup>/Mpz<sup>+</sup>  [background:] FVB.129S2(Cg)-Mpz<sup>tm3.1Wra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22689911	20190307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909317	Mpz<sup>tm3.1Wra</sup>	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6191698	Mpz<sup>tm3.1Wra</sup>/Mpz<sup>tm3.1Wra</sup>  [background:] FVB.129S2(Cg)-Mpz<sup>tm1.1Wra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22689911	20190307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909317	Mpz<sup>tm3.1Wra</sup>	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:23250879	20190307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26626081	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23160193	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27995895	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27601642	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26642438	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24951540	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25619660	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24376631	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25740845	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:32387649	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27008868	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26908618	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23209424	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26920069	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23123142	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25271967	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27140644	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26508634	20200828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800779	Tg(HTT*97Q)IXwy	is_implicated_in	DOID:12858	Huntington's disease		MGI:3800927	Tg(HTT*97Q)IXwy/0  [background:] FVB-Tg(HTT*97Q)IXwy			ECO:0000033	author statement supported by traceable reference	PMID:18550760	20200828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824119	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25155956	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285183	Gnas<sup>tm1Gwa</sup>/Gnas<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae	is_model_of	DOID:4183	pseudopseudohypoparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:21747923	20110913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5614816	Tnfsf11<sup>gum</sup>	is_implicated_in	DOID:0110943	autosomal recessive osteopetrosis 2		MGI:5691824	Tnfsf11<sup>gum</sup>/Tnfsf11<sup>gum</sup>  [background:] STOCK Tnfsf11<sup>gum</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26234751	20151020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3607794	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:12893739	20051220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3607794	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:15025677	20051220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6140086	Tafa3<sup>em1Hssh</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6164125	Tafa3<sup>em1Hssh</sup>/Tafa3<sup>em1Hssh</sup>  [background:] C57BL/6NTac-Tafa3<sup>em1Hssh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29184127	20180704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003461	Tg(Thy1-APPLon)2Vln/0  [background:] involves: C57BL/6 * CBA * FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27298335	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27452466	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30674677	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27373157	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20190226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778526	Dnah5<sup>hlb612</sup>/Dnah5<sup>hlb612</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:18037990	20101001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621461	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:16510575	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621461	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129 * BALB/c * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:15798202	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7261448	Tg(Col2a1*G574S)1Waho	is_implicated_in	DOID:0080044	hypochondrogenesis						ECO:0000033	author statement supported by traceable reference	PMID:10100048	20220415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7261448	Tg(Col2a1*G574S)1Waho	is_implicated_in	DOID:0080044	hypochondrogenesis		MGI:7261449	Tg(Col2a1*G574S)1Waho/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9022054	20220415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644691	Tg(CAG-lacZ,-FUS*R521G,-EGFP)682Gyu	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:5644693	Meox2<sup>tm1(cre)Sor</sup>/Meox2<sup>+</sup> Tg(CAG-lacZ,-FUS*R521G,-EGFP)682Gyu/0  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25324524	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4833641	Serpina6<sup>tm1.1Mmp</sup>	is_implicated_in	DOID:0090030	corticosteroid-binding globulin deficiency		MGI:4833684	Serpina6<sup>tm1.1Mmp</sup>/Serpina6<sup>tm1.1Mmp</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20022933	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4833641	Serpina6<sup>tm1.1Mmp</sup>	is_implicated_in	DOID:0090030	corticosteroid-binding globulin deficiency		MGI:4833684	Serpina6<sup>tm1.1Mmp</sup>/Serpina6<sup>tm1.1Mmp</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22930537	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294943	Pitx1<sup>tm1Rsd</sup>/Pitx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:21775501	20111104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569754	Tg(TG-TPR/NTRK1)#Rstn	is_implicated_in	DOID:1781	thyroid cancer		MGI:5581425	Tg(TG-TPR/NTRK1)#Rstn/0  [background:] involves: 129S4/SvJaeSor * C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19261681	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909327	Tg(Myh6-Tnni3*R146G)133Rbns	is_implicated_in	DOID:0110313	hypertrophic cardiomyopathy 7		MGI:5909329	Tg(Myh6-Tnni3*R146G)133Rbns/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11055985	20170918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424980	Casr<sup>BCH003</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425919	Casr<sup>BCH003</sup>/Casr<sup>BCH003</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH003</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:28827223	20181128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:23470631	20181128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:24692543	20181128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3691620	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12746448	20181128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3611043	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15472122	20181128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5555034	Tg(DUX4*)1Maar	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27744317	20180604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5555034	Tg(DUX4*)1Maar	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23593020	20180604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857160	Edn3<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:25487064	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857160	Edn3<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857160	Edn3<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2174947	Edn3<sup>tm1Ywa</sup>/Edn3<sup>tm1Ywa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8001160	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950076	Fmr1<sup>tm1Usdn</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21220020	20110514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579804	Ccl3<sup>tm1Unc</sup>/Ccl3<sup>tm1Unc</sup> Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:15155903	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174949	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:0110953	Waardenburg syndrome type 4A						ECO:0000033	author statement supported by traceable reference	PMID:15294878	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119464	Tubb5<sup>tm2.1Dak</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:6119481	Tubb5<sup>tm2.1Dak</sup>/Tubb5<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26903504	20180305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910333	Tg(Myh6-LDB3*S196L)93Mva	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910333	Tg(Myh6-LDB3*S196L)93Mva	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C		MGI:5910334	Tg(Myh6-LDB3*S196L)93Mva/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20852297	20170926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028001	Pde6b<sup>atrd2</sup>/Pde6b<sup>atrd2</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286085	Tg(Myh6*)131Lnwd/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:8585273	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790094	Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>/Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110764	hereditary spastic paraplegia 11						ECO:0000033	author statement supported by traceable reference	PMID:26284655	20160829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686939	Galns<sup>tm1Toma</sup>/Galns<sup>tm1Toma</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:12804	mucopolysaccharidosis IV						ECO:0000033	author statement supported by traceable reference	PMID:14583446	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28666707	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25148207	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27069115	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25731615	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32522344	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30554086	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32678276	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28262325	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27425031	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31221985	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3618601	Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9212102	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:22301060	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:25055824	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15580285	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11773599	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583451	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] C3.FVB-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11773599	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583453	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: C3H * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11773599	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8952527	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3046284	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11062270	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3046284	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15226261	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583451	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] C3.FVB-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8191288	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157527	Ift88<sup>Tg737Rpw</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8191288	20150715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665257	Ryr2<sup>tm1Slh</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:31155924	20201006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665257	Ryr2<sup>tm1Slh</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:6278119	Ryr2<sup>tm1Slh</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27482086	20201006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665257	Ryr2<sup>tm1Slh</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:3689179	Ryr2<sup>tm1Slh</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16873551	20201006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774727	Col8a2<sup>tm2.1Asj</sup>	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24952277	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774727	Col8a2<sup>tm2.1Asj</sup>	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:5796114	Col8a2<sup>tm2.1Asj</sup>/Col8a2<sup>tm2.1Asj</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:7698753	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828597	Tg(CAG-cat,-Ptpn11*Q510E)#Krnz	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines		MGI:5828598	Tg(CAG-cat,-Ptpn11*Q510E)#Krnz/0 Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25359717	20170315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641338	Ryr2<sup>tm1Sgp</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:26121139	20160816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641338	Ryr2<sup>tm1Sgp</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:3653876	Ryr2<sup>tm1Sgp</sup>/Ryr2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15890976	20160816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524276	Tg(tetO-BRAF*V600E)26Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5524277	Tg(tetO-BRAF*V600E)26Jaf/0 Tg(TG-rtTA)30Jaf/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22105174	20181109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524276	Tg(tetO-BRAF*V600E)26Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29990309	20181109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524276	Tg(tetO-BRAF*V600E)26Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23372702	20181109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:2246770	20140110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20140110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20140110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711773	Bmp4<sup>tm1Blh</sup>/Bmp4<sup>+</sup>  [background:] B6.129S2-Bmp4<sup>tm1Blh</sup>	is_model_of	DOID:0110122	Axenfeld-Rieger syndrome type 3						ECO:0000033	author statement supported by traceable reference	PMID:11722794	20080318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573194	Tg(Thy1-Snca)1S13Putt	is_implicated_in	DOID:0060895	Parkinson's disease 4		MGI:5573196	Tg(Thy1-Snca)1S13Putt/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21966373	20140718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014340	Bscl2<sup>tm1.2Gliu</sup>/Bscl2<sup>tm1.2Gliu</sup>  [background:] involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:21551454	20150417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014340	Bscl2<sup>tm1.2Gliu</sup>/Bscl2<sup>tm1.2Gliu</sup>  [background:] involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:24778225	20150417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624982	X/Yaa  [background:] BXSB/MpJScr	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:1991974	20060621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4415196	Idua<sup>tm1.1Kmke</sup>/Idua<sup>tm1.1Kmke</sup>  [background:] B6.129-Idua<sup>tm1.1Kmke</sup>	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:19751987	20100106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18495771	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18452964	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26184451	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19091867	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:2945	severe acute respiratory syndrome		MGI:6399965	Tg(K18-ACE2)2Prlmn/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:17079315	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32498696	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25337879	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23873940	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28363999	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25174400	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25704820	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28790158	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26909577	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:27212033	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:29241546	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25519892	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25713296	20180124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441311	Tg(Igkv3-5*-MYC)#Plbe	is_implicated_in	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:30198908	20181106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441311	Tg(Igkv3-5*-MYC)#Plbe	is_implicated_in	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:26859080	20181106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441311	Tg(Igkv3-5*-MYC)#Plbe	is_implicated_in	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:22451422	20181106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706167	Brca1<sup>tm1Aash</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:35393420	20220708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706167	Brca1<sup>tm1Aash</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27653681	20220708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706167	Brca1<sup>tm1Aash</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3710355	Brca1<sup>tm1Aash</sup>/Brca1<sup>tm1Aash</sup> Tg(LGB-cre)74Acl/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17212342	20220708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412050	Nfkb2<sup>Lym1</sup>/Nfkb2<sup>Lym1</sup>  [background:] involves: BALB/c	is_model_of	DOID:12177	common variable immunodeficiency						ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5499110	Tg(Myl1-SOD1*G93A)#Amu	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23471914	20130801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5499110	Tg(Myl1-SOD1*G93A)#Amu	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5499112	Tg(Myl1-SOD1*G93A)#Amu/0  [background:] FVB/NJ-Tg(Myl1-SOD1*G93A)#Amu			ECO:0000033	author statement supported by traceable reference	PMID:19046573	20130801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438059	Pkd1<sup>b2b1585Clo</sup>	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5445215	Pkd1<sup>b2b1585Clo</sup>/Pkd1<sup>b2b1585Clo</sup>  [background:] C57BL/6J-Pkd1<sup>b2b1585Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23467932	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:26244298	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:28263189	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:26095930	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:32652549	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:31001259	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23616572	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:25871979	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:31826980	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:34831390	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:24623145	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:36345939	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:24040398	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:26791485	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:762500	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12486097	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76424	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:309911	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6304486	Tnnc1<sup>tm1.1Jrpi</sup>	is_implicated_in	DOID:0110319	hypertrophic cardiomyopathy 13		MGI:6304488	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26304555	20190522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6304486	Tnnc1<sup>tm1.1Jrpi</sup>	is_implicated_in	DOID:0110319	hypertrophic cardiomyopathy 13		MGI:6304487	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>tm1.1Jrpi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26304555	20190522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6304486	Tnnc1<sup>tm1.1Jrpi</sup>	is_implicated_in	DOID:0110319	hypertrophic cardiomyopathy 13		MGI:6304487	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>tm1.1Jrpi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28235781	20190522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629751	Ar<sup>tm1(AR)Dmr</sup>/Y Tg(TRAMP)8247Ng/0  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:16601069	20060721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5460859	Fgd4<sup>tm1.1Ics</sup>/Fgd4<sup>tm1.1Ics</sup>  [background:] Not Specified	is_model_of	DOID:0110192	Charcot-Marie-Tooth disease type 4H						ECO:0000033	author statement supported by traceable reference	PMID:23171661	20130128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574665	Enam<sup>Rgsc395</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:33753288	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:25768905	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:25595967	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:22884877	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:29192206	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:30507379	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429435	Atxn1<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1		MGI:3774931	Atxn1<sup>tm1Hzo</sup>/Atxn1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12086639	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308970	Asl<sup>tm1Brle</sup>	is_implicated_in	DOID:14755	argininosuccinic aciduria						ECO:0000033	author statement supported by traceable reference	PMID:22541557	20130912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308970	Asl<sup>tm1Brle</sup>	is_implicated_in	DOID:14755	argininosuccinic aciduria		MGI:5308984	Asl<sup>tm1Brle</sup>/Asl<sup>tm1Brle</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:22541557	20130912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706581	Rbl2<sup>tm2Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27298335	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706581	Rbl2<sup>tm2Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27373157	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706581	Rbl2<sup>tm2Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706581	Rbl2<sup>tm2Tyj</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27452466	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:29391529	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26264577	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23263861	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28916199	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:29016853	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27170316	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27621445	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23268200	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27557711	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:33693569	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28426667	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:35159369	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:30188931	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31060774	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056903	Tg(SMN2)2Hung	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:33931501	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:28860175	20190718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I		MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20675713	20190718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:31091146	20190718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:28663375	20190718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:27561302	20190718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789333	Tg(SFTPC-EGFR*L858R)4-3Kkiu	is_implicated_in	DOID:1324	lung cancer		MGI:5789334	Tg(SFTPC-EGFR*L858R)4-3Kkiu/0  [background:] involves: C57BL/6Cr			ECO:0000033	author statement supported by traceable reference	PMID:19690148	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789333	Tg(SFTPC-EGFR*L858R)4-3Kkiu	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24768699	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258221	Tg(KRT5-Terf2)PMBlas	is_implicated_in	DOID:0050427	xeroderma pigmentosum		MGI:6258254	Tg(KRT5-Terf2)PMBlas/Y  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16142233	20181129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444198	Pparg<sup>tm2Rev</sup>/Pparg<sup>tm2Rev</sup> Tg(Tagln-cre)1Her/?  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:18382765	20130416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907159	Tg(Myh6-NEBL*G202R)#Jato	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23632046	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907159	Tg(Myh6-NEBL*G202R)#Jato	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907159	Tg(Myh6-NEBL*G202R)#Jato	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907161	Tg(Myh6-NEBL*G202R)#Jato/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20951326	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623521	Pomgnt1<sup>Gt(OST179231)Lex</sup>	is_implicated_in	DOID:0050560	Walker-Warburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22728091	20130805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623521	Pomgnt1<sup>Gt(OST179231)Lex</sup>	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:3624438	Pomgnt1<sup>Gt(OST179231)Lex</sup>/Pomgnt1<sup>Gt(OST179231)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23454088	20130805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623521	Pomgnt1<sup>Gt(OST179231)Lex</sup>	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:3624438	Pomgnt1<sup>Gt(OST179231)Lex</sup>/Pomgnt1<sup>Gt(OST179231)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16458488	20130805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007651	Tg(Myh6-Tpm1*E180G)57Dfw/0  [background:] involves: FVB/N	is_model_of	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:11603924	20120319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007651	Tg(Myh6-Tpm1*E180G)57Dfw/0  [background:] involves: FVB/N	is_model_of	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:14575301	20120319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007651	Tg(Myh6-Tpm1*E180G)57Dfw/0  [background:] involves: FVB/N	is_model_of	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:21056571	20120319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:10802658	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:12506090	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:11528395	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:14517541	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:9843205	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850972	Ppm1k<sup>tm1Yiwa</sup>/Ppm1k<sup>tm1Yiwa</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:9269	maple syrup urine disease						ECO:0000033	author statement supported by traceable reference	PMID:19411760	20090722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644514	Tg(H2-K<sup>b</sup>-Tcra,-Tcrb)1640Kurs	is_implicated_in	DOID:2377	multiple sclerosis		MGI:5644517	Tg(H2-K<sup>b</sup>-Tcra,-Tcrb)1640Kurs/0  [background:] SJL.FVB-Tg(H2-K<sup>b</sup>-Tcra,-Tcrb)1640Kurs			ECO:0000033	author statement supported by traceable reference	PMID:19487416	20150721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6378540	Best1<sup>tm2.1Web</sup>	is_not_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:6378557	Best1<sup>tm2.1Web</sup>/Best1<sup>tm2.1Web</sup>  [background:] B6.129S1(Cg)-Best1<sup>tm2.1Web</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31201163	20191126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5828598	Tg(CAG-cat,-Ptpn11*Q510E)#Krnz/0 Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * FVB/N * SJL	is_model_of	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:25359717	20170315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6394064	Cchcr1<sup>em1Aoka</sup>	is_implicated_in	DOID:986	alopecia areata		MGI:6782396	Cchcr1<sup>em1Aoka</sup>/Cchcr1<sup>em1Aoka</sup>  [background:] C57BL/6NJcl-Cchcr1<sup>em1Aoka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32580135	20211027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838361	Gt(ROSA)26Sor<sup>tm1(CAG-Kcnj11*,-GFP)Nich</sup>	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24458355	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838361	Gt(ROSA)26Sor<sup>tm1(CAG-Kcnj11*,-GFP)Nich</sup>	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:21813803	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838361	Gt(ROSA)26Sor<sup>tm1(CAG-Kcnj11*,-GFP)Nich</sup>	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus		MGI:4430413	Gt(ROSA)26Sor<sup>tm1(CAG-Kcnj11*,-GFP)Nich</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:19187772	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5495412	Kif7<sup>dda</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5495415	Kif7<sup>dda</sup>/Kif7<sup>dda</sup>  [background:] FVB.A-Kif7<sup>dda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23650387	20130717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361017	Tg(MMTV-Erbb2*,-cre)1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26721874	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361017	Tg(MMTV-Erbb2*,-cre)1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28096336	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361017	Tg(MMTV-Erbb2*,-cre)1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:32393835	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361017	Tg(MMTV-Erbb2*,-cre)1Mul	is_implicated_in	DOID:1612	breast cancer		MGI:4361922	Tg(MMTV-Erbb2*,-cre)1Mul/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18273058	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057332	Ret<sup>tm2(RET)Jmi</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278934	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>	is_implicated_in	DOID:0111227	chromosome 3-linked frontotemporal dementia		MGI:6278939	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27329763	20210201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278934	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>	is_implicated_in	DOID:0111227	chromosome 3-linked frontotemporal dementia		MGI:6278937	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27329763	20210201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692746	Gfap<sup>tm2Mes</sup>/Gfap<sup>+</sup> Tg(GFAP)10Mes/0  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:17065456	20070108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810875	Fkrp<sup>tvrm53</sup>	is_implicated_in	DOID:9884	muscular dystrophy		MGI:6093458	Fkrp<sup>tvrm53</sup>/Fkrp<sup>tvrm53</sup>  [background:] C57BL/6J-Fkrp<sup>tvrm53</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7484418	Gba1<sup>tm1.1Smoc</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:7484465	Gba1<sup>tm1.1Smoc</sup>/Gba1<sup>tm1.1Smoc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:35711931	20230524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:26825707	20180514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:26864340	20180514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:29420734	20180514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:26518437	20180514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2		MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23160464	20180514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2		MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15069016	20180514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836256	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>tm3Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm3Maag</sup>	is_model_of	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:19104150	20090318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617439	Hgd<sup>aku</sup>/Hgd<sup>aku</sup>  [background:] either: (involves: 129/Sv * BALB/cByJ * NB) or (involves: 129/Sv * C57BL/6J * NB)	is_model_of	DOID:9270	alkaptonuria						ECO:0000033	author statement supported by traceable reference	PMID:8188247	20060323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5547756	Tg(Utg-TAg)#Fjd/?  [background:] involves: FVB	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:9040936	20140304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624685	Mecp2<sup>tm1Jae</sup>/Y Tg(Camk2a-cre)93Kln/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242118	20060619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563494	Dzip1l<sup>warpy</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:6107228	Dzip1l<sup>warpy</sup>/Dzip1l<sup>warpy</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28530676	20180102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563494	Dzip1l<sup>warpy</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:6107229	Dzip1l<sup>warpy</sup>/Dzip1l<sup>warpy</sup>  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28530676	20180102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314412	Tg(MECP2)3Hzo/0  [background:] either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1	is_model_of	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000033	author statement supported by traceable reference	PMID:22231481	20120408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5816464	Rai1<sup>tm2.1Luo</sup>	is_implicated_in	DOID:0060768	Smith-Magenis syndrome		MGI:5817471	Rai1<sup>tm2.1Luo</sup>/Rai1<sup>tm2.1Luo</sup> Tg(Nes-cre)1Kln/?  [background:] either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)			ECO:0000033	author statement supported by traceable reference	PMID:27693255	20170113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797739	Tg(FXN)YG8Pook	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25113747	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797739	Tg(FXN)YG8Pook	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25681319	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797739	Tg(FXN)YG8Pook	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:27079523	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797739	Tg(FXN)YG8Pook	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25070719	20160801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579532	Mdk<sup>tm1Tmu</sup>/Mdk<sup>tm1Tmu</sup>  [background:] B6.129S2-Mdk<sup>tm1Tmu</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19217924	20090818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26237041	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25878291	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098756	Mecp2<sup>tm1Jae</sup>/Y Chat<sup>tm2(cre)Lowl</sup>/Chat<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624680	Mecp2<sup>tm1Jae</sup>/Y Tg(Nes-cre)1Atp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11242118	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158353	Mecp2<sup>tm1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624685	Mecp2<sup>tm1Jae</sup>/Y Tg(Camk2a-cre)93Kln/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11242118	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052072	Crb1<sup>tm1Wij</sup>	is_implicated_in	DOID:0110358	retinitis pigmentosa 12						ECO:0000033	author statement supported by traceable reference	PMID:24565864	20140917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3783471	Sirt1<sup>tm1Mcby</sup>/Sirt1<sup>tm1Mcby</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:18687325	20100728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794201	Tg(Pbsn-TAg)15Tvd	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794201	Tg(Pbsn-TAg)15Tvd	is_implicated_in	DOID:10283	prostate cancer		MGI:4836241	Tg(Pbsn-TAg)15Tvd/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16288012	20140529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856327	Col1a2<sup>oim</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:22910579	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856327	Col1a2<sup>oim</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:27821779	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856327	Col1a2<sup>oim</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:26707242	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856327	Col1a2<sup>oim</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:2664353	Col1a2<sup>oim</sup>/Col1a2<sup>oim</sup>  [background:] involves: C3H/HeJ * C57BL/6JLe			ECO:0000033	author statement supported by traceable reference	PMID:8446583	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856327	Col1a2<sup>oim</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:3720802	Col1a2<sup>oim</sup>/Col1a2<sup>oim</sup>  [background:] B6C3Fe a/a-Col1a2<sup>oim</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8968022	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:25904800	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:22849820	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:23404611	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:28531236	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:25533112	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:25236689	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:27638600	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:25240259	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:24057669	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:25749991	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:21809420	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7417782	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20441793	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7437911	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856218	Galc<sup>twi</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21389217	20200217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5767124	Gbe1<sup>tm2.1Hoa</sup>/Gbe1<sup>tm2.1Hoa</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:2750	glycogen storage disease IV						ECO:0000033	author statement supported by traceable reference	PMID:26385640	20160511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694660	Map6<sup>tm1Job</sup>/Map6<sup>tm1Job</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23002183	20151104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716968	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:16288016	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716968	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19847165	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716968	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24239348	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716968	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23565506	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433323	Ap1b1<sup>b2b1660Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818807	Tg(Myh6-PRKAG2*T400N)1Feah	is_implicated_in	DOID:0090101	lethal congenital glycogen storage disease of heart		MGI:4818886	Tg(Myh6-PRKAG2*T400N)1Feah/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20005292	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438061	b2b1639Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5442129	b2b1639Clo/b2b1639Clo  [background:] C57BL/6J-b2b1639Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7437928	Snrpb<sup>em1Lajm</sup>	is_implicated_in	DOID:0111248	cerebrocostomandibular syndrome		MGI:7437965	E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup> Snrpb<sup>em1Lajm</sup>/Snrpb<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6J * CD1			ECO:0000033	author statement supported by traceable reference	PMID:35593225	20230224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15593201	20150604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25447050	20150604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10793067	20150604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8077681	20150604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2658880	Cyp19a1<sup>tm1Sih</sup>/Cyp19a1<sup>tm1Sih</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25447050	20150604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680727	Il4ra<sup>tm1Tch</sup>/Il4ra<sup>tm1Tch</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:14557412	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438020	Slc39a4<sup>tm2Gka</sup>	is_implicated_in	DOID:0050605	acrodermatitis enteropathica						ECO:0000033	author statement supported by traceable reference	PMID:24015258	20140630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438020	Slc39a4<sup>tm2Gka</sup>	is_implicated_in	DOID:0050605	acrodermatitis enteropathica		MGI:5438021	Slc39a4<sup>tm2Gka</sup>/Slc39a4<sup>tm2Gka</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22737083	20140630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930939	Psen2<sup>tm1Ber</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23792007	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930939	Psen2<sup>tm1Ber</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34758364	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930939	Psen2<sup>tm1Ber</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29867447	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646292	b2b2966Clo	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:5646375	b2b2966Clo/b2b2966Clo  [background:] C57BL/6J-b2b2966Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5524087	Tg(MMTV-Myc*T58A)TA41Jrn/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707419	Disc1<sup>Rgsc1393</sup>	is_implicated_in	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:26768401	20160712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707419	Disc1<sup>Rgsc1393</sup>	is_implicated_in	DOID:1595	melancholic depression		MGI:3707972	Disc1<sup>Rgsc1393</sup>/Disc1<sup>Rgsc1393</sup>  [background:] B6.Cg-Disc1<sup>Rgsc1393</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17481393	20160712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23565247	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25914642	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24337465	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31306446	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25878270	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26235435	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23470163	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33137399	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16049335	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32450297	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29782905	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25830951	20221108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3722063	Tg(Thy1-APPSwDutIowa)BWevn/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14985348	20221108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811453	Gnptab<sup>tm1Dkji</sup>/Gnptab<sup>tm1Dkji</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000033	author statement supported by traceable reference	PMID:26857995	20161208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662716	Plau<sup>tm1Mlg</sup>/Plau<sup>tm1Mlg</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15615772	20070928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461798	Fgfr2<sup>m1Sgg</sup>	is_implicated_in	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22872266	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461798	Fgfr2<sup>m1Sgg</sup>	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:4461807	Fgfr2<sup>m1Sgg</sup>/Fgfr2<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20503384	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461798	Fgfr2<sup>m1Sgg</sup>	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:4461806	Fgfr2<sup>m1Sgg</sup>/Fgfr2<sup>m1Sgg</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20503384	20220617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682252	Krt2<sup>Mhdadsk2</sup>/Krt2<sup>+</sup>  [background:] C3HeB/FeJ-Krt2<sup>Mhdadsk2</sup>/Ieg	is_model_of	DOID:0060877	bullous congenital ichthyosiform erythroderma						ECO:0000033	author statement supported by traceable reference	PMID:12533510	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:31462499	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6694906	Dnah17<sup>em1Qsh</sup>	is_implicated_in	DOID:0111926	spermatogenic failure 39		MGI:6695074	Dnah17<sup>em1Qsh</sup>/Dnah17<sup>em1Qsh</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:31658987	20210427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5621061	Tg(SOD1*L126Z)45Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5621062	Tg(SOD1*L126Z)45Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16000321	20150408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764813	Tg(CAG-SNCA*)1.1Ccs	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:24204848	20140821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764813	Tg(CAG-SNCA*)1.1Ccs	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3764817	Tg(CAG-SNCA*)1.1Ccs/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21212098	20140821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5642117	Fgfr1<sup>tm1Upir</sup>/Fgfr1<sup>tm1Upir</sup> Fgfr2<sup>tm1Dor</sup>/Fgfr2<sup>tm1Dor</sup> Tg(KRT5-cre)5132Jlj/0  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:25843682	20150630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618244	Atp7a<sup>Mo-Tohm</sup>/Atp7a<sup>+</sup>  [background:] B6.Cg-Atp7a<sup>Mo-Tohm</sup>	is_model_of	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:16338116	20060330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705759	Fhl1<sup>tm1.1Mihi</sup>	is_implicated_in	DOID:0060253	scapuloperoneal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705759	Fhl1<sup>tm1.1Mihi</sup>	is_implicated_in	DOID:0060253	scapuloperoneal myopathy		MGI:5706792	Fhl1<sup>tm1.1Mihi</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J * C57BL/6NJ			ECO:0000033	author statement supported by traceable reference	PMID:25274776	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6156567	Stat2<sup>tm1.1(STAT2)Diam</sup>	is_implicated_in	DOID:0060478	Zika fever		MGI:6192490	Stat2<sup>tm1.1(STAT2)Diam</sup>/Stat2<sup>tm1.1(STAT2)Diam</sup>  [background:] C57BL/6-Stat2<sup>tm1.1(STAT2)Diam</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29746837	20230821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6116281	Tg(Plp1-Eif2ak3*)18Pop	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6116285	Tg(Plp1-Eif2ak3*)18Pop/Tg(Plp1-Eif2ak3*)18Pop  [background:] C57BL/6J-Tg(Plp1-Eif2ak3*)18Pop			ECO:0000033	author statement supported by traceable reference	PMID:25186761	20180214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:28063983	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:23663739	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:28536304	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:27107699	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:26976331	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:24430976	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:28973665	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:30135927	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease		MGI:3054886	Epm2a<sup>tm1Kzy</sup>/Epm2a<sup>tm1Kzy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21493628	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182627	Epm2a<sup>tm1Kzy</sup>	is_implicated_in	DOID:3534	Lafora disease		MGI:3054886	Epm2a<sup>tm1Kzy</sup>/Epm2a<sup>tm1Kzy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12019206	20190410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:9950794	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:12528192	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:23843985	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:6257302	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:18160655	20140204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:24121738	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21448290	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26577758	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21267465	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23473812	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21969553	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5689331	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] B6J.D2-Dtnbp1<sup>sdy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25677649	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5689331	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] B6J.D2-Dtnbp1<sup>sdy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23261874	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:4358724	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] DBA/2J-Dtnbp1<sup>sdy</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18984010	20160705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360692	Tg(Eno2-ATN1)14Tx/0  [background:] B6.Cg-Tg(Eno2-ATN1)14Tx	is_model_of	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000033	author statement supported by traceable reference	PMID:16407196	20091007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30126037	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28827321	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23029293	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29776378	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28408124	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28760828	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31982202	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34039738	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24631720	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4819951	Tg(Camk2a-tTA)1Mmay/? Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/?  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16020737	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33402227	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32623260	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28654636	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26508157	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35513476	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28500878	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5511058	Tg(Camk2a-tTA)1Mmay/0 Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/Fgf14<sup>+</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16291936	20230803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437086	Tmem67<sup>b2b1291.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437111	Tmem67<sup>b2b1291.1Clo</sup>/Tmem67<sup>b2b1291.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1291.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586967	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311364	Megf8<sup>b2b288Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5311833	Megf8<sup>b2b288Clo</sup>/Megf8<sup>b2b288Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b288Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5902220	Braf<sup>tm1Tumg</sup>	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:6164161	Braf<sup>tm1Tumg</sup>/Braf<sup>+</sup> Tg(CAG-cre)2Osb/0  [background:] involves: C57BL * C57BL/6J * DBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:26472072	20180704	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5902220	Braf<sup>tm1Tumg</sup>	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:5902221	Braf<sup>tm1Tumg</sup>/Braf<sup>+</sup> Tg(CAG-cre)2Osb/0  [background:] involves: C57BL * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:25035421	20180704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577096	Tg(MMTVneu)202Mul/0  [background:] FVB/N-Tg(MMTVneu)202Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:1359541	20080617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285078	Dnah5<sup>b2b016Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684306	F13a1<sup>tm1Gdi</sup>/F13a1<sup>tm1Gdi</sup>  [background:] involves: 129P2/OlaHsd * CBA/Ca	is_model_of	DOID:2211	factor XIII deficiency						ECO:0000033	author statement supported by traceable reference	PMID:12529747	20111107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3770518	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:18493606	20110404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3770518	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:11323676	20110404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438059	Pkd1<sup>b2b1585Clo</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5445215	Pkd1<sup>b2b1585Clo</sup>/Pkd1<sup>b2b1585Clo</sup>  [background:] C57BL/6J-Pkd1<sup>b2b1585Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461044	Abca12<sup>el12</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:4461053	Abca12<sup>el12</sup>/Abca12<sup>el12</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18802465	20100721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6315194	Tg(Vav1-Asxl1*Y588X)#Fcy	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:6315197	Tg(Vav1-Asxl1*Y588X)#Fcy/0  [background:] C57BL/6-Tg(Vav1-Asxl1*Y588X)#Fcy			ECO:0000033	author statement supported by traceable reference	PMID:29113963	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24107773	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25164016	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27292643	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28504653	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23770012	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511877	Tg(TetO-Erbb2)1Lach	is_implicated_in	DOID:1612	breast cancer		MGI:5506798	Tg(MMTV-rtTA)1Lach/0 Tg(TetO-Erbb2)1Lach/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:12498714	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661920	Tg(Alb-HRAS*G12V)28Yu	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5695608	Tg(Alb-HRAS*G12V)28Yu/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:16087271	20170208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661920	Tg(Alb-HRAS*G12V)28Yu	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16405947	20170208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661920	Tg(Alb-HRAS*G12V)28Yu	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5695608	Tg(Alb-HRAS*G12V)28Yu/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26131558	20170208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661920	Tg(Alb-HRAS*G12V)28Yu	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25218146	20170208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311370	Dync2h1<sup>b2b414Clo</sup>	is_implicated_in	DOID:0110087	asphyxiating thoracic dystrophy 3		MGI:5311880	Dync2h1<sup>b2b414Clo</sup>/Dync2h1<sup>b2b414Clo</sup>  [background:] C57BL/6J-Dync2h1<sup>b2b414Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6256806	Tg(tetO-EGFR*)#Kkw	is_implicated_in	DOID:1324	lung cancer		MGI:6256808	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*)#Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27251290	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6256806	Tg(tetO-EGFR*)#Kkw	is_implicated_in	DOID:1324	lung cancer		MGI:6256808	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*)#Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20033049	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835236	Tg(MMTV-LPAR3)#Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763113	Tg(MMTV-LPAR3)#Gbm/Tg(MMTV-LPAR3)#Gbm  [background:] FVB/N-Tg(MMTV-LPAR3)#Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694079	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:17932107	20151029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819724	Tg(Myh6-TNNT2*R141W)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR	is_model_of	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:18349139	20100819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910501	Tg(Myh6-Tnni3*L184)#Rste	is_implicated_in	DOID:0110313	hypertrophic cardiomyopathy 7		MGI:5910505	Tg(Myh6-Tnni3*L184)#Rste/0  [background:] B6.Cg-Tg(Myh6-Tnni3*L184)#Rste			ECO:0000033	author statement supported by traceable reference	PMID:18096573	20170927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476535	Tg(Eno2-MFN2*R94Q)L87Ugfm	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A		MGI:5476673	Tg(Eno2-MFN2*R94Q)L87Ugfm/Tg(Eno2-MFN2*R94Q)L87Ugfm  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20418531	20130501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055190	Pla2g6<sup>tm1Turk</sup>/Pla2g6<sup>tm1Turk</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:18202189	20100219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175836	Dysf<sup>im</sup>/Dysf<sup>im</sup>  [background:] involves: SJL	is_model_of	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:10508505	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462543	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup> Tg(CBS)11181Eri/0  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:20638879	20130211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857388	Dsg3<sup>tm1Stan</sup>	is_implicated_in	DOID:0060851	pemphigus vulgaris						ECO:0000033	author statement supported by traceable reference	PMID:25695683	20151215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857388	Dsg3<sup>tm1Stan</sup>	is_implicated_in	DOID:0060851	pemphigus vulgaris		MGI:2175834	Dsg3<sup>tm1Stan</sup>/Dsg3<sup>tm1Stan</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9166409	20151215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28916199	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:29016853	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27621445	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27557711	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:30188931	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23263861	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26311784	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:29391529	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26264577	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:33693569	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28426667	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31060774	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383990	Smn1<sup>tm1Hung</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:35159369	20220309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3828308	Plp1<sup>tm1Frca</sup>/Y  [background:] B6.129-Plp1<sup>tm1Frca</sup>	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:18835559	20090122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417827	Gata1<sup>tm2Sho</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:12149188	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183931	Xpa<sup>tm1Tnka</sup>	is_implicated_in	DOID:0110843	xeroderma pigmentosum group A						ECO:0000033	author statement supported by traceable reference	PMID:28528167	20190819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183931	Xpa<sup>tm1Tnka</sup>	is_implicated_in	DOID:0110843	xeroderma pigmentosum group A		MGI:4361117	Xpa<sup>tm1Tnka</sup>/Xpa<sup>tm1Tnka</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8751968	20190819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287464	Clcn7<sup>tm1.1Aros</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:6466741	Clcn7<sup>tm1.1Aros</sup>/Clcn7<sup>tm1.1Aros</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30865697	20201013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450728	Hbb<sup>tm1Unc</sup>/Hbb<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:8475058	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6458475	Tg(Thy1/THY1)T6Gsv	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21719782	20201104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6458475	Tg(Thy1/THY1)T6Gsv	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6458735	Tg(Thy1/THY1)T6Gsv/0  [background:] involves: C57BL/10 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15034095	20201104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6458475	Tg(Thy1/THY1)T6Gsv	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:16968721	20201104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6458475	Tg(Thy1/THY1)T6Gsv	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6458735	Tg(Thy1/THY1)T6Gsv/0  [background:] involves: C57BL/10 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14605274	20201104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6458475	Tg(Thy1/THY1)T6Gsv	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:31029503	20201104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6458475	Tg(Thy1/THY1)T6Gsv	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis						ECO:0000033	author statement supported by traceable reference	PMID:12081570	20201104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22079083	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26758873	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22798624	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:23656793	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26438828	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31060774	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27488123	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26911699	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26258776	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26134627	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:25878277	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26502195	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22763238	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:33382987	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26030275	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28062667	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26733414	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:31127156	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22037760	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28379354	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24191055	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22422766	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:36619669	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26276812	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056918	Tg(SMN2*delta7)4299Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24691550	20230331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437709	Tg(SERPINC1-SV40)BPbr	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20971743	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437709	Tg(SERPINC1-SV40)BPbr	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437710	X/Tg(SERPINC1-SV40)BPbr  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:1660504	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437709	Tg(SERPINC1-SV40)BPbr	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437710	X/Tg(SERPINC1-SV40)BPbr  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12763373	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857499	Gja8<sup>No2</sup>	is_implicated_in	DOID:0110231	cataract 1 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:27317663	20161104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857499	Gja8<sup>No2</sup>	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:2175043	Gja8<sup>No2</sup>/Gja8<sup>No2</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:1277597	20161104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857499	Gja8<sup>No2</sup>	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:2175044	Gja8<sup>No2</sup>/Gja8<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:1277597	20161104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906284	Sap130<sup>b2b635.2Clo</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:5906294	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup> Pcdha9<sup>b2b635.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906284	Sap130<sup>b2b635.2Clo</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:5906296	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857544	Cftr<sup>tm1Cam</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:25680200	20160303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857544	Cftr<sup>tm1Cam</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:26365583	20160303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857544	Cftr<sup>tm1Cam</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177436	Cftr<sup>tm1Cam</sup>/Cftr<sup>tm1Cam</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:1355249	20160303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828833	Nkx2-5<sup>tm2.1Mwc</sup>	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6476759	Cd2ap<sup>em1Irgu</sup>	is_implicated_in	DOID:0112245	focal segmental glomerulosclerosis 3		MGI:6476763	Cd2ap<sup>em1Irgu</sup>/Cd2ap<sup>em1Irgu</sup>  [background:] C57BL/6-Cd2ap<sup>em1Irgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30612599	20210727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:24737887	20180110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:25078979	20180110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:26964623	20180110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:27159635	20180110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412280	Prnp<sup>tm2Lnq</sup>/Prnp<sup>tm2Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:0050433	fatal familial insomnia						ECO:0000033	author statement supported by traceable reference	PMID:19709627	20140227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412280	Prnp<sup>tm2Lnq</sup>/Prnp<sup>tm2Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:0050433	fatal familial insomnia						ECO:0000033	author statement supported by traceable reference	PMID:23959875	20140227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19187267	20150420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:18997009	20150420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:12384220	20150420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822033	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25024188	20150420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:10746634	20061019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:9241280	20061019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:25524704	20150410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:23049915	20150410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:22096577	20150410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:2651509	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10588735	20150410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:2651494	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12576554	20150410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:3777760	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17712420	20150410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014325	Bscl2<sup>tm1.2Gliu</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:25866184	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014325	Bscl2<sup>tm1.2Gliu</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5014340	Bscl2<sup>tm1.2Gliu</sup>/Bscl2<sup>tm1.2Gliu</sup>  [background:] involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24778225	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014325	Bscl2<sup>tm1.2Gliu</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:27806294	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014325	Bscl2<sup>tm1.2Gliu</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5014340	Bscl2<sup>tm1.2Gliu</sup>/Bscl2<sup>tm1.2Gliu</sup>  [background:] involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21551454	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23722545	20180213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28530657	20180213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25176624	20180213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23975428	20180213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20180213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24075993	20180213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1890080	Tg(Wnt1)1Hev	is_implicated_in	DOID:1612	breast cancer		MGI:4819121	Tg(Wnt1)1Hev/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10713683	20180213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174965	Irs1<sup>tm1Tka</sup>/Irs1<sup>tm1Tka</sup>  [background:] Not Specified	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:7969452	20050811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706555	Tg(Pbsn-Tag)12T7fRjm	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23423848	20140925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706555	Tg(Pbsn-Tag)12T7fRjm	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706555	Tg(Pbsn-Tag)12T7fRjm	is_implicated_in	DOID:10283	prostate cancer		MGI:4358596	Tg(Pbsn-Tag)12T7fRjm/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9645768	20140925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717464	Cm/+  [background:] C3Sn.Cg-Cm/J	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:1613559	20090731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25301067	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:29241546	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28381544	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24706787	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:27212033	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:35332150	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23873940	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25843002	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28363999	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23475959	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26567140	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25339352	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:34143182	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25704820	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26030593	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26909577	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25337879	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28007785	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28790158	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:29195074	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25713296	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26751774	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25519892	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:5528689	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24239348	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3716404	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:24430184	20220525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810590	Aipl1<sup>tvrm127</sup>	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:5922033	Aipl1<sup>tvrm127</sup>/Aipl1<sup>tvrm127</sup>  [background:] C57BL/6J-Aipl1<sup>tvrm127</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576493	Trp53<sup>tm3.1Glo</sup>/Trp53<sup>+</sup>  [background:] B6.129S7-Trp53<sup>tm3.1Glo</sup>	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607981	20101019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697374	Hdc<sup>tm1Nagy</sup>/Hdc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24411733	20151130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25561290	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23142422	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5805821	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] B6.129S1-Pten<sup>tm1Rps</sup>/Nci			ECO:0000033	author statement supported by traceable reference	PMID:25561290	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620663	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup> Tg(CMV-GAA*P545L)#Kjv/0  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:25036864	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6403442	Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31296843	20200409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6403442	Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6403447	Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>/Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>  [background:] C57BL/6-Gt(ROSA)26Sor<sup>em1(DPP4)Yowa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30142928	20200409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6885539	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:14780	KBG syndrome		MGI:7336829	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>/Ankrd11<sup>+</sup> E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33996804	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6885539	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:14780	KBG syndrome		MGI:6885557	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>/Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup> E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33996804	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569747	Tg(TG-TPR/NTRK1)5215Rstn	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5578560	Tg(TG-TPR/NTRK1)5215Rstn/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11126359	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836993	Tg(Prnp*D177N*M128V)A21Rchi/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:19038218	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053711	Tg(TNF)197Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:25111378	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053711	Tg(TNF)197Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:25896020	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053711	Tg(TNF)197Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:34305946	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053711	Tg(TNF)197Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3053718	Tg(TNF)197Gkl/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:1721867	20220325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5006991	Slurp2<sup>tm1Lex</sup>	is_implicated_in	DOID:3390	palmoplantar keratosis		MGI:6159890	Slurp2<sup>tm1Lex</sup>/Slurp2<sup>tm1Lex</sup>  [background:] involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26967477	20180607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5315427	Tg(Myh6-MYL2*A13T)L1Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10		MGI:5315430	Tg(Myh6-MYL2*A13T)L1Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22091967	20120418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618859	Dock1<sup>b2b3190Clo</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5618862	Dock1<sup>b2b3190Clo</sup>/Dock1<sup>b2b3190Clo</sup>  [background:] C57BL/6J-Dock1<sup>b2b3190Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6798111	Gnat2<sup>cpfl3-2J</sup>	is_implicated_in	DOID:13911	achromatopsia		MGI:6798143	Gnat2<sup>cpfl3-2J</sup>/Gnat2<sup>cpfl3-2J</sup>  [background:] B6.Cg-Gnat2<sup>cpfl3-2J</sup>/Boc			ECO:0000033	author statement supported by traceable reference	MGI:6798134	20211110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689841	Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo  [background:] C57BL/6-Tg(Thy1-TARDBP*)BOddo	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:26002100	20151012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521583	Pkd1<sup>tm1Djmp</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25961459	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521583	Pkd1<sup>tm1Djmp</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25877301	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521583	Pkd1<sup>tm1Djmp</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3521730	Pkd1<sup>tm1Djmp</sup>/Pkd1<sup>tm1Djmp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15496422	20160128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613525	Tg(YAC128)53Hay/0  [background:] FVB/N-Tg(YAC128)53Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16697652	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613525	Tg(YAC128)53Hay/0  [background:] FVB/N-Tg(YAC128)53Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:12812983	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613525	Tg(YAC128)53Hay/0  [background:] FVB/N-Tg(YAC128)53Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16230019	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305254	Sirt1<sup>tm1.2Cxd</sup>/Sirt1<sup>tm1.2Cxd</sup> Tg(Alb1-cre)1Dlr/?  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:21103071	20120209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180054	Abcb1a<sup>tm1Bor</sup>	is_implicated_in	DOID:0110893	inflammatory bowel disease 13						ECO:0000033	author statement supported by traceable reference	PMID:25882614	20160815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180054	Abcb1a<sup>tm1Bor</sup>	is_implicated_in	DOID:0110893	inflammatory bowel disease 13						ECO:0000033	author statement supported by traceable reference	PMID:26431947	20160815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180054	Abcb1a<sup>tm1Bor</sup>	is_implicated_in	DOID:0110893	inflammatory bowel disease 13		MGI:5693947	Abcb1a<sup>tm1Bor</sup>/Abcb1a<sup>tm1Bor</sup>  [background:] FVB.129P2-Abcb1a<sup>tm1Bor</sup>/TacImx			ECO:0000033	author statement supported by traceable reference	PMID:9820555	20160815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663711	Bmpr1a<sup>tm1Bhr</sup>/Bmpr1a<sup>tm2.1Bhr</sup> Tg(GATA6-cre)#Jbeb/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:14289	Ebstein anomaly						ECO:0000033	author statement supported by traceable reference	PMID:16037571	20061016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3757609	Ophn1<sup>tm1Bill</sup>	is_implicated_in	DOID:0050888	syndromic intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:27146843	20161220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3757609	Ophn1<sup>tm1Bill</sup>	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:3758489	Ophn1<sup>tm1Bill</sup>/Y  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:17728457	20161220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5049965	Tg(PDGF-S100B)36Cqin	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5049966	Tg(PDGF-S100B)36Cqin/0  [background:] C57BL/6-Tg(PDGF-S100B)36Cqin			ECO:0000033	author statement supported by traceable reference	PMID:21376255	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430075	Tbc1d20<sup>bs</sup>/Tbc1d20<sup>bs</sup>  [background:] 129S;AKR-Tbc1d20<sup>bs</sup>/J	is_model_of	DOID:0110719	Warburg micro syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:24239381	20140327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693250	Tg(Myh6-Tnnt2*R92W)1Jcf	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:30586744	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693250	Tg(Myh6-Tnnt2*R92W)1Jcf	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:5908988	Tg(Myh6-Tnnt2*R92W)1Jcf/0  [background:] B6.Cg-Tg(Myh6-Tnnt2*R92W)1Jcf			ECO:0000033	author statement supported by traceable reference	PMID:16326803	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857935	Ptch1<sup>tm1Zim</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:26935062	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857935	Ptch1<sup>tm1Zim</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3040327	Ptch1<sup>tm1Zim</sup>/Ptch1<sup>+</sup>  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12386820	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817496	Sqstm1<sup>tm1Jjw</sup>	is_implicated_in	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:24339057	20170307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817496	Sqstm1<sup>tm1Jjw</sup>	is_implicated_in	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:26878170	20170307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043224	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15109498	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6355949	Hvf	is_implicated_in	DOID:0060249	scoliosis		MGI:6356523	Hvf/Hvf<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30283900	20220518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3662854	Fgg<sup>tm1Fjc</sup>/Fgg<sup>tm1Fjc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:2236	congenital afibrinogenemia						ECO:0000033	author statement supported by traceable reference	PMID:11891199	20061005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711215	Fmr1<sup>tm1Usdn</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25886163	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711215	Fmr1<sup>tm1Usdn</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24657592	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711215	Fmr1<sup>tm1Usdn</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27427765	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711215	Fmr1<sup>tm1Usdn</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22470123	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711215	Fmr1<sup>tm1Usdn</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4950076	Fmr1<sup>tm1Usdn</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21220020	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711215	Fmr1<sup>tm1Usdn</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:5617140	Fmr1<sup>tm1Usdn</sup>/Fmr1<sup>tm1Usdn</sup>  [background:] B6.129S6(Cg)-Fmr1<sup>tm1Usdn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22470123	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445938	Fbn2<sup>tm1Rmz</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:26408953	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445938	Fbn2<sup>tm1Rmz</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:3652413	Fbn2<sup>tm1Rmz</sup>/Fbn2<sup>tm1Rmz</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11470817	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445938	Fbn2<sup>tm1Rmz</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:4850046	Fbn2<sup>tm1Rmz</sup>/Fbn2<sup>tm1Rmz</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:20729550	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868217	Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050471	Carney complex						ECO:0000033	author statement supported by traceable reference	PMID:20421483	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6471956	Bbs2<sup>tm1.1Huss</sup>	is_implicated_in	DOID:0110124	Bardet-Biedl syndrome 2		MGI:6471957	Bbs2<sup>tm1.1Huss</sup>/Bbs2<sup>tm1.1Huss</sup>  [background:] involves: 129S6/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32620959	20201113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044770	Cln3<sup>tm1.1Mem</sup>/Cln3<sup>tm1.1Mem</sup>  [background:] involves: 129S/SvEv * CD-1	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:12374761	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932265	F9<sup>tm1Ver</sup>	is_implicated_in	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:28202722	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932265	F9<sup>tm1Ver</sup>	is_implicated_in	DOID:12259	hemophilia B		MGI:2175873	F9<sup>tm1Ver</sup>/F9<sup>tm1Ver</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9326649	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32343226	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27328325	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22174313	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22653753	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27803317	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26842955	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27458802	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624719	Mecp2<sup>tm1Bird</sup>/Y Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3817462	Mecp2<sup>tm1Bird</sup>/Y  [background:] (129S6.129P2-Mecp2<sup>tm1Bird</sup> x FVB/N)F1			ECO:0000033	author statement supported by traceable reference	PMID:18321864	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137555	Mecp2<sup>tm1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3817461	Mecp2<sup>tm1Bird</sup>/Y  [background:] (129S6.129P2-Mecp2<sup>tm1Bird</sup> x C57BL/6)F1			ECO:0000033	author statement supported by traceable reference	PMID:18321864	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:29602770	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:27432952	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:30397118	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:26420842	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:22886305	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:24231350	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease		MGI:2653823	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10412977	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20181214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23524344	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23892607	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26677864	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28205547	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:32239723	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22338085	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28887310	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793791	Pkd1<sup>tm2Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:6317327	Pkd1<sup>tm2Som</sup>/Pkd1<sup>tm2Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJae * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20210715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3808026	Gja1<sup>tm3Gfi</sup>/Gja1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:18077386	20080929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692446	Acadm<sup>tm1Uab</sup>	is_implicated_in	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:31601874	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692446	Acadm<sup>tm1Uab</sup>	is_implicated_in	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency		MGI:3693216	Acadm<sup>tm1Uab</sup>/Acadm<sup>tm1Uab</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16121256	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:30760495	20190410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6455516	Elmod3<sup>em1Jili</sup>	is_implicated_in	DOID:0110533	autosomal recessive nonsyndromic deafness 88		MGI:6455517	Elmod3<sup>em1Jili</sup>/Elmod3<sup>em1Jili</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31628468	20200916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5641919	Tg(MYOC*Y437H)#Sit	is_implicated_in	DOID:1067	open-angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:25740847	20150629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5641919	Tg(MYOC*Y437H)#Sit	is_implicated_in	DOID:1067	open-angle glaucoma		MGI:5641920	Tg(MYOC*Y437H)#Sit/0  [background:] B6.FVB-Tg(MYOC*T437C)#Sit			ECO:0000033	author statement supported by traceable reference	PMID:18436825	20150629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461062	Mog<sup>tm1Dpd</sup>/Mog<sup>tm1Dpd</sup> Rag2<sup>tm1Cgn</sup>/Rag2<sup>tm1Cgn</sup> Tg(Tcra2D2,Tcrb2D2)1Kuch/0  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19483694	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433613	Pin1<sup>tm1Tuc</sup>/Pin1<sup>tm1Tuc</sup> Tg(APPSWE)2576Kha/0  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16554819	20120912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:35969769	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:23446829	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:22661702	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:25706118	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:25931013	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:22042865	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:23118216	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:32817286	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26330244	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790753	Hbb<sup>tm2(HBG1,HBB*)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:32533970	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22084065	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26209539	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25119024	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22975374	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24561622	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27893715	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23540692	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21903772	20160714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:26279473	20160714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311375	Dnaaf4<sup>b2b811.1Clo</sup>	is_implicated_in	DOID:0060254	Robinow syndrome		MGI:5312334	Dnaaf4<sup>b2b811.1Clo</sup>/Dnaaf4<sup>b2b811.1Clo</sup>  [background:] C57BL/6J-Dnaaf4<sup>b2b811.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6849996	Clcn2<sup>em1Uis</sup>	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:6850120	Clcn2<sup>em1Uis</sup>/Clcn2<sup>+</sup>  [background:] C57BL/6N-Clcn2<sup>em1Uis</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31727896	20220110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15475948	20180910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19105207	20180910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21573126	20180910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045186	Psen1<sup>tm1Jzt</sup>/Psen1<sup>tm1Jzt</sup> Psen2<sup>tm1Ber</sup>/Psen2<sup>tm1Ber</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15148382	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487278	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:22144569	20130526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2441654	Nr3c2<sup>tm1Gsc</sup>	is_implicated_in	DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2441654	Nr3c2<sup>tm1Gsc</sup>	is_implicated_in	DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1		MGI:3041700	Nr3c2<sup>tm1Gsc</sup>/Nr3c2<sup>tm1Gsc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9689096	20131230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3026839	Mmut<sup>tm1Pai</sup>	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:22792386	20121220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3026839	Mmut<sup>tm1Pai</sup>	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:3026845	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1Pai</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14555645	20121220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24790210	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29892074	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22522472	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27233938	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22737234	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22257369	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808885	Fmr1<sup>tm1.2Cidz</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:5292357	Fmr1<sup>tm1.2Cidz</sup>/Y  [background:] involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19103683	20180705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867484	Gjb2<sup>tm2.2Kwi</sup>/Gjb2<sup>+</sup> Tg(Pgk1-cre)1Lni/0  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6	is_model_of	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20926451	20110111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825019	Slc6a8<sup>tm1.2Lbar</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:37063368	20230918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825019	Slc6a8<sup>tm1.2Lbar</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:5825026	Slc6a8<sup>tm1.2Lbar</sup>/Y  [background:] involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27466184	20230918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825019	Slc6a8<sup>tm1.2Lbar</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:31029731	20230918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825019	Slc6a8<sup>tm1.2Lbar</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:5825021	Slc6a8<sup>tm1.2Lbar</sup>/Y  [background:] involves: 129 * 129S1/Sv * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25485098	20230918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5750095	Cntnap2<sup>tm2Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5750217	Cntnap2<sup>tm2Pele</sup>/Cntnap2<sup>tm2Pele</sup>  [background:] B6.129(Cg)-Cntnap2<sup>tm2Pele</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26647347	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5750095	Cntnap2<sup>tm2Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30679017	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5750095	Cntnap2<sup>tm2Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:32889171	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5750095	Cntnap2<sup>tm2Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:38027494	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447142	Tshr<sup>tm1Rmar</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:27179782	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447142	Tshr<sup>tm1Rmar</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3766096	Tshr<sup>tm1Rmar</sup>/Tshr<sup>tm1Rmar</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12432094	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30679017	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20220603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5824119	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25155956	20220603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654122	Acvr2b<sup>tm1Enl</sup>/Acvr2b<sup>tm1Enl</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:0060856	right atrial isomerism						ECO:0000033	author statement supported by traceable reference	PMID:9242489	20060424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386438	Wrn<sup>tm1Lgu</sup>	is_implicated_in	DOID:5688	Werner syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18028256	20150723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179766	Tbr1<sup>tm1Jlr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179766	Tbr1<sup>tm1Jlr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25981743	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179766	Tbr1<sup>tm1Jlr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5752313	Tbr1<sup>tm1Jlr</sup>/Tbr1<sup>+</sup>  [background:] B6.129X1-Tbr1<sup>tm1Jlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24441682	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:26432840	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:21047515	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:23960072	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:17416600	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3		MGI:5007651	Tg(Myh6-Tpm1*E180G)57Dfw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21056571	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:21840315	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3		MGI:5007651	Tg(Myh6-Tpm1*E180G)57Dfw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11603924	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:23800848	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007645	Tg(Myh6-Tpm1*E180G)57Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3		MGI:5007651	Tg(Myh6-Tpm1*E180G)57Dfw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14575301	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5699838	Tg(PDGFB-SNCA*A53T)8Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5699839	Tg(PDGFB-SNCA*A53T)8Ema/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26201615	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491622	Tg(Thy1-APPSweLon)41Ema	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28298456	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491622	Tg(Thy1-APPSweLon)41Ema	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5491627	Tg(Thy1-APPSweLon)41Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11746377	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491622	Tg(Thy1-APPSweLon)41Ema	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27313503	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491622	Tg(Thy1-APPSweLon)41Ema	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22863679	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491622	Tg(Thy1-APPSweLon)41Ema	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25406061	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491622	Tg(Thy1-APPSweLon)41Ema	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33482356	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23437388	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:22021912	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23664616	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:35858542	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:26224859	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27425891	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:25639352	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:28183733	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23749404	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3802584	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(GFAP-cre)8Gtm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17714952	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3802584	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(GFAP-cre)8Gtm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21062901	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3588988	Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup> Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15601645	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428215	Tg(Disc1/EGFP)M19Sshe	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428215	Tg(Disc1/EGFP)M19Sshe	is_implicated_in	DOID:5419	schizophrenia		MGI:5428306	Tg(Disc1/EGFP)M19Sshe/0  [background:] involves: C57BL/6JCrl * CBA/CaCrl			ECO:0000033	author statement supported by traceable reference	PMID:18945897	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428215	Tg(Disc1/EGFP)M19Sshe	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21821099	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774845	Chd7<sup>tm1.1Dmm</sup>/Chd7<sup>tm1.1Dmm</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26670829	20161116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26604152	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26826269	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25822630	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:21414903	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24280221	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26384962	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671112	Tg(SOD1*G93A)<sup>dl</sup>1Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3813319	Tg(SOD1*G93A)<sup>dl</sup>1Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9382875	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4889192	Ank<sup>tm1.1Ejr</sup>	is_implicated_in	DOID:0080033	craniometaphyseal dysplasia		MGI:4889220	Ank<sup>tm1.1Ejr</sup>/Ank<sup>tm1.1Ejr</sup>  [background:] B6.129-Ank<sup>tm1.1Ejr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19257826	20151207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4889192	Ank<sup>tm1.1Ejr</sup>	is_implicated_in	DOID:0080033	craniometaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:23160629	20151207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4889192	Ank<sup>tm1.1Ejr</sup>	is_implicated_in	DOID:0080033	craniometaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:24663682	20151207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3779036	Lyst<sup>bg-Btlr</sup>/Lyst<sup>bg-Btlr</sup>  [background:] C57BL/6J-Lyst<sup>bg-Btlr</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	MGI:3778945	20080428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027853	skc3/skc3  [background:] involves: C57BL/6J	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:12955145	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428331	Tg(Prnp*)#Rgab	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:23922744	20210122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428331	Tg(Prnp*)#Rgab	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:5428334	Tg(Prnp*)#Rgab/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22072968	20210122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428331	Tg(Prnp*)#Rgab	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:28847567	20210122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428331	Tg(Prnp*)#Rgab	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:23349890	20210122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428331	Tg(Prnp*)#Rgab	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:32861834	20210122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26139429	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24445867	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24947019	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25252690	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:28515090	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25482129	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:27843137	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:27055869	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25564405	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:35296093	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26522085	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29725010	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:27728807	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25293770	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22001392	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26522084	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26825709	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia		MGI:5571378	Tg(Igh-V186.2-TCL1A)3Cro/0  [background:] B6.Cg-Tg(Igh-V186.2-TCL1A)3Cro			ECO:0000033	author statement supported by traceable reference	PMID:24379361	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527221	Tg(Igh-V186.2-TCL1A)3Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia		MGI:3841692	Tg(Igh-V186.2-TCL1A)3Cro/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12011454	20220323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6455416	Frem3<sup>em1Osb</sup>	is_not_implicated_in	DOID:0090001	Fraser syndrome		MGI:6455426	Frem3<sup>em1Osb</sup>/Frem3<sup>em1Osb</sup>  [background:] involves: C57BL/6NJcl * DBA/2NJcl			ECO:0000033	author statement supported by traceable reference	PMID:31554749	20200916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027066	Pklr<sup>char4</sup>	is_implicated_in	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:19865104	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027066	Pklr<sup>char4</sup>	is_implicated_in	DOID:12365	malaria		MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17466543	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027066	Pklr<sup>char4</sup>	is_implicated_in	DOID:12365	malaria		MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14595440	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5450965	Fgfr2<sup>tm3Ewj</sup>/Fgfr2<sup>+</sup>  [background:] B6.129-Fgfr2<sup>tm3Ewj</sup>	is_model_of	DOID:0050660	Beare-Stevenson cutis gyrata syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22585574	20130124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793715	Tg(Myh6*)140Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793715	Tg(Myh6*)140Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:22778230	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793715	Tg(Myh6*)140Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:23352598	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793715	Tg(Myh6*)140Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:27199124	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793715	Tg(Myh6*)140Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3799202	Tg(Myh6*)140Lnwd/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8898372	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793715	Tg(Myh6*)140Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3799202	Tg(Myh6*)140Lnwd/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8585273	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25298424	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22427904	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:36099033	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25652448	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31506484	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148589	Utrn<sup>tm1Ked</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25865621	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5662101	Pax3<sup>Rwa</sup>	is_implicated_in	DOID:9258	Waardenburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28043919	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25315299	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30215697	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22206846	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25027328	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36639708	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23838176	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35649351	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20404004	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23405115	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32061032	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29274751	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28391636	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31394196	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24587388	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25592972	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29158413	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23577177	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27856911	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25706990	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26542217	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720731	Tg(Thy1-APP)3Somm/0  [background:] B6.Cg-Tg(Thy1-APP)3Somm			ECO:0000033	author statement supported by traceable reference	PMID:12426044	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652447	Tg(Thy1-APP)3Somm/0  [background:] involves: C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9371838	20230901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805498	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:6392337	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>/Sdhc<sup>tm1c(EUCOMM)Wtsi</sup> Gt(ROSA)26Sor<sup>tm1.1(rtTA,tetO-cre)Bkmn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31469588	20200302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437122	Lgi1<sup>tm1Mafu</sup>/Lgi1<sup>tm1Mafu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0060748	familial temporal lobe epilepsy 1						ECO:0000033	author statement supported by traceable reference	PMID:20133599	20100312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6392908	Scn11a<sup>em1Akoi</sup>	is_implicated_in	DOID:0111731	familial episodic pain syndrome 3		MGI:6392909	Scn11a<sup>em1Akoi</sup>/Scn11a<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27224030	20210120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7495583	Ighmbp2<sup>em1Cx</sup>	is_implicated_in	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S		MGI:7495585	Ighmbp2<sup>em1Cx</sup>/Ighmbp2<sup>em1Cx</sup>  [background:] C57BL/6J-Ighmbp2<sup>em1Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:36413117	20230706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437302	Tg(GFAP-HTT*160Q)31Xjl/0  [background:] either: (involves: FVB/NCrl) or (involves: C3H * C57BL/6 * FVB/NCrl)	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20018729	20100316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445215	Pkd1<sup>b2b1585Clo</sup>/Pkd1<sup>b2b1585Clo</sup>  [background:] C57BL/6J-Pkd1<sup>b2b1585Clo</sup>	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437083	Dnah11<sup>b2b1289Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5437114	Dnah11<sup>b2b1289Clo</sup>/Dnah11<sup>b2b1289Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1289Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526971	Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz	is_implicated_in	DOID:1612	breast cancer		MGI:5526972	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21822287	20170203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526971	Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27292631	20170203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526971	Tg(tetO-PIK3CA*H1047R,-luc)2239Jjz	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23940356	20170203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699259	Ush1c<sup>tm1Bkts</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699259	Ush1c<sup>tm1Bkts</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:23380860	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699259	Ush1c<sup>tm1Bkts</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:3700039	Ush1c<sup>tm1Bkts</sup>/Ush1c<sup>tm1Bkts</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17174357	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687640	Nlgn3<sup>tm1Bros</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687640	Nlgn3<sup>tm1Bros</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4353654	Nlgn3<sup>tm1Bros</sup>/Nlgn3<sup>tm1Bros</sup>  [background:] B6.Cg-Nlgn3<sup>tm1Bros</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19243448	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794294	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] B6.Cg-Pmp22<sup>Tr-J</sup> Krt25<sup>Re</sup>/+ +/J	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:15363066	20080818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794294	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] B6.Cg-Pmp22<sup>Tr-J</sup> Krt25<sup>Re</sup>/+ +/J	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:1303281	20080818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663270	cl/cl  [background:] Not Specified	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	MGI:48832	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429211	Mboat7<sup>tm1Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429558	Mboat7<sup>tm1Lex</sup>/Mboat7<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513454	Mtmr2<sup>tm1.1Abol</sup>	is_implicated_in	DOID:0110191	Charcot-Marie-Tooth disease type 4B1						ECO:0000033	author statement supported by traceable reference	PMID:20878767	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513454	Mtmr2<sup>tm1.1Abol</sup>	is_implicated_in	DOID:0110191	Charcot-Marie-Tooth disease type 4B1						ECO:0000033	author statement supported by traceable reference	PMID:16162938	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513454	Mtmr2<sup>tm1.1Abol</sup>	is_implicated_in	DOID:0110191	Charcot-Marie-Tooth disease type 4B1		MGI:3513600	Mtmr2<sup>tm1.1Abol</sup>/Mtmr2<sup>tm1.1Abol</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15557122	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707421	Disc1<sup>Rgsc1390</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23637159	20160712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707421	Disc1<sup>Rgsc1390</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25487992	20160712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707421	Disc1<sup>Rgsc1390</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26768401	20160712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707421	Disc1<sup>Rgsc1390</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3707975	Disc1<sup>Rgsc1390</sup>/Disc1<sup>Rgsc1390</sup>  [background:] B6.Cg-Disc1<sup>Rgsc1390</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17481393	20160712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590232	Apc<sup>tm1Kk</sup>/Apc<sup>tm1Kk</sup> Tg(Lck-cre)1Cwi/?  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:18077429	20141010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458373	Scn1a<sup>tm1.1Aesc</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:33189882	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458373	Scn1a<sup>tm1.1Aesc</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:24704313	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458373	Scn1a<sup>tm1.1Aesc</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:25378155	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458373	Scn1a<sup>tm1.1Aesc</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:4458389	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>tm1.1Aesc</sup>  [background:] involves: 129X1/SvJ * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20100831	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458373	Scn1a<sup>tm1.1Aesc</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:4458390	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20100831	20220309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2668459	Ilk<sup>tm1Star</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2668459	Ilk<sup>tm1Star</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907206	Ilk<sup>tm1Star</sup>/Ilk<sup>tm1Star</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16951252	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697073	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup>  [background:] B6J.129P2-Ercc6<sup>tm1Gvh</sup>	is_model_of	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25762674	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5707003	Chrnb2<sup>tm1.1Cont</sup>	is_implicated_in	DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3		MGI:5789945	Chrnb2<sup>tm1.1Cont</sup>/Chrnb2<sup>tm1.1Cont</sup>  [background:] B6.129-Chrnb2<sup>tm1.1Cont</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20603624	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285643	Myh9<sup>tm7.1Rsad</sup>	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499738	Myh9<sup>tm7.1Rsad</sup>/Myh9<sup>+</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285643	Myh9<sup>tm7.1Rsad</sup>	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499740	Myh9<sup>tm7.1Rsad</sup>/Myh9<sup>tm7.1Rsad</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450132	Fancc<sup>tm1Mgo</sup>/Fancc<sup>tm1Mgo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:0111087	Fanconi anemia complementation group C						ECO:0000033	author statement supported by traceable reference	PMID:8704201	20110518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764510	Gba1<sup>tm2Karl</sup>	is_implicated_in	DOID:0110958	Gaucher's disease type II						ECO:0000033	author statement supported by traceable reference	PMID:22912851	20130109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764510	Gba1<sup>tm2Karl</sup>	is_implicated_in	DOID:0110958	Gaucher's disease type II		MGI:3764515	Gba1<sup>tm2Karl</sup>/Gba1<sup>tm2Karl</sup> Tg(KRT14-cre)8Brn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17954912	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5499736	Myh9<sup>tm1.1(MYH9*)Mjk</sup>/Myh9<sup>tm1.1(MYH9*)Mjk</sup>  [background:] B6.129-Myh9<sup>tm1.1(MYH9*)Mjk</sup>	is_model_of	DOID:0060651	MYH-9 related disease						ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543795	Tgfbr1<sup>tm1.1Hcd</sup>	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome		MGI:5543898	Tgfbr1<sup>tm1.1Hcd</sup>/Tgfbr1<sup>+</sup>  [background:] 129S6(Cg)-Tgfbr1<sup>tm1.1Hcd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24355923	20140212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428666	Nemf<sup>tvrm116</sup>	is_implicated_in	DOID:440	neuromuscular disease		MGI:6718876	Nemf<sup>tvrm116</sup>/Nemf<sup>tvrm116</sup>  [background:] C57BL/6J-Nemf<sup>tvrm116</sup>/PjnCx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6489964	Ano5<sup>em1Huyi</sup>	is_implicated_in	DOID:0111533	gnathodiaphyseal dysplasia		MGI:6489966	Ano5<sup>em1Huyi</sup>/Ano5<sup>em1Huyi</sup>  [background:] C57BL/6N-Ano5<sup>em1Huyi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30712070	20210105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699097	Htt<sup>tm1.1Tna</sup>/Htt<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11494364	20070307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23382946	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25092570	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:27001837	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:31358653	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26839406	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29743672	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888382	Snca<sup>tm1Rosl</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3720759	Snca<sup>tm1Rosl</sup>/Snca<sup>tm1Rosl</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10707987	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461737	Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6717362	Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>/Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32877400	20210625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456236	Prkar1a<sup>tm1Lsk</sup>	is_implicated_in	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000033	author statement supported by traceable reference	PMID:24865460	20150929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456236	Prkar1a<sup>tm1Lsk</sup>	is_implicated_in	DOID:0060280	primary pigmented nodular adrenocortical disease		MGI:4819186	Prkar1a<sup>tm1Lsk</sup>/Prkar1a<sup>tm1Lsk</sup> Tg(Akr1b7-cre)1Anm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20548949	20150929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306612	Trp53<sup>tm1.1Dgk</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:35803738	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5903084	Cic<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:150	disease of mental health		MGI:6275604	Cic<sup>tm1c(KOMP)Wtsi</sup>/Cic<sup>tm1c(KOMP)Wtsi</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28288114	20190201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692450	Tg(Myh6-Tnnt2*R92Q)2Lnwd	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:26092120	20160331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692450	Tg(Myh6-Tnnt2*R92Q)2Lnwd	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:5755254	Tg(Myh6-Tnnt2*R92Q)2Lnwd/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10449439	20160331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447068	Tg(Neurod2-Smo*A2)#Jols/0  [background:] C57BL/6-Tg(Neurod2-Smo*A2)#Jols	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22869526	20121228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491260	Ndst1<sup>b2b2230Clo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5505393	Ndst1<sup>b2b2230Clo</sup>/Ndst1<sup>b2b2230Clo</sup>  [background:] C57BL/6J-Ndst1<sup>b2b2230Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5508894	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup>  [background:] C.B6N-Ins2<sup>Akita</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22297672	20130927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5775113	Ido1<sup>tm1.1Mkks</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:5823026	Ido1<sup>tm1.1Mkks</sup>/Ido1<sup>tm1.1Mkks</sup>  [background:] B6.Cg-Ido1<sup>tm1.1Mkks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25602015	20170201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4458389	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>tm1.1Aesc</sup>  [background:] involves: 129X1/SvJ * C57BL/6J * SJL	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:20100831	20110514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7439058	Iigp1c<sup>M2Btlr</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:7439145	Iigp1c<sup>M2Btlr</sup>/Iigp1c<sup>M2Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>M2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523235	Tg(Pcp2-ATXN3*69Q)bHirai	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:5523236	Tg(Pcp2-ATXN3*69Q)bHirai/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18344973	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523235	Tg(Pcp2-ATXN3*69Q)bHirai	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:23349684	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523235	Tg(Pcp2-ATXN3*69Q)bHirai	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:19103174	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523235	Tg(Pcp2-ATXN3*69Q)bHirai	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:26220979	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856707	Hps3<sup>coa</sup>	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:23043085	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856707	Hps3<sup>coa</sup>	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:27777976	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856707	Hps3<sup>coa</sup>	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3		MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:3408670	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856707	Hps3<sup>coa</sup>	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3		MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20200805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037904	Col6a1<sup>tm1Gmb</sup>/Col6a1<sup>tm1Gmb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050663	Bethlem myopathy						ECO:0000033	author statement supported by traceable reference	PMID:9817932	20120117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037904	Col6a1<sup>tm1Gmb</sup>/Col6a1<sup>tm1Gmb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050663	Bethlem myopathy						ECO:0000033	author statement supported by traceable reference	PMID:14625552	20120117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3783887	Sbf2<sup>Gt(RRF511)Byg</sup>/Sbf2<sup>Gt(RRF511)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110190	Charcot-Marie-Tooth disease type 4B2						ECO:0000033	author statement supported by traceable reference	PMID:18349142	20080506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868696	Nphp4<sup>nmf192</sup>/Nphp4<sup>nmf192</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0111115	nephronophthisis 4						ECO:0000033	author statement supported by traceable reference	PMID:21078623	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5919933	Tg(C9orf72)500Lpwr	is_implicated_in	DOID:0060213	frontotemporal dementia and/or amyotrophic lateral sclerosis-1						ECO:0000033	author statement supported by traceable reference	PMID:33378537	20210806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5919933	Tg(C9orf72)500Lpwr	is_implicated_in	DOID:0060213	frontotemporal dementia and/or amyotrophic lateral sclerosis-1		MGI:6101187	Tg(C9orf72)500Lpwr/0  [background:] FVB/NJ-Tg(C9orf72)500Lpwr			ECO:0000033	author statement supported by traceable reference	PMID:27112499	20210806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22542623	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27913616	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:20357106	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26546830	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28628038	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24948797	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33370315	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23284626	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27995895	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:30061661	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33113354	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33940179	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23223017	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:31666698	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27236020	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22508027	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:29259100	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22044764	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24955833	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:30451892	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28578004	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:34884918	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23209424	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23341618	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27147652	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27147650	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25619660	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:33556538	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26210937	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28031289	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23284644	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26282324	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:2675620	Htt<sup>tm1Mfc</sup>/Htt<sup>tm1Mfc</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17239451	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675580	Htt<sup>tm1Mfc</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:2675620	Htt<sup>tm1Mfc</sup>/Htt<sup>tm1Mfc</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12926013	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056058	Rs1<sup>tm1Sie</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:28297725	20180320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056058	Rs1<sup>tm1Sie</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:3056342	Rs1<sup>tm1Sie</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15326152	20180320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056058	Rs1<sup>tm1Sie</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:3056343	Rs1<sup>tm1Sie</sup>/Rs1<sup>tm1Sie</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15326152	20180320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805451	Tg(CD2-Rorc)#Staka	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5805456	Tg(CD2-Rorc)#Staka/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25411202	20161027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155985	Adora2a<sup>tm1Jfc</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20130410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155985	Adora2a<sup>tm1Jfc</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5473699	Adora2a<sup>tm1Jfc</sup>/Adora2a<sup>tm1Jfc</sup>  [background:] B6.129S4-Adora2a<sup>tm1Jfc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20938208	20130410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286070	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: 129T2/SvEms * C57BL/6 * CBA	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294566	Tg(Fabp4-Il22)#Ychn	is_implicated_in	DOID:3382	liposarcoma		MGI:5294574	Tg(Fabp4-Il22)#Ychn/0  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:21897855	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611211	Psen1<sup>tm1Dgf</sup>/Psen1<sup>tm1Dgf</sup> Tg(APPSWE)2576Kha/?  [background:] involves: 129 * C57BL/6 * CD-1 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11959395	20060125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038727	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup> Tg(CMV-Rpgr)1Tili/0  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0111008	X-linked cone-rod dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:14691151	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5788420	Tg(TNFSF11)5519Edou	is_implicated_in	DOID:11476	osteoporosis		MGI:5788426	Tg(TNFSF11)5519Edou/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24127173	20160810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7532855	Best3<sup>tm1.1Zhoj</sup>	is_implicated_in	DOID:0080685	aortic dissection		MGI:7536982	Best3<sup>tm1.1Zhoj</sup>/Best3<sup>tm1.1Zhoj</sup> Tg(Tagln-cre)1Her/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:37203562	20231005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311366	b2b370Clo	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5313541	b2b370Clo/b2b370Clo  [background:] C57BL/6J-b2b370Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523495	Sptlc2<sup>tm1Yhir</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523495	Sptlc2<sup>tm1Yhir</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:5563659	Sptlc2<sup>tm1Yhir</sup>/Sptlc2<sup>tm1Yhir</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23633022	20140515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367989	Cngb3<sup>tm1Dgen</sup>	is_implicated_in	DOID:0110008	achromatopsia 3						ECO:0000033	author statement supported by traceable reference	PMID:26567794	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367989	Cngb3<sup>tm1Dgen</sup>	is_implicated_in	DOID:0110008	achromatopsia 3		MGI:4367994	Cngb3<sup>tm1Dgen</sup>/Cngb3<sup>tm1Dgen</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19767295	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22223655	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25281316	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31537705	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28973916	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26819275	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25766678	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17928448	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25024183	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19234123	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23524966	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:3818175	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:17881658	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16921370	20191203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701082	Hamp<sup>tm1Svl</sup>	is_implicated_in	DOID:0111032	hemochromatosis type 2B						ECO:0000033	author statement supported by traceable reference	PMID:22045566	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701082	Hamp<sup>tm1Svl</sup>	is_implicated_in	DOID:0111032	hemochromatosis type 2B						ECO:0000033	author statement supported by traceable reference	PMID:24970260	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701082	Hamp<sup>tm1Svl</sup>	is_implicated_in	DOID:0111032	hemochromatosis type 2B						ECO:0000033	author statement supported by traceable reference	PMID:22128145	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701082	Hamp<sup>tm1Svl</sup>	is_implicated_in	DOID:0111032	hemochromatosis type 2B		MGI:3702021	Hamp<sup>tm1Svl</sup>/Hamp<sup>tm1Svl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16574947	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046866	Capn3<sup>Gt(OST141731)Lex</sup>	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A						ECO:0000033	author statement supported by traceable reference	PMID:27005420	20161220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046866	Capn3<sup>Gt(OST141731)Lex</sup>	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A		MGI:3047138	Capn3<sup>Gt(OST141731)Lex</sup>/Capn3<sup>Gt(OST141731)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15138196	20161220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516463	Tg(Prnp-ATXN3*148Q)NLS.28Olri/0  [background:] involves: C57BL/6N	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:17626202	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692603	Tg(Myh6-Tnnt2)191Lnwd	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692603	Tg(Myh6-Tnnt2)191Lnwd	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:3719611	Tg(Myh6-Tnnt2)191Lnwd/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9637714	20170915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604025	Fgfr2<sup>tm1Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:15975938	20100421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604025	Fgfr2<sup>tm1Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:20077479	20100421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888378	Psap<sup>tm1Suz</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:26312487	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888378	Psap<sup>tm1Suz</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:22167193	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5546407	Prnp<sup>tm3Lnq</sup>	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:5546408	Prnp<sup>tm3Lnq</sup>/Prnp<sup>tm3Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23959875	20140227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033164	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] involves: HRS/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:61833	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033164	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] involves: HRS/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:2250094	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651647	Ttn<sup>tm1Her</sup>/Ttn<sup>tm1Her</sup> Tg(Ckmm-cre)5Khn/0  [background:] Not Specified	is_model_of	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J						ECO:0000033	author statement supported by traceable reference	PMID:12464612	20050919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524234	Tg(TG-BRAF*V600E)2Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5524236	Tg(TG-BRAF*V600E)2Jaf/0  [background:] FVB/N-Tg(TG-BRAF*V600E)2Jaf			ECO:0000033	author statement supported by traceable reference	PMID:23372702	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524234	Tg(TG-BRAF*V600E)2Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5524236	Tg(TG-BRAF*V600E)2Jaf/0  [background:] FVB/N-Tg(TG-BRAF*V600E)2Jaf			ECO:0000033	author statement supported by traceable reference	PMID:15899815	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313375	Fbn1<sup>tm3.2Lysa</sup>	is_not_implicated_in	DOID:14323	Marfan syndrome		MGI:5313384	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313375	Fbn1<sup>tm3.2Lysa</sup>	is_not_implicated_in	DOID:14323	Marfan syndrome		MGI:5313383	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>tm3.2Lysa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614341	Tg(MMTV-PyVT*Y250F)250-2Mul/?  [background:] FVB/N-Tg(MMTV-PyVT*Y250F)250-2Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:9528804	20101110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427579	Pik3ca<sup>tm1.1Waph</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:5755852	Pik3ca<sup>tm1.1Waph</sup>/Pik3ca<sup>+</sup> Tg(MMTV-cre)#Mam/0  [background:] involves: 129S1/Sv * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:22666336	20160407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427579	Pik3ca<sup>tm1.1Waph</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26266985	20160407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23341618	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26247199	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23372043	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:30179155	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24021477	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24302884	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28069792	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:30587542	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23861892	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23122961	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22984513	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:36574405	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25411494	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28550168	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25748626	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26908614	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3043476	Htt<sup>tm2Detl</sup>/Htt<sup>tm2Detl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17715336	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177757	Htt<sup>tm2Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5698523	Htt<sup>tm2Detl</sup>/Htt<sup>+</sup>  [background:] B6J.129P2-Htt<sup>tm2Detl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25609071	20230921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:21875900	20141017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:22030750	20141017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23690466	20141017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7465211	Vps35<sup>tm1.1Hlw</sup>	is_implicated_in	DOID:0060897	Parkinson's disease 17		MGI:7466182	Vps35<sup>tm1.1Hlw</sup>/Vps35<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33257649	20230425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432147	Tg(YAC128)55Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27072890	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432147	Tg(YAC128)55Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24588402	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432147	Tg(YAC128)55Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432190	Tg(YAC128)55Hay/Tg(YAC128)55Hay  [background:] FVB/N-Tg(YAC128)55Hay			ECO:0000033	author statement supported by traceable reference	PMID:16165367	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432147	Tg(YAC128)55Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24269729	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432147	Tg(YAC128)55Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432192	Tg(YAC128)55Hay/0  [background:] FVB/N-Tg(YAC128)55Hay			ECO:0000033	author statement supported by traceable reference	PMID:16230019	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432147	Tg(YAC128)55Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432190	Tg(YAC128)55Hay/Tg(YAC128)55Hay  [background:] FVB/N-Tg(YAC128)55Hay			ECO:0000033	author statement supported by traceable reference	PMID:16230019	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821824	Ift172<sup>avc1</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:5290081	Ift172<sup>avc1</sup>/Ift172<sup>avc1</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21653639	20111011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:18182166	20090708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:14755333	20090708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5607782	Gjb6<sup>tm2.2Kwi</sup>/Gjb6<sup>tm2.2Kwi</sup>  [background:] involves: 129P2/OlaHsd * BALB/c * C57BL/6 * CD-1 * SJL	is_model_of	DOID:14693	Clouston syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24685692	20150106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:5590154	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:4601767	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:408	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:4589319	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1523694	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7366734	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:4697831	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1113502	20130107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441585	Atp6v0a4<sup>tm1.1Fekf</sup>/Atp6v0a4<sup>tm1.1Fekf</sup>  [background:] involves: C57BL/6	is_model_of	DOID:14219	renal tubular acidosis						ECO:0000033	author statement supported by traceable reference	PMID:22872862	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806080	Nbeal2<sup>gps</sup>/Nbeal2<sup>gps</sup>  [background:] 129S1/SvImJ-Nbeal2<sup>gps</sup>	is_model_of	DOID:0111044	gray platelet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26950939	20161103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622905	Pitx2<sup>tm1Rsd</sup>/Pitx2<sup>tm1Rsd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10499586	20060522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6403115	Tg(DPP4)2Nnag	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6403118	Tg(DPP4)2Nnag/0  [background:] B6.Cg-Tg(DPP4)2Nnag			ECO:0000033	author statement supported by traceable reference	PMID:30626685	20200407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836985	Smn1<sup>tm1.1Dscd</sup>/Smn1<sup>tm1.1Dscd</sup>  [background:] involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:12376	juvenile spinal muscular atrophy						ECO:0000033	author statement supported by traceable reference	PMID:20705738	20101102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052116	Tg(Eno2-PSEN2)2348Ykk	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5052119	Tg(Eno2-PSEN2)2348Ykk/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12039862	20110804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517485	Syn3<sup>tm1Pggd</sup>/Syn3<sup>tm1Pggd</sup>  [background:] B6.129X1-Syn3<sup>tm1Jfe</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6276321	Tg(CAG-Ncoa6)87Hwl	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276334	Tg(CAG-Ncoa6)87Hwl/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624551	Mecp2<sup>tm1Hzo</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12160743	20060616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611751	Postn<sup>tm1Sjc</sup>	is_implicated_in	DOID:1474	aggressive periodontitis						ECO:0000033	author statement supported by traceable reference	PMID:25757567	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611751	Postn<sup>tm1Sjc</sup>	is_implicated_in	DOID:1474	aggressive periodontitis		MGI:3629331	Postn<sup>tm1Sjc</sup>/Postn<sup>tm1Sjc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16314533	20151030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4835907	Clcn1<sup>adr</sup>/Clcn1<sup>adr</sup>  [background:] A2G-Clcn1<sup>adr</sup>	is_model_of	DOID:2106	myotonia congenita						ECO:0000033	author statement supported by traceable reference	PMID:1653899	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800596	Mecp2<sup>tm1Pplt</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25424712	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800596	Mecp2<sup>tm1Pplt</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800596	Mecp2<sup>tm1Pplt</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26237041	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800596	Mecp2<sup>tm1Pplt</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3801487	Mecp2<sup>tm1Pplt</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18557922	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800596	Mecp2<sup>tm1Pplt</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3801488	Mecp2<sup>tm1Pplt</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18557922	20170110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665286	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16899370	20061031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22231738	20161011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25034600	20161011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24107778	20161011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24143217	20161011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651679	Rr320<sup>tm2Mkg</sup>/Rr320<sup>tm2Mkg</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:7557375	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513831	Gars1<sup>Nmf249</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:31557132	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513831	Gars1<sup>Nmf249</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:28351971	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513831	Gars1<sup>Nmf249</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:27288508	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513831	Gars1<sup>Nmf249</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:5308205	Gars1<sup>Nmf249</sup>/Gars1<sup>+</sup>  [background:] involves: C57BL/6J * CAST/Ei			ECO:0000033	author statement supported by traceable reference	PMID:22144914	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513831	Gars1<sup>Nmf249</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:3513833	Gars1<sup>Nmf249</sup>/Gars1<sup>+</sup>  [background:] C57BL/6J-Gars1<sup>Nmf249</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16982418	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824055	Tg(Mpz*S63X)30Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:18255032	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824055	Tg(Mpz*S63X)30Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:20878767	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824055	Tg(Mpz*S63X)30Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6276575	Tg(Mpz*S63X)30Mes/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824055	Tg(Mpz*S63X)30Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:27807175	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675356	Ptch1<sup>tm1Bjw</sup>	is_implicated_in	DOID:2513	basal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28263978	20171120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675356	Ptch1<sup>tm1Bjw</sup>	is_implicated_in	DOID:2513	basal cell carcinoma		MGI:5925369	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129T2/SvEms * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23404854	20171120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5760384	Bag3<sup>tm1c(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0110448	dilated cardiomyopathy 1HH		MGI:6107901	Bag3<sup>tm1c(EUCOMM)Hmgu</sup>/Bag3<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Myhca-cre)1Abel/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28737513	20180109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809583	Tg(RCAN1)M9Mapr/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22511596	20120726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6850156	Nemf<sup>em8Cx</sup>	is_implicated_in	DOID:870	neuropathy		MGI:6850159	Nemf<sup>em8Cx</sup>/Nemf<sup>em8Cx</sup>  [background:] C57BL/6J-Nemf<sup>em8Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525444	Erbb2<sup>tm8(Erbb2)Mul</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525444	Erbb2<sup>tm8(Erbb2)Mul</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28096336	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525444	Erbb2<sup>tm8(Erbb2)Mul</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23720052	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525444	Erbb2<sup>tm8(Erbb2)Mul</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3714371	Erbb2<sup>tm8(Erbb2)Mul</sup>/Erbb2<sup>+</sup> Tg(MMTV-cre)7Mul/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20961995	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804114	Tg(Mafg-Nfe2l1)1Mym	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5804115	Tg(Mafg-Nfe2l1)1Mym/0  [background:] involves: C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25041126	20161019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438064	b2b1709Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5445972	b2b1709Clo/b2b1709Clo  [background:] C57BL/6J-b2b1709Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804124	Tg(Mafg-Nfe2l1)6Mym	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5804125	Tg(Mafg-Nfe2l1)6Mym/0  [background:] involves: C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25041126	20161019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157453	Klhl3<sup>tm2.1Esoh</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6157462	Klhl3<sup>tm2.1Esoh</sup>/Klhl3<sup>tm2.1Esoh</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28052936	20180522	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586560	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup>  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9150142	20050901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:2763211	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:14170406	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838167	Tg(ATXN3*)84.2Cce/Tg(ATXN3*)84.2Cce  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:11978767	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693491	Tg(PSEN1H163R)G9Btla/0  [background:] involves: 129S4/SvJae	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10412057	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388945	Ctns<sup>tm1Antc</sup>	is_implicated_in	DOID:1064	cystinosis						ECO:0000033	author statement supported by traceable reference	PMID:23716592	20160707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388945	Ctns<sup>tm1Antc</sup>	is_implicated_in	DOID:1064	cystinosis						ECO:0000033	author statement supported by traceable reference	PMID:25586965	20160707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388945	Ctns<sup>tm1Antc</sup>	is_implicated_in	DOID:1064	cystinosis		MGI:2672886	Ctns<sup>tm1Antc</sup>/Ctns<sup>tm1Antc</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12370309	20160707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836619	Jak2<sup>tm1(JAK2)Argr</sup>/Jak2<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CBA	is_model_of	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:20489053	20101028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5585638	Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:7545539	Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>  [background:] STOCK Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:37158461	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5811451	Gnptab<sup>tm1Dkji</sup>	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:5811453	Gnptab<sup>tm1Dkji</sup>/Gnptab<sup>tm1Dkji</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26857995	20161208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717173	Prex1<sup>tm1Hcew</sup>/Prex1<sup>tm1Hcew</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26621702	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038607	Aspa<sup>tm1Mata</sup>/Aspa<sup>tm1Mata</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:10894262	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038607	Aspa<sup>tm1Mata</sup>/Aspa<sup>tm1Mata</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:14572139	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838994	Atp8a2<sup>wl</sup>/Atp8a2<sup>wl</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949224	C1qtnf5<sup>tm1.1Itl</sup>	is_implicated_in	DOID:0060869	late-onset retinal degeneration						ECO:0000033	author statement supported by traceable reference	PMID:25814825	20160104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949224	C1qtnf5<sup>tm1.1Itl</sup>	is_implicated_in	DOID:0060869	late-onset retinal degeneration		MGI:4949225	C1qtnf5<sup>tm1.1Itl</sup>/C1qtnf5<sup>+</sup>  [background:] C57BL/6-C1qtnf5<sup>tm1.1Itl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21349921	20160104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794206	Tg(ACTA1-Ar)141Kyjo	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:25929689	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794206	Tg(ACTA1-Ar)141Kyjo	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:29897452	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794206	Tg(ACTA1-Ar)141Kyjo	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:27493028	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794206	Tg(ACTA1-Ar)141Kyjo	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:25719894	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794206	Tg(ACTA1-Ar)141Kyjo	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:27147661	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794206	Tg(ACTA1-Ar)141Kyjo	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:3794207	Tg(ACTA1-Ar)141Kyjo/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17984063	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157363	Mmut<sup>tm1.1Mrb</sup>	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:6157364	Mmut<sup>tm1.1Mrb</sup>/Mmut<sup>tm1.1Mrb</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27519416	20180521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558103	Tg(CMV-SALL4_iB)#Chai	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24051379	20140411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558103	Tg(CMV-SALL4_iB)#Chai	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5558108	Tg(CMV-SALL4_iB)#Chai/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16763212	20140411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543796	Tgfbr2<sup>tm1.1Hcd</sup>	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome		MGI:5543899	Tgfbr2<sup>tm1.1Hcd</sup>/Tgfbr2<sup>+</sup>  [background:] 129S6(Cg)-Tgfbr2<sup>tm1.1Hcd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24355923	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543796	Tgfbr2<sup>tm1.1Hcd</sup>	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26173585	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183949	Ercc2<sup>tm2(ERCC2)Jhjh</sup>	is_implicated_in	DOID:2960	photosensitive trichothiodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25340339	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183949	Ercc2<sup>tm2(ERCC2)Jhjh</sup>	is_implicated_in	DOID:2960	photosensitive trichothiodystrophy		MGI:2386444	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11950998	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183949	Ercc2<sup>tm2(ERCC2)Jhjh</sup>	is_implicated_in	DOID:2960	photosensitive trichothiodystrophy		MGI:2386444	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9651581	20160728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800678	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup> Tgfb1<sup>tm1N</sup>/Tgfb1<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J * C57BL/10 * DBA/2	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:11168809	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:22595426	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21223590	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:23520473	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:28432149	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:23297226	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:22167193	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:24079945	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:17509920	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:31233883	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:28225753	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:27598339	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21257328	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21730160	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680328	Gba1<sup>tm4Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680509	Gba1<sup>tm4Ggb</sup>/Gba1<sup>tm4Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437480	Shank2<sup>tm1Mgle</sup>/Shank2<sup>tm1Mgle</sup>  [background:] B6.129S4-Shank2<sup>tm1Mgle</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22699620	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437480	Shank2<sup>tm1Mgle</sup>/Shank2<sup>tm1Mgle</sup>  [background:] B6.129S4-Shank2<sup>tm1Mgle</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27903723	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613376	Tg(TTR-V30M)15Imeg/0  [background:] Not Specified	is_model_of	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:1992765	20130104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856392	Edn3<sup>ls</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856392	Edn3<sup>ls</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3589107	Edn3<sup>ls</sup>/Edn3<sup>ls</sup>  [background:] involves: C57BL			ECO:0000033	author statement supported by traceable reference	PMID:5917257	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5513111	Mnx1<sup>tm4(cre)Tmj</sup>/Mnx1<sup>+</sup> Tardbp<sup>tm1.1Ckjs</sup>/Tardbp<sup>tm1.2Cjks</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:22718760	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5564916	Tg(APOC1)1Lmh/Tg(APOC1)1Lmh  [background:] involves: C57BL/6	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:18049452	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4421709	Tg(CAG-SYVN1)1Tn/?  [background:] D1.Cg-Tg(CAG-SYVN1)1Tn	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:12975321	20100212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324174	Hmgcs2<sup>em1(IMPC)Tcp</sup>	is_implicated_in	DOID:0081168	HMG-CoA synthase 2 deficiency		MGI:7329792	Hmgcs2<sup>em1(IMPC)Tcp</sup>/Hmgcs2<sup>+</sup>  [background:] C57BL/6NCrl-Hmgcs2<sup>em1(IMPC)Tcp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35421611	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324174	Hmgcs2<sup>em1(IMPC)Tcp</sup>	is_implicated_in	DOID:0081168	HMG-CoA synthase 2 deficiency		MGI:7329791	Hmgcs2<sup>em1(IMPC)Tcp</sup>/Hmgcs2<sup>em1(IMPC)Tcp</sup>  [background:] C57BL/6NCrl-Hmgcs2<sup>em1(IMPC)Tcp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35421611	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:23863460	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:21956219	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:23221341	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:24163128	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25535838	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25786243	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:23318430	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:23434321	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25043591	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3710237	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3710235	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Mpz-cre)94Imeg/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3710236	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Pax3-cre)1Joe/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:5493228	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:22868293	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3810648	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Fabp7-cre,-lacZ)3Gtm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18614544	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:5492109	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:21478499	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2176767	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11297510	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515634	Prdm1<sup>tm1Clme</sup>/Prdm1<sup>tm1Clme</sup> Tg(Itgax-cre)1-1Reiz/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:21948081	20131030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491207	Tg(Plp1-Lmnb1)#Yfu/0  [background:] involves: FVB	is_model_of	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23676464	20130621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446158	Dnah11<sup>b2b1775Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5446426	Dnah11<sup>b2b1775Clo</sup>/Dnah11<sup>b2b1775Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1775Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711122	Col1a2<sup>tm1.1Mcbr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:28461254	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711122	Col1a2<sup>tm1.1Mcbr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:30579604	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711122	Col1a2<sup>tm1.1Mcbr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300564	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (BALB/cByJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711122	Col1a2<sup>tm1.1Mcbr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300566	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (FVB/NJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711122	Col1a2<sup>tm1.1Mcbr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300563	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (A/J x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711122	Col1a2<sup>tm1.1Mcbr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300565	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (C3H/HeJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20200722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10049712	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10213384	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:9182763	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587737	Nhs<sup>Xcat</sup>/Y  [background:] involves: DBA/2 * T STOCK	is_model_of	DOID:0060599	Nance-Horan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587737	Nhs<sup>Xcat</sup>/Y  [background:] involves: DBA/2 * T STOCK	is_model_of	DOID:0060599	Nance-Horan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450916	Phex<sup>Ska1</sup>/Phex<sup>+</sup>  [background:] C57BL/6-Phex<sup>Ska1</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:12414538	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851145	Atm<sup>tm2.1Fwa</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:33608602	20210508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835822	Tg(Dspp-TGFB1)3Kul/?  [background:] FVB/N-Tg(Dspp-TGFB1)3Kul	is_model_of	DOID:701	dentin dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:11116156	20090316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586756	Lepr<sup>db-3J</sup>/Lepr<sup>db-3J</sup>  [background:] 129P3/J-Lepr<sup>db-3J</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:6993269	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856574	Atcay<sup>ji</sup>	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:23226316	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856574	Atcay<sup>ji</sup>	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia		MGI:3719716	Atcay<sup>ji</sup>/Atcay<sup>ji</sup>  [background:] JIGR			ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771037	Aec1<sup>NOD/Uf</sup>/Aec1<sup>NOD/Uf</sup> Aec2<sup>NOD/Uf</sup>/Aec2<sup>NOD/Uf</sup>  [background:] B6.NOD-Aec2<sup>NOD/Uf</sup> Aec1<sup>NOD/Uf</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12614028	20140812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771037	Aec1<sup>NOD/Uf</sup>/Aec1<sup>NOD/Uf</sup> Aec2<sup>NOD/Uf</sup>/Aec2<sup>NOD/Uf</sup>  [background:] B6.NOD-Aec2<sup>NOD/Uf</sup> Aec1<sup>NOD/Uf</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16918699	20140812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771037	Aec1<sup>NOD/Uf</sup>/Aec1<sup>NOD/Uf</sup> Aec2<sup>NOD/Uf</sup>/Aec2<sup>NOD/Uf</sup>  [background:] B6.NOD-Aec2<sup>NOD/Uf</sup> Aec1<sup>NOD/Uf</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12115247	20140812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014491	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup> Tg(ACTB-Fig4*I41T)705Mm/0  [background:] involves: 129 * C3H * C57BL/6J * CAST/Ei * SJL	is_model_of	DOID:0110184	Charcot-Marie-Tooth disease type 4J						ECO:0000033	author statement supported by traceable reference	PMID:21655088	20110715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849591	Gpc3<sup>tm1Snd</sup>/Gpc3<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850412	Cdkn2a<sup>tm1.1Brn</sup>/Cdkn2a<sup>tm1.1Brn</sup> Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:4586	familial meningioma						ECO:0000033	author statement supported by traceable reference	PMID:17924978	20090715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21587206	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:25174876	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:33398092	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:26563932	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:33065077	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:7336151	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] WSB.Cg-Tg(APPswe,PSEN1dE9)85Dbo/How			ECO:0000033	author statement supported by traceable reference	PMID:31150388	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:7336146	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] CAST.Cg-Tg(APPswe,PSEN1dE9)85Dbo/How			ECO:0000033	author statement supported by traceable reference	PMID:31150388	20220915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043699	Ercc5<sup>tm1Shm</sup>/Ercc5<sup>tm1Shm</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0110849	xeroderma pigmentosum group G						ECO:0000033	author statement supported by traceable reference	PMID:10022922	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522319	Lama2<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:22943509	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522319	Lama2<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:21652631	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522319	Lama2<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:24009313	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522319	Lama2<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3522485	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9710454	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522319	Lama2<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:4947712	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:20876525	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522319	Lama2<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3522483	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10616210	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904947	Tg(Myh6-Rab1a)medGwd	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5904950	Tg(Myh6-Rab1a)medGwd/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11739277	20170718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819405	Tg(PMP22)C61Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:25150498	20160628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819405	Tg(PMP22)C61Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:4819492	Tg(PMP22)C61Clh/0  [background:] B6.Cg-Tg(PMP22)C61Clh			ECO:0000033	author statement supported by traceable reference	PMID:20093502	20160628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809430	Col7a1<sup>tm1Lbt</sup>/Col7a1<sup>tm1Lbt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6Crl	is_model_of	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:18382769	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046834	Cdkn1a<sup>tm1(HBsAg)Xya</sup>/Cdkn1a<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5881966	Acvr1<sup>tm2.1Vlcg</sup>/Acvr1<sup>+</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: C57BL/6J * C57BL/6NTac * SJL/J	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:26896819	20170330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467734	Cacna1a<sup>tm2.1Kewa</sup>/Cacna1a<sup>tm2.1Kewa</sup>  [background:] B6.Cg-Cacna1a<sup>tm2.1Kewa</sup>	is_model_of	DOID:0050956	spinocerebellar ataxia type 6						ECO:0000033	author statement supported by traceable reference	PMID:23054835	20130306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440238	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Stk11<sup>tm1Rdp</sup>/Stk11<sup>tm1Rdp</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22791749	20121031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618096	Cd86<sup>tm1Shr</sup>/Cd86<sup>tm1Shr</sup>  [background:] NOD.129S4-Cd86<sup>tm1Shr</sup>	is_model_of	DOID:12842	Guillain-Barre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11535635	20090325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618096	Cd86<sup>tm1Shr</sup>/Cd86<sup>tm1Shr</sup>  [background:] NOD.129S4-Cd86<sup>tm1Shr</sup>	is_model_of	DOID:12842	Guillain-Barre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19050296	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316719	Tg(ACTA1*D286G/EGFP)#Kjno	is_implicated_in	DOID:0110927	nemaline myopathy 3		MGI:5316720	Tg(ACTA1*D286G/EGFP)#Kjno/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:22174871	20120427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367909	Dp(17Abcg1-Cbs)1Yah/0  [background:] B6.129P2-Dp(17Abcg1-Cbs1)1Yah	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19783846	20170220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28386018	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30938713	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28408354	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:36256464	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27506299	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437428	Tg(Lrrk2*G2019S)2Yue	is_implicated_in	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:26310625	20151207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437428	Tg(Lrrk2*G2019S)2Yue	is_implicated_in	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:26251043	20151207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437428	Tg(Lrrk2*G2019S)2Yue	is_implicated_in	DOID:0060371	Parkinson's disease 8		MGI:4437437	Tg(Lrrk2*G2019S)2Yue/0  [background:] involves: C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20130188	20151207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544444	Pde6b<sup>tm1Eye</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:28468800	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287842	Gprasp2<sup>tm1.1Jpe</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6287871	Gprasp2<sup>tm1.1Jpe</sup>/Y  [background:] B6.129(FVB)-Gprasp2<sup>tm1.1Jpe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30926797	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157626	Tardbp<sup>em1Rhbr</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:6187717	Tardbp<sup>em1Rhbr</sup>/Tardbp<sup>em1Rhbr</sup>  [background:] C57BL/6J-Tardbp<sup>em1Rhbr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29556029	20180709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5767288	Tg(Ckm-DNAJB6_ib*F93L)#Ccwe	is_implicated_in	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1		MGI:5767290	Tg(Ckm-DNAJB6_ib*F93L)#Ccwe/0  [background:] B6.Cg-Tg(Ckm-DNAJB6_ib*F93L)#Ccwe			ECO:0000033	author statement supported by traceable reference	PMID:26362252	20160513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6364882	Tfap2b<sup>em1Fenli</sup>	is_implicated_in	DOID:13832	patent ductus arteriosus		MGI:6393314	Tfap2b<sup>em1Fenli</sup>/Tfap2b<sup>em1Fenli</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29804851	20200305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836921	Tcrb<sup>tm1Mom</sup>/Tcrb<sup>tm1Mom</sup> Tcrd<sup>tm1Mom</sup>/Tcrd<sup>tm1Mom</sup> Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>/Igh-J<sup>+</sup>  [background:] B6.129P2-Tcrb<sup>tm1Mom</sup> Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup> Tcrd<sup>tm1Mom</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:19017966	20090324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579805	Ccl3<sup>tm1Unc</sup>/Ccl3<sup>+</sup> Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:15155903	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861771	Abcd1<sup>tm1Kan</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27779191	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861771	Abcd1<sup>tm1Kan</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446583	Abcd1<sup>tm1Kan</sup>/Abcd1<sup>tm1Kan</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9418970	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861771	Abcd1<sup>tm1Kan</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446586	Abcd1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9418970	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5460881	Hbb-b1<sup>Rbc13</sup>	is_implicated_in	DOID:12241	beta thalassemia		MGI:5460885	Hbb-b1<sup>Rbc13</sup>/Hbb-b1<sup>Rbc13</sup>  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23040355	20130128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430185	Fgfr2<sup>tm2Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:24580805	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430185	Fgfr2<sup>tm2Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:4430189	Fgfr2<sup>tm2Ewj</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20077479	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430185	Fgfr2<sup>tm2Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:4440856	Fgfr2<sup>tm2Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] B6.Cg-Fgfr2<sup>tm2Ewj</sup> Tg(EIIa-cre)C5379Lmgd			ECO:0000033	author statement supported by traceable reference	PMID:20175913	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3703793	Tg(tetO-BMPR2*T504)1Jwst	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3703793	Tg(tetO-BMPR2*T504)1Jwst	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:24951762	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3703793	Tg(tetO-BMPR2*T504)1Jwst	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:3703798	Tg(Tagln-rtTA)E1Jwst/0 Tg(tetO-BMPR2*T504)1Jwst/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15031260	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317589	Dnai1<sup>b2b1526Clo</sup>	is_implicated_in	DOID:0110594	primary ciliary dyskinesia 1		MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676545	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup>  [background:] either: B6SJL.129-Chrd<sup>tm1Emdr</sup> or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12810603	20070104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678247	Prkn<sup>tm1Roo</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:19680561	20180323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678247	Prkn<sup>tm1Roo</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:21113145	20180323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678247	Prkn<sup>tm1Roo</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:25486126	20180323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678247	Prkn<sup>tm1Roo</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:3757750	Prkn<sup>tm1Roo</sup>/Prkn<sup>tm1Roo</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:17623040	20180323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678247	Prkn<sup>tm1Roo</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:2678248	Prkn<sup>tm1Roo</sup>/Prkn<sup>tm1Roo</sup>  [background:] either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12915482	20180323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851507	Nsd2<sup>tm1Ykan</sup>	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26092122	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851507	Nsd2<sup>tm1Ykan</sup>	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome		MGI:3851517	Nsd2<sup>tm1Ykan</sup>/Nsd2<sup>tm1Ykan</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19483677	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851507	Nsd2<sup>tm1Ykan</sup>	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome		MGI:3851518	Nsd2<sup>tm1Ykan</sup>/Nsd2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19483677	20230106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796117	Col8a2<sup>tm1.1Asj</sup>/Col8a2<sup>tm1.1Asj</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23422828	20160929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28768803	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:33705688	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:32126198	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25951243	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:38027494	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26403076	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:31768051	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5295268	Cntnap2<sup>tm1Pele</sup>/Cntnap2<sup>tm1Pele</sup>  [background:] B6.129-Cntnap2<sup>tm1Pele</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21962519	20231228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014211	Tg(Gfap-rtTA,tetO-MAOB,-lacZ)1Jkan	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5014212	Tg(Gfap-rtTA,tetO-MAOB,-lacZ)1Jkan/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18286173	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014211	Tg(Gfap-rtTA,tetO-MAOB,-lacZ)1Jkan	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:27185595	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3844550	Tg(CAG-PKD2)#Hwl	is_implicated_in	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:24515114	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3844550	Tg(CAG-PKD2)#Hwl	is_implicated_in	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:25934702	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3844550	Tg(CAG-PKD2)#Hwl	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:3844551	Tg(CAG-PKD2)#Hwl/?  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:19098310	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717718	Tg(PDGFB-APPSwInd)J9Lms	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26615780	20191127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717718	Tg(PDGFB-APPSwInd)J9Lms	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22197104	20191127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717718	Tg(PDGFB-APPSwInd)J9Lms	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24760838	20191127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717718	Tg(PDGFB-APPSwInd)J9Lms	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19664757	20191127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717718	Tg(PDGFB-APPSwInd)J9Lms	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25878292	20191127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717718	Tg(PDGFB-APPSwInd)J9Lms	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3784684	Tg(PDGFB-APPSwInd)J9Lms/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10818140	20191127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580533	Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050471	Carney complex						ECO:0000033	author statement supported by traceable reference	PMID:15930266	20050701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680653	Kcnq1<sup>tm1Kpfe</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26084842	20160808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680653	Kcnq1<sup>tm1Kpfe</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3618869	Kcnq1<sup>tm1Kpfe</sup>/Kcnq1<sup>tm1Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11226272	20160808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5517707	Nlrp3<sup>tm3.1Hhf</sup>	is_implicated_in	DOID:0090029	CINCA Syndrome		MGI:5517789	Nlrp3<sup>tm3.1Hhf</sup>/Nlrp3<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:22558291	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2387109	Crygd<sup>Aey4</sup>/Crygd<sup>Aey4</sup>  [background:] C3HeB/FeJ-Crygd<sup>Aey4</sup>	is_model_of	DOID:0110234	cataract 4 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:12226711	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367049	Sh3tc2<sup>tm1.1Rchr</sup>/Sh3tc2<sup>tm1.1Rchr</sup>  [background:] involves: 129/Sv * FVB/N	is_model_of	DOID:0110183	Charcot-Marie-Tooth disease type 4C						ECO:0000033	author statement supported by traceable reference	PMID:19805030	20091112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581208	Tshr<sup>hyt</sup>/Tshr<sup>hyt</sup>  [background:] CBy.RF-Tshr<sup>hyt</sup>/J	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:10575115	20151029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581208	Tshr<sup>hyt</sup>/Tshr<sup>hyt</sup>  [background:] CBy.RF-Tshr<sup>hyt</sup>/J	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:17932107	20151029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308126	Tg(Prnp-AR*112Q)#Deme	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:5308127	Tg(Prnp-AR*112Q)#Deme/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15152038	20120301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308126	Tg(Prnp-AR*112Q)#Deme	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:21954065	20120301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5498230	Kif7<sup>b2b2254Clo</sup>	is_implicated_in	DOID:0050779	hydrolethalus syndrome		MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444200	Grn<sup>tm1.1Far</sup>/Grn<sup>tm1.1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * FVB/N	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:25155018	20150918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654804	Cdh23<sup>v-Alb</sup>/Cdh23<sup>v-Alb</sup>  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:11138008	20090504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5461515	Cerkl<sup>tm1.1Geno</sup>	is_implicated_in	DOID:0110368	retinitis pigmentosa 26						ECO:0000033	author statement supported by traceable reference	PMID:34048907	20210910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26082468	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26908607	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:30926669	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:16864772	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:33503262	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:28369518	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:22859208	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:32504084	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:22846424	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763907	Tg(HSA*LR)20bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3763917	Tg(HSA*LR)20bCath/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10976074	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849286	Myo3a<sup>tm1.1Mckg</sup>	is_implicated_in	DOID:0110489	autosomal recessive nonsyndromic deafness 30		MGI:4849847	Myo3a<sup>tm1.1Mckg</sup>/Myo3a<sup>tm1.1Mckg</sup>  [background:] C57BL/6-Myo3a<sup>tm1.1Mckg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21165622	20101230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887400	Ryr1<sup>m1Nisw</sup>	is_implicated_in	DOID:3529	congenital myopathy 1A		MGI:5749228	Ryr1<sup>m1Nisw</sup>/Ryr1<sup>+</sup>  [background:] 129S1.B6-Ryr1<sup>m1Nisw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25564733	20160218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716083	Pink1<sup>tm1Shn</sup>	is_implicated_in	DOID:0060369	Parkinson's disease 6						ECO:0000033	author statement supported by traceable reference	PMID:22511790	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716083	Pink1<sup>tm1Shn</sup>	is_implicated_in	DOID:0060369	Parkinson's disease 6						ECO:0000033	author statement supported by traceable reference	PMID:21839811	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716083	Pink1<sup>tm1Shn</sup>	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:3716639	Pink1<sup>tm1Shn</sup>/Pink1<sup>tm1Shn</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17563363	20121112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618631	Zic3<sup>tm1Bca</sup>/Zic3<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5013830	Tg(MMTV-ERBB2*,-luc)6157Aami	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20170215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5013830	Tg(MMTV-ERBB2*,-luc)6157Aami	is_implicated_in	DOID:1612	breast cancer		MGI:5013911	Tg(MMTV-ERBB2*,-luc)6157Aami/0  [background:] FVB-Tg(MMTV-ERBB2*,-luc)6157Aami			ECO:0000033	author statement supported by traceable reference	PMID:21559085	20170215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5013830	Tg(MMTV-ERBB2*,-luc)6157Aami	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27475932	20170215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7957574	20080729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1565490	20080729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8163351	20080729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449928	Adk<sup>tm1Bois</sup>/Adk<sup>tm1Bois</sup>  [background:] involves: 129P3/JEmsJ * C57BL/6	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:11997462	20050526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716137	Ins2<sup>tm1Jja</sup>/Ins2<sup>tm1Jja</sup>  [background:] NOD.129S2-Ins2<sup>tm1Jja</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12925730	20070726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639605	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/MpJ-Fas<sup>lpr</sup>/J	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17208228	20080806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4420396	Scn4a<sup>tm1.1Ljh</sup>/Scn4a<sup>+</sup>  [background:] B6.129S4-Scn4a<sup>tm1.1Ljh</sup>	is_model_of	DOID:14451	hyperkalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7451121	Sox9<sup>tm1.2Ksec</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:7451325	Sox9<sup>tm1.2Ksec</sup>/Sox9<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:36343245	20230407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718076	Tg(PDGFB-MAPT*V337M)1Atak/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:11756496	20140313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:23132636	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:23527181	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:22469986	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:27913199	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:22761823	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:34520730	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:26121046	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2665504	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] C57BL/6J-Apc<sup>Min</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14522940	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856318	Apc<sup>Min</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2175903	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] involves: AKR/J * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:1350108	20230207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135928	Kras<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25038189	20150714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135928	Kras<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23913633	20150714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135928	Kras<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3770518	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:18493606	20150714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135928	Kras<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3770518	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20150714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135928	Kras<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3770515	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20150714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039042	Tg(MMTV-Erbb2)1Pv	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28300085	20190819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039042	Tg(MMTV-Erbb2)1Pv	is_implicated_in	DOID:1612	breast cancer		MGI:5796560	Tg(MMTV-Erbb2)1Pv/0  [background:] involves: BALB/c * C57BL/6 * CD-1 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:26941084	20190819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612485	Lrp5<sup>tm1Grw</sup>	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612485	Lrp5<sup>tm1Grw</sup>	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome		MGI:3615357	Lrp5<sup>tm1Grw</sup>/Lrp5<sup>tm1Grw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651594	Tg(Lck-Tnfsf4)1Nish/0  [background:] B6.Cg-Tg(Lck-Tnfsf4)1Nish	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22171643	20130423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7564405	Dram2<sup>em1Jean</sup>	is_implicated_in	DOID:0050572	cone-rod dystrophy		MGI:7564407	Dram2<sup>em1Jean</sup>/Dram2<sup>em1Jean</sup>  [background:] C57BL/6J-Dram2<sup>em1Jean</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37691820	20231208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5469980	Atp6v1b1<sup>vtx</sup>	is_implicated_in	DOID:0050332	enlarged vestibular aqueduct		MGI:5910007	Atp6v1b1<sup>vtx</sup>/Atp6v1b1<sup>vtx</sup>  [background:] MRL/MpJ-Atp6v1b1<sup>vtx</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	PMID:28934385	20170920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763757	Kl<sup>ecalc1</sup>	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:5903776	Kl<sup>ecalc1</sup>/Kl<sup>ecalc1</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25860694	20170703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6272833	Pgrmc1<sup>em1Ejho</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6272838	Pgrmc1<sup>em1Ejho</sup>/Pgrmc1<sup>em1Ejho</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30356113	20190110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29674739	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28832675	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33633159	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5638672	App<sup>tm2.1Tcs</sup>/App<sup>tm2.1Tcs</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24728269	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29510211	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36001964	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27656030	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637816	App<sup>tm2.1Tcs</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31407772	20220915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617386	Pkd1<sup>tm1Ggg</sup>/Pkd1<sup>tm1Ggg</sup>  [background:] Not Specified	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12007403	20060323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431500	b2b1436Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5431539	b2b1436Clo/b2b1436Clo  [background:] C57BL/6J-b2b1436Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695364	Srsf2<sup>tm1.1Oaw</sup>/Srsf2<sup>+</sup> Tg(Mx1-cre)1Cgn/?  [background:] B6.Cg-Tg(Mx1-cre)1Cgn Srsf2<sup>tm1.1Oaw</sup>	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25965569	20151110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437081	Psme4<sup>b2b1508Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437116	Psme4<sup>b2b1508Clo</sup>/Psme4<sup>b2b1508Clo</sup>  [background:] C57BL/6J-Psme4<sup>b2b1508Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824061	Tg(Mpz*S63C)33Mes	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000033	author statement supported by traceable reference	PMID:20878767	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824061	Tg(Mpz*S63C)33Mes	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3		MGI:6276573	Tg(Mpz*S63C)33Mes/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662096	Tg(Pcp2-tTA)3Horr/0 Tg(tetO-SPTBN2*)#Lpwr/0  [background:] involves: FVB/N	is_model_of	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000033	author statement supported by traceable reference	PMID:25057192	20150918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5305729	Fgf23<sup>tm1.1Kew</sup>	is_implicated_in	DOID:0050948	autosomal dominant hypophosphatemic rickets		MGI:5305730	Fgf23<sup>tm1.1Kew</sup>/Fgf23<sup>tm1.1Kew</sup>  [background:] B6.129-Fgf23<sup>tm1.1Kew</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22006328	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5305729	Fgf23<sup>tm1.1Kew</sup>	is_implicated_in	DOID:0050948	autosomal dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:23873717	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856694	Flt4<sup>Chy</sup>	is_implicated_in	DOID:0050580	hereditary lymphedema						ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856694	Flt4<sup>Chy</sup>	is_implicated_in	DOID:0050580	hereditary lymphedema		MGI:3620108	Flt4<sup>Chy</sup>/Flt4<sup>+</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:11592985	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437050	Mirc30<sup>tm1.2Rdf</sup>/Mirc30<sup>tm1.2Rdf</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20060366	20110103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565224	Prkdc<sup>scid</sup>/Prkdc<sup>scid</sup> Tg(INS-HBEGF*L148S*P149T)70Rin/0  [background:] C.BKa-Prkdc<sup>scid</sup> Tg(INS-HBEGF*L148S*P149T)70Rin	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23747725	20140523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447073	Tg(Th-Twnk*,-EGFP)2Gcor/0  [background:] involves: C57BL/6J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22949510	20121228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6681833	Myo9a<sup>em1Atuf</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6681843	Myo9a<sup>em1Atuf</sup>/Myo9a<sup>+</sup>  [background:] C57BL/6J-Myo9a<sup>em1Atuf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33412162	20210408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6220715	Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>	is_implicated_in	DOID:12705	Friedreich ataxia		MGI:6220717	Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] B6.129-Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29257745	20181102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438063	b2b1700Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4436745	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] B6.C-Npc1<sup>m1N</sup>	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:20007718	20100310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5551435	Fgfr3<sup>tm1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:23200862	20140317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5812797	Ctnnb1<sup>tm2Kem</sup>/Ctnnb1<sup>tm2Kem</sup> Pvalb<sup>tm1(cre)Arbr</sup>/Pvalb<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27131348	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25461194	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26577758	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22300668	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:2175046	Grin1<sup>tm1Bhk</sup>/Grin1<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10481908	20181203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2687217	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14681207	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2687217	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16585505	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31875547	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35065251	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28959956	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22423084	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32778793	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:36609445	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33346120	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35662390	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35496999	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34039738	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23425014	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:35765058	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31852801	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25132556	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31951013	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22984603	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31664089	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31601677	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31160584	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768407	Tg(Prnp-MAPT*P301S)PS19Vle	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5512699	Tg(Prnp-MAPT*P301S)PS19Vle/0  [background:] B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle			ECO:0000033	author statement supported by traceable reference	PMID:21698260	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456082	Actb<sup>tm3.1(Sirt1)Npa</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20655472	20120216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1929642	Tg(Trp53R172H)8512Jmr	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11156526	20211209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1929642	Tg(Trp53R172H)8512Jmr	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20211209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1929642	Tg(Trp53R172H)8512Jmr	is_implicated_in	DOID:1612	breast cancer		MGI:3799369	Tg(Trp53R172H)8512Jmr/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:9519874	20211209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616342	Stk11<sup>tm1.1Mlfr</sup>/Stk11<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16357136	20060315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151181	Sgsh<sup>mps3a</sup>	is_implicated_in	DOID:0111395	mucopolysaccharidosis type IIIA						ECO:0000033	author statement supported by traceable reference	PMID:37891179	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705326	Alk<sup>tm2.1Ics</sup>	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29321660	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625688	Ctse<sup>tm1Kjy</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625688	Ctse<sup>tm1Kjy</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625688	Ctse<sup>tm1Kjy</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3629084	Ctse<sup>tm1Kjy</sup>/Ctse<sup>tm1Kjy</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14769879	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305067	App<sup>tm1Dbo</sup>/App<sup>tm1Dbo</sup> Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] C.Cg-App<sup>tm1Dbo</sup> Npc1<sup>m1N</sup>	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:21303697	20120207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32817939	20210331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:0080600	COVID-19		MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J			ECO:0000033	author statement supported by traceable reference	MGI:6467226	20210331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:33465158	20210331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:0080600	COVID-19		MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J			ECO:0000033	author statement supported by traceable reference	PMID:33257679	20210331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:0080600	COVID-19		MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J			ECO:0000033	author statement supported by traceable reference	PMID:33465158	20210331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389235	Tg(K18-ACE2)2Prlmn	is_implicated_in	DOID:0080600	COVID-19		MGI:6455041	Tg(K18-ACE2)2Prlmn/0  [background:] B6.Cg-Tg(K18-ACE2)2Prlmn/J			ECO:0000033	author statement supported by traceable reference	PMID:32841215	20210331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798621	Dmd<sup>mdx-5Cv</sup>/Y  [background:] B6Ros.Cg-Dmd<sup>mdx-5Cv</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21893021	20120723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441538	Gata4<sup>tm1.2Wtp</sup>/Gata4<sup>+</sup>  [background:] B6.Cg-Gata4<sup>tm1.2Wtp</sup>	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:17069789	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683906	Blm<sup>tm3Brd</sup>/Blm<sup>tm3Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11101838	20050714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343355	Tg(Thy1-APP*)2Tbay	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31156407	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343355	Tg(Thy1-APP*)2Tbay	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:6392258	Tg(Thy1-APP*)2Tbay/0  [background:] C57BL/6J-Tg(Thy1-APP*)2Tbay			ECO:0000033	author statement supported by traceable reference	PMID:23685882	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343355	Tg(Thy1-APP*)2Tbay	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30670962	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343355	Tg(Thy1-APP*)2Tbay	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23685882	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510681	Zic1/Zic4<sup>tm1Kjmi</sup>	is_implicated_in	DOID:2785	Dandy-Walker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22947655	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510681	Zic1/Zic4<sup>tm1Kjmi</sup>	is_implicated_in	DOID:2785	Dandy-Walker syndrome		MGI:3511195	Zic1/Zic4<sup>tm1Kjmi</sup>/Zic4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15338008	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934013	Hfe<sup>tm1Gfn</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30427936	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934013	Hfe<sup>tm1Gfn</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22531912	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934013	Hfe<sup>tm1Gfn</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:20976594	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934013	Hfe<sup>tm1Gfn</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3839772	Hfe<sup>tm1Gfn</sup>/Hfe<sup>tm1Gfn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10557317	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934013	Hfe<sup>tm1Gfn</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3839772	Hfe<sup>tm1Gfn</sup>/Hfe<sup>tm1Gfn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20976594	20181217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523927	Tg(SFTPC-EZR/ROS1)AShiba/0  [background:] C57BL/6-Tg(SFTPC-EZR/ROS1)AShiba	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23418494	20131216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723272	Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub  [background:] involves: FVB/N	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:21684039	20150612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723272	Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub  [background:] involves: FVB/N	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22722052	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5546373	Tg(KRT14-Hmgn2)#Baam	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:5546382	Tg(KRT14-Hmgn2)#Baam/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:23975681	20140227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447335	Tg(PSEN1)5Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28484012	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447335	Tg(PSEN1)5Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22522613	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447335	Tg(PSEN1)5Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33998138	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447335	Tg(PSEN1)5Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28934252	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447335	Tg(PSEN1)5Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23260124	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401292	Tg(Ace2-ACE2)1Cqin	is_implicated_in	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32498696	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401292	Tg(Ace2-ACE2)1Cqin	is_implicated_in	DOID:0080600	COVID-19		MGI:6402641	Tg(Ace2-ACE2)1Cqin/0  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:32444876	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401292	Tg(Ace2-ACE2)1Cqin	is_implicated_in	DOID:0080600	COVID-19		MGI:6402641	Tg(Ace2-ACE2)1Cqin/0  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:32380511	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438058	Cntrl<sup>b2b1468.1Clo</sup>	is_implicated_in	DOID:12712	nephronophthisis		MGI:5442123	Cntrl<sup>b2b1468.1Clo</sup>/Cntrl<sup>b2b1468.1Clo</sup>  [background:] C57BL/6J-Cntrl<sup>b2b1468.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037431	Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] C3H/HeJ-Fasl<sup>gld</sup>/J	is_model_of	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:6693832	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037431	Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] C3H/HeJ-Fasl<sup>gld</sup>/J	is_model_of	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	MGI:77345	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772866	Tg(Prnp-TBP*)71-16Xjl	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000033	author statement supported by traceable reference	PMID:23665119	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772866	Tg(Prnp-TBP*)71-16Xjl	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:3772883	Tg(Prnp-TBP*)71-16Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)71-16Xjl			ECO:0000033	author statement supported by traceable reference	PMID:17994014	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6100933	Fus<sup>tm1.1Emcf</sup>	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:6101467	Fus<sup>tm1.1Emcf</sup>/Fus<sup>+</sup>  [background:] involves: C3H * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29053787	20171215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574538	Dok1<sup>tm1Yyam</sup>/Dok1<sup>tm1Yyam</sup> Dok2<sup>tm1Yyam</sup>/Dok2<sup>tm1Yyam</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: C57BL/6	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611294	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553464	Tg(Prnp-APPSweArc)#Rmni	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5553465	Tg(Prnp-APPSweArc)#Rmni/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:27836896	20190724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810681	Tg(Hsf4/EGFP)N7Spbh	is_implicated_in	DOID:0110255	cataract 5 multiple types		MGI:5810684	Tg(Hsf4/EGFP)N7Spbh/0  [background:] C57BL/6-Tg(Hsf4/EGFP)N7Spbh			ECO:0000033	author statement supported by traceable reference	PMID:25168898	20161202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720943	Bace1<sup>tm1Pcw</sup>/Bace1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:18385378	20161101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386210	Epor<sup>tm1.4Jtp</sup>/Epor<sup>tm1.4Jtp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060652	familial erythrocytosis 1						ECO:0000033	author statement supported by traceable reference	PMID:11158582	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J	is_model_of	DOID:0060545	Hermansky-Pudlak syndrome 7						ECO:0000033	author statement supported by traceable reference	PMID:1936982	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J	is_model_of	DOID:0060545	Hermansky-Pudlak syndrome 7						ECO:0000033	author statement supported by traceable reference	PMID:12923531	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:27105383	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24150608	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:37681411	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:25633666	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:31530849	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:29035364	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:27176632	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:27479085	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:33370564	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:22275362	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:25193594	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24695736	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity		MGI:3623749	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16394172	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity		MGI:3655835	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] D2.Cg-Lep<sup>ob</sup>/Chua			ECO:0000033	author statement supported by traceable reference	PMID:12136396	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9970	obesity		MGI:3623749	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12885755	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26686669	20191219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24698766	20191219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31601677	20191219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27559087	20191219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26372964	20191219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27085394	20191219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23738020	20191219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772798	Etv6<sup>tm3(NTRK3)Sho</sup>/Etv6<sup>+</sup> Tg(Wap-cre)11738Mam/0  [background:] involves: 129S1/Sv * C57BL/6 * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18068631	20160426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317102	Tg(Pcp2-tTA)3Horr/0 Tg(tetO-ATXN1*82Q)#Horr/Tg(tetO-ATXN1*82Q)#Horr  [background:] involves: FVB/N	is_model_of	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:15470152	20120502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181878	Ins2<sup>tm1Jja</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22427377	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181878	Ins2<sup>tm1Jja</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26696124	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181878	Ins2<sup>tm1Jja</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3716137	Ins2<sup>tm1Jja</sup>/Ins2<sup>tm1Jja</sup>  [background:] NOD.129S2-Ins2<sup>tm1Jja</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12925730	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931018	Rb1<sup>tm2Brn</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5800408	Tg(PDGFB-LRRK2*R1441C)31Hlw	is_implicated_in	DOID:0060371	Parkinson's disease 8		MGI:5800410	Tg(PDGFB-LRRK2*R1441C)31Hlw/0  [background:] FVB/N-Tg(PDGFB-LRRK2*R1441C)31Hlw			ECO:0000033	author statement supported by traceable reference	PMID:26363496	20161012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5790962	Myo5b<sup>tm1.1Cle</sup>	is_implicated_in	DOID:0060775	microvillus inclusion disease		MGI:5790964	Myo5b<sup>tm1.1Cle</sup>/Myo5b<sup>tm1.1Cle</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26392529	20160909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824254	Tg(Erbb2-Erbb2*V664E)#Led/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:10803404	20170215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5320442	Cdc42<sup>tm1.1Ayam</sup>	is_implicated_in	DOID:674	cleft palate		MGI:7335182	Cdc42<sup>tm1.1Ayam</sup>/Cdc42<sup>tm1.1Ayam</sup> Tg(Mpz-cre)94Imeg/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28326341	20220909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6451090	Cfap65<sup>em1Fzh</sup>	is_implicated_in	DOID:0111918	spermatogenic failure 40		MGI:6451096	Cfap65<sup>em1Fzh</sup>/Cfap65<sup>em1Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31501240	20200821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555835	b2b2025Clo/b2b2025Clo  [background:] C57BL/6J-b2b2025Clo	is_model_of	DOID:0110598	primary ciliary dyskinesia 14						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435698	Shank2<sup>tm1.1Tmb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23994547	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435698	Shank2<sup>tm1.1Tmb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435698	Shank2<sup>tm1.1Tmb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23583105	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435698	Shank2<sup>tm1.1Tmb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5435702	Shank2<sup>tm1.1Tmb</sup>/Shank2<sup>tm1.1Tmb</sup>  [background:] B6.129-Shank2<sup>tm1.1Tmb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22699619	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435698	Shank2<sup>tm1.1Tmb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27581745	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435698	Shank2<sup>tm1.1Tmb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:33491217	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530234	Tg(HDexon1)62Gpb/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:8898202	20060602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3639702	Tg(tetO-APPSwInd)885Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22855807	20120824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154521	Cdk4<sup>tm1.1Bbd</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26354726	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154521	Cdk4<sup>tm1.1Bbd</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26511633	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154521	Cdk4<sup>tm1.1Bbd</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25088201	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154521	Cdk4<sup>tm1.1Bbd</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:22742762	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0110635	muscular dystrophy-dystroglycanopathy type B5		MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20675713	20101011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820083	Tcte1<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6111404	Tcte1<sup>tm1a(KOMP)Wtsi</sup>/Tcte1<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Tcte1<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28630322	20180123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416159	Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:6437232	Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>/Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>  [background:] B6N(Cg)-Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31844321	20210427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5568128	Lrrk1<sup>tm1.1Smo</sup>	is_implicated_in	DOID:13533	osteopetrosis		MGI:5568131	Lrrk1<sup>tm1.1Smo</sup>/Lrrk1<sup>tm1.1Smo</sup>  [background:] involves: 129S/Sv			ECO:0000033	author statement supported by traceable reference	PMID:23526378	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295259	Muc5ac<sup>tm1.1Evns</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:5295260	Muc5ac<sup>tm1.1Evns</sup>/Muc5ac<sup>tm1.1Evns</sup>  [background:] B6.129S1-Muc5ac<sup>tm1.1Evns</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23272068	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619415	Fbn1<sup>tm1Rmz</sup>/Fbn1<sup>tm1Rmz</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9326947	20060413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700794	Tg(Tcra2D2,Tcrb2D2)1Kuch	is_implicated_in	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:24819960	20140821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677318	Recql4<sup>tm1Abe</sup>/Recql4<sup>tm1Abe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:2732	Rothmund-Thomson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12915449	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566993	Tg(CAG-A4GALT)#Sais	is_implicated_in	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:20961863	20140606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559448	Tg(Thy1-APPSweAut)A7Tiwa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33287899	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559448	Tg(Thy1-APPSweAut)A7Tiwa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27466196	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559448	Tg(Thy1-APPSweAut)A7Tiwa	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5559449	Tg(Thy1-APPSweAut)A7Tiwa/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:19741145	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559448	Tg(Thy1-APPSweAut)A7Tiwa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19741145	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559448	Tg(Thy1-APPSweAut)A7Tiwa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25937280	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559448	Tg(Thy1-APPSweAut)A7Tiwa	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23636056	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430050	b2b243.1Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5430322	b2b243.1Clo/b2b243.1Clo  [background:] C57BL/6J-b2b243.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6444205	Psap<sup>tm2.1Juma</sup>	is_not_implicated_in	DOID:1926	Gaucher's disease		MGI:6444206	Psap<sup>tm2.1Juma</sup>/Psap<sup>tm2.1Juma</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20175216	20200724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476174	b2b1929Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5476437	b2b1929Clo/b2b1929Clo  [background:] C57BL/6J-b2b1929Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582929	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] involves: BALB/c * CAST/EiJ	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3032531	Tg(Pdx1-cre)6Tuv	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23076356	20130128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3032531	Tg(Pdx1-cre)6Tuv	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22738914	20130128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715607	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11069286	20070723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317649	Dnah11<sup>b2b1279Clo</sup>/Dnah11<sup>b2b1279Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1279Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461155	Nrcam<sup>tm1Gmt</sup>/Nrcam<sup>tm1Gmt</sup>  [background:] involves: 129S6/SvEvTac * Swiss Webster	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:19540269	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942392	Ift80<sup>Gt(AN0245)Wtsi</sup>/Ift80<sup>Gt(AN0245)Wtsi</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0110086	asphyxiating thoracic dystrophy 2						ECO:0000033	author statement supported by traceable reference	PMID:21227999	20110329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950568	Prpf31<sup>tm1.1Bha</sup>/Prpf31<sup>+</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:0110408	retinitis pigmentosa 11						ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6231206	Tg(H2-K-Hmga1)#Lmsr	is_implicated_in	DOID:5603	T-cell acute lymphoblastic leukemia		MGI:6231210	Tg(H2-K-Hmga1)#Lmsr/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15150086	20230724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6231206	Tg(H2-K-Hmga1)#Lmsr	is_implicated_in	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22053823	20230724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7282115	Tardbp<sup>tm1.1Hiok</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:7284280	Tardbp<sup>tm1.1Hiok</sup>/Tardbp<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154650	Col7a1<sup>tm1Uit</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:23321329	20220207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154650	Col7a1<sup>tm1Uit</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:26203639	20220207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154650	Col7a1<sup>tm1Uit</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:25640200	20220207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154650	Col7a1<sup>tm1Uit</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:4417895	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:19893033	20220207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154650	Col7a1<sup>tm1Uit</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:3037979	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10523500	20220207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584464	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm2.1Tyj</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJae	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693334	Crtap<sup>tm1Brle</sup>	is_implicated_in	DOID:0110337	osteogenesis imperfecta type 7						ECO:0000033	author statement supported by traceable reference	PMID:19895918	20150724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693334	Crtap<sup>tm1Brle</sup>	is_implicated_in	DOID:0110337	osteogenesis imperfecta type 7		MGI:3693839	Crtap<sup>tm1Brle</sup>/Crtap<sup>tm1Brle</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:17055431	20150724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5550581	Tg(PDGFB-APPInd)F17Plhn	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5550582	Tg(PDGFB-APPInd)F17Plhn/0  [background:] C57BL/6-Tg(PDGFB-APPInd)F17Plhn			ECO:0000033	author statement supported by traceable reference	PMID:16289866	20140314	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5550581	Tg(PDGFB-APPInd)F17Plhn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20140314	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559368	Tg(KRT14-HPV8)9Vuc	is_implicated_in	DOID:4159	skin cancer		MGI:5559461	Tg(KRT14-HPV8)9Vuc/0  [background:] FVB.Cg-Tg(KRT14-HPV8)9Vuc			ECO:0000033	author statement supported by traceable reference	PMID:15735026	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775427	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>/?  [background:] B6.Cg-Cox10<sup>tm1Ctm</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:27038906	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5471642	Acvr1<sup>tm1Emsh</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:23115204	20131028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5471642	Acvr1<sup>tm1Emsh</sup>	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5471728	Acvr1<sup>tm1Emsh</sup>/Acvr1<sup>+</sup>  [background:] chimera involves: BALB/c * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:22508565	20131028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4455027	Rho<sup>Tvrm4</sup>/Rho<sup>+</sup> Rpe65<sup>rd12</sup>/Rpe65<sup>rd12</sup>  [background:] B6.Cg-Rpe65<sup>rd12</sup> Rho<sup>Tvrm4</sup>	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:20207741	20100616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312925	Nhlrc1<sup>tm1.2Geno</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:10384102	20180208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312925	Nhlrc1<sup>tm1.2Geno</sup>	is_implicated_in	DOID:3534	Lafora disease		MGI:5312936	Nhlrc1<sup>tm1.2Geno</sup>/Nhlrc1<sup>tm1.2Geno</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22186026	20180208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5501108	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060688	arteriovenous malformations of the brain						ECO:0000033	author statement supported by traceable reference	PMID:22571958	20130814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:25859855	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:29743593	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3347	osteosarcoma		MGI:5521544	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23486187	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441584	Atp6v0a4<sup>tm1.1Fekf</sup>	is_implicated_in	DOID:14219	renal tubular acidosis						ECO:0000033	author statement supported by traceable reference	PMID:23065636	20131028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441584	Atp6v0a4<sup>tm1.1Fekf</sup>	is_implicated_in	DOID:14219	renal tubular acidosis		MGI:5441585	Atp6v0a4<sup>tm1.1Fekf</sup>/Atp6v0a4<sup>tm1.1Fekf</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22872862	20131028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6118174	C9orf72<sup>em1Eggn</sup>	is_implicated_in	DOID:417	autoimmune disease		MGI:6278556	C9orf72<sup>em1Eggn</sup>/C9orf72<sup>em1Eggn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5787576	Aspa<sup>deaf14</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:5787605	Aspa<sup>deaf14</sup>/Aspa<sup>deaf14</sup>  [background:] BALB/c-Aspa<sup>deaf14</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24682784	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296904	Cacna1c<sup>tm2Itl</sup>	is_implicated_in	DOID:0060173	Timothy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23313911	20181218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296904	Cacna1c<sup>tm2Itl</sup>	is_implicated_in	DOID:0060173	Timothy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24371506	20181218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296904	Cacna1c<sup>tm2Itl</sup>	is_implicated_in	DOID:0060173	Timothy syndrome		MGI:5296910	Cacna1c<sup>tm2Itl</sup>/Cacna1c<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:21878566	20181218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296904	Cacna1c<sup>tm2Itl</sup>	is_implicated_in	DOID:0060173	Timothy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30151840	20181218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296904	Cacna1c<sup>tm2Itl</sup>	is_implicated_in	DOID:0060173	Timothy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20181218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825287	Wdfy3<sup>disc</sup>/Wdfy3<sup>disc</sup>  [background:] involves: C57BL/6J * FVB/NJ	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25198012	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926379	Tg(APOC1)1Lmh	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926379	Tg(APOC1)1Lmh	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5564916	Tg(APOC1)1Lmh/Tg(APOC1)1Lmh  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18049452	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384494	Pitx2<sup>tm1Rsd</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:12015277	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384494	Pitx2<sup>tm1Rsd</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3622905	Pitx2<sup>tm1Rsd</sup>/Pitx2<sup>tm1Rsd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10499586	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5604542	Brinp1<sup>tm1.1Pib</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5770244	Brinp1<sup>tm1.1Pib</sup>/Brinp1<sup>tm1.1Pib</sup>  [background:] involves: BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27042284	20160517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:29878125	20180906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:28069793	20180906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:29849091	20180906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:3527796	Lmna<sup>tm1Gbon</sup>/Lmna<sup>tm1Gbon</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22773734	20180906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053090	Vip<sup>tm1Clw</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20130417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053090	Vip<sup>tm1Clw</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:3054170	Vip<sup>tm1Clw</sup>/Vip<sup>tm1Clw</sup>  [background:] involves: 129S/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17309917	20130417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906016	Tg(Myh6-Tpm1*E54K)30Dfw	is_implicated_in	DOID:0110457	dilated cardiomyopathy 1Y		MGI:5906019	Tg(Myh6-Tpm1*E54K)30Dfw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17556658	20170801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0111103	maturity-onset diabetes of the young type 4						ECO:0000033	author statement supported by traceable reference	PMID:12697734	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527094	Tecta<sup>tm3.1Gpr</sup>	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:5527171	Tecta<sup>tm3.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5581489	Tg(Myh6-MYOZ2*I246M)#Ajm	is_implicated_in	DOID:0110322	hypertrophic cardiomyopathy 16						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5581489	Tg(Myh6-MYOZ2*I246M)#Ajm	is_implicated_in	DOID:0110322	hypertrophic cardiomyopathy 16		MGI:5581491	Tg(Myh6-MYOZ2*I246M)#Ajm/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22987565	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195004	Col17a1<sup>tm1.1(COL17A1)Zliu</sup>	is_implicated_in	DOID:8506	bullous pemphigoid		MGI:6195005	Col17a1<sup>tm1.1(COL17A1)Zliu</sup>/Col17a1<sup>tm1.1(COL17A1)Zliu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18922680	20180820	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311383	Daw1<sup>b2b1116Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:936	brain disease						ECO:0000033	author statement supported by traceable reference	PMID:25752454	20180801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:936	brain disease						ECO:0000033	author statement supported by traceable reference	PMID:29476105	20180801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:936	brain disease		MGI:3714016	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Gfap-cre)1Sbk/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:19470613	20180801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640329	Gnmt<sup>tm1Cwa</sup>/Gnmt<sup>tm1Cwa</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0111037	glycine N-methyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16779654	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769902	Scn5a<sup>tm1Care</sup>	is_implicated_in	DOID:0110218	Brugada syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24700869	20170922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769902	Scn5a<sup>tm1Care</sup>	is_implicated_in	DOID:0110218	Brugada syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23661717	20170922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769902	Scn5a<sup>tm1Care</sup>	is_implicated_in	DOID:0110218	Brugada syndrome 1		MGI:3769904	Scn5a<sup>tm1Care</sup>/Scn5a<sup>+</sup>  [background:] FVB.129P2-Scn5a<sup>tm1Care</sup>/Care			ECO:0000033	author statement supported by traceable reference	PMID:17145985	20170922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042286	Fst<sup>tm1Zuk</sup>/Fst<sup>tm1Zuk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060762	restrictive dermopathy						ECO:0000033	author statement supported by traceable reference	PMID:7885475	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942165	Tg(Ins2-Hnf1a)#Cbw	is_implicated_in	DOID:0111102	maturity-onset diabetes of the young type 3		MGI:4942179	Tg(Ins2-Hnf1a)#Cbw/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11713231	20110328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435562	Porcn<sup>tm1.1Vdv</sup>/Y Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5140078	Trp53<sup>tm4Att</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5750594	Tg(CMV-cre)1Cgn/0 Trp53<sup>tm4Att</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25119037	20160229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6147714	Dnaaf11<sup>tm1.2Hmd</sup>	is_implicated_in	DOID:0110608	primary ciliary dyskinesia 19		MGI:6285740	Dnaaf11<sup>tm1.2Hmd</sup>/Dnaaf11<sup>tm1.2Hmd</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27353389	20190402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433725	Pklr<sup>slc</sup>/Pklr<sup>slc</sup>  [background:] CBA/NSlc-Pklr<sup>slc</sup>	is_model_of	DOID:0111077	pyruvate kinase deficiency of red cells						ECO:0000033	author statement supported by traceable reference	PMID:7579416	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5762986	Tg(MMTV-NCOA3)#Mybr	is_implicated_in	DOID:1612	breast cancer		MGI:5762988	Tg(MMTV-NCOA3)#Mybr/0  [background:] FVB/N-Tg(MMTV-NCOA3)#Mybr			ECO:0000033	author statement supported by traceable reference	PMID:15380517	20160422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5762986	Tg(MMTV-NCOA3)#Mybr	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837855	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup> Col1a1<sup>tm1(CAG-EGFR)Char</sup>/Col1a1<sup>tm1(CAG-EGFR)Char</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:19196966	20130322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5547618	Tg(CKMM-tTA)A3Rhvh/0 Tg(tetO-H2-K1)#Papl/0  [background:] B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl	is_model_of	DOID:633	myositis						ECO:0000033	author statement supported by traceable reference	PMID:10922072	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5788094	Dpp4<sup>tm1(DPP4)Vlcg</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400455	Dpp4<sup>tm1(DPP4)Vlcg</sup>/?  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26124093	20200619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5788094	Dpp4<sup>tm1(DPP4)Vlcg</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6435210	Dpp4<sup>tm1(DPP4)Vlcg</sup>/?  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:27795435	20200619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637741	Tg(MMTV-Espl1)1Pati	is_implicated_in	DOID:1612	breast cancer		MGI:5637742	Tg(MMTV-Espl1)1Pati/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24276237	20150529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586988	Ndn<sup>tm1Ky</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586988	Ndn<sup>tm1Ky</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3607781	Ndn<sup>tm1Ky</sup>/Ndn<sup>+</sup>  [background:] involves: C57BL/6 * CBA * ICR/Slc			ECO:0000033	author statement supported by traceable reference	PMID:16049186	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7486783	Chd7<sup>Trooper</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493334	Chd7<sup>Trooper</sup>/Chd7<sup>+</sup>  [background:] BALB/c-Chd7<sup>Trooper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29615807	20230627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306914	Tg(Thy1-GLRA1*R271Q)382Wha	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:5306916	Tg(Thy1-GLRA1*R271Q)382Wha/Tg(Thy1-GLRA1*R271Q)382Wha  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11923415	20120223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450128	Cyp19a1<sup>tm1Esi</sup>/Cyp19a1<sup>tm1Esi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15314222	20150603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26742432	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24414704	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27881875	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26847026	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23643835	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22927245	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357686	Tg(Vav1-NUP98/HOXD13)G2Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:4357767	Tg(Vav1-NUP98/HOXD13)G2Apla/0  [background:] C57BL/6-Tg(Vav1-NUP98/HOXD13)G2Apla			ECO:0000033	author statement supported by traceable reference	PMID:15755899	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5003453	Tg(PDGFB-APPSwDutLon)46Lpr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5003463	Tg(PDGFB-APPSwDutLon)46Lpr/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624520	Dnah5<sup>Tg1Htz</sup>/Dnah5<sup>Tg1Htz</sup>  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:11912187	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524274	Tg(TG-rtTA)30Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22105174	20131220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524274	Tg(TG-rtTA)30Jaf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23372702	20131220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5525131	Tg(Prnp-ITM2B*)1Ruvi/Tg(Prnp-ITM2B*)1Ruvi Tg(Prnp-MAPT*P301L)#Ruvi/Tg(Prnp-MAPT*P301L)#Ruvi  [background:] involves: C3HeB/FeJ * C57BL/6	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:23418567	20131226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762253	Tg(CMV-Msx2*P7H)1Rem/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:2340	craniosynostosis						ECO:0000033	author statement supported by traceable reference	PMID:7597092	20071126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897617	Tg(TG-RET/CCDC6)42Cled/0  [background:] involves: FVB/N	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:10380889	20170518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897617	Tg(TG-RET/CCDC6)42Cled/0  [background:] involves: FVB/N	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:8536638	20170518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694081	Hpse2<sup>Gt(OST411605)Lex</sup>/Hpse2<sup>Gt(OST411605)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0050816	urofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25510506	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432227	Grm1<sup>Tg(p18A4.B)1352Szc</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:30987979	20210115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432227	Grm1<sup>Tg(p18A4.B)1352Szc</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:23913827	20210115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432227	Grm1<sup>Tg(p18A4.B)1352Szc</sup>	is_implicated_in	DOID:8923	skin melanoma		MGI:5432229	Grm1<sup>Tg(p18A4.B)1352Szc</sup>/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12704387	20210115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:25143484	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:21841818	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:26941288	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:23966158	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:29870403	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:24368766	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:26888257	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:33608271	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3811798	Tg(IghMyc)22Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22081075	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447604	Tg(IghMyc)22Bri	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3811798	Tg(IghMyc)22Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:3906410	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26058840	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32858248	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24278307	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29669277	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33482356	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057129	Tg(MAPT)8cPdav	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:30508732	20210722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6297004	Tg(Col1a1-FGF2*,-Sapphire)203Mmh	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:6297005	Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27732085	20190509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6297004	Tg(Col1a1-FGF2*,-Sapphire)203Mmh	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:28938491	20190509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:26279473	20160714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21903772	20160714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476838	Tg(TARDBP*G348C)#Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:21752789	20130502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3761174	Tg(MMTV-neu/OT-I/OT-II)CBnel/?  [background:] involves: C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:17616705	20080617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:17641777	20150330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689841	Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo  [background:] C57BL/6-Tg(Thy1-TARDBP*)BOddo	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:26002100	20151012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4453304	Cldn16<sup>tm1.1Dmu</sup>/Cldn16<sup>tm1.1Dmu</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6	is_model_of	DOID:0060880	renal hypomagnesemia 3						ECO:0000033	author statement supported by traceable reference	PMID:20147368	20151122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5643859	Wfs1<sup>tm1Koks</sup>/Wfs1<sup>tm1Koks</sup>  [background:] 129S6/SvEvTac-Wfs1<sup>tm1Koks</sup>	is_model_of	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:21031341	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5643859	Wfs1<sup>tm1Koks</sup>/Wfs1<sup>tm1Koks</sup>  [background:] 129S6/SvEvTac-Wfs1<sup>tm1Koks</sup>	is_model_of	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24710642	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3026845	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1Pai</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:14555645	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526095	Jak1<sup>M1Mhda</sup>/Jak1<sup>+</sup>  [background:] C3HeB/FeJ-Jak1<sup>M1Mhda</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23791841	20140103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438065	Fbn2<sup>mz</sup>/Fbn2<sup>mz</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:20161761	20100329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038633	Gad2<sup>tm1Miya</sup>/Gad2<sup>tm1Miya</sup>  [background:] NOD.129P2-Gad2<sup>tm1Miya</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14676944	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2659140	Mocs1<sup>tm1Jre</sup>	is_implicated_in	DOID:0111164	molybdenum cofactor deficiency type A						ECO:0000033	author statement supported by traceable reference	PMID:17236133	20230619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2659140	Mocs1<sup>tm1Jre</sup>	is_implicated_in	DOID:0111164	molybdenum cofactor deficiency type A						ECO:0000033	author statement supported by traceable reference	PMID:15862276	20230619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2659140	Mocs1<sup>tm1Jre</sup>	is_implicated_in	DOID:0111164	molybdenum cofactor deficiency type A		MGI:2659147	Mocs1<sup>tm1Jre</sup>/Mocs1<sup>tm1Jre</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12471057	20230619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437082	Cep290<sup>b2b1454Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437115	Cep290<sup>b2b1454Clo</sup>/Cep290<sup>b2b1454Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1454Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614453	Ar<sup>tm4(AR)Dmr</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:16400023	20081107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614453	Ar<sup>tm4(AR)Dmr</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:16981011	20081107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153356	Col6a1<sup>tm1Gmb</sup>	is_implicated_in	DOID:0050663	Bethlem myopathy						ECO:0000033	author statement supported by traceable reference	PMID:26945058	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153356	Col6a1<sup>tm1Gmb</sup>	is_implicated_in	DOID:0050663	Bethlem myopathy						ECO:0000033	author statement supported by traceable reference	PMID:14625552	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153356	Col6a1<sup>tm1Gmb</sup>	is_implicated_in	DOID:0050663	Bethlem myopathy						ECO:0000033	author statement supported by traceable reference	PMID:19293339	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153356	Col6a1<sup>tm1Gmb</sup>	is_implicated_in	DOID:0050663	Bethlem myopathy						ECO:0000033	author statement supported by traceable reference	PMID:9817932	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153356	Col6a1<sup>tm1Gmb</sup>	is_implicated_in	DOID:0050663	Bethlem myopathy		MGI:3037904	Col6a1<sup>tm1Gmb</sup>/Col6a1<sup>tm1Gmb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9817932	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153356	Col6a1<sup>tm1Gmb</sup>	is_implicated_in	DOID:0050663	Bethlem myopathy		MGI:3037904	Col6a1<sup>tm1Gmb</sup>/Col6a1<sup>tm1Gmb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14625552	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:29700358	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28195574	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25689854	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27799523	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24922526	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23831727	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856331	Dmd<sup>mdx-4Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:33175853	20201221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28825599	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28300085	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:33097662	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21996747	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25972601	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27601049	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24909172	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26729790	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28373182	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22038845	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24435044	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26833123	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23720051	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11156526	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28536279	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26554829	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer		MGI:2654501	Tg(MMTVneu)202Mul/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12483526	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930204	Tg(MMTVneu)202Mul	is_implicated_in	DOID:1612	breast cancer		MGI:3577096	Tg(MMTVneu)202Mul/0  [background:] FVB/N-Tg(MMTVneu)202Mul			ECO:0000033	author statement supported by traceable reference	PMID:1359541	20220926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7545269	Lepr<sup>db-Nokl</sup>	is_implicated_in	DOID:9970	obesity		MGI:7545546	Lepr<sup>db-Nokl</sup>/Lepr<sup>db-Nokl</sup>  [background:] C57BL/6N-Lepr<sup>db-Nokl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400999	Dpp4<sup>tm1.1(DPP4)Pbmj</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6401000	Dpp4<sup>tm1.1(DPP4)Pbmj</sup>/Dpp4<sup>tm1.1(DPP4)Pbmj</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:28348219	20200522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400999	Dpp4<sup>tm1.1(DPP4)Pbmj</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32265331	20200522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856067	Plp1<sup>jp-rsh</sup>	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:20091761	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856067	Plp1<sup>jp-rsh</sup>	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3711148	Plp1<sup>jp-rsh</sup>/Y  [background:] involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr			ECO:0000033	author statement supported by traceable reference	PMID:17394578	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708462	Tg(tetO-APPSwInd)107Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22855807	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708462	Tg(tetO-APPSwInd)107Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33412147	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708462	Tg(tetO-APPSwInd)107Dbo	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21411653	20210819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708462	Tg(tetO-APPSwInd)107Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3709152	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)107Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16279840	20210819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:9501313	20050914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450918	Best1<sup>tm1.1Amar</sup>/Best1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:0050661	vitelliform macular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7494069	Stmn2<sup>em1Jmi</sup>	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:7523314	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>+</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7494069	Stmn2<sup>em1Jmi</sup>	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:7523309	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>em1Jmi</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713721	Nr4a1<sup>tm1Jmi</sup>/Nr4a1<sup>tm1Jmi</sup> Nr4a3<sup>tm1Omc</sup>/Nr4a3<sup>tm1Omc</sup>  [background:] involves: 129S/SvEv * 129S2/SvPas * C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:17515897	20070704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:17101178	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808349	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:34962634	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808349	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:3534	Lafora disease		MGI:4839642	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>/Nhlrc1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:20538597	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808349	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:3534	Lafora disease		MGI:4839642	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>/Nhlrc1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:21882344	20230427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398901	Acvrl1<sup>tm2.1Spo</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398901	Acvrl1<sup>tm2.1Spo</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775199	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Tg(Tal1-cre/ERT)1Jrg/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398901	Acvrl1<sup>tm2.1Spo</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5431571	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19805914	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398901	Acvrl1<sup>tm2.1Spo</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5431572	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19805914	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29036344	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:32477098	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:32929122	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:24392030	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23297226	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22537068	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29899409	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29776378	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:33677035	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:27126635	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26797281	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26324905	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3603037	Tg(Prnp-SNCA*A53T)83Vle/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12062037	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057167	Tg(Prnp-SNCA*A53T)83Vle	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3603036	Tg(Prnp-SNCA*A53T)83Vle/Tg(Prnp-SNCA*A53T)83Vle  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12062037	20210708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818266	Tg(TNF)3647Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:24421350	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818266	Tg(TNF)3647Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:5449076	Tg(TNF)3647Gkl/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21809421	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818266	Tg(TNF)3647Gkl	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:30510188	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692741	Gfap<sup>tm2Mes</sup>	is_implicated_in	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:24806671	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692741	Gfap<sup>tm2Mes</sup>	is_implicated_in	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:22693571	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692741	Gfap<sup>tm2Mes</sup>	is_implicated_in	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:26190408	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692741	Gfap<sup>tm2Mes</sup>	is_implicated_in	DOID:4252	Alexander disease		MGI:3692745	Gfap<sup>tm2Mes</sup>/Gfap<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17065456	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:27466204	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:23954172	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:26330466	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:33031745	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:22203986	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:36716828	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:24154542	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:29458840	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:4361717	Tg(Prnp-TARDBP*A315T)95Balo/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19833869	20230914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6163749	Klhl31<sup>em1Eno</sup>	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:6201559	Klhl31<sup>em1Eno</sup>/Klhl31<sup>em1Eno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28872460	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7569243	Dnaaf5<sup>em1Slb</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:7569326	Dnaaf5<sup>em1Slb</sup>/Dnaaf5<sup>em1Slb</sup>  [background:] C57BL/6-Dnaaf5<sup>em1Slb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37104040	20231229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587739	Nhs<sup>Xcat</sup>/Nhs<sup>+</sup>  [background:] involves: DBA/2 * T STOCK	is_model_of	DOID:0060599	Nance-Horan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587739	Nhs<sup>Xcat</sup>/Nhs<sup>+</sup>  [background:] involves: DBA/2 * T STOCK	is_model_of	DOID:0060599	Nance-Horan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5812298	Snap29<sup>tm1b(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060337	CEDNIK syndrome		MGI:5812299	Snap29<sup>tm1b(EUCOMM)Wtsi</sup>/Snap29<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26747696	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693366	Gata3<sup>tm1Gsv</sup>/Gata3<sup>+</sup>  [background:] FVB.129(B6)-Gata3<sup>tm1Gsv</sup>	is_model_of	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15994092	20070112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715214	Gnat2<sup>cpfl3</sup>/Gnat2<sup>cpfl3</sup>  [background:] ALS/LtJ	is_model_of	DOID:0110010	achromatopsia 4						ECO:0000033	author statement supported by traceable reference	PMID:17065522	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6727113	Trpm3<sup>em1Alsh</sup>	is_implicated_in	DOID:83	cataract		MGI:6727359	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>em1Alsh</sup>  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7541100	Wwox<sup>em1Mald</sup>	is_implicated_in	DOID:0080060	autosomal recessive spinocerebellar ataxia 12		MGI:7541130	Wwox<sup>em1Mald</sup>/Wwox<sup>em1Mald</sup>  [background:] FVB/N-Wwox<sup>em1Mald</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36828035	20231019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850536	Gfap<sup>tm2Mes</sup>/Gfap<sup>+</sup> Tg(GFAP)10Mes/0  [background:] involves: 129S7/SvEvBrd * FVB/N	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:19129171	20090716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:28432149	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:28225753	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:24079945	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21223590	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:27598339	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:22595426	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042586	Rps6ka3<sup>tm1.1Kry</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24416220	20140822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042586	Rps6ka3<sup>tm1.1Kry</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:5578346	Rps6ka3<sup>tm1.1Kry</sup>/Y  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042586	Rps6ka3<sup>tm1.1Kry</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3043224	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042586	Rps6ka3<sup>tm1.1Kry</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3043197	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>tm1.1Kry</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042586	Rps6ka3<sup>tm1.1Kry</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:5529680	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>tm1.1Kry</sup>  [background:] B6.129X1(Cg)-Rps6ka3<sup>tm1.1Kry</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23742761	20140822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042586	Rps6ka3<sup>tm1.1Kry</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:5578346	Rps6ka3<sup>tm1.1Kry</sup>/Y  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24416220	20140822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857648	Ighmbp2<sup>nmd-2J</sup>	is_implicated_in	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:23295857	20130715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857648	Ighmbp2<sup>nmd-2J</sup>	is_implicated_in	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1		MGI:3603515	Ighmbp2<sup>nmd-2J</sup>/Ighmbp2<sup>nmd-2J</sup>  [background:] B6.BKS-Ighmbp2<sup>nmd-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15269181	20130715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6500762	Slc26a4<sup>em1Jgao</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:6500763	Slc26a4<sup>em1Jgao</sup>/Slc26a4<sup>em1Jgao</sup>  [background:] involves: CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:31155292	20210118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4839388	Tg(Sox3)1Pqt	is_implicated_in	DOID:10908	hydrocephalus		MGI:5428462	Tg(Sox3)1Pqt/0 Tg(Sox3-EGFP)NrPqt/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22291885	20120720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832875	bpck/bpck  [background:] B6C3Fe a/a-bpck/J	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19211713	20090226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438492	Tg(Thy1-TARDBP)4Singh/Tg(Thy1-TARDBP)4Singh  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:20133711	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808273	Krt16<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0050428	nonepidermolytic palmoplantar keratoderma						ECO:0000033	author statement supported by traceable reference	PMID:24218583	20140305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808273	Krt16<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0050428	nonepidermolytic palmoplantar keratoderma		MGI:5426823	Krt16<sup>tm1(KOMP)Vlcg</sup>/Krt16<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Krt16<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22336941	20140305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182346	Hmbs<sup>tm2Uam</sup>	is_implicated_in	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:23562909	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182346	Hmbs<sup>tm2Uam</sup>	is_implicated_in	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:26908609	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6358539	Eftud2<sup>em2Lajm</sup>	is_not_implicated_in	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type		MGI:6358540	Eftud2<sup>em2Lajm</sup>/Eftud2<sup>+</sup>  [background:] involves: CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31276534	20190906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856523	Prph2<sup>Rd2</sup>	is_implicated_in	DOID:0110383	retinitis pigmentosa 7						ECO:0000033	author statement supported by traceable reference	PMID:28053051	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856523	Prph2<sup>Rd2</sup>	is_implicated_in	DOID:0110383	retinitis pigmentosa 7						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856523	Prph2<sup>Rd2</sup>	is_implicated_in	DOID:0110383	retinitis pigmentosa 7		MGI:3620587	Prph2<sup>Rd2</sup>/Prph2<sup>+</sup>  [background:] either: (involves: BALB/c * O20/A) or (involves: GR/A * O20/A) or (involves: O20/A * STS/A)			ECO:0000033	author statement supported by traceable reference	PMID:3830736	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617823	Snrpn<sup>tm1Kaj</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617823	Snrpn<sup>tm1Kaj</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3618137	Snrpn<sup>tm1Kaj</sup>/Snrpn<sup>+</sup>  [background:] either: 129S1-Snrpn<sup>tm1Kaj</sup> or (involves: 129S1/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:16368707	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569629	Tg(Myh6-2A)#Know	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905888	A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup> Tg(Myh6-2A)#Know/0  [background:] involves: BALB/c * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17190866	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5469411	Otoa<sup>tm1Gpr</sup>	is_implicated_in	DOID:0110480	autosomal recessive nonsyndromic deafness 22		MGI:5469422	Otoa<sup>tm1Gpr</sup>/Otoa<sup>tm1Gpr</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:23129639	20130329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532923	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6.129S1-Tor1a<sup>tm2Wtd</sup>	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:21464304	20140131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532923	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6.129S1-Tor1a<sup>tm2Wtd</sup>	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:24121114	20140131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24454278	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26508157	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28173111	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29776378	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720701	Tg(Prnp-MAPT*P301L)JNPL3Hlmc/0  [background:] involves: C57BL/6 * DBA/2 * SJL * SW			ECO:0000033	author statement supported by traceable reference	PMID:11520987	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040314	Tg(WapTAg)1Knw	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040314	Tg(WapTAg)1Knw	is_implicated_in	DOID:1612	breast cancer		MGI:3581641	Tg(WapTAg)1Knw/0  [background:] C57BL/6J-Tg(WapTAg)1Knw/J			ECO:0000033	author statement supported by traceable reference	PMID:9859214	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28455451	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29471108	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30306735	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19814726	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25086405	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26042521	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32824919	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28947563	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28347539	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31402541	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25614286	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27824871	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30004239	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29433732	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36577770	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28539414	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26506064	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31284709	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30571378	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26371162	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28385916	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26945079	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25238161	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30359839	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25988230	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29769563	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28768908	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25541192	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19814725	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29300219	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3690327	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15546004	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690325	Fbn1<sup>tm1Hcd</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3690327	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15254584	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5286585	Tg(SOD1*G127X)716Mrkl	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5286592	Tg(SOD1*G127X)716Mrkl/Tg(SOD1*G127X)716Mrkl  [background:] B6JBom.Cg-Tg(SOD1*G127X)716Mrkl			ECO:0000033	author statement supported by traceable reference	PMID:14534160	20110926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715142	Ldb1<sup>tm1Witz</sup>/Ldb1<sup>tm1Witz</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:9467	nail-patella syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17316599	20070718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119764	Rhbdf2<sup>em2Mvw</sup>	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30022999	20220516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119764	Rhbdf2<sup>em2Mvw</sup>	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome		MGI:6256973	Rhbdf2<sup>em2Mvw</sup>/Rhbdf2<sup>em2Mvw</sup>  [background:] C57BL/6J-Rhbdf2<sup>em2Mvw</sup>/Mvw			ECO:0000033	author statement supported by traceable reference	PMID:28655741	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052120	Tg(Eno2-PSEN2*)1480Ykk/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12039862	20110804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797844	Fxn<sup>tm1Mkn</sup>/Fxn<sup>tm1Mkn</sup> Tg(FXN)YG8Pook/0  [background:] involves: 129/Sv * C57BL/6 * CBA	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25104852	20150316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797844	Fxn<sup>tm1Mkn</sup>/Fxn<sup>tm1Mkn</sup> Tg(FXN)YG8Pook/0  [background:] involves: 129/Sv * C57BL/6 * CBA	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:16919418	20150316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5803880	Gas8<sup>Gt(CH0760)Wtsi</sup>/Gas8<sup>em1Bky</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110619	primary ciliary dyskinesia 33						ECO:0000033	author statement supported by traceable reference	PMID:27472056	20161018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785794	Tg(Camk2a-ESR1/Disc1*)2698.1Sva	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785794	Tg(Camk2a-ESR1/Disc1*)2698.1Sva	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21821099	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785794	Tg(Camk2a-ESR1/Disc1*)2698.1Sva	is_implicated_in	DOID:5419	schizophrenia		MGI:3785829	Tg(Camk2a-ESR1/Disc1*)2698.1Sva/0  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:17984054	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832641	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm2(FCMD)Ttd</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:19017726	20101116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037641	Phex<sup>Hyp-2J</sup>/Phex<sup>+</sup>  [background:] C57BL/6-Phex<sup>Hyp-2J</sup>/J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446456	Abcc8<sup>tm1Jbry</sup>/Abcc8<sup>tm1Jbry</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060334	transient neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10734066	20130415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6356300	Cep250<sup>tm1Jzb</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:6357191	Cep250<sup>tm1Jzb</sup>/Cep250<sup>tm1Jzb</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30998843	20190827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450997	Mtm1<sup>tm1.1Jman</sup>	is_implicated_in	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:23307925	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450997	Mtm1<sup>tm1.1Jman</sup>	is_implicated_in	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:30451841	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450997	Mtm1<sup>tm1.1Jman</sup>	is_implicated_in	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:24452262	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450997	Mtm1<sup>tm1.1Jman</sup>	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:2451017	Mtm1<sup>tm1.1Jman</sup>/Y  [background:] involves: 129T1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12391329	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451004	Del(16Es2el-Ufd1l)217Bld/+  [background:] B6.129S7-Del(16Es2el-Ufd1l)217Bld	is_model_of	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000033	author statement supported by traceable reference	PMID:23055483	20140416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451004	Del(16Es2el-Ufd1l)217Bld/+  [background:] B6.129S7-Del(16Es2el-Ufd1l)217Bld	is_model_of	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000033	author statement supported by traceable reference	PMID:24101523	20140416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804654	Camkmt<sup>tm1Rpav</sup>/Camkmt<sup>tm1Rpav</sup>  [background:] B6.129S7-Camkmt<sup>tm1Rpav</sup>	is_model_of	DOID:0060858	hypotonia-cystinuria syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25548191	20161024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361186	Tg(Krt19-Ptgs2,Krt19-Ptges)8Tko	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:23975421	20140911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7388494	Mettl23<sup>em2Itwa</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:7388557	Mettl23<sup>em2Itwa</sup>/Mettl23<sup>+</sup>  [background:] C57BL/6J-Mettl23<sup>em2Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7388494	Mettl23<sup>em2Itwa</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:7388558	Mettl23<sup>em2Itwa</sup>/Mettl23<sup>em2Itwa</sup>  [background:] C57BL/6J-Mettl23<sup>em2Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722063	Tg(Thy1-APPSwDutIowa)BWevn/0  [background:] involves: C57BL/6	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:14985348	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432190	Tg(YAC128)55Hay/Tg(YAC128)55Hay  [background:] FVB/N-Tg(YAC128)55Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16165367	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432190	Tg(YAC128)55Hay/Tg(YAC128)55Hay  [background:] FVB/N-Tg(YAC128)55Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16230019	20120824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5496051	Robo1<sup>b2b872Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5496284	Robo1<sup>b2b872Clo</sup>/Robo1<sup>b2b872Clo</sup>  [background:] C57BL/6J-Robo1<sup>b2b872Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680668	Foxn1<sup>nu</sup>/Foxn1<sup>nu</sup>  [background:] Not Specified	is_model_of	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:4547146	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559071	Tmem79<sup>ma</sup>/Tmem79<sup>ma</sup>  [background:] involves: C57BL/6JJcl * CBA/CaGr	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24060273	20140418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430362	Tg(Dyrk1a)189N3Yah	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25490145	20151231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430362	Tg(Dyrk1a)189N3Yah	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23920041	20151231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430362	Tg(Dyrk1a)189N3Yah	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24453307	20151231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430362	Tg(Dyrk1a)189N3Yah	is_implicated_in	DOID:14250	Down syndrome		MGI:5430593	Tg(Dyrk1a)189N3Yah/0  [background:] B6.129P2-Tg(Dyrk1a)189N3Yah/Yah			ECO:0000033	author statement supported by traceable reference	PMID:22293606	20151231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827768	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)20Fwan/?  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/NCrl	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:27345403	20170307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831195	Tg(Pbsn-Ar*E231G)7353Ng/0  [background:] involves: FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:15657128	20090210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639354	Mc3r<sup>tm1Cone</sup>/Mc3r<sup>tm1Cone</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:10965927	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619005	Elk3<sup>tm1Wlyk</sup>/Elk3<sup>tm1Wlyk</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0060646	congenital chylothorax						ECO:0000033	author statement supported by traceable reference	PMID:11566878	20060411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559582	Tg(CAG-dsRed2/RNAi:Tardbp)6Zxu	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5563078	Tg(CAG-dsRed2/RNAi:Tardbp)6Zxu/0  [background:] involves: C57BL/6 * C57BL/6J * FVB/NJ * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24616503	20140509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6285753	Glul<sup>tm1.1Ncd</sup>	is_implicated_in	DOID:3328	temporal lobe epilepsy		MGI:6285755	Glul<sup>tm1.1Ncd</sup>/Glul<sup>tm1.1Ncd</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] B6.Cg-Glul<sup>tm1.1Ncd</sup> Emx1<sup>tm1(cre)Krj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30053506	20190402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712734	Arsb<sup>tm1Cptr</sup>/Arsb<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas	is_model_of	DOID:12800	mucopolysaccharidosis VI						ECO:0000033	author statement supported by traceable reference	PMID:12904606	20070625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5692888	Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0110660	congenital myasthenic syndrome 12		MGI:6277926	Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup>/Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * C57BL/6N * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:29905857	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5692888	Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0110660	congenital myasthenic syndrome 12						ECO:0000033	author statement supported by traceable reference	PMID:29905857	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:31059522	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25145933	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28604386	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25961459	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29463793	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:33852874	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25139996	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5430604	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Nes-cre)Wme/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20075061	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617392	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15579506	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:6188648	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Hoxb7-cre)13Amc/0  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21465620	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612341	Pkd1<sup>tm2Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5502373	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Col1a1-cre)1Bek/0  [background:] involves: 129S4/SvJae * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23029375	20210721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720702	Tg(APPSWE)2576Kha/0 Tg(Prnp-MAPT*P301L)JNPL3Hlmc/0  [background:] involves: C57BL/6 * DBA/2 * SJL * SW	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11520987	20070907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510606	Tg(Thy1-APP<sup>SL</sup>)28Lpr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25018730	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510606	Tg(Thy1-APP<sup>SL</sup>)28Lpr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20813165	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510606	Tg(Thy1-APP<sup>SL</sup>)28Lpr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5003460	Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14637096	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510606	Tg(Thy1-APP<sup>SL</sup>)28Lpr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5003460	Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15972962	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768645	Tg(Tyr-NRAS*Q61K)1Bee	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25088201	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768645	Tg(Tyr-NRAS*Q61K)1Bee	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:31039140	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768645	Tg(Tyr-NRAS*Q61K)1Bee	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26354726	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768645	Tg(Tyr-NRAS*Q61K)1Bee	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:22742762	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768645	Tg(Tyr-NRAS*Q61K)1Bee	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:28463229	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768645	Tg(Tyr-NRAS*Q61K)1Bee	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25629959	20200710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832406	Tg(SOD1*G85R)148Dwc/?  [background:] Not Specified	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:9052802	20090218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5503192	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Twist2<sup>tm1.1(cre)Dor</sup>/Twist2<sup>+</sup>  [background:] B6.129-Twist2<sup>tm1.1(cre)Dor</sup> Pten<sup>tm1Hwu</sup>	is_model_of	DOID:13042	persistent fetal circulation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23023706	20130830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639711	Zbtb20<sup>Tg(PDGFB-APPSwInd)20Lms</sup>/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10818140	20060802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618859	Dock1<sup>b2b3190Clo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5618862	Dock1<sup>b2b3190Clo</sup>/Dock1<sup>b2b3190Clo</sup>  [background:] C57BL/6J-Dock1<sup>b2b3190Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806144	Lmna<sup>tm12Lgf</sup>/Lmna<sup>tm12Lgf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:26999604	20161103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837566	Tg(CSNK1D*,-EGFP)827Yfu	is_implicated_in	DOID:0110012	advanced sleep phase syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:23636092	20141001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837566	Tg(CSNK1D*,-EGFP)827Yfu	is_implicated_in	DOID:0110012	advanced sleep phase syndrome 2		MGI:3837652	Tg(CSNK1D*,-EGFP)827Yfu/?  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15800623	20141001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620841	Gja1<sup>M1Jrt</sup>/Gja1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/N	is_model_of	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:16155213	20060502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6822330	Abcc9<sup>em3Nich</sup>	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6825757	Abcc9<sup>em3Nich</sup>/Abcc9<sup>+</sup>  [background:] B6.Cg-Abcc9<sup>em3Nich</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33529173	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6822330	Abcc9<sup>em3Nich</sup>	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6825756	Abcc9<sup>em3Nich</sup>/Abcc9<sup>em3Nich</sup>  [background:] B6.Cg-Abcc9<sup>em3Nich</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33529173	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5698356	Tg(MMTV-DMTF1_i2)7Kai	is_implicated_in	DOID:1612	breast cancer		MGI:5698359	Tg(MMTV-DMTF1_i2)7Kai/0  [background:] FVB/NJ-Tg(MMTV-DMTF1_i2)7Kai			ECO:0000033	author statement supported by traceable reference	PMID:25537728	20151208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:1852	intrahepatic cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:11113093	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:1852	intrahepatic cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:32332110	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:1852	intrahepatic cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:32994489	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:1852	intrahepatic cholestasis		MGI:3694478	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21292027	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7464270	Got2<sup>em2Pcamp</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:7464549	Got2<sup>em2Pcamp</sup>/Got2<sup>em2Pcamp</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31422819	20230421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5576170	Tg(Myh6-TNNT2*R141W)#Lian	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:22198484	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5576170	Tg(Myh6-TNNT2*R141W)#Lian	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:21352494	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5576170	Tg(Myh6-TNNT2*R141W)#Lian	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:23539503	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5576170	Tg(Myh6-TNNT2*R141W)#Lian	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:5576171	Tg(Myh6-TNNT2*R141W)#Lian/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18606313	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:26387748	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:24012986	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11528395	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10802658	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9843205	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14517541	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:5501103	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18296659	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181399	Rpe65<sup>tm1Tmr</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12506090	20161109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577843	Mme<sup>tm1Cge</sup>/Mme<sup>tm1Cge</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11375493	20050524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180033	Zmpste24<sup>tm1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23217256	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180033	Zmpste24<sup>tm1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:30157432	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180033	Zmpste24<sup>tm1Otin</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:26214134	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180033	Zmpste24<sup>tm1Otin</sup>	is_implicated_in	DOID:3911	progeria		MGI:4834358	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20805469	20190221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397674	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158359	Slc12a1<sup>tm1Tkh</sup>	is_implicated_in	DOID:0110142	Bartter disease type 1						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158359	Slc12a1<sup>tm1Tkh</sup>	is_implicated_in	DOID:0110142	Bartter disease type 1		MGI:3036453	Slc12a1<sup>tm1Tkh</sup>/Slc12a1<sup>tm1Tkh</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10779555	20131223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:9736651	20070509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675737	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19185848	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620501	Gnao1<sup>tm2.1Rneu</sup>	is_implicated_in	DOID:0080450	developmental and epileptic encephalopathy 17		MGI:5620503	Gnao1<sup>tm2.1Rneu</sup>/Gnao1<sup>+</sup>  [background:] B6.129S-Gnao1<sup>tm2.1Rneu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24700286	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5790694	Glra1<sup>spd-ot9J</sup>	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:5790702	Glra1<sup>spd-ot9J</sup>/Glra1<sup>spd-ot9J</sup>  [background:] B6.Cg-Glra1<sup>spd-ot9J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5790609	20160907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5647918	Tg(Tff3-Tmem207)1Tamo	is_implicated_in	DOID:2433	epidermal appendage tumor		MGI:5647920	Tg(Tff3-Tmem207)1Tamo/0  [background:] C57BL/6-Tg(Tff3-Tmem207)1Tamo			ECO:0000033	author statement supported by traceable reference	PMID:25305140	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949272	Grid2<sup>tm1(cre)Mwa</sup>	is_implicated_in	DOID:0080042	autosomal recessive spinocerebellar ataxia 18		MGI:4949279	Grid2<sup>tm1(cre)Mwa</sup>/Grid2<sup>tm1(cre)Mwa</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24078737	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:16497528	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:28842642	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:25298037	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:21076027	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:9660052	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:25410057	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:26427607	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:26710715	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:28171706	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:18022143	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:19903883	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:17920451	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:3839661	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] B6.129-Idua<sup>tm1Clk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18022143	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:3587410	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9097952	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176236	Idua<sup>tm1Clk</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:3587410	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9660052	20180209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286246	Tg(Prnp-MAPT*P301S)50Hiw	is_implicated_in	DOID:680	tauopathy		MGI:6286248	Tg(Prnp-MAPT*P301S)50Hiw/0  [background:] B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw			ECO:0000033	author statement supported by traceable reference	PMID:24406748	20190405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653766	Ass1<sup>tm1Bay</sup>/Ass1<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:8197477	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6477377	Trp63<sup>tm3Aam</sup>	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:6477390	Trp63<sup>tm3Aam</sup>/Trp63<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:23775923	20201203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258950	Cfap43<sup>em2Fzh</sup>	is_implicated_in	DOID:0070170	spermatogenic failure 19		MGI:6258953	Cfap43<sup>em2Fzh</sup>/Cfap43<sup>em2Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603012	Gck<sup>tm1.1Mgn</sup>/Gck<sup>+</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437102	Slit2<sup>b2b1200.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824730	Dlg3<sup>tm1Grnt</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:27466188	20170221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285080	Dnai1<sup>b2b284Clo</sup>	is_implicated_in	DOID:0110594	primary ciliary dyskinesia 1		MGI:5285345	Dnai1<sup>b2b284Clo</sup>/Dnai1<sup>b2b284Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20110926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659881	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.2Rdp</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:3908	lung non-small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17676035	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3704920	Dbt<sup>tm1Geh</sup>/Dbt<sup>tm1Geh</sup> Tg(tetO-DBT)525AGeh/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB * NMRI	is_model_of	DOID:9269	maple syrup urine disease						ECO:0000033	author statement supported by traceable reference	PMID:16579849	20070426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385353	Hfe<sup>tm2Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23705020	20131025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385353	Hfe<sup>tm2Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23223430	20131025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385353	Hfe<sup>tm2Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655482	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20131025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385353	Hfe<sup>tm2Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655506	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20131025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385353	Hfe<sup>tm2Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655482	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10791995	20131025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285394	Shank3<sup>tm1.2Bux</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23583105	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285394	Shank3<sup>tm1.2Bux</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285394	Shank3<sup>tm1.2Bux</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5285395	Shank3<sup>tm1.2Bux</sup>/Shank3<sup>+</sup>  [background:] C57BL/6-Shank3<sup>tm1.2Bux</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21167025	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285394	Shank3<sup>tm1.2Bux</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2671158	Tg(HD82Gln)81Gschi/0  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9949199	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6431098	Rcbtb2<sup>tm1.1Xyw</sup>	is_implicated_in	DOID:2570	malignant histiocytic disease		MGI:6431136	Rcbtb2<sup>tm1.1Xyw</sup>/Rcbtb2<sup>tm1.1Xyw</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26291700	20200602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6431098	Rcbtb2<sup>tm1.1Xyw</sup>	is_implicated_in	DOID:2570	malignant histiocytic disease		MGI:6431137	Rcbtb2<sup>tm1.1Xyw</sup>/Rcbtb2<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26291700	20200602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613056	Wfs1<sup>tm1Perm</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:25422446	20150220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613056	Wfs1<sup>tm1Perm</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:3614209	Wfs1<sup>tm1Perm</sup>/Wfs1<sup>tm1Perm</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:16215705	20150220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830993	Del(7Gabrb3-Ube3a)1Yhj/+  [background:] B6.129S7-Del(7Gabrb3-Ube3a)1Yhj	is_model_of	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20808828	20150701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763921	Tg(HSA*LR)32aCath/?  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648533	Gt(ROSA)26Sor<sup>tm1(rtTA,EGFP)Nagy</sup>/Gt(ROSA)26Sor<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup> Tg(tetO-Kras*G12D)#Rdp/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22541435	20150814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438921	Srr<sup>tm1.2Jtc</sup>/Srr<sup>tm1.2Jtc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19065142	20100407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304754	Col1a1<sup>tm1(tetO-RNAi:Rps19)Karl</sup>	is_implicated_in	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:25987256	20160519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843212	Tg(Thy1-APPSw)10Jiri	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23273572	20190604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843212	Tg(Thy1-APPSw)10Jiri	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4843219	Tg(Thy1-APPSw)10Jiri/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14596862	20190604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843212	Tg(Thy1-APPSw)10Jiri	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20600435	20190604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843212	Tg(Thy1-APPSw)10Jiri	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22863679	20190604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7278809	Optn<sup>em1Hyua</sup>	is_implicated_in	DOID:13544	low tension glaucoma		MGI:7279070	Optn<sup>em1Hyua</sup>/Optn<sup>em1Hyua</sup>  [background:] C57BL/6J-Optn<sup>em1Hyua</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33723228	20231003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7278809	Optn<sup>em1Hyua</sup>	is_implicated_in	DOID:13544	low tension glaucoma		MGI:7279070	Optn<sup>em1Hyua</sup>/Optn<sup>em1Hyua</sup>  [background:] C57BL/6J-Optn<sup>em1Hyua</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35436991	20231003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574061	Tg(Stat3*)9199Alau/0  [background:] involves: C57BL/6	is_model_of	DOID:3261	hyper IgE recurrent infection syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24632714	20140721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625122	Ids<sup>tm1Muen</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:28334757	20180914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625122	Ids<sup>tm1Muen</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:17876721	20180914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625122	Ids<sup>tm1Muen</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:6198013	Ids<sup>tm1Muen</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17876721	20180914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625122	Ids<sup>tm1Muen</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:3625957	Ids<sup>tm1Muen</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16505002	20180914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625122	Ids<sup>tm1Muen</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:3625957	Ids<sup>tm1Muen</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12572850	20180914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433294	b2b1519Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433295	b2b1519Clo/b2b1519Clo  [background:] C57BL/6J-b2b1519Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829878	Nfkbia<sup>tm1.1Pjc</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4829879	Nfkbia<sup>tm1.1Pjc</sup>/Nfkbia<sup>tm1.1Pjc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20696914	20100917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6163634	Dmd<sup>em1Eno</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6163637	Dmd<sup>em1Eno</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29187645	20180628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6474168	Cln3<sup>em1Dprc</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:6474170	Cln3<sup>em1Dprc</sup>/Cln3<sup>em1Dprc</sup>  [background:] C57BL/6-Cln3<sup>em1Dprc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32601357	20201130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713764	Sumf1<sup>Gt(RST760)Byg</sup>/Sumf1<sup>Gt(RST760)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050441	mucosulfatidosis						ECO:0000033	author statement supported by traceable reference	PMID:17360554	20070705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5750594	Tg(CMV-cre)1Cgn/0 Trp53<sup>tm4Att</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/cJ * C57BL/6J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25119037	20160229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5897172	Tg(CAG-Ppard*E411P)#Als	is_implicated_in	DOID:12858	Huntington's disease		MGI:5897176	Tg(CAG-Ppard*E411P)#Als/0 Tg(Nes-cre)1Kln/0  [background:] B6J.Cg-Tg(Nes-cre)1Kln Tg(CAG-Ppard*E411P)#Als			ECO:0000033	author statement supported by traceable reference	PMID:26642438	20170511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312923	Nhlrc1<sup>tm1Bmin</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:28063983	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312923	Nhlrc1<sup>tm1Bmin</sup>	is_implicated_in	DOID:3534	Lafora disease		MGI:5313256	Nhlrc1<sup>tm1Bmin</sup>/Nhlrc1<sup>tm1Bmin</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:21077101	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312923	Nhlrc1<sup>tm1Bmin</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:27107699	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312923	Nhlrc1<sup>tm1Bmin</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:23663739	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312923	Nhlrc1<sup>tm1Bmin</sup>	is_implicated_in	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:28536304	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158456	Akt2<sup>tm1.1Mbb</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24622975	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158456	Akt2<sup>tm1.1Mbb</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25740694	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158456	Akt2<sup>tm1.1Mbb</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:20728450	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158456	Akt2<sup>tm1.1Mbb</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3629188	Akt2<sup>tm1.1Mbb</sup>/Akt2<sup>tm1.1Mbb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11387480	20181217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681526	Fbln5<sup>tm1Eno</sup>/Fbln5<sup>tm1Eno</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:3144	cutis laxa						ECO:0000033	author statement supported by traceable reference	PMID:11805834	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896637	Hba<sup>tm1(HBA)Tow</sup>/Hba<sup>tm1(HBA)Tow</sup> Hbb<sup>tm2(HBG1,HBB*)Tow</sup>/Hbb<sup>tm2(HBG1,HBB*)Tow</sup> Slc12a4<sup>Rbc10</sup>/Slc12a4<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6J	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26450986	20170504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840234	Kdm3a<sup>tm1.1Yzha</sup>/Kdm3a<sup>tm1.1Yzha</sup>  [background:] B6.129P2-Kdm3a<sup>tm1.1Yzha</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:19194461	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856108	Foxn1<sup>nu</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:7604876	20131122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856108	Foxn1<sup>nu</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23091413	20131122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856108	Foxn1<sup>nu</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22474479	20131122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856108	Foxn1<sup>nu</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:2680668	Foxn1<sup>nu</sup>/Foxn1<sup>nu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:4547146	20131122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575755	Tg(KRT5-tTA)1216Glk	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:22418873	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575755	Tg(KRT5-tTA)1216Glk	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:21471984	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2660658	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:15386278	20060523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5691394	Hap1<sup>tm2Xjl</sup>/Hap1<sup>tm2Xjl</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129 * C57BL/6 * CBA	is_model_of	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:25875952	20151015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946396	Selenon<sup>tm1.2Mred</sup>	is_implicated_in	DOID:0110633	rigid spine muscular dystrophy 1		MGI:5298009	Selenon<sup>tm1.2Mred</sup>/Selenon<sup>tm1.2Mred</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21858002	20111212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152376	Nrl<sup>tm1Asw</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:24671090	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152376	Nrl<sup>tm1Asw</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:30332642	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177177	Fxn<sup>tm2.1Mkn</sup>	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:23169664	20130219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447704	Pmp22<sup>tm1Ueli</sup>	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies						ECO:0000033	author statement supported by traceable reference	PMID:29315582	20180516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447704	Pmp22<sup>tm1Ueli</sup>	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies		MGI:3794447	Pmp22<sup>tm1Ueli</sup>/Pmp22<sup>tm1Ueli</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:7581450	20180516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:25595737	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:8997	polycythemia vera		MGI:5553472	Tg(JAK2*V617F)FF1Rsko/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18160670	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:27401344	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:25339357	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429212	Fzd3<sup>tm1(FZD3)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429559	Fzd3<sup>tm1(FZD3)Lex</sup>/Fzd3<sup>tm1(FZD3)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27378338	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25803479	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26300749	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25852455	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25879444	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17559418	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857070	Itpr3<sup>tf</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18728777	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668611	Slc45a2<sup>uw</sup>/Slc45a2<sup>uw</sup>  [background:] C57BL/6J-Slc45a2<sup>uw</sup>/J	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2180831	Zic3<sup>tm1Bca</sup>/Y  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6390206	Pex1<sup>tm1.1Hrw</sup>	is_implicated_in	DOID:905	Zellweger syndrome		MGI:6390207	Pex1<sup>tm1.1Hrw</sup>/Pex1<sup>tm1.1Hrw</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31207289	20200217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197466	Tg(APCS-Tnfsf11*)#aKhs	is_implicated_in	DOID:11476	osteoporosis		MGI:6197473	Tg(APCS-Tnfsf11*)#aKhs/0  [background:] C57BL/6J-Tg(APCS-Tnfsf11*)#aKhs			ECO:0000033	author statement supported by traceable reference	PMID:12434161	20180911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5499734	Myh9<sup>tm1.1(MYH9*)Mjk</sup>/Myh9<sup>+</sup>  [background:] B6.Cg-Myh9<sup>tm1.1(MYH9*)Mjk</sup>	is_model_of	DOID:0060651	MYH-9 related disease						ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5489760	Gja8<sup>R205G</sup>/Gja8<sup>R205G</sup>  [background:] B6.Cg-Gja8<sup>R205G</sup>	is_model_of	DOID:0110231	cataract 1 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:23300808	20130610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926253	Chrnb2<sup>tm1Jpc</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926253	Chrnb2<sup>tm1Jpc</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5318689	Chrnb2<sup>tm1Jpc</sup>/Chrnb2<sup>tm1Jpc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12876201	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438033	Tg(tetO-CUGBP1)3413Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:23901116	20140106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438033	Tg(tetO-CUGBP1)3413Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:4438035	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-CUGBP1)3413Coop/0  [background:] involves: FVB * FVB/N * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:20051426	20140106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476821	Tg(TARDBP)#Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23238732	20131021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:1247	blood coagulation disease		MGI:5558876	Tg(JAK2*V617F)FF1Rsko/0 Tg(Tek-cre)1Arnd/0  [background:] involves: C57BL/6 * CBA * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:24469804	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416441	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:33370388	20210924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416441	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:6416454	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>/Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:28230213	20210924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416441	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:6416462	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:28230213	20210924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416441	Fgfr3<sup>tm1.1(FGFR3*)Ytc</sup>	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:33784257	20210924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6315233	Npc1<sup>tm1Tacf</sup>	is_implicated_in	DOID:0070113	Niemann-Pick disease type C1		MGI:6359477	Npc1<sup>tm1Tacf</sup>/Npc1<sup>tm1Tacf</sup>  [background:] B6(Cg)-Npc1<sup>tm1Tacf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28167839	20190911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402828	Tg(CAG-ACE2)AC70Ctkt	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19297479	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402828	Tg(CAG-ACE2)AC70Ctkt	is_implicated_in	DOID:2945	severe acute respiratory syndrome		MGI:6402832	Tg(CAG-ACE2)AC70Ctkt/0  [background:] either: (involves: BALB/c * C3H/HeJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6 * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17108019	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402828	Tg(CAG-ACE2)AC70Ctkt	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32498696	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402828	Tg(CAG-ACE2)AC70Ctkt	is_implicated_in	DOID:2945	severe acute respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26184451	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867517	Tg(CAG-ELN*)60Zu	is_implicated_in	DOID:3144	cutis laxa		MGI:4867519	Tg(CAG-ELN*)60Zu/0  [background:] C57BL/6J-Tg(CAG-ELN*)60Zu			ECO:0000033	author statement supported by traceable reference	PMID:20600892	20110111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619460	Fbn1<sup>tm2Rmz</sup>/Fbn1<sup>tm2Rmz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10097121	20060414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:31306463	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:25695521	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28428273	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28493878	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23348745	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28249898	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23624841	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23687346	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:25411967	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:27207648	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23575960	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26645563	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23873027	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:24018560	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22052531	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23131993	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26723876	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:24549646	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:27207661	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26107383	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:24509905	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:27872095	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28162974	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23423848	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28346424	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:25797291	20220121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384595	Tg(TRAMP)8247Ng	is_implicated_in	DOID:10283	prostate cancer		MGI:3718580	Tg(TRAMP)8247Ng/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7724580	20220121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2182801	Smad4<sup>tm1Mmt</sup>/Smad4<sup>+</sup>  [background:] B6.129S2-Smad4<sup>tm1Mmt</sup>	is_model_of	DOID:0050787	juvenile polyposis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10626800	20071105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174906	Col11a1<sup>cho</sup>/Col11a1<sup>cho</sup>  [background:] involves: C57BL/6Fr	is_model_of	DOID:0080046	Stickler syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7859283	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5548208	Tg(Vav1-ERG)#Jpim/0  [background:] involves: C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23974202	20140312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5486142	Tg(Camk2a-DISC1)37Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)37Asaw	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23314019	20130524	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5486142	Tg(Camk2a-DISC1)37Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)37Asaw	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17675407	20130524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055492	Bbs4<sup>Gt1Nk</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:31479441	20191107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055492	Bbs4<sup>Gt1Nk</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:6370045	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] B6.129S7-Bbs4<sup>Gt1Nk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31479441	20191107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055492	Bbs4<sup>Gt1Nk</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3608977	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16794820	20191107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055492	Bbs4<sup>Gt1Nk</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3055585	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20191107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766122	Timo/Timo  [background:] either: B6.Cg-Timo or (involves: C57BL/6J * CBA/CaJ)	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:17652166	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:12697734	20051104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:9637677	20051104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856898	Atcay<sup>ji-hes</sup>	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:23226316	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856898	Atcay<sup>ji-hes</sup>	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia		MGI:3719706	Atcay<sup>ji-hes</sup>/Atcay<sup>ji-hes</sup>  [background:] C3H/HeJ-Atcay<sup>ji-hes</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4034281	Hgsnat<sup>Gt(IST11912G1)Tigm</sup>	is_implicated_in	DOID:0111393	mucopolysaccharidosis type IIIC						ECO:0000033	author statement supported by traceable reference	PMID:36858249	20231108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158503	Bmpr2<sup>tm1Kmi</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22371328	20130726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158503	Bmpr2<sup>tm1Kmi</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5438770	Bmpr2<sup>tm1Kmi</sup>/Bmpr2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16027259	20130726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620629	Dhcr7<sup>tm1Gst</sup>/Dhcr7<sup>tm1Gst</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11560960	20060428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570647	Tg(Slc1a2-tTA)#Waw	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24107773	20140701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506271	Uox<sup>em1Cli</sup>	is_implicated_in	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:35276331	20230629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506271	Uox<sup>em1Cli</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:6506273	Uox<sup>em1Cli</sup>/Uox<sup>em1Cli</sup>  [background:] C57BL/6J-Uox<sup>em1Cli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28729031	20230629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506271	Uox<sup>em1Cli</sup>	is_implicated_in	DOID:1920	hyperuricemia						ECO:0000033	author statement supported by traceable reference	PMID:30690853	20230629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576605	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:7581451	20050511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5645262	Zfp366<sup>b2b2834Clo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5645264	Zfp366<sup>b2b2834Clo</sup>/Zfp366<sup>b2b2834Clo</sup>  [background:] C57BL/6J-Zfp366<sup>b2b2834Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6781911	Scn2a<sup>em1Gsp</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6783448	Scn2a<sup>em1Gsp</sup>/Scn2a<sup>+</sup>  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:34156984	20211029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441546	Tg(Ins2-Tag*,-flpe)#Gne	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5441548	Tg(Ins2-Tag*,-flpe)#Gne/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20554752	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441546	Tg(Ins2-Tag*,-flpe)#Gne	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5441547	Tg(Ins2-Tag*,-flpe)#Gne/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22611036	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560911	Cplane2<sup>b2b2827Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561553	Cplane2<sup>b2b2827Clo</sup>/Cplane2<sup>b2b2827Clo</sup>  [background:] C57BL/6J-Cplane2<sup>b2b2827Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808750	Tk2<sup>tm1Mihi</sup>	is_implicated_in	DOID:0080120	mitochondrial DNA depletion syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:24968719	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808750	Tk2<sup>tm1Mihi</sup>	is_implicated_in	DOID:0080120	mitochondrial DNA depletion syndrome 2		MGI:3808758	Tk2<sup>tm1Mihi</sup>/Tk2<sup>tm1Mihi</sup>  [background:] involves: 129S6/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20940150	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808750	Tk2<sup>tm1Mihi</sup>	is_implicated_in	DOID:0080120	mitochondrial DNA depletion syndrome 2		MGI:3808758	Tk2<sup>tm1Mihi</sup>/Tk2<sup>tm1Mihi</sup>  [background:] involves: 129S6/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18467430	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831201	Pten<sup>tm1Rdp</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28321130	20171120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831201	Pten<sup>tm1Rdp</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20171120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7513830	Ank2<sup>em1Melr</sup>	is_implicated_in	DOID:0111700	ankyrin-B-related cardiac arrhythmia		MGI:7514498	Ank2<sup>em1Melr</sup>/Ank2<sup>em1Melr</sup>  [background:] B6.Cg-Ank2<sup>em1Melr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37182735	20230804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459448	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20406986	20100713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530740	Ppp3r1<sup>tm1Stl</sup>/Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl/0  [background:] C57BL/6-Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:11733061	20070514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530740	Ppp3r1<sup>tm1Stl</sup>/Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl/0  [background:] C57BL/6-Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:12851457	20070514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042272	Gh<sup>Sma1</sup>/Gh<sup>Sma1</sup>  [background:] C3HeB/FeJ-Gh<sup>Sma1</sup>	is_model_of	DOID:0060872	isolated growth hormone deficiency type II						ECO:0000033	author statement supported by traceable reference	PMID:14726450	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698401	Sh3bp2<sup>tm1Bjro</sup>	is_implicated_in	DOID:1856	cherubism						ECO:0000033	author statement supported by traceable reference	PMID:20691350	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698401	Sh3bp2<sup>tm1Bjro</sup>	is_implicated_in	DOID:1856	cherubism						ECO:0000033	author statement supported by traceable reference	PMID:25220465	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698401	Sh3bp2<sup>tm1Bjro</sup>	is_implicated_in	DOID:1856	cherubism		MGI:3699094	Sh3bp2<sup>tm1Bjro</sup>/Sh3bp2<sup>tm1Bjro</sup>  [background:] involves: 129S4/SvJae * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17218256	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6193913	Tg(Myh6-Prkaca)2Eno	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6193917	Tg(Myh6-Prkaca)2Eno/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11717156	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437686	Tg(SERPINC1-SV40)A1Pbr	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437688	Tg(SERPINC1-SV40)A1Pbr/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:1660504	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437686	Tg(SERPINC1-SV40)A1Pbr	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437689	Tg(SERPINC1-SV40)A1Pbr/Tg(SERPINC1-SV40)A1Pbr  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:1660504	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521182	Slc6a4<sup>tm2.1Rbl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6316332	Slc6a4<sup>tm2.1Rbl</sup>/Slc6a4<sup>tm2.1Rbl</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:27111230	20190708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521182	Slc6a4<sup>tm2.1Rbl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6316332	Slc6a4<sup>tm2.1Rbl</sup>/Slc6a4<sup>tm2.1Rbl</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:22431635	20190708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:26505994	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:5646304	Tg(CMV-ATXN3*135Q)CPama/0  [background:] C57BL/6-Tg(CMV-ATXN3*135Q)CPama			ECO:0000033	author statement supported by traceable reference	PMID:24477711	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:26601773	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:28448548	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:27717809	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:25633985	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646300	Tg(CMV-ATXN3*135Q)CPama	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:28624196	20220913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834525	Aspm<sup>Gt(AJ0069)Wtsi</sup>/Aspm<sup>Gt(AJ0069)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:20823249	20101011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317863	Tg(tetO/CMV-Tslp)#Sfz	is_implicated_in	DOID:718	autoimmune hemolytic anemia		MGI:5317912	Tg(KRT5-rtTA)1Glk/0 Tg(tetO/CMV-Tslp)#Sfz/0  [background:] C.Cg-Tg(KRT5-rtTA)1Glk Tg(tetO/CMV-Tslp)#Sfz			ECO:0000033	author statement supported by traceable reference	PMID:22281511	20120510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766948	Del(16Dgcr2-Hira)3Aam/+  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18836441	20160510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045972	Aga<sup>tm1Vk</sup>/Aga<sup>tm1Vk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:0050461	aspartylglucosaminuria						ECO:0000033	author statement supported by traceable reference	PMID:8946839	20050526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905765	Tg(Myh6-Rest*)474Ysai	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19687356	20170818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905765	Tg(Myh6-Rest*)474Ysai	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905766	Tg(Myh6-Rest*)474Ysai/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14633990	20170818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905765	Tg(Myh6-Rest*)474Ysai	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25100767	20170818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905765	Tg(Myh6-Rest*)474Ysai	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19346456	20170818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6444679	Ikbkb<sup>em1Macc</sup>	is_implicated_in	DOID:0111960	immunodeficiency 15A		MGI:6444680	Ikbkb<sup>em1Macc</sup>/Ikbkb<sup>em1Macc</sup>  [background:] involves: C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:30337470	20210120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6444679	Ikbkb<sup>em1Macc</sup>	is_implicated_in	DOID:0111960	immunodeficiency 15A		MGI:6444681	Ikbkb<sup>em1Macc</sup>/Ikbkb<sup>+</sup>  [background:] involves: C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:30337470	20210120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317077	Tg(tetO-ATXN1*82Q)#Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1		MGI:5317102	Tg(Pcp2-tTA)3Horr/0 Tg(tetO-ATXN1*82Q)#Horr/Tg(tetO-ATXN1*82Q)#Horr  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15470152	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317077	Tg(tetO-ATXN1*82Q)#Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:28979190	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317077	Tg(tetO-ATXN1*82Q)#Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:27147646	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317077	Tg(tetO-ATXN1*82Q)#Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:33436887	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317077	Tg(tetO-ATXN1*82Q)#Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:21963649	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294807	Cdh5<sup>tm1Dvst</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:7467143	Cdh5<sup>tm1Dvst</sup>/Cdh5<sup>tm1Dvst</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3639517	Tg(Myh6-Acsl1)O7Jesc	is_implicated_in	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:16603124	20170822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3639517	Tg(Myh6-Acsl1)O7Jesc	is_implicated_in	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:15347805	20170822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3639517	Tg(Myh6-Acsl1)O7Jesc	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:3639520	Tg(Myh6-Acsl1)O7Jesc/0  [background:] FVB/N-Tg(Myh6-Acsl1)O7Jesc			ECO:0000033	author statement supported by traceable reference	PMID:11285300	20170822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655257	Col3a1<sup>Tsk2</sup>/Col3a1<sup>+</sup>  [background:] C3H101H-Col3a1<sup>Tsk2</sup>/H	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:8849351	20160420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7493416	Foxi3<sup>em1Ybz</sup>	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:7493642	Foxi3<sup>em1Ybz</sup>/Foxi3<sup>em1Ybz</sup>  [background:] C57BL/6-Foxi3<sup>em1Ybz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37041148	20230628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397677	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] FVB.129-Kcnq3<sup>tm1.1Naas</sup>	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7509517	Csrp3<sup>tm1.1Kage</sup>	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:7509544	Csrp3<sup>tm1.1Kage</sup>/Csrp3<sup>tm1.1Kage</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:30048712	20230719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175037	Gabrb3<sup>tm1Geh</sup>/Gabrb3<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:17983671	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614946	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] multiple strains	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:7416238	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6357166	Mir199a-2<sup>tm1Kinn</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:6357214	Mir199a-2<sup>tm1Kinn</sup>/Mir199a-2<sup>tm1Kinn</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:26344767	20190827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5310727	Mecp2<sup>tm1.1Joez</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5310735	Mecp2<sup>tm1.1Joez</sup>/Y  [background:] B6.129-Mecp2<sup>tm1.1Joez</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22119903	20181227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5310727	Mecp2<sup>tm1.1Joez</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28394263	20181227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6828598	Zfp804a<sup>em1Yqd</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6828730	Zfp804a<sup>em1Yqd</sup>/Zfp804a<sup>em1Yqd</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:33303946	20211201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603464	Fgfr2<sup>tm1Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:24632501	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603464	Fgfr2<sup>tm1Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:24580805	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603464	Fgfr2<sup>tm1Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:3604025	Fgfr2<sup>tm1Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20077479	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603464	Fgfr2<sup>tm1Ewj</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:3604025	Fgfr2<sup>tm1Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15975938	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:26216423	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:22848611	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:23874435	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:25907690	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:18829978	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:28002460	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:21841819	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2665845	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8402911	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3759844	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] B6.129P2-Il10<sup>tm1Cgn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17617560	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2665845	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8770874	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857199	Il10<sup>tm1Cgn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3759844	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] B6.129P2-Il10<sup>tm1Cgn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17574631	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5141088	Tg(NEFL*E397K)#Milg	is_implicated_in	DOID:0110165	Charcot-Marie-Tooth disease type 2E						ECO:0000033	author statement supported by traceable reference	PMID:26423936	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5141088	Tg(NEFL*E397K)#Milg	is_implicated_in	DOID:0110165	Charcot-Marie-Tooth disease type 2E		MGI:5141091	Tg(NEFL*E397K)#Milg/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21493625	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5141088	Tg(NEFL*E397K)#Milg	is_implicated_in	DOID:0110165	Charcot-Marie-Tooth disease type 2E						ECO:0000033	author statement supported by traceable reference	PMID:22288874	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:20570219	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:26283735	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:25114233	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:26092868	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:25680200	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:27035618	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:5445420	Cftr<sup>tm1Eur</sup>/Cftr<sup>tm1Eur</sup>  [background:] B6.129P2-Cftr<sup>tm1Eur</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22711878	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857899	Cftr<sup>tm1Eur</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:5445419	Cftr<sup>tm1Eur</sup>/Cftr<sup>tm1Eur</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:7556083	20180402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6370001	Phf8<sup>tm1.1Cdcn</sup>	is_implicated_in	DOID:0060812	syndromic X-linked intellectual disability Siderius type		MGI:6370003	Phf8<sup>tm1.1Cdcn</sup>/Y  [background:] B6.129S6(Cg)-Phf8<sup>tm1.1Cdcn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29317619	20191107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767672	Bbs1<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:33886537	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767672	Bbs1<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:31479441	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767672	Bbs1<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23160237	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767672	Bbs1<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1		MGI:3767679	Bbs1<sup>tm1Vcs</sup>/Bbs1<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18032602	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618818	Dnah5<sup>b2b2925Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584122	Crygs<sup>Opj</sup>/Crygs<sup>Opj</sup>  [background:] involves: 102 * C3H/He * T STOCK	is_model_of	DOID:0110240	cataract 20 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:8812411	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584122	Crygs<sup>Opj</sup>/Crygs<sup>Opj</sup>  [background:] involves: 102 * C3H/He * T STOCK	is_model_of	DOID:0110240	cataract 20 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11121426	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654422	Mybpc3<sup>tm1.1Jse</sup>/Mybpc3<sup>tm1.1Jse</sup>  [background:] Not Specified	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:10545522	20060609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716208	Rpgrip1l<sup>tm1Urt</sup>	is_implicated_in	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26071364	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716208	Rpgrip1l<sup>tm1Urt</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:3716631	Rpgrip1l<sup>tm1Urt</sup>/Rpgrip1l<sup>tm1Urt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17558409	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661474	Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt	is_implicated_in	DOID:417	autoimmune disease		MGI:5661482	Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25182415	20150911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512911	Tpp1<sup>m1J</sup>/Tpp1<sup>m1J</sup>  [background:] STOCK Tpp1<sup>m1J</sup>/GrsrJ	is_model_of	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000033	author statement supported by traceable reference	MGI:5511005	20131017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4460267	Msh2<sup>tm2.1Rak</sup>/Msh2<sup>tm3.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * C57BL/6 * DBA/2 * SJL	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19931261	20111104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840003	Fgfr3<sup>tm1Llm</sup>	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:24419316	20140627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840003	Fgfr3<sup>tm1Llm</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:5551435	Fgfr3<sup>tm1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:23200862	20140627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3758489	Ophn1<sup>tm1Bill</sup>/Y  [background:] involves: 129S2/SvPas	is_model_of	DOID:0050888	syndromic intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:17728457	20090714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905048	Tg(Myh6-Gnaq*Q209L)44Ejne	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18466775	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905048	Tg(Myh6-Gnaq*Q209L)44Ejne	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18674539	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905048	Tg(Myh6-Gnaq*Q209L)44Ejne	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905050	Tg(Myh6-Gnaq*Q209L)44Ejne/Tg(Myh6-Gnaq*Q209L)44Ejne  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:11448136	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905048	Tg(Myh6-Gnaq*Q209L)44Ejne	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905051	Tg(Myh6-Gnaq*Q209L)44Ejne/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:11448136	20170816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046796	Tbx1<sup>tm2Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778685	Gata4<sup>tm1.1Sad</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:27565037	20180118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4462383	Ecel1<sup>tm1Hiki</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6160055	Ecel1<sup>tm1Hiki</sup>/Ecel1<sup>tm1Hiki</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26951213	20180608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679886	Pten<sup>tm2.1Ppp</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:28433543	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679886	Pten<sup>tm2.1Ppp</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:27341128	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796264	Fan1<sup>tm1d(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060911	karyomegalic interstitial nephritis		MGI:5897864	Fan1<sup>tm1d(KOMP)Wtsi</sup>/Fan1<sup>tm1d(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26980189	20170523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149910	Golgb1<sup>em8Lanyu</sup>	is_implicated_in	DOID:674	cleft palate		MGI:6151466	Golgb1<sup>em8Lanyu</sup>/Golgb1<sup>em8Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655191	Tlx2<sup>tm1Sjk</sup>/Tlx2<sup>tm1Sjk</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0080072	intestinal pseudo-obstruction						ECO:0000033	author statement supported by traceable reference	PMID:9176491	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554185	Tg(tetO-MAPT*K280,-luc)#Eman	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5554193	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-MAPT*K280,-luc)#Eman/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21325519	20140402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554185	Tg(tetO-MAPT*K280,-luc)#Eman	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23158765	20140402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554185	Tg(tetO-MAPT*K280,-luc)#Eman	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5554193	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-MAPT*K280,-luc)#Eman/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18199773	20140402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714532	Dp(16Lipi-Zbtb21)1Yey/0  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:17412756	20101001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136268	Pitx2<sup>tm1Jfm</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:12015277	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136268	Pitx2<sup>tm1Jfm</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:23975681	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136268	Pitx2<sup>tm1Jfm</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2172351	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm1Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:14623826	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136268	Pitx2<sup>tm1Jfm</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2172351	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm1Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:10499585	20190503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175162	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6N	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175162	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6N	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17183066	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28802916	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23326437	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27552480	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:31034974	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24361736	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23382922	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25852545	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27312772	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28242605	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28628896	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26365177	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22959727	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747948	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3665287	Tg(PRNP-APPSweInd)8Dwst/?  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:16899370	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589475	Tg(PRNP-APPSweInd)8Dwst	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3722160	Tg(PRNP-APPSweInd)8Dwst/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20682779	20200131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009551	Tg(Th-MYCN)41Waw/0  [background:] involves: BALB/c * C57BL/6J * FVB/N	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18842883	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3528946	Ap3d1<sup>mh</sup>/Ap3d1<sup>mh</sup>  [background:] B6.C3-Grxcr1<sup>pi</sup>	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521545	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CD-1	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942392	Ift80<sup>Gt(AN0245)Wtsi</sup>/Ift80<sup>Gt(AN0245)Wtsi</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0110087	asphyxiating thoracic dystrophy 3						ECO:0000033	author statement supported by traceable reference	PMID:21227999	20140216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622113	Jup<sup>tm1Kem</sup>/Jup<sup>tm1Kem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:4603	epidermolytic hyperkeratosis						ECO:0000033	author statement supported by traceable reference	PMID:8954745	20060512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653501	Gata1<sup>tm2Sho</sup>/Gata1<sup>tm2Sho</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:12149188	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680324	Gba1<sup>tm3Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21257328	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680324	Gba1<sup>tm3Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:23520473	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680324	Gba1<sup>tm3Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:26312487	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680324	Gba1<sup>tm3Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:22167193	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680324	Gba1<sup>tm3Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680502	Gba1<sup>tm3Ggb</sup>/Gba1<sup>tm3Ggb</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512701	Tg(tetO-SNCA)0Olri	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22814000	20131015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512701	Tg(tetO-SNCA)0Olri	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5512702	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA)0Olri/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18322092	20131015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513373	Plec<sup>tm2Gwi</sup>/Plec<sup>tm2Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060736	epidermolysis bullosa simplex Ogna type						ECO:0000033	author statement supported by traceable reference	PMID:9389647	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834850	Cp<sup>tm1Yos</sup>/Cp<sup>tm1Yos</sup>  [background:] C.129P2-Cp<sup>tm1Yos</sup>	is_model_of	DOID:0050711	aceruloplasminemia						ECO:0000033	author statement supported by traceable reference	PMID:18804145	20090309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:25339357	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:27401344	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:25595737	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553468	Tg(JAK2*V617F)FF1Rsko	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:5553469	Tg(JAK2*V617F)FF1Rsko/0 Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:18160670	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5812299	Snap29<sup>tm1b(EUCOMM)Wtsi</sup>/Snap29<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:0060337	CEDNIK syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26747696	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028926	Spg7<sup>tm1Eir</sup>/Spg7<sup>tm1Eir</sup>  [background:] either: 129/Sv-Spg7<sup>tm1Eir</sup> or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0110816	hereditary spastic paraplegia 7						ECO:0000033	author statement supported by traceable reference	PMID:14722615	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790755	Hba<sup>tm1(HBA)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26330244	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790755	Hba<sup>tm1(HBA)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:32533970	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790755	Hba<sup>tm1(HBA)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:35969769	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790755	Hba<sup>tm1(HBA)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:32817286	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790755	Hba<sup>tm1(HBA)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:25931013	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790755	Hba<sup>tm1(HBA)Tow</sup>	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:22661702	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444670	Gt(ROSA)26Sor<sup>tm13(CAG-MYC,-CD2*)Rsky</sup>	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22897848	20130214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506458	Gt(ROSA)26Sor<sup>tm1.1(Alb-PCSK9)Mby</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:6506468	Gt(ROSA)26Sor<sup>tm1.1(Alb-PCSK9)Mby</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30646909	20210216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3654648	Ubr1<sup>tm1Avar</sup>/Ubr1<sup>tm1Avar</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:14694	Johanson-Blizzard syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16311597	20100309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936849	Itm2b<sup>tm2.1Ldad</sup>/Itm2b<sup>+</sup>  [background:] B6.129-Itm2b<sup>tm2.1Ldad</sup>	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21098268	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7262690	Tg(KRT18*R89C)30Rgo	is_implicated_in	DOID:2237	hepatitis		MGI:7262709	Tg(KRT18*R89C)30Rgo/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8522591	20220419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25176624	20230505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:36611809	20230505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:10713685	20230505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25195861	20230505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20230505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:1612	breast cancer		MGI:3835423	Tg(C3-1-TAg)cJeg/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:7972041	20230505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7339258	Rreb1<sup>em1Rtpl</sup>	is_implicated_in	DOID:0080690	RASopathy		MGI:7339281	Rreb1<sup>em1Rtpl</sup>/Rreb1<sup>+</sup>  [background:] C57BL/6J-Rreb1<sup>em1Rtpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32938917	20220926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660416	Dsp<sup>tm1Efu</sup>/Dsp<sup>tm1Efu</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129 * 129S4/SvJae * C57BL/6	is_model_of	DOID:0110076	arrhythmogenic right ventricular dysplasia 8						ECO:0000033	author statement supported by traceable reference	PMID:24108106	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848937	Tg(Pcp2-FMR1*)1Dln	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24108107	20140305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848937	Tg(Pcp2-FMR1*)1Dln	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome		MGI:3848946	Tg(Pcp2-FMR1*)1Dln/0  [background:] C57BL/6-Tg(Pcp2-Fmr1*)1Dln			ECO:0000033	author statement supported by traceable reference	PMID:19377084	20140305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295045	Ppp1r13l<sup>tm1.1Xlu</sup>	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy		MGI:5910392	Ppp1r13l<sup>tm1.1Xlu</sup>/Ppp1r13l<sup>tm1.1Xlu</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25691752	20170926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295045	Ppp1r13l<sup>tm1.1Xlu</sup>	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27766308	20170926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302421	Tg(Mt1-IL6)28Gci	is_implicated_in	DOID:9120	amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:30377267	20181217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302421	Tg(Mt1-IL6)28Gci	is_implicated_in	DOID:9120	amyloidosis		MGI:5302497	Tg(Mt1-IL6)28Gci/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10233864	20181217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3770516	Kras<sup>tm3Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:11323676	20080212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:22054871	20181130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:29852407	20181130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:26949217	20181130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:3722379	Tg(Prnp-MAPT*P301L)JNPL3Hlmc/?  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10932182	20181130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448356	Syn1<sup>tm1Pggd</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:23236212	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448356	Syn1<sup>tm1Pggd</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:27005990	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085315	Ccm2<sup>tm2.1Sbn</sup>	is_not_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:5085318	Ccm2<sup>tm2.1Sbn</sup>/Ccm2<sup>tm2.1Sbn</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21596842	20110812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177945	Nyx<sup>nob</sup>	is_implicated_in	DOID:0110870	congenital stationary night blindness 1A						ECO:0000033	author statement supported by traceable reference	PMID:31513577	20191009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177945	Nyx<sup>nob</sup>	is_implicated_in	DOID:0110870	congenital stationary night blindness 1A		MGI:3055970	Nyx<sup>nob</sup>/Nyx<sup>nob</sup>  [background:] BALB/c-Nyx<sup>nob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9804152	20191009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525504	Tg(MMTV-PyVT)#Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:33097605	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525504	Tg(MMTV-PyVT)#Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24589775	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525504	Tg(MMTV-PyVT)#Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25048202	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525504	Tg(MMTV-PyVT)#Mul	is_implicated_in	DOID:1612	breast cancer		MGI:5644499	Tg(MMTV-PyVT)#Mul/0  [background:] B6.FVB-Tg(MMTV-PyVT)#Mul			ECO:0000033	author statement supported by traceable reference	PMID:18317964	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5445385	Tg(Prnp-FUS)WT3Cshw	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:5445435	Tg(Prnp-FUS)WT3Cshw/Tg(Prnp-FUS)WT3Cshw  [background:] involves: C57BL/6 * Crl:CD-1(ICR)			ECO:0000033	author statement supported by traceable reference	PMID:22961620	20121212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14690057	20070625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17299139	20070625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15320950	20070625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6513138	Gnao1<sup>em2Rneu</sup>	is_implicated_in	DOID:0112276	neurodevelopmental disorder with involuntary movements		MGI:6513140	Gnao1<sup>em2Rneu</sup>/Gnao1<sup>+</sup>  [background:] C57BL/6J-Gnao1<sup>em2Rneu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31907305	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790635	Pdgfrb<sup>tm1Msas</sup>/Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu/0  [background:] B6J.Cg-Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25803852	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698861	Gne<sup>tm1Sngi</sup>/Gne<sup>tm1Sngi</sup> Tg(ACTB-GNE*D176V)9Sngi/0  [background:] involves: C57BL/6	is_model_of	DOID:3429	inclusion body myositis						ECO:0000033	author statement supported by traceable reference	PMID:17164266	20070306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6783463	Washc4<sup>em1Ssod</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:6783465	Washc4<sup>em1Ssod</sup>/Washc4<sup>em1Ssod</sup>  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:33749590	20211029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512699	Tg(Prnp-MAPT*P301S)PS19Vle/0  [background:] B6.Cg-Tg(Prnp-MAPT*P301S)PS19Vle	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21698260	20131015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5902816	Adamtsl4<sup>tvrm267</sup>	is_implicated_in	DOID:110	lens disease		MGI:5902990	Adamtsl4<sup>tvrm267</sup>/Adamtsl4<sup>tvrm267</sup>  [background:] C57BL/6J-Adamtsl4<sup>tvrm267</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26405179	20170620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149153	Ano5<sup>tm1Lrk</sup>	is_implicated_in	DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L		MGI:6149568	Ano5<sup>tm1Lrk</sup>/Ano5<sup>tm1Lrk</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26911675	20180405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763078	Tg(MMTV-ENPP2)21Gbm/0  [background:] FVB/N-Tg(MMTV-ENPP2)21Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696968	Lmx1b<sup>tm1Zfc</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:27407143	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720098	Glis2<sup>tm1Tre</sup>/Glis2<sup>tm1Tre</sup>  [background:] B6.129P2-Glis2<sup>tm1Tre</sup>	is_model_of	DOID:0111116	nephronophthisis 7						ECO:0000033	author statement supported by traceable reference	PMID:17618285	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:7437911	20110606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:7417782	20110606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:20441793	20110606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J	is_model_of	DOID:10587	Krabbe disease						ECO:0000033	author statement supported by traceable reference	PMID:21389217	20110606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693287	Zfp423<sup>nur12</sup>/Zfp423<sup>nur12</sup>  [background:] involves: BALB/c * C57BL/6 * C3H	is_model_of	DOID:2785	Dandy-Walker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17151198	20070111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5704141	Pcdh15<sup>roda</sup>	is_implicated_in	DOID:0110832	Usher syndrome type 1F		MGI:5704195	Pcdh15<sup>roda</sup>/Pcdh15<sup>roda</sup>  [background:] BALB/c-Pcdh15<sup>roda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24044941	20160226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574545	Dok1<sup>tm1Ppp</sup>/Dok1<sup>+</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: 129S1/Sv	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611295	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176466	Runx2<sup>tm1Kish</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:23702614	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176466	Runx2<sup>tm1Kish</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10049712	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176466	Runx2<sup>tm1Kish</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10213384	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176466	Runx2<sup>tm1Kish</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9182763	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176466	Runx2<sup>tm1Kish</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678410	Runx2<sup>tm1Kish</sup>/Runx2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9182763	20160801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5051941	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/?  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21356380	20110802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5319644	Tg(NPHS2-Trpc6)F419Walz/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0111129	focal segmental glomerulosclerosis 2						ECO:0000033	author statement supported by traceable reference	PMID:20877463	20120530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4415286	Pla2g6<sup>m1Sein</sup>/Pla2g6<sup>m1Sein</sup>  [background:] C57BL/6JJcl-Pla2g6<sup>m1Sein</sup>	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:19893029	20100108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6492300	Prph2<sup>tm4.1Itl</sup>	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6492344	Prph2<sup>tm4.1Itl</sup>/Prph2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:31914632	20210115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6492300	Prph2<sup>tm4.1Itl</sup>	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6492346	Prph2<sup>tm4.1Itl</sup>/Prph2<sup>tm4.1Itl</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:31914632	20210115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6715576	Elp2<sup>em2Bjw</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6754173	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6715576	Elp2<sup>em2Bjw</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6754175	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471728	Acvr1<sup>tm1Emsh</sup>/Acvr1<sup>+</sup>  [background:] chimera involves: BALB/c * C57BL/6 * CD-1	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:22508565	20130403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851105	Otc<sup>spf</sup>/Y  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8750014	20090723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054886	Epm2a<sup>tm1Kzy</sup>/Epm2a<sup>tm1Kzy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:21493628	20110826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054886	Epm2a<sup>tm1Kzy</sup>/Epm2a<sup>tm1Kzy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:12019206	20110826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141084	Mtss1<sup>Gt(CSC156)Byg</sup>/Mtss1<sup>Gt(CSC156)Byg</sup>  [background:] B6.129P2-Mtss1<sup>Gt(CSC156)Byg</sup>	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22081072	20120912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680187	Fas<sup>tm1Vbo</sup>/Fas<sup>tm1Vbo</sup> Tg(Ins2-cre)25Mgn/0 Tg(Ins2-HA)165Bri/0 Tg(Tcra/Tcrb)1Vbo/0  [background:] Not Specified	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14530378	20060531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4939884	Rxra<sup>tm1Krc</sup>/Rxra<sup>tm1Krc</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:21135166	20110307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:6234993	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:6841965	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5754490	Lmna<sup>tm10Lgf</sup>/Lmna<sup>tm10Lgf</sup> Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:9164	achalasia						ECO:0000033	author statement supported by traceable reference	PMID:25652409	20160324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:14699048	20140912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:16720837	20140912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181261	Csf2rb<sup>tm1Mur</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:25143363	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181261	Csf2rb<sup>tm1Mur</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3604113	Csf2rb<sup>tm1Mur</sup>/Csf2rb<sup>tm1Mur</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8839836	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181261	Csf2rb<sup>tm1Mur</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3604114	Csf2rb<sup>tm1Mur</sup>/Csf2rb<sup>tm1Mur</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:7697542	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285200	Tg(Thy1-HSPB1*S135F)#Lvdb	is_implicated_in	DOID:0110163	Charcot-Marie-Tooth disease axonal type 2F		MGI:5285207	Tg(Thy1-HSPB1*S135F)#Lvdb/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21785432	20110913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883451	Katnip<sup>Gt(RRG309)Byg</sup>/Katnip<sup>Gt(RRG309)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110995	Joubert syndrome 26						ECO:0000033	author statement supported by traceable reference	PMID:26714646	20170419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700037	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup> Spry4<sup>tm1Ayos</sup>/Spry4<sup>tm1Ayos</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:17156747	20070315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446426	Dnah11<sup>b2b1775Clo</sup>/Dnah11<sup>b2b1775Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1775Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665413	Zfpm2<sup>tm1Sho</sup>/Zfpm2<sup>tm1Sho</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:10892744	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665413	Zfpm2<sup>tm1Sho</sup>/Zfpm2<sup>tm1Sho</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:12223418	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438063	b2b1700Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052171	Pomgnt1<sup>tm1.1Cfg</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5615582	Pomgnt1<sup>tm1.1Cfg</sup>/Pomgnt1<sup>tm1.1Cfg</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26306834	20190515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6489960	Frmd7<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:0111790	congenital nystagmus 1		MGI:6491490	Frmd7<sup>tm1b(KOMP)Wtsi</sup>/Y  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33007925	20210112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6489960	Frmd7<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:0111790	congenital nystagmus 1		MGI:6491489	Frmd7<sup>tm1b(KOMP)Wtsi</sup>/Frmd7<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33007925	20210112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673970	Dspp<sup>tm1Kul</sup>/Dspp<sup>tm1Kul</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:4154	dentinogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:12721295	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6758642	Cerkl<sup>em1Gmar</sup>	is_implicated_in	DOID:0110368	retinitis pigmentosa 26						ECO:0000033	author statement supported by traceable reference	PMID:34048907	20210910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6780038	Dnah10<sup>em1Yxc</sup>	is_implicated_in	DOID:0111910	spermatogenic failure		MGI:6780172	Dnah10<sup>em1Yxc</sup>/Dnah10<sup>em1Yxc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34237282	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620801	Ap1s2<sup>tm1Pschu</sup>	is_implicated_in	DOID:0060800	syndromic X-linked intellectual disability 5		MGI:5661462	Ap1s2<sup>tm1Pschu</sup>/Ap1s2<sup>tm1Pschu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20203623	20150911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838409	Col13a1<sup>tm3.1Pih</sup>	is_implicated_in	DOID:0110673	congenital myasthenic syndrome 19		MGI:6316981	Col13a1<sup>tm3.1Pih</sup>/Col13a1<sup>tm3.1Pih</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:28369367	20190710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5901846	Phkb<sup>em1(IMPC)J</sup>	is_implicated_in	DOID:0111041	glycogen storage disease IXb		MGI:6263156	Phkb<sup>em1(IMPC)J</sup>/Phkb<sup>+</sup>  [background:] C57BL/6NJ-Phkb<sup>em1(IMPC)J</sup>/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:36077341	20221108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2671154	Rdx<sup>tm1Sts</sup>/Rdx<sup>tm1Sts</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12308	Dubin-Johnson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12068294	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174917	App<sup>tm1Dbo</sup>/App<sup>tm1Dbo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10188929	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:1576433	20080811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:11168809	20080811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:7271067	20080811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:6562869	20080811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:6971670	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437101	b2b1200Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038212	Gck<sup>Rgsc210</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J	is_model_of	DOID:0060547	Hermansky-Pudlak syndrome 9						ECO:0000033	author statement supported by traceable reference	PMID:25477496	20151231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474570	Bbs1<sup>tm2Vcs</sup>/Bbs1<sup>tm2Vcs</sup> Tg(Pdgfra-cre)1Clc/0  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23160237	20130418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5550095	Marveld2<sup>tm1.1Sria</sup>	is_implicated_in	DOID:0110506	autosomal recessive nonsyndromic deafness 49		MGI:5550096	Marveld2<sup>tm1.1Sria</sup>/Marveld2<sup>tm1.1Sria</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23979167	20140310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634713	Tg(CAG-Mtor*)#Atai	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5634715	Emx1<sup>tm1(cre)Ito</sup>/Emx1<sup>+</sup> Tg(CAG-Mtor*)#Atai/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:24857653	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:27614205	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:20223998	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:25217571	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:23041258	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:22815812	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:23457523	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3033756	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9668092	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148550	Gaa<sup>tm1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3033756	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10838256	20190121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431996	Col1a1<sup>Aga2</sup>/Col1a1<sup>+</sup>  [background:] C3HeB/FeJ-Col1a1<sup>Aga2</sup>	is_model_of	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:22589248	20120822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661919	Tg(SFTPC-KIF5B/RET)1Tkoh/0  [background:] involves: C57BL/6J	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25064355	20150917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437687	Ceacam16<sup>tm1Wzm</sup>/Ceacam16<sup>tm1Wzm</sup>  [background:] BALB/cJ-Ceacam16<sup>tm1Wzm</sup>	is_model_of	DOID:0110573	autosomal dominant nonsyndromic deafness 4A						ECO:0000033	author statement supported by traceable reference	PMID:22544735	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359177	Arx<sup>tm4Kki</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:33711494	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359177	Arx<sup>tm4Kki</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:22565167	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359177	Arx<sup>tm4Kki</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:6196032	Arx<sup>tm4Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6NHsd			ECO:0000033	author statement supported by traceable reference	PMID:28602636	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359177	Arx<sup>tm4Kki</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:4359207	Arx<sup>tm4Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22565167	20210720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523468	Tg(DMWD,DMPK*,SIX5)328Ggo/Tg(DMWD,DMPK*,SIX5)328Ggo  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:11726559	20131212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523468	Tg(DMWD,DMPK*,SIX5)328Ggo/Tg(DMWD,DMPK*,SIX5)328Ggo  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:23180777	20131212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3770247	Tcirg1<sup>oc</sup>/Tcirg1<sup>oc</sup>  [background:] C57BL/6J-Vps33a<sup>bf</sup>	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	MGI:76073	20110125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:12651621	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:11883932	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:12205028	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:24189943	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:33483253	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:24761004	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:22854956	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:24532665	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:25008174	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria		MGI:3623008	Cbs<sup>tm1Unc</sup>/Cbs<sup>+</sup>  [background:] B6.129P2-Cbs<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25016930	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria		MGI:2660658	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15386278	20220805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6336104	Mocos<sup>em2(IMPC)Ics</sup>	is_implicated_in	DOID:0070453	xanthinuria type II		MGI:7495807	Mocos<sup>em2(IMPC)Ics</sup>/Mocos<sup>em2(IMPC)Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35372998	20230731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3841167	Tg(Myh6-PRKAG2*N488I)4623Jse	is_implicated_in	DOID:0110312	hypertrophic cardiomyopathy 6						ECO:0000033	author statement supported by traceable reference	PMID:28009297	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3841167	Tg(Myh6-PRKAG2*N488I)4623Jse	is_implicated_in	DOID:0110312	hypertrophic cardiomyopathy 6		MGI:3841175	Tg(Myh6-PRKAG2*N488I)4623Jse/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:12782567	20170921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437727	Dnah11<sup>b2b1727Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6716871	Yap1<sup>tm1.1Hmc</sup>	is_implicated_in	DOID:0050795	cone dystrophy		MGI:6716878	Yap1<sup>tm1.1Hmc</sup>/Yap1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6 * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:32801350	20210622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3770517	Kras<sup>tm3Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:11323676	20080212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512906	Tpp1<sup>m1J</sup>	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:5512911	Tpp1<sup>m1J</sup>/Tpp1<sup>m1J</sup>  [background:] STOCK Tpp1<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5511005	20131017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042794	Nrxn1<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042794	Nrxn1<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21262241	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042794	Nrxn1<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042794	Nrxn1<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5428133	Nrxn1<sup>tm1Sud</sup>/Nrxn1<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19822762	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:25218179	20190415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:28282402	20190415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:30875376	20190415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:26822703	20190415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:22951387	20190415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria		MGI:5300789	Pah<sup>enu2</sup>/Pah<sup>enu2</sup>  [background:] BTBR-Pah<sup>enu2</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21640623	20190415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857272	Pah<sup>enu2</sup>	is_implicated_in	DOID:9281	phenylketonuria		MGI:3587815	Pah<sup>enu2</sup>/Pah<sup>enu2</sup>  [background:] involves: BTBR			ECO:0000033	author statement supported by traceable reference	PMID:9119379	20190415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838433	Stk39<sup>tm1.2Slin</sup>/Stk39<sup>tm1.2Slin</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20813865	20101115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431572	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:19805914	20120816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387399	Tcf4<sup>tm1Zhu</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32015540	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387399	Tcf4<sup>tm1Zhu</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6479882	Tcf4<sup>tm1Zhu</sup>/Tcf4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27568567	20201217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660857	Nlgn3<sup>tm2.1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:24995986	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5811315	Pus1<sup>tm1.1Mdf</sup>	is_implicated_in	DOID:0080099	myopathy, lactic acidosis, and sideroblastic anemia		MGI:5811553	Pus1<sup>tm1.1Mdf</sup>/Pus1<sup>tm1.1Mdf</sup>  [background:] B6.129S7(C)-Pus1<sup>tm1.1Mdf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27197761	20161209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432231	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605471	Tg(Scgb1a1-Scnn1b)6608Bouc	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:21658636	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605471	Tg(Scgb1a1-Scnn1b)6608Bouc	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:26185363	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605471	Tg(Scgb1a1-Scnn1b)6608Bouc	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:28062483	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605471	Tg(Scgb1a1-Scnn1b)6608Bouc	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3605476	Tg(Scgb1a1-Scnn1b)6608Bouc/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15077107	20171116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867515	Tg(DYRK1A)36Wjs/0  [background:] involves: C57BL/6NCrjBgi	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16455265	20110111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028923	Spg7<sup>tm1Eir</sup>	is_implicated_in	DOID:0110816	hereditary spastic paraplegia 7						ECO:0000033	author statement supported by traceable reference	PMID:22563492	20121008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028923	Spg7<sup>tm1Eir</sup>	is_implicated_in	DOID:0110816	hereditary spastic paraplegia 7		MGI:3028926	Spg7<sup>tm1Eir</sup>/Spg7<sup>tm1Eir</sup>  [background:] either: 129/Sv-Spg7<sup>tm1Eir</sup> or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:14722615	20121008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662000	Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129/Sv * CD-1	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444502	Tg(tetO-IL1B)KBry	is_implicated_in	DOID:0050161	lower respiratory tract disease		MGI:5444503	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IL1B)KBry/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16888287	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25218145	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23418438	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:31341969	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22773734	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27131347	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527206	Lmna<sup>tm1Gbon</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:3527796	Lmna<sup>tm1Gbon</sup>/Lmna<sup>tm1Gbon</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15548545	20220429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5319640	Tg(NPHS2-Trpc6*E896K)F75aWalz	is_implicated_in	DOID:0111129	focal segmental glomerulosclerosis 2		MGI:5319646	Tg(NPHS2-Trpc6*E896K)F75aWalz/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20877463	20120530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6313615	Tg(Itgam-FCAR)83Rcmo	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:6313621	Tg(Itgam-FCAR)83Rcmo/0  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:10839814	20190611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819790	Fkbp8<sup>tm1Kei</sup>/Fkbp8<sup>tm1Kei</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:18459960	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437082	Cep290<sup>b2b1454Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437115	Cep290<sup>b2b1454Clo</sup>/Cep290<sup>b2b1454Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1454Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581190	Pcdh15<sup>av-3J</sup>/Pcdh15<sup>av-3J</sup>  [background:] C57BL/6J-Pcdh15<sup>av-3J</sup>/J	is_model_of	DOID:0110832	Usher syndrome type 1F						ECO:0000033	author statement supported by traceable reference	PMID:15537665	20090219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5803879	Gas8<sup>Gt(CH0760)Wtsi</sup>/Gas8<sup>Gt(CH0760)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110619	primary ciliary dyskinesia 33						ECO:0000033	author statement supported by traceable reference	PMID:27472056	20161018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6273991	Tg(RP11-578M14)5Mkru	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:6273993	Tg(RP11-578M14)5Mkru/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29206867	20190121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999626	Col2a1<sup>M2J</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5292535	Col2a1<sup>M2J</sup>/Col2a1<sup>+</sup>  [background:] B6;C3Fe-Col2a1<sup>M2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442117	Dnaaf3<sup>b2b1739Clo</sup>	is_implicated_in	DOID:0110626	primary ciliary dyskinesia 2		MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852559	Tg(DBH-SNCA)#Dwei	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6852560	Tg(DBH-SNCA)#Dwei/0  [background:] C57BL/6N-Tg(DBH-SNCA)#Dwei			ECO:0000033	author statement supported by traceable reference	PMID:32868457	20220112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400423	Dpp4<sup>em1Rba</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400425	Dpp4<sup>em1Rba</sup>/Dpp4<sup>em1Rba</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31339932	20200615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400423	Dpp4<sup>em1Rba</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29277291	20200615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400423	Dpp4<sup>em1Rba</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31883094	20200615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400423	Dpp4<sup>em1Rba</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400427	Dpp4<sup>em1Rba</sup>/Dpp4<sup>+</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27892925	20200615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400423	Dpp4<sup>em1Rba</sup>	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400425	Dpp4<sup>em1Rba</sup>/Dpp4<sup>em1Rba</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27892925	20200615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5690110	Gdap1<sup>tm1.2Geno</sup>	is_implicated_in	DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K		MGI:5690112	Gdap1<sup>tm1.2Geno</sup>/Gdap1<sup>tm1.2Geno</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25860513	20151014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5319218	Spink5<sup>m1Btlr</sup>	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:5319225	Spink5<sup>m1Btlr</sup>/Spink5<sup>m1Btlr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:5319224	20120525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695543	Alx4<sup>Lst-2J</sup>/Alx4<sup>Lst-2J</sup>  [background:] C57BL/6J-Alx4<sup>Lst-2J</sup>/J	is_model_of	DOID:0060285	parietal foramina						ECO:0000033	author statement supported by traceable reference	PMID:25673119	20151112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5697198	Tg(ATXN2*72Q)#Plt	is_implicated_in	DOID:0050955	spinocerebellar ataxia type 2		MGI:5697200	Tg(ATXN2*72Q)#Plt/0  [background:] FVB/N-Tg(ATXN2*72Q)#Plt			ECO:0000033	author statement supported by traceable reference	PMID:25902068	20151125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476822	Pkd1<sup>tm1.1Pcha</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:33852874	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476822	Pkd1<sup>tm1.1Pcha</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29463793	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476822	Pkd1<sup>tm1.1Pcha</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:28205547	20210721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476822	Pkd1<sup>tm1.1Pcha</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5476836	Pkd1<sup>tm1.1Pcha</sup>/Pkd1<sup>tm1.1Pcha</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23064367	20210721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624438	Pomgnt1<sup>Gt(OST179231)Lex</sup>/Pomgnt1<sup>Gt(OST179231)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:0050560	Walker-Warburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16458488	20130805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624438	Pomgnt1<sup>Gt(OST179231)Lex</sup>/Pomgnt1<sup>Gt(OST179231)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:0050560	Walker-Warburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23454088	20130805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800485	Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0  [background:] involves: C57BL/6 * CBA * FVB/NTac	is_model_of	DOID:0110433	dilated cardiomyopathy 1E						ECO:0000033	author statement supported by traceable reference	PMID:26595809	20161013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510920	Tg(ALB-cre,CMV-rtTA)#Wcyy/0 Tg(CMV-EGFP,Rnu6-siAbca1)#Wcyy/0  [background:] involves: ICR	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:15509524	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654781	Axl<sup>tm1Grl</sup>/Axl<sup>tm1Grl</sup> Mertk<sup>tm1Grl</sup>/Mertk<sup>tm1Grl</sup> Tyro3<sup>tm1Grl</sup>/Tyro3<sup>tm1Grl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:11452127	20120330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316786	Ccdc39<sup>b2b1304Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622652	Scn5a<sup>tm1Pec</sup>/Scn5a<sup>+</sup>  [background:] involves: Swiss	is_model_of	DOID:0110646	long QT syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:11533705	20060518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027206	Aspa<sup>nur7</sup>/Aspa<sup>nur7</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:26511242	20160525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027206	Aspa<sup>nur7</sup>/Aspa<sup>nur7</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:18987190	20160525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5751860	Tg(tetO-FMR1*,-EGFP)#Rkhu	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28369393	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5751860	Tg(tetO-FMR1*,-EGFP)#Rkhu	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome		MGI:5751863	Tg(Hnrnpa2b1-rtTA2S*M2)9Jstr/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0  [background:] involves: C57BL/6JRj * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25486200	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5751860	Tg(tetO-FMR1*,-EGFP)#Rkhu	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome		MGI:5752054	Tg(Prnp-rtTA2S*M2)#Rkhu/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0  [background:] involves: C57BL/6JRj			ECO:0000033	author statement supported by traceable reference	PMID:26060190	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5901732	Cul3<sup>tm2Suc</sup>	is_not_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:5901736	Cul3<sup>tm2Suc</sup>/Cul3<sup>tm2Suc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26490675	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6281438	Borcs7<sup>Q87X</sup>	is_implicated_in	DOID:2476	hereditary spastic paraplegia		MGI:6302764	Borcs7<sup>Q87X</sup>/Borcs7<sup>Q87X</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30067980	20190513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491026	Tg(Prnp*P101L)2862Sbp	is_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:5491044	Tg(Prnp*P101L)2862Sbp/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774447	Tg(Sox3-GFP,Tyr)HolNpln	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774447	Tg(Sox3-GFP,Tyr)HolNpln	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5774474	Tg(Sox3-GFP,Tyr)HolNpln/Tg(Sox3-GFP,Tyr)HolNpln  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26571399	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566851	Rho<sup>tm1.1Eye</sup>/Rho<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:22252712	20140605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437084	b2b1146Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654027	Upk3a<sup>tm1Tsun</sup>/Upk3a<sup>tm1Tsun</sup>  [background:] either: (involves: 129S/SvEv) or (involves: 129S/SvEv * Swiss Webster)	is_model_of	DOID:9620	vesicoureteral reflux						ECO:0000033	author statement supported by traceable reference	PMID:11085999	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192450	Cftr<sup>em3Cwr</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:6192451	Cftr<sup>em3Cwr</sup>/Cftr<sup>em3Cwr</sup>  [background:] C57BL/6J-Cftr<sup>em3Cwr</sup>/Cwr			ECO:0000033	author statement supported by traceable reference	PMID:29924856	20180801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179045	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9990064	20050708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295267	Spef2<sup>bgh</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5295270	Spef2<sup>bgh</sup>/Spef2<sup>bgh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:21715716	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295267	Spef2<sup>bgh</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5295269	Spef2<sup>bgh</sup>/Spef2<sup>bgh</sup>  [background:] involves: C57BL/6J * C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:21715716	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295267	Spef2<sup>bgh</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia						ECO:0000033	author statement supported by traceable reference	PMID:24360193	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301407	Abcc1<sup>tm1Bor</sup>/Abcc1<sup>tm1Bor</sup> Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/0  [background:] FVB.Cg-Abcc1<sup>tm1Bor</sup> Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21881209	20120115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430054	b2b1470Clo	is_implicated_in	DOID:674	cleft palate		MGI:5430328	b2b1470Clo/b2b1470Clo  [background:] C57BL/6J-b2b1470Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722925	Alpl<sup>Hpp</sup>/Alpl<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:17539739	20120620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857927	Gjb1<sup>tm1Kwi</sup>	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1						ECO:0000033	author statement supported by traceable reference	PMID:26865613	20160708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857927	Gjb1<sup>tm1Kwi</sup>	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:2176915	Gjb1<sup>tm1Kwi</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8790370	20160708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857927	Gjb1<sup>tm1Kwi</sup>	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:2176912	Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8790370	20160708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857927	Gjb1<sup>tm1Kwi</sup>	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:4821790	Gjb1<sup>tm1Kwi</sup>/Y  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9169515	20160708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857927	Gjb1<sup>tm1Kwi</sup>	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:4821788	Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9169515	20160708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4888744	Kif20b<sup>magoo</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:6095619	Kif20b<sup>magoo</sup>/Kif20b<sup>magoo</sup>  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28359322	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835226	Cep290<sup>tm1.1Jgg</sup>	is_implicated_in	DOID:0111000	Joubert syndrome 5		MGI:5007766	Cep290<sup>tm1.1Jgg</sup>/Cep290<sup>tm1.1Jgg</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21623382	20110616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431495	b2b904.1Clo	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5431511	b2b904.1Clo/b2b904.1Clo  [background:] C57BL/6J-b2b904.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:28416184	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25526314	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:27758879	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:27797827	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:3844311	Apc<sup>tm1Tno</sup>/Apc<sup>+</sup> Tg(CDX2-cre)101Erf/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17942902	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796248	Col7a1<sup>tm1Lbt</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:26194911	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796248	Col7a1<sup>tm1Lbt</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:26676755	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796248	Col7a1<sup>tm1Lbt</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:3809430	Col7a1<sup>tm1Lbt</sup>/Col7a1<sup>tm1Lbt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6Crl			ECO:0000033	author statement supported by traceable reference	PMID:18382769	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6479074	Col4a5<sup>em1Keha</sup>	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:6479076	Col4a5<sup>em1Keha</sup>/Y  [background:] C57BL/6J-Col4a5<sup>em1Keha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30582011	20201214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6479074	Col4a5<sup>em1Keha</sup>	is_implicated_in	DOID:0110034	X-linked Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32488001	20201214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297388	Prickle1<sup>b2b019Clo</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5300249	Prickle1<sup>b2b019Clo</sup>/Prickle1<sup>b2b019Clo</sup>  [background:] C57BL/6J-Prickle1<sup>b2b019Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618357	Gadd45a<sup>tm1Ajf</sup>/Gadd45a<sup>tm1Ajf</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179992	Tg(tetO-Kras2)12Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27292643	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179992	Tg(tetO-Kras2)12Hev	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28504653	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179992	Tg(tetO-Kras2)12Hev	is_implicated_in	DOID:1612	breast cancer		MGI:5827756	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Kras2)12Hev/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18356293	20180306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426228	Lepr<sup>tm1Jke</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25157166	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426228	Lepr<sup>tm1Jke</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5620891	Lepr<sup>tm1Jke</sup>/Lepr<sup>tm1Jke</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:25157166	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182347	Hmbs<sup>tm3Uam</sup>	is_implicated_in	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:23562909	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182347	Hmbs<sup>tm3Uam</sup>	is_implicated_in	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:26908609	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796023	Tg(Bglap2-TAg)1Rkho	is_implicated_in	DOID:3347	osteosarcoma		MGI:5796036	Tg(Bglap2-TAg)1Rkho/0  [background:] FVB/N-Tg(Bglap2-TAg)1Rkho			ECO:0000033	author statement supported by traceable reference	PMID:20697156	20160930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796023	Tg(Bglap2-TAg)1Rkho	is_implicated_in	DOID:3347	osteosarcoma		MGI:5796170	Tg(Bglap2-TAg)1Rkho/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26659571	20160930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442315	Prkcsh<sup>tm1Som</sup>/Prkcsh<sup>tm1Som</sup> Tg(CAG-cre/Esr1*)1Lbe/0  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050770	polycystic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:21685914	20121120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:37649609	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27506299	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27180906	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29050937	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29237705	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29798841	20230921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811260	Cdkn1b<sup>tm1Ako</sup>/Cdkn1b<sup>tm1Ako</sup> Kit<sup>W-v</sup>/Kit<sup>W-v</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:27354067	20161207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044774	Npc2<sup>tm1Plob</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:23843985	20140811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044774	Npc2<sup>tm1Plob</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:24076310	20140811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044774	Npc2<sup>tm1Plob</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5538404	Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:23843985	20140811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044774	Npc2<sup>tm1Plob</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3044881	Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15071184	20140811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7378850	Dnm2<sup>Rbc12</sup>	is_implicated_in	DOID:11252	microcytic anemia		MGI:7378853	Dnm2<sup>Rbc12</sup>/Dnm2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28466468	20221107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574666	Enam<sup>Rgsc514</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523906	Cntn1<sup>usl</sup>/Cntn1<sup>usl</sup>  [background:] MRL/MpJ-Fas<sup>lpr</sup> Cntn1<sup>usl</sup>/GrsrJ	is_model_of	DOID:0080101	Compton-North congenital myopathy						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6394017	Dmd<sup>em#Tve</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6394025	Dmd<sup>em#Tve</sup>/Y  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:31028078	20200312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680509	Gba1<sup>tm4Ggb</sup>/Gba1<sup>tm4Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424981	Casr<sup>BCH004</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425920	Casr<sup>BCH004</sup>/Casr<sup>BCH004</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH004</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635524	Tg(tetO-GJB2*G45E,-EGFP)#Tww	is_implicated_in	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26777423	20160420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635524	Tg(tetO-GJB2*G45E,-EGFP)#Tww	is_implicated_in	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome		MGI:5635532	Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-GJB2*G45E,-EGFP)#Tww/0  [background:] involves: FVB/N * SKH1			ECO:0000033	author statement supported by traceable reference	PMID:22031297	20160420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635524	Tg(tetO-GJB2*G45E,-EGFP)#Tww	is_implicated_in	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25229253	20160420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386444	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2960	photosensitive trichothiodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9651581	20050825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386444	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2960	photosensitive trichothiodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11950998	20050825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5546026	Sox9<sup>Bbfc</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:5659902	Sox9<sup>Bbfc</sup>/Sox9<sup>+</sup>  [background:] C57BL/6J-Sox9<sup>Bbfc</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26234751	20150825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4336382	Mto1<sup>Gt(G019A03)Wrst</sup>	is_implicated_in	DOID:0060286	combined oxidative phosphorylation deficiency						ECO:0000033	author statement supported by traceable reference	PMID:25552653	20160324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4336382	Mto1<sup>Gt(G019A03)Wrst</sup>	is_implicated_in	DOID:0060286	combined oxidative phosphorylation deficiency		MGI:5659847	Mto1<sup>Gt(G019A03)Wrst</sup>/Mto1<sup>Gt(G019A03)Wrst</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25506927	20160324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432130	Clrn1<sup>tm2.1Kuna</sup>	is_implicated_in	DOID:0110841	Usher syndrome type 3A		MGI:5432139	Clrn1<sup>tm2.1Kuna</sup>/Clrn1<sup>tm2.1Kuna</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22787034	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432130	Clrn1<sup>tm2.1Kuna</sup>	is_implicated_in	DOID:0110841	Usher syndrome type 3A						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5642118	Neb<sup>tm2Hgra</sup>	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:5883288	Neb<sup>tm2Hgra</sup>/Neb<sup>tm2Hgra</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S6/SvEvTac * FVB			ECO:0000033	author statement supported by traceable reference	PMID:26123491	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5642118	Neb<sup>tm2Hgra</sup>	is_implicated_in	DOID:0110928	nemaline myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:36528760	20230330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045236	Abcc6<sup>tm1Jfk</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:22846719	20221205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045236	Abcc6<sup>tm1Jfk</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:23014343	20221205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045236	Abcc6<sup>tm1Jfk</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:36400944	20221205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045236	Abcc6<sup>tm1Jfk</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum		MGI:3605029	Abcc6<sup>tm1Jfk</sup>/Abcc6<sup>tm1Jfk</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16135817	20221205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389228	Bace1<sup>tm1Pcw</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25912880	20161101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389228	Bace1<sup>tm1Pcw</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3720943	Bace1<sup>tm1Pcw</sup>/Bace1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18385378	20161101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6469362	Foxf1<sup>em1Vvk</sup>	is_implicated_in	DOID:13042	persistent fetal circulation syndrome		MGI:6470789	Foxf1<sup>em1Vvk</sup>/Foxf1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:31199666	20201105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5707492	Slc2a9<sup>tm1Khm</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5760132	Slc2a9<sup>tm1Khm</sup>/Slc2a9<sup>tm1Khm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25100214	20210319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433409	Tmem67<sup>b2b1163.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433489	Tmem67<sup>b2b1163.1Clo</sup>/Tmem67<sup>b2b1163.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1163.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6188634	Tpi1<sup>rbc19</sup>	is_implicated_in	DOID:0050884	triosephosphate isomerase deficiency		MGI:6188637	Tpi1<sup>rbc19</sup>/Tpi1<sup>rbc19</sup>  [background:] SJL-Tpi1<sup>rbc19</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29720471	20180716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527455	Mmut<sup>tm1Cpv</sup>/Mmut<sup>tm1Cpv</sup> Tg(Alb-Mut)#Cpv/0  [background:] involves: C57BL/6	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:23898205	20140110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177436	Cftr<sup>tm1Cam</sup>/Cftr<sup>tm1Cam</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:1355249	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177755	Htt<sup>tm2Szi</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:31968243	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177755	Htt<sup>tm2Szi</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24019939	20200529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628821	Eng<sup>tm1Mle</sup>/Eng<sup>+</sup>  [background:] 129P2/OlaHsd-Eng<sup>tm1Mle</sup>	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:10562296	20060712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837478	Trim32<sup>Gt(BGA355)Byg</sup>/Trim32<sup>Gt(BGA355)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H						ECO:0000033	author statement supported by traceable reference	PMID:19155210	20090327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5478554	G6pc1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:5823404	G6pc1<sup>tm1.1Ics</sup>/G6pc1<sup>tm1.1Ics</sup> Tg(Kap-icre)29066/2Sig/0  [background:] involves: 129S2/SvPas * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24717294	20170207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5478554	G6pc1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:5478556	G6pc1<sup>tm1.1Ics</sup>/G6pc1<sup>tm1.1Ics</sup> Alb<sup>tm1(cre/ERT2)Mtz</sup>/Alb<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21109326	20170207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5478554	G6pc1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:22013018	20170207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820518	Tg(Myh6-MYL2*R58Q)#Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10		MGI:5904628	Tg(Myh6-MYL2*R58Q)#Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19150977	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820518	Tg(Myh6-MYL2*R58Q)#Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:26906074	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5292658	Tg(tetO-TAg)2-5Hiwa	is_implicated_in	DOID:769	neuroblastoma		MGI:5292662	Tg(tetO-TAg)2-5Hiwa/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20664939	20111020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5292658	Tg(tetO-TAg)2-5Hiwa	is_implicated_in	DOID:769	neuroblastoma		MGI:5292662	Tg(tetO-TAg)2-5Hiwa/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19020752	20111020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182078	Ctsd<sup>tm1Cptr</sup>	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10						ECO:0000033	author statement supported by traceable reference	PMID:36122205	20230323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182078	Ctsd<sup>tm1Cptr</sup>	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:3040187	Ctsd<sup>tm1Cptr</sup>/Ctsd<sup>tm1Cptr</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd)			ECO:0000033	author statement supported by traceable reference	PMID:18498441	20230323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5613978	Tg(CMV-Plaur*)19Lbh	is_not_implicated_in	DOID:0111128	focal segmental glomerulosclerosis 1		MGI:5649016	Tg(CMV-Plaur*)19Lbh/0  [background:] FVB/N-Tg(CMV-Plaur*)19Lbh			ECO:0000033	author statement supported by traceable reference	PMID:25354239	20150818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6209388	Slc9a9<sup>tm1.1Yzj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6209392	Slc9a9<sup>tm1.1Yzj</sup>/Slc9a9<sup>tm1.1Yzj</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26755066	20181026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31299345	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26733386	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25941473	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23015442	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27352031	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25147297	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26237041	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31291284	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26821816	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5306241	Mecp2<sup>tm1.1Jae</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16446138	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624674	Mecp2<sup>tm1.1Jae</sup>/Y  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242118	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158354	Mecp2<sup>tm1.1Jae</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624676	Mecp2<sup>tm1.1Jae</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22302819	20200131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038333	Rp1<sup>tm1Jnz</sup>/Rp1<sup>tm1Jnz</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110390	retinitis pigmentosa 1						ECO:0000033	author statement supported by traceable reference	PMID:11960024	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5700345	Tg(Plp1-HTT*150Q)4aXjl/0  [background:] Not Specified	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25789755	20151231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:23577145	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:23326332	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:25481823	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:22005682	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:22144569	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:25447936	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:25716839	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3037958	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15003170	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3836258	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm1Maag</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19104150	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3037859	Cacna1a<sup>tm1Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3836258	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm1Maag</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22144569	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446162	b2b1941Clo	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5487398	b2b1941Clo/b2b1941Clo  [background:] C57BL/6J-b2b1941Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620118	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup> Tg(Ins2-NP)25-3Olds/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10553062	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824305	Tg(PDGFB-SNCA/EGFP)78Ema	is_implicated_in	DOID:12217	Lewy body dementia		MGI:5824306	Tg(PDGFB-SNCA/EGFP)78Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15765523	20170216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429701	Hexb<sup>tm1Grv</sup>	is_implicated_in	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:26467605	20180717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429701	Hexb<sup>tm1Grv</sup>	is_implicated_in	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:28007910	20180717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429701	Hexb<sup>tm1Grv</sup>	is_implicated_in	DOID:3323	Sandhoff disease		MGI:2668046	Hexb<sup>tm1Grv</sup>/Hexb<sup>tm1Grv</sup>  [background:] either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)			ECO:0000033	author statement supported by traceable reference	PMID:8789434	20180717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302187	Crbn<sup>tm1.1Jjh</sup>	is_implicated_in	DOID:0060308	autosomal recessive intellectual developmental disorder		MGI:5302203	Crbn<sup>tm1.1Jjh</sup>/Crbn<sup>tm1.1Jjh</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21995942	20190703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949134	Hcrtr2<sup>tm1Tesc</sup>/Hcrtr2<sup>tm1Tesc</sup>  [background:] B6.Cg-Hcrtr2<sup>tm1Tesc</sup>	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:21368172	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5292220	Tmem67<sup>tm1Dgen</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5292226	Tmem67<sup>tm1Dgen</sup>/Tmem67<sup>tm1Dgen</sup>  [background:] B6.129P2-Tmem67<sup>tm1Dgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23283079	20131104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6201439	Slc9a9<sup>tm2c(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6201594	Slc9a9<sup>tm2c(KOMP)Wtsi</sup>/Slc9a9<sup>tm2c(KOMP)Wtsi</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29362376	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905614	Mdm1<sup>m1J</sup>	is_implicated_in	DOID:10871	age related macular degeneration		MGI:3826270	Mdm1<sup>m1J</sup>/Mdm1<sup>m1J</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18805803	20170721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836596	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:15619626	20101028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174726	Hps5<sup>ru2-J</sup>/Hps5<sup>ru2-J</sup>  [background:] C57BL/6J-Hps5<sup>ru2-J</sup>/J	is_model_of	DOID:0060543	Hermansky-Pudlak syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589459	Lmna<sup>tm3Stw</sup>/Lmna<sup>tm3Stw</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * C57BL	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:15972724	20051013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543418	Tg(Myh6-ACTC1*E99K)#Sbm/0  [background:] involves: C57BL/10 * CBA/Ca	is_model_of	DOID:0110317	hypertrophic cardiomyopathy 11						ECO:0000033	author statement supported by traceable reference	PMID:21622575	20140207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278014	Tg(Actb-Ptma)T12Clwu	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:6278015	Tg(Actb-Ptma)T12Clwu/Tg(Actb-Ptma)T12Clwu  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15840017	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629937	Bscl2<sup>tm1.1Gliu</sup>	is_implicated_in	DOID:12336	male infertility		MGI:5629954	Bscl2<sup>tm1.1Gliu</sup>/Bscl2<sup>tm1.1Gliu</sup> Tg(Fabp4-cre)1Rev/0  [background:] involves: 129 * 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:24778225	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:16735375	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:16147464	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:15544612	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:16178852	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:21191418	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5564943	Tg(KRT14-Il4)#Lsch	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5564982	Tg(KRT14-Il4)#Lsch/0  [background:] involves: BALB/cBy * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11676841	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569537	Tg(CMV-HTT*89Q)ATag/Tg(CMV-HTT*89Q)ATag  [background:] involves: FVB/N	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767716	Tg(CAG-AR*97Q)7-8Sobue	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:25929689	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767716	Tg(CAG-AR*97Q)7-8Sobue	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:27147661	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767716	Tg(CAG-AR*97Q)7-8Sobue	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:23637164	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767716	Tg(CAG-AR*97Q)7-8Sobue	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:25168383	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767716	Tg(CAG-AR*97Q)7-8Sobue	is_implicated_in	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:29897452	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767716	Tg(CAG-AR*97Q)7-8Sobue	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:3767789	Tg(CAG-AR*97Q)7-8Sobue/?  [background:] involves: C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17991424	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5792731	Asah1<sup>tm1Medin</sup>	is_implicated_in	DOID:0050464	Farber lipogranulomatosis						ECO:0000033	author statement supported by traceable reference	PMID:29167126	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5792731	Asah1<sup>tm1Medin</sup>	is_implicated_in	DOID:0050464	Farber lipogranulomatosis		MGI:5800675	Asah1<sup>tm1Medin</sup>/Asah1<sup>tm1Medin</sup>  [background:] involves: 129S6/SvEvTac * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23681708	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523466	Tg(DMWD,DMPK*,SIX5)1177Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:5523475	Tg(DMWD,DMPK*,SIX5)1177Ggo/Tg(DMWD,DMPK*,SIX5)1177Ggo  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11726559	20160902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523466	Tg(DMWD,DMPK*,SIX5)1177Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:25799359	20160902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152894	Pkd1<sup>m1Bei</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:22859406	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152894	Pkd1<sup>m1Bei</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:14600027	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152894	Pkd1<sup>m1Bei</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:17108316	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152894	Pkd1<sup>m1Bei</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2181896	Pkd1<sup>m1Bei</sup>/Pkd1<sup>m1Bei</sup>  [background:] involves: A/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774945	Tg(Prnp-SMN)92Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:27466204	20170209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774945	Tg(Prnp-SMN)92Ahmb	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22732506	20170209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706664	Neb<sup>tm1Slbt</sup>/Neb<sup>tm1Slbt</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0110928	nemaline myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:19346529	20090625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20962742	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25111226	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14507670	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24915008	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25777062	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22739976	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34341345	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32822386	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:3510458	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] 129X1/SvJ-Col4a3<sup>tm1Dec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9682811	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:4452030	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] 129-Col4a3<sup>tm1Dec</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20197625	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857432	Col4a3<sup>tm1Dec</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:3510446	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8956999	20220412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867688	Gba1<sup>tm1.1Pmis</sup>/Gba1<sup>tm1.1Pmis</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:20962279	20110113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906238	Tg(Myh6-ACTC1*E361G)361.20Sbm	is_implicated_in	DOID:0110456	dilated cardiomyopathy 1R						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906238	Tg(Myh6-ACTC1*E361G)361.20Sbm	is_implicated_in	DOID:0110456	dilated cardiomyopathy 1R		MGI:5906239	Tg(Myh6-ACTC1*E361G)361.20Sbm/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20600154	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906238	Tg(Myh6-ACTC1*E361G)361.20Sbm	is_implicated_in	DOID:0110456	dilated cardiomyopathy 1R						ECO:0000033	author statement supported by traceable reference	PMID:26432839	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5574085	Kcna10<sup>tm1Lex</sup>	is_implicated_in	DOID:3426	vestibular disease		MGI:5574086	Kcna10<sup>tm1Lex</sup>/Kcna10<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23528307	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6696138	Trappc9<sup>em1Xyli</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6715154	Trappc9<sup>em1Xyli</sup>/Trappc9<sup>em1Xyli</sup>  [background:] C57BL/6J-Trappc9<sup>em1Xyli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33208359	20210611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:23223430	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:33941818	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:28151426	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:26276665	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:22490864	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:24880340	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:24282296	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857295	Hbb-b1<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:27154187	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7444112	Dnajb4<sup>em2Sngi</sup>	is_implicated_in	DOID:11720	distal myopathy		MGI:7444385	Dnajb4<sup>em2Sngi</sup>/Dnajb4<sup>em2Sngi</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:36512060	20230315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947988	Ank1<sup>M1Wlst</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:4948066	Ank1<sup>M1Wlst</sup>/Ank1<sup>M1Wlst</sup>  [background:] involves: 129S1/SvImJ * C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21193012	20110426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797591	Phox2b<sup>tm2Jbr</sup>/Phox2b<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18198276	20080717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785389	Tg(Thy1-SOD1*G93A)T1Hgrd/0 Tg(Thy1-SOD1*G93A)T3Hgrd/0  [background:] involves: C57BL/6 * CBA * FVB	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:18305242	20080516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397670	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538531	Smarcb1<sup>tm1Sho</sup>/Smarcb1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J	is_model_of	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634090	Tg(Mbp-SNCA)29Ema	is_implicated_in	DOID:4752	multiple system atrophy		MGI:5634093	Tg(Mbp-SNCA)29Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16291942	20200825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634090	Tg(Mbp-SNCA)29Ema	is_implicated_in	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:32302677	20200825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856880	Flg<sup>ft</sup>	is_implicated_in	DOID:0110098	atopic dermatitis 2						ECO:0000033	author statement supported by traceable reference	PMID:24480880	20170202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856880	Flg<sup>ft</sup>	is_implicated_in	DOID:0110098	atopic dermatitis 2						ECO:0000033	author statement supported by traceable reference	PMID:23792461	20170202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856880	Flg<sup>ft</sup>	is_implicated_in	DOID:0110098	atopic dermatitis 2						ECO:0000033	author statement supported by traceable reference	PMID:27381887	20170202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856880	Flg<sup>ft</sup>	is_implicated_in	DOID:0110098	atopic dermatitis 2		MGI:5532944	Flg<sup>ft</sup>/Flg<sup>ft</sup>  [background:] STOCK a/a Tmem79<sup>ma</sup> Flg<sup>ft</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23844115	20170202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687258	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:16492673	20220719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687258	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:34740257	20220719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698627	Sall4<sup>tm1Brd</sup>/Sall4<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060747	Duane-radial ray syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17216607	20070305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769341	Ahsp<sup>tm1Mjwe</sup>/Ahsp<sup>tm1Mjwe</sup> Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:15545996	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5568998	Mecp2<sup>tm1.1Jtc</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24283265	20170308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3760264	Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] B6.129P2-Il2<sup>tm1Hor</sup>/J	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17207605	20170417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0050794	multiple synostoses syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587758	Myo7a<sup>3336SB</sup>/Myo7a<sup>3336SB</sup>  [background:] involves: BALB/cRl	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755852	Pik3ca<sup>tm1.1Waph</sup>/Pik3ca<sup>+</sup> Tg(MMTV-cre)#Mam/0  [background:] involves: 129S1/Sv * C57BL/6 * FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22666336	20160407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688743	Scarb2<sup>tm1Psa</sup>/Scarb2<sup>tm1Psa</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:891	progressive myoclonus epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:25316793	20151001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663447	Tg(Prnp-MAPT)43Vle/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10595524	20110502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388028	Tg(Plp)66Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:22706386	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388028	Tg(Plp)66Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:26676415	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388028	Tg(Plp)66Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:4887901	Tg(Plp)66Kan/0  [background:] B6NCrl.Cg-Tg(Plp)66Kan			ECO:0000033	author statement supported by traceable reference	PMID:17133418	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388028	Tg(Plp)66Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:4887891	Tg(Plp)66Kan/Tg(Plp)66Kan  [background:] B6NCrl.Cg-Tg(Plp)66Kan			ECO:0000033	author statement supported by traceable reference	PMID:17133418	20160819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437484	Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15885355	20121003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437484	Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11042693	20121003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437484	Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857930	Terc<sup>tm1Rdp</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23831727	20170303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857930	Terc<sup>tm1Rdp</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27799523	20170303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5882421	Tg(EmuSR-HDAC9)1468Kpet	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5882422	Tg(EmuSR-HDAC9)1468Kpet/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:27799148	20170406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6509462	Ppil1<sup>em4Jgg</sup>	is_implicated_in	DOID:0112325	pontocerebellar hypoplasia type 14		MGI:6509640	Ppil1<sup>em4Jgg</sup>/Ppil1<sup>em4Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em4Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655819	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4441292	Gla<sup>tm1Kul</sup>/Y Itpr1<sup>wblo</sup>/Itpr1<sup>wblo</sup>  [background:] B6;129-Gla<sup>tm1Kul</sup> Itpr1<sup>wblo</sup>/GrsrJ	is_model_of	DOID:0050965	spinocerebellar ataxia type 15						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637814	Lgals3<sup>tm1Ftl</sup>/Lgals3<sup>tm1Ftl</sup>  [background:] involves: 129S2/SvPas * CD-1	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:17029217	20150601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637814	Lgals3<sup>tm1Ftl</sup>/Lgals3<sup>tm1Ftl</sup>  [background:] involves: 129S2/SvPas * CD-1	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:18637146	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:23056165	20161208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:26172853	20161208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857212	Ldlr<sup>tm1Her</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:3611043	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21690266	20161208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825057	Tg(BAC144D14)5D3Masu	is_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:6199144	Tg(BAC144D14)5D3Masu/0  [background:] B6.Cg-Tg(BAC144D14)5D3Masu			ECO:0000033	author statement supported by traceable reference	PMID:27798108	20180924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825057	Tg(BAC144D14)5D3Masu	is_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:5825059	Tg(BAC144D14)5D3Masu/0  [background:] B6J.Cg-Tg(BAC144D14)5D3Masu			ECO:0000033	author statement supported by traceable reference	PMID:26963625	20180924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5085985	Zic2<sup>tm1Jaru</sup>/Zic2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22355535	20110815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29311329	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21875659	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35129866	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26670829	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493591	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] 129S1.129S4(B6)-Chd7<sup>Gt(S20-7E1)Sor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21596839	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3708348	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>Gt(S20-7E1)Sor</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17334657	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3708350	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17334657	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7496091	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:36288662	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5807347	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26670829	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3719118	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6J) or (involves: 129S1/SvImJ * 129S4/SvJae C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17701983	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493591	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] 129S1.129S4(B6)-Chd7<sup>Gt(S20-7E1)Sor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19279158	20230707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707678	Chd7<sup>Gt(S20-7E1)Sor</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7496044	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:21875659	20230707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583529	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/JUnc	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:6624875	20050812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909970	Tg(Myh6/tetO-Mybpc3*)#Rbns	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5909973	Tg(Myh6/tetO-Mybpc3*)#Rbns/0 Tg(Myh6-tTA)55Rbns/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23852539	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796560	Tg(MMTV-Erbb2)1Pv/0  [background:] involves: BALB/c * C57BL/6 * CD-1 * DBA	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26941084	20161005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559563	Arx<sup>tm5Kki</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:6196031	Arx<sup>tm5Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6NHsd			ECO:0000033	author statement supported by traceable reference	PMID:28602636	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559563	Arx<sup>tm5Kki</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:33711494	20210720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175186	Ntrk1<sup>tm1Par</sup>/Ntrk1<sup>tm1Par</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0050548	hereditary sensory neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:10681461	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:26792657	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22930691	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22886699	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:26784541	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:30002128	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:29635291	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11159866	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3779061	Phex<sup>Hyp</sup>/?  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15976027	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764685	Phex<sup>Hyp</sup>/Phex<sup>+</sup>  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857312	Phex<sup>Hyp</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9063736	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5299425	Scrib<sup>tm1.1Phum</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6414871	Wnk4<sup>em1Cjc</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6414873	Wnk4<sup>em1Cjc</sup>/Wnk4<sup>em1Cjc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30765526	20200505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818801	Jak2<sup>tm1.2Ble</sup>	is_implicated_in	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:27154187	20170123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818801	Jak2<sup>tm1.2Ble</sup>	is_implicated_in	DOID:8997	polycythemia vera		MGI:4818803	Jak2<sup>tm1.2Ble</sup>/Jak2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20541703	20170123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818801	Jak2<sup>tm1.2Ble</sup>	is_implicated_in	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:25552701	20170123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579768	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] B6.129S-Col4a1<sup>deltaex40</sup>	is_model_of	DOID:0060263	porencephaly						ECO:0000033	author statement supported by traceable reference	PMID:15905400	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402443	Tg(CAG-DPP4)4Yuzh	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6402445	Tg(CAG-DPP4)4Yuzh/0  [background:] C57BL/6-Tg(CAG-DPP4)4Yuzh			ECO:0000033	author statement supported by traceable reference	PMID:26701103	20200406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575018	Pcdh15<sup>av-Jfb</sup>/Pcdh15<sup>av-Jfb</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110832	Usher syndrome type 1F						ECO:0000033	author statement supported by traceable reference	PMID:12782354	20090220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135675	Fgfr3<sup>tm4Cxd</sup>	is_implicated_in	DOID:13481	thanatophoric dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:27506979	20170222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135675	Fgfr3<sup>tm4Cxd</sup>	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3640323	Fgfr3<sup>tm4Cxd</sup>/Fgfr3<sup>+</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * NIH Black Swiss * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10861287	20170222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446328	Sbds<sup>tm1Jrom</sup>/Sbds<sup>tm3.1Jrom</sup> Ptf1a<sup>tm1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	is_model_of	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22510201	20121227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699155	Spast<sup>tm1.1Jme</sup>/Spast<sup>tm1.1Jme</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000033	author statement supported by traceable reference	PMID:17101632	20070308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524978	Tg(tetORo1-lacZ)3Conk	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:11247776	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524978	Tg(tetORo1-lacZ)3Conk	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905901	Tg(Myh6-tTA)6Smbf/0 Tg(tetORo1-lacZ)3Conk/0  [background:] FVB.Cg-Tg(Myh6-tTA)6Smbf Tg(tetORo1-lacZ)3Conk			ECO:0000033	author statement supported by traceable reference	PMID:10781088	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357688	Tg(Vav1-NUP98/HOXD13)C1Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23643835	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357688	Tg(Vav1-NUP98/HOXD13)C1Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22613470	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357688	Tg(Vav1-NUP98/HOXD13)C1Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24414704	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357688	Tg(Vav1-NUP98/HOXD13)C1Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18648006	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357688	Tg(Vav1-NUP98/HOXD13)C1Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26637787	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4357688	Tg(Vav1-NUP98/HOXD13)C1Apla	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:4357766	Tg(Vav1-NUP98/HOXD13)C1Apla/0  [background:] FVB/N-Tg(Vav1-NUP98/HOXD13)C1Apla			ECO:0000033	author statement supported by traceable reference	PMID:15755899	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629821	Slurp1<sup>tm1Lex</sup>	is_implicated_in	DOID:0060862	mal de Meleda		MGI:5629822	Slurp1<sup>tm1Lex</sup>/Slurp1<sup>tm1Lex</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24499735	20150415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5753079	Aspm<sup>tm1(cre)Mrc</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:5753081	Aspm<sup>tm1(cre)Mrc</sup>/Aspm<sup>tm1(cre)Mrc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26581405	20160323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412040	Opa1<sup>M1Bewi</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6	is_model_of	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:17314202	20091217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7435277	Lztfl1<sup>tm1.3Zpl</sup>	is_implicated_in	DOID:0110139	Bardet-Biedl syndrome 17		MGI:7435338	Lztfl1<sup>tm1.3Zpl</sup>/Lztfl1<sup>tm1.3Zpl</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30423168	20230217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4941776	Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>	is_implicated_in	DOID:0060861	microphthalmia with limb anomalies		MGI:4941783	Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>/Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>  [background:] involves: C3H * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21194678	20110323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819955	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:9041192	20081215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5002631	Pdcd10<sup>tm1.1Wami</sup>	is_implicated_in	DOID:0060671	cerebral cavernous malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:29295866	20190509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570240	Tg(TG-NRAS*Q61K)#Msnt	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:5578522	Tg(TG-NRAS*Q61K)#Msnt/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16785999	20140826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014516	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:20505730	20110715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789953	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Stk11<sup>tm1Keis</sup>/Stk11<sup>tm1Keis</sup> Tg(Cyp1a1-cre/ERT)1Dwi/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:21283818	20160826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	MGI:1274824	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560494	Rfx3<sup>b2b1213Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5560505	Rfx3<sup>b2b1213Clo</sup>/Rfx3<sup>b2b1213Clo</sup>  [background:] C57BL/6J-Rfx3<sup>b2b1213Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624136	Cep290<sup>rd16</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:30332642	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624136	Cep290<sup>rd16</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:24051377	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624136	Cep290<sup>rd16</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:24671090	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624136	Cep290<sup>rd16</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10		MGI:5557989	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup>  [background:] involves: BXD24/TyJ			ECO:0000033	author statement supported by traceable reference	PMID:17898177	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624136	Cep290<sup>rd16</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10		MGI:5557979	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup>  [background:] involves: BXD24/TyJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21245082	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388456	Ngf<sup>tm1(NGF*)Cat</sup>	is_implicated_in	DOID:0070145	hereditary sensory and autonomic neuropathy type 5						ECO:0000033	author statement supported by traceable reference	PMID:30612733	20200227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388456	Ngf<sup>tm1(NGF*)Cat</sup>	is_implicated_in	DOID:0070145	hereditary sensory and autonomic neuropathy type 5		MGI:6388458	Ngf<sup>tm1(NGF*)Cat</sup>/Ngf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:31685654	20200227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388456	Ngf<sup>tm1(NGF*)Cat</sup>	is_implicated_in	DOID:0070145	hereditary sensory and autonomic neuropathy type 5		MGI:6388457	Ngf<sup>tm1(NGF*)Cat</sup>/Ngf<sup>tm1(NGF*)Cat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:30612733	20200227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6108137	Otud7a<sup>em1Cpsc</sup>	is_implicated_in	DOID:0060394	chromosome 15q13.3 microdeletion syndrome		MGI:6115021	Otud7a<sup>em1Cpsc</sup>/Otud7a<sup>em1Cpsc</sup>  [background:] C57BL/6J-Otud7a<sup>em1Cpsc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29395075	20180418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433858	Slc4a4<sup>tm1.1Slin</sup>/Slc4a4<sup>tm1.1Slin</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:14219	renal tubular acidosis						ECO:0000033	author statement supported by traceable reference	PMID:21228764	20120914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007926	Mefv<sup>tm3.1(MEFV)Chae</sup>/Mefv<sup>tm3.1(MEFV)Chae</sup>  [background:] B6.129S6-Mefv<sup>tm3.1(MEFV)Chae</sup>	is_model_of	DOID:2987	familial mediterranean fever						ECO:0000033	author statement supported by traceable reference	PMID:21600797	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824267	Wt1<sup>tm1.1Ndha</sup>/Wt1<sup>tm1.1Ndha</sup> Tg(Gata4*G2-cre)#Roja/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:27642710	20170216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767418	Map3k14<sup>aly</sup>/Map3k14<sup>aly</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:12236	primary biliary cholangitis						ECO:0000033	author statement supported by traceable reference	PMID:9620319	20091015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3045711	Htr1a<sup>tm1Rhn</sup>/Htr1a<sup>tm1Rhn</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:2030	anxiety disorder						ECO:0000033	author statement supported by traceable reference	PMID:9826725	20110201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710763	Tg(Prnp-ITM2B/APP695*42)A12Emcg/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16039562	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910771	Tnnt2<sup>tm2.1Feah</sup>	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:5910772	Tnnt2<sup>tm2.1Feah</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27936050	20171002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699329	Tg(SOD1*H46R)IAra/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25762155	20151216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617271	Htt<sup>tm1Hay</sup>/Htt<sup>tm1Hay</sup> Tg(HTT*97Q)IXwy/0 Tg(YAC18)18Hay/Tg(YAC18)18Hay  [background:] FVB.Cg-Htt<sup>tm1Hay</sup> Tg(HTT*97Q)IXwy Tg(YAC18)18Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24728353	20150303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617271	Htt<sup>tm1Hay</sup>/Htt<sup>tm1Hay</sup> Tg(HTT*97Q)IXwy/0 Tg(YAC18)18Hay/Tg(YAC18)18Hay  [background:] FVB.Cg-Htt<sup>tm1Hay</sup> Tg(HTT*97Q)IXwy Tg(YAC18)18Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23001568	20150303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2385830	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11152663	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036209	Junb<sup>tm3Wag</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:24574341	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036209	Junb<sup>tm3Wag</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:24332034	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036209	Junb<sup>tm3Wag</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:25216727	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544447	Pde6b<sup>atrd1</sup>/Pde6b<sup>tm1Eye</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:23946405	20140218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4940531	Dag1<sup>tm4.1Kcam</sup>	is_implicated_in	DOID:0110293	autosomal recessive limb-girdle muscular dystrophy type 2P		MGI:4940545	Dag1<sup>tm4.1Kcam</sup>/Dag1<sup>tm4.1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21388311	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:24882209	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:26269637	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:20869591	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:23630944	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:30507379	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:27466200	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:25595967	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:30718999	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447854	Tg(Pcp2-ATXN1*82Q)5Horr	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1		MGI:5518618	Tg(Pcp2-ATXN1*82Q)5Horr/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20869591	20190801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157626	Tardbp<sup>em1Rhbr</sup>	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6187717	Tardbp<sup>em1Rhbr</sup>/Tardbp<sup>em1Rhbr</sup>  [background:] C57BL/6J-Tardbp<sup>em1Rhbr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29556029	20180709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698026	Glra1<sup>tm1Betz</sup>/Glra1<sup>tm1Betz</sup>  [background:] B6.129P2-Glra1<sup>tm1Betz</sup>	is_model_of	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	PMID:17114051	20070227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358337	Cacna2d2<sup>du</sup>/Cacna2d2<sup>du</sup>  [background:] TKDU/DnJ	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:11487633	20110707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3041878	Kcnj1<sup>tm1Ges</sup>/Kcnj1<sup>tm1Ges</sup>  [background:] involves: 129X1/SvJ * Black Swiss	is_model_of	DOID:0110143	Bartter disease type 2						ECO:0000033	author statement supported by traceable reference	PMID:12122007	20050913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705251	Tg(tetO-EGFR*T790M*L858R)51Paow	is_implicated_in	DOID:1324	lung cancer		MGI:5705253	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)51Paow/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17726540	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705251	Tg(tetO-EGFR*T790M*L858R)51Paow	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26744526	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705251	Tg(tetO-EGFR*T790M*L858R)51Paow	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25870145	20160713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763919	Tg(HSA*LR)41Cath/?  [background:] involves: FVB/N	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2182596	Cln6<sup>nclf</sup>/Cln6<sup>nclf</sup>  [background:] involves: C57BL/6J * C57BL/10J * C3HeB/FeJLe	is_model_of	DOID:0110729	neuronal ceroid lipofuscinosis 6A						ECO:0000033	author statement supported by traceable reference	PMID:11791207	20081009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856399	Col11a1<sup>cho</sup>	is_implicated_in	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:21855682	20190102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856399	Col11a1<sup>cho</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:5294332	Col11a1<sup>cho</sup>/Col11a1<sup>+</sup>  [background:] involves: C57BL/6Fr			ECO:0000033	author statement supported by traceable reference	PMID:13130470	20190102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432016	Tg(Ly6e-MALT1)#Isg	is_implicated_in	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue		MGI:5432017	Tg(Ly6e-MALT1)#Isg/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22689981	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26934227	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29464015	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28432125	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26966191	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:21573126	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:15475948	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:19105207	20210922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838645	Tg(tetO-DISC1*)1001Plet	is_implicated_in	DOID:0070085	schizophrenia 9						ECO:0000033	author statement supported by traceable reference	PMID:20048751	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838645	Tg(tetO-DISC1*)1001Plet	is_implicated_in	DOID:0070085	schizophrenia 9						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838645	Tg(tetO-DISC1*)1001Plet	is_implicated_in	DOID:0070085	schizophrenia 9		MGI:3838963	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-DISC1*)1001Plet/0  [background:] involves: C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17848917	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:26450969	20160520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:25490446	20160520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3810322	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Tg(Atoh1-cre/Esr1*)14Fsh/0  [background:] involves: 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18691547	20160520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3810317	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18691547	20160520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3810319	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Tlx3<sup>tm1(cre)Qima</sup>/Tlx3<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18691547	20160520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3810318	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup> Olig2<sup>tm2(TVA,cre)Rth</sup>/Olig2<sup>+</sup>  [background:] involves: 129 * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18691547	20160520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20190724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:28082400	20190724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818800	Jak2<sup>tm1.1Ble</sup>	is_implicated_in	DOID:2226	myeloproliferative neoplasm		MGI:6356966	Jak2<sup>tm1.1Ble</sup>/Jak2<sup>+</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:29202466	20190826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867909	Myb<sup>boo</sup>	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:4868118	Myb<sup>boo</sup>/Myb<sup>boo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20610815	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175834	Dsg3<sup>tm1Stan</sup>/Dsg3<sup>tm1Stan</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060851	pemphigus vulgaris						ECO:0000033	author statement supported by traceable reference	PMID:9166409	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553464	Tg(Prnp-APPSweArc)#Rmni	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:5553465	Tg(Prnp-APPSweArc)#Rmni/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:23840405	20140331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:309911	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:762500	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	MGI:76424	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12486097	20081002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6162645	Atp1a3<sup>tm1Ute</sup>	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:6162678	Atp1a3<sup>tm1Ute</sup>/Atp1a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25523819	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10699173	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16697652	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638793	Col1a1<sup>tm2(tetO-LIN28B)Gqda</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA,EGFP)Nagy</sup>/Gt(ROSA)26Sor<sup>+</sup> Wt1<sup>tm2(cre/ERT2)Wtp</sup>/Wt1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:2154	nephroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24732380	20150609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806781	Gt(ROSA)26Sor<sup>tm4(CAG-hsb5)Nki</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Mx1-cre)1Cgn/0 Tg(Tal1-tTA)19Dgt/0 Tg(tetO-BCR/ABL1)2Dgt/0 TgTn(pb-sb-GrOnc)#aGsva/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA/J * DBA/2 * FVB/N	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26304963	20161110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:8774148	20070202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:16274458	20070202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:8362989	20070202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:18037434	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:20202977	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:15385543	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:6000	congestive heart failure						ECO:0000033	author statement supported by traceable reference	PMID:20157292	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284885	Tg(Myh6-Mtpn)4Ssen	is_implicated_in	DOID:6000	congestive heart failure		MGI:5908182	Tg(Myh6-Mtpn)4Ssen/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:14970239	20170905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176892	Dmd<sup>mdx</sup>/Y Dtna<sup>tm1Jrs</sup>/Dtna<sup>tm1Jrs</sup>  [background:] involves: 129X1/SvJ * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:10559919	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052685	Pdx1<sup>tm1Cvw</sup>/Pdx1<sup>+</sup> Pbx1<sup>tm1Mlc</sup>/Pbx1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11912494	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581437	Itgb6<sup>tm1Des</sup>/Itgb6<sup>tm1Des</sup>  [background:] involves: 129T2/SvEms	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:12634787	20050712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897270	Lbr<sup>ic-J</sup>/Lbr<sup>+</sup>  [background:] (NZW/LacJ x C57BL/6J-Lbr<sup>ic-J</sup>/J)F1	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:27483354	20170512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5468686	Tg(Ckm-Chrne*L269F)5Cgz	is_implicated_in	DOID:0110678	congenital myasthenic syndrome 4A						ECO:0000033	author statement supported by traceable reference	PMID:16973214	20151103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5468686	Tg(Ckm-Chrne*L269F)5Cgz	is_implicated_in	DOID:0110678	congenital myasthenic syndrome 4A		MGI:5478770	Tg(Ckm-Chrne*L269F)5Cgz/?  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:9151734	20151103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5468686	Tg(Ckm-Chrne*L269F)5Cgz	is_implicated_in	DOID:0110678	congenital myasthenic syndrome 4A						ECO:0000033	author statement supported by traceable reference	PMID:25448156	20151103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5468686	Tg(Ckm-Chrne*L269F)5Cgz	is_implicated_in	DOID:0110678	congenital myasthenic syndrome 4A						ECO:0000033	author statement supported by traceable reference	PMID:17853947	20151103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689179	Ryr2<sup>tm1Slh</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:16873551	20061129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949848	Mecp2<sup>tm1Vnar</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:4949888	Mecp2<sup>tm1Vnar</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:20163734	20110512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5461654	Ube3a<sup>tm1Alb</sup>/Ube3a<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22916201	20130201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3578633	Spry2<sup>tm1.1Mrt</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23434594	20131022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6110833	Tg(TTR)#Jbux	is_implicated_in	DOID:0050638	transthyretin amyloidosis		MGI:6110836	Tg(TTR)#Jbux/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11310831	20180118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304449	Tg(RP11-209M4)AGglo	is_implicated_in	DOID:0080036	SOST-related sclerosing bone dysplasia		MGI:5304472	Tg(RP11-209M4)AGglo/0  [background:] FVB-Tg(RP11-209M4)4Gglo			ECO:0000033	author statement supported by traceable reference	PMID:15965026	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304449	Tg(RP11-209M4)AGglo	is_implicated_in	DOID:0080036	SOST-related sclerosing bone dysplasia		MGI:5304474	Tg(RP11-209M4)AGglo/Tg(RP11-209M4)AGglo  [background:] FVB-Tg(RP11-209M4)4Gglo			ECO:0000033	author statement supported by traceable reference	PMID:15965026	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029314	Slc34a1<sup>tm1Hten</sup>/Slc34a1<sup>tm1Hten</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria						ECO:0000033	author statement supported by traceable reference	PMID:9560283	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6369410	Adamtsl2<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:0111725	geleophysic dysplasia 1		MGI:6378827	Adamtsl2<sup>tm1c(KOMP)Wtsi</sup>/Adamtsl2<sup>tm1c(KOMP)Wtsi</sup> Tg(Prrx1-cre)1Cjt/0  [background:] B6.Cg-Adamtsl2<sup>tm1c(KOMP)Wtsi</sup> Tg(Prrx1-cre)1Cjt			ECO:0000033	author statement supported by traceable reference	PMID:30738849	20200518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665566	F11<sup>tm1Gjb</sup>/F11<sup>tm1Gjb</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2229	factor XI deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9518045	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:9063736	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:11159866	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304695	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup>  [background:] B6.129-Kras<sup>tm4Tyj</sup> Tgfbr2<sup>tm1.2Hlm</sup>	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:21911454	20120202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574668	Enam<sup>Rgsc521</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J	is_model_of	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046797	Tbx1<sup>tm2Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809674	Abca12<sup>tm1Shzu</sup>/Abca12<sup>tm1Shzu</sup>  [background:] B6.129S-Abca12<sup>tm1Shzu</sup>	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:18632686	20081006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6695910	Rab39b<sup>em1Jfch</sup>	is_implicated_in	DOID:0060309	syndromic X-linked intellectual disability		MGI:6695982	Rab39b<sup>em1Jfch</sup>/Y  [background:] C57BL/6N-Rab39b<sup>em1Jfch</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32115408	20210503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361520	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0  [background:] involves: C57BL/6J * CBA/J * FVB/N	is_model_of	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19706403	20091015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587187	Hps4<sup>le</sup>/Hps4<sup>le</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5086221	Shank3<sup>tm1.1Pfw</sup>/Shank3<sup>+</sup>  [background:] B6.129S6-Shank3<sup>tm1.1Pfw</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	MGI:5499103	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25237101	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:10579712	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5287715	Trim32<sup>tm1Spc</sup>	is_implicated_in	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H		MGI:5287716	Trim32<sup>tm1Spc</sup>/Trim32<sup>tm1Spc</sup>  [background:] involves: 129S/SvEvBrd * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21775502	20110930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821827	avc3	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822144	avc3/avc3  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437479	Shank2<sup>tm1Mgle</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23583105	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437479	Shank2<sup>tm1Mgle</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22699620	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437479	Shank2<sup>tm1Mgle</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5437480	Shank2<sup>tm1Mgle</sup>/Shank2<sup>tm1Mgle</sup>  [background:] B6.129S4-Shank2<sup>tm1Mgle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27903723	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437479	Shank2<sup>tm1Mgle</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437479	Shank2<sup>tm1Mgle</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25981743	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437479	Shank2<sup>tm1Mgle</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5437480	Shank2<sup>tm1Mgle</sup>/Shank2<sup>tm1Mgle</sup>  [background:] B6.129S4-Shank2<sup>tm1Mgle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22699620	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577900	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm1Ttd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:15837576	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814717	Tc(HSA21)1TybEmcf/0  [background:] involves: 129S2/SvPas * 129S8/SvEv * C57BL/6J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16179473	20081112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156187	Spint2<sup>Gt(KST272)Byg</sup>	is_implicated_in	DOID:0060781	congenital secretory sodium diarrhea 3						ECO:0000033	author statement supported by traceable reference	PMID:31628112	20201208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183770	Tg(PMP22)C22Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:29202483	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183770	Tg(PMP22)C22Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3845794	Tg(PMP22)C22Clh/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:12090404	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183770	Tg(PMP22)C22Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3845794	Tg(PMP22)C22Clh/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:8733121	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526031	Tg(Snca-SNCA)#Galt	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:27509067	20180125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526031	Tg(Snca-SNCA)#Galt	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5526032	Tg(Snca-SNCA)#Galt/?  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:23573275	20180125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818630	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S5/SvEvBrd * FVB/N	is_model_of	DOID:206	hereditary multiple exostoses						ECO:0000033	author statement supported by traceable reference	PMID:20534475	20100809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324681	Tg(Thy1-APP*Swe*Ind)fAccu	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21414686	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324681	Tg(Thy1-APP*Swe*Ind)fAccu	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:6324682	Tg(Thy1-APP*Swe*Ind)fAccu/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21143159	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324681	Tg(Thy1-APP*Swe*Ind)fAccu	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27681803	20190725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6187668	Atp1a2<sup>tm1.1Tmklh</sup>	is_implicated_in	DOID:0111182	familial hemiplegic migraine 2		MGI:6314222	Atp1a2<sup>tm1.1Tmklh</sup>/Atp1a2<sup>+</sup>  [background:] B6.129S1(Cg)-Atp1a2<sup>tm1.1Tmklh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26911348	20210810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6187668	Atp1a2<sup>tm1.1Tmklh</sup>	is_implicated_in	DOID:0111182	familial hemiplegic migraine 2						ECO:0000033	author statement supported by traceable reference	PMID:30446731	20210810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805033	Brca1<sup>tm1Thl</sup>/Brca1<sup>tm1Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6188930	Tg(Myh6-Pkp2*/mRuby)4Rbrug	is_implicated_in	DOID:0110077	arrhythmogenic right ventricular dysplasia 9		MGI:6188933	Tg(Myh6-Pkp2*/mRuby)4Rbrug/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:27412010	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682002	Nbn<sup>tm1Zqw</sup>/Nbn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14612522	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835231	Tg(MMTV-LPAR1)7Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763094	Tg(MMTV-LPAR1)7Gbm/Tg(MMTV-LPAR1)7Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)7Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5307228	Tg(Lgi1*)#Mpan	is_implicated_in	DOID:0060748	familial temporal lobe epilepsy 1		MGI:5307230	Tg(Lgi1*)#Mpan/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:19701204	20120227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4973916	Adgrl3<sup>Gt(S17-5H1)Sor</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5430804	Adgrl3<sup>Gt(S17-5H1)Sor</sup>/Adgrl3<sup>Gt(S17-5H1)Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27247960	20190718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779562	Tg(ACTA1-Ctss)1Jmol/?  [background:] FVB/N-Tg(ACTA1-Ctss)1Jmol	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26966179	20160630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5577182	Tg(Thy1-FUS*)19Vlb/0  [background:] B6.Cg-Tg(Thy1-FUS*)19Vlb	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:23867462	20140815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23540693	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25422452	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24819516	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:2653844	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:7977654	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817313	Dym<sup>Gt(GTR1.3)1Rul</sup>/Dym<sup>Gt(GTR1.3)1Rul</sup>  [background:] involves: 129	is_model_of	DOID:0060247	Smith-McCort dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:18852472	20081120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774583	Pdx1<sup>tm1Cvw</sup>/Pdx1<sup>tm4Cvw</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 * DBA	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:18155690	20080321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906381	rd21	is_implicated_in	DOID:8466	retinal degeneration		MGI:5906382	rd21/rd21  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:5906378	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781013	Tg(Mup3-Plau)350-2Eps	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27166937	20161017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781013	Tg(Mup3-Plau)350-2Eps	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5781017	Tg(Mup3-Plau)350-2Eps/?  [background:] C57BL/6-Tg(Mup3-Plau)350-2Eps			ECO:0000033	author statement supported by traceable reference	PMID:25132496	20161017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781013	Tg(Mup3-Plau)350-2Eps	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27211490	20161017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867020	Dchs1<sup>tm1.2Irv</sup>	is_implicated_in	DOID:988	mitral valve prolapse		MGI:5695318	Dchs1<sup>tm1.2Irv</sup>/Dchs1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26258302	20151110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6885945	Prickle1<sup>em1Yzou</sup>	is_implicated_in	DOID:0111448	progressive myoclonus epilepsy 1B		MGI:6890374	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>+</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448372	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] involves: C3H	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:14451913	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646612	b2b3077Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5648026	b2b3077Clo/b2b3077Clo  [background:] C57BL/6J-b2b3077Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850354	Hr<sup>rh-8J</sup>/Hr<sup>rh-8J</sup>  [background:] B10.D2/nSnJ-Hr<sup>rh-8J</sup>	is_model_of	DOID:0060689	atrichia with papular lesions						ECO:0000033	author statement supported by traceable reference	PMID:9799606	20090714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772334	Sgca<sup>tm2Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:31430305	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772334	Sgca<sup>tm2Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D		MGI:7278768	Sgca<sup>tm2Kcam</sup>/Sgca<sup>tm2Kcam</sup>  [background:] B6.129S6-Sgca<sup>tm2Kcam</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28797108	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7261361	Tshz3<sup>tm2.1Lafa</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:35292625	20220414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7261361	Tshz3<sup>tm2.1Lafa</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:7261388	Tshz3<sup>tm2.1Lafa</sup>/Tshz3<sup>tm2.1Lafa</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31060802	20220414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511167	Tg(Ela1-Myc)159Bri	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22024988	20120828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511167	Tg(Ela1-Myc)159Bri	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5432345	Tg(Ela1-Myc)159Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1986386	20120828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825461	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Nes-cre/ERT2,-ALPP)1Sbk/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27815386	20170302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6476958	Tg(Thy1-FUS*)1Dit	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:7278827	Tg(Thy1-FUS*)1Dit/0  [background:] B6.Cg-Tg(Thy1-FUS*)1Dit			ECO:0000033	author statement supported by traceable reference	PMID:28928015	20220519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6476958	Tg(Thy1-FUS*)1Dit	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:7278827	Tg(Thy1-FUS*)1Dit/0  [background:] B6.Cg-Tg(Thy1-FUS*)1Dit			ECO:0000033	author statement supported by traceable reference	PMID:27368346	20220519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571374	Tg(Igh-ROR1)1Kip/0 Tg(Igh-V186.2-TCL1A)3Cro/0  [background:] B6.Cg-Tg(Igh-ROR1)1Kip Tg(Igh-V186.2-TCL1A)3Cro	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24379361	20140707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824305	Tg(PDGFB-SNCA/EGFP)78Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5824306	Tg(PDGFB-SNCA/EGFP)78Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15765523	20170216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644279	Tg(Prnp-lacZ/ATXN10*)#Teas	is_implicated_in	DOID:0050960	spinocerebellar ataxia type 10		MGI:5644283	Tg(Prnp-lacZ/ATXN10*)#Teas/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22065565	20150812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644279	Tg(Prnp-lacZ/ATXN10*)#Teas	is_implicated_in	DOID:0050960	spinocerebellar ataxia type 10						ECO:0000033	author statement supported by traceable reference	PMID:24533179	20150812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438062	Drc1<sup>b2b1654Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384151	Smn1<sup>tm1Jme</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:24463453	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384151	Smn1<sup>tm1Jme</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:26276812	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384151	Smn1<sup>tm1Jme</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:5287852	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1Jme</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15076752	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7529021	Cfap57<sup>em1Qsh</sup>	is_implicated_in	DOID:12336	male infertility		MGI:7529045	Cfap57<sup>em1Qsh</sup>/Cfap57<sup>em1Qsh</sup>  [background:] C57BL/6-Cfap57<sup>em1Qsh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36752199	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6404929	Rs1<sup>tm3.1Rom</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6404948	Rs1<sup>tm3.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796111	Gt(ROSA)26Sor<sup>tm1(DTA)Jpmb</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Plp1-cre/ERT)3Pop/0  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:26656646	20160929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672959	Lyst<sup>bg-14J</sup>/Lyst<sup>bg-14J</sup>  [background:] C3Fe;B6-Lyst<sup>bg-14J</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	MGI:2673072	20051103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6194707	Ttr<sup>tm1.1Smoc</sup>	is_implicated_in	DOID:0050638	transthyretin amyloidosis		MGI:6194720	Ttr<sup>tm1.1Smoc</sup>/?  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29360446	20180816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526881	Mybpc3<sup>tm1Rmos</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526881	Mybpc3<sup>tm1Rmos</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:3527229	Mybpc3<sup>tm1Rmos</sup>/Mybpc3<sup>tm1Rmos</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11909824	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671905	Kmt2a<sup>tm2(MLLT3)Thr</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26847026	20170316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671905	Kmt2a<sup>tm2(MLLT3)Thr</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:4455033	Kmt2a<sup>tm2(MLLT3)Thr</sup>/Kmt2a<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:10393173	20170316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182126	Tg(CMV-Scnn1a)1352Rss	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:9326675	20140103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5547617	Tg(tetO-H2-K1)#Papl	is_implicated_in	DOID:633	myositis		MGI:5547618	Tg(CKMM-tTA)A3Rhvh/0 Tg(tetO-H2-K1)#Papl/0  [background:] B6.Cg-Tg(CKMM-tTA)A3Rhvh Tg(tetO-H2-K1)#Papl			ECO:0000033	author statement supported by traceable reference	PMID:10922072	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5547617	Tg(tetO-H2-K1)#Papl	is_implicated_in	DOID:633	myositis						ECO:0000033	author statement supported by traceable reference	PMID:23785461	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5547617	Tg(tetO-H2-K1)#Papl	is_implicated_in	DOID:633	myositis						ECO:0000033	author statement supported by traceable reference	PMID:26551678	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5002476	Tg(Prnp-TARDBP)3cPtrc	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5308055	Tg(Prnp-TARDBP)3cPtrc/Tg(Prnp-TARDBP)3cPtrc  [background:] C57BL/6-Tg(Prnp-TARDBP)3cPtrc			ECO:0000033	author statement supported by traceable reference	PMID:20702714	20120229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056093	Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>/Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>	is_model_of	DOID:0060861	microphthalmia with limb anomalies						ECO:0000033	author statement supported by traceable reference	PMID:21750680	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148229	Neurod1<sup>tm1Mjts</sup>	is_implicated_in	DOID:0110746	type 1 diabetes mellitus 7						ECO:0000033	author statement supported by traceable reference	PMID:24411943	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148229	Neurod1<sup>tm1Mjts</sup>	is_implicated_in	DOID:0110746	type 1 diabetes mellitus 7		MGI:2174973	Neurod1<sup>tm1Mjts</sup>/Neurod1<sup>tm1Mjts</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9308961	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6391198	Hnrnpf<sup>tm1Jsdc</sup>	is_implicated_in	DOID:9432	renal glycosuria		MGI:6392034	Hnrnpf<sup>tm1Jsdc</sup>/Hnrnpf<sup>tm1Jsdc</sup> Pax8<sup>tm1.1(cre)Mbu</sup>/Pax8<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31673025	20200226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624435	Myo5a<sup>d-n</sup>/Myo5a<sup>d-n</sup>  [background:] B10.D2-H2<sup>d</sup>/nSnJ	is_model_of	DOID:0060832	Griscelli syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:21508232	20110606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857132	Atm<sup>tm1Awb</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:25646414	20150428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857132	Atm<sup>tm1Awb</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175703	Atm<sup>tm1Awb</sup>/Atm<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Atm<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:10449794	20150428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857132	Atm<sup>tm1Awb</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175703	Atm<sup>tm1Awb</sup>/Atm<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Atm<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:8689683	20150428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7331422	Sar1b<sup>em2Emle</sup>	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:7331489	Sar1b<sup>em2Emle</sup>/Sar1b<sup>+</sup>  [background:] C57BL/6N-Sar1b<sup>em2Emle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33964306	20220824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428306	Tg(Disc1/EGFP)M19Sshe/0  [background:] involves: C57BL/6JCrl * CBA/CaCrl	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:18945897	20120719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575509	Tg(Prnp-SNAP25/HTT*150Q)8Xjl/0  [background:] involves: FVB	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24081492	20140730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158863	Col1a1<sup>tm1.1Jcm</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:26264579	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158863	Col1a1<sup>tm1.1Jcm</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:22511244	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158863	Col1a1<sup>tm1.1Jcm</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:26769006	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158863	Col1a1<sup>tm1.1Jcm</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:24022296	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158863	Col1a1<sup>tm1.1Jcm</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4		MGI:3623489	Col1a1<sup>tm1.1Jcm</sup>/Col1a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:10608859	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:27777976	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23043085	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:26121745	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:26719147	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24361037	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:3586967	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6232310	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:3588311	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] B6.C3Fe-Hps1<sup>ep</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20200805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5510724	Hbb<sup>d3th</sup>/Hbb<sup>+</sup> Tg(LCR-HBA1,LCR-HBB*)1Tow/0  [background:] involves: C57BL/6 * DBA/2J * SJL	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:2154033	20131009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882127	Tg(CMV-Tsc2*)1Arbi/0  [background:] involves: C57BL/6	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15576369	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882127	Tg(CMV-Tsc2*)1Arbi/0  [background:] involves: C57BL/6	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21827857	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:8325377	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	MGI:62459	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:8155735	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:3352223	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:9837751	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:9140816	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:1996978	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>	is_model_of	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:10100867	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304359	Samd9l<sup>tm1Homy</sup>	is_not_implicated_in	DOID:0080170	normophosphatemic familial tumoral calcinosis		MGI:5694935	Samd9l<sup>tm1Homy</sup>/Samd9l<sup>tm1Homy</sup>  [background:] B6N.129P2-Samd9l<sup>tm1Homy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22716256	20151105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30104343	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29127345	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28556246	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5523996	Scn1a<sup>tm1Kea</sup>/Scn1a<sup>+</sup>  [background:] (C57BL/6J x 129S6/SvEvTac-Scn1a<sup>tm1Kea</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:24152123	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30347190	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27768696	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24434335	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510417	Scn1a<sup>tm1Kea</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:37901435	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7567698	Atp6v1b2<sup>em1Pcamp</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:7567701	Atp6v1b2<sup>em1Pcamp</sup>/Atp6v1b2<sup>em1Pcamp</sup>  [background:] C57BL/6N-Atp6v1b2<sup>em1Pcamp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37628590	20231220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5577178	Tg(Thy1-FUS*)19Vlb	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:31383794	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5577178	Tg(Thy1-FUS*)19Vlb	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:5577182	Tg(Thy1-FUS*)19Vlb/0  [background:] B6.Cg-Tg(Thy1-FUS*)19Vlb			ECO:0000033	author statement supported by traceable reference	PMID:23867462	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5577178	Tg(Thy1-FUS*)19Vlb	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:24334610	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5086230	Tg(Thy1-GLRA1*R271Q)300Wha	is_implicated_in	DOID:9091	REM sleep behavior disorder		MGI:5140029	Tg(Thy1-GLRA1*R271Q)300Wha/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21562273	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857931	Brca1<sup>tm1Bhk</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18068631	20160422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6356292	Mast1<sup>em1Dak</sup>	is_implicated_in	DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		MGI:6358832	Mast1<sup>em1Dak</sup>/Mast1<sup>+</sup>  [background:] B6.Cg-Mast1<sup>em1Dak</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30449657	20200518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5776537	Cap2<sup>tm1e(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907446	Cap2<sup>tm1e(EUCOMM)Wtsi</sup>/Cap2<sup>tm1e(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Cap2<sup>tm1e(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22945801	20170825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763090	Tg(MMTV-LPAR1)2Gbm/Tg(MMTV-LPAR1)2Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)2Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857164	En2<sup>tm1Alj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30980901	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857164	En2<sup>tm1Alj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23360806	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857164	En2<sup>tm1Alj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23142422	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857164	En2<sup>tm1Alj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26987954	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857164	En2<sup>tm1Alj</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3719798	En2<sup>tm1Alj</sup>/En2<sup>tm1Alj</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16935268	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448770	Tg(SOD1)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26853136	20210209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448770	Tg(SOD1)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30460537	20210209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448770	Tg(SOD1)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24154542	20210209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7531287	Nsf<sup>tm1Himat</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:7531415	Nsf<sup>tm1Himat</sup>/Nsf<sup>+</sup>  [background:] C57BL/6N-Nsf<sup>tm1Himat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34745222	20230928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653187	Ikzf3<sup>tm1Kge</sup>/Ikzf3<sup>tm1Kge</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:9806640	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653187	Ikzf3<sup>tm1Kge</sup>/Ikzf3<sup>tm1Kge</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12574333	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461705	Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0111044	gray platelet syndrome		MGI:5608466	Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>/Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:25258341	20150526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697652	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] D2.B10-Dmd<sup>mdx</sup>/J	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:26566673	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5288470	Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>/Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>  [background:] involves: FVB/N	is_model_of	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15466487	20111006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610503	Col4a5<sup>tm1Yseg</sup>/Y  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>	is_model_of	DOID:0110034	X-linked Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23707242	20140709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610503	Col4a5<sup>tm1Yseg</sup>/Y  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>	is_model_of	DOID:0110034	X-linked Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15153557	20140709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906192	Tg(Myh6-Tnni3*)1Ammu	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906193	Tg(Myh6-Tnni3*)1Ammu/0  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15863459	20170803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5604241	Tg(tetO-Fgfr3*R248C/Fgfr1)#Dor	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5604242	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Fgfr3*R248C/Fgfr1)#Dor/0  [background:] involves: 129 * C57BL/6 * FVB/N * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:24349409	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524081	Tg(MMTV-Myc)WT21Jrn	is_implicated_in	DOID:1612	breast cancer		MGI:5524085	Tg(MMTV-Myc)WT21Jrn/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22525269	20220628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524081	Tg(MMTV-Myc)WT21Jrn	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26474282	20220628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157622	Notch2<sup>tm2.1Ecan</sup>	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:6157651	Notch2<sup>tm2.1Ecan</sup>/Notch2<sup>tm2.1Ecan</sup> Tg(BGLAP-cre)1Clem/0  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:28592489	20180523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524080	Tg(MMTV-Myc)WT13Jrn	is_implicated_in	DOID:1612	breast cancer		MGI:5524084	Tg(MMTV-Myc)WT13Jrn/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473556	Eml1<sup>tm1.2Ics</sup>	is_implicated_in	DOID:0111169	subcortical band heterotopia		MGI:6473560	Eml1<sup>tm1.2Ics</sup>/Eml1<sup>tm1.2Ics</sup>  [background:] C57BL/6N-Eml1<sup>tm1.2Ics</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31173351	20201123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5811610	Camk2a<sup>em1Rjco</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6324924	Camk2a<sup>em1Rjco</sup>/Camk2a<sup>em1Rjco</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:28130356	20190726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687167	H2<sup>g7</sup>/H2<sup>g7</sup> Ins2<sup>tm1Jja</sup>/Ins2<sup>tm1Jja</sup> Rag1<sup>tm1Mom</sup>/Rag1<sup>tm1Mom</sup> Tg(TcraBDC12-4.1)10Jos/0 Tg(TcrbBDC12-4.1)82Gse/0  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6 * FVB * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16804066	20061109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908395	Gabrb3<sup>tm2.1Uru</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5908397	Gabrb3<sup>tm2.1Uru</sup>/Gabrb3<sup>tm2.1Uru</sup>  [background:] B6J.129S6(Cg)-Gabrb3<sup>tm2.1Uru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26627235	20170906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:22983217	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:21956219	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25184332	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:24163128	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2175141	Nf1<sup>tm1Fcr</sup>/Nf1<sup>tm1Fcr</sup>  [background:] either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7926784	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7281840	Hsf2bp<sup>em2Amp</sup>	is_implicated_in	DOID:0112278	primary ovarian insufficiency 19		MGI:7282037	Hsf2bp<sup>em2Amp</sup>/Hsf2bp<sup>em2Amp</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:32845237	20220603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285350	Bicc1<sup>b2b222Clo</sup>/Bicc1<sup>b2b222Clo</sup>  [background:] C57BL/6J-Bicc1<sup>b2b222Clo</sup>	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5307058	Tg(CTSG-NUMA1/RARA)#Skr	is_implicated_in	DOID:0060318	acute promyelocytic leukemia		MGI:5307063	Tg(CTSG-NUMA1/RARA)#Skr/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14737102	20120224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444399	Tg(Tlr7)1Boll	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5488510	Tg(Tlr7)1Boll/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23382559	20130603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175102	Lim2<sup>To3</sup>/Lim2<sup>To3</sup>  [background:] involves: 102 * C3H/He * T STOCK	is_model_of	DOID:0110263	cataract 19 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:9238094	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838322	Ttn<sup>tm1.1Isrd</sup>	is_implicated_in	DOID:0111078	tibial muscular dystrophy		MGI:4838323	Ttn<sup>tm1.1Isrd</sup>/Ttn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20855473	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838322	Ttn<sup>tm1.1Isrd</sup>	is_implicated_in	DOID:0111078	tibial muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473606	Frem1<sup>eyes2</sup>/Frem1<sup>eyes2</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:23221805	20130410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6336104	Mocos<sup>em2(IMPC)Ics</sup>	is_implicated_in	DOID:0070314	obstructive nephropathy		MGI:7495807	Mocos<sup>em2(IMPC)Ics</sup>/Mocos<sup>em2(IMPC)Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35372998	20230706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909257	Tg(Myh6-MYL3*A57G)#Dsc	is_implicated_in	DOID:0110314	hypertrophic cardiomyopathy 8		MGI:5909258	Tg(Myh6-MYL3*A57G)#Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23748425	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433408	b2b1163Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433487	b2b1163Clo/b2b1163Clo  [background:] C57BL/6J-b2b1163Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431136	Gt(ROSA)26Sor<sup>tm1(tTA,tetO-Mir155)Fjsl</sup>	is_implicated_in	DOID:0060058	lymphoma		MGI:5431138	Gt(ROSA)26Sor<sup>tm1(tTA,tetO-Mir155)Fjsl</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Nes-cre)1Wmz/0  [background:] involves: 129 * C57BL/6 * FVB/N * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:22685206	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043584	Aga<sup>tm1Pltn</sup>/Aga<sup>tm1Pltn</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0050461	aspartylglucosaminuria						ECO:0000033	author statement supported by traceable reference	PMID:9425233	20050526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052119	Tg(Eno2-PSEN2)2348Ykk/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12039862	20110804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6501733	Cpa1<sup>tm1.1Satom</sup>	is_implicated_in	DOID:4989	pancreatitis		MGI:6501768	Cpa1<sup>tm1.1Satom</sup>/Cpa1<sup>tm1.1Satom</sup>  [background:] involves: C57BL/6NCrl * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:30045879	20210125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5486141	Tg(Camk2a-DISC1)37Asaw	is_implicated_in	DOID:5419	schizophrenia		MGI:5486142	Tg(Camk2a-DISC1)37Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)37Asaw			ECO:0000033	author statement supported by traceable reference	PMID:17675407	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5486141	Tg(Camk2a-DISC1)37Asaw	is_implicated_in	DOID:5419	schizophrenia		MGI:5486680	Tg(Camk2a-DISC1)37Asaw/Tg(Camk2a-DISC1)37Asaw  [background:] C57BL/6-Tg(Camk2a-DISC1)37Asaw			ECO:0000033	author statement supported by traceable reference	PMID:23314019	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5486141	Tg(Camk2a-DISC1)37Asaw	is_implicated_in	DOID:5419	schizophrenia		MGI:5486142	Tg(Camk2a-DISC1)37Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)37Asaw			ECO:0000033	author statement supported by traceable reference	PMID:23314019	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5486141	Tg(Camk2a-DISC1)37Asaw	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720113	Tg(Thy1-MAPT)1Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720113	Tg(Thy1-MAPT)1Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720209	Tg(Thy1-MAPT)1Vln/Tg(Thy1-MAPT)1Vln  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:11007782	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720113	Tg(Thy1-MAPT)1Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720209	Tg(Thy1-MAPT)1Vln/Tg(Thy1-MAPT)1Vln  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:10595944	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934009	Cd14<sup>tm1Frm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21084593	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432255	Tg(tetO-IGF1R)1Ramo	is_implicated_in	DOID:1324	lung cancer		MGI:7265160	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-IGF1R)1Ramo/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:19568412	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432255	Tg(tetO-IGF1R)1Ramo	is_implicated_in	DOID:1324	lung cancer		MGI:7266256	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IGF1R)1Ramo/0  [background:] involves: 129 * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19568412	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432255	Tg(tetO-IGF1R)1Ramo	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:30412601	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635256	Tnnt1<sup>tm1.2Jin</sup>	is_implicated_in	DOID:0110936	nemaline myopathy 5A		MGI:5697946	Tnnt1<sup>tm1.2Jin</sup>/Tnnt1<sup>tm1.2Jin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24445317	20151203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804183	Ednrb<sup>tm1.1Nrd</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5804451	Ednrb<sup>tm1.1Nrd</sup>/Ednrb<sup>tm1.1Nrd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26240367	20161021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0110977	brachydactyly type A1C		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384513	Tgfbr2<sup>tm1.2Hlm</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384513	Tgfbr2<sup>tm1.2Hlm</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:5543401	Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup> Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22904682	20140207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4356193	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp*A116V*M128V)1309Jama/0  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19675240	20090909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613050	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm1Fdp</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11230174	20101102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613050	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm1Fdp</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20670678	20101102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777399	Uros<sup>tm2Rjde</sup>/Uros<sup>tm3Rjde</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:13271	cutaneous porphyria						ECO:0000033	author statement supported by traceable reference	PMID:16532394	20080623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6118143	Fuca1<sup>tm1Tlub</sup>	is_implicated_in	DOID:14500	fucosidosis						ECO:0000033	author statement supported by traceable reference	PMID:29706874	20190606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6118143	Fuca1<sup>tm1Tlub</sup>	is_implicated_in	DOID:14500	fucosidosis		MGI:6188994	Fuca1<sup>tm1Tlub</sup>/Fuca1<sup>tm1Tlub</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27491075	20190606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4880665	Fbn1<sup>tm1Lper</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29765495	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4880665	Fbn1<sup>tm1Lper</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:4880671	Fbn1<sup>tm1Lper</sup>/Fbn1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21152435	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4880665	Fbn1<sup>tm1Lper</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:4880670	Fbn1<sup>tm1Lper</sup>/Fbn1<sup>+</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21152435	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4880665	Fbn1<sup>tm1Lper</sup>	is_implicated_in	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28395026	20210106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580089	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512741	Lgr5<sup>tm1Ah</sup>/Lgr5<sup>tm1Ah</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0060604	ankyloglossia						ECO:0000033	author statement supported by traceable reference	PMID:15509778	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296511	Jup<sup>tm1.1Shou</sup>	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12		MGI:5296512	Jup<sup>tm1.1Shou</sup>/Jup<sup>tm1.1Shou</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21880664	20111123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312336	Dnah11<sup>b2b598Clo</sup>/Dnah11<sup>b2b598Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b598Clo</sup>	is_model_of	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046779	Srf<sup>tm1Zli</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23436819	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046779	Srf<sup>tm1Zli</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23771945	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046779	Srf<sup>tm1Zli</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5575856	Srf<sup>tm1Zli</sup>/Srf<sup>tm1Zli</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16260633	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820821	Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro/0  [background:] FVB/N-Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20566844	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857228	Nos2<sup>tm1Lau</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33137399	20210702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857228	Nos2<sup>tm1Lau</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25878270	20210702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437087	b2b1291.2Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437112	b2b1291.2Clo/b2b1291.2Clo  [background:] C57BL/6J-b2b1291.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861811	Cdkn1c<sup>tm1Sje</sup>	is_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21729874	20230127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861811	Cdkn1c<sup>tm1Sje</sup>	is_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:2175768	Cdkn1c<sup>tm1Sje</sup>/Cdkn1c<sup>tm1Sje</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9144284	20230127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857299	Hprt1<sup>b-m3</sup>	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24804781	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857299	Hprt1<sup>b-m3</sup>	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29305058	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857299	Hprt1<sup>b-m3</sup>	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome		MGI:3625335	Hprt1<sup>b-m3</sup>/Y  [background:] B6.129P2-Hprt1<sup>b-m3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7509865	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857299	Hprt1<sup>b-m3</sup>	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome		MGI:5637726	Hprt1<sup>b-m3</sup>/Hprt1<sup>b-m3</sup>  [background:] B6.129P2-Hprt1<sup>b-m3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7509865	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857299	Hprt1<sup>b-m3</sup>	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome		MGI:3625335	Hprt1<sup>b-m3</sup>/Y  [background:] B6.129P2-Hprt1<sup>b-m3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11297820	20190501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623584	Gk<sup>tm1Wjc</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060363	glycerol kinase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16105550	20060531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623584	Gk<sup>tm1Wjc</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060363	glycerol kinase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9302256	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23678045	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:29634312	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23508046	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26908870	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23132297	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3576767	Tg(Cryaa-TAg,Ins2-CALM1)26Ove/0  [background:] FVB(Cg)-Tg(Cryaa-Tag,Ins2-CALM1)26Ove/PneJ			ECO:0000033	author statement supported by traceable reference	PMID:2673540	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576672	Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:4360179	Tg(Cryaa-TAg,Ins2-CALM1)26Ove/0  [background:] FVB-Tg(Cryaa-TAg,Ins2-CALM1)26Ove			ECO:0000033	author statement supported by traceable reference	PMID:15561957	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852752	Smpx<sup>em1Jgao</sup>	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852759	Smpx<sup>em1Jgao</sup>/Smpx<sup>em1Jgao</sup>  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852752	Smpx<sup>em1Jgao</sup>	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852756	Smpx<sup>em1Jgao</sup>/Y  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852752	Smpx<sup>em1Jgao</sup>	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852761	Smpx<sup>em1Jgao</sup>/Smpx<sup>+</sup>  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3652413	Fbn2<sup>tm1Rmz</sup>/Fbn2<sup>tm1Rmz</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6J)	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:11470817	20060822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476832	Tg(TARDBP*A315T)#Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:21752789	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429704	Tg(Cd4-CD4)2362Litt/0 Tg(HLA-DR2)#Lfug/0 Tg(TCROb.1A12)#Lfug/0  [background:] involves: C57BL/6 * DBA/2 * SJL	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:10610182	20120731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5289968	Tg(tetO-SNCA*A53T)33Vle	is_implicated_in	DOID:12217	Lewy body dementia		MGI:5289971	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA*A53T)33Vle/0  [background:] involves: C3H/HeH * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21734300	20111011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:11689485	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:9988265	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:9326937	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437099	Odad2<sup>b2b227.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437109	Odad2<sup>b2b227.1Clo</sup>/Odad2<sup>b2b227.1Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b227.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521822	Apc<sup>tm2.1Cip</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:31194980	20200626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521822	Apc<sup>tm2.1Cip</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3522324	Apc<sup>tm2.1Cip</sup>/Apc<sup>tm2.1Cip</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:15563600	20200626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6277079	B3glct<sup>tm1.2Nari</sup>	is_implicated_in	DOID:0080201	Peters plus syndrome		MGI:6406868	B3glct<sup>tm1.2Nari</sup>/B3glct<sup>tm1.2Nari</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J * DBA/2 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:31600785	20200429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624719	Mecp2<sup>tm1Bird</sup>/Y Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242117	20060619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611043	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:15472122	20120221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified	is_model_of	DOID:6406	double outlet right ventricle						ECO:0000033	author statement supported by traceable reference	PMID:10574770	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7520866	Tmem98<sup>em1Siggs</sup>	is_not_implicated_in	DOID:0080634	nanophthalmos		MGI:7520868	Tmem98<sup>em1Siggs</sup>/Tmem98<sup>em1Siggs</sup>  [background:] C57BL/6J-Tmem98<sup>em1Siggs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37419942	20230828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033772	Hoxa3<sup>tm1Mrc</sup>/Hoxa3<sup>tm1Mrc</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1673020	20050701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749788	Tg(Camk2a-MAPT)601Ymot	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:21324362	20160223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749788	Tg(Camk2a-MAPT)601Ymot	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5749790	Tg(Camk2a-MAPT)601Ymot/0  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21324362	20160223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5805971	Hoga1<sup>tm2a(KOMP)Wtsi</sup>/Hoga1<sup>tm2a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:2977	primary hyperoxaluria						ECO:0000033	author statement supported by traceable reference	PMID:26428388	20161102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044679	Fgfr2<sup>tm1Dor</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:26081170	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700191	Mecp2<sup>tm2Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24009314	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700191	Mecp2<sup>tm2Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27328325	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700191	Mecp2<sup>tm2Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700191	Mecp2<sup>tm2Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:3712286	Mecp2<sup>tm2Bird</sup>/Mecp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17289941	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700191	Mecp2<sup>tm2Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098754	Mecp2<sup>tm2Bird</sup>/Y  [background:] B6.129P2-Mecp2<sup>tm2Bird</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6256428	Washc5<sup>tm1.2Cbee</sup>	is_not_implicated_in	DOID:0110823	hereditary spastic paraplegia 8		MGI:6256431	Washc5<sup>tm1.2Cbee</sup>/Washc5<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26572744	20181115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824245	Tg(Erbb2-Erbb2*V664E)#Led	is_implicated_in	DOID:1612	breast cancer		MGI:5824254	Tg(Erbb2-Erbb2*V664E)#Led/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10803404	20170215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824245	Tg(Erbb2-Erbb2*V664E)#Led	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20170215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402178	Tg(KRT18-DPP4)3Pbmj	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6402203	Tg(KRT18-DPP4)3Pbmj/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:29152574	20200617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402178	Tg(KRT18-DPP4)3Pbmj	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6402203	Tg(KRT18-DPP4)3Pbmj/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:26486634	20200617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857590	Trp53<sup>tm1Brd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25176624	20220708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857590	Trp53<sup>tm1Brd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:35393420	20220708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857590	Trp53<sup>tm1Brd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20220708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387763	Tg(HCRT-MJD)1Stak	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:28507129	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387763	Tg(HCRT-MJD)1Stak	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:28396432	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387763	Tg(HCRT-MJD)1Stak	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:23922890	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387763	Tg(HCRT-MJD)1Stak	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:27919403	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387763	Tg(HCRT-MJD)1Stak	is_implicated_in	DOID:8986	narcolepsy		MGI:3767400	Tg(HCRT-MJD)1Stak/?  [background:] involves: C57BL/6 * DBA/1			ECO:0000033	author statement supported by traceable reference	PMID:11394998	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686741	Npc1<sup>nmf164</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26707209	20210429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686741	Npc1<sup>nmf164</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:31862414	20210429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686741	Npc1<sup>nmf164</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:25979674	20210429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686741	Npc1<sup>nmf164</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:31605022	20210429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686741	Npc1<sup>nmf164</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2686745	Npc1<sup>nmf164</sup>/Npc1<sup>nmf164</sup>  [background:] C57BL/6J-Npc1<sup>nmf164</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22048958	20210429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703798	Tg(Tagln-rtTA)E1Jwst/0 Tg(tetO-BMPR2*T504)1Jwst/0  [background:] involves: FVB/N	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:15031260	20130409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713665	Hr<sup>rh-Chr</sup>/Hr<sup>rh-Chr</sup>  [background:] Not Specified	is_model_of	DOID:0050634	alopecia universalis						ECO:0000033	author statement supported by traceable reference	PMID:9832318	20070703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437595	Ceacam16<sup>tm1Wzm</sup>	is_implicated_in	DOID:0110573	autosomal dominant nonsyndromic deafness 4A		MGI:5437687	Ceacam16<sup>tm1Wzm</sup>/Ceacam16<sup>tm1Wzm</sup>  [background:] BALB/cJ-Ceacam16<sup>tm1Wzm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22544735	20121004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444462	Map2k7<sup>tm1Pngr</sup>/Map2k7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22899651	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037342	Sftpc<sup>tm1Swg</sup>/Sftpc<sup>tm1Swg</sup>  [background:] either: 129 or (involves: 129 * Black Swiss)	is_model_of	DOID:0050158	desquamative interstitial pneumonia						ECO:0000033	author statement supported by traceable reference	PMID:12519727	20080910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384177	Cdkn2a<sup>tm2.1Rdp</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22052106	20220401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4457064	Irf6<sup>clft1</sup>/Irf6<sup>clft1</sup>  [background:] involves: A/J * FVB	is_model_of	DOID:0060239	Van der Woude syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20196077	20100629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297587	Tg(SOD1*H46R)#Maw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27439389	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297587	Tg(SOD1*H46R)#Maw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5297589	Tg(SOD1*H46R)#Maw/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15899257	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297587	Tg(SOD1*H46R)#Maw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22438926	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297587	Tg(SOD1*H46R)#Maw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24498180	20170131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6121103	Cdyl<sup>tm1.1Yuw</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:6121112	Cdyl<sup>tm1.1Yuw</sup>/Cdyl<sup>tm1.1Yuw</sup> Emx1<sup>tm1(cre)Yql</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28076783	20180313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856098	Atp7a<sup>Mo-br</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:26269458	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856098	Atp7a<sup>Mo-br</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:10332039	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856098	Atp7a<sup>Mo-br</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:21878905	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856098	Atp7a<sup>Mo-br</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:3793780	Atp7a<sup>Mo-br</sup>/Y  [background:] involves: C57BL			ECO:0000033	author statement supported by traceable reference	PMID:4858102	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6360453	Rab28<sup>tm1d(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0111024	cone-rod dystrophy 18		MGI:6360454	Rab28<sup>tm1d(EUCOMM)Hmgu</sup>/Rab28<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30228185	20190919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5529273	Slc26a4<sup>tm2.1Dontu</sup>	is_not_implicated_in	DOID:0060744	Pendred Syndrome		MGI:5529274	Slc26a4<sup>tm2.1Dontu</sup>/Slc26a4<sup>tm2.1Dontu</sup>  [background:] B6.129-Slc26a4<sup>tm2.1Dontu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23755160	20140120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857448	Rbl1<sup>tm1Tyj</sup>	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:26628093	20170424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857448	Rbl1<sup>tm1Tyj</sup>	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24227978	20170424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491025	Tg(Prnp*P101L)2866Sbp	is_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:5491033	Tg(Prnp*P101L)2866Sbp/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007929	Mefv<sup>tm5.1(MEFV)Chae</sup>/Mefv<sup>tm5.1(MEFV)Chae</sup>  [background:] B6.129S6-Mefv<sup>tm5.1(MEFV)Chae</sup>	is_model_of	DOID:2987	familial mediterranean fever						ECO:0000033	author statement supported by traceable reference	PMID:21600797	20110617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527179	Adgrv1<sup>tm1Msat</sup>	is_implicated_in	DOID:0110839	Usher syndrome type 2C						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527179	Adgrv1<sup>tm1Msat</sup>	is_implicated_in	DOID:0110839	Usher syndrome type 2C		MGI:3527887	Adgrv1<sup>tm1Msat</sup>/Adgrv1<sup>tm1Msat</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17567809	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5301528	Scn4a<sup>tm1.1Cann</sup>	is_implicated_in	DOID:14452	hypokalemic periodic paralysis		MGI:5301550	Scn4a<sup>tm1.1Cann</sup>/Scn4a<sup>tm1.1Cann</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21881211	20120116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720208	Tg(Thy1-MAPT)2Vln/Tg(Thy1-MAPT)2Vln  [background:] involves: FVB	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10595944	20071023	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720208	Tg(Thy1-MAPT)2Vln/Tg(Thy1-MAPT)2Vln  [background:] involves: FVB	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11007782	20071023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6152666	Cabyr<sup>em1Osb</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6152755	Cabyr<sup>em1Osb</sup>/Cabyr<sup>em1Osb</sup>  [background:] involves: C57BL/6NJcl * DBA/2NJcl			ECO:0000033	author statement supported by traceable reference	PMID:27802166	20180423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665106	Pde6b<sup>rd1-2J</sup>/Pde6b<sup>rd1-2J</sup>  [background:] C57BL/6J-Pde6b<sup>rd1-2J</sup>/J	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	MGI:2651853	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447845	Tg(RHO-SCA7)R7EJman	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:20600911	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447845	Tg(RHO-SCA7)R7EJman	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:30625334	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447845	Tg(RHO-SCA7)R7EJman	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:17189700	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447845	Tg(RHO-SCA7)R7EJman	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:3774852	Tg(RHO-SCA7)R7EJman/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11030754	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451184	Del(13Simc1-B4galt7)2Dja/+  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:14748	Sotos syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22926222	20130125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5050632	Mrgprd<sup>tm5Mjz</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6275457	Mrgprd<sup>tm5Mjz</sup>/Mrgprd<sup>tm5Mjz</sup>  [background:] B6.129S1-Mrgprd<sup>tm5Mjz</sup>/Mmnc			ECO:0000033	author statement supported by traceable reference	PMID:30339496	20190131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784200	Sbf2<sup>Gt(XH212)Byg</sup>/Sbf2<sup>Gt(XH212)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110190	Charcot-Marie-Tooth disease type 4B2						ECO:0000033	author statement supported by traceable reference	PMID:5955164	20080507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>	is_model_of	DOID:0110594	primary ciliary dyskinesia 1						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574636	Tg(Msmb-TAg)183-2Xuan/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:12424611	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287441	Cenpf<sup>em3Bko</sup>	is_not_implicated_in	DOID:0110595	Stromme syndrome		MGI:6287445	Cenpf<sup>em3Bko</sup>/Cenpf<sup>em3Bko</sup>  [background:] involves: C57BL/6 * C57BL/6NTac * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30856164	20190415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700984	Tbx6<sup>rv</sup>/Tbx6<sup>rv</sup>  [background:] involves: C57BL/J * C57BL/6J	is_model_of	DOID:0050568	spondylocostal dysostosis						ECO:0000033	author statement supported by traceable reference	PMID:4073528	20070327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182456	Nppc<sup>tm1Yog</sup>	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:20610569	20220512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182456	Nppc<sup>tm1Yog</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3522090	Nppc<sup>tm1Yog</sup>/Nppc<sup>tm1Yog</sup>  [background:] either: 129X1/SvJ or (involves: 129 * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11259675	20220512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044706	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] B6.Cg-Wfs1<sup>tm1Yoka</sup>	is_model_of	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15056606	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687750	Btk<sup>xid</sup>/Y  [background:] CBA/HN-Btk<sup>xid</sup>	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515890	Pmp22<sup>Tr-2J</sup>	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7311560	Tardbp<sup>tm1.1Sobue</sup>	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:7311612	Tardbp<sup>tm1.1Sobue</sup>/Tardbp<sup>tm1.1Sobue</sup> Tg(SLC18A3-cre)Misa/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:23449777	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463441	b2b1456Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5463447	b2b1456Clo/b2b1456Clo  [background:] C57BL/6J-b2b1456Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528437	Fgfr1<sup>tm1Upir</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:26081170	20160720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446588	Abcd1<sup>tm1Kds</sup>/Abcd1<sup>tm1Kds</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9256488	20050823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827840	Bmpr2<sup>tm1Mmue</sup>/Bmpr2<sup>+</sup>  [background:] B6.129S1-Bmpr2<sup>tm1Mmue</sup>	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:26076038	20170307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763424	Flt3<sup>tm1Dgg</sup>/Flt3<sup>tm1Dgg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:17936561	20160111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3696354	Ercc2<sup>tm3Jhjh</sup>/Ercc2<sup>tm3Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:0110845	xeroderma pigmentosum group D						ECO:0000033	author statement supported by traceable reference	PMID:16904611	20070209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178322	Des<sup>tm1Cap</sup>/Des<sup>tm1Cap</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0110431	dilated cardiomyopathy 1I						ECO:0000033	author statement supported by traceable reference	PMID:8794866	20060523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491023	Tg(Prnp*P101L)2247Sbp	is_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:5491030	Tg(Prnp*P101L)2247Sbp/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5465569	Tg(APOE-FGF23*R176Q)#Ack	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5466160	Tg(APOE-FGF23*R176Q)#Ack/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15284207	20130225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451169	Sox9<sup>tm2Crm</sup>/Sox9<sup>+</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680503	Hlb228/?  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:2656149	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799202	Tg(Myh6*)140Lnwd/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:8898372	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3799202	Tg(Myh6*)140Lnwd/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:8585273	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312912	b2b954Clo/b2b954Clo  [background:] C57BL/6J-b2b954Clo	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:6971670	20060414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26748053	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:24211371	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928280	Grin1<sup>tm1Bhk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6258771	Grin1<sup>tm1Bhk</sup>/Grin1<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22726567	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5004866	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16951148	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197715	Trem2<sup>em2Bwef</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5904595	Trem2<sup>em2Bwef</sup>/Trem2<sup>em2Bwef</sup>  [background:] involves: C57BL/6J * DBA/2J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28559417	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544755	Cdkn1b<sup>tm1Mlf</sup>/Cdkn1b<sup>tm1Mlf</sup> Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19147535	20140220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6342637	Rit1<sup>tm1.1Tumg</sup>	is_implicated_in	DOID:0060586	Noonan syndrome 8		MGI:6356633	Rit1<sup>tm1.1Tumg</sup>/Rit1<sup>+</sup>  [background:] B6.Cg-Rit1<sup>tm1.1Tumg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30898653	20190822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5478770	Tg(Ckm-Chrne*L269F)5Cgz/?  [background:] involves: FVB/NJ	is_model_of	DOID:0110678	congenital myasthenic syndrome 4A						ECO:0000033	author statement supported by traceable reference	PMID:9151734	20150511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442284	Tg(OMP-SV40T)13Bse/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:7923140	20121120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6501716	Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0110081	arrhythmogenic right ventricular dysplasia 10		MGI:6501726	Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>/Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27170944	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:8441253	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781130	Tg(tetO-EGFR*T790M*L858R)19Kkw	is_implicated_in	DOID:1324	lung cancer		MGI:5781131	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)19Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17613438	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781130	Tg(tetO-EGFR*T790M*L858R)19Kkw	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25767874	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781130	Tg(tetO-EGFR*T790M*L858R)19Kkw	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781130	Tg(tetO-EGFR*T790M*L858R)19Kkw	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26883990	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781130	Tg(tetO-EGFR*T790M*L858R)19Kkw	is_implicated_in	DOID:1324	lung cancer		MGI:5781131	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)19Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27251290	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781130	Tg(tetO-EGFR*T790M*L858R)19Kkw	is_implicated_in	DOID:1324	lung cancer		MGI:5781131	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)19Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20033049	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713111	Sp4<sup>tm3(Sp4)Krc</sup>/Sp4<sup>tm3(Sp4)Krc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:20634195	20140319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6726263	Tcf20<sup>em1Jwji</sup>	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6726265	Tcf20<sup>em1Jwji</sup>/Tcf20<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32510763	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318525	Gfi1<sup>Gen</sup>/Gfi1<sup>+</sup>  [background:] C57BL/6J-Gfi1<sup>Gen</sup>	is_model_of	DOID:0050590	severe congenital neutropenia						ECO:0000033	author statement supported by traceable reference	PMID:22393124	20121114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177176	Fxn<sup>tm2Mkn</sup>	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:22736457	20130325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5883222	Otog<sup>vbd</sup>	is_implicated_in	DOID:0110474	autosomal recessive nonsyndromic deafness 18B		MGI:5883223	Otog<sup>vbd</sup>/Otog<sup>vbd</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26636018	20170414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5319638	Tg(NPHS2-Trpc6*P111Q)F615Walz	is_implicated_in	DOID:0111129	focal segmental glomerulosclerosis 2		MGI:5319645	Tg(NPHS2-Trpc6*P111Q)F615Walz/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20877463	20120530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830980	Mecp2<sup>tm1.1Irsf</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5751707	Mecp2<sup>tm1.1Irsf</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25634563	20160310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830980	Mecp2<sup>tm1.1Irsf</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5751716	Mecp2<sup>tm1.1Irsf</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25634563	20160310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587786	Ndst1<sup>tm1Ekf</sup>/Ndst1<sup>tm1Ekf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:12716	newborn respiratory distress syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10852901	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702409	Sacs<sup>tm2Bebr</sup>/Sacs<sup>tm2Bebr</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050946	Charlevoix-Saguenay spastic ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25260547	20160216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:27777976	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:23043085	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:26719147	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:3702286	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] B6.C3-Ap3b1<sup>pe</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25477496	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:2655702	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] involves: C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20200805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:2655702	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] involves: C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:9931340	20200805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588064	Thrb<sup>tm2Few</sup>/Thrb<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11274423	20050921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6690504	Gcgr<sup>em2Smoc</sup>	is_implicated_in	DOID:0112306	Mahvash Disease						ECO:0000033	author statement supported by traceable reference	PMID:32785645	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6690504	Gcgr<sup>em2Smoc</sup>	is_implicated_in	DOID:0112306	Mahvash Disease		MGI:6690506	Gcgr<sup>em2Smoc</sup>/Gcgr<sup>em2Smoc</sup>  [background:] C57BL/6J-Gcgr<sup>em2Smoc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32677665	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5619347	Rhot1<sup>tm1.1Jmsu</sup>	is_implicated_in	DOID:231	motor neuron disease		MGI:5619354	Rhot1<sup>tm1.1Jmsu</sup>/Rhot1<sup>tm1.1Jmsu</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25136135	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29474906	20180621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:25175806	20180621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:26766587	20180621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:2675737	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19185848	20180621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3836962	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup> Tg(Atoh1-GFP)1Jejo/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19185848	20180621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037642	Phex<sup>Hyp-Duk</sup>/Y  [background:] involves: BALB/cAnBomUrd	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6384248	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:6488227	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32446853	20201223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6384248	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:6488233	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1c(EUCOMM)Wtsi</sup> Emx1<sup>tm1(cre)Yql</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31715135	20201223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934922	Sgca<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:10981665	20130823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934922	Sgca<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:23418438	20130823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934922	Sgca<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:9744877	20130823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934922	Sgca<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:12855815	20130823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934922	Sgca<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D		MGI:2176866	Sgca<sup>tm1Kcam</sup>/Sgca<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9744877	20130823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506267	Tuba1a<sup>em1Rstot</sup>	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:6507151	Tuba1a<sup>em1Rstot</sup>/Tuba1a<sup>em1Rstot</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669096	Tlx3<sup>tm1Sjk</sup>/Tlx3<sup>tm1Sjk</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10700185	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7484703	Adar<sup>em3Qwan</sup>	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome		MGI:7485763	Adar<sup>em3Qwan</sup>/Adar<sup>em3Qwan</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:34332594	20230530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822800	Phyh<sup>tm1Safe</sup>/Phyh<sup>tm1Safe</sup>  [background:] involves: 129P2/OlaHsd * 129X1/SvJ * Black Swiss * FVB/N	is_model_of	DOID:10582	Refsum disease						ECO:0000033	author statement supported by traceable reference	PMID:19004801	20090112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908193	Tg(Myh6-POLG*Y955C)DWcc	is_implicated_in	DOID:0050700	cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23090637	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908193	Tg(Myh6-POLG*Y955C)DWcc	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5908194	Tg(Myh6-POLG*Y955C)DWcc/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17310215	20170905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5086003	Amer1<sup>tm1.1Nbar</sup>	is_implicated_in	DOID:0060886	osteopathia striata with cranial sclerosis		MGI:5086009	Amer1<sup>tm1.1Nbar</sup>/Y Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21571217	20110815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604891	Tg(MMTV-Erbb2)12Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526657	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>/Ctsg<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:14636558	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526657	Ctsg<sup>tm2.1(PML/RARA)Ley</sup>/Ctsg<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:12750176	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6490339	Matr3<sup>em1Tcp</sup>	is_implicated_in	DOID:0060212	amyotrophic lateral sclerosis type 21		MGI:6490343	Matr3<sup>em1Tcp</sup>/Matr3<sup>em1Tcp</sup>  [background:] C57BL/6J-Matr3<sup>em1Tcp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33082323	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5049894	Tg(CMV-Tsc2*)1Arbi	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5882127	Tg(CMV-Tsc2*)1Arbi/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21827857	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5049894	Tg(CMV-Tsc2*)1Arbi	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5882127	Tg(CMV-Tsc2*)1Arbi/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15576369	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033300	Tg(PML-RARA)556Kog	is_implicated_in	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29795382	20180710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033300	Tg(PML-RARA)556Kog	is_implicated_in	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26108692	20180710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033300	Tg(PML-RARA)556Kog	is_implicated_in	DOID:0060318	acute promyelocytic leukemia		MGI:3815135	Tg(PML-RARA)556Kog/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9122233	20180710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3845065	Hras<sup>tm1Jaf</sup>/Hras<sup>+</sup> Tg(CAG-cre)13Miya/0  [background:] involves: 129S6/SvEvTac * Black Swiss * C57BL/6	is_model_of	DOID:0050469	Costello syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24057668	20140429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614409	Abcc6<sup>tm1Aabb</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:28416300	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614409	Abcc6<sup>tm1Aabb</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:27826008	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614409	Abcc6<sup>tm1Aabb</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:23935882	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614409	Abcc6<sup>tm1Aabb</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:23041262	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614409	Abcc6<sup>tm1Aabb</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:24675664	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614409	Abcc6<sup>tm1Aabb</sup>	is_implicated_in	DOID:2738	pseudoxanthoma elasticum		MGI:3615174	Abcc6<sup>tm1Aabb</sup>/Abcc6<sup>tm1Aabb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15888484	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775189	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775189	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:24520391	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:22960170	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:24453992	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295419	Mcm9<sup>Gt(AW0655)Wtsi</sup>/Mcm9<sup>Gt(XG743)Byg</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857113	Prkdc<sup>scid</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26644351	20160509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5310744	Arl6<sup>tm2Vcs</sup>	is_implicated_in	DOID:0110125	Bardet-Biedl syndrome 3		MGI:7449243	Arl6<sup>tm2Vcs</sup>/Arl6<sup>tm2Vcs</sup>  [background:] B6.129-Arl6<sup>tm2Vcs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27170093	20230403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857896	Cftr<sup>tm2Cam</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24367540	20141002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857896	Cftr<sup>tm2Cam</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177534	Cftr<sup>tm2Cam</sup>/Cftr<sup>tm2Cam</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:7545494	20141002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5465558	Tg(Thy1-APPArc)M8Cagr/Tg(Thy1-APPArc)M8Cagr  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21880397	20130222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046091	Slc37a4<sup>tm1Jyc</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:27864142	20170725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046091	Slc37a4<sup>tm1Jyc</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:28334808	20170725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046091	Slc37a4<sup>tm1Jyc</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:3046092	Slc37a4<sup>tm1Jyc</sup>/Slc37a4<sup>tm1Jyc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12925567	20170725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813633	Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6	is_model_of	DOID:1380	endometrial cancer						ECO:0000033	author statement supported by traceable reference	PMID:18632614	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582934	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] involves: 101 * BALB/c * C3H * C57BL/6J * T STOCK	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604728	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR	is_model_of	DOID:1380	endometrial cancer						ECO:0000033	author statement supported by traceable reference	PMID:24930886	20141118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856220	Atp7b<sup>tx</sup>	is_implicated_in	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:25634697	20150514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856220	Atp7b<sup>tx</sup>	is_implicated_in	DOID:893	Wilson disease		MGI:3793277	Atp7b<sup>tx</sup>/Atp7b<sup>tx</sup>  [background:] DL-Atp7b<sup>tx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8894697	20150514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3487369	Pax3<sup>tm1Mrc</sup>	is_implicated_in	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:22960170	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3487369	Pax3<sup>tm1Mrc</sup>	is_implicated_in	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:24453992	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3487369	Pax3<sup>tm1Mrc</sup>	is_implicated_in	DOID:4051	alveolar rhabdomyosarcoma		MGI:3844656	Myf6<sup>tm1(cre)Mrc</sup>/Myf6<sup>+</sup> Pax3<sup>tm1Mrc</sup>/Pax3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15489287	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663382	Scnn1g<sup>tm1Bhk</sup>	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663382	Scnn1g<sup>tm1Bhk</sup>	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1		MGI:3664199	Scnn1g<sup>tm1Bhk</sup>/Scnn1g<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9788978	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000265	Tg(AR*100Q)C25Als	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:5000279	Tg(AR*100Q)C25Als/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15003169	20110527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3821613	Baz1b<sup>MommeD10</sup>/Baz1b<sup>MommeD10</sup>  [background:] involves: FVB/N	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19099580	20081230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796925	Slc6a5<sup>trsl</sup>	is_implicated_in	DOID:0060698	hyperekplexia 3		MGI:5796931	Slc6a5<sup>trsl</sup>/Slc6a5<sup>trsl</sup>  [background:] C57BL/6J-Slc6a5<sup>trsl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5796923	20161007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476824	Tg(TARDBP*A315T)#Jpj	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5476832	Tg(TARDBP*A315T)#Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21752789	20130502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515418	Tg(Eno2-Bmp4)3Jake	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5515421	Tg(Eno2-Bmp4)3Jake/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15466378	20131030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515418	Tg(Eno2-Bmp4)3Jake	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:23115204	20131030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5013917	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20807812	20110711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6342430	Cwc27<sup>em1Bay</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:6342435	Cwc27<sup>em1Bay</sup>/Cwc27<sup>em1Bay</sup>  [background:] C57BL/6J-Cwc27<sup>em1Bay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28285769	20190807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136169	Kras<sup>tm3Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25450481	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136169	Kras<sup>tm3Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136169	Kras<sup>tm3Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28381544	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136169	Kras<sup>tm3Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:21807965	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136169	Kras<sup>tm3Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3770517	Kras<sup>tm3Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136169	Kras<sup>tm3Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3770516	Kras<sup>tm3Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808273	Krt16<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0050449	pachyonychia congenita						ECO:0000033	author statement supported by traceable reference	PMID:24218583	20140305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808273	Krt16<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0050449	pachyonychia congenita		MGI:5426823	Krt16<sup>tm1(KOMP)Vlcg</sup>/Krt16<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Krt16<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22336941	20140305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5003364	Raf1<sup>tm1.1Bgn</sup>	is_implicated_in	DOID:0060583	Noonan syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:28548091	20171212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5003364	Raf1<sup>tm1.1Bgn</sup>	is_implicated_in	DOID:0060583	Noonan syndrome 5		MGI:5003451	Raf1<sup>tm1.1Bgn</sup>/Raf1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:21339642	20171212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621818	Ikbkg<sup>tm1Mka</sup>/Ikbkg<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:12305	Bloch-Sulzberger syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10911991	20060509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605621	Prdm1<sup>tm1Clme</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23298838	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605621	Prdm1<sup>tm1Clme</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:28692065	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605621	Prdm1<sup>tm1Clme</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5515634	Prdm1<sup>tm1Clme</sup>/Prdm1<sup>tm1Clme</sup> Tg(Itgax-cre)1-1Reiz/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21948081	20180404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838199	Col4a4<sup>m1Btlr</sup>/Col4a4<sup>m1Btlr</sup>  [background:] C57BL/6J-Col4a4<sup>m1Btlr</sup>	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21196518	20110509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838199	Col4a4<sup>m1Btlr</sup>/Col4a4<sup>m1Btlr</sup>  [background:] C57BL/6J-Col4a4<sup>m1Btlr</sup>	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	MGI:4440633	20110509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6164702	Clcnkb<sup>em1Haca</sup>	is_implicated_in	DOID:0110144	Bartter disease type 3		MGI:6198300	Clcnkb<sup>em1Haca</sup>/Clcnkb<sup>em1Haca</sup>  [background:] C57BL/6-Clcnkb<sup>em1Haca</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27421685	20180917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:10541472	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625335	Hprt1<sup>b-m3</sup>/Y  [background:] B6.129P2-Hprt1<sup>b-m3</sup>	is_model_of	DOID:1919	Lesch-Nyhan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7509865	20150529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625335	Hprt1<sup>b-m3</sup>/Y  [background:] B6.129P2-Hprt1<sup>b-m3</sup>	is_model_of	DOID:1919	Lesch-Nyhan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11297820	20150529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858008	Ctnnb1<sup>tm1Mmt</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858008	Ctnnb1<sup>tm1Mmt</sup>	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5546509	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Msx2-rtTA)885Lma/0 Tg(tetO-cre)1Jaw/0  [background:] involves: 129 * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23928991	20160823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584121	Tg(TcraTcrbNY8.3)1Pesa	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22890824	20130802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584121	Tg(TcraTcrbNY8.3)1Pesa	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22190647	20130802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584121	Tg(TcraTcrbNY8.3)1Pesa	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3584136	Tg(TcraTcrbNY8.3)1Pesa/?  [background:] involves: C57BL/6 * NOD * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9362527	20130802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7466960	Lrp5<sup>em1Xjz</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:7467137	Lrp5<sup>em1Xjz</sup>/Lrp5<sup>em1Xjz</sup>  [background:] C57BL/6J-Lrp5<sup>em1Xjz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827761	Tg(MMTV-KRAS*G12V)3025Mrl/0 Tg(MMTV-rtTA)1Lach/0 Tg(tetO-MYC)1Lach/0  [background:] involves: C57BL/6 * FVB/N * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18356293	20170306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044565	Kras<sup>tm4.1Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:28685754	20181206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812200	Krt14<sup>tm1Der</sup>/Krt14<sup>+</sup> Tg(KRT14-cre/PGR)1Der/?  [background:] involves: 129X1/SvJ * FVB * ICR	is_model_of	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type						ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:30591714	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21103359	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10678833	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5784536	Tg(tetO-NRG1_i4)6Ajla	is_implicated_in	DOID:5419	schizophrenia		MGI:5784537	Tg(Eno2tTA)5030Nes/0 Tg(tetO-NRG1_i4)6Ajla/0  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:27122041	20160726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6330734	Tg(KRT14-VP16/NR1I2)13Sdub	is_implicated_in	DOID:3310	atopic dermatitis		MGI:6330737	Tg(KRT14-VP16/NR1I2)13Sdub/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28927887	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4462398	Whrn<sup>tm1Tili</sup>	is_implicated_in	DOID:0110840	Usher syndrome type 2D		MGI:4462829	Whrn<sup>tm1Tili</sup>/Whrn<sup>tm1Tili</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20502675	20100803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6887964	Tubb4a<sup>Jit</sup>	is_implicated_in	DOID:0060798	hypomyelinating leukodystrophy 6		MGI:6888382	Tubb4a<sup>Jit</sup>/Tubb4a<sup>+</sup>  [background:] FVB.B6-Tubb4a<sup>Jit</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35171680	20220316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6887964	Tubb4a<sup>Jit</sup>	is_implicated_in	DOID:0060798	hypomyelinating leukodystrophy 6		MGI:6888378	Tubb4a<sup>Jit</sup>/Tubb4a<sup>Jit</sup>  [background:] FVB.B6-Tubb4a<sup>Jit</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35171680	20220316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583451	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] C3.FVB-Ift88<sup>Tg737Rpw</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11773599	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583451	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] C3.FVB-Ift88<sup>Tg737Rpw</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8191288	20050812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387812	Ptf1a<sup>tm1.1(cre)Cvw</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23912455	20140911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387812	Ptf1a<sup>tm1.1(cre)Cvw</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22975374	20140911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713297	Gck<sup>tm3Mgn</sup>/Gck<sup>+</sup>  [background:] B6.129S6-Gck<sup>tm3Mgn</sup>	is_model_of	DOID:13317	hyperinsulinemic hypoglycemia						ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5925306	Bcor<sup>tm1.1Vjba</sup>	is_implicated_in	DOID:0111809	syndromic microphthalmia 2		MGI:7343893	Bcor<sup>tm1.1Vjba</sup>/Bcor<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/Tmem163<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:32692983	20221006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:7523551	20060510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:6847727	20060510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:4048170	20060510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:6604585	20060510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044747	Runx2<sup>tm1Mjo</sup>/Runx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:9182764	20050722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044747	Runx2<sup>tm1Mjo</sup>/Runx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10204840	20050722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617977	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup>  [background:] C.129S2-Stat4<sup>tm1Gru</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15596856	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4887579	Mks1<sup>hlb614</sup>/Mks1<sup>hlb614</sup>  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21045211	20110211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679609	Lamc2<sup>tm1Uit</sup>/Lamc2<sup>tm1Uit</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060737	junctional epidermolysis bullosa Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:14632187	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695904	Lep<sup>ob</sup>/Lep<sup>ob</sup> Pparg<sup>tm1Avp</sup>/Pparg<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0050440	familial partial lipodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17003330	20070207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762600	Gja3<sup>tm1.1Vmb</sup>/Gja3<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110253	cataract 14 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:25103261	20160419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777556	Ret<sup>tm2.1Heno</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:31818953	20210222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777556	Ret<sup>tm2.1Heno</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:4820803	Ret<sup>tm2.1Heno</sup>/Ret<sup>tm2.1Heno</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18414682	20210222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6467011	Ikzf4<sup>tm1Djr</sup>	is_implicated_in	DOID:640	encephalomyelitis		MGI:6467272	Foxp3<sup>tm4(YFP/icre)Ayr</sup>/Foxp3<sup>tm4(YFP/icre)Ayr</sup> Ikzf4<sup>tm1Djr</sup>/Ikzf4<sup>tm1Djr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:31296356	20201015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768525	Tg(Thy1-MAPT*P301L)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24498342	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768525	Tg(Thy1-MAPT*P301L)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23977276	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768525	Tg(Thy1-MAPT*P301L)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24704314	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768525	Tg(Thy1-MAPT*P301L)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3771317	Tg(Thy1-MAPT*P301L)2Vln/Tg(Thy1-MAPT*P301L)2Vln  [background:] FVB/N-Tg(Thy1-MAPT*P301L)2Vln			ECO:0000033	author statement supported by traceable reference	PMID:15509565	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491272	Dnah11<sup>b2b2349Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5445346	b2b1432Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5445971	b2b1432Clo/b2b1432Clo  [background:] C57BL/6J-b2b1432Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446583	Abcd1<sup>tm1Kan</sup>/Abcd1<sup>tm1Kan</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9418970	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424982	Casr<sup>BCH007</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425921	Casr<sup>BCH007</sup>/Casr<sup>BCH007</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH007</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361028	Tg(Col2a1-rtTA,tetO-COMP*)2Jath	is_implicated_in	DOID:0080047	pseudoachondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:22154935	20160810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361028	Tg(Col2a1-rtTA,tetO-COMP*)2Jath	is_implicated_in	DOID:0080047	pseudoachondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:24194321	20160810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361028	Tg(Col2a1-rtTA,tetO-COMP*)2Jath	is_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:4361030	Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0  [background:] C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath			ECO:0000033	author statement supported by traceable reference	PMID:24194321	20160810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361028	Tg(Col2a1-rtTA,tetO-COMP*)2Jath	is_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:4361030	Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0  [background:] C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath			ECO:0000033	author statement supported by traceable reference	PMID:19762713	20160810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574014	Tg(SOD1*G37R)42Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22371592	20140319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574014	Tg(SOD1*G37R)42Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23043510	20140319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574014	Tg(SOD1*G37R)42Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24381160	20140319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574014	Tg(SOD1*G37R)42Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3814058	Tg(SOD1*G37R)42Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7605627	20140319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839508	Erbb2<sup>tm8(Erbb2)Mul</sup>/Erbb2<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(MMTV-cre)7Mul/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18381417	20101123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435565	Porcn<sup>tm1.1Vdv</sup>/Porcn<sup>+</sup> Hprt1<sup>tm1(CAG-cre)Mnn</sup>/Hprt1<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6J	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047131	Fanca<sup>tm1Wong</sup>/Fanca<sup>tm1Wong</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0111095	Fanconi anemia complementation group A						ECO:0000033	author statement supported by traceable reference	PMID:12913077	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887237	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>	is_implicated_in	DOID:0050476	Barth syndrome		MGI:5288490	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21091282	20180810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887237	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>	is_implicated_in	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26030409	20180810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887237	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>	is_implicated_in	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26697888	20180810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887237	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>	is_implicated_in	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30008435	20180810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887237	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>	is_implicated_in	DOID:0050476	Barth syndrome		MGI:4943692	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21068380	20180810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860840	Pkd2<sup>tm1Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:26677864	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860840	Pkd2<sup>tm1Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174703	Pkd2<sup>tm1Som</sup>/Pkd2<sup>tm1Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9568711	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860840	Pkd2<sup>tm1Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174704	Pkd2<sup>tm1Som</sup>/Pkd2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9568711	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5648017	Plxnd1<sup>b2b3150Clo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5648021	Plxnd1<sup>b2b3150Clo</sup>/Plxnd1<sup>b2b3150Clo</sup>  [background:] C57BL/6J-Plxnd1<sup>b2b3150Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543906	Snca<sup>tm1Rosl</sup>/Snca<sup>tm1Rosl</sup> Tg(SNCA*A30P)192Rwm/0  [background:] B6.Cg-Snca<sup>tm1Rosl</sup> Tg(SNCA*A30P)#Rwm	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:24121116	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813525	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr/0  [background:] involves: 129S4/SvJae * C57BL/6J * SJL/J	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18757421	20081103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5662095	Tg(tetO-SPTBN2*)#Lpwr	is_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:5662096	Tg(Pcp2-tTA)3Horr/0 Tg(tetO-SPTBN2*)#Lpwr/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25057192	20150918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome						ECO:0000033	author statement supported by traceable reference	PMID:37699442	20231004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949738	Shank3<sup>tm2Gfng</sup>	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6324047	Shank3<sup>tm2Gfng</sup>/Shank3<sup>+</sup>  [background:] B6.129-Shank3<sup>tm2Gfng</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27189882	20231004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836979	Smn1<sup>tm1.1Dscd</sup>	is_implicated_in	DOID:12376	juvenile spinal muscular atrophy		MGI:4836985	Smn1<sup>tm1.1Dscd</sup>/Smn1<sup>tm1.1Dscd</sup>  [background:] involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20705738	20101102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560813	b2b2736Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561115	b2b2736Clo/b2b2736Clo  [background:] C57BL/6J-b2b2736Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461031	Tg(Igh-V-CD40lg)#Tsub/0  [background:] C57BL/6-Tg(Igh-V-CD40lg)#Tsub	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11751940	20100721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687865	Uox<sup>tm1Bay</sup>/Uox<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:11316859	20061116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637726	Hprt1<sup>b-m3</sup>/Hprt1<sup>b-m3</sup>  [background:] B6.129P2-Hprt1<sup>b-m3</sup>	is_model_of	DOID:1919	Lesch-Nyhan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7509865	20150529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397672	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] FVB.129-Kcnq2<sup>tm1.1Naas</sup>	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544077	Tg(Snca-SNCA/GFP)#Jyl	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5544078	Tg(Snca-SNCA/GFP)#Jyl/Tg(Snca-SNCA/GFP)#Jyl  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23643841	20140214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587743	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:22723523	20130313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428952	Ndufs6<sup>Gt(AR0138)Wtsi</sup>/Ndufs6<sup>Gt(AR0138)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060536	mitochondrial complex I deficiency						ECO:0000033	author statement supported by traceable reference	PMID:22474353	20120726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5811153	Tg(tetO-MYC,-OVAL)#Gtgm	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:6197223	Tg(Cebpb-tTA)5Bjd/0 Tg(tetO-MYC,-OVAL)#Gtgm/0  [background:] B6J.Cg-Tg(Cebpb-tTA)5Bjd Tg(tetO-MYC,-OVAL)#Gtgm			ECO:0000033	author statement supported by traceable reference	PMID:19105207	20180910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584494	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup>  [background:] B6.Cg-Spry2<sup>tm1Ayos</sup>	is_model_of	DOID:9164	achalasia						ECO:0000033	author statement supported by traceable reference	PMID:15937482	20050829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25742698	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29898385	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:32929022	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26621336	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26878174	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22184410	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693328	Tg(Tal1-tTA)19Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:32001531	20220711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7260353	Lmna<sup>tm1.1Vde</sup>	is_not_implicated_in	DOID:0110156	Charcot-Marie-Tooth disease type 2B1		MGI:7260355	Lmna<sup>tm1.1Vde</sup>/Lmna<sup>tm1.1Vde</sup>  [background:] B6.129(Cg)-Lmna<sup>tm1.1Vde</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22331516	20220411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311378	Cfc1<sup>b2b970Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312921	Cfc1<sup>b2b970Clo</sup>/Cfc1<sup>b2b970Clo</sup>  [background:] C57BL/6J-Cfc1<sup>b2b970Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845880	Tg(Slc6a3-PARK2*Q311X)AXwy	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:25316086	20171205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845880	Tg(Slc6a3-PARK2*Q311X)AXwy	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:3846703	Tg(Slc6a3-PARK2*Q311X)AXwy/0  [background:] FVB/NJ-Tg(Slc6a3-PARK2*Q311X)AXwy			ECO:0000033	author statement supported by traceable reference	PMID:19228951	20171205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2384061	Jag1<sup>tm1Grid</sup>/Jag1<sup>+</sup> Notch2<sup>tm1Grid</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11861489	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7282116	Chmp2b<sup>tm1.1Hiok</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:7284279	Chmp2b<sup>tm1.1Hiok</sup>/Chmp2b<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828148	Tg(Fabp4-ENPP1)#Naba	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1		MGI:5828153	Tg(Fabp4-ENPP1)#Naba/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21810932	20170310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828148	Tg(Fabp4-ENPP1)#Naba	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:25640170	20170310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428913	Tg(Pklr-Myc)73Ak	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5428914	Tg(Pklr-Myc)73Ak/0  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:1620553	20120807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428913	Tg(Pklr-Myc)73Ak	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5430592	Tg(Pklr-Myc)73Ak/0  [background:] B6.Cg-Tg(Pklr-Myc)73Ak			ECO:0000033	author statement supported by traceable reference	PMID:22251704	20120807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836992	Tg(Prnp*D177N*M128V)A21Rchi/Tg(Prnp*D177N*M128V)A21Rchi  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:19038218	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158686	Irs2<sup>tm1Mfw</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:23478411	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158686	Irs2<sup>tm1Mfw</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27013528	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158686	Irs2<sup>tm1Mfw</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24760140	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158686	Irs2<sup>tm1Mfw</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583763	Irs2<sup>tm1Mfw</sup>/Irs2<sup>tm1Mfw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9495343	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829538	Jak2<sup>tm1.1Jlvl</sup>	is_implicated_in	DOID:8997	polycythemia vera		MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5697874	Tg(Plp1-LMNB1)1108Qsp	is_implicated_in	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy		MGI:5697875	Tg(Plp1-LMNB1)1108Qsp/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26311780	20151203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427868	Cdc42<sup>tm1Brak</sup>/Cdc42<sup>tm1Brak</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:0060775	microvillus inclusion disease						ECO:0000033	author statement supported by traceable reference	PMID:22354172	20120713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663736	Lepr<sup>db-Pas</sup>/Lepr<sup>db-Pas</sup>  [background:] involves: DW/Pas	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:78566	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176849	Fgf8<sup>tm1.3Mrt</sup>/Fgf8<sup>tm1.4Mrt</sup> Tg(Msx2-cre)5Rem/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:11101846	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:28433543	20200903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:27341128	20200903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:32620791	20200903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:24737887	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:26964623	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:25078979	20160609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040322	Ccn1<sup>tm1Lfl</sup>/Ccn1<sup>tm1Lfl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:17023674	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7437687	Cwh43<sup>em1Mdj</sup>	is_implicated_in	DOID:1572	normal pressure hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:34380733	20230222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7437687	Cwh43<sup>em1Mdj</sup>	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:7437706	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>+</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7437687	Cwh43<sup>em1Mdj</sup>	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:7437702	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em1Mdj</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386978	Twist1<sup>tm1Bhr</sup>/Twist1<sup>tm1Bhr</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8988167	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446159	b2b1801Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5465102	b2b1801Clo/b2b1801Clo  [background:] C57BL/6J-b2b1801Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6273758	Gt(ROSA)26Sor<sup>tm1(DUX4)Sqh</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:6280332	Gt(ROSA)26Sor<sup>tm1(DUX4)Sqh</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(ACTA1-cre/Esr1*)2Kesr/0  [background:] involves: 129S6/SvEvTac * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30429376	20190226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305070	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/c-Npc1<sup>m1N</sup>	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:21303697	20120207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857113	Prkdc<sup>scid</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21854253	20120315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619409	Tg(Ins2*Y16A)3Ell/0  [background:] NOD-Tg(Ins2*Y16A)3Ell	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15889095	20060606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361717	Tg(Prnp-TARDBP*A315T)95Balo/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:19833869	20111207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838164	Tg(ATXN3*)67.2Cce/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:11978767	20090401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5696597	Ppox<sup>tm1Had</sup>	is_implicated_in	DOID:4346	variegate porphyria		MGI:5697204	Ppox<sup>tm1Had</sup>/Ppox<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11929050	20151125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437646	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>+</sup> Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437646	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>+</sup> Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:15885355	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575878	Tg(Prnp-Immt/SOD1*G93A)7Gmnf	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:6286689	Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf  [background:] involves: C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22049426	20190410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832390	Ldb3<sup>tm4Chen</sup>/Ldb3<sup>tm4Chen</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * FVB/N	is_model_of	DOID:0110423	dilated cardiomyopathy 1C						ECO:0000033	author statement supported by traceable reference	PMID:19028670	20090218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710989	Fkbp4<sup>tm1Shou</sup>/Fkbp4<sup>tm1Shou</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17142810	20070605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644332	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] B6J.129-Wfs1<sup>tm1Yoka</sup>	is_model_of	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:18343518	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687203	Cdkn2a<sup>tm4Rdp</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26438693	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687203	Cdkn2a<sup>tm4Rdp</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687203	Cdkn2a<sup>tm4Rdp</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21996748	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687203	Cdkn2a<sup>tm4Rdp</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16397221	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5550566	Comp<sup>tm2.1Mbri</sup>	is_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:5550573	Comp<sup>tm2.1Mbri</sup>/Comp<sup>tm2.1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:22006726	20140314	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834482	Tg(Ly6a-BCR/ABL1)IS1BIsg/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:19037256	20090305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27163546	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:28334820	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26143143	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26681807	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24040016	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24282028	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26295712	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:24992836	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26908605	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27217211	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27913616	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23598407	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698041	Htt<sup>tm5Mem</sup>/Htt<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:16697652	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861935	Htt<sup>tm5Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20171207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836922	Cd4<sup>tm1Mak</sup>/Cd4<sup>tm1Mak</sup> Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>/Igh-J<sup>+</sup>  [background:] B6.Cg-Cd4<sup>tm1Mak</sup> Igh-J<sup>tm2(3H9-VDJ*)Mwg</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:19017966	20090324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J	is_model_of	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:3408670	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J	is_model_of	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6209826	Polr3a<sup>tm1.1Bebr</sup>	is_not_implicated_in	DOID:0060794	hypomyelinating leukodystrophy 7		MGI:6209828	Polr3a<sup>tm1.1Bebr</sup>/Polr3a<sup>tm1.1Bebr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28407788	20181030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:26858440	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:27806304	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5807153	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/JRj			ECO:0000033	author statement supported by traceable reference	PMID:25621497	20170804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769132	Tg(HBx)3Yu	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24941955	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769132	Tg(HBx)3Yu	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22986746	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769132	Tg(HBx)3Yu	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26392315	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769132	Tg(HBx)3Yu	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5509206	Tg(HBx)3Yu/0  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:10424292	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856041	Gusb<sup>mps</sup>	is_implicated_in	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32102934	20220615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856041	Gusb<sup>mps</sup>	is_implicated_in	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23412092	20220615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856041	Gusb<sup>mps</sup>	is_implicated_in	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25559179	20220615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856041	Gusb<sup>mps</sup>	is_implicated_in	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22403656	20220615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856041	Gusb<sup>mps</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:3784505	Gusb<sup>mps</sup>/Gusb<sup>mps</sup>  [background:] B6.Cg-Gusb<sup>mps</sup>/BrkJ			ECO:0000033	author statement supported by traceable reference	PMID:2111021	20220615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856041	Gusb<sup>mps</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:3758717	Gusb<sup>mps</sup>/Gusb<sup>mps</sup>  [background:] B6.C-H2-K<sup>bm1</sup>/ByBir-Gusb<sup>mps</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2495302	20220615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677759	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1.1Lss</sup> Tg(ACTB-cre)1Tes/0  [background:] involves: 129X1/SvJ * C3H * C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:14500363	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5696384	Tg(Cd74-Nlrc4*)1Kyas	is_implicated_in	DOID:0090065	familial cold autoinflammatory syndrome 4		MGI:5696385	Tg(Cd74-Nlrc4*)1Kyas/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25385754	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840080	Fgfr3<sup>tm1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:13481	thanatophoric dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19073250	20090415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654886	Tulp1<sup>tm1Pjn</sup>/Tulp1<sup>tm1Pjn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110381	retinitis pigmentosa 14						ECO:0000033	author statement supported by traceable reference	PMID:10607826	20090429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5762597	Gja3<sup>tm1.1Vmb</sup>	is_implicated_in	DOID:0110253	cataract 14 multiple types		MGI:5762599	Gja3<sup>tm1.1Vmb</sup>/Gja3<sup>tm1.1Vmb</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25103261	20160419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5762597	Gja3<sup>tm1.1Vmb</sup>	is_implicated_in	DOID:0110253	cataract 14 multiple types		MGI:5762600	Gja3<sup>tm1.1Vmb</sup>/Gja3<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25103261	20160419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4443335	Best1<sup>tm1.1Amar</sup>/Best1<sup>tm1.1Amar</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:0050662	bestrophinopathy						ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429538	Tg(Notch3*R169C)88Bbb	is_implicated_in	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:27821617	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429538	Tg(Notch3*R169C)88Bbb	is_implicated_in	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:27476853	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429538	Tg(Notch3*R169C)88Bbb	is_implicated_in	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:31647781	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429538	Tg(Notch3*R169C)88Bbb	is_implicated_in	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:25555543	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429538	Tg(Notch3*R169C)88Bbb	is_implicated_in	DOID:0111035	CADASIL 1		MGI:4429555	Tg(Notch3*R169C)88Bbb/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25646445	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7388493	Mettl23<sup>em1Itwa</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:7388555	Mettl23<sup>em1Itwa</sup>/Mettl23<sup>em1Itwa</sup>  [background:] C57BL/6J-Mettl23<sup>em1Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7388493	Mettl23<sup>em1Itwa</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:7388554	Mettl23<sup>em1Itwa</sup>/Mettl23<sup>+</sup>  [background:] C57BL/6J-Mettl23<sup>em1Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3630163	Sgcg<sup>tm1Oza</sup>/Sgcg<sup>tm1Oza</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:12609501	20060725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6360451	Rab28<sup>tm1d(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0111024	cone-rod dystrophy 18		MGI:6360455	Rab28<sup>tm1d(EUCOMM)Wtsi</sup>/Rab28<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30228185	20190919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700039	Ush1c<sup>tm1Bkts</sup>/Ush1c<sup>tm1Bkts</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N	is_model_of	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:17174357	20070315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311383	Daw1<sup>b2b1116Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056282	Foxi1<sup>tm1Sven</sup>/Foxi1<sup>tm1Sven</sup>  [background:] involves: CD-1	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12706902	20050622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366442	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8844056	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366442	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16055059	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294354	Trib2<sup>Tg(Thy1-Trh/APP*)2.1Ingm</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5294357	Trib2<sup>Tg(Thy1-Trh/APP*)2.1Ingm</sup>/Trib2<sup>Tg(Thy1-Trh/APP*)2.1Ingm</sup>  [background:] involves: C57BL/6 * DBA/1			ECO:0000033	author statement supported by traceable reference	PMID:21900558	20111031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476821	Tg(TARDBP)#Jpj	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5476847	Tg(TARDBP)#Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21752789	20130502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5699091	Tg(EIF1AX-Aldh2*E487K)101Oht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25698614	20151223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999580	Cryab<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0080093	myofibrillar myopathy 2		MGI:4999584	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21445271	20110523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999580	Cryab<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0080093	myofibrillar myopathy 2		MGI:4999583	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>tm1.1Ady</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21445271	20110523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654707	Grip1<sup>tm1Paw</sup>/Grip1<sup>tm1Paw</sup>  [background:] involves: 129X1/SvJ * ICR	is_model_of	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:11983858	20050719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25843002	20171129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26751774	20171129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:28790158	20171129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047689	Lum<sup>tm1Chak</sup>/Lum<sup>tm1Chak</sup>  [background:] involves: 129S/Sv * CD-1	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:9606218	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720209	Tg(Thy1-MAPT)1Vln/Tg(Thy1-MAPT)1Vln  [background:] involves: FVB	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10595944	20071023	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720209	Tg(Thy1-MAPT)1Vln/Tg(Thy1-MAPT)1Vln  [background:] involves: FVB	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11007782	20071023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828833	Nkx2-5<sup>tm2.1Mwc</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300249	Prickle1<sup>b2b019Clo</sup>/Prickle1<sup>b2b019Clo</sup>  [background:] C57BL/6J-Prickle1<sup>b2b019Clo</sup>	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491051	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23452848	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183025	Npr2<sup>cn-2J</sup>/Npr2<sup>cn-2J</sup>  [background:] B6;CBACa-A<sup>w-J</sup>/A-Kcnj6<sup>wv</sup>/+	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	MGI:2152911	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794207	Tg(ACTA1-Ar)141Kyjo/0  [background:] Not Specified	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:17984063	20080618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6156852	Marveld2<sup>tm1Sats</sup>	is_implicated_in	DOID:0110506	autosomal recessive nonsyndromic deafness 49		MGI:6156912	Marveld2<sup>tm1Sats</sup>/Marveld2<sup>tm1Sats</sup>  [background:] B6.Cg-Marveld2<sup>tm1Sats</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26677943	20180517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814906	Six3<sup>tm4(cre/ERT2)Gco</sup>/Six3<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0110872	holoprosencephaly 2						ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605490	Asl<sup>tm1Wjc</sup>/Asl<sup>tm1Wjc</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:14755	argininosuccinic aciduria						ECO:0000033	author statement supported by traceable reference	PMID:12559843	20051122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710689	Tg(Prnp-ITM2B/APP695*42)A12Emcg	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33161213	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710689	Tg(Prnp-ITM2B/APP695*42)A12Emcg	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710689	Tg(Prnp-ITM2B/APP695*42)A12Emcg	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33766652	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710689	Tg(Prnp-ITM2B/APP695*42)A12Emcg	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3710763	Tg(Prnp-ITM2B/APP695*42)A12Emcg/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16039562	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181671	Tg(RHO-P23H)DTpd	is_implicated_in	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:24825107	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181671	Tg(RHO-P23H)DTpd	is_implicated_in	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:27149983	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181671	Tg(RHO-P23H)DTpd	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:5440289	Tg(RHO-P23H)DTpd/?  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:1418997	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515936	Tg(Shank3-EGFP)1Hzo	is_implicated_in	DOID:0060437	chromosome 22q13 duplication syndrome		MGI:5570964	Tg(Shank3-EGFP)1Hzo/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24153177	20140702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473983	Dnah8<sup>em1Osb</sup>	is_implicated_in	DOID:0112164	spermatogenic failure 46		MGI:6473984	Dnah8<sup>em1Osb</sup>/Dnah8<sup>em1Osb</sup>  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:32619401	20210118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705328	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22350410	20160126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441312	Tg(Vav1-JAK2*V617F)AZjz/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:18334677	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529680	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>tm1.1Kry</sup>  [background:] B6.129X1(Cg)-Rps6ka3<sup>tm1.1Kry</sup>	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23742761	20140123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3041643	Pomc<sup>tm1Sora</sup>/Pomc<sup>tm1Sora</sup>  [background:] involves: 129S2/SvHsd * 129S6/SvEvTac	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15070780	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819453	Tg(tetO-TAg,CMV-rtTA)123Yihu/0  [background:] involves: FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18271920	20081211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907160	Tg(Myh6-NEBL*A592E)#Jato	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907160	Tg(Myh6-NEBL*A592E)#Jato	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907162	Tg(Myh6-NEBL*A592E)#Jato/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20951326	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907160	Tg(Myh6-NEBL*A592E)#Jato	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23632046	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384332	Insr<sup>tm1Khn</sup>	is_implicated_in	DOID:11612	polycystic ovary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24379345	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461887	Pgap1<sup>m1Nisw</sup>	is_implicated_in	DOID:4621	holoprosencephaly		MGI:5432254	Pgap1<sup>m1Nisw</sup>/Pgap1<sup>m1Nisw</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23213481	20190927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29898385	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26878174	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22184410	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26621336	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:28481221	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25742698	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:32929022	20201023	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387680	Tg(tetO-BCR/ABL1)2Dgt	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3693373	Tg(tetO-BCR/ABL1)2Dgt/0 Tg(Tal1-tTA)19Dgt/0  [background:] involves: C57BL/6 * DBA/2 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15331442	20201023	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883282	Shank3<sup>tm1Cmpl</sup>/Shank3<sup>tm1Cmpl</sup>  [background:] B6J.129S6-Shank3<sup>tm1Cmpl</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26134648	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544754	Cdkn1b<sup>tm1Mlf</sup>/Cdkn1b<sup>+</sup> Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19147535	20140220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448078	Nrg1<sup>tm2Zhou</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26707035	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448078	Nrg1<sup>tm2Zhou</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448078	Nrg1<sup>tm2Zhou</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22450046	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448078	Nrg1<sup>tm2Zhou</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3530450	Nrg1<sup>tm2Zhou</sup>/Nrg1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12145742	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449422	Tg(SOD1*)DF7Yaw/Tg(SOD1*)DF7Yaw  [background:] C57BL/6-Tg(SOD1*)DF7Yaw	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:15857664	20130117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665504	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] C57BL/6J-Apc<sup>Min</sup>	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:14522940	20131206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384606	Tg(UPII-SV40T)29Xrw	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384606	Tg(UPII-SV40T)29Xrw	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5141747	Tg(UPII-SV40T)29Xrw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10416618	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179992	Tg(tetO-Kras2)12Hev	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24097820	20140620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867660	Gba1<sup>tm1.2Pmis</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:22665763	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5707492	Slc2a9<sup>tm1Khm</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:5760132	Slc2a9<sup>tm1Khm</sup>/Slc2a9<sup>tm1Khm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25100214	20210319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7339104	Lamp2<sup>tm1.2Ces</sup>	is_implicated_in	DOID:0050437	Danon disease						ECO:0000033	author statement supported by traceable reference	PMID:36027926	20220923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7339104	Lamp2<sup>tm1.2Ces</sup>	is_implicated_in	DOID:0050437	Danon disease		MGI:7339154	Lamp2<sup>tm1.2Ces</sup>/Y  [background:] involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:34459252	20220923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3622169	Dicer1<sup>tm1Tara</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:27159635	20180110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506268	Tuba1a<sup>em2Rstot</sup>	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:6507152	Tuba1a<sup>em2Rstot</sup>/Tuba1a<sup>em2Rstot</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524144	Tg(MMTV-Myc*T58A)TA39Jrn	is_implicated_in	DOID:1612	breast cancer		MGI:5524146	Tg(MMTV-Myc*T58A)TA39Jrn/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620185	b2b2696Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5620189	b2b2696Clo/b2b2696Clo  [background:] C57BL/6J-b2b2696Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6280442	Phf6<sup>em1Azbi</sup>	is_implicated_in	DOID:0050681	Borjeson-Forssman-Lehmann syndrome		MGI:6295127	Phf6<sup>em1Azbi</sup>/Y  [background:] B6.Cg-Phf6<sup>em1Azbi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30403997	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25892237	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23486940	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27796305	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:30320556	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26621731	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3629233	Tg(ITGAM-cre)2781Gkl/0 Tg(SOD1*G37R)1Dwc/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16741123	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629226	Tg(SOD1*G37R)1Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3629232	Isl1<sup>tm1(cre)Tmj</sup>/Isl1<sup>+</sup> Tg(SOD1*G37R)1Dwc/0  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16741123	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426930	Gt(ROSA)26Sor<sup>tm50(HTT)Arte</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432178	Gt(ROSA)26Sor<sup>tm50(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6760662	Syce1<sup>em1Rrca</sup>	is_implicated_in	DOID:0080869	primary ovarian insufficiency 12		MGI:6760664	Syce1<sup>em1Rrca</sup>/Syce1<sup>em1Rrca</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32402064	20210920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639713	Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110040	Alzheimer's disease 4						ECO:0000033	author statement supported by traceable reference	PMID:16354928	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811989	Arhgap32<sup>tm1Taki</sup>/Arhgap32<sup>tm1Taki</sup>  [background:] B6N.Cg-Arhgap32<sup>tm1Taki</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26979507	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425920	Casr<sup>BCH004</sup>/Casr<sup>BCH004</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH004</sup>	is_model_of	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655526	Arsa<sup>tm1Gie</sup>/Arsa<sup>tm1Gie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:10581	metachromatic leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9728336	20070823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655526	Arsa<sup>tm1Gie</sup>/Arsa<sup>tm1Gie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:10581	metachromatic leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:8962139	20070823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644329	Chordc1<sup>tm1Mbra</sup>/Chordc1<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25678499	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4867518	Tg(CAG-ELN*)2Zu/0  [background:] C57BL/6J-Tg(CAG-ELN*)2Zu	is_model_of	DOID:3144	cutis laxa						ECO:0000033	author statement supported by traceable reference	PMID:20600892	20110111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511193	Zic1/Zic4<sup>tm1Kjmi</sup>/Zic1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:2785	Dandy-Walker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15338008	20050830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183431	Pkd1<sup>tm1Shh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:29463793	20180801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424920	Alpl<sup>BAP023</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425670	Alpl<sup>BAP023</sup>/Alpl<sup>BAP023</sup>  [background:] C3HeB/FeJ-Alpl<sup>BAP023</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5691406	Ildr1<sup>tm1(KOMP)Wtsi</sup>/Ildr1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0110500	autosomal recessive nonsyndromic deafness 42						ECO:0000033	author statement supported by traceable reference	PMID:25822906	20151125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5691406	Ildr1<sup>tm1(KOMP)Wtsi</sup>/Ildr1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0110500	autosomal recessive nonsyndromic deafness 42						ECO:0000033	author statement supported by traceable reference	PMID:25217574	20151125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646614	b2b3077.2Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5648030	b2b3077.2Clo/b2b3077.2Clo  [background:] C57BL/6J-b2b3077.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5501229	Wdr35<sup>yeti</sup>/Wdr35<sup>yeti</sup>  [background:] Not Specified	is_model_of	DOID:0110090	short-rib thoracic dysplasia 7 with or without polydactyly						ECO:0000033	author statement supported by traceable reference	PMID:21473986	20130815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183403	Fgf14<sup>tm1Dor</sup>	is_implicated_in	DOID:0050976	spinocerebellar ataxia type 27						ECO:0000033	author statement supported by traceable reference	PMID:25926453	20150703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183403	Fgf14<sup>tm1Dor</sup>	is_implicated_in	DOID:0050976	spinocerebellar ataxia type 27		MGI:3663129	Fgf14<sup>tm1Dor</sup>/Fgf14<sup>tm1Dor</sup>  [background:] B6.129S6-Fgf14<sup>tm1Dor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17236779	20150703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712064	Tsc2<sup>tm1.2Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23749404	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712064	Tsc2<sup>tm1.2Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712064	Tsc2<sup>tm1.2Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23123587	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850084	Baz1b<sup>tm1Ska</sup>/Baz1b<sup>tm1Ska</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19470456	20090710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510654	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup> Mmp9<sup>tm1Tvu</sup>/Mmp9<sup>tm1Tvu</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10880400	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6257844	Tg(Alb-SND1)3aDsar	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:6257845	Tg(Alb-SND1)3aDsar/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28428278	20181126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311373	Odad2<sup>b2b643Clo</sup>	is_implicated_in	DOID:0110609	primary ciliary dyskinesia 23		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311373	Odad2<sup>b2b643Clo</sup>	is_implicated_in	DOID:0110609	primary ciliary dyskinesia 23		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23850584	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620941	Col1a1<sup>M1Jrt</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4		MGI:5791061	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26277094	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620941	Col1a1<sup>M1Jrt</sup>	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4		MGI:5689511	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:24443344	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661319	Col1a1<sup>tm4(CAG-FGFR2_iIIIb*K660N)Kkw</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:5661329	Col1a1<sup>tm4(CAG-FGFR2_iIIIb*K660N)Kkw</sup>/Col1a1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25035393	20150909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437727	Dnah11<sup>b2b1727Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444189	Prss56<sup>glcr4</sup>	is_implicated_in	DOID:0060835	isolated microphthalmia 6		MGI:5444192	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] C3A.Cg-Prss56<sup>glcr4</sup> Pde6b<sup>+</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444189	Prss56<sup>glcr4</sup>	is_implicated_in	DOID:0060835	isolated microphthalmia 6		MGI:5444190	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] involves: C3H/HeA * C57BL/6J * C57BL/LiA			ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444189	Prss56<sup>glcr4</sup>	is_implicated_in	DOID:0060835	isolated microphthalmia 6		MGI:5444191	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] C57BL/6J-Prss56<sup>glcr4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426998	Bscl2<sup>tm1.1Lchan</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:30521848	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426998	Bscl2<sup>tm1.1Lchan</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:27185876	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426998	Bscl2<sup>tm1.1Lchan</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5427014	Bscl2<sup>tm1.1Lchan</sup>/Bscl2<sup>tm1.1Lchan</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24358199	20190416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6849808	Pla2g6<sup>tm1.1Hlw</sup>	is_implicated_in	DOID:0060900	Parkinson's disease 14		MGI:6849976	Pla2g6<sup>tm1.1Hlw</sup>/Pla2g6<sup>tm1.1Hlw</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30088174	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860962	Tfam<sup>tm1Lrsn</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22251459	20161028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860962	Tfam<sup>tm1Lrsn</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:25752644	20161028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860962	Tfam<sup>tm1Lrsn</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:27053209	20161028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860962	Tfam<sup>tm1Lrsn</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3702932	Slc6a3<sup>tm1(cre)Lrsn</sup>/Slc6a3<sup>+</sup> Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17227870	20161028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796166	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>+</sup> Rb1<sup>tm2Brn</sup>/Rb1<sup>+</sup> Tg(Col1a1-cre)1Kry/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129 * 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:26659571	20160930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175833	Dsg3<sup>bal</sup>/Dsg3<sup>bal</sup>  [background:] C57BL/6J-Dsg3<sup>bal</sup>/J	is_model_of	DOID:0060851	pemphigus vulgaris						ECO:0000033	author statement supported by traceable reference	PMID:9284099	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6315194	Tg(Vav1-Asxl1*Y588X)#Fcy	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:6315197	Tg(Vav1-Asxl1*Y588X)#Fcy/0  [background:] C57BL/6-Tg(Vav1-Asxl1*Y588X)#Fcy			ECO:0000033	author statement supported by traceable reference	PMID:29113963	20190626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359221	Slc34a1<sup>tm1Hten</sup>/Slc34a1<sup>tm1Hten</sup> Slc34a3<sup>tm1Kimi</sup>/Slc34a3<sup>tm1Kimi</sup>  [background:] B6.129-Slc34a3<sup>tm1Kimi</sup> Slc34a1<sup>tm1Hten</sup>	is_model_of	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria						ECO:0000033	author statement supported by traceable reference	PMID:19570882	20090928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857265	Twist1<sup>tm1Bhr</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24585549	20140618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857265	Twist1<sup>tm1Bhr</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23354436	20140618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857265	Twist1<sup>tm1Bhr</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2667352	Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12221714	20140618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857265	Twist1<sup>tm1Bhr</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2386979	Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8988167	20140618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857265	Twist1<sup>tm1Bhr</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2386978	Twist1<sup>tm1Bhr</sup>/Twist1<sup>tm1Bhr</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8988167	20140618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388821	Tg(KRT14-CASP1)1Miz	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388821	Tg(KRT14-CASP1)1Miz	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388821	Tg(KRT14-CASP1)1Miz	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5563662	Tg(KRT14-CASP1)1Miz/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12151598	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4127237	Btbd9<sup>Gt(RRE078)Byg</sup>	is_implicated_in	DOID:0050425	restless legs syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31704978	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4127237	Btbd9<sup>Gt(RRE078)Byg</sup>	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:5438092	Btbd9<sup>Gt(RRE078)Byg</sup>/Btbd9<sup>Gt(RRE078)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22678064	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7547217	Rab39b<sup>tm1Pdad</sup>	is_implicated_in	DOID:0112059	non-syndromic X-linked intellectual disability 72		MGI:7547388	Rab39b<sup>tm1Pdad</sup>/Y  [background:] B6N.Cg-Rab39b<sup>tm1Pdad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34761259	20231113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196103	F9<sup>em3Dlli</sup>	is_implicated_in	DOID:12259	hemophilia B		MGI:6196105	F9<sup>em3Dlli</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26964564	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5465282	Srgap3<sup>tm1.1Zi</sup>/Srgap3<sup>tm1.1Zi</sup>  [background:] B6.129(SJL)-Srgap3<sup>tm1.1Zi</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22820399	20130221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175101	Lepr<sup>Tg(Mth11)1Aig</sup>/Lepr<sup>Tg(Mth11)1Aig</sup>  [background:] involves: Him:OF1	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10708583	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5787924	Alpl<sup>tm1Jlm</sup>/Alpl<sup>tm1Jlm</sup>  [background:] involves: 129S1/SvImJ * 129S2/SvPas * C57BL/6	is_model_of	DOID:0110914	infantile hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:22991301	20160804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181896	Pkd1<sup>m1Bei</sup>/Pkd1<sup>m1Bei</sup>  [background:] involves: A/J * FVB/N	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11818962	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5498230	Kif7<sup>b2b2254Clo</sup>	is_implicated_in	DOID:9250	acrocallosal syndrome		MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176166	Tg(MMTV-cre)4Mam	is_implicated_in	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22915751	20130408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177545	Cftr<sup>tm2Hgu</sup>/Cftr<sup>tm2Hgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:11823443	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159000	Oprm1<sup>tm1Kff</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27274875	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159000	Oprm1<sup>tm1Kff</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23327738	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159000	Oprm1<sup>tm1Kff</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5538574	Oprm1<sup>tm1Kff</sup>/Oprm1<sup>tm1Kff</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20503133	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5314995	Tmc1<sup>nice</sup>	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:5314998	Tmc1<sup>nice</sup>/Tmc1<sup>nice</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814575	Tg(MT1A-Dyrk1a)#Xest	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22215728	20160610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814575	Tg(MT1A-Dyrk1a)#Xest	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27030752	20160610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814575	Tg(MT1A-Dyrk1a)#Xest	is_implicated_in	DOID:14250	Down syndrome		MGI:3814581	Tg(MT1A-Dyrk1a)#Xest/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11555628	20160610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5708531	Enam<sup>tm1.1Jcch</sup>/Enam<sup>tm1.1Jcch</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000033	author statement supported by traceable reference	PMID:24603688	20160216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5496902	Tg(Myh6-cre)TG9Pjay	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:29691457	20180710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5496902	Tg(Myh6-cre)TG9Pjay	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:22038742	20180710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5496902	Tg(Myh6-cre)TG9Pjay	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907012	Tg(Myh6-cre)TG9Pjay/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17202264	20180710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000280	Tg(AR*100Q)C32Als/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:15003169	20110527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3041700	Nr3c2<sup>tm1Gsc</sup>/Nr3c2<sup>tm1Gsc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:9689096	20050913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176880	Dmd<sup>Gt(ROSABetageo)1Mpd</sup>/Y  [background:] involves: 129S1/Sv	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9626497	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942358	Tg(Kit*D814V)2Roer	is_implicated_in	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:24788138	20150309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4942358	Tg(Kit*D814V)2Roer	is_implicated_in	DOID:350	mastocytosis		MGI:4942361	Tg(Kit*D814V)2Roer/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21148330	20150309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575511	Tg(CAG-Diaph3)771Lesp/0  [background:] FVB/NJ-Tg(CAG-Diaph3)771Lesp	is_model_of	DOID:0060690	autosomal dominant auditory neuropathy 1						ECO:0000033	author statement supported by traceable reference	PMID:23441200	20140730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859921	Tulp1<sup>tm1Pjn</sup>	is_implicated_in	DOID:0110381	retinitis pigmentosa 14						ECO:0000033	author statement supported by traceable reference	PMID:23746204	20160711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859921	Tulp1<sup>tm1Pjn</sup>	is_implicated_in	DOID:0110381	retinitis pigmentosa 14						ECO:0000033	author statement supported by traceable reference	PMID:26911694	20160711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859921	Tulp1<sup>tm1Pjn</sup>	is_implicated_in	DOID:0110381	retinitis pigmentosa 14		MGI:2654886	Tulp1<sup>tm1Pjn</sup>/Tulp1<sup>tm1Pjn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10607826	20160711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692444	Jag1<sup>tm2Grid</sup>	is_implicated_in	DOID:9245	Alagille syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24491691	20140508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692444	Jag1<sup>tm2Grid</sup>	is_implicated_in	DOID:9245	Alagille syndrome		MGI:5318528	Jag1<sup>tm2Grid</sup>/Jag1<sup>tm2Grid</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22156581	20140508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6860354	Sbf1<sup>em1Frobi</sup>	is_implicated_in	DOID:0110194	Charcot-Marie-Tooth disease type 4B3		MGI:7316771	Sbf1<sup>em1Frobi</sup>/Sbf1<sup>em1Frobi</sup>  [background:] C57BL/6N-Sbf1<sup>em1Frobi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34718573	20220729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5606283	mt-Tk<sup>m1</sup>	is_implicated_in	DOID:700	mitochondrial metabolism disease						ECO:0000033	author statement supported by traceable reference	PMID:24510903	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5606283	mt-Tk<sup>m1</sup>	is_implicated_in	DOID:700	mitochondrial metabolism disease		MGI:5606285	mt-Tk<sup>m1</sup>  [background:] involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:24510903	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6273991	Tg(RP11-578M14)5Mkru	is_implicated_in	DOID:9970	obesity		MGI:6273993	Tg(RP11-578M14)5Mkru/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29206867	20190121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3763455	Hcrt<sup>tm1Ywa</sup>/Hcrt<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:10481909	20071210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437134	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437134	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17283114	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5305225	Sirt1<sup>tm1.2Cxd</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5305254	Sirt1<sup>tm1.2Cxd</sup>/Sirt1<sup>tm1.2Cxd</sup> Tg(Alb1-cre)1Dlr/?  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21103071	20120209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6294292	Tg(Prnp-HTT*82Q)61Gschi	is_implicated_in	DOID:12858	Huntington's disease		MGI:6294294	Tg(Prnp-HTT*82Q)61Gschi/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15190011	20190424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5630056	Tg(SOD1*G85R/EYFP)737Alho	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5630057	Tg(SOD1*G85R/EYFP)737Alho/Tg(SOD1*G85R/EYFP)737Alho  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:25024188	20160725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5630056	Tg(SOD1*G85R/EYFP)737Alho	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27114530	20160725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575505	Ehmt1<sup>tm1Yshk</sup>	is_implicated_in	DOID:0060352	Kleefstra syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:28071689	20190423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575505	Ehmt1<sup>tm1Yshk</sup>	is_implicated_in	DOID:0060352	Kleefstra syndrome 1		MGI:4461144	Ehmt1<sup>tm1Yshk</sup>/Ehmt1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:19896504	20190423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575505	Ehmt1<sup>tm1Yshk</sup>	is_implicated_in	DOID:0060352	Kleefstra syndrome 1		MGI:4461144	Ehmt1<sup>tm1Yshk</sup>/Ehmt1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23175442	20190423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838322	Ttn<sup>tm1.1Isrd</sup>	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J		MGI:4838324	Ttn<sup>tm1.1Isrd</sup>/Ttn<sup>tm1.1Isrd</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20855473	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838322	Ttn<sup>tm1.1Isrd</sup>	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5699326	Tg(SOD1*H46R)LAra	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5699330	Tg(SOD1*H46R)LAra/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25762155	20151216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793792	Pkd1<sup>tm2.1Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23524344	20140408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793792	Pkd1<sup>tm2.1Som</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22338085	20140408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174904	Fgfr1<sup>tm1Led</sup>/Fgfr1<sup>tm1Led</sup>  [background:] involves: 129S4/SvJae * NIH Black Swiss	is_model_of	DOID:14705	Pfeiffer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8001823	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887578	Mks1<sup>hlb614</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:4887579	Mks1<sup>hlb614</sup>/Mks1<sup>hlb614</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21045211	20110211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110156	Charcot-Marie-Tooth disease type 2B1						ECO:0000033	author statement supported by traceable reference	PMID:11799477	20060502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560472	Tg(Cela1-luc,Cela1-TAg)#Nzh	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5560479	Tg(Cela1-luc,Cela1-TAg)#Nzh/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19622581	20140528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560472	Tg(Cela1-luc,Cela1-TAg)#Nzh	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23801758	20140528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709041	Myo7a<sup>polka</sup>/Myo7a<sup>polka</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:20016096	20100312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679967	Id3<sup>tm1Zhu</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17472721	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679967	Id3<sup>tm1Zhu</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26382297	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679967	Id3<sup>tm1Zhu</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23904442	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679967	Id3<sup>tm1Zhu</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5000526	Id3<sup>tm1Zhu</sup>/Id3<sup>tm1Zhu</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:15485632	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907885	Tg(Myh6-HBEGF)#Iko	is_implicated_in	DOID:6000	congestive heart failure		MGI:5907886	Tg(Myh6-HBEGF)#Iko/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15272002	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5086116	Tg(AMELX*P70T)2Gibs/?  [background:] Not Specified	is_model_of	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000033	author statement supported by traceable reference	PMID:17384027	20110816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23538858	20140627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575311	Sh2d1a<sup>tm1Lyin</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575311	Sh2d1a<sup>tm1Lyin</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:5515317	Sh2d1a<sup>tm1Lyin</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575311	Sh2d1a<sup>tm1Lyin</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3575716	Sh2d1a<sup>tm1Lyin</sup>/Sh2d1a<sup>tm1Lyin</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544197	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0  [background:] C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	is_model_of	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000033	author statement supported by traceable reference	PMID:23771029	20140214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625035	Pmp22<sup>tm1Lnot</sup>/Pmp22<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0060843	hereditary neuropathy with liability to pressure palsies						ECO:0000033	author statement supported by traceable reference	PMID:16436605	20060621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5298019	Tg(Ggt1-Hif1a*)43Log/0  [background:] involves: C57BL/6	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:21908555	20111213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5648733	Dph1<sup>tm1.1Cmch</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:5659970	Dph1<sup>tm1.1Cmch</sup>/Dph1<sup>tm1.1Cmch</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5648733	Dph1<sup>tm1.1Cmch</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:5659973	Dph1<sup>tm1.1Cmch</sup>/Dph1<sup>tm1.1Cmch</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5511058	Tg(Camk2a-tTA)1Mmay/0 Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/Fgf14<sup>+</sup>  [background:] involves: FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16291936	20131011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580088	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:24234649	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23332367	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:20542988	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21824387	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:20705734	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798621	Dmd<sup>mdx-5Cv</sup>/Y  [background:] B6Ros.Cg-Dmd<sup>mdx-5Cv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21893021	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856332	Dmd<sup>mdx-5Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798788	Dmd<sup>mdx-5Cv</sup>/Dmd<sup>mdx-5Cv</sup>  [background:] B6Ros.Cg-Dmd<sup>mdx-5Cv</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16857961	20140407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622062	Tnf<sup>tm1Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:10204494	20060511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5571366	Tg(Igh-ROR1)1Kip	is_implicated_in	DOID:1040	chronic lymphocytic leukemia		MGI:5571369	Tg(Igh-ROR1)1Kip/0  [background:] C57BL/6-Tg(Igh-ROR1)1Kip			ECO:0000033	author statement supported by traceable reference	PMID:24379361	20140707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050284	Ptpn11<sup>tm1Bgn</sup>	is_implicated_in	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24590274	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050284	Ptpn11<sup>tm1Bgn</sup>	is_implicated_in	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:30089263	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050284	Ptpn11<sup>tm1Bgn</sup>	is_implicated_in	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:22371576	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050284	Ptpn11<sup>tm1Bgn</sup>	is_implicated_in	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24865967	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050284	Ptpn11<sup>tm1Bgn</sup>	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:3050469	Ptpn11<sup>tm1Bgn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15273746	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760297	Gars1<sup>C201R</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:28351971	20170720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760297	Gars1<sup>C201R</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:26503042	20170720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760297	Gars1<sup>C201R</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:27288508	20170720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760297	Gars1<sup>C201R</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:3849420	Gars1<sup>C201R</sup>/Gars1<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22144914	20170720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760297	Gars1<sup>C201R</sup>	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:3849420	Gars1<sup>C201R</sup>/Gars1<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19470612	20170720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4944273	Errfi1<sup>tm1Jwj</sup>/Errfi1<sup>tm1Jwj</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ	is_model_of	DOID:1380	endometrial cancer						ECO:0000033	author statement supported by traceable reference	PMID:20418913	20110409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471586	Insr<sup>tm1Khn</sup>/Insr<sup>tm1Khn</sup> Lepr<sup>tm1.1Chua</sup>/Lepr<sup>tm1.1Chua</sup> Tg(Pomc1-cre)16Lowl/0  [background:] involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * FVB/N	is_model_of	DOID:11612	polycystic ovary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23119079	20130403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:1018005	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:10861288	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:16589192	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:10942421	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:63130	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446796	Bcs1l<sup>tm1.1Levp</sup>	is_implicated_in	DOID:0080111	mitochondrial complex III deficiency nuclear type 1		MGI:6387277	Bcs1l<sup>tm1.1Levp</sup>/Bcs1l<sup>tm1.1Levp</sup>  [background:] B6.129-Bcs1l<sup>tm1.1Levp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28424480	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609549	Cacna1f<sup>tm1Ntbh</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:33117610	20210326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609549	Cacna1f<sup>tm1Ntbh</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3611755	Cacna1f<sup>tm1Ntbh</sup>/Y  [background:] B6.129-Cacna1f<sup>tm1Ntbh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16155113	20210326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609549	Cacna1f<sup>tm1Ntbh</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3611756	Cacna1f<sup>tm1Ntbh</sup>/Cacna1f<sup>tm1Ntbh</sup>  [background:] B6.129-Cacna1f<sup>tm1Ntbh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16155113	20210326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044685	Amacr<sup>tm1Jkh</sup>/Amacr<sup>tm1Jkh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060602	alpha-methylacyl-CoA racemase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:15016763	20111031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7311664	Rarres1<sup>tm1d(KOMP)Wtsi</sup>	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:7311758	Rarres1<sup>tm1d(KOMP)Wtsi</sup>/Rarres1<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543401	Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup> Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:22904682	20140207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447489	Scn1a<sup>tm2.1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23524966	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447489	Scn1a<sup>tm2.1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26017580	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447489	Scn1a<sup>tm2.1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5447490	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:22908258	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447489	Scn1a<sup>tm2.1Wac</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:6274702	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447029	Tg(Plp)72Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:5776501	Tg(Plp)72Kan/Tg(Plp)72Kan  [background:] B6N.Cg-Tg(Plp)72Kan			ECO:0000033	author statement supported by traceable reference	PMID:20091761	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447029	Tg(Plp)72Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:24680886	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447029	Tg(Plp)72Kan	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:20091761	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284898	Pdlim5<sup>tm1.1Chen</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5284902	Pdlim5<sup>tm1.1Chen</sup>/Pdlim5<sup>tm1.1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:20538684	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179545	Relb<sup>tm1Brv</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179545	Relb<sup>tm1Brv</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179545	Relb<sup>tm1Brv</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3588865	Relb<sup>tm1Brv</sup>/Relb<sup>tm1Brv</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: C57BL/6) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10940923	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817969	Ccm2<sup>tm1Kwhi</sup>	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2						ECO:0000033	author statement supported by traceable reference	PMID:25486933	20160831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6231206	Tg(H2-K-Hmga1)#Lmsr	is_implicated_in	DOID:363	uterine cancer		MGI:6231210	Tg(H2-K-Hmga1)#Lmsr/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17483309	20181107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6727102	Cfap47<sup>em1Fzh</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6727110	Cfap47<sup>em1Fzh</sup>/Y  [background:] C57BL/6-Cfap47<sup>em1Fzh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33472045	20210729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6510292	Rpl11<sup>tm1.1Srn</sup>	is_implicated_in	DOID:0111878	Diamond-Blackfan anemia 7		MGI:6510523	Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/Ndor1<sup>+</sup> Rpl11<sup>tm1.1Srn</sup>/Rpl11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:26489471	20210316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424983	Casr<sup>BCH011</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425922	Casr<sup>BCH011</sup>/Casr<sup>BCH011</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH011</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175783	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:10527801	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834526	Aspm<sup>Gt(AA0137)Wtsi</sup>/Aspm<sup>Gt(AA0137)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:20823249	20101011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565602	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0  [background:] FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:18068632	20140529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441310	Tg(Vav1-JAK2*V617F)AZjz	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:5441312	Tg(Vav1-JAK2*V617F)AZjz/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18334677	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524121	Fat1<sup>tm1.2Fhel</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:5524138	Fat1<sup>tm1.2Fhel</sup>/Fat1<sup>tm1.2Fhel</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176410	Ppt1<sup>tm1Hof</sup>/Ppt1<sup>tm1Hof</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:11717424	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6268324	Dhtkd1<sup>em1Hpr</sup>	is_implicated_in	DOID:0111453	2-aminoadipic 2-oxoadipic aciduria		MGI:6268326	Dhtkd1<sup>em1Hpr</sup>/Dhtkd1<sup>em1Hpr</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28545977	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5496902	Tg(Myh6-cre)TG9Pjay	is_implicated_in	DOID:6000	congestive heart failure		MGI:5907012	Tg(Myh6-cre)TG9Pjay/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16762803	20170815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623422	Tor1a<sup>tm2Wtd</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:27769743	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623422	Tor1a<sup>tm2Wtd</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:24503369	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623422	Tor1a<sup>tm2Wtd</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:5532923	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6.129S1-Tor1a<sup>tm2Wtd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24121114	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623422	Tor1a<sup>tm2Wtd</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:5532923	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6.129S1-Tor1a<sup>tm2Wtd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21464304	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623422	Tor1a<sup>tm2Wtd</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:3624527	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:23748075	20190729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777397	Uros<sup>tm3Rjde</sup>/Uros<sup>tm3Rjde</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:13271	cutaneous porphyria						ECO:0000033	author statement supported by traceable reference	PMID:16532394	20080623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178096	Hoxd13<sup>tm1Ddu</sup>/Hoxd13<sup>tm1Ddu</sup>  [background:] either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6)	is_model_of	DOID:0060242	synpolydactyly						ECO:0000033	author statement supported by traceable reference	PMID:8106170	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603148	Crygb<sup>Clapper</sup>/Crygb<sup>+</sup>  [background:] C57BL/6J-Crygb<sup>Clapper</sup>	is_model_of	DOID:0110236	cataract 39 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:15878859	20130513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5532204	Gtf2i<sup>tm1Vcam</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5532293	Gtf2i<sup>tm1Vcam</sup>/Gtf2i<sup>tm1Vcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:20403157	20140127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462246	Tg(Myh6-Tpm1*D175N)#Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462246	Tg(Myh6-Tpm1*D175N)#Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3		MGI:5906030	Tg(Myh6-Tpm1*D175N)#Dfw/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10400910	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462246	Tg(Myh6-Tpm1*D175N)#Dfw	is_implicated_in	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:21743000	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26908607	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:17950578	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:23209425	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:19436705	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:25799359	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:25211016	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26339785	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:5523468	Tg(DMWD,DMPK*,SIX5)328Ggo/Tg(DMWD,DMPK*,SIX5)328Ggo  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:23180777	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:5523468	Tg(DMWD,DMPK*,SIX5)328Ggo/Tg(DMWD,DMPK*,SIX5)328Ggo  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11726559	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:21378394	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:21044947	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523461	Tg(DMWD,DMPK*,SIX5)328Ggo	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:33503262	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5649273	Gt(ROSA)26Sor<sup>tm5(ASPSCR1/TFE3)Mrc</sup>	is_implicated_in	DOID:4239	alveolar soft part sarcoma		MGI:5649275	Gt(ROSA)26Sor<sup>tm5(ASPSCR1/TFE3)Mrc</sup>/Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25453902	20150819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12885755	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12590922	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:8177042	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5546509	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Msx2-rtTA)885Lma/0 Tg(tetO-cre)1Jaw/0  [background:] involves: 129 * 129X1/SvJ * C57BL/6	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:23928991	20140228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824056	Tg(Mpz*S63X)31Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6276576	Tg(Mpz*S63X)31Mes/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824056	Tg(Mpz*S63X)31Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:20878767	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824056	Tg(Mpz*S63X)31Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:27807175	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824056	Tg(Mpz*S63X)31Mes	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:18255032	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5925410	Emp2<sup>tm1.1Tac</sup>	is_implicated_in	DOID:3891	placental insufficiency		MGI:5925411	Emp2<sup>tm1.1Tac</sup>/Emp2<sup>tm1.1Tac</sup> Tg(Zp3-cre)93Knw/0  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28295343	20171121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425670	Alpl<sup>BAP023</sup>/Alpl<sup>BAP023</sup>  [background:] C3HeB/FeJ-Alpl<sup>BAP023</sup>	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317863	Tg(tetO/CMV-Tslp)#Sfz	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317863	Tg(tetO/CMV-Tslp)#Sfz	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5317865	Tg(KRT5-rtTA)1Glk/0 Tg(tetO/CMV-Tslp)#Sfz/0  [background:] involves: C3H * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16103410	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317863	Tg(tetO/CMV-Tslp)#Sfz	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438111	Ncf1<sup>tm1Shl</sup>/Ncf1<sup>tm1Shl</sup>  [background:] B6.129S2-Ncf1<sup>tm1Shl</sup>	is_model_of	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:16843452	20100330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450635	Hbb<sup>d3th</sup>/Hbb<sup>d3th</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:6313205	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448547	Tg(SOD1*G85R)#Roos	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22668777	20160804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448547	Tg(SOD1*G85R)#Roos	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:20962037	20160804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448547	Tg(SOD1*G85R)#Roos	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24368417	20160804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448547	Tg(SOD1*G85R)#Roos	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5448548	Tg(SOD1*G85R)#Roos/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19233858	20160804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784582	Cryaa<sup>tm1.1Ady</sup>/Cryaa<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:18056999	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559371	Tg(KRT14-HPV8)#Vuc	is_implicated_in	DOID:4159	skin cancer		MGI:5559468	Tg(KRT14-HPV8)#Vuc/0  [background:] involves: C57BL/6 * DBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15735026	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587760	Myo7a<sup>816SB</sup>/Myo7a<sup>816SB</sup>  [background:] involves: BALB/cRl	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157129	Lyn<sup>tm1Ard</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:29463843	20180320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157129	Lyn<sup>tm1Ard</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3767995	Lyn<sup>tm1Ard</sup>/Lyn<sup>tm1Ard</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20512127	20180320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525443	Tg(MMTV-cre)7Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23720052	20130916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837824	Col1a1<sup>tm1(CAG-EGFR)Char</sup>	is_implicated_in	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:22020333	20120828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569528	Tg(CMV-HTT*48Q)BTag	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569528	Tg(CMV-HTT*48Q)BTag	is_implicated_in	DOID:12858	Huntington's disease		MGI:5569533	Tg(CMV-HTT*48Q)BTag/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569528	Tg(CMV-HTT*48Q)BTag	is_implicated_in	DOID:12858	Huntington's disease		MGI:5569535	Tg(CMV-HTT*48Q)BTag/Tg(CMV-HTT*48Q)BTag  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699377	Ctnna1<sup>Tvrm5</sup>/Ctnna1<sup>+</sup>  [background:] C57BL/6J-Ctnna1<sup>Tvrm5</sup>/Pjn	is_model_of	DOID:0060864	patterned macular dystrophy 2						ECO:0000033	author statement supported by traceable reference	PMID:26691986	20161209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829605	Trip11<sup>m1Mawa</sup>	is_implicated_in	DOID:0080054	achondrogenesis type IA		MGI:4829609	Trip11<sup>m1Mawa</sup>/Trip11<sup>m1Mawa</sup>  [background:] C57BL/6J-Trip11<sup>m1Mawa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20089971	20100915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696738	Tg(Camk2a-SNCA*)2Mgsp/0 Del(6Snca)1Slab/Del(6Snca)1Slab  [background:] B6JOlaHsd.Cg-Tg(Camk2a-SNCA*)2Mgsp	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:25450466	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440895	Tg(Eno2-MFN2*R94Q)L51Ugfm	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	PMID:30659145	20190228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440895	Tg(Eno2-MFN2*R94Q)L51Ugfm	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	PMID:20418531	20190228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440895	Tg(Eno2-MFN2*R94Q)L51Ugfm	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A		MGI:4440922	Tg(Eno2-MFN2*R94Q)L51Ugfm/0  [background:] involves: C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	MGI:4440898	20190228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440895	Tg(Eno2-MFN2*R94Q)L51Ugfm	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A		MGI:5476672	Tg(Eno2-MFN2*R94Q)L51Ugfm/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20418531	20190228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>	is_model_of	DOID:0110609	primary ciliary dyskinesia 23						ECO:0000033	author statement supported by traceable reference	PMID:23850584	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>	is_model_of	DOID:0110609	primary ciliary dyskinesia 23						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7280685	Nphp1<sup>em1Lisu</sup>	is_implicated_in	DOID:0111112	nephronophthisis 1		MGI:7280905	Nphp1<sup>em1Lisu</sup>/Nphp1<sup>em1Lisu</sup>  [background:] C57BL/6J-Nphp1<sup>em1Lisu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34415307	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861106	Cm	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861106	Cm	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:3717464	Cm/+  [background:] C3Sn.Cg-Cm/J			ECO:0000033	author statement supported by traceable reference	PMID:1613559	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258768	Adamts10<sup>em1Cbal</sup>	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:6258769	Adamts10<sup>em1Cbal</sup>/Adamts10<sup>em1Cbal</sup>  [background:] involves: C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30060141	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302192	Crbn<sup>tm1.2Jjh</sup>	is_implicated_in	DOID:0060308	autosomal recessive intellectual developmental disorder		MGI:5302204	Crbn<sup>tm1.2Jjh</sup>/Crbn<sup>tm1.2Jjh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29459374	20190703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779551	Tg(PMP22-tTA)JY13Clh/0 Tg(tetO/CMV-Pmp22)JP18Clh/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:11331611	20160630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618363	Cdkn1a<sup>tm1Led</sup>/Cdkn1a<sup>tm1Led</sup> Gadd45a<sup>tm1Ajf</sup>/Gadd45a<sup>tm1Ajf</sup>  [background:] either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324028	Tg(Myh6-BAG3*P209L)#Mswi	is_implicated_in	DOID:0080097	myofibrillar myopathy 6		MGI:6324029	Tg(Myh6-BAG3*P209L)#Mswi/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:27321750	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716631	Rpgrip1l<sup>tm1Urt</sup>/Rpgrip1l<sup>tm1Urt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0111002	Joubert syndrome 7						ECO:0000033	author statement supported by traceable reference	PMID:17558409	20150903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695897	Tg(SOD1*)125Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25054289	20150408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695897	Tg(SOD1*)125Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16000321	20150408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695897	Tg(SOD1*)125Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5056450	Tg(SOD1*)125Dbo/?  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12966034	20150408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6164675	Clcnkb<sup>tm1.1Doel</sup>	is_implicated_in	DOID:445	Bartter disease		MGI:6200350	Clcnkb<sup>tm1.1Doel</sup>/Clcnkb<sup>tm1.1Doel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:27335120	20180928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4850046	Fbn2<sup>tm1Rmz</sup>/Fbn2<sup>tm1Rmz</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:20729550	20110103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5699320	Tg(SOD1*H46R)IAra	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5699329	Tg(SOD1*H46R)IAra/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25762155	20151216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698924	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Gt(ROSA)26Sor<sup>tm1Sho</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S4/SvJaeSor	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23696872	20151214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822129	Tg(CAG-cat,-Ptpn11*Q97R)1Rbns	is_implicated_in	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24599474	20140613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822129	Tg(CAG-cat,-Ptpn11*Q97R)1Rbns	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:3822157	Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0 Tg(Tek-cre)12Flv/0  [background:] involves: C3H * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19017799	20140613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822129	Tg(CAG-cat,-Ptpn11*Q97R)1Rbns	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:4361520	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0  [background:] involves: C57BL/6J * CBA/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19706403	20140613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524082	Tg(MMTV-Myc*T58A)TA14Jrn	is_implicated_in	DOID:1612	breast cancer		MGI:5524086	Tg(MMTV-Myc*T58A)TA14Jrn/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:18728777	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25879444	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:17559418	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819096	Tg(Umod*C147W)958Lura	is_implicated_in	DOID:0060062	familial juvenile hyperuricemic nephropathy		MGI:4819114	Tg(Umod*C147W)958Lura/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:20472742	20100813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417919	Slc1a1<sup>tm1Wst</sup>/Slc1a1<sup>tm1Wst</sup>  [background:] B6.129-Slc1a1<sup>tm1Wst</sup>	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:17607354	20100115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028851	Tg(aP2-SREBF1c)9884Reh/0  [background:] involves: C57BL/6J * SJL	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9784493	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2182802	Apc<sup>tm1Mmt</sup>/Apc<sup>+</sup> Smad4<sup>tm1Mmt</sup>/Smad4<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:9506519	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639115	Aqp2<sup>cph</sup>/Aqp2<sup>cph</sup>  [background:] C57BL/6J-Aqp2<sup>cph</sup>	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:16641094	20060727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587738	Nhs<sup>Xcat</sup>/Nhs<sup>Xcat</sup>  [background:] involves: DBA/2 * T STOCK	is_model_of	DOID:0060599	Nance-Horan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587738	Nhs<sup>Xcat</sup>/Nhs<sup>Xcat</sup>  [background:] involves: DBA/2 * T STOCK	is_model_of	DOID:0060599	Nance-Horan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6682022	Ryr2<sup>em1Swch</sup>	is_implicated_in	DOID:114	heart disease		MGI:6682030	Ryr2<sup>em1Swch</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33536282	20210409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6469320	Kbtbd13<sup>em1Coeo</sup>	is_implicated_in	DOID:0110935	nemaline myopathy 6		MGI:6469361	Kbtbd13<sup>em1Coeo</sup>/Kbtbd13<sup>em1Coeo</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31671076	20201026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6469320	Kbtbd13<sup>em1Coeo</sup>	is_implicated_in	DOID:0110935	nemaline myopathy 6						ECO:0000033	author statement supported by traceable reference	PMID:31671076	20201026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515353	Chd2<sup>Gt(RRBO46)Byg</sup>/Chd2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18386809	20140818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681404	Prkn<sup>tm1Shn</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:26182419	20190528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681404	Prkn<sup>tm1Shn</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:28086194	20190528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681404	Prkn<sup>tm1Shn</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:21839811	20190528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681404	Prkn<sup>tm1Shn</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:26546471	20190528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681404	Prkn<sup>tm1Shn</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:25154397	20190528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681404	Prkn<sup>tm1Shn</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:2681434	Prkn<sup>tm1Shn</sup>/Prkn<sup>tm1Shn</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:12930822	20190528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26231800	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27581300	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22381732	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26485287	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31503547	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29431654	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28576709	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31730795	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25848016	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome		MGI:5461654	Ube3a<sup>tm1Alb</sup>/Ube3a<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22916201	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181811	Ube3a<sup>tm1Alb</sup>	is_implicated_in	DOID:1932	Angelman syndrome		MGI:3694359	Ube3a<sup>tm1Alb</sup>/Ube3a<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9808466	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177162	Fxn<sup>tm1Mkn</sup>	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25113747	20150507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177162	Fxn<sup>tm1Mkn</sup>	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25681319	20150507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177162	Fxn<sup>tm1Mkn</sup>	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:11714098	20150507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0060648	anterior segment dysgenesis						ECO:0000033	author statement supported by traceable reference	PMID:4970465	20190929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0060648	anterior segment dysgenesis						ECO:0000033	author statement supported by traceable reference	PMID:12655058	20190929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0060648	anterior segment dysgenesis						ECO:0000033	author statement supported by traceable reference	PMID:12702666	20190929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491272	Dnah11<sup>b2b2349Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431496	b2b904.2Clo	is_implicated_in	DOID:114	heart disease		MGI:5431512	b2b904.2Clo/b2b904.2Clo  [background:] C57BL/6J-b2b904.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036915	Sh2d1a<sup>tm1Pls</sup>/Sh2d1a<sup>tm1Pls</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11404475	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157962	Tcf4<sup>em1Bdph</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157969	Tcf4<sup>em1Bdph</sup>/?  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157962	Tcf4<sup>em1Bdph</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32015540	20201216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042292	Gh<sup>Sma1</sup>/Gh<sup>+</sup>  [background:] C3HeB/FeJ-Gh<sup>Sma1</sup>	is_model_of	DOID:0060872	isolated growth hormone deficiency type II						ECO:0000033	author statement supported by traceable reference	PMID:14726450	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444038	Tg(H2-K<sup>b</sup>-Jak2*V617F)2Shmd/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:18033315	20121130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5487460	Myo7a<sup>dmbo2</sup>/Myo7a<sup>dmbo2</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110477	autosomal recessive nonsyndromic deafness 2						ECO:0000033	author statement supported by traceable reference	PMID:23251483	20130529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473659	Gt(ROSA)26Sor<sup>tm1(CAG-SNCA)Tanj</sup>	is_implicated_in	DOID:4752	multiple system atrophy		MGI:6473661	Gt(ROSA)26Sor<sup>tm1(CAG-SNCA)Tanj</sup>/Gt(ROSA)26Sor<sup>tm1(CAG-SNCA)Tanj</sup> Tg(Plp1-cre/ERT)3Pop/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30910745	20201124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857846	Pitx2<sup>tm2Sac</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:12015277	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857846	Pitx2<sup>tm2Sac</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3589210	Pitx2<sup>tm2Sac</sup>/Pitx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10498698	20190503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5619363	Rp2<sup>tm1.2Asw</sup>/Rp2<sup>tm1.2Asw</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110415	retinitis pigmentosa 2						ECO:0000033	author statement supported by traceable reference	PMID:23745007	20150330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511141	Trp63<sup>tm2Brd</sup>/Trp63<sup>tm2Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0080174	bladder exstrophy						ECO:0000033	author statement supported by traceable reference	PMID:17079275	20121109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5318684	Tg(CMV-IGL@AL080)55Dcs	is_implicated_in	DOID:9120	amyloidosis		MGI:5318687	Tg(CMV-IGL@AL080)55Dcs/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:21998211	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3608784	Ext2<sup>tm1Werb</sup>/Ext2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:206	hereditary multiple exostoses						ECO:0000033	author statement supported by traceable reference	PMID:16236767	20051230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835229	Tg(MMTV-LPAR1)#Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763097	Tg(MMTV-LPAR1)#Gbm/Tg(MMTV-LPAR1)#Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)#Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604880	Tg(MMTV-Erbb2)10Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4941901	Pink1<sup>tm1Hbu</sup>	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:4941907	Pink1<sup>tm1Hbu</sup>/Pink1<sup>tm1Hbu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21249202	20150303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461029	Tg(Igh-V-CD40lg)#Tsub	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4461031	Tg(Igh-V-CD40lg)#Tsub/0  [background:] C57BL/6-Tg(Igh-V-CD40lg)#Tsub			ECO:0000033	author statement supported by traceable reference	PMID:11751940	20100721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4840220	Igha<sup>tm1(Myc)Janz</sup>/Igha<sup>+</sup> Tg(Tnfsf13b)1Fma/0  [background:] involves: 129S1/Sv * C57BL/6 * DBA/2J	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20956327	20101203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624036	Tg(Ins1-Cat,Tyr)25Pne/0  [background:] NOD.FVB-Tg(Ins1-Cat,Tyr)25Pne	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16731821	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6147690	Spata16<sup>em2Osb</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6162247	Spata16<sup>em2Osb</sup>/Spata16<sup>em2Osb</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:29065458	20180625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946082	Lrp5<sup>tm1Dgen</sup>/Lrp5<sup>tm1Dgen</sup>  [background:] B6.129P2-Lrp5<sup>tm1Dgen</sup>/J	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:27524797	20161101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605230	Large1<sup>myd</sup>/Large1<sup>myd</sup>  [background:] B6.Cg-Large1<sup>myd</sup>/Pjn	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:16111892	20101116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857733	Colq<sup>tm1Jrs</sup>	is_implicated_in	DOID:0110667	congenital myasthenic syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:26993635	20170324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857733	Colq<sup>tm1Jrs</sup>	is_implicated_in	DOID:0110667	congenital myasthenic syndrome 5		MGI:2176897	Colq<sup>tm1Jrs</sup>/Colq<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10087275	20170324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5697353	Evc2<sup>tm1.1Mis</sup>	is_implicated_in	DOID:12714	Ellis-Van Creveld syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27090777	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5697353	Evc2<sup>tm1.1Mis</sup>	is_implicated_in	DOID:12714	Ellis-Van Creveld syndrome		MGI:5697977	Evc2<sup>tm1.1Mis</sup>/Evc2<sup>tm1.1Mis</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26219237	20160819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949225	C1qtnf5<sup>tm1.1Itl</sup>/C1qtnf5<sup>+</sup>  [background:] C57BL/6-C1qtnf5<sup>tm1.1Itl</sup>	is_model_of	DOID:0060869	late-onset retinal degeneration						ECO:0000033	author statement supported by traceable reference	PMID:21349921	20110506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719098	Neu1<sup>tm1Adz</sup>/Neu1<sup>tm1Adz</sup>  [background:] either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * NMRI)	is_model_of	DOID:3343	glycoproteinosis						ECO:0000033	author statement supported by traceable reference	PMID:12023988	20070824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6490502	Ppp3r1<sup>tm1.1Jhon</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6490510	Ppp3r1<sup>tm1.1Jhon</sup>/Ppp3r1<sup>tm1.1Jhon</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:32882262	20210107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5621058	Tg(SOD1*G85R/EYFP)641Alho/Tg(SOD1*G85R/EYFP)641Alho  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19171884	20150408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910326	Mypn<sup>tm1.1Epu</sup>	is_implicated_in	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910326	Mypn<sup>tm1.1Epu</sup>	is_implicated_in	DOID:397	restrictive cardiomyopathy		MGI:5910329	Mypn<sup>tm1.1Epu</sup>/Mypn<sup>+</sup>  [background:] either: (involves: 129S6/SvEv) or (involves: 129S6/SvEv * C57BL/6NCrl)			ECO:0000033	author statement supported by traceable reference	PMID:25541130	20170926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634330	Tg(Eno2-APP*Ind)#Kakiz	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5634332	Tg(Eno2-APP*Ind)#Kakiz/Tg(Eno2-APP*Ind)#Kakiz  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24489866	20150503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624423	Gaa<sup>tm2Rabn</sup>/Gaa<sup>tm2Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5475005	Tg(Msr1-MMP9)#Apar	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:5475008	Tg(Msr1-MMP9)#Apar/0  [background:] B6.Cg-Tg(Msr1-MMP9)#Apar			ECO:0000033	author statement supported by traceable reference	PMID:18408070	20130423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857930	Terc<sup>tm1Rdp</sup>	is_implicated_in	DOID:5688	Werner syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18028256	20150723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856066	Plp1<sup>jp-msd</sup>	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:22436581	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856066	Plp1<sup>jp-msd</sup>	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3711151	Plp1<sup>jp-msd</sup>/Y  [background:] involves: BALB/c * C3H * C57BL/6 * C57BL/10			ECO:0000033	author statement supported by traceable reference	PMID:17394578	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5615244	Foxh1<sup>b2b2662Clo</sup>	is_implicated_in	DOID:0060341	agnathia-otocephaly complex		MGI:5615273	Foxh1<sup>b2b2662Clo</sup>/Foxh1<sup>b2b2662Clo</sup>  [background:] C57BL/6J-Foxh1<sup>b2b2662Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3810811	Tg(tetO-MET)23Rwng/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:11381087	20090323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581491	Tg(Myh6-MYOZ2*I246M)#Ajm/0  [background:] involves: FVB	is_model_of	DOID:0110322	hypertrophic cardiomyopathy 16						ECO:0000033	author statement supported by traceable reference	PMID:22987565	20140902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5649285	Kras<sup>tm4.1Bbd</sup>	is_implicated_in	DOID:0060581	Noonan syndrome 3		MGI:5649287	Kras<sup>tm4.1Bbd</sup>/Kras<sup>tm4.1Bbd</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25359213	20150819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311373	Odad2<sup>b2b643Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6275554	Tg(tetO-TGFA)22.1Kor	is_implicated_in	DOID:3770	pulmonary fibrosis		MGI:6275557	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-TGFA)22.1Kor/0  [background:] involves: 129 * C57BL/6 * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:28130263	20211119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6275554	Tg(tetO-TGFA)22.1Kor	is_implicated_in	DOID:3770	pulmonary fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:34520400	20211119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5049887	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>+</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:21768372	20110720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587759	Myo7a<sup>4494SB</sup>/Myo7a<sup>4494SB</sup>  [background:] involves: BALB/cRl	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5776380	Shank3<sup>tm4.1Gfng</sup>/Shank3<sup>tm4.1Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26687841	20160620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657065	Mip<sup>Cat-Tohm</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:24120416	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657065	Mip<sup>Cat-Tohm</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2657109	Mip<sup>Cat-Tohm</sup>/Mip<sup>Cat-Tohm</sup>  [background:] involves: DDI			ECO:0000033	author statement supported by traceable reference	PMID:12676560	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857942	Cdkn2a<sup>tm1Rdp</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:31039140	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448088	Tg(CKMM-tTA)A3Rhvh	is_implicated_in	DOID:633	myositis						ECO:0000033	author statement supported by traceable reference	PMID:23785461	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448088	Tg(CKMM-tTA)A3Rhvh	is_implicated_in	DOID:633	myositis						ECO:0000033	author statement supported by traceable reference	PMID:26551678	20160322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606787	Tg(Lim2*G15V)1Rlc/Tg(Lim2*G15V)1Rlc  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110263	cataract 19 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:10851259	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6307777	Prss3b<sup>tm1.1Satom</sup>	is_implicated_in	DOID:4989	pancreatitis		MGI:6307806	Prss3b<sup>tm1.1Satom</sup>/Prss3b<sup>+</sup>  [background:] B6(FVB)-Prss3b<sup>tm1.1Satom</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30487519	20190607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388566	Tg(Ins1-GAS)1Sbr	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:25143365	20150403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388566	Tg(Ins1-GAS)1Sbr	is_implicated_in	DOID:10534	stomach cancer		MGI:2665288	Tg(Ins1-GAS)1Sbr/0  [background:] involves: FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:10611152	20150403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449985	Fas<sup>lpr-cg</sup>/Fas<sup>lpr-cg</sup>  [background:] CBA/KlJms-Fas<sup>lpr-cg</sup>/J	is_model_of	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:2302830	20051011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449985	Fas<sup>lpr-cg</sup>/Fas<sup>lpr-cg</sup>  [background:] CBA/KlJms-Fas<sup>lpr-cg</sup>/J	is_model_of	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:2406366	20051011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5819052	Apob<sup>tm2Sgy</sup>/Apob<sup>tm2Sgy</sup> Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:18160459	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311393	Dnah11<sup>b2b1279Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5317649	Dnah11<sup>b2b1279Clo</sup>/Dnah11<sup>b2b1279Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1279Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287154	Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:6287156	Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>/Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28666097	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287154	Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:6287155	Mitf<sup>Tg(Tff3-Tmem207)2Tamo</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28666097	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774670	Tg(KRT14-Snai1)1Efu	is_implicated_in	DOID:4159	skin cancer						ECO:0000033	author statement supported by traceable reference	PMID:29769563	20180831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774670	Tg(KRT14-Snai1)1Efu	is_implicated_in	DOID:4159	skin cancer		MGI:3774672	Tg(KRT14-Snai1)1Efu/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24162662	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586912	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242110	20050908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6313626	Tg(MMTV-Scgb1a1)#Abm	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:6313628	Tg(MMTV-Scgb1a1)#Abm/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10470078	20190611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>	is_model_of	DOID:0110490	autosomal recessive nonsyndromic deafness 31						ECO:0000033	author statement supported by traceable reference	PMID:5538400	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>	is_model_of	DOID:0110490	autosomal recessive nonsyndromic deafness 31						ECO:0000033	author statement supported by traceable reference	PMID:12124769	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>	is_model_of	DOID:0110490	autosomal recessive nonsyndromic deafness 31						ECO:0000033	author statement supported by traceable reference	PMID:14098314	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>	is_model_of	DOID:0110490	autosomal recessive nonsyndromic deafness 31						ECO:0000033	author statement supported by traceable reference	PMID:6034501	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177542	Cftr<sup>tm1Hsc</sup>/Cftr<sup>tm1Hsc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:8589719	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039434	Sell<sup>tm1Flv</sup>/Sell<sup>+</sup>  [background:] involves: C57BL/6 * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710322	Cdkn2c<sup>tm1Bbd</sup>/Cdkn2c<sup>tm1Bbd</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Tyj</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16260494	20110921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149776	Dyrk1a<sup>em1Kzy</sup>	is_implicated_in	DOID:0070037	autosomal dominant intellectual developmental disorder 7		MGI:7264822	Dyrk1a<sup>em1Kzy</sup>/Dyrk1a<sup>+</sup>  [background:] C57BL/6J-Dyrk1a<sup>em1Kzy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29223763	20220428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7262691	Tg(KRT18*R89C)50Rgo	is_implicated_in	DOID:2237	hepatitis		MGI:7262713	Tg(KRT18*R89C)50Rgo/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8522591	20220419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696200	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] 129S1.NON(NZO)-Col4a4<sup>bwk</sup>/PgnJ	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24522496	20151116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652508	Tg(CEACAM5-Tag)L5496Wzm	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:26333534	20160222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652508	Tg(CEACAM5-Tag)L5496Wzm	is_implicated_in	DOID:10534	stomach cancer		MGI:4819864	Tg(CEACAM5-Tag)L5496Wzm/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:10842202	20160222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672839	Tg(Thy1-MAPT)183Gotz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27475227	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672839	Tg(Thy1-MAPT)183Gotz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:32278495	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672839	Tg(Thy1-MAPT)183Gotz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25558816	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672839	Tg(Thy1-MAPT)183Gotz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:28160413	20201217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618139	Snrpn<sup>tm2Cbr</sup>/Snrpn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9590284	20060329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009035	Ncstn<sup>tm1.1Akli</sup>	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5779426	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(Upk2-cre,-EGFP)#Akli/0  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:25194568	20160823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009035	Ncstn<sup>tm1.1Akli</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530127	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22399753	20230908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530127	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:33296726	20230908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530127	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:36647152	20230908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530127	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:36230952	20230908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530127	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5297858	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12084935	20230908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053579	Fgfr2<sup>tm4Lni</sup>/Fgfr2<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25966306	20161025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053579	Fgfr2<sup>tm4Lni</sup>/Fgfr2<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15316116	20161025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578354	Tg(Prnp-MAPT*)2652Gds	is_implicated_in	DOID:680	tauopathy		MGI:6317190	Tg(Prnp-MAPT*)2652Gds/0  [background:] B6.Cg-Tg(Prnp-MAPT*)2652Gds			ECO:0000033	author statement supported by traceable reference	PMID:26041339	20190711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749799	Nefl<sup>tm2.1Liem</sup>	is_implicated_in	DOID:0110165	Charcot-Marie-Tooth disease type 2E		MGI:5751579	Nefl<sup>tm2.1Liem</sup>/Nefl<sup>+</sup>  [background:] B6.Cg-Nefl<sup>tm2.1Liem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25552649	20160310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851387	Tg(Mt1-CBS)25Waku	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:25008174	20161006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387750	Axl<sup>tm1Grl</sup>	is_implicated_in	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:23840307	20140130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824306	Tg(PDGFB-SNCA/EGFP)78Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:15765523	20170216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679886	Pten<sup>tm2.1Ppp</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679886	Pten<sup>tm2.1Ppp</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23428429	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618847	Ednra<sup>m1Mhda</sup>	is_implicated_in	DOID:0060365	mandibulofacial dysostosis with alopecia		MGI:5817772	Ednra<sup>m1Mhda</sup>/Ednra<sup>m1Mhda</sup>  [background:] C3HeB/FeJ-Ednra<sup>m1Mhda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27671791	20170116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618847	Ednra<sup>m1Mhda</sup>	is_implicated_in	DOID:0060365	mandibulofacial dysostosis with alopecia		MGI:5817760	Ednra<sup>m1Mhda</sup>/Ednra<sup>+</sup>  [background:] C3HeB/FeJ-Ednra<sup>m1Mhda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27671791	20170116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4889198	Tg(CD2-Lmo2)#Thr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:1461647	20110223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22614361	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:25251606	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:25092414	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12213735	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7670466	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11454988	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8706124	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12594290	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183206	Smpd1<sup>tm1Esc</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9382882	20180403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836591	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C3H/HeJ)	is_model_of	DOID:289	endometriosis						ECO:0000033	author statement supported by traceable reference	PMID:15619626	20101028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720114	Tg(Thy1-MAPT)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720114	Tg(Thy1-MAPT)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720208	Tg(Thy1-MAPT)2Vln/Tg(Thy1-MAPT)2Vln  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:10595944	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720114	Tg(Thy1-MAPT)2Vln	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720208	Tg(Thy1-MAPT)2Vln/Tg(Thy1-MAPT)2Vln  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:11007782	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515890	Pmp22<sup>Tr-2J</sup>	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668037	Hexa<sup>tm1Grv</sup>/Hexa<sup>tm1Grv</sup>  [background:] involves: 129P2/Ola * C57BL/6J	is_model_of	DOID:3320	Tay-Sachs disease						ECO:0000033	author statement supported by traceable reference	PMID:8789434	20050613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0110015	age related macular degeneration 2						ECO:0000033	author statement supported by traceable reference	PMID:29602770	20181009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0110015	age related macular degeneration 2						ECO:0000033	author statement supported by traceable reference	PMID:30126999	20181009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717470	Abca3<sup>tm1Holz</sup>/Abca3<sup>tm1Holz</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:17577581	20070807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449903	Tg(SOD1)2Gur/0 Tg(SOD1*L126Z)#Deng/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16636275	20130122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949110	Grn<sup>tm1.1Far</sup>	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:28438992	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949110	Grn<sup>tm1.1Far</sup>	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:26361634	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949110	Grn<sup>tm1.1Far</sup>	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5444200	Grn<sup>tm1.1Far</sup>/Grn<sup>tm1.1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25155018	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5538516	Tg(tetO-Fgf9,-EGFP)#Dor	is_implicated_in	DOID:4769	pleuropulmonary blastoma		MGI:5538520	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:25978641	20160311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038935	Lrat<sup>tm1Kpal</sup>	is_implicated_in	DOID:0110188	Leber congenital amaurosis 14						ECO:0000033	author statement supported by traceable reference	PMID:22531707	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038935	Lrat<sup>tm1Kpal</sup>	is_implicated_in	DOID:0110188	Leber congenital amaurosis 14						ECO:0000033	author statement supported by traceable reference	PMID:26387748	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038935	Lrat<sup>tm1Kpal</sup>	is_implicated_in	DOID:0110188	Leber congenital amaurosis 14						ECO:0000033	author statement supported by traceable reference	PMID:16250670	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038935	Lrat<sup>tm1Kpal</sup>	is_implicated_in	DOID:0110188	Leber congenital amaurosis 14		MGI:3039274	Lrat<sup>tm1Kpal</sup>/Lrat<sup>tm1Kpal</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:18296659	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5775620	Shank3<sup>tm3.1Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5776377	Shank3<sup>tm3.1Gfng</sup>/Shank3<sup>tm3.1Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26687841	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6115637	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>	is_not_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:6160754	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>/Y Neurod6<sup>tm1(cre)Kan</sup>/Neurod6<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427873	Tg(Ckm-CUGBP1)1039Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:5427874	Tg(Ckm-CUGBP1)1039Coop/0  [background:] FVB-Tg(Ckm-CUGBP1)1039Coop			ECO:0000033	author statement supported by traceable reference	PMID:15843400	20120713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668609	Slc45a2<sup>Uw-dbr</sup>/Slc45a2<sup>Uw-dbr</sup>  [background:] B10.PL-H2<sup>u</sup>/(73NS)Sn	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c	is_model_of	DOID:0110354	retinitis pigmentosa 19						ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661482	Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0  [background:] involves: C57BL/6	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:25182415	20150911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5803721	Notch2<sup>tm1.1Ecan</sup>/Notch2<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * C57BL/6J	is_model_of	DOID:2736	Hajdu-Cheney syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26627824	20161017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5641735	Npc1<sup>tm1.1Dso</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26908626	20191216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5641735	Npc1<sup>tm1.1Dso</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:31141688	20191216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5641735	Npc1<sup>tm1.1Dso</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5642030	Npc1<sup>tm1.1Dso</sup>/Npc1<sup>tm1.1Dso</sup>  [background:] B6.129-Npc1<sup>tm1.1Dso</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26019327	20191216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438699	Ank1<sup>MRI23420</sup>	is_implicated_in	DOID:12365	malaria		MGI:5438702	Ank1<sup>MRI23420</sup>/Ank1<sup>MRI23420</sup>  [background:] SJL/J-Ank1<sup>MRI23420</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22723917	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5500910	Hps1<sup>ep-7J</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:5501040	Hps1<sup>ep-7J</sup>/Hps1<sup>ep-7J</sup>  [background:] CAST/EiJ-Hps1<sup>ep-7J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5499306	20130814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003464	Tg(Hmgcr-PSEN1*M146L)#Lpr/0 Tg(PDGFB-APPSwDutLon)46Lpr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527316	Tg(MMTV-ERBB2)5Erick	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:31484792	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527316	Tg(MMTV-ERBB2)5Erick	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27553713	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527316	Tg(MMTV-ERBB2)5Erick	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23940356	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527316	Tg(MMTV-ERBB2)5Erick	is_implicated_in	DOID:1612	breast cancer		MGI:5527317	Tg(MMTV-ERBB2)5Erick/?  [background:] FVB/N-Tg(MMTV-ERBB2)5Erick			ECO:0000033	author statement supported by traceable reference	PMID:15073130	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527316	Tg(MMTV-ERBB2)5Erick	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:28396358	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705123	Tg(Prnp-ATXN7*92Q)1963Als	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5705127	Tg(Prnp-ATXN7*92Q)1963Als/0  [background:] B6J.Cg-Tg(Prnp-ATXN7*92Q)1963Als			ECO:0000033	author statement supported by traceable reference	PMID:25859008	20160125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619459	Tg(IGL-MYC)3Hm/0  [background:] C57BL/6N-Tg(IGL-MYC)3Hm/Nci	is_model_of	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:11034608	20060413	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941783	Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>/Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>  [background:] involves: C3H * C57BL/6J * DBA/2	is_model_of	DOID:0060861	microphthalmia with limb anomalies						ECO:0000033	author statement supported by traceable reference	PMID:21194678	20110323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687994	Tg(Sod1*G86R)M1Jwg/0  [background:] involves: FVB/N	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10578106	20061121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687994	Tg(Sod1*G86R)M1Jwg/0  [background:] involves: FVB/N	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:7846037	20061121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687994	Tg(Sod1*G86R)M1Jwg/0  [background:] involves: FVB/N	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:15263088	20061121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296756	Tg(tetO-Esr1)#Paf	is_implicated_in	DOID:1612	breast cancer		MGI:5296806	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Esr1)#Paf/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15705859	20111129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038221	Gck<sup>Rgsc702</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444033	Dcc<sup>Tg(H2-Kb-Jak2*V617F)1Shmd</sup>/Dcc<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:18033315	20121130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821884	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:33705358	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821884	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:23572558	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821884	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:23115204	20220330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821884	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:3821886	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19029982	20220330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620650	Ofd1<sup>tm2.1Bfra</sup>/Y Tg(CAG-cre)1Nagy/0  [background:] involves: 129S2/SvPas	is_model_of	DOID:0060316	orofaciodigital syndrome I						ECO:0000033	author statement supported by traceable reference	PMID:16311594	20060428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009711	Id3<sup>tm2.1Zhu</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5009805	Id3<sup>tm2.1Zhu</sup>/Id3<sup>tm2.1Zhu</sup> Tg(Lck-cre)#Zhu/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:20932862	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526863	Rsc1a1<sup>tm1Koep</sup>/Rsc1a1<sup>tm1Koep</sup>  [background:] B6.129-Rsc1a1<sup>tm1Koep</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15601832	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6766469	Notch2<sup>tm1.1Hhtg</sup>	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:6766538	Notch2<sup>tm1.1Hhtg</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28856714	20211012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003463	Tg(PDGFB-APPSwDutLon)46Lpr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14637096	20110607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176950	Gck<sup>tm1Ts</sup>/Gck<sup>+</sup>  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J)	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:7553875	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691062	Kmt2a<sup>tm1Clgr</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23660685	20150520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691062	Kmt2a<sup>tm1Clgr</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24994068	20150520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718580	Tg(TRAMP)8247Ng/0  [background:] involves: C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:7724580	20070817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6860325	Thap11<sup>em1Poche</sup>	is_implicated_in	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC		MGI:6860682	Thap11<sup>em1Poche</sup>/Thap11<sup>em1Poche</sup>  [background:] C57BL/6J-Thap11<sup>em1Poche</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35013307	20220131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:11689485	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:9326937	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12514735	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009550	Tg(Th-MYCN)41Waw/Tg(Th-MYCN)41Waw  [background:] involves: BALB/c * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:9214616	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659902	Sox9<sup>Bbfc</sup>/Sox9<sup>+</sup>  [background:] C57BL/6J-Sox9<sup>Bbfc</sup>/GrsrJ	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:26234751	20150825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530031	Tg(Th-SNCA*A30P*A53T)39Eric	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:28771510	20190709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530031	Tg(Th-SNCA*A30P*A53T)39Eric	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:26317511	20190709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530031	Tg(Th-SNCA*A30P*A53T)39Eric	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6099058	Tg(Th-SNCA*A30P*A53T)39Eric/0  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15009131	20190709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183031	Crybb2<sup>Phil</sup>/Crybb2<sup>Phil</sup>  [background:] Swiss Webster	is_model_of	DOID:0110269	cataract 3 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:1707874	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637028	Cibar1<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:1148	polydactyly		MGI:5797530	Cibar1<sup>tm1b(KOMP)Wtsi</sup>/Cibar1<sup>tm1b(KOMP)Wtsi</sup>  [background:] C57BL/6N-Cibar1<sup>tm1b(KOMP)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:30395363	20190523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818953	Suco<sup>Gt(KST050)Byg</sup>/Suco<sup>Gt(KST050)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1	is_model_of	DOID:0110344	osteogenesis imperfecta type 5						ECO:0000033	author statement supported by traceable reference	PMID:20440000	20100811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603013	Gck<sup>tm1.1Mgn</sup>/Gck<sup>tm1.1Mgn</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451086	Fmr1<sup>tm2Cgr</sup>	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28444183	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451086	Fmr1<sup>tm2Cgr</sup>	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23553633	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451086	Fmr1<sup>tm2Cgr</sup>	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23390134	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451086	Fmr1<sup>tm2Cgr</sup>	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451086	Fmr1<sup>tm2Cgr</sup>	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome		MGI:3815023	Fmr1<sup>tm2Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15876460	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6850156	Nemf<sup>em8Cx</sup>	is_implicated_in	DOID:440	neuromuscular disease		MGI:6850159	Nemf<sup>em8Cx</sup>/Nemf<sup>em8Cx</sup>  [background:] C57BL/6J-Nemf<sup>em8Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829975	Scn1b<sup>tm1.1Bion</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:4830676	Scn1b<sup>tm1.1Bion</sup>/Scn1b<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20628201	20100927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5518769	Mybl2<sup>tm1.1Jof</sup>/Mybl2<sup>+</sup> Tg(Zp3-cre)3Mrt/0  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22910183	20131120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:21103359	20120919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:10678833	20120919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:12111846	20120919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430751	Inpp5b<sup>tm1Nbm</sup>/Inpp5b<sup>tm1Nbm</sup> Ocrl<sup>tm1Nbm</sup>/Ocrl<sup>tm1Nbm</sup> Tg(INPP5B)CNbm/0  [background:] involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	is_model_of	DOID:0050699	Dent disease						ECO:0000033	author statement supported by traceable reference	PMID:21183592	20120809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5707775	Senp1<sup>tm1Wami</sup>/Senp1<sup>tm1Wami</sup> Tg(Fabp4-cre)#Abel/0  [background:] B6.Cg-Senp1<sup>tm1Wami</sup> Tg(Fabp4-cre)#Abel	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26596471	20160210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437475	Cryaa<sup>tm1Ady</sup>/Cryaa<sup>tm1Ady</sup>  [background:] involves: 129	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:19619312	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000261	Tg(tetO-TARDBP*)4Vle	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5448853	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-TARDBP*)4Vle/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21206091	20151111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000261	Tg(tetO-TARDBP*)4Vle	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5695547	Tg(NEFH-tTA)8Vle/0 Tg(tetO-TARDBP*)4Vle/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26197969	20151111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000261	Tg(tetO-TARDBP*)4Vle	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:25392493	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722277	Tg(YAC72)2511Hay/?  [background:] involves: FVB/N	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10402204	20070921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7569243	Dnaaf5<sup>em1Slb</sup>	is_implicated_in	DOID:12336	male infertility		MGI:7569326	Dnaaf5<sup>em1Slb</sup>/Dnaaf5<sup>em1Slb</sup>  [background:] C57BL/6-Dnaaf5<sup>em1Slb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37104040	20231229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028003	Pde6b<sup>atrd3</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5568837	Iqgap2<sup>tm1Vs</sup>/Iqgap2<sup>tm1Vs</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23951254	20140619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527175	Tecta<sup>tm5.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0110544	autosomal dominant nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196127	Gt(ROSA)26Sor<sup>tm1(CAG-MYCN,-luc)Jhsc</sup>	is_implicated_in	DOID:769	neuroblastoma		MGI:6196129	Gt(ROSA)26Sor<sup>tm1(CAG-MYCN,-luc)Jhsc</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Dbh-icre)1Gsc/0  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25174395	20180831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196127	Gt(ROSA)26Sor<sup>tm1(CAG-MYCN,-luc)Jhsc</sup>	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29769563	20180831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620796	Tg(Camk2a-Magi2)1Shlee	is_implicated_in	DOID:5419	schizophrenia		MGI:5620953	Tg(Camk2a-Magi2)1Shlee/?  [background:] C57BL/6J-Tg(Camk2a-Magi2)1Shlee			ECO:0000033	author statement supported by traceable reference	PMID:25653350	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6314797	Cfh<sup>tm1.1Song</sup>	is_implicated_in	DOID:0080301	atypical hemolytic-uremic syndrome		MGI:6314805	Cfh<sup>tm1.1Song</sup>/Cfh<sup>tm1.1Song</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28057640	20190625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819096	Tg(Umod*C147W)958Lura	is_implicated_in	DOID:557	kidney disease		MGI:4819114	Tg(Umod*C147W)958Lura/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:20472742	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4947241	Jup<sup>tm1.1Glr</sup>/Jup<sup>tm1.1Glr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:21245375	20110420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664995	Hcrtr2<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:29784823	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664995	Hcrtr2<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:28396432	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664995	Hcrtr2<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy		MGI:2669895	Hcrtr2<sup>tm1Ywa</sup>/Hcrtr2<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12797957	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835235	Tg(MMTV-LPAR2)6Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763104	Tg(MMTV-LPAR2)6Gbm/Tg(MMTV-LPAR2)6Gbm  [background:] FVB/N-Tg(MMTV-LPAR2)6Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947230	Rho<sup>tm1.1Kpal</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:24214395	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947230	Rho<sup>tm1.1Kpal</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4947235	Rho<sup>tm1.1Kpal</sup>/Rho<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21224384	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947230	Rho<sup>tm1.1Kpal</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:27149983	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5570748	Tg(Slc1a2-tTA)#Waw/0 Tg(tetO-MYCN,-luc)#Waw/Tg(tetO-MYCN,-luc)#Waw  [background:] involves: FVB/NJ	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:20478998	20140701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6159285	Abca4<sup>tm1.1Rsmy</sup>	is_implicated_in	DOID:0050817	Stargardt disease		MGI:6159288	Abca4<sup>tm1.1Rsmy</sup>/Abca4<sup>tm1.1Rsmy</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29145636	20180601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183212	Gucy2e<sup>tm1Gar</sup>	is_implicated_in	DOID:0110078	Leber congenital amaurosis 1						ECO:0000033	author statement supported by traceable reference	PMID:26387748	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4129208	Zdhhc17<sup>Gt(RRJ233)Byg</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22649491	20120927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4129208	Zdhhc17<sup>Gt(RRJ233)Byg</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5292519	Zdhhc17<sup>Gt(RRJ233)Byg</sup>/Zdhhc17<sup>Gt(RRJ233)Byg</sup>  [background:] FVB.129P2-Zdhhc17<sup>Gt(RRJ233)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21775500	20120927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6515829	Ryr1<sup>tm3.1Alle</sup>	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:6515831	Ryr1<sup>tm3.1Alle</sup>/Ryr1<sup>tm3.1Alle</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30236258	20210407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6515829	Ryr1<sup>tm3.1Alle</sup>	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:6515830	Ryr1<sup>tm3.1Alle</sup>/Ryr1<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30236258	20210407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805200	Hras<sup>tm2Xbr</sup>/Hras<sup>tm2Xbr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:0050469	Costello syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18483625	20080910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	MGI:78359	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660859	Nlgn3<sup>tm1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:24995986	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6715267	Pah<sup>em1Skym</sup>	is_implicated_in	DOID:9281	phenylketonuria		MGI:6715269	Pah<sup>em1Skym</sup>/Pah<sup>em1Skym</sup>  [background:] C57BL/6J-Pah<sup>em1Skym</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33790381	20210611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052118	Tg(Eno2-PSEN2*)1480Ykk	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5052120	Tg(Eno2-PSEN2*)1480Ykk/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12039862	20120330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052118	Tg(Eno2-PSEN2*)1480Ykk	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20969897	20120330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6275111	Pitx2<sup>egl1</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:6275112	Pitx2<sup>egl1</sup>/Pitx2<sup>egl1</sup>  [background:] C57BL/6J-Pitx2<sup>egl1</sup>/Boc			ECO:0000033	author statement supported by traceable reference	MGI:6275025	20190129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5499996	Cacna1a<sup>smrl</sup>	is_implicated_in	DOID:0050956	spinocerebellar ataxia type 6		MGI:5500085	Cacna1a<sup>smrl</sup>/Cacna1a<sup>smrl</sup>  [background:] CXB10/HiAJ-Cacna1a<sup>smrl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4365644	Sh3pxd2b<sup>nee</sup>/Sh3pxd2b<sup>nee</sup>  [background:] B10.Cg-H2<sup>h4</sup> Sh3pxd2b<sup>nee</sup>/GrsrJ	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:19669234	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708562	Des<sup>tm1.1Ccrs</sup>	is_implicated_in	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708562	Des<sup>tm1.1Ccrs</sup>	is_implicated_in	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:32126091	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708562	Des<sup>tm1.1Ccrs</sup>	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:5762537	Des<sup>tm1.1Ccrs</sup>/Des<sup>tm1.1Ccrs</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25394388	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708562	Des<sup>tm1.1Ccrs</sup>	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:5762541	Des<sup>tm1.1Ccrs</sup>/Des<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25394388	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:23412344	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25242307	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:23863460	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1						ECO:0000033	author statement supported by traceable reference	PMID:26000738	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3580056	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9054942	20231019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576227	Park7<sup>tm1Dsp</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:32999308	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576227	Park7<sup>tm1Dsp</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3576369	Park7<sup>tm1Dsp</sup>/Park7<sup>tm1Dsp</sup>  [background:] B6.129P2-Park7<sup>tm1Dsp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23019375	20201022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814580	Tg(MT1A-Dyrk1a)33Xest/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11555628	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6780039	Dnah10<sup>em2Yxc</sup>	is_implicated_in	DOID:0111910	spermatogenic failure		MGI:6780173	Dnah10<sup>em2Yxc</sup>/Dnah10<sup>em2Yxc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34237282	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463435	Tg(Thy1-APPArc)M8Cagr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5463438	Tg(Thy1-APPArc)M8Cagr/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19329229	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463435	Tg(Thy1-APPArc)M8Cagr	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26500157	20160321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463435	Tg(Thy1-APPArc)M8Cagr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5465558	Tg(Thy1-APPArc)M8Cagr/Tg(Thy1-APPArc)M8Cagr  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21880397	20160321	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5632129	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:1790	malignant mesothelioma						ECO:0000033	author statement supported by traceable reference	PMID:23851502	20150421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449268	Tg(tetO-EGFR*L858R)#Hev	is_implicated_in	DOID:1324	lung cancer		MGI:5634289	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)#Hev/0  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24535670	20230208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449268	Tg(tetO-EGFR*L858R)#Hev	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:36612121	20230208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449268	Tg(tetO-EGFR*L858R)#Hev	is_implicated_in	DOID:1324	lung cancer		MGI:5634289	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)#Hev/0  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17726540	20230208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449268	Tg(tetO-EGFR*L858R)#Hev	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25870145	20230208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449268	Tg(tetO-EGFR*L858R)#Hev	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26759237	20230208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665272	Frem1<sup>bat</sup>/Frem1<sup>bat</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>	is_model_of	DOID:0060732	chromosome 9p deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21931569	20111118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857229	Nos3<sup>tm1Unc</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25499815	20150519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857229	Nos3<sup>tm1Unc</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24864273	20150519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007410	Zdhhc9<sup>tm1Lex</sup>	is_implicated_in	DOID:0060824	syndromic X-linked intellectual disability Raymond type		MGI:6315636	Zdhhc9<sup>tm1Lex</sup>/Y  [background:] B6.129S5-Zdhhc9<sup>tm1Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29944857	20190701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527336	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25173427	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527336	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:5527337	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>/Col1a1<sup>+</sup> Tg(Scgb1a1-rtTA)1Jaw/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20952506	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527336	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6467540	Tg(SERPINA1-TAg)1812Jtsb	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:6467541	Tg(SERPINA1-TAg)1812Jtsb/0  [background:] involves: C3H * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:2551499	20201019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183718	Tg(SOD1*G93A)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24324755	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183718	Tg(SOD1*G93A)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:28844763	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183718	Tg(SOD1*G93A)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2446420	Tg(SOD1*G93A)2Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:7992831	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183718	Tg(SOD1*G93A)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2446420	Tg(SOD1*G93A)2Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8209258	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183718	Tg(SOD1*G93A)2Gur	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2446420	Tg(SOD1*G93A)2Gur/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12802201	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693973	Slc26a4<sup>pdsm</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693973	Slc26a4<sup>pdsm</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3712949	Slc26a4<sup>pdsm</sup>/Slc26a4<sup>pdsm</sup>  [background:] BXA7/PgnJ-Slc26a4<sup>pdsm</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3712813	20131230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930612	Brca1<sup>tm1Cxd</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25176624	20141204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181812	Rho<sup>tm1Phm</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:24825107	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181812	Rho<sup>tm1Phm</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:27149983	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181812	Rho<sup>tm1Phm</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181812	Rho<sup>tm1Phm</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22549882	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181812	Rho<sup>tm1Phm</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22169101	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648857	Prickle1<sup>tm1Asw</sup>/Prickle1<sup>tm1.2Asw</sup>  [background:] Not Specified	is_model_of	DOID:0060764	autosomal recessive Robinow syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25190059	20150818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6466711	Impg2<sup>em1Xjz</sup>	is_implicated_in	DOID:0110371	retinitis pigmentosa 56		MGI:6466733	Impg2<sup>em1Xjz</sup>/Impg2<sup>em1Xjz</sup>  [background:] C57BL/6J-Impg2<sup>em1Xjz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32242237	20201013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5314798	Chrne<sup>tm2Vwi</sup>	is_implicated_in	DOID:0110678	congenital myasthenic syndrome 4A		MGI:5314815	Chrne<sup>tm2Vwi</sup>/Chrne<sup>tm2Vwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22178625	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856667	Pitx3<sup>ak</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:16269007	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856667	Pitx3<sup>ak</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:25281315	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856667	Pitx3<sup>ak</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3712364	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] involves: 129S1/Sv * C57BL/6 * C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:15728853	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800675	Asah1<sup>tm1Medin</sup>/Asah1<sup>tm1Medin</sup>  [background:] involves: 129S6/SvEvTac * CD-1	is_model_of	DOID:0050464	Farber lipogranulomatosis						ECO:0000033	author statement supported by traceable reference	PMID:23681708	20161014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644693	Meox2<sup>tm1(cre)Sor</sup>/Meox2<sup>+</sup> Tg(CAG-lacZ,-FUS*R521G,-EGFP)682Gyu/0  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:25324524	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5301553	Cxcr4<sup>tm1.1Bala</sup>	is_implicated_in	DOID:0060591	WHIM syndrome		MGI:5301555	Cxcr4<sup>tm1.1Bala</sup>/Cxcr4<sup>+</sup>  [background:] B6.129S2-Cxcr4<sup>tm1.1Bala</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22438253	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5301553	Cxcr4<sup>tm1.1Bala</sup>	is_implicated_in	DOID:0060591	WHIM syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25662009	20150508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577939	Rai1<sup>tm1Jrl</sup>/Rai1<sup>+</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6	is_model_of	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15746153	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856149	Ednrb<sup>s-l</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856149	Ednrb<sup>s-l</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:26863197	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856149	Ednrb<sup>s-l</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3589108	Ednrb<sup>s-l</sup>/Ednrb<sup>s-l</sup>  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:5917257	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315442	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>tm1Hzo</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:22002997	20120418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6726365	Abcg2<sup>em1Omw</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:6726370	Abcg2<sup>em1Omw</sup>/Abcg2<sup>em1Omw</sup>  [background:] C57BL/6J-Abcg2<sup>em1Omw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32488095	20210727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5896437	Col4a1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:557	kidney disease		MGI:5905035	Col4a1<sup>tm1.1Ics</sup>/Col4a1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26260163	20170719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5896437	Col4a1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:557	kidney disease		MGI:5905032	Col4a1<sup>tm1.1Ics</sup>/Col4a1<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26260163	20170719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5700344	Tg(Plp1-HTT*150Q)4aXjl	is_implicated_in	DOID:12858	Huntington's disease		MGI:5700345	Tg(Plp1-HTT*150Q)4aXjl/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25789755	20151231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442620	Kit<sup>tm4.1Bsm</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:5442707	Kit<sup>tm4.1Bsm</sup>/Kit<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22652566	20121126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5617727	Pdgfrb<sup>redeye</sup>	is_implicated_in	DOID:8946	severe nonproliferative diabetic retinopathy		MGI:5661928	Pdgfrb<sup>redeye</sup>/Pdgfrb<sup>redeye</sup>  [background:] C3N.C-Pdgfrb<sup>redeye</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23633653	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7384686	Smc3<sup>tm1.2Toshi</sup>	is_implicated_in	DOID:0080507	Cornelia de Lange syndrome 3		MGI:7489810	Smc3<sup>tm1.2Toshi</sup>/Smc3<sup>+</sup>  [background:] B6.Cg-Smc3<sup>tm1.2Toshi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28408410	20230615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>	is_model_of	DOID:11044	gastroschisis						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814436	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Glo</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:17486075	20081111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580456	Prkdc<sup>scid</sup>/Prkdc<sup>scid</sup> Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] NOD.Cg-Prkdc<sup>scid</sup> Idua<sup>tm1Clk</sup>/J	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:17920451	20090410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620587	Prph2<sup>Rd2</sup>/Prph2<sup>+</sup>  [background:] either: (involves: BALB/c * O20/A) or (involves: GR/A * O20/A) or (involves: O20/A * STS/A)	is_model_of	DOID:0110383	retinitis pigmentosa 7						ECO:0000033	author statement supported by traceable reference	PMID:3830736	20090318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6491679	Coasy<sup>tm1.1Vtr</sup>	is_implicated_in	DOID:0110740	neurodegeneration with brain iron accumulation 6		MGI:6491890	Coasy<sup>tm1.1Vtr</sup>/Coasy<sup>tm1.1Vtr</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129 * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33352696	20210114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7522151	Kif23<sup>tm1.1Igo</sup>	is_not_implicated_in	DOID:0111399	congenital dyserythropoietic anemia type III		MGI:7522155	Kif23<sup>tm1.1Igo</sup>/Kif23<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:32818800	20230829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7522151	Kif23<sup>tm1.1Igo</sup>	is_not_implicated_in	DOID:0111399	congenital dyserythropoietic anemia type III		MGI:7522153	Kif23<sup>tm1.1Igo</sup>/Kif23<sup>tm1.1Igo</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:32818800	20230829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5466324	Crb2<sup>tm1.1Wij</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5466335	Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Chx10-EGFP/cre,-ALPP)2Clc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23001562	20141007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5466324	Crb2<sup>tm1.1Wij</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:24565864	20141007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5466324	Crb2<sup>tm1.1Wij</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5586690	Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24493795	20141007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4460262	Msh2<sup>tm2.1Rak</sup>	is_implicated_in	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:34224739	20211102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4460262	Msh2<sup>tm2.1Rak</sup>	is_implicated_in	DOID:3883	Lynch syndrome		MGI:4460266	Msh2<sup>tm2.1Rak</sup>/Msh2<sup>tm2.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19931261	20211102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620632	Hdc<sup>tm1Nagy</sup>/Hdc<sup>tm1Nagy</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24411733	20151130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840340	Mmut<sup>tm1Cpv</sup>/Mmut<sup>tm1Cpv</sup>  [background:] Not Specified	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:17937813	20090417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6693686	Impg2<sup>em1Visu</sup>	is_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:6693692	Impg2<sup>em1Visu</sup>/Impg2<sup>em1Visu</sup>  [background:] involves: C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:32265257	20210420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3802545	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1.1Djk</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:18495876	20080815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:26545928	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:22496568	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:24057669	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:27018595	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease		MGI:2177468	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7550345	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease		MGI:2177468	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23028353	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857438	Hexb<sup>tm1Rlp</sup>	is_implicated_in	DOID:3323	Sandhoff disease		MGI:3579385	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14722612	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473718	Tg(tetO-CTGF)#Swu	is_implicated_in	DOID:0050161	lower respiratory tract disease		MGI:5473834	Tg(SFTPC-rtTA)2Jaw/0 Tg(tetO-CTGF)#Swu/0  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21239535	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473718	Tg(tetO-CTGF)#Swu	is_implicated_in	DOID:0050161	lower respiratory tract disease		MGI:5473719	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-CTGF)#Swu/0  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19541844	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661962	Ncf1<sup>m1J</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:25689796	20160411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446499	Tg(Fabp4-SREBF1)#Dajl	is_implicated_in	DOID:811	lipodystrophy		MGI:5446500	Tg(Fabp4-SREBF1)#Dajl/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22792234	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5142235	Tg(Pcp2-TBP*)69Hmhl	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:5142236	Tg(Pcp2-TBP*)69Hmhl/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21554323	20110906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5619358	Rp2<sup>tm1.2Asw</sup>	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:5619363	Rp2<sup>tm1.2Asw</sup>/Rp2<sup>tm1.2Asw</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23745007	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5619358	Rp2<sup>tm1.2Asw</sup>	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:5620352	Rp2<sup>tm1.2Asw</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23745007	20150330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:6841965	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:6234993	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438066	Ccdc39<sup>b2b1735Clo</sup>	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712949	Slc26a4<sup>pdsm</sup>/Slc26a4<sup>pdsm</sup>  [background:] BXA7/PgnJ-Slc26a4<sup>pdsm</sup>/J	is_model_of	DOID:0060744	Pendred Syndrome						ECO:0000033	author statement supported by traceable reference	MGI:3712813	20070627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698754	Htt<sup>tm2.1Pfs</sup>/Htt<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10196365	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702870	Gt(ROSA)26Sor<sup>tm1(GNAQ*)Cvrk</sup>	is_implicated_in	DOID:6039	uveal melanoma		MGI:5702873	Gt(ROSA)26Sor<sup>tm1(GNAQ*)Cvrk</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Mitf-cre)7114Gsb/0  [background:] C3FeJ.Cg-Gt(ROSA)26Sor<sup>tm1(GNAQ*)Cvkr</sup> Tg(Mitf-cre)7114Gsb/Cvrk			ECO:0000033	author statement supported by traceable reference	PMID:26113083	20160115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785397	Ugt1<sup>tm1Rhtu</sup>/Ugt1<sup>tm1Rhtu</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:3803	Crigler-Najjar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18180294	20080516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441753	Tg(LMNA*G608G)HClns/?  [background:] C57BL/6-Tg(LMNA*G608G)HClns/J	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:16492728	20121116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6501795	Col4a4<sup>m1H</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:6501951	Col4a4<sup>m1H</sup>/Col4a4<sup>m1H</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31892712	20210126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467305	Pten<sup>tm2.1Ppp</sup>/Pten<sup>+</sup> Spry1<sup>tm1Jdli</sup>/Spry1<sup>tm1.1Jdli</sup> Spry2<sup>tm1Mrt</sup>/Spry2<sup>tm1.1Mrt</sup> Tg(Osr1-cre)4Mrt/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23150596	20130304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157831	Cfap418<sup>em3Jyang</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:6157954	Cfap418<sup>em3Jyang</sup>/Cfap418<sup>em3Jyang</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29440555	20180524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6115370	Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:12236	primary biliary cholangitis		MGI:6717173	Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup>/Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA			ECO:0000033	author statement supported by traceable reference	PMID:33513427	20210623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636739	Dok7<sup>tm2Yyam</sup>/Dok7<sup>tm2Yyam</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0110668	congenital myasthenic syndrome 10						ECO:0000033	author statement supported by traceable reference	PMID:25237101	20150521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155978	Psen1<sup>tm1Jzt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29867447	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155978	Psen1<sup>tm1Jzt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23792007	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155978	Psen1<sup>tm1Jzt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18834536	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155978	Psen1<sup>tm1Jzt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:34758364	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155978	Psen1<sup>tm1Jzt</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3045183	Psen1<sup>tm1Jzt</sup>/Psen1<sup>tm1Jzt</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11738035	20220303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149903	Golgb1<sup>m1Lanyu</sup>	is_implicated_in	DOID:674	cleft palate		MGI:6151463	Golgb1<sup>m1Lanyu</sup>/Golgb1<sup>m1Lanyu</sup>  [background:] A/J-Golgb1<sup>m1Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793713	Ndufs4<sup>tm1.1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:26363424	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793713	Ndufs4<sup>tm1.1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:28483998	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793713	Ndufs4<sup>tm1.1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:26917594	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793713	Ndufs4<sup>tm1.1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:37883842	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793713	Ndufs4<sup>tm1.1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:5451011	Ndufs4<sup>tm1.1Rpa</sup>/Ndufs4<sup>tm1.1Rpa</sup>  [background:] B6.129S4-Ndufs4<sup>tm1.1Rpa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22653057	20231201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5460858	Fgd4<sup>tm1.1Ics</sup>	is_implicated_in	DOID:0110192	Charcot-Marie-Tooth disease type 4H		MGI:5460859	Fgd4<sup>tm1.1Ics</sup>/Fgd4<sup>tm1.1Ics</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:23171661	20130128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3696558	Serpinc1<sup>tm1Dwr</sup>/Serpinc1<sup>tm1Dwr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:3755	antithrombin III deficiency						ECO:0000033	author statement supported by traceable reference	PMID:14592998	20091123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491206	Tg(Lmnb1)1Yfu/0  [background:] involves: C57BL/6J	is_model_of	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23676464	20130621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831527	Gtf2i<sup>Gt(XE029)Byg</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:36152627	20230329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831527	Gtf2i<sup>Gt(XE029)Byg</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3831546	Gtf2i<sup>Gt(XE029)Byg</sup>/Gtf2i<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19109438	20230329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530076	Atrx<sup>tm1Rjg</sup>/Y Tg(Nes-cre)2472Pick/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15668733	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5803717	Notch2<sup>tm1.1Ecan</sup>	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:5803721	Notch2<sup>tm1.1Ecan</sup>/Notch2<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26627824	20161017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429852	Frem2<sup>b2b1562Clo</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:5429856	Frem2<sup>b2b1562Clo</sup>/Frem2<sup>b2b1562Clo</sup>  [background:] C57BL/6J-Frem2<sup>b2b1562Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523971	Kit<sup>Wps</sup>/Kit<sup>Wps</sup>  [background:] involves: C57BL/6J * CBA/CaJ	is_model_of	DOID:3263	piebaldism						ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619149	Tbx1<sup>tm2.1Bem</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28346476	20171206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950567	Prpf8<sup>tm1.1Eap</sup>/Prpf8<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:0110403	retinitis pigmentosa 13						ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5085321	Ccm2<sup>tm2.1Sbn</sup>/Ccm2<sup>tm2.1Sbn</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0060670	cerebral cavernous malformation 2						ECO:0000033	author statement supported by traceable reference	PMID:21596842	20110812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554193	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-MAPT*K280,-luc)#Eman/0  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21325519	20140402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554193	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-MAPT*K280,-luc)#Eman/0  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18199773	20140402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6784038	Ank2<sup>em1Bnt</sup>	is_implicated_in	DOID:12849	autistic disorder		MGI:6790238	Ank2<sup>em1Bnt</sup>/Ank2<sup>em1Bnt</sup>  [background:] C57BL/6J-Ank2<sup>em1Bnt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31285321	20211102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693941	Edar<sup>dl</sup>/Edar<sup>dl</sup>  [background:] involves: A/H	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:17148670	20070118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	MGI:78279	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	MGI:63097	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607604	Myo5a<sup>d-l34J</sup>	is_implicated_in	DOID:0060832	Griscelli syndrome type 1		MGI:5607614	Myo5a<sup>d-l34J</sup>/Myo5a<sup>d-l34J</sup>  [background:] BALB/cJ-Myo5a<sup>d-l34J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5607575	20141222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435319	Lepr<sup>db</sup>/Lepr<sup>+</sup> Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H * C57BL/6 * C57BLKS/J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22414803	20120919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785390	Tg(Thy1-SOD1*G93A)T3Hgrd/Tg(Thy1-SOD1*G93A)T3Hgrd  [background:] involves: C57BL/6 * CBA * FVB	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:18305242	20080516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428689	Hprt1<sup>tm1(Nphs1-CMIP)Dsah</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:5428692	Hprt1<sup>tm1(Nphs1-CMIP)Dsah</sup>/Hprt1<sup>+</sup>  [background:] B6.Cg-Hprt1<sup>tm1(Nphs1-CMIP)Dsah</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20484117	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678410	Runx2<sup>tm1Kish</sup>/Runx2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:9182763	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703450	Ts(17<sup>16</sup>)65Dn/0  [background:] involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15859352	20080626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3703450	Ts(17<sup>16</sup>)65Dn/0  [background:] involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15515178	20080626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860866	Pkd2<sup>tm2Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:23892607	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860866	Pkd2<sup>tm2Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:25934702	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860866	Pkd2<sup>tm2Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:24515114	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860866	Pkd2<sup>tm2Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174705	Pkd2<sup>tm2Som</sup>/Pkd2<sup>tm2Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10615132	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860866	Pkd2<sup>tm2Som</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174706	Pkd2<sup>tm2Som</sup>/Pkd2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10615132	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437098	b2b227Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702397	Sacs<sup>tm1(NCOM)Mfgc</sup>	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25260547	20190710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702397	Sacs<sup>tm1(NCOM)Mfgc</sup>	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia		MGI:6316985	Sacs<sup>tm1(NCOM)Mfgc</sup>/Sacs<sup>tm1(NCOM)Mfgc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22307627	20190710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6110825	Tg(CAG-Bmp4,-EGFP)1Ypc	is_implicated_in	DOID:0080313	cleft palate-lateral synechia syndrome		MGI:6110828	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(CAG-Bmp4,-EGFP)1Ypc/0  [background:] involves: C57BL/6J * CBA/J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24785830	20180725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908892	Tg(Myh6-MYL2*E22K)4Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10		MGI:5908893	Tg(Myh6-MYL2*E22K)4Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16076902	20170912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908892	Tg(Myh6-MYL2*E22K)4Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:17606808	20170912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908892	Tg(Myh6-MYL2*E22K)4Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:16751284	20170912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774594	Spr<sup>tm1Lex</sup>/Spr<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:18201550	20110629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695129	Tg(Syn1-ADCY7)11004Btab/0  [background:] B6.Cg-Tg(Syn1-ADCY7)11004Btab	is_model_of	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:17135423	20070130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819108	Tg(Thy1-APPDutch)#Jckr/0 Tg(Thy1-PSEN1*G384A)45Jckr/0  [background:] involves: C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:15311281	20100818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806788	Tg(Thy1-SNCA*E57K)16Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5806789	Tg(Thy1-SNCA*E57K)16Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:24662516	20161110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806788	Tg(Thy1-SNCA*E57K)16Ema	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26341908	20161110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474481	Bbs1<sup>tm2Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:33886537	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474481	Bbs1<sup>tm2Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:26926121	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474481	Bbs1<sup>tm2Vcs</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1		MGI:5474570	Bbs1<sup>tm2Vcs</sup>/Bbs1<sup>tm2Vcs</sup> Tg(Pdgfra-cre)1Clc/0  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23160237	20210712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388062	Fgfr3<sup>tm1.1Iwa</sup>	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:22634226	20120927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7258399	Ryr1<sup>em1Tmur</sup>	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:7260233	Ryr1<sup>em1Tmur</sup>/Ryr1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:34257294	20220408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6108878	Trmu<sup>tm1Tomik</sup>	is_implicated_in	DOID:409	liver disease		MGI:6108884	Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup> Trmu<sup>tm1Tomik</sup>/Trmu<sup>tm1Tomik</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:27689697	20180112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435319	Lepr<sup>db</sup>/Lepr<sup>+</sup> Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H * C57BL/6 * C57BLKS/J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22414803	20120919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439278	Nlgn3<sup>tm1Rhn</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439278	Nlgn3<sup>tm1Rhn</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5440731	Nlgn3<sup>tm1Rhn</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22983708	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397669	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582830	Kras<sup>tm1Bbd</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:27775074	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582830	Kras<sup>tm1Bbd</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:4844193	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Polr2a<sup>tm1(cre/ERT2)Bbd</sup>/Polr2a<sup>tm1(cre/ERT2)Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20609353	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582830	Kras<sup>tm1Bbd</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:5508232	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21514245	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5546597	Prmt5<sup>tm2c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7277815	Prmt5<sup>tm2c(EUCOMM)Wtsi</sup>/Prmt5<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Col2a1-cre)#Amc/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31848143	20220516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5288006	Notch2<sup>tm3Grid</sup>/Notch2<sup>tm3Grid</sup> Tg(Tpbpa-cre,-EGFP)5Jcc/0  [background:] involves: 129S1/Sv	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:21693515	20111003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686931	Galns<sup>tm1Toma</sup>	is_implicated_in	DOID:12804	mucopolysaccharidosis IV						ECO:0000033	author statement supported by traceable reference	PMID:24953405	20150428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686931	Galns<sup>tm1Toma</sup>	is_implicated_in	DOID:12804	mucopolysaccharidosis IV		MGI:2686939	Galns<sup>tm1Toma</sup>/Galns<sup>tm1Toma</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14583446	20150428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8341011	20050803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8476712	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7516354	Rab33b<sup>em1Rmr</sup>	is_implicated_in	DOID:0081271	Smith-McCort dysplasia 2		MGI:7517090	Rab33b<sup>em1Rmr</sup>/Rab33b<sup>em1Rmr</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:37359363	20230814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7516354	Rab33b<sup>em1Rmr</sup>	is_implicated_in	DOID:0081271	Smith-McCort dysplasia 2		MGI:7517091	Rab33b<sup>em1Rmr</sup>/Rab33b<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:37359363	20230814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3820200	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16293761	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5694344	Tg(Ckm-Chrnd*S262T)40Cgz/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110666	congenital myasthenic syndrome 3A						ECO:0000033	author statement supported by traceable reference	PMID:8538674	20151102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437688	Tg(SERPINC1-SV40)A1Pbr/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1660504	20121004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819193	Brca2<sup>tm1Brn</sup>/Brca2<sup>tm1Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:20585617	20100813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459475	Gnasas1<sup>tm1.1Hju</sup>	is_implicated_in	DOID:4184	pseudohypoparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22496590	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459475	Gnasas1<sup>tm1.1Hju</sup>	is_implicated_in	DOID:4184	pseudohypoparathyroidism		MGI:4459500	Gnasas1<sup>tm1.1Hju</sup>/Gnasas1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:20427744	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:27353086	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:25125170	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:28717008	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:23708682	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M		MGI:3037157	Csrp3<sup>tm1Crni</sup>/Csrp3<sup>tm1Crni</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9039266	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387850	Tbx5<sup>tm1Jse</sup>	is_implicated_in	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28164238	20180508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387850	Tbx5<sup>tm1Jse</sup>	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3692774	Tbx5<sup>tm1Jse</sup>/Tbx5<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:16870172	20180508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693295	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:17021169	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575890	Tg(Myh6-KCNQ1_i2)H02Desc	is_implicated_in	DOID:0110644	long QT syndrome 1		MGI:5575893	Tg(Myh6-KCNQ1_i2)H02Desc/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:11334835	20140801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764818	Tg(Th-SNCA*)1.2Ccs/?  [background:] involves: C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:21212098	20110307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778191	Tg(Thy1-MAPT*P301S)2541Godt	is_implicated_in	DOID:680	tauopathy						ECO:0000033	author statement supported by traceable reference	PMID:32008854	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:24015215	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793703	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] SJL.129S2-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793700	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] B6.129S2-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793701	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] NOD.129S2(B6)-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793702	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] C.129S2-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661910	Aire<sup>tm1.1Doi</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:2661915	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12376594	20140317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883024	Tg(EEF1A1-Gnas*R201C)184Pabi/0  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * FVB/N)	is_model_of	DOID:1858	McCune Albright syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24764158	20170413	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814533	Stk11<sup>tm1.2Rdp</sup>/Stk11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18172296	20081112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814533	Stk11<sup>tm1.2Rdp</sup>/Stk11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12226664	20081112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009680	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	is_implicated_in	DOID:10283	prostate cancer		MGI:5565602	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp/0  [background:] FVB-Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp			ECO:0000033	author statement supported by traceable reference	PMID:18068632	20140529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009680	Tg(Pbsn-Fgfr1/Fkbp1a)#aDmsp	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25693568	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21389115	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27035958	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22388814	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22262900	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:17581637	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653679	Tg(tetO-CDK5R1/GFP)337Lht	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3653709	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-CDK5R1/GFP)337Lht/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22049418	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388388	Cnga3<sup>tm1Biel</sup>	is_implicated_in	DOID:0110007	achromatopsia 2						ECO:0000033	author statement supported by traceable reference	PMID:26740549	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388388	Cnga3<sup>tm1Biel</sup>	is_implicated_in	DOID:0110007	achromatopsia 2		MGI:2663832	Cnga3<sup>tm1Biel</sup>/Cnga3<sup>tm1Biel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10377453	20160909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7494069	Stmn2<sup>em1Jmi</sup>	is_implicated_in	DOID:870	neuropathy		MGI:7523309	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>em1Jmi</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6358537	Eftud2<sup>em1Lajm</sup>	is_not_implicated_in	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type		MGI:6358542	Eftud2<sup>em1Lajm</sup>/Eftud2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31276534	20190906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559486	m12Anu	is_implicated_in	DOID:0050563	nonsyndromic deafness		MGI:5582638	m12Anu/m12Anu  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24086324	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444190	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] involves: C3H/HeA * C57BL/6J * C57BL/LiA	is_model_of	DOID:0060835	isolated microphthalmia 6						ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386959	Cdk4<sup>tm1Bbd</sup>/Cdk4<sup>tm1Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10319860	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0090130	cortical dysplasia-focal epilepsy syndrome						ECO:0000033	author statement supported by traceable reference	PMID:37699442	20231004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677631	Cntnap2<sup>tm1Pele</sup>	is_implicated_in	DOID:0090130	cortical dysplasia-focal epilepsy syndrome		MGI:5295268	Cntnap2<sup>tm1Pele</sup>/Cntnap2<sup>tm1Pele</sup>  [background:] B6.129-Cntnap2<sup>tm1Pele</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21962519	20231004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525159	Nfatc2<sup>tm1Glm</sup>/Nfatc2<sup>tm1Glm</sup> Nfatc3<sup>tm1Glm</sup>/Nfatc3<sup>tm1Glm</sup> Nfatc4<sup>tm1Grc</sup>/Nfatc4<sup>tm1Grc</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16554754	20060720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5788295	Tg(CD4-CIITA)357Ccum/?  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:24038328	20160809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720810	Prkci<sup>tm1Rfar</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:22225955	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720810	Prkci<sup>tm1Rfar</sup>	is_implicated_in	DOID:9970	obesity		MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17641777	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618818	Dnah5<sup>b2b2925Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5140723	Ttc8<sup>tm1Reed</sup>	is_implicated_in	DOID:0110130	Bardet-Biedl syndrome 8		MGI:5140726	Ttc8<sup>tm1Reed</sup>/Ttc8<sup>tm1Reed</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21646512	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387401	Stk11<sup>tm1Rdp</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25190708	20150807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387401	Stk11<sup>tm1Rdp</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:5440238	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Stk11<sup>tm1Rdp</sup>/Stk11<sup>tm1Rdp</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22791749	20150807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835239	Tg(MMTV-LPAR3)22Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763109	Tg(MMTV-LPAR3)22Gbm/Tg(MMTV-LPAR3)22Gbm  [background:] FVB/N-Tg(MMTV-LPAR3)22Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845228	Tg(Six2-EGFP/cre)1Amc	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:32484794	20211102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618724	Nos3<sup>tm1Gdk</sup>/Nos3<sup>tm1Gdk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10825	essential hypertension						ECO:0000033	author statement supported by traceable reference	PMID:9468189	20060406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538528	Tg(LPV-TAg121)2Tvd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J	is_model_of	DOID:2626	choroid plexus papilloma						ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512655	Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:5512667	Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>/Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23502960	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512655	Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:5512665	Gt(ROSA)26Sor<sup>tm3(tetO-Mir193)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23502960	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5806505	Tg(SFTPC-CD74/ROS1)125Tno/0  [background:] C57BL/6J-Tg(SFTPC-CD74/ROS1)125Tno	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:26964870	20161108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554389	Tshr<sup>hyt-3J</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5572798	Tshr<sup>hyt-3J</sup>/Tshr<sup>hyt-3J</sup>  [background:] CXB10/HiAJ-Tshr<sup>hyt-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5571363	20140714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554389	Tshr<sup>hyt-3J</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5572808	Tshr<sup>hyt-3J</sup>/Tshr<sup>hyt-3J</sup>  [background:] CByJ;CXB10-Tshr<sup>hyt-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5571363	20140714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441310	Tg(Vav1-JAK2*V617F)AZjz	is_implicated_in	DOID:4971	myelofibrosis		MGI:5441312	Tg(Vav1-JAK2*V617F)AZjz/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18334677	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441310	Tg(Vav1-JAK2*V617F)AZjz	is_implicated_in	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:32294178	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441310	Tg(Vav1-JAK2*V617F)AZjz	is_implicated_in	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:22796437	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5638104	Tg(Tcrb-TCF3/PBX1)23Gusa	is_implicated_in	DOID:12603	acute leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24503485	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512882	Tg(CAG-Lyn*)#Paau	is_implicated_in	DOID:8893	psoriasis		MGI:5512884	Tg(CAG-Lyn*)#Paau/0  [background:] B6.Cg-Tg(CAG-Lyn*)#Paau			ECO:0000033	author statement supported by traceable reference	PMID:19590497	20131016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512882	Tg(CAG-Lyn*)#Paau	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:23071785	20131016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:22704978	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:28334871	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:32938982	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:19416667	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000033	author statement supported by traceable reference	PMID:24014511	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1		MGI:5296508	Ppt1<sup>tm1Hof</sup>/Ppt1<sup>tm1Hof</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22031903	20201021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3806486	Lrp5<sup>r18</sup>/Lrp5<sup>r18</sup>  [background:] C57BL/6J-Lrp5<sup>r18</sup>	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:18263894	20120326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5141633	Tg(Vav1-ERG)#Jpim	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5548208	Tg(Vav1-ERG)#Jpim/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23974202	20140313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5141633	Tg(Vav1-ERG)#Jpim	is_implicated_in	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23974202	20140313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817454	Arid4a<sup>tm1Alb</sup>/Arid4a<sup>tm1Alb</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:18728284	20081121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196853	Gt(ROSA)26Sor<sup>tm1(OVAL/fla,GFP)Vnce</sup>	is_implicated_in	DOID:612	primary immunodeficiency disease		MGI:6196856	Gt(ROSA)26Sor<sup>tm1(OVAL/fla,GFP)Vnce</sup>/Gt(ROSA)26Sor<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29263322	20180906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690090	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)57Hev/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:16705038	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311376	Mmp21<sup>b2b873Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313515	Mmp21<sup>b2b873Clo</sup>/Mmp21<sup>b2b873Clo</sup>  [background:] C57BL/6J-Mmp21<sup>b2b873Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444031	Dcc<sup>Tg(H2-Kb-Jak2*V617F)1Shmd</sup>	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:5444033	Dcc<sup>Tg(H2-Kb-Jak2*V617F)1Shmd</sup>/Dcc<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18033315	20121130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5696972	Pygm<sup>tm1.1Adru</sup>	is_implicated_in	DOID:2746	glycogen storage disease V						ECO:0000033	author statement supported by traceable reference	PMID:25762569	20200221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5696972	Pygm<sup>tm1.1Adru</sup>	is_implicated_in	DOID:2746	glycogen storage disease V		MGI:5696978	Pygm<sup>tm1.1Adru</sup>/Pygm<sup>tm1.1Adru</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22730558	20200221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5696972	Pygm<sup>tm1.1Adru</sup>	is_implicated_in	DOID:2746	glycogen storage disease V						ECO:0000033	author statement supported by traceable reference	PMID:31848135	20200221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5703732	Tg(Prnp-MAPT*R406W)21807Dwst/?  [background:] FVB/N-Tg(Prnp-MAPT*R406W)21807Dwst	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:15681835	20160118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1575747	20090716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8041507	20090716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7816342	20090716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702318	Ctsd<sup>tm1.1Thre</sup>	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:5702327	Ctsd<sup>tm1.1Thre</sup>/Ctsd<sup>tm1.1Thre</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26232697	20160111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702318	Ctsd<sup>tm1.1Thre</sup>	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:5702324	Ctsd<sup>tm1.1Thre</sup>/Ctsd<sup>tm1.1Thre</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26232697	20160111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7427368	Tnfrsf11a<sup>tm1.1Sral</sup>	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:7427405	Tnfrsf11a<sup>tm1.1Sral</sup>/Tnfrsf11a<sup>+</sup>  [background:] B6.129P2(Cg)-Tnfrsf11a<sup>tm1.1Sral</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33724536	20230117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176897	Colq<sup>tm1Jrs</sup>/Colq<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110667	congenital myasthenic syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:10087275	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176966	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:15798202	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176966	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:11171994	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5518618	Tg(Pcp2-ATXN1*82Q)5Horr/0  [background:] involves: FVB/N	is_model_of	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:20869591	20131119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311153	Dnah5<sup>b2b601Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720000	Cacna1f<sup>nob2</sup>/Cacna1f<sup>nob2</sup>  [background:] AXB6/PgnJ	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:16597347	20070830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640358	Fgfr3<sup>tm5.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:13481	thanatophoric dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:11181569	20060810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789335	Lama2<sup>dy-2J</sup>/Lama2<sup>dy-2J</sup>  [background:] B6.WK-Lama2<sup>dy-2J</sup>	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:15823249	20080527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432255	Tg(tetO-IGF1R)1Ramo	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22020329	20120828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432255	Tg(tetO-IGF1R)1Ramo	is_implicated_in	DOID:1612	breast cancer		MGI:5432258	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-IGF1R)1Ramo/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:16953219	20120828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182171	Tg(SOD1*G85R)148Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25054289	20161026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182171	Tg(SOD1*G85R)148Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22371592	20161026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182171	Tg(SOD1*G85R)148Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26416261	20161026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182171	Tg(SOD1*G85R)148Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26853136	20161026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182171	Tg(SOD1*G85R)148Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:27551074	20161026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182171	Tg(SOD1*G85R)148Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3832406	Tg(SOD1*G85R)148Dwc/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9052802	20161026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639355	Mc3r<sup>tm1Cone</sup>/Mc3r<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:10965927	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141009	Cdh23<sup>12J</sup>/Cdh23<sup>12J</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110467	autosomal recessive nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:20644563	20110825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5470234	Pkd1<sup>tm1.1Fqi</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23524344	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5470234	Pkd1<sup>tm1.1Fqi</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5471141	Pkd1<sup>tm1.1Fqi</sup>/Pkd1<sup>tm1.1Fqi</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23236168	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5470234	Pkd1<sup>tm1.1Fqi</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25234309	20150406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634274	Cacna1f<sup>tm1.2Sdie</sup>/Cacna1f<sup>tm1.2Sdie</sup>  [background:] B6.Cg-Cacna1f<sup>tm1.2Sdie</sup>/J	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833393	Tg(Thy1-SERPINI1*G392E)333Icka/Tg(Thy1-SERPINI1*G392E)333Icka  [background:] involves: C57BL * CD-1 * DBA	is_model_of	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000033	author statement supported by traceable reference	PMID:18940798	20090224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861959	Kcna1<sup>tm1Tem</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:28334922	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861959	Kcna1<sup>tm1Tem</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:27346881	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861959	Kcna1<sup>tm1Tem</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:29193044	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861959	Kcna1<sup>tm1Tem</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:4833820	Kcna1<sup>tm1Tem</sup>/Kcna1<sup>tm1Tem</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:20392939	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25559195	20150513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7282124	Sdhb<sup>tm1c(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:7314952	Sdhb<sup>tm1c(EUCOMM)Hmgu</sup>/Sdhb<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: C57BL/6J * C57BL/6N * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:35472723	20220725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821979	Sptbn2<sup>tm1Mjac</sup>	is_not_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:5426692	Sptbn2<sup>tm1Mjac</sup>/Sptbn2<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20603325	20120702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857226	Ngfr<sup>tm1Jae</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21307265	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672889	Serpinf2<sup>tm1Hrl</sup>/Serpinf2<sup>tm1Hrl</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060601	alpha-2-plasmin inhibitor deficiency						ECO:0000033	author statement supported by traceable reference	PMID:10090937	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672889	Serpinf2<sup>tm1Hrl</sup>/Serpinf2<sup>tm1Hrl</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060601	alpha-2-plasmin inhibitor deficiency						ECO:0000033	author statement supported by traceable reference	PMID:10318667	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654712	Dkc1<sup>tm1Ppp</sup>/Dkc1<sup>+</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:2729	dyskeratosis congenita						ECO:0000033	author statement supported by traceable reference	PMID:12522253	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430527	Gt(ROSA)26Sor<sup>tm7(Pik3ca*,EGFP)Rsky</sup>	is_implicated_in	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22897848	20130214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137421	Gabra1<sup>tm1.1Geh</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:23744069	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137421	Gabra1<sup>tm1.1Geh</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:25447232	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137421	Gabra1<sup>tm1.1Geh</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5433047	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] B6.129(Cg)-Gabra1<sup>tm1.1Geh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26054439	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137421	Gabra1<sup>tm1.1Geh</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5433031	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] D2.129(Cg)-Gabra1<sup>tm1.1Geh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22812724	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137421	Gabra1<sup>tm1.1Geh</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5433047	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] B6.129(Cg)-Gabra1<sup>tm1.1Geh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22812724	20180404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153007	Eln<sup>tm1Dyl</sup>	is_implicated_in	DOID:1929	supravalvular aortic stenosis						ECO:0000033	author statement supported by traceable reference	PMID:26858344	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153007	Eln<sup>tm1Dyl</sup>	is_implicated_in	DOID:1929	supravalvular aortic stenosis						ECO:0000033	author statement supported by traceable reference	PMID:23493289	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153007	Eln<sup>tm1Dyl</sup>	is_implicated_in	DOID:1929	supravalvular aortic stenosis		MGI:3619994	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9819363	20160720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153007	Eln<sup>tm1Dyl</sup>	is_implicated_in	DOID:1929	supravalvular aortic stenosis		MGI:3620001	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] B6.129-Eln<sup>tm1Dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14597767	20160720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4457497	Sav1<sup>tm2.1Dlim</sup>/Sav1<sup>tm2.1Dlim</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26131558	20170208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785495	Tg(ARR2/Pbsn-MYC)7Key	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785495	Tg(ARR2/Pbsn-MYC)7Key	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23348745	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785495	Tg(ARR2/Pbsn-MYC)7Key	is_implicated_in	DOID:10283	prostate cancer		MGI:5486199	Tg(ARR2/Pbsn-MYC)7Key/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14522256	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459898	Tg(tetO-MYC)36Bop	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5521486	Tg(CAG-Bgeo,-tTA,-EGFP)2A11Kuw/0 Tg(Pdx1-cre)6Tuv/0 X/Tg(tetO-MYC)36Bop  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23467612	20131204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22892246	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23217740	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:29078331	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33848635	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24747018	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:6257025	Tg(APPV717F)109Ili/0  [background:] B6.Cg-Tg(APPV717F)109Ili			ECO:0000033	author statement supported by traceable reference	PMID:28806762	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5427915	Tg(APPV717F)109Ili/0  [background:] involves: BALB/c * C57BL * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:22623685	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174818	Tg(APPV717F)109Ili/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7845465	20210617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151935	Tg(APPV717F)109Ili	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3721531	Tg(APPV717F)109Ili/Tg(APPV717F)109Ili  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12145324	20210617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589108	Ednrb<sup>s-l</sup>/Ednrb<sup>s-l</sup>  [background:] involves: C3H/HeJ * C57BL/6	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:5917257	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360797	Tg(RBP3-ELOVL4*)2Kzh/0  [background:] C57BL/6-Tg(RBP3-ELOVL4*)2Kzh	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:15749821	20091008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749385	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7339183	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:34732824	20230815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749385	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7518241	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Neurod1-cre)RZ24Gsat/0  [background:] involves: C57BL/6J * C57BL/6N * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:34732824	20230815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749385	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7496108	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Slc1a3<sup>tm1(cre/ERT2)Mgoe</sup>/Slc1a3<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25183173	20230815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749385	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493449	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: C57BL/6 * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28317875	20230815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26266985	20211008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27775073	20211008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25421310	20211008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27571409	20211008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:30222135	20211008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22515648	20211008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175873	F9<sup>tm1Ver</sup>/F9<sup>tm1Ver</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:12259	hemophilia B						ECO:0000033	author statement supported by traceable reference	PMID:9326649	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4868492	Gbe1<sup>m1Yty</sup>	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:4868493	Gbe1<sup>m1Yty</sup>/Gbe1<sup>m1Yty</sup>  [background:] C3HeB/FeJ-Gbe1<sup>m1Yty</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21075835	20110119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285078	Dnah5<sup>b2b016Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702925	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15207348	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950068	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21195751	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044667	Foxl2<sup>tm1Gpil</sup>/Foxl2<sup>tm1Gpil</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)	is_model_of	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15056605	20071022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512461	Fgf23<sup>tm1Blan</sup>/Fgf23<sup>+</sup> Phex<sup>Hyp</sup>/Y  [background:] Not Specified	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15579309	20090728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178057	Gria1<sup>tm1Rsp</sup>	is_implicated_in	DOID:5418	schizoaffective disorder						ECO:0000033	author statement supported by traceable reference	PMID:21693126	20170718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178057	Gria1<sup>tm1Rsp</sup>	is_implicated_in	DOID:5418	schizoaffective disorder		MGI:4888960	Gria1<sup>tm1Rsp</sup>/Gria1<sup>tm1Rsp</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20699120	20170718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178057	Gria1<sup>tm1Rsp</sup>	is_implicated_in	DOID:5418	schizoaffective disorder		MGI:4888959	Gria1<sup>tm1Rsp</sup>/Gria1<sup>tm1Rsp</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20699120	20170718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401292	Tg(Ace2-ACE2)1Cqin	is_implicated_in	DOID:2945	severe acute respiratory syndrome		MGI:6402641	Tg(Ace2-ACE2)1Cqin/0  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:17974127	20200402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417921	Slc1a3<sup>tm1Kta</sup>/Slc1a3<sup>tm1Kta</sup>  [background:] B6.129P2-Slc1a3<sup>tm1Kta</sup>	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:17607354	20100115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6198713	Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A		MGI:6198715	Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17959936	20180919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607162	Oca2<sup>p-6Btlr</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5607163	Oca2<sup>p-6Btlr</sup>/Oca2<sup>p-6Btlr</sup>  [background:] C57BL/6J-Oca2<sup>p-6Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5607140	20141215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177551	Hexa<sup>tm1Rlp</sup>/Hexa<sup>tm1Rlp</sup> Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8896570	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653048	Ndn<sup>tm2Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653048	Ndn<sup>tm2Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22776820	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653048	Ndn<sup>tm2Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653055	Ndn<sup>tm2Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12629158	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653048	Ndn<sup>tm2Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2654656	Ndn<sup>tm2Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10508517	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153004	Lama2<sup>tm1Stk</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:24631023	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153004	Lama2<sup>tm1Stk</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789197	Lama2<sup>tm1Stk</sup>/Lama2<sup>tm1Stk</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR			ECO:0000033	author statement supported by traceable reference	PMID:21084425	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153004	Lama2<sup>tm1Stk</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789197	Lama2<sup>tm1Stk</sup>/Lama2<sup>tm1Stk</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9326364	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311372	Dnah11<sup>b2b598Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312336	Dnah11<sup>b2b598Clo</sup>/Dnah11<sup>b2b598Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b598Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440450	Tg(CAG-VCP*A232E)93Jpat/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:20147319	20100414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358596	Tg(Pbsn-Tag)12T7fRjm/0  [background:] involves: CD-1	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:9645768	20140603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510594	Tg(APPSw)40Btla	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22413000	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510594	Tg(APPSw)40Btla	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3722393	Tg(APPSw)40Btla/Tg(APPSw)40Btla  [background:] B6.129-Tg(APPSw)40Btla			ECO:0000033	author statement supported by traceable reference	PMID:14506131	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510594	Tg(APPSw)40Btla	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3693439	Tg(APPSw)40Btla/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9285791	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6443611	Tg(Tk1-DPP4)27Ysj	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6443613	Tg(Tk1-DPP4)27Ysj/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31838832	20200721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438065	b2b1714Clo	is_implicated_in	DOID:114	heart disease		MGI:5442137	b2b1714Clo/b2b1714Clo  [background:] C57BL/6J-b2b1714Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431942	Tert<sup>tm3Rdp</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5436308	Pink1<sup>tm1.1Wrst</sup>	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:5436309	Pink1<sup>tm1.1Wrst</sup>/Pink1<sup>tm1.1Wrst</sup>  [background:] involves: 129S2/SvPas * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22265660	20120926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294675	Scn3b<sup>tm1Clhh</sup>/Scn3b<sup>tm1Clhh</sup>  [background:] 129S/SvEv-Scn3b<sup>tm1Clhh</sup>	is_model_of	DOID:0110224	Brugada syndrome 7						ECO:0000033	author statement supported by traceable reference	PMID:19351516	20111103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0080052	acromesomelic dysplasia, Grebe type						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850443	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd	is_model_of	DOID:1790	malignant mesothelioma						ECO:0000033	author statement supported by traceable reference	PMID:18328429	20090716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23221339	20140213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:23221337	20140213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176057	Nf1<sup>tm1Par</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:5544056	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14982883	20140213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867514	Tg(DYRK1A)36Wjs	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27538963	20180119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867514	Tg(DYRK1A)36Wjs	is_implicated_in	DOID:14250	Down syndrome		MGI:4867515	Tg(DYRK1A)36Wjs/0  [background:] involves: C57BL/6NCrjBgi			ECO:0000033	author statement supported by traceable reference	PMID:16455265	20180119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426792	Tg(CAG-DMPK*)1323Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:22371589	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426792	Tg(CAG-DMPK*)1323Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:5426794	A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup> Tg(CAG-DMPK*)1323Coop/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:17823658	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426792	Tg(CAG-DMPK*)1323Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:28369378	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426792	Tg(CAG-DMPK*)1323Coop	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:5426828	Tg(ACTA1-cre/ERT2)97.16Mtz/0 Tg(CAG-DMPK*)1323Coop/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:18272483	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569504	Msrb3<sup>tm1Hyk</sup>	is_implicated_in	DOID:0110523	autosomal recessive nonsyndromic deafness 74		MGI:5569513	Msrb3<sup>tm1Hyk</sup>/Msrb3<sup>tm1Hyk</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24191262	20140625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857043	Muc19<sup>sld</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26343329	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857043	Muc19<sup>sld</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25447050	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857043	Muc19<sup>sld</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8077681	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857043	Muc19<sup>sld</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15593201	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857043	Muc19<sup>sld</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10793067	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7366891	Ndrg1<sup>em1Lxli</sup>	is_implicated_in	DOID:0110186	Charcot-Marie-Tooth disease type 4D		MGI:7366893	Ndrg1<sup>em1Lxli</sup>/Ndrg1<sup>em1Lxli</sup>  [background:] C57BL/6N-Ndrg1<sup>em1Lxli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35708320	20221025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694004	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:9590297	20070119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694004	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:14981357	20070119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820827	Traf3ip2<sup>adjm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820831	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] A.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820827	Traf3ip2<sup>adjm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820830	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820827	Traf3ip2<sup>adjm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820832	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] B6.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820827	Traf3ip2<sup>adjm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820834	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] AK.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820827	Traf3ip2<sup>adjm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820833	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] C.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5550582	Tg(PDGFB-APPInd)F17Plhn/0  [background:] C57BL/6-Tg(PDGFB-APPInd)F17Plhn	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16289866	20140314	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5688522	Lrp4<sup>mdig-3J</sup>	is_implicated_in	DOID:0060757	sclerosteosis 2		MGI:5688562	Lrp4<sup>mdig-3J</sup>/Lrp4<sup>mdig-3J</sup>  [background:] B6.Cg-Lrp4<sup>mdig-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5688518	20150930	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705651	Col1a1<sup>tm1(tetO-YAP1*)Fcam</sup>/Col1a1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(rtTA,EGFP)Nagy</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26058078	20160128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3578958	Irf8<sup>myls</sup>/Irf8<sup>myls</sup> Slc11a1<sup>r</sup>/Slc11a1<sup>r</sup>  [background:] involves: A/J * BXH2/TyJ	is_model_of	DOID:0060761	familial chronic myelocytic leukemia-like syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15781580	20050607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4842225	Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0112247	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		MGI:6451664	Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>/Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31440507	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037339	Ece1<sup>tm1Reh</sup>/Ece1<sup>tm1Reh</sup> Ece2<sup>tm1Ywa</sup>/Ece2<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:6406	double outlet right ventricle						ECO:0000033	author statement supported by traceable reference	PMID:10811845	20110509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258222	Tg(KRT5-Terf2)POBlas	is_implicated_in	DOID:0050427	xeroderma pigmentosum		MGI:6258418	Tg(KRT5-Terf2)POBlas/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16142233	20181129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447591	Tg(APP)8.9Btla	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22413000	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447591	Tg(APP)8.9Btla	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3718515	Tg(APP)8.9Btla/Tg(APP)8.9Btla  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15016076	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775814	Nlgn4l<sup>Gt(XST093)Byg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775814	Nlgn4l<sup>Gt(XST093)Byg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775814	Nlgn4l<sup>Gt(XST093)Byg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3783593	Nlgn4l<sup>Gt(XST093)Byg</sup>/Nlgn4l<sup>Gt(XST093)Byg</sup>  [background:] B6.129P2-Nlgn4x<sup>Gt(XST093)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18227507	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4947712	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:20876525	20110422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651448	Pax8<sup>tm1(cre)Mbu</sup>/Pax8<sup>tm1(cre)Mbu</sup>  [background:] involves: 129P2/OlaHsd * C3H/He * C57BL/6	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:12435636	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412048	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:27889678	20210325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412048	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22805202	20210325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412048	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	MGI:6512372	20210325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412048	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25706990	20210325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412048	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24806669	20210325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620242	Plp1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110773	hereditary spastic paraplegia 2						ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620242	Plp1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110773	hereditary spastic paraplegia 2						ECO:0000033	author statement supported by traceable reference	PMID:9616125	20180613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584030	Ap3b1<sup>pe-rim2</sup>/Ap3b1<sup>pe-rim2</sup>  [background:] involves: B10.A(R201) * C57BL/10Slc	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9434937	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6509459	Ppil1<sup>em3Jgg</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:6509636	Ppil1<sup>em3Jgg</sup>/Ppil1<sup>em3Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em3Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467729	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup> Slc6a4<sup>tm1Kpl</sup>/Slc6a4<sup>+</sup>  [background:] B6.129-Slc6a4<sup>tm1Kpl</sup> Pten<sup>tm1Rps</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:19208814	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7464491	mrs1	is_implicated_in	DOID:8465	retinoschisis		MGI:7465150	mrs1/Y  [background:] B6.Cg-mrs1/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:7464180	20230424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5518640	Sox11<sup>tm1.1Gan</sup>	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:5827939	Sox11<sup>tm1.1Gan</sup>/Sox11<sup>tm1.1Gan</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26826126	20170308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10541472	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044184	App<sup>tm1Ini</sup>/App<sup>+</sup>  [background:] involves: C57BL/6 * CBA * CD-1	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15147316	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7314199	Col5a1<sup>em1Brle</sup>	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:7314211	Col5a1<sup>em1Brle</sup>/Col5a1<sup>+</sup>  [background:] C57BL/6-Col5a1<sup>em1Brle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34740257	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6885945	Prickle1<sup>em1Yzou</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6890373	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>em1Yzou</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6885945	Prickle1<sup>em1Yzou</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6890374	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>+</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820839	Gck<sup>m1Rge</sup>/Gck<sup>+</sup>  [background:] involves: C3HeB/FeJ	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:19952346	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:0111394	mucopolysaccharidosis type IIIB						ECO:0000033	author statement supported by traceable reference	PMID:37794029	20231108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527451	Spink5<sup>tm1Drh</sup>/Spink5<sup>tm1Drh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15590704	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717246	Ar<sup>tm1Jdz</sup>	is_implicated_in	DOID:11612	polycystic ovary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32229702	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717246	Ar<sup>tm1Jdz</sup>	is_implicated_in	DOID:11612	polycystic ovary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28320971	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6316982	Sacs<sup>tm2Bebr</sup>	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia		MGI:5702409	Sacs<sup>tm2Bebr</sup>/Sacs<sup>tm2Bebr</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25260547	20160216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673460	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] 129S4/SvJae-Fancd2<sup>tm1Hou</sup>	is_model_of	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000033	author statement supported by traceable reference	PMID:12893777	20110518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430750	Bmpr2<sup>tm1.1Enl</sup>/Bmpr2<sup>tm1.1Enl</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129S4/SvJae * FVB	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:18663089	20120809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297554	Elp1<sup>tm1Id</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome		MGI:5444514	Elp1<sup>tm1Id</sup>/Elp1<sup>tm1Id</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22922231	20150306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297554	Elp1<sup>tm1Id</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24760006	20150306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307256	Brca1<sup>tm1Brn</sup>/Brca1<sup>tm1.1Jjon</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22172724	20120227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301555	Cxcr4<sup>tm1.1Bala</sup>/Cxcr4<sup>+</sup>  [background:] B6.129S2-Cxcr4<sup>tm1.1Bala</sup>	is_model_of	DOID:0060591	WHIM syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22438253	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045984	Syn2<sup>tm1Pggd</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:23236212	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045984	Syn2<sup>tm1Pggd</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:24962993	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045984	Syn2<sup>tm1Pggd</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:3045985	Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24009558	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452245	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Csnk1d)#Mfla/0  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:20145109	20100518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028388	Pde6b<sup>rd1-3H</sup>/Pde6b<sup>rd1-3H</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5006763	Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050679	blue cone monochromacy		MGI:6259805	Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>/Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28751656	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620122	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup> Tg(Ins2-GP)34-20Olds/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10553062	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857940	Msh2<sup>tm1Mak</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25036629	20150521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6887477	Litaf<sup>tm1.1Cwc</sup>	is_implicated_in	DOID:0110151	Charcot-Marie-Tooth disease type 1C		MGI:6887866	Litaf<sup>tm1.1Cwc</sup>/Litaf<sup>tm1.1Cwc</sup>  [background:] B6.Cg-Litaf<sup>tm1.1Cwc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23576546	20220310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6725084	Clcn1<sup>m1Btlr</sup>	is_implicated_in	DOID:2106	myotonia congenita		MGI:6725719	Clcn1<sup>m1Btlr</sup>/Clcn1<sup>m1Btlr</sup>  [background:] C57BL/6J-Clcn1<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302242	Tg(CMV-MYOC*Y437H)#Vcs	is_implicated_in	DOID:1070	primary open angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:22328638	20130611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302242	Tg(CMV-MYOC*Y437H)#Vcs	is_implicated_in	DOID:1070	primary open angle glaucoma		MGI:5302243	Tg(CMV-MYOC*Y437H)#Vcs/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:21821918	20130611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5704141	Pcdh15<sup>roda</sup>	is_implicated_in	DOID:0110481	autosomal recessive nonsyndromic deafness 23		MGI:5704195	Pcdh15<sup>roda</sup>/Pcdh15<sup>roda</sup>  [background:] BALB/c-Pcdh15<sup>roda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24044941	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693255	Tg(Myh6-Tnnt2*R92L)1Jcf	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:30586744	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693255	Tg(Myh6-Tnnt2*R92L)1Jcf	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:5908986	Tg(Myh6-Tnnt2*R92L)1Jcf/0  [background:] B6.Cg-Tg(Myh6-Tnnt2*R92L)1Jcf			ECO:0000033	author statement supported by traceable reference	PMID:16326803	20200623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646170	Tg(Thy1-PSEN1*M146V)#Jiri	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16774924	20190604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646170	Tg(Thy1-PSEN1*M146V)#Jiri	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20600435	20190604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582784	Ighm<sup>tm1(Bcl6)Rdf</sup>/?  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:15894265	20160427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819719	Tg(Tnnt2-TNNT2*R92Q)M-2Ajm	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819719	Tg(Tnnt2-TNNT2*R92Q)M-2Ajm	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:4819727	Tg(Tnnt2-TNNT2*R92Q)M-2Ajm/0  [background:] involves: C3H * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9788962	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679024	Ikbkg<sup>tm1.1Mpa</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:24802098	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679024	Ikbkg<sup>tm1.1Mpa</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:3700375	Ikbkg<sup>tm1.1Mpa</sup>/Ikbkg<sup>tm1.1Mpa</sup> Tg(Alb1-cre)7Gsc/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17292824	20150601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177208	Fxn<sup>tm2Mkn</sup>/Fxn<sup>tm2.1Mkn</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:11175786	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6715338	Fmr1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:6715340	Fmr1<sup>tm1.1Ics</sup>/Fmr1<sup>tm1.1Ics</sup>  [background:] C57BL/6-Fmr1<sup>tm1.1Ics</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33692361	20210614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6766586	Hand1<sup>tm5Abfi</sup>	is_not_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6766587	Hand1<sup>tm5Abfi</sup>/Hand1<sup>+</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:29016838	20211012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6766586	Hand1<sup>tm5Abfi</sup>	is_not_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6766588	Hand1<sup>tm5Abfi</sup>/Hand1<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29016838	20211012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6766586	Hand1<sup>tm5Abfi</sup>	is_not_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6766589	Hand1<sup>tm5Abfi</sup>/Hand1<sup>+</sup> Tg(Mef2c-cre)2Blk/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29016838	20211012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5780077	Braf<sup>tm1Mmcm</sup>/Braf<sup>+</sup> Tg(Tg-cre/ERT2)#Mmcm/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21512141	20160708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702269	Ush2a<sup>tm1Tili</sup>/Ush2a<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110838	Usher syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:17360538	20070409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613518	Mtmr2<sup>tm1Ueli</sup>/Mtmr2<sup>tm1Ueli</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110191	Charcot-Marie-Tooth disease type 4B1						ECO:0000033	author statement supported by traceable reference	PMID:16249189	20060224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7518551	Lmna<sup>em1Fenz</sup>	is_implicated_in	DOID:3911	progeria		MGI:7518590	Lmna<sup>em1Fenz</sup>/Lmna<sup>+</sup>  [background:] C57BL/6-Lmna<sup>em1Fenz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36583724	20230816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849420	Gars1<sup>C201R</sup>/Gars1<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH * C57BL/6J	is_model_of	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:22144914	20120302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849420	Gars1<sup>C201R</sup>/Gars1<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH * C57BL/6J	is_model_of	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000033	author statement supported by traceable reference	PMID:19470612	20120302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427084	Polb<sup>tm1.1Jbsw</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5427085	Polb<sup>tm1.1Jbsw</sup>/Polb<sup>tm1.1Jbsw</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24388753	20140715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5605699	Prom1<sup>rd19</sup>	is_implicated_in	DOID:0110376	retinitis pigmentosa 41		MGI:5605714	Prom1<sup>rd19</sup>/Prom1<sup>rd19</sup>  [background:] B6.BXD83-Prom1<sup>rd19</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:5605698	20141205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6783437	Adamts10<sup>em1Jku</sup>	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:6783439	Adamts10<sup>em1Jku</sup>/Adamts10<sup>em1Jku</sup>  [background:] C57BL/6J-Adamts10<sup>em1Jku</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34424262	20211029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7258422	Alx1<sup>em1Jian</sup>	is_implicated_in	DOID:0081047	frontonasal dysplasia 3		MGI:7336692	Alx1<sup>em1Jian</sup>/Alx1<sup>em1Jian</sup>  [background:] C57BL/6N-Alx1<sup>em1Jian</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35127681	20220920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5689121	Tfrc<sup>tm3.1Nca</sup>	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:7339041	Tfrc<sup>tm3.1Nca</sup>/Tfrc<sup>tm3.1Nca</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:27362800	20220922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908402	Gt(ROSA)26Sor<sup>tm2(CARD11*L225LI)Jrld</sup>	is_implicated_in	DOID:0050745	diffuse large B-cell lymphoma		MGI:5908453	Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup> Gt(ROSA)26Sor<sup>tm2(CARD11*L225LI)Jrld</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26668357	20170907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5660917	Slc7a8<sup>tm1Geno</sup>	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:6323255	Slc7a8<sup>tm1Geno</sup>/Slc7a8<sup>tm1Geno</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29355479	20190716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907163	Flnc<sup>tm1.1Rsdf</sup>	is_implicated_in	DOID:0080096	myofibrillar myopathy 5		MGI:5907165	Flnc<sup>tm1.1Rsdf</sup>/Flnc<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26472074	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907163	Flnc<sup>tm1.1Rsdf</sup>	is_implicated_in	DOID:0080096	myofibrillar myopathy 5						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491268	Tbc1d32<sup>b2b2284Clo</sup>	is_implicated_in	DOID:1935	Bardet-Biedl syndrome		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415584	Scn5a<sup>tm1.1Iba</sup>	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:6415595	Scn5a<sup>tm1.1Iba</sup>/Scn5a<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30144447	20200508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302222	Lzts2<sup>tm1.1Zsu</sup>	is_implicated_in	DOID:18	urinary system disease		MGI:5302224	Lzts2<sup>tm1.1Zsu</sup>/Lzts2<sup>tm1.1Zsu</sup>  [background:] B6.Cg-Lzts2<sup>tm1.1Zsu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21949185	20170619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4462423	Sall1<sup>tm1.1Mrau</sup>/Sall1<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0050887	Townes-Brocks syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18470945	20100730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934893	Col4a3<sup>tm1Jhm</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23303673	20140416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934893	Col4a3<sup>tm1Jhm</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24262794	20140416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934893	Col4a3<sup>tm1Jhm</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:2176903	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24262794	20140416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934893	Col4a3<sup>tm1Jhm</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:2176903	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8947561	20140416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763763	Kl<sup>ecalc2</sup>	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:5903847	Kl<sup>ecalc2</sup>/Kl<sup>ecalc2</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25860694	20170703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563124	Clcn7<sup>tm1.1Mjec</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:29501587	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563124	Clcn7<sup>tm1.1Mjec</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563125	Clcn7<sup>tm1.1Mjec</sup>/Clcn7<sup>+</sup>  [background:] involves: 129 * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563124	Clcn7<sup>tm1.1Mjec</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563141	Clcn7<sup>tm1.1Mjec</sup>/Clcn7<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157964	Tcf4<sup>em2Bdph</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157970	Tcf4<sup>em2Bdph</sup>/?  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157964	Tcf4<sup>em2Bdph</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32015540	20201216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844658	Myf6<sup>tm1(cre)Mrc</sup>/Myf6<sup>+</sup> Pax3<sup>tm1Mrc</sup>/Pax3<sup>tm1Mrc</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:15489287	20090519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431984	Tg(SNCA*E46K)3Elan	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5509299	Tg(SNCA*E46K)3Elan/?  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	MGI:5509204	20131003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437296	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Smad1<sup>tm2Rob</sup>/Smad1<sup>tm2.1Rob</sup> Smad5<sup>tm1Huy</sup>/Smad5<sup>tm1Huy</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:19819941	20100316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7442138	Ccdc34<sup>em1Fzg</sup>	is_implicated_in	DOID:0111910	spermatogenic failure		MGI:7442184	Ccdc34<sup>em1Fzg</sup>/Ccdc34<sup>em1Fzg</sup>  [background:] C57BL/6-Ccdc34<sup>em1Fzg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34348960	20230308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6492209	Lrrc7<sup>Tg(Myl2-TSPYL)1Sich</sup>	is_implicated_in	DOID:0060037	developmental disorder of mental health		MGI:6492211	Lrrc7<sup>Tg(Myl2-TSPYL)1Sich</sup>/Lrrc7<sup>Tg(Myl2-TSPYL)1Sich</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31582721	20210115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705135	Slc7a14<sup>em1Jqu</sup>	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:5705137	Slc7a14<sup>em1Jqu</sup>/Slc7a14<sup>em1Jqu</sup>  [background:] C57BL/6-Slc7a14<sup>em1Jqu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6501143	Atrip<sup>tm1.1Pof</sup>	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:6505486	Atrip<sup>tm1.1Pof</sup>/Atrip<sup>tm1.1Pof</sup> Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32994318	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7336100	Sdccag8<sup>em2Lji</sup>	is_implicated_in	DOID:0110138	Bardet-Biedl syndrome 16		MGI:7336110	Sdccag8<sup>em2Lji</sup>/Sdccag8<sup>em2Lji</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:35503560	20220914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3821619	A<sup>iy</sup>/A<sup>iy</sup>  [background:] C3H/HeJ-A<sup>iy</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:5798139	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432223	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819006	Igh<sup>tm1(Myc)Janz</sup>/Igh<sup>+</sup> Tg(Emu-FGFR3)A5Wmk/0  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:20393505	20100812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5565209	Col6a3<sup>tm2.1Chu</sup>	is_implicated_in	DOID:0050558	Ullrich congenital muscular dystrophy		MGI:5565211	Col6a3<sup>tm2.1Chu</sup>/Col6a3<sup>+</sup>  [background:] B6.129(Cg)-Col6a3<sup>tm2.1Chu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24563484	20140522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:24046374	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:28255463	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22633921	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25347860	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5660859	Nlgn3<sup>tm1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24995986	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758949	Nlgn3<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3758961	Nlgn3<sup>tm1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17823315	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6511094	Agtrap<sup>tm1Tamk</sup>	is_implicated_in	DOID:0060158	acquired metabolic disease		MGI:6511096	Agtrap<sup>tm1Tamk</sup>/Agtrap<sup>tm1Tamk</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23902639	20210318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681522	Ar<sup>tm1Ska</sup>/Y Tg(CMV-cre)1Ipc/?  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12943692	20081106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040285	Tg(TagRb)1Plm	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24227978	20140918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040285	Tg(TagRb)1Plm	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:21571674	20140918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040285	Tg(TagRb)1Plm	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:22266512	20140918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040285	Tg(TagRb)1Plm	is_implicated_in	DOID:768	retinoblastoma		MGI:5009467	Tg(TagRb)1Plm/?  [background:] involves: BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:1689463	20140918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5301410	Abcc1<sup>tm1Bor</sup>/Abcc1<sup>tm1Bor</sup> Tg(Thy1-APPDutch)#Jckr/0  [background:] FVB.Cg-Abcc1<sup>tm1Bor</sup> Tg(Thy1-AppDutch)#Jckr	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21881209	20120115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:26104662	20160111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3763424	Flt3<sup>tm1Dgg</sup>/Flt3<sup>tm1Dgg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17936561	20160111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763385	Flt3<sup>tm1Dgg</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3763425	Flt3<sup>tm1Dgg</sup>/Flt3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17936561	20160111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5629811	Pten<sup>tm1Engc</sup>/Pten<sup>tm1Engc</sup>  [background:] involves: CD-1	is_model_of	DOID:0060867	macrocephaly-autism syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24470394	20150415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4410603	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp-tTA)F959Sbp/Tg(Prnp-tTA)F959Sbp Tg(tetO-ATXN3)2904Olri/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:19666958	20091215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154534	Thbs1<sup>tm1Hyn</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24086667	20140619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154534	Thbs1<sup>tm1Hyn</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4361456	Thbs1<sup>tm1Hyn</sup>/Thbs1<sup>tm1Hyn</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19700744	20140619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6492321	Alkbh7<sup>tm1.1Klng</sup>	is_implicated_in	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:23572141	20210119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5776377	Shank3<sup>tm3.1Gfng</sup>/Shank3<sup>tm3.1Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26687841	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629538	Asb4<sup>tm1.2Cpat</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:5703970	Asb4<sup>tm1.2Cpat</sup>/Asb4<sup>tm1.2Cpat</sup>  [background:] involves: 129/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:27821757	20170317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5615575	Qsox1<sup>b2b2673Clo</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:5615576	Qsox1<sup>b2b2673Clo</sup>/Qsox1<sup>b2b2673Clo</sup>  [background:] C57BL/6J-Qsox1<sup>b2b2673Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451011	Ndufs4<sup>tm1.1Rpa</sup>/Ndufs4<sup>tm1.1Rpa</sup>  [background:] B6.129S4-Ndufs4<sup>tm1.1Rpa</sup>	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:22653057	20130124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5818893	Alpl<sup>tm2.1Jlm</sup>/Alpl<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:25716980	20170124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932102	Ercc6<sup>tm1Gvh</sup>	is_implicated_in	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25440059	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932102	Ercc6<sup>tm1Gvh</sup>	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:3586560	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:9150142	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932102	Ercc6<sup>tm1Gvh</sup>	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:5697073	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup>  [background:] B6J.129P2-Ercc6<sup>tm1Gvh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25762674	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6281180	Cmas<sup>tm1.1Bwei</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6402523	Cmas<sup>tm1.1Bwei</sup>/Cmas<sup>tm1.1Bwei</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:31040189	20200402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177312	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] STOCK Grhl3<sup>ct</sup>/J	is_model_of	DOID:0110563	autosomal dominant nonsyndromic deafness 36						ECO:0000033	author statement supported by traceable reference	MGI:48774	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710766	Tg(APPSWE)2576Kha/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:17215356	20071005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620949	Wasl<sup>tm1.1Ttha</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:6295452	Wasl<sup>tm1.1Ttha</sup>/Wasl<sup>tm1.1Ttha</sup> Tg(KRT14-cre)1Amc/0  [background:] involves: C57BL/6 * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28779153	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6118179	Apela<sup>tm1.2Brre</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:6118197	Apela<sup>tm1.2Brre</sup>/Apela<sup>tm1.2Brre</sup>  [background:] B6(Cg)-Apela<sup>tm1.2Brre</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28663440	20180301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857090	Whrn<sup>wi</sup>	is_implicated_in	DOID:0110840	Usher syndrome type 2D						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5819211	Rad54l<sup>em1Murr</sup>	is_implicated_in	DOID:0060252	sclerocornea						ECO:0000033	author statement supported by traceable reference	MGI:5443917	20200108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5819211	Rad54l<sup>em1Murr</sup>	is_implicated_in	DOID:0060252	sclerocornea		MGI:6288687	Rad54l<sup>em1Murr</sup>/Rad54l<sup>+</sup>  [background:] C57BL/6N-Rad54l<sup>em1Murr</sup>/MurrJ			ECO:0000033	author statement supported by traceable reference	MGI:5576271	20200108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308055	Tg(Prnp-TARDBP)3cPtrc/Tg(Prnp-TARDBP)3cPtrc  [background:] C57BL/6-Tg(Prnp-TARDBP)3cPtrc	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:20702714	20120229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5478640	Npm1<sup>tm1Hft</sup>	is_not_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5478730	Npm1<sup>tm1Hft</sup>/Npm1<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:23226219	20130507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2182592	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:9311916	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3713766	Rag2<sup>tm1Avla</sup>	is_implicated_in	DOID:0060010	Omenn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24052573	20140611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3713766	Rag2<sup>tm1Avla</sup>	is_implicated_in	DOID:0060010	Omenn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22723555	20140611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3713766	Rag2<sup>tm1Avla</sup>	is_implicated_in	DOID:0060010	Omenn syndrome		MGI:3714069	Rag2<sup>tm1Avla</sup>/Rag2<sup>tm1Avla</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17476358	20140611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664740	Add2<sup>tm1Llp</sup>/Add2<sup>tm1Llp</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10485892	20061026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814581	Tg(MT1A-Dyrk1a)#Xest/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11555628	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400348	Dnase1<sup>tm2092.1Arte</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6400352	Dnase1<sup>tm2092.1Arte</sup>/Dnase1<sup>tm2092.1Arte</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30758851	20200317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028639	Slc25a13<sup>tm1Lct</sup>	is_implicated_in	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:21908222	20120315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175121	Msx2<sup>tm1Rilm</sup>/Msx2<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:0060285	parietal foramina						ECO:0000033	author statement supported by traceable reference	PMID:10742104	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587766	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Balb/cOlaHsd * C57BL/6JOlaHsd	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:15888477	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437085	b2b1291Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437110	b2b1291Clo/b2b1291Clo  [background:] C57BL/6J-b2b1291Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5818891	Alpl<sup>tm2.1Jlm</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5818893	Alpl<sup>tm2.1Jlm</sup>/Alpl<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25716980	20170124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424918	Phex<sup>Mhdabap012</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5425546	Phex<sup>Mhdabap012</sup>/Phex<sup>Mhdabap012</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap012</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154694	Sgcd<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000033	author statement supported by traceable reference	PMID:18495669	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154694	Sgcd<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:3618464	Sgcd<sup>tm1Kcam</sup>/Sgcd<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10481911	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1115	sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:31462499	20191007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680668	Foxn1<sup>nu</sup>/Foxn1<sup>nu</sup>  [background:] Not Specified	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:596425	20131203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7263374	Cftr<sup>tm1.1Sdw</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:7263380	Cftr<sup>tm1.1Sdw</sup>/Cftr<sup>tm1.1Sdw</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:35392567	20220425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838502	Hmx1<sup>mpe</sup>/Hmx1<sup>mpe</sup>  [background:] C3H/HeJ-Hmx1<sup>mpe</sup>/J	is_model_of	DOID:0060482	oculoauricular syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19379485	20090501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3821614	Baz1b<sup>MommeD10</sup>/Baz1b<sup>+</sup>  [background:] involves: FVB/N	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19099580	20081230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5645783	Tg(Myh6-Htr2b)1Lum	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5907236	Tg(Myh6-Htr2b)1Lum/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12810613	20170822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N	is_model_of	DOID:10016	multiple endocrine neoplasia type 2B						ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027999	Pde6b<sup>atrd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5754842	Grm6<sup>nob7</sup>	is_implicated_in	DOID:0110865	congenital stationary night blindness 1B		MGI:5754843	Grm6<sup>nob7</sup>/Grm6<sup>nob7</sup>  [background:] C57BL/6J-Grm6<sup>nob7</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26241901	20160329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590308	Pax6<sup>4Neu</sup>/Pax6<sup>+</sup>  [background:] either: (involves: 102 * C3H) or (involves: C3H)	is_model_of	DOID:0060673	Peters anomaly						ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:10746634	20061019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663620	Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9354339	20061015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3051907	Ptprn2<sup>tm1Aln</sup>/Ptprn2<sup>tm1Aln</sup>  [background:] involves: 129S4/SvJae * C57BL/6N * NOD/LtJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12535631	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008418	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26780512	20161004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008418	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20445063	20161004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008418	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6.Cg-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21573167	20161004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521534	Scn1a<sup>tm1.1Kzy</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:6154327	Scn1a<sup>tm1.1Kzy</sup>/Scn1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:29329111	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521534	Scn1a<sup>tm1.1Kzy</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33069731	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521534	Scn1a<sup>tm1.1Kzy</sup>	is_implicated_in	DOID:0080422	Dravet syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32126198	20210204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053718	Tg(TNF)197Gkl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:1721867	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23123587	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:25613864	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23749404	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5140843	Tg(Pcp2-cre)2Mpin/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21419848	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:4880715	Tg(GFAP-cre)8Gtm/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup>  [background:] involves: 129X1/SvJ * 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21062901	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590686	Gck<sup>tm1.2Mgn</sup>/Gck<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763241	Tg(Fabp4-Phb)#Smis/0  [background:] involves: CD-1	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:24947361	20160426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175787	Hps3<sup>coa-6J</sup>/Hps3<sup>coa-6J</sup>  [background:] C3H/HeJ-Hps3<sup>coa-6J</sup>/J	is_model_of	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000033	author statement supported by traceable reference	MGI:1861465	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583530	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] involves: C57BL/6J * CD-1	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8800407	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652361	App<sup>tm1Cep</sup>/App<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811151	Vhl<sup>tm1Mcs</sup>/Vhl<sup>tm1Mcs</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:0060474	familial erythrocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:17992257	20081020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629728	Nfatc2<sup>tm1Glm</sup>/Nfatc2<sup>tm1Glm</sup> Nfatc4<sup>tm1Grc</sup>/Nfatc4<sup>tm1Grc</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16554754	20060720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7277696	Slc7a14<sup>em1Jin</sup>	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:7277716	Slc7a14<sup>em1Jin</sup>/Slc7a14<sup>em1Jin</sup>  [background:] C57BL/6J-Slc7a14<sup>em1Jin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766909	Car8<sup>wdl</sup>/Car8<sup>wdl</sup>  [background:] C57BLKS/J-Car8<sup>wdl</sup>/GrsrJ	is_model_of	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26586559	20160509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8191288	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11773599	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8952527	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:15580285	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:10204494	20060511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463579	Anks6<sup>b2b1801.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5465103	Anks6<sup>b2b1801.1Clo</sup>/Anks6<sup>b2b1801.1Clo</sup>  [background:] C57BL/6J-Anks6<sup>b2b1801.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634817	Del(7Slx1b-Sept1)4Aam/0  [background:] B6129S-Del(7Slx1b-Sept1)4Aam/J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25698753	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6431857	Cfap69<sup>em1Fzh</sup>	is_implicated_in	DOID:0111929	spermatogenic failure 24		MGI:6431858	Cfap69<sup>em1Fzh</sup>/Cfap69<sup>em1Fzh</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30415212	20200911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7280773	Ppp4c<sup>em1Qys</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7281440	Ppp4c<sup>em1Qys</sup>/Ppp4c<sup>em1Qys</sup> Tg(Stra8-icre)1Reb/0  [background:] involves: 129S/SvEv * C57BL/6 * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:33543287	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687965	Gba1<sup>tm1Karl</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:28186340	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687965	Gba1<sup>tm1Karl</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:27234572	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687965	Gba1<sup>tm1Karl</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:24064337	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7491944	Ano5<sup>em2Huyi</sup>	is_implicated_in	DOID:0111533	gnathodiaphyseal dysplasia		MGI:7492024	Ano5<sup>em2Huyi</sup>/Ano5<sup>em2Huyi</sup>  [background:] C57BL/6-Ano5<sup>em2Huyi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34841576	20230622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192354	Hprt1<sup>tm1(MAPT)Dph</sup>	is_implicated_in	DOID:680	tauopathy		MGI:6192446	Hprt1<sup>tm1(MAPT)Dph</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27297240	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619388	Ins1<sup>tm1Jja</sup>/Ins1<sup>tm1Jja</sup> Tg(Ins2*Y16A)1Ell/0  [background:] NOD.Cg-Ins1<sup>tm1Jja</sup> Tg(Ins2*Y16A)1Ell	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15889095	20060526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583531	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] C.B6(Cg)-Cys1<sup>cpk</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11004214	20050812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179136	Tbx1<sup>tm1Bld</sup>	is_implicated_in	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000033	author statement supported by traceable reference	PMID:25452432	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:24232002	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:19773742	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:20971723	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:22574107	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:24094090	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease		MGI:2183938	Gla<sup>tm1Kul</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22574107	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861794	Gla<sup>tm1Kul</sup>	is_implicated_in	DOID:14499	Fabry disease		MGI:2183938	Gla<sup>tm1Kul</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9122231	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183411	Alpl<sup>tm1Jlm</sup>	is_implicated_in	DOID:0110914	infantile hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:27466191	20170222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183411	Alpl<sup>tm1Jlm</sup>	is_implicated_in	DOID:0110914	infantile hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:23427088	20170222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183411	Alpl<sup>tm1Jlm</sup>	is_implicated_in	DOID:0110914	infantile hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:26605996	20170222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183411	Alpl<sup>tm1Jlm</sup>	is_implicated_in	DOID:0110914	infantile hypophosphatasia		MGI:5787924	Alpl<sup>tm1Jlm</sup>/Alpl<sup>tm1Jlm</sup>  [background:] involves: 129S1/SvImJ * 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22991301	20170222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183411	Alpl<sup>tm1Jlm</sup>	is_implicated_in	DOID:0110914	infantile hypophosphatasia		MGI:2654850	Alpl<sup>tm1Jlm</sup>/Alpl<sup>tm1Jlm</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9056646	20170222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680502	Gba1<sup>tm3Ggb</sup>/Gba1<sup>tm3Ggb</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705324	Alk<sup>tm1.1Ics</sup>	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29321660	20180904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805029	Bard1<sup>tm2Thl</sup>/Bard1<sup>tm2Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129/Sv * 129S1/Sv * C57BL/6J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18443292	20130918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661818	Celsr1<sup>Crsh</sup>/Celsr1<sup>+</sup> Scrib<sup>Crc</sup>/Scrib<sup>+</sup>  [background:] C3H.Cg-Scrib<sup>Crc</sup> Celsr1<sup>Crsh</sup>	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:25128525	20150915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712362	Duox2<sup>thyd</sup>/Duox2<sup>thyd</sup>  [background:] B6(129)-Duox2<sup>thyd</sup>/J	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:17440044	20070622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4940545	Dag1<sup>tm4.1Kcam</sup>/Dag1<sup>tm4.1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110293	autosomal recessive limb-girdle muscular dystrophy type 2P						ECO:0000033	author statement supported by traceable reference	PMID:21388311	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796605	Tg(Alb-TAg)1Gjh	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23661267	20140113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796605	Tg(Alb-TAg)1Gjh	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3797588	Tg(Alb-TAg)1Gjh/0  [background:] C3.Cg-Tg(Alb-TAg)1Gjh			ECO:0000033	author statement supported by traceable reference	PMID:16397233	20140113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136847	App<sup>tm1Dbo</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24919190	20150313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136847	App<sup>tm1Dbo</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174917	App<sup>tm1Dbo</sup>/App<sup>tm1Dbo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10188929	20150313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388888	Cln3<sup>tm1.1Mem</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:30837943	20190621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388888	Cln3<sup>tm1.1Mem</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:24736558	20190621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388888	Cln3<sup>tm1.1Mem</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:30086172	20190621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388888	Cln3<sup>tm1.1Mem</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:22701626	20190621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388888	Cln3<sup>tm1.1Mem</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3044770	Cln3<sup>tm1.1Mem</sup>/Cln3<sup>tm1.1Mem</sup>  [background:] involves: 129S/SvEv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12374761	20190621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6682077	Prkar1a<sup>tm1.1Geno</sup>	is_implicated_in	DOID:14669	acrodysostosis		MGI:6682080	Prkar1a<sup>tm1.1Geno</sup>/Prkar1a<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27589370	20210409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793714	Tg(Myh6*)131Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793714	Tg(Myh6*)131Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:27199124	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793714	Tg(Myh6*)131Lnwd	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:5286085	Tg(Myh6*)131Lnwd/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8585273	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311563	Plec<sup>tm7.1Gwi</sup>	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:5311585	Plec<sup>tm7.1Gwi</sup>/Plec<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22144912	20120321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311563	Plec<sup>tm7.1Gwi</sup>	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:5311582	Plec<sup>tm7.1Gwi</sup>/Plec<sup>tm7.1Gwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22144912	20120321	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5289692	Slc6a19<sup>tm1Dgen</sup>/Slc6a19<sup>tm1Dgen</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:1060	Hartnup disease						ECO:0000033	author statement supported by traceable reference	PMID:21636576	20111007	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14645205	20061031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:17029828	20061031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6441050	Hdac4<sup>em1Hcu</sup>	is_implicated_in	DOID:8670	eating disorder		MGI:6441085	Hdac4<sup>em1Hcu</sup>/Hdac4<sup>em1Hcu</sup>  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:32153359	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6441050	Hdac4<sup>em1Hcu</sup>	is_implicated_in	DOID:8670	eating disorder		MGI:6441077	Hdac4<sup>em1Hcu</sup>/Hdac4<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:27884425	20200710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384594	Tg(Mpz)88.4Mfel	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:20878767	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384594	Tg(Mpz)88.4Mfel	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6276671	Tg(Mpz)88.4Mfel/0  [background:] FVB/N-Tg(Mpz)88.4Mfel			ECO:0000033	author statement supported by traceable reference	PMID:11086005	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0050790	fibular hypoplasia and complex brachydactyly						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558103	Tg(CMV-SALL4_iB)#Chai	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5558108	Tg(CMV-SALL4_iB)#Chai/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16763212	20140411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:12576554	20070829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:15111796	20070829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:15979918	20070829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5517595	Snca<sup>tm1.1Koks</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23219665	20131114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5517595	Snca<sup>tm1.1Koks</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5517669	Snca<sup>tm1.1Koks</sup>/Snca<sup>+</sup>  [background:] either: B6.129P2-Snca<sup>tm1.1Koks</sup> or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:18622040	20131114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896835	Tg(Thy1-UBQLN2*P497S)3Mont/?  [background:] involves: C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000033	author statement supported by traceable reference	PMID:27834214	20170509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677400	Slc7a9<sup>tm1Nune</sup>/Slc7a9<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:12915471	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5552945	Dnah5<sup>b2b2395Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796438	Scnn1b<sup>tm1.1Ipt</sup>/Scnn1b<sup>tm1.1Ipt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N	is_model_of	DOID:0050477	Liddle syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10589691	20080709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583662	Psen1<sup>tm1Tak</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:27143420	20160926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583662	Psen1<sup>tm1Tak</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:5795582	Psen1<sup>tm1Tak</sup>/Psen1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16377636	20160926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5829037	Tg(Thy1-UBQLN2*P497S)3Mont	is_implicated_in	DOID:0060206	amyotrophic lateral sclerosis type 15		MGI:5896835	Tg(Thy1-UBQLN2*P497S)3Mont/?  [background:] involves: C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27834214	20170509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5489751	Gja8<sup>R205G</sup>	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:5489760	Gja8<sup>R205G</sup>/Gja8<sup>R205G</sup>  [background:] B6.Cg-Gja8<sup>R205G</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23300808	20130610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908700	Ssu2<sup>tm1.1Xmx</sup>	is_implicated_in	DOID:701	dentin dysplasia		MGI:5908863	Ssu2<sup>tm1.1Xmx</sup>/Ssu2<sup>tm1.1Xmx</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27680507	20170913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908700	Ssu2<sup>tm1.1Xmx</sup>	is_implicated_in	DOID:701	dentin dysplasia		MGI:5908862	Ssu2<sup>tm1.1Xmx</sup>/Ssu2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27680507	20170913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311385	Dnah5<sup>b2b1134Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4839313	Tg(CAG-RPS19*R62W)#Dmb	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:4839332	Tg(CAG-RPS19*R62W)#Dmb/0 Tg(Prnp-GFP/cre)1Blw/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20606162	20101122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6390917	Chd8<sup>tm1.1Csbd</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6390918	Chd8<sup>tm1.1Csbd</sup>/Chd8<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30104731	20200218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665845	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:8770874	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2665845	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:8402911	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7488215	St6galnac1<sup>em1Len</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:7488220	St6galnac1<sup>em1Len</sup>/St6galnac1<sup>em1Len</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:35303419	20230608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763101	Tg(MMTV-LPAR2)3Gbm/Tg(MMTV-LPAR2)3Gbm  [background:] FVB/N-Tg(MMTV-LPAR2)3Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710691	Tg(Prnp-ITM2B/APP695*40)1Emcg	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:33766652	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710691	Tg(Prnp-ITM2B/APP695*40)1Emcg	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3710761	Tg(Prnp-ITM2B/APP695*40)1Emcg/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16039562	20210720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388388	Cnga3<sup>tm1Biel</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20160419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858040	Fancc<sup>tm1Mab</sup>	is_implicated_in	DOID:0111087	Fanconi anemia complementation group C						ECO:0000033	author statement supported by traceable reference	PMID:26676373	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858040	Fancc<sup>tm1Mab</sup>	is_implicated_in	DOID:0111087	Fanconi anemia complementation group C						ECO:0000033	author statement supported by traceable reference	PMID:25056314	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858040	Fancc<sup>tm1Mab</sup>	is_implicated_in	DOID:0111087	Fanconi anemia complementation group C		MGI:2450130	Fancc<sup>tm1Mab</sup>/Fancc<sup>tm1Mab</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8630504	20160819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052111	Tg(Mapt-MAPT*)#Hanr	is_implicated_in	DOID:680	tauopathy		MGI:5052112	Tg(Mapt-MAPT*)#Hanr/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18490011	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4939894	Rassf5<sup>tm1Kina</sup>/Rassf5<sup>tm1Kina</sup>  [background:] B6.Cg-Rassf5<sup>tm1Kina</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:21194982	20110307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849030	Fgfrl1<sup>tm1.1Ptew</sup>/Fgfrl1<sup>tm1.1Ptew</sup>  [background:] B6.129-Fgfrl1<sup>tm1.1Ptew</sup>	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19383940	20090626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843174	Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup> Ep300<sup>tm2Reck</sup>/Ep300<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:17513743	20090506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526160	Rai1<sup>tm1Jrl</sup>	is_implicated_in	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22578325	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526160	Rai1<sup>tm1Jrl</sup>	is_implicated_in	DOID:0060768	Smith-Magenis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25127133	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526160	Rai1<sup>tm1Jrl</sup>	is_implicated_in	DOID:0060768	Smith-Magenis syndrome		MGI:4835032	Rai1<sup>tm1Jrl</sup>/Rai1<sup>+</sup>  [background:] B6.129S7-Rai1<sup>tm1Jrl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20663924	20150402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526160	Rai1<sup>tm1Jrl</sup>	is_implicated_in	DOID:0060768	Smith-Magenis syndrome		MGI:3577939	Rai1<sup>tm1Jrl</sup>/Rai1<sup>+</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15746153	20150402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5636613	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(KLK3-cre)13Saa/0  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:24986896	20150520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6118180	Slc25a46<sup>atc</sup>	is_implicated_in	DOID:0080068	Charcot-Marie-Tooth disease type 6		MGI:6286393	Slc25a46<sup>atc</sup>/Slc25a46<sup>atc</sup>  [background:] B6.Cg-Slc25a46<sup>atc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28376086	20190408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819230	Ikzf1<sup>tm1Kast</sup>/Ikzf1<sup>+</sup> Tg(BCR/ABL)623Hkp/0  [background:] involves: 129S2/SvPas * C57BL/6 * CBA	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20393504	20100816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412061	Tg(SNCA*A53T)1Nbm	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25351739	20150818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582588	Dock7<sup>m</sup>/Dock7<sup>m</sup>  [background:] B6.D(Cg)-Dock7<sup>m</sup>	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9475748	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2388398	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] B6.KB2/Rn-Cln8<sup>mnd</sup>	is_model_of	DOID:0110723	neuronal ceroid lipofuscinosis 8						ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2388398	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] B6.KB2/Rn-Cln8<sup>mnd</sup>	is_model_of	DOID:0110723	neuronal ceroid lipofuscinosis 8						ECO:0000033	author statement supported by traceable reference	PMID:7683855	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926960	Nkx3-1<sup>tm1Mms</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:28775169	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926960	Nkx3-1<sup>tm1Mms</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23538858	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926960	Nkx3-1<sup>tm1Mms</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:2175152	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>tm1Mms</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10215624	20181101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926960	Nkx3-1<sup>tm1Mms</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:2175153	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10215624	20181101	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292662	Tg(tetO-TAg)2-5Hiwa/0  [background:] involves: C57BL/6	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:20664939	20111020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292662	Tg(tetO-TAg)2-5Hiwa/0  [background:] involves: C57BL/6	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19020752	20111020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857192	Il2ra<sup>tm1Dw</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27085137	20170417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857192	Il2ra<sup>tm1Dw</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5883306	Il2ra<sup>tm1Dw</sup>/Il2ra<sup>tm1Dw</sup>  [background:] B6.129S4-Il2ra<sup>tm1Dw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17207605	20170417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387402	Stk11<sup>tm1.1Rdp</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25519892	20150825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807705	Hmx1<sup>dmbo</sup>	is_implicated_in	DOID:0060482	oculoauricular syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22736458	20130325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807705	Hmx1<sup>dmbo</sup>	is_implicated_in	DOID:0060482	oculoauricular syndrome		MGI:3838401	Hmx1<sup>dmbo</sup>/Hmx1<sup>dmbo</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19379485	20130325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784993	Lepr<sup>Db-2Btlr</sup>/Lepr<sup>Db-2Btlr</sup>  [background:] C57BL/6J-Lepr<sup>Db-2Btlr</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:3778962	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838162	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>tm1Kat</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:12468647	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576369	Park7<sup>tm1Dsp</sup>/Park7<sup>tm1Dsp</sup>  [background:] B6.129P2-Park7<sup>tm1Dsp</sup>	is_model_of	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:23019375	20150303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056368	Ccdc39<sup>prh</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5056384	Ccdc39<sup>prh</sup>/Ccdc39<sup>prh</sup>  [background:] involves: A/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29317443	20180222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714853	Lig4<sup>tiny</sup>/Lig4<sup>tiny</sup>  [background:] C57BL/6-Lig4<sup>tiny</sup>	is_model_of	DOID:0060021	DNA ligase IV deficiency						ECO:0000033	author statement supported by traceable reference	PMID:17554302	20090727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177237	Brca2<sup>tm1Arge</sup>/Brca2<sup>tm2Arge</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11494122	20060807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176876	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup> Utrn<sup>tm1Jrs</sup>/Utrn<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9288752	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176876	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup> Utrn<sup>tm1Jrs</sup>/Utrn<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:10559919	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5800483	Tg(Myh6*/tetO-SCN5A*F1759A)#Marx	is_implicated_in	DOID:0050650	familial atrial fibrillation		MGI:5800485	Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0  [background:] involves: C57BL/6 * CBA * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:26595809	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431499	Gm572<sup>b2b1167Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660499	Jup<sup>tm1Ruiz</sup>/Jup<sup>+</sup> Tg(Myh6-Jup*)1Ajm/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:22021931	20150831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5576520	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Wap-cre)11738Mam/0 Tg(Wap-Hgf)402Mig/0  [background:] FVB.Cg-Ctnnb1<sup>tm1Mmt</sup> Tg(Wap-cre)11738Mam Tg(Wap-Hgf)402Mig	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24290754	20140808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385350	Hfe<sup>tm1.1Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22531912	20121029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385350	Hfe<sup>tm1.1Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655513	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20121029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385350	Hfe<sup>tm1.1Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655512	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20121029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385350	Hfe<sup>tm1.1Nca</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655503	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10791995	20121029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471773	Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>/Khdrbs2<sup>+</sup>  [background:] FVB/N-Khdrbs2<sup>Tg(LRRK2*R1441G)135Cjli</sup>/J	is_model_of	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:23936174	20140528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431494	b2b904Clo	is_implicated_in	DOID:114	heart disease		MGI:5431510	b2b904Clo/b2b904Clo  [background:] C57BL/6J-b2b904Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5780982	Nexn<sup>tm1.1Zhh</sup>	is_implicated_in	DOID:0110326	hypertrophic cardiomyopathy 20		MGI:5780987	Nexn<sup>tm1.1Zhh</sup>/Nexn<sup>tm1.1Zhh</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26659360	20160721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5475270	Gclc<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:83	cataract						ECO:0000033	author statement supported by traceable reference	PMID:28177569	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5475270	Gclc<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:83	cataract		MGI:5475286	Gclc<sup>tm1c(EUCOMM)Wtsi</sup>/Gclc<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Cryaa-cre)10Mlr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23226398	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044171	Amacr<sup>tm1Jkh</sup>	is_implicated_in	DOID:0060602	alpha-methylacyl-CoA racemase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:26248199	20160623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044171	Amacr<sup>tm1Jkh</sup>	is_implicated_in	DOID:0060602	alpha-methylacyl-CoA racemase deficiency		MGI:3044685	Amacr<sup>tm1Jkh</sup>/Amacr<sup>tm1Jkh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15016763	20160623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665286	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:16899370	20061031	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836169	Rho<sup>tm1Phm</sup>/Rho<sup>tm1Phm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:9020854	20130619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6368631	Afg3l2<sup>tm1.1Alfb</sup>	is_implicated_in	DOID:0050977	spinocerebellar ataxia type 28						ECO:0000033	author statement supported by traceable reference	PMID:30389403	20191030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583788	Itga6<sup>tm1Egl</sup>/Itga6<sup>tm1Egl</sup>  [background:] either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129S2/SvPas * C57BL/6 * CD-1)	is_model_of	DOID:0060737	junctional epidermolysis bullosa Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:8673141	20050817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439490	Ccm2<sup>tm1Mlkn</sup>	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:6279212	Ccm2<sup>tm1Mlkn</sup>/Ccm2<sup>tm1Mlkn</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:27513872	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176850	Gm2a<sup>tm1Rlp</sup>/Gm2a<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:4795	GM2 gangliosidosis, AB variant						ECO:0000033	author statement supported by traceable reference	PMID:9223328	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009553	Rb1<sup>tm1Tyj</sup>/Rb1<sup>+</sup> Tg(Th-MYCN)41Waw/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:9199335	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622656	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup> Ldlr<sup>tm1Her</sup>	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:11445560	20120221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420229	Tg(Thy1-APPSweArc)BLngn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:26892305	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420229	Tg(Thy1-APPSweArc)BLngn	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25089901	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420229	Tg(Thy1-APPSweArc)BLngn	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5708587	Tg(Thy1-APPSweArc)BLngn/0  [background:] B6J.Cg-Tg(Thy1-APPSweArc)BLngn			ECO:0000033	author statement supported by traceable reference	PMID:20615433	20160908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286246	Tg(Prnp-MAPT*P301S)50Hiw	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:6286248	Tg(Prnp-MAPT*P301S)50Hiw/0  [background:] B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw			ECO:0000033	author statement supported by traceable reference	PMID:24406748	20190405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286246	Tg(Prnp-MAPT*P301S)50Hiw	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:30510257	20190405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149780	Daam1<sup>tm1.1Tpy</sup>	is_implicated_in	DOID:0060036	intrinsic cardiomyopathy		MGI:6150918	Daam1<sup>tm1.1Tpy</sup>/Daam1<sup>tm1.1Tpy</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:26526197	20180417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:9501313	20050914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819394	Gt(ROSA)26Sor<sup>tm1(Kcnj11*V59M)Fmas</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:20595581	20100817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2388134	Rxfp2<sup>tm1Aia</sup>/Rxfp2<sup>tm1Aia</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:12217959	20151207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530450	Nrg1<sup>tm2Zhou</sup>/Nrg1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:12145742	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2183672	Tg(NEFH)200Jpj/Tg(NEFH)200Jpj  [background:] Not Specified	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651673	Btk<sup>tm1Wk</sup>/Btk<sup>tm1Wk</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:7552994	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576767	Tg(Cryaa-TAg,Ins2-CALM1)26Ove/0  [background:] FVB(Cg)-Tg(Cryaa-Tag,Ins2-CALM1)26Ove/PneJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:2673540	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449063	Tg(Krt18-EGFP,-TAg121)36Ysng	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7309151	Zng1<sup>em2Skan</sup>	is_implicated_in	DOID:0080205	CAKUT		MGI:7309156	Zng1<sup>em2Skan</sup>/Zng1<sup>em2Skan</sup>  [background:] C57BL/6N-Zng1<sup>em2Skan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31862704	20220705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715473	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] 129S6/SvEvTac-Cln3<sup>tm1Nbm</sup>	is_model_of	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000033	author statement supported by traceable reference	PMID:15326100	20070720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587727	Nphs1<sup>tm1Rkl</sup>/Nphs1<sup>tm1Rkl</sup>  [background:] involves: 129S2/SvPasCrl	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12039968	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3715982	Inpp5d<sup>tm1Rav</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:31451659	20191113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3715982	Inpp5d<sup>tm1Rav</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6376530	Cd79a<sup>tm1(cre)Reth</sup>/Cd79a<sup>+</sup> Inpp5d<sup>tm1Rav</sup>/Inpp5d<sup>tm1Rav</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22078222	20191113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584120	Crygs<sup>Opj</sup>/Crygs<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK	is_model_of	DOID:0110240	cataract 20 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11121426	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584120	Crygs<sup>Opj</sup>/Crygs<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK	is_model_of	DOID:0110240	cataract 20 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:8812411	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449076	Tg(TNF)3647Gkl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:21809421	20150430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529521	Tg(ACTB-THRB*)#Syc/0  [background:] involves: CD-1	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:10454355	20140122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5490471	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] involves: C57BL/6J * C57BL/Fa	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:20643756	20130614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5490471	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] involves: C57BL/6J * C57BL/Fa	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23539154	20130614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521972	Tpp1<sup>tm1Plob</sup>	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000033	author statement supported by traceable reference	PMID:19429009	20160701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521972	Tpp1<sup>tm1Plob</sup>	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000033	author statement supported by traceable reference	PMID:22792360	20160701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521972	Tpp1<sup>tm1Plob</sup>	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:3522157	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15483130	20160701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521972	Tpp1<sup>tm1Plob</sup>	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:3804722	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1Plob</sup>  [background:] B6.129S1-Tpp1<sup>tm1Plob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18343701	20160701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259176	Tg(Eno2-Thrsp)#Cheo	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:6259179	Tg(Eno2-Thrsp)#Cheo/0  [background:] C57BL/6-Tg(Eno2-Thrsp)#Cheo			ECO:0000033	author statement supported by traceable reference	PMID:30138648	20181205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3760289	Otof<sup>deaf5Jcs</sup>/Otof<sup>deaf5Jcs</sup>  [background:] STOCK Otof<sup>deaf5Jcs</sup>/Kjn	is_model_of	DOID:0110535	autosomal recessive nonsyndromic deafness 9						ECO:0000033	author statement supported by traceable reference	PMID:17967520	20071207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610388	Hnf1a<sup>tm1Mya</sup>/Hnf1a<sup>tm1Mya</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:8598044	20060119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3050469	Ptpn11<sup>tm1Bgn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15273746	20090416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055194	Rasgrp2<sup>tm1Amg</sup>/Rasgrp2<sup>tm1Amg</sup>  [background:] Not Specified	is_model_of	DOID:0110912	leukocyte adhesion deficiency 3						ECO:0000033	author statement supported by traceable reference	PMID:17492052	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N	is_model_of	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:20675713	20101011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4880671	Fbn1<sup>tm1Lper</sup>/Fbn1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6 * CD-1	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21152435	20110127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6193977	Tg(Myh6-MYL2*K104E)2Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10		MGI:6193978	Tg(Myh6-MYL2*K104E)2Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24992035	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6193977	Tg(Myh6-MYL2*K104E)2Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:26906074	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444031	Dcc<sup>Tg(H2-Kb-Jak2*V617F)1Shmd</sup>	is_implicated_in	DOID:8997	polycythemia vera		MGI:5444033	Dcc<sup>Tg(H2-Kb-Jak2*V617F)1Shmd</sup>/Dcc<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18033315	20121130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560901	b2b2140Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561311	b2b2140Clo/b2b2140Clo  [background:] C57BL/6J-b2b2140Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367272	Rho<sup>R3</sup>/Rho<sup>R3</sup>  [background:] C57BL/6J-Rho<sup>R3</sup>	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:19741247	20130619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491275	b2b2350Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300204	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Scrib<sup>tm1.1Phum</sup>/Scrib<sup>tm1.1Phum</sup> Tg(Pbsn-cre)20Fwan/0  [background:] involves: 129S4/SvJae * FVB/NCrl	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:21965329	20140603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6099051	Clrn1<sup>tm1.1Ugpa</sup>	is_implicated_in	DOID:0110841	Usher syndrome type 3A		MGI:6467338	Clrn1<sup>tm1.1Ugpa</sup>/Clrn1<sup>tm1.1Ugpa</sup> Myo15a<sup>tm1.1(cre)Ugds</sup>/Myo15a<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29985171	20201016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295754	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23690466	20141017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789553	Tg(KRT19-TAg)7Eps	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5789554	Tg(KRT19-TAg)7Eps/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10980120	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789553	Tg(KRT19-TAg)7Eps	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5495816	Ddc<sup>tm1.1Nwlh</sup>	is_implicated_in	DOID:0090123	aromatic L-amino acid decarboxylase deficiency		MGI:5495915	Ddc<sup>tm1.1Nwlh</sup>/Ddc<sup>tm1.1Nwlh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23275025	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715788	Rb(12.Ts17<sup>16</sup>65Dn)2Cje/0  [background:] involves: C3H/HeSnJ * C57BL/6JEi	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15859352	20080626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3590082	Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell	is_implicated_in	DOID:820	myocarditis						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5450851	Slc45a2<sup>uw-6J</sup>/Slc45a2<sup>uw-6J</sup>  [background:] CAST/EiJ-Slc45a2<sup>uw-6J</sup>/GrsrJ	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	MGI:5449587	20130123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037943	Trf<sup>hpx</sup>/Trf<sup>+</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>	is_model_of	DOID:0050649	atransferrinemia						ECO:0000033	author statement supported by traceable reference	PMID:3681112	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037943	Trf<sup>hpx</sup>/Trf<sup>+</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>	is_model_of	DOID:0050649	atransferrinemia						ECO:0000033	author statement supported by traceable reference	MGI:1889268	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040574	Cstb<sup>tm1Rm</sup>/Cstb<sup>tm1Rm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:3535	Unverricht-Lundborg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11555622	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040574	Cstb<sup>tm1Rm</sup>/Cstb<sup>tm1Rm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:3535	Unverricht-Lundborg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9806543	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6511815	Ttn<sup>em1Kage</sup>	is_implicated_in	DOID:0110430	dilated cardiomyopathy 1G						ECO:0000033	author statement supported by traceable reference	PMID:33637999	20210323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085999	Shank3<sup>tm1.1Pfw</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5086221	Shank3<sup>tm1.1Pfw</sup>/Shank3<sup>+</sup>  [background:] B6.129S6-Shank3<sup>tm1.1Pfw</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5499103	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085999	Shank3<sup>tm1.1Pfw</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26847545	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085999	Shank3<sup>tm1.1Pfw</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20190719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3521730	Pkd1<sup>tm1Djmp</sup>/Pkd1<sup>tm1Djmp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:15496422	20050530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606460	Ppm1g<sup>tm1Dgen</sup>/Ppm1g<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846426	Cisd2<sup>tm1Tfts</sup>/Cisd2<sup>tm1Tfts</sup>  [background:] B6.129S7-Cisd2<sup>tm1Tfts</sup>	is_model_of	DOID:0110630	Wolfram syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:19451219	20090602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528480	Atrx<sup>tm1Rjg</sup>	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25452430	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528480	Atrx<sup>tm1Rjg</sup>	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome		MGI:3834848	Atrx<sup>tm1Rjg</sup>/Y Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19088125	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528480	Atrx<sup>tm1Rjg</sup>	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome		MGI:3530074	Atrx<sup>tm1Rjg</sup>/Y Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15668733	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528480	Atrx<sup>tm1Rjg</sup>	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome		MGI:3530076	Atrx<sup>tm1Rjg</sup>/Y Tg(Nes-cre)2472Pick/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15668733	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311153	Dnah5<sup>b2b601Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764832	Epm2a<sup>Tg(TcraK,TcrbK)TG-BFlv</sup>	is_implicated_in	DOID:0060058	lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:22751135	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764832	Epm2a<sup>Tg(TcraK,TcrbK)TG-BFlv</sup>	is_implicated_in	DOID:0060058	lymphoma		MGI:5461066	Epm2a<sup>Tg(TcraK,TcrbK)TG-BFlv</sup>/Epm2a<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * C57BR/cd * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:16959610	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>	is_model_of	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	MGI:76424	20050527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610986	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242049	20060123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3035835	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:14966562	20140912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655832	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] FVB.BKS-Lepr<sup>db</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12136396	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521202	Tg(Thy1-Tcf4)1Mjro/0  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23069005	20131203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046284	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: FVB/N	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:15226261	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046284	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: FVB/N	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11062270	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851237	Tg(Acta2-RAC1*G12V)33Pjgc/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:8632	Kaposi's sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:19429708	20090727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657251	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1Df</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8673137	20070306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657251	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1Df</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8670802	20070306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909303	Tg(Myh6-Tnni3*R193H)42Xhu	is_implicated_in	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:18408133	20171102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909303	Tg(Myh6-Tnni3*R193H)42Xhu	is_implicated_in	DOID:397	restrictive cardiomyopathy		MGI:5909304	Tg(Myh6-Tnni3*R193H)42Xhu/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17027633	20171102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909303	Tg(Myh6-Tnni3*R193H)42Xhu	is_implicated_in	DOID:397	restrictive cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25813360	20171102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999580	Cryab<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0110250	cataract 16 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:32833997	20200909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999580	Cryab<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0110250	cataract 16 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:26542570	20200909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999580	Cryab<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0110250	cataract 16 multiple types		MGI:5571860	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>tm1.1Ady</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23872361	20200909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934143	Ncf1<sup>tm1Shl</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:24549323	20140624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934143	Ncf1<sup>tm1Shl</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:2175140	Ncf1<sup>tm1Shl</sup>/Ncf1<sup>tm1Shl</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7650482	20140624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934143	Ncf1<sup>tm1Shl</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:4438111	Ncf1<sup>tm1Shl</sup>/Ncf1<sup>tm1Shl</sup>  [background:] B6.129S2-Ncf1<sup>tm1Shl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16843452	20140624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450928	Gata1<sup>tm1Mym</sup>/Gata1<sup>tm1Mym</sup> Tg(Gata1*)#Mym/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	is_model_of	DOID:0060888	transient myeloproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19682090	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2663995	Kit<sup>tm2Bsm</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:25572173	20150803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2663995	Kit<sup>tm2Bsm</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:25836719	20150803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2663995	Kit<sup>tm2Bsm</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor						ECO:0000033	author statement supported by traceable reference	PMID:20736294	20150803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2663995	Kit<sup>tm2Bsm</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:2663997	Kit<sup>tm2Bsm</sup>/Kit<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12754375	20150803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5532580	Clpp<sup>Gt(IST13563G11)Tigm</sup>/Clpp<sup>Gt(IST13563G11)Tigm</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0050857	Perrault syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23851121	20140129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819252	Tg(Ela1-TAg)19Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1316086	20100816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677399	Slc7a9<sup>tm1Nune</sup>/Slc7a9<sup>tm1Nune</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:12915471	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3795721	Tg(Myh6-Des*)641Rbns	is_implicated_in	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3795721	Tg(Myh6-Des*)641Rbns	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:5905194	Tg(Myh6-Des*)641Rbns/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11352891	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906252	Tg(Myh6-Snai1)B10Jcc	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906259	Tg(Myh6-Snai1)B10Jcc/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17512504	20170807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906252	Tg(Myh6-Snai1)B10Jcc	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906253	Tg(Myh6-Snai1)B10Jcc/Tg(Myh6-Snai1)B10Jcc  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17512504	20170807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5621057	Tg(SOD1*G85R/EYFP)641Alho	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5621058	Tg(SOD1*G85R/EYFP)641Alho/Tg(SOD1*G85R/EYFP)641Alho  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:19171884	20150408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663269	ckr/ckr  [background:] involves: C3H/HeRos * C57BL/10Ros	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:14709346	20081212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435702	Shank2<sup>tm1.1Tmb</sup>/Shank2<sup>tm1.1Tmb</sup>  [background:] B6.129-Shank2<sup>tm1.1Tmb</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22699619	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856917	Dnah11<sup>iv</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000033	author statement supported by traceable reference	PMID:22102620	20171107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856917	Dnah11<sup>iv</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:2172625	Dnah11<sup>iv</sup>/Dnah11<sup>iv</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	MGI:48750	20171107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192642	Cib2<sup>tm1.1Aela</sup>	is_implicated_in	DOID:0110505	autosomal recessive nonsyndromic deafness 48		MGI:6192643	Cib2<sup>tm1.1Aela</sup>/Cib2<sup>tm1.1Aela</sup>  [background:] involves: BALB/c * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29084757	20180803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581429	Tg(CMV-IgkvaD11)BCat/Tg(CMV-IgkvaD11)BCat  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22986780	20140901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843456	Avp<sup>tm1Hari</sup>	is_implicated_in	DOID:12388	neurohypophyseal diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:24675466	20210218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843456	Avp<sup>tm1Hari</sup>	is_implicated_in	DOID:12388	neurohypophyseal diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:19955494	20210218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843456	Avp<sup>tm1Hari</sup>	is_implicated_in	DOID:12388	neurohypophyseal diabetes insipidus		MGI:3843460	Avp<sup>tm1Hari</sup>/Avp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19297548	20210218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461468	Myo5b<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060775	microvillus inclusion disease		MGI:5752734	Myo5b<sup>tm1a(KOMP)Wtsi</sup>/Myo5b<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Myo5b<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26201991	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437083	Dnah11<sup>b2b1289Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437114	Dnah11<sup>b2b1289Clo</sup>/Dnah11<sup>b2b1289Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1289Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332076	Kmt2d<sup>Gt(RRT024)Byg</sup>	is_implicated_in	DOID:0060473	Kabuki syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31557133	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332076	Kmt2d<sup>Gt(RRT024)Byg</sup>	is_implicated_in	DOID:0060473	Kabuki syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31465303	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332076	Kmt2d<sup>Gt(RRT024)Byg</sup>	is_implicated_in	DOID:0060473	Kabuki syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27999180	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332076	Kmt2d<sup>Gt(RRT024)Byg</sup>	is_implicated_in	DOID:0060473	Kabuki syndrome		MGI:6515623	Kmt2d<sup>Gt(RRT024)Byg</sup>/Kmt2d<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:33431871	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332076	Kmt2d<sup>Gt(RRT024)Byg</sup>	is_implicated_in	DOID:0060473	Kabuki syndrome		MGI:5829566	Kmt2d<sup>Gt(RRT024)Byg</sup>/Kmt2d<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25273096	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809545	Tg(RCAN1)M9Mapr	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23644448	20131022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809545	Tg(RCAN1)M9Mapr	is_implicated_in	DOID:14250	Down syndrome		MGI:3809583	Tg(RCAN1)M9Mapr/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22511596	20131022	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429703	Tg(HLA-DR2)#Lfug/0 Tg(TCROb.1A12)#Lfug/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:10610182	20120731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175882	Fech<sup>m1Pas</sup>/Fech<sup>m1Pas</sup>  [background:] involves: 129/Sv * BALB/c	is_model_of	DOID:13270	erythropoietic protoporphyria						ECO:0000033	author statement supported by traceable reference	PMID:1939658	20090108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152744	Gnas<sup>tm1Gwa</sup>	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:35079678	20220510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152744	Gnas<sup>tm1Gwa</sup>	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy		MGI:5285183	Gnas<sup>tm1Gwa</sup>/Gnas<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:21747923	20220510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401408	Asah1<sup>tm1.2Geno</sup>	is_implicated_in	DOID:0050464	Farber lipogranulomatosis						ECO:0000033	author statement supported by traceable reference	PMID:31835809	20200709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401408	Asah1<sup>tm1.2Geno</sup>	is_implicated_in	DOID:0050464	Farber lipogranulomatosis		MGI:6401409	Asah1<sup>tm1.2Geno</sup>/Asah1<sup>tm1.2Geno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29908121	20200709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618534	Tg(Prnp-FUS*R521C)3313Ejh/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:24509083	20150313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836590	Jak2<sup>tm1(JAK2)Argr</sup>	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:4836619	Jak2<sup>tm1(JAK2)Argr</sup>/Jak2<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20489053	20140908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836590	Jak2<sup>tm1(JAK2)Argr</sup>	is_implicated_in	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:24692758	20140908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442117	Dnaaf3<sup>b2b1739Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670462	Gnpat<sup>tm1Just</sup>/Gnpat<sup>tm1Just</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110852	rhizomelic chondrodysplasia punctata type 2						ECO:0000033	author statement supported by traceable reference	PMID:12874108	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525574	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	is_model_of	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697838	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653131	Krt14<sup>tm2Der</sup>/Krt14<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type						ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433326	Dnah5<sup>b2b1537Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655715	Rpgrip1<sup>tm1Tili</sup>/Rpgrip1<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110329	Leber congenital amaurosis 6						ECO:0000033	author statement supported by traceable reference	PMID:12651948	20110502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676253	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050535	exudative vitreoretinopathy						ECO:0000033	author statement supported by traceable reference	PMID:20159112	20100420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947957	Csrp3<sup>tm1.1Rkn</sup>	is_implicated_in	DOID:0110318	hypertrophic cardiomyopathy 12						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4947957	Csrp3<sup>tm1.1Rkn</sup>	is_implicated_in	DOID:0110318	hypertrophic cardiomyopathy 12		MGI:4947966	Csrp3<sup>tm1.1Rkn</sup>/Csrp3<sup>tm1.1Rkn</sup>  [background:] either: (involves: Black Swiss) or (involves: C57BL/6N)			ECO:0000033	author statement supported by traceable reference	PMID:20044516	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432240	Apc<sup>tm2Rak</sup>/Apc<sup>tm2Rak</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129 * 129S4/SvJae * C57BL/6J * SJL	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:20080688	20120827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:14982859	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:10485893	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:9732288	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183404	Vdr<sup>tm1Mbd</sup>	is_implicated_in	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:25147982	20150917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183404	Vdr<sup>tm1Mbd</sup>	is_implicated_in	DOID:10609	rickets		MGI:3588584	Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9275211	20150917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183404	Vdr<sup>tm1Mbd</sup>	is_implicated_in	DOID:10609	rickets		MGI:3779048	Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15976027	20150917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6711468	Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0112321	alacrima, achalasia, and impaired intellectual development syndrome		MGI:6711469	Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>/Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33755596	20220301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774117	Snord116<sup>tm1.1Uta</sup>/Snord116<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18320030	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635067	Grid2<sup>ho-15J</sup>/Grid2<sup>ho-15J</sup>  [background:] involves: C3HeB/Fe	is_model_of	DOID:0080042	autosomal recessive spinocerebellar ataxia 18						ECO:0000033	author statement supported by traceable reference	PMID:24078737	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708157	Atxn3<sup>tm2.1(ATXN3*)Mfig</sup>	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:5750701	Atxn3<sup>tm2.1(ATXN3*)Mfig</sup>/Atxn3<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25301414	20160301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6193912	Tg(Myh6-Prkaca)33Eno	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6193916	Tg(Myh6-Prkaca)33Eno/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11717156	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4941021	Tg(Col2a1*R789C)#Waho	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:4941022	Tg(Col2a1*R789C)#Waho/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11771668	20110315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442116	b2b1723Clo	is_implicated_in	DOID:114	heart disease		MGI:5442140	b2b1723Clo/b2b1723Clo  [background:] C57BL/6J-b2b1723Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:10332039	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:3674914	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:6441865	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:6542992	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:6324209	Atp7a<sup>Mo-blo</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6685755	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:6324210	Atp7a<sup>Mo-blo</sup>/Atp7a<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6685755	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5516451	Tg(Prnp-ATXN3*70Q)70.61Olri	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:5516453	Tg(Prnp-ATXN3*70Q)70.61Olri/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:17626202	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4822570	Tg(CMV-ATXN3*94Q)94Pama	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:4822572	Tg(CMV-ATXN3*94Q)94Pama/Tg(CMV-ATXN3*94Q)94Pama  [background:] B6.FVB-Tg(CMV-ATXN3*94Q)94Pama			ECO:0000033	author statement supported by traceable reference	PMID:20510362	20100913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4822570	Tg(CMV-ATXN3*94Q)94Pama	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:4822571	Tg(CMV-ATXN3*94Q)94Pama/0  [background:] B6.FVB-Tg(CMV-ATXN3*94Q)94Pama			ECO:0000033	author statement supported by traceable reference	PMID:20510362	20100913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158420	H2-Ab1<sup>b-tm1Gru</sup>	is_implicated_in	DOID:820	myocarditis						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5700531	Tg(PGK1-FTL*)#Sle	is_implicated_in	DOID:0110737	neurodegeneration with brain iron accumulation 3		MGI:5700536	Tg(PGK1-FTL*)#Sle/0  [background:] B6J.FVB-Tg(PGK1-FTL*)#Sle			ECO:0000033	author statement supported by traceable reference	PMID:25689865	20160105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6294041	Hgf<sup>tm1Tbf</sup>	is_implicated_in	DOID:0110497	autosomal recessive nonsyndromic deafness 39		MGI:6446736	Hgf<sup>tm1Tbf</sup>/Hgf<sup>tm1Tbf</sup>  [background:] B6.Cg-Hgf<sup>tm1Tbf</sup>/Tbf			ECO:0000033	author statement supported by traceable reference	PMID:32152201	20200730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815537	Musk<sup>tm1.1Vwi</sup>/Musk<sup>tm2Vwi</sup>  [background:] Not Specified	is_model_of	DOID:0110670	congenital myasthenic syndrome 9						ECO:0000033	author statement supported by traceable reference	PMID:18718936	20150511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4443126	Pex7<sup>tm1Nbra</sup>/Pex7<sup>tm1Nbra</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110851	rhizomelic chondrodysplasia punctata type 1						ECO:0000033	author statement supported by traceable reference	PMID:20060764	20100512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294340	Dnah5<sup>b2b002Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5749650	Kif1a<sup>lgdg</sup>	is_implicated_in	DOID:0110781	hereditary spastic paraplegia 30		MGI:5752905	Kif1a<sup>lgdg</sup>/Kif1a<sup>lgdg</sup>  [background:] C3.Cg-Kif1a<sup>lgdg</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5752885	20160323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435409	Tg(Thy1-SNCA)61Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12111846	20120919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5752892	Kif1a<sup>lgdg-2J</sup>	is_implicated_in	DOID:0110781	hereditary spastic paraplegia 30		MGI:5752897	Kif1a<sup>lgdg-2J</sup>/Kif1a<sup>lgdg-2J</sup>  [background:] C57BL/6J-Kif1a<sup>lgdg-2J</sup>/CxJ			ECO:0000033	author statement supported by traceable reference	MGI:5752885	20160323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd	is_model_of	DOID:5394	prolactinoma						ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554792	Clp1<sup>tm1.1Pngr</sup>	is_implicated_in	DOID:0060279	pontocerebellar hypoplasia type 10		MGI:5554934	Clp1<sup>tm1.1Pngr</sup>/Clp1<sup>tm1.1Pngr</sup>  [background:] CBA.Cg-Clp1<sup>tm1.1Pngr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24766809	20150507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575012	Umod<sup>tm1Kuma</sup>/Umod<sup>tm1Kuma</sup>  [background:] involves: 129	is_model_of	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:15522986	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6726263	Tcf20<sup>em1Jwji</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6726265	Tcf20<sup>em1Jwji</sup>/Tcf20<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32510763	20210727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664515	Serpinf1<sup>tm1Craw</sup>	is_implicated_in	DOID:0110350	osteogenesis imperfecta type 6						ECO:0000033	author statement supported by traceable reference	PMID:26693895	20160411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664515	Serpinf1<sup>tm1Craw</sup>	is_implicated_in	DOID:0110350	osteogenesis imperfecta type 6		MGI:5758948	Serpinf1<sup>tm1Craw</sup>/Serpinf1<sup>tm1Craw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:23413146	20160411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580085	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3529938	Vangl2<sup>Lp</sup>/Vangl2<sup>Lp</sup>  [background:] involves: CBA/Ca * LPT/Le	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:9545534	20130429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177702	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9262482	20060118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4948066	Ank1<sup>M1Wlst</sup>/Ank1<sup>M1Wlst</sup>  [background:] involves: 129S1/SvImJ * C3H/HeJ * C57BL/6	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:21193012	20110426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174949	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:15294878	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694235	Acan<sup>cmd</sup>/Acan<sup>cmd</sup>  [background:] involves: STOCK T t<sup>low</sup> Itpr3<sup>tf</sup>	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	MGI:78375	20070122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694235	Acan<sup>cmd</sup>/Acan<sup>cmd</sup>  [background:] involves: STOCK T t<sup>low</sup> Itpr3<sup>tf</sup>	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:632744	20070122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670755	Ywhae<sup>tm1Awb</sup>/Ywhae<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12796778	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5617217	Ifih1<sup>Rgsc422</sup>	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000033	author statement supported by traceable reference	PMID:33165593	20210205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J	is_model_of	DOID:0080121	mitochondrial DNA depletion syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:18818194	20090224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438113	Shank3<sup>tm3.2Cmpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6438117	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438113	Shank3<sup>tm3.2Cmpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6438116	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>tm3.2Cmpl</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843497	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19342371	20090511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673421	Hoxb8<sup>tm1.1Mrc</sup>/Hoxb8<sup>tm1.1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050587	trichotillomania						ECO:0000033	author statement supported by traceable reference	PMID:11779477	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437297	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Smad1<sup>tm2Rob</sup>/Smad1<sup>tm2Rob</sup> Smad5<sup>tm1Huy</sup>/Smad5<sup>tm1Zuk</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:19819941	20100316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316778	b2b520Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5316792	b2b520Clo/b2b520Clo  [background:] C57BL/6J-b2b520Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308013	Tg(ED-L2-IL1RN/IL1B)#Tcw/?  [background:] B6.Cg-Tg(ED-L2-IL1RN/IL1B)#Tcw	is_model_of	DOID:5041	esophageal cancer						ECO:0000033	author statement supported by traceable reference	PMID:22264787	20120229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292663	Tfap2b<sup>tm1Rbu</sup>/Tfap2b<sup>tm1Rbu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060563	Char syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21829553	20111020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706582	Rbl2<sup>tm2.1Tyj</sup>	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24227978	20140918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3692945	Tg(Tnfsf13b)1Fma/0  [background:] B6.Cg-Tg(Tnfsf13b)1Fma	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11781351	20070109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037061	Sgsh<sup>mps3a</sup>/Sgsh<sup>mps3a</sup>  [background:] involves: 129X1/SvJ * CD-1 * C57BL/6 * SJL	is_model_of	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:10561464	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682251	Krt2<sup>Mhdadsk2</sup>/Krt2<sup>Mhdadsk2</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0060877	bullous congenital ichthyosiform erythroderma						ECO:0000033	author statement supported by traceable reference	PMID:12533510	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175797	Crkl<sup>tm1Imo</sup>/Crkl<sup>tm1Imo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242111	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4936851	Tg(tetO-S100a7a)#Yus	is_implicated_in	DOID:8893	psoriasis		MGI:4936856	Tg(KRT5-rtTA)#Glk/0 Tg(tetO-S100a7a)#Yus/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21148126	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5779548	Tg(tetO/CMV-Pmp22)JP18Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:5779551	Tg(PMP22-tTA)JY13Clh/0 Tg(tetO/CMV-Pmp22)JP18Clh/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:11331611	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5445347	Odad3<sup>b2b1885Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5445974	Odad3<sup>b2b1885Clo</sup>/Odad3<sup>b2b1885Clo</sup>  [background:] C57BL/6J-Odad3<sup>b2b1885Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311386	Dnah5<sup>b2b1154Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5314017	Dnah5<sup>b2b1154Clo</sup>/Dnah5<sup>b2b1154Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1154Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621905	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:0111074	progressive familial heart block type IA						ECO:0000033	author statement supported by traceable reference	PMID:11972032	20060817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850439	Cdkn2a<sup>tm1.1Brn</sup>/Cdkn2a<sup>tm1.1Brn</sup> Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd	is_model_of	DOID:1790	malignant mesothelioma						ECO:0000033	author statement supported by traceable reference	PMID:18328429	20090716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5637144	Minar2<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5756630	Minar2<sup>tm1b(KOMP)Wtsi</sup>/Minar2<sup>tm1b(KOMP)Wtsi</sup>  [background:] C57BL/6N-Minar2<sup>tm1b(KOMP)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:32954300	20210113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4848043	Dnm2<sup>tm1.1Ics</sup>	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:4848149	Dnm2<sup>tm1.1Ics</sup>/Dnm2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27870637	20170105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5315307	Wnt7a<sup>px-J</sup>	is_implicated_in	DOID:0090067	Fuhrmann syndrome		MGI:5440902	Wnt7a<sup>px-J</sup>/Wnt7a<sup>px-J</sup>  [background:] C57BL/6J-Wnt7a<sup>px-J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5440718	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832410	Prlh<sup>tm1Taon</sup>/Prlh<sup>tm1Taon</sup>  [background:] B6N.129X1-Prlh<sup>tm1Taon</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:19033670	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014305	Tg(Upk2-TAg)1Rkl	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5014310	Tg(Upk2-TAg)1Rkl/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21388952	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014305	Tg(Upk2-TAg)1Rkl	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835008	Cdkn2a<sup>tm2.1Nesh</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:27236105	20190123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308056	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0050560	Walker-Warburg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21625620	20120229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767861	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup> Xpa<sup>tm1Hvs</sup>/Xpa<sup>tm1Hvs</sup>  [background:] B6.129P2-Xpa<sup>tm1Hvs</sup> Ercc6<sup>tm1Gvh</sup>	is_model_of	DOID:2962	Cockayne syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17326724	20080118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655090	Dmd<sup>mdx</sup>/Y Foxk1<sup>tm1Djg</sup>/Foxk1<sup>tm1Djg</sup>  [background:] involves: 129S4/SvJae * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:10792059	20060919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055585	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:15322545	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707975	Disc1<sup>Rgsc1390</sup>/Disc1<sup>Rgsc1390</sup>  [background:] B6.Cg-Disc1<sup>Rgsc1390</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17481393	20070514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461807	Fgfr2<sup>m1Sgg</sup>/Fgfr2<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20503384	20100726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529520	Tg(ACTB-THRB*)DSyc/0  [background:] Not Specified	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9205946	20140122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566998	Gla<sup>tm1Kul</sup>/Gla<sup>tm1Kul</sup> Tg(CAG-A4GALT)#Sais/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	is_model_of	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:24094090	20140606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3578783	Bmpr1a<sup>tm2.1Bhr</sup>/Bmpr1a<sup>tm2.2Bhr</sup> Tg(Gdf5-cre,-ALPP)1Kng/0  [background:] involves: 129 * C57BL/6 * FVB/N-Tg(Gdf5-cre-ALPP)1Kng	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:15492776	20050603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5585301	Ppt1<sup>tm1.1Dprc</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1		MGI:5585410	Ppt1<sup>tm1.1Dprc</sup>/Ppt1<sup>tm1.1Dprc</sup>  [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25205113	20150521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5574592	Fbn2<sup>fp-4J</sup>/Fbn2<sup>fp-4J</sup>  [background:] BALB/cByJ-Fbn2<sup>fp-4J</sup>/GrsrJ	is_model_of	DOID:0050646	distal arthrogryposis						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313375	Fbn1<sup>tm3.2Lysa</sup>	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:5313383	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>tm3.2Lysa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313375	Fbn1<sup>tm3.2Lysa</sup>	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:5313384	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906918	Tg(Myh6-Rxra)41Pcn	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906919	Tg(Myh6-Rxra)41Pcn/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10675365	20170814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195702	Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup>	is_implicated_in	DOID:5602	T-cell adult acute lymphocytic leukemia		MGI:6195751	Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup>/Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup> Tg(Cd4-cre)1Cwi/0  [background:] involves: C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25565005	20180827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195702	Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup>	is_implicated_in	DOID:5602	T-cell adult acute lymphocytic leukemia		MGI:6195746	Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup>/Gt(ROSA)26Sor<sup>tm18(Zeb2)Jhai</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25565005	20180827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5779859	Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694867	Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157623	Notch2<sup>tm2.2Ecan</sup>	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:6157629	Notch2<sup>tm2.2Ecan</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28592489	20180523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437221	Sox7<sup>tm1.1Dsco</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5437224	Sox7<sup>tm1.1Dsco</sup>/Sox7<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22723016	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838155	Tg(ATXN3*)84.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:31157458	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838155	Tg(ATXN3*)84.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:30086154	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838155	Tg(ATXN3*)84.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:28624196	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838155	Tg(ATXN3*)84.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:29908063	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838155	Tg(ATXN3*)84.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:3838166	Tg(ATXN3*)84.2Cce/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11978767	20220913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838155	Tg(ATXN3*)84.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:3838167	Tg(ATXN3*)84.2Cce/Tg(ATXN3*)84.2Cce  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11978767	20220913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624553	Mecp2<sup>tm1Hzo</sup>/Y  [background:] 129S7/SvEvBrd-Mecp2<sup>tm1Hzo</sup>	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12160743	20060616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718115	Tg(Camk2a-MAPT*R406W)748Atak/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:12368474	20070814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655190	Slc1a1<sup>tm1Wst</sup>	is_implicated_in	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:28703795	20210118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655190	Slc1a1<sup>tm1Wst</sup>	is_implicated_in	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:26230766	20210118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655190	Slc1a1<sup>tm1Wst</sup>	is_implicated_in	DOID:13544	low tension glaucoma		MGI:4417919	Slc1a1<sup>tm1Wst</sup>/Slc1a1<sup>tm1Wst</sup>  [background:] B6.129-Slc1a1<sup>tm1Wst</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17607354	20210118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3771372	Stat1<sup>tm1Rds</sup>/Stat1<sup>tm1Rds</sup>  [background:] 129S6/SvEv-Stat1<sup>tm1Rds</sup>/Tac	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22264274	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882507	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] 129S5/SvEvBrd-S1pr2<sup>tm1Ajml</sup>	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:19903857	20170406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified	is_model_of	DOID:0110341	osteogenesis imperfecta type 2						ECO:0000033	author statement supported by traceable reference	PMID:8456819	20130702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5528981	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15983791	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513416	Apc<sup>tm1Cip</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:27816490	20170302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513416	Apc<sup>tm1Cip</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:3513849	Apc<sup>tm1Cip</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15502862	20170302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442115	b2b1594Clo	is_implicated_in	DOID:674	cleft palate		MGI:5442125	b2b1594Clo/b2b1594Clo  [background:] C57BL/6J-b2b1594Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760092	Magel2<sup>tm1Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25926624	20160725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760092	Magel2<sup>tm1Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20160725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760092	Magel2<sup>tm1Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:5781308	Magel2<sup>tm1Stw</sup>/Magel2<sup>tm1Stw</sup>  [background:] C57BL/6-Magel2<sup>tm1Stw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27436578	20160725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3760092	Magel2<sup>tm1Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3834842	Magel2<sup>tm1Stw</sup>/Magel2<sup>+</sup>  [background:] C57BL/6-Magel2<sup>tm1Stw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19172181	20160725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516430	Gucy1a1<sup>tm1.1Brou</sup>/Gucy1a1<sup>tm1.1Brou</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ	is_model_of	DOID:1070	primary open angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:23527308	20131107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316003	Ezh2<sup>tm2Sho</sup>/Ezh2<sup>tm2.1Sho</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22431509	20120422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311388	Dnah11<sup>b2b1203Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5318339	Dnah11<sup>b2b1203Clo</sup>/Dnah11<sup>b2b1203Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1203Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531468	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:8614836	20100521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3531468	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:15001446	20100521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702286	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] B6.C3-Ap3b1<sup>pe</sup>/J	is_model_of	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:25477496	20151231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5621062	Tg(SOD1*L126Z)45Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16000321	20150408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2385751	Tg(UcpDta)1Kz/?  [background:] involves: FVB/N	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:8264795	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5552945	Dnah5<sup>b2b2395Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175703	Atm<sup>tm1Awb</sup>/Atm<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Atm<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Black Swiss)	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:8689683	20071012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175703	Atm<sup>tm1Awb</sup>/Atm<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Atm<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Black Swiss)	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:10449794	20071012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306919	Lmna<sup>tm2.1Gbon</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:5906504	Lmna<sup>tm2.1Gbon</sup>/Lmna<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23575224	20170810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316782	b2b913Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5316796	b2b913Clo/b2b913Clo  [background:] C57BL/6J-b2b913Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:11825062	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:22209984	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:18023223	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:16317004	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:16581029	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:3617447	Fah<sup>tm1Mgo</sup>/Fah<sup>tm1Mgo</sup>  [background:] involves: 129S7/SvEvBrd * PT			ECO:0000033	author statement supported by traceable reference	PMID:10518553	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429529	Fah<sup>tm1Mgo</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:5558898	Fah<sup>tm1Mgo</sup>/Fah<sup>tm1Mgo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:7545495	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680217	Erbb4<sup>tm1Fej</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26577758	20160705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259431	Tg(Alb-SREBF1_ic)#Jkot	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6259432	Tg(Alb-SREBF1_ic)#Jkot/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28490610	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461144	Ehmt1<sup>tm1Yshk</sup>/Ehmt1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:0060352	Kleefstra syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23175442	20130305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461144	Ehmt1<sup>tm1Yshk</sup>/Ehmt1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:0060352	Kleefstra syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19896504	20130305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448548	Tg(SOD1*G85R)#Roos/0  [background:] involves: C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19233858	20130110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438493	Tg(Thy1-TARDBP)6Singh/Tg(Thy1-TARDBP)6Singh  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:20133711	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926343	Atm<sup>tm1Bal</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:33734555	20210504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926343	Atm<sup>tm1Bal</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175706	Atm<sup>tm1Bal</sup>/Atm<sup>tm1Bal</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9356511	20210504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926343	Atm<sup>tm1Bal</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175706	Atm<sup>tm1Bal</sup>/Atm<sup>tm1Bal</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:8843193	20210504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606580	Avpr1a<sup>tm1Dgen</sup>/Avpr1a<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720676	Tg(DMD-APP*)7Neve/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:8744400	20070906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720676	Tg(DMD-APP*)7Neve/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:1438289	20070906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5287721	Gba1<sup>tm2Ggb</sup>/Gba1<sup>tm2Ggb</sup> Psap<sup>tm1Suz</sup>/Psap<sup>tm1Suz</sup>  [background:] involves: 129P2/OlaHsd * 129S5/SvEvBrd	is_model_of	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21700325	20171211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620907	Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:15608054	20060502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6202022	Slc3a1<sup>tm1Jat</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:6202041	Slc3a1<sup>tm1Jat</sup>/Slc3a1<sup>tm1Jat</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28165480	20181015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6202022	Slc3a1<sup>tm1Jat</sup>	is_implicated_in	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:25443947	20181015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6202022	Slc3a1<sup>tm1Jat</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:6202041	Slc3a1<sup>tm1Jat</sup>/Slc3a1<sup>tm1Jat</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19484501	20181015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527896	Cngb1<sup>tm1.1Biel</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:25392995	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527896	Cngb1<sup>tm1.1Biel</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:22802073	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527896	Cngb1<sup>tm1.1Biel</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:29202463	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527896	Cngb1<sup>tm1.1Biel</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:26740549	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527896	Cngb1<sup>tm1.1Biel</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3528030	Cngb1<sup>tm1.1Biel</sup>/Cngb1<sup>tm1.1Biel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:15634774	20180622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7336745	Copa<sup>tm1.1Shum</sup>	is_implicated_in	DOID:0081242	autoimmune interstitial lung, joint, and kidney disease		MGI:7336761	Copa<sup>tm1.1Shum</sup>/Copa<sup>+</sup>  [background:] B6(CBA)-Copa<sup>tm1.1Shum</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32198142	20230113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6150321	Kifbp<sup>em1Hmy</sup>	is_implicated_in	DOID:0060481	Goldberg-Shprintzen syndrome		MGI:6154375	Kifbp<sup>em1Hmy</sup>/Kifbp<sup>em1Hmy</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29192291	20180503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5620891	Lepr<sup>tm1Jke</sup>/Lepr<sup>tm1Jke</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25157166	20150403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361924	Tg(MMTV-PyVT)634Mul/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27264173	20170301	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794044	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050645	arterial tortuosity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17293478	20080617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3773702	Cftr<sup>tm1Hgu</sup>/Cftr<sup>tm1Hgu</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:7540910	20080314	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798288	Del(5D5Mit73-D5Mit351)5Jcs/+  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11152656	20080722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582068	Scn5a<sup>tm1Clhh</sup>/Scn5a<sup>+</sup>  [background:] involves: 129/SvEv	is_model_of	DOID:0110646	long QT syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:22287583	20140910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828836	Nkx2-5<sup>tm3.1Mwc</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570746	Tg(tetO-MYCN,-luc)#Waw	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24107773	20160809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570746	Tg(tetO-MYCN,-luc)#Waw	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5570748	Tg(Slc1a2-tTA)#Waw/0 Tg(tetO-MYCN,-luc)#Waw/Tg(tetO-MYCN,-luc)#Waw  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:20478998	20160809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570746	Tg(tetO-MYCN,-luc)#Waw	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5570747	Tg(Slc1a2-tTA)#Waw/0 Tg(tetO-MYCN,-luc)#Waw/0  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:20478998	20160809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570746	Tg(tetO-MYCN,-luc)#Waw	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:25785590	20160809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710098	Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>	is_implicated_in	DOID:5485	synovial sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:22797074	20131111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710098	Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>	is_implicated_in	DOID:5485	synovial sarcoma		MGI:3843451	Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19351831	20131111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710098	Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>	is_implicated_in	DOID:5485	synovial sarcoma		MGI:3711004	Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup>/Gt(ROSA)26Sor<sup>tm3(SS18/EGFP)Mrc</sup> Myf5<sup>tm1(cre)Mrc</sup>/Myf5<sup>tm1(cre)Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17418413	20131111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5586970	Cd46<sup>tm1Atk</sup>	is_implicated_in	DOID:10871	age related macular degeneration		MGI:5586971	Cd46<sup>tm1Atk</sup>/Cd46<sup>tm1Atk</sup>  [background:] B6.129-Cd46<sup>tm1Atk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27295359	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908882	Tg(Rho-GUCY2D*R838S)362Amd	is_implicated_in	DOID:0111011	cone-rod dystrophy 6		MGI:6154646	Tg(Rho-GUCY2D*R838S)362Amd/0  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:27703005	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354847	Adam17<sup>tm1.2Bbl</sup>	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:29751002	20181112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354847	Adam17<sup>tm1.2Bbl</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:6241552	Adam17<sup>tm1.2Bbl</sup>/Adam17<sup>tm1.2Bbl</sup> Sox9<sup>tm3(cre)Crm</sup>/Sox9<sup>+</sup>  [background:] B6.129(SJL)-Sox9<sup>tm3(cre)Crm</sup> Adam17<sup>tm1.2Bbl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25902485	20181112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644542	Atm<sup>tm1Pmc</sup>/Atm<sup>tm1Pmc</sup>  [background:] B6.Cg-Atm<sup>tm1Pmc</sup>	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:25683718	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6376284	Gna11<sup>em1Mman</sup>	is_implicated_in	DOID:0090108	autosomal dominant hypocalcemia 2		MGI:6376303	Gna11<sup>em1Mman</sup>/Gna11<sup>+</sup>  [background:] C57BL/6NCrl-Gna11<sup>em1Mman</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28194446	20191112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6376284	Gna11<sup>em1Mman</sup>	is_implicated_in	DOID:0090108	autosomal dominant hypocalcemia 2		MGI:6376290	Gna11<sup>em1Mman</sup>/Gna11<sup>em1Mman</sup>  [background:] C57BL/6NCrl-Gna11<sup>em1Mman</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28194446	20191112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183509	Gjb2<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000033	author statement supported by traceable reference	PMID:25451287	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183509	Gjb2<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000033	author statement supported by traceable reference	PMID:24333301	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183509	Gjb2<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:3588875	Gjb2<sup>tm1Ugds</sup>/Gjb2<sup>tm1Ugds</sup> Tg(Otog-cre)1Ugds/0  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12121617	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183509	Gjb2<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:5571190	Gjb2<sup>tm1Ugds</sup>/Gjb2<sup>tm1Ugds</sup> Tg(Sox10-cre)1Wdr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24333301	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4943309	Tg(Csf1r-Tnfsf15,-EGFP)#Targ	is_implicated_in	DOID:0110896	inflammatory bowel disease 16		MGI:4943327	Tg(Csf1r-Tnfsf15,-EGFP)#Targ/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21264313	20110331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3641169	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:0110218	Brugada syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:21097662	20101221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6690810	Dysf<sup>tm1.1Mdcb</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:6690813	Dysf<sup>tm1.1Mdcb</sup>/Dysf<sup>tm1.1Mdcb</sup>  [background:] B6.129P2(Cg)-Dysf<sup>tm1.1Mdcb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30292141	20220304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6690810	Dysf<sup>tm1.1Mdcb</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:35028538	20220304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618925	Tg(Ins2-NP)25-3Olds/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:1901765	20060411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5498329	Dnm2<sup>b2b2159Clo</sup>/Dnm2<sup>b2b2159Clo</sup>  [background:] C57BL/6J-Dnm2<sup>b2b2159Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798287	Del(5D5Mit388-D5Mit351)4Jcs/+  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11152656	20080722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689583	Mecom<sup>Jbo</sup>/Mecom<sup>+</sup>  [background:] C3N.C-Mecom<sup>Jbo</sup>	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:17029558	20071008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174985	Pik3r1<sup>tm1Tka</sup>/Pik3r1<sup>tm1Tka</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:9888854	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046274	Adgrv1<sup>tm1Pwh</sup>/Adgrv1<sup>tm1Pwh</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0110839	Usher syndrome type 2C						ECO:0000033	author statement supported by traceable reference	PMID:16775142	20070109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777621	Tg(MUC1)79.24Gend	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29462213	20180403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4889196	Tg(CD2-Lmo2)#Thr	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:4889198	Tg(CD2-Lmo2)#Thr/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:1461647	20110223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7329776	Tg(Zfhx2*R1907K)#Jcox	is_implicated_in	DOID:0081075	Marsili syndrome		MGI:7329778	Tg(Zfhx2*R1907K)#Jcox/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29253101	20220816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763104	Tg(MMTV-LPAR2)6Gbm/Tg(MMTV-LPAR2)6Gbm  [background:] FVB/N-Tg(MMTV-LPAR2)6Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000472	Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26400062	20160526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000472	Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000472	Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:5000477	Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(MMTV-cre)#Tfln/0  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:21324922	20160526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7447439	Hpdl<sup>em1Jgg</sup>	is_implicated_in	DOID:1289	neurodegenerative disease		MGI:7447442	Hpdl<sup>em1Jgg</sup>/Hpdl<sup>em1Jgg</sup>  [background:] C57BL/6-Hpdl<sup>em1Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33188300	20230327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308951	Cdkn2a<sup>tm2.1Rdp</sup>/Cdkn2a<sup>+</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * CBA * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16585505	20180730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355227	Apoe<sup>tm3(APOE*4)Mae</sup>/Apoe<sup>tm3(APOE*4)Mae</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:16079201	20110906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653134	Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:12620190	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439329	Tg(HCRT-tTA)1Ahky	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:27919403	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5461578	Tg(Myh6-Erbb2)6Kaga	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5461579	Tg(Myh6-Erbb2)6Kaga/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:22912742	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845397	Rho<sup>Tvrm4</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:33046772	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845397	Rho<sup>Tvrm4</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4455025	Rho<sup>Tvrm4</sup>/Rho<sup>+</sup>  [background:] B6.Cg-Rho<sup>Tvrm4</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:20207741	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6690662	Gck<sup>tm1Ydor</sup>	is_implicated_in	DOID:0070216	familial hyperinsulinemic hypoglycemia 3		MGI:6690664	Gck<sup>tm1Ydor</sup>/Gck<sup>+</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:33558985	20210414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5707848	Gata5<sup>tm1.2Nemr</sup>/Gata5<sup>tm1.2Nemr</sup>  [background:] Not Specified	is_model_of	DOID:10825	essential hypertension						ECO:0000033	author statement supported by traceable reference	PMID:26617239	20160210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314754	Tg(CAG-GLVP)#Cath/0 Tg(GAL4-PABPN1*A16)#Cath/0  [background:] involves: C57BL/6 * FVB	is_model_of	DOID:11719	oculopharyngeal muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21964252	20120411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6368816	Armc2<sup>em1Pfr</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6369630	Armc2<sup>em1Pfr</sup>/Armc2<sup>em1Pfr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30686508	20191105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690327	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15254584	20061211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690327	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15546004	20061211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175808	Crygd<sup>Lop12</sup>/Crygd<sup>+</sup>  [background:] involves: BALB/cJ * SJL/J	is_model_of	DOID:0110235	cataract 2 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:10704279	20050718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5637298	Cryba1<sup>tm1.1Dbsa</sup>/Cryba1<sup>tm1.1Dbsa</sup> Tg(BEST1-cre)1Jdun/0  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:25257511	20150525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661118	Dysf<sup>tm1Kcam</sup>/Dysf<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:12736685	20090630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412066	Tg(SNCA*A53T)2Nbm	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25351739	20150818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687751	Btk<sup>xid</sup>/Btk<sup>xid</sup>  [background:] involves: CBA/HN * DBA/2N	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806231	Plekhm1<sup>tm1.1Hzhao</sup>	is_implicated_in	DOID:0110945	autosomal recessive osteopetrosis 6		MGI:5896640	Ctsk<sup>tm1(cre)Ska</sup>/Ctsk<sup>+</sup> Plekhm1<sup>tm1.1Hzhao</sup>/Plekhm1<sup>tm1.1Hzhao</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:27777970	20170712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818381	Gnptab<sup>tm1Kkol</sup>	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000033	author statement supported by traceable reference	PMID:22961545	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818381	Gnptab<sup>tm1Kkol</sup>	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:5544331	Gnptab<sup>tm1Kkol</sup>/Gnptab<sup>tm1Kkol</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24127423	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818381	Gnptab<sup>tm1Kkol</sup>	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000033	author statement supported by traceable reference	PMID:25601403	20171116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5621175	Tg(SOD1)2Gur/0 Tg(SOD1*)D-14Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25305079	20150409	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4939025	Tg(Igh-Maf)524Staka/0  [background:] involves: C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:21224354	20110228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178287	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup> Tyrp1<sup>isa</sup>/Tyrp1<sup>isa</sup>  [background:] DBA/2J	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10192392	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7378548	Setd1a<sup>em1Yzhg</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:7378550	Setd1a<sup>em1Yzhg</sup>/Setd1a<sup>+</sup>  [background:] B6.Cg-Setd1a<sup>em1Yzhg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35245111	20221103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5775083	Pclo<sup>tm1.1Mver</sup>	is_not_implicated_in	DOID:1595	melancholic depression		MGI:5819105	Pclo<sup>tm1.1Mver</sup>/Pclo<sup>tm1.1Mver</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26045179	20170126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5752221	Ctsd<sup>m1J</sup>	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:5752257	Ctsd<sup>m1J</sup>/Ctsd<sup>m1J</sup>  [background:] C3HeB/FeJ-Ctsd<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5751705	20160317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148539	Utrn<sup>tm1Jrs</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22266080	20161005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148539	Utrn<sup>tm1Jrs</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25921779	20161005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148539	Utrn<sup>tm1Jrs</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25940966	20161005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834218	Tg(Myh7-Pln)2Egk	is_implicated_in	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:28278204	20180112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834218	Tg(Myh7-Pln)2Egk	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:5052046	Tg(Myh7-Pln)2Egk/0  [background:] FVB/N-Tg(Myh7-Pln)2Egk			ECO:0000033	author statement supported by traceable reference	PMID:26035394	20180112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624713	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20633611	20101102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624713	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242117	20101102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538574	Oprm1<sup>tm1Kff</sup>/Oprm1<sup>tm1Kff</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:20503133	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829786	Tg(SOD1*G93A)1Gur/0  [background:] B6SJL-Tg(SOD1*G93A)1Gur	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19116365	20100916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813634	Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:1380	endometrial cancer						ECO:0000033	author statement supported by traceable reference	PMID:18632614	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5519084	Tg(Pkd1*)39Mtru/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23439951	20131121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445420	Cftr<sup>tm1Eur</sup>/Cftr<sup>tm1Eur</sup>  [background:] B6.129P2-Cftr<sup>tm1Eur</sup>	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:22711878	20121212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398734	Smn1<sup>tm1Rako</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28069797	20180202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398734	Smn1<sup>tm1Rako</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:28062667	20180202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820832	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] B6.KOR-Traf3ip2<sup>adjm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448998	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup>  [background:] B6.129S4-Fcgr2b<sup>tm1Ttk</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:10981970	20051011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4454555	Gtf2ird1<sup>tm1Hrd</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25248400	20170105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4454555	Gtf2ird1<sup>tm1Hrd</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27295951	20170105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4454555	Gtf2ird1<sup>tm1Hrd</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5428426	Gtf2ird1<sup>tm1Hrd</sup>/Gtf2ird1<sup>tm1Hrd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22198572	20170105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5529361	Mecp2<sup>tm4.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5702941	Mecp2<sup>tm4.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26647311	20160115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424984	Casr<sup>BCH013</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425923	Casr<sup>BCH013</sup>/Casr<sup>BCH013</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH013</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618464	Sgcd<sup>tm1Kcam</sup>/Sgcd<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000033	author statement supported by traceable reference	PMID:10481911	20060404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355581	Galnt3<sup>tm1Mjec</sup>/Galnt3<sup>tm1Mjec</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0111063	hyperphosphatemic familial tumoral calcinosis						ECO:0000033	author statement supported by traceable reference	PMID:19213845	20090901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424983	Casr<sup>BCH011</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425922	Casr<sup>BCH011</sup>/Casr<sup>BCH011</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH011</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651821	Lpl<sup>tm1Sem</sup>/Lpl<sup>tm1Sem</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7759497	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838032	Col4a4<sup>m1Btlr</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:4838199	Col4a4<sup>m1Btlr</sup>/Col4a4<sup>m1Btlr</sup>  [background:] C57BL/6J-Col4a4<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:4440633	20110509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838032	Col4a4<sup>m1Btlr</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:4838199	Col4a4<sup>m1Btlr</sup>/Col4a4<sup>m1Btlr</sup>  [background:] C57BL/6J-Col4a4<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21196518	20110509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450518	Hba<sup>th-J</sup>/Hba<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:6950407	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450518	Hba<sup>th-J</sup>/Hba<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	MGI:1195879	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668607	Slc45a2<sup>uw-bls</sup>/Slc45a2<sup>uw-bls</sup>  [background:] wild Corsican mouse	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	MGI:61984	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:1696177	20070128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10233845	20070128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332250	Nipbl<sup>Gt(RRS564)Byg</sup>	is_implicated_in	DOID:11725	Cornelia de Lange syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25255084	20160222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3613052	Nphs1<sup>tm1Ktry</sup>/Nphs1<sup>tm1Ktry</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11136707	20060221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615174	Abcc6<sup>tm1Aabb</sup>/Abcc6<sup>tm1Aabb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2738	pseudoxanthoma elasticum						ECO:0000033	author statement supported by traceable reference	PMID:15888484	20060307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709038	Cdh23<sup>sals</sup>/Cdh23<sup>sals</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110467	autosomal recessive nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:19270079	20090504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566909	Tg(ACTA1*D286G)#Kjno	is_implicated_in	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:23977274	20160919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566909	Tg(ACTA1*D286G)#Kjno	is_implicated_in	DOID:0110927	nemaline myopathy 3		MGI:5566910	Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21303860	20160919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566909	Tg(ACTA1*D286G)#Kjno	is_implicated_in	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:23736297	20160919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719609	Tg(Myh6-Tnnt2)117Lnwd/0  [background:] involves: C57BL/6	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:9637714	20100521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155926	Abcd1<sup>tm1Kds</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23604518	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155926	Abcd1<sup>tm1Kds</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446588	Abcd1<sup>tm1Kds</sup>/Abcd1<sup>tm1Kds</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9256488	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155926	Abcd1<sup>tm1Kds</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446589	Abcd1<sup>tm1Kds</sup>/Y  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9256488	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155926	Abcd1<sup>tm1Kds</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2680904	Abcd1<sup>tm1Kds</sup>/Abcd1<sup>tm1Kds</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11875044	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155926	Abcd1<sup>tm1Kds</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:3617307	Abcd1<sup>tm1Kds</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15489218	20131217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292357	Fmr1<sup>tm1.2Cidz</sup>/Y  [background:] involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N	is_model_of	DOID:14261	fragile X syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19103683	20111017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429609	Msh2<sup>tm1Htr</sup>/Msh2<sup>tm1Htr</sup> Tap1<sup>tm1Hpl</sup>/Tap1<sup>tm1Hpl</sup>  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9443401	20110923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384507	Stat3<sup>tm1Vpo</sup>	is_implicated_in	DOID:9997	peripartum cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:23619365	20170814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384507	Stat3<sup>tm1Vpo</sup>	is_implicated_in	DOID:9997	peripartum cardiomyopathy		MGI:5906908	Stat3<sup>tm1Vpo</sup>/Stat3<sup>tm1Vpo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17289576	20170814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389010	Abcc9<sup>em1Nich</sup>	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6389024	Abcc9<sup>em1Nich</sup>/Abcc9<sup>em1Nich</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389010	Abcc9<sup>em1Nich</sup>	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6389016	Abcc9<sup>em1Nich</sup>/Abcc9<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664130	Pafah1b1<sup>tm2.2Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177316	Tmc1<sup>Mhdabth</sup>/Tmc1<sup>+</sup>  [background:] C3HeB/FeJ-Tmc1<sup>Mhdabth</sup>/Ieg	is_model_of	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000033	author statement supported by traceable reference	MGI:2681078	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:37649609	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26929329	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27506299	20230921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5556393	Tinf2<sup>tm2.2Tdl</sup>	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:5556400	Tinf2<sup>tm2.2Tdl</sup>/Tinf2<sup>+</sup>  [background:] involves: BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24449270	20140415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5818291	Gnas<sup>tm5.1Lsw</sup>/Gnas<sup>tm5.1Lsw</sup> Tg(Slc5a2-cre)1Tauc/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:4184	pseudohypoparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:26671181	20170119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491030	Tg(Prnp*P101L)2247Sbp/0  [background:] involves: FVB/N	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5817401	Cacna1f<sup>nob9</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:6259768	Cacna1f<sup>nob9</sup>/Cacna1f<sup>nob9</sup>  [background:] B6(PWD)-Cacna1f<sup>nob9</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	PMID:30445045	20181211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778393	Tg(DRD1-ctxA)7Burt/0  [background:] C.Cg-Tg(DRD1-ctxA)7Burt	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12140785	20080423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778393	Tg(DRD1-ctxA)7Burt/0  [background:] C.Cg-Tg(DRD1-ctxA)7Burt	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10636303	20080423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3797214	Pcsk5<sup>vcc</sup>/Pcsk5<sup>vcc</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:14679	VACTERL association						ECO:0000033	author statement supported by traceable reference	PMID:18519639	20150724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6404913	Rs1<sup>tm1.1Rom</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6404937	Rs1<sup>tm1.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5621172	Tg(SOD1*)D-14Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5621173	Tg(SOD1*)D-14Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25305079	20150409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857844	Pitx2<sup>tm1Sac</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:12015277	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857844	Pitx2<sup>tm1Sac</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2170004	Pitx2<sup>tm1Sac</sup>/Pitx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10498698	20190503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679221	Atcay<sup>swd</sup>	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:23226316	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679221	Atcay<sup>swd</sup>	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia		MGI:3719717	Atcay<sup>swd</sup>/Atcay<sup>swd</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950072	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>+</sup> Tg(Eno2-Scn2a1*)Q54Mm/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * SJL/J	is_model_of	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:21156207	20110514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5751448	Ifng<sup>tm1.1Hayg</sup>	is_implicated_in	DOID:12449	aplastic anemia		MGI:5792659	Ifng<sup>tm1.1Hayg</sup>/Ifng<sup>tm1.1Hayg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25342713	20160919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033756	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033756	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:9668092	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5811645	Grn<sup>tm2.1Far</sup>	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:6314154	Grn<sup>tm2.1Far</sup>/Grn<sup>tm2.1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29511098	20190613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810589	Aipl1<sup>tvrm119</sup>	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:5922030	Aipl1<sup>tvrm119</sup>/Aipl1<sup>tvrm119</sup>  [background:] C57BL/6J-Aipl1<sup>tvrm119</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6107687	Thap1<sup>tm1.1Meeh</sup>	is_implicated_in	DOID:0090039	torsion dystonia 6		MGI:6107696	Thap1<sup>tm1.1Meeh</sup>/Thap1<sup>+</sup>  [background:] involves: 129S/SvEv * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26376866	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7469825	Tbl1xr1<sup>em2H</sup>	is_implicated_in	DOID:0081362	Pierpont syndrome		MGI:7469827	Tbl1xr1<sup>em2H</sup>/Tbl1xr1<sup>em2H</sup>  [background:] C57BL/6J-Tbl1xr1<sup>em2H</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35416977	20231020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4355008	Atr<sup>tm1Ofc</sup>	is_implicated_in	DOID:0050569	Seckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22370720	20120724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4355008	Atr<sup>tm1Ofc</sup>	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:4355020	Atr<sup>tm1Ofc</sup>/Atr<sup>tm1Ofc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:19620979	20120724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4415702	Dnai1<sup>tm1.1Leo</sup>/Dnai1<sup>tm1.1Leo</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110594	primary ciliary dyskinesia 1						ECO:0000033	author statement supported by traceable reference	PMID:19675306	20100823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781017	Tg(Mup3-Plau)350-2Eps/?  [background:] C57BL/6-Tg(Mup3-Plau)350-2Eps	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25132496	20160722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30674677	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27373157	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27298335	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27452466	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5466584	Tg(Pnkd*A7V*A9V,-DsRed)704Ljp	is_implicated_in	DOID:0090049	paroxysmal nonkinesigenic dyskinesia 1		MGI:5469979	Tg(Pnkd*A7V*A9V,-DsRed)704Ljp/0  [background:] B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)704Ljp			ECO:0000033	author statement supported by traceable reference	PMID:22214848	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833385	Tg(Thy1-MAPT*K369I)K3Gotz/0  [background:] B6.Cg-Tg(Thy1-MAPT*K369I)K3Gotz	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:18832465	20090224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563141	Clcn7<sup>tm1.1Mjec</sup>/Clcn7<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2J	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:24185277	20140509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6471171	Glra1<sup>m1Cpai</sup>	is_implicated_in	DOID:0060695	hyperekplexia						ECO:0000033	author statement supported by traceable reference	PMID:29910711	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6471171	Glra1<sup>m1Cpai</sup>	is_implicated_in	DOID:0060695	hyperekplexia		MGI:6471172	Glra1<sup>m1Cpai</sup>/Glra1<sup>m1Cpai</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28724750	20210121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513101	Slc12a3<sup>tm1Ges</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513101	Slc12a3<sup>tm1Ges</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:3513541	Slc12a3<sup>tm1Ges</sup>/Slc12a3<sup>tm1Ges</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9786924	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6156948	Auts2<sup>tm1Mhos</sup>	is_implicated_in	DOID:0070056	autosomal dominant intellectual developmental disorder 26		MGI:6156953	Auts2<sup>tm1Mhos</sup>/Auts2<sup>+</sup>  [background:] C57BL/6N-Auts2<sup>tm1Mhos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26717414	20180518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5616147	Cplane2<sup>b2b2804Clo</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:5616148	Cplane2<sup>b2b2804Clo</sup>/Cplane2<sup>b2b2804Clo</sup>  [background:] C57BL/6J-Cplane2<sup>b2b2804Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052308	Hr<sup>rhsl</sup>/Hr<sup>rhsl</sup>  [background:] involves: BALB/c	is_model_of	DOID:0060689	atrichia with papular lesions						ECO:0000033	author statement supported by traceable reference	PMID:15955095	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5704111	Ube3a<sup>tm1Yelg</sup>/Ube3a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPasCrl	is_model_of	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25866966	20160120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830477	Tg(HP-MMP1a)34-1Cha/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:1458541	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4943692	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21068380	20110405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559219	Slx4<sup>tm1.2Jrou</sup>	is_not_implicated_in	DOID:0111092	Fanconi anemia complementation group P		MGI:5559492	Slx4<sup>tm1.2Jrou</sup>/Slx4<sup>tm1.2Jrou</sup>  [background:] B6.129P2-Slx4<sup>tm1.2Jrou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24076219	20140421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583344	Irs2<sup>tm1Tka</sup>/Irs2<sup>tm1Tka</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11078455	20050811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805498	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:6392337	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>/Sdhc<sup>tm1c(EUCOMM)Wtsi</sup> Gt(ROSA)26Sor<sup>tm1.1(rtTA,tetO-cre)Bkmn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31469588	20200302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297398	Cplane1<sup>b2b012Clo</sup>	is_implicated_in	DOID:0110986	Joubert syndrome 17		MGI:5309129	Cplane1<sup>b2b012Clo</sup>/Cplane1<sup>b2b012Clo</sup>  [background:] C57BL/6J-Cplane1<sup>b2b012Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25877302	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430343	Pcsk5<sup>b2b1549Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5430345	Pcsk5<sup>b2b1549Clo</sup>/Pcsk5<sup>b2b1549Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b1549Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052922	Mbnl1<sup>tm1Sws</sup>	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:23901116	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052922	Mbnl1<sup>tm1Sws</sup>	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:25263597	20210420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052922	Mbnl1<sup>tm1Sws</sup>	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:33503262	20210420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028383	Pde6b<sup>rd1-4H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5775596	Tg(tetO-ERBB2)#Jjz	is_implicated_in	DOID:1612	breast cancer		MGI:5775603	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-ERBB2)#Jjz/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26977878	20160610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652059	Ldb3<sup>tm1Chen</sup>/Ldb3<sup>tm1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss	is_model_of	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:11696561	20060404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6509462	Ppil1<sup>em4Jgg</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:6509640	Ppil1<sup>em4Jgg</sup>/Ppil1<sup>em4Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em4Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007914	Mefv<sup>tm5.1(MEFV)Chae</sup>	is_implicated_in	DOID:2987	familial mediterranean fever		MGI:5007929	Mefv<sup>tm5.1(MEFV)Chae</sup>/Mefv<sup>tm5.1(MEFV)Chae</sup>  [background:] B6.129S6-Mefv<sup>tm5.1(MEFV)Chae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21600797	20110617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388158	Scn5a<sup>tm1Pec</sup>	is_implicated_in	DOID:0110646	long QT syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:25343952	20150527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388158	Scn5a<sup>tm1Pec</sup>	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:3622652	Scn5a<sup>tm1Pec</sup>/Scn5a<sup>+</sup>  [background:] involves: Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11533705	20150527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611443	Wt1<sup>tm2Hst</sup>/Wt1<sup>+</sup>  [background:] chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16245160	20060130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611443	Wt1<sup>tm2Hst</sup>/Wt1<sup>+</sup>  [background:] chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10077614	20060130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5607163	Oca2<sup>p-6Btlr</sup>/Oca2<sup>p-6Btlr</sup>  [background:] C57BL/6J-Oca2<sup>p-6Btlr</sup>	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	MGI:5607140	20141215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662356	Slit3<sup>tm1Dor</sup>/Slit3<sup>tm1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:12702769	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5466155	Kxd1<sup>tm1Wli</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:5466156	Kxd1<sup>tm1Wli</sup>/Kxd1<sup>tm1Wli</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22554196	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5819053	Apob<sup>tm2Sgy</sup>/Apob<sup>tm2Sgy</sup> Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:18160459	20170125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4441385	Fli1<sup>tm1Matr</sup>/Fli1<sup>tm1Matr</sup> Tg(Tek-cre)12Flv/0  [background:] B6.Cg-Fli1<sup>tm1Matr</sup> Tg(Tek-cre)12Flv	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:20228226	20100428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657248	Pde6c<sup>cpfl1</sup>/Pde6c<sup>cpfl1</sup>  [background:] involves: CXB1/ByJ	is_model_of	DOID:13911	achromatopsia						ECO:0000033	author statement supported by traceable reference	PMID:11853768	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6466590	Pak3<sup>tm1.1Rpo</sup>	is_implicated_in	DOID:0112051	non-syndromic X-linked intellectual disability 30		MGI:6466594	Pak3<sup>tm1.1Rpo</sup>/Y  [background:] B6.129S2(Cg)-Pak3<sup>tm1.1Rpo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31943058	20201012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5708587	Tg(Thy1-APPSweArc)BLngn/0  [background:] B6J.Cg-Tg(Thy1-APPSweArc)BLngn	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20615433	20160216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285078	Dnah5<sup>b2b016Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618869	Kcnq1<sup>tm1Kpfe</sup>/Kcnq1<sup>tm1Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11226272	20060410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584247	Irak3<sup>tm1Flv</sup>/Irak3<sup>tm1Flv</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:15809356	20050825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5707297	Slc3a1<sup>m1Crl</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:5707340	Slc3a1<sup>m1Crl</sup>/Slc3a1<sup>m1Crl</sup>  [background:] 129S2/SvPasCrl			ECO:0000033	author statement supported by traceable reference	PMID:25048459	20160205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5642051	Tg(Ly6a-GCSAM)102AIsg	is_implicated_in	DOID:9120	amyloidosis		MGI:5642052	Tg(Ly6a-GCSAM)102AIsg/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:23299888	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175031	Foxn1<sup>tm1Tbo</sup>/Foxn1<sup>tm1Tbo</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:8629026	20050701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433326	Dnah5<sup>b2b1537Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710595	Slc16a2<sup>tm1Dgen</sup>/Y  [background:] either: (involves: C57BL/6N) or (involves: NMRI)	is_model_of	DOID:0050631	Allan-Herndon-Dudley syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17318265	20070531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175729	Car2<sup>n</sup>/Car2<sup>n</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0110941	autosomal recessive osteopetrosis 3						ECO:0000033	author statement supported by traceable reference	PMID:3126501	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822571	Tg(CMV-ATXN3*94Q)94Pama/0  [background:] B6.FVB-Tg(CMV-ATXN3*94Q)94Pama	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:20510362	20100913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775617	Afg3l2<sup>Emv66</sup>	is_implicated_in	DOID:0050977	spinocerebellar ataxia type 28						ECO:0000033	author statement supported by traceable reference	PMID:25485680	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775617	Afg3l2<sup>Emv66</sup>	is_implicated_in	DOID:0050977	spinocerebellar ataxia type 28		MGI:5696777	Afg3l2<sup>Emv66</sup>/Afg3l2<sup>+</sup>  [background:] involves: MEV/2Ty			ECO:0000033	author statement supported by traceable reference	PMID:19625515	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618808	Atp8b1<sup>tm1Nbf</sup>/Atp8b1<sup>tm1Nbf</sup> Por<sup>tm1Wolf</sup>/Por<sup>tm1Wolf</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA	is_model_of	DOID:1852	intrahepatic cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:25068656	20150316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5552738	Drc1<sup>b2b2237Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5554187	Drc1<sup>b2b2237Clo</sup>/Drc1<sup>b2b2237Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b2237Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3821886	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000033	author statement supported by traceable reference	PMID:19029982	20090102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815135	Tg(PML-RARA)556Kog/?  [background:] involves: FVB/N	is_model_of	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:9122233	20081117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5752218	Lmna<sup>tm11Lgf</sup>	is_implicated_in	DOID:9164	achalasia		MGI:5754489	Lmna<sup>tm11Lgf</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25652409	20160324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820836	Gck<sup>m1Rge</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:4820839	Gck<sup>m1Rge</sup>/Gck<sup>+</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:19952346	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909085	Tg(Myh7-Ptpn11*Q510E)#Krnz	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines		MGI:5909088	Tg(Myh7-Ptpn11*Q510E)#Krnz/0  [background:] FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz			ECO:0000033	author statement supported by traceable reference	PMID:25724491	20180126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830454	P3h1<sup>tm1Dgen</sup>/P3h1<sup>tm1Dgen</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110336	osteogenesis imperfecta type 8						ECO:0000033	author statement supported by traceable reference	PMID:20363744	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792957	Tg(Alb1-Myc)#Sst/0 Tg(MtTGFA)Lmb/0  [background:] involves: C57BL/6 * CBA * CD-1	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21771728	20160923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3588578	Lmna<sup>tm3Stw</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3588578	Lmna<sup>tm3Stw</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:3589459	Lmna<sup>tm3Stw</sup>/Lmna<sup>tm3Stw</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:15972724	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5795894	Tnf<sup>Bpsm1</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:6272035	Tnf<sup>Bpsm1</sup>/Tnf<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5795894	Tnf<sup>Bpsm1</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:6272036	Tnf<sup>Bpsm1</sup>/Tnf<sup>Bpsm1</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3777760	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:17712420	20080417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174994	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9883847	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842791	Tg(Ckm-IGF1R*K1003R)1Dlr/0  [background:] FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11485987	20150416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842791	Tg(Ckm-IGF1R*K1003R)1Dlr/0  [background:] FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24598803	20150416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640522	Tg(APCS-Ifng)5Imeg	is_implicated_in	DOID:2237	hepatitis						ECO:0000033	author statement supported by traceable reference	PMID:10202184	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640522	Tg(APCS-Ifng)5Imeg	is_implicated_in	DOID:2237	hepatitis		MGI:5906283	Tg(APCS-Ifng)5Imeg/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:8290572	20170808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5642030	Npc1<sup>tm1.1Dso</sup>/Npc1<sup>tm1.1Dso</sup>  [background:] B6.129-Npc1<sup>tm1.1Dso</sup>	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26019327	20150629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818604	Atg16l1<sup>Gt(XR0164)Wtsi</sup>/Atg16l1<sup>Gt(XR0164)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110885	inflammatory bowel disease 10						ECO:0000033	author statement supported by traceable reference	PMID:18849966	20081208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5570964	Tg(Shank3-EGFP)1Hzo/0  [background:] involves: FVB/N	is_model_of	DOID:0060437	chromosome 22q13 duplication syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24153177	20140702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441745	Tg(LMNA*G608G)HClns	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441745	Tg(LMNA*G608G)HClns	is_implicated_in	DOID:3911	progeria		MGI:5441753	Tg(LMNA*G608G)HClns/?  [background:] C57BL/6-Tg(LMNA*G608G)HClns/J			ECO:0000033	author statement supported by traceable reference	PMID:16492728	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838422	Stk39<sup>tm1.2Slin</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24039833	20140424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838422	Stk39<sup>tm1.2Slin</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:4838433	Stk39<sup>tm1.2Slin</sup>/Stk39<sup>tm1.2Slin</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20813865	20140424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6446228	Prss8<sup>em1Bug</sup>	is_implicated_in	DOID:0060781	congenital secretory sodium diarrhea 3						ECO:0000033	author statement supported by traceable reference	PMID:31628112	20201208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4397671	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] B6.129-Kcnq2<sup>tm1.1Naas</sup>	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717577	Tg(Thy1-APPLon)2Vln/0  [background:] involves: FVB/N	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15509532	20080122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563691	Tg(SV40-KLK7)1010Teg	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5563692	Tg(SV40-KLK7)1010Teg/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11874483	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563691	Tg(SV40-KLK7)1010Teg	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563691	Tg(SV40-KLK7)1010Teg	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3845794	Tg(PMP22)C22Clh/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:8733121	20160629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3845794	Tg(PMP22)C22Clh/0  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:12090404	20160629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765977	Scn5a<sup>tm1Clhh</sup>	is_implicated_in	DOID:0110646	long QT syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:24705556	20140910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3765977	Scn5a<sup>tm1Clhh</sup>	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:5582068	Scn5a<sup>tm1Clhh</sup>/Scn5a<sup>+</sup>  [background:] involves: 129/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:22287583	20140910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622418	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] NOD.Cg-H2<sup>b</sup> Il4<sup>tm1Cgn</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16413168	20060516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522704	pta/pta  [background:] C57BL/6J-pta	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:15548583	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:10579712	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582824	Crb1<sup>tm1Wij</sup>/Crb1<sup>tm1Wij</sup> Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Chx10-EGFP/cre,-ALPP)2Clc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL	is_model_of	DOID:0110079	Leber congenital amaurosis 8						ECO:0000033	author statement supported by traceable reference	PMID:24339791	20140918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629742	Yme1l1<sup>tm1Tlan</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5805256	Yme1l1<sup>tm1Tlan</sup>/Yme1l1<sup>tm1Tlan</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: C57BL/6 * C57BL/6NCrl * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26785494	20170929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526094	Jak1<sup>M1Mhda</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5526095	Jak1<sup>M1Mhda</sup>/Jak1<sup>+</sup>  [background:] C3HeB/FeJ-Jak1<sup>M1Mhda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23791841	20140103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452236	Tg(tetO-Csnk1d)#Mfla	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452236	Tg(tetO-Csnk1d)#Mfla	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:4452245	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Csnk1d)#Mfla/0  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20145109	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784684	Tg(PDGFB-APPSwInd)J9Lms/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10818140	20090818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354601	Tsc2<sup>tm2.2Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354601	Tsc2<sup>tm2.2Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:4358058	Tsc2<sup>tm2.2Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19357198	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6115637	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:6160757	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>/Y Cnp<sup>tm1(cre)Kan</sup>/Cnp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446796	Bcs1l<sup>tm1.1Levp</sup>	is_implicated_in	DOID:0111455	GRACILE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22829922	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446796	Bcs1l<sup>tm1.1Levp</sup>	is_implicated_in	DOID:0111455	GRACILE syndrome		MGI:5446806	Bcs1l<sup>tm1.1Levp</sup>/Bcs1l<sup>tm1.1Levp</sup>  [background:] involves: 129 * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21274865	20200131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3808758	Tk2<sup>tm1Mihi</sup>/Tk2<sup>tm1Mihi</sup>  [background:] involves: 129S6/SvEv * C57BL/6J	is_model_of	DOID:0080120	mitochondrial DNA depletion syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:20940150	20110117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3808758	Tk2<sup>tm1Mihi</sup>/Tk2<sup>tm1Mihi</sup>  [background:] involves: 129S6/SvEv * C57BL/6J	is_model_of	DOID:0080120	mitochondrial DNA depletion syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:18467430	20110117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047402	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0110887	inflammatory bowel disease 12						ECO:0000033	author statement supported by traceable reference	PMID:7663509	20081208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6759477	Cilk1<sup>tm1.1Zfu</sup>	is_implicated_in	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome		MGI:6759479	Cilk1<sup>tm1.1Zfu</sup>/Cilk1<sup>tm1.1Zfu</sup>  [background:] B6.Cg-Cilk1<sup>tm1.1Zfu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29098359	20210917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6759477	Cilk1<sup>tm1.1Zfu</sup>	is_implicated_in	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome		MGI:6759479	Cilk1<sup>tm1.1Zfu</sup>/Cilk1<sup>tm1.1Zfu</sup>  [background:] B6.Cg-Cilk1<sup>tm1.1Zfu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28380258	20210917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6501730	Tg(Myh6-JUP*)1Dpju	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12		MGI:6501732	Tg(Myh6-JUP*)1Dpju/0  [background:] FVB/N-Tg(Myh6-JUP*)1Dpju			ECO:0000033	author statement supported by traceable reference	PMID:27170944	20210125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638047	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Scrib<sup>tm1.1Phum</sup>/Scrib<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24276238	20150602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850173	Otc<sup>spf</sup>/Y  [background:] involves: C57BL/6	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:1531355	20090713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604251	Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>/Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0110722	neuronal ceroid lipofuscinosis 7						ECO:0000033	author statement supported by traceable reference	PMID:24423645	20141112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433047	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] B6.129(Cg)-Gabra1<sup>tm1.1Geh</sup>	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:22812724	20160601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433047	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] B6.129(Cg)-Gabra1<sup>tm1.1Geh</sup>	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:26054439	20160601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044705	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0110629	Wolfram syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15056606	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444502	Tg(tetO-IL1B)KBry	is_implicated_in	DOID:2841	asthma		MGI:5444503	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IL1B)KBry/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15668323	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611755	Cacna1f<sup>tm1Ntbh</sup>/Y  [background:] B6.129-Cacna1f<sup>tm1Ntbh</sup>	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:16155113	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829382	Lbr<sup>ic-J</sup>/Lbr<sup>ic-J</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:9631	Pelger-Huet anomaly						ECO:0000033	author statement supported by traceable reference	PMID:17403717	20090129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618699	Tg(TcraAI4)1Dvs/0 Tg(TcrbAI4)1Dvs/0  [background:] NOD-Tg(TcraAI4)1Dvs Tg(TcrbAI4)1Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6509459	Ppil1<sup>em3Jgg</sup>	is_implicated_in	DOID:0112325	pontocerebellar hypoplasia type 14		MGI:6509636	Ppil1<sup>em3Jgg</sup>/Ppil1<sup>em3Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em3Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473963	Vwf<sup>tm1.1Vhf</sup>	is_implicated_in	DOID:12531	von Willebrand's disease		MGI:6473965	Vwf<sup>tm1.1Vhf</sup>/Vwf<sup>tm1.1Vhf</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30565388	20201124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473963	Vwf<sup>tm1.1Vhf</sup>	is_implicated_in	DOID:12531	von Willebrand's disease		MGI:6473967	Vwf<sup>tm1.1Vhf</sup>/Vwf<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30565388	20201124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806092	Tg(Rho-Arl3*Q71L)#Visu	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:5806094	Tg(Rho-Arl3*Q71L)#Visu/0  [background:] involves: 129 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26936825	20161103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625060	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] either: NOD.129-Il4<sup>tm1Cgn</sup> or (involves: 129 * NOD)	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9703318	20060622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528279	Trp53<sup>tm3.1Glo</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27869650	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528279	Trp53<sup>tm3.1Glo</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3576493	Trp53<sup>tm3.1Glo</sup>/Trp53<sup>+</sup>  [background:] B6.129S7-Trp53<sup>tm3.1Glo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15607981	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385681	Myd88<sup>tm1Aki</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21763676	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476838	Tg(TARDBP*G348C)#Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:21752789	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437079	Lrp1<sup>b2b1554Clo</sup>	is_implicated_in	DOID:0060327	omphalocele		MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654122	Acvr2b<sup>tm1Enl</sup>/Acvr2b<sup>tm1Enl</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:9242489	20110307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941778	Slc6a8<sup>tm1.2Clar</sup>/Y  [background:] involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:21249153	20110323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668046	Hexb<sup>tm1Grv</sup>/Hexb<sup>tm1Grv</sup>  [background:] either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:8789434	20050613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831728	Ts(16C-tel)1Cje/0  [background:] involves: C3H/HeSnJ * C57BL/6J * CD-1 * Rb(16.17)32Lub * STOCK Rb(11.16)2H/H	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9600952	20090213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5703730	Tg(Prnp-MAPT*R406W)21807Dwst	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5703732	Tg(Prnp-MAPT*R406W)21807Dwst/?  [background:] FVB/N-Tg(Prnp-MAPT*R406W)21807Dwst			ECO:0000033	author statement supported by traceable reference	PMID:15681835	20160118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6729716	Awat2<sup>tm1.2Golc</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:6729736	Awat2<sup>tm1.2Golc</sup>/Y  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32851726	20210809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6729716	Awat2<sup>tm1.2Golc</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:6729732	Awat2<sup>tm1.2Golc</sup>/Awat2<sup>tm1.2Golc</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32851726	20210809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589555	Psen1<sup>tm1Tak</sup>/Psen1<sup>tm1Tak</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15908021	20051014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583907	Ins2<sup>Akita</sup>/Ins2<sup>+</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>/J	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:15914643	20060626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046092	Slc37a4<sup>tm1Jyc</sup>/Slc37a4<sup>tm1Jyc</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:12925567	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424775	Acta1<sup>tm1Hrd</sup>	is_implicated_in	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:27102768	20160919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424775	Acta1<sup>tm1Hrd</sup>	is_implicated_in	DOID:0110927	nemaline myopathy 3		MGI:5424992	Acta1<sup>tm1Hrd</sup>/Acta1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6JArc)			ECO:0000033	author statement supported by traceable reference	PMID:22067542	20160919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424775	Acta1<sup>tm1Hrd</sup>	is_implicated_in	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:23736297	20160919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435560	Porcn<sup>tm1Vdv</sup>/Y  [background:] chimera involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623489	Col1a1<sup>tm1.1Jcm</sup>/Col1a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1)	is_model_of	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000033	author statement supported by traceable reference	PMID:10608859	20160510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5516452	Tg(Prnp-ATXN3*148Q)148.19Olri	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:5516455	Tg(Prnp-ATXN3*148Q)148.19Olri/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:17626202	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5516452	Tg(Prnp-ATXN3*148Q)148.19Olri	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:23100324	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177586	Gata1<sup>tm2Sho</sup>	is_implicated_in	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:23462118	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177586	Gata1<sup>tm2Sho</sup>	is_implicated_in	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:16109774	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177586	Gata1<sup>tm2Sho</sup>	is_implicated_in	DOID:4971	myelofibrosis		MGI:2653501	Gata1<sup>tm2Sho</sup>/Gata1<sup>tm2Sho</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12149188	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177586	Gata1<sup>tm2Sho</sup>	is_implicated_in	DOID:4971	myelofibrosis		MGI:4417827	Gata1<sup>tm2Sho</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12149188	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23873941	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:5506904	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr/0  [background:] FVB.Cg-Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr			ECO:0000033	author statement supported by traceable reference	PMID:23873941	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4836620	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17237784	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:3813525	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr/0  [background:] involves: 129S4/SvJae * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:18757421	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4829793	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:12163417	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6187993	Tg(RHO*P347S)A1Tili	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:6188004	Tg(RHO*P347S)A1Tili/0  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29242588	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7262689	Tg(KRT18*R89C)22Rgo	is_implicated_in	DOID:2237	hepatitis		MGI:7262692	Tg(KRT18*R89C)22Rgo/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8522591	20220419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:24802098	20160113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5702658	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15199412	20160113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6693810	Dhdds<sup>tm1.1Sjpi</sup>	is_implicated_in	DOID:0110352	retinitis pigmentosa 59		MGI:6693811	Dhdds<sup>tm1.1Sjpi</sup>/Dhdds<sup>tm1.1Sjpi</sup> Tg(BEST1-rtTA,tetO-cre)1Yzl/0  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:32245241	20210421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400993	Nlgn1<sup>em1Taku</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6400995	Nlgn1<sup>em1Taku</sup>/Nlgn1<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28841651	20200323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400993	Nlgn1<sup>em1Taku</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6400998	Nlgn1<sup>em1Taku</sup>/Nlgn1<sup>em1Taku</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28841651	20200323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5523900	Cntn1<sup>usl</sup>/Cntn1<sup>usl</sup>  [background:] B6.MRL-Cntn1<sup>usl</sup>/GrsrJ	is_model_of	DOID:0080101	Compton-North congenital myopathy						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386674	Rpgr<sup>tm1Tili</sup>	is_implicated_in	DOID:0110414	retinitis pigmentosa 3						ECO:0000033	author statement supported by traceable reference	PMID:25877300	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386674	Rpgr<sup>tm1Tili</sup>	is_implicated_in	DOID:0110414	retinitis pigmentosa 3						ECO:0000033	author statement supported by traceable reference	PMID:26908598	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386674	Rpgr<sup>tm1Tili</sup>	is_implicated_in	DOID:0110414	retinitis pigmentosa 3		MGI:3038416	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10725384	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578541	Lamb2<sup>npht</sup>	is_implicated_in	DOID:0060852	Pierson syndrome		MGI:5578543	Lamb2<sup>npht</sup>/Lamb2<sup>npht</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24293254	20140826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793464	Aire<sup>tm1Mand</sup>	is_implicated_in	DOID:12842	Guillain-Barre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23487421	20130503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793464	Aire<sup>tm1Mand</sup>	is_implicated_in	DOID:12842	Guillain-Barre syndrome		MGI:3803199	Aire<sup>tm1Mand</sup>/Aire<sup>+</sup>  [background:] NOD.129P2-Aire<sup>tm1Mand</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22490868	20130503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690971	Tg(KRT5-Stat3*A661C*N663C)1Jdg	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:23543761	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690971	Tg(KRT5-Stat3*A661C*N663C)1Jdg	is_implicated_in	DOID:8893	psoriasis		MGI:4430194	Tg(KRT5-Stat3*A661C*N663C)1Jdg/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:15592573	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:22020333	20120828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043322	Etv4<sup>tm1Hass</sup>/Etv4<sup>tm1Hass</sup> Tg(MMTVneu)202Mul/Tg(MMTVneu)202Mul  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:14635793	20080617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179981	F8<sup>tm1Kaz</sup>	is_implicated_in	DOID:12134	factor VIII deficiency						ECO:0000033	author statement supported by traceable reference	PMID:31594977	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179981	F8<sup>tm1Kaz</sup>	is_implicated_in	DOID:12134	factor VIII deficiency		MGI:2449544	F8<sup>tm1Kaz</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7647782	20200219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522144	Tg(Tyrp1-TAg)3434Bee	is_implicated_in	DOID:4645	retinal cancer						ECO:0000033	author statement supported by traceable reference	PMID:9840923	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522144	Tg(Tyrp1-TAg)3434Bee	is_implicated_in	DOID:4645	retinal cancer						ECO:0000033	author statement supported by traceable reference	PMID:19098995	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522144	Tg(Tyrp1-TAg)3434Bee	is_implicated_in	DOID:4645	retinal cancer		MGI:3763734	Tg(Tyrp1-TAg)3434Bee/?  [background:] involves: BALB/c * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11896616	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693665	Fbxo11<sup>Jf</sup>/Fbxo11<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeN * C57BL/6J	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:17035249	20080721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623958	Cd38<sup>tm1Lnd</sup>/Cd38<sup>tm1Lnd</sup>  [background:] NOD.129P2(B6)-Cd38<sup>tm1Lnd</sup>/LtJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16585549	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583695	Itga9<sup>tm1Des</sup>/Itga9<sup>tm1Des</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060646	congenital chylothorax						ECO:0000033	author statement supported by traceable reference	PMID:10866676	20100302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24227978	20140918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817475	Lepr<sup>m3Btlr</sup>/Lepr<sup>m3Btlr</sup>  [background:] C57BL/6J-Lepr<sup>m3Btlr</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:3815208	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5538511	Mecp2<sup>tm3Meg</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5538526	Mecp2<sup>tm3Meg</sup>/Y  [background:] B6.129-Mecp2<sup>tm3Meg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23770587	20140205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5478742	Tg(CMV-LITAF*W116G)#Lli	is_implicated_in	DOID:0110151	Charcot-Marie-Tooth disease type 1C		MGI:5478744	Tg(CMV-LITAF*W116G)#Lli/Tg(CMV-LITAF*W116G)#Lli  [background:] FVB-Tg(CMV-LITAF*W116G)#Lli			ECO:0000033	author statement supported by traceable reference	PMID:23359569	20130507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774663	Klhl40<sup>tm1(KOMP)Vlcg</sup>/Klhl40<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Klhl40<sup>tm1(KOMP)Vlcg</sup>	is_model_of	DOID:0110930	nemaline myopathy 8						ECO:0000033	author statement supported by traceable reference	PMID:24960163	20160601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437103	b2b1200.2Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437106	b2b1200.2Clo/b2b1200.2Clo  [background:] C57BL/6J-b2b1200.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038214	Gck<sup>Rgsc272</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558945	Tg(Camk2a-tTA)1Mmay/0 Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/Fgf14<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:24503275	20140415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5882799	Clcn7<sup>tm1.1Mawa</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:6259526	Clcn7<sup>tm1.1Mawa</sup>/Clcn7<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28942122	20181207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5688299	Tg(tetO-PTPN11*E76K)#Jiwu	is_implicated_in	DOID:1324	lung cancer		MGI:5688300	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-PTPN11*E76K)#Jiwu/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24480804	20150925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5636649	Tg(Lck-Tax)53Hall	is_implicated_in	DOID:5602	T-cell adult acute lymphocytic leukemia		MGI:5636650	Tg(Lck-Tax)53Hall/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16550188	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5636649	Tg(Lck-Tax)53Hall	is_implicated_in	DOID:5602	T-cell adult acute lymphocytic leukemia		MGI:5636650	Tg(Lck-Tax)53Hall/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25035162	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5451025	Ndufs4<sup>tm1Rpa</sup>/Ndufs4<sup>tm1Rpa</sup> Tg(Nes-cre)1Kln/0  [background:] B6.Cg-Tg(Nes-cre)1Kln Ndufs4<sup>tm1Rpa</sup>	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:22653057	20130124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831375	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] CBACa.129P2-Fgfr3<sup>tm1.1Aomw</sup>	is_model_of	DOID:0060703	Muenke Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712469	Thbd<sup>tm2Emc</sup>/Thbd<sup>tm2Emc</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:2452	thrombophilia						ECO:0000033	author statement supported by traceable reference	PMID:12208873	20120305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652447	Tg(Thy1-APP)3Somm/0  [background:] involves: C57BL/6J * DBA/2	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:11222652	20101005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425687	Phex<sup>Mhdabap024</sup>/Phex<sup>Mhdabap024</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7427681	Defb19<sup>em1Cya</sup>	is_implicated_in	DOID:229	female reproductive system disease		MGI:7427684	Defb19<sup>em1Cya</sup>/Defb19<sup>em1Cya</sup>  [background:] C57BL/6-Defb19<sup>em1Cya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36513070	20230120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578654	Crh<sup>m1H</sup>	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:5578736	Crh<sup>m1H</sup>/Crh<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24302625	20200321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578654	Crh<sup>m1H</sup>	is_implicated_in	DOID:446	primary hyperaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:31827172	20200321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449894	Tg(SOD1*L126Z)#Deng	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5449895	Tg(SOD1*L126Z)#Deng/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16636275	20130122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474459	Tg(Tagln-SLC6A4)#Edd	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20160824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474459	Tg(Tagln-SLC6A4)#Edd	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:19679640	20160824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474459	Tg(Tagln-SLC6A4)#Edd	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:25550449	20160824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474459	Tg(Tagln-SLC6A4)#Edd	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5474460	Tg(Tagln-SLC6A4)#Edd/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16614302	20160824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474459	Tg(Tagln-SLC6A4)#Edd	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:23513067	20160824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4410604	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-ATXN3)2904Olri/Tg(tetO-ATXN3)2904Olri  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:19666958	20091215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046533	Clcn5<sup>tm1Tjj</sup>/Y  [background:] B6.129-Clcn5<sup>tm1Tjj</sup>	is_model_of	DOID:0050699	Dent disease						ECO:0000033	author statement supported by traceable reference	PMID:11099045	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056450	Tg(SOD1*)125Dbo/?  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:12966034	20110810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693895	Gucy2e<sup>tm1Gar</sup>/Gucy2e<sup>tm1Gar</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0111011	cone-rod dystrophy 6						ECO:0000033	author statement supported by traceable reference	PMID:10407028	20090604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819864	Tg(CEACAM5-Tag)L5496Wzm/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:10842202	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427702	Wnk4<sup>tm1Pfi</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:5427703	Wnk4<sup>tm1Pfi</sup>/Wnk4<sup>tm1Pfi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22550170	20120713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5439173	Barx2<sup>tm1Rsd</sup>/Barx2<sup>tm1Rsd</sup> Dmd<sup>mdx</sup>/Y  [background:] involves: 129 * C57BL/6 * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22076929	20121024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580087	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3762252	Tg(Timp1-Msx2*P7H)1Rem/0  [background:] involves: C57BL/6 * CBA/J	is_model_of	DOID:2340	craniosynostosis						ECO:0000033	author statement supported by traceable reference	PMID:7597092	20071126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4834518	Fkrp<sup>tm1Itl</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20675713	20101116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544078	Tg(Snca-SNCA/GFP)#Jyl/Tg(Snca-SNCA/GFP)#Jyl  [background:] involves: C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:23643841	20140214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661527	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:25255451	20150911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711235	Cadps2<sup>tm1Tfr</sup>/Cadps2<sup>tm1Tfr</sup>  [background:] C57BL/6-Cadps2<sup>tm1Tfr</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:17380209	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042794	Nrxn1<sup>tm1Sud</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:21262241	20120718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042794	Nrxn1<sup>tm1Sud</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5428133	Nrxn1<sup>tm1Sud</sup>/Nrxn1<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19822762	20120718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22198154	20130222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3027999	Pde6b<sup>atrd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7286340	Specc1l<sup>em4Kumc</sup>	is_implicated_in	DOID:0080698	Teebi hypertelorism syndrome 1		MGI:7286353	Specc1l<sup>em4Kumc</sup>/Specc1l<sup>em4Kumc</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6276041	Tg(Myh6-Camk2d_ic)LJhb	is_implicated_in	DOID:6000	congestive heart failure		MGI:6276046	Tg(Myh6-Camk2d_ic)LJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5494450	Far2<sup>tm2b(KOMP)Wtsi</sup>	is_implicated_in	DOID:987	alopecia		MGI:6267296	Far2<sup>tm2b(KOMP)Wtsi</sup>/Far2<sup>tm2b(KOMP)Wtsi</sup>  [background:] B6N(Cg)-Far2<sup>tm2b(KOMP)Wtsi</sup>/2J			ECO:0000033	author statement supported by traceable reference	PMID:30372477	20181219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5754382	Psen1<sup>tm4.1Shn</sup>/Psen1<sup>+</sup> Psen2<sup>tm1Haa</sup>/Psen2<sup>tm1Haa</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25741723	20160324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183900	Tsc1<sup>tm1.1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183900	Tsc1<sup>tm1.1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3588773	Tsc1<sup>tm1.1Djk</sup>/Tsc1<sup>+</sup>  [background:] either: 129S4/SvJae-Tsc1<sup>tm1Djk</sup> or (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11875047	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694660	Itgb4<sup>tm1Fgg</sup>/Itgb4<sup>tm1Fgg</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060733	junctional epidermolysis bullosa with pyloric atresia						ECO:0000033	author statement supported by traceable reference	PMID:9670011	20090319	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675251	Men1<sup>tm1.2Zqw</sup>/Men1<sup>tm1.2Zqw</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * CBA/J	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:12941803	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804729	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1.1Plob</sup>  [background:] B6.129S1-Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1.1Plob</sup>	is_model_of	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000033	author statement supported by traceable reference	PMID:18343701	20080908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:23687340	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29321660	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:28455243	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:26914605	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma		MGI:5009551	Tg(Th-MYCN)41Waw/0  [background:] involves: BALB/c * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18842883	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma		MGI:5009549	Tg(Th-MYCN)41Waw/0  [background:] involves: BALB/c * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9214616	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma		MGI:5009550	Tg(Th-MYCN)41Waw/Tg(Th-MYCN)41Waw  [background:] involves: BALB/c * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9214616	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039395	Tg(Th-MYCN)41Waw	is_implicated_in	DOID:769	neuroblastoma		MGI:5009555	Tg(Th-MYCN)41Waw/0  [background:] involves: 129X1/SvJ * BALB/c * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21559450	20180904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435555	Porcn<sup>tm1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435560	Porcn<sup>tm1Vdv</sup>/Y  [background:] chimera involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435555	Porcn<sup>tm1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435559	Porcn<sup>tm1Vdv</sup>/Porcn<sup>+</sup>  [background:] chimera involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605225	Large1<sup>vls</sup>/Large1<sup>vls</sup>  [background:] B6.CAST(Cg)-Large1<sup>vls</sup>/Pjn	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:16111892	20101116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910536	Tg(CMV-cat,-ROCK2*)3-1Koba	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27766308	20170928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910536	Tg(CMV-cat,-ROCK2*)3-1Koba	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy		MGI:5910538	Tg(CMV-cat,-ROCK2*)3-1Koba/0 Tg(Tagln-cre)1Her/0  [background:] involves: C57BL/6 * C57BL/6JJcl * DBA/2 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26315406	20170928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387762	Tyro3<sup>tm1Grl</sup>	is_implicated_in	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:23840307	20140130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152755	Pdx1<sup>tm1Ted</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:24411943	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152755	Pdx1<sup>tm1Ted</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12697734	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152755	Pdx1<sup>tm1Ted</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9637677	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5508226	Gnao1<sup>tm2Rneu</sup>	is_implicated_in	DOID:0080450	developmental and epileptic encephalopathy 17		MGI:6295359	Gnao1<sup>tm2Rneu</sup>/Gnao1<sup>+</sup>  [background:] B6.129S1-Gnao1<sup>tm2Rneu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30682176	20190502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6392157	Iqsec2<sup>em1Frk</sup>	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:6392615	Iqsec2<sup>em1Frk</sup>/Y  [background:] involves: C3HeB/FeJ * C57BL/6NJ			ECO:0000033	author statement supported by traceable reference	PMID:31978606	20200303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2675118	Rasgrp1<sup>lag</sup>/Rasgrp1<sup>lag</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12932358	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527173	Tecta<sup>tm4.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0110544	autosomal dominant nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195494	Tbc1d24<sup>em2Tbf</sup>	is_implicated_in	DOID:0080449	developmental and epileptic encephalopathy 16		MGI:6306133	Tbc1d24<sup>em2Tbf</sup>/Tbc1d24<sup>em2Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em2Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30602030	20190529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588420	Hjv<sup>tm1Nca</sup>/Hjv<sup>tm1Nca</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac	is_model_of	DOID:0111027	hemochromatosis type 2A						ECO:0000033	author statement supported by traceable reference	PMID:16075059	20050927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5287978	Lmx1a<sup>tm1Tpe</sup>	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:27407143	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028002	Pde6b<sup>atrd2</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817455	Arid4a<sup>tm1Alb</sup>/Arid4a<sup>tm1Alb</sup> Arid4b<sup>tm1Alb</sup>/Arid4b<sup>+</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:18728284	20081121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491268	Tbc1d32<sup>b2b2284Clo</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20150727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430747	Tg(Emu-TXLNA)1Amjr	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26365984	20190125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430747	Tg(Emu-TXLNA)1Amjr	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23772034	20190125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430747	Tg(Emu-TXLNA)1Amjr	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20952683	20190125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430747	Tg(Emu-TXLNA)1Amjr	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:6274721	Tg(Emu-TXLNA)1Amjr/0  [background:] B6.Cg-Tg(Emu-TXLNA)1Amjr			ECO:0000033	author statement supported by traceable reference	PMID:19038581	20190125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:24587158	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:32239698	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:16049335	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:23470163	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721992	Tg(Thy1-APPSwDutIowa)BWevn	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:3722063	Tg(Thy1-APPSwDutIowa)BWevn/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14985348	20210715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7279292	Glyr1<sup>em1Dsr</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:7279300	Glyr1<sup>em1Dsr</sup>/Glyr1<sup>em1Dsr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:35182466	20220523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046056	Rs1<sup>tm1Web</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:11983912	20070912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424984	Casr<sup>BCH013</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425923	Casr<sup>BCH013</sup>/Casr<sup>BCH013</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH013</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3802703	Gusb<sup>mps-3J</sup>/Gusb<sup>mps-3J</sup>  [background:] C57BL/6J-Gusb<sup>mps-3J</sup>/J	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	MGI:3801433	20080819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437080	Megf8<sup>b2b1702.2Clo</sup>	is_implicated_in	DOID:0060234	Carpenter syndrome		MGI:5437117	Megf8<sup>b2b1702.2Clo</sup>/Megf8<sup>b2b1702.2Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b1702.2Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6274278	Tg(Krt14-Rac1*G12V)#Mrnk	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:32615123	20210422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6274278	Tg(Krt14-Rac1*G12V)#Mrnk	is_implicated_in	DOID:8893	psoriasis		MGI:6274282	Tg(Krt14-Rac1*G12V)#Mrnk/0  [background:] either: B6.CBACa-Tg(Krt14-Rac1*G12V)#Mrnk or C.CBACa-Tg(Krt14-Rac1*G12V)#Mrnk			ECO:0000033	author statement supported by traceable reference	PMID:27294528	20210422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6274278	Tg(Krt14-Rac1*G12V)#Mrnk	is_implicated_in	DOID:8893	psoriasis		MGI:6274280	Tg(Krt14-Rac1*G12V)#Mrnk/0  [background:] involves: CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:27294528	20210422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415610	Itm2b<sup>tm2.1Ldad</sup>	is_implicated_in	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21587206	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415610	Itm2b<sup>tm2.1Ldad</sup>	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4936849	Itm2b<sup>tm2.1Ldad</sup>/Itm2b<sup>+</sup>  [background:] B6.129-Itm2b<sup>tm2.1Ldad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21098268	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6117774	Cpox<sup>Rbc16</sup>	is_implicated_in	DOID:13269	hereditary coproporphyria		MGI:6160805	Cpox<sup>Rbc16</sup>/Cpox<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28600349	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5754533	Grm6<sup>nob8</sup>	is_implicated_in	DOID:0110865	congenital stationary night blindness 1B		MGI:5897563	Grm6<sup>nob8</sup>/Grm6<sup>nob8</sup>  [background:] CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:28490646	20170522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774863	Exoc5<sup>tm1c(KOMP)Mbp</sup>	is_implicated_in	DOID:0070314	obstructive nephropathy		MGI:5774940	Exoc5<sup>tm1c(KOMP)Mbp</sup>/Exoc5<sup>tm1c(KOMP)Mbp</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:27511831	20190705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774863	Exoc5<sup>tm1c(KOMP)Mbp</sup>	is_implicated_in	DOID:0070314	obstructive nephropathy		MGI:5774940	Exoc5<sup>tm1c(KOMP)Mbp</sup>/Exoc5<sup>tm1c(KOMP)Mbp</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:26046524	20190705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693809	Irf6<sup>tm1Mjd</sup>/Irf6<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060055	popliteal pterygium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17041603	20070326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655551	Asah1<sup>tm1Esc</sup>/Asah1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0050464	Farber lipogranulomatosis						ECO:0000033	author statement supported by traceable reference	PMID:11829492	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5789748	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Rbl1<sup>tm1Tyj</sup>/Rbl1<sup>tm1Tyj</sup> Rbl2<sup>tm2Tyj</sup>/Rbl2<sup>tm2Tyj</sup>  [background:] involves: 129 * 129S2/SvPas * 129S4/SvJae	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25252918	20160823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680573	Pax6<sup>1Jrt</sup>/Pax6<sup>+</sup>  [background:] C3.B6-Pax6<sup>1Jrt</sup>	is_model_of	DOID:0060673	Peters anomaly						ECO:0000033	author statement supported by traceable reference	MGI:2680583	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5805519	Tg(PyLT)1Vb/0  [background:] Not Specified	is_model_of	DOID:7004	ACTH-secreting pituitary adenoma						ECO:0000033	author statement supported by traceable reference	PMID:1316082	20161028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839791	Men1<sup>tm1Gfk</sup>/Men1<sup>tm1Gfk</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:15060136	20170324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697200	Tg(ATXN2*72Q)#Plt/0  [background:] FVB/N-Tg(ATXN2*72Q)#Plt	is_model_of	DOID:0050955	spinocerebellar ataxia type 2						ECO:0000033	author statement supported by traceable reference	PMID:25902068	20151125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774163	Gja1<sup>tm3Gfi</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:32320893	20200819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774163	Gja1<sup>tm3Gfi</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3808026	Gja1<sup>tm3Gfi</sup>/Gja1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:18077386	20200819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461135	Tnfrsf1a<sup>tm2.1Rsie</sup>	is_implicated_in	DOID:0090018	autosomal dominant familial periodic fever		MGI:4461160	Tnfrsf1a<sup>tm2.1Rsie</sup>/Tnfrsf1a<sup>+</sup>  [background:] B6.Cg-Tnfrsf1a<sup>tm2.1Rsie</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20457915	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664353	Col1a2<sup>oim</sup>/Col1a2<sup>oim</sup>  [background:] involves: C3H/HeJ * C57BL/6JLe	is_model_of	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:8446583	20070907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442645	Ryr2<sup>tm1.1Maya</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:24755079	20150504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442645	Ryr2<sup>tm1.1Maya</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:4443207	Ryr2<sup>tm1.1Maya</sup>/Ryr2<sup>+</sup>  [background:] C57BL/6J-Ryr2<sup>tm1.1Maya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20224043	20150504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5707975	Zfyve26<sup>tm1.1Cahb</sup>	is_implicated_in	DOID:0110768	hereditary spastic paraplegia 15		MGI:5749268	Zfyve26<sup>tm1.1Cahb</sup>/Zfyve26<sup>tm1.1Cahb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24367272	20160219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629227	Kat6a<sup>tm1Avo</sup>/Kat6a<sup>tm1Avo</sup>  [background:] involves: 129/Sv * BALB/c * FVB/N	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22921202	20121228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181289	Gpd2<sup>tm1Tka</sup>	is_implicated_in	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:21908222	20120315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6272829	Thra<sup>em1Ffla</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:6317178	Thra<sup>em1Ffla</sup>/Thra<sup>+</sup>  [background:] C57BL/6-Thra<sup>em1Ffla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29205102	20190711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806093	Myo15a<sup>tm1.1Jebd</sup>	is_implicated_in	DOID:0110488	autosomal recessive nonsyndromic deafness 3		MGI:6192743	Myo15a<sup>tm1.1Jebd</sup>/Myo15a<sup>tm1.1Jebd</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26302205	20180806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560815	Cfc1<sup>b2b2736.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561116	Cfc1<sup>b2b2736.1Clo</sup>/Cfc1<sup>b2b2736.1Clo</sup>  [background:] C57BL/6J-Cfc1<sup>b2b2736.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5544056	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:14982883	20140213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2674087	P2ry12<sup>tm1Pcon</sup>/P2ry12<sup>tm1Pcon</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060692	platelet-type bleeding disorder 8						ECO:0000033	author statement supported by traceable reference	PMID:12897207	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867516	Tg(CAG-ELN*)2Zu	is_implicated_in	DOID:3144	cutis laxa		MGI:4867518	Tg(CAG-ELN*)2Zu/0  [background:] C57BL/6J-Tg(CAG-ELN*)2Zu			ECO:0000033	author statement supported by traceable reference	PMID:20600892	20110111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4848149	Dnm2<sup>tm1.1Ics</sup>/Dnm2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:14717	centronuclear myopathy						ECO:0000033	author statement supported by traceable reference	PMID:27870637	20170105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6392623	Hspb8<sup>tm1Vti</sup>	is_implicated_in	DOID:0111208	obsolete distal hereditary motor neuronopathy type 2A		MGI:6392628	Hspb8<sup>tm1Vti</sup>/Hspb8<sup>tm1Vti</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:28780615	20200303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2451065	Gusb<sup>tm2Sly</sup>/Gusb<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784504	Pparg<sup>tm3(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6	is_model_of	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178322	Des<sup>tm1Cap</sup>/Des<sup>tm1Cap</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0080092	myofibrillar myopathy 1						ECO:0000033	author statement supported by traceable reference	PMID:8794866	20060523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179819	Scnn1b<sup>tm1Wsh</sup>	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179819	Scnn1b<sup>tm1Wsh</sup>	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1		MGI:2181800	Scnn1b<sup>tm1Wsh</sup>/Scnn1b<sup>tm1Wsh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9990092	20131223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836577	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:19117991	20090320	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307127	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] 129S6/SvEvTac-Was<sup>tm1Sbs</sup>/J	is_model_of	DOID:2986	IgA glomerulonephritis						ECO:0000033	author statement supported by traceable reference	PMID:22079330	20120226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838172	Tg(Myh6-MYL2*D166V)1Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:26124132	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838172	Tg(Myh6-MYL2*D166V)1Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:26906074	20180809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838172	Tg(Myh6-MYL2*D166V)1Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10		MGI:3838173	Tg(Myh6-MYL2*D166V)1Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18987303	20180809	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834842	Magel2<sup>tm1Stw</sup>/Magel2<sup>+</sup>  [background:] C57BL/6-Magel2<sup>tm1Stw</sup>	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19172181	20090309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5605714	Prom1<sup>rd19</sup>/Prom1<sup>rd19</sup>  [background:] B6.BXD83-Prom1<sup>rd19</sup>/BocJ	is_model_of	DOID:0110376	retinitis pigmentosa 41						ECO:0000033	author statement supported by traceable reference	MGI:5605698	20141205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4999643	Chd7<sup>Ome</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5437367	Chd7<sup>Ome</sup>/Chd7<sup>+</sup>  [background:] involves: BALB/cByJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22539951	20121003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587024	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] involves: MYA/Hu	is_model_of	DOID:0060739	hand-foot-genital syndrome						ECO:0000033	author statement supported by traceable reference	PMID:5519671	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587024	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] involves: MYA/Hu	is_model_of	DOID:0060739	hand-foot-genital syndrome						ECO:0000033	author statement supported by traceable reference	MGI:1889019	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5298093	Tg(CAG-cat,-Dcn*)#Debi	is_implicated_in	DOID:0060445	congenital stromal corneal dystrophy		MGI:5298094	Tg(CAG-cat,-Dcn*)#Debi/0 Tg(Kera-cre)KC4.3Wwk/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21893019	20111213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559369	Tg(KRT14-HPV8)85Vuc	is_implicated_in	DOID:4159	skin cancer		MGI:5559465	Tg(KRT14-HPV8)85Vuc/0  [background:] FVB.Cg-Tg(KRT14-HPV8)85Vuc			ECO:0000033	author statement supported by traceable reference	PMID:15735026	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5302243	Tg(CMV-MYOC*Y437H)#Vcs/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:1070	primary open angle glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:21821918	20120121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583951	Hmga1<sup>tm1Brun</sup>/Hmga1<sup>tm1Brun</sup>  [background:] Not Specified	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15924147	20050819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270415	Tnni2<sup>tm1Sgao</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6272014	Tnni2<sup>tm1Sgao</sup>/Tnni2<sup>tm1Sgao</sup>  [background:] involves: 129 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:25340332	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270415	Tnni2<sup>tm1Sgao</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6272015	Tnni2<sup>tm1Sgao</sup>/Tnni2<sup>+</sup>  [background:] involves: 129 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:25340332	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646621	Tg(Camk2a-MAPT*P301L)D35Jiri	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5646623	Tg(Camk2a-MAPT*P301L)D35Jiri/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25620700	20150807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812462	Krt14<sup>tm1Efu</sup>/Krt14<sup>tm1Efu</sup>  [background:] involves: 129	is_model_of	DOID:4644	epidermolysis bullosa simplex						ECO:0000033	author statement supported by traceable reference	PMID:7539810	20081029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575580	Apc<sup>Min</sup>/Apc<sup>+</sup> Recql4<sup>tm1Glu</sup>/Recql4<sup>tm1Glu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:2732	Rothmund-Thomson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15703196	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5292220	Tmem67<sup>tm1Dgen</sup>	is_implicated_in	DOID:0111001	Joubert syndrome 6		MGI:5292226	Tmem67<sup>tm1Dgen</sup>/Tmem67<sup>tm1Dgen</sup>  [background:] B6.129P2-Tmem67<sup>tm1Dgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23283079	20131104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793277	Atp7b<sup>tx</sup>/Atp7b<sup>tx</sup>  [background:] DL-Atp7b<sup>tx</sup>	is_model_of	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:8894697	20080611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:23223430	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:26276665	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:33941818	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:28151426	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:27154187	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:24880340	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857296	Hbb-b2<sup>tm1Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:24282296	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:22426494	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:34852229	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5315439	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16936724	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5315442	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>tm1Hzo</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:22002997	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5315439	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:22002997	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:2651696	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12575948	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651378	Atxn7<sup>tm1Hzo</sup>	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:3774850	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16494529	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6363552	Pianp<sup>tm1d(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6364110	Pianp<sup>tm1d(KOMP)Wtsi</sup>/Pianp<sup>tm1d(KOMP)Wtsi</sup>  [background:] involves: BALB/cJ * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:31511635	20210817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582952	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk</sup>  [background:] involves: 101 * C3H * T STOCK	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:7723240	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888773	Prnp<sup>tm1Cwe</sup>	is_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22956830	20150701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5508232	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:21514245	20130925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706513	Tg(Ins2-Nos2)31Okam/0  [background:] involves: C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9446547	20070501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287122	Tg(tetO-DISC1*)70Plet	is_implicated_in	DOID:0070085	schizophrenia 9		MGI:6287125	Tg(tetO-DISC1*)70Plet/0 Tg(Camk2a-tTA)1Mmay/0  [background:] involves: C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17848917	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655835	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] D2.Cg-Lep<sup>ob</sup>/Chua	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12136396	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779541	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup> Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:17418409	20160630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007482	Abhd5<sup>tm1.1Rze</sup>/Abhd5<sup>tm1.1Rze</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20023287	20110614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426928	Gt(ROSA)26Sor<sup>tm48(HTT)Arte</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432176	Gt(ROSA)26Sor<sup>tm48(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036311	Ddb2<sup>tm1Linn</sup>/Ddb2<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110846	xeroderma pigmentosum group E						ECO:0000033	author statement supported by traceable reference	PMID:14769931	20070509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5464281	Tg(MUT)AHlps	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:22792386	20130215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522485	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv * Black Swiss * FVB/N	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:9710454	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6389009	Kcnj8<sup>em1Nich</sup>	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6389011	Kcnj8<sup>em1Nich</sup>/Kcnj8<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4358724	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] DBA/2J-Dtnbp1<sup>sdy</sup>/J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:18984010	20151007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445420	Jun<sup>tm4Wag</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:25216727	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445420	Jun<sup>tm4Wag</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:24332034	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445420	Jun<sup>tm4Wag</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:24574341	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834358	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:20805469	20101008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836388	Mybpc3<sup>tm2.1Lcrr</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5909891	Mybpc3<sup>tm2.1Lcrr</sup>/Mybpc3<sup>+</sup>  [background:] involves: 129S2/SvPasCrl * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:22465693	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836388	Mybpc3<sup>tm2.1Lcrr</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5909888	Mybpc3<sup>tm2.1Lcrr</sup>/Mybpc3<sup>tm2.1Lcrr</sup>  [background:] involves: 129S2/SvPasCrl * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:22465693	20220107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836388	Mybpc3<sup>tm2.1Lcrr</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:33957110	20220107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174900	Oat<sup>tm1Dva</sup>/Oat<sup>tm1Dva</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1415	gyrate atrophy						ECO:0000033	author statement supported by traceable reference	PMID:7550347	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857697	Smad4<sup>tm1Mmt</sup>	is_implicated_in	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25559195	20150513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295995	Frem1<sup>bat</sup>/Frem1<sup>+</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>	is_model_of	DOID:0060732	chromosome 9p deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21931569	20111118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653295	Lepr<sup>tm1Mgmj</sup>/Lepr<sup>tm1Mgmj</sup>  [background:] B6.129-Lepr<sup>tm1Mgmj</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:12594516	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796775	Tg(Ins2-GLUD1*H454Y)1Csta/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:13317	hyperinsulinemic hypoglycemia						ECO:0000033	author statement supported by traceable reference	PMID:16574664	20161006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831310	Tg(Pbsn-IGF1*)5305Ng/0 Tg(TRAMP)8247Ng/0  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:18026134	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820820	Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro	is_implicated_in	DOID:1040	chronic lymphocytic leukemia		MGI:4820821	Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro/0  [background:] FVB/N-Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro			ECO:0000033	author statement supported by traceable reference	PMID:20566844	20100826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844311	Apc<sup>tm1Tno</sup>/Apc<sup>+</sup> Tg(CDX2-cre)101Erf/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:17942902	20160803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7484403	Sbds<sup>em1(SBDS*)Dbau</sup>	is_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:7485960	Sbds<sup>em1(SBDS*)Dbau</sup>/Sbds<sup>em1(SBDS*)Dbau</sup>  [background:] C57BL/6J-Sbds<sup>em1(SBDS*)Dbau</sup>/Dbau			ECO:0000033	author statement supported by traceable reference	MGI:7485797	20230609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5604910	Rp1<sup>m1Jdun</sup>	is_implicated_in	DOID:0110390	retinitis pigmentosa 1		MGI:5604912	Rp1<sup>m1Jdun</sup>/Rp1<sup>m1Jdun</sup>  [background:] C57BL/6-Rp1<sup>m1Jdun</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25088982	20141121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712947	Tg(Myh6-rtTA)8585Jam	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:23901116	20140106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5766488	Tg(tetO-NPM1/ALK,-luc)2Gde	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5766492	Tg(EmuSR-tTa)83Bop/Tg(EmuSR-tTa)83Bop Tg(tetO-NPM1/ALK,-luc)2Gde/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20223922	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5766488	Tg(tetO-NPM1/ALK,-luc)2Gde	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:26258416	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6359448	Coq8a<sup>tm1.1Ics</sup>	is_implicated_in	DOID:0070241	primary coenzyme Q10 deficiency 4		MGI:6359449	Coq8a<sup>tm1.1Ics</sup>/Coq8a<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27499294	20190911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509044	Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>/Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] B6Brd;B6N-Tyr<sup>c-Brd</sup> Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi	is_model_of	DOID:0050569	Seckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23166506	20131001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543909	Tg(Amh-SMAD2*)#Jebu	is_implicated_in	DOID:5117	dermoid cyst of ovary		MGI:5543910	Tg(Amh-SMAD2*)#Jebu/0  [background:] FVB/N-Tg(Amh-SMAD2*)#Jebu			ECO:0000033	author statement supported by traceable reference	PMID:23741457	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721530	Clu<sup>tm1Jakh</sup>/Clu<sup>tm1Jakh</sup> Tg(APPV717F)109Ili/Tg(APPV717F)109Ili  [background:] involves: 129S2/SvPas	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12145324	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946647	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21383153	20110415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3759029	Matn3<sup>tm1Mbri</sup>	is_implicated_in	DOID:0070299	multiple epiphyseal dysplasia 5						ECO:0000033	author statement supported by traceable reference	PMID:31260448	20190807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3759029	Matn3<sup>tm1Mbri</sup>	is_implicated_in	DOID:0070299	multiple epiphyseal dysplasia 5						ECO:0000033	author statement supported by traceable reference	PMID:22083516	20190807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3759029	Matn3<sup>tm1Mbri</sup>	is_implicated_in	DOID:0070299	multiple epiphyseal dysplasia 5		MGI:3759051	Matn3<sup>tm1Mbri</sup>/Matn3<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17517694	20190807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5775645	Shank3<sup>tm4.1Gfng</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5776380	Shank3<sup>tm4.1Gfng</sup>/Shank3<sup>tm4.1Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26687841	20160620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179025	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697695	20050708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651806	Lpl<sup>tm1Bres</sup>/Lpl<sup>tm1Bres</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8675619	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569532	Tg(CMV-HTT*89Q)ATag	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569532	Tg(CMV-HTT*89Q)ATag	is_implicated_in	DOID:12858	Huntington's disease		MGI:5569537	Tg(CMV-HTT*89Q)ATag/Tg(CMV-HTT*89Q)ATag  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569532	Tg(CMV-HTT*89Q)ATag	is_implicated_in	DOID:12858	Huntington's disease		MGI:5569536	Tg(CMV-HTT*89Q)ATag/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7516790	Fgfr3<sup>tm3.1Llm</sup>	is_implicated_in	DOID:0080041	hypochondroplasia		MGI:7517089	Fgfr3<sup>tm3.1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:37345656	20230812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491275	b2b2350Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581517	Ighm<sup>tm1(Bcl6)Rdf</sup>	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:25921526	20160427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581517	Ighm<sup>tm1(Bcl6)Rdf</sup>	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:3582784	Ighm<sup>tm1(Bcl6)Rdf</sup>/?  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15894265	20160427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6331092	Tg(Thy1-DCTN1*G71A)#Ytsu	is_implicated_in	DOID:0060486	Perry syndrome		MGI:6331093	Tg(Thy1-DCTN1*G71A)#Ytsu/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29154962	20190730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5505596	Epg5<sup>tm1Ygz</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5505671	Epg5<sup>tm1Ygz</sup>/Epg5<sup>tm1Ygz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27715390	20200127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:15190012	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6467464	Pqbp1<sup>tm1.1Hiok</sup>	is_implicated_in	DOID:0060179	Renpenning syndrome		MGI:6474216	Pqbp1<sup>tm1.1Hiok</sup>/Y Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25070536	20201130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315430	Tg(Myh6-MYL2*A13T)L1Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:22091967	20120418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603638	Errfi1<sup>tm1Gvw</sup>/Errfi1<sup>tm1Gvw</sup>  [background:] Not Specified	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:16087873	20051107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5436309	Pink1<sup>tm1.1Wrst</sup>/Pink1<sup>tm1.1Wrst</sup>  [background:] involves: 129S2/SvPas * BALB/cJ * C57BL/6J	is_model_of	DOID:0060369	Parkinson's disease 6						ECO:0000033	author statement supported by traceable reference	PMID:22265660	20120926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4441061	Tubb3<sup>tm1.1Ece</sup>/Tubb3<sup>tm1.1Ece</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0080143	congenital fibrosis of the extraocular muscles						ECO:0000033	author statement supported by traceable reference	PMID:20074521	20100423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476622	Stx11<sup>tm1.2Ics</sup>	is_implicated_in	DOID:0110924	familial hemophagocytic lymphohistiocytosis 4		MGI:5476653	Stx11<sup>tm1.2Ics</sup>/Stx11<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:23160464	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009035	Ncstn<sup>tm1.1Akli</sup>	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5009037	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21562564	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009035	Ncstn<sup>tm1.1Akli</sup>	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5009036	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129 * C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21562564	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6162240	Shank3<sup>tm2.1Bux</sup>	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6394127	Shank3<sup>tm2.1Bux</sup>/Shank3<sup>tm2.1Bux</sup>  [background:] B6(Cg)-Shank3<sup>tm2.1Bux</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30302388	20200313	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655859	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * Black Swiss * C57BL/6	is_model_of	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16199475	20060927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566834	Rho<sup>tm1.1Eye</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:5566851	Rho<sup>tm1.1Eye</sup>/Rho<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22252712	20140605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839782	Hfe<sup>tm1.1Gfn</sup>/Hfe<sup>tm1.1Gfn</sup>  [background:] B6.129P2-Hfe<sup>tm1.1Gfn</sup>	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16491649	20090413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159328	Cln6<sup>nclf</sup>	is_implicated_in	DOID:0110729	neuronal ceroid lipofuscinosis 6A						ECO:0000033	author statement supported by traceable reference	PMID:25992714	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159328	Cln6<sup>nclf</sup>	is_implicated_in	DOID:0110729	neuronal ceroid lipofuscinosis 6A						ECO:0000033	author statement supported by traceable reference	PMID:24124525	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159328	Cln6<sup>nclf</sup>	is_implicated_in	DOID:0110729	neuronal ceroid lipofuscinosis 6A		MGI:2182596	Cln6<sup>nclf</sup>/Cln6<sup>nclf</sup>  [background:] involves: C57BL/6J * C57BL/10J * C3HeB/FeJLe			ECO:0000033	author statement supported by traceable reference	PMID:11791207	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424922	Alpl<sup>Mhdabap26</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425671	Alpl<sup>Mhdabap26</sup>/Alpl<sup>Mhdabap26</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap26</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ	is_model_of	DOID:0060843	hereditary neuropathy with liability to pressure palsies						ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6158645	Nlgn2<sup>tm1.1Gchn</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6294898	Nlgn2<sup>tm1.1Gchn</sup>/Nlgn2<sup>tm1.1Gchn</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29859117	20190429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5614904	Ephb4<sup>b2b2412Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5614941	Ephb4<sup>b2b2412Clo</sup>/Ephb4<sup>b2b2412Clo</sup>  [background:] C57BL/6J-Ephb4<sup>b2b2412Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716838	Fig4<sup>plt1</sup>	is_implicated_in	DOID:0110184	Charcot-Marie-Tooth disease type 4J						ECO:0000033	author statement supported by traceable reference	PMID:25187576	20150814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716838	Fig4<sup>plt1</sup>	is_implicated_in	DOID:0110184	Charcot-Marie-Tooth disease type 4J		MGI:3717180	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup>  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17572665	20150814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429214	Tg(SNCA)ARyot	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5429329	Tg(SNCA)ARyot/0  [background:] C57BL/6J-Tg(SNCA)ARyot			ECO:0000033	author statement supported by traceable reference	PMID:22475625	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6378616	Lamb2<sup>em1Jhm</sup>	is_not_implicated_in	DOID:0060852	Pierson syndrome		MGI:6378620	Lamb2<sup>em1Jhm</sup>/Lamb2<sup>em1Jhm</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:29263159	20191127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618705	Cd4<sup>tm1Knw</sup>/Cd4<sup>tm1Knw</sup> Tg(TcraAI4)1Dvs/0 Tg(TcrbAI4)1Dvs/0  [background:] NOD.Cg-Cd4<sup>tm1Knw</sup> Tg(TcraAI4)1Dvs Tg(TcrbAI4)1Dvs	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828833	Nkx2-5<sup>tm2.1Mwc</sup>	is_implicated_in	DOID:0110112	atrial heart septal defect 7		MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5704195	Pcdh15<sup>roda</sup>/Pcdh15<sup>roda</sup>  [background:] BALB/c-Pcdh15<sup>roda</sup>	is_model_of	DOID:0110832	Usher syndrome type 1F						ECO:0000033	author statement supported by traceable reference	PMID:24044941	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796770	Tg(Ins2-GLUD1*H454Y)1Csta	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:5796775	Tg(Ins2-GLUD1*H454Y)1Csta/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16574664	20161107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796770	Tg(Ins2-GLUD1*H454Y)1Csta	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia						ECO:0000033	author statement supported by traceable reference	PMID:25024374	20161107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297426	Dnah5<sup>b2b1003Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763080	Tg(MMTV-ENPP2)#Gbm/0  [background:] FVB/N-Tg(MMTV-ENPP2)#Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620185	b2b2696Clo	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5620189	b2b2696Clo/b2b2696Clo  [background:] C57BL/6J-b2b2696Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5529365	Mecp2<sup>tm5.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5702951	Mecp2<sup>tm5.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26647311	20160115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693849	Otof<sup>tm1Ugds</sup>/Otof<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0110535	autosomal recessive nonsyndromic deafness 9						ECO:0000033	author statement supported by traceable reference	PMID:17055430	20070116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428448	Snap25<sup>Bdr</sup>/Snap25<sup>+</sup>  [background:] involves: BALB/cAnNCrl	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17283335	20120720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6163735	Kdm5c<sup>tm1.2Yshi</sup>	is_implicated_in	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type		MGI:6163736	Kdm5c<sup>tm1.2Yshi</sup>/Y  [background:] involves: 129 * 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26804915	20180629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119708	Dst<sup>dt-23Rbrc</sup>	is_implicated_in	DOID:0070151	hereditary sensory and autonomic neuropathy type 6		MGI:6160388	Dst<sup>dt-23Rbrc</sup>/Dst<sup>dt-23Rbrc</sup>  [background:] involves: C3H/HeN * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27693510	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5585621	Sucla2<sup>Gt(SAbetageo)1Bhg</sup>/Sucla2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0080124	mitochondrial DNA depletion syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:24271779	20141003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5499740	Myh9<sup>tm7.1Rsad</sup>/Myh9<sup>tm7.1Rsad</sup>  [background:] involves: BALB/cJ	is_model_of	DOID:0060651	MYH-9 related disease						ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4962718	Rnf168<sup>Gt(405F11)Cmhd</sup>	is_implicated_in	DOID:0090113	RIDDLE syndrome		MGI:5505901	Rnf168<sup>Gt(405F11)Cmhd</sup>/Rnf168<sup>Gt(405F11)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21552324	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628806	Shox2<sup>tm1Ddu</sup>/Shox2<sup>tm1.1Ddu</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S2/SvPas * C57BL/6J * SJL/J	is_model_of	DOID:0060847	Leri-Weill dyschondrosteosis						ECO:0000033	author statement supported by traceable reference	PMID:16537395	20060712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752734	Myo5b<sup>tm1a(KOMP)Wtsi</sup>/Myo5b<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Myo5b<sup>tm1a(KOMP)Wtsi</sup>	is_model_of	DOID:0060775	microvillus inclusion disease						ECO:0000033	author statement supported by traceable reference	PMID:26201991	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6441508	Scamp5<sup>tm1Smoc</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:6441509	Scamp5<sup>tm1Smoc</sup>/Scamp5<sup>tm1Smoc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32020363	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530620	Lcat<sup>tm1Nsa</sup>/Lcat<sup>tm1Nsa</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:1391	Norum disease						ECO:0000033	author statement supported by traceable reference	PMID:9054454	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384163	Cdkn2a<sup>tm2Brn</sup>	is_implicated_in	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26139534	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856394	Pcdh15<sup>av-3J</sup>	is_implicated_in	DOID:0110481	autosomal recessive nonsyndromic deafness 23						ECO:0000033	author statement supported by traceable reference	PMID:35830793	20231106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654522	Slc6a3<sup>tm2Mca</sup>/Slc6a3<sup>tm2Mca</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15710042	20111021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359175	Arx<sup>tm2Kki</sup>	is_implicated_in	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:22565167	20130716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359175	Arx<sup>tm2Kki</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:4359205	Arx<sup>tm2Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22565167	20130716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4356192	Tg(Prnp*A116V*M128V)1309Jama	is_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22956830	20150701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656910	Sgca<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:12620894	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656910	Sgca<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:15689353	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656910	Sgca<sup>tm1Eeng</sup>	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D		MGI:2656914	Sgca<sup>tm1Eeng</sup>/Sgca<sup>tm1Eeng</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12620894	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5450850	Slc45a2<sup>uw-7J</sup>/Slc45a2<sup>uw-7J</sup>  [background:] C3H/HeJ-Slc45a2<sup>uw-7J</sup>/GrsrJ	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	MGI:5449588	20130123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5788543	Tg(Igh-HMGA2)#Cro/0  [background:] FVB/N-Tg(Igh-HMGA2)#Cro	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:25014774	20160811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603529	Rxfp2<sup>tm1Aia</sup>/crsp  [background:] involves: 129S7/SvEvBrd * C57BL/6J * FVB/N	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:12217959	20151207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850836	Mc3r<sup>tm1Lvp</sup>/Mc3r<sup>tm1Lvp</sup> Mc4r<sup>tm1Dhu</sup>/Mc4r<sup>tm1Dhu</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:10973258	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4970574	Rnf168<sup>Gt(156B6)Cmhd</sup>	is_implicated_in	DOID:0090113	RIDDLE syndrome		MGI:5505899	Rnf168<sup>Gt(156B6)Cmhd</sup>/Rnf168<sup>Gt(156B6)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21552324	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5306241	Mecp2<sup>tm1.1Jae</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16446138	20120216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700746	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0050990	episodic ataxia type 2						ECO:0000033	author statement supported by traceable reference	PMID:25855180	20150702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587028	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11239417	20050909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430590	Lect2<sup>tm1Ymg</sup>/Lect2<sup>tm1Ymg</sup> Tg(Pklr-Myc)73Ak/0  [background:] B6.Cg-Lect2<sup>tm1Ymg</sup> Tg(Pklr-Myc)73Ak	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22251704	20120807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6515598	Vcpip1<sup>em1Zlou</sup>	is_implicated_in	DOID:3911	progeria		MGI:6515750	Vcpip1<sup>em1Zlou</sup>/Vcpip1<sup>em1Zlou</sup>  [background:] C57BL/6NHsd-Vcpip1<sup>em1Zlou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32649882	20210407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6515598	Vcpip1<sup>em1Zlou</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:32649882	20210407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672029	Gp1ba<sup>tm1Ware</sup>/Gp1ba<sup>tm1Ware</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:2217	Bernard-Soulier syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10706630	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440731	Nlgn3<sup>tm1Rhn</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22983708	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774265	Efemp1<sup>tm1Eap</sup>	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23943789	20140102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774265	Efemp1<sup>tm1Eap</sup>	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3800794	Efemp1<sup>tm1Eap</sup>/Efemp1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17666404	20140102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774265	Efemp1<sup>tm1Eap</sup>	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3800793	Efemp1<sup>tm1Eap</sup>/Efemp1<sup>tm1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17666404	20140102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311368	b2b954Clo	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5312912	b2b954Clo/b2b954Clo  [background:] C57BL/6J-b2b954Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359814	Ttn<sup>tm1Brge</sup>/Ttn<sup>+</sup>  [background:] B6.Cg-Ttn<sup>tm1Brge</sup>	is_model_of	DOID:0110430	dilated cardiomyopathy 1G						ECO:0000033	author statement supported by traceable reference	PMID:19406126	20091001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690087	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)56Hev/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:16705038	20150501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663832	Cnga3<sup>tm1Biel</sup>/Cnga3<sup>tm1Biel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110007	achromatopsia 2						ECO:0000033	author statement supported by traceable reference	PMID:10377453	20160909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522157	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000033	author statement supported by traceable reference	PMID:15483130	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318542	Slc12a6<sup>tm1Garo</sup>/Slc12a6<sup>tm1Garo</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129 * C57BL/6 * CBA	is_model_of	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:22423107	20180617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343570	Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:6343572	Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30520996	20190815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343570	Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:6343571	Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>/Gt(ROSA)26Sor<sup>tm1.1(CAG-SPAST*C448Y)Baas</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30520996	20190815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603015	Myc<sup>tm1Lbox</sup>/Myc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N	is_model_of	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:15687498	20051026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009703	Ar<sup>tm1Verh</sup>/Y Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:21620777	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415223	Tg(FOXJ1-ACE2)1Rba	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6415340	Tg(FOXJ1-ACE2)1Rba/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26976607	20200507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835842	Tg(Scgb1a1-IL6)9Flv	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:24951765	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835842	Tg(Scgb1a1-IL6)9Flv	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835842	Tg(Scgb1a1-IL6)9Flv	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5474461	Tg(Scgb1a1-IL6)9Flv/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19074475	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835266	Chd7<sup>tm1.1Dmm</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5774943	Chd7<sup>tm1.1Dmm</sup>/Chd7<sup>+</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:26670829	20161116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835266	Chd7<sup>tm1.1Dmm</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5774845	Chd7<sup>tm1.1Dmm</sup>/Chd7<sup>tm1.1Dmm</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:26670829	20161116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5792156	Sgcd<sup>tm1Ojml</sup>	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:5911874	Sgcd<sup>tm1Ojml</sup>/Sgcd<sup>+</sup>  [background:] B6.129-Sgcd<sup>tm1Ojml</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23695275	20171026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624942	X/Yaa  [background:] (NZB x BXSB)F1	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:315777	20060621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589210	Pitx2<sup>tm2Sac</sup>/Pitx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:10498698	20051011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7281146	Myd88<sup>em1.1Rsky</sup>	is_implicated_in	DOID:7442	monoclonal gammopathy of uncertain significance		MGI:7281484	Ighg1<sup>tm1(cre)Cgn</sup>/Ighg1<sup>+</sup> Myd88<sup>em1.1Rsky</sup>/Myd88<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:33343574	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7281146	Myd88<sup>em1.1Rsky</sup>	is_implicated_in	DOID:7442	monoclonal gammopathy of uncertain significance		MGI:7281485	Cd19<sup>tm1(cre/ERT2)Rsky</sup>/Cd19<sup>+</sup> Myd88<sup>em1.1Rsky</sup>/Myd88<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:33343574	20220601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3849442	Arsb<sup>m1J</sup>/Arsb<sup>m1J</sup>  [background:] C57BL/6J-Arsb<sup>m1J</sup>/GrsrJ	is_model_of	DOID:12800	mucopolysaccharidosis VI						ECO:0000033	author statement supported by traceable reference	MGI:3849437	20090702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629752	Ar<sup>tm2(AR)Dmr</sup>/Y Tg(TRAMP)8247Ng/0  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:16601069	20060721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5529516	Tg(ACTB-THRB*)#Syc	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5529521	Tg(ACTB-THRB*)#Syc/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10454355	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7494070	Stmn2<sup>em2Jmi</sup>	is_implicated_in	DOID:2477	motor peripheral neuropathy		MGI:7523313	Chat<sup>tm2(cre)Lowl</sup>/Chat<sup>+</sup> Stmn2<sup>em2Jmi</sup>/Stmn2<sup>em2Jmi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604912	Rp1<sup>m1Jdun</sup>/Rp1<sup>m1Jdun</sup>  [background:] C57BL/6-Rp1<sup>m1Jdun</sup>	is_model_of	DOID:0110390	retinitis pigmentosa 1						ECO:0000033	author statement supported by traceable reference	PMID:25088982	20141121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3612955	Pax9<sup>tm1Hpt</sup>/Pax9<sup>tm1Rbal</sup>  [background:] involves: 129 * C57BL/6 * CD-1	is_model_of	DOID:0050591	tooth agenesis						ECO:0000033	author statement supported by traceable reference	PMID:16236760	20060216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722379	Tg(Prnp-MAPT*P301L)JNPL3Hlmc/?  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:10932182	20090422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5555964	Tg(tetO-Rai1,-EGFP)463Walz	is_implicated_in	DOID:0060853	Potocki-Lupski syndrome		MGI:5555966	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Rai1,-EGFP)463Walz/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24218365	20140408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857104	Mip<sup>Cat-Fr</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:24120416	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857104	Mip<sup>Cat-Fr</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175110	Mip<sup>Cat-Fr</sup>/Mip<sup>Cat-Fr</sup>  [background:] involves: A/J			ECO:0000033	author statement supported by traceable reference	PMID:8563764	20141009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834263	Abca12<sup>tm1Lex</sup>/Abca12<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J	is_model_of	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000033	author statement supported by traceable reference	PMID:18957418	20090304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085889	Lrrtm1<sup>tm1.1Jaru</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5085920	Lrrtm1<sup>tm1.1Jaru</sup>/Lrrtm1<sup>tm1.1Jaru</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21818371	20110815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450098	Fas<sup>tm1Osa</sup>/Fas<sup>tm1Osa</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8700897	20051011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904946	Tg(Myh6-Rab1a)highGwd	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5904949	Tg(Myh6-Rab1a)highGwd/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11739277	20170718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587816	Pah<sup>enu3</sup>/Pah<sup>enu3</sup>  [background:] involves: BTBR	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:8375656	20050916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582593	Ryr2<sup>tm3.1Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:22828895	20140915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285211	Bsnd<sup>tm1.1Suc</sup>	is_implicated_in	DOID:0110145	Bartter disease type 4a						ECO:0000033	author statement supported by traceable reference	PMID:31362893	20210223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285211	Bsnd<sup>tm1.1Suc</sup>	is_implicated_in	DOID:0110145	Bartter disease type 4a		MGI:5285220	Bsnd<sup>tm1.1Suc</sup>/Bsnd<sup>tm1.1Suc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21593186	20210223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285211	Bsnd<sup>tm1.1Suc</sup>	is_implicated_in	DOID:0110145	Bartter disease type 4a						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20210223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805980	Per2<sup>M1Btlr</sup>	is_implicated_in	DOID:0110011	advanced sleep phase syndrome 1		MGI:5906447	Per2<sup>M1Btlr</sup>/Per2<sup>M1Btlr</sup>  [background:] C57BL/6J-Per2<sup>M1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:6197761	20180913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7495802	Ighmbp2<sup>em5Cx</sup>	is_implicated_in	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S		MGI:7495806	Ighmbp2<sup>em5Cx</sup>/Ighmbp2<sup>em5Cx</sup>  [background:] C57BL/6J-Ighmbp2<sup>em5Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:36413117	20230706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4820519	Tg(Myh6-MYL2*N47K)#Dsc	is_implicated_in	DOID:0110316	hypertrophic cardiomyopathy 10		MGI:5904627	Tg(Myh6-MYL2*N47K)#Dsc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19150977	20170714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778899	Pnp<sup>f</sup>/Pnp<sup>f</sup>  [background:] involves: C3H/HeHa * C57BL/6J	is_model_of	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:2516826	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834666	Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834666	Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:25877214	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834666	Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:21902803	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834666	Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:18708427	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834666	Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer	is_implicated_in	DOID:3911	progeria		MGI:3834667	Tg(KRT5-tTA)1216Glk/0 Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18334552	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858040	Fancc<sup>tm1Mab</sup>	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A						ECO:0000033	author statement supported by traceable reference	PMID:23315168	20130509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5696741	Tg(Prl-EGFR)#Sme	is_implicated_in	DOID:5394	prolactinoma		MGI:5696742	Tg(Prl-EGFR)#Sme/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25375038	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5776726	Bmpr2<sup>tm1Mmue</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5827840	Bmpr2<sup>tm1Mmue</sup>/Bmpr2<sup>+</sup>  [background:] B6.129S1-Bmpr2<sup>tm1Mmue</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26076038	20170307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056342	Rs1<sup>tm1Sie</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:15326152	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946650	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] B6.129-Braf<sup>tm1Bbd</sup>	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21383153	20110415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5819097	Adgrg6<sup>tm1Arte</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7266840	Adgrg6<sup>tm1Arte</sup>/Adgrg6<sup>tm1Arte</sup> Tg(Scx-GFP/cre)1Stzr/0  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:34318745	20220506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5819097	Adgrg6<sup>tm1Arte</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7266813	Adgrg6<sup>tm1Arte</sup>/Adgrg6<sup>tm1Arte</sup> Tg(Col2a1-cre)#Amc/0  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:25954032	20220506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424921	Phex<sup>Mhdabap024</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:6198726	Phex<sup>Mhdabap024</sup>/Phex<sup>+</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29735309	20180920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424921	Phex<sup>Mhdabap024</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:6198725	Phex<sup>Mhdabap024</sup>/Y  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29735309	20180920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424921	Phex<sup>Mhdabap024</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5425687	Phex<sup>Mhdabap024</sup>/Phex<sup>Mhdabap024</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793274	Atp7b<sup>tx-J</sup>/Atp7b<sup>tx-J</sup>  [background:] C3H/HeJ-Atp7b<sup>tx-J</sup>/J	is_model_of	DOID:893	Wilson disease						ECO:0000033	author statement supported by traceable reference	PMID:17981064	20080611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177313	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] involves: STOCK Grhl3<sup>ct</sup> * M. m. molossinus	is_model_of	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000033	author statement supported by traceable reference	PMID:7719036	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554444	Ccdc39<sup>b2b2025.1Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5555837	Ccdc39<sup>b2b2025.1Clo</sup>/Ccdc39<sup>b2b2025.1Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b2025.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7261176	Csf2ra<sup>em1Szut</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:7261196	Csf2ra<sup>em1Szut</sup>/Csf2ra<sup>em1Szut</sup>  [background:] C57BL/6-Csf2ra<sup>em1Szut</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35043685	20220412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7264666	Cant1<sup>tm1.1Aros</sup>	is_implicated_in	DOID:0060462	Desbuquois dysplasia		MGI:7264676	Cant1<sup>tm1.1Aros</sup>/Cant1<sup>tm1.1Aros</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30439444	20220427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474461	Tg(Scgb1a1-IL6)9Flv/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:19074475	20130417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841484	Ptprc<sup>tm1Weis</sup>/Ptprc<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:11163182	20090428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680322	Gba1<sup>tm2Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:23520473	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680322	Gba1<sup>tm2Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:26312487	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680322	Gba1<sup>tm2Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21257328	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680322	Gba1<sup>tm2Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:22167193	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680322	Gba1<sup>tm2Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:21223590	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680322	Gba1<sup>tm2Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680393	Gba1<sup>tm2Ggb</sup>/Gba1<sup>tm2Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5645929	Prickle1<sup>tm1Asw</sup>	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:5648842	Prickle1<sup>tm1Asw</sup>/Prickle1<sup>tm1Asw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25190059	20150818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705132	Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:5902766	Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>/Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27939640	20170619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430640	Arsg<sup>tm1Tdi</sup>	is_implicated_in	DOID:12798	mucopolysaccharidosis						ECO:0000033	author statement supported by traceable reference	PMID:25452429	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430640	Arsg<sup>tm1Tdi</sup>	is_implicated_in	DOID:12798	mucopolysaccharidosis		MGI:5430642	Arsg<sup>tm1Tdi</sup>/Arsg<sup>tm1Tdi</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22689975	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23386687	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23966835	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3811791	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:18568033	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857938	Tsc2<sup>tm1Djk</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:2174788	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10491404	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5447056	Kat6a<sup>tm1Avo</sup>/Kat6a<sup>+</sup> Tbx1<sup>tm1Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129 * 129S7/SvEvBrd * BALB/c * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22921202	20121228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618619	Pdgfrb<sup>b2b2903Clo</sup>	is_implicated_in	DOID:2226	myeloproliferative neoplasm		MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830316	Hap1<sup>tm2Xjl</sup>	is_implicated_in	DOID:1595	melancholic depression		MGI:5691394	Hap1<sup>tm2Xjl</sup>/Hap1<sup>tm2Xjl</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:25875952	20151112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830316	Hap1<sup>tm2Xjl</sup>	is_implicated_in	DOID:1595	melancholic depression		MGI:5695752	Hap1<sup>tm2Xjl</sup>/Hap1<sup>tm2Xjl</sup> Tg(Camk2a-cre)159Kln/0  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25875952	20151112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5614979	Dnah5<sup>b2b2570Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5614980	Dnah5<sup>b2b2570Clo</sup>/Dnah5<sup>b2b2570Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2570Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177756	Htt<sup>tm1Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23341618	20131011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177756	Htt<sup>tm1Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3573928	Htt<sup>tm1Detl</sup>/Htt<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11152661	20131011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177756	Htt<sup>tm1Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3573927	Htt<sup>tm1Detl</sup>/Htt<sup>tm1Detl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11152661	20131011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6153609	Fat1<sup>tm1.1Nsib</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:6160427	Fat1<sup>tm1.1Nsib</sup>/Fat1<sup>tm1.1Nsib</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129/Sv * 129S4/SvJaeSor * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26905694	20180612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820834	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] AK.KOR-Traf3ip2<sup>adjm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524119	Fat1<sup>tm1Fhel</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:5524136	Fat1<sup>tm1Fhel</sup>/Fat1<sup>tm1Fhel</sup> Pax3<sup>tm1(cre)Joe</sup>/Pax3<sup>+</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N	is_model_of	DOID:0110635	muscular dystrophy-dystroglycanopathy type B5						ECO:0000033	author statement supported by traceable reference	PMID:20675713	20101011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521185	Tg(Thy1-Tcf4)1Mjro	is_implicated_in	DOID:5419	schizophrenia		MGI:5521202	Tg(Thy1-Tcf4)1Mjro/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23069005	20131203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850032	Sost<sup>tm1Paz</sup>/Sost<sup>tm1Paz</sup>  [background:] involves: 129/Sv * Black Swiss	is_model_of	DOID:0060756	sclerosteosis 1						ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5812297	Snap29<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060337	CEDNIK syndrome		MGI:5812300	Snap29<sup>tm1c(EUCOMM)Wtsi</sup>/Snap29<sup>tm1c(EUCOMM)Wtsi</sup> Tg(KRT14-cre)1Cgn/0  [background:] involves: C57BL/6 * C57BL/6N * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26747696	20161216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554544	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup>  [background:] involves: 129P2/OlaHsd * C3H * SJL	is_model_of	DOID:0060589	Yunis-Varon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23623387	20140402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5795894	Tnf<sup>Bpsm1</sup>	is_implicated_in	DOID:4079	heart valve disease		MGI:6272038	Tnf<sup>Bpsm1</sup>/Tnf<sup>+</sup>  [background:] C.Cg-Tnf<sup>Bpsm1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491272	Dnah11<sup>b2b2349Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20131014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824743	Tg(PMP22)C3Fbas/?  [background:] B6.Cg-Tg(PMP22)C3Fbas	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	PMID:21487305	20170222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752786	Disc1<sup>m1H</sup>/Disc1<sup>m1H</sup>  [background:] B6N.C(C3H)-Disc1<sup>m1H</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:26728762	20160322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644517	Tg(H2-K<sup>b</sup>-Tcra,-Tcrb)1640Kurs/0  [background:] SJL.FVB-Tg(H2-K<sup>b</sup>-Tcra,-Tcrb)1640Kurs	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19487416	20150721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314953	Eif4h<sup>Gt(Ex279)Byg</sup>/Eif4h<sup>Gt(Ex279)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22234171	20120412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384179	Cfh<sup>tm1Mbo</sup>	is_implicated_in	DOID:0110017	age related macular degeneration 4						ECO:0000033	author statement supported by traceable reference	PMID:24370827	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384179	Cfh<sup>tm1Mbo</sup>	is_implicated_in	DOID:0110017	age related macular degeneration 4		MGI:5546609	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup>  [background:] B6.129-Cfh<sup>tm1Mbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23799019	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5558945	Tg(Camk2a-tTA)1Mmay/0 Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/Fgf14<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24503275	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5511058	Tg(Camk2a-tTA)1Mmay/0 Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/Fgf14<sup>+</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16291936	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819866	Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:24631720	20141013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621458	Dhcr7<sup>tm2Fdp</sup>/Dhcr7<sup>tm2Fdp</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16446309	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433487	b2b1163Clo/b2b1163Clo  [background:] C57BL/6J-b2b1163Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360909	Adam9<sup>tm1Bbl</sup>/Adam9<sup>tm1Bbl</sup>  [background:] involves: 129	is_model_of	DOID:0111020	cone-rod dystrophy 9						ECO:0000033	author statement supported by traceable reference	PMID:19409519	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574185	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Tg(Il1rn)1Dih/Tg(Il1rn)1Dih  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CBA	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	PMID:11983917	20120221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316396	Fmr1<sup>tm1Cgr</sup>/Y  [background:] B6.129P2-Fmr1<sup>tm1Cgr</sup>/Nwu	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21364941	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720700	Tg(APPSWE)2576Kha/0  [background:] involves: C57BL/6 * DBA/2 * SJL * SW	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19041304	20110823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579498	Stk11<sup>tm1Keis</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6144040	Chd8<sup>tm2.1Kei</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6189103	Chd8<sup>tm2.1Kei</sup>/Chd8<sup>+</sup>  [background:] B6J.129P2-Chd8<sup>tm2.1Kei</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27602517	20180720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819267	Chrna7<sup>tm1Bay</sup>/Chrna7<sup>tm1Bay</sup>  [background:] B6.129S7-Chrna7<sup>tm1Bay</sup>/J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:24983521	20141106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840300	Mmut<sup>tm1Cpv</sup>	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:23898205	20140110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840300	Mmut<sup>tm1Cpv</sup>	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:3840340	Mmut<sup>tm1Cpv</sup>/Mmut<sup>tm1Cpv</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17937813	20140110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7444110	Dnajb4<sup>em1Sngi</sup>	is_implicated_in	DOID:11720	distal myopathy		MGI:7444383	Dnajb4<sup>em1Sngi</sup>/Dnajb4<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:36512060	20230315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491275	b2b2350Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766495	Snap25<sup>tm1.1Bark</sup>/Snap25<sup>tm1.1Bark</sup>  [background:] Not Specified	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:26195742	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438113	Shank3<sup>tm3.2Cmpl</sup>	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6438116	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>tm3.2Cmpl</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438113	Shank3<sup>tm3.2Cmpl</sup>	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6438117	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5288597	Nrp1<sup>tm1.1Cruh</sup>	is_implicated_in	DOID:1727	retinal vein occlusion		MGI:5288598	Nrp1<sup>tm1.1Cruh</sup>/Nrp1<sup>tm1.1Cruh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21852397	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655695	Kcna1<sup>tm1Jmay</sup>/Kcna1<sup>+</sup>  [background:] B6.129S4-Kcna1<sup>tm1Jmay</sup>	is_model_of	DOID:0050989	episodic ataxia type 1						ECO:0000033	author statement supported by traceable reference	PMID:12612586	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654420	Mybpc3<sup>tm1.1Jse</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:24464755	20170919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654420	Mybpc3<sup>tm1.1Jse</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:2654422	Mybpc3<sup>tm1.1Jse</sup>/Mybpc3<sup>tm1.1Jse</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10545522	20170919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618625	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10825	essential hypertension						ECO:0000033	author statement supported by traceable reference	PMID:11457755	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7510181	Chd4<sup>em1Flc</sup>	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:7511685	Chd4<sup>em1Flc</sup>/Chd4<sup>em1Flc</sup>  [background:] C57BL/6J-Chd4<sup>em1Flc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37254794	20230804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712286	Mecp2<sup>tm2Bird</sup>/Mecp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17289941	20070621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5690112	Gdap1<sup>tm1.2Geno</sup>/Gdap1<sup>tm1.2Geno</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K						ECO:0000033	author statement supported by traceable reference	PMID:25860513	20151014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588183	Trp63<sup>tm1Brd</sup>/Trp63<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:10227293	20050922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136894	Ret<sup>tm1Cos</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136894	Ret<sup>tm1Cos</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2175009	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:7595168	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136894	Ret<sup>tm1Cos</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2175009	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:8114940	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136894	Ret<sup>tm1Cos</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:4820806	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18414682	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836258	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm1Maag</sup>	is_model_of	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:22144569	20130526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836258	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm1Maag</sup>	is_model_of	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:19104150	20130526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6726554	Tsga8<sup>em2Ohbo</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6727062	Tsga8<sup>em2Ohbo</sup>/Tsga8<sup>em2Ohbo</sup>  [background:] C57BL/6-Tsga8<sup>em2Ohbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33766931	20210729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308378	Tg(RP3-340H11)29Kel	is_implicated_in	DOID:0060334	transient neonatal diabetes mellitus		MGI:5308379	Tg(RP3-340H11)29Kel/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:15286800	20120307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582680	Mafa<sup>tm1Staka</sup>/Mafa<sup>tm1Staka</sup>  [background:] involves: ICR	is_model_of	DOID:0050524	maturity-onset diabetes of the young						ECO:0000033	author statement supported by traceable reference	PMID:15923615	20050729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430187	Del(8A4-B3)7H/+  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:0050580	hereditary lymphedema						ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588311	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] B6.C3Fe-Hps1<sup>ep</sup>/J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432111	Ryr2<sup>tm1.1Clhh</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5432115	Ryr2<sup>tm1.1Clhh</sup>/Ryr2<sup>tm1.1Clhh</sup>  [background:] 129S/SvEv-Ryr2<sup>tm1.1Clhh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18419777	20120823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036310	Ddb2<sup>tm1Linn</sup>/Ddb2<sup>tm1Linn</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110846	xeroderma pigmentosum group E						ECO:0000033	author statement supported by traceable reference	PMID:14769931	20070509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442286	Tg(rTH-Tag)20Dmc/0  [background:] involves: C57BL/6NTac * DBA/2NTac	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:7680068	20121120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819094	Tg(tetO-NEFL)173.2Jpj/0 Tg(THY1-tTA)177Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0110165	Charcot-Marie-Tooth disease type 2E						ECO:0000033	author statement supported by traceable reference	PMID:20421365	20100812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5896606	Tg(Thy1-UBQLN2*P506T)6Mont	is_implicated_in	DOID:0060206	amyotrophic lateral sclerosis type 15		MGI:5896834	Tg(Thy1-UBQLN2*P506T)6Mont/?  [background:] involves: C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27834214	20170509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315001	Tmc1<sup>baringo</sup>/Tmc1<sup>baringo</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140950	Cdh23<sup>v-bus</sup>/Cdh23<sup>v-bus</sup>  [background:] involves: KYF/MsIdr	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5639081	Ptpn11<sup>tm1.1Ics</sup>	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines		MGI:5639083	Ptpn11<sup>tm1.1Ics</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25288766	20150610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838011	Col4a4<sup>bwk</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:5696188	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] NON;NZO-Col4a4<sup>bwk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24522496	20151116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838011	Col4a4<sup>bwk</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:5696196	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] D2.NON(NZO)-Col4a4<sup>bwk</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:24522496	20151116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838011	Col4a4<sup>bwk</sup>	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:5696200	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] 129S1.NON(NZO)-Col4a4<sup>bwk</sup>/PgnJ			ECO:0000033	author statement supported by traceable reference	PMID:24522496	20151116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821832	Mks1<sup>avc6</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:4822147	Mks1<sup>avc6</sup>/Mks1<sup>avc6</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20101008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558037	Elp1<sup>tm1c(KOMP)Wtsi</sup>/Elp1<sup>tm1c(KOMP)Wtsi</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N * CBA/J	is_model_of	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24173031	20140410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835232	Tg(MMTV-LPAR1)27Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763087	Tg(MMTV-LPAR1)27Gbm/Tg(MMTV-LPAR1)27Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)27Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5565506	Flt3<sup>tm2.1Dosm</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5565510	Flt3<sup>tm2.1Dosm</sup>/Flt3<sup>+</sup>  [background:] B6.129(C)-Flt3<sup>tm2.1Dosm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24255108	20140529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175110	Mip<sup>Cat-Fr</sup>/Mip<sup>Cat-Fr</sup>  [background:] involves: A/J	is_model_of	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:8563764	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758077	Tg(Camk2a-DISC1)10Asaw	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758077	Tg(Camk2a-DISC1)10Asaw	is_implicated_in	DOID:5419	schizophrenia		MGI:3758089	Tg(Camk2a-DISC1)10Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)10Asaw			ECO:0000033	author statement supported by traceable reference	PMID:17675407	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758077	Tg(Camk2a-DISC1)10Asaw	is_implicated_in	DOID:5419	schizophrenia		MGI:3758089	Tg(Camk2a-DISC1)10Asaw/0  [background:] C57BL/6-Tg(Camk2a-DISC1)10Asaw			ECO:0000033	author statement supported by traceable reference	PMID:23314019	20190411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949205	Foxo3<sup>mommeR1</sup>/Foxo3<sup>mommeR1</sup> Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew  [background:] FVB/NJ-Foxo3<sup>mommeR1</sup> Tg(HBA1-Gfp)1Ew	is_model_of	DOID:5117	dermoid cyst of ovary						ECO:0000033	author statement supported by traceable reference	PMID:21347845	20110505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>	is_model_of	DOID:0110626	primary ciliary dyskinesia 2						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5602879	Tg(IKBKAP*)#Sasl	is_implicated_in	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30905397	20200204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6331299	Tg(tetO-GFP,-APOL1*S342G*I384M)#Susz	is_implicated_in	DOID:557	kidney disease		MGI:6331339	Tg(Nphs1-rtTA*3G)8Jhm/0 Tg(tetO-GFP,-APOL1*S342G*I384M)#Susz/0  [background:] involves: C57BL/6J * CBA/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28218918	20190731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5639272	Tg(Prnp-SNCA*A53T)AAub/?  [background:] involves: FVB/N	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25297088	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386185	Tcof1<sup>tm1Mjd</sup>	is_implicated_in	DOID:2908	Treacher Collins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23283078	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386185	Tcof1<sup>tm1Mjd</sup>	is_implicated_in	DOID:2908	Treacher Collins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22479190	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386185	Tcof1<sup>tm1Mjd</sup>	is_implicated_in	DOID:2908	Treacher Collins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26792133	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386185	Tcof1<sup>tm1Mjd</sup>	is_implicated_in	DOID:2908	Treacher Collins syndrome		MGI:3029251	Tcof1<sup>tm1Mjd</sup>/Tcof1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10888597	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386185	Tcof1<sup>tm1Mjd</sup>	is_implicated_in	DOID:2908	Treacher Collins syndrome		MGI:3513306	Tcof1<sup>tm1Mjd</sup>/Tcof1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/1			ECO:0000033	author statement supported by traceable reference	PMID:16938878	20190212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583956	Pthlh<sup>tm1Hmk</sup>/Pthlh<sup>tm1Hmk</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:8314082	20050819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175710	Atm<sup>tm1Pmc</sup>/Atm<sup>tm1Pmc</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:9582124	20050603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029285	Tg(APPSWE)2576Kha/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22085694	20120309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029285	Tg(APPSWE)2576Kha/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16236385	20120309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513849	Apc<sup>tm1Cip</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:15502862	20170302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640338	Fgfr3<sup>tm3.1Cxd</sup>/Fgfr3<sup>tm3.1Cxd</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:10587515	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856027	Lama2<sup>dy-2J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:24631023	20201027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856027	Lama2<sup>dy-2J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:31348492	20201027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856027	Lama2<sup>dy-2J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:28218617	20201027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856027	Lama2<sup>dy-2J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789335	Lama2<sup>dy-2J</sup>/Lama2<sup>dy-2J</sup>  [background:] B6.WK-Lama2<sup>dy-2J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15823249	20201027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5465030	Foxn1<sup>nu-2J</sup>/Foxn1<sup>nu-2J</sup>  [background:] B6(SJL)-Foxn1<sup>nu-2J</sup>/GrsrJ	is_model_of	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618630	Zic3<sup>tm1Bca</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659501	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] CAnNCrl.12P2(FVB)-Abcb4<sup>tm1Bor</sup>	is_model_of	DOID:0060643	primary sclerosing cholangitis						ECO:0000033	author statement supported by traceable reference	PMID:25478810	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462364	Tg(tetO-HMOX1)6Hyms	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:28746897	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462364	Tg(tetO-HMOX1)6Hyms	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5462366	Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22881289	20171213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449420	Tg(SOD1*)DF7Yaw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5449421	Tg(SOD1*)DF7Yaw/0  [background:] C57BL/6-Tg(SOD1*)DF7Yaw			ECO:0000033	author statement supported by traceable reference	PMID:15857664	20130117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5449420	Tg(SOD1*)DF7Yaw	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5449422	Tg(SOD1*)DF7Yaw/Tg(SOD1*)DF7Yaw  [background:] C57BL/6-Tg(SOD1*)DF7Yaw			ECO:0000033	author statement supported by traceable reference	PMID:15857664	20130117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615834	Nbn<sup>tm1Jpt</sup>/Nbn<sup>tm1Jpt</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11967151	20060313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6363715	Dspp<sup>em1Yolu</sup>	is_implicated_in	DOID:4154	dentinogenesis imperfecta						ECO:0000033	author statement supported by traceable reference	PMID:31173534	20191016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183736	Tg(Sod1*G86R)M1Jwg	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23874395	20180702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183736	Tg(Sod1*G86R)M1Jwg	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:29458840	20180702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183736	Tg(Sod1*G86R)M1Jwg	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3687994	Tg(Sod1*G86R)M1Jwg/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:7846037	20180702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183736	Tg(Sod1*G86R)M1Jwg	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3687994	Tg(Sod1*G86R)M1Jwg/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15263088	20180702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183736	Tg(Sod1*G86R)M1Jwg	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3687994	Tg(Sod1*G86R)M1Jwg/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10578106	20180702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0050794	multiple synostoses syndrome		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6359826	Ush1c<sup>dfcr-4J</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:6359828	Ush1c<sup>dfcr-4J</sup>/Ush1c<sup>dfcr-4J</sup>  [background:] 129P3/J-Ush1c<sup>dfcr-4J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:6359814	20190913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7286337	Specc1l<sup>em3Kumc</sup>	is_implicated_in	DOID:674	cleft palate		MGI:7286375	Specc1l<sup>em3Kumc</sup>/Specc1l<sup>+</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706992	Tlr4<sup>tm1Aki</sup>/Tlr4<sup>tm1Aki</sup>  [background:] B6.129P2-Tlr4<sup>tm1Aki</sup>	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:17053835	20091216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810760	Rpgrip1<sup>tvrm111</sup>	is_implicated_in	DOID:0110329	Leber congenital amaurosis 6		MGI:5924950	Rpgrip1<sup>tvrm111</sup>/Rpgrip1<sup>tvrm111</sup>  [background:] C57BL/6J-Rpgrip1<sup>tvrm111</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847801	Tg(SERPINA1*E342K)#Slcw	is_implicated_in	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:25210780	20170324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847801	Tg(SERPINA1*E342K)#Slcw	is_implicated_in	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:27102560	20170324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847801	Tg(SERPINA1*E342K)#Slcw	is_implicated_in	DOID:13372	alpha 1-antitrypsin deficiency		MGI:5562921	Tg(SERPINA1*E342K)#Slcw/Tg(SERPINA1*E342K)#Slcw  [background:] involves: C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:24355919	20170324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388126	Ghr<sup>tm1Jjk</sup>	is_implicated_in	DOID:9521	Laron syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23456957	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388126	Ghr<sup>tm1Jjk</sup>	is_implicated_in	DOID:9521	Laron syndrome		MGI:3796418	Ghr<sup>tm1Jjk</sup>/Ghr<sup>tm1Jjk</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:19269870	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388126	Ghr<sup>tm1Jjk</sup>	is_implicated_in	DOID:9521	Laron syndrome		MGI:3796418	Ghr<sup>tm1Jjk</sup>/Ghr<sup>tm1Jjk</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:9371826	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473821	Tg(CAG-Bmpr1a*,-lacZ)1Nobs	is_implicated_in	DOID:0050787	juvenile polyposis syndrome		MGI:5473901	Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22773757	20130411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653482	Fgf23<sup>tm1Sliu</sup>/Fgf23<sup>+</sup> Phex<sup>Hyp</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:16449303	20060905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430347	Notch3<sup>hpbk</sup>/Notch3<sup>hpbk</sup>  [background:] C57BL/6J-Notch3<sup>hpbk</sup>/GrsrJ	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448372	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] involves: C3H	is_model_of	DOID:0110916	hereditary spherocytosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14451913	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176786	Brca1<sup>tm1Cxd</sup>/Brca1<sup>tm2Cxd</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:10319859	20130408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183923	Muc2<sup>tm1Avel</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:26121642	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183923	Muc2<sup>tm1Avel</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3574621	Muc2<sup>tm1Avel</sup>/Muc2<sup>tm1Avel</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24945909	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836472	Ercc3<sup>tm2Jhjh</sup>/Ercc3<sup>tm2Jhjh</sup>  [background:] B6.129P2-Ercc3<sup>tm2Jhjh</sup>	is_model_of	DOID:0110850	xeroderma pigmentosum group B						ECO:0000033	author statement supported by traceable reference	PMID:19114557	20090320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5619080	Dnai2<sup>b2b3405Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5619081	Dnai2<sup>b2b3405Clo</sup>/Dnai2<sup>b2b3405Clo</sup>  [background:] C57BL/6J-Dnai2<sup>b2b3405Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5552738	Drc1<sup>b2b2237Clo</sup>	is_implicated_in	DOID:0110596	primary ciliary dyskinesia 21		MGI:5554187	Drc1<sup>b2b2237Clo</sup>/Drc1<sup>b2b2237Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b2237Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819110	Tg(Thy1-APPDutch)#Jckr/0  [background:] involves: C57BL/6J	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:15311281	20100818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819110	Tg(Thy1-APPDutch)#Jckr/0  [background:] involves: C57BL/6J	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:17596707	20100818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831332	Nek1<sup>kat</sup>/Nek1<sup>kat</sup>  [background:] involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:9070925	20090212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621007	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/Ola * C57BL/6	is_model_of	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11923874	20060503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5006985	Tg(Mov1/Tyr)OVE876BPay/Tg(Mov1/Tyr)OVE876BPay  [background:] FVB/N-Tg(Mov1/Tyr)OVE876BPay	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21093492	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712799	Gjb3<sup>tm2.1Kwi</sup>/Gjb3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050467	erythrokeratodermia variabilis						ECO:0000033	author statement supported by traceable reference	PMID:17446259	20070626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819007	Igh<sup>tm1(Myc)Janz</sup>/Igh<sup>+</sup> Tg(Emu-FGFR3)D3Wmk/0  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:9538	multiple myeloma						ECO:0000033	author statement supported by traceable reference	PMID:20393505	20100812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5565690	Tg(UBC-GFP/HTT*84Q)22Shya	is_implicated_in	DOID:12858	Huntington's disease		MGI:5565691	Tg(UBC-GFP/HTT*84Q)22Shya/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22422149	20140530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5565690	Tg(UBC-GFP/HTT*84Q)22Shya	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:23810380	20140530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3807710	Gja1<sup>tm8Kwi</sup>/Gja1<sup>+</sup> Tg(Pgk1-cre)1Lni/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:18003637	20080926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155245	Snrpn<sup>tm2Cbr</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155245	Snrpn<sup>tm2Cbr</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3618139	Snrpn<sup>tm2Cbr</sup>/Snrpn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9590284	20130729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819157	Zfp36l1<sup>tm1.1Tnr</sup>/Zfp36l1<sup>tm1.1Tnr</sup> Zfp36l2<sup>tm1.1Tnr</sup>/Zfp36l2<sup>tm1.1Tnr</sup> Tg(CD2-icre)4Kio/0  [background:] involves: C57BL/6 * C57BL/10 * CBA/Ca * SJL	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20622884	20100813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622093	Alms1<sup>foz</sup>/Alms1<sup>foz</sup>  [background:] involves: NOD	is_model_of	DOID:0050473	Alstrom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16516152	20060606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5487621	Abhd12<sup>tm1Crv</sup>	is_implicated_in	DOID:0080181	PHARC syndrome		MGI:5487655	Abhd12<sup>tm1Crv</sup>/Abhd12<sup>tm1Crv</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23297193	20211116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5487621	Abhd12<sup>tm1Crv</sup>	is_implicated_in	DOID:0080181	PHARC syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31213981	20211116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772884	Tg(Prnp-TBP*)71-27Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)71-27Xjl	is_model_of	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000033	author statement supported by traceable reference	PMID:17994014	20080305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559449	Tg(Thy1-APPSweAut)A7Tiwa/0  [background:] Not Specified	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19741145	20140418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774646	Snap25<sup>tm1Mcw</sup>/Snap25<sup>+</sup>  [background:] B6N.Cg-Snap25<sup>tm1Mcw</sup>	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:26300453	20161107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3801487	Mecp2<sup>tm1Pplt</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18557922	20150610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438236	Cul4b<sup>tm1Swl</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:5438241	Cul4b<sup>tm1Swl</sup>/Y Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] B6.Cg-Edil3<sup>Tg(Sox2-cre)1Amc</sup> Cul4b<sup>tm1Swl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22763239	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037157	Csrp3<sup>tm1Crni</sup>/Csrp3<sup>tm1Crni</sup>  [background:] Not Specified	is_model_of	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000033	author statement supported by traceable reference	PMID:9039266	20060518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6277991	Nrg3<sup>tm1.1Plet</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6283412	Nrg3<sup>tm1.1Plet</sup>/Nrg3<sup>tm1.1Plet</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27606322	20190318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476847	Tg(TARDBP)#Jpj/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:21752789	20130502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646378	Klhl3<sup>tm1.1Esoh</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:5646380	Klhl3<sup>tm1.1Esoh</sup>/Klhl3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24821705	20181031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646378	Klhl3<sup>tm1.1Esoh</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism						ECO:0000033	author statement supported by traceable reference	PMID:28743496	20181031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527095	Tecta<sup>tm4.1Gpr</sup>	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:5527173	Tecta<sup>tm4.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7506302	G6pc1<sup>em1Jyc</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:7506311	G6pc1<sup>em1Jyc</sup>/G6pc1<sup>em1Jyc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33359667	20230711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908875	Tg(Rho-GUCY2D*R838S)379Amd	is_implicated_in	DOID:0111011	cone-rod dystrophy 6		MGI:6154645	Tg(Rho-GUCY2D*R838S)379Amd/0  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:27703005	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806089	Tcf3<sup>tm1(PBX1)Mlc</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5825357	Tcf3<sup>tm1(PBX1)Mlc</sup>/Tcf3<sup>+</sup> Cd79a<sup>tm1(cre)Reth</sup>/Cd79a<sup>+</sup>  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26301816	20170301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806089	Tcf3<sup>tm1(PBX1)Mlc</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5825359	Tcf3<sup>tm1(PBX1)Mlc</sup>/Tcf3<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26301816	20170301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806089	Tcf3<sup>tm1(PBX1)Mlc</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5825356	Tcf3<sup>tm1(PBX1)Mlc</sup>/Tcf3<sup>+</sup> Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26301816	20170301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806089	Tcf3<sup>tm1(PBX1)Mlc</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:27758892	20170301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:2571	Langerhans-cell histiocytosis						ECO:0000033	author statement supported by traceable reference	PMID:33075814	20220204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:2571	Langerhans-cell histiocytosis		MGI:6192275	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Tg(Itgax-cre)1-1Reiz/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24638167	20220204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:2571	Langerhans-cell histiocytosis		MGI:6192274	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Cd207<sup>tm2.1(cre)Bjec</sup>/Cd207<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24638167	20220204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306919	Lmna<sup>tm2.1Gbon</sup>	is_implicated_in	DOID:0110640	congenital muscular dystrophy due to LMNA mutation		MGI:5306920	Lmna<sup>tm2.1Gbon</sup>/Lmna<sup>tm2.1Gbon</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22090424	20120223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405013	Tgfbi<sup>em1Yaou</sup>	is_implicated_in	DOID:2566	corneal dystrophy		MGI:6405015	Tgfbi<sup>em1Yaou</sup>/Tgfbi<sup>em1Yaou</sup>  [background:] involves: C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:32029872	20200422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6739867	Ppdpf<sup>tm1Nju</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6739868	Ppdpf<sup>tm1Nju</sup>/Ppdpf<sup>tm1Nju</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:34031390	20210816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6502626	Prrt2<sup>tm1d(KOMP)Wtsi</sup>	is_implicated_in	DOID:0090053	episodic kinesigenic dyskinesia 1		MGI:6502639	Prrt2<sup>tm1d(KOMP)Wtsi</sup>/Prrt2<sup>tm1d(KOMP)Wtsi</sup>  [background:] B6(Cg)-Prrt2<sup>tm1d(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32891704	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6502626	Prrt2<sup>tm1d(KOMP)Wtsi</sup>	is_implicated_in	DOID:0090053	episodic kinesigenic dyskinesia 1		MGI:6502640	Prrt2<sup>tm1d(KOMP)Wtsi</sup>/Prrt2<sup>+</sup>  [background:] B6(Cg)-Prrt2<sup>tm1d(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32891704	20210128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3702859	Psen1<sup>tm1Bdes</sup>/Psen1<sup>+</sup> Psen2<sup>tm1Bdes</sup>/Psen2<sup>tm1Bdes</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:6498	seborrheic keratosis						ECO:0000033	author statement supported by traceable reference	PMID:15128703	20070413	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175103	Lim2<sup>To3</sup>/Lim2<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK	is_model_of	DOID:0110263	cataract 19 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:9238094	20130617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654709	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:25144618	20151001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569727	Tg(TG-RET/CCDC6)42Cled	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5897617	Tg(TG-RET/CCDC6)42Cled/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10380889	20170518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569727	Tg(TG-RET/CCDC6)42Cled	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5897617	Tg(TG-RET/CCDC6)42Cled/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8536638	20170518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4398918	Acvrl1<sup>tm2Spo</sup>/Acvrl1<sup>tm2Spo</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:17911384	20110519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623677	Tg(INS-MT2A,Tyr)1Pne/0  [background:] FVB-Tg(INS-MT2A,Tyr)1Pne	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9836515	20060601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702868	Mecp2<sup>tm6.1Bird</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5702952	Mecp2<sup>tm6.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26647311	20160115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318689	Chrnb2<sup>tm1Jpc</sup>/Chrnb2<sup>tm1Jpc</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:12876201	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149904	Golgb1<sup>em33Lanyu</sup>	is_implicated_in	DOID:674	cleft palate		MGI:6151467	Golgb1<sup>em33Lanyu</sup>/Golgb1<sup>em33Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906017	Tg(Myh6-Tpm1*E54K)67Dfw	is_implicated_in	DOID:0110457	dilated cardiomyopathy 1Y		MGI:5906020	Tg(Myh6-Tpm1*E54K)67Dfw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17556658	20170801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286052	Dis3l2<sup>em3Jtm</sup>	is_implicated_in	DOID:0060476	Perlman syndrome		MGI:6286061	Dis3l2<sup>em3Jtm</sup>/Dis3l2<sup>em3Jtm</sup>  [background:] C57BL/6J-Dis3l2<sup>em3Jtm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29950491	20190404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829629	Gon4l<sup>justy</sup>	is_implicated_in	DOID:8850	salivary gland cancer		MGI:4829639	Gon4l<sup>justy</sup>/Gon4l<sup>justy</sup>  [background:] C3HeB/FeJ-Gon4l<sup>justy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23608756	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009552	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup> Tg(Th-MYCN)41Waw/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6J	is_model_of	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:9214616	20110702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809472	Cebpa<sup>tm8.1Nerl</sup>/Cebpa<sup>tm8.1Nerl</sup>  [background:] involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:18394553	20081003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587791	Lmna<sup>tm1Lgf</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587791	Lmna<sup>tm1Lgf</sup>	is_implicated_in	DOID:3911	progeria		MGI:3817506	Lmna<sup>tm1Lgf</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16862216	20150330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2671994	Chrne<sup>tm1Vwi</sup>/Chrne<sup>tm1Vwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110679	congenital myasthenic syndrome 4C						ECO:0000033	author statement supported by traceable reference	PMID:10998094	20090428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651858	Ush1c<sup>dfcr</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651858	Ush1c<sup>dfcr</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:2676319	Ush1c<sup>dfcr</sup>/Ush1c<sup>dfcr</sup>  [background:] involves: BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790748	Tg(H2-Ea-G6pc2)69Tkay	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22190647	20130325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790748	Tg(H2-Ea-G6pc2)69Tkay	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3790760	Tg(H2-Ea-G6pc2)69Tkay/?  [background:] NOD-Tg(H2-Ea-G6pc2)69Tkay			ECO:0000033	author statement supported by traceable reference	PMID:17143333	20130325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809245	Tg(Gfap-GFAP*R239H)60TMIke/0  [background:] involves: C57BL/6J	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:18602179	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809245	Tg(Gfap-GFAP*R239H)60TMIke/0  [background:] involves: C57BL/6J	is_model_of	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:17299771	20081002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3590082	Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677136	Itga2b<sup>tm1Tlr</sup>/Itga2b<sup>tm1Tlr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:0060691	platelet-type bleeding disorder 16						ECO:0000033	author statement supported by traceable reference	PMID:10942384	20050705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047138	Capn3<sup>Gt(OST141731)Lex</sup>/Capn3<sup>Gt(OST141731)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A						ECO:0000033	author statement supported by traceable reference	PMID:15138196	20161220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111539	Arpc4<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:6115481	Arpc4<sup>tm1c(EUCOMM)Wtsi</sup>/Arpc4<sup>tm1c(EUCOMM)Wtsi</sup> Krt14<sup>tm1(cre)Wbm</sup>/Krt14<sup>+</sup>  [background:] B6.Cg-Arpc4<sup>tm1c(EUCOMM)Wtsi</sup> Krt14<sup>tm1(cre)Wbm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29113991	20180209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766494	Tg(EmuSR-tTa)83Bop/Tg(EmuSR-tTa)83Bop Tg(tetO-TPM3/ALK,-luc)2Gde/0  [background:] involves: FVB/N	is_model_of	DOID:0060060	non-Hodgkin lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:20223922	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634270	Cacna1f<sup>tm1.1Sdie</sup>/Y  [background:] B6.Cg-Cacna1f<sup>tm1.1Sdie</sup>/J	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752897	Kif1a<sup>lgdg-2J</sup>/Kif1a<sup>lgdg-2J</sup>  [background:] C57BL/6J-Kif1a<sup>lgdg-2J</sup>/CxJ	is_model_of	DOID:0110781	hereditary spastic paraplegia 30						ECO:0000033	author statement supported by traceable reference	MGI:5752885	20160323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5284897	Pdlim5<sup>tm1Chen</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5284901	Pdlim5<sup>tm1Chen</sup>/Pdlim5<sup>tm1Chen</sup> Tg(Tnnt2-cre)5Blh/?  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20538684	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491627	Tg(Thy1-APPSweLon)41Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11746377	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949132	Hcrtr2<sup>tm1Tesc</sup>	is_implicated_in	DOID:8986	narcolepsy		MGI:4949134	Hcrtr2<sup>tm1Tesc</sup>/Hcrtr2<sup>tm1Tesc</sup>  [background:] B6.Cg-Hcrtr2<sup>tm1Tesc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21368172	20151120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4889220	Ank<sup>tm1.1Ejr</sup>/Ank<sup>tm1.1Ejr</sup>  [background:] B6.129-Ank<sup>tm1.1Ejr</sup>	is_model_of	DOID:0080033	craniometaphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19257826	20110223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946808	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>	is_implicated_in	DOID:3614	Kallmann syndrome		MGI:6162486	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>/Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>  [background:] B6.Cg-Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29263200	20180626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6162644	Slc19a3<sup>tm1.1Nwak</sup>	is_implicated_in	DOID:0050659	biotin-responsive basal ganglia disease		MGI:6162647	Slc19a3<sup>tm1.1Nwak</sup>/Slc19a3<sup>tm1.1Nwak</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28665968	20180627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21909131	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:23840792	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22919057	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22797060	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:3715723	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15231697	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491268	Tbc1d32<sup>b2b2284Clo</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111481	Snx10<sup>em2Ael</sup>	is_implicated_in	DOID:0110940	autosomal recessive osteopetrosis 8		MGI:6441471	Snx10<sup>em2Ael</sup>/Snx10<sup>em2Ael</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:32278070	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607779	Vps35<sup>tm1.1Mjff</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:7378801	Vps35<sup>tm1.1Mjff</sup>/Vps35<sup>tm1.1Mjff</sup>  [background:] B6.Cg-Vps35<sup>tm1.1Mjff</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33745227	20221107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5293442	Rtn4r<sup>rgsc1836</sup>	is_not_implicated_in	DOID:5419	schizophrenia		MGI:5293444	Rtn4r<sup>rgsc1836</sup>/Rtn4r<sup>rgsc1836</sup>  [background:] C57BL/6JJcl-Rtn4r<sup>rgsc1836</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21645550	20111026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856106	Bloc1s5<sup>mu</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:25673877	20160726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850221	Errfi1<sup>tm1Jwj</sup>/Errfi1<sup>tm1Jwj</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1380	endometrial cancer						ECO:0000033	author statement supported by traceable reference	PMID:19439667	20090713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4354296	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Lpl<sup>tm1Sem</sup>/Lpl<sup>tm1Sem</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:13809	familial combined hyperlipidemia						ECO:0000033	author statement supported by traceable reference	PMID:19481534	20090821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6460299	Akt1<sup>tm1Mjl</sup>	is_implicated_in	DOID:13482	Proteus syndrome		MGI:6460345	Akt1<sup>tm1Mjl</sup>/Akt1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31194862	20201008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401814	Col6a1<sup>tm1Sngi</sup>	is_implicated_in	DOID:0050558	Ullrich congenital muscular dystrophy		MGI:6401817	Col6a1<sup>tm1Sngi</sup>/Col6a1<sup>tm1Sngi</sup>  [background:] B6.Cg-Col6a1<sup>tm1Sngi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28043812	20200327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850819	Ts(17<sup>16</sup>)65Dn/0  [background:] B6EiC3Sn a/A-Ts(17<sup>16</sup>)65Dn/J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20875841	20110412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836294	Itgb4<sup>tm1Efu</sup>/Itgb4<sup>tm1Efu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:8707838	20090319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6164037	Tg(Vav1-STAT5B*N642H)726Biat	is_implicated_in	DOID:0060058	lymphoma		MGI:6164043	Tg(Vav1-STAT5B*N642H)726Biat/0  [background:] C57BL/6NCrl-Tg(Vav1-STAT5B*N642H)726Biat			ECO:0000033	author statement supported by traceable reference	PMID:29200404	20180703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6194622	Tg(GFAP-ATXN7*92Q)2542Als	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:6194625	Tg(GFAP-ATXN7*92Q)2542Als/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445966	Raf1<sup>tm2.1Ara</sup>/Raf1<sup>tm2.1Ara</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCr	is_model_of	DOID:0060583	Noonan syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:22826437	20121214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5639083	Ptpn11<sup>tm1.1Ics</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N	is_model_of	DOID:14291	Noonan syndrome with multiple lentigines						ECO:0000033	author statement supported by traceable reference	PMID:25288766	20150610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359169	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup> Nr1h2<sup>tm1Djm</sup>/Nr1h2<sup>tm1Djm</sup>  [background:] involves: 129S6/SvEvTac * BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:18160655	20090925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7310129	Aqp5<sup>em1Cya</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:7310130	Aqp5<sup>em1Cya</sup>/Aqp5<sup>em1Cya</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33013441	20220706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575410	Phox2b<sup>tm1Rth</sup>	is_implicated_in	DOID:0060731	congenital central hypoventilation syndrome		MGI:7397263	Phox2b<sup>tm1Rth</sup>/Phox2b<sup>+</sup> Hprt1<sup>tm1(CAG-cre)Mnn</sup>/?  [background:] involves: 129 * 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25975378	20221205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635983	Mitf<sup>mi-bw</sup>/Mitf<sup>mi-bw</sup> Tg(Dct-lacZ)A12Jkn/0  [background:] involves: C3H * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:22563733	20150514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814590	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18227155	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6881754	Tg(Prnp-SETX*R2136H)1920Als	is_implicated_in	DOID:0060196	amyotrophic lateral sclerosis type 4		MGI:6883568	Tg(Prnp-SETX*R2136H)1920Als/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29725819	20220225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5532525	Krit1<sup>tm1Kwhi</sup>	is_implicated_in	DOID:0060669	cerebral cavernous malformation		MGI:6279211	Krit1<sup>tm1Kwhi</sup>/Krit1<sup>tm1Kwhi</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27027284	20190220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5532525	Krit1<sup>tm1Kwhi</sup>	is_implicated_in	DOID:0060669	cerebral cavernous malformation		MGI:6279211	Krit1<sup>tm1Kwhi</sup>/Krit1<sup>tm1Kwhi</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27513872	20190220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838091	Ass1<sup>bar</sup>/Ass1<sup>fold</sup>  [background:] involves: C57BL/6Ei * C57BL/6J * OF1 * P/J	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307230	Tg(Lgi1*)#Mpan/0  [background:] Not Specified	is_model_of	DOID:0060748	familial temporal lobe epilepsy 1						ECO:0000033	author statement supported by traceable reference	PMID:19701204	20120227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7311668	Rarres1<sup>tm1.2Mhl</sup>	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:7311738	Rarres1<sup>tm1.2Mhl</sup>/Rarres1<sup>tm1.2Mhl</sup>  [background:] involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7311668	Rarres1<sup>tm1.2Mhl</sup>	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:7311756	Rarres1<sup>tm1.2Mhl</sup>/Rarres1<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857151	Cftr<sup>tm1Kth</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24303840	20170515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857151	Cftr<sup>tm1Kth</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24801204	20170515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857151	Cftr<sup>tm1Kth</sup>	is_implicated_in	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:20570219	20170515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857151	Cftr<sup>tm1Kth</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177536	Cftr<sup>tm1Kth</sup>/Cftr<sup>tm1Kth</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7560099	20170515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857151	Cftr<sup>tm1Kth</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3689378	Cftr<sup>tm1Kth</sup>/Cftr<sup>tm1Kth</sup>  [background:] B6.129S7-Cftr<sup>tm1Kth</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20170515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000250	Tg(Alb-TAg)#Arnd	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:31291357	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000250	Tg(Alb-TAg)#Arnd	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5000253	Tg(Alb-TAg)#Arnd/0  [background:] C3Fe.Cg-Tg(Alb-TAg)#Arnd			ECO:0000033	author statement supported by traceable reference	PMID:19428549	20190812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856919	Nek8<sup>jck</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:26967905	20161214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856919	Nek8<sup>jck</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:23973373	20161214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856919	Nek8<sup>jck</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:27053712	20161214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856919	Nek8<sup>jck</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:25934702	20161214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856919	Nek8<sup>jck</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2429561	Nek8<sup>jck</sup>/Nek8<sup>jck</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8510385	20161214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437461	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14522252	20160121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437461	Rb1<sup>tm2Brn</sup>/Rb1<sup>tm2Brn</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19765830	20160121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437102	Slit2<sup>b2b1200.1Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:13481	thanatophoric dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10545953	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5439657	Bap1<sup>tm1.1Geno</sup>/Bap1<sup>tm1.1Geno</sup> Gt(ROSA)26Sor<sup>tm9(cre/ESR1)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6NTac	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22878500	20121026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5501040	Hps1<sup>ep-7J</sup>/Hps1<sup>ep-7J</sup>  [background:] CAST/EiJ-Hps1<sup>ep-7J</sup>/GrsrJ	is_model_of	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	MGI:5499306	20130814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834658	Ccn1<sup>tm1Lfl</sup>/Ccn1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110106	atrial heart septal defect 1						ECO:0000033	author statement supported by traceable reference	PMID:17023674	20101013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838173	Tg(Myh6-MYL2*D166V)1Dsc/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000033	author statement supported by traceable reference	PMID:18987303	20141112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5642333	Atp13a2<sup>tm1.2Wtd</sup>	is_implicated_in	DOID:0060556	Kufor-Rakeb syndrome		MGI:5642335	Atp13a2<sup>tm1.2Wtd</sup>/Atp13a2<sup>tm1.2Wtd</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25855184	20150702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287205	Arhgef10<sup>tm1.1Ssfg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6287207	Arhgef10<sup>tm1.1Ssfg</sup>/Arhgef10<sup>tm1.1Ssfg</sup>  [background:] B6.129S1-Arhgef10<sup>tm1.1Ssfg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29456827	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7511793	Rtf1<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:7523000	Rtf1<sup>tm1c(KOMP)Wtsi</sup>/Rtf1<sup>tm1c(KOMP)Wtsi</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:37233188	20230831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5825056	Tg(BAC144D14)5A2Masu	is_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:5825063	Tg(BAC144D14)5A2Masu/0  [background:] B6J.Cg-Tg(BAC144D14)5A2Masu			ECO:0000033	author statement supported by traceable reference	PMID:26963625	20170224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814057	Tg(SOD1*G37R)29Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:12127151	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814057	Tg(SOD1*G37R)29Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:7605627	20130109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5463442	Fras1<sup>bfb</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:5564953	Fras1<sup>bfb</sup>/Fras1<sup>bfb</sup>  [background:] involves: C57BL/6JAnu			ECO:0000033	author statement supported by traceable reference	PMID:24143185	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5538516	Tg(tetO-Fgf9,-EGFP)#Dor	is_implicated_in	DOID:1324	lung cancer		MGI:5538520	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:23867472	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949537	Agps<sup>bs2</sup>/Agps<sup>bs2</sup>  [background:] STOCK Agps<sup>bs2</sup>/J	is_model_of	DOID:0110853	rhizomelic chondrodysplasia punctata type 3						ECO:0000033	author statement supported by traceable reference	PMID:21353609	20120615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6315194	Tg(Vav1-Asxl1*Y588X)#Fcy	is_implicated_in	DOID:2226	myeloproliferative neoplasm		MGI:6315197	Tg(Vav1-Asxl1*Y588X)#Fcy/0  [background:] C57BL/6-Tg(Vav1-Asxl1*Y588X)#Fcy			ECO:0000033	author statement supported by traceable reference	PMID:29113963	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575668	Asxl1<sup>tm1.1Mjxu</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575760	Asxl1<sup>tm1.1Mjxu</sup>/Asxl1<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24255920	20140731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575668	Asxl1<sup>tm1.1Mjxu</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575759	Asxl1<sup>tm1.1Mjxu</sup>/Asxl1<sup>tm1.1Mjxu</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24255920	20140731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578131	Tg(Alb-PDGFC)#Jcam	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5578132	Tg(Alb-PDGFC)#Jcam/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23929039	20140822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029167	Tgm1<sup>tm1Kfyn</sup>/Tgm1<sup>tm1Kfyn</sup>  [background:] involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060656	autosomal recessive congenital ichthyosis 1						ECO:0000033	author statement supported by traceable reference	PMID:11805136	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029167	Tgm1<sup>tm1Kfyn</sup>/Tgm1<sup>tm1Kfyn</sup>  [background:] involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060656	autosomal recessive congenital ichthyosis 1						ECO:0000033	author statement supported by traceable reference	PMID:9448282	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177239	Brca2<sup>tm2Arge</sup>/Brca2<sup>tm2Arge</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>tm1(cre)Arge</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11494122	20060807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5582511	Ryr2<sup>tm4.1Amks</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5582594	Ryr2<sup>tm4.1Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22828895	20140915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6193897	Tg(Myh6-MYL2*D94A)1Dsc	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6193898	Tg(Myh6-MYL2*D94A)1Dsc/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29463717	20180808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476170	Plxnd1<sup>b2b1863Clo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5476432	Plxnd1<sup>b2b1863Clo</sup>/Plxnd1<sup>b2b1863Clo</sup>  [background:] C57BL/6J-Plxnd1<sup>b2b1863Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7279260	Tlr7<sup>em2Anu</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:7284944	Tlr7<sup>em2Anu</sup>/Tlr7<sup>em2Anu</sup>  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7279260	Tlr7<sup>em2Anu</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:7284986	Tlr7<sup>em2Anu</sup>/Y  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7279260	Tlr7<sup>em2Anu</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:7284974	Tlr7<sup>em2Anu</sup>/Tlr7<sup>+</sup>  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429405	Tg(Htt-ATXN3*148Q)3746Thsc/0  [background:] involves: C57BL/6N	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:19699305	20100218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655642	Atp2a2<sup>tm1Ges</sup>/Atp2a2<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss	is_model_of	DOID:2734	keratosis follicularis						ECO:0000033	author statement supported by traceable reference	PMID:11389134	20130610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6466713	Impg2<sup>em2Xjz</sup>	is_implicated_in	DOID:0110371	retinitis pigmentosa 56		MGI:6466735	Impg2<sup>em2Xjz</sup>/Impg2<sup>em2Xjz</sup>  [background:] C57BL/6J-Impg2<sup>em2Xjz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32242237	20201013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719798	En2<sup>tm1Alj</sup>/En2<sup>tm1Alj</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:16935268	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818990	Tg(Prnp-APP*)1Hmor/0  [background:] B6.Cg-Tg(Prnp-APP*)1Hmor	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20371804	20100812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618433	Slc7a5<sup>tm1.1Daca</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5829465	Slc7a5<sup>tm1.1Daca</sup>/Slc7a5<sup>tm1.1Daca</sup> Tg(Tek-cre)12Flv/0  [background:] B6J.Cg-Slc7a5<sup>tm1.1Daca</sup> Tg(Tek-cre)12Flv			ECO:0000033	author statement supported by traceable reference	PMID:27912058	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431477	Gpr179<sup>nob5</sup>	is_implicated_in	DOID:0110869	congenital stationary night blindness 1E		MGI:5431492	Gpr179<sup>nob5</sup>/Gpr179<sup>nob5</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:22325362	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699108	Col9a1<sup>tm1Jae</sup>/Col9a1<sup>tm1Jae</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:8398	osteoarthritis						ECO:0000033	author statement supported by traceable reference	PMID:11680679	20070308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5424158	Dot1l<sup>tm1Tche</sup>/Dot1l<sup>tm1.1Tche</sup> Tg(Myhca-cre)1Abel/0  [background:] Not Specified	is_model_of	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:21289070	20120613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716404	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24430184	20140508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512883	Wt1<sup>tm1Vih</sup>/Wt1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * MF1	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15509792	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425920	Casr<sup>BCH004</sup>/Casr<sup>BCH004</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH004</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476653	Stx11<sup>tm1.2Ics</sup>/Stx11<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0110924	familial hemophagocytic lymphohistiocytosis 4						ECO:0000033	author statement supported by traceable reference	PMID:23160464	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527452	Tg(Alb-Mut)#Cpv	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:23898205	20140110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6331300	Tg(tetO-GFP,-APOL1*)#Susz	is_implicated_in	DOID:557	kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:30226866	20190731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6331300	Tg(tetO-GFP,-APOL1*)#Susz	is_implicated_in	DOID:557	kidney disease		MGI:6331363	Tg(Nphs1-rtTA*3G)8Jhm/0 Tg(tetO-GFP,-APOL1*)#Susz/0  [background:] involves: C57BL/6J * CBA/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28218918	20190731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195852	Arx<sup>tm1.1Ics</sup>	is_implicated_in	DOID:0060309	syndromic X-linked intellectual disability		MGI:6195853	Arx<sup>tm1.1Ics</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29659809	20180829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439833	Ids<sup>tm1Eto</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II						ECO:0000033	author statement supported by traceable reference	PMID:22704483	20121106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439833	Ids<sup>tm1Eto</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:5440736	Ids<sup>tm1Eto</sup>/Ids<sup>tm1Eto</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22704483	20121106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664199	Scnn1g<sup>tm1Bhk</sup>/Scnn1g<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1						ECO:0000033	author statement supported by traceable reference	PMID:9788978	20100302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604072	Fgfr2<sup>tm2Cxd</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:24259495	20160830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604072	Fgfr2<sup>tm2Cxd</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:3604078	Fgfr2<sup>tm2Cxd</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14499350	20160830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604072	Fgfr2<sup>tm2Cxd</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:5790180	Fgfr2<sup>tm2Cxd</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21538817	20160830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819720	Tg(Myh6-TNNT2*R92Q)#Ajm	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:4819722	Tg(Myh6-TNNT2*R92Q)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18349139	20100819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819720	Tg(Myh6-TNNT2*R92Q)#Ajm	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:4819722	Tg(Myh6-TNNT2*R92Q)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11171784	20100819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6467991	Vps13b<sup>tm1.2Ics</sup>	is_implicated_in	DOID:83	cataract		MGI:6468047	Vps13b<sup>tm1.2Ics</sup>/Vps13b<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32915983	20201021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6103872	Tg(Myh6-CRYAB*R120G)7302Ijb	is_implicated_in	DOID:0080093	myofibrillar myopathy 2		MGI:6103873	Tg(Myh6-CRYAB*R120G)7302Ijb/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17693254	20171220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5792687	Ptchd1<sup>tm2.2Gfng</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5792693	Ptchd1<sup>tm2.2Gfng</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27007844	20170712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3530074	Atrx<sup>tm1Rjg</sup>/Y Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15668733	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388817	Tg(KRT14-Il18)#Knak	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388817	Tg(KRT14-Il18)#Knak	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:19078986	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388817	Tg(KRT14-Il18)#Knak	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5563665	Tg(KRT14-Il18)#Knak/0  [background:] C57BL/6-Tg(KRT14-Il18)#Knak			ECO:0000033	author statement supported by traceable reference	PMID:12151598	20140520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856798	A<sup>y</sup>	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:23583377	20131205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856965	Large1<sup>myd</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25710816	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856965	Large1<sup>myd</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:3607259	Large1<sup>myd</sup>/Large1<sup>myd</sup>  [background:] B6C3Fe a/a-Large1<sup>myd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7602333	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695720	Krt4<sup>Bcc1</sup>/Krt4<sup>+</sup>  [background:] C3HeB/FeJ-Krt4<sup>Bcc1</sup>	is_model_of	DOID:0050448	white sponge nevus						ECO:0000033	author statement supported by traceable reference	PMID:16858417	20070206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181203	Tg(TcraBDC2.5,TcrbBDC2.5)1Doi	is_implicated_in	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:28292965	20171212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563665	Tg(KRT14-Il18)#Knak/0  [background:] C57BL/6-Tg(KRT14-Il18)#Knak	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:12151598	20140515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857942	Cdkn2a<sup>tm1Rdp</sup>	is_implicated_in	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000033	author statement supported by traceable reference	PMID:27333032	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660030	Tg(Pcp2-tTA)3Horr/0 Tg(tetO-PRKCG*S361G,-GFP)3Jpka/0  [background:] involves: FVB/N	is_model_of	DOID:0050964	spinocerebellar ataxia type 14						ECO:0000033	author statement supported by traceable reference	PMID:24937631	20150827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670767	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup> Ywhae<sup>tm1Awb</sup>/Ywhae<sup>+</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12796778	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582615	Mkks<sup>tm1Vcs</sup>/Mkks<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15772095	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5516082	Slc6a2<sup>tm1.1Mkh</sup>	is_implicated_in	DOID:10273	heart conduction disease		MGI:5516191	Slc6a2<sup>tm1.1Mkh</sup>/Slc6a2<sup>+</sup>  [background:] B6.129S6-Slc6a2<sup>tm1.1Mkh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23580201	20170710	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672030	Hic1<sup>tm1Sbb</sup>/Hic1<sup>tm1Sbb</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10655551	20150831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311582	Plec<sup>tm7.1Gwi</sup>/Plec<sup>tm7.1Gwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060736	epidermolysis bullosa simplex Ogna type						ECO:0000033	author statement supported by traceable reference	PMID:22144912	20120321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135673	Fgfr3<sup>tm3.1Cxd</sup>	is_implicated_in	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:22634226	20120927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135673	Fgfr3<sup>tm3.1Cxd</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3640338	Fgfr3<sup>tm3.1Cxd</sup>/Fgfr3<sup>tm3.1Cxd</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10587515	20120927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135673	Fgfr3<sup>tm3.1Cxd</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3640343	Fgfr3<sup>tm3.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10587515	20120927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5560479	Tg(Cela1-luc,Cela1-TAg)#Nzh/0  [background:] involves: FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19622581	20140429	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3770515	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:11323676	20080212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702951	Mecp2<sup>tm5.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26647311	20160115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007799	Gt(ROSA)26Sor<sup>tm3(NOTCH3*R1031C)Sat</sup>	is_implicated_in	DOID:0111035	CADASIL 1		MGI:5007819	Gt(ROSA)26Sor<sup>tm3(NOTCH3*R1031C)Sat</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21555590	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5320595	Ugt1<sup>tm1.1Afmu</sup>/Ugt1<sup>tm1.1Afmu</sup>  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:3803	Crigler-Najjar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22094718	20120607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785289	Cybb<sup>tm1Din</sup>/Cybb<sup>tm1Din</sup>  [background:] B6.129S-Cybb<sup>tm1Din</sup>	is_model_of	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:19234224	20100414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590228	Tg(H2-Ea-Ins2)1Wehi/0  [background:] NOD/ShiLtJWehi-Tg(H2-Ea-Ins2)1Wehi	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9836515	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6406986	Fgfr2<sup>tm3.1Cxd</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:6407058	Fgfr2<sup>tm3.1Cxd</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18242159	20200430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5463438	Tg(Thy1-APPArc)M8Cagr/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19329229	20130212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555837	Ccdc39<sup>b2b2025.1Clo</sup>/Ccdc39<sup>b2b2025.1Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b2025.1Clo</sup>	is_model_of	DOID:0110598	primary ciliary dyskinesia 14						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612533	Braf<sup>tm1Cpri</sup>	is_implicated_in	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:28463229	20181220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612533	Braf<sup>tm1Cpri</sup>	is_implicated_in	DOID:1909	melanoma		MGI:3843341	Braf<sup>tm1Cpri</sup>/Braf<sup>tm1Cpri</sup> Tg(Tyr-cre/ERT2)1Lru/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19345328	20181220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661588	Lyst<sup>bg-18J</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:6383409	Lyst<sup>bg-18J</sup>/Lyst<sup>bg-18J</sup>  [background:] B6.Cg-Lyst<sup>bg-18J</sup>/Boc			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20200106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5461308	Men1<sup>tm1Rvt</sup>/Men1<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:19620250	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5519083	Tg(Pkd1*)39Mtru	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5519084	Tg(Pkd1*)39Mtru/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:23439951	20131121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5553469	Tg(JAK2*V617F)FF1Rsko/0 Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * CBA/Ca	is_model_of	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:18160670	20140329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950068	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB	is_model_of	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21195751	20110514	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435246	Crybb2<sup>Lop19</sup>/Crybb2<sup>+</sup>  [background:] SJL/J-Crybb2<sup>Lop19</sup>/BocJ	is_model_of	DOID:0110269	cataract 3 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:5435169	20120918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640323	Fgfr3<sup>tm4Cxd</sup>/Fgfr3<sup>+</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * NIH Black Swiss * SJL	is_model_of	DOID:13481	thanatophoric dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10861287	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818906	Dnm1l<sup>Py</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4818928	Dnm1l<sup>Py</sup>/Dnm1l<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:20585624	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618137	Snrpn<sup>tm1Kaj</sup>/Snrpn<sup>+</sup>  [background:] either: 129S1-Snrpn<sup>tm1Kaj</sup> or (involves: 129S1/Sv * C57BL/6J)	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16368707	20060329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777403	Cryaa<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:32833997	20200909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777403	Cryaa<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:3784582	Cryaa<sup>tm1.1Ady</sup>/Cryaa<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18056999	20200909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777403	Cryaa<sup>tm1.1Ady</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:3784583	Cryaa<sup>tm1.1Ady</sup>/Cryaa<sup>tm1.1Ady</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18056999	20200909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620609	Ryr1<sup>tm1Tno</sup>/Ryr1<sup>tm1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:3529	congenital myopathy 1A						ECO:0000033	author statement supported by traceable reference	PMID:7515481	20060823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304755	Col1a1<sup>tm2(tetO-RNAi:Rps19)Karl</sup>	is_implicated_in	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:22791294	20160519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304755	Col1a1<sup>tm2(tetO-RNAi:Rps19)Karl</sup>	is_implicated_in	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:25987256	20160519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766495	Snap25<sup>tm1.1Bark</sup>/Snap25<sup>tm1.1Bark</sup>  [background:] Not Specified	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:26195742	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6704950	Mkrn3<sup>em1Rhu</sup>	is_implicated_in	DOID:0112309	central precocious puberty 2		MGI:6704951	Mkrn3<sup>em1Rhu</sup>/Mkrn3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34692086	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629843	Slurp1<sup>tm1.1Sgy</sup>	is_implicated_in	DOID:0060862	mal de Meleda		MGI:5629846	Slurp1<sup>tm1.1Sgy</sup>/Slurp1<sup>tm1.1Sgy</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24499735	20150416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007912	Mefv<sup>tm3.1(MEFV)Chae</sup>	is_implicated_in	DOID:2987	familial mediterranean fever		MGI:5007926	Mefv<sup>tm3.1(MEFV)Chae</sup>/Mefv<sup>tm3.1(MEFV)Chae</sup>  [background:] B6.129S6-Mefv<sup>tm3.1(MEFV)Chae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21600797	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676317	Ush1c<sup>dfcr-2J</sup>/Ush1c<sup>dfcr-2J</sup>  [background:] B6;129S4	is_model_of	DOID:0110473	autosomal recessive nonsyndromic deafness 18A						ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835411	Fkrp<sup>tm1Scbr</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:6303809	Fkrp<sup>tm1Scbr</sup>/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26306834	20190515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5607261	Slc40a1<sup>tm1.1Mmfe</sup>/Slc40a1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111028	hemochromatosis type 4						ECO:0000033	author statement supported by traceable reference	PMID:25100063	20141216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431501	Daw1<sup>b2b1584Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3689004	Tg(Myh6-PRKAG2*R302Q)#Rro/0  [background:] involves: FVB	is_model_of	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15611370	20061129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909328	Tg(Myh6-Tnni3*R146G)121Rbns	is_implicated_in	DOID:0110313	hypertrophic cardiomyopathy 7		MGI:5909332	Tg(Myh6-Tnni3*R146G)121Rbns/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11055985	20170918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046801	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm3Bld</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689331	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] B6J.D2-Dtnbp1<sup>sdy</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25677649	20151009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689331	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] B6J.D2-Dtnbp1<sup>sdy</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23261874	20151009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430049	b2b243Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5430325	b2b243Clo/b2b243Clo  [background:] C57BL/6J-b2b243Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6758566	Tg(Umod*C217G)1Xrw	is_implicated_in	DOID:0060062	familial juvenile hyperuricemic nephropathy		MGI:6758622	Tg(Umod*C217G)1Xrw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29145399	20210910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0110354	retinitis pigmentosa 19						ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620001	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] B6.129-Eln<sup>tm1Dyl</sup>	is_model_of	DOID:10825	essential hypertension						ECO:0000033	author statement supported by traceable reference	PMID:14597767	20060418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912306	Clcn2<sup>nmf289</sup>	is_implicated_in	DOID:10579	leukodystrophy		MGI:5925277	Clcn2<sup>nmf289</sup>/Clcn2<sup>nmf289</sup>  [background:] CByJ.Cg-Clcn2<sup>nmf289</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:3892	insulinoma						ECO:0000033	author statement supported by traceable reference	PMID:25978773	20181120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429941	Tg(RIP1-Tag)2Dh	is_implicated_in	DOID:3892	insulinoma		MGI:5431966	Tg(RIP1-Tag)2Dh/0  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:22562956	20181120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640318	Fgfr3<sup>tm4.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:13481	thanatophoric dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:10861287	20060810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510312	Tbx1<sup>tm1Dsr</sup>/Tbx1<sup>tm1Dsr</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589477	Zfpm2<sup>lil</sup>/Zfpm2<sup>lil</sup>  [background:] involves: A/J	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:16103912	20051013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832388	Ldb3<sup>tm4Chen</sup>	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832388	Ldb3<sup>tm4Chen</sup>	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C		MGI:3832389	Ldb3<sup>tm4Chen</sup>/Ldb3<sup>tm4Chen</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:19028670	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832388	Ldb3<sup>tm4Chen</sup>	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C		MGI:3832390	Ldb3<sup>tm4Chen</sup>/Ldb3<sup>tm4Chen</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19028670	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575507	Tg(Prnp-SNAP25/HTT*150Q)8Xjl	is_implicated_in	DOID:12858	Huntington's disease		MGI:5575509	Tg(Prnp-SNAP25/HTT*150Q)8Xjl/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:24081492	20140730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706544	Ager<sup>tm1.1Hyam</sup>/Ager<sup>tm1.1Hyam</sup> Tg(Ins2-Nos2)40Okam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1 * DBA/2	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:16936199	20070502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653055	Ndn<sup>tm2Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12629158	20091026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6116819	Arid1b<sup>em1Hzhu</sup>	is_implicated_in	DOID:0070042	Coffin-Siris syndrome 1		MGI:6159715	Arid1b<sup>em1Hzhu</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Hzhu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28695822	20180606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5766489	Tg(tetO-TPM3/ALK,-luc)2Gde	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5766494	Tg(EmuSR-tTa)83Bop/Tg(EmuSR-tTa)83Bop Tg(tetO-TPM3/ALK,-luc)2Gde/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20223922	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430593	Tg(Dyrk1a)189N3Yah/0  [background:] B6.129P2-Tg(Dyrk1a)189N3Yah/Yah	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22293606	20120807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624974	X/Yaa  [background:] (NZW x SB)F1	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:6690614	20060621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5004866	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:16951148	20110608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2656914	Sgca<sup>tm1Eeng</sup>/Sgca<sup>tm1Eeng</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ	is_model_of	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:12620894	20100330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850190	Tg(KRT5-tTA)1216Glk/0 Tg(tetO-Il13)1Tazh/0  [background:] B6.Cg-Tg(KRT5-tTA)1216Glk Tg(tetO-Il13)1Tazh	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:18830273	20090713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318856	Smn1<sup>tm1Cdid</sup>/Smn1<sup>tm1Cdid</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22423102	20120521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720810	Prkci<sup>tm1Rfar</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22225955	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720810	Prkci<sup>tm1Rfar</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17641777	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270401	Mecp2<sup>tm1Nlnd</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266283	Mecp2<sup>tm1Nlnd</sup>/Mecp2<sup>+</sup>  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270401	Mecp2<sup>tm1Nlnd</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266266	Mecp2<sup>tm1Nlnd</sup>/Y  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270401	Mecp2<sup>tm1Nlnd</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266261	Mecp2<sup>tm1Nlnd</sup>/Y  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111355	Tg(Ins2-IAPP)L13Gjsc	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:6111393	Tg(Ins2-IAPP)L13Gjsc/0  [background:] FVB/N-Tg(Ins2-IAPP)L13Gjsc			ECO:0000033	author statement supported by traceable reference	PMID:18633116	20180122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111355	Tg(Ins2-IAPP)L13Gjsc	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:19794060	20180122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111355	Tg(Ins2-IAPP)L13Gjsc	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:27865831	20180122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576739	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11323694	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6406374	Chn1<sup>tm1.1Ece</sup>	is_implicated_in	DOID:12557	Duane retraction syndrome		MGI:6406385	Chn1<sup>tm1.1Ece</sup>/Chn1<sup>tm1.1Ece</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28346224	20200427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6508538	Pank4<sup>em1Nju</sup>	is_implicated_in	DOID:83	cataract		MGI:6508539	Pank4<sup>em1Nju</sup>/Pank4<sup>em1Nju</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30585370	20210303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426931	Gt(ROSA)26Sor<sup>tm51(HTT)Arte</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432179	Gt(ROSA)26Sor<sup>tm51(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360273	Tg(Myh6-CREB1*S133A)1Jml	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12054854	20170824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360273	Tg(Myh6-CREB1*S133A)1Jml	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:9616213	20170824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360273	Tg(Myh6-CREB1*S133A)1Jml	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4360302	Tg(Myh6-CREB1*S133A)1Jml/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9616213	20170824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664917	Actn4<sup>tm1Mrpk</sup>	is_implicated_in	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000033	author statement supported by traceable reference	PMID:25962121	20161117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664917	Actn4<sup>tm1Mrpk</sup>	is_implicated_in	DOID:0111128	focal segmental glomerulosclerosis 1		MGI:2669775	Actn4<sup>tm1Mrpk</sup>/Actn4<sup>tm1Mrpk</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12782671	20161117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5141270	Slc32a1<sup>tm2(cre)Lowl</sup>	is_implicated_in	DOID:3328	temporal lobe epilepsy		MGI:6730293	Slc32a1<sup>tm2(cre)Lowl</sup>/Slc32a1<sup>tm2(cre)Lowl</sup>  [background:] either: B6J.129S6(FVB)-Slc32a1<sup>tm2(cre)Lowl</sup> or (involves: 129S6/SvEvTac * C57BL/6J * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:32954490	20210812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813896	Kras<sup>tm5Tyj</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813896	Kras<sup>tm5Tyj</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:5007794	Kras<sup>tm5Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21512139	20171108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3710321	Cdkn2c<sup>tm1Bbd</sup>/Cdkn2c<sup>tm1Bbd</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16260494	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5500068	Vcp<sup>tm1Itl</sup>/Vcp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:23029473	20130808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047080	Tg(TTR-V30M)15Imeg	is_implicated_in	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:27338109	20180905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047080	Tg(TTR-V30M)15Imeg	is_implicated_in	DOID:0050638	transthyretin amyloidosis						ECO:0000033	author statement supported by traceable reference	PMID:25693163	20180905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047080	Tg(TTR-V30M)15Imeg	is_implicated_in	DOID:0050638	transthyretin amyloidosis		MGI:3613376	Tg(TTR-V30M)15Imeg/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:1992765	20180905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047080	Tg(TTR-V30M)15Imeg	is_implicated_in	DOID:0050638	transthyretin amyloidosis		MGI:6196487	Tg(TTR-V30M)15Imeg/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29330472	20180905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473902	Cacna1s<sup>tm1.1Cann</sup>	is_implicated_in	DOID:14452	hypokalemic periodic paralysis		MGI:5474008	Cacna1s<sup>tm1.1Cann</sup>/Cacna1s<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:23187123	20130411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473902	Cacna1s<sup>tm1.1Cann</sup>	is_implicated_in	DOID:14452	hypokalemic periodic paralysis		MGI:5474009	Cacna1s<sup>tm1.1Cann</sup>/Cacna1s<sup>tm1.1Cann</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:7962166	20130411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836195	Cacna1a<sup>tm3Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:22144569	20150506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836195	Cacna1a<sup>tm3Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine						ECO:0000033	author statement supported by traceable reference	PMID:25716839	20150506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836195	Cacna1a<sup>tm3Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:5487277	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>tm3Maag</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22144569	20150506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836195	Cacna1a<sup>tm3Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:5487278	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22144569	20150506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836195	Cacna1a<sup>tm3Maag</sup>	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3836256	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>tm3Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm3Maag</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19104150	20150506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806143	Lmna<sup>tm12Lgf</sup>	is_implicated_in	DOID:3911	progeria		MGI:5806144	Lmna<sup>tm12Lgf</sup>/Lmna<sup>tm12Lgf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26999604	20211020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806143	Lmna<sup>tm12Lgf</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:34423791	20211020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668598	Grk1<sup>tm1Citb</sup>/Grk1<sup>tm1Citb</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110713	Oguchi disease-2						ECO:0000033	author statement supported by traceable reference	PMID:10097103	20100707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857590	Trp53<sup>tm1Brd</sup>	is_implicated_in	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:30202050	20190109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5467321	Tg(Pcp2-ATXN2*127Q)#Plt	is_implicated_in	DOID:0050955	spinocerebellar ataxia type 2		MGI:5467323	Tg(Pcp2-ATXN2*127Q)#Plt/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:23087021	20130305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7442161	Kcnt1<sup>em1Pqt</sup>	is_implicated_in	DOID:0080439	developmental and epileptic encephalopathy 14		MGI:7442320	Kcnt1<sup>em1Pqt</sup>/Kcnt1<sup>em1Pqt</sup>  [background:] C57BL/6J-Kcnt1<sup>em1Pqt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36173683	20230308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5803807	Tg(tetO/Prnp-APP*Swe*Lon)9191Krz	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5803810	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO/Prnp-APP*Swe*Lon)9191Krz/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25946042	20161017	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817243	Tlx2<sup>tm1Htno</sup>/Tlx2<sup>tm1Htno</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0080072	intestinal pseudo-obstruction						ECO:0000033	author statement supported by traceable reference	PMID:9259577	20081120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694478	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:1852	intrahepatic cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:21292027	20150312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2429561	Nek8<sup>jck</sup>/Nek8<sup>jck</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8510385	20050805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6276040	Tg(Myh6-Camk2d_ic)MJhb	is_implicated_in	DOID:6000	congestive heart failure		MGI:6276042	Tg(Myh6-Camk2d_ic)MJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722095	Tg(GSK3B*S9A)1Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24498342	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722095	Tg(GSK3B*S9A)1Vln	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24704314	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5883590	C9orf72<sup>tm1.1Eggn</sup>	is_implicated_in	DOID:417	autoimmune disease		MGI:6278554	C9orf72<sup>tm1.1Eggn</sup>/C9orf72<sup>tm1.1Eggn</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5582277	Tg(Cryaa-APEH)KKS4Kksha	is_implicated_in	DOID:83	cataract		MGI:5582278	Tg(Cryaa-APEH)KKS4Kksha/0  [background:] FVB/N-Tg(Cryaa-APEH)KKS4Kksha			ECO:0000033	author statement supported by traceable reference	PMID:24554718	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616632	Galns<sup>tm2(GALNS)Toma</sup>/Galns<sup>tm2(GALNS)Toma</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:12804	mucopolysaccharidosis IV						ECO:0000033	author statement supported by traceable reference	PMID:16219627	20060316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3699817	Fgfr2<sup>tm1Schl</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17132737	20070315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5556065	Fkrp<sup>tm1Scbr</sup>/Fkrp<sup>tm1Scbr</sup> Sox1<sup>tm1(cre)Take</sup>/Sox1<sup>+</sup> Tg(CAG-LARGE)126Fmu/0  [background:] involves: C57BL/6NCrlj * C57BL/10 * CBA/Ca * CBA/JNCrlj	is_model_of	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000033	author statement supported by traceable reference	PMID:24234655	20140408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5762599	Gja3<sup>tm1.1Vmb</sup>/Gja3<sup>tm1.1Vmb</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110253	cataract 14 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:25103261	20160419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449063	C3<sup>tm1Hrc</sup>/C3<sup>tm1Hrc</sup>  [background:] either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	is_model_of	DOID:8354	complement component 3 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:10408374	20151118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514345	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] B6.Cg-Fasl<sup>gld</sup> Apoe<sup>tm1Unc</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:15096538	20131024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514345	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] B6.Cg-Fasl<sup>gld</sup> Apoe<sup>tm1Unc</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23577189	20131024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2388401	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] involves: AKR/J * B6.KB2	is_model_of	DOID:0110723	neuronal ceroid lipofuscinosis 8						ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769780	Del(7Herc2-Mkrn3)13FRdni/+  [background:] involves: C57BL/6 * CD-1 * SJL	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10430930	20080205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697171	Ass1<sup>fold</sup>/Ass1<sup>fold</sup>  [background:] involves: C57BL/6JEiJ * P/J	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6162681	Umod<sup>em1Duf</sup>	is_implicated_in	DOID:557	kidney disease		MGI:6162682	Umod<sup>em1Duf</sup>/Umod<sup>+</sup>  [background:] C57BL/6J-Umod<sup>em1Duf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28990932	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827598	Zic2<sup>Ku</sup>/Zic2<sup>Ku</sup>  [background:] 129S.CAnNCrl(C3)-Zic2<sup>Ku</sup>	is_model_of	DOID:0110878	holoprosencephaly 5						ECO:0000033	author statement supported by traceable reference	PMID:27466203	20170303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785162	Enpp1<sup>asj</sup>	is_implicated_in	DOID:0050644	arterial calcification of infancy						ECO:0000033	author statement supported by traceable reference	PMID:26624227	20160210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785162	Enpp1<sup>asj</sup>	is_implicated_in	DOID:0050644	arterial calcification of infancy		MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:23798568	20160210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693326	Tg(ACTA1-PABPN1*A17)1Drub/0  [background:] involves: FVB/N	is_model_of	DOID:11719	oculopharyngeal muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:15864313	20070111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655540	Arsb<sup>tm1Cptr</sup>/Arsb<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12800	mucopolysaccharidosis VI						ECO:0000033	author statement supported by traceable reference	PMID:8710849	20070625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412047	Nfkb2<sup>Lym1</sup>/Nfkb2<sup>+</sup>  [background:] BALB/c-Nfkb2<sup>Lym1</sup>	is_model_of	DOID:12177	common variable immunodeficiency						ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832389	Ldb3<sup>tm4Chen</sup>/Ldb3<sup>tm4Chen</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	is_model_of	DOID:0110423	dilated cardiomyopathy 1C						ECO:0000033	author statement supported by traceable reference	PMID:19028670	20090218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:5566610	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17363566	20140602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044095	Sox9<sup>tm1Crm</sup>/Sox9<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CD-1	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:11371614	20060614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800565	Dnm1<sup>Ftfl</sup>/Dnm1<sup>tm1.2Frk</sup>  [background:] involves: 129 * C57BL/6J * FVB	is_model_of	DOID:1827	idiopathic generalized epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:27363778	20161014	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584475	Ihh<sup>tm1Amc</sup>/Ihh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:0060850	annular pancreas						ECO:0000033	author statement supported by traceable reference	PMID:10821773	20081215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635264	Kif21a<sup>tm1.1Ece</sup>	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:6241435	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>tm1.1Ece</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635264	Kif21a<sup>tm1.1Ece</sup>	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:6241434	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635264	Kif21a<sup>tm1.1Ece</sup>	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:6241436	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>tm1.1Ece</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663863	Mlh1<sup>tm1Rak</sup>/Mlh1<sup>tm1Rak</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10096563	20091216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3785825	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup> Tg(SMN2*delta7)4299Ahmb/Tg(SMN2*delta7)4299Ahmb  [background:] FVB.Cg-Grm7<sup>Tg(SMN2)89Ahmb</sup> Smn1<sup>tm1Msd</sup> Tg(SMN2*delta7)4299Ahmb	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:15703193	20090505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6107688	Thap1<sup>tm1.2Meeh</sup>	is_implicated_in	DOID:0090039	torsion dystonia 6		MGI:6107698	Thap1<sup>tm1.2Meeh</sup>/Thap1<sup>+</sup>  [background:] involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26376866	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906059	Tg(Myh7-Phc1)#Yota	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906061	Tg(Myh7-Phc1)#Yota/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11950896	20170802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5425295	Smarcal1<sup>tm1.1Cfbo</sup>	is_implicated_in	DOID:0060490	Schimke immuno-osseous dysplasia		MGI:5425315	Smarcal1<sup>tm1.1Cfbo</sup>/Smarcal1<sup>tm1.1Cfbo</sup>  [background:] either: B6.129-Smarcal1<sup>tm1.1Cfbo</sup> or (involves: 129 * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:22378147	20120620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620941	Col1a1<sup>M1Jrt</sup>	is_implicated_in	DOID:13359	Ehlers-Danlos syndrome		MGI:5689511	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:24443344	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437727	Dnah11<sup>b2b1727Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386464	Kif3a<sup>tm2Gsn</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23759744	20140619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386464	Kif3a<sup>tm2Gsn</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23892607	20140619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653121	Rhbdf2<sup>cub</sup>	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:30022999	20220516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653121	Rhbdf2<sup>cub</sup>	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome		MGI:6256982	Rhbdf2<sup>cub</sup>/Rhbdf2<sup>cub</sup>  [background:] MRL.Cg-Rhbdf2<sup>cub</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29116018	20220516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653121	Rhbdf2<sup>cub</sup>	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome		MGI:2653142	Rhbdf2<sup>cub</sup>/Rhbdf2<sup>cub</sup>  [background:] B6.Cg-Rhbdf2<sup>cub</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29116018	20220516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835240	Tg(MMTV-ENPP2)#Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763080	Tg(MMTV-ENPP2)#Gbm/0  [background:] FVB/N-Tg(MMTV-ENPP2)#Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428741	Tg(Wap-TAg)NP8Depp	is_implicated_in	DOID:0060074	ductal carcinoma in situ						ECO:0000033	author statement supported by traceable reference	PMID:22235331	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428741	Tg(Wap-TAg)NP8Depp	is_implicated_in	DOID:0060074	ductal carcinoma in situ		MGI:5428747	Tg(Wap-TAg)NP8Depp/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10713686	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699086	Zfp521<sup>tm1Nohk</sup>/Zfp521<sup>tm1Nohk</sup>  [background:] B6J.Cg-Zfp521<sup>tm1Nohk</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:24676388	20151215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:1018005	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:10942421	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:16589192	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	MGI:63130	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:10861288	20050608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529468	Mecp2<sup>tm2.1Meg</sup>/Y  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23770565	20140121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558867	Fbn1<sup>tm2.1Hcd</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:5558879	Fbn1<sup>tm2.1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24107997	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5645238	Dnah5<sup>b2b2451Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5645239	Dnah5<sup>b2b2451Clo</sup>/Dnah5<sup>b2b2451Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2451Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447065	Tg(Neurod2-Smo*A2)#Jols	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5447068	Tg(Neurod2-Smo*A2)#Jols/0  [background:] C57BL/6-Tg(Neurod2-Smo*A2)#Jols			ECO:0000033	author statement supported by traceable reference	PMID:22869526	20140701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447065	Tg(Neurod2-Smo*A2)#Jols	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24107773	20140701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140726	Ttc8<sup>tm1Reed</sup>/Ttc8<sup>tm1Reed</sup>  [background:] involves: 129	is_model_of	DOID:0110130	Bardet-Biedl syndrome 8						ECO:0000033	author statement supported by traceable reference	PMID:21646512	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623404	Eng<sup>tm1Hma</sup>/Eng<sup>+</sup>  [background:] 129P2/OlaHsd-Eng<sup>tm1Hma</sup>	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:10625534	20060529	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693373	Tg(tetO-BCR/ABL1)2Dgt/0 Tg(Tal1-tTA)19Dgt/0  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15331442	20070112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814059	Tg(SOD1*G37R)9Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:7605627	20081106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659847	Mto1<sup>Gt(G019A03)Wrst</sup>/Mto1<sup>Gt(G019A03)Wrst</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0060286	combined oxidative phosphorylation deficiency						ECO:0000033	author statement supported by traceable reference	PMID:25506927	20150825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604147	Tg(PDGFB-MAPT*V337M)1Atak	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23833557	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604147	Tg(PDGFB-MAPT*V337M)1Atak	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604147	Tg(PDGFB-MAPT*V337M)1Atak	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3718076	Tg(PDGFB-MAPT*V337M)1Atak/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11756496	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4462422	Sall1<sup>tm1.1Mrau</sup>	is_implicated_in	DOID:0050887	Townes-Brocks syndrome		MGI:4462423	Sall1<sup>tm1.1Mrau</sup>/Sall1<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18470945	20100730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707513	Ass1<sup>fold</sup>/Ass1<sup>fold</sup>  [background:] B6Ei.P-Ass1<sup>fold</sup>/GrsrJ	is_model_of	DOID:9273	citrullinemia						ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857144	Cd4<sup>tm1Mak</sup>	is_implicated_in	DOID:2752	glycogen storage disease II						ECO:0000033	author statement supported by traceable reference	PMID:34737297	20220204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774799	Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>	is_implicated_in	DOID:0110931	nemaline myopathy 10		MGI:5819051	Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26035871	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6718838	Gabrg2<sup>tm1.2Rmac</sup>	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:6740192	Gabrg2<sup>tm1.2Rmac</sup>/Gabrg2<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:33582225	20210817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831537	Gtf2ird1<sup>Gt(XE465)Byg</sup>/Gtf2ird1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19109438	20090212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6726546	Macroh2a1<sup>tm1.1Oxbo</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:6726548	Macroh2a1<sup>tm1.1Oxbo</sup>/Macroh2a1<sup>tm1.1Oxbo</sup>  [background:] B6.Cg-Macroh2a1<sup>tm1.1Oxbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31439048	20210728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4818803	Jak2<sup>tm1.2Ble</sup>/Jak2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:20541703	20100810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838149	Tg(Myh7-RARA/lacZ)30Mcco	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:12393001	20170831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838149	Tg(Myh7-RARA/lacZ)30Mcco	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3838153	Tg(Myh7-RARA/lacZ)30Mcco/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9329959	20170831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676199	Ndp<sup>tm1Wbrg</sup>	is_implicated_in	DOID:0060844	Norrie disease						ECO:0000033	author statement supported by traceable reference	PMID:29654250	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676199	Ndp<sup>tm1Wbrg</sup>	is_implicated_in	DOID:0060844	Norrie disease		MGI:3695277	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12040033	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676199	Ndp<sup>tm1Wbrg</sup>	is_implicated_in	DOID:0060844	Norrie disease		MGI:2676253	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8789439	20180705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6509649	Krt13<sup>em1Hcha</sup>	is_implicated_in	DOID:0050448	white sponge nevus		MGI:6509651	Krt13<sup>em1Hcha</sup>/Krt13<sup>em1Hcha</sup>  [background:] C57BL/6-Krt13<sup>em1Hcha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32758484	20210311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6163746	Gnat2<sup>m1Erica</sup>	is_implicated_in	DOID:0110010	achromatopsia 4		MGI:6163747	Gnat2<sup>m1Erica</sup>/Gnat2<sup>m1Erica</sup>  [background:] C.Cg-Gnat2<sup>m1Erica</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23580486	20180629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897680	Sox10<sup>Dom</sup>/Sox10<sup>+</sup>  [background:] C57BL/6J-Sox10<sup>Dom</sup>	is_model_of	DOID:0110955	Waardenburg syndrome type 4C						ECO:0000033	author statement supported by traceable reference	PMID:20739296	20170519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5607614	Myo5a<sup>d-l34J</sup>/Myo5a<sup>d-l34J</sup>  [background:] BALB/cJ-Myo5a<sup>d-l34J</sup>/GrsrJ	is_model_of	DOID:0060832	Griscelli syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:5607575	20141222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515890	Pmp22<sup>Tr-2J</sup>	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6116463	Vps16<sup>em1Weli</sup>	is_implicated_in	DOID:543	dystonia						ECO:0000033	author statement supported by traceable reference	PMID:27174565	20180215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6459753	Tg(CAG-EPM2A*C266S)1Bmin	is_implicated_in	DOID:3534	Lafora disease		MGI:6459755	Tg(CAG-EPM2A*C266S)1Bmin/0  [background:] involves: 129 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15102711	20201005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6459753	Tg(CAG-EPM2A*C266S)1Bmin	is_implicated_in	DOID:3534	Lafora disease		MGI:6459755	Tg(CAG-EPM2A*C266S)1Bmin/0  [background:] involves: 129 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17118331	20201005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360798	Tg(RBP3-ELOVL4*)3Kzh/0  [background:] C57BL/6-Tg(RBP3-ELOVL4*)3Kzh	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:15749821	20091008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931018	Rb1<sup>tm2Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931018	Rb1<sup>tm2Brn</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195290	Ifitm5<sup>em1Pmof</sup>	is_not_implicated_in	DOID:0110344	osteogenesis imperfecta type 5		MGI:6195291	Ifitm5<sup>em1Pmof</sup>/Ifitm5<sup>+</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:29174564	20180822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140843	Tg(Pcp2-cre)2Mpin/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21419848	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2667352	Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12221714	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910506	Erg<sup>tm1.1Iwamo</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:5910547	Erg<sup>tm1.1Iwamo</sup>/Erg<sup>tm1.1Iwamo</sup> Tg(Gdf5-cre,-ALPP)1Kng/?  [background:] involves: 129S4/SvJaeSor * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26097038	20170928	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179030	Pten<sup>tm1Mak</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10910075	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438062	Drc1<sup>b2b1654Clo</sup>	is_implicated_in	DOID:0110596	primary ciliary dyskinesia 21		MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5293607	Tg(MAPT*V337M)1Gds	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5750141	Tg(MAPT*V337M)1Gds/0  [background:] B6J.Cg-Tg(MAPT*V337M)1Gds			ECO:0000033	author statement supported by traceable reference	PMID:25471585	20160225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634289	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)#Hev/0  [background:] involves: 129 * C57BL/6 * CBA	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:17726540	20160125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634289	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)#Hev/0  [background:] involves: 129 * C57BL/6 * CBA	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:24535670	20160125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6117138	Opa1<sup>tm1.1Geno</sup>	is_implicated_in	DOID:5723	optic atrophy		MGI:6188926	Opa1<sup>tm1.1Geno</sup>/Opa1<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:23250881	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883223	Otog<sup>vbd</sup>/Otog<sup>vbd</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0110474	autosomal recessive nonsyndromic deafness 18B						ECO:0000033	author statement supported by traceable reference	PMID:26636018	20170414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588307	Bloc1s3<sup>rp</sup>/Bloc1s3<sup>rp</sup>  [background:] involves: C57BL/10ScSn * C57BL/Tb	is_model_of	DOID:0060546	Hermansky-Pudlak syndrome 8						ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258949	Cfap43<sup>em1Fzh</sup>	is_implicated_in	DOID:0070170	spermatogenic failure 19		MGI:6258952	Cfap43<sup>em1Fzh</sup>/Cfap43<sup>em1Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448551	Slc45a2<sup>uw-7J</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5450850	Slc45a2<sup>uw-7J</sup>/Slc45a2<sup>uw-7J</sup>  [background:] C3H/HeJ-Slc45a2<sup>uw-7J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5449588	20130123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437084	b2b1146Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6386115	Fscn2<sup>em1Fhan</sup>	is_implicated_in	DOID:2742	auditory system disease		MGI:6386243	Fscn2<sup>em1Fhan</sup>/Fscn2<sup>em1Fhan</sup>  [background:] C57BL/6J-Fscn2<sup>em1Fhan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30082328	20200124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175907	Apc<sup>tm1Mmt</sup>/Apc<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:7753829	20050822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3834483	Tg(Ly6a-TK,-BCR/ABL1)IS9AIsg/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:19037256	20090305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831388	Nek1<sup>kat-2J</sup>/Nek1<sup>kat-2J</sup>  [background:] C57BL/6J-Nek1<sup>kat-2J</sup>/J	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:9070925	20090212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946403	Aqp4<sup>tm1.1Lmno</sup>	is_implicated_in	DOID:12365	malaria		MGI:4946419	Aqp4<sup>tm1.1Lmno</sup>/Aqp4<sup>tm1.1Lmno</sup>  [background:] B6.Cg-Aqp4<sup>tm1.1Lmno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23277579	20131001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448415	Slc6a8<sup>tm1.1Clar</sup>/Y Tg(Camk2a-cre)2Gsc/0  [background:] involves: C57BL/6 * C57BL/6J * FVB/N	is_model_of	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:22751104	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640343	Fgfr3<sup>tm3.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:10587515	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5690250	Hexb<sup>lysd</sup>	is_implicated_in	DOID:3323	Sandhoff disease		MGI:6507051	Hexb<sup>lysd</sup>/Hexb<sup>lysd</sup>  [background:] B6.Cg-Hexb<sup>lysd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:31547903	20210219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432215	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup> Tg(MUC1)79.24Gend/0  [background:] B6.Cg-Il10<sup>tm1Cgn</sup> Tg(MUC1)79.24Gend	is_model_of	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:17617560	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2180790	Tbx21<sup>tm1Glm</sup>/Tbx21<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:11786643	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5469319	mt-Nd6<sup>m3Dwa</sup>	is_implicated_in	DOID:705	Leber hereditary optic neuropathy		MGI:5469320	mt-Nd6<sup>m3Dwa</sup>  [background:] B6.129S-mt-Nd6<sup>m3Dwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23129651	20130320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6294291	Tg(Prnp-HTT*82Q)8AGschi	is_implicated_in	DOID:12858	Huntington's disease		MGI:6294293	Tg(Prnp-HTT*82Q)8AGschi/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15190011	20190424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695247	Vps35<sup>Gt(RRK261)Byg</sup>/Vps35<sup>+</sup>  [background:] B6.129P2-Vps35<sup>Gt(RRK261)Byg</sup>	is_model_of	DOID:0060897	Parkinson's disease 17						ECO:0000033	author statement supported by traceable reference	PMID:26203154	20151109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3716366	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:9467	nail-patella syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15562281	20070727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297555	Elp1<sup>tm1.1Id</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24760006	20150306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429942	Dmd<sup>tm1Mok</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25027324	20150609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429942	Dmd<sup>tm1Mok</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3722314	Dmd<sup>tm1Mok</sup>/Y  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:9299538	20150609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179753	Scn5a<sup>tm1Agrc</sup>	is_implicated_in	DOID:0111074	progressive familial heart block type IA						ECO:0000033	author statement supported by traceable reference	PMID:28339646	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179753	Scn5a<sup>tm1Agrc</sup>	is_implicated_in	DOID:0111074	progressive familial heart block type IA		MGI:3641169	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:15809371	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179753	Scn5a<sup>tm1Agrc</sup>	is_implicated_in	DOID:0111074	progressive familial heart block type IA		MGI:3621905	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11972032	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5788539	Tg(Igh-HMGA2)#Cro	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5788543	Tg(Igh-HMGA2)#Cro/0  [background:] FVB/N-Tg(Igh-HMGA2)#Cro			ECO:0000033	author statement supported by traceable reference	PMID:25014774	20160811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042284	Fst<sup>tm1Zuk</sup>/Fst<sup>tm1Zuk</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060762	restrictive dermopathy						ECO:0000033	author statement supported by traceable reference	PMID:7885475	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438148	Dmd<sup>em4Eno</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:32128412	20200709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438148	Dmd<sup>em4Eno</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6438177	Dmd<sup>em4Eno</sup>/Dmd<sup>em4Eno</sup>  [background:] C57BL/6-Dmd<sup>em4Eno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30854433	20200709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6438148	Dmd<sup>em4Eno</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6438180	Dmd<sup>em4Eno</sup>/Y  [background:] C57BL/6-Dmd<sup>em4Eno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30854433	20200709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428741	Tg(Wap-TAg)NP8Depp	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22235331	20120724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428741	Tg(Wap-TAg)NP8Depp	is_implicated_in	DOID:1612	breast cancer		MGI:5428747	Tg(Wap-TAg)NP8Depp/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10713686	20120724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437079	Lrp1<sup>b2b1554Clo</sup>	is_implicated_in	DOID:11044	gastroschisis		MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6163619	Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:6163706	Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] FVB/NJ-Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29247744	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5565508	Flt3<sup>tm1.1Dosm</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5565512	Flt3<sup>tm1.1Dosm</sup>/Flt3<sup>+</sup>  [background:] B6.129(C)-Flt3<sup>tm1.1Dosm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24255108	20140529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4845889	Nphs2<sup>tm3.1Antc</sup>	is_implicated_in	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:37556557	20231226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841015	Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>  [background:] C57BL/6-Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>	is_model_of	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:8563760	20200312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841015	Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>  [background:] C57BL/6-Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>	is_model_of	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:30615115	20200312	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430189	Fgfr2<sup>tm2Ewj</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:20077479	20100225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174785	Trp63<sup>tm1Fmc</sup>/Trp63<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:10227294	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563089	Clcn7<sup>tm1.1Teti</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:29501587	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563089	Clcn7<sup>tm1.1Teti</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563101	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>tm1.1Teti</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563089	Clcn7<sup>tm1.1Teti</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563097	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>tm1.1Teti</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563089	Clcn7<sup>tm1.1Teti</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563098	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857166	Fcgr2b<sup>tm1Ttk</sup>	is_implicated_in	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:21187399	20130312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857166	Fcgr2b<sup>tm1Ttk</sup>	is_implicated_in	DOID:12365	malaria		MGI:2448997	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup>  [background:] C.129S4-Fcgr2b<sup>tm1Ttk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17435165	20130312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7316653	Serac1<sup>em1Bcgen</sup>	is_implicated_in	DOID:0110001	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome		MGI:7316678	Serac1<sup>em1Bcgen</sup>/Serac1<sup>em1Bcgen</sup>  [background:] C57BL/6N-Serac1<sup>em1Bcgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35235340	20220728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311380	b2b997Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312933	b2b997Clo/b2b997Clo  [background:] C57BL/6J-b2b997Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618601	Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:9212102	20060405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522019	Cln5<sup>tm1Pltn</sup>/Cln5<sup>tm1Pltn</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110728	neuronal ceroid lipofuscinosis 5						ECO:0000033	author statement supported by traceable reference	PMID:15459177	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759457	Sufu<sup>Gt(XB699)Byg</sup>/Sufu<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19076778	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699096	Tg(APPSWE)2576Kha/? Tg(EIF1AX-Aldh2*E487K)101Oht/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25529196	20151215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437367	Chd7<sup>Ome</sup>/Chd7<sup>+</sup>  [background:] involves: BALB/cByJ * C57BL/6J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22539951	20121003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175029	Foxn1<sup>nu-Y</sup>/Foxn1<sup>nu-Y</sup>  [background:] 101/HY-Foxn1<sup>nu-Y</sup>	is_model_of	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000033	author statement supported by traceable reference	MGI:76644	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709152	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)107Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16279840	20120824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559903	Tg(PDGFB-LRRK2*G2019S)32Hlw	is_implicated_in	DOID:0060371	Parkinson's disease 8		MGI:5559904	Tg(PDGFB-LRRK2*G2019S)32Hlw/?  [background:] FVB/N-Tg(PDGFB-LRRK2*G2019S)32Hlw			ECO:0000033	author statement supported by traceable reference	PMID:22539006	20140425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515890	Pmp22<sup>Tr-2J</sup>	is_implicated_in	DOID:0110153	Charcot-Marie-Tooth disease type 1E		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7520216	Tafazzin<sup>em1Xfa</sup>	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:7520358	Tafazzin<sup>em1Xfa</sup>/Y Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: C57BL/6NCrl * MF1			ECO:0000033	author statement supported by traceable reference	PMID:34129362	20230824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827939	Sox11<sup>tm1.1Gan</sup>/Sox11<sup>tm1.1Gan</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:4258	Weissenbacher-Zweymuller syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26826126	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5178248	Clpp<sup>Gt(IST13563G11)Tigm</sup>	is_implicated_in	DOID:0050857	Perrault syndrome		MGI:5532580	Clpp<sup>Gt(IST13563G11)Tigm</sup>/Clpp<sup>Gt(IST13563G11)Tigm</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23851121	20140129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628445	Def6<sup>Gt(OST307148)Lex</sup>/Def6<sup>Gt(OST307148)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:16470246	20060707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822143	avc2/avc2  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0110106	atrial heart septal defect 1						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20101008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566610	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:17363566	20140602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6295353	Gnao1<sup>em1Rneu</sup>	is_implicated_in	DOID:0080450	developmental and epileptic encephalopathy 17		MGI:6295357	Gnao1<sup>em1Rneu</sup>/Gnao1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:30682176	20190501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711074	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup> Rab27b<sup>tm1.2Seab</sup>/Rab27b<sup>tm1.2Seab</sup>  [background:] involves: 129X1/SvJ * C3H/HeSn * C57BL/6J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:17384153	20070605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821826	avc2	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:4822143	avc2/avc2  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20101008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6154324	Nup35<sup>m1Apb</sup>	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:6154633	Nup35<sup>m1Apb</sup>/Nup35<sup>m1Apb</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27427419	20200621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5822820	Fras1<sup>rdf</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:6443692	Fras1<sup>rdf</sup>/Fras1<sup>rdf</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:26813283	20221116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789953	Tg(ACTA1-MYOT*T57I)71Mah/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0080094	myofibrillar myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:16801328	20080602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4836355	Urah<sup>plt2</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:4836356	Urah<sup>plt2</sup>/Urah<sup>plt2</sup>  [background:] C57BL/6-Urah<sup>plt2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30383838	20220415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433408	b2b1163Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5433487	b2b1163Clo/b2b1163Clo  [background:] C57BL/6J-b2b1163Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428914	Tg(Pklr-Myc)73Ak/0  [background:] involves: C57BL/6 * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1620553	20120731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696057	Brca1<sup>tm1Brn</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27943283	20170718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056451	Sqstm1<sup>tm1.1Sral</sup>	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:5056475	Sqstm1<sup>tm1.1Sral</sup>/Sqstm1<sup>tm1.1Sral</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21515589	20110811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056451	Sqstm1<sup>tm1.1Sral</sup>	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:5056476	Sqstm1<sup>tm1.1Sral</sup>/Sqstm1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21515589	20110811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510446	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8956999	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	MGI:2662103	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20190724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:28082400	20190724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444192	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] C3A.Cg-Prss56<sup>glcr4</sup> Pde6b<sup>+</sup>	is_model_of	DOID:0060835	isolated microphthalmia 6						ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6273244	Ubiad1<sup>em1Wwk</sup>	is_implicated_in	DOID:0060456	Schnyder corneal dystrophy		MGI:6273246	Ubiad1<sup>em1Wwk</sup>/Ubiad1<sup>em1Wwk</sup>  [background:] C57BL/6N-Ubiad1<sup>em1Wwk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29977031	20190111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6273244	Ubiad1<sup>em1Wwk</sup>	is_implicated_in	DOID:0060456	Schnyder corneal dystrophy		MGI:6273247	Ubiad1<sup>em1Wwk</sup>/Ubiad1<sup>+</sup>  [background:] C57BL/6N-Ubiad1<sup>em1Wwk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29977031	20190111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582674	Apc<sup>Min</sup>/Apc<sup>+</sup> Blm<sup>tm1Grdn</sup>/Blm<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * Black Swiss * C57BL/6J	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12242442	20050729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5766543	Slc24a1<sup>tm1Xen</sup>/Slc24a1<sup>tm1Xen</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110868	congenital stationary night blindness 1D						ECO:0000033	author statement supported by traceable reference	PMID:26246500	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6220701	Lama2<sup>dy-Pas</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:6226150	Lama2<sup>dy-Pas</sup>/Lama2<sup>dy-Pas</sup>  [background:] involves: non-inbred stock			ECO:0000033	author statement supported by traceable reference	PMID:12609503	20181106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000269	Tg(AR*100Q)#Als	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:5000281	Tg(AR*100Q)#Als/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21317158	20110527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558025	Scn11a<sup>tm1.1Ikth</sup>	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:5558028	Scn11a<sup>tm1.1Ikth</sup>/Scn11a<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24036948	20140410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6469363	Sdr9c7<sup>em1Maak</sup>	is_implicated_in	DOID:0080257	autosomal recessive congenital ichthyosis 13						ECO:0000033	author statement supported by traceable reference	PMID:31671075	20201027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6469363	Sdr9c7<sup>em1Maak</sup>	is_implicated_in	DOID:0080257	autosomal recessive congenital ichthyosis 13		MGI:6469470	Sdr9c7<sup>em1Maak</sup>/Sdr9c7<sup>em1Maak</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31671075	20201027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428762	Tg(Pklr-HRAS*G12V)21Ak	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5428841	Tg(Pklr-HRAS*G12V)21Ak/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9398057	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158420	H2-Ab1<sup>b-tm1Gru</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27679742	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7448443	Cfap61<sup>em1Yqt</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7448446	Cfap61<sup>em1Yqt</sup>/Cfap61<sup>em1Yqt</sup>  [background:] C57BL/6-Cfap61<sup>em1Yqt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35387802	20230328	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5320791	Jak2<sup>tm1Mohi</sup>/Jak2<sup>tm1Mohi</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:8997	polycythemia vera						ECO:0000033	author statement supported by traceable reference	PMID:22144185	20120608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789135	Htr2c<sup>tm1Jul</sup>/Y  [background:] B6.129S-Htr2c<sup>tm1Jul</sup>	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9771748	20100129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3525158	Nfatc3<sup>tm1Glm</sup>/Nfatc3<sup>tm1Glm</sup> Nfatc4<sup>tm1Grc</sup>/Nfatc4<sup>tm1Grc</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16554754	20060720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906284	Sap130<sup>b2b635.2Clo</sup>	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5906294	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup> Pcdha9<sup>b2b635.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523787	Scn1a<sup>tm2.1Kzy</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5523889	Scn1a<sup>tm2.1Kzy</sup>/Scn1a<sup>tm2.1Kzy</sup> Tg(Pvalb-cre)1Tama/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:23922229	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523787	Scn1a<sup>tm2.1Kzy</sup>	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5523888	Scn1a<sup>tm2.1Kzy</sup>/Scn1a<sup>+</sup> Tg(Pvalb-cre)1Tama/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:23922229	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798999	None [background:] DBA/1J	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:9364191	20141105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711151	Plp1<sup>jp-msd</sup>/Y  [background:] involves: BALB/c * C3H * C57BL/6 * C57BL/10	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:17394578	20070606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179721	Lamb3<sup>IAP</sup>/Lamb3<sup>IAP</sup>  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:9271670	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815542	In(15)4H/In(15)4H  [background:] involves: C3H/HeH	is_model_of	DOID:0111060	Ambras type hypertrichosis universalis congenita						ECO:0000033	author statement supported by traceable reference	PMID:18713754	20081119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579773	Nkx3-2<sup>tm1(cre)Tsa</sup>/Nkx3-2<sup>+</sup> Nr2f2<sup>tm2.1Tsa</sup>/Nr2f2<sup>tm2.1Tsa</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:16251273	20100614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837707	Eef1a1<sup>tm1(Kras*)Arge</sup>/Eef1a1<sup>+</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>+</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19174523	20090330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393997	Hmbs<sup>tm1.1Rjde</sup>	is_implicated_in	DOID:3890	acute intermittent porphyria						ECO:0000033	author statement supported by traceable reference	PMID:32197664	20210220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393997	Hmbs<sup>tm1.1Rjde</sup>	is_implicated_in	DOID:3890	acute intermittent porphyria		MGI:6394002	Hmbs<sup>tm1.1Rjde</sup>/Hmbs<sup>tm1.1Rjde</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30615115	20210220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437100	b2b227.2Clo	is_implicated_in	DOID:114	heart disease		MGI:5437108	b2b227.2Clo/b2b227.2Clo  [background:] C57BL/6J-b2b227.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660194	Mapk1<sup>tm1Gela</sup>/Mapk1<sup>tm1Gela</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18952847	20150827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6431142	Myo6<sup>em1Bcgen</sup>	is_implicated_in	DOID:0110552	autosomal dominant nonsyndromic deafness 22		MGI:6431144	Myo6<sup>em1Bcgen</sup>/Myo6<sup>+</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:31103816	20200602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433326	Dnah5<sup>b2b1537Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286071	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(Atoh1-cre/Esr1*)14Fsh/0  [background:] involves: 129T2/SvEms * FVB/N	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784677	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>tm1.1Mag</sup> Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S6/SvEvTac * CD-1	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:25625625	20160727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907885	Tg(Myh6-HBEGF)#Iko	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907886	Tg(Myh6-HBEGF)#Iko/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15272002	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5630054	Itpr2<sup>tm1Kmik</sup>/Itpr2<sup>tm1Kmik</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:0060603	isolated anhidrosis with normal sweat glands						ECO:0000033	author statement supported by traceable reference	PMID:25329695	20150417	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610502	Col4a5<sup>tm1Yseg</sup>/Col4a5<sup>+</sup>  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>	is_model_of	DOID:0110034	X-linked Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23707242	20140709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610502	Col4a5<sup>tm1Yseg</sup>/Col4a5<sup>+</sup>  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>	is_model_of	DOID:0110034	X-linked Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15153557	20140709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680164	Tgfbr1<sup>tm1.1Karl</sup>	is_implicated_in	DOID:5520	head and neck squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25723392	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6741516	Myt1l<sup>em1Jdd</sup>	is_implicated_in	DOID:0070069	autosomal dominant intellectual developmental disorder 39		MGI:7265077	Myt1l<sup>em1Jdd</sup>/Myt1l<sup>+</sup>  [background:] C57BL/6-Myt1l<sup>em1Jdd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:34614421	20220502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4456351	Gnptab<sup>Gt(OST97730)Lex</sup>/Gnptab<sup>Gt(OST97730)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J	is_model_of	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000033	author statement supported by traceable reference	PMID:17962477	20100623	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586704	Fzd9<sup>tm1Sjp</sup>/Fzd9<sup>tm1Sjp</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15930120	20050906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311374	Ift74<sup>b2b796Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5311937	Ift74<sup>b2b796Clo</sup>/Ift74<sup>b2b796Clo</sup>  [background:] C57BL/6J-Ift74<sup>b2b796Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178321	Des<sup>tm1Cap</sup>	is_implicated_in	DOID:0110431	dilated cardiomyopathy 1I						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20180604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178321	Des<sup>tm1Cap</sup>	is_implicated_in	DOID:0110431	dilated cardiomyopathy 1I						ECO:0000033	author statement supported by traceable reference	PMID:27566162	20180604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178321	Des<sup>tm1Cap</sup>	is_implicated_in	DOID:0110431	dilated cardiomyopathy 1I		MGI:2178322	Des<sup>tm1Cap</sup>/Des<sup>tm1Cap</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8794866	20180604	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441312	Tg(Vav1-JAK2*V617F)AZjz/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:18334677	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4941330	Lhx3<sup>tm1.1Sjr</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:4941332	Lhx3<sup>tm1.1Sjr</sup>/Lhx3<sup>tm1.1Sjr</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21149718	20110317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574812	Bmpr2<sup>tm1.1Enl</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:24951762	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574812	Bmpr2<sup>tm1.1Enl</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574812	Bmpr2<sup>tm1.1Enl</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5430750	Bmpr2<sup>tm1.1Enl</sup>/Bmpr2<sup>tm1.1Enl</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:18663089	20171127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566827	Myo7a<sup>sh1-13J</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:5566830	Myo7a<sup>sh1-13J</sup>/Myo7a<sup>sh1-13J</sup>  [background:] C.Cg-Myo7a<sup>sh1-13J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6507035	Phf6<sup>tm1.2Avo</sup>	is_implicated_in	DOID:0050681	Borjeson-Forssman-Lehmann syndrome		MGI:6507205	Phf6<sup>tm1.2Avo</sup>/Y  [background:] involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:32994169	20210219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178613	Slc6a4<sup>tm1Kpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23142422	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178613	Slc6a4<sup>tm1Kpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3640114	Slc6a4<sup>tm1Kpl</sup>/Slc6a4<sup>tm1Kpl</sup>  [background:] B6.129-Slc6a4<sup>tm1Kpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23142422	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7277680	Eef1a2<sup>em#Abb</sup>	is_implicated_in	DOID:0070068	autosomal dominant intellectual developmental disorder 38		MGI:7277684	Eef1a2<sup>em#Abb</sup>/Eef1a2<sup>+</sup>  [background:] C57BL/6JCrl-Eef1a2<sup>em#Abb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32160274	20220513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793424	Gata4<sup>tm1.2Sad</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:27565037	20180118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526090	Tg(ACTB-KRAS*G12V,-luc)#Lche	is_implicated_in	DOID:1324	lung cancer		MGI:5526091	Tg(ACTB-KRAS*G12V,-luc)#Lche/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23536778	20140102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471136	Gpsm1<sup>tm1.1Lajb</sup>/Gpsm1<sup>tm1.1Lajb</sup> Pkd1<sup>tm1.1Fqi</sup>/Pkd1<sup>tm1.1Fqi</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23236168	20130401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5574060	Tg(Stat3*)9199Alau	is_implicated_in	DOID:3261	hyper IgE recurrent infection syndrome 1		MGI:5574061	Tg(Stat3*)9199Alau/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24632714	20181008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5574060	Tg(Stat3*)9199Alau	is_implicated_in	DOID:3261	hyper IgE recurrent infection syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:30035749	20181008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558022	Elp1<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28439028	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558022	Elp1<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28167615	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558022	Elp1<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome		MGI:5558037	Elp1<sup>tm1c(KOMP)Wtsi</sup>/Elp1<sup>tm1c(KOMP)Wtsi</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24173031	20170726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512698	Tg(APPV717F)109Ili/0 Tg(Prnp-MAPT*P301S)PS19Vle/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20802182	20131015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4837367	Myh6<sup>tm3.1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:4837384	Myh6<sup>tm3.1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20811150	20190823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4837367	Myh6<sup>tm3.1Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:6356707	Myh6<sup>tm3.1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6376642	Arl2bp<sup>em1Visu</sup>	is_implicated_in	DOID:0110419	retinitis pigmentosa with or without situs inversus		MGI:6376646	Arl2bp<sup>em1Visu</sup>/Arl2bp<sup>em1Visu</sup>  [background:] involves: 129S2/SvPasCrl * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29718757	20191114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5445347	Odad3<sup>b2b1885Clo</sup>	is_implicated_in	DOID:0110624	primary ciliary dyskinesia 30		MGI:5445974	Odad3<sup>b2b1885Clo</sup>/Odad3<sup>b2b1885Clo</sup>  [background:] C57BL/6J-Odad3<sup>b2b1885Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003451	Raf1<sup>tm1.1Bgn</sup>/Raf1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCr	is_model_of	DOID:0060583	Noonan syndrome 5						ECO:0000033	author statement supported by traceable reference	PMID:21339642	20110607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6359826	Ush1c<sup>dfcr-4J</sup>	is_implicated_in	DOID:0110473	autosomal recessive nonsyndromic deafness 18A		MGI:6359828	Ush1c<sup>dfcr-4J</sup>/Ush1c<sup>dfcr-4J</sup>  [background:] 129P3/J-Ush1c<sup>dfcr-4J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:6359814	20190913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2169285	Pax3<sup>Sp-2H</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:62273	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622553	Invs<sup>inv</sup>/Invs<sup>inv</sup>  [background:] FVB/N-Invs<sup>inv</sup>	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:9664638	20101001	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5630057	Tg(SOD1*G85R/EYFP)737Alho/Tg(SOD1*G85R/EYFP)737Alho  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25024188	20150420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5474008	Cacna1s<sup>tm1.1Cann</sup>/Cacna1s<sup>+</sup>  [background:] involves: 129	is_model_of	DOID:14452	hypokalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:23187123	20130411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861112	Il1r1<sup>tm1Imx</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24143217	20140812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646613	Wnt5a<sup>b2b3077.1Clo</sup>	is_implicated_in	DOID:0060254	Robinow syndrome		MGI:5648028	Wnt5a<sup>b2b3077.1Clo</sup>/Wnt5a<sup>b2b3077.1Clo</sup>  [background:] C57BL/6J-Wnt5a<sup>b2b3077.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445442	Tg(GFAP-Hras1)2Agu	is_implicated_in	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:26617336	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445442	Tg(GFAP-Hras1)2Agu	is_implicated_in	DOID:3070	high grade glioma		MGI:5286097	Tg(GFAP-Hras1)2Agu/Tg(GFAP-Hras1)2Agu  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11325859	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6150889	Grn<sup>tm1.1Hiok</sup>	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:6199038	Grn<sup>tm1.1Hiok</sup>/Grn<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29382817	20180921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7260342	Msh5<sup>em1Jzc</sup>	is_implicated_in	DOID:0080870	primary ovarian insufficiency 13		MGI:7260343	Msh5<sup>em1Jzc</sup>/Msh5<sup>em1Jzc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28175301	20220411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5700536	Tg(PGK1-FTL*)#Sle/0  [background:] B6J.FVB-Tg(PGK1-FTL*)#Sle	is_model_of	DOID:0110737	neurodegeneration with brain iron accumulation 3						ECO:0000033	author statement supported by traceable reference	PMID:25689865	20160105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429693	Arx<sup>tm1Kki</sup>	is_implicated_in	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:22565167	20130716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429693	Arx<sup>tm1Kki</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:2451237	Arx<sup>tm1Kki</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:12379852	20130716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505393	Ndst1<sup>b2b2230Clo</sup>/Ndst1<sup>b2b2230Clo</sup>  [background:] C57BL/6J-Ndst1<sup>b2b2230Clo</sup>	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5643943	Slc6a3<sup>tm1Rbl</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5643944	Slc6a3<sup>tm1Rbl</sup>/Slc6a3<sup>tm1Rbl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25331903	20150709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817462	Mecp2<sup>tm1Bird</sup>/Y  [background:] (129S6.129P2-Mecp2<sup>tm1Bird</sup> x FVB/N)F1	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18321864	20081121	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459466	Lmna<sup>Dhe</sup>/Lmna<sup>+</sup>  [background:] B6(D2)-Lmna<sup>Dhe</sup>/TyGrsrJ	is_model_of	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:21464947	20110606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295418	Mcm9<sup>Gt(XG743)Byg</sup>/Mcm9<sup>Gt(XG743)Byg</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720088	Hba<sup>b3(th)</sup>/Hba<sup>+</sup>  [background:] SEC-Hba<sup>b3(th)</sup>	is_model_of	DOID:1099	alpha thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:7450330	20070831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700665	Slc40a1<sup>ffe</sup>/Slc40a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6J)	is_model_of	DOID:0111028	hemochromatosis type 4						ECO:0000033	author statement supported by traceable reference	PMID:17289807	20070322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715252	Tub<sup>tub</sup>/Tub<sup>tub</sup>  [background:] C57BL/6J-Tub<sup>tub</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:61951	20091105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5617494	Tg(Krt18-EGFP,-TAg121)36Ysng/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm2Tyj</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286225	Nkx2-5<sup>tm1.1Burg</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:6286233	Nkx2-5<sup>tm1.1Burg</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S2/SvPasCrl * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:28302382	20190405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5922010	Tg(tetO-TARDBP*A315T)13Lmit	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6095155	Tg(tetO-TARDBP*A315T)13Lmit/0 Tg(Thy1-tTA)6Lmit/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28334913	20171206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5922010	Tg(tetO-TARDBP*A315T)13Lmit	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6095155	Tg(tetO-TARDBP*A315T)13Lmit/0 Tg(Thy1-tTA)6Lmit/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26437864	20171206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800793	Efemp1<sup>tm1Eap</sup>/Efemp1<sup>tm1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17666404	20080808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6715576	Elp2<sup>em2Bjw</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6754175	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6715576	Elp2<sup>em2Bjw</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6754173	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5614979	Dnah5<sup>b2b2570Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5614980	Dnah5<sup>b2b2570Clo</sup>/Dnah5<sup>b2b2570Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2570Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20190214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867482	Gjb2<sup>tm2.2Kwi</sup>	is_implicated_in	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome		MGI:4867484	Gjb2<sup>tm2.2Kwi</sup>/Gjb2<sup>+</sup> Tg(Pgk1-cre)1Lni/0  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20926451	20160420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867482	Gjb2<sup>tm2.2Kwi</sup>	is_implicated_in	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26777423	20160420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805223	Tg(tetO-PyVT,-cre)1Mul	is_implicated_in	DOID:1612	breast cancer		MGI:5903421	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-PyVT,-cre)1Mul/0  [background:] FVB/N-Tg(MMTV-rtTA)1Lach Tg(tetO-PyVT,-cre)#Mul			ECO:0000033	author statement supported by traceable reference	PMID:24457046	20190628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805223	Tg(tetO-PyVT,-cre)1Mul	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26719528	20190628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259433	Shank3<sup>em1Hzo</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6715314	Shank3<sup>em1Hzo</sup>/Shank3<sup>em1Hzo</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30610205	20210614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6363203	Mrap<sup>tm1.2Geno</sup>	is_implicated_in	DOID:9553	adrenal gland disease		MGI:6363217	Mrap<sup>tm1.2Geno</sup>/Mrap<sup>tm1.2Geno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29879378	20191010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6118044	Reep6<sup>em1Ruch</sup>	is_implicated_in	DOID:0080350	retinitis pigmentosa 77		MGI:6189553	Reep6<sup>em1Ruch</sup>/Reep6<sup>em1Ruch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27889058	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861958	Jup<sup>tm1Ruiz</sup>	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:24276085	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5509327	Tg(LCR-HBA2,LCR-HBB*)1Cos	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:26967481	20160524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5509327	Tg(LCR-HBA2,LCR-HBB*)1Cos	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:22976952	20160524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5796776	Tg(Ins2-GLUD1*H454Y)2Csta	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:5796777	Tg(Ins2-GLUD1*H454Y)2Csta/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16574664	20161006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693304	Tg(ACTA1-PABPN1*A17)1Drub	is_implicated_in	DOID:11719	oculopharyngeal muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:28361972	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693304	Tg(ACTA1-PABPN1*A17)1Drub	is_implicated_in	DOID:11719	oculopharyngeal muscular dystrophy		MGI:3693326	Tg(ACTA1-PABPN1*A17)1Drub/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15864313	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155980	Acvrl1<sup>tm1Enl</sup>	is_implicated_in	DOID:0070314	obstructive nephropathy						ECO:0000033	author statement supported by traceable reference	PMID:23945497	20210218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438359	Mcph1<sup>Gt(RRO608)Byg</sup>/Mcph1<sup>Gt(RRO608)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:20169082	20110428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5529515	Tg(ACTB-THRB*)DSyc	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:5529520	Tg(ACTB-THRB*)DSyc/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9205946	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5319631	Tg(NPHS2-Trpc6)F419Walz	is_implicated_in	DOID:0111129	focal segmental glomerulosclerosis 2		MGI:5319644	Tg(NPHS2-Trpc6)F419Walz/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20877463	20120530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181774	Atm<sup>tm1Mfl</sup>/Atm<sup>tm1Mfl</sup>  [background:] involves: 129T2/SvEms * C57BL/6J	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:11389091	20050603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829966	Capn3<sup>tm1.1Hiso</sup>	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A		MGI:4829971	Capn3<sup>tm1.1Hiso</sup>/Capn3<sup>tm1.1Hiso</sup>  [background:] B6.129P2-Capn3<sup>tm1.1Hiso</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20592470	20100920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5582510	Ryr2<sup>tm3.1Amks</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5582593	Ryr2<sup>tm3.1Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22828895	20140915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196043	Tg(CAG-Alk*F1174L,-luc)60Jhsc	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:29769563	20180831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196043	Tg(CAG-Alk*F1174L,-luc)60Jhsc	is_implicated_in	DOID:769	neuroblastoma		MGI:6196044	Tg(CAG-Alk*F1174L,-luc)60Jhsc/0 Tg(Dbh-icre)1Gsc/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22764207	20180831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196043	Tg(CAG-Alk*F1174L,-luc)60Jhsc	is_implicated_in	DOID:769	neuroblastoma		MGI:6196045	Tg(CAG-Alk*F1174L,-luc)60Jhsc/0 Th<sup>tm1(cre)Te</sup>/Th<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22764207	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5306592	Jun<sup>tm4Wag</sup>/Jun<sup>tm4Wag</sup> Tg(Sftpc-cre)1Blh/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:22265050	20120220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033302	Tg(S100b-v-erbB)4496Waw	is_implicated_in	DOID:3181	oligodendroglioma						ECO:0000033	author statement supported by traceable reference	PMID:30202050	20190109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033302	Tg(S100b-v-erbB)4496Waw	is_implicated_in	DOID:3181	oligodendroglioma		MGI:3822319	Tg(S100b-v-erbB)4496Waw/0  [background:] involves: C57BL/6J * DBA/2J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12670909	20190109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183817	Acta1<sup>tm1Jll</sup>	is_implicated_in	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:23736297	20160919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056729	Tg(FCGR2A)11Mkz	is_implicated_in	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:25061875	20150603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056729	Tg(FCGR2A)11Mkz	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3839558	Tg(FCGR2A)11Mkz/Tg(FCGR2A)11Mkz  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16200626	20150603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946808	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>	is_implicated_in	DOID:0060340	ciliopathy		MGI:6162486	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>/Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>  [background:] B6.Cg-Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29263200	20180626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6105932	Mlc1<sup>tm1.1Vdk</sup>	is_implicated_in	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1		MGI:6105933	Mlc1<sup>tm1.1Vdk</sup>/Mlc1<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28695146	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6105932	Mlc1<sup>tm1.1Vdk</sup>	is_implicated_in	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1		MGI:6105933	Mlc1<sup>tm1.1Vdk</sup>/Mlc1<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25382142	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634092	Tg(Mbp-SNCA)1Ema	is_implicated_in	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:24310907	20150430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634092	Tg(Mbp-SNCA)1Ema	is_implicated_in	DOID:4752	multiple system atrophy		MGI:5634095	Tg(Mbp-SNCA)1Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:24310907	20150430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182395	Tacr1<sup>tm1Sph</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182395	Tacr1<sup>tm1Sph</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:4821001	Tacr1<sup>tm1Sph</sup>/Tacr1<sup>tm1Sph</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9748515	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620067	Neil1<sup>tm1Rsld</sup>/Neil1<sup>+</sup>  [background:] either: B6.129S1-Neil1<sup>tm1Rsld</sup> or (involves: 129S1/Sv * C57BL/6)	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16446448	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155424	Fah<sup>1R</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I						ECO:0000033	author statement supported by traceable reference	PMID:20162619	20140423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155424	Fah<sup>1R</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:2655553	Fah<sup>1R</sup>/Fah<sup>1R</sup>  [background:] involves: BALB/cRl * C3H/Rl * C57BL/10Rl			ECO:0000033	author statement supported by traceable reference	PMID:11209059	20140423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908353	Tg(Myh6-EGFR*)9-12Iko	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5908356	Tg(Myh6-EGFR*)9-12Iko/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22216087	20170906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575771	Sod1<sup>m1H</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5749248	Sod1<sup>m1H</sup>/Sod1<sup>m1H</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25468678	20160218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6423627	Stk39<sup>tm1Pawe</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6423631	Stk39<sup>tm1Pawe</sup>/Stk39<sup>tm1Pawe</sup> Pvalb<sup>tm1(cre)Arbr</sup>/Pvalb<sup>+</sup>  [background:] B6.129-Stk39<sup>tm1Pawe</sup> Pvalb<sup>tm1(cre)Arbr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28442491	20200521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6355946	Brd4<sup>M1Rvt</sup>	is_implicated_in	DOID:12679	nephrocalcinosis		MGI:6368208	Brd4<sup>M1Rvt</sup>/Brd4<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:30830987	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5758948	Serpinf1<sup>tm1Craw</sup>/Serpinf1<sup>tm1Craw</sup>  [background:] Not Specified	is_model_of	DOID:0110350	osteogenesis imperfecta type 6						ECO:0000033	author statement supported by traceable reference	PMID:23413146	20160411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4880715	Tg(GFAP-cre)8Gtm/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup>  [background:] involves: 129X1/SvJ * 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21062901	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696057	Brca1<sup>tm1Brn</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:24748377	20150304	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699839	Tg(PDGFB-SNCA*A53T)8Ema/0  [background:] Not Specified	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26201615	20151222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3766996	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] either: (B6.D1-Spta1<sup>sph-ha</sup> x WB.D1-Spta1<sup>sph-ha</sup>)F1 or (WB.D1-Spta1<sup>sph-ha</sup> x B6.D1-Spta1<sup>sph-ha</sup>)F1	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:8355480	20080109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7309144	Zng1<sup>em1Skan</sup>	is_implicated_in	DOID:0080205	CAKUT		MGI:7309153	Zng1<sup>em1Skan</sup>/Zng1<sup>em1Skan</sup>  [background:] C57BL/6N-Zng1<sup>em1Skan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31862704	20220705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5464997	Foxn1<sup>nu-2J</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:5465030	Foxn1<sup>nu-2J</sup>/Foxn1<sup>nu-2J</sup>  [background:] B6(SJL)-Foxn1<sup>nu-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6456056	Diaph3<sup>tm1.1Pji</sup>	is_implicated_in	DOID:1338	congenital dyserythropoietic anemia		MGI:6456066	Diaph3<sup>tm1.1Pji</sup>/Diaph3<sup>tm1.1Pji</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26471482	20200918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653596	Slc6a3<sup>tm1Hhg</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653596	Slc6a3<sup>tm1Hhg</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5318772	Slc6a3<sup>tm1Hhg</sup>/Slc6a3<sup>tm1Hhg</sup>  [background:] B6.129X1-Slc6a3<sup>tm1Hhg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22034972	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5817396	Tg(PMP22)C3Fbas	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:5824743	Tg(PMP22)C3Fbas/?  [background:] B6.Cg-Tg(PMP22)C3Fbas			ECO:0000033	author statement supported by traceable reference	PMID:21487305	20170222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361187	Tg(Krt19-Wnt1)2Maos	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:23975421	20140911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620108	Flt4<sup>Chy</sup>/Flt4<sup>+</sup>  [background:] involves: C3H	is_model_of	DOID:0050580	hereditary lymphedema						ECO:0000033	author statement supported by traceable reference	PMID:11592985	20060420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856173	Pax3<sup>Sp</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:7801299	20220215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822146	l11Jus16/l11Jus16  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2384126	C1qa<sup>tm1Mjw</sup>/C1qa<sup>tm1Mjw</sup>  [background:] involves: 129P2/Ola * 129S/SvEv * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:9590289	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181388	Hfe<sup>tm1Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22370144	20230518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181388	Hfe<sup>tm1Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22858058	20230518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181388	Hfe<sup>tm1Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:26707700	20230518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181388	Hfe<sup>tm1Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033464	Hfe<sup>tm1Sly</sup>/Hfe<sup>tm1Sly</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20230518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286495	Tg(Myoc*Y423H)#Sit	is_implicated_in	DOID:1067	open-angle glaucoma		MGI:6286497	Tg(Myoc*Y423H)#Sit/0  [background:] B6.FVB-Tg(Myoc*Y423H)#Sit			ECO:0000033	author statement supported by traceable reference	PMID:17108164	20190409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5751702	Pcare<sup>tm1Kpal</sup>	is_implicated_in	DOID:0110364	retinitis pigmentosa 54		MGI:5755292	Pcare<sup>tm1Kpal</sup>/Pcare<sup>tm1Kpal</sup>  [background:] involves: C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:25616964	20160401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317193	Cacna1f<sup>tm1.2Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634274	Cacna1f<sup>tm1.2Sdie</sup>/Cacna1f<sup>tm1.2Sdie</sup>  [background:] B6.Cg-Cacna1f<sup>tm1.2Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317193	Cacna1f<sup>tm1.2Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634279	Cacna1f<sup>tm1.2Sdie</sup>/Y  [background:] B6.Cg-Cacna1f<sup>tm1.2Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6490517	Tbc1d24<sup>em3Tbf</sup>	is_not_implicated_in	DOID:0110532	autosomal recessive nonsyndromic deafness 86		MGI:6490523	Tbc1d24<sup>em3Tbf</sup>/Tbc1d24<sup>em3Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em3Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32987832	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4841616	Gas2<sup>tm1a(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:7282200	Gas2<sup>tm1a(EUCOMM)Hmgu</sup>/Gas2<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Gas2<sup>tm1a(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33964205	20220606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781131	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)19Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:20033049	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781131	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)19Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:17613438	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781131	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)19Kkw/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:27251290	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694681	Tg(HDexon1)62Gpb/0  [background:] B6CBA-Tg(HDexon1)62Gpb/1J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694681	Tg(HDexon1)62Gpb/0  [background:] B6CBA-Tg(HDexon1)62Gpb/1J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:16697652	20070302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0080051	acromesomelic dysplasia, Hunter-Thompson type		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3757843	Tg(Th-SNCA*)1702Yosh/0  [background:] involves: C3H * C57BL/6J	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:17174013	20101129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3603677	Smarcb1<sup>tm1Gvk</sup>/Smarcb1<sup>tm1Gvk</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL/J	is_model_of	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000033	author statement supported by traceable reference	PMID:16099835	20051107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3608986	Fut8<sup>tm1Nta</sup>/Fut8<sup>tm1Nta</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:16236725	20060104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2387110	Crygd<sup>Aey4</sup>/Crygd<sup>+</sup>  [background:] C3HeB/FeJ-Crygd<sup>Aey4</sup>	is_model_of	DOID:0110234	cataract 4 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:12226711	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175208	Pax6<sup>Sey-Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 102 * C3H	is_model_of	DOID:12271	aniridia						ECO:0000033	author statement supported by traceable reference	PMID:12714618	20080218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6391169	Slc7a7<sup>em1Lbu</sup>	is_implicated_in	DOID:0060439	lysinuric protein intolerance		MGI:7380585	Slc7a7<sup>em1Lbu</sup>/Slc7a7<sup>em1Lbu</sup>  [background:] involves: 129/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32504080	20221109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476825	Tg(TARDBP*G348C)#Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22230045	20131021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476825	Tg(TARDBP*G348C)#Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:23238732	20131021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578147	Idh2<sup>tm1Jwpk</sup>	is_implicated_in	DOID:0080005	bone remodeling disease		MGI:5578156	Idh2<sup>tm1Jwpk</sup>/Idh2<sup>tm1Jwpk</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29527922	20220527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:5520	head and neck squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25723392	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4850020	Tg(Lck-TNFSF13)3919Mhah	is_implicated_in	DOID:1040	chronic lymphocytic leukemia		MGI:4850030	Tg(Lck-TNFSF13)3919Mhah/0  [background:] B6.Cg-Tg(Lck-TNFSF13)3919Mhah			ECO:0000033	author statement supported by traceable reference	PMID:15488762	20180111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4850020	Tg(Lck-TNFSF13)3919Mhah	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:28460208	20180111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526032	Tg(Snca-SNCA)#Galt/?  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:23573275	20131231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838346	Agpat2<sup>tm1Garg</sup>	is_implicated_in	DOID:0111135	congenital generalized lipodystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26880786	20160708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838346	Agpat2<sup>tm1Garg</sup>	is_implicated_in	DOID:0111135	congenital generalized lipodystrophy type 1		MGI:3838352	Agpat2<sup>tm1Garg</sup>/Agpat2<sup>tm1Garg</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:19187773	20160708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621357	Uros<sup>tm1Cged</sup>/Uros<sup>tm1Cged</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:13271	cutaneous porphyria						ECO:0000033	author statement supported by traceable reference	PMID:16314073	20060504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838352	Agpat2<sup>tm1Garg</sup>/Agpat2<sup>tm1Garg</sup>  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0111135	congenital generalized lipodystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:19187773	20090402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5706755	Col1a1<sup>tm1(tetO-URI1)Ndj</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:6378447	Col1a1<sup>tm1(tetO-URI1)Ndj</sup>/Col1a1<sup>tm1(tetO-URI1)Ndj</sup> Tg(Cebpb-tTA)#Bjd/0  [background:] B6.Cg-Col1a1<sup>tm1(tetO-URI1)Ndj</sup> Tg(Cebpb-tTA)#Bjd			ECO:0000033	author statement supported by traceable reference	PMID:25453901	20191125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5706755	Col1a1<sup>tm1(tetO-URI1)Ndj</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:6378441	Col1a1<sup>tm1(tetO-URI1)Ndj</sup>/Col1a1<sup>+</sup> Tg(Cebpb-tTA)#Bjd/0  [background:] B6.Cg-Col1a1<sup>tm1(tetO-URI1)Ndj</sup> Tg(Cebpb-tTA)#Bjd			ECO:0000033	author statement supported by traceable reference	PMID:25453901	20191125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5050413	Sorl1<sup>tm1Tew</sup>/Sorl1<sup>tm1Tew</sup> Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] involves: 129 * C3H/HeJ * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19036982	20110725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183470	Fanca<sup>tm1Faw</sup>	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A						ECO:0000033	author statement supported by traceable reference	PMID:25261197	20150526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183470	Fanca<sup>tm1Faw</sup>	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A		MGI:3618892	Fanca<sup>tm1Faw</sup>/Fanca<sup>tm1Faw</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10915769	20150526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046553	Col18a1<sup>tm1Hms</sup>/Col18a1<sup>tm1Hms</sup>  [background:] B6.129S4-Col18a1<sup>tm1Hms</sup>	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12766032	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6336196	Gas2l2<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:6343406	Gas2l2<sup>tm1c(KOMP)Wtsi</sup>/Gas2l2<sup>tm1c(KOMP)Wtsi</sup> Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/Foxj1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30665704	20190814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641392	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] B6J.129S4-Tsc1<sup>tm1Hin</sup>	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23250422	20150622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690019	Casq2<sup>tm1Kpfe</sup>	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000033	author statement supported by traceable reference	PMID:23295832	20160816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690019	Casq2<sup>tm1Kpfe</sup>	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000033	author statement supported by traceable reference	PMID:26121139	20160816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690019	Casq2<sup>tm1Kpfe</sup>	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:3691621	Casq2<sup>tm1Kpfe</sup>/Casq2<sup>tm1Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16932808	20160816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835423	Tg(C3-1-TAg)cJeg/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:7972041	20141204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678505	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>/Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12039988	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772780	Etv6<sup>tm3(NTRK3)Sho</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772780	Etv6<sup>tm3(NTRK3)Sho</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3772798	Etv6<sup>tm3(NTRK3)Sho</sup>/Etv6<sup>+</sup> Tg(Wap-cre)11738Mam/0  [background:] involves: 129S1/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18068631	20160426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857448	Rbl1<sup>tm1Tyj</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3803665	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18040647	20080828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804682	Slc17a8<sup>tm1Selm</sup>/Slc17a8<sup>tm1Selm</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0110555	autosomal dominant nonsyndromic deafness 25						ECO:0000033	author statement supported by traceable reference	PMID:18674745	20090520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433323	Ap1b1<sup>b2b1660Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3717676	Tg(Gfap-TGFB1)64Lms	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23954171	20140815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3046808	Cdkn1a<sup>tm2(HBx)Xya</sup>/Cdkn1a<sup>tm2(HBx)Xya</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7286337	Specc1l<sup>em3Kumc</sup>	is_implicated_in	DOID:0080698	Teebi hypertelorism syndrome 1		MGI:7286352	Specc1l<sup>em3Kumc</sup>/Specc1l<sup>em3Kumc</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708063	Cc2d2a<sup>tm1Asw</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5775312	Cc2d2a<sup>tm1Asw</sup>/Cc2d2a<sup>tm1Asw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24947469	20160608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4950565	Prpf3<sup>tm1.1Eap</sup>/Prpf3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:0110356	retinitis pigmentosa 18						ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653120	Cdon<sup>tm1Rsk</sup>	is_implicated_in	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21802063	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653120	Cdon<sup>tm1Rsk</sup>	is_implicated_in	DOID:0110877	holoprosencephaly 11		MGI:2653134	Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12620190	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442701	Mirc1<sup>tm1.2Tyj</sup>/Mirc1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060464	Feingold syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21892160	20121126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4359732	Dp(7Herc2-Mkrn3)1Taku/0  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:19563756	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000526	Id3<sup>tm1Zhu</sup>/Id3<sup>tm1Zhu</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15485632	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2673461	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000033	author statement supported by traceable reference	PMID:12893777	20110518	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838401	Hmx1<sup>dmbo</sup>/Hmx1<sup>dmbo</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J	is_model_of	DOID:0060482	oculoauricular syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19379485	20090501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0110965	brachydactyly type A2		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3803707	Hba<sup>tm1(HBA)Tow</sup>/Hba<sup>tm1(HBA)Tow</sup> Hbb<sup>tm2(HBG1,HBB*)Tow</sup>/Hbb<sup>tm2(HBG1,HBB*)Tow</sup>  [background:] Not Specified	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:16638928	20080829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182322	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26239478	20160407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6437154	Rbm20<sup>em1Hide</sup>	is_implicated_in	DOID:0110447	dilated cardiomyopathy 1DD		MGI:6477029	Rbm20<sup>em1Hide</sup>/Rbm20<sup>em1Hide</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33110103	20201202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560903	b2b2459Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5561312	b2b2459Clo/b2b2459Clo  [background:] C57BL/6J-b2b2459Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286560	Tg(Ckmm-Cav3)1Ysu/0  [background:] involves: C57BL/Slc * DBA/Slc	is_model_of	DOID:0060255	rippling muscle disease 2						ECO:0000033	author statement supported by traceable reference	PMID:11159934	20190224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3609030	Chuk<sup>tm1Mka</sup>/Chuk<sup>tm1Mka</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA	is_model_of	DOID:0060647	fetal encasement syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510652	Psen1<sup>tm1Lpr</sup>/Psen1<sup>tm1Lpr</sup> Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:15466394	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140734	Ts(17<sup>16</sup>)65Dn/0  [background:] involves: C3H/HeJ * C57BL/6J * DBA/2J	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19041304	20110823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000310	Sos1<sup>tm1.2Rak</sup>/Sos1<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:0060582	Noonan syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:21041952	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056757	Kcnq1<sup>tm2Kpfe</sup>/Kcnq1<sup>tm2Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15498462	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308012	Tg(ED-L2-IL1RN/IL1B)#Tcw	is_implicated_in	DOID:9206	Barrett's esophagus		MGI:5308013	Tg(ED-L2-IL1RN/IL1B)#Tcw/?  [background:] B6.Cg-Tg(ED-L2-IL1RN/IL1B)#Tcw			ECO:0000033	author statement supported by traceable reference	PMID:22264787	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308012	Tg(ED-L2-IL1RN/IL1B)#Tcw	is_implicated_in	DOID:9206	Barrett's esophagus						ECO:0000033	author statement supported by traceable reference	PMID:32325086	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553119	Neb<sup>tm1.1Hgra</sup>	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:5553123	Neb<sup>tm1.1Hgra</sup>/Neb<sup>tm1.1Hgra</sup>  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23715096	20170110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5553119	Neb<sup>tm1.1Hgra</sup>	is_implicated_in	DOID:0110928	nemaline myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:27890461	20170110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655827	Foxc1<sup>tm1Blh</sup>/Foxc1<sup>+</sup>  [background:] B6.Cg-Foxc1<sup>tm1Blh</sup>	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654613	Invs<sup>inv</sup>/Invs<sup>inv</sup>  [background:] involves: FVB/N	is_model_of	DOID:0111113	nephronophthisis 2						ECO:0000033	author statement supported by traceable reference	PMID:15213262	20120926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839642	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>/Nhlrc1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6J * C57BL/6NTac	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:20538597	20150709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839642	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>/Nhlrc1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6J * C57BL/6NTac	is_model_of	DOID:3534	Lafora disease						ECO:0000033	author statement supported by traceable reference	PMID:21882344	20150709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317912	Tg(KRT5-rtTA)1Glk/0 Tg(tetO/CMV-Tslp)#Sfz/0  [background:] C.Cg-Tg(KRT5-rtTA)1Glk Tg(tetO/CMV-Tslp)#Sfz	is_model_of	DOID:718	autoimmune hemolytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:22281511	20120510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038219	Gck<sup>Rgsc392</sup>/Gck<sup>Rgsc392</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428665	Nemf<sup>pdft</sup>	is_implicated_in	DOID:870	neuropathy		MGI:6719084	Nemf<sup>pdft</sup>/Nemf<sup>pdft</sup>  [background:] B6(C3)-Nemf<sup>pdft</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5566832	Tg(Pbsn-MYC)#Tt	is_implicated_in	DOID:10283	prostate cancer		MGI:5566833	Tg(Pbsn-MYC)#Tt/?  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22144662	20140605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523955	Kit<sup>Wps</sup>	is_implicated_in	DOID:3263	piebaldism		MGI:5523971	Kit<sup>Wps</sup>/Kit<sup>Wps</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619802	Tbx1<sup>tm2.1Bem</sup>/Tbx1<sup>tm2.2Bem</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129 * C57BL/6J * SJL * Swiss Webster	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16452092	20070423	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619802	Tbx1<sup>tm2.1Bem</sup>/Tbx1<sup>tm2.2Bem</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129 * C57BL/6J * SJL * Swiss Webster	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16600992	20070423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294340	Dnah5<sup>b2b002Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5050420	Cdh23<sup>v-4J</sup>/Cdh23<sup>v-4J</sup>  [background:] involves: C57BLKS/J	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2387931	Kif1b<sup>tm1Noh</sup>/Kif1b<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0110154	Charcot-Marie-Tooth disease type 2A1						ECO:0000033	author statement supported by traceable reference	PMID:11389829	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:5409	lung small cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:30674677	20190226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180816	Pcca<sup>tm1Tmiy</sup>	is_implicated_in	DOID:14701	propionic acidemia						ECO:0000033	author statement supported by traceable reference	PMID:33087718	20201215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180816	Pcca<sup>tm1Tmiy</sup>	is_implicated_in	DOID:14701	propionic acidemia		MGI:3052741	Pcca<sup>tm1Tmiy</sup>/Pcca<sup>tm1Tmiy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11461925	20201215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179220	Tff1<sup>tm1Mrio</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:22034055	20210929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179220	Tff1<sup>tm1Mrio</sup>	is_implicated_in	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:25980439	20210929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179220	Tff1<sup>tm1Mrio</sup>	is_implicated_in	DOID:10534	stomach cancer		MGI:5433072	Tff1<sup>tm1Mrio</sup>/Tff1<sup>tm1Mrio</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:12768581	20210929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819968	Bmal1<sup>tm2Bra</sup>	is_implicated_in	DOID:9351	diabetes mellitus		MGI:5576883	Bmal1<sup>tm2Bra</sup>/Bmal1<sup>tm2Bra</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * CBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:20562852	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5646612	b2b3077Clo	is_implicated_in	DOID:0060254	Robinow syndrome		MGI:5648026	b2b3077Clo/b2b3077Clo  [background:] C57BL/6J-b2b3077Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830474	Tg(HP-MMP1a)34-1Cha	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:4830477	Tg(HP-MMP1a)34-1Cha/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:1458541	20100923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830474	Tg(HP-MMP1a)34-1Cha	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:4830478	Tg(HP-MMP1a)34-1Cha/Tg(HP-MMP1a)34-1Cha  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:1458541	20100923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828836	Nkx2-5<sup>tm3.1Mwc</sup>	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5464901	Ndufs4<sup>tm1Capt</sup>/Ndufs4<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac	is_model_of	DOID:0060536	mitochondrial complex I deficiency						ECO:0000033	author statement supported by traceable reference	PMID:19460290	20130218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527214	Spink5<sup>tm1Drh</sup>	is_implicated_in	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31255470	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527214	Spink5<sup>tm1Drh</sup>	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:3527451	Spink5<sup>tm1Drh</sup>/Spink5<sup>tm1Drh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15590704	20200722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311377	b2b942Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313520	b2b942Clo/b2b942Clo  [background:] C57BL/6J-b2b942Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857397	Hoxd13<sup>spdh</sup>	is_implicated_in	DOID:0060242	synpolydactyly						ECO:0000033	author statement supported by traceable reference	PMID:24161848	20140225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857397	Hoxd13<sup>spdh</sup>	is_implicated_in	DOID:0060242	synpolydactyly		MGI:3587188	Hoxd13<sup>spdh</sup>/Hoxd13<sup>spdh</sup>  [background:] B6C3Fe a/a-Hoxd13<sup>spdh</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9580668	20140225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447072	Tg(Th-Twnk*,-EGFP)2Gcor	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5447073	Tg(Th-Twnk*,-EGFP)2Gcor/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22949510	20121228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623449	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] NOD.129S7(B6)-Ifng<sup>tm1Ts</sup>/DvsJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11714835	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386740	Abcb1a<sup>tm1Bor</sup>/Abcb1a<sup>tm1Bor</sup> Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: 129/Ola * BALB/c	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:11984826	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692598	Tg(Myh6-Tnnt2)117Lnwd	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:10562721	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692598	Tg(Myh6-Tnnt2)117Lnwd	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:3719609	Tg(Myh6-Tnnt2)117Lnwd/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9637714	20170915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5770088	Vps33b<sup>tm1.1Arte</sup>	is_implicated_in	DOID:0050763	ARC syndrome		MGI:5770121	Vps33b<sup>tm1.1Arte</sup>/Vps33b<sup>tm1.1Arte</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25947942	20170112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624718	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242117	20060619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842765	Tg(Ckm-IGF1R*K1003R)1Dlr	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:24585709	20210716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842765	Tg(Ckm-IGF1R*K1003R)1Dlr	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:33148881	20210716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842765	Tg(Ckm-IGF1R*K1003R)1Dlr	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25029527	20210716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842765	Tg(Ckm-IGF1R*K1003R)1Dlr	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3842791	Tg(Ckm-IGF1R*K1003R)1Dlr/0  [background:] FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr			ECO:0000033	author statement supported by traceable reference	PMID:11485987	20210716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842765	Tg(Ckm-IGF1R*K1003R)1Dlr	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3842791	Tg(Ckm-IGF1R*K1003R)1Dlr/0  [background:] FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr			ECO:0000033	author statement supported by traceable reference	PMID:24598803	20210716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623789	Kcne1<sup>pkr</sup>/Kcne1<sup>pkr</sup>  [background:] C57BL/10J-Kcne1<sup>pkr</sup>	is_model_of	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11003695	20130308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432239	Apc<sup>tm2Rak</sup>/Apc<sup>tm2Rak</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:20080688	20120827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5464284	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1Pai</sup> Tg(MUT*R403X)#Hlps/0  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:23024777	20130215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677133	G6pc1<sup>tm1Jyc</sup>/G6pc1<sup>tm1Jyc</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:2749	glycogen storage disease Ia						ECO:0000033	author statement supported by traceable reference	PMID:8640227	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604148	Tg(Prnp-MAPT*P301L)JNPL3Hlmc	is_implicated_in	DOID:680	tauopathy						ECO:0000033	author statement supported by traceable reference	PMID:34929160	20230629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039265	Trp53<sup>tm3Tyj</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:26196479	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039265	Trp53<sup>tm3Tyj</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:27571409	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039265	Trp53<sup>tm3Tyj</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:5759821	Trp53<sup>tm3Tyj</sup>/Trp53<sup>+</sup> Tg(Wap-cre)11738Mam/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16166291	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4941332	Lhx3<sup>tm1.1Sjr</sup>/Lhx3<sup>tm1.1Sjr</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:21149718	20110317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476825	Tg(TARDBP*G348C)#Jpj	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5476838	Tg(TARDBP*G348C)#Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21752789	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:22617326	20150304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531484	Dmd<sup>tm1.1Khan</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25511460	20150420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531484	Dmd<sup>tm1.1Khan</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3573782	Dmd<sup>tm1.1Khan</sup>/Y  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15694376	20150420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3573782	Dmd<sup>tm1.1Khan</sup>/Y  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:15694376	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822572	Tg(CMV-ATXN3*94Q)94Pama/Tg(CMV-ATXN3*94Q)94Pama  [background:] B6.FVB-Tg(CMV-ATXN3*94Q)94Pama	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:20510362	20100913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3779061	Phex<sup>Hyp</sup>/?  [background:] involves: C57BL/6J	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15976027	20080428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6423595	Lmna<sup>tm1Bliu</sup>	is_implicated_in	DOID:3911	progeria		MGI:6423604	Lmna<sup>tm1Bliu</sup>/Lmna<sup>+</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:32128409	20200521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316786	Ccdc39<sup>b2b1304Clo</sup>	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311367	b2b635Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5312337	b2b635Clo/b2b635Clo  [background:] C57BL/6J-b2b635Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573756	Spink5<sup>tm1Hov</sup>	is_implicated_in	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32442469	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573756	Spink5<sup>tm1Hov</sup>	is_implicated_in	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573756	Spink5<sup>tm1Hov</sup>	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:3575519	Spink5<sup>tm1Hov</sup>/Spink5<sup>tm1Hov</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15619623	20210204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7511620	Aicda<sup>em1Jaych</sup>	is_implicated_in	DOID:0060758	immunodeficiency with hyper-IgM type 2		MGI:7511767	Aicda<sup>em1Jaych</sup>/Aicda<sup>em1Jaych</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33098766	20230726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5306916	Tg(Thy1-GLRA1*R271Q)382Wha/Tg(Thy1-GLRA1*R271Q)382Wha  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	PMID:11923415	20120223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5305275	Col8a2<sup>tm1.1Asj</sup>	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:5305276	Col8a2<sup>tm1.1Asj</sup>/Col8a2<sup>tm1.1Asj</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22002996	20160929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5305275	Col8a2<sup>tm1.1Asj</sup>	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:5796117	Col8a2<sup>tm1.1Asj</sup>/Col8a2<sup>tm1.1Asj</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23422828	20160929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824069	Mpz<sup>tm1.1Wra</sup>	is_implicated_in	DOID:870	neuropathy		MGI:6273176	Mpz<sup>tm1.1Wra</sup>/Mpz<sup>+</sup>  [background:] FVB.129S2-Mpz<sup>tm1.1Wra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30239779	20190111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3801152	Tph2<sup>tm1Mca</sup>/Tph2<sup>tm1Mca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:23467366	20130805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461059	Igh-J<sup>tm1Aigl</sup>/Igh-J<sup>+</sup> Tg(Tcra2D2,Tcrb2D2)1Kuch/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19483694	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722160	Tg(PRNP-APPSweInd)8Dwst/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20682779	20110104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6147816	Slc39a8<sup>tm1.2Mrl</sup>	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:6360946	Slc39a8<sup>tm1.2Mrl</sup>/Slc39a8<sup>tm1.2Mrl</sup>  [background:] B6(Cg)-Slc39a8<sup>tm1.2Mrl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29337306	20190925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5787927	Emg1<sup>tm1.1Btr</sup>	is_implicated_in	DOID:0050684	Bowen-Conradi syndrome		MGI:5787933	Emg1<sup>tm1.1Btr</sup>/Emg1<sup>tm1.1Btr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25708872	20160804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4881048	Gns<sup>tm1e(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:6105949	Gns<sup>tm1e(EUCOMM)Hmgu</sup>/Gns<sup>tm1e(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-A<sup>tm1Brd</sup> Gns<sup>tm1e(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28334745	20171222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:25948589	20160210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26640144	20160210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20160210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311373	Odad2<sup>b2b643Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814907	Six3<sup>tm3.1Gco</sup>/Six3<sup>+</sup> Shh<sup>tm1Chg</sup>/Shh<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110872	holoprosencephaly 2						ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4417910	Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25456500	20150813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4417910	Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4417912	Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte/Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19936202	20150813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5475548	Tg(tetO-Spp1)5Gad	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5485272	Tg(Myh6-tTA)6Smbf/0 Tg(tetO-Spp1)5Gad/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20200330	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428682	Tg(H2-K1-HLA-A*)28Mpla	is_implicated_in	DOID:0111079	birdshot chorioretinopathy		MGI:5428686	Tg(H2-K1-HLA-A*)28Mpla/0  [background:] B10.Cg-Tg(H2-K1-HLA-A*)28Mpla			ECO:0000033	author statement supported by traceable reference	PMID:11226280	20120723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111480	Snx10<sup>em1Ael</sup>	is_implicated_in	DOID:0110940	autosomal recessive osteopetrosis 8		MGI:6441464	Snx10<sup>em1Ael</sup>/Snx10<sup>em1Ael</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:32278070	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717256	Ar<sup>tm1.1Jdz</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17317769	20081107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850185	Tg(tetO-Il13)1Tazh	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850185	Tg(tetO-Il13)1Tazh	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3850190	Tg(KRT5-tTA)1216Glk/0 Tg(tetO-Il13)1Tazh/0  [background:] B6.Cg-Tg(KRT5-tTA)1216Glk Tg(tetO-Il13)1Tazh			ECO:0000033	author statement supported by traceable reference	PMID:18830273	20140514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904771	Clcn7<sup>tm2.1Mjec</sup>	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:27746321	20170718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6441136	Card14<sup>em2Tshu</sup>	is_implicated_in	DOID:0080475	psoriasis 2		MGI:6441186	Card14<sup>em2Tshu</sup>/Card14<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29980436	20200713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435571	Fktn<sup>tm1Kcam</sup>	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:5435674	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Tg(CAG-cre/Esr1*)5Amc/?  [background:] involves: 129S/SvEv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435571	Fktn<sup>tm1Kcam</sup>	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:5435676	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435571	Fktn<sup>tm1Kcam</sup>	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:5435675	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S/SvEv * FVB			ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442117	Dnaaf3<sup>b2b1739Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669895	Hcrtr2<sup>tm1Ywa</sup>/Hcrtr2<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:12797957	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5697201	Ppox<sup>tm1.1Had</sup>	is_implicated_in	DOID:4346	variegate porphyria		MGI:5697205	Ppox<sup>tm1.1Had</sup>/Ppox<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11929050	20151125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569019	Tg(Ins1-Cd80)378Psoh/0 Tg(Ins2-GP)#Psoh/0 Tg(TcrLCMV)327Sdz/0  [background:] involves: C57BL/6 * DBA/2 * FVB/N	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:7512724	20140620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857590	Trp53<sup>tm1Brd</sup>	is_implicated_in	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22915751	20130408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4462257	Kit<sup>W-sh</sup>/Kit<sup>W-sh</sup> Lyn<sup>tm1Ard</sup>/Lyn<sup>tm1Ard</sup>  [background:] involves: 101 * 129P2/OlaHsd * C3H/HeH	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:20512127	20100729	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054824	Aipl1<sup>tm1Visu</sup>/Aipl1<sup>tm1Visu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110332	Leber congenital amaurosis 4						ECO:0000033	author statement supported by traceable reference	PMID:15365178	20050531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3713302	Gck<sup>tm2Mgn</sup>/Gck<sup>tm2Mgn</sup>  [background:] 129S6/SvEvTac-Gck<sup>tm2Mgn</sup>	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839653	Tg(Prnp-TARDBP*A315T)23Jlel/0  [background:] involves: C57BL/6 * CD-1 * SJL	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:20621187	20101130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814540	Coch<sup>tm1Mrtn</sup>/Coch<sup>tm1Mrtn</sup>  [background:] CBACa.129S4-Coch<sup>tm1Mrtn</sup>	is_model_of	DOID:0110593	autosomal dominant nonsyndromic deafness 9						ECO:0000033	author statement supported by traceable reference	PMID:18697796	20110128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814540	Coch<sup>tm1Mrtn</sup>/Coch<sup>tm1Mrtn</sup>  [background:] CBACa.129S4-Coch<sup>tm1Mrtn</sup>	is_model_of	DOID:0110593	autosomal dominant nonsyndromic deafness 9						ECO:0000033	author statement supported by traceable reference	PMID:21073934	20110128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174705	Pkd2<sup>tm2Som</sup>/Pkd2<sup>tm2Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:10615132	20091021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197540	Pnpla3<sup>tm2.1Hobb</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6197548	Pnpla3<sup>tm2.1Hobb</sup>/Pnpla3<sup>tm2.1Hobb</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24917523	20180911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5770788	Tg(CAG-TRIM29)ADims	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5770790	Tg(CAG-TRIM29)ADims/0  [background:] FVB/NJ-Tg(CAG-TRIM29)ADims			ECO:0000033	author statement supported by traceable reference	PMID:26471361	20160523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618431	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:0060643	primary sclerosing cholangitis						ECO:0000033	author statement supported by traceable reference	PMID:20921947	20150312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4950563	Prpf8<sup>tm1.1Eap</sup>	is_implicated_in	DOID:0110403	retinitis pigmentosa 13		MGI:4950567	Prpf8<sup>tm1.1Eap</sup>/Prpf8<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4950563	Prpf8<sup>tm1.1Eap</sup>	is_implicated_in	DOID:0110403	retinitis pigmentosa 13		MGI:4950566	Prpf8<sup>tm1.1Eap</sup>/Prpf8<sup>tm1.1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5816979	Vipas39<sup>tm1c(KOMP)Mbp</sup>	is_implicated_in	DOID:0050763	ARC syndrome		MGI:5817425	Vipas39<sup>tm1c(KOMP)Mbp</sup>/Vipas39<sup>tm1c(KOMP)Mbp</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27435297	20170112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431499	Gm572<sup>b2b1167Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459456	Tg(PLP1*)4Rsj/0  [background:] involves: CD-1	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:7505836	20131024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459456	Tg(PLP1*)4Rsj/0  [background:] involves: CD-1	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21228378	20131024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587744	Myo7a<sup>26SB</sup>/Myo7a<sup>26SB</sup>  [background:] involves: BALB/cRl	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312616	Myo7a<sup>sh1-11J</sup>/Myo7a<sup>sh1-11J</sup>  [background:] 129.B6-Myo7a<sup>sh1-11J</sup>	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:21447681	20120325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3843604	Bcl2l1<sup>tm1.1Mam</sup>/Bcl2l1<sup>tm1.1Mam</sup> Tg(Ins2-cre)25Mgn/0 Tg(RIP1-Tag)2Dh/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19209227	20090511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4940057	Tg(Prnp-ATXN3*79Q)#Hlw	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:4940059	Tg(Prnp-ATXN3*79Q)#Hlw/0  [background:] FVB/N-Tg(Prnp-ATXN3*79Q)#Hlw			ECO:0000033	author statement supported by traceable reference	PMID:18502140	20110308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720782	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup> Tg(APPSwe,tauP301L)1Lfa/Tg(APPSwe,tauP301L)1Lfa  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:15748844	20080310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831378	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] 129S6.129P2-Fgfr3<sup>tm1.1Aomw</sup>	is_model_of	DOID:0060703	Muenke Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665287	Tg(PRNP-APPSweInd)8Dwst/?  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16899370	20061031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5310969	Tg(Thy1-TARDBP*)BOddo	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5689841	Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo  [background:] C57BL/6-Tg(Thy1-TARDBP*)BOddo			ECO:0000033	author statement supported by traceable reference	PMID:26002100	20151012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7327433	Acad9<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:0112072	nuclear type mitochondrial complex I deficiency 20		MGI:7378413	Acad9<sup>tm1c(KOMP)Wtsi</sup>/Acad9<sup>tm1c(KOMP)Wtsi</sup> Tg(ACTA1-cre)79Jme/0  [background:] involves: C57BL/6J * C57BL/6N * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:34556413	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7327433	Acad9<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:0112072	nuclear type mitochondrial complex I deficiency 20		MGI:7378415	Acad9<sup>tm1c(KOMP)Wtsi</sup>/Acad9<sup>tm1c(KOMP)Wtsi</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:34556413	20221102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5286114	Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo	is_implicated_in	DOID:12858	Huntington's disease		MGI:5286128	Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21515588	20110923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614806	Muc2<sup>wnn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease						ECO:0000033	author statement supported by traceable reference	PMID:27881401	20180201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614806	Muc2<sup>wnn</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3615592	Muc2<sup>wnn</sup>/Muc2<sup>wnn</sup>  [background:] C57BL/6-Muc2<sup>wnn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18318598	20180201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386184	Pdcd1<sup>tm1Hon</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:14595408	20170803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386184	Pdcd1<sup>tm1Hon</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3054645	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] C.129S2(B6)-Pdcd1<sup>tm1Hon</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11209085	20170803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5517702	Tg(Pax6-TAg)1796Hur	is_implicated_in	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24227978	20140918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5517702	Tg(Pax6-TAg)1796Hur	is_implicated_in	DOID:768	retinoblastoma		MGI:5517703	Tg(Pax6-TAg)1796Hur/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22562503	20140918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5310969	Tg(Thy1-TARDBP*)BOddo	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5689841	Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo  [background:] C57BL/6-Tg(Thy1-TARDBP*)BOddo			ECO:0000033	author statement supported by traceable reference	PMID:26002100	20151012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5310969	Tg(Thy1-TARDBP*)BOddo	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5310970	Tg(Thy1-TARDBP*)BOddo/0  [background:] C57BL/6-Tg(Thy1-TARDBP*)BOddo			ECO:0000033	author statement supported by traceable reference	PMID:22067910	20151012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5616922	Gnptab<sup>nym</sup>	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:5790646	Gnptab<sup>nym</sup>/Gnptab<sup>nym</sup>  [background:] involves: BALB/cAnNHsd * C3H/HeNHsd			ECO:0000033	author statement supported by traceable reference	PMID:25107912	20160906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620065	Neil1<sup>tm1Rsld</sup>/Neil1<sup>tm1Rsld</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16446448	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555966	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Rai1,-EGFP)463Walz/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060853	Potocki-Lupski syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24218365	20140408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663375	Smn1<sup>tm1Hung</sup>/Smn1<sup>tm1Hung</sup> Tg(SMN2)2Hung/Tg(SMN2)2Hung  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:10615130	20061012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433857	Slc4a4<sup>tm1.1Slin</sup>	is_implicated_in	DOID:14219	renal tubular acidosis		MGI:5433858	Slc4a4<sup>tm1.1Slin</sup>/Slc4a4<sup>tm1.1Slin</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21228764	20120914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4460266	Msh2<sup>tm2.1Rak</sup>/Msh2<sup>tm2.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19931261	20111104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2659090	Dhh<sup>tm1Amc</sup>/Dhh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * C57BL/6J * Swiss Webster	is_model_of	DOID:14448	46,XY sex reversal						ECO:0000033	author statement supported by traceable reference	PMID:11090455	20050923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6108898	Tg(CAG-Calr)#Mlk	is_implicated_in	DOID:6000	congestive heart failure		MGI:6108900	Tg(CAG-Calr)#Mlk/0 Tg(Myh6-cre/Esr1*)1Liao/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27441395	20180112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6437154	Rbm20<sup>em1Hide</sup>	is_implicated_in	DOID:0060224	atrial fibrillation		MGI:6477029	Rbm20<sup>em1Hide</sup>/Rbm20<sup>em1Hide</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33110103	20201202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6765940	Zfp469<sup>em1Chms</sup>	is_implicated_in	DOID:14775	brittle cornea syndrome 1		MGI:6765943	Zfp469<sup>em1Chms</sup>/Zfp469<sup>em1Chms</sup>  [background:] C57BL/6J-Zfp469<sup>em1Chms</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34368841	20211007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7331421	Sar1b<sup>em1Emle</sup>	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:7331486	Sar1b<sup>em1Emle</sup>/Sar1b<sup>+</sup>  [background:] C57BL/6N-Sar1b<sup>em1Emle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33964306	20220824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931875	Smarcb1<sup>tm1Sho</sup>	is_implicated_in	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000033	author statement supported by traceable reference	PMID:23197309	20140205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931875	Smarcb1<sup>tm1Sho</sup>	is_implicated_in	DOID:2129	atypical teratoid rhabdoid tumor		MGI:5538531	Smarcb1<sup>tm1Sho</sup>/Smarcb1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516455	Tg(Prnp-ATXN3*148Q)148.19Olri/0  [background:] involves: C57BL/6N	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:17626202	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437085	b2b1291Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437110	b2b1291Clo/b2b1291Clo  [background:] C57BL/6J-b2b1291Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511901	Myo7a<sup>Hdb</sup>/Myo7a<sup>4626SB</sup>  [background:] involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:15389316	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857287	Serpine1<sup>tm1Mlg</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19604604	20120201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033883	Loxl1<sup>tm1Tili</sup>	is_implicated_in	DOID:13641	exfoliation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29419647	20200506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033883	Loxl1<sup>tm1Tili</sup>	is_implicated_in	DOID:13641	exfoliation syndrome		MGI:3033884	Loxl1<sup>tm1Tili</sup>/Loxl1<sup>tm1Tili</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24425853	20200506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835308	Hbb<sup>tm2Unc</sup>/Hbb<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:9490703	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709182	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)102Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16279840	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652363	App<sup>tm1.1Cep</sup>/App<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5582594	Ryr2<sup>tm4.1Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:22828895	20140915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695885	Tg(SOD1*H46R*H48Q)139Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16000321	20150408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695885	Tg(SOD1*H46R*H48Q)139Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5448463	Tg(SOD1*H46R*H48Q)139Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12127151	20150408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3610987	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm1Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242049	20060123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447548	Lep<sup>m1Btlr</sup>	is_implicated_in	DOID:9970	obesity		MGI:5447549	Lep<sup>m1Btlr</sup>/Lep<sup>m1Btlr</sup>  [background:] C57BL/6J-Lep<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5447547	20130104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6690860	Eml1<sup>tvrm360</sup>	is_implicated_in	DOID:0111169	subcortical band heterotopia		MGI:6690862	Eml1<sup>tvrm360</sup>/Eml1<sup>tvrm360</sup>  [background:] C57BL/6J-Eml1<sup>tvrm360</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:32221352	20210418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433072	Tff1<sup>tm1Mrio</sup>/Tff1<sup>tm1Mrio</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:12768581	20120906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575656	Asxl1<sup>tm1.1Iaai</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575662	Asxl1<sup>tm1.1Iaai</sup>/Asxl1<sup>tm1.1Iaai</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24218140	20140731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575656	Asxl1<sup>tm1.1Iaai</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575661	Asxl1<sup>tm1.1Iaai</sup>/Asxl1<sup>tm1.1Iaai</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S/SvEv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24218140	20140731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5516453	Tg(Prnp-ATXN3*70Q)70.61Olri/0  [background:] involves: C57BL/6N	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:17626202	20131107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722083	Cdh23<sup>v-J</sup>/Cdh23<sup>v-J</sup>  [background:] B6.C-H2-K<sup>bm1</sup>/ByJ	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5320164	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22302806	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085354	Pnpla1<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060719	autosomal recessive congenital ichthyosis 10		MGI:6286487	Pnpla1<sup>tm1a(KOMP)Wtsi</sup>/Pnpla1<sup>tm1a(KOMP)Wtsi</sup>  [background:] B6NTac;B6N-A<sup>tm1Brd</sup> Pnpla1<sup>tm1a(KOMP)Wtsi</sup>/Ics			ECO:0000033	author statement supported by traceable reference	PMID:28369476	20190409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044558	Gck<sup>Gena348</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:35046471	20220302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044558	Gck<sup>Gena348</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3044561	Gck<sup>Gena348</sup>/Gck<sup>Gena348</sup>  [background:] involves: BALB/c * C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:15161764	20220302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044558	Gck<sup>Gena348</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3044560	Gck<sup>Gena348</sup>/Gck<sup>+</sup>  [background:] involves: BALB/c * C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:15161764	20220302	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4456472	Gstm1<sup>tm1Gcw</sup>/Gstm1<sup>tm1Gcw</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:20178820	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842652	Gnmt<sup>tm1Ymac</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25754535	20150807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842652	Gnmt<sup>tm1Ymac</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3842683	Gnmt<sup>tm1Ymac</sup>/Gnmt<sup>tm1Ymac</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19035462	20150807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313524	Lox<sup>b2b370.2Clo</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5313544	Lox<sup>b2b370.2Clo</sup>/Lox<sup>b2b370.2Clo</sup>  [background:] C57BL/6J-Lox<sup>b2b370.2Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6474226	Ids<sup>tm1Dkji</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:6476699	Ids<sup>tm1Dkji</sup>/Y  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22847837	20201201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6474226	Ids<sup>tm1Dkji</sup>	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:6474227	Ids<sup>tm1Dkji</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20652491	20201201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438263	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Sprr2f-cre)1Dcas/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:1380	endometrial cancer						ECO:0000033	author statement supported by traceable reference	PMID:20142330	20100331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815024	Ece1<sup>tm1Reh</sup>/Ece1<sup>tm1Reh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:6406	double outlet right ventricle						ECO:0000033	author statement supported by traceable reference	PMID:10811845	20110509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311370	Dync2h1<sup>b2b414Clo</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:5311880	Dync2h1<sup>b2b414Clo</sup>/Dync2h1<sup>b2b414Clo</sup>  [background:] C57BL/6J-Dync2h1<sup>b2b414Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695608	Tg(Alb-HRAS*G12V)28Yu/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26131558	20170208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695608	Tg(Alb-HRAS*G12V)28Yu/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16087271	20170208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640479	Tnfsf4<sup>tm1Shr</sup>/Tnfsf4<sup>tm1Shr</sup>  [background:] NOD.129S4-Tnfsf4<sup>tm1Shr</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:14662903	20060811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5751490	Ush1c<sup>tm1Xzl</sup>/Ush1c<sup>tm1Xzl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110830	Usher syndrome type 1C						ECO:0000033	author statement supported by traceable reference	PMID:24725409	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0110970	brachydactyly type C		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449114	Aprt<sup>tm1Jat</sup>/Aprt<sup>tm1Jat</sup>  [background:] involves: 129S2/SvPas * Black Swiss	is_model_of	DOID:0060350	adenine phosphoribosyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8643571	20120924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3573789	Vps13a<sup>tm1Asan</sup>/Vps13a<sup>tm1Asan</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0050766	choreaacanthocytosis						ECO:0000033	author statement supported by traceable reference	PMID:15686477	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4843038	Klhl40<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0110930	nemaline myopathy 8		MGI:5774663	Klhl40<sup>tm1(KOMP)Vlcg</sup>/Klhl40<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Klhl40<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24960163	20160601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4367205	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Tg(APPSWE)2576Kha/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16236385	20110802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452396	Ptch1<sup>tm1Hahn</sup>/Ptch1<sup>tm1Hahn</sup> Gt(ROSA)26Sor<sup>tm2(cre/ERT2)Brn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	is_model_of	DOID:2513	basal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:20233865	20100519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037942	Trf<sup>hpx</sup>/Trf<sup>hpx</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>	is_model_of	DOID:0050649	atransferrinemia						ECO:0000033	author statement supported by traceable reference	MGI:1889268	20050610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037942	Trf<sup>hpx</sup>/Trf<sup>hpx</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>	is_model_of	DOID:0050649	atransferrinemia						ECO:0000033	author statement supported by traceable reference	PMID:3681112	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857942	Cdkn2a<sup>tm1Rdp</sup>	is_implicated_in	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:22020333	20161010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857942	Cdkn2a<sup>tm1Rdp</sup>	is_implicated_in	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:24147027	20161010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857942	Cdkn2a<sup>tm1Rdp</sup>	is_implicated_in	DOID:3070	high grade glioma						ECO:0000033	author statement supported by traceable reference	PMID:25683249	20161010	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028380	Pde6b<sup>rd1-1H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5528981	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:15983791	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278934	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:6278939	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27329763	20190219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278934	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:6278937	Atp2b1<sup>Tg(Thy1-CHMP2B*)1Rene</sup>/Atp2b1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27329763	20190219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830506	Otc<sup>spf-J</sup>/Y  [background:] C57BL/6J-Otc<sup>spf-J</sup>/J	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:25647322	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3835423	Tg(C3-1-TAg)cJeg/0  [background:] involves: FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:7972041	20141204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538520	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0  [background:] involves: FVB	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23867472	20140204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615437	Polh<sup>tm1.1Rak</sup>/Polh<sup>tm1.1Rak</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:0110847	xeroderma pigmentosum variant type						ECO:0000033	author statement supported by traceable reference	PMID:16397220	20060310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843447	Tg(Lck-Notch3)#Issc/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:10880446	20121024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J	is_model_of	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:15069016	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J	is_model_of	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000033	author statement supported by traceable reference	PMID:23160464	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5433612	Pin1<sup>tm1Tuc</sup>/Pin1<sup>tm1Tuc</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16554819	20120912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4881336	Gfi1<sup>Gen</sup>	is_implicated_in	DOID:0050590	severe congenital neutropenia		MGI:5318525	Gfi1<sup>Gen</sup>/Gfi1<sup>+</sup>  [background:] C57BL/6J-Gfi1<sup>Gen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22393124	20121114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007765	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>tm1Jgg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110998	Joubert syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:21623382	20110616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5805518	Tg(PyLT)1Vb	is_implicated_in	DOID:7004	ACTH-secreting pituitary adenoma		MGI:5805519	Tg(PyLT)1Vb/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:1316082	20161028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405410	Mir140<sup>em1Tkob</sup>	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:6423511	Mir140<sup>em1Tkob</sup>/Mir140<sup>+</sup>  [background:] C57BL/6-Mir140<sup>em1Tkob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30804514	20200520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405410	Mir140<sup>em1Tkob</sup>	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:6423510	Mir140<sup>em1Tkob</sup>/Mir140<sup>em1Tkob</sup>  [background:] C57BL/6-Mir140<sup>em1Tkob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30804514	20200520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6383470	Rs1<sup>em1Fegu</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6383471	Rs1<sup>em1Fegu</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29379415	20200106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197908	Alms1<sup>m3Btlr</sup>	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:6197910	Alms1<sup>m3Btlr</sup>/Alms1<sup>m3Btlr</sup>  [background:] C57BL/6J-Alms1<sup>m3Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:6197907	20180914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5309003	C1qtnf5<sup>tm1.1Geno</sup>	is_not_implicated_in	DOID:0060869	late-onset retinal degeneration		MGI:5309011	C1qtnf5<sup>tm1.1Geno</sup>/C1qtnf5<sup>tm1.1Geno</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22110650	20120312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180079	Acadl<sup>tm1Uab</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:24648546	20150112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180079	Acadl<sup>tm1Uab</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:2448162	Acadl<sup>tm1Uab</sup>/Acadl<sup>tm1Uab</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:9861014	20150112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5911931	Tg(Ckm-Sgcg)4Mcn	is_implicated_in	DOID:11724	limb-girdle muscular dystrophy		MGI:5911937	Tg(Ckm-Sgcg)4Mcn/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11287429	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428133	Nrxn1<sup>tm1Sud</sup>/Nrxn1<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:19822762	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6856586	Tg(Igkv3-5*-MYC)24Plbe	is_implicated_in	DOID:9538	multiple myeloma		MGI:5441332	Tg(Igkv3-5*-MYC)24Plbe/0  [background:] C57BL/6J-Tg(Igkv3-5*-MYC)24Plbe/PlbeMmmh			ECO:0000033	author statement supported by traceable reference	PMID:18242516	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755966	Tg(Alb-HBx)A112Tfts/0  [background:] involves: C57BL/6	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16403455	20160407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428133	Nrxn1<sup>tm1Sud</sup>/Nrxn1<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19822762	20120718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:12217	Lewy body dementia						ECO:0000033	author statement supported by traceable reference	PMID:30591714	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:12217	Lewy body dementia		MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10678833	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:12217	Lewy body dementia		MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21103359	20190104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528873	Tg(PDGFB-SNCA)4Ema	is_implicated_in	DOID:12217	Lewy body dementia		MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12111846	20190104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3653876	Ryr2<sup>tm1Sgp</sup>/Ryr2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:15890976	20060907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695752	Hap1<sup>tm2Xjl</sup>/Hap1<sup>tm2Xjl</sup> Tg(Camk2a-cre)159Kln/0  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6	is_model_of	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:25875952	20151112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5527171	Tecta<sup>tm3.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0110544	autosomal dominant nonsyndromic deafness 12						ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822147	Mks1<sup>avc6</sup>/Mks1<sup>avc6</sup>  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20101008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044881	Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:15071184	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644690	Tg(CAG-lacZ,-FUS,-EGFP)629Gyu	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:5644692	Meox2<sup>tm1(cre)Sor</sup>/Meox2<sup>+</sup> Tg(CAG-lacZ,-FUS,-EGFP)629Gyu/0  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25324524	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:27143420	20160926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930937	Psen1<sup>tm1Mpm</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2174994	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9883847	20160926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313383	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>tm3.2Lysa</sup>  [background:] Not Specified	is_model_of	DOID:0050475	Weill-Marchesani syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183532	Ncoa1<sup>tm1Bwo</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24550004	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183532	Ncoa1<sup>tm1Bwo</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3527794	Ncoa1<sup>tm1Bwo</sup>/Ncoa1<sup>tm1Bwo</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10202153	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4868120	Dicer1<sup>tm1Bdh</sup>/Dicer1<sup>tm1Bdh</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * CBA/J	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21098571	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5555965	Tg(tetO-Rai1,-EGFP)479Walz	is_implicated_in	DOID:0060853	Potocki-Lupski syndrome		MGI:5555967	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Rai1,-EGFP)479Walz/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24218365	20140408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720796	Tg(Ckm-APPSw)A6Lfa	is_implicated_in	DOID:3429	inclusion body myositis						ECO:0000033	author statement supported by traceable reference	PMID:22518836	20120930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720796	Tg(Ckm-APPSw)A6Lfa	is_implicated_in	DOID:3429	inclusion body myositis		MGI:3720804	Tg(Ckm-APPSw)A6Lfa/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11972038	20120930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429195	Nme5<sup>tm1Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429549	Nme5<sup>tm1Lex</sup>/Nme5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844324	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:19261747	20090515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604078	Fgfr2<sup>tm2Cxd</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:14499350	20051109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386211	Epor<sup>tm1.4Jtp</sup>/Epor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060652	familial erythrocytosis 1						ECO:0000033	author statement supported by traceable reference	PMID:11158582	20051003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590307	Pax6<sup>3Neu</sup>/Pax6<sup>+</sup>  [background:] either: (involves: 102 * C3H) or (involves: C3H)	is_model_of	DOID:0060673	Peters anomaly						ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717244	Ar<sup>tm1.1Jdz</sup>/Y  [background:] B6.129X1-Ar<sup>tm1.1Jdz</sup>	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16326839	20081107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3612480	Fscn2<sup>tm1Sykk</sup>/Fscn2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110406	retinitis pigmentosa 30						ECO:0000033	author statement supported by traceable reference	PMID:16043865	20060210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3774850	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:16494529	20080324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5528705	Tg(Amh-SMAD2*)2Tkw	is_implicated_in	DOID:11427	endosalpingiosis		MGI:5528706	Tg(Amh-SMAD2*)2Tkw/?  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:16141389	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440865	Rab25<sup>tm1Jrgo</sup>/Rab25<sup>tm1Jrgo</sup> Smad3<sup>tm1Par</sup>/Smad3<sup>+</sup>  [background:] 129-Rab25<sup>tm1Jrgo</sup> Smad3<sup>tm1Par</sup>	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:20197623	20100421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763240	Tg(Fabp4-Phb)#Smis	is_implicated_in	DOID:9970	obesity		MGI:5763241	Tg(Fabp4-Phb)#Smis/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24947361	20160426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398901	Acvrl1<sup>tm2.1Spo</sup>	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain						ECO:0000033	author statement supported by traceable reference	PMID:35663401	20220621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398901	Acvrl1<sup>tm2.1Spo</sup>	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:5501106	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:22571958	20220621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5466160	Tg(APOE-FGF23*R176Q)#Ack/0  [background:] involves: C57BL/6J * CBA	is_model_of	DOID:0050949	autosomal recessive hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:23038738	20130226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6473850	Rac2<sup>em1Shl</sup>	is_implicated_in	DOID:0112061	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia		MGI:6473858	Rac2<sup>em1Shl</sup>/Rac2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30723080	20210909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698703	Rab18<sup>m1Hongc</sup>/Rab18<sup>m1Hongc</sup>  [background:] C57BL/6J-Rab18<sup>m1Hongc</sup>	is_model_of	DOID:0110718	Warburg micro syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:25779931	20151211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6121104	Lama3<sup>tm1Arte</sup>	is_implicated_in	DOID:3209	junctional epidermolysis bullosa		MGI:6277933	Lama3<sup>tm1Arte</sup>/Lama3<sup>tm1Arte</sup> Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:27729280	20190212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644074	Tbp<sup>tm1Xjl</sup>	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:5693885	Tbp<sup>tm1Xjl</sup>/Tbp<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129S/SvEv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24462098	20151028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5704099	Ube3a<sup>tm1Yelg</sup>	is_implicated_in	DOID:1932	Angelman syndrome		MGI:5704111	Ube3a<sup>tm1Yelg</sup>/Ube3a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPasCrl			ECO:0000033	author statement supported by traceable reference	PMID:25866966	20160120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622060	Tnf<sup>tm2Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:10204494	20060511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6825765	Npnt<sup>em1Zhwe</sup>	is_implicated_in	DOID:0080200	bilateral renal aplasia		MGI:6825769	Npnt<sup>em1Zhwe</sup>/Npnt<sup>em1Zhwe</sup>  [background:] C57BL/6-Npnt<sup>em1Zhwe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34049960	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856026	Lama2<sup>dy</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:31308722	20200326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856026	Lama2<sup>dy</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3783638	Lama2<sup>dy</sup>/Lama2<sup>dy</sup>  [background:] involves: 129P1/Re			ECO:0000033	author statement supported by traceable reference	PMID:16589799	20200326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811522	Lztfl1<sup>tm1e(KOMP)Wtsi</sup>/Lztfl1<sup>tm1e(KOMP)Wtsi</sup>  [background:] involves: 129S/SvEv * C57BL/6N	is_model_of	DOID:0110139	Bardet-Biedl syndrome 17						ECO:0000033	author statement supported by traceable reference	PMID:26216965	20161209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672848	Kcnq2<sup>tm1Hsa</sup>/Kcnq2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14264	benign neonatal seizures						ECO:0000033	author statement supported by traceable reference	PMID:10854243	20050913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663620	Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:9354339	20061015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179025	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697695	20050708	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4830478	Tg(HP-MMP1a)34-1Cha/Tg(HP-MMP1a)34-1Cha  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:1458541	20100923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6155597	Magt1<sup>Gt(IST13422E1)Tigm</sup>	is_implicated_in	DOID:612	primary immunodeficiency disease		MGI:6155603	Magt1<sup>Gt(IST13422E1)Tigm</sup>/Y  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29581357	20180510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749248	Sod1<sup>m1H</sup>/Sod1<sup>m1H</sup>  [background:] involves: C3H/HeH * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25468678	20160218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588773	Tsc1<sup>tm1.1Djk</sup>/Tsc1<sup>+</sup>  [background:] either: 129S4/SvJae-Tsc1<sup>tm1Djk</sup> or (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:11875047	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720810	Prkci<sup>tm1Rfar</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22225955	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720810	Prkci<sup>tm1Rfar</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17641777	20150330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445720	Tg(Thy1-SNCA*A30P)18Pjk	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:31422098	20200113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445720	Tg(Thy1-SNCA*A30P)18Pjk	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:2652214	Tg(Thy1-SNCA*A30P)18Pjk/Tg(Thy1-SNCA*A30P)18Pjk  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12438441	20200113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148259	Dmd<sup>Gt(ROSABetageo)1Mpd</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25260053	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148259	Dmd<sup>Gt(ROSABetageo)1Mpd</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:2176880	Dmd<sup>Gt(ROSABetageo)1Mpd</sup>/Y  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:9626497	20150821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804696	Cox6a1<sup>tm1(KOMP)Wtsi</sup>/Cox6a1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6JJcl * C57BL/6N	is_model_of	DOID:0110203	Charcot-Marie-Tooth disease recessive intermediate D						ECO:0000033	author statement supported by traceable reference	PMID:25152455	20161024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5646623	Tg(Camk2a-MAPT*P301L)D35Jiri/0  [background:] Not Specified	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:25620700	20150807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473683	Coq9<sup>tm1.1Lcl</sup>/Coq9<sup>tm1.1Lcl</sup>  [background:] involves: C57BL/6 * C57BL/6NTac * SJL	is_model_of	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:23255162	20130410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417912	Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte/Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19936202	20100115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5662267	Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:11612	polycystic ovary syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25211588	20150922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052377	Tg(HTT*/EGFP)190Nn	is_implicated_in	DOID:12858	Huntington's disease		MGI:5052380	Tg(HTT*/EGFP)190Nn/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15836623	20150303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052377	Tg(HTT*/EGFP)190Nn	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25305080	20150303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5689425	Tg(LONP1-mt-ND4*,-mCherry*)#Jguy	is_implicated_in	DOID:705	Leber hereditary optic neuropathy		MGI:5690061	Tg(LONP1-mt-ND4*,-mCherry*)#Jguy  [background:] B6(D2)-Tg(LONP1-mt-ND4*,-mCherry*)#Jguy			ECO:0000033	author statement supported by traceable reference	PMID:26438859	20151014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909983	Tmigd3<sup>Tg(H2-K-CALR*)del52Shmd</sup>	is_implicated_in	DOID:2224	essential thrombocythemia						ECO:0000033	author statement supported by traceable reference	PMID:27807369	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5629689	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0 Tg(Prnp-MAPT*P301S)PS19Vle/0  [background:] B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas Tg(Prnp-MAPT*P301S)PS19Vle	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23747045	20150415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384513	Tgfbr2<sup>tm1.2Hlm</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:35332150	20220418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6153138	Nf1<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:6275138	Nf1<sup>tm1c(KOMP)Wtsi</sup>/Nf1<sup>tm1c(KOMP)Wtsi</sup> Tg(Dhh-cre)1Mejr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27482814	20231018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4357766	Tg(Vav1-NUP98/HOXD13)C1Apla/0  [background:] FVB/N-Tg(Vav1-NUP98/HOXD13)C1Apla	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15755899	20130926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790497	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>tm1Mmt</sup> Tg(Upk2-cre)6Xrw/0 Tg(Upk2-HRAS*Q61L)5Xrw/0  [background:] involves: 129X1/SvJ * FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:21368895	20160902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5468661	Trp63<sup>tm1Cmis</sup>	is_implicated_in	DOID:0090119	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		MGI:5468673	Trp63<sup>tm1Cmis</sup>/Trp63<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23108156	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6720362	Wdr45<sup>em1Wrst</sup>	is_implicated_in	DOID:0110739	neurodegeneration with brain iron accumulation 5		MGI:6721005	Wdr45<sup>em1Wrst</sup>/Wdr45<sup>em1Wrst</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:34043061	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6720362	Wdr45<sup>em1Wrst</sup>	is_implicated_in	DOID:0110739	neurodegeneration with brain iron accumulation 5		MGI:6721006	Wdr45<sup>em1Wrst</sup>/Y  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:34043061	20210714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5431238	Tg(Thy1-Sncg)HvP36Putt/?  [background:] C57BL/6-Tg(Thy1-Sncg)HvP36Putt	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:22750530	20120815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429756	Tg(YAC72)2511Hay	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:22633949	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429756	Tg(YAC72)2511Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:3722277	Tg(YAC72)2511Hay/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10402204	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429756	Tg(YAC72)2511Hay	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432191	Tg(YAC72)2511Hay/Tg(YAC72)2511Hay  [background:] FVB/N-Tg(YAC72)2511Hay			ECO:0000033	author statement supported by traceable reference	PMID:16165367	20140626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838323	Ttn<sup>tm1.1Isrd</sup>/Ttn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:0111078	tibial muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:20855473	20101115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177529	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] B6.129P2-Cftr<sup>tm1Unc</sup>/J	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:10570187	20070827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177529	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] B6.129P2-Cftr<sup>tm1Unc</sup>/J	is_model_of	DOID:1485	cystic fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:15246977	20070827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663021	Fas<sup>lpr</sup>/Fas<sup>lpr</sup> Tg(Ins2-Fasl)24Ach/0  [background:] NOD.Cg-Fas<sup>lpr</sup> Tg(Ins2-Fasl)24Ach	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12525697	20061006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510458	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] 129X1/SvJ-Col4a3<sup>tm1Dec</sup>	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9682811	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5750701	Atxn3<sup>tm2.1(ATXN3*)Mfig</sup>/Atxn3<sup>+</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:25301414	20160301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830510	Tg(Camk2a-Tardbp)#Ckjs	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:20660618	20130131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830510	Tg(Camk2a-Tardbp)#Ckjs	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:4830521	Tg(Camk2a-Tardbp)#Ckjs/Tg(Camk2a-Tardbp)#Ckjs  [background:] FVB/N-Tg(Camk2a-Tardbp)#Ckjs			ECO:0000033	author statement supported by traceable reference	PMID:20660618	20130131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6881752	Setx<sup>tm1.1Als</sup>	is_implicated_in	DOID:0060196	amyotrophic lateral sclerosis type 4		MGI:6883565	Setx<sup>tm1.1Als</sup>/Setx<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29725819	20220225	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838185	Ethe1<sup>tm1.1Zev</sup>/Ethe1<sup>tm1.1Zev</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0060640	ethylmalonic encephalopathy						ECO:0000033	author statement supported by traceable reference	PMID:19136963	20090401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3036892	Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:8524813	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842819	Tg(TcraR28,TcrbR28)KRNDim/0  [background:] involves: C57BL/6 * NOD * SJL	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:8945509	20090505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6390909	Col7a1<sup>em#Jtol</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:6390913	Col7a1<sup>em#Jtol</sup>/Col7a1<sup>em#Jtol</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/Ka * NOD			ECO:0000033	author statement supported by traceable reference	PMID:28892093	20200218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624973	X/Yaa  [background:] BXSB/MpJ	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:6363600	20121219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624973	X/Yaa  [background:] BXSB/MpJ	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:762500	20121219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624973	X/Yaa  [background:] BXSB/MpJ	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:315777	20121219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587642	Myo7a<sup>sh1-9J</sup>/Myo7a<sup>sh1-9J</sup>  [background:] involves: C3.MRL-Fas<sup>lpr</sup>/J	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:1276604	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7439059	Iigp1c<sup>em1Btlr</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:7439148	Iigp1c<sup>em1Btlr</sup>/Iigp1c<sup>em1Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>em1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6510879	Nexn<sup>em1Chen</sup>	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6511077	Nexn<sup>em1Chen</sup>/Nexn<sup>em1Chen</sup>  [background:] C57BL/6J-Nexn<sup>em1Chen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32814711	20210318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259993	Col10a1<sup>tm2.1Rpbh</sup>	is_implicated_in	DOID:0080021	Schmid metaphyseal chondrodysplasia		MGI:6259995	Col10a1<sup>tm2.1Rpbh</sup>/Col10a1<sup>tm2.1Rpbh</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:30010889	20181213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259993	Col10a1<sup>tm2.1Rpbh</sup>	is_implicated_in	DOID:0080021	Schmid metaphyseal chondrodysplasia		MGI:6259994	Col10a1<sup>tm2.1Rpbh</sup>/Col10a1<sup>+</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:30010889	20181213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821828	Dnah11<sup>avc4</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822145	Dnah11<sup>avc4</sup>/Dnah11<sup>avc4</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4936750	Tg(CAG-Rpgr)mRDefWrght	is_implicated_in	DOID:0110414	retinitis pigmentosa 3		MGI:5313503	Tg(CAG-Rpgr)mRDefWrght/0  [background:] C57BL/6-Tg(CAG-Rpgr)mRDefWrght			ECO:0000033	author statement supported by traceable reference	PMID:21546531	20120330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450918	Best1<sup>tm1.1Amar</sup>/Best1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c	is_model_of	DOID:0050662	bestrophinopathy						ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835242	Tg(MMTV-ENPP2)21Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763078	Tg(MMTV-ENPP2)21Gbm/0  [background:] FVB/N-Tg(MMTV-ENPP2)21Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690366	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup> Ptch2<sup>tm1Pmc</sup>/Ptch2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:16849540	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804652	Camkmt<sup>tm1Rpav</sup>/Camkmt<sup>tm1Rpav</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0060858	hypotonia-cystinuria syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25548191	20161024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5526981	Dnaaf2<sup>tm1.1Mkis</sup>	is_implicated_in	DOID:0110612	primary ciliary dyskinesia 10		MGI:5526986	Dnaaf2<sup>tm1.1Mkis</sup>/Dnaaf2<sup>tm1.1Mkis</sup>  [background:] involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23525783	20191107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698855	Htt<sup>tm2Msl</sup>/Htt<sup>tm2Msl</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:12223581	20070306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698855	Htt<sup>tm2Msl</sup>/Htt<sup>tm2Msl</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10533044	20070306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510680	Zic1/Zic4<sup>tm1Kjmi</sup>	is_implicated_in	DOID:2785	Dandy-Walker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22947655	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510680	Zic1/Zic4<sup>tm1Kjmi</sup>	is_implicated_in	DOID:2785	Dandy-Walker syndrome		MGI:3511193	Zic1/Zic4<sup>tm1Kjmi</sup>/Zic1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15338008	20130129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5426823	Krt16<sup>tm1(KOMP)Vlcg</sup>/Krt16<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Krt16<sup>tm1(KOMP)Vlcg</sup>	is_model_of	DOID:0050428	nonepidermolytic palmoplantar keratoderma						ECO:0000033	author statement supported by traceable reference	PMID:22336941	20120703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722926	Alpl<sup>Hpp</sup>/Alpl<sup>Hpp</sup>  [background:] involves: BALB/cAnN * C3H/HeH	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:17539739	20120620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449488	Btk<sup>tm1Gsv</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:8890160	20081222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2663842	Bloc1s4<sup>cno</sup>/Bloc1s4<sup>cno</sup>  [background:] C3H/HeJ-Bloc1s4<sup>cno</sup>	is_model_of	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11110696	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670271	Ro60<sup>tm1Woln</sup>/Ro60<sup>tm1Woln</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462465	Tg(CBS)11181Eri	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:22854956	20130211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6117472	Eif2b5<sup>tm1.1Vdk</sup>	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6160484	Eif2b5<sup>tm1.1Vdk</sup>/Eif2b5<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448404	Tg(Col11a2-Npr2*)28Keoz	is_implicated_in	DOID:0080006	bone development disease		MGI:5448405	Tg(Col11a2-Npr2*)28Keoz/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22870295	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857267	Vldlr<sup>tm1Her</sup>	is_implicated_in	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:23978600	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857267	Vldlr<sup>tm1Her</sup>	is_implicated_in	DOID:0110014	age related macular degeneration 1						ECO:0000033	author statement supported by traceable reference	PMID:28980001	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857267	Vldlr<sup>tm1Her</sup>	is_implicated_in	DOID:0110014	age related macular degeneration 1		MGI:3797222	Vldlr<sup>tm1Her</sup>/Vldlr<sup>tm1Her</sup>  [background:] B6;129S7-Vldlr<sup>tm1Her</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18172119	20180315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7256880	Mybpc1<sup>em1Lbmc</sup>	is_implicated_in	DOID:0081337	congenital myopathy		MGI:7258345	Mybpc1<sup>em1Lbmc</sup>/Mybpc1<sup>+</sup>  [background:] C57BL/6NTac-Mybpc1<sup>em1Lbmc</sup>/Lmcb			ECO:0000033	author statement supported by traceable reference	MGI:7256878	20230605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156542	Dsp<sup>tm1Efu</sup>	is_implicated_in	DOID:0110076	arrhythmogenic right ventricular dysplasia 8						ECO:0000033	author statement supported by traceable reference	PMID:33857019	20220722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156542	Dsp<sup>tm1Efu</sup>	is_implicated_in	DOID:0110076	arrhythmogenic right ventricular dysplasia 8						ECO:0000033	author statement supported by traceable reference	PMID:24276085	20220722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156542	Dsp<sup>tm1Efu</sup>	is_implicated_in	DOID:0110076	arrhythmogenic right ventricular dysplasia 8		MGI:5660416	Dsp<sup>tm1Efu</sup>/Dsp<sup>tm1Efu</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129 * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24108106	20220722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449115	Aprt<sup>tm1Jat</sup>/Aprt<sup>tm1Jat</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:0060350	adenine phosphoribosyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8643571	20120924	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805720	Gp1bb<sup>tm1Frla</sup>/Gp1bb<sup>tm1Frla</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:2217	Bernard-Soulier syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17095718	20111110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5828836	Nkx2-5<sup>tm3.1Mwc</sup>	is_implicated_in	DOID:0110112	atrial heart septal defect 7		MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5775294	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL	is_model_of	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:24520391	20160607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842820	H2<sup>b</sup>/H2<sup>g7</sup> Tg(TcraR28,TcrbR28)KRNDim/0  [background:] involves: C57BL/6 * NOD * SJL	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:8945509	20090505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691068	Tg(tetO-Tek)1Dmt	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:22418873	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691068	Tg(tetO-Tek)1Dmt	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:21471984	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691068	Tg(tetO-Tek)1Dmt	is_implicated_in	DOID:8893	psoriasis		MGI:6268445	Tg(Tek-tTA)1Dmt/0 Tg(tetO-Tek)1Dmt/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15743796	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691068	Tg(tetO-Tek)1Dmt	is_implicated_in	DOID:8893	psoriasis		MGI:3842959	Tg(KRT5-tTA)1216Glk/0 Tg(tetO-Tek)1Dmt/0  [background:] involves: CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19342373	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5465281	Srgap3<sup>tm1.1Zi</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5465282	Srgap3<sup>tm1.1Zi</sup>/Srgap3<sup>tm1.1Zi</sup>  [background:] B6.129(SJL)-Srgap3<sup>tm1.1Zi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22820399	20130221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6510877	Nexn<sup>tm1Chen</sup>	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6514899	Nexn<sup>tm1Chen</sup>/Nexn<sup>tm1Chen</sup> Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: MF1			ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6510877	Nexn<sup>tm1Chen</sup>	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6514900	Nexn<sup>tm1Chen</sup>/Nexn<sup>tm1Chen</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683845	Blm<sup>tm1Ches</sup>/Blm<sup>tm3Brd</sup>  [background:] involves: 129S/SvEv * C57BL/6 * NIH Black Swiss	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14642567	20050714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839772	Hfe<sup>tm1Gfn</sup>/Hfe<sup>tm1Gfn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10557317	20180801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839772	Hfe<sup>tm1Gfn</sup>/Hfe<sup>tm1Gfn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:20976594	20180801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4843272	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Gnas)1593Mpke/0  [background:] B6.Cg-Tg(Camk2a-tTA)1Mmay Tg(tetO-Gnas)1593Mpke	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19030002	20101209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054666	Eya1<sup>tm1Rilm</sup>/Eya1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c)	is_model_of	DOID:14702	branchiootorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5698701	Rab18<sup>m1Hongc</sup>	is_implicated_in	DOID:0110718	Warburg micro syndrome 3		MGI:5698703	Rab18<sup>m1Hongc</sup>/Rab18<sup>m1Hongc</sup>  [background:] C57BL/6J-Rab18<sup>m1Hongc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25779931	20151211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5616630	Mbnl2<sup>tm1.1Sws</sup>	is_implicated_in	DOID:450	myotonic disease						ECO:0000033	author statement supported by traceable reference	PMID:29331264	20181107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794044	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:14323	Marfan syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17293478	20080617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3640114	Slc6a4<sup>tm1Kpl</sup>/Slc6a4<sup>tm1Kpl</sup>  [background:] B6.129-Slc6a4<sup>tm1Kpl</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23142422	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575899	Igh<sup>tm1(Myc)Janz</sup>/Igh<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:8584	Burkitt lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:15735016	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055578	Dysf<sup>tm1Meho</sup>/Dysf<sup>tm1Meho</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:15254015	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037661	Gy/Y  [background:] involves: C3H/Sn * C57BL/6Ei	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15029877	20100308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037661	Gy/Y  [background:] involves: C3H/Sn * C57BL/6Ei	is_model_of	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:9063736	20100308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5563473	Bbip1<sup>tm1.1Gne</sup>	is_implicated_in	DOID:0110140	Bardet-Biedl syndrome 18		MGI:5563481	Bbip1<sup>tm1.1Gne</sup>/Bbip1<sup>tm1.1Gne</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24316073	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5315747	Wdr19<sup>twto</sup>	is_implicated_in	DOID:0060340	ciliopathy		MGI:5315749	Wdr19<sup>twto</sup>/Wdr19<sup>twto</sup>  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:22228095	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695719	Krt4<sup>Bcc1</sup>/Krt4<sup>Bcc1</sup>  [background:] C3HeB/FeJ-Krt4<sup>Bcc1</sup>	is_model_of	DOID:0050448	white sponge nevus						ECO:0000033	author statement supported by traceable reference	PMID:16858417	20070206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5583981	Ryr2<sup>tm2Hhv</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000033	author statement supported by traceable reference	PMID:23152493	20140922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861915	Cstb<sup>tm1Rm</sup>	is_implicated_in	DOID:3535	Unverricht-Lundborg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24603771	20150518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861915	Cstb<sup>tm1Rm</sup>	is_implicated_in	DOID:3535	Unverricht-Lundborg syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24586687	20150518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861915	Cstb<sup>tm1Rm</sup>	is_implicated_in	DOID:3535	Unverricht-Lundborg syndrome		MGI:3040574	Cstb<sup>tm1Rm</sup>/Cstb<sup>tm1Rm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11555622	20150518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861915	Cstb<sup>tm1Rm</sup>	is_implicated_in	DOID:3535	Unverricht-Lundborg syndrome		MGI:3040574	Cstb<sup>tm1Rm</sup>/Cstb<sup>tm1Rm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9806543	20150518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6116819	Arid1b<sup>em1Hzhu</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6159715	Arid1b<sup>em1Hzhu</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Hzhu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28695822	20180606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821824	Ift172<sup>avc1</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822142	Ift172<sup>avc1</sup>/Ift172<sup>avc1</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5467982	Atxn2<sup>tm2.1Aub</sup>	is_implicated_in	DOID:0050955	spinocerebellar ataxia type 2		MGI:5467984	Atxn2<sup>tm2.1Aub</sup>/Atxn2<sup>tm2.1Aub</sup>  [background:] B6.129S2-Atxn2<sup>tm2.1Aub</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22956915	20130307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798607	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:19535499	20180205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798607	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:21893021	20180205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome		MGI:2179045	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9990064	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767789	Tg(CAG-AR*97Q)7-8Sobue/?  [background:] involves: C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:17991424	20080117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5707946	Tg(Thy1-DCTN1*G59S)M2Pcw/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:18305234	20160211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639581	Zic2<sup>Ku</sup>/Zic2<sup>Ku</sup>  [background:] C3.CAnNCrl-Zic2<sup>Ku</sup>	is_model_of	DOID:0110878	holoprosencephaly 5						ECO:0000033	author statement supported by traceable reference	PMID:18617531	20170303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046580	Bub1b<sup>tm1Jvd</sup>	is_implicated_in	DOID:0080141	mosaic variegated aneuploidy syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:37900274	20231110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6117465	Eif2b4<sup>tm1.1Vdk</sup>	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6160483	Eif2b4<sup>tm1.1Vdk</sup>/Eif2b4<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424980	Casr<sup>BCH003</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425919	Casr<sup>BCH003</sup>/Casr<sup>BCH003</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH003</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641251	Fxn<sup>tm1Pand</sup>	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25113747	20150317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819012	Tg(tetO-NEFL)173.2Jpj	is_implicated_in	DOID:0110165	Charcot-Marie-Tooth disease type 2E		MGI:4819094	Tg(tetO-NEFL)173.2Jpj/0 Tg(THY1-tTA)177Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20421365	20100812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3826786	Pkhd1<sup>tm1Gwu</sup>/Pkhd1<sup>tm1Gwu</sup>  [background:] Not Specified	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:18235088	20090116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774474	Tg(Sox3-GFP,Tyr)HolNpln/Tg(Sox3-GFP,Tyr)HolNpln  [background:] involves: FVB/N	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:26571399	20160531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723649	Ndn<sup>tm1.1Mus</sup>/Ndn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11115855	20071008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6718491	Dzip1<sup>tm1Sasl</sup>	is_implicated_in	DOID:988	mitral valve prolapse		MGI:6718507	Dzip1<sup>tm1Sasl</sup>/Dzip1<sup>tm1Sasl</sup> Nfatc1<sup>tm1.1(cre)Bz</sup>/Nfatc1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856608	Mip<sup>Hfi</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:24120416	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856608	Mip<sup>Hfi</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175114	Mip<sup>Hfi</sup>/Mip<sup>Hfi</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:62456	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856608	Mip<sup>Hfi</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175115	Mip<sup>Hfi</sup>/Mip<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:62456	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857105	Mip<sup>Cat-Lop</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:24120416	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857105	Mip<sup>Cat-Lop</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175113	Mip<sup>Cat-Lop</sup>/Mip<sup>+</sup>  [background:] involves: STOCK Rb(6.15)1Ald			ECO:0000033	author statement supported by traceable reference	PMID:8563764	20141009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5514339	Tg(CTSG-RARA/ZBTB16)#Ppp/0 Tg(CTSG-ZBTB16/RARA)#Ppp/0  [background:] Not Specified	is_model_of	DOID:0060318	acute promyelocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:11106752	20131024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511195	Zic1/Zic4<sup>tm1Kjmi</sup>/Zic4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:2785	Dandy-Walker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15338008	20050830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437101	b2b1200Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529794	Tg(Thy1-MAPT*)1Avil/Tg(Thy1-MAPT*)1Avil  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:23774255	20140123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5781001	Ptch1<sup>tm1Yy</sup>/Ptch1<sup>+</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup> Tg(BGLAP-cre)1Clem/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:24141783	20160721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857873	Sod1<sup>tm1Leb</sup>	is_implicated_in	DOID:10140	dry eye syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24991185	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857873	Sod1<sup>tm1Leb</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:3820405	Sod1<sup>tm1Leb</sup>/Sod1<sup>tm1Leb</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25036096	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856575	Ush1g<sup>js</sup>	is_implicated_in	DOID:0110834	Usher syndrome type 1G						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20150916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856575	Ush1g<sup>js</sup>	is_implicated_in	DOID:0110834	Usher syndrome type 1G		MGI:3581211	Ush1g<sup>js</sup>/Ush1g<sup>js</sup>  [background:] B6.A-Ush1g<sup>js</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12588793	20150916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857936	Pten<sup>tm1Ppp</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618825	1700093K21Rik<sup>b2b3025Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5618826	1700093K21Rik<sup>b2b3025Clo</sup>/1700093K21Rik<sup>b2b3025Clo</sup>  [background:] C57BL/6J-1700093K21Rik<sup>b2b3025Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810960	Cdc14a<sup>em1Tbf</sup>	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694869	Cdc14a<sup>em1Tbf</sup>/Cdc14a<sup>em1Tbf</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3654321	Pjvk<sup>tm1Ugds</sup>/Pjvk<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:0110511	autosomal recessive nonsyndromic deafness 59						ECO:0000033	author statement supported by traceable reference	PMID:16804542	20060912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5800483	Tg(Myh6*/tetO-SCN5A*F1759A)#Marx	is_implicated_in	DOID:0110433	dilated cardiomyopathy 1E		MGI:5800485	Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0  [background:] involves: C57BL/6 * CBA * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:26595809	20161013	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3707433	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Rbl1<sup>tm1Tyj</sup>/Rbl1<sup>tm1Tyj</sup> Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129S2/SvPas * 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:17235288	20080501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438494	Tg(Thy1-TARDBP)4Singh/0  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:20133711	20100402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052754	Trex1<sup>tm1Tld</sup>	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24218451	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052754	Trex1<sup>tm1Tld</sup>	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome		MGI:3053060	Trex1<sup>tm1Tld</sup>/Trex1<sup>tm1Tld</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:18724932	20140407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425921	Casr<sup>BCH007</sup>/Casr<sup>BCH007</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH007</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055584	Bbs1<sup>Gt1Nk</sup>/Bbs1<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15322545	20050603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623593	Ighm<sup>tm1Cgn</sup>/Ighm<sup>+</sup> Tg(Igh-6/Igh-V281)3Jwt/0  [background:] NOD.Cg-Ighm<sup>tm1Cgn</sup> Tg(Igh-6/Igh-V281)3Jwt	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:11698422	20060601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661024	Lyst<sup>bg-slt</sup>/Lyst<sup>bg-slt</sup>  [background:] YZ57/Ch	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:13943454	20051103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949204	Foxo3<sup>mommeR1</sup>	is_implicated_in	DOID:5117	dermoid cyst of ovary		MGI:4949205	Foxo3<sup>mommeR1</sup>/Foxo3<sup>mommeR1</sup> Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew  [background:] FVB/NJ-Foxo3<sup>mommeR1</sup> Tg(HBA1-Gfp)1Ew			ECO:0000033	author statement supported by traceable reference	PMID:21347845	20110505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4887395	Ryr1<sup>tm2.1Alle</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:8545	malignant hyperthermia						ECO:0000033	author statement supported by traceable reference	PMID:17122579	20110210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6195852	Arx<sup>tm1.1Ics</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:6195853	Arx<sup>tm1.1Ics</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29659809	20180829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3802584	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(GFAP-cre)8Gtm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:17714952	20110128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3802584	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(GFAP-cre)8Gtm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:21062901	20110128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560263	Ift140<sup>b2b1283Clo</sup>	is_implicated_in	DOID:0110097	short-rib thoracic dysplasia 9 with or without polydactyly		MGI:5560283	Ift140<sup>b2b1283Clo</sup>/Ift140<sup>b2b1283Clo</sup>  [background:] C57BL/6J-Ift140<sup>b2b1283Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3026650	Vegfc<sup>tm1Ali</sup>	is_implicated_in	DOID:0050580	hereditary lymphedema						ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3026650	Vegfc<sup>tm1Ali</sup>	is_implicated_in	DOID:0050580	hereditary lymphedema		MGI:3026664	Vegfc<sup>tm1Ali</sup>/Vegfc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5502687	Ar<sup>tm1Verh</sup>/Y Tg(Fabp4-cre)1Rev/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:22415878	20130827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574539	Dok2<sup>tm1Yyam</sup>/Dok2<sup>tm1Yyam</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: C57BL/6	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611294	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028633	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm1Antc</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14701729	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5484771	Ap3d1<sup>mh-4J</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:5559208	Ap3d1<sup>mh-4J</sup>/Ap3d1<sup>mh-4J</sup>  [background:] involves: 129P2/OlaHsd * BALB/cByJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:5558048	20140416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0080052	acromesomelic dysplasia, Grebe type		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789526	Tg(Myh6-Pln*R9C)#Ces	is_implicated_in	DOID:0110439	dilated cardiomyopathy 1P						ECO:0000033	author statement supported by traceable reference	PMID:19139388	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789526	Tg(Myh6-Pln*R9C)#Ces	is_implicated_in	DOID:0110439	dilated cardiomyopathy 1P		MGI:5883140	Tg(Myh6-Pln*R9C)#Ces/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12610310	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183146	Tsc1<sup>tm1Hin</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183146	Tsc1<sup>tm1Hin</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5641392	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] B6J.129S4-Tsc1<sup>tm1Hin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183146	Tsc1<sup>tm1Hin</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3708979	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11438694	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698734	Zap70<sup>m1Saka</sup>/Zap70<sup>m1Saka</sup>  [background:] involves: BALB/c	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:14647385	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7314213	Ighmbp2<sup>em1Cll</sup>	is_implicated_in	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1		MGI:7314416	Ighmbp2<sup>em1Cll</sup>/Ighmbp2<sup>em1Cll</sup>  [background:] FVB/NJ-Ighmbp2<sup>em1Cll</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34726235	20220720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367784	Tg(PRNP-APPSweInd)19959Dwst	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:23209315	20131101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367784	Tg(PRNP-APPSweInd)19959Dwst	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4367786	Tg(PRNP-APPSweInd)19959Dwst/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21925470	20131101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5788680	Bbs10<sup>tm1.2Vmar</sup>	is_implicated_in	DOID:0110132	Bardet-Biedl syndrome 10		MGI:5792863	Bbs10<sup>tm1.2Vmar</sup>/Bbs10<sup>tm1.2Vmar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26273430	20160922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5817903	Col5a2<sup>tm1.2Dgr</sup>/Col5a2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * DBA/2	is_model_of	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000033	author statement supported by traceable reference	PMID:25987251	20170117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722314	Dmd<sup>tm1Mok</sup>/Y  [background:] involves: 129S/SvEv	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9299538	20070921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5694699	Srsf2<sup>tm1.1Oaw</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5695364	Srsf2<sup>tm1.1Oaw</sup>/Srsf2<sup>+</sup> Tg(Mx1-cre)1Cgn/?  [background:] B6.Cg-Tg(Mx1-cre)1Cgn Srsf2<sup>tm1.1Oaw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25965569	20151110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819721	Tg(Myh6-TNNT2*R141W)#Ajm	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:4819724	Tg(Myh6-TNNT2*R141W)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18349139	20100819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822157	Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0 Tg(Tek-cre)12Flv/0  [background:] involves: C3H * C57BL/6 * FVB/N	is_model_of	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:19017799	20090105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822779	Hesx1<sup>tm2Jpmb</sup>/Hesx1<sup>tm2Jpmb</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N	is_model_of	DOID:0060857	septooptic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19093031	20090113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311372	Dnah11<sup>b2b598Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5312336	Dnah11<sup>b2b598Clo</sup>/Dnah11<sup>b2b598Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b598Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6510878	Nexn<sup>tm1.1Chen</sup>	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6514898	Nexn<sup>tm1.1Chen</sup>/Nexn<sup>tm1.1Chen</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832567	Tg(SOD1*G85R)74Dwc/?  [background:] Not Specified	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:9052802	20090220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620543	Maoa<sup>Tg(H2-K1-Ifnb1)8Seif</sup>/Y  [background:] involves: C3H/HeJ	is_model_of	DOID:0060693	Brunner Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:7792602	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676096	Tg(Tyr-HRAS)60Lc	is_implicated_in	DOID:6039	uveal melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26354726	20160812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5306920	Lmna<sup>tm2.1Gbon</sup>/Lmna<sup>tm2.1Gbon</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0110640	congenital muscular dystrophy due to LMNA mutation						ECO:0000033	author statement supported by traceable reference	PMID:22090424	20120223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821790	Gjb1<sup>tm1Kwi</sup>/Y  [background:] involves: 129S4/SvJae	is_model_of	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1						ECO:0000033	author statement supported by traceable reference	PMID:9169515	20100906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663671	Sp4<sup>tm3(Sp4)Krc</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:23823008	20140319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663671	Sp4<sup>tm3(Sp4)Krc</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3713111	Sp4<sup>tm3(Sp4)Krc</sup>/Sp4<sup>tm3(Sp4)Krc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:20634195	20140319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308732	Becn1<sup>tm1Ebr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287976	Becn1<sup>tm1Ebr</sup>/Becn1<sup>tm1Ebr</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5575891	Tg(Myh6-KCNQ1_i2)H05Desc	is_implicated_in	DOID:0110644	long QT syndrome 1		MGI:5575895	Tg(Myh6-KCNQ1_i2)H05Desc/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:23542581	20140805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5648530	Tg(tetO-Kras*G12D)#Rdp	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25119024	20150814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867909	Myb<sup>boo</sup>	is_implicated_in	DOID:4971	myelofibrosis		MGI:4868118	Myb<sup>boo</sup>/Myb<sup>boo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20610815	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388241	Sh2d1a<sup>tm1Pls</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:26764158	20160824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388241	Sh2d1a<sup>tm1Pls</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3036915	Sh2d1a<sup>tm1Pls</sup>/Sh2d1a<sup>tm1Pls</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11404475	20160824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:24802098	20150331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:4829790	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:24802098	20150331	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295417	Mcm9<sup>Gt(AW0655)Wtsi</sup>/Mcm9<sup>Gt(AW0655)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446570	Trps1<sup>tm1.1Shiv</sup>	is_implicated_in	DOID:14743	trichorhinophalangeal syndrome type I						ECO:0000033	author statement supported by traceable reference	PMID:31130868	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446570	Trps1<sup>tm1.1Shiv</sup>	is_implicated_in	DOID:14743	trichorhinophalangeal syndrome type I		MGI:3723222	Trps1<sup>tm1.1Shiv</sup>/Trps1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12446778	20200629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794861	Tg(LCR-HBA2,LCR-HBB)11Cos	is_implicated_in	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:25706118	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569533	Tg(CMV-HTT*48Q)BTag/0  [background:] involves: FVB/N	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:9771716	20140625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6279851	Sh3rf2<sup>tm1Zhxu</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6430624	Sh3rf2<sup>tm1Zhxu</sup>/Sh3rf2<sup>+</sup> Tg(Thy1-EGFP)MJrs/0  [background:] involves: C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:30540932	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6279851	Sh3rf2<sup>tm1Zhxu</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6430623	Sh3rf2<sup>tm1Zhxu</sup>/Sh3rf2<sup>+</sup>  [background:] C57BL/6-Sh3rf2<sup>tm1Zhxu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30540932	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7284431	Npsr1<sup>em1Yfu</sup>	is_implicated_in	DOID:535	sleep disorder		MGI:7284791	Npsr1<sup>em1Yfu</sup>/Npsr1<sup>+</sup>  [background:] C57BL/6J-Npsr1<sup>em1Yfu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31619542	20220610	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5790500	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>tm1Mmt</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Upk2-cre)6Xrw/0  [background:] involves: 129S4/SvJae * 129X1/SvJ * FVB/N	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:21368895	20160902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6729893	Atp1a2<sup>tm1.1Gica</sup>	is_implicated_in	DOID:0111182	familial hemiplegic migraine 2						ECO:0000033	author statement supported by traceable reference	PMID:33321071	20210810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6729893	Atp1a2<sup>tm1.1Gica</sup>	is_implicated_in	DOID:0111182	familial hemiplegic migraine 2		MGI:6729923	Atp1a2<sup>tm1.1Gica</sup>/Atp1a2<sup>+</sup>  [background:] B6.Cg-Atp1a2<sup>tm1.1Gica</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21731499	20210810	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584471	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm3.1Tyj</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJae	is_model_of	DOID:3012	Li-Fraumeni syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897176	Tg(CAG-Ppard*E411P)#Als/0 Tg(Nes-cre)1Kln/0  [background:] B6J.Cg-Tg(Nes-cre)1Kln Tg(CAG-Ppard*E411P)#Als	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:26642438	20170511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440289	Tg(RHO-P23H)DTpd/?  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:1418997	20121101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313511	Tg(Myh6-Actc1*R312H)307Iko	is_implicated_in	DOID:0110456	dilated cardiomyopathy 1R		MGI:5313516	Tg(Myh6-Actc1*R312H)307Iko/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20713897	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313511	Tg(Myh6-Actc1*R312H)307Iko	is_implicated_in	DOID:0110456	dilated cardiomyopathy 1R						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038222	Gck<sup>Rgsc702</sup>/Gck<sup>Rgsc702</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663312	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Tg(SMN1*A2G)2023Ahmb/0 Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:12376	juvenile spinal muscular atrophy						ECO:0000033	author statement supported by traceable reference	PMID:12515823	20061011	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755045	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas  [background:] B6.Cg-Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25697701	20160330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5563101	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>tm1.1Teti</sup>  [background:] involves: 129S2/SvPas * CD-1	is_model_of	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:24185277	20140509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491040	Mecp2<sup>tm1.1Bird</sup>/Y Tg(MECP2*R270X/GFP)AHzo/0  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23452848	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5429329	Tg(SNCA)ARyot/0  [background:] C57BL/6J-Tg(SNCA)ARyot	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:22475625	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5634777	Tg(EIF1AX-Lin28a)#Gqda	is_implicated_in	DOID:2154	nephroblastoma		MGI:5638792	Tg(Ddx4-cre)1Dcas/0 Tg(EIF1AX-Lin28a)#Gqda/0  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24732380	20150609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5295268	Cntnap2<sup>tm1Pele</sup>/Cntnap2<sup>tm1Pele</sup>  [background:] B6.129-Cntnap2<sup>tm1Pele</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21962519	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040629	Dmp1<sup>tm1Mis</sup>	is_implicated_in	DOID:0050949	autosomal recessive hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:26721590	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040629	Dmp1<sup>tm1Mis</sup>	is_implicated_in	DOID:0050949	autosomal recessive hypophosphatemic rickets		MGI:5694692	Dmp1<sup>tm1Mis</sup>/Dmp1<sup>tm1Mis</sup>  [background:] involves: 129S7/SvEvBrd * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21542006	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6324050	Tg(CAG-Ptafr)1Tksh	is_implicated_in	DOID:8923	skin melanoma		MGI:6324051	Tg(CAG-Ptafr)1Tksh/0  [background:] B6;D2-Tg(CAG-Ptafr)1Tksh/TkshRbrc			ECO:0000033	author statement supported by traceable reference	PMID:9009274	20190719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5002630	Pdcd10<sup>tm1Wami</sup>	is_implicated_in	DOID:0060671	cerebral cavernous malformation 3						ECO:0000033	author statement supported by traceable reference	PMID:28500274	20180122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5002630	Pdcd10<sup>tm1Wami</sup>	is_implicated_in	DOID:0060671	cerebral cavernous malformation 3		MGI:5002697	Pdcd10<sup>tm1Wami</sup>/Pdcd10<sup>tm1Wami</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21321212	20180122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386937	Dyrk1a<sup>tm1Mla</sup>	is_implicated_in	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23512985	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5505450	Chd7<sup>Looper</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:6281675	Chd7<sup>Looper</sup>/Chd7<sup>+</sup>  [background:] BALB/c-Chd7<sup>Looper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24840056	20190308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385566	Tg(Prnp-MAPT)43Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22464332	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385566	Tg(Prnp-MAPT)43Vle	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3663447	Tg(Prnp-MAPT)43Vle/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10595524	20120918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838640	Sav1<sup>tm1.1Dupa</sup>	is_implicated_in	DOID:5353	colonic disease		MGI:4838642	Sav1<sup>tm1.1Dupa</sup>/Sav1<sup>tm1.1Dupa</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21041407	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7414300	Ubap1<sup>em1Yta</sup>	is_implicated_in	DOID:0112341	hereditary spastic paraplegia 80		MGI:7414333	Ubap1<sup>em1Yta</sup>/Ubap1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:35962060	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437098	b2b227Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5505596	Epg5<sup>tm1Ygz</sup>	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:5505671	Epg5<sup>tm1Ygz</sup>/Epg5<sup>tm1Ygz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23479740	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3841005	Ccr2<sup>tm1Mae</sup>/Ccr2<sup>tm1Mae</sup>  [background:] B6.129P2-Ccr2<sup>tm1Mae</sup>	is_model_of	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:14566334	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428742	Tg(Wap-TAg)1Depp	is_implicated_in	DOID:0060074	ductal carcinoma in situ		MGI:5428746	Tg(Wap-TAg)1Depp/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10713686	20170713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177468	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:7550345	20130125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177468	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:3323	Sandhoff disease						ECO:0000033	author statement supported by traceable reference	PMID:23028353	20130125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294944	Tg(CAG-NRIP1)51Row	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5294945	Tg(CAG-NRIP1)51Row/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20083575	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038695	Hapln1<sup>tm1Nid</sup>/Hapln1<sup>tm1Nid</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:9988279	20051006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3696575	Tg(APP695)3Dbo/0  [background:] B6.C3-Tg(APP695)3Dbo	is_model_of	DOID:0110040	Alzheimer's disease 4						ECO:0000033	author statement supported by traceable reference	PMID:12742740	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3715440	Rd3<sup>rd3</sup>/Rd3<sup>rd3</sup>  [background:] RBF/DnJ-Rd3<sup>rd3</sup>	is_model_of	DOID:0110080	Leber congenital amaurosis 12						ECO:0000033	author statement supported by traceable reference	PMID:23687432	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7494069	Stmn2<sup>em1Jmi</sup>	is_implicated_in	DOID:2477	motor peripheral neuropathy		MGI:7523314	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>+</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623218	Disc1<sup>tm1Kara</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623218	Disc1<sup>tm1Kara</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:27613435	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623218	Disc1<sup>tm1Kara</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3623253	Disc1<sup>tm1Kara</sup>/Disc1<sup>tm1Kara</sup>  [background:] B6.129S6-Disc1<sup>tm1Kara</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16484369	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623218	Disc1<sup>tm1Kara</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3623286	Disc1<sup>tm1Kara</sup>/Disc1<sup>+</sup>  [background:] B6.129S6-Disc1<sup>tm1Kara</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16484369	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6161436	b2b3183Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6161438	b2b3183Clo/b2b3183Clo  [background:] C57BL/6J-b2b3183Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20180618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317113	Lgi1<sup>tm1.1Ics</sup>	is_implicated_in	DOID:0060748	familial temporal lobe epilepsy 1		MGI:5317116	Lgi1<sup>tm1.1Ics</sup>/Lgi1<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20659958	20120502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5586972	Krt71<sup>Ca-19J</sup>	is_implicated_in	DOID:0110710	hypotrichosis 13		MGI:5586979	Krt71<sup>Ca-19J</sup>/Krt71<sup>+</sup>  [background:] BALB/cJ-Krt71<sup>Ca-19J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5586973	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679597	Lamc2<sup>tm1Uit</sup>	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:23321329	20220207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679597	Lamc2<sup>tm1Uit</sup>	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:2679609	Lamc2<sup>tm1Uit</sup>/Lamc2<sup>tm1Uit</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14632187	20220207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:3627	aortic aneurysm						ECO:0000033	author statement supported by traceable reference	PMID:7769737	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:3627	aortic aneurysm		MGI:3793728	Atp7a<sup>Mo-blo</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:3385878	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:3627	aortic aneurysm		MGI:3793784	Atp7a<sup>Mo-blo</sup>/Atp7a<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:1115218	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:3627	aortic aneurysm		MGI:3793728	Atp7a<sup>Mo-blo</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:1115218	20190722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6198748	Zfp462<sup>Tn(pb-Act-RFP)1.090115023-HRAZhu</sup>	is_implicated_in	DOID:14320	generalized anxiety disorder		MGI:6198752	Zfp462<sup>Tn(pb-Act-RFP)1.090115023-HRAZhu</sup>/Zfp462<sup>+</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27621227	20180920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512702	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA)0Olri/0  [background:] involves: C57BL/6	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:18322092	20131015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7464273	Got2<sup>em3Pcamp</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:7464550	Got2<sup>em3Pcamp</sup>/Got2<sup>em3Pcamp</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31422819	20230421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4949279	Grid2<sup>tm1(cre)Mwa</sup>/Grid2<sup>tm1(cre)Mwa</sup>  [background:] involves: C57BL/6N	is_model_of	DOID:0080042	autosomal recessive spinocerebellar ataxia 18						ECO:0000033	author statement supported by traceable reference	PMID:24078737	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5908461	Tg(Myh6-Mybpc3*)24Rbns	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5908514	Tg(Myh6-Mybpc3*)24Rbns/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10532952	20170907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175097	Lamb2<sup>tm1Jrs</sup>/Lamb2<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060852	Pierson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16452099	20061018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4462803	Ppib<sup>tm1.1Rjb</sup>	is_implicated_in	DOID:0110349	osteogenesis imperfecta type 9		MGI:4462833	Ppib<sup>tm1.1Rjb</sup>/Ppib<sup>tm1.1Rjb</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:19997487	20160815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5318538	Slc12a6<sup>tm1Garo</sup>	is_implicated_in	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy		MGI:5318542	Slc12a6<sup>tm1Garo</sup>/Slc12a6<sup>tm1Garo</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22423107	20180617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400521	Cacna1g<sup>em1Ftan</sup>	is_implicated_in	DOID:0111742	cerebellar ataxia type 42		MGI:6400524	Cacna1g<sup>em1Ftan</sup>/Cacna1g<sup>+</sup>  [background:] C57BL/6NCrSlc-Cacna1g<sup>em1Ftan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31229688	20200702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400521	Cacna1g<sup>em1Ftan</sup>	is_implicated_in	DOID:0111742	cerebellar ataxia type 42		MGI:6400523	Cacna1g<sup>em1Ftan</sup>/Cacna1g<sup>em1Ftan</sup>  [background:] C57BL/6NCrSlc-Cacna1g<sup>em1Ftan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31229688	20200702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682016	Gja1<sup>M1Jrt</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:22947655	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682016	Gja1<sup>M1Jrt</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:21716323	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682016	Gja1<sup>M1Jrt</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3620827	Gja1<sup>M1Jrt</sup>/Gja1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16155213	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682016	Gja1<sup>M1Jrt</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3620841	Gja1<sup>M1Jrt</sup>/Gja1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16155213	20130129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6150887	Rnf146<sup>tm1.1Rtpl</sup>	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:6150914	Rnf146<sup>tm1.1Rtpl</sup>/Rnf146<sup>tm1.1Rtpl</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28581440	20221010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033459	Hfe<sup>tm2Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:24439478	20141009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033459	Hfe<sup>tm2Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033466	Hfe<sup>tm2Sly</sup>/Hfe<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20141009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174706	Pkd2<sup>tm2Som</sup>/Pkd2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:10615132	20091021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698038	Spast<sup>tm1.1Jme</sup>	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000033	author statement supported by traceable reference	PMID:22773755	20130325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698038	Spast<sup>tm1.1Jme</sup>	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:3699155	Spast<sup>tm1.1Jme</sup>/Spast<sup>tm1.1Jme</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17101632	20130325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154693	Sgcg<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:28823869	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154693	Sgcg<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:24717843	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154693	Sgcg<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000033	author statement supported by traceable reference	PMID:23418438	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154693	Sgcg<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14982859	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154693	Sgcg<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9732288	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154693	Sgcg<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10485893	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554444	Ccdc39<sup>b2b2025.1Clo</sup>	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5555837	Ccdc39<sup>b2b2025.1Clo</sup>/Ccdc39<sup>b2b2025.1Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b2025.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459499	Del(2Nespas-Gnas)1Hju/+  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)	is_model_of	DOID:4184	pseudohypoparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:20427744	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5689483	Runx3<sup>tm3Yg</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7281829	Runx3<sup>tm3Yg</sup>/Runx3<sup>tm3Yg</sup> Tg(Pou4f1-cre/ERT2)2Jiz/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5689483	Runx3<sup>tm3Yg</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7281828	Runx3<sup>tm3Yg</sup>/Runx3<sup>tm3Yg</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3764497	Hba<sup>tm1Paz</sup>/Hba<sup>tm1Paz</sup> Hbb<sup>tm1Tow</sup>/Hbb<sup>tm1Tow</sup> Tg(HBA-HBBs)41Paz/?  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * Black Swiss * C57BL/6 * DBA/2* FVB/N	is_model_of	DOID:10923	sickle cell anemia						ECO:0000033	author statement supported by traceable reference	PMID:9346488	20071214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856330	Dmd<sup>mdx-3Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:27792813	20180319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856330	Dmd<sup>mdx-3Cv</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798606	Dmd<sup>mdx-3Cv</sup>/Y  [background:] involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus			ECO:0000033	author statement supported by traceable reference	PMID:7843915	20180319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304359	Samd9l<sup>tm1Homy</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5308655	Samd9l<sup>tm1Homy</sup>/Samd9l<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:24029230	20140701	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0080051	acromesomelic dysplasia, Hunter-Thompson type						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5763094	Tg(MMTV-LPAR1)7Gbm/Tg(MMTV-LPAR1)7Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)7Gbm	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418566	Ehmt1<sup>tm1.1Tara</sup>/Ehmt1<sup>tm1.1Tara</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:0060352	Kleefstra syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:20005824	20100125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3039683	Rpsa<sup>tp1</sup>/Rpsa<sup>tp1</sup>  [background:] involves: KK	is_model_of	DOID:0110074	arrhythmogenic right ventricular dysplasia 5						ECO:0000033	author statement supported by traceable reference	PMID:14730304	20110420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767679	Bbs1<sup>tm1Vcs</sup>/Bbs1<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:18032602	20080116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509299	Tg(SNCA*E46K)3Elan/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	MGI:5509204	20131003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805034	Hps5<sup>ru2-mr</sup>/Hps5<sup>ru2-mr</sup>  [background:] B6.Cg-Hps5<sup>ru2-mr</sup>/Re	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3847256	Tnfrsf13b<sup>tm1Vmd</sup>/Tnfrsf13b<sup>tm1Vmd</sup>  [background:] involves: C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12594954	20090609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491244	Dnm2<sup>b2b2159Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5498329	Dnm2<sup>b2b2159Clo</sup>/Dnm2<sup>b2b2159Clo</sup>  [background:] C57BL/6J-Dnm2<sup>b2b2159Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676553	Pkd2<sup>tm1Dwo</sup>/Pkd2<sup>tm1Dwo</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:12062060	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441554	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461029	Tg(Igh-V-CD40lg)#Tsub	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:4461233	Tg(Igh-V-CD40lg)#Tsub/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15128830	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3773293	Hoxa1<sup>tm3.1Mrc</sup>/Hoxa1<sup>tm3.1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0050682	Athabaskan brainstem dysgenesis syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21940751	20120408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6457568	Cfap43<sup>em1Sono</sup>	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:6457570	Cfap43<sup>em1Sono</sup>/Cfap43<sup>em1Sono</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:31004071	20200925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824059	Tg(Mpz*S63C)32Mes	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000033	author statement supported by traceable reference	PMID:20878767	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5824059	Tg(Mpz*S63C)32Mes	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3		MGI:6276568	Tg(Mpz*S63C)32Mes/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16495463	20190208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:24190659	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:3583142	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:8700894	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:2651381	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:8700894	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:2651381	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:14634077	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:3583142	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814331	Prkn<sup>tm1Ykt</sup>/Prkn<sup>tm1Ykt</sup> Tg(Prp-GPR37)1Ryot/Tg(Prp-GPR37)1Ryot  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:18691389	20081110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312681	Opa3<sup>m1Votr</sup>/Opa3<sup>m1Votr</sup>  [background:] involves: C3H * C57BL/6JCrl	is_model_of	DOID:0110004	3-methylglutaconic aciduria type 3						ECO:0000033	author statement supported by traceable reference	PMID:22869679	20121115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5312681	Opa3<sup>m1Votr</sup>/Opa3<sup>m1Votr</sup>  [background:] involves: C3H * C57BL/6JCrl	is_model_of	DOID:0110004	3-methylglutaconic aciduria type 3						ECO:0000033	author statement supported by traceable reference	PMID:18222992	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036170	Tcf4<sup>tm1Hmb</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32015540	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036170	Tcf4<sup>tm1Hmb</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157967	Tcf4<sup>tm1Hmb</sup>/Tcf4<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/Tmem163<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036170	Tcf4<sup>tm1Hmb</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157968	Tcf4<sup>tm1Hmb</sup>/Tcf4<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312669	Opa3<sup>m1Votr</sup>	is_implicated_in	DOID:0110004	3-methylglutaconic aciduria type 3		MGI:5312681	Opa3<sup>m1Votr</sup>/Opa3<sup>m1Votr</sup>  [background:] involves: C3H * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:22869679	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312669	Opa3<sup>m1Votr</sup>	is_implicated_in	DOID:0110004	3-methylglutaconic aciduria type 3		MGI:5312681	Opa3<sup>m1Votr</sup>/Opa3<sup>m1Votr</sup>  [background:] involves: C3H * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:18222992	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5312669	Opa3<sup>m1Votr</sup>	is_implicated_in	DOID:0110004	3-methylglutaconic aciduria type 3						ECO:0000033	author statement supported by traceable reference	PMID:27106103	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5086004	Amer1<sup>tm1.2Nbar</sup>	is_implicated_in	DOID:0060886	osteopathia striata with cranial sclerosis		MGI:5086005	Amer1<sup>tm1.2Nbar</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21571217	20110815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316416	Kiss1r<sup>tm1.1Lex</sup>	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:5316427	Kiss1r<sup>tm1.1Lex</sup>/Kiss1r<sup>tm1.1Lex</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:22067321	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444488	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup> Tgfb2<sup>tm1Doe</sup>/Tgfb2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050466	Loeys-Dietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22772368	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822318	Lepr<sup>tm2Yli</sup>/Lepr<sup>tm2Yli</sup>  [background:] B6.129-Lepr<sup>tm2Yli</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:19015522	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491238	b2b2059Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5555838	b2b2059Clo/b2b2059Clo  [background:] C57BL/6J-b2b2059Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4838205	Tg(Eno2-TOR1A*)13Shas/0  [background:] involves: C3H * C57BL/6J	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:15548549	20101111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444028	Tg(H2-K<sup>b</sup>-Jak2*V617F)2Shmd	is_implicated_in	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:27401345	20161208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444028	Tg(H2-K<sup>b</sup>-Jak2*V617F)2Shmd	is_implicated_in	DOID:4971	myelofibrosis		MGI:5444038	Tg(H2-K<sup>b</sup>-Jak2*V617F)2Shmd/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18033315	20161208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5543910	Tg(Amh-SMAD2*)#Jebu/0  [background:] FVB/N-Tg(Amh-SMAD2*)#Jebu	is_model_of	DOID:5117	dermoid cyst of ovary						ECO:0000033	author statement supported by traceable reference	PMID:23741457	20140212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3706580	Ctnnb1<sup>tm2(Nfkbia)Rsu</sup>/Ctnnb1<sup>+</sup> Tg(CMV-cre)1Cgn/0  [background:] involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:11585809	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5569820	Tg(AGER)#Eca	is_implicated_in	DOID:0050161	lower respiratory tract disease		MGI:5569826	Tg(AGER)#Eca/Tg(AGER)#Eca  [background:] C57BL/6J-Tg(AGER)#Eca			ECO:0000033	author statement supported by traceable reference	PMID:23144333	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764690	Prkn<sup>tm1Ccs</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:24204848	20140821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764690	Prkn<sup>tm1Ccs</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:4939781	Prkn<sup>tm1Ccs</sup>/Prkn<sup>tm1Ccs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21212098	20140821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:21103359	20110704	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723224	Tg(PDGFB-SNCA)4Ema/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:10678833	20110704	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5660027	Tg(tetO-PRKCG*S361G,-GFP)3Jpka	is_implicated_in	DOID:0050964	spinocerebellar ataxia type 14		MGI:5660030	Tg(Pcp2-tTA)3Horr/0 Tg(tetO-PRKCG*S361G,-GFP)3Jpka/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24937631	20150827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6119737	Sgcb<sup>em1Isrd</sup>	is_not_implicated_in	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E		MGI:6323188	Sgcb<sup>em1Isrd</sup>/Sgcb<sup>em1Isrd</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29360879	20190716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629779	Gpc3<sup>tm1Arge</sup>/Y  [background:] either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)	is_model_of	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:11846487	20060724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428442	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup> Il1r1<sup>tm1Imx</sup>/Il1r1<sup>tm1Imx</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * NOD	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20696775	20120720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4940059	Tg(Prnp-ATXN3*79Q)#Hlw/0  [background:] FVB/N-Tg(Prnp-ATXN3*79Q)#Hlw	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:18502140	20110308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714069	Rag2<sup>tm1Avla</sup>/Rag2<sup>tm1Avla</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:0060010	Omenn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17476358	20070709	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3811281	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>tm2Jzh</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:18385665	20081020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447500	Tg(MMTV-Myc)141-3Led	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11156526	20160104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197903	Alms1<sup>m2Btlr</sup>	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:6197905	Alms1<sup>m2Btlr</sup>/Alms1<sup>m2Btlr</sup>  [background:] C57BL/6J-Alms1<sup>m2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:6197902	20180914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175713	Avpr2<sup>tm1Jwe</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * CF-1	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:11104789	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6886215	P2rx2<sup>em1Xzl</sup>	is_implicated_in	DOID:0110567	autosomal dominant nonsyndromic deafness 41		MGI:6886231	P2rx2<sup>em1Xzl</sup>/P2rx2<sup>+</sup>  [background:] CBA/J-P2rx2<sup>em1Xzl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33791800	20220307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6188931	Tg(Myh6-Pkp2*/mRuby)5Rbrug	is_implicated_in	DOID:0110077	arrhythmogenic right ventricular dysplasia 9		MGI:6188936	Tg(Myh6-Pkp2*/mRuby)5Rbrug/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:27412010	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3584494	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup>  [background:] B6.Cg-Spry2<sup>tm1Ayos</sup>	is_model_of	DOID:0080072	intestinal pseudo-obstruction						ECO:0000033	author statement supported by traceable reference	PMID:15937482	20050829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5450938	Fgfr2<sup>tm3Ewj</sup>	is_implicated_in	DOID:0050660	Beare-Stevenson cutis gyrata syndrome		MGI:5450965	Fgfr2<sup>tm3Ewj</sup>/Fgfr2<sup>+</sup>  [background:] B6.129-Fgfr2<sup>tm3Ewj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22585574	20130124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5897147	Fan1<sup>tm1.1Jrou</sup>	is_implicated_in	DOID:0060911	karyomegalic interstitial nephritis		MGI:5897798	Fan1<sup>tm1.1Jrou</sup>/Fan1<sup>tm1.1Jrou</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26980188	20170519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578357	Cep290<sup>tm2.1Rwjc</sup>	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:24223178	20140822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5441254	Col2a1<sup>Lpk</sup>/Col2a1<sup>+</sup>  [background:] C.B6(C3)-Col2a1<sup>Lpk</sup>	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:22028304	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618601	Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9212102	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5779857	Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694858	Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5698523	Htt<sup>tm2Detl</sup>/Htt<sup>+</sup>  [background:] B6J.129P2-Htt<sup>tm2Detl</sup>	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:25609071	20151210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438492	Tg(Thy1-TARDBP)4Singh/Tg(Thy1-TARDBP)4Singh  [background:] involves: C57BL/6J * SJL/J	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:20133711	20100402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5547757	Tg(Utg-TAg)7593Fjd/?  [background:] involves: FVB	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:9040936	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7429117	Arb2a<sup>Tg(Tyr)TpNpin</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7429209	Arb2a<sup>Tg(Tyr)TpNpin</sup>/Arb2a<sup>Tg(Tyr)TpNpin</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29311329	20230131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7429117	Arb2a<sup>Tg(Tyr)TpNpin</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:35129866	20230131	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5638675	App<sup>tm3.1Tcs</sup>/App<sup>tm3.1Tcs</sup>  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24728269	20150608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040884	Tg(WapTAg)3Knw	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040884	Tg(WapTAg)3Knw	is_implicated_in	DOID:1612	breast cancer		MGI:3835117	Tg(WapTAg)3Knw/0  [background:] C57BL/6J-Tg(WapTAg)3Knw			ECO:0000033	author statement supported by traceable reference	PMID:9859214	20170623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635152	Tg(HTT*)NXwy	is_implicated_in	DOID:12858	Huntington's disease		MGI:5635158	Tg(HTT*)NXwy/0  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:25661181	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405040	Mc4r<sup>tm1Matsu</sup>	is_implicated_in	DOID:0080547	metabolic dysfunction-associated steatohepatitis		MGI:6405042	Mc4r<sup>tm1Matsu</sup>/Mc4r<sup>tm1Matsu</sup>  [background:] C57BL/6J-Mc4r<sup>tm1Matsu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31990961	20200422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473699	Adora2a<sup>tm1Jfc</sup>/Adora2a<sup>tm1Jfc</sup>  [background:] B6.129S4-Adora2a<sup>tm1Jfc</sup>	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:20938208	20130410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6759435	Clp1<sup>em1Slac</sup>	is_implicated_in	DOID:0060279	pontocerebellar hypoplasia type 10		MGI:6771475	Clp1<sup>em1Slac</sup>/Clp1<sup>em1Slac</sup>  [background:] C57BL/6J-Clp1<sup>em1Slac</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:34548404	20211014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829538	Jak2<sup>tm1.1Jlvl</sup>	is_implicated_in	DOID:4971	myelofibrosis		MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755254	Tg(Myh6-Tnnt2*R92Q)2Lnwd/0  [background:] involves: C57BL/6	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:10449439	20160331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6431336	Ace2<sup>em1(ACE2)Yowa</sup>	is_implicated_in	DOID:0080600	COVID-19		MGI:6431340	Ace2<sup>em1(ACE2)Yowa</sup>/Ace2<sup>em1(ACE2)Yowa</sup>  [background:] C57BL/6-Ace2<sup>em1(ACE2)Yowa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32485164	20200603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815199	Ar<sup>Tfm</sup>/Y  [background:] involves: NMRI * STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>	is_model_of	DOID:4674	androgen insensitivity syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819722	Tg(Myh6-TNNT2*R92Q)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:11171784	20100819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819722	Tg(Myh6-TNNT2*R92Q)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:18349139	20100819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861703	Htt<sup>tm2Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27913616	20171207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575519	Spink5<sup>tm1Hov</sup>/Spink5<sup>tm1Hov</sup>  [background:] involves: 129P2/OlaHsd * FVB	is_model_of	DOID:0050474	Netherton syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15619623	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662836	Lmna<sup>tm2Stw</sup>	is_implicated_in	DOID:3911	progeria						ECO:0000033	author statement supported by traceable reference	PMID:23095062	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662836	Lmna<sup>tm2Stw</sup>	is_implicated_in	DOID:3911	progeria		MGI:2662910	Lmna<sup>tm2Stw</sup>/Lmna<sup>tm2Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12748643	20150601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574274	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:0060668	anencephaly						ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5903729	Map3k20<sup>em2Smun</sup>	is_implicated_in	DOID:0090020	split hand-foot malformation		MGI:5903753	Map3k20<sup>em2Smun</sup>/Map3k20<sup>em2Smun</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:26755636	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297859	Tg(Prnp-SNCA*A53T)25Mkle/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12084935	20111210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405195	Tardbp<sup>tm2.1Neas</sup>	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6405401	Tardbp<sup>tm2.1Neas</sup>/Tardbp<sup>tm2.1Neas</sup>  [background:] B6(C3)-Tardbp<sup>tm2.1Neas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30625319	20200423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6276041	Tg(Myh6-Camk2d_ic)LJhb	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276046	Tg(Myh6-Camk2d_ic)LJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5559904	Tg(PDGFB-LRRK2*G2019S)32Hlw/?  [background:] FVB/N-Tg(PDGFB-LRRK2*G2019S)32Hlw	is_model_of	DOID:0060371	Parkinson's disease 8						ECO:0000033	author statement supported by traceable reference	PMID:22539006	20140425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611807	Alms1<sup>bbb</sup>/Alms1<sup>bbb</sup>  [background:] C57BL/6JSfdAnu-Alms1<sup>bbb</sup>/Anu	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	MGI:3611487	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793788	Tg(Eno2-Scn2a1*)Q54Mm	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000033	author statement supported by traceable reference	PMID:22471526	20131111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4839645	Tg(Prnp-TARDBP)4Jlel	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:4839655	Tg(Prnp-TARDBP)4Jlel/0  [background:] involves: C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20621187	20101130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007203	Jam3<sup>tm1Lex</sup>	is_not_implicated_in	DOID:0111723	Jacobsen Syndrome		MGI:6388692	Jam3<sup>tm1Lex</sup>/Jam3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19533782	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157831	Cfap418<sup>em3Jyang</sup>	is_implicated_in	DOID:0111022	cone-rod dystrophy 16		MGI:6157954	Cfap418<sup>em3Jyang</sup>/Cfap418<sup>em3Jyang</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29440555	20180524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5750602	Ryr2<sup>tm3.1Hhv</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:6104247	Ryr2<sup>tm3.1Hhv</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25775566	20171221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2687183	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup> Urod<sup>tm1Kush</sup>/Urod<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:3132	porphyria cutanea tarda						ECO:0000033	author statement supported by traceable reference	PMID:11134514	20050609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796036	Tg(Bglap2-TAg)1Rkho/0  [background:] FVB/N-Tg(Bglap2-TAg)1Rkho	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:20697156	20160929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676332	Col2a1<sup>sedc</sup>/Col2a1<sup>sedc</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:12968670	20051006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4820833	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] C.KOR-Traf3ip2<sup>adjm</sup>	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428020	Fam20c<sup>tm1.1Cqi</sup>	is_implicated_in	DOID:10609	rickets		MGI:5428021	Fam20c<sup>tm1.1Cqi</sup>/Fam20c<sup>tm1.1Cqi</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22615579	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387765	Mertk<sup>tm1Grl</sup>	is_implicated_in	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:23840307	20140130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5552945	Dnah5<sup>b2b2395Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5755288	Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln  [background:] involves: FVB/N	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:25786024	20160401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850449	Cdkn2a<sup>tm1.1Brn</sup>/Cdkn2a<sup>+</sup> Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S7/SvEvBrd	is_model_of	DOID:1790	malignant mesothelioma						ECO:0000033	author statement supported by traceable reference	PMID:18328429	20090716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800941	Tnfsf11<sup>tm1Ywc</sup>/Tnfsf11<sup>tm1Ywc</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0110943	autosomal recessive osteopetrosis 2						ECO:0000033	author statement supported by traceable reference	PMID:22836362	20160804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5763309	Tg(Fabp4-Phb*Y114F)#Smis	is_implicated_in	DOID:9970	obesity		MGI:5763310	Tg(Fabp4-Phb*Y114F)#Smis/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26751773	20160427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7442161	Kcnt1<sup>em1Pqt</sup>	is_not_implicated_in	DOID:0080439	developmental and epileptic encephalopathy 14		MGI:7442319	Kcnt1<sup>em1Pqt</sup>/Kcnt1<sup>+</sup>  [background:] C57BL/6J-Kcnt1<sup>em1Pqt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36173683	20230308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415727	Scn5a<sup>em1Coop</sup>	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:6415732	Scn5a<sup>em1Coop</sup>/Scn5a<sup>em1Coop</sup>  [background:] involves: C57BL/6NJ * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:30371314	20200511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415727	Scn5a<sup>em1Coop</sup>	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:6415731	Scn5a<sup>em1Coop</sup>/Scn5a<sup>+</sup>  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:30371314	20200511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285079	Bicc1<sup>b2b222Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5285350	Bicc1<sup>b2b222Clo</sup>/Bicc1<sup>b2b222Clo</sup>  [background:] C57BL/6J-Bicc1<sup>b2b222Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6164037	Tg(Vav1-STAT5B*N642H)726Biat	is_implicated_in	DOID:1240	leukemia		MGI:6164043	Tg(Vav1-STAT5B*N642H)726Biat/0  [background:] C57BL/6NCrl-Tg(Vav1-STAT5B*N642H)726Biat			ECO:0000033	author statement supported by traceable reference	PMID:29200404	20180703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438066	Ccdc39<sup>b2b1735Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617451	Pkd2<sup>tm1Som</sup>/Pkd2<sup>tm2Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:9568711	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3617976	Stat4<sup>tm1Gru</sup>/Stat4<sup>+</sup>  [background:] NOD.129S2-Stat4<sup>tm1Gru</sup>	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15041039	20060526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583134	T(2;10)67Gso/T(2;10)67Gso  [background:] involves: 101 * C3H * C3H/Rl * C57BL/RlGso * SEC/RlGso	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11944981	20050808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311385	Dnah5<sup>b2b1134Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5469980	Atp6v1b1<sup>vtx</sup>	is_implicated_in	DOID:0050565	autosomal recessive nonsyndromic deafness		MGI:5910007	Atp6v1b1<sup>vtx</sup>/Atp6v1b1<sup>vtx</sup>  [background:] MRL/MpJ-Atp6v1b1<sup>vtx</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	PMID:28934385	20170920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385811	Lamp2<sup>tm1Psa</sup>	is_implicated_in	DOID:0050437	Danon disease						ECO:0000033	author statement supported by traceable reference	PMID:11427988	20181207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385811	Lamp2<sup>tm1Psa</sup>	is_implicated_in	DOID:0050437	Danon disease						ECO:0000033	author statement supported by traceable reference	PMID:29463847	20181207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385811	Lamp2<sup>tm1Psa</sup>	is_implicated_in	DOID:0050437	Danon disease		MGI:3042186	Lamp2<sup>tm1Psa</sup>/Lamp2<sup>tm1Psa</sup>  [background:] either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)			ECO:0000033	author statement supported by traceable reference	PMID:10972293	20181207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385811	Lamp2<sup>tm1Psa</sup>	is_implicated_in	DOID:0050437	Danon disease		MGI:6259615	Lamp2<sup>tm1Psa</sup>/Lamp2<sup>tm1Psa</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:28526246	20181207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3054643	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:9796923	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424982	Casr<sup>BCH007</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425921	Casr<sup>BCH007</sup>/Casr<sup>BCH007</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH007</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677767	Vhl<sup>tm1.1Lss</sup>/Vhl<sup>+</sup>  [background:] involves: BALB/c	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:14500363	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6452242	Cfh<sup>tm1.1Mcp</sup>	is_implicated_in	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26374608	20200831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451080	Lipa<sup>tm1Ggb</sup>	is_implicated_in	DOID:14497	Wolman disease						ECO:0000033	author statement supported by traceable reference	PMID:16380916	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451080	Lipa<sup>tm1Ggb</sup>	is_implicated_in	DOID:14497	Wolman disease		MGI:2451081	Lipa<sup>tm1Ggb</sup>/Lipa<sup>tm1Ggb</sup>  [background:] involves: 129P2/OlaHsd * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:9700186	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6116844	Reep1<sup>Gt(OST398247)Tigm</sup>	is_implicated_in	DOID:0110782	hereditary spastic paraplegia 31		MGI:6199190	Reep1<sup>Gt(OST398247)Tigm</sup>/Reep1<sup>Gt(OST398247)Tigm</sup>  [background:] B6J.Cg-Reep1<sup>Gt(OST398247)Tigm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27638887	20180924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182940	Aire<sup>tm1Pltn</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:23991207	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182940	Aire<sup>tm1Pltn</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:2182941	Aire<sup>tm1Pltn</sup>/Aire<sup>tm1Pltn</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11854172	20140317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5828524	Lepr<sup>db</sup>/Lepr<sup>db</sup> Tg(SHBG)4-aGlha/0  [background:] involves: C57BL/6 * C57BLKS/J * CBA	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:26441241	20170315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5525128	Tg(Prnp-ITM2B*)1Ruvi/Tg(Prnp-ITM2B*)1Ruvi  [background:] involves: C3HeB/FeJ * C57BL/6	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:23418567	20131226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825304	Wdfy3<sup>tm1a(KOMP)Mbp</sup>/Wdfy3<sup>tm1a(KOMP)Mbp</sup>  [background:] C57BL/6N-Wdfy3<sup>tm1a(KOMP)Mbp</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:25198012	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285345	Dnai1<sup>b2b284Clo</sup>/Dnai1<sup>b2b284Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b284Clo</sup>	is_model_of	DOID:0110594	primary ciliary dyskinesia 1						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20110926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3757580	Tg(Ins2-CD80)3B7Flv/?  [background:] involves: C57BL/6 * CBA/Ca * NOD/Caj	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:7533734	20071009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311393	Dnah11<sup>b2b1279Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5317649	Dnah11<sup>b2b1279Clo</sup>/Dnah11<sup>b2b1279Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1279Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544595	Ptch1<sup>dl</sup>	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:5544602	Ptch1<sup>dl</sup>/Ptch1<sup>dl</sup>  [background:] involves: 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23897749	20140512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056760	Kcnq1<sup>tm3Kpfe</sup>/Kcnq1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	is_model_of	DOID:0110644	long QT syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15498462	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5582513	Tg(H2-K-IL6)2Srj	is_implicated_in	DOID:934	viral infectious disease		MGI:5582588	Tg(H2-K-IL6)2Srj/0  [background:] B6.Cg-Tg(H2-K-IL6)2Srj			ECO:0000033	author statement supported by traceable reference	PMID:22490805	20170705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5752193	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(MMTV-cre)#Tfln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:25330770	20160316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313507	Tg(CRYBB1-CRYGC*)#Jfhe	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:5313510	Tg(CRYBB1-CRYGC*)#Jfhe/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21436266	20130429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424981	Casr<sup>BCH004</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425920	Casr<sup>BCH004</sup>/Casr<sup>BCH004</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH004</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714016	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Gfap-cre)1Sbk/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11726926	20070709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5776276	Crppa<sup>em2Mbp</sup>	is_implicated_in	DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U		MGI:7279103	Crppa<sup>em2Mbp</sup>/Crppa<sup>em2Mbp</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] B6.Cg-Myf5<sup>tm3(cre)Sor</sup> Crppa<sup>em2Mbp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35422047	20220519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440955	Itga7<sup>tm1Burk</sup>/Itga7<sup>tm1Burk</sup> Sspn<sup>tm1Kcam</sup>/Sspn<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22798625	20121108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278302	Tg(tetO-CHMP2B*)3Fbga	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:6278310	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-CHMP2B*)3Fbga/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25401692	20190215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5441362	Tg(Rho*G90D*A337V)202Sie	is_implicated_in	DOID:0110862	congenital stationary night blindness autosomal dominant 1		MGI:5441373	Tg(Rho*G90D*A337V)202Sie/0  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:11466416	20121114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175120	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae-Msx1<sup>tm1Rilm</sup>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J)	is_model_of	DOID:0050591	tooth agenesis						ECO:0000033	author statement supported by traceable reference	PMID:7914451	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438332	Pkhd1<sup>tm2Cjwa</sup>/Pkhd1<sup>tm2Cjwa</sup>  [background:] either: B6.129(Cg)-Pkhd1<sup>tm2Cjwa</sup> or C.129(Cg)-Pkhd1<sup>tm2Cjwa</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:22021705	20121012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5584016	Mecp2<sup>tm1.1Dhy</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5584025	Mecp2<sup>tm1.1Dhy</sup>/Y  [background:] C57BL/6N-Mecp2<sup>tm1.1Dhy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24352790	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432032	Tg(CAG-Cfh*)#Mcp	is_implicated_in	DOID:12554	hemolytic-uremic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21148255	20120823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5555967	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-Rai1,-EGFP)479Walz/0  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:0060853	Potocki-Lupski syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24218365	20140408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3521968	Cnga3<sup>tm1Biel</sup>/Cnga3<sup>tm1Biel</sup> Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:11528395	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196512	Rubcn<sup>em1Dgre</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287978	Rubcn<sup>em1Dgre</sup>/Rubcn<sup>em1Dgre</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5817760	Ednra<sup>m1Mhda</sup>/Ednra<sup>+</sup>  [background:] C3HeB/FeJ-Ednra<sup>m1Mhda</sup>	is_model_of	DOID:0060365	mandibulofacial dysostosis with alopecia						ECO:0000033	author statement supported by traceable reference	PMID:27671791	20170116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5301441	Cdkal1<sup>tm1.1Tomik</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5301577	Cdkal1<sup>tm1.1Tomik</sup>/Cdkal1<sup>tm1.1Tomik</sup> Tg(Ins2-cre)25Mgn/0  [background:] B6.Cg-Cdkal1<sup>tm1.1Tomik</sup> Tg(Ins2-cre)25Mgn			ECO:0000033	author statement supported by traceable reference	PMID:21841312	20130415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4839563	Tg(Amhr2-SV40TAg)1Dcco/0  [background:] (C57BL/6 x C3H)F1	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:12649204	20101128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:23610450	20140317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677978	Slc3a1<sup>pbl</sup>/Slc3a1<sup>pbl</sup>  [background:] C3HeB/FeJ-Slc3a1<sup>pbl</sup>	is_model_of	DOID:9266	cystinuria						ECO:0000033	author statement supported by traceable reference	PMID:12923163	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559221	Slx1b<sup>tm1.1Jrou</sup>	is_implicated_in	DOID:0090066	Fanconi-like syndrome		MGI:5559491	Slx1b<sup>tm1.1Jrou</sup>/Slx1b<sup>tm1.1Jrou</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24076219	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581179	Lyst<sup>bg-J</sup>/Lyst<sup>bg-J</sup>  [background:] C57BL/6J-Lyst<sup>bg-J</sup>/J	is_model_of	DOID:13641	exfoliation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19029039	20110715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5320677	Jak2<sup>tm1Mohi</sup>	is_implicated_in	DOID:8997	polycythemia vera		MGI:5320791	Jak2<sup>tm1Mohi</sup>/Jak2<sup>tm1Mohi</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22144185	20120608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5320677	Jak2<sup>tm1Mohi</sup>	is_implicated_in	DOID:8997	polycythemia vera		MGI:5320790	Jak2<sup>tm1Mohi</sup>/Jak2<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22144185	20120608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5751707	Mecp2<sup>tm1.1Irsf</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25634563	20160310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5467354	b2b1963Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5467392	b2b1963Clo/b2b1963Clo  [background:] C57BL/6J-b2b1963Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176915	Gjb1<sup>tm1Kwi</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1						ECO:0000033	author statement supported by traceable reference	PMID:8790370	20100906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5439652	Bap1<sup>tm1.1Geno</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5439657	Bap1<sup>tm1.1Geno</sup>/Bap1<sup>tm1.1Geno</sup> Gt(ROSA)26Sor<sup>tm9(cre/ESR1)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:22878500	20121026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4887389	Ryr1<sup>tm2.1Alle</sup>	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:4887395	Ryr1<sup>tm2.1Alle</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17122579	20110210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4357767	Tg(Vav1-NUP98/HOXD13)G2Apla/0  [background:] C57BL/6-Tg(Vav1-NUP98/HOXD13)G2Apla	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15755899	20130926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5699330	Tg(SOD1*H46R)LAra/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:25762155	20151216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491268	Tbc1d32<sup>b2b2284Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6163502	Atp1a3<sup>tm1.1Tmklh</sup>	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:6163608	Atp1a3<sup>tm1.1Tmklh</sup>/Atp1a3<sup>+</sup>  [background:] B6JRj.129S1-Atp1a3<sup>tm1.1Tmklh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27549929	20180628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5140884	Cdh23<sup>Jera</sup>	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12		MGI:5140886	Cdh23<sup>Jera</sup>/Cdh23<sup>Jera</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5559165	Tg(Myh6-Gnaq*Q209L)52Ejne	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5559168	Tg(Myh6-Gnaq*Q209L)52Ejne/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:9811897	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4413664	Sco2<sup>tm1.1Easc</sup>/Sco2<sup>tm2.1Easc</sup>  [background:] 129X1/SvJ-Sco2<sup>tm1.1Easc</sup>/Sco2<sup>tm2.1Easc</sup>	is_model_of	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:19837698	20091229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176947	Gck<sup>tm1Ts</sup>/Gck<sup>tm1Ts</sup>  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J)	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:7553875	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7282271	Avpr2<sup>tm2.1Jwe</sup>	is_implicated_in	DOID:0081060	X-linked nephrogenic diabetes insipidus		MGI:7282305	Avpr2<sup>tm2.1Jwe</sup>/Y Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19729836	20220606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136846	Gdnf<sup>tm1Lmgd</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136846	Gdnf<sup>tm1Lmgd</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3588431	Gdnf<sup>tm1Lmgd</sup>/Gdnf<sup>tm1Lmgd</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S1/Sv * 129X1/SvJ)			ECO:0000033	author statement supported by traceable reference	PMID:8657307	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136846	Gdnf<sup>tm1Lmgd</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3588490	Gdnf<sup>tm1Lmgd</sup>/Gdnf<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:11774071	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936846	Itm2b<sup>tm1.1Ldad</sup>/Itm2b<sup>+</sup>  [background:] B6.129-Itm2b<sup>tm1.1Ldad</sup>	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:21098268	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6105945	Tg(Myh6-Gnaq*Q209L/Esr1*)7Rzl	is_implicated_in	DOID:6000	congestive heart failure		MGI:6105947	Tg(Myh6-Gnaq*Q209L/Esr1*)7Rzl/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16210321	20171222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433409	Tmem67<sup>b2b1163.1Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5433489	Tmem67<sup>b2b1163.1Clo</sup>/Tmem67<sup>b2b1163.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1163.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831341	Brca2<sup>tm1Brn</sup>/Brca2<sup>tm1Brn</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:19164512	20110921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576734	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] B6.129S4-Sh2d1a<sup>tm1Cpt</sup>	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15749842	20050513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576734	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] B6.129S4-Sh2d1a<sup>tm1Cpt</sup>	is_model_of	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:15774582	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6274478	Cngb3<sup>cpfl10</sup>	is_implicated_in	DOID:0110008	achromatopsia 3		MGI:6275192	Cngb3<sup>cpfl10</sup>/Cngb3<sup>cpfl10</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30592498	20190130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7507065	Cfi<sup>em1Jiwe</sup>	is_implicated_in	DOID:2921	glomerulonephritis		MGI:7507073	Cfi<sup>em1Jiwe</sup>/Cfi<sup>em1Jiwe</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34149444	20230714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151804	Pten<sup>tm1Rps</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:2179045	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9990064	20170403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5424992	Acta1<sup>tm1Hrd</sup>/Acta1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6JArc)	is_model_of	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:22067542	20120618	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5784494	Foxo1<sup>tm1Rdp</sup>/Foxo1<sup>tm1.1Rdp</sup> Foxo3<sup>tm1Rdp</sup>/Foxo3<sup>tm1.1Rdp</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:26061565	20160726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389489	Snca<sup>tm1Nbm</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:25351739	20151222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389489	Snca<sup>tm1Nbm</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:26324905	20151222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5792863	Bbs10<sup>tm1.2Vmar</sup>/Bbs10<sup>tm1.2Vmar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110132	Bardet-Biedl syndrome 10						ECO:0000033	author statement supported by traceable reference	PMID:26273430	20160922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:5825461	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Nes-cre/ERT2,-ALPP)1Sbk/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27815386	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:3714016	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Gfap-cre)1Sbk/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11726926	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629558	Lrit3<sup>tm1Lex</sup>	is_implicated_in	DOID:0110864	congenital stationary night blindness 1F		MGI:5688660	Lrit3<sup>tm1Lex</sup>/Lrit3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24598786	20151001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581819	Tg(GFAP)10Mes	is_implicated_in	DOID:4252	Alexander disease						ECO:0000033	author statement supported by traceable reference	PMID:26190408	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581819	Tg(GFAP)10Mes	is_implicated_in	DOID:4252	Alexander disease		MGI:3581822	Tg(GFAP)10Mes/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9466565	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270168	Tg(Camk2a-Polg*D181A)BTkato	is_implicated_in	DOID:3312	bipolar disorder		MGI:6270171	Tg(Camk2a-Polg*D181A)BTkato/0  [background:] C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato			ECO:0000033	author statement supported by traceable reference	PMID:16619054	20181231	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672093	Krt10<sup>tm1Tmm</sup>/Krt10<sup>tm1Tmm</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6)	is_model_of	DOID:4603	epidermolytic hyperkeratosis						ECO:0000033	author statement supported by traceable reference	PMID:8603923	20090224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587103	Hps3<sup>coa</sup>/Hps3<sup>coa</sup> Myo5a<sup>d</sup>/Myo5a<sup>d</sup> Mreg<sup>dsu</sup>/Mreg<sup>dsu</sup>  [background:] involves: C57BL/10J	is_model_of	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000033	author statement supported by traceable reference	PMID:2379821	20110705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836731	Egr2<sup>tm2Jmi</sup>/Egr2<sup>tm2Jmi</sup>  [background:] B6.Cg-Egr2<sup>tm2Jmi</sup>	is_model_of	DOID:0110195	Charcot-Marie-Tooth disease type 4E						ECO:0000033	author statement supported by traceable reference	PMID:19244508	20090323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:32661395	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27050589	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5641483	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22763451	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6188888	Itsn2<sup>tm1Kure</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:6188890	Itsn2<sup>tm1Kure</sup>/Itsn2<sup>tm1Kure</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29773874	20180718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3839661	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] B6.129-Idua<sup>tm1Clk</sup>/J	is_model_of	DOID:12802	mucopolysaccharidosis I						ECO:0000033	author statement supported by traceable reference	PMID:18022143	20090413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909085	Tg(Myh7-Ptpn11*Q510E)#Krnz	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5909088	Tg(Myh7-Ptpn11*Q510E)#Krnz/0  [background:] FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz			ECO:0000033	author statement supported by traceable reference	PMID:22058153	20170920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5909085	Tg(Myh7-Ptpn11*Q510E)#Krnz	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:25724491	20170920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833851	Park7<sup>tm1Cai</sup>/Park7<sup>tm1Cai</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:18187333	20090226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311385	Dnah5<sup>b2b1134Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856953	Ttn<sup>mdm</sup>	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J						ECO:0000033	author statement supported by traceable reference	PMID:23824195	20140108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856953	Ttn<sup>mdm</sup>	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J		MGI:3041561	Ttn<sup>mdm</sup>/Ttn<sup>mdm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11829483	20140108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829507	Nos2<sup>tm1Lau</sup>/Nos2<sup>tm1Lau</sup> Tg(Thy1-APPSwDutIowa)BWevn/?  [background:] involves: C57BL/6	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18272675	20150703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386308	Itga9<sup>tm1Des</sup>	is_implicated_in	DOID:0060646	congenital chylothorax						ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386308	Itga9<sup>tm1Des</sup>	is_implicated_in	DOID:0060646	congenital chylothorax		MGI:3583695	Itga9<sup>tm1Des</sup>/Itga9<sup>tm1Des</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10866676	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769767	Tg(Igh-Lmp2a)13FRdni	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769767	Tg(Igh-Lmp2a)13FRdni	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3769776	Tg(Igh-Lmp2a)13FRdni/0  [background:] involves: C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10430930	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6121113	Lrch1<sup>em1Hwa</sup>	is_implicated_in	DOID:2377	multiple sclerosis		MGI:6140058	Lrch1<sup>em1Hwa</sup>/Lrch1<sup>em1Hwa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28028151	20180316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7327648	Bag5<sup>em1Asay</sup>	is_implicated_in	DOID:0081162	dilated cardiomyopathy 2F		MGI:7328939	Bag5<sup>em1Asay</sup>/Bag5<sup>em1Asay</sup>  [background:] C57BL/6JJcl-Bag5<sup>em1Asay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35044787	20220921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583335	Ret<sup>tm2.1Cos</sup>/Ret<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N	is_model_of	DOID:10016	multiple endocrine neoplasia type 2B						ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5006974	Tg(Pnkd*A7V*A9V,-DsRed)671Ljp	is_implicated_in	DOID:0090049	paroxysmal nonkinesigenic dyskinesia 1		MGI:5469978	Tg(Pnkd*A7V*A9V,-DsRed)671Ljp/0  [background:] B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)671Ljp			ECO:0000033	author statement supported by traceable reference	PMID:22214848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888408	Hbb<sup>tm2Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:27782131	20170811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888408	Hbb<sup>tm2Unc</sup>	is_implicated_in	DOID:12241	beta thalassemia		MGI:3835308	Hbb<sup>tm2Unc</sup>/Hbb<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9490703	20170811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5086280	Lca5<sup>Gt(AG0283)Wtsi</sup>/Lca5<sup>Gt(AG0283)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110215	Leber congenital amaurosis 5						ECO:0000033	author statement supported by traceable reference	PMID:21606596	20110816	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285220	Bsnd<sup>tm1.1Suc</sup>/Bsnd<sup>tm1.1Suc</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110145	Bartter disease type 4a						ECO:0000033	author statement supported by traceable reference	PMID:21593186	20110913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412181	Tg(FXN)YG22Pook	is_implicated_in	DOID:12705	Friedreich ataxia						ECO:0000033	author statement supported by traceable reference	PMID:25198290	20160104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5701399	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] D2.Cg-Tg(APPswe,PSEN1dE9)85Dbo	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:25933409	20160106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818698	Taar1<sup>tm1Tdw</sup>/Taar1<sup>tm1Tdw</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17212650	20081208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574546	Dok2<sup>tm1Ppp</sup>/Dok2<sup>+</sup> Tg(Tec-BCR/ABL1)5Hhi/0  [background:] involves: 129S1/Sv	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611295	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386303	Slc6a3<sup>tm1Mca</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:10637574	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386303	Slc6a3<sup>tm1Mca</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386303	Slc6a3<sup>tm1Mca</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:2654500	Slc6a3<sup>tm1Mca</sup>/Slc6a3<sup>tm1Mca</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9888856	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5557979	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup>  [background:] involves: BXD24/TyJ * C57BL/6	is_model_of	DOID:0110291	Leber congenital amaurosis 10						ECO:0000033	author statement supported by traceable reference	PMID:21245082	20140410	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588063	Thrb<sup>tm2Few</sup>/Thrb<sup>tm2Few</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:11633	thyroid hormone resistance syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11274423	20050921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5491033	Tg(Prnp*P101L)2866Sbp/0  [background:] involves: FVB/N	is_model_of	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8698234	20130620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461138	Tg(Gfap-TNF*)K21Gkl/0 Tnfrsf1a<sup>tm1Blt</sup>/Tnfrsf1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:9736029	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813538	Men1<sup>tm1.1Gfk</sup>/Men1<sup>+</sup>  [background:] involves: 129T2/SvEms * C57BL/6	is_model_of	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:17044021	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5553123	Neb<sup>tm1.1Hgra</sup>/Neb<sup>tm1.1Hgra</sup>  [background:] involves: C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0110928	nemaline myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:23715096	20140326	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3820248	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>+</sup> Tg(MtTGFA)42Lmb/0  [background:] involves: C57BL/6 * CBA * CD-1	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:8701981	20090619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580495	Sod1<sup>tm1Leb</sup>/Sod1<sup>tm1Leb</sup>  [background:] B6;129S-Sod1<sup>tm1Leb</sup>/J	is_model_of	DOID:13544	low tension glaucoma						ECO:0000033	author statement supported by traceable reference	PMID:21421868	20120325	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663621	Tg(APP695)3Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14645205	20061017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845883	Tg(CD2-Stat6*V625A*T626A)78Mhk	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:27554818	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845883	Tg(CD2-Stat6*V625A*T626A)78Mhk	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4818943	Tg(CD2-Stat6*V625A*T626A)78Mhk/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20147633	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:8923	skin melanoma						ECO:0000033	author statement supported by traceable reference	PMID:32620791	20200903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474981	Pikfyve<sup>tm2.1Tssk</sup>	is_implicated_in	DOID:8778	Crohn's disease		MGI:5474983	Pikfyve<sup>tm2.1Tssk</sup>/Pikfyve<sup>tm2.1Tssk</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:23322734	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:3360305	20060726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca	is_model_of	DOID:9281	phenylketonuria						ECO:0000033	author statement supported by traceable reference	PMID:15144277	20060726	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3056343	Rs1<sup>tm1Sie</sup>/Rs1<sup>tm1Sie</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:15326152	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3717637	Efnb1<sup>tm1.1Sor</sup>/Efnb1<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:14737	craniofrontonasal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16968134	20070809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4441373	Fli1<sup>tm1Matr</sup>	is_implicated_in	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:27777101	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4441373	Fli1<sup>tm1Matr</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:4441385	Fli1<sup>tm1Matr</sup>/Fli1<sup>tm1Matr</sup> Tg(Tek-cre)12Flv/0  [background:] B6.Cg-Fli1<sup>tm1Matr</sup> Tg(Tek-cre)12Flv			ECO:0000033	author statement supported by traceable reference	PMID:20228226	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837468	Trim32<sup>Gt(BGA355)Byg</sup>	is_implicated_in	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H						ECO:0000033	author statement supported by traceable reference	PMID:22505452	20120718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837468	Trim32<sup>Gt(BGA355)Byg</sup>	is_implicated_in	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H		MGI:3837478	Trim32<sup>Gt(BGA355)Byg</sup>/Trim32<sup>Gt(BGA355)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19155210	20120718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5758867	Sco1<sup>tm1c(KOMP)Wtsi</sup>	is_implicated_in	DOID:3762	cytochrome-c oxidase deficiency disease		MGI:5758892	Sco1<sup>tm1c(KOMP)Wtsi</sup>/Sco1<sup>tm1c(KOMP)Wtsi</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA			ECO:0000033	author statement supported by traceable reference	PMID:25683716	20160411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:25132272	20150807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24027047	20150807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4829790	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:20837017	20150807	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5811262	Kit<sup>W-v</sup>/Kit<sup>W-v</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:27354067	20161207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654656	Ndn<sup>tm2Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10508517	20091026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5288490	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>/?  [background:] Not Specified	is_model_of	DOID:0050476	Barth syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21091282	20111006	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5440213	Traf3ip2<sup>tm1.1Lix</sup>/Traf3ip2<sup>tm1.1Lix</sup>  [background:] B6.129-Traf3ip2<sup>tm1.1Lix</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:22585710	20121031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5508556	Tg(Thy1-VCP*A232E)BMaki	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:5508557	Tg(Thy1-VCP*A232E)BMaki/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23747512	20130926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3848057	Glis3<sup>tm1Amj</sup>/Glis3<sup>tm1Amj</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:19273592	20090616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6728807	Fgf13<sup>em1Xuzh</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6729187	Fgf13<sup>em1Xuzh</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34184986	20210806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5013911	Tg(MMTV-ERBB2*,-luc)6157Aami/0  [background:] FVB-Tg(MMTV-ERBB2*,-luc)6157Aami	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21559085	20110711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809288	Nphp3<sup>pcy</sup>/Nphp3<sup>tm1Cbe</sup>  [background:] involves: C57BL/6 * CD-1 * KK/Upj	is_model_of	DOID:0111114	nephronophthisis 3						ECO:0000033	author statement supported by traceable reference	PMID:18371931	20081002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677921	Gusb<sup>mps-2J</sup>/Gusb<sup>mps-2J</sup>  [background:] C3H/HeOuJ-Gusb<sup>mps-2J</sup>/BrkJ	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9774663	20050629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677921	Gusb<sup>mps-2J</sup>/Gusb<sup>mps-2J</sup>  [background:] C3H/HeOuJ-Gusb<sup>mps-2J</sup>/BrkJ	is_model_of	DOID:12803	Sly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11228259	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431002	Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5431005	Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>/Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>  [background:] FVB/N-Ak7<sup>Tg(tetO-Hmox1)67Sami</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18776131	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772885	Tg(Prnp-TBP*)105Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)105Xjl	is_model_of	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000033	author statement supported by traceable reference	PMID:17994014	20080305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5568409	Abcc8<sup>tm1.1Fmas</sup>	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:5568494	Abcc8<sup>tm1.1Fmas</sup>/Abcc8<sup>tm1.1Fmas</sup>  [background:] B6.129S2(Cg)-Abcc8<sup>tm1.1Fmas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23903354	20140616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5582192	Col1a1<sup>tm3(CAG-IDH2*R140Q)Kkw</sup>	is_implicated_in	DOID:0050575	D-2-hydroxyglutaric aciduria		MGI:5582197	Col1a1<sup>tm3(CAG-IDH2*R140Q)Kkw</sup>/Col1a1<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24589777	20140911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3718111	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] 129S.129X1-Myh6<sup>tm1Jse</sup>	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:16332958	20100521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663749	Mapt<sup>tm1(EGFP)Klt</sup>/Mapt<sup>tm1(EGFP)Klt</sup> Tg(MAPT)8cPdav/?  [background:] involves: 129S4/SvJae * C57BL/6 * Swiss Webster	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19041304	20110823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663749	Mapt<sup>tm1(EGFP)Klt</sup>/Mapt<sup>tm1(EGFP)Klt</sup> Tg(MAPT)8cPdav/?  [background:] involves: 129S4/SvJae * C57BL/6 * Swiss Webster	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:12859672	20110823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844657	Myf6<sup>tm1(cre)Mrc</sup>/Myf6<sup>+</sup> Pax3<sup>tm1Mrc</sup>/Pax3<sup>tm1Mrc</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:15489287	20090519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491238	b2b2059Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5555838	b2b2059Clo/b2b2059Clo  [background:] C57BL/6J-b2b2059Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560734	Eml1<sup>heco</sup>	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:5648122	Eml1<sup>heco</sup>/?  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24859200	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560734	Eml1<sup>heco</sup>	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:5560741	Eml1<sup>heco</sup>/Eml1<sup>heco</sup>  [background:] involves: NOR			ECO:0000033	author statement supported by traceable reference	PMID:18562329	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5560734	Eml1<sup>heco</sup>	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:5560742	Eml1<sup>heco</sup>/Eml1<sup>heco</sup>  [background:] involves: C57BL/6 * NOR			ECO:0000033	author statement supported by traceable reference	PMID:18562329	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4955130	Fam161a<sup>Gt(462E7)Cmhd</sup>	is_implicated_in	DOID:0110365	retinitis pigmentosa 28		MGI:5609024	Fam161a<sup>Gt(462E7)Cmhd</sup>/Fam161a<sup>Gt(462E7)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24833722	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912483	Tg(tetO-ERBB2*)26Kkw	is_implicated_in	DOID:4829	adenosquamous lung carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22464334	20171108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912483	Tg(tetO-ERBB2*)26Kkw	is_implicated_in	DOID:4829	adenosquamous lung carcinoma		MGI:5912488	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-ERBB2*)26Kkw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19122144	20171108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661330	Col1a1<sup>tm4(CAG-FGFR2_iIIIb*K660N)Kkw</sup>/Col1a1<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25035393	20150909	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042186	Lamp2<sup>tm1Psa</sup>/Lamp2<sup>tm1Psa</sup>  [background:] either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)	is_model_of	DOID:0050437	Danon disease						ECO:0000033	author statement supported by traceable reference	PMID:10972293	20050913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3614634	Abca1<sup>tm2Jp</sup>/Abca1<sup>tm2Jp</sup> Tg(APOA1)427Bres/?  [background:] involves: 129X1/SvJ * C57BL/6J * CBA/J	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:16024913	20060306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified	is_model_of	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:8456819	20130702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829468	Bckdk<sup>Gt(OST79912)Lex</sup>/Bckdk<sup>Gt(OST79912)Lex</sup>  [background:] involves: 129S5/SvEvBrd	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27912058	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5788281	Shank3<sup>tm1Cmpl</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5883282	Shank3<sup>tm1Cmpl</sup>/Shank3<sup>tm1Cmpl</sup>  [background:] B6J.129S6-Shank3<sup>tm1Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26134648	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5752774	Rnf213<sup>tm1.1Mfuji</sup>	is_not_implicated_in	DOID:13099	Moyamoya disease		MGI:5752779	Rnf213<sup>tm1.1Mfuji</sup>/Rnf213<sup>tm1.1Mfuji</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26315378	20160322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819727	Tg(Tnnt2-TNNT2*R92Q)M-2Ajm/0  [background:] involves: C3H * C57BL/6 * ICR	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:9788962	20100819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3806086	Npr2<sup>slw</sup>/Npr2<sup>slw</sup>  [background:] involves: C57BL/6 * DDY	is_model_of	DOID:0080050	acromesomelic dysplasia, Maroteaux type						ECO:0000033	author statement supported by traceable reference	PMID:17728275	20080916	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4410605	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup> Tg(Prnp-tTA)F959Sbp/Tg(Prnp-tTA)F959Sbp Tg(tetO-ATXN3)2904Olri/Tg(tetO-ATXN3)2904Olri  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:19666958	20091215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5754843	Grm6<sup>nob7</sup>/Grm6<sup>nob7</sup>  [background:] C57BL/6J-Grm6<sup>nob7</sup>	is_model_of	DOID:0110865	congenital stationary night blindness 1B						ECO:0000033	author statement supported by traceable reference	PMID:26241901	20160329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306612	Trp53<sup>tm1.1Dgk</sup>	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:22611036	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452338	Tg(Myh6-STK4)28Jusa	is_implicated_in	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:19679877	20170831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452338	Tg(Myh6-STK4)28Jusa	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4452351	Tg(Myh6-STK4)28Jusa/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12750396	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832988	Tg(CMV-TOR1A*)1Nush/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:15930383	20090223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5704195	Pcdh15<sup>roda</sup>/Pcdh15<sup>roda</sup>  [background:] BALB/c-Pcdh15<sup>roda</sup>	is_model_of	DOID:0110481	autosomal recessive nonsyndromic deafness 23						ECO:0000033	author statement supported by traceable reference	PMID:24044941	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6160000	Ecel1<sup>em1Hiki</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6160009	Ecel1<sup>em1Hiki</sup>/Ecel1<sup>em1Hiki</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26951213	20180608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5646215	Tg(Thy1-APPSw)10Jiri/0 Tg(Thy1-PSEN1*M146V)#Jiri/0  [background:] B6.Cg-Tg(Thy1-APPSw)10Jiri Tg(Thy1-PSEN1*M146V)#Jiri	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:19272356	20150805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3815540	Tg(MECP2)1Hzo	is_implicated_in	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000033	author statement supported by traceable reference	PMID:35248529	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3815540	Tg(MECP2)1Hzo	is_implicated_in	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000033	author statement supported by traceable reference	PMID:26237041	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3815540	Tg(MECP2)1Hzo	is_implicated_in	DOID:0060799	syndromic X-linked intellectual disability Lubs type		MGI:6305084	Tg(MECP2)1Hzo/0  [background:] FVB-Tg(MECP2)1Hzo/J			ECO:0000033	author statement supported by traceable reference	PMID:28743991	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3815540	Tg(MECP2)1Hzo	is_implicated_in	DOID:0060799	syndromic X-linked intellectual disability Lubs type		MGI:5314411	Tg(MECP2)1Hzo/0  [background:] either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1			ECO:0000033	author statement supported by traceable reference	PMID:22231481	20230810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5014809	Trp53<sup>tm1.2Awbr</sup>	is_implicated_in	DOID:0050745	diffuse large B-cell lymphoma		MGI:5014832	Trp53<sup>tm1.2Awbr</sup>/Trp53<sup>tm1.2Awbr</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21411755	20170621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3840644	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] FVB.129P2-Abcb4<sup>tm1Bor</sup>/J	is_model_of	DOID:1949	cholecystitis						ECO:0000033	author statement supported by traceable reference	PMID:14752830	20150311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3607258	Eif4ebp2<sup>tm1Klan</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:26245973	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3607258	Eif4ebp2<sup>tm1Klan</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3610950	Eif4ebp2<sup>tm1Klan</sup>/Eif4ebp2<sup>tm1Klan</sup>  [background:] B6.129S4(C)-Eif4ebp2<sup>tm1Klan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23172145	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5645238	Dnah5<sup>b2b2451Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5645239	Dnah5<sup>b2b2451Clo</sup>/Dnah5<sup>b2b2451Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2451Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6404009	Fkrp<sup>tm1.1Pg</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I		MGI:6404021	Fkrp<sup>tm1.1Pg</sup>/Fkrp<sup>tm1.1Pg</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26574668	20200415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589869	Ndst1<sup>tm1Je</sup>/Ndst1<sup>tm1Je</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:24355925	20140507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6472627	Mecp2<sup>em1Jlzn</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:6472629	Mecp2<sup>em1Jlzn</sup>/Y  [background:] C57BL/6-Mecp2<sup>em1Jlzn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32469049	20201116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856914	Tshr<sup>hyt</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:9183515	20151029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856914	Tshr<sup>hyt</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3581208	Tshr<sup>hyt</sup>/Tshr<sup>hyt</sup>  [background:] CBy.RF-Tshr<sup>hyt</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10575115	20151029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856914	Tshr<sup>hyt</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3581208	Tshr<sup>hyt</sup>/Tshr<sup>hyt</sup>  [background:] CBy.RF-Tshr<sup>hyt</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17932107	20151029	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651509	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6) or (involves: C57BL/6)	is_model_of	DOID:12801	mucopolysaccharidosis III						ECO:0000033	author statement supported by traceable reference	PMID:10588735	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5646304	Tg(CMV-ATXN3*135Q)CPama/0  [background:] C57BL/6-Tg(CMV-ATXN3*135Q)CPama	is_model_of	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:24477711	20150806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5882591	Tg(Col1a1-Ifitm5*)1Brle	is_implicated_in	DOID:0110344	osteogenesis imperfecta type 5		MGI:5882592	Tg(Col1a1-Ifitm5*)1Brle/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25251575	20170407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664440	Blm<sup>tm1Ches</sup>/Blm<sup>tm4Ches</sup> Tg(LGB-cre)74Acl/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL	is_model_of	DOID:2717	Bloom syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16914751	20061024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175044	Gja8<sup>No2</sup>/Gja8<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:0110231	cataract 1 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:1277597	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3783638	Lama2<sup>dy</sup>/Lama2<sup>dy</sup>  [background:] involves: 129P1/Re	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:16589799	20080502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583131	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:0110910	leukocyte adhesion deficiency 1						ECO:0000033	author statement supported by traceable reference	PMID:8101543	20050808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313530	Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/0  [background:] C57BL/6-Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21228171	20120330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759458	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129 * 129S2/SvPas * C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:11212243	20110922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3589405	Edn3<sup>tmgc48</sup>/Edn3<sup>tmgc48</sup>  [background:] C57BL/6-19<sup>PWK</sup>	is_model_of	DOID:0110954	Waardenburg syndrome type 4B						ECO:0000033	author statement supported by traceable reference	PMID:17516928	20100330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6386115	Fscn2<sup>em1Fhan</sup>	is_implicated_in	DOID:8466	retinal degeneration		MGI:6386243	Fscn2<sup>em1Fhan</sup>/Fscn2<sup>em1Fhan</sup>  [background:] C57BL/6J-Fscn2<sup>em1Fhan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30082328	20200124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654850	Alpl<sup>tm1Jlm</sup>/Alpl<sup>tm1Jlm</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6J)	is_model_of	DOID:0110914	infantile hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:9056646	20090219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4848154	Gjb6<sup>tm1.1Fama</sup>	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:4848186	Gjb6<sup>tm1.1Fama</sup>/Gjb6<sup>tm1.1Fama</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20858605	20101221	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5759821	Trp53<sup>tm3Tyj</sup>/Trp53<sup>+</sup> Tg(Wap-cre)11738Mam/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:16166291	20160412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437047	Del(14Trim13-Dleu2)4Rdf/Del(14Trim13-Dleu2)4Rdf  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:20060366	20100311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862014	Snap25<sup>Bdr</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22264613	20120720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862014	Snap25<sup>Bdr</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5428448	Snap25<sup>Bdr</sup>/Snap25<sup>+</sup>  [background:] involves: BALB/cAnNCrl			ECO:0000033	author statement supported by traceable reference	PMID:17283335	20120720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5644302	Tg(SFTPC-Tnf)2Pva	is_implicated_in	DOID:0050156	idiopathic pulmonary fibrosis		MGI:5644303	Tg(SFTPC-Tnf)2Pva/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:7542280	20150716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007819	Gt(ROSA)26Sor<sup>tm3(NOTCH3*R1031C)Sat</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:21555590	20110617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6343233	Lrp4<sup>tm1.1Pg</sup>	is_implicated_in	DOID:0060757	sclerosteosis 2		MGI:6404118	Lrp4<sup>tm1.1Pg</sup>/Lrp4<sup>tm1.1Pg</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28477420	20200415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558880	Fbn1<sup>tm3.1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:24107997	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6725087	Hes7<sup>M1Btlr</sup>	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:6725725	Hes7<sup>M1Btlr</sup>/Hes7<sup>+</sup>  [background:] C57BL/6J-Hes7<sup>M1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586839	Htt<sup>tm1Hay</sup>/Htt<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:7774020	20050907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661331	Col1a1<sup>tm5(CAG-FGFR2_iIIIb*W290C)Kkw</sup>/Col1a1<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25035393	20150909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491242	b2b2153Clo	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5516012	b2b2153Clo/b2b2153Clo  [background:] C57BL/6J-b2b2153Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5791914	Tg(Neurod2-Smo*A1)199Jols/0  [background:] involves: C57BL/6	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:25348795	20160912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3702040	Ush2a<sup>tm1Tili</sup>	is_implicated_in	DOID:0110838	Usher syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3702040	Ush2a<sup>tm1Tili</sup>	is_implicated_in	DOID:0110838	Usher syndrome type 2A		MGI:3702269	Ush2a<sup>tm1Tili</sup>/Ush2a<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17360538	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6280004	Kcnh6<sup>em2Jkya</sup>	is_implicated_in	DOID:4194	glucose metabolism disease		MGI:6402419	Kcnh6<sup>em2Jkya</sup>/Kcnh6<sup>em2Jkya</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30590050	20200401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635155	Tg(HTT*)LXwy	is_implicated_in	DOID:12858	Huntington's disease		MGI:5635161	Tg(HTT*)LXwy/0  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:25661181	20150508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575893	Tg(Myh6-KCNQ1_i2)H02Desc/0  [background:] involves: FVB	is_model_of	DOID:0110644	long QT syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11334835	20140801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393578	Ezh2<sup>tm1.1Nesh</sup>	is_implicated_in	DOID:707	B-cell lymphoma		MGI:6393679	Ezh2<sup>tm1.1Nesh</sup>/Ezh2<sup>+</sup> Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27135738	20200310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N	is_model_of	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000033	author statement supported by traceable reference	PMID:20675713	20101116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668857	Arg1<sup>tm1Rki</sup>/Arg1<sup>tm1Rki</sup>  [background:] Not Specified	is_model_of	DOID:9278	hyperargininemia						ECO:0000033	author statement supported by traceable reference	PMID:12052859	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5701634	Sh3bp2<sup>tm1.1Ics</sup>	is_implicated_in	DOID:1856	cherubism		MGI:5701638	Sh3bp2<sup>tm1.1Ics</sup>/Sh3bp2<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25705883	20160108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904948	Tg(Myh6-Rab1a)lowGwd	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5904951	Tg(Myh6-Rab1a)lowGwd/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11739277	20170718	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611756	Cacna1f<sup>tm1Ntbh</sup>/Cacna1f<sup>tm1Ntbh</sup>  [background:] B6.129-Cacna1f<sup>tm1Ntbh</sup>	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:16155113	20060201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5770244	Brinp1<sup>tm1.1Pib</sup>/Brinp1<sup>tm1.1Pib</sup>  [background:] involves: BALB/cJ * C57BL/6	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:27042284	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581675	Rc3h1<sup>san</sup>	is_implicated_in	DOID:0050749	peripheral T-cell lymphoma						ECO:0000033	author statement supported by traceable reference	PMID:31013298	20190531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581675	Rc3h1<sup>san</sup>	is_implicated_in	DOID:0050749	peripheral T-cell lymphoma		MGI:5445374	Rc3h1<sup>san</sup>/Rc3h1<sup>+</sup>  [background:] involves: C57BL/6JSfdAnu			ECO:0000033	author statement supported by traceable reference	PMID:22700722	20190531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7333014	Kmt2d<sup>tm2.1Kaig</sup>	is_implicated_in	DOID:0060473	Kabuki syndrome		MGI:7333170	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Kmt2d<sup>tm2.1Kaig</sup>/Kmt2d<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:32541010	20220902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4410618	Mks1<sup>krc</sup>/Mks1<sup>krc</sup>  [background:] involves: C3HeB/FeJ * C57BL/6 * CD-1	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19776033	20091215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3723505	Tg(HD)63Aron/?  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11717344	20071004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435556	Porcn<sup>tm1.1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435567	Porcn<sup>tm1.1Vdv</sup>/Y Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435556	Porcn<sup>tm1.1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435562	Porcn<sup>tm1.1Vdv</sup>/Y Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435556	Porcn<sup>tm1.1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435565	Porcn<sup>tm1.1Vdv</sup>/Porcn<sup>+</sup> Hprt1<sup>tm1(CAG-cre)Mnn</sup>/Hprt1<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435556	Porcn<sup>tm1.1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435561	Porcn<sup>tm1.1Vdv</sup>/Porcn<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5435556	Porcn<sup>tm1.1Vdv</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435568	Porcn<sup>tm1.1Vdv</sup>/Y Tg(KRT14-cre)1Efu/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702952	Mecp2<sup>tm6.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26647311	20160115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5487544	Tg(Prnp*P101L)174Sbp	is_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:5487546	Tg(Prnp*P101L)174Sbp/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1980379	20130529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4421295	Myd88<sup>tm1.1Defr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28951424	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4421295	Myd88<sup>tm1.1Defr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31993047	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297426	Dnah5<sup>b2b1003Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314017	Dnah5<sup>b2b1154Clo</sup>/Dnah5<sup>b2b1154Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1154Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430946	Spart<sup>tm1.1Xen</sup>	is_implicated_in	DOID:0050886	Troyer syndrome		MGI:5430992	Spart<sup>tm1.1Xen</sup>/Spart<sup>tm1.1Xen</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22619377	20120813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442115	b2b1594Clo	is_implicated_in	DOID:11193	syndactyly		MGI:5442125	b2b1594Clo/b2b1594Clo  [background:] C57BL/6J-b2b1594Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566682	Tg(YAC128)#Hay/0  [background:] FVB/N-Tg(YAC128)#Hay	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15843620	20140603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435561	Porcn<sup>tm1.1Vdv</sup>/Porcn<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176925	Crygc<sup>Chl3</sup>/Crygc<sup>+</sup>  [background:] involves: 102/El * C3H/El	is_model_of	DOID:0110235	cataract 2 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11773036	20050923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817970	Ccm2<sup>tm1.1Kwhi</sup>	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2						ECO:0000033	author statement supported by traceable reference	PMID:25486933	20160831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5517669	Snca<sup>tm1.1Koks</sup>/Snca<sup>+</sup>  [background:] either: B6.129P2-Snca<sup>tm1.1Koks</sup> or (involves: 129P2/OlaHsd * C57BL/6)	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:18622040	20131114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5765989	Tg(ACTA1-Ctss)1Jmol	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5779562	Tg(ACTA1-Ctss)1Jmol/?  [background:] FVB/N-Tg(ACTA1-Ctss)1Jmol			ECO:0000033	author statement supported by traceable reference	PMID:26966179	20160630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856155	Pax6<sup>Sey</sup>	is_implicated_in	DOID:12271	aniridia						ECO:0000033	author statement supported by traceable reference	PMID:24290376	20140506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856155	Pax6<sup>Sey</sup>	is_implicated_in	DOID:12271	aniridia						ECO:0000033	author statement supported by traceable reference	PMID:24355924	20140506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575660	Lmo4<sup>tm1.1Gng</sup>/Lmo4<sup>tm1.1Gng</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0060668	anencephaly						ECO:0000033	author statement supported by traceable reference	PMID:15691703	20050525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851599	Cngb1<sup>tm1Sjpi</sup>/Cngb1<sup>tm1Sjpi</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:19339551	20100720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5755963	Tg(Alb-HBx)A112Tfts	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5755966	Tg(Alb-HBx)A112Tfts/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16403455	20160407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5755963	Tg(Alb-HBx)A112Tfts	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26206949	20160407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7511852	Pigk<sup>em2Linwu</sup>	is_not_implicated_in	DOID:0112202	developmental and epileptic encephalopathy		MGI:7511860	Pigk<sup>em2Linwu</sup>/Pigk<sup>em2Linwu</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33392778	20230727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888950	Cdkn1a<sup>tm1Led</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052529	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: Black Swiss)	is_model_of	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16870172	20150821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052529	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: Black Swiss)	is_model_of	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15289437	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5519934	Bscl2<sup>tm1Geno</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5519974	Bscl2<sup>tm1Geno</sup>/Bscl2<sup>tm1Geno</sup>  [background:] B6.129P2-Bscl2<sup>tm1Geno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23680914	20131126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5825059	Tg(BAC144D14)5D3Masu/0  [background:] B6J.Cg-Tg(BAC144D14)5D3Masu	is_model_of	DOID:14681	Silver-Russell syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26963625	20170224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292519	Zdhhc17<sup>Gt(RRJ233)Byg</sup>/Zdhhc17<sup>Gt(RRJ233)Byg</sup>  [background:] FVB.129P2-Zdhhc17<sup>Gt(RRJ233)Byg</sup>	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21775500	20111019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513849	Apc<sup>tm1Cip</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:15502862	20170302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317589	Dnai1<sup>b2b1526Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428666	Nemf<sup>tvrm116</sup>	is_implicated_in	DOID:870	neuropathy		MGI:6718876	Nemf<sup>tvrm116</sup>/Nemf<sup>tvrm116</sup>  [background:] C57BL/6J-Nemf<sup>tvrm116</sup>/PjnCx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177634	Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12934	Kearns-Sayre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9916807	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6488172	Kcnq2<sup>tm1.1Lvi</sup>	is_implicated_in	DOID:0080462	developmental and epileptic encephalopathy 7		MGI:6488175	Kcnq2<sup>tm1.1Lvi</sup>/Kcnq2<sup>+</sup>  [background:] 129-Kcnq2<sup>tm1.1Lvi</sup>/Lvi			ECO:0000033	author statement supported by traceable reference	PMID:32239694	20201222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5774860	Tg(Thy1-MAPT*L266V*G272V)13Ema	is_implicated_in	DOID:11870	Pick's disease		MGI:5774862	Tg(Thy1-MAPT*L266V*G272V)13Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25803611	20160602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3803199	Aire<sup>tm1Mand</sup>/Aire<sup>+</sup>  [background:] NOD.129P2-Aire<sup>tm1Mand</sup>	is_model_of	DOID:12842	Guillain-Barre syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22490868	20130503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821260	Phka1<sup>I/FnLn</sup>	is_implicated_in	DOID:0111040	glycogen storage disease IXd		MGI:4821261	Phka1<sup>I/FnLn</sup>/Phka1<sup>I/FnLn</sup>  [background:] I/FnLn			ECO:0000033	author statement supported by traceable reference	PMID:7874115	20100913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821260	Phka1<sup>I/FnLn</sup>	is_implicated_in	DOID:0111040	glycogen storage disease IXd		MGI:4821274	Phka1<sup>I/FnLn</sup>/Y  [background:] I/FnLn			ECO:0000033	author statement supported by traceable reference	PMID:7874115	20100913	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510438	Nbn<sup>tm1Md</sup>/Nbn<sup>tm1Zqw</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15333589	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3828513	Fermt1<sup>tm1Ref</sup>/Fermt1<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0060472	Kindler syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19057668	20090123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5643754	Gt(ROSA)26Sor<sup>tm5(ACTB-tTA)Luo</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Col2a1-cre)1Bhr/0 Tg(tetO/CMV-Col2a1*R992C,-GFP)#Afe/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000033	author statement supported by traceable reference	PMID:25451152	20150707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438068	Cep290<sup>b2b1752Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5442145	Cep290<sup>b2b1752Clo</sup>/Cep290<sup>b2b1752Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1752Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856716	Myo7a<sup>sh1</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20150916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856716	Myo7a<sup>sh1</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:2449164	Myo7a<sup>sh1</sup>/Myo7a<sup>sh1</sup>  [background:] involves: BALB			ECO:0000033	author statement supported by traceable reference	MGI:63673	20150916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856716	Myo7a<sup>sh1</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:2449164	Myo7a<sup>sh1</sup>/Myo7a<sup>sh1</sup>  [background:] involves: BALB			ECO:0000033	author statement supported by traceable reference	PMID:4187938	20150916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835238	Tg(MMTV-LPAR3)3Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763111	Tg(MMTV-LPAR3)3Gbm/Tg(MMTV-LPAR3)3Gbm  [background:] FVB/N-Tg(MMTV-LPAR3)3Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461777	Ttll1<sup>tm1Seto</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:4461790	Ttll1<sup>tm1Seto</sup>/Ttll1<sup>tm1Seto</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20498047	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5469591	Pik3ca<sup>tm1Gne</sup>/Pik3ca<sup>+</sup> Tg(MMTV-cre)1Mam/0  [background:] involves: C57BL/6N * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:22370636	20130321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4874654	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:6115250	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>/Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25422369	20180208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4874654	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:6115249	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>/Y  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25422369	20180208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055667	Dysf<sup>prmd</sup>/Dysf<sup>prmd</sup>  [background:] A/J	is_model_of	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000033	author statement supported by traceable reference	PMID:15254015	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6358416	Nsmf<sup>tm1.2Mrkr</sup>	is_not_implicated_in	DOID:3614	Kallmann syndrome		MGI:6358417	Nsmf<sup>tm1.2Mrkr</sup>/Nsmf<sup>tm1.2Mrkr</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26977770	20190905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7449316	Gt(ROSA)26Sor<sup>tm1.1(CAG-ATP1A3*D591V,-EGFP)Bcgen</sup>	is_implicated_in	DOID:0050572	cone-rod dystrophy		MGI:7449370	Gt(ROSA)26Sor<sup>tm1.1(CAG-ATP1A3*D591V,-EGFP)Bcgen</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32440726	20230403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641393	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] B6J.129S4-Tsc2<sup>tm1Tno</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23250422	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5752280	Ildr1<sup>tm1.1Lwa</sup>	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5903891	Ildr1<sup>tm1.1Lwa</sup>/Ildr1<sup>tm1.1Lwa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25819842	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856656	Rab27a<sup>ash</sup>	is_implicated_in	DOID:0050120	hemophagocytic lymphohistiocytosis						ECO:0000033	author statement supported by traceable reference	PMID:18991284	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856656	Rab27a<sup>ash</sup>	is_implicated_in	DOID:0050120	hemophagocytic lymphohistiocytosis		MGI:5476655	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] B6.C3Sn-Rab27a<sup>ash</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23160464	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5469422	Otoa<sup>tm1Gpr</sup>/Otoa<sup>tm1Gpr</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0110480	autosomal recessive nonsyndromic deafness 22						ECO:0000033	author statement supported by traceable reference	PMID:23129639	20130329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7444804	Lemd2<sup>em1Eno</sup>	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:7444862	Lemd2<sup>em1Eno</sup>/Lemd2<sup>em1Eno</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:36377660	20230317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388372	Kcnj1<sup>tm1Ges</sup>	is_implicated_in	DOID:0110143	Bartter disease type 2						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388372	Kcnj1<sup>tm1Ges</sup>	is_implicated_in	DOID:0110143	Bartter disease type 2		MGI:3041878	Kcnj1<sup>tm1Ges</sup>/Kcnj1<sup>tm1Ges</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12122007	20131223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2429606	C3<sup>tm1Crr</sup>/C3<sup>tm1Crr</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:8354	complement component 3 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:8524789	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304797	Tg(Prnp-HTT*82Q)52Caro	is_implicated_in	DOID:12858	Huntington's disease		MGI:5304801	Tg(Prnp-HTT*82Q)52Caro/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22219281	20120203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175792	Crebbp<sup>Gt(U-San)112Imeg</sup>/Crebbp<sup>+</sup>  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9949198	20050929	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444484	Tgfb2<sup>tm1Doe</sup>/Tgfb2<sup>+</sup>  [background:] STOCK Tgfb2<sup>tm1Doe</sup>/J	is_model_of	DOID:0050466	Loeys-Dietz syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22772368	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3691621	Casq2<sup>tm1Kpfe</sup>/Casq2<sup>tm1Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000033	author statement supported by traceable reference	PMID:16932808	20090821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835233	Tg(MMTV-LPAR2)#Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763106	Tg(MMTV-LPAR2)#Gbm/Tg(MMTV-LPAR2)#Gbm  [background:] FVB/N-Tg(MMTV-LPAR2)#Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772702	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] C3H/HeJ	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:18776951	20140218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5558868	Fbn1<sup>tm3.1Hcd</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:5558880	Fbn1<sup>tm3.1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24107997	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5607149	Enpp1<sup>asj-2J</sup>	is_implicated_in	DOID:0050644	arterial calcification of infancy		MGI:5607167	Enpp1<sup>asj-2J</sup>/Enpp1<sup>asj-2J</sup>  [background:] BALB/cJ-Enpp1<sup>asj-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25479107	20141215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618813	Tg(H2-Ea<sup>d</sup>)12Lt/0  [background:] NOD/ShiLt-Tg(H2-Ea<sup>d</sup>)12Lt	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:8757636	20060531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5430752	Inpp5b<sup>tm1Nbm</sup>/Inpp5b<sup>tm1Nbm</sup> Ocrl<sup>tm1Nbm</sup>/Y Tg(INPP5B)CNbm/0  [background:] involves: 129S/SvEv * 129S6/SvEvTac * FVB/N	is_model_of	DOID:1056	oculocerebrorenal syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21183592	20120809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4842354	Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:906	peroxisomal disease		MGI:6502847	Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>/Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-A<sup>tm1Brd</sup> Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>/WtsiCnbc			ECO:0000033	author statement supported by traceable reference	PMID:33244184	20210129	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5567000	Gla<sup>tm1Kul</sup>/Y Tg(CAG-A4GALT)#Sais/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6JJms	is_model_of	DOID:14499	Fabry disease						ECO:0000033	author statement supported by traceable reference	PMID:24094090	20140606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4829971	Capn3<sup>tm1.1Hiso</sup>/Capn3<sup>tm1.1Hiso</sup>  [background:] B6.129P2-Capn3<sup>tm1.1Hiso</sup>	is_model_of	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A						ECO:0000033	author statement supported by traceable reference	PMID:20592470	20100920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037831	Gjb6<sup>tm1Kwi</sup>/Gjb6<sup>tm1Kwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000033	author statement supported by traceable reference	PMID:12490528	20051005	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720802	Col1a2<sup>oim</sup>/Col1a2<sup>oim</sup>  [background:] B6C3Fe a/a-Col1a2<sup>oim</sup>/J	is_model_of	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:8968022	20070907	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3040187	Ctsd<sup>tm1Cptr</sup>/Ctsd<sup>tm1Cptr</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd)	is_model_of	DOID:0110725	neuronal ceroid lipofuscinosis 10						ECO:0000033	author statement supported by traceable reference	PMID:18498441	20081009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5490865	Rho<sup>tm4.1(RHO*/EGFP)Jhw</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:5490868	Rho<sup>tm4.1(RHO*/EGFP)Jhw</sup>/Rho<sup>+</sup>  [background:] B6.129S7-Rho<sup>tm4.1(RHO*/EGFP)Jhw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22110080	20130619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910441	Fgf9<sup>tm1Zgwg</sup>	is_implicated_in	DOID:0050794	multiple synostoses syndrome		MGI:6161223	Fgf9<sup>tm1Zgwg</sup>/Fgf9<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:28169396	20180615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910441	Fgf9<sup>tm1Zgwg</sup>	is_implicated_in	DOID:0050794	multiple synostoses syndrome		MGI:6161224	Fgf9<sup>tm1Zgwg</sup>/Fgf9<sup>tm1Zgwg</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:28169396	20180615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842290	Ptpn22<sup>tm2Achn</sup>/Ptpn22<sup>tm2Achn</sup> Ptprc<sup>tm1Weis</sup>/Ptprc<sup>tm1Weis</sup>  [background:] B6.Cg-Ptprc<sup>tm1Weis</sup> Ptpn22<sup>tm2Achn</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:19299707	20090430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907607	E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>	is_implicated_in	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome		MGI:5907679	E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24565867	20170829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285646	Myh9<sup>tm1.1(MYH9*)Mjk</sup>	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499736	Myh9<sup>tm1.1(MYH9*)Mjk</sup>/Myh9<sup>tm1.1(MYH9*)Mjk</sup>  [background:] B6.129-Myh9<sup>tm1.1(MYH9*)Mjk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285646	Myh9<sup>tm1.1(MYH9*)Mjk</sup>	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499734	Myh9<sup>tm1.1(MYH9*)Mjk</sup>/Myh9<sup>+</sup>  [background:] B6.Cg-Myh9<sup>tm1.1(MYH9*)Mjk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5086230	Tg(Thy1-GLRA1*R271Q)300Wha	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:5140029	Tg(Thy1-GLRA1*R271Q)300Wha/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11923415	20140501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5086230	Tg(Thy1-GLRA1*R271Q)300Wha	is_implicated_in	DOID:0060696	hyperekplexia 1						ECO:0000033	author statement supported by traceable reference	PMID:24390226	20140501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1927833	Fgf10<sup>tm1Wss</sup>	is_implicated_in	DOID:0050331	lacrimoauriculodentodigital syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:33363172	20221006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1927833	Fgf10<sup>tm1Wss</sup>	is_implicated_in	DOID:0050331	lacrimoauriculodentodigital syndrome 1		MGI:5816495	Fgf10<sup>tm1Wss</sup>/Fgf10<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:27590203	20221006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462364	Tg(tetO-HMOX1)6Hyms	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5462366	Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22881289	20130208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4881773	Triobp<sup>tm1Tbf</sup>	is_implicated_in	DOID:0110486	autosomal recessive nonsyndromic deafness 28		MGI:4881776	Triobp<sup>tm1Tbf</sup>/Triobp<sup>tm1Tbf</sup>  [background:] C57BL/6-Triobp<sup>tm1Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20510926	20220308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5521542	Tg(tetO-RNAi:Trp53)ASlowe	is_implicated_in	DOID:3347	osteosarcoma		MGI:5521546	Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 Tg(tetO-RNAi:Trp53)ASlowe/0  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623394	Hnf1a<sup>tm1.1Ylee</sup>/Hnf1a<sup>tm1.1Ylee</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111102	maturity-onset diabetes of the young type 3						ECO:0000033	author statement supported by traceable reference	PMID:9566924	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175905	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/J	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:7062441	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175905	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/J	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:3404974	20050812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851249	Tg(Kera-PITX2*A)AHjal/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:15509533	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430344	Dnah5<sup>b2b1565Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5430346	Dnah5<sup>b2b1565Clo</sup>/Dnah5<sup>b2b1565Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1565Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420801	Tg(tetO-SNCA*A53T)E2Cai	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:26317866	20171211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5581488	Tg(Myh6-MYOZ2*S48P)114Ajm	is_implicated_in	DOID:0110322	hypertrophic cardiomyopathy 16						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5581488	Tg(Myh6-MYOZ2*S48P)114Ajm	is_implicated_in	DOID:0110322	hypertrophic cardiomyopathy 16		MGI:5581490	Tg(Myh6-MYOZ2*S48P)114Ajm/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22987565	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670276	Ro60<sup>tm1Woln</sup>/Ro60<sup>tm1Woln</sup>  [background:] B6.129S1-Ro60<sup>tm1Woln</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440922	Tg(Eno2-MFN2*R94Q)L51Ugfm/0  [background:] involves: C57BL/6 * C57BL/6J * DBA/2	is_model_of	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	MGI:4440898	20110919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5486199	Tg(ARR2/Pbsn-MYC)7Key/?  [background:] involves: FVB/N	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:14522256	20130521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384133	Mpz<sup>tm1Msch</sup>	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000033	author statement supported by traceable reference	PMID:27215377	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384133	Mpz<sup>tm1Msch</sup>	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:3576602	Mpz<sup>tm1Msch</sup>/Mpz<sup>tm1Msch</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7581451	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384133	Mpz<sup>tm1Msch</sup>	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:3576605	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7581451	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:31484823	20211102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:5636613	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(KLK3-cre)13Saa/0  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24986896	20211102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405194	Tardbp<sup>tm1.1Neas</sup>	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6405398	Tardbp<sup>tm1.1Neas</sup>/Tardbp<sup>tm1.1Neas</sup>  [background:] B6(C3)-Tardbp<sup>tm1.1Neas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30625319	20200423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4950562	Prpf3<sup>tm1.1Eap</sup>	is_implicated_in	DOID:0110356	retinitis pigmentosa 18		MGI:4950564	Prpf3<sup>tm1.1Eap</sup>/Prpf3<sup>tm1.1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4950562	Prpf3<sup>tm1.1Eap</sup>	is_implicated_in	DOID:0110356	retinitis pigmentosa 18		MGI:4950565	Prpf3<sup>tm1.1Eap</sup>/Prpf3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705250	Tg(tetO-EGFR*T790M)8Paow	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:25870145	20160126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705250	Tg(tetO-EGFR*T790M)8Paow	is_implicated_in	DOID:1324	lung cancer		MGI:5705252	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M)8Paow/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17726540	20160126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043695	Ercc5<sup>tm4Shm</sup>/Ercc5<sup>tm4Shm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0110849	xeroderma pigmentosum group G						ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5803980	Tg(Dct-Grm1)ESzc/0  [background:] C57BL/6J-Tg(Dct-Grm1)ESzc	is_model_of	DOID:6039	uveal melanoma						ECO:0000033	author statement supported by traceable reference	PMID:25051141	20161018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5550383	Cacna1f<sup>tm1.1Sdie</sup>/Y  [background:] involves: C57BL/6	is_model_of	DOID:0110871	congenital stationary night blindness 2A						ECO:0000033	author statement supported by traceable reference	PMID:24163243	20140312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830837	Tymp<sup>tm1Mihi</sup>	is_implicated_in	DOID:0080119	mitochondrial DNA depletion syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24362886	20140813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3041140	Map6<sup>tm1Job</sup>/Map6<sup>tm1Job</sup>  [background:] either: 129S2/SvPas or (involves: 129S2/SvPas * BALB/c)	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:12231625	20090223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522715	vsd/vsd<sup>+</sup>  [background:] C57BL/6J-vsd	is_model_of	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6474002	Gch1<sup>em1Ypt</sup>	is_implicated_in	DOID:0112225	BH4-deficient hyperphenylalaninemia B		MGI:6474005	Gch1<sup>em1Ypt</sup>/Gch1<sup>em1Ypt</sup>  [background:] C57BL/6-Gch1<sup>em1Ypt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30742839	20210727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5693797	Apc<sup>Min</sup>/Apc<sup>+</sup> Ccdc80<sup>tm1.1Ftk</sup>/Ccdc80<sup>tm1.1Ftk</sup>  [background:] involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * C57BL/6J * C57BL/6N	is_model_of	DOID:9256	colorectal cancer						ECO:0000033	author statement supported by traceable reference	PMID:25053805	20151028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926345	Tsc2<sup>tm1Tno</sup>	is_implicated_in	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:27889578	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926345	Tsc2<sup>tm1Tno</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:2174790	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10096549	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926345	Tsc2<sup>tm1Tno</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5641393	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] B6J.129S4-Tsc2<sup>tm1Tno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20170403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5532530	Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0110612	primary ciliary dyskinesia 10		MGI:6369967	Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>/Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>  [background:] B6N(Cg)-Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:31107948	20191107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5474282	Efnb3<sup>m1Btlr</sup>	is_implicated_in	DOID:480	movement disease		MGI:5474304	Efnb3<sup>m1Btlr</sup>/Efnb3<sup>m1Btlr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:5474302	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677574	Vhl<sup>tm1Lss</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:23384121	20131118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677574	Vhl<sup>tm1Lss</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3844062	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Ins2-cre)25Mgn/0  [background:] either: (involves: 129X1/SvJ * C57BL/6 * DBA) or (involves: 129X1/SvJ * A/J * C57BL/6 * DBA)			ECO:0000033	author statement supported by traceable reference	PMID:19340311	20131118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677574	Vhl<sup>tm1Lss</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3844061	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Gcg-cre)1Slib/0  [background:] either: (involves: 129X1/SvJ * A/J) or (involves: 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:19340311	20131118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677574	Vhl<sup>tm1Lss</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3844065	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19340311	20131118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5495415	Kif7<sup>dda</sup>/Kif7<sup>dda</sup>  [background:] FVB.A-Kif7<sup>dda</sup>	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:23650387	20130717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393452	Spast<sup>tm1.1Evre</sup>	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:6393456	Spast<sup>tm1.1Evre</sup>/Spast<sup>tm1.1Evre</sup>  [background:] C57BL/6-Spast<sup>tm1.1Evre</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27019090	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437079	Lrp1<sup>b2b1554Clo</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851236	Tg(Acta2-RAC1*G12V)33Pjgc/Tg(Acta2-RAC1*G12V)33Pjgc  [background:] involves: C57BL/6 * FVB/N	is_model_of	DOID:8632	Kaposi's sarcoma						ECO:0000033	author statement supported by traceable reference	PMID:19429708	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446156	b2b1430Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5446380	b2b1430Clo/b2b1430Clo  [background:] C57BL/6J-b2b1430Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6400708	Htt<sup>tm5Detl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:6400710	Htt<sup>tm5Detl</sup>/Htt<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28927719	20200320	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285395	Shank3<sup>tm1.2Bux</sup>/Shank3<sup>+</sup>  [background:] C57BL/6-Shank3<sup>tm1.2Bux</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21167025	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437101	b2b1200Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669009	Wt1<sup>tm1Jae</sup>/Wt1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * MF1	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:17071579	20161003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476825	Tg(TARDBP*G348C)#Jpj	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5476838	Tg(TARDBP*G348C)#Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21752789	20130502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476825	Tg(TARDBP*G348C)#Jpj	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000033	author statement supported by traceable reference	PMID:22230045	20130502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705131	Brpf1<sup>tm1c(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:5896655	Brpf1<sup>tm1c(EUCOMM)Wtsi</sup>/Brpf1<sup>tm1c(EUCOMM)Wtsi</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27939640	20170619	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662011	Ar<sup>Tfm</sup>/Y Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129/Sv * CD-1 * STOCK Eda<sup>Ta</sup>	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705252	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M)8Paow/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:17726540	20160125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3772883	Tg(Prnp-TBP*)71-16Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)71-16Xjl	is_model_of	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000033	author statement supported by traceable reference	PMID:17994014	20080305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2386447	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup> Xpa<sup>tm1Hvs</sup>/Xpa<sup>tm1Hvs</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2960	photosensitive trichothiodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:11950998	20050825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849047	Etv5<sup>tm1.1Xsun</sup>	is_implicated_in	DOID:5602	T-cell adult acute lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29769563	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3821602	Hbb-b1<sup>MommeD7</sup>/Hbb-b1<sup>MommeD7</sup>  [background:] involves: FVB/N	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:23040355	20130128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576602	Mpz<sup>tm1Msch</sup>/Mpz<sup>tm1Msch</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000033	author statement supported by traceable reference	PMID:7581451	20050511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>	is_model_of	DOID:0110598	primary ciliary dyskinesia 14						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5621006	Lrp6<sup>tm1Arma</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5694491	Lrp6<sup>tm1Arma</sup>/Lrp6<sup>tm1Arma</sup>  [background:] C57BL/6-Lrp6<sup>tm1Arma</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25917329	20151103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521585	Apc<sup>tm2Tno</sup>/Apc<sup>+</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0050424	familial adenomatous polyposis						ECO:0000033	author statement supported by traceable reference	PMID:14522940	20131206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849863	Glis3<sup>tm1Hiha</sup>	is_implicated_in	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:24411943	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849863	Glis3<sup>tm1Hiha</sup>	is_implicated_in	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism		MGI:3849867	Glis3<sup>tm1Hiha</sup>/Glis3<sup>tm1Hiha</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19481545	20140923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5568206	Mecp2<sup>tm1.1Jtc</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5568994	Mecp2<sup>tm1.1Jtc</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24283265	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5568206	Mecp2<sup>tm1.1Jtc</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5568998	Mecp2<sup>tm1.1Jtc</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24283265	20170308	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3044750	Mnt<sup>tm1.1Awb</sup>/Mnt<sup>tm1.1Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15028671	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5548820	Cfap69<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:0111929	spermatogenic failure 24		MGI:6865772	Cfap69<sup>tm1b(KOMP)Wtsi</sup>/Cfap69<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29606301	20220209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5616117	Bmp10<sup>b2b2711Clo</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5616119	Bmp10<sup>b2b2711Clo</sup>/Bmp10<sup>b2b2711Clo</sup>  [background:] C57BL/6J-Bmp10<sup>b2b2711Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712038	Opa1<sup>Q285X</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6JCrl	is_model_of	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:17428816	20130104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3712038	Opa1<sup>Q285X</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6JCrl	is_model_of	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:21803037	20130104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705650	Tg(Pbsn-ERG*)1Vv/0  [background:] involves: 129S1/SvImJ * C57BL/6J * CBA	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:26058078	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6276040	Tg(Myh6-Camk2d_ic)MJhb	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276042	Tg(Myh6-Camk2d_ic)MJhb/0  [background:] either: (involves: Black Swiss) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12676814	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5693885	Tbp<sup>tm1Xjl</sup>/Tbp<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129S/SvEv * C57BL/6 * CBA	is_model_of	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000033	author statement supported by traceable reference	PMID:24462098	20151028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789190	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup> Nos2<sup>tm1Mrl</sup>/Nos2<sup>tm1Mrl</sup> Nos3<sup>tm1Plh</sup>/Nos3<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:16024729	20080527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6467991	Vps13b<sup>tm1.2Ics</sup>	is_implicated_in	DOID:0111590	Cohen syndrome		MGI:6468047	Vps13b<sup>tm1.2Ics</sup>/Vps13b<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32915983	20201021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176866	Sgca<sup>tm1Kcam</sup>/Sgca<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000033	author statement supported by traceable reference	PMID:9744877	20050622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317116	Lgi1<sup>tm1.1Ics</sup>/Lgi1<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6	is_model_of	DOID:0060748	familial temporal lobe epilepsy 1						ECO:0000033	author statement supported by traceable reference	PMID:20659958	20120502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800675	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup> Il4ra<sup>tm1Sz</sup>/Il4ra<sup>tm1Sz</sup>  [background:] involves: BALB/cJ * C57BL/6J * C57BL/10 * DBA/2	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:11168809	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177824	Eng<sup>tm1Mle</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:23074273	20130311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177824	Eng<sup>tm1Mle</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:2669003	Eng<sup>tm1Mle</sup>/Eng<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10562296	20130311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177824	Eng<sup>tm1Mle</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:3628821	Eng<sup>tm1Mle</sup>/Eng<sup>+</sup>  [background:] 129P2/OlaHsd-Eng<sup>tm1Mle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10562296	20130311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5704132	Cacna1a<sup>tm1.1Ehess</sup>	is_implicated_in	DOID:0050990	episodic ataxia type 2		MGI:5707183	Cacna1a<sup>tm1.1Ehess</sup>/Cacna1a<sup>tm1.1Ehess</sup>  [background:] C57BL/6-Cacna1a<sup>tm1.1Ehess</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25109669	20160203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437099	Odad2<sup>b2b227.1Clo</sup>	is_implicated_in	DOID:0110609	primary ciliary dyskinesia 23		MGI:5437109	Odad2<sup>b2b227.1Clo</sup>/Odad2<sup>b2b227.1Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b227.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388567	Tg(MtTGFA)42Lmb	is_implicated_in	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26239478	20160407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5476673	Tg(Eno2-MFN2*R94Q)L87Ugfm/Tg(Eno2-MFN2*R94Q)L87Ugfm  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000033	author statement supported by traceable reference	PMID:20418531	20130501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2684657	Psen1<sup>tm1Vln</sup>/Psen1<sup>tm1Vln</sup> Tg(Thy1-cre)1Vln/0  [background:] involves: FVB/N	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:11978821	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197036	Atp1a3<sup>tm1Mika</sup>	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:6197063	Atp1a3<sup>tm1Mika</sup>/Atp1a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30071271	20180907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4941753	Slc6a8<sup>tm1.1Clar</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:5448415	Slc6a8<sup>tm1.1Clar</sup>/Y Tg(Camk2a-cre)2Gsc/0  [background:] involves: C57BL/6 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22751104	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694359	Ube3a<sup>tm1Alb</sup>/Ube3a<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9808466	20070123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440440	Tg(CAG-VCP*A232E)93Jpat	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:27009270	20171218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440440	Tg(CAG-VCP*A232E)93Jpat	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:4440450	Tg(CAG-VCP*A232E)93Jpat/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20147319	20171218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5085315	Ccm2<sup>tm2.1Sbn</sup>	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:5085321	Ccm2<sup>tm2.1Sbn</sup>/Ccm2<sup>tm2.1Sbn</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21596842	20110812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6405407	Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:6405698	Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>/Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] B6J.Cg-Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31824252	20200424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6355913	Polg2<sup>M1Rvt</sup>	is_implicated_in	DOID:12679	nephrocalcinosis		MGI:6368626	Polg2<sup>M1Rvt</sup>/Polg2<sup>+</sup>  [background:] involves: BALB/c * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:30395686	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412021	Apc<sup>tm1Rak</sup>/Apc<sup>+</sup> Mlh1<sup>tm1Rak</sup>/Mlh1<sup>tm1Rak</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10096563	20091216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5771865	Apob<sup>tm2Sgy</sup>/Apob<sup>tm2Sgy</sup> Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup> Tg(Ins-Igf2)1Fbos/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:0110741	type 1 diabetes mellitus 2						ECO:0000033	author statement supported by traceable reference	PMID:25231636	20160526	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5702941	Mecp2<sup>tm4.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1206	Rett syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26647311	20160115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6110860	Pabpn1<sup>tm1.2Gpvl</sup>	is_implicated_in	DOID:11719	oculopharyngeal muscular dystrophy		MGI:6111174	Pabpn1<sup>tm1.2Gpvl</sup>/Pabpn1<sup>+</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28575395	20180119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5810761	Rho<sup>Tvrm334</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:5924952	Rho<sup>Tvrm334</sup>/Rho<sup>+</sup>  [background:] B6.Cg-Rho<sup>Tvrm334</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354013	Tg(Tyr-cre/ERT,-Hras1*,-Trap1a)10BJvde	is_implicated_in	DOID:1909	melanoma						ECO:0000033	author statement supported by traceable reference	PMID:26139534	20170627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5635532	Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-GJB2*G45E,-EGFP)#Tww/0  [background:] involves: FVB/N * SKH1	is_model_of	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22031297	20150512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5604542	Brinp1<sup>tm1.1Pib</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5770244	Brinp1<sup>tm1.1Pib</sup>/Brinp1<sup>tm1.1Pib</sup>  [background:] involves: BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27042284	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3767061	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] either: (B6.C3-Spta1<sup>sph</sup> x WB.C3-Spta1<sup>sph</sup>)F1 or (WB.C3-Spta1<sup>sph</sup> x B6.C3-Spta1<sup>sph</sup>)F1	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	PMID:7059672	20080110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151182	Hcrt<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:28396432	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151182	Hcrt<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:23993842	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151182	Hcrt<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:29784823	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151182	Hcrt<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:28507129	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151182	Hcrt<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy		MGI:3763455	Hcrt<sup>tm1Ywa</sup>/Hcrt<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10481909	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151182	Hcrt<sup>tm1Ywa</sup>	is_implicated_in	DOID:8986	narcolepsy		MGI:4949137	Hcrt<sup>tm1Ywa</sup>/Hcrt<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:12797957	20180711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259647	Pmfbp1<sup>em1Wli</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6259651	Pmfbp1<sup>em1Wli</sup>/Pmfbp1<sup>em1Wli</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:30032984	20181210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5770425	Stk39<sup>tm2.1Arte</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:5804131	Stk39<sup>tm2.1Arte</sup>/Stk39<sup>tm2.1Arte</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25994507	20161020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297858	2310039L15Rik<sup>Tg(Prnp-SNCA*A53T)23Mkle</sup>/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060367	Parkinson's disease 1						ECO:0000033	author statement supported by traceable reference	PMID:12084935	20111210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688533	Flna<sup>Dilp2</sup>/Y  [background:] involves: BALB/cAnN * C3H/HeN * C57BL/6	is_model_of	DOID:0050454	periventricular nodular heterotopia						ECO:0000033	author statement supported by traceable reference	PMID:16825286	20061124	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437110	b2b1291Clo/b2b1291Clo  [background:] C57BL/6J-b2b1291Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620975	Lyst<sup>bg-grey</sup>/Lyst<sup>bg-grey</sup>  [background:] C57BL/6-Lyst<sup>bg-grey</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16518687	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806503	Tg(SFTPC-SDC4/ROS1)141Tno	is_implicated_in	DOID:1324	lung cancer		MGI:5806507	Tg(SFTPC-SDC4/ROS1)141Tno/0  [background:] C57BL/6J-Tg(SFTPC-SDC4/ROS1)141Tno			ECO:0000033	author statement supported by traceable reference	PMID:26964870	20161108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5795594	Wdfy3<sup>disc</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5825287	Wdfy3<sup>disc</sup>/Wdfy3<sup>disc</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:25198012	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946645	Braf<sup>tm1Bbd</sup>	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:4946646	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21383153	20110415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946645	Braf<sup>tm1Bbd</sup>	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:4946647	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21383153	20110415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4946645	Braf<sup>tm1Bbd</sup>	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:4946650	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] B6.129-Braf<sup>tm1Bbd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21383153	20110415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5450673	Tg(Thy1-MAPT*P301S)2541Godt/Tg(Thy1-MAPT*P301S)2541Godt  [background:] involves: C57BL/6J * CBA/Ca	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:12417659	20160419	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175807	Crygb<sup>Nop</sup>/Crygb<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0110236	cataract 39 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:6479248	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711776	Col17a1<sup>tm1Shzu</sup>	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:22044750	20120719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711776	Col17a1<sup>tm1Shzu</sup>	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:3711939	Col17a1<sup>tm1Shzu</sup>/Col17a1<sup>tm1Shzu</sup>  [background:] B6.129S-Col17a1<sup>tm1Shzu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17322897	20120719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176465	Runx2<sup>tm1Mjo</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:36599929	20230907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176465	Runx2<sup>tm1Mjo</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3044747	Runx2<sup>tm1Mjo</sup>/Runx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9182764	20230907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176465	Runx2<sup>tm1Mjo</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3044747	Runx2<sup>tm1Mjo</sup>/Runx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204840	20230907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4362969	Ulk4<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:24284070	20140820	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6491215	Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0080768	pyridoxine-dependent epilepsy		MGI:6491217	Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>/Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] B6(FVB)-Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32969477	20210111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192374	Kdm6a<sup>tm1Cdcn</sup>	is_implicated_in	DOID:0080188	chronic myelomonocytic leukemia		MGI:6192376	Kdm6a<sup>tm1Cdcn</sup>/Kdm6a<sup>tm1Cdcn</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29479066	20180731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192374	Kdm6a<sup>tm1Cdcn</sup>	is_implicated_in	DOID:0080188	chronic myelomonocytic leukemia		MGI:6192375	Kdm6a<sup>tm1Cdcn</sup>/Y Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29479066	20180731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664790	Gja5<sup>tm1Paul</sup>/Gja5<sup>tm1Paul</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:6419	tetralogy of Fallot						ECO:0000033	author statement supported by traceable reference	PMID:12842919	20061030	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793282	Ror2<sup>tm1Anec</sup>/Ror2<sup>tm1Anec</sup>  [background:] B6.129S1-Ror2<sup>tm1Anec</sup>	is_model_of	DOID:0060764	autosomal recessive Robinow syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18353862	20080611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3607259	Large1<sup>myd</sup>/Large1<sup>myd</sup>  [background:] B6C3Fe a/a-Large1<sup>myd</sup>/J	is_model_of	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:7602333	20051215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5911918	Tg(Myh6-Sgcd*S151A)5Mcn	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:5911924	Tg(Myh6-Sgcd*S151A)5Mcn/0  [background:] involves: 129T2/SvEms * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17164264	20171027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5488915	Cpox<sup>nct</sup>/Cpox<sup>nct</sup>  [background:] involves: BALB/cCrSlc	is_model_of	DOID:13269	hereditary coproporphyria						ECO:0000033	author statement supported by traceable reference	PMID:23631845	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5304758	Col1a1<sup>tm2(tetO-RNAi:Rps19)Karl</sup>/Col1a1<sup>tm2(tetO-RNAi:Rps19)Karl</sup> Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>/Gt(ROSA)26Sor<sup>tm1(rtTA*M2)Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1339	Diamond-Blackfan anemia						ECO:0000033	author statement supported by traceable reference	PMID:21989989	20120202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6269452	Npr3<sup>kylb</sup>	is_implicated_in	DOID:0080001	bone disease		MGI:6269453	Npr3<sup>kylb</sup>/Npr3<sup>kylb</sup>  [background:] involves: BALB/c * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27959934	20181227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573154	Tg(Cnp-SNCA)M2Vle	is_implicated_in	DOID:4752	multiple system atrophy						ECO:0000033	author statement supported by traceable reference	PMID:24405769	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5573154	Tg(Cnp-SNCA)M2Vle	is_implicated_in	DOID:4752	multiple system atrophy		MGI:5573172	Tg(Cnp-SNCA)M2Vle/Tg(Cnp-SNCA)M2Vle  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15797547	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813896	Kras<sup>tm5Tyj</sup>	is_implicated_in	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:35803738	20220801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7511851	Pigk<sup>em1Linwu</sup>	is_not_implicated_in	DOID:0112202	developmental and epileptic encephalopathy		MGI:7511857	Pigk<sup>em1Linwu</sup>/Pigk<sup>em1Linwu</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33392778	20230727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175708	Atm<sup>tm1Led</sup>/Atm<sup>tm1Led</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss	is_model_of	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:8917548	20050603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655962	Tg(YACW408A5)1952Ricc/0  [background:] involves: 129/Sv * SD7	is_model_of	DOID:5572	Beckwith-Wiedemann syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15640248	20060927	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655825	Foxc1<sup>tm1Blh</sup>/Foxc1<sup>+</sup> Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6.Cg-Tyr<sup>c-2J</sup> Foxc1<sup>tm1Blh</sup>	is_model_of	DOID:11211	buphthalmos						ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586593	Fgfr3<sup>tm1Cxd</sup>/Fgfr3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss	is_model_of	DOID:4480	achondroplasia						ECO:0000033	author statement supported by traceable reference	PMID:9887329	20050901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3846848	Npc1<sup>spm</sup>/Npc1<sup>spm</sup>  [background:] C57BLKS/J-Npc1<sup>spm</sup>/J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:7202025	20111205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590140	Gck<sup>Rgsc735</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462250	Tg(CAG-Diap3)924Lesp	is_implicated_in	DOID:0060690	autosomal dominant auditory neuropathy 1		MGI:5575514	Tg(CAG-Diap3)924Lesp/0  [background:] FVB/NJ-Tg(CAG-Diap3)924Lesp			ECO:0000033	author statement supported by traceable reference	PMID:23441200	20140730	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850161	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15385444	20130130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796418	Ghr<sup>tm1Jjk</sup>/Ghr<sup>tm1Jjk</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:9521	Laron syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9371826	20110127	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3796418	Ghr<sup>tm1Jjk</sup>/Ghr<sup>tm1Jjk</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:9521	Laron syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19269870	20110127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699313	Fgfr2<sup>tm1Schl</sup>	is_implicated_in	DOID:2339	Crouzon syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22872266	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699313	Fgfr2<sup>tm1Schl</sup>	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:3699817	Fgfr2<sup>tm1Schl</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:17132737	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857174	Gabrb3<sup>tm1Geh</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23142422	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857174	Gabrb3<sup>tm1Geh</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23010509	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857174	Gabrb3<sup>tm1Geh</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:2175037	Gabrb3<sup>tm1Geh</sup>/Gabrb3<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17983671	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4361526	Ifngr1<sup>tm1Agt</sup>/Ifngr1<sup>tm1Agt</sup>  [background:] B6.129S7-Ifngr1<sup>tm1Agt</sup>/J	is_model_of	DOID:11476	osteoporosis						ECO:0000033	author statement supported by traceable reference	PMID:21308779	20170515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6490519	Tbc1d24<sup>em4Tbf</sup>	is_not_implicated_in	DOID:0110586	autosomal dominant nonsyndromic deafness 65		MGI:6490525	Tbc1d24<sup>em4Tbf</sup>/Tbc1d24<sup>em4Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em4Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32987832	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5293611	Gbe1<sup>tm1Hoa</sup>	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:5293613	Gbe1<sup>tm1Hoa</sup>/Gbe1<sup>tm1Hoa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:21856731	20111027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427874	Tg(Ckm-CUGBP1)1039Coop/0  [background:] FVB-Tg(Ckm-CUGBP1)1039Coop	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:15843400	20120713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5286128	Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo/0  [background:] Not Specified	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21515588	20110923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6441735	Dhtkd1<sup>tm1Mmgu</sup>	is_implicated_in	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q		MGI:6441736	Dhtkd1<sup>tm1Mmgu</sup>/Dhtkd1<sup>tm1Mmgu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32169121	20200715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5467564	Cenpf<sup>tm1Dbdr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5467575	Cenpf<sup>tm1Dbdr</sup>/Cenpf<sup>tm1Dbdr</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:22563055	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476824	Tg(TARDBP*A315T)#Jpj	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5476832	Tg(TARDBP*A315T)#Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21752789	20160504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2670767	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup> Ywhae<sup>tm1Awb</sup>/Ywhae<sup>+</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:12796778	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047228	Vegfa<sup>tm1Pec</sup>/Vegfa<sup>tm1Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12716	newborn respiratory distress syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12053176	20110217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2681992	Prnp<sup>tm1(PRNP)Tkit</sup>/Prnp<sup>tm1(PRNP)Tkit</sup>  [background:] Not Specified	is_model_of	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000033	author statement supported by traceable reference	PMID:14633630	20050620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471363	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> En1<sup>tm2(cre)Wrst</sup>/En1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:23152632	20130402	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695547	Tg(NEFH-tTA)8Vle/0 Tg(tetO-TARDBP*)4Vle/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:26197969	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc	is_model_of	DOID:0110112	atrial heart septal defect 7						ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	MGI:63097	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J	is_model_of	DOID:0110918	hereditary spherocytosis type 3						ECO:0000033	author statement supported by traceable reference	MGI:78279	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700824	Gli3<sup>tm1Urt</sup>/Gli3<sup>tm1Urt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9248	Pallister-Hall syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11978771	20070324	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527887	Adgrv1<sup>tm1Msat</sup>/Adgrv1<sup>tm1Msat</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0110839	Usher syndrome type 2C						ECO:0000033	author statement supported by traceable reference	PMID:17567809	20070821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5002476	Tg(Prnp-TARDBP)3cPtrc	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5308055	Tg(Prnp-TARDBP)3cPtrc/Tg(Prnp-TARDBP)3cPtrc  [background:] C57BL/6-Tg(Prnp-TARDBP)3cPtrc			ECO:0000033	author statement supported by traceable reference	PMID:20702714	20120229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5585619	Sucla2<sup>Gt(SAbetageo)1Bhg</sup>	is_implicated_in	DOID:0080124	mitochondrial DNA depletion syndrome 5		MGI:5585621	Sucla2<sup>Gt(SAbetageo)1Bhg</sup>/Sucla2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24271779	20141003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4868581	Lmna<sup>tm8Lgf</sup>	is_not_implicated_in	DOID:3911	progeria		MGI:4868583	Lmna<sup>tm8Lgf</sup>/Lmna<sup>tm8Lgf</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21088111	20110119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5752777	Disc1<sup>m1H</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5752786	Disc1<sup>m1H</sup>/Disc1<sup>m1H</sup>  [background:] B6N.C(C3H)-Disc1<sup>m1H</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26728762	20160322	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618987	Tg(Ins2-GP)34-20Olds/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:7889411	20060411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432139	Clrn1<sup>tm2.1Kuna</sup>/Clrn1<sup>tm2.1Kuna</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6J	is_model_of	DOID:0110841	Usher syndrome type 3A						ECO:0000033	author statement supported by traceable reference	PMID:22787034	20120824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5755287	Tg(SRY-YFP,Tyr)TashTNpln	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5755288	Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25786024	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5755287	Tg(SRY-YFP,Tyr)TashTNpln	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437101	b2b1200Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3028004	Pde6b<sup>atrd3</sup>/Pde6b<sup>atrd3</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110375	retinitis pigmentosa 40						ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583453	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: C3H * FVB/N	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:11773599	20050812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5635813	Zfp521<sup>tm1Nohk</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5699086	Zfp521<sup>tm1Nohk</sup>/Zfp521<sup>tm1Nohk</sup>  [background:] B6J.Cg-Zfp521<sup>tm1Nohk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24676388	20151215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5749268	Zfyve26<sup>tm1.1Cahb</sup>/Zfyve26<sup>tm1.1Cahb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	is_model_of	DOID:0110768	hereditary spastic paraplegia 15						ECO:0000033	author statement supported by traceable reference	PMID:24367272	20160219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543406	Tg(Myh6-ACTC1*E99K)#Sbm	is_implicated_in	DOID:0110317	hypertrophic cardiomyopathy 11						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543406	Tg(Myh6-ACTC1*E99K)#Sbm	is_implicated_in	DOID:0110317	hypertrophic cardiomyopathy 11		MGI:5543418	Tg(Myh6-ACTC1*E99K)#Sbm/0  [background:] involves: C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:21622575	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5543406	Tg(Myh6-ACTC1*E99K)#Sbm	is_implicated_in	DOID:0110317	hypertrophic cardiomyopathy 11						ECO:0000033	author statement supported by traceable reference	PMID:23604709	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6476759	Cd2ap<sup>em1Irgu</sup>	is_implicated_in	DOID:783	end stage renal disease		MGI:6476763	Cd2ap<sup>em1Irgu</sup>/Cd2ap<sup>em1Irgu</sup>  [background:] C57BL/6-Cd2ap<sup>em1Irgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30612599	20201201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6287842	Gprasp2<sup>tm1.1Jpe</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6287871	Gprasp2<sup>tm1.1Jpe</sup>/Y  [background:] B6.129(FVB)-Gprasp2<sup>tm1.1Jpe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30926797	20190418	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581423	Glb1<sup>tm1Adz</sup>/Glb1<sup>tm1Adz</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:3322	GM1 gangliosidosis						ECO:0000033	author statement supported by traceable reference	PMID:15687347	20050712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4460281	Ap5z1<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110800	hereditary spastic paraplegia 48		MGI:6458731	Ap5z1<sup>tm1(KOMP)Wtsi</sup>/Ap5z1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30930081	20200930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311386	Dnah5<sup>b2b1154Clo</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5314017	Dnah5<sup>b2b1154Clo</sup>/Dnah5<sup>b2b1154Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1154Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5750673	Gt(ROSA)26Sor<sup>tm1(CAG-Nr2f2)Tsa</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906002	Gt(ROSA)26Sor<sup>tm1(CAG-Nr2f2)Tsa</sup>/Gt(ROSA)26Sor<sup>+</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26356605	20170731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856100	Atp7a<sup>Mo-ms</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:25247420	20150819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856100	Atp7a<sup>Mo-ms</sup>	is_implicated_in	DOID:1838	Menkes disease						ECO:0000033	author statement supported by traceable reference	PMID:22815746	20150819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856100	Atp7a<sup>Mo-ms</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:4940051	Atp7a<sup>Mo-ms</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20831904	20150819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2182941	Aire<sup>tm1Pltn</sup>/Aire<sup>tm1Pltn</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:11854172	20050531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526798	Dnase2a<sup>tm1Osa</sup>/Dnase2a<sup>tm1Osa</sup> Ifnar1<sup>tm1Agt</sup>/Ifnar1<sup>tm1Agt</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:17066036	20170208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3526798	Dnase2a<sup>tm1Osa</sup>/Dnase2a<sup>tm1Osa</sup> Ifnar1<sup>tm1Agt</sup>/Ifnar1<sup>tm1Agt</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:26114879	20170208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3832577	Gt(ROSA)26Sor<sup>tm1(Kcnj11*V59M)Fmas</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:19065048	20090220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6260051	Dhtkd1<sup>tm1Zgwg</sup>	is_implicated_in	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q		MGI:6260058	Dhtkd1<sup>tm1Zgwg</sup>/Dhtkd1<sup>tm1Zgwg</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29661920	20181213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2668610	Slc45a2<sup>Uw-dbr</sup>/Slc45a2<sup>+</sup>  [background:] B10.PL-H2<sup>u</sup>/(73NS)Sn	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3050555	Prkn<sup>tm1Tmd</sup>/Prkn<sup>tm1Tmd</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:15249681	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664295	Myh6<sup>tm2Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000033	author statement supported by traceable reference	PMID:15001446	20100521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2660662	Ccd/Ccd<sup>+</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	MGI:62184	20050817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618414	Tg(Prnp-FUS*R521C)3313Ejh	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:5618534	Tg(Prnp-FUS*R521C)3313Ejh/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24509083	20150313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5565217	Tg(Ins2-HBEGF)5Rin	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5565220	Tg(Ins2-HBEGF)5Rin/?  [background:] C57BL/6-Tg(Ins2-HBEGF)5Rin			ECO:0000033	author statement supported by traceable reference	PMID:23747725	20140523	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5538520	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0  [background:] involves: FVB	is_model_of	DOID:4769	pleuropulmonary blastoma						ECO:0000033	author statement supported by traceable reference	PMID:25978641	20160311	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3655854	Krt1<sup>Mhdadsk12</sup>/Krt1<sup>+</sup>  [background:] C3HeB/FeJ-Krt1<sup>Mhdadsk12</sup>	is_model_of	DOID:4603	epidermolytic hyperkeratosis						ECO:0000033	author statement supported by traceable reference	PMID:16528356	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7336099	Sdccag8<sup>em1Lji</sup>	is_implicated_in	DOID:0110138	Bardet-Biedl syndrome 16		MGI:7336104	Sdccag8<sup>em1Lji</sup>/Sdccag8<sup>em1Lji</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:35503560	20220914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4999583	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>tm1.1Ady</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J	is_model_of	DOID:0080093	myofibrillar myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:21445271	20110523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5581668	Mafb<sup>tm1.2Good</sup>	is_implicated_in	DOID:12557	Duane retraction syndrome		MGI:6278261	Mafb<sup>tm1.2Good</sup>/Mafb<sup>tm1.2Good</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27181683	20190215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5581668	Mafb<sup>tm1.2Good</sup>	is_implicated_in	DOID:12557	Duane retraction syndrome		MGI:6278262	Mafb<sup>tm1.2Good</sup>/Mafb<sup>+</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27181683	20190215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007913	Mefv<sup>tm4.1(MEFV)Chae</sup>	is_implicated_in	DOID:2987	familial mediterranean fever		MGI:5007927	Mefv<sup>tm4.1(MEFV)Chae</sup>/Mefv<sup>tm4.1(MEFV)Chae</sup>  [background:] B6.129S6-Mefv<sup>tm4.1(MEFV)Chae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21600797	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5693602	Cilk1<sup>tm1a(KOMP)Mbp</sup>/Cilk1<sup>tm1a(KOMP)Mbp</sup>  [background:] C57BL/6N-Cilk1<sup>tm1a(KOMP)Mbp</sup>	is_model_of	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24853502	20151027	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2181617	Kl<sup>kl</sup>/Kl<sup>kl</sup>  [background:] either: C.Cg-Kl<sup>kl</sup> or (involves: C3H/HeJ * C57BL/6J)	is_model_of	DOID:9675	pulmonary emphysema						ECO:0000033	author statement supported by traceable reference	PMID:9363890	20060905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3053453	Slit3<sup>Gt(OST106158)Lex</sup>/Slit3<sup>Gt(OST106158)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:14550534	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360796	Tg(RBP3-ELOVL4*)1Kzh/0  [background:] C57BL/6-Tg(RBP3-ELOVL4*)1Kzh	is_model_of	DOID:0050817	Stargardt disease						ECO:0000033	author statement supported by traceable reference	PMID:15749821	20091008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5288516	Slc6a19<sup>tm1Dgen</sup>	is_implicated_in	DOID:1060	Hartnup disease		MGI:5289692	Slc6a19<sup>tm1Dgen</sup>/Slc6a19<sup>tm1Dgen</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21636576	20111007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856228	Cdh23<sup>v</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856228	Cdh23<sup>v</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3778632	Cdh23<sup>v</sup>/Cdh23<sup>v</sup>  [background:] involves: fancier's stocks			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20160226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4437308	Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] B6.Cg-Tg(APP695)3Dbo Tg(PSEN1dE9)S9Dbo/Mmjax	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:20092570	20100317	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3817221	Sox9<sup>tm1Gsr</sup>/Sox9<sup>+</sup> Tg(Pdx1-cre)6Cvw/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA * FVB/N	is_model_of	DOID:0050463	campomelic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:18723011	20081120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179753	Scn5a<sup>tm1Agrc</sup>	is_implicated_in	DOID:0110218	Brugada syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:31291141	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179753	Scn5a<sup>tm1Agrc</sup>	is_implicated_in	DOID:0110218	Brugada syndrome 1		MGI:3641169	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21097662	20191007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157844	Slc12a6<sup>em1Dlp</sup>	is_implicated_in	DOID:2477	motor peripheral neuropathy		MGI:6157847	Slc12a6<sup>em1Dlp</sup>/Slc12a6<sup>em1Dlp</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27485015	20180523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4410556	Tg(tetO-ATXN3)2904Olri	is_implicated_in	DOID:1440	Machado-Joseph disease						ECO:0000033	author statement supported by traceable reference	PMID:29476013	20180406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5313384	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>+</sup>  [background:] Not Specified	is_model_of	DOID:0050475	Weill-Marchesani syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4431253	Npc1<sup>tm1.2Apl</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:26908626	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438063	b2b1700Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708705	Arid1a<sup>tm1.1Mag</sup>	is_implicated_in	DOID:1925	Coffin-Siris syndrome		MGI:5784729	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>+</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26806701	20171117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708705	Arid1a<sup>tm1.1Mag</sup>	is_implicated_in	DOID:1925	Coffin-Siris syndrome		MGI:5784730	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>tm1.1Mag</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26806701	20171117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805032	Brca1<sup>tm1Arge</sup>/Brca1<sup>tm1Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3708979	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:11438694	20070516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850371	Pink1<sup>tm1Aub</sup>/Pink1<sup>tm1Aub</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0060369	Parkinson's disease 6						ECO:0000033	author statement supported by traceable reference	PMID:19492057	20090714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6476743	Zfhx2<sup>tm3Ymri</sup>	is_implicated_in	DOID:0081075	Marsili syndrome		MGI:7329779	Zfhx2<sup>tm3Ymri</sup>/Zfhx2<sup>tm3Ymri</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29253101	20220816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5583016	Tg(IVL-KLK5)#Hov	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:5583018	Tg(IVL-KLK5)#Hov/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24534191	20140919	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5014310	Tg(Upk2-TAg)1Rkl/0  [background:] involves: C57BL/6	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:21388952	20110714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4353812	Plcb1<sup>tm1Hssh</sup>/Plcb1<sup>tm1Hssh</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:17667964	20090819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5562921	Tg(SERPINA1*E342K)#Slcw/Tg(SERPINA1*E342K)#Slcw  [background:] involves: C57BL/6 * ICR	is_model_of	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000033	author statement supported by traceable reference	PMID:24355919	20140508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652553	Plcb1<sup>tm1Hssh</sup>/Plcb1<sup>tm1Hssh</sup>  [background:] Not Specified	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9305844	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652447	Tg(Thy1-APP)3Somm/0  [background:] involves: C57BL/6J * DBA/2	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9371838	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622480	Tg(Fabp4-Hsd11b1)7Jesf/0  [background:] FVB-Tg(Fabp4-Hsd11b1)7Jesf	is_model_of	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:11739957	20150504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4939021	Tg(Igh-Maf)524Staka	is_implicated_in	DOID:9538	multiple myeloma		MGI:4939025	Tg(Igh-Maf)524Staka/0  [background:] involves: C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21224354	20110228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174704	Pkd2<sup>tm1Som</sup>/Pkd2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL	is_model_of	DOID:0110859	polycystic kidney disease 2						ECO:0000033	author statement supported by traceable reference	PMID:9568711	20091021	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620124	Cd80<sup>tm1Shr</sup>/Cd80<sup>tm1Shr</sup> Cd86<sup>tm2Shr</sup>/Cd86<sup>tm2Shr</sup>  [background:] involves: 129S4/SvJae * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10795741	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904006	Lrfn2<sup>tm1.1Jaru</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5904009	Lrfn2<sup>tm1.1Jaru</sup>/Lrfn2<sup>tm1.1Jaru</sup>  [background:] B6J.129P2-Lrfn2<sup>tm1.1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28604739	20170706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796931	Slc6a5<sup>trsl</sup>/Slc6a5<sup>trsl</sup>  [background:] C57BL/6J-Slc6a5<sup>trsl</sup>/GrsrJ	is_model_of	DOID:0060698	hyperekplexia 3						ECO:0000033	author statement supported by traceable reference	MGI:5796923	20161007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7435644	Dzip1<sup>em1Yxc</sup>	is_implicated_in	DOID:0112175	spermatogenic failure 47		MGI:7435649	Dzip1<sup>em1Yxc</sup>/Dzip1<sup>em1Yxc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32051257	20230220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835241	Tg(MMTV-ENPP2)20Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763076	Tg(MMTV-ENPP2)20Gbm/0  [background:] FVB/N-Tg(MMTV-ENPP2)20Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6444834	Tubb4a<sup>em1Avan</sup>	is_implicated_in	DOID:0060798	hypomyelinating leukodystrophy 6		MGI:6444908	Tubb4a<sup>em1Avan</sup>/Tubb4a<sup>em1Avan</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32463361	20200727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4881158	Mocs2<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0111163	molybdenum cofactor deficiency type B		MGI:5904770	Mocs2<sup>tm1(KOMP)Vlcg</sup>/Mocs2<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:27138983	20230619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7282107	Vcp<sup>tm1.1Hiok</sup>	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:7284278	Vcp<sup>tm1.1Hiok</sup>/Vcp<sup>+</sup>  [background:] B6(Cg)-Vcp<sup>tm1.1Hiok</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5285079	Bicc1<sup>b2b222Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5285350	Bicc1<sup>b2b222Clo</sup>/Bicc1<sup>b2b222Clo</sup>  [background:] C57BL/6J-Bicc1<sup>b2b222Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:17641777	20150330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	MGI:2662101	20050627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5449900	Tg(SOD1)2Gur/0 Tg(SOD1*A4V)A1073Gur/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:16636275	20130122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644692	Meox2<sup>tm1(cre)Sor</sup>/Meox2<sup>+</sup> Tg(CAG-lacZ,-FUS,-EGFP)629Gyu/0  [background:] involves: 129S4/SvJaeSor * C57BL/6	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:25324524	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5905137	Tg(Myh6-Pln*)#Egk	is_implicated_in	DOID:0110439	dilated cardiomyopathy 1P		MGI:5905138	Tg(Myh6-Pln*)#Egk/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16432188	20170720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5689559	Ctnna1<sup>Tvrm5</sup>	is_implicated_in	DOID:0060864	patterned macular dystrophy 2		MGI:5699377	Ctnna1<sup>Tvrm5</sup>/Ctnna1<sup>+</sup>  [background:] C57BL/6J-Ctnna1<sup>Tvrm5</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26691986	20161209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5689559	Ctnna1<sup>Tvrm5</sup>	is_implicated_in	DOID:0060864	patterned macular dystrophy 2		MGI:5699376	Ctnna1<sup>Tvrm5</sup>/Ctnna1<sup>Tvrm5</sup>  [background:] C57BL/6J-Ctnna1<sup>Tvrm5</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26691986	20161209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175798	Cryaa<sup>lop18</sup>/Cryaa<sup>lop18</sup>  [background:] involves: CBA/CaGnLeJ	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:8812430	20130528	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3708348	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>Gt(S20-7E1)Sor</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17334657	20070515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433854	Crybb2<sup>Lop19</sup>	is_implicated_in	DOID:0110269	cataract 3 multiple types		MGI:5435246	Crybb2<sup>Lop19</sup>/Crybb2<sup>+</sup>  [background:] SJL/J-Crybb2<sup>Lop19</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:5435169	20120918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582826	Krt5<sup>tm1Tmm</sup>/Krt5<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd * BALB/c	is_model_of	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type						ECO:0000033	author statement supported by traceable reference	PMID:11408584	20050802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3029380	Slc2a2<sup>tm1Thor</sup>/Slc2a2<sup>tm1Thor</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9354799	20061012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5445892	Scn5a<sup>tm3(SCN5A*)Rdn</sup>	is_implicated_in	DOID:0110433	dilated cardiomyopathy 1E		MGI:5445935	Scn5a<sup>tm3(SCN5A*)Rdn</sup>/Scn5a<sup>tm3(SCN5A*)Rdn</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:21824921	20170802	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3619449	Sufu<sup>tm1Rto</sup>/Sufu<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16459298	20060413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:5602	T-cell adult acute lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:29769563	20180831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038218	Gck<sup>Rgsc392</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838153	Tg(Myh7-RARA/lacZ)30Mcco/0  [background:] Not Specified	is_model_of	DOID:12930	dilated cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:9329959	20170831	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3697463	Crb1<sup>tm1Wij</sup>/Crb1<sup>tm2Wij</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110358	retinitis pigmentosa 12						ECO:0000033	author statement supported by traceable reference	PMID:17234588	20070222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491236	b2b2025Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5555835	b2b2025Clo/b2b2025Clo  [background:] C57BL/6J-b2b2025Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050973	Cyb5r4<sup>tm1Hfb</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:21839170	20120225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050973	Cyb5r4<sup>tm1Hfb</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3051529	Cyb5r4<sup>tm1Hfb</sup>/Cyb5r4<sup>tm1Hfb</sup>  [background:] involves: 129S4/SvJae * BALB/cAnN			ECO:0000033	author statement supported by traceable reference	PMID:15247412	20120225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5547954	Fbn2<sup>fp-4J</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:5574592	Fbn2<sup>fp-4J</sup>/Fbn2<sup>fp-4J</sup>  [background:] BALB/cByJ-Fbn2<sup>fp-4J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5514346	Fktn<sup>tm3.1Ttd</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5514353	Fktn<sup>tm3.1Ttd</sup>/Fktn<sup>tm3.1Ttd</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23562821	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5514346	Fktn<sup>tm3.1Ttd</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5514355	Fktn<sup>tm3.1Ttd</sup>/Fktn<sup>tm3.1Ttd</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23562821	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446591	Abcd1<sup>tm1Ymd</sup>/Abcd1<sup>tm1Ymd</sup>  [background:] involves: 129S/SvEv * C57BL/6J * DBA/2J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9126326	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6194621	Tg(GFAP-ATXN7*92Q)2521Als	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:6194624	Tg(GFAP-ATXN7*92Q)2521Als/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4821261	Phka1<sup>I/FnLn</sup>/Phka1<sup>I/FnLn</sup>  [background:] I/FnLn	is_model_of	DOID:0111040	glycogen storage disease IXd						ECO:0000033	author statement supported by traceable reference	PMID:7874115	20100913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527096	Tecta<sup>tm5.1Gpr</sup>	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:5527175	Tecta<sup>tm5.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4942361	Tg(Kit*D814V)2Roer/0 Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:350	mastocytosis						ECO:0000033	author statement supported by traceable reference	PMID:21148330	20110328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5572816	Tg(ASL1/Cryaa-Ralbp1)24Yca	is_implicated_in	DOID:10629	microphthalmia		MGI:5572817	Tg(ASL1/Cryaa-Ralbp1)24Yca/0  [background:] involves: C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24188744	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6392092	Fancd2<sup>em1Tzh</sup>	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:6392094	Fancd2<sup>em1Tzh</sup>/Fancd2<sup>em1Tzh</sup>  [background:] C57BL/6-Fancd2<sup>em1Tzh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31078270	20200226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5446655	Agtpbp1<sup>pcd</sup>/Agtpbp1<sup>pcd</sup>  [background:] involves: C57BL/6J * C57BR/cdJ * DBA/2J	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:21824473	20121219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6276066	Tg(Myh6-Camk2d_ic)#Jhb	is_implicated_in	DOID:6000	congestive heart failure		MGI:6276135	Tg(Myh6-Camk2d_ic)#Jhb/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17124532	20190206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285951	Ccdc66<sup>Gt(E021F10)Wrst</sup>/Ccdc66<sup>Gt(E021F10)Wrst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:21680557	20110920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3510314	Tbx1<sup>tm1.1Dsr</sup>/Tbx1<sup>tm1.1Dsr</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6478807	Ins2<sup>em#Arak</sup>	is_implicated_in	DOID:11717	neonatal diabetes		MGI:6478875	Ins2<sup>em#Arak</sup>/Ins2<sup>+</sup>  [background:] C.129-Rag2<sup>tm1Fwa</sup> Ins2<sup>em#Arak</sup> Jak3<sup>tm1Tks</sup>/Arak			ECO:0000033	author statement supported by traceable reference	PMID:32699230	20201210	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2166570	Ednra<sup>tm1Ywa</sup>/Ednra<sup>tm1Ywa</sup>  [background:] 129S/SvEv-Ednra<sup>tm1Ywa</sup>	is_model_of	DOID:12583	velocardiofacial syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9449664	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462093	Notch3<sup>tm1.1Dwr</sup>	is_implicated_in	DOID:0111035	CADASIL 1		MGI:5462095	Notch3<sup>tm1.1Dwr</sup>/Notch3<sup>tm1.1Dwr</sup>  [background:] involves: 129S/SvEv * Swiss			ECO:0000033	author statement supported by traceable reference	PMID:21940951	20130206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462093	Notch3<sup>tm1.1Dwr</sup>	is_implicated_in	DOID:0111035	CADASIL 1		MGI:5462096	Notch3<sup>tm1.1Dwr</sup>/Notch3<sup>+</sup>  [background:] involves: 129S/SvEv * Swiss			ECO:0000033	author statement supported by traceable reference	PMID:21940951	20130206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4819718	Tg(Tnnt2-TNNT2*R92Q)#Ajm	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:4819725	Tg(Tnnt2-TNNT2*R92Q)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9788962	20100819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5568494	Abcc8<sup>tm1.1Fmas</sup>/Abcc8<sup>tm1.1Fmas</sup>  [background:] B6.129S2(Cg)-Abcc8<sup>tm1.1Fmas</sup>	is_model_of	DOID:13317	hyperinsulinemic hypoglycemia						ECO:0000033	author statement supported by traceable reference	PMID:23903354	20140616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803587	Hras<sup>tm2Xbr</sup>	is_implicated_in	DOID:0050469	Costello syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28455524	20190514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803587	Hras<sup>tm2Xbr</sup>	is_implicated_in	DOID:0050469	Costello syndrome		MGI:3805200	Hras<sup>tm2Xbr</sup>/Hras<sup>tm2Xbr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18483625	20190514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5056364	Tubb2b<sup>brdp</sup>	is_implicated_in	DOID:0090132	complex cortical dysplasia with other brain malformations 7		MGI:5522833	Tubb2b<sup>brdp</sup>/Tubb2b<sup>brdp</sup>  [background:] involves: A/J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23727838	20170630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679083	Bmp4<sup>tm3.1Blh</sup>/Bmp4<sup>tm3.1Blh</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * ICR	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:12975322	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5315309	Wnt7a<sup>px-2J</sup>	is_implicated_in	DOID:0090067	Fuhrmann syndrome		MGI:5440925	Wnt7a<sup>px-2J</sup>/Wnt7a<sup>px-2J</sup>  [background:] B6;C3Fe-Wnt7a<sup>px-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5440720	20170629	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3802581	Psap<sup>tm2Ggb</sup>/Psap<sup>tm2Ggb</sup>  [background:] involves: 129S/SvEv * C57BL/6J	is_model_of	DOID:10581	metachromatic leukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:18480170	20080818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5707183	Cacna1a<sup>tm1.1Ehess</sup>/Cacna1a<sup>tm1.1Ehess</sup>  [background:] C57BL/6-Cacna1a<sup>tm1.1Ehess</sup>	is_model_of	DOID:0050990	episodic ataxia type 2						ECO:0000033	author statement supported by traceable reference	PMID:25109669	20160203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491149	Tg(Plp1-Lmnb1)#Yfu	is_implicated_in	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy		MGI:5491207	Tg(Plp1-Lmnb1)#Yfu/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:23676464	20130621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5544194	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai	is_implicated_in	DOID:0050752	amyotrophic lateral sclerosis type 8		MGI:5544197	Tg(Thy1-VAPB*P56S,-EGFP)D3Cai/0  [background:] C57BL/6-Tg(Thy1-VAPB*P56S,-EGFP)D3Cai			ECO:0000033	author statement supported by traceable reference	PMID:23771029	20140214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622102	Ldlr<sup>Hlb301</sup>/Ldlr<sup>+</sup>  [background:] C57BL/6J-Ldlr<sup>Hlb301</sup>/J	is_model_of	DOID:13810	familial hypercholesterolemia						ECO:0000033	author statement supported by traceable reference	MGI:2656149	20060511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651696	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:12575948	20070622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6508399	Spg21<sup>tm1Mchan</sup>	is_implicated_in	DOID:0060245	Mast syndrome		MGI:6508400	Spg21<sup>tm1Mchan</sup>/Spg21<sup>tm1Mchan</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20661613	20210302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6159751	Slurp2<sup>tm1.1Sgy</sup>	is_implicated_in	DOID:3390	palmoplantar keratosis		MGI:6159891	Slurp2<sup>tm1.1Sgy</sup>/Slurp2<sup>tm1.1Sgy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26967477	20180607	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3694548	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] BKS.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:6991317	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5430343	Pcsk5<sup>b2b1549Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5430345	Pcsk5<sup>b2b1549Clo</sup>/Pcsk5<sup>b2b1549Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b1549Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431494	b2b904Clo	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5431510	b2b904Clo/b2b904Clo  [background:] C57BL/6J-b2b904Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654421	Mybpc3<sup>tm1Jse</sup>/Mybpc3<sup>tm1Jse</sup>  [background:] Not Specified	is_model_of	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000033	author statement supported by traceable reference	PMID:10545522	20060609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5824005	Stk3<sup>tm1Jav</sup>/Stk3<sup>tm1Jav</sup> Stk4<sup>Gt(AJ0315)Wtsi</sup>/Stk4<sup>Gt(AJ0315)Wtsi</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6 * DBA	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26131558	20170213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844659	Cdkn2a<sup>tm4Rdp</sup>/Cdkn2a<sup>tm4Rdp</sup> Myf6<sup>tm1(cre)Mrc</sup>/Myf6<sup>+</sup> Pax3<sup>tm1Mrc</sup>/Pax3<sup>tm1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	is_model_of	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:15489287	20090519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037334	Zfp36<sup>tm1Pjb</sup>/Zfp36<sup>tm1Pjb</sup>  [background:] B6.Cg-Zfp36<sup>tm1Pjb</sup>	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:24727475	20141024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6723864	Tmem53<sup>em1Ikeg</sup>	is_implicated_in	DOID:0112340	craniotubular dysplasia Ikegawa type		MGI:6854714	Tmem53<sup>em1Ikeg</sup>/Tmem53<sup>em1Ikeg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:33824347	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6272834	Thra<sup>em2Ffla</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:6317180	Thra<sup>em2Ffla</sup>/Thra<sup>+</sup>  [background:] C57BL/6-Thra<sup>em2Ffla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29205102	20190711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623411	Tgfbr2<sup>tm1Karl</sup>/Tgfbr2<sup>tm1Karl</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15741317	20060529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429196	Stk36<sup>tm1Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429551	Stk36<sup>tm1Lex</sup>/Stk36<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857161	Ednrb<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:25487064	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857161	Ednrb<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:24945437	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857161	Ednrb<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:27370713	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857161	Ednrb<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2174949	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15294878	20161222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857161	Ednrb<sup>tm1Ywa</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5617944	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] B6;129-Ednrb<sup>tm1Ywa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24945437	20161222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719353	Gadd45a<sup>tm1Ajf</sup>/Gadd45a<sup>tm1Ajf</sup> Xpc<sup>tm1Ecf</sup>/Xpc<sup>tm1Ecf</sup>  [background:] either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:16141330	20070827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5780987	Nexn<sup>tm1.1Zhh</sup>/Nexn<sup>tm1.1Zhh</sup>  [background:] involves: C57BL/6NTac	is_model_of	DOID:0110326	hypertrophic cardiomyopathy 20						ECO:0000033	author statement supported by traceable reference	PMID:26659360	20160721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258948	Cfap44<sup>em1Fzh</sup>	is_implicated_in	DOID:0070166	spermatogenic failure 20		MGI:6258951	Cfap44<sup>em1Fzh</sup>/Cfap44<sup>em1Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446518	Slc6a3<sup>tm2Mca</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446518	Slc6a3<sup>tm2Mca</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:2654522	Slc6a3<sup>tm2Mca</sup>/Slc6a3<sup>tm2Mca</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11172062	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711062	Bicc1<sup>tm1Emdr</sup>/Bicc1<sup>tm1Emdr</sup>  [background:] B6SJL-Bicc1<sup>tm1Emdr</sup>	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:3710978	20070605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4439299	p23-ST1/p23-ST1  [background:] C57BL/6J-p23-ST1	is_model_of	DOID:1572	normal pressure hydrocephalus						ECO:0000033	author statement supported by traceable reference	PMID:19924295	20100412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623405	H2-Ab1<sup>b-tm1Gru</sup>/H2-Ab1<sup>b-tm1Gru</sup> Tg(HLA-DQA1,HLA-DQB1)1Dv/0 Tg(Ins2-CD80)3B7Flv/0  [background:] B6.Cg-H2-Ab1<sup>b-tm1Gru</sup> Tg(HLA-DQA1,HLA-DQB1)1Dv Tg(Ins2-CD80)3B7Flv	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10620608	20060906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655513	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10381492	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2660562	Tlr9<sup>tm1Aki</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23467932	20130506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491077	Tg(Lmnb1)1Yfu	is_implicated_in	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy		MGI:5491206	Tg(Lmnb1)1Yfu/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23676464	20130621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6883575	Pbx1<sup>em1Dunw</sup>	is_implicated_in	DOID:0112359	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		MGI:7264531	Pbx1<sup>em1Dunw</sup>/Pbx1<sup>em1Dunw</sup>  [background:] C57BL/6J-Pbx1<sup>em1Dunw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31625560	20220502	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696978	Pygm<sup>tm1.1Adru</sup>/Pygm<sup>tm1.1Adru</sup>  [background:] involves: 129 * C57BL/6J	is_model_of	DOID:2746	glycogen storage disease V						ECO:0000033	author statement supported by traceable reference	PMID:22730558	20151123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437084	b2b1146Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7528727	Poc1b<sup>em1Xjzha</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7530054	Poc1b<sup>em1Xjzha</sup>/Poc1b<sup>em1Xjzha</sup>  [background:] C57BL/6J-Poc1b<sup>em1Xjzha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37070736	20230925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2653233	Cryaa<sup>Aey7</sup>/Cryaa<sup>Aey7</sup>  [background:] C3HeB/FeJ-Cryaa<sup>Aey7</sup>/Ieg	is_model_of	DOID:0110266	cataract 9 multiple types						ECO:0000033	author statement supported by traceable reference	PMID:11687536	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5636485	Tg(Th-ALK*F1174L)2Loch	is_implicated_in	DOID:769	neuroblastoma						ECO:0000033	author statement supported by traceable reference	PMID:24667968	20150519	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3709154	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)18Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16279840	20120824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3803666	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] 129P2/OlaHsd-Wt1<sup>tm1Mlh</sup>	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18040647	20080828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428425	Hprt1<sup>tm1(Camk2a-APP*Swe*Lon,-MAPT*P301L*R406W)Geno</sup>/Hprt1<sup>+</sup> Tg(PSEN1)5Dbo/0  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22096518	20120720	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698432	Tpo<sup>R479C</sup>/Tpo<sup>R479C</sup>  [background:] involves: ICR	is_model_of	DOID:0050328	congenital hypothyroidism						ECO:0000033	author statement supported by traceable reference	PMID:16762971	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437098	b2b227Clo	is_implicated_in	DOID:114	heart disease		MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5469320	mt-Nd6<sup>m3Dwa</sup>  [background:] B6.129S-mt-Nd6<sup>m3Dwa</sup>	is_model_of	DOID:705	Leber hereditary optic neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:23129651	20130320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506870	Gabrg1<sup>em1Ktka</sup>	is_implicated_in	DOID:12098	trigeminal neuralgia		MGI:6506871	Gabrg1<sup>em1Ktka</sup>/Gabrg1<sup>em1Ktka</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33083721	20210217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437086	Tmem67<sup>b2b1291.1Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437111	Tmem67<sup>b2b1291.1Clo</sup>/Tmem67<sup>b2b1291.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1291.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3622764	Prf1<sup>tm1Clrk</sup>/Prf1<sup>tm1Clrk</sup> Tg(INS-Il10)#Sar/0  [background:] involves: 129S7/SvEvBrd * BALB/c * NOD	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10946317	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418339	Tg(CAG-SPTLC1*C133W)8EAmcc	is_implicated_in	DOID:0050548	hereditary sensory neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:22045570	20120719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418339	Tg(CAG-SPTLC1*C133W)8EAmcc	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:4418351	Tg(CAG-SPTLC1*C133W)8EAmcc/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16210380	20120719	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5294357	Trib2<sup>Tg(Thy1-Trh/APP*)2.1Ingm</sup>/Trib2<sup>Tg(Thy1-Trh/APP*)2.1Ingm</sup>  [background:] involves: C57BL/6 * DBA/1	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21900558	20111031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6226076	Cacna1a<sup>tm1Lory</sup>	is_implicated_in	DOID:0050990	episodic ataxia type 2		MGI:6226089	Cacna1a<sup>tm1Lory</sup>/Cacna1a<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28688851	20181106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682556	Slc6a5<sup>tm1Betz</sup>/Slc6a5<sup>tm1Betz</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0060698	hyperekplexia 3						ECO:0000033	author statement supported by traceable reference	PMID:14622583	20120514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5789380	Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5796293	Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27274810	20170818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4460268	Msh2<sup>tm1Rak</sup>/Msh2<sup>tm2.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19931261	20111104	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831376	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] CBACa.129P2-Fgfr3<sup>tm1.1Aomw</sup>	is_model_of	DOID:0060703	Muenke Syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5701345	Lmod3<sup>em1Eno</sup>	is_implicated_in	DOID:0110931	nemaline myopathy 10		MGI:5701349	Lmod3<sup>em1Eno</sup>/Lmod3<sup>em1Eno</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25774500	20160106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6810185	Ppara<sup>em1Tyrb</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6810192	Ppara<sup>em1Tyrb</sup>/Ppara<sup>em1Tyrb</sup>  [background:] C57BL/6J-Ppara<sup>em1Tyrb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33279456	20211115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444503	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-IL1B)KBry/0  [background:] involves: 129 * C57BL/6	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:15668323	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2449173	Myo7a<sup>sh1-6J</sup>/Myo7a<sup>sh1-6J</sup>  [background:] involves: C57BLKS/J	is_model_of	DOID:0110826	Usher syndrome type 1						ECO:0000033	author statement supported by traceable reference	MGI:65387	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680317	Gba1<sup>tm1Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease						ECO:0000033	author statement supported by traceable reference	PMID:23520473	20181026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680317	Gba1<sup>tm1Ggb</sup>	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680386	Gba1<sup>tm1Ggb</sup>/Gba1<sup>tm1Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286071	Arid1b<sup>em1Iha</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6286096	Arid1b<sup>em1Iha</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Iha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28867767	20190404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6401825	Mafb<sup>em1Staka</sup>	is_implicated_in	DOID:0111534	multicentric carpotarsal osteolysis syndrome		MGI:6401826	Mafb<sup>em1Staka</sup>/Mafb<sup>em1Staka</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30369533	20200327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5823562	Tmco1<sup>em1Smoc</sup>	is_implicated_in	DOID:0081072	craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome		MGI:5823987	Tmco1<sup>em1Smoc</sup>/Tmco1<sup>em1Smoc</sup>  [background:] C57BL/6J-Tmco1<sup>em1Smoc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27212239	20220616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5911893	Src<sup>inl</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5911896	Src<sup>inl</sup>/Src<sup>inl</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:26464974	20171026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5529628	Dp(XTceal3-Plp1)1Gmh/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:23864668	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512050	Mc4r<sup>tm1Lowl</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:37681411	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512050	Mc4r<sup>tm1Lowl</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:3692534	Mc4r<sup>tm1Lowl</sup>/Mc4r<sup>tm1Lowl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21906580	20231117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781149	Dmd<sup>tm1Kmf</sup>	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5897011	Dmd<sup>tm1Kmf</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26365037	20170510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433323	Ap1b1<sup>b2b1660Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6402836	Enpp1<sup>ttw-Ham</sup>	is_implicated_in	DOID:0060887	ossification of the posterior longitudinal ligament of spine		MGI:6402953	Enpp1<sup>ttw-Ham</sup>/Enpp1<sup>ttw-Ham</sup>  [background:] Jcl:ICR-Enpp1<sup>ttw-Ham</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24770645	20200406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4949465	Tg(tetO-TPR/MET,-EGFP)12Tcre	is_implicated_in	DOID:6000	congestive heart failure		MGI:5911349	Tg(Myh6-tTA)6Smbf/0 Tg(tetO-TPR/MET,-EGFP)12Tcre/0  [background:] FVB.Cg-Tg(Myh6-tTA)6Smbf Tg(tetO-TPR/MET,-EGFP)12Tcre			ECO:0000033	author statement supported by traceable reference	PMID:27298830	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849838	Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:4849842	Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo/Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16046140	20101230	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3798284	Del(5D5Mit148-Qdpr)2Jcs/+  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11152656	20080722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052111	Tg(Mapt-MAPT*)#Hanr	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5052112	Tg(Mapt-MAPT*)#Hanr/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18490011	20110804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5588576	None [background:] NOD/ShiLtJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	MGI:61003	20141022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612533	Braf<sup>tm1Cpri</sup>	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26501867	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612533	Braf<sup>tm1Cpri</sup>	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5779643	Braf<sup>tm1Cpri</sup>/Braf<sup>tm1Cpri</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129P2/OlaHsd * FVB/NCr			ECO:0000033	author statement supported by traceable reference	PMID:21220306	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6270168	Tg(Camk2a-Polg*D181A)BTkato	is_implicated_in	DOID:3324	mood disorder		MGI:6270171	Tg(Camk2a-Polg*D181A)BTkato/0  [background:] C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato			ECO:0000033	author statement supported by traceable reference	PMID:16619054	20181231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6718494	Dzip1<sup>em1Sasl</sup>	is_implicated_in	DOID:988	mitral valve prolapse		MGI:6718509	Dzip1<sup>em1Sasl</sup>/Dzip1<sup>+</sup>  [background:] C57BL/6J-Dzip1<sup>em1Sasl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5461232	Men1<sup>tm1Rvt</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:5461308	Men1<sup>tm1Rvt</sup>/Men1<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19620250	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5461232	Men1<sup>tm1Rvt</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000033	author statement supported by traceable reference	PMID:23024266	20130130	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2179721	Lamb3<sup>IAP</sup>/Lamb3<sup>IAP</sup>  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0060737	junctional epidermolysis bullosa Herlitz type						ECO:0000033	author statement supported by traceable reference	PMID:9271670	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5007262	Nbeal2<sup>tm1Lex</sup>	is_implicated_in	DOID:0111044	gray platelet syndrome		MGI:5527439	Nbeal2<sup>tm1Lex</sup>/Nbeal2<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23863626	20140110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2173244	Pkd1<sup>tm1Rsa</sup>/Pkd1<sup>+</sup>  [background:] involves: 129S4/SvJaeSor	is_model_of	DOID:0110858	polycystic kidney disease 1						ECO:0000033	author statement supported by traceable reference	PMID:11593033	20050530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5529372	Mecp2<sup>tm2.1Meg</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5529468	Mecp2<sup>tm2.1Meg</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:23770565	20140121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311364	Megf8<sup>b2b288Clo</sup>	is_implicated_in	DOID:0060234	Carpenter syndrome		MGI:5311833	Megf8<sup>b2b288Clo</sup>/Megf8<sup>b2b288Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b288Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121217	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5305067	App<sup>tm1Dbo</sup>/App<sup>tm1Dbo</sup> Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] C.Cg-App<sup>tm1Dbo</sup> Npc1<sup>m1N</sup>	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:21303697	20120207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446158	Dnah11<sup>b2b1775Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5446426	Dnah11<sup>b2b1775Clo</sup>/Dnah11<sup>b2b1775Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1775Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176912	Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1						ECO:0000033	author statement supported by traceable reference	PMID:8790370	20100906	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3606654	Csf2<sup>tm1Mlg</sup>/Csf2<sup>tm1Mlg</sup>  [background:] involves: 129S2/SvPas	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:8171324	20051207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180562	Tg(Ckmm-Cav3)1Ysu	is_implicated_in	DOID:0060255	rippling muscle disease 2						ECO:0000033	author statement supported by traceable reference	PMID:22584670	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180562	Tg(Ckmm-Cav3)1Ysu	is_implicated_in	DOID:0060255	rippling muscle disease 2		MGI:5286560	Tg(Ckmm-Cav3)1Ysu/0  [background:] involves: C57BL/Slc * DBA/Slc			ECO:0000033	author statement supported by traceable reference	PMID:11159934	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459812	Timd4<sup>tm1Kuch</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287981	Timd4<sup>tm1Kuch</sup>/Timd4<sup>tm1Kuch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6111331	Myo9a<sup>tm1.2Bah</sup>	is_implicated_in	DOID:14159	obstructive hydrocephalus		MGI:6120521	Myo9a<sup>tm1.2Bah</sup>/Myo9a<sup>tm1.2Bah</sup>  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19828736	20180309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3038919	Kcnj10<sup>tm1Lst</sup>/Kcnj10<sup>tm1Lst</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0060484	EAST syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11466414	20151117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574277	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] C.129P2-Cecr2<sup>Gt(pGT1)1Hemc</sup>	is_model_of	DOID:0060668	anencephaly						ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317589	Dnai1<sup>b2b1526Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821832	Mks1<sup>avc6</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822147	Mks1<sup>avc6</sup>/Mks1<sup>avc6</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000477	Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(MMTV-cre)#Tfln/0  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21324922	20110531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3851332	Otc<sup>spf-ash</sup>/Y  [background:] B6EiC3Sn a/A-Otc<sup>spf-ash</sup>/J	is_model_of	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:16497529	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192642	Cib2<sup>tm1.1Aela</sup>	is_not_implicated_in	DOID:0110836	Usher syndrome type 1J		MGI:6192643	Cib2<sup>tm1.1Aela</sup>/Cib2<sup>tm1.1Aela</sup>  [background:] involves: BALB/c * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29084757	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427681	Nr1d2<sup>tm1Dgen</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:5804180	Nr1d2<sup>tm1Dgen</sup>/Nr1d2<sup>tm1Dgen</sup>  [background:] B6;129P2-Nr1d2<sup>tm1Dgen</sup>/H			ECO:0000033	author statement supported by traceable reference	PMID:27058611	20161020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3487371	Myf6<sup>tm1(cre)Mrc</sup>	is_implicated_in	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:22960170	20130109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6197751	Pomt1<sup>tm1c(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:6197758	Pomt1<sup>tm1c(EUCOMM)Hmgu</sup>/Pomt1<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29867208	20180912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3611217	Pdss2<sup>kd</sup>/Pdss2<sup>kd</sup>  [background:] CBA/H-Pdss2<sup>kd</sup>	is_model_of	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:23150520	20130711	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4836243	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup> Tg(Pbsn-TAg)15Tvd/0  [background:] involves: 129S1/Sv * C57BL/6 * DBA/2	is_model_of	DOID:10283	prostate cancer						ECO:0000033	author statement supported by traceable reference	PMID:16288012	20101025	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5661462	Ap1s2<sup>tm1Pschu</sup>/Ap1s2<sup>tm1Pschu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060800	syndromic X-linked intellectual disability 5						ECO:0000033	author statement supported by traceable reference	PMID:20203623	20150911	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3804498	Tnnt2<sup>tm2Mmto</sup>/Tnnt2<sup>tm2Mmto</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000033	author statement supported by traceable reference	PMID:17556660	20080904	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688419	Gba1<sup>tm1.1Karl</sup>/Gba1<sup>tm1.1Karl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110957	Gaucher's disease type I						ECO:0000033	author statement supported by traceable reference	PMID:16954197	20061121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708309	Lamb3<sup>tm1.1Hosc</sup>	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:5749252	Lamb3<sup>tm1.1Hosc</sup>/Lamb3<sup>tm1.1Hosc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25350318	20160218	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581209	Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6(Cg)-Tyr<sup>c-2J</sup>/J	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	PMID:21968110	20120426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2658930	Cyp27b1<sup>tm1Dgo</sup>/Cyp27b1<sup>tm1Dgo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c	is_model_of	DOID:10609	rickets						ECO:0000033	author statement supported by traceable reference	PMID:11416220	20050616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462096	Notch3<sup>tm1.1Dwr</sup>/Notch3<sup>+</sup>  [background:] involves: 129S/SvEv * Swiss	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:21940951	20130206	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623769	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] involves: 129/Sv * Black Swiss	is_model_of	DOID:0060468	Holt-Oram syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11572777	20060602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7547409	Slitrk2<sup>tm1.1Jwum</sup>	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:7547513	Slitrk2<sup>tm1.1Jwum</sup>/Y Tg(Nes-cre)1Atp/0  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:35840571	20231113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4418351	Tg(CAG-SPTLC1*C133W)8EAmcc/0  [background:] involves: C3H * C57BL/6	is_model_of	DOID:0050548	hereditary sensory neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:16210380	20100121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856685	Rpl24<sup>Bst</sup>	is_implicated_in	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:26035379	20150908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856685	Rpl24<sup>Bst</sup>	is_implicated_in	DOID:5723	optic atrophy		MGI:2658856	Rpl24<sup>Bst</sup>/Rpl24<sup>+</sup>  [background:] involves: C57BLKS			ECO:0000033	author statement supported by traceable reference	PMID:8589526	20150908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819186	Prkar1a<sup>tm1Lsk</sup>/Prkar1a<sup>tm1Lsk</sup> Tg(Akr1b7-cre)1Anm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	is_model_of	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000033	author statement supported by traceable reference	PMID:20548949	20100813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569760	Tg(Prnp-MAPT)7Vle/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:10595524	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5470152	Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0080074	neural tube defect		MGI:5470154	Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>/Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23267094	20130327	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5604887	Tg(MMTV-Erbb2)9Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897391	Ada<sup>tm1Mw</sup>/Ada<sup>tm1Mw</sup> Tg(Afp-ADA)#Xiay/0  [background:] involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J	is_model_of	DOID:10591	pre-eclampsia						ECO:0000033	author statement supported by traceable reference	PMID:25538227	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5707276	Gt(ROSA)26Sor<sup>tm1.1(DUX4*)Plj</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:6120564	Gt(ROSA)26Sor<sup>tm1.1(DUX4*)Plj</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(ACTA1-cre/Esr1*)2Kesr/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29415061	20180309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693439	Tg(APPSw)40Btla/0  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:9285791	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4441291	Gla<sup>tm1Kul</sup>/Gla<sup>tm1Kul</sup> Itpr1<sup>wblo</sup>/Itpr1<sup>wblo</sup>  [background:] B6;129-Gla<sup>tm1Kul</sup> Itpr1<sup>wblo</sup>/GrsrJ	is_model_of	DOID:0050965	spinocerebellar ataxia type 15						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856973	Tcirg1<sup>oc</sup>	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000033	author statement supported by traceable reference	PMID:20091929	20120224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856973	Tcirg1<sup>oc</sup>	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1		MGI:2174761	Tcirg1<sup>oc</sup>/Tcirg1<sup>oc</sup>  [background:] B6C3Fe a/a-Tcirg1<sup>oc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10709991	20120224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858114	Fech<sup>m1Pas</sup>	is_implicated_in	DOID:13270	erythropoietic protoporphyria						ECO:0000033	author statement supported by traceable reference	PMID:27507172	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858114	Fech<sup>m1Pas</sup>	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:2175882	Fech<sup>m1Pas</sup>/Fech<sup>m1Pas</sup>  [background:] involves: 129/Sv * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:1939658	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5526862	Crx<sup>Rip</sup>/Crx<sup>+</sup>  [background:] C57BL/6J-Crx<sup>Rip</sup>	is_model_of	DOID:0110333	Leber congenital amaurosis 7						ECO:0000033	author statement supported by traceable reference	PMID:24382353	20140106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5439179	Barx2<sup>tm1Rsd</sup>/Barx2<sup>tm1Rsd</sup> Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] involves: 129 * C57BL/6 * C57BL/10ScSn	is_model_of	DOID:11723	Duchenne muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22076929	20121024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5444459	Map2k7<sup>tm1Pngr</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5444462	Map2k7<sup>tm1Pngr</sup>/Map2k7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22899651	20121205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3759225	Pkhd1<sup>tm1.1Ggg</sup>/Pkhd1<sup>tm1.1Ggg</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae * C57BL/6	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:17575307	20071025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5296243	Gata5<sup>tm1.2Nemr</sup>	is_implicated_in	DOID:10825	essential hypertension		MGI:5707848	Gata5<sup>tm1.2Nemr</sup>/Gata5<sup>tm1.2Nemr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26617239	20160210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855969	Lyst<sup>bg-J</sup>	is_implicated_in	DOID:13641	exfoliation syndrome						ECO:0000033	author statement supported by traceable reference	PMID:29419647	20200506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855969	Lyst<sup>bg-J</sup>	is_implicated_in	DOID:13641	exfoliation syndrome		MGI:3581179	Lyst<sup>bg-J</sup>/Lyst<sup>bg-J</sup>  [background:] C57BL/6J-Lyst<sup>bg-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:19029039	20200506	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5703863	Dp(16Lipi-Zbtb21)1TybEmcf/0  [background:] B6JNimr.129P2-Dp(16Lipi-Zbtb21)1TybEmcf/Nimr	is_model_of	DOID:14250	Down syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26765563	20160119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711758	Opa1<sup>Q285X</sup>	is_implicated_in	DOID:5723	optic atrophy						ECO:0000033	author statement supported by traceable reference	PMID:23409176	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711758	Opa1<sup>Q285X</sup>	is_implicated_in	DOID:5723	optic atrophy		MGI:3712038	Opa1<sup>Q285X</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:21803037	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711758	Opa1<sup>Q285X</sup>	is_implicated_in	DOID:5723	optic atrophy		MGI:3712038	Opa1<sup>Q285X</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:17428816	20130624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3695277	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1	is_model_of	DOID:0060844	Norrie disease						ECO:0000033	author statement supported by traceable reference	PMID:12040033	20070201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5695545	Abcd3<sup>tm1Safe</sup>	is_implicated_in	DOID:0111066	congenital bile acid synthesis defect 5		MGI:5695549	Abcd3<sup>tm1Safe</sup>/Abcd3<sup>tm1Safe</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25168382	20151111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437224	Sox7<sup>tm1.1Dsco</sup>/Sox7<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:3827	congenital diaphragmatic hernia						ECO:0000033	author statement supported by traceable reference	PMID:22723016	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311388	Dnah11<sup>b2b1203Clo</sup>	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5318339	Dnah11<sup>b2b1203Clo</sup>/Dnah11<sup>b2b1203Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1203Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6388548	Tbr1<sup>tm1.1Csbd</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6388550	Tbr1<sup>tm1.1Csbd</sup>/Tbr1<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31680851	20200204	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445345	Flt3<sup>tm1Dgg</sup>/Flt3<sup>tm1Dgg</sup> Kmt2a<sup>tm1Clgr</sup>/Kmt2a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6J	is_model_of	DOID:9119	acute myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:22674806	20121211	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052075	Slc29a1<sup>tm1Msg</sup>/Slc29a1<sup>tm1Msg</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0050741	alcohol dependence						ECO:0000033	author statement supported by traceable reference	PMID:15258586	20080206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586525	Upp1<sup>tm1Gp</sup>	is_implicated_in	DOID:0080119	mitochondrial DNA depletion syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:24362886	20140813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445949	Tg(LPV-TAg121)2Tvd	is_implicated_in	DOID:2626	choroid plexus papilloma						ECO:0000033	author statement supported by traceable reference	PMID:21385880	20140221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445949	Tg(LPV-TAg121)2Tvd	is_implicated_in	DOID:2626	choroid plexus papilloma		MGI:5538528	Tg(LPV-TAg121)2Tvd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657247	Pde6c<sup>cpfl1</sup>	is_implicated_in	DOID:0110007	achromatopsia 2						ECO:0000033	author statement supported by traceable reference	PMID:25183393	20150714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5528981	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:15983791	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5473821	Tg(CAG-Bmpr1a*,-lacZ)1Nobs	is_implicated_in	DOID:0060389	chromosome 10q23 deletion syndrome		MGI:5473901	Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22773757	20130411	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842833	Tg(KRT14-cre)8Brn/0 Tg(KRT5-Akt1*)Jmpa/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	is_model_of	DOID:5520	head and neck squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19176372	20090505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450162	Rb1<sup>tm3Tyj</sup>	is_implicated_in	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:29743593	20220203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5437102	Slit2<sup>b2b1200.1Clo</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3586915	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster	is_model_of	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11242110	20050908	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800513	Tg(Prnp-PFN1*C71G)22Zxu/0 Tg(Thy1-PFN1*C71G)67Zxu/Tg(Thy1-PFN1*C71G)67Zxu  [background:] involves: FVB/N	is_model_of	DOID:0060209	amyotrophic lateral sclerosis type 18						ECO:0000033	author statement supported by traceable reference	PMID:27681617	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661962	Ncf1<sup>m1J</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:25188296	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661962	Ncf1<sup>m1J</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:2661972	Ncf1<sup>m1J</sup>/Ncf1<sup>m1J</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10670582	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603948	Tg(Camk2a-MAPT*R406W)748Atak	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:26949217	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603948	Tg(Camk2a-MAPT*R406W)748Atak	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:3718115	Tg(Camk2a-MAPT*R406W)748Atak/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12368474	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425669	Alpl<sup>Mhdabap020</sup>/Alpl<sup>Mhdabap020</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap020</sup>/Ieg	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425919	Casr<sup>BCH003</sup>/Casr<sup>BCH003</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH003</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653064	Ndn<sup>tm1.1Mus</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653064	Ndn<sup>tm1.1Mus</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3723649	Ndn<sup>tm1.1Mus</sup>/Ndn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11115855	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653064	Ndn<sup>tm1.1Mus</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3773672	Ndn<sup>tm1.1Mus</sup>/Ndn<sup>+</sup>  [background:] B6.129S2-Ndn<sup>tm1.1Mus</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17116257	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664242	Psen2<sup>tm1Haa</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:18834536	20121015	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308962	Cdkn2a<sup>tm2.1Rdp</sup>/Cdkn2a<sup>tm2.1Rdp</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * CBA * FVB/N	is_model_of	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16585505	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840248	Ptpn11<sup>tm6Bgn</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24553178	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840248	Ptpn11<sup>tm6Bgn</sup>	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3845014	Ptpn11<sup>tm6Bgn</sup>/Ptpn11<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19179468	20140716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415223	Tg(FOXJ1-ACE2)1Rba	is_implicated_in	DOID:0080600	COVID-19						ECO:0000033	author statement supported by traceable reference	PMID:32498696	20200609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415223	Tg(FOXJ1-ACE2)1Rba	is_implicated_in	DOID:0080600	COVID-19		MGI:6415340	Tg(FOXJ1-ACE2)1Rba/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32516571	20200609	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3590139	Gck<sup>Rgsc553</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J	is_model_of	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3521856	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:9406	hypopituitarism						ECO:0000033	author statement supported by traceable reference	PMID:15459176	20060111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360179	Tg(Cryaa-TAg,Ins2-CALM1)26Ove/0  [background:] FVB-Tg(Cryaa-TAg,Ins2-CALM1)26Ove	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:15561957	20130620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821356	Hfe<sup>tm1.1Gfn</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3839782	Hfe<sup>tm1.1Gfn</sup>/Hfe<sup>tm1.1Gfn</sup>  [background:] B6.129P2-Hfe<sup>tm1.1Gfn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16491649	20090413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582830	Kras<sup>tm1Bbd</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:22975375	20140627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582830	Kras<sup>tm1Bbd</sup>	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5502430	Kras<sup>tm1Bbd</sup>/Kras<sup>tm1Bbd</sup> Tg(Cela1-tTA)#Eps/? Tg(tetO-cre)3Jig/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17349585	20140627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040305	Tg(Utg-TAg)7736Fjd	is_implicated_in	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:23851682	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040305	Tg(Utg-TAg)7736Fjd	is_implicated_in	DOID:1324	lung cancer		MGI:5547758	Tg(Utg-TAg)7736Fjd/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:9040936	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6887761	Anapc7<sup>tm1.1Azbi</sup>	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:6887846	Anapc7<sup>tm1.1Azbi</sup>/Anapc7<sup>tm1.1Azbi</sup>  [background:] B6.129S6(CBA)-Anapc7<sup>tm1.1Azbi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34942119	20220310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767624	Tg(tetO-DTA)1Gfi	is_implicated_in	DOID:8986	narcolepsy						ECO:0000033	author statement supported by traceable reference	PMID:27919403	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767624	Tg(tetO-DTA)1Gfi	is_implicated_in	DOID:8986	narcolepsy		MGI:5582929	Tg(HCRT-tTA)1Ahky/0 Tg(tetO-DTA)1Gfi/0  [background:] B6.Cg-Tg(HCRT-tTA)1Ahky Tg(tetO-DTA)1Gfi			ECO:0000033	author statement supported by traceable reference	PMID:24806676	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3767624	Tg(tetO-DTA)1Gfi	is_implicated_in	DOID:8986	narcolepsy		MGI:5582929	Tg(HCRT-tTA)1Ahky/0 Tg(tetO-DTA)1Gfi/0  [background:] B6.Cg-Tg(HCRT-tTA)1Ahky Tg(tetO-DTA)1Gfi			ECO:0000033	author statement supported by traceable reference	PMID:24806675	20230124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5427934	Gata4<sup>tm1Grg</sup>	is_implicated_in	DOID:0110107	atrial heart septal defect 2		MGI:5427936	Gata4<sup>tm1Grg</sup>/Gata4<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22589735	20120716	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc	is_model_of	DOID:9955	hypoplastic left heart syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4822147	Mks1<sup>avc6</sup>/Mks1<sup>avc6</sup>  [background:] involves: C57BL/6J * FVB/N	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3579508	Park7<sup>tm1Shn</sup>/Park7<sup>tm1Shn</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060370	Parkinson's disease 7						ECO:0000033	author statement supported by traceable reference	PMID:15721235	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574536	Dok1<sup>tm1Yyam</sup>/Dok1<sup>tm1Yyam</sup> Dok2<sup>tm1Yyam</sup>/Dok2<sup>tm1Yyam</sup>  [background:] B6.129-Dok1<sup>tm1Yyam</sup> Dok2<sup>tm1Yyam</sup>	is_model_of	DOID:8552	chronic myeloid leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15611294	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5618619	Pdgfrb<sup>b2b2903Clo</sup>	is_implicated_in	DOID:0080109	infantile myofibromatosis		MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574278	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] 129P2(C)-Cecr2<sup>Gt(pGT1)1Hemc</sup>	is_model_of	DOID:0060668	anencephaly						ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5659970	Dph1<sup>tm1.1Cmch</sup>/Dph1<sup>tm1.1Cmch</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720803	Tg(Ckm-APPSw)A2Lfa/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:3429	inclusion body myositis						ECO:0000033	author statement supported by traceable reference	PMID:11972038	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814175	Pkhd1<sup>tm1Cjwa</sup>/Pkhd1<sup>tm1Cjwa</sup>  [background:] involves: 129S6/SvEvTac * FVB/N	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:17519956	20081107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907738	Mlx<sup>tm1.2Rne</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7444296	Mlx<sup>tm1.2Rne</sup>/Mlx<sup>tm1.2Rne</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:34669700	20230315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297135	Brca1<sup>tm2Cxd</sup>/Brca1<sup>tm2Cxd</sup> Tg(MMTV-cre)4Mam/0 Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Esr1)#Paf/0 Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17653086	20130408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857263	Trp53<sup>tm1Tyj</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:25175806	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857263	Trp53<sup>tm1Tyj</sup>	is_implicated_in	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:26766587	20160713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5613243	Cryba1<sup>tm1.1Dbsa</sup>	is_implicated_in	DOID:0110014	age related macular degeneration 1		MGI:5637298	Cryba1<sup>tm1.1Dbsa</sup>/Cryba1<sup>tm1.1Dbsa</sup> Tg(BEST1-cre)1Jdun/0  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25257511	20150525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623286	Disc1<sup>tm1Kara</sup>/Disc1<sup>+</sup>  [background:] B6.129S6-Disc1<sup>tm1Kara</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:16484369	20060525	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316479	Tyr<sup>c-h</sup>/Tyr<sup>c-h</sup>  [background:] B6.Cg-Tyr<sup>c-h</sup>/J	is_model_of	DOID:0050632	oculocutaneous albinism						ECO:0000033	author statement supported by traceable reference	PMID:21968110	20120426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386938	Lgals3<sup>tm1Ftl</sup>	is_implicated_in	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:24802098	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386938	Lgals3<sup>tm1Ftl</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5637814	Lgals3<sup>tm1Ftl</sup>/Lgals3<sup>tm1Ftl</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:18637146	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386938	Lgals3<sup>tm1Ftl</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5637814	Lgals3<sup>tm1Ftl</sup>/Lgals3<sup>tm1Ftl</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:17029217	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442170	Prkcsh<sup>tm1Som</sup>	is_implicated_in	DOID:0050770	polycystic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:21685914	20121120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5442170	Prkcsh<sup>tm1Som</sup>	is_implicated_in	DOID:0050770	polycystic liver disease		MGI:5442315	Prkcsh<sup>tm1Som</sup>/Prkcsh<sup>tm1Som</sup> Tg(CAG-cre/Esr1*)1Lbe/0  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21685914	20121120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5662251	Ddhd2<sup>tm1Crv</sup>	is_implicated_in	DOID:0110806	hereditary spastic paraplegia 54		MGI:5662254	Ddhd2<sup>tm1Crv</sup>/Ddhd2<sup>tm1Crv</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25267624	20150921	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2672094	Krt10<sup>tm1Tmm</sup>/Krt10<sup>+</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6)	is_model_of	DOID:4603	epidermolytic hyperkeratosis						ECO:0000033	author statement supported by traceable reference	PMID:8603923	20090224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814329	Prkn<sup>tm1Ykt</sup>/Prkn<sup>tm1Ykt</sup> Tg(Prp-GPR37)1Ryot/0  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:18691389	20081110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429555	Tg(Notch3*R169C)88Bbb/0  [background:] involves: FVB/N	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:25646445	20151123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425672	Alpl<sup>Mhdabap27</sup>/Alpl<sup>Mhdabap27</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap27</sup>	is_model_of	DOID:0110913	adult hypophosphatasia						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677456	Sall1<sup>tm1Mrau</sup>/Sall1<sup>+</sup>  [background:] involves: 129X1/SvJ * ICR	is_model_of	DOID:0050887	Townes-Brocks syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12915476	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039263	Trp53<sup>tm2Tyj</sup>	is_implicated_in	DOID:3587	pancreatic ductal carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:29050937	20180123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393876	Tmprss9<sup>tm1.3Hzo</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6393881	Tmprss9<sup>tm1.3Hzo</sup>/Tmprss9<sup>tm1.3Hzo</sup>  [background:] involves: 129S1/Sv * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31943016	20200311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706581	Rbl2<sup>tm2Tyj</sup>	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6727113	Trpm3<sup>em1Alsh</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:6727359	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>em1Alsh</sup>  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5516462	Tg(Prnp-ATXN3*148Q)NLS.28Olri	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:5516463	Tg(Prnp-ATXN3*148Q)NLS.28Olri/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:17626202	20131107	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831546	Gtf2i<sup>Gt(XE029)Byg</sup>/Gtf2i<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19109438	20090212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800222	Fas<sup>lpr</sup>/Fas<sup>lpr</sup> Tnfrsf9<sup>tm1Byk</sup>/Tnfrsf9<sup>tm1Byk</sup>  [background:] MRL.Cg-Tnfrsf9<sup>tm1Byk</sup> Fas<sup>lpr</sup>	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:10878371	20080813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5008419	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21573126	20110621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5648842	Prickle1<sup>tm1Asw</sup>/Prickle1<sup>tm1Asw</sup>  [background:] Not Specified	is_model_of	DOID:0060764	autosomal recessive Robinow syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25190059	20150818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5509194	Pten<sup>tm1Engc</sup>	is_implicated_in	DOID:0060867	macrocephaly-autism syndrome		MGI:5629811	Pten<sup>tm1Engc</sup>/Pten<sup>tm1Engc</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24470394	20201216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5509194	Pten<sup>tm1Engc</sup>	is_implicated_in	DOID:0060867	macrocephaly-autism syndrome						ECO:0000033	author statement supported by traceable reference	PMID:32015540	20201216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432232	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	is_model_of	DOID:2394	ovarian cancer						ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393654	Atp7a<sup>tm1.2Mlke</sup>	is_implicated_in	DOID:0111196	X-linked distal spinal muscular atrophy 3		MGI:6393655	Atp7a<sup>tm1.2Mlke</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27293072	20200310	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3513510	Rpe65<sup>rd12</sup>/Rpe65<sup>rd12</sup>  [background:] B6(A)-Rpe65<sup>rd12</sup>/J	is_model_of	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:15823427	20120118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613019	Tor1a<sup>tm1Yql</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:27404940	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613019	Tor1a<sup>tm1Yql</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:3613373	Tor1a<sup>tm1Yql</sup>/Tor1a<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16242683	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912453	Pde6a<sup>tm1.1Bewi</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:26188004	20171106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437111	Tmem67<sup>b2b1291.1Clo</sup>/Tmem67<sup>b2b1291.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1291.1Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2682001	Nbn<sup>tm1Zqw</sup>/Nbn<sup>tm1Zqw</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:7400	Nijmegen breakage syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14612522	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3822143	Tg(Myh7-Ptpn11*Q79R)11Rbns/0  [background:] FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns	is_model_of	DOID:0060578	Noonan syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:17641779	20090105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857284	Cybb<sup>tm1Din</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease						ECO:0000033	author statement supported by traceable reference	PMID:25188296	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857284	Cybb<sup>tm1Din</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:2449556	Cybb<sup>tm1Din</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7719350	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857284	Cybb<sup>tm1Din</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:3785289	Cybb<sup>tm1Din</sup>/Cybb<sup>tm1Din</sup>  [background:] B6.129S-Cybb<sup>tm1Din</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19234224	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5570186	Pex1<sup>tm1.1Sjms</sup>	is_implicated_in	DOID:905	Zellweger syndrome		MGI:5571189	Pex1<sup>tm1.1Sjms</sup>/Pex1<sup>tm1.1Sjms</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24503136	20140702	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5292226	Tmem67<sup>tm1Dgen</sup>/Tmem67<sup>tm1Dgen</sup>  [background:] B6.129P2-Tmem67<sup>tm1Dgen</sup>	is_model_of	DOID:0050778	Meckel syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23283079	20131104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431501	Daw1<sup>b2b1584Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819172	Tg(Lck-LMO1)11Sjk/0 Tg(STIL-TAL1)A5(3)Alpa/0  [background:] involves: C3H * C3H/HeRos * C57BL/6 * C57BL/10Ros	is_model_of	DOID:9952	acute lymphoblastic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:9171354	20100813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4867721	Mapk8ip2<sup>tm1.1Gol</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:30696733	20210115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5521546	Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 Tg(tetO-RNAi:Trp53)ASlowe/0  [background:] involves: C57BL/6 * CD-1	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5511058	Tg(Camk2a-tTA)1Mmay/0 Fgf14<sup>Tg(tetO-MAPT*P301L)4510Kha</sup>/Fgf14<sup>+</sup>  [background:] involves: FVB/N	is_model_of	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:16291936	20131011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5432204	Srgap1<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:7442509	Srgap1<sup>tm1a(KOMP)Wtsi</sup>/Srgap1<sup>tm1a(KOMP)Wtsi</sup> Six2<sup>tm1(tTA,tetO-EGFP/cre)Amc</sup>/Six2<sup>+</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33514561	20230309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5467984	Atxn2<sup>tm2.1Aub</sup>/Atxn2<sup>tm2.1Aub</sup>  [background:] B6.129S2-Atxn2<sup>tm2.1Aub</sup>	is_model_of	DOID:0050955	spinocerebellar ataxia type 2						ECO:0000033	author statement supported by traceable reference	PMID:22956915	20130307	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571378	Tg(Igh-V186.2-TCL1A)3Cro/0  [background:] B6.Cg-Tg(Igh-V186.2-TCL1A)3Cro	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24379361	20140707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4438035	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-CUGBP1)3413Coop/0  [background:] involves: FVB * FVB/N * FVB/NTac	is_model_of	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:20051426	20100331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907285	Tg(Myh6-LMNA*E82K)35Lizh	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:5907286	Tg(Myh6-LMNA*E82K)35Lizh/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21151901	20170823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150441	Oat<sup>tm1Dva</sup>	is_implicated_in	DOID:1415	gyrate atrophy						ECO:0000033	author statement supported by traceable reference	MGI:5811568	20161209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150441	Oat<sup>tm1Dva</sup>	is_implicated_in	DOID:1415	gyrate atrophy		MGI:3719126	Oat<sup>tm1Dva</sup>/Oat<sup>tm1Dva</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10655512	20161209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150441	Oat<sup>tm1Dva</sup>	is_implicated_in	DOID:1415	gyrate atrophy		MGI:2174900	Oat<sup>tm1Dva</sup>/Oat<sup>tm1Dva</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7550347	20161209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664093	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>tm2Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	is_model_of	DOID:0060469	Miller-Dieker lissencephaly syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523802	Cntn1<sup>usl</sup>	is_implicated_in	DOID:0080101	Compton-North congenital myopathy		MGI:5523900	Cntn1<sup>usl</sup>/Cntn1<sup>usl</sup>  [background:] B6.MRL-Cntn1<sup>usl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523802	Cntn1<sup>usl</sup>	is_implicated_in	DOID:0080101	Compton-North congenital myopathy		MGI:5523906	Cntn1<sup>usl</sup>/Cntn1<sup>usl</sup>  [background:] MRL/MpJ-Fas<sup>lpr</sup> Cntn1<sup>usl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4847559	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm3.1Antc</sup> Tg(CAG-cre/Esr1*)86Lbgn/0  [background:] involves: 129 * C57BL/6 * DBA	is_model_of	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19713307	20101216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655506	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:10381492	20050630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5566913	Acta1<sup>tm1Jll</sup>/Acta1<sup>+</sup> Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:0110927	nemaline myopathy 3						ECO:0000033	author statement supported by traceable reference	PMID:21303860	20140606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3789306	Gt(ROSA)26Sor<sup>tm1(Tgfbr1*)Crm</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * DBA/2	is_model_of	DOID:418	systemic scleroderma						ECO:0000033	author statement supported by traceable reference	PMID:17195237	20080527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6358819	Atp6v1b2<sup>tm1Yoyu</sup>	is_implicated_in	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy		MGI:6359427	Atp6v1b2<sup>tm1Yoyu</sup>/Atp6v1b2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31257146	20210120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6358819	Atp6v1b2<sup>tm1Yoyu</sup>	is_implicated_in	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy		MGI:6359426	Atp6v1b2<sup>tm1Yoyu</sup>/Atp6v1b2<sup>tm1Yoyu</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31257146	20210120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4429602	Msh2<sup>tm1Htr</sup>/Msh2<sup>tm1Htr</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:3883	Lynch syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9443401	20110923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042280	Rps6ka3<sup>tm1Ljg</sup>/Y  [background:] involves: 129 * C57BL/6	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12765942	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3042280	Rps6ka3<sup>tm1Ljg</sup>/Y  [background:] involves: 129 * C57BL/6	is_model_of	DOID:3783	Coffin-Lowry syndrome						ECO:0000033	author statement supported by traceable reference	PMID:11113183	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442747	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup> Tg(Wnt1)1Hev/0  [background:] involves: 129S1/Sv * C57BL/6 * FVB/N * SJL	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11178110	20121126	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3711148	Plp1<sup>jp-rsh</sup>/Y  [background:] involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr	is_model_of	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000033	author statement supported by traceable reference	PMID:17394578	20070606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896834	Tg(Thy1-UBQLN2*P506T)6Mont/?  [background:] involves: C3H * C57BL/6 * C57BL/6J	is_model_of	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000033	author statement supported by traceable reference	PMID:27834214	20170509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384039	Snrpn<sup>tm2Alb</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23609791	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384039	Snrpn<sup>tm2Alb</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3719120	Snrpn<sup>tm2Alb</sup>/Snrpn<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11431693	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5465569	Tg(APOE-FGF23*R176Q)#Ack	is_implicated_in	DOID:0050949	autosomal recessive hypophosphatemic rickets		MGI:5466160	Tg(APOE-FGF23*R176Q)#Ack/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:23038738	20130226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3762634	Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:23681253	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3762634	Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5000121	Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>/Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21499268	20140115	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3580086	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	is_model_of	DOID:10629	microphthalmia						ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2175911	Ccl2<sup>tm1Rol</sup>	is_implicated_in	DOID:10871	age related macular degeneration						ECO:0000033	author statement supported by traceable reference	PMID:23982842	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2175911	Ccl2<sup>tm1Rol</sup>	is_implicated_in	DOID:10871	age related macular degeneration		MGI:3815114	Ccl2<sup>tm1Rol</sup>/Ccl2<sup>tm1Rol</sup>  [background:] B6.129S4-Ccl2<sup>tm1Rol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14566334	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447039	Tg(BCL2/IGH)#Jcre	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15545599	20121227	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5697205	Ppox<sup>tm1.1Had</sup>/Ppox<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:4346	variegate porphyria						ECO:0000033	author statement supported by traceable reference	PMID:11929050	20151125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623483	Tg(Ins1-Cat,Tyr)25Pne/0  [background:] involves: FVB	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:10515587	20060530	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052307	Cnr1<sup>tm1Map</sup>/Cnr1<sup>tm1Map</sup> Tg(HD82Gln)81Gschi/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:21406230	20110805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182618	Hdc<sup>tm1Nagy</sup>	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome						ECO:0000033	author statement supported by traceable reference	PMID:28117842	20190507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182618	Hdc<sup>tm1Nagy</sup>	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:5697374	Hdc<sup>tm1Nagy</sup>/Hdc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24411733	20190507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182618	Hdc<sup>tm1Nagy</sup>	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:3620632	Hdc<sup>tm1Nagy</sup>/Hdc<sup>tm1Nagy</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24411733	20190507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3794447	Pmp22<sup>tm1Ueli</sup>/Pmp22<sup>tm1Ueli</sup>  [background:] involves: 129S/SvEv	is_model_of	DOID:0060843	hereditary neuropathy with liability to pressure palsies						ECO:0000033	author statement supported by traceable reference	PMID:7581450	20080620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5896991	Ednrb<sup>tm1Nrd</sup>/Ednrb<sup>tm1Nrd</sup> Gt(ROSA)26Sor<sup>tm14(CAG-tdTomato)Hze</sup>/Gt(ROSA)26Sor<sup>+</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * CBA/J	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:26061883	20170510	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620090	Chm<sup>tm1.3Seab</sup>/Chm<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:9821	choroideremia						ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5759931	Tor1a<sup>tm1Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6;129-Tor1a<sup>tm1Wtd</sup>/J	is_model_of	DOID:0060730	torsion dystonia 1						ECO:0000033	author statement supported by traceable reference	PMID:26183317	20160412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7466919	Ctnnb1<sup>em1V</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:7467133	Ctnnb1<sup>em1V</sup>/Ctnnb1<sup>em1V</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5052381	Tg(HTT*/EGFP)150Nn/0  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:15836623	20110805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4366153	Tg(SFTPC-env)1Yhch/0  [background:] FVB/N-Tg(SFTPC-env)1Yhch	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:19695657	20091103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5442413	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c * C3H/HeJ * C57BL/6J	is_model_of	DOID:14504	Niemann-Pick disease						ECO:0000033	author statement supported by traceable reference	PMID:22869680	20121120	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3803667	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * MF1	is_model_of	DOID:3764	Denys-Drash syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18040647	20080828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2446595	Abcd1<sup>tm1Ymd</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J * DBA/2J	is_model_of	DOID:10588	adrenoleukodystrophy						ECO:0000033	author statement supported by traceable reference	PMID:9126326	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5498230	Kif7<sup>b2b2254Clo</sup>	is_implicated_in	DOID:0060340	ciliopathy		MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835230	Tg(MMTV-LPAR1)2Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763090	Tg(MMTV-LPAR1)2Gbm/Tg(MMTV-LPAR1)2Gbm  [background:] FVB/N-Tg(MMTV-LPAR1)2Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6149962	Zfp106<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:6150431	Zfp106<sup>tm1b(KOMP)Wtsi</sup>/Zfp106<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28072389	20180411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5615244	Foxh1<sup>b2b2662Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5615273	Foxh1<sup>b2b2662Clo</sup>/Foxh1<sup>b2b2662Clo</sup>  [background:] C57BL/6J-Foxh1<sup>b2b2662Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5462364	Tg(tetO-HMOX1)6Hyms	is_implicated_in	DOID:5419	schizophrenia		MGI:5462366	Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22875919	20130207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5812676	Pten<sup>tm1Mro</sup>/Pten<sup>tm1Mro</sup> Sdhb<sup>tm1.1Ics</sup>/Sdhb<sup>+</sup> Tg(KLK3-cre)D4Trp/0  [background:] involves: 129S2/SvPas * FVB	is_model_of	DOID:0050771	pheochromocytoma						ECO:0000033	author statement supported by traceable reference	PMID:26123588	20161220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639668	Dnase1<sup>tm1Tmo</sup>/Dnase1<sup>tm1Tmo</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:10835632	20060802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6120904	Cabp2<sup>tm1b(KOMP)Mbp</sup>	is_implicated_in	DOID:0110537	autosomal recessive nonsyndromic deafness 93		MGI:6155766	Cabp2<sup>tm1b(KOMP)Mbp</sup>/Cabp2<sup>tm1b(KOMP)Mbp</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28183797	20180511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6200023	Patl2<sup>tm1b(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:1100	ovarian disease		MGI:6200082	Patl2<sup>tm1b(EUCOMM)Hmgu</sup>/Patl2<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29661911	20180927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448620	Scnn1b<sup>tm1.1Ipt</sup>	is_implicated_in	DOID:0050477	Liddle syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23684652	20131223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448620	Scnn1b<sup>tm1.1Ipt</sup>	is_implicated_in	DOID:0050477	Liddle syndrome		MGI:3796438	Scnn1b<sup>tm1.1Ipt</sup>/Scnn1b<sup>tm1.1Ipt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10589691	20131223	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437689	Tg(SERPINC1-SV40)A1Pbr/Tg(SERPINC1-SV40)A1Pbr  [background:] involves: C57BL/6 * DBA/2	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1660504	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5583980	Ryr2<sup>tm2Hhv</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5583981	Ryr2<sup>tm2Hhv</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23152493	20140922	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3037979	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup>  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:0060642	recessive dystrophic epidermolysis bullosa						ECO:0000033	author statement supported by traceable reference	PMID:10523500	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4818971	Tg(Prnp-APP*)1Hmor	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4818990	Tg(Prnp-APP*)1Hmor/0  [background:] B6.Cg-Tg(Prnp-APP*)1Hmor			ECO:0000033	author statement supported by traceable reference	PMID:20371804	20100812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827756	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Kras2)12Hev/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18356293	20170306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3813506	Tg(H2-K-Fosl2,-EGFP)13Wag/0  [background:] either: 129.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag or B6.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag	is_model_of	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000033	author statement supported by traceable reference	PMID:18641127	20081103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6281657	Tg(Eif1a-LUM*L199P,-hrGFP)#Fzha	is_implicated_in	DOID:11830	myopia		MGI:6281659	Tg(Eif1a-LUM*L199P,-hrGFP)#Fzha/0  [background:] B6.Cg-Tg(Eif1a-LUM*L199P,-hrGFP)#Fzha			ECO:0000033	author statement supported by traceable reference	PMID:27711221	20190308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5314997	Tmc1<sup>baringo</sup>	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:5315001	Tmc1<sup>baringo</sup>/Tmc1<sup>baringo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3722102	Tg(GSK3B*S9A)1Vln/0 Tg(Thy1-MAPT)2Vln/Tg(Thy1-MAPT)2Vln  [background:] involves: FVB	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:11007782	20070920	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5007812	Gt(ROSA)26Sor<sup>tm2(NOTCH3*C455R)Sat</sup>/Gt(ROSA)26Sor<sup>+</sup> Notch3<sup>Gt(PST033)Byg</sup>/Notch3<sup>Gt(PST033)Byg</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129 * C57BL/6 * SJL	is_model_of	DOID:0111035	CADASIL 1						ECO:0000033	author statement supported by traceable reference	PMID:21555590	20110617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5883288	Neb<sup>tm2Hgra</sup>/Neb<sup>tm2Hgra</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S6/SvEvTac * FVB	is_model_of	DOID:0110928	nemaline myopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:26123491	20170414	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5510810	Ift140<sup>cauli</sup>/Ift140<sup>cauli</sup>  [background:] involves: C3H/HeH * C57BL/6JAnu	is_model_of	DOID:0110085	asphyxiating thoracic dystrophy 1						ECO:0000033	author statement supported by traceable reference	PMID:24009529	20151209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5629846	Slurp1<sup>tm1.1Sgy</sup>/Slurp1<sup>tm1.1Sgy</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0060862	mal de Meleda						ECO:0000033	author statement supported by traceable reference	PMID:24499735	20150416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5141741	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Fgfr3<sup>tm4Cxd</sup>/Fgfr3<sup>+</sup> Tg(Upk2-cre)6Xrw/0  [background:] involves: 129S6/SvEvTac * 129X1/SvJ * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:21504907	20110902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5200558	Arhgef2<sup>Gt(IST13976A8)Tigm</sup>	is_implicated_in	DOID:0080312	neurodevelopmental disorder with midbrain and hindbrain malformations		MGI:5576781	Arhgef2<sup>Gt(IST13976A8)Tigm</sup>/Arhgef2<sup>Gt(IST13976A8)Tigm</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28453519	20180725	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4850030	Tg(Lck-TNFSF13)3919Mhah/0  [background:] B6.Cg-Tg(Lck-TNFSF13)3919Mhah	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15488762	20110103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5796170	Tg(Bglap2-TAg)1Rkho/0  [background:] involves: FVB/N	is_model_of	DOID:3347	osteosarcoma						ECO:0000033	author statement supported by traceable reference	PMID:26659571	20160930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047406	Tg(KRT14-HPV16)wt1Dh	is_implicated_in	DOID:3151	skin squamous cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:24523442	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047406	Tg(KRT14-HPV16)wt1Dh	is_implicated_in	DOID:3151	skin squamous cell carcinoma		MGI:4849989	Tg(KRT14-HPV16)wt1Dh/0  [background:] either: FVB.Cg-Tg(KRT14-HPV16)wt1Dh or (involves: C57BL/6 * DBA/2 * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:8952526	20170728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3784690	Lyst<sup>bg-Lac</sup>/Lyst<sup>bg-Lac</sup>  [background:] CBA/CaLac-Lyst<sup>bg-Lac</sup>	is_model_of	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	MGI:77347	20080512	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605770	Htt<sup>tm1Szi</sup>/Htt<sup>tm2Szi</sup> Tg(Camk2a-cre)2Szi/0  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11062468	20051128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793702	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] C.129S2-Aire<sup>tm1.1Doi</sup>/Doi	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3850389	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)2Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5293422	Mapk1<sup>tm1.2Kuta</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5293439	Mapk1<sup>tm1.2Kuta</sup>/Mapk1<sup>tm1.2Kuta</sup> Tg(Nes-cre)1Kag/0  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21849556	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641393	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] B6J.129S4-Tsc2<sup>tm1Tno</sup>	is_model_of	DOID:13515	tuberous sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23250422	20150622	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435674	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Tg(CAG-cre/Esr1*)5Amc/?  [background:] involves: 129S/SvEv * C57BL/6 * CBA	is_model_of	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4442333	Pten<sup>tm1.1Gle</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N	is_model_of	DOID:6457	Cowden syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20194734	20100504	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5505784	a/a Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] involves: C3H/HeSnJ * C57BL/6J	is_model_of	DOID:0060833	Griscelli syndrome type 2						ECO:0000033	author statement supported by traceable reference	PMID:12070017	20130912	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3041561	Ttn<sup>mdm</sup>/Ttn<sup>mdm</sup>  [background:] Not Specified	is_model_of	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J						ECO:0000033	author statement supported by traceable reference	PMID:11829483	20060222	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5581490	Tg(Myh6-MYOZ2*S48P)114Ajm/0  [background:] involves: FVB	is_model_of	DOID:0110322	hypertrophic cardiomyopathy 16						ECO:0000033	author statement supported by traceable reference	PMID:22987565	20140902	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829652	Flcn<sup>tm1Btt</sup>/Flcn<sup>tm1Btt</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * ICR	is_model_of	DOID:0050387	nonpapillary renal cell carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:18974783	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857129	Apoe<sup>tm1Unc</sup>	is_implicated_in	DOID:9263	homocystinuria						ECO:0000033	author statement supported by traceable reference	PMID:25008174	20161006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4850018	Tg(H2-K/Igh-Traf2*)#Ywc	is_implicated_in	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:15545599	20121227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856158	Pax6<sup>Sey-Neu</sup>	is_implicated_in	DOID:12271	aniridia						ECO:0000033	author statement supported by traceable reference	PMID:24355924	20140506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856158	Pax6<sup>Sey-Neu</sup>	is_implicated_in	DOID:12271	aniridia		MGI:2175208	Pax6<sup>Sey-Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:12714618	20140506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835411	Fkrp<sup>tm1Scbr</sup>	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I		MGI:5556062	Fkrp<sup>tm1Scbr</sup>/Fkrp<sup>tm1Scbr</sup> Sox1<sup>tm1(cre)Take</sup>/Sox1<sup>+</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:24234655	20140408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6192630	Tg(Erbb2*)#Maed	is_implicated_in	DOID:0060072	benign neoplasm		MGI:6192631	Tg(Erbb2*)#Maed/0 Tg(Foxa3-cre)1Khk/0  [background:] involves: C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:29670173	20180803	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639781	Npy1r<sup>tm1Tped</sup>/Npy1r<sup>tm1Tped</sup>  [background:] B6.129P2-Npy1r<sup>tm1Tped</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:14525913	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5318589	Rhag<sup>tm1Goo</sup>	is_not_implicated_in	DOID:0050641	Rh deficiency syndrome		MGI:5318592	Rhag<sup>tm1Goo</sup>/Rhag<sup>tm1Goo</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19807729	20120517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2678248	Prkn<sup>tm1Roo</sup>/Prkn<sup>tm1Roo</sup>  [background:] either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:12915482	20100505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424923	Alpl<sup>Mhdabap27</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425672	Alpl<sup>Mhdabap27</sup>/Alpl<sup>Mhdabap27</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap27</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5308127	Tg(Prnp-AR*112Q)#Deme/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060161	Kennedy's disease						ECO:0000033	author statement supported by traceable reference	PMID:15152038	20120301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429777	b2b1528Clo	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5429854	b2b1528Clo/b2b1528Clo  [background:] C57BL/6J-b2b1528Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523956	Pax3<sup>Sp-1Wli</sup>	is_implicated_in	DOID:0080074	neural tube defect		MGI:5523973	Pax3<sup>Sp-1Wli</sup>/Pax3<sup>Sp-1Wli</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609234	App<sup>tm1Ck</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:24278307	20140904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311153	Dnah5<sup>b2b601Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5308012	Tg(ED-L2-IL1RN/IL1B)#Tcw	is_implicated_in	DOID:5041	esophageal cancer		MGI:5308013	Tg(ED-L2-IL1RN/IL1B)#Tcw/?  [background:] B6.Cg-Tg(ED-L2-IL1RN/IL1B)#Tcw			ECO:0000033	author statement supported by traceable reference	PMID:22264787	20120229	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448463	Tg(SOD1*H46R*H48Q)139Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:12127151	20130109	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4355901	Tg(GFAP-tTA)67Pop/0 Tg(tetO-Ifng)184Pop/0  [background:] B6.Cg-Tg(GFAP-tTA)67Pop Tg(tetO-Ifng)184Pop	is_model_of	DOID:0050902	medulloblastoma						ECO:0000033	author statement supported by traceable reference	PMID:15537876	20090903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7331342	Osbpl2<sup>em1Cya</sup>	is_implicated_in	DOID:0110588	autosomal dominant nonsyndromic deafness 67		MGI:7331344	Osbpl2<sup>em1Cya</sup>/Osbpl2<sup>em1Cya</sup>  [background:] C57BL/6-Osbpl2<sup>em1Cya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35041619	20220823	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814330	Prkn<sup>tm1Ykt</sup>/Prkn<sup>tm1Ykt</sup> Tg(PDGFB-GPR37)20Ryot/Tg(PDGFB-GPR37)20Ryot  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060368	Parkinson's disease 2						ECO:0000033	author statement supported by traceable reference	PMID:18691389	20081110	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3604114	Csf2rb<sup>tm1Mur</sup>/Csf2rb<sup>tm1Mur</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:12120	pulmonary alveolar proteinosis						ECO:0000033	author statement supported by traceable reference	PMID:7697542	20051110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6860324	Hcfc1<sup>em1Poche</sup>	is_implicated_in	DOID:0111814	methylmalonic acidemia and homocysteinemia cblX type		MGI:6860681	Hcfc1<sup>em1Poche</sup>/Y  [background:] C57BL/6J-Hcfc1<sup>em1Poche</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35013307	20220131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5465108	Nlrp3<sup>tm1Bhk</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6256432	Nlrp3<sup>tm1Bhk</sup>/Nlrp3<sup>tm1Bhk</sup>  [background:] B6.129S6-Nlrp3<sup>tm1Bhk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28939830	20190117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778902	Pnp<sup>g</sup>/Pnp<sup>g</sup>  [background:] involves: C57BL/6 * DBA/2J	is_model_of	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6423627	Stk39<sup>tm1Pawe</sup>	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:6423629	Stk39<sup>tm1Pawe</sup>/Stk39<sup>tm1Pawe</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28442491	20200521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3693839	Crtap<sup>tm1Brle</sup>/Crtap<sup>tm1Brle</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0110337	osteogenesis imperfecta type 7						ECO:0000033	author statement supported by traceable reference	PMID:17055431	20070116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5706939	Tg(IRS1)1Mhep/0 Tg(SERPINA1-HBVX)1655Jtsb/0  [background:] involves: C3H * C57BL/6 * FVB * ICR	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:26433160	20160202	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3721542	Apoe<sup>tm1Unc</sup>/Apoe<sup>tm1Unc</sup> Tg(APPV717F)109Ili/Tg(APPV717F)109Ili  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:14741101	20070914	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3773274	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] B6.D2-Gpnmb<sup>R150X</sup>	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16827931	20080310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856877	Smpd3<sup>fro</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000033	author statement supported by traceable reference	PMID:22910579	20130802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856877	Smpd3<sup>fro</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8456819	20130802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179136	Tbx1<sup>tm1Bld</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25197075	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179136	Tbx1<sup>tm1Bld</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3610986	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242049	20150406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179136	Tbx1<sup>tm1Bld</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3610987	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm1Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242049	20150406	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3574963	Fgfr1<sup>Hspy</sup>/Fgfr1<sup>+</sup>  [background:] C3HeB/FeJ-Hspy	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:15630379	20110303	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461061	Mog<sup>tm1(cre)Gkl</sup>/Mog<sup>tm1(cre)Gkl</sup> Tg(Tcra2D2,Tcrb2D2)1Kuch/0  [background:] C57BL/6-Mog<sup>tm1(cre)Gkl</sup> Tg(Tcra2D2,Tcrb2D2)1Kuch	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19483694	20100722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000290	Sos1<sup>tm1.2Rak</sup>	is_implicated_in	DOID:0060582	Noonan syndrome 4		MGI:5000309	Sos1<sup>tm1.2Rak</sup>/Sos1<sup>tm1.2Rak</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21041952	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000290	Sos1<sup>tm1.2Rak</sup>	is_implicated_in	DOID:0060582	Noonan syndrome 4		MGI:5000310	Sos1<sup>tm1.2Rak</sup>/Sos1<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21041952	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5912298	Tg(Myh6-Tnni3*R193H)594Jmme	is_implicated_in	DOID:397	restrictive cardiomyopathy		MGI:5912300	Tg(Myh6-Tnni3*R193H)594Jmme/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22683325	20171102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2174943	Clcnka<sup>tm1Suc</sup>/Clcnka<sup>tm1Suc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:9916798	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3836724	Efhc1<sup>tm1Kzy</sup>/Efhc1<sup>tm1Kzy</sup>  [background:] B6.129P2-Efhc1<sup>tm1Kzy</sup>	is_model_of	DOID:4890	juvenile myoclonic epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:19147686	20090323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5438062	Drc1<sup>b2b1654Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5302829	Ccn6<sup>tm1(cre)Mawa</sup>	is_implicated_in	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood		MGI:5317004	Ccn6<sup>tm1(cre)Mawa</sup>/Ccn6<sup>tm1(cre)Mawa</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24040393	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817488	Tg(ACTA1-FRG1)highRotu	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25695429	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817488	Tg(ACTA1-FRG1)highRotu	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:23300487	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817488	Tg(ACTA1-FRG1)highRotu	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:3817494	Tg(ACTA1-FRG1)highRotu/0  [background:] C57BL/6-Tg(ACTA1-FRG1)highRotu			ECO:0000033	author statement supported by traceable reference	PMID:16341202	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3663129	Fgf14<sup>tm1Dor</sup>/Fgf14<sup>tm1Dor</sup>  [background:] B6.129S6-Fgf14<sup>tm1Dor</sup>	is_model_of	DOID:0050976	spinocerebellar ataxia type 27						ECO:0000033	author statement supported by traceable reference	PMID:17236779	20150703	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3687752	Btk<sup>xid</sup>/Y  [background:] involves: CBA/HN * DBA/2N	is_model_of	DOID:14179	X-linked agammaglobulinemia						ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3625140	Prkar1a<sup>tm1Gsm</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0050471	Carney complex						ECO:0000033	author statement supported by traceable reference	PMID:15371594	20060622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693661	Cdh1<sup>tm1Jjon</sup>	is_implicated_in	DOID:3457	invasive lobular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27411687	20190507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800794	Efemp1<sup>tm1Eap</sup>/Efemp1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:17666404	20080808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588582	Gcm2<sup>tm1Kry</sup>/Gcm2<sup>tm1Kry</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:11199	hypoparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:10910362	20050929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806502	Tg(SFTPC-CD74/ROS1)125Tno	is_implicated_in	DOID:1324	lung cancer		MGI:5806505	Tg(SFTPC-CD74/ROS1)125Tno/0  [background:] C57BL/6J-Tg(SFTPC-CD74/ROS1)125Tno			ECO:0000033	author statement supported by traceable reference	PMID:26964870	20161108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4829538	Jak2<sup>tm1.1Jlvl</sup>	is_not_implicated_in	DOID:2224	essential thrombocythemia		MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6392262	Tulp3<sup>m1Kflj</sup>	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:6392266	Tulp3<sup>m1Kflj</sup>/Tulp3<sup>m1Kflj</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:30799240	20200228	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5318858	Mnx1<sup>tm4(cre)Tmj</sup>/Mnx1<sup>+</sup> Smn1<sup>tm1Cdid</sup>/Smn1<sup>tm1Cdid</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * C57BL/6 * FVB	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:22423102	20120521	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618629	Zic3<sup>tm1Bca</sup>/Zic3<sup>tm1Bca</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6	is_model_of	DOID:0050545	visceral heterotaxy						ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6849722	Lss<sup>em1Zhaol</sup>	is_implicated_in	DOID:83	cataract		MGI:6849724	Lss<sup>em1Zhaol</sup>/Lss<sup>em1Zhaol</sup>  [background:] C57BL/6J-Lss<sup>em1Zhaol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34926465	20220106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3837032	Il6st<sup>tm1Ern</sup>/Il6st<sup>tm1Ern</sup>  [background:] involves: 129S1/Sv * C57BL/6	is_model_of	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:14699500	20130521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259828	Ezh2<sup>em1Jbn</sup>	is_implicated_in	DOID:14731	Weaver syndrome		MGI:6275998	Ezh2<sup>em1Jbn</sup>/Ezh2<sup>+</sup>  [background:] C57BL/6J-Ezh2<sup>em1Jbn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29244146	20190205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6259828	Ezh2<sup>em1Jbn</sup>	is_implicated_in	DOID:14731	Weaver syndrome		MGI:6275997	Ezh2<sup>em1Jbn</sup>/Ezh2<sup>em1Jbn</sup>  [background:] C57BL/6J-Ezh2<sup>em1Jbn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29244146	20190205	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4946646	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21383153	20110415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907641	Tg(HBx-HCV)C5Tto	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5907647	Tg(HBx-HCV)C5Tto/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15618537	20170829	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588431	Gdnf<sup>tm1Lmgd</sup>/Gdnf<sup>tm1Lmgd</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S1/Sv * 129X1/SvJ)	is_model_of	DOID:10487	Hirschsprung's disease						ECO:0000033	author statement supported by traceable reference	PMID:8657307	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6286049	Dis3l2<sup>em1Jtm</sup>	is_implicated_in	DOID:0060476	Perlman syndrome		MGI:6286056	Dis3l2<sup>em1Jtm</sup>/Dis3l2<sup>em1Jtm</sup>  [background:] C57BL/6J-Dis3l2<sup>em1Jtm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29950491	20190404	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576120	Egr2<sup>tm1Jmi</sup>/Egr2<sup>tm1Jmi</sup>  [background:] Not Specified	is_model_of	DOID:0110195	Charcot-Marie-Tooth disease type 4E						ECO:0000033	author statement supported by traceable reference	PMID:15695336	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6294039	Hgf<sup>tm1.1Tbf</sup>	is_implicated_in	DOID:0110497	autosomal recessive nonsyndromic deafness 39		MGI:6446738	Hgf<sup>tm1.1Tbf</sup>/Hgf<sup>tm1.1Tbf</sup>  [background:] B6.Cg-Hgf<sup>tm1.1Tbf</sup>/Tbf			ECO:0000033	author statement supported by traceable reference	PMID:32152201	20200730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295199	Tg(Thy1-BSCL2*N88S)1Dit	is_implicated_in	DOID:231	motor neuron disease		MGI:5295210	Tg(Thy1-BSCL2*N88S)1Dit/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21750110	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5647995	Tfap2a<sup>tm1Will</sup>/Tfap2a<sup>tm2.1Will</sup>  [background:] involves: 129S1/Sv * Black Swiss	is_model_of	DOID:0050567	orofacial cleft						ECO:0000033	author statement supported by traceable reference	PMID:25381013	20150812	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4936868	Adh7<sup>tm1Gdu</sup>/Adh7<sup>tm1Gdu</sup>  [background:] B6.129(Cg)-Adh7<sup>tm1Gdu</sup>	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:21075145	20110224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3527796	Lmna<sup>tm1Gbon</sup>/Lmna<sup>tm1Gbon</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:15548545	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5478744	Tg(CMV-LITAF*W116G)#Lli/Tg(CMV-LITAF*W116G)#Lli  [background:] FVB-Tg(CMV-LITAF*W116G)#Lli	is_model_of	DOID:0110151	Charcot-Marie-Tooth disease type 1C						ECO:0000033	author statement supported by traceable reference	PMID:23359569	20130507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3575579	Recql4<sup>tm1Glu</sup>/Recql4<sup>tm1Glu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:2732	Rothmund-Thomson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15703196	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3664785	Grm1<sup>crv4</sup>/Grm1<sup>crv4</sup>  [background:] BALB/cPas-Grm1<sup>crv4</sup>	is_model_of	DOID:0080062	autosomal recessive spinocerebellar ataxia 13						ECO:0000033	author statement supported by traceable reference	PMID:16964410	20151117	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000247	Boc<sup>tm2Rsk</sup>/Boc<sup>tm2Rsk</sup> Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] B6.129-Boc<sup>tm2Rsk</sup> Cdon<sup>tm1Rsk</sup>	is_model_of	DOID:0110877	holoprosencephaly 11						ECO:0000033	author statement supported by traceable reference	PMID:21183473	20140825	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4819725	Tg(Tnnt2-TNNT2*R92Q)#Ajm/0  [background:] involves: C3H * C57BL/6 * ICR	is_model_of	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000033	author statement supported by traceable reference	PMID:9788962	20100819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3522714	vsd/vsd  [background:] C57BL/6J-vsd	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:15548583	20110125	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5753081	Aspm<sup>tm1(cre)Mrc</sup>/Aspm<sup>tm1(cre)Mrc</sup>  [background:] Not Specified	is_model_of	DOID:10907	microcephaly						ECO:0000033	author statement supported by traceable reference	PMID:26581405	20160323	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5086118	Amelx<sup>tm1Kul</sup>/Amelx<sup>tm1Kul</sup> Tg(AMELX*P70T)2Gibs/?  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000033	author statement supported by traceable reference	PMID:17384027	20110816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5907138	Rnf170<sup>Gt(OST104375)Lex</sup>	is_implicated_in	DOID:0050951	hereditary ataxia		MGI:5907140	Rnf170<sup>Gt(OST104375)Lex</sup>/Rnf170<sup>Gt(OST104375)Lex</sup>  [background:] B6.129S-Rnf170<sup>Gt(OST104375)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26433933	20170817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655355	None [background:] DBA/2J	is_model_of	DOID:0060680	pigment dispersion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22859742	20150601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3605769	Htt<sup>tm1Szi</sup>/Htt<sup>tm2Szi</sup> Tg(Camk2a-cre)1Szi/0  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11062468	20051128	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2657302	Fras1<sup>bl</sup>/Fras1<sup>bl</sup>  [background:] involves: 101/H * C3H/HeH	is_model_of	DOID:11836	clubfoot						ECO:0000033	author statement supported by traceable reference	PMID:12766769	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5910326	Mypn<sup>tm1.1Epu</sup>	is_implicated_in	DOID:0110933	nemaline myopathy 11		MGI:6283403	Mypn<sup>tm1.1Epu</sup>/Mypn<sup>tm1.1Epu</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:28017374	20190318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4940765	Fan1<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060911	karyomegalic interstitial nephritis		MGI:6281646	Fan1<sup>tm1a(KOMP)Wtsi</sup>/Fan1<sup>tm1a(KOMP)Wtsi</sup>  [background:] 129S1.B6-Fan1<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27026368	20190307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575755	Tg(KRT5-tTA)1216Glk	is_implicated_in	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:24473265	20140514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179190	Tbx1<sup>tm1Pa</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22396765	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179190	Tbx1<sup>tm1Pa</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3586915	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179190	Tbx1<sup>tm1Pa</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3586912	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179190	Tbx1<sup>tm1Pa</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3586914	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179190	Tbx1<sup>tm1Pa</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3850161	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15385444	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5009280	Clec16a<sup>curt</sup>	is_implicated_in	DOID:1289	neurodegenerative disease		MGI:5009333	Clec16a<sup>curt</sup>/Clec16a<sup>curt</sup>  [background:] SWR/J-Clec16a<sup>curt</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26987296	20191217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4882077	Ofd1<sup>tm2.1Bfra</sup>	is_implicated_in	DOID:0060316	orofaciodigital syndrome I		MGI:3620649	Ofd1<sup>tm2.1Bfra</sup>/Ofd1<sup>+</sup> Tg(CAG-cre)1Nagy/0  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16311594	20060428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4882077	Ofd1<sup>tm2.1Bfra</sup>	is_implicated_in	DOID:0060316	orofaciodigital syndrome I		MGI:3620650	Ofd1<sup>tm2.1Bfra</sup>/Y Tg(CAG-cre)1Nagy/0  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16311594	20060428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5906301	Mdga2<sup>Tg(Prnp-PFN1*G118V)838Kiaei</sup>	is_implicated_in	DOID:0060209	amyotrophic lateral sclerosis type 18		MGI:6275631	Mdga2<sup>Tg(Prnp-PFN1*G118V)838Kiaei</sup>/Mdga2<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28040732	20190201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676549	Stk11<sup>tm1.1Jish</sup>/Stk11<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12060709	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6274710	Gucy2e<sup>cpfl9</sup>	is_implicated_in	DOID:0110078	Leber congenital amaurosis 1		MGI:6274727	Gucy2e<sup>cpfl9</sup>/Gucy2e<sup>cpfl9</sup>  [background:] B6;129P2-Gucy2e<sup>cpfl9</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:6274742	20190125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6404633	Tardbp<sup>tm3.1Ckjs</sup>	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6404636	Tardbp<sup>tm3.1Ckjs</sup>/Tardbp<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31964415	20200420	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623773	Kcnq1<sup>tm1Apf</sup>/Kcnq1<sup>tm1Apf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15891643	20070116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5285350	Bicc1<sup>b2b222Clo</sup>/Bicc1<sup>b2b222Clo</sup>  [background:] C57BL/6J-Bicc1<sup>b2b222Clo</sup>	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7432734	Cdh2<sup>em1Obir</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:7434319	Cdh2<sup>em1Obir</sup>/Cdh2<sup>em1Obir</sup>  [background:] C57BL/6JRcc-Cdh2<sup>em1Obir</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34702855	20230214	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778824	Vangl1<sup>Gt(XL802)Byg</sup>/Vangl1<sup>+</sup> Vangl2<sup>Lp</sup>/Vangl2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * LPT/LeJ	is_model_of	DOID:0080074	neural tube defect						ECO:0000033	author statement supported by traceable reference	PMID:18296642	20080424	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5432346	Tg(Ela1-Myc)160Bri/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:1986386	20120828	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2450673	Abca1<sup>tm1Wpfl</sup>/Abca1<sup>tm1Wpfl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:1388	Tangier disease						ECO:0000033	author statement supported by traceable reference	PMID:10980140	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431501	Daw1<sup>b2b1584Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175082	Itgb6<sup>tm1Des</sup>/Itgb6<sup>tm1Des</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:2841	asthma						ECO:0000033	author statement supported by traceable reference	PMID:8666675	20050706	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4947235	Rho<sup>tm1.1Kpal</sup>/Rho<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:21224384	20130619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6150323	Kifbp<sup>em2Hmy</sup>	is_implicated_in	DOID:0060481	Goldberg-Shprintzen syndrome		MGI:6154376	Kifbp<sup>em2Hmy</sup>/Kifbp<sup>em2Hmy</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29192291	20180503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177288	Gpi1<sup>b-m2Neu</sup>/Gpi1<sup>b-m2Neu</sup>  [background:] C3.Cg-Gpi1<sup>b-m2Neu</sup>	is_model_of	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000033	author statement supported by traceable reference	PMID:8417789	20110309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3838969	Atp8a2<sup>wl</sup>/Atp8a2<sup>wl</sup>  [background:] Not Specified	is_model_of	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861934	Htt<sup>tm4Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27913616	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861934	Htt<sup>tm4Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861934	Htt<sup>tm4Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698040	Htt<sup>tm4Mem</sup>/Htt<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861934	Htt<sup>tm4Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:16697652	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861934	Htt<sup>tm4Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20171207	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705622	Pcnt<sup>Gt(RRU388)Byg</sup>/Pcnt<sup>Gt(RRU388)Byg</sup>  [background:] B6.129P2-Pcnt<sup>Gt(RRU388)Byg</sup>	is_model_of	DOID:0060609	microcephalic osteodysplastic primordial dwarfism type II						ECO:0000033	author statement supported by traceable reference	PMID:25220058	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5502183	Gdf5<sup>Bp-5J</sup>	is_implicated_in	DOID:0050790	fibular hypoplasia and complex brachydactyly		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5435567	Porcn<sup>tm1.1Vdv</sup>/Y Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J	is_model_of	DOID:2120	focal dermal hypoplasia						ECO:0000033	author statement supported by traceable reference	PMID:22412863	20120920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054417	Tg(DM15)26Bew	is_implicated_in	DOID:11722	myotonic dystrophy type 1						ECO:0000033	author statement supported by traceable reference	PMID:26908607	20160728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054417	Tg(DM15)26Bew	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3054527	Tg(DM15)26Bew/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:15317754	20160728	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5499112	Tg(Myl1-SOD1*G93A)#Amu/0  [background:] FVB/NJ-Tg(Myl1-SOD1*G93A)#Amu	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:19046573	20130801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6506378	Dnm2<sup>tm2.1Ics</sup>	is_implicated_in	DOID:423	myopathy		MGI:6506379	Dnm2<sup>tm2.1Ics</sup>/Dnm2<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32129442	20210216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5445435	Tg(Prnp-FUS)WT3Cshw/Tg(Prnp-FUS)WT3Cshw  [background:] involves: C57BL/6 * Crl:CD-1(ICR)	is_model_of	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000033	author statement supported by traceable reference	PMID:22961620	20121212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5583020	Nbeal2<sup>gps</sup>	is_implicated_in	DOID:0111044	gray platelet syndrome		MGI:5806080	Nbeal2<sup>gps</sup>/Nbeal2<sup>gps</sup>  [background:] 129S1/SvImJ-Nbeal2<sup>gps</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26950939	20161103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4943308	Tg(Lck-Tnfsf15,-EGFP)#Targ	is_implicated_in	DOID:0110896	inflammatory bowel disease 16		MGI:4943326	Tg(Lck-Tnfsf15,-EGFP)#Targ/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21264313	20110331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856987	Nphp3<sup>pcy</sup>	is_implicated_in	DOID:0111114	nephronophthisis 3						ECO:0000033	author statement supported by traceable reference	PMID:24815352	20140804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856987	Nphp3<sup>pcy</sup>	is_implicated_in	DOID:0111114	nephronophthisis 3		MGI:3583125	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:12872122	20140804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4360685	Apc<sup>tm2Rfo</sup>/Apc<sup>+</sup>  [background:] (C57BL/6J x 129P2/OlaHsd)F1	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23955540	20140430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856108	Foxn1<sup>nu</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome						ECO:0000033	author statement supported by traceable reference	PMID:596425	20140213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856108	Foxn1<sup>nu</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2680668	Foxn1<sup>nu</sup>/Foxn1<sup>nu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:596425	20140213	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5140117	Gjc2<sup>tm2.1Kwi</sup>/Gjc2<sup>tm2.1Kwi</sup>  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:0060787	hypomyelinating leukodystrophy 2						ECO:0000033	author statement supported by traceable reference	PMID:21750683	20110818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804675	Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup>	is_implicated_in	DOID:2526	prostate adenocarcinoma		MGI:6193619	Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Osr1-cre)4Mrt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21795710	20180807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804675	Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup>	is_implicated_in	DOID:2526	prostate adenocarcinoma		MGI:6193618	Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup>/Gt(ROSA)26Sor<sup>tm1(CAG-AR)Zsu</sup> Tg(Osr1-cre)4Mrt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21795710	20180807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4461396	Tg(CAG-Map3k7*K63W)1232Mds	is_implicated_in	DOID:384	Wolff-Parkinson-White syndrome		MGI:4461321	Tg(CAG-Map3k7*K63W)1232Mds/0 Tg(Myh6-cre)2182Mds/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17085580	20100723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5316006	Slc6a3<sup>tm2(tTA)Xz</sup>/Slc6a3<sup>+</sup> Tg(tetO-COX8A/PstI*)1Ctm/0  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:22131425	20120422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5471581	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0 Tg(Tagln-cre)1Her/0  [background:] involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6 * C57BL/6J * SJL	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:23152628	20130403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6681928	Pmfbp1<sup>em#Jfw</sup>	is_implicated_in	DOID:0111922	spermatogenic failure 31		MGI:6681929	Pmfbp1<sup>em#Jfw</sup>/Pmfbp1<sup>em#Jfw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30298696	20210408	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5882592	Tg(Col1a1-Ifitm5*)1Brle/0  [background:] involves: FVB/N	is_model_of	DOID:0110344	osteogenesis imperfecta type 5						ECO:0000033	author statement supported by traceable reference	PMID:25251575	20170407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5883023	Tg(EEF1A1-Gnas*R201C)184Pabi	is_implicated_in	DOID:1858	McCune Albright syndrome		MGI:5883024	Tg(EEF1A1-Gnas*R201C)184Pabi/0  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:24764158	20170413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4839643	Tg(Prnp-TARDBP*A315T)23Jlel	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:4839653	Tg(Prnp-TARDBP*A315T)23Jlel/0  [background:] involves: C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20621187	20101130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6865661	Prkcg<sup>em1Jpka</sup>	is_implicated_in	DOID:0050964	spinocerebellar ataxia type 14		MGI:6865686	Prkcg<sup>em1Jpka</sup>/Prkcg<sup>em1Jpka</sup>  [background:] FVB/N-Prkcg<sup>em1Jpka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33478986	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6865661	Prkcg<sup>em1Jpka</sup>	is_implicated_in	DOID:0050964	spinocerebellar ataxia type 14		MGI:6865691	Prkcg<sup>em1Jpka</sup>/Prkcg<sup>+</sup>  [background:] FVB/N-Prkcg<sup>em1Jpka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33478986	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4835234	Tg(MMTV-LPAR2)3Gbm	is_implicated_in	DOID:1612	breast cancer		MGI:5763101	Tg(MMTV-LPAR2)3Gbm/Tg(MMTV-LPAR2)3Gbm  [background:] FVB/N-Tg(MMTV-LPAR2)3Gbm			ECO:0000033	author statement supported by traceable reference	PMID:19477432	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5295154	Tg(tetO-APPSwInd)Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5812135	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27109181	20161215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5487403	Myo7a<sup>dmbo2</sup>	is_implicated_in	DOID:0110477	autosomal recessive nonsyndromic deafness 2		MGI:5487460	Myo7a<sup>dmbo2</sup>/Myo7a<sup>dmbo2</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23251483	20130529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4821979	Sptbn2<sup>tm1Mjac</sup>	is_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:4821985	Sptbn2<sup>tm1Mjac</sup>/Sptbn2<sup>tm1Mjac</sup>  [background:] B6.129P2-Sptbn2<sup>tm1Mjac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20371805	20100908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5304394	Lim2<sup>Aca47</sup>	is_implicated_in	DOID:83	cataract		MGI:5304399	Lim2<sup>Aca47</sup>/Lim2<sup>Aca47</sup>  [background:] C57BL/6J-Lim2<sup>Aca47</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21617753	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000266	Tg(AR*100Q)C32Als	is_implicated_in	DOID:0060161	Kennedy's disease		MGI:5000280	Tg(AR*100Q)C32Als/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15003169	20110527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6725088	Galc<sup>m4Btlr</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:6725727	Galc<sup>m4Btlr</sup>/Galc<sup>m4Btlr</sup>  [background:] C57BL/6J-Galc<sup>m4Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6256800	Col1a1<sup>tm1(CAG-EGFR*T790M*C797S*L858R)Mje</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:6256822	Col1a1<sup>tm1(CAG-EGFR*T790M*C797S*L858R)Mje</sup>/Col1a1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27251290	20181119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583763	Irs2<sup>tm1Mfw</sup>/Irs2<sup>tm1Mfw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:9495343	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933762	Cdkn2c<sup>tm1Yxi</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160422	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5502432	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup> Tg(Cela1-tTA)#Eps/? Tg(tetO-cre)3Jig/?  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:17349585	20130822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5572940	Rpe65<sup>450L</sup>/Rpe65<sup>450L</sup> Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] 129.Cg(B6)-Whrn<sup>wi</sup>	is_model_of	DOID:0110840	Usher syndrome type 2D						ECO:0000033	author statement supported by traceable reference	PMID:24211856	20140715	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2655154	Tbx19<sup>tm1Jdr</sup>/Tbx19<sup>tm1Jdr</sup>  [background:] either: (involves: 129/Sv) or (involves: BALB/c)	is_model_of	DOID:0080150	adrenocorticotropic hormone deficiency						ECO:0000033	author statement supported by traceable reference	PMID:12651888	20050621	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050811	congenital adrenal hyperplasia						ECO:0000033	author statement supported by traceable reference	PMID:9326645	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050811	congenital adrenal hyperplasia						ECO:0000033	author statement supported by traceable reference	PMID:10976923	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0050811	congenital adrenal hyperplasia						ECO:0000033	author statement supported by traceable reference	PMID:9888583	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675750	Syn3<sup>tm1Pggd</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:23236212	20190213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5298013	Tg(Ggt1-Hif1a*)43Log	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:5298019	Tg(Ggt1-Hif1a*)43Log/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21908555	20111213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5514357	Col6a3<sup>tm1Chu</sup>	is_implicated_in	DOID:0050557	congenital muscular dystrophy		MGI:5514360	Col6a3<sup>tm1Chu</sup>/Col6a3<sup>tm1Chu</sup>  [background:] B6.129-Col6a3<sup>tm1Chu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23564457	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5689835	Reln<sup>rl</sup>/Reln<sup>+</sup>  [background:] B6.Cg-Reln<sup>rl</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:25845740	20151012	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719126	Oat<sup>tm1Dva</sup>/Oat<sup>tm1Dva</sup>  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:1415	gyrate atrophy						ECO:0000033	author statement supported by traceable reference	PMID:10655512	20070827	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5309129	Cplane1<sup>b2b012Clo</sup>/Cplane1<sup>b2b012Clo</sup>  [background:] C57BL/6J-Cplane1<sup>b2b012Clo</sup>	is_model_of	DOID:0110986	Joubert syndrome 17						ECO:0000033	author statement supported by traceable reference	PMID:25877302	20160609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429194	Ulk4<sup>tm1Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429215	Ulk4<sup>tm1Lex</sup>/Ulk4<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6093469	Ccn6<sup>tm1.1Cgkl</sup>	is_implicated_in	DOID:4680	breast metaplastic carcinoma		MGI:6093470	Ccn6<sup>tm1.1Cgkl</sup>/Ccn6<sup>tm1.1Cgkl</sup> Tg(MMTV-cre)1Mam/0  [background:] FVB/N-Ccn6<sup>tm1.1Cgkl</sup> Tg(MMTV-cre)1Mam			ECO:0000033	author statement supported by traceable reference	PMID:27819674	20171130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7332932	Tg(KRT14-Shh)#Cobm	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:7332935	Tg(KRT14-Shh)#Cobm/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19394325	20220830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5050725	Cntn1<sup>m1J</sup>	is_implicated_in	DOID:0080101	Compton-North congenital myopathy		MGI:5300199	Cntn1<sup>m1J</sup>/Cntn1<sup>m1J</sup>  [background:] B6;C-Cntn1<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6198574	Dync1h1<sup>tm1.1Sjki</sup>	is_implicated_in	DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O		MGI:6198577	Dync1h1<sup>tm1.1Sjki</sup>/Dync1h1<sup>+</sup>  [background:] involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29379136	20180918	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3511748	Lepr<sup>tm1.2Chua</sup>/Lepr<sup>tm1.2Chua</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:15389315	20050707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3573928	Htt<sup>tm1Detl</sup>/Htt<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:11152661	20090223	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6509315	Kcnt1<sup>em8Frk</sup>	is_implicated_in	DOID:1826	epilepsy						ECO:0000033	author statement supported by traceable reference	PMID:33113364	20210309	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3842982	Ihh<sup>tm1.1Dcha</sup>/Ihh<sup>tm1.1Dcha</sup>  [background:] either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR)	is_model_of	DOID:0110964	brachydactyly type A1						ECO:0000033	author statement supported by traceable reference	PMID:19252479	20090505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3524999	Bbs2<sup>tm1Vcs</sup>/Bbs2<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	is_model_of	DOID:0110124	Bardet-Biedl syndrome 2						ECO:0000033	author statement supported by traceable reference	PMID:15539463	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ	is_model_of	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6196100	F9<sup>em1Dlli</sup>	is_implicated_in	DOID:12259	hemophilia B		MGI:6196101	F9<sup>em1Dlli</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26964564	20180830	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>	is_model_of	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641392	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] B6J.129S4-Tsc1<sup>tm1Hin</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23250422	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5491236	b2b2025Clo	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5555835	b2b2025Clo/b2b2025Clo  [background:] C57BL/6J-b2b2025Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140407	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5704429	Madd<sup>tm1Bpra</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5789257	Madd<sup>tm1Bpra</sup>/Madd<sup>tm1Bpra</sup> Tg(Ins2-cre/ERT)1Dam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24379354	20160818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4430084	Uaca<sup>tm1Kiy</sup>/Uaca<sup>tm1Kiy</sup>  [background:] B6.129P2-Uaca<sup>tm1Kiy</sup>	is_model_of	DOID:684	hepatocellular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:19637241	20100224	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3615358	Trak1<sup>hyrt</sup>/Trak1<sup>hyrt</sup>  [background:] involves: AKR * C3HeB/FeJ * C57BL/6J	is_model_of	DOID:13366	Stiff-Person syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16380713	20060309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707315	Cadps2<sup>tm1Tfr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:23159942	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707315	Cadps2<sup>tm1Tfr</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3711235	Cadps2<sup>tm1Tfr</sup>/Cadps2<sup>tm1Tfr</sup>  [background:] C57BL/6-Cadps2<sup>tm1Tfr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17380209	20211019	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>	is_model_of	DOID:0110545	autosomal dominant nonsyndromic deafness 13						ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3819135	Nog<sup>tm1Amc</sup>/Nog<sup>tm1Amc</sup>  [background:] either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1 * ICR)	is_model_of	DOID:0080171	esophageal atresia/tracheoesophageal fistula						ECO:0000033	author statement supported by traceable reference	PMID:17260385	20081212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183279	Lrp5<sup>tm1Kry</sup>	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23901037	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183279	Lrp5<sup>tm1Kry</sup>	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome		MGI:3664614	Lrp5<sup>tm1Kry</sup>/Lrp5<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11956231	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183279	Lrp5<sup>tm1Kry</sup>	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome		MGI:3664613	Lrp5<sup>tm1Kry</sup>/Lrp5<sup>tm1Kry</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11956231	20160801	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3629805	Pcsk1<sup>N222D</sup>/Pcsk1<sup>N222D</sup>  [background:] C57BL/6-Pcsk1<sup>N222D</sup>	is_model_of	DOID:9970	obesity						ECO:0000033	author statement supported by traceable reference	PMID:16644867	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5447640	Atp7a<sup>tm1.1Mjp</sup>	is_implicated_in	DOID:0111196	X-linked distal spinal muscular atrophy 3		MGI:6324372	Atp7a<sup>tm1.1Mjp</sup>/Y Mnx1<sup>tm4(cre)Tmj</sup>/Mnx1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25639447	20191122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5695740	Ppard<sup>tm1Dsvg</sup>/Ppard<sup>tm1Dsvg</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:25279796	20151112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3587188	Hoxd13<sup>spdh</sup>/Hoxd13<sup>spdh</sup>  [background:] B6C3Fe a/a-Hoxd13<sup>spdh</sup>/J	is_model_of	DOID:0060242	synpolydactyly						ECO:0000033	author statement supported by traceable reference	PMID:9580668	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4841281	Hgd<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:9270	alkaptonuria		MGI:6416345	Hgd<sup>tm1a(KOMP)Wtsi</sup>/Hgd<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31600782	20200513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857974	Psen1<sup>tm1Shn</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:27143420	20160926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857974	Psen1<sup>tm1Shn</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2174998	Psen1<sup>tm1Shn</sup>/Psen1<sup>tm1Shn</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9160754	20160926	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5473901	Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0 Tg(Mpz-cre)94Imeg/0  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0060389	chromosome 10q23 deletion syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22773757	20130411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578131	Tg(Alb-PDGFC)#Jcam	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5578132	Tg(Alb-PDGFC)#Jcam/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15728360	20140819	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660497	Tg(Myh6-Jup*)1Ajm/0  [background:] involves: FVB/N	is_model_of	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000033	author statement supported by traceable reference	PMID:22021931	20150831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857444	Nf1<sup>tm1Fcr</sup>	is_implicated_in	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000033	author statement supported by traceable reference	PMID:27333032	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7266849	Rbm20<sup>em1Hgra</sup>	is_implicated_in	DOID:0110447	dilated cardiomyopathy 1DD		MGI:7275232	Rbm20<sup>em1Hgra</sup>/Rbm20<sup>+</sup>  [background:] C57BL/6-Rbm20<sup>em1Hgra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35041844	20220509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7266849	Rbm20<sup>em1Hgra</sup>	is_implicated_in	DOID:0110447	dilated cardiomyopathy 1DD		MGI:7275231	Rbm20<sup>em1Hgra</sup>/Rbm20<sup>em1Hgra</sup>  [background:] C57BL/6-Rbm20<sup>em1Hgra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35041844	20220509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5319508	Tg(Myh6-MYPN*Y20C)#Jato	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5319509	Tg(Myh6-MYPN*Y20C)#Jato/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22286171	20170925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5319508	Tg(Myh6-MYPN*Y20C)#Jato	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy						ECO:0000033	author statement supported by traceable reference	PMID:27171814	20170925	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3720946	Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J	is_model_of	DOID:0110042	Alzheimer's disease 3						ECO:0000033	author statement supported by traceable reference	PMID:16354928	20071026	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5558082	Bpifa1<sup>m1Ingm</sup>/Bpifa1<sup>m1Ingm</sup>  [background:] involves: C3HeB/FeJ	is_model_of	DOID:10754	otitis media						ECO:0000033	author statement supported by traceable reference	PMID:25765466	20151216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5315461	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>tm1Hzo</sup> Kat2a<sup>tm3.1Roth</sup>/Kat2a<sup>+</sup>  [background:] involves: 129 * 129S7/SvEvBrd	is_model_of	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000033	author statement supported by traceable reference	PMID:22002997	20120418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5512768	Elp1<sup>tm1.1Gilas</sup>	is_implicated_in	DOID:11589	Riley-Day syndrome		MGI:6274313	Elp1<sup>tm1.1Gilas</sup>/Elp1<sup>tm1.1Gilas</sup> Tg(Dct-cre)1Apdn/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27997532	20190123	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3618910	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae	is_model_of	DOID:9164	achalasia						ECO:0000033	author statement supported by traceable reference	PMID:11438492	20091111	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J	is_model_of	DOID:2223	platelet storage pool deficiency						ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297424	b2b464Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5311117	b2b464Clo/b2b464Clo  [background:] C57BL/6J-b2b464Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2173405	Shh<sup>tm1Chg</sup>/Shh<sup>tm1Chg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110875	holoprosencephaly 3						ECO:0000033	author statement supported by traceable reference	PMID:8837770	20050817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5314996	Tmc1<sup>stitch</sup>	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:5314999	Tmc1<sup>stitch</sup>/Tmc1<sup>stitch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3783528	Rb1<sup>tm3Tyj</sup>/Rb1<sup>tm3Tyj</sup> Rbl2<sup>tm1Tyj</sup>/Rbl2<sup>tm1Tyj</sup> Tg(Nes-cre)1Atp/0  [background:] involves: 129S2/SvPas * 129S4/SvJae * FVB/N	is_model_of	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:15231717	20080501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5438770	Bmpr2<sup>tm1Kmi</sup>/Bmpr2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J	is_model_of	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:16027259	20121018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314815	Chrne<sup>tm2Vwi</sup>/Chrne<sup>tm2Vwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0110678	congenital myasthenic syndrome 4A						ECO:0000033	author statement supported by traceable reference	PMID:22178625	20150511	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176903	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24262794	20140416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2176903	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:8947561	20140416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2448896	Rs1<sup>tmgc1</sup>/Rs1<sup>tmgc1</sup>  [background:] involves: C3H/Rl * C57BL/6	is_model_of	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000033	author statement supported by traceable reference	PMID:16088326	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4850003	Tg(Igh-TCL1A)1Ypek	is_implicated_in	DOID:1040	chronic lymphocytic leukemia		MGI:4850007	Tg(Igh-TCL1A)1Ypek/0  [background:] FVB/N-Tg(Igh-TCL1A)1Ypek			ECO:0000033	author statement supported by traceable reference	PMID:20357824	20110103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6406985	Fgfr2<sup>tm3Cxd</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:6415627	Fgfr2<sup>tm3Cxd</sup>/Fgfr2<sup>+</sup> Tg(Col2a1-cre)1Xya/0  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28123344	20200508	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3719716	Atcay<sup>ji</sup>/Atcay<sup>ji</sup>  [background:] JIGR	is_model_of	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3512452	Fgf23<sup>tm1Blan</sup>/Fgf23<sup>tm1Blan</sup> Phex<sup>Hyp</sup>/Y  [background:] Not Specified	is_model_of	DOID:0050948	autosomal dominant hypophosphatemic rickets						ECO:0000033	author statement supported by traceable reference	PMID:15579309	20090728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6094271	Tuba8<sup>tm1.2Ctpd</sup>	is_not_implicated_in	DOID:0090132	complex cortical dysplasia with other brain malformations 7		MGI:6094276	Tuba8<sup>tm1.2Ctpd</sup>/Tuba8<sup>tm1.2Ctpd</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28388629	20171204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5286986	Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:5288470	Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>/Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15466487	20111006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359275	Sirt1<sup>tm3Fwa</sup>	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:20655472	20120201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581193	Pde6b<sup>rd10</sup>/Pde6b<sup>rd10</sup>  [background:] B6.CXB1-Pde6b<sup>rd10</sup>/J	is_model_of	DOID:10584	retinitis pigmentosa						ECO:0000033	author statement supported by traceable reference	PMID:17267005	20081103	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3581453	Lama2<sup>dy-7J</sup>/Lama2<sup>dy-7J</sup>  [background:] C57BL/6J-Lama2<sup>dy-7J</sup>/J	is_model_of	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000033	author statement supported by traceable reference	PMID:18430779	20090626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311383	Daw1<sup>b2b1116Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3795785	Fermt3<sup>tm1Ref</sup>/Fermt3<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:0110912	leukocyte adhesion deficiency 3						ECO:0000033	author statement supported by traceable reference	PMID:19234461	20151119	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2683669	Icos<sup>tm1Shr</sup>/Icos<sup>tm1Shr</sup>  [background:] Not Specified	is_model_of	DOID:12177	common variable immunodeficiency						ECO:0000033	author statement supported by traceable reference	PMID:11343122	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6858119	Fstl1<sup>tm1Ajn</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:7256886	Fstl1<sup>tm1Ajn</sup>/Fstl1<sup>tm1Ajn</sup>  [background:] B6.Cg-Fstl1<sup>tm1Ajn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31834999	20220328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6404921	Rs1<sup>tm2.1Rom</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6404946	Rs1<sup>tm2.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2677374	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:9467	nail-patella syndrome						ECO:0000033	author statement supported by traceable reference	PMID:9590288	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6110171	Odad4<sup>em#Omra</sup>	is_implicated_in	DOID:0110620	primary ciliary dyskinesia 35		MGI:6110172	Odad4<sup>em#Omra</sup>/Odad4<sup>em#Omra</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27486780	20180116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3582933	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk</sup>  [background:] involves: 101 * C3H * C57BL/6J * T STOCK	is_model_of	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7257843	Yars1<sup>tm1.1Rwb</sup>	is_implicated_in	DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C		MGI:7258133	Yars1<sup>tm1.1Rwb</sup>/Yars1<sup>tm1.1Rwb</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:34516839	20220330	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698040	Htt<sup>tm4Mem</sup>/Htt<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1	is_model_of	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:10699173	20070227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804590	Camkmt<sup>tm1Rpav</sup>	is_implicated_in	DOID:0060858	hypotonia-cystinuria syndrome		MGI:5804652	Camkmt<sup>tm1Rpav</sup>/Camkmt<sup>tm1Rpav</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25548191	20161024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5804590	Camkmt<sup>tm1Rpav</sup>	is_implicated_in	DOID:0060858	hypotonia-cystinuria syndrome		MGI:5804654	Camkmt<sup>tm1Rpav</sup>/Camkmt<sup>tm1Rpav</sup>  [background:] B6.129S7-Camkmt<sup>tm1Rpav</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25548191	20161024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5317146	Del(5Gtf2i-Limk1)1Uta/Del(5Limk1-Trim50)2Uta  [background:] involves: 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:1928	Williams-Beuren syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20049703	20120503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852753	Smpx<sup>em2Jgao</sup>	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852757	Smpx<sup>em2Jgao</sup>/Y  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852753	Smpx<sup>em2Jgao</sup>	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852762	Smpx<sup>em2Jgao</sup>/Smpx<sup>+</sup>  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6852753	Smpx<sup>em2Jgao</sup>	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852760	Smpx<sup>em2Jgao</sup>/Smpx<sup>em2Jgao</sup>  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586327	Rdh8<sup>tm1Kpal</sup>	is_implicated_in	DOID:0110015	age related macular degeneration 2						ECO:0000033	author statement supported by traceable reference	PMID:29602770	20180515	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3624851	Dcx<sup>tm1.2Ffr</sup>/Y  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	is_model_of	DOID:0050453	lissencephaly						ECO:0000033	author statement supported by traceable reference	PMID:16571605	20060620	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5804204	Cyp4v3<sup>tm1(KOMP)Vlcg</sup>/Cyp4v3<sup>tm1(KOMP)Vlcg</sup>  [background:] B6(Cg)-Cyp4v3<sup>tm1(KOMP)Vlcg</sup>	is_model_of	DOID:0050664	Bietti crystalline corneoretinal dystrophy						ECO:0000033	author statement supported by traceable reference	PMID:25118264	20161020	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3665495	Ccr2<sup>tm1Blck</sup>/Ccr2<sup>tm1Blck</sup> Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL.Cg-Ccr2<sup>tm1Blck</sup> Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:16267157	20061103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6515762	Dhcr7<sup>tm1.1Sbpa</sup>	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:6690698	Dhcr7<sup>tm1.1Sbpa</sup>/Dhcr7<sup>tm1.1Sbpa</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] B6.Cg-Dhcr7<sup>tm1.1Sbpa</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33410752	20210414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7314724	Mdfic<sup>em#Nlh</sup>	is_implicated_in	DOID:0081030	central conducting lymphatic anomaly		MGI:7314827	Mdfic<sup>em#Nlh</sup>/Mdfic<sup>em#Nlh</sup>  [background:] C57BL/6J-Mdfic<sup>em#Nlh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35235341	20220722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5641483	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:22763451	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5660617	Efemp2<sup>tm1.1Chu</sup>/Efemp2<sup>tm1.1Chu</sup>  [background:] B6(SJL)-Efemp2<sup>tm1.1Chu</sup>	is_model_of	DOID:3144	cutis laxa						ECO:0000033	author statement supported by traceable reference	PMID:26178373	20150901	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>	is_model_of	DOID:9250	acrocallosal syndrome						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5469577	Pik3ca<sup>tm1Gne</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:5469591	Pik3ca<sup>tm1Gne</sup>/Pik3ca<sup>+</sup> Tg(MMTV-cre)1Mam/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22370636	20130321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5617217	Ifih1<sup>Rgsc422</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5617218	Ifih1<sup>Rgsc422</sup>/Ifih1<sup>Rgsc422</sup>  [background:] D2JJcl.B6JJcl-Ifih1<sup>Rgsc422</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24530055	20150302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5617217	Ifih1<sup>Rgsc422</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5617219	Ifih1<sup>Rgsc422</sup>/Ifih1<sup>+</sup>  [background:] D2JJcl.B6JJcl-Ifih1<sup>Rgsc422</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24530055	20150302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4939022	Tg(Igh-Maf)68Staka	is_implicated_in	DOID:9538	multiple myeloma		MGI:4939026	Tg(Igh-Maf)68Staka/0  [background:] C57BL/6-Tg(Igh-Maf)68Staka			ECO:0000033	author statement supported by traceable reference	PMID:21224354	20110228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856398	Reln<sup>rl</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856398	Reln<sup>rl</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5661067	Reln<sup>rl</sup>/Reln<sup>+</sup>  [background:] B6C3Fe a/a-Reln<sup>rl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11982630	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856398	Reln<sup>rl</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5689835	Reln<sup>rl</sup>/Reln<sup>+</sup>  [background:] B6.Cg-Reln<sup>rl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25845740	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416103	Eif2b5<sup>tm1.1Sidr</sup>	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6416112	Eif2b5<sup>tm1.1Sidr</sup>/Eif2b5<sup>tm1.1Sidr</sup>  [background:] B6(Cg)-Eif2b5<sup>tm1.1Sidr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30624206	20200512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554255	Slc22a4<sup>tm1Atsu</sup>	is_implicated_in	DOID:0110892	inflammatory bowel disease 1						ECO:0000033	author statement supported by traceable reference	PMID:20224991	20140401	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4844193	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Polr2a<sup>tm1(cre/ERT2)Bbd</sup>/Polr2a<sup>tm1(cre/ERT2)Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:20609353	20130820	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258653	Vwf<sup>tm1.1Geno</sup>	is_implicated_in	DOID:0060574	von Willebrand's disease 2		MGI:6258654	Vwf<sup>tm1.1Geno</sup>/Vwf<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27212476	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6258653	Vwf<sup>tm1.1Geno</sup>	is_implicated_in	DOID:0060574	von Willebrand's disease 2		MGI:6258657	Vwf<sup>tm1.1Geno</sup>/Vwf<sup>tm1.1Geno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27212476	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5605963	b2b386.1Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5605970	b2b386.1Clo/b2b386.1Clo  [background:] C57BL/6J-b2b386.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3800222	Fas<sup>lpr</sup>/Fas<sup>lpr</sup> Tnfrsf9<sup>tm1Byk</sup>/Tnfrsf9<sup>tm1Byk</sup>  [background:] MRL.Cg-Tnfrsf9<sup>tm1Byk</sup> Fas<sup>lpr</sup>	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:10878371	20080813	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4455026	Rho<sup>Tvrm1</sup>/Rho<sup>+</sup>  [background:] C57BL/6J-Rho<sup>Tvrm1</sup>	is_model_of	DOID:0110372	retinitis pigmentosa 4						ECO:0000033	author statement supported by traceable reference	PMID:20207741	20130619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6323000	Tg(HBB-Myc)#Cos	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:6323048	Tg(HBB-Myc)#Cos/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:9422539	20190715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6323000	Tg(HBB-Myc)#Cos	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000033	author statement supported by traceable reference	PMID:9422539	20190715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5306912	Col3a1<sup>m1Lsmi</sup>	is_implicated_in	DOID:14756	vascular type Ehlers-Danlos syndrome		MGI:5307019	Col3a1<sup>m1Lsmi</sup>/Col3a1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21071432	20120224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5697527	Auts2<sup>tm1.1Dare</sup>	is_implicated_in	DOID:0060307	autosomal dominant intellectual developmental disorder		MGI:5697531	Auts2<sup>tm1.1Dare</sup>/Auts2<sup>tm1.1Dare</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25519132	20151201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578543	Lamb2<sup>npht</sup>/Lamb2<sup>npht</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0060852	Pierson syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24293254	20140826	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4417874	Comp<sup>tm1Mbri</sup>/Comp<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:12721	multiple epiphyseal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:19808781	20100115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6158669	Ube3a<sup>em1Yelg</sup>	is_implicated_in	DOID:1932	Angelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:31235931	20191206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5897817	Tprn<sup>em1Pghu</sup>	is_implicated_in	DOID:0110526	autosomal recessive nonsyndromic deafness 79		MGI:5897821	Tprn<sup>em1Pghu</sup>/Tprn<sup>em1Pghu</sup>  [background:] B6.Cg-Tprn<sup>em1Pghu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27693694	20170712	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5297134	Brca1<sup>tm2Cxd</sup>/Brca1<sup>tm2Cxd</sup> Trp53<sup>tm1Brd</sup>/Trp53<sup>+</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB	is_model_of	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17653086	20130408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524083	Tg(MMTV-Myc*T58A)TA41Jrn	is_implicated_in	DOID:1612	breast cancer		MGI:5524087	Tg(MMTV-Myc*T58A)TA41Jrn/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22525269	20131219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3818860	Tg(Psp-Rbbp4)1Yoha/0  [background:] involves: C57BL/6	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19015307	20081209	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5496257	Lrsam1<sup>Gt(RRK461)Byg</sup>/Lrsam1<sup>Gt(RRK461)Byg</sup>  [background:] involves: 129P2/OlaHsd	is_model_of	DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P						ECO:0000033	author statement supported by traceable reference	PMID:23519028	20130723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3043046	Cfc1<sup>tm1Mms</sup>/Cfc1<sup>tm1Mms</sup>  [background:] either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)	is_model_of	DOID:0060856	right atrial isomerism						ECO:0000033	author statement supported by traceable reference	PMID:10521397	20060503	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5800485	Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0  [background:] involves: C57BL/6 * CBA * FVB/NTac	is_model_of	DOID:0050650	familial atrial fibrillation						ECO:0000033	author statement supported by traceable reference	PMID:26595809	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459455	Tg(PLP1*)4Rsj	is_implicated_in	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:23281397	20131024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459455	Tg(PLP1*)4Rsj	is_implicated_in	DOID:2377	multiple sclerosis		MGI:4459456	Tg(PLP1*)4Rsj/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21228378	20131024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459455	Tg(PLP1*)4Rsj	is_implicated_in	DOID:2377	multiple sclerosis		MGI:4459456	Tg(PLP1*)4Rsj/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:7505836	20131024	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4450929	Gata1<sup>tm1Mym</sup>/Y Tg(Gata1*)#Mym/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2J	is_model_of	DOID:0060888	transient myeloproliferative syndrome						ECO:0000033	author statement supported by traceable reference	PMID:19682090	20100513	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5578132	Tg(Alb-PDGFC)#Jcam/0  [background:] involves: C57BL/6	is_model_of	DOID:9452	steatotic liver disease						ECO:0000033	author statement supported by traceable reference	PMID:15728360	20140819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5615094	Trappc10<sup>b2b2613Clo</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5615097	Trappc10<sup>b2b2613Clo</sup>/Trappc10<sup>b2b2613Clo</sup>  [background:] C57BL/6J-Trappc10<sup>b2b2613Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5426929	Gt(ROSA)26Sor<sup>tm49(HTT)Arte</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5432177	Gt(ROSA)26Sor<sup>tm49(HTT)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26025364	20180601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5433294	b2b1519Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5433295	b2b1519Clo/b2b1519Clo  [background:] C57BL/6J-b2b1519Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3052846	Pex7<sup>tm1Rjaw</sup>/Pex7<sup>tm1Rjaw</sup>  [background:] Swiss	is_model_of	DOID:0110851	rhizomelic chondrodysplasia punctata type 1						ECO:0000033	author statement supported by traceable reference	PMID:12915479	20050713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6725092	Large1<sup>m1Btlr</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:7264454	Large1<sup>m1Btlr</sup>/Large1<sup>m1Btlr</sup>  [background:] C57BL/6J-Large1<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5512884	Tg(CAG-Lyn*)#Paau/0  [background:] B6.Cg-Tg(CAG-Lyn*)#Paau	is_model_of	DOID:8893	psoriasis						ECO:0000033	author statement supported by traceable reference	PMID:19590497	20131016	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5003501	Psen1<sup>tm1Lpr</sup>/Psen1<sup>tm1Lpr</sup> Tg(Thy1-APP<sup>SL</sup>)28Lpr/0  [background:] involves: 129 * C57BL/6 * CBA	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:16963164	20110608	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5448853	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-TARDBP*)4Vle/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000033	author statement supported by traceable reference	PMID:21206091	20130114	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829994	Ncor2<sup>tm1Rev</sup>/Ncor2<sup>tm1Rev</sup>  [background:] involves: 129/Sv * C57BL/6	is_model_of	DOID:4971	myelofibrosis						ECO:0000033	author statement supported by traceable reference	PMID:24191050	20140306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5554934	Clp1<sup>tm1.1Pngr</sup>/Clp1<sup>tm1.1Pngr</sup>  [background:] CBA.Cg-Clp1<sup>tm1.1Pngr</sup>	is_model_of	DOID:0060279	pontocerebellar hypoplasia type 10						ECO:0000033	author statement supported by traceable reference	PMID:24766809	20150507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527336	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>	is_implicated_in	DOID:3908	lung non-small cell carcinoma		MGI:5527337	Col1a1<sup>tm1(tetO-EML4/ALK)Kkw</sup>/Col1a1<sup>+</sup> Tg(Scgb1a1-rtTA)1Jaw/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20952506	20171106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5554438	Mmp21<sup>b2b2458Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5555841	Mmp21<sup>b2b2458Clo</sup>/Mmp21<sup>b2b2458Clo</sup>  [background:] C57BL/6J-Mmp21<sup>b2b2458Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3577344	inad/inad  [background:] C57BL/6-inad	is_model_of	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000033	author statement supported by traceable reference	PMID:15859351	20050519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5888869	Plekhm1<sup>tm1.2Hzhao</sup>	is_implicated_in	DOID:0110945	autosomal recessive osteopetrosis 6		MGI:5896639	Plekhm1<sup>tm1.2Hzhao</sup>/Plekhm1<sup>tm1.2Hzhao</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27777970	20170712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415223	Tg(FOXJ1-ACE2)1Rba	is_implicated_in	DOID:2945	severe acute respiratory syndrome		MGI:6415340	Tg(FOXJ1-ACE2)1Rba/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26976607	20200507	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4440856	Fgfr2<sup>tm2Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] B6.Cg-Fgfr2<sup>tm2Ewj</sup> Tg(EIIa-cre)C5379Lmgd	is_model_of	DOID:12960	acrocephalosyndactylia						ECO:0000033	author statement supported by traceable reference	PMID:20175913	20100421	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4940096	Brca2<sup>tm1Brn</sup>/Brca2<sup>tm1Cam</sup> Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Trp53<sup>tm3Tyj</sup>/Trp53<sup>+</sup> Tg(Pdx1-cre)6Tuv/0  [background:] involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * C57BL/6 * FVB/N	is_model_of	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:21056012	20110309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6153554	Pik3r1<sup>tm1.1Geno</sup>	is_implicated_in	DOID:0111454	SHORT syndrome		MGI:6275834	Pik3r1<sup>tm1.1Geno</sup>/Pik3r1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26974159	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5429197	Ak8<sup>Gt(OST16378)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429555	Ak8<sup>Gt(OST16378)Lex</sup>/Ak8<sup>Gt(OST16378)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4462529	Cilk1<sup>tm1a(KOMP)Mbp</sup>	is_implicated_in	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome		MGI:5693602	Cilk1<sup>tm1a(KOMP)Mbp</sup>/Cilk1<sup>tm1a(KOMP)Mbp</sup>  [background:] C57BL/6N-Cilk1<sup>tm1a(KOMP)Mbp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24853502	20151027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome						ECO:0000033	author statement supported by traceable reference	PMID:23043085	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4601767	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7366734	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1113502	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3588316	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7089489	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5590154	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1523694	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4697831	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4589319	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855968	Lyst<sup>bg</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:408	20170516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5425228	Zbtb18<sup>tm1.1Nda</sup>	is_implicated_in	DOID:0060307	autosomal dominant intellectual developmental disorder		MGI:5425229	Zbtb18<sup>tm1.1Nda</sup>/Zbtb18<sup>tm1.1Nda</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22095278	20120620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388240	Rpe65<sup>rd12</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2						ECO:0000033	author statement supported by traceable reference	PMID:26387748	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388240	Rpe65<sup>rd12</sup>	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3513510	Rpe65<sup>rd12</sup>/Rpe65<sup>rd12</sup>  [background:] B6(A)-Rpe65<sup>rd12</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15823427	20161109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7277696	Slc7a14<sup>em1Jin</sup>	is_implicated_in	DOID:1432	blindness		MGI:7277716	Slc7a14<sup>em1Jin</sup>/Slc7a14<sup>em1Jin</sup>  [background:] C57BL/6J-Slc7a14<sup>em1Jin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5901731	Cul3<sup>tm1Suc</sup>	is_not_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:5901734	Cul3<sup>tm1Suc</sup>/Cul3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26490675	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5648248	Dnah5<sup>b2b3491Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5649319	Dnah5<sup>b2b3491Clo</sup>/Dnah5<sup>b2b3491Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b3491Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3055578	Dysf<sup>tm1Meho</sup>/Dysf<sup>tm1Meho</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:11720	distal myopathy						ECO:0000033	author statement supported by traceable reference	PMID:15254015	20050624	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300199	Cntn1<sup>m1J</sup>/Cntn1<sup>m1J</sup>  [background:] B6;C-Cntn1<sup>m1J</sup>/GrsrJ	is_model_of	DOID:0080101	Compton-North congenital myopathy						ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5694343	Tg(Ckm-Chrnd*S262T)40Cgz	is_implicated_in	DOID:0110666	congenital myasthenic syndrome 3A		MGI:5694344	Tg(Ckm-Chrnd*S262T)40Cgz/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:8538674	20151102	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5569760	Tg(Prnp-MAPT)7Vle/0  [background:] involves: C57BL/6 * SJL	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:10595524	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5578212	Scn8a<sup>em1Mm</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:5578216	Scn8a<sup>em1Mm</sup>/Scn8a<sup>+</sup>  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24288358	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5767122	Gbe1<sup>tm2.1Hoa</sup>	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:5767124	Gbe1<sup>tm2.1Hoa</sup>/Gbe1<sup>tm2.1Hoa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:26385640	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4948864	Slc19a3<sup>tm1Said</sup>	is_implicated_in	DOID:0050659	biotin-responsive basal ganglia disease		MGI:6162677	Slc19a3<sup>tm1Said</sup>/Slc19a3<sup>tm1Said</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28665968	20180627	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3815023	Fmr1<sup>tm2Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB	is_model_of	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000033	author statement supported by traceable reference	PMID:15876460	20081114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5547589	Dnaaf4<sup>tm1.2Jjlo</sup>	is_implicated_in	DOID:0110615	primary ciliary dyskinesia 25		MGI:5547595	Dnaaf4<sup>tm1.2Jjlo</sup>/Dnaaf4<sup>tm1.2Jjlo</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23872636	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7564565	Tnfaip2<sup>tm1.1Ohno</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:7564569	Tnfaip2<sup>tm1.1Ohno</sup>/Tnfaip2<sup>tm1.1Ohno</sup>  [background:] C.Cg-Tnfaip2<sup>tm1.1Ohno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33722931	20231211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5052379	Tg(HTT*/EGFP)150Nn	is_implicated_in	DOID:12858	Huntington's disease		MGI:5052381	Tg(HTT*/EGFP)150Nn/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15836623	20110805	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3050895	Msx2<sup>tm1Rilm</sup>/Msx2<sup>+</sup> Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S7/SvEvBrd * BALB/c * C57BL/6	is_model_of	DOID:14768	Saethre-Chotzen syndrome						ECO:0000033	author statement supported by traceable reference	PMID:14597577	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5639127	Prkcq<sup>rpea1</sup>	is_implicated_in	DOID:5327	retinal detachment		MGI:5817744	Prkcq<sup>rpea1</sup>/Prkcq<sup>rpea1</sup>  [background:] B6.ABJ-Prkcq<sup>rpea1</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	PMID:26978024	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4420228	Scn4a<sup>tm1.1Ljh</sup>/Scn4a<sup>tm1.1Ljh</sup>  [background:] B6.129S4-Scn4a<sup>tm1.1Ljh</sup>	is_model_of	DOID:14451	hyperkalemic periodic paralysis						ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5307019	Col3a1<sup>m1Lsmi</sup>/Col3a1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:14756	vascular type Ehlers-Danlos syndrome						ECO:0000033	author statement supported by traceable reference	PMID:21071432	20120224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838202	Tg(Eno2-TOR1A*)13Shas	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:4838205	Tg(Eno2-TOR1A*)13Shas/0  [background:] involves: C3H * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15548549	20101111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5293759	Npc1<sup>tm1Mbjg</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5293760	Npc1<sup>tm1Mbjg</sup>/Npc1<sup>tm1Mbjg</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21896731	20111028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830457	Htr2c<sup>tm1.1Eme</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:4830462	Htr2c<sup>tm1.1Eme</sup>/Y  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20394819	20100923	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5300032	Sptbn2<sup>Gt(XK442)Byg</sup>/Sptbn2<sup>Gt(XK442)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000033	author statement supported by traceable reference	PMID:20231455	20151118	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652360	App<sup>tm1Cep</sup>/App<sup>tm1Cep</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5619080	Dnai2<sup>b2b3405Clo</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5619081	Dnai2<sup>b2b3405Clo</sup>/Dnai2<sup>b2b3405Clo</sup>  [background:] C57BL/6J-Dnai2<sup>b2b3405Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5779426	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(Upk2-cre,-EGFP)#Akli/0  [background:] involves: 129	is_model_of	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25194568	20160629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933746	Atm<sup>tm1Pmc</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia						ECO:0000033	author statement supported by traceable reference	PMID:25683718	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933746	Atm<sup>tm1Pmc</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175710	Atm<sup>tm1Pmc</sup>/Atm<sup>tm1Pmc</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9582124	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933746	Atm<sup>tm1Pmc</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:5644542	Atm<sup>tm1Pmc</sup>/Atm<sup>tm1Pmc</sup>  [background:] B6.Cg-Atm<sup>tm1Pmc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25683718	20150722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5781013	Tg(Mup3-Plau)350-2Eps	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5781017	Tg(Mup3-Plau)350-2Eps/?  [background:] C57BL/6-Tg(Mup3-Plau)350-2Eps			ECO:0000033	author statement supported by traceable reference	PMID:25132496	20160722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2661992	Insl3<sup>tm1Par</sup>/Insl3<sup>+</sup>  [background:] involves: 129/Sv * CD-1	is_model_of	DOID:11383	cryptorchidism						ECO:0000033	author statement supported by traceable reference	PMID:10391220	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429784	Hmox1<sup>tm1Mlee</sup>	is_implicated_in	DOID:12365	malaria						ECO:0000033	author statement supported by traceable reference	PMID:17496899	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429784	Hmox1<sup>tm1Mlee</sup>	is_implicated_in	DOID:12365	malaria		MGI:2429786	Hmox1<sup>tm1Mlee</sup>/Hmox1<sup>tm1Mlee</sup>  [background:] involves: 129S2/SvPas * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:19706490	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620880	Apc<sup>M1Tno</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:5688288	Apc<sup>M1Tno</sup>/Apc<sup>+</sup>  [background:] either: B6JJcl.B6(D2JJcl)-Apc<sup>M1Tno</sup> or (involves: C57BL/6 * C57BL/6JJcl * DBA/2JJcl)			ECO:0000033	author statement supported by traceable reference	PMID:23551873	20150924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6256754	Tg(Myh6-Tpm1*D230N)HJcf	is_implicated_in	DOID:0110457	dilated cardiomyopathy 1Y		MGI:6256757	Tg(Myh6-Tpm1*D230N)HJcf/0  [background:] B6.FVB-Tg(Myh6-Tpm1*D230N)HJcf			ECO:0000033	author statement supported by traceable reference	PMID:28600229	20181116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5524270	Slc4a11<sup>tm1.1Jrcy</sup>	is_implicated_in	DOID:0060649	congenital hereditary endothelial dystrophy of cornea		MGI:5524271	Slc4a11<sup>tm1.1Jrcy</sup>/Slc4a11<sup>tm1.1Jrcy</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23942972	20150515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5705748	Tg(OPTN*E50K,-EGFP)1Mde	is_implicated_in	DOID:1070	primary open angle glaucoma		MGI:5705749	Tg(OPTN*E50K,-EGFP)1Mde/0  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25818176	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7354967	Far2<sup>em1Akih</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:7355994	Far2<sup>em1Akih</sup>/Far2<sup>em1Akih</sup>  [background:] C57BL/6J-Far2<sup>em1Akih</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35238077	20221018	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5000479	Gt(ROSA)26Sor<sup>tm1(Pik3ca*H1047R)Egan</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(MMTV-cre)#Tfln/0 Trp53<sup>tm1Brn</sup>/Trp53<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:21324922	20110531	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461060	Igh-J<sup>tm1Aigl</sup>/Igh-J<sup>+</sup> Mog<sup>tm1Dpd</sup>/Mog<sup>tm1Dpd</sup> Tg(Tcra2D2,Tcrb2D2)1Kuch/0  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:19483694	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5701638	Sh3bp2<sup>tm1.1Ics</sup>/Sh3bp2<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6	is_model_of	DOID:1856	cherubism						ECO:0000033	author statement supported by traceable reference	PMID:25705883	20160108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5515375	Crx<sup>Rip</sup>	is_implicated_in	DOID:0110333	Leber congenital amaurosis 7		MGI:5526862	Crx<sup>Rip</sup>/Crx<sup>+</sup>  [background:] C57BL/6J-Crx<sup>Rip</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24382353	20140106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5488510	Tg(Tlr7)1Boll/0  [background:] involves: C57BL/6	is_model_of	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:23382559	20130603	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5428747	Tg(Wap-TAg)NP8Depp/0  [background:] involves: BALB/c * C57BL/6	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:10713686	20120724	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5575759	Asxl1<sup>tm1.1Mjxu</sup>/Asxl1<sup>tm1.1Mjxu</sup>  [background:] involves: 129 * C57BL/6	is_model_of	DOID:0050908	myelodysplastic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24255920	20140731	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3688000	Apob<sup>tm1Mae</sup>/Apob<sup>tm1Mae</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:0111061	familial hypobetalipoproteinemia 2						ECO:0000033	author statement supported by traceable reference	PMID:8921909	20061117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830452	P3h1<sup>tm1Dgen</sup>	is_implicated_in	DOID:0110336	osteogenesis imperfecta type 8		MGI:4830454	P3h1<sup>tm1Dgen</sup>/P3h1<sup>tm1Dgen</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20363744	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4830452	P3h1<sup>tm1Dgen</sup>	is_implicated_in	DOID:0110336	osteogenesis imperfecta type 8						ECO:0000033	author statement supported by traceable reference	PMID:26808442	20160511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6367794	Prph2<sup>tm1.1Itl</sup>	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6423338	Prph2<sup>tm1.1Itl</sup>/Prph2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25001182	20200519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6367794	Prph2<sup>tm1.1Itl</sup>	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6423341	Prph2<sup>tm1.1Itl</sup>/Prph2<sup>tm1.1Itl</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25001182	20200519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393409	Klhl3<sup>tm1.1Slin</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6393415	Klhl3<sup>tm1.1Slin</sup>/Klhl3<sup>tm1.1Slin</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30148674	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6393409	Klhl3<sup>tm1.1Slin</sup>	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6393411	Klhl3<sup>tm1.1Slin</sup>/Klhl3<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30148674	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3703755	Tg(Tagln-rtTA)E1Jwst	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20130409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5902155	Krt12<sup>tm1.1(KRT12*L132P)Arte</sup>	is_implicated_in	DOID:0060451	Meesmann corneal dystrophy		MGI:5902157	Krt12<sup>tm1.1(KRT12*L132P)Arte</sup>/Krt12<sup>tm1.1(KRT12*L132P)Arte</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26758872	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5548687	Odad3<sup>tm1b(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0110624	primary ciliary dyskinesia 30		MGI:6360703	Odad3<sup>tm1b(EUCOMM)Hmgu</sup>/Odad3<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Odad3<sup>tm1b(EUCOMM)Hmgu</sup>/Cnrm			ECO:0000033	author statement supported by traceable reference	PMID:31383820	20190924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671733	Aspa<sup>nur7</sup>	is_implicated_in	DOID:3613	Canavan disease						ECO:0000033	author statement supported by traceable reference	PMID:29456021	20190806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671733	Aspa<sup>nur7</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:3027206	Aspa<sup>nur7</sup>/Aspa<sup>nur7</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26511242	20190806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671733	Aspa<sup>nur7</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:3027206	Aspa<sup>nur7</sup>/Aspa<sup>nur7</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18987190	20190806	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2660751	Fancl<sup>gcd</sup>/Fancl<sup>gcd</sup>  [background:] involves: C57BL/6J * CBA/J	is_model_of	DOID:14450	46 XX gonadal dysgenesis						ECO:0000033	author statement supported by traceable reference	PMID:8373945	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6231206	Tg(H2-K-Hmga1)#Lmsr	is_implicated_in	DOID:0060058	lymphoma		MGI:6231210	Tg(H2-K-Hmga1)#Lmsr/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15150086	20181107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5140116	Gjc2<sup>tm2.1Kwi</sup>	is_implicated_in	DOID:0060787	hypomyelinating leukodystrophy 2		MGI:5140117	Gjc2<sup>tm2.1Kwi</sup>/Gjc2<sup>tm2.1Kwi</sup>  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21750683	20110818	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5897118	Fnip1<sup>tm1.2Baba</sup>/Fnip1<sup>+</sup> Fnip2<sup>tm1.2Lss</sup>/Fnip2<sup>tm1.2Lss</sup>  [background:] involves: C57BL/6	is_model_of	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000033	author statement supported by traceable reference	PMID:25775561	20170510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384608	Tg(UPII-SV40T)2Xrw	is_implicated_in	DOID:11054	urinary bladder cancer						ECO:0000033	author statement supported by traceable reference	PMID:25533675	20160822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384608	Tg(UPII-SV40T)2Xrw	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5141744	Tg(UPII-SV40T)2Xrw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10416618	20160822	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583813	Itga7<sup>tm1Umr</sup>/Itga7<sup>tm1Umr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency						ECO:0000033	author statement supported by traceable reference	PMID:12588796	20100614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6508689	Hsd17b3<sup>tm1.2Mpo</sup>	is_implicated_in	DOID:0112248	17-beta hydroxysteroid dehydrogenase 3 deficiency		MGI:6508693	Hsd17b3<sup>tm1.2Mpo</sup>/Hsd17b3<sup>tm1.2Mpo</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:32190925	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4849364	Wt1<sup>tm1.1Ndha</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5824267	Wt1<sup>tm1.1Ndha</sup>/Wt1<sup>tm1.1Ndha</sup> Tg(Gata4*G2-cre)#Roja/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27642710	20170216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850171	Clrn1<sup>tm1.1Kuna</sup>	is_implicated_in	DOID:0110841	Usher syndrome type 3A						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850171	Clrn1<sup>tm1.1Kuna</sup>	is_implicated_in	DOID:0110841	Usher syndrome type 3A		MGI:3850181	Clrn1<sup>tm1.1Kuna</sup>/Clrn1<sup>tm1.1Kuna</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19414487	20160226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5437106	b2b1200.2Clo/b2b1200.2Clo  [background:] C57BL/6J-b2b1200.2Clo	is_model_of	DOID:2975	cystic kidney disease						ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7328725	Myt1l<sup>em1Mwer</sup>	is_implicated_in	DOID:0070069	autosomal dominant intellectual developmental disorder 39		MGI:7328859	Myt1l<sup>em1Mwer</sup>/Myt1l<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35538503	20220811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3628949	Unc13d<sup>Jinx</sup>/Unc13d<sup>Jinx</sup>  [background:] C57BL/6J-Unc13d<sup>Jinx</sup>/Mmucd	is_model_of	DOID:0110923	familial hemophagocytic lymphohistiocytosis 3						ECO:0000033	author statement supported by traceable reference	PMID:17420270	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6696392	Polr3h<sup>em2Cfe</sup>	is_implicated_in	DOID:5426	primary ovarian insufficiency		MGI:6696394	Polr3h<sup>em2Cfe</sup>/Polr3h<sup>em2Cfe</sup>  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:30830215	20210506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4840236	Cth<sup>tm1Iish</sup>	is_implicated_in	DOID:0090142	cystathioninuria		MGI:4840250	Cth<sup>tm1Iish</sup>/Cth<sup>tm1Iish</sup>  [background:] B6.129-Cth<sup>tm1Iish</sup>/Iish			ECO:0000033	author statement supported by traceable reference	PMID:20566639	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6415560	Flvcr2<sup>tm1.2Tda</sup>	is_implicated_in	DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		MGI:6415690	Flvcr2<sup>tm1.2Tda</sup>/Flvcr2<sup>tm1.2Tda</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32369453	20200511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5476821	Tg(TARDBP)#Jpj	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5476847	Tg(TARDBP)#Jpj/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21752789	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5428665	Nemf<sup>pdft</sup>	is_implicated_in	DOID:440	neuromuscular disease		MGI:6719084	Nemf<sup>pdft</sup>/Nemf<sup>pdft</sup>  [background:] B6(C3)-Nemf<sup>pdft</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856544	Hps6<sup>ru</sup>	is_implicated_in	DOID:0060544	Hermansky-Pudlak syndrome 6						ECO:0000033	author statement supported by traceable reference	PMID:25593336	20160105	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793301	Tg(IghelMD4)4Ccg/Tg(IghelMD4)4Ccg  [background:] NOD.B6-Tg(IghelMD4)4Ccg/DvsJ	is_model_of	DOID:9744	type 1 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:12516557	20080611	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5571369	Tg(Igh-ROR1)1Kip/0  [background:] C57BL/6-Tg(Igh-ROR1)1Kip	is_model_of	DOID:1040	chronic lymphocytic leukemia						ECO:0000033	author statement supported by traceable reference	PMID:24379361	20140707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838083	Ass1<sup>bar</sup>	is_implicated_in	DOID:9273	citrullinemia		MGI:4838087	Ass1<sup>bar</sup>/Ass1<sup>bar</sup>  [background:] FVB.BAR-Ass1<sup>bar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4838083	Ass1<sup>bar</sup>	is_implicated_in	DOID:9273	citrullinemia		MGI:4838089	Ass1<sup>bar</sup>/Ass1<sup>bar</sup>  [background:] B6.BAR-Ass1<sup>bar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764815	Tg(Th-SNCA*)1.2Ccs	is_implicated_in	DOID:14330	Parkinson's disease						ECO:0000033	author statement supported by traceable reference	PMID:24204848	20140821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764815	Tg(Th-SNCA*)1.2Ccs	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3764818	Tg(Th-SNCA*)1.2Ccs/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21212098	20140821	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3833428	Gdi1<sup>tm1Toni</sup>/Y  [background:] B6N.129S7-Gdi1<sup>tm1Toni</sup>	is_model_of	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000033	author statement supported by traceable reference	PMID:18829665	20131021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5317822	Ush1g<sup>js-3J</sup>	is_implicated_in	DOID:0110834	Usher syndrome type 1G		MGI:5320445	Ush1g<sup>js-3J</sup>/Ush1g<sup>js-3J</sup>  [background:] B6.Cg-Ush1g<sup>js-3J</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	MGI:5320439	20120606	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ	is_model_of	DOID:0110970	brachydactyly type C						ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045473	Bbs4<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000033	author statement supported by traceable reference	PMID:23554981	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045473	Bbs4<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3525001	Bbs4<sup>tm1Vcs</sup>/Bbs4<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15539463	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045473	Bbs4<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3045547	Bbs4<sup>tm1Vcs</sup>/Bbs4<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15173597	20141028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5425923	Casr<sup>BCH013</sup>/Casr<sup>BCH013</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH013</sup>	is_model_of	DOID:13543	hyperparathyroidism						ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5311382	Cc2d2a<sup>b2b1035Clo</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313509	Cc2d2a<sup>b2b1035Clo</sup>/Cc2d2a<sup>b2b1035Clo</sup>  [background:] C57BL/6J-Cc2d2a<sup>b2b1035Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5311585	Plec<sup>tm7.1Gwi</sup>/Plec<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060736	epidermolysis bullosa simplex Ogna type						ECO:0000033	author statement supported by traceable reference	PMID:22144912	20120321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5487826	Bub1b<sup>tm2.1Jvd</sup>	is_implicated_in	DOID:0080141	mosaic variegated aneuploidy syndrome 1		MGI:5487831	Bub1b<sup>tm2.1Jvd</sup>/Bub1b<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23300461	20130531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778191	Tg(Thy1-MAPT*P301S)2541Godt	is_implicated_in	DOID:9255	frontotemporal dementia						ECO:0000033	author statement supported by traceable reference	PMID:26949217	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778191	Tg(Thy1-MAPT*P301S)2541Godt	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5450673	Tg(Thy1-MAPT*P301S)2541Godt/Tg(Thy1-MAPT*P301S)2541Godt  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:12417659	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5523909	Trp53<sup>tm1.1Tldo</sup>	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:5524023	Trp53<sup>tm1.1Tldo</sup>/Trp53<sup>tm1.1Tldo</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23770245	20131220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7408183	Rbm24<sup>tm1.1Xixu</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:7408196	Rbm24<sup>tm1.1Xixu</sup>/Rbm24<sup>tm1.1Xixu</sup> Tg(Myhc-cre)1Xya/0  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:30267374	20221215	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3776087	Flcn<sup>tm1Baba</sup>/Flcn<sup>tm1.1Lss</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: C57BL/6 * FVB/N * ICR * SJL	is_model_of	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000033	author statement supported by traceable reference	PMID:18182616	20080404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4840554	Adarb1<sup>tm1.1Skwa</sup>	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:4843114	Adarb1<sup>tm1.1Skwa</sup>/Adarb1<sup>tm1.1Skwa</sup> Tg(SLC18A3-cre)KMisa/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20826656	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5629288	Gt(ROSA)26Sor<sup>tm1(CAG-MFN2*T105M)Dple</sup>	is_implicated_in	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A		MGI:6198662	Gt(ROSA)26Sor<sup>tm1(CAG-MFN2*T105M)Dple</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:27907123	20180919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5471473	Muc2<sup>eey</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5471480	Muc2<sup>eey</sup>/Muc2<sup>eey</sup>  [background:] C57BL/6-Muc2<sup>eey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18318598	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5424919	Alpl<sup>Mhdabap020</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425669	Alpl<sup>Mhdabap020</sup>/Alpl<sup>Mhdabap020</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap020</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2669172	Trpv4<sup>tm1Msz</sup>/Trpv4<sup>tm1Msz</sup>  [background:] involves: 129X1/SvJ * C57BL/6	is_model_of	DOID:0110555	autosomal dominant nonsyndromic deafness 25						ECO:0000033	author statement supported by traceable reference	PMID:15925108	20070112	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814058	Tg(SOD1*G37R)42Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:7605627	20081106	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J	is_model_of	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714532	Dp(16Lipi-Zbtb21)1Yey/0  [background:] involves: 129S7/SvEvBrd	is_model_of	DOID:0060850	annular pancreas						ECO:0000033	author statement supported by traceable reference	PMID:17412756	20081215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6477396	Cfap58<sup>em1Fzh</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:6477412	Cfap58<sup>em1Fzh</sup>/Cfap58<sup>em1Fzh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32791035	20201203	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5462366	Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0  [background:] involves: FVB/N	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:22875919	20130207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829386	Crtc1<sup>Gt(XK522)Byg</sup>	is_implicated_in	DOID:1470	major depressive disorder						ECO:0000033	author statement supported by traceable reference	PMID:27404284	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829386	Crtc1<sup>Gt(XK522)Byg</sup>	is_implicated_in	DOID:1470	major depressive disorder		MGI:6098717	Crtc1<sup>Gt(XK522)Byg</sup>/Crtc1<sup>Gt(XK522)Byg</sup>  [background:] B6N.129P2-Crtc1<sup>Gt(XK522)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22592058	20171208	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576859	Cd200<sup>tm1Jods</sup>/Cd200<sup>tm1Jods</sup>  [background:] C57BL/6-Cd200<sup>tm1Jods</sup>	is_model_of	DOID:417	autoimmune disease						ECO:0000033	author statement supported by traceable reference	PMID:11099416	20050516	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2679084	Bmp4<sup>tm1Blh</sup>/Bmp4<sup>tm3.1Blh</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: 129S/Sv * Black Swiss * C57BL/6 * DBA/2 * ICR	is_model_of	DOID:0050651	atrioventricular septal defect						ECO:0000033	author statement supported by traceable reference	PMID:12975322	20110808	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3047777	Avpr2<sup>tm1Jwe</sup>/Avpr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CF-1	is_model_of	DOID:12387	nephrogenic diabetes insipidus						ECO:0000033	author statement supported by traceable reference	PMID:11104789	20050602	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3690458	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*delta19)11Hev/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:16705038	20150501	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3583772	Ccd/Ccd<sup>+</sup>  [background:] B10Rl.101-Ccd	is_model_of	DOID:13994	cleidocranial dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:8270769	20050817	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3714862	Cdh23<sup>v-ngt</sup>/Cdh23<sup>v-ngt</sup>  [background:] involves: ICR * MSM	is_model_of	DOID:0110831	Usher syndrome type 1D						ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3844062	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Ins2-cre)25Mgn/0  [background:] either: (involves: 129X1/SvJ * C57BL/6 * DBA) or (involves: 129X1/SvJ * A/J * C57BL/6 * DBA)	is_model_of	DOID:14175	von Hippel-Lindau disease						ECO:0000033	author statement supported by traceable reference	PMID:19340311	20090514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6157680	Map2k1<sup>tm2.1Chrn</sup>	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:6159581	Map2k1<sup>tm2.1Chrn</sup>/Map2k1<sup>tm2.1Chrn</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:29590634	20180605	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4461137	Tg(Gfap-TNF*)K21Gkl/0  [background:] involves: C57BL/6 * CBA	is_model_of	DOID:2377	multiple sclerosis						ECO:0000033	author statement supported by traceable reference	PMID:9736029	20100722	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5577168	Dst<sup>Tg4</sup>/Dst<sup>Tg4</sup>  [background:] involves: C57BL/6 * CD-1	is_model_of	DOID:0050548	hereditary sensory neuropathy						ECO:0000033	author statement supported by traceable reference	PMID:24381311	20140814	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2652979	Kcnh2<sup>tm1Hjd</sup>/Kcnh2<sup>tm1Hjd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0050793	short QT syndrome						ECO:0000033	author statement supported by traceable reference	PMID:12612061	20060419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5448202	Tg(NES/TK-PDGFB,-lacZ)310Kfn	is_implicated_in	DOID:0060282	persistent hyperplastic primary vitreous		MGI:5448462	Tg(NES/TK-PDGFB,-lacZ)310Kfn/0  [background:] B6.Cg-Tg(NES/TK-PDGFB,-lacZ)310Kfn			ECO:0000033	author statement supported by traceable reference	PMID:22880002	20170707	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651823	Lpl<sup>tm1Sem</sup>/Lpl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J	is_model_of	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:7759497	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845022	Hras<sup>tm1Jaf</sup>	is_implicated_in	DOID:0050469	Costello syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26740656	20160225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845022	Hras<sup>tm1Jaf</sup>	is_implicated_in	DOID:0050469	Costello syndrome		MGI:3845065	Hras<sup>tm1Jaf</sup>/Hras<sup>+</sup> Tg(CAG-cre)13Miya/0  [background:] involves: 129S6/SvEvTac * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24057668	20160225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4356167	Atp1a3<sup>Myk</sup>	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood						ECO:0000033	author statement supported by traceable reference	PMID:26501181	20190520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4356167	Atp1a3<sup>Myk</sup>	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26463346	20190520	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3616343	Stk11<sup>tm1.1Mlfr</sup>/Stk11<sup>+</sup> Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	is_model_of	DOID:3852	Peutz-Jeghers syndrome						ECO:0000033	author statement supported by traceable reference	PMID:16357136	20060315	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3793703	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] SJL.129S2-Aire<sup>tm1.1Doi</sup>/Doi	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009805	Id3<sup>tm2.1Zhu</sup>/Id3<sup>tm2.1Zhu</sup> Tg(Lck-cre)#Zhu/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL * SJL/J	is_model_of	DOID:12894	Sjogren's syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20932862	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5468143	Tg(CAG-Diaph3)771Lesp	is_implicated_in	DOID:0060690	autosomal dominant auditory neuropathy 1		MGI:5575511	Tg(CAG-Diaph3)771Lesp/0  [background:] FVB/NJ-Tg(CAG-Diaph3)771Lesp			ECO:0000033	author statement supported by traceable reference	PMID:23441200	20140730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297423	b2b386Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312335	b2b386Clo/b2b386Clo  [background:] C57BL/6J-b2b386Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179129	Rp1<sup>tm1Jnz</sup>	is_implicated_in	DOID:0110390	retinitis pigmentosa 1						ECO:0000033	author statement supported by traceable reference	PMID:23281133	20140220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179129	Rp1<sup>tm1Jnz</sup>	is_implicated_in	DOID:0110390	retinitis pigmentosa 1		MGI:3038333	Rp1<sup>tm1Jnz</sup>/Rp1<sup>tm1Jnz</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:11960024	20140220	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4835061	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Msd</sup> Grm7<sup>Tg(SMN2)89Ahmb</sup>/Grm7<sup>Tg(SMN2)89Ahmb</sup> Tg(SMN2*delta7)4299Ahmb/Tg(SMN2*delta7)4299Ahmb  [background:] involves: 129P2/OlaHsd * FVB/N	is_model_of	DOID:13137	Werdnig-Hoffmann disease						ECO:0000033	author statement supported by traceable reference	PMID:20696672	20101014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6460342	Akt1<sup>tm1.1Mjl</sup>	is_implicated_in	DOID:13482	Proteus syndrome		MGI:6460379	Akt1<sup>tm1.1Mjl</sup>/Akt1<sup>+</sup>  [background:] chimera involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31194862	20201008	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2674081	Cldn14<sup>tm1Tbf</sup>/Cldn14<sup>tm1Tbf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110487	autosomal recessive nonsyndromic deafness 29						ECO:0000033	author statement supported by traceable reference	PMID:12913076	20110613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5527601	Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:6695122	Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>/Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31844321	20210427	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2654522	Slc6a3<sup>tm2Mca</sup>/Slc6a3<sup>tm2Mca</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ	is_model_of	DOID:1094	attention deficit hyperactivity disorder						ECO:0000033	author statement supported by traceable reference	PMID:11172062	20050614	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5688778	Gjb1<sup>tm1Kwi</sup>/Y Gjc2<sup>tm1(EGFP)Kwi</sup>/Gjc2<sup>tm1(EGFP)Kwi</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	is_model_of	DOID:0060787	hypomyelinating leukodystrophy 2						ECO:0000033	author statement supported by traceable reference	PMID:25524707	20151002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5661918	Tg(SFTPC-KIF5B/RET)1Tkoh	is_implicated_in	DOID:1324	lung cancer		MGI:5661919	Tg(SFTPC-KIF5B/RET)1Tkoh/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25064355	20150917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7329914	Usp45<sup>em1Qzha</sup>	is_implicated_in	DOID:0081169	Leber congenital amaurosis 19		MGI:7329919	Usp45<sup>em1Qzha</sup>/Usp45<sup>em1Qzha</sup>  [background:] C57BL/6J-Usp45<sup>em1Qzha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30573563	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651542	Krt17<sup>tm1Cou</sup>	is_implicated_in	DOID:0050449	pachyonychia congenita						ECO:0000033	author statement supported by traceable reference	PMID:24218583	20140102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5708388	Tg(Prnp-MAPT*K274Q*K281Q)286Lgn	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5829782	Tg(Prnp-MAPT*K274Q*K281Q)286Lgn/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27041503	20170329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5902816	Adamtsl4<sup>tvrm267</sup>	is_implicated_in	DOID:0111149	autosomal recessive isolated ectopia lentis 2		MGI:5902990	Adamtsl4<sup>tvrm267</sup>/Adamtsl4<sup>tvrm267</sup>  [background:] C57BL/6J-Adamtsl4<sup>tvrm267</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26405179	20180306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3698637	Zic3<sup>tm1Jwb</sup>/Zic3<sup>tm1Jwb</sup>  [background:] either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)	is_model_of	DOID:2907	Goldenhar syndrome						ECO:0000033	author statement supported by traceable reference	PMID:17127413	20070305	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2676253	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6	is_model_of	DOID:0060844	Norrie disease						ECO:0000033	author statement supported by traceable reference	PMID:8789439	20050617	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5009467	Tg(TagRb)1Plm/?  [background:] involves: BALB/cJ * C57BL/6J	is_model_of	DOID:768	retinoblastoma						ECO:0000033	author statement supported by traceable reference	PMID:1689463	20110630	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5427703	Wnk4<sup>tm1Pfi</sup>/Wnk4<sup>tm1Pfi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J	is_model_of	DOID:0050450	Gitelman syndrome						ECO:0000033	author statement supported by traceable reference	PMID:22550170	20120713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5696188	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] NON;NZO-Col4a4<sup>bwk</sup>/J	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:24522496	20151116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5904804	Tg(Myh6-CACNA1C)M1Aschw	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5904828	Tg(Myh6-CACNA1C)M1Aschw/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11136699	20170717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857166	Fcgr2b<sup>tm1Ttk</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus						ECO:0000033	author statement supported by traceable reference	PMID:30889825	20200723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857166	Fcgr2b<sup>tm1Ttk</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2448998	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup>  [background:] B6.129S4-Fcgr2b<sup>tm1Ttk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10981970	20200723	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5314147	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] B6.Cg-Tbx1<sup>tm1Bem</sup>	is_model_of	DOID:0060041	autism spectrum disorder						ECO:0000033	author statement supported by traceable reference	PMID:21908517	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5565367	Met<sup>tm4Gvw</sup>/Met<sup>+</sup>  [background:] involves: 129 * C57BL/6J * FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:19567831	20140527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861699	Htt<sup>tm3Mem</sup>	is_implicated_in	DOID:12858	Huntington's disease						ECO:0000033	author statement supported by traceable reference	PMID:27913616	20171207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5620186	b2b2696.1Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5620190	b2b2696.1Clo/b2b2696.1Clo  [background:] C57BL/6J-b2b2696.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651605	Pparg<sup>tm2Rev</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension						ECO:0000033	author statement supported by traceable reference	PMID:22307907	20130416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651605	Pparg<sup>tm2Rev</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5444198	Pparg<sup>tm2Rev</sup>/Pparg<sup>tm2Rev</sup> Tg(Tagln-cre)1Her/?  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18382765	20130416	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2686996	Mitf<sup>Mi-H</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN	is_model_of	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5297426	Dnah5<sup>b2b1003Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521924	Tph2<sup>Arg447</sup>	is_implicated_in	DOID:1595	melancholic depression						ECO:0000033	author statement supported by traceable reference	PMID:23467366	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5313702	Pcsk5<sup>b2b585Clo</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:5313813	Pcsk5<sup>b2b585Clo</sup>/Pcsk5<sup>b2b585Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b585Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120403	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2651426	Surf1<sup>tm1Zev</sup>/Surf1<sup>tm1Zev</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * DBA/2	is_model_of	DOID:3652	Leigh disease						ECO:0000033	author statement supported by traceable reference	PMID:12566387	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5431499	Gm572<sup>b2b1167Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3829382	Lbr<sup>ic-J</sup>/Lbr<sup>ic-J</sup>  [background:] involves: 129S4/SvJae * C57BL/6	is_model_of	DOID:1702	ichthyosis vulgaris						ECO:0000033	author statement supported by traceable reference	PMID:17403717	20090129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6416171	Muc4<sup>tm1Unc</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6423102	Muc4<sup>tm1Unc</sup>/Muc4<sup>tm1Unc</sup>  [background:] B6NTac.129(FVB)-Muc4<sup>tm1Unc</sup>/Rand			ECO:0000033	author statement supported by traceable reference	MGI:6416514	20200714	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4452030	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] 129-Col4a3<sup>tm1Dec</sup>/J	is_model_of	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000033	author statement supported by traceable reference	PMID:20197625	20100517	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5618809	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup> Por<sup>tm1Wolf</sup>/Por<sup>tm1Wolf</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA * FVB/N	is_model_of	DOID:1852	intrahepatic cholestasis						ECO:0000033	author statement supported by traceable reference	PMID:25068656	20150316	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3809475	Tg(HLA-DRA*0101,HLA-DRB1*0101)1Dmz/Tg(HLA-DRA*0101,HLA-DRB1*0101)1Dmz  [background:] involves: C57BL/6 * C57BL/10Sn * SJL/J	is_model_of	DOID:7148	rheumatoid arthritis						ECO:0000033	author statement supported by traceable reference	PMID:9091584	20081003	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4459458	Eda<sup>Ta</sup>/Y  [background:] Not Specified	is_model_of	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:27590203	20170104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5446134	Arsk<sup>tm1b(KOMP)Wtsi</sup>	is_implicated_in	DOID:12798	mucopolysaccharidosis		MGI:5797380	Arsk<sup>tm1b(KOMP)Wtsi</sup>/Arsk<sup>tm1b(KOMP)Wtsi</sup>  [background:] B6N(Cg)-Arsk<sup>tm1b(KOMP)Wtsi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:32856704	20210405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5702426	Ccdc154<sup>ntl</sup>	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1		MGI:5702613	Ccdc154<sup>ntl</sup>/Ccdc154<sup>ntl</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20121924	20160113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5551861	Col2a1<sup>M3J</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5553144	Col2a1<sup>M3J</sup>/Col2a1<sup>+</sup>  [background:] B6(Cg)-Col2a1<sup>M3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3033466	Hfe<sup>tm2Sly</sup>/Hfe<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J	is_model_of	DOID:0111029	hemochromatosis type 1						ECO:0000033	author statement supported by traceable reference	PMID:14673107	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512112	Prkar1a<sup>tm1.2Lsk</sup>	is_implicated_in	DOID:0050471	Carney complex						ECO:0000033	author statement supported by traceable reference	PMID:23045281	20131230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512112	Prkar1a<sup>tm1.2Lsk</sup>	is_implicated_in	DOID:0050471	Carney complex		MGI:3580534	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Tg(Tyr-cre)3Gfk/0  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15930266	20131230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4941025	Tg(Mt1-GH1)#Jjk	is_implicated_in	DOID:2449	acromegaly		MGI:4941028	Tg(Mt1-GH1)#Jjk/0  [background:] C57BL/6J-Tg(Mt1-GH1)#Jjk			ECO:0000033	author statement supported by traceable reference	PMID:19269870	20170727	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3778900	Pnp<sup>f</sup>/Pnp<sup>f</sup>  [background:] C57BL/6J-Pnp<sup>f</sup>	is_model_of	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448890	Brca2<sup>tm1Kamc</sup>	is_implicated_in	DOID:0111089	Fanconi anemia complementation group D1						ECO:0000033	author statement supported by traceable reference	PMID:27037238	20160711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448890	Brca2<sup>tm1Kamc</sup>	is_implicated_in	DOID:0111089	Fanconi anemia complementation group D1		MGI:3833153	Brca2<sup>tm1Kamc</sup>/Brca2<sup>tm1Kamc</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:16859999	20160711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157566	Nr4a2<sup>tm1Tpe</sup>	is_implicated_in	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:19379776	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157566	Nr4a2<sup>tm1Tpe</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3841583	Nr4a2<sup>tm1Tpe</sup>/Nr4a2<sup>+</sup>  [background:] B6.129P2-Nr4a2<sup>tm1Tpe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17457314	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360671	Nphs2<sup>tm2.1Antc</sup>	is_implicated_in	DOID:1184	nephrotic syndrome						ECO:0000033	author statement supported by traceable reference	PMID:37556557	20231226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6315994	Tg(Myh6-MYL3*E143K)2Dsc	is_implicated_in	DOID:397	restrictive cardiomyopathy		MGI:6315995	Tg(Myh6-MYL3*E143K)2Dsc/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28371863	20190704	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7286340	Specc1l<sup>em4Kumc</sup>	is_implicated_in	DOID:674	cleft palate		MGI:7286374	Specc1l<sup>em4Kumc</sup>/Specc1l<sup>+</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5000260	Tg(tetO-TARDBP)12Vle	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5448852	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-TARDBP)12Vle/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21206091	20130114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7550686	Hnrnpu<sup>em1Frk</sup>	is_implicated_in	DOID:0080418	developmental and epileptic encephalopathy 54		MGI:7550770	Hnrnpu<sup>em1Frk</sup>/Hnrnpu<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:37782669	20231122	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3814365	Brca2<sup>tm1Mbn</sup>/Brca2<sup>+</sup>  [background:] B6.Cg-Brca2<sup>tm1Mbn</sup> Apc<sup>Min</sup>	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:11215675	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574926	Slc26a2<sup>tm1Aros</sup>	is_implicated_in	DOID:14687	diastrophic dysplasia						ECO:0000033	author statement supported by traceable reference	PMID:23369989	20130917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574926	Slc26a2<sup>tm1Aros</sup>	is_implicated_in	DOID:14687	diastrophic dysplasia		MGI:3575650	Slc26a2<sup>tm1Aros</sup>/Slc26a2<sup>tm1Aros</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15703192	20130917	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3831884	Pot1b<sup>tm1.1Schg</sup>/Pot1b<sup>tm1.1Schg</sup> Terc<sup>tm1Rdp</sup>/Terc<sup>+</sup>  [background:] involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL	is_model_of	DOID:2729	dyskeratosis congenita						ECO:0000033	author statement supported by traceable reference	PMID:18936156	20090216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3588311	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] B6.C3Fe-Hps1<sup>ep</sup>/J	is_model_of	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5660409	Efemp2<sup>tm1.1Chu</sup>	is_implicated_in	DOID:3144	cutis laxa		MGI:5660617	Efemp2<sup>tm1.1Chu</sup>/Efemp2<sup>tm1.1Chu</sup>  [background:] B6(SJL)-Efemp2<sup>tm1.1Chu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26178373	20150901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6188327	Abca12<sup>smsk</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:6188328	Abca12<sup>smsk</sup>/Abca12<sup>smsk</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27551807	20180713	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5504442	Ins2<sup>Akita</sup>/?  [background:] involves: C57BL/6NSlc	is_model_of	DOID:9352	type 2 diabetes mellitus						ECO:0000033	author statement supported by traceable reference	PMID:17911348	20130905	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3620558	Zfpm2<sup>tm1Jml</sup>/Zfpm2<sup>tm1Jml</sup>  [background:] involves: 129X1/SvJ	is_model_of	DOID:0080169	tricuspid atresia						ECO:0000033	author statement supported by traceable reference	PMID:10888889	20060427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5806788	Tg(Thy1-SNCA*E57K)16Ema	is_implicated_in	DOID:12217	Lewy body dementia		MGI:5806789	Tg(Thy1-SNCA*E57K)16Ema/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:24662516	20161110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046273	Adgrv1<sup>tm1Pwh</sup>	is_implicated_in	DOID:0110839	Usher syndrome type 2C						ECO:0000033	author statement supported by traceable reference	PMID:24239741	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046273	Adgrv1<sup>tm1Pwh</sup>	is_implicated_in	DOID:0110839	Usher syndrome type 2C		MGI:3046274	Adgrv1<sup>tm1Pwh</sup>/Adgrv1<sup>tm1Pwh</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16775142	20160226	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5644499	Tg(MMTV-PyVT)#Mul/0  [background:] B6.FVB-Tg(MMTV-PyVT)#Mul	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18317964	20150721	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2175043	Gja8<sup>No2</sup>/Gja8<sup>No2</sup>  [background:] involves: 101 * C3H	is_model_of	DOID:0110231	cataract 1 multiple types						ECO:0000033	author statement supported by traceable reference	MGI:1277597	20050628	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3812201	Krt14<sup>tm1Der</sup>/Krt14<sup>+</sup> Tg(KRT5-cre/PGR)1Der/?  [background:] involves: 129X1/SvJ * FVB * ICR	is_model_of	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type						ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5705253	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*T790M*L858R)51Paow/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:1324	lung cancer						ECO:0000033	author statement supported by traceable reference	PMID:17726540	20160125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385580	Tg(Prnp-MAPT)7Vle	is_implicated_in	DOID:10652	Alzheimer's disease						ECO:0000033	author statement supported by traceable reference	PMID:22687952	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385580	Tg(Prnp-MAPT)7Vle	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5569760	Tg(Prnp-MAPT)7Vle/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10595524	20140626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5775650	Shank3<sup>tm5.1Gfng</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5776354	Shank3<sup>tm5.1Gfng</sup>/Shank3<sup>tm5.1Gfng</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26886798	20190430	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3700172	Nfkbia<sup>tm1Stw</sup>/Nfkbia<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv	is_model_of	DOID:3310	atopic dermatitis						ECO:0000033	author statement supported by traceable reference	PMID:8628301	20070318	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5774943	Chd7<sup>tm1.1Dmm</sup>/Chd7<sup>+</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S6/SvEvTac	is_model_of	DOID:0050834	CHARGE syndrome						ECO:0000033	author statement supported by traceable reference	PMID:26670829	20161116	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3769340	Ahsp<sup>tm1Mjwe</sup>/Ahsp<sup>+</sup> Hbb-b1<sup>tm1Unc</sup>/Hbb-b1<sup>+</sup> Hbb-b2<sup>tm1Unc</sup>/Hbb-b2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	is_model_of	DOID:12241	beta thalassemia						ECO:0000033	author statement supported by traceable reference	PMID:15545996	20121113	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5444474	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Tg(Camk2a-cre)#Szi/0  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J * CBA	is_model_of	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000033	author statement supported by traceable reference	PMID:22914734	20130415	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2177138	Gba1<sup>tm1Nsb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * C57BL/6	is_model_of	DOID:0110958	Gaucher's disease type II						ECO:0000033	author statement supported by traceable reference	PMID:1594045	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5464892	Ndufs4<sup>tm1Capt</sup>	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:5464901	Ndufs4<sup>tm1Capt</sup>/Ndufs4<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:19460290	20130218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5294639	Scn3b<sup>tm1Clhh</sup>	is_implicated_in	DOID:0110224	Brugada syndrome 7		MGI:5294675	Scn3b<sup>tm1Clhh</sup>/Scn3b<sup>tm1Clhh</sup>  [background:] 129S/SvEv-Scn3b<sup>tm1Clhh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19351516	20111103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5316786	Ccdc39<sup>b2b1304Clo</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6390920	Cfap276<sup>em1Fuxi</sup>	is_implicated_in	DOID:0050543	Charcot-Marie-Tooth disease intermediate type						ECO:0000033	author statement supported by traceable reference	PMID:31199454	20200219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5827758	Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Kras2)12Hev/0 Tg(tetO-MYC)1Lach/0  [background:] involves: FVB/N	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:16236385	20170306	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3805024	Bard1<sup>tm1Thl</sup>/Bard1<sup>tm2Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S1/Sv * C57BL/6J	is_model_of	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4888510	Btd<sup>tm1Bwol</sup>	is_implicated_in	DOID:856	biotinidase deficiency		MGI:4888512	Btd<sup>tm1Bwol</sup>/Btd<sup>tm1Bwol</sup>  [background:] B6.Cg-Btd<sup>tm1Bwol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21051254	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6376642	Arl2bp<sup>em1Visu</sup>	is_implicated_in	DOID:12336	male infertility		MGI:6377057	Arl2bp<sup>em1Visu</sup>/Arl2bp<sup>em1Visu</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31425546	20191115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7341380	Ftsj1<sup>tm1Tomik</sup>	is_implicated_in	DOID:0112034	non-syndromic X-linked intellectual disability 9		MGI:7341464	Ftsj1<sup>tm1Tomik</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:33771871	20220928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5510863	Bpifa1<sup>m1Ingm</sup>	is_implicated_in	DOID:10754	otitis media		MGI:5558082	Bpifa1<sup>m1Ingm</sup>/Bpifa1<sup>m1Ingm</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:25765466	20151216	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:2680800	Clcn7<sup>tm2Tjj</sup>/Clcn7<sup>tm2Tjj</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6	is_model_of	DOID:0110944	autosomal recessive osteopetrosis 4						ECO:0000033	author statement supported by traceable reference	PMID:11207362	20120117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278978	Tg(TBK1)#Andm	is_implicated_in	DOID:13544	low tension glaucoma		MGI:6278980	Tg(TBK1)#Andm/0  [background:] B6J.Cg-Tg(TBK1)#Andm			ECO:0000033	author statement supported by traceable reference	PMID:28025332	20190219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6278978	Tg(TBK1)#Andm	is_implicated_in	DOID:13544	low tension glaucoma		MGI:6278981	Tg(TBK1)#Andm/Tg(TBK1)#Andm  [background:] B6J.Cg-Tg(TBK1)#Andm			ECO:0000033	author statement supported by traceable reference	PMID:28025332	20190219	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:4412052	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz/0  [background:] C57BL/6-Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_model_of	DOID:9246	cerebral amyloid angiopathy						ECO:0000033	author statement supported by traceable reference	PMID:20615468	20101130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6280002	Kcnh6<sup>em1Jkya</sup>	is_implicated_in	DOID:4194	glucose metabolism disease		MGI:6402390	Kcnh6<sup>em1Jkya</sup>/Kcnh6<sup>em1Jkya</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30590050	20200401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:3457	invasive lobular carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:27411687	20190507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449466	Tg(Ela1-Tgfa)150Bri	is_implicated_in	DOID:4905	pancreatic carcinoma						ECO:0000033	author statement supported by traceable reference	PMID:16397221	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:7279192	Pcsk1<sup>em2Irli</sup>	is_implicated_in	DOID:28	endocrine system disease		MGI:7279194	Pcsk1<sup>em2Irli</sup>/Pcsk1<sup>em2Irli</sup>  [background:] C57BL/6J-Pcsk1<sup>em2Irli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35245347	20220520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521830	Met<sup>tm4Gvw</sup>	is_implicated_in	DOID:1612	breast cancer						ECO:0000033	author statement supported by traceable reference	PMID:23928995	20140527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521830	Met<sup>tm4Gvw</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:5565367	Met<sup>tm4Gvw</sup>/Met<sup>+</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19567831	20140527	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5056476	Sqstm1<sup>tm1.1Sral</sup>/Sqstm1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6	is_model_of	DOID:5408	Paget's disease of bone						ECO:0000033	author statement supported by traceable reference	PMID:21515589	20110811	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:5634400	Cdh1<sup>tm2Kem</sup>/Cdh1<sup>+</sup> Smad4<sup>tm2.1Cxd</sup>/Smad4<sup>tm2.1Cxd</sup> Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Pdx1-cre)6Tuv/0  [background:] involves: 129 * C57BL/6 * FVB/N	is_model_of	DOID:10534	stomach cancer						ECO:0000033	author statement supported by traceable reference	PMID:24784840	20150504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:6164625	Card14<sup>em9Lutzy</sup>	is_implicated_in	DOID:0080475	psoriasis 2		MGI:6314145	Card14<sup>em9Lutzy</sup>/Card14<sup>+</sup>  [background:] C57BL/6J-Card14<sup>em9Lutzy</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:29689250	20190613	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3621470	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N	is_model_of	DOID:11721	glycogen storage disease VII						ECO:0000033	author statement supported by traceable reference	PMID:15328538	20060505	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3576481	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] C.Cg-Aire<sup>tm1Mmat</sup>	is_model_of	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	affected_genomic_model	MGI:3623253	Disc1<sup>tm1Kara</sup>/Disc1<sup>tm1Kara</sup>  [background:] B6.129S6-Disc1<sup>tm1Kara</sup>	is_model_of	DOID:5419	schizophrenia						ECO:0000033	author statement supported by traceable reference	PMID:16484369	20060525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:5307891	Tnfsf11<sup>tles</sup>	is_implicated_in	DOID:0110943	autosomal recessive osteopetrosis 2		MGI:5307894	Tnfsf11<sup>tles</sup>/Tnfsf11<sup>tles</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22068587	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425922	Casr<sup>BCH011</sup>/Casr<sup>BCH011</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH011</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425923	Casr<sup>BCH013</sup>/Casr<sup>BCH013</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH013</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425918	Casr<sup>BCH002</sup>/Casr<sup>BCH002</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH002</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425920	Casr<sup>BCH004</sup>/Casr<sup>BCH004</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH004</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425919	Casr<sup>BCH003</sup>/Casr<sup>BCH003</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH003</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:5425921	Casr<sup>BCH007</sup>/Casr<sup>BCH007</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH007</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:2176761	Casr<sup>tm1Ces</sup>/Casr<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:7493018	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915213	Npc2	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3044881	Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15071184	20140204	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915213	Npc2	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5538404	Npc2<sup>tm1Plob</sup>/Npc2<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:23843985	20140204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655730	Casp8<sup>tm1Raz</sup>	is_implicated_in	DOID:0110116	autoimmune lymphoproliferative syndrome type 2B		MGI:2655731	Casp8<sup>tm1Raz</sup>/Casp8<sup>tm1Raz</sup> Tg(Lck-cre)548Jxm/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16157684	20060822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182914	Hivep2<sup>tm1Sis</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6189202	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] either: (involves: BALB/cA * C57BL/6NCrlj * CBA/JNCrlj) or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)			ECO:0000033	author statement supported by traceable reference	PMID:23389689	20190403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182914	Hivep2<sup>tm1Sis</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6189180	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:29233179	20190403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387358	Dag1<sup>tm2Kcam</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4946226	Dag1<sup>tm2Kcam</sup>/Dag1<sup>tm2Kcam</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19797173	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857446	Plp1<sup>tm1Kan</sup>	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3838180	Plp1<sup>tm1Kan</sup>/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11872612	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354962	Copb2	is_implicated_in	DOID:10907	microcephaly		MGI:6107893	Copb2<sup>em1Rstot</sup>/Copb2<sup>em2Rstot</sup>  [background:] involves: C57BL/6 * C57BL/6J * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:29036432	20180109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857091	Vps54<sup>wr</sup>	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:3614946	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] multiple strains			ECO:0000033	author statement supported by traceable reference	PMID:7416238	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690438	Fkbp4<sup>tm1Shou</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3710989	Fkbp4<sup>tm1Shou</sup>/Fkbp4<sup>tm1Shou</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:17142810	20070605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857401	Sox10<sup>Dom</sup>	is_implicated_in	DOID:0110955	Waardenburg syndrome type 4C		MGI:5897680	Sox10<sup>Dom</sup>/Sox10<sup>+</sup>  [background:] C57BL/6J-Sox10<sup>Dom</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20739296	20170519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:5313384	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:5313383	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>tm3.2Lysa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	MGI:62459	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8325377	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8155735	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9140816	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10100867	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3352223	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9837751	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856926	Slc22a5<sup>jvs</sup>	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1996978	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5296515	Sh2b3<sup>tm1Paw</sup>/Sh2b3<sup>tm1Paw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20458146	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	is_implicated_in	DOID:0090116	spondylocarpotarsal synostosis syndrome		MGI:3785077	Flnb<sup>Gt(XD076)Byg</sup>/Flnb<sup>Gt(XD076)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17606870	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	is_implicated_in	DOID:0090116	spondylocarpotarsal synostosis syndrome		MGI:3775522	Flnb<sup>Gt(RRF239)Byg</sup>/Flnb<sup>Gt(RRF239)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17635842	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856465	Acan<sup>cmd</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3694235	Acan<sup>cmd</sup>/Acan<sup>cmd</sup>  [background:] involves: STOCK T t<sup>low</sup> Itpr3<sup>tf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:632744	20070122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856465	Acan<sup>cmd</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3694235	Acan<sup>cmd</sup>/Acan<sup>cmd</sup>  [background:] involves: STOCK T t<sup>low</sup> Itpr3<sup>tf</sup>			ECO:0000033	author statement supported by traceable reference	MGI:78375	20070122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	is_implicated_in	DOID:0050887	Townes-Brocks syndrome		MGI:4462423	Sall1<sup>tm1.1Mrau</sup>/Sall1<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18470945	20100730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	is_implicated_in	DOID:0050887	Townes-Brocks syndrome		MGI:2677455	Sall1<sup>tm1Mrau</sup>/Sall1<sup>tm1Mrau</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12915476	20100730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	is_implicated_in	DOID:0050887	Townes-Brocks syndrome		MGI:2677456	Sall1<sup>tm1Mrau</sup>/Sall1<sup>+</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12915476	20100730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856667	Pitx3<sup>ak</sup>	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12655058	20190929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856667	Pitx3<sup>ak</sup>	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:4970465	20190929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856667	Pitx3<sup>ak</sup>	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12702666	20190929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96298	Hyal1	is_implicated_in	DOID:0050809	mucopolysaccharidosis IX		MGI:3797579	Hyal1<sup>tm1Stn</sup>/Hyal1<sup>tm1Stn</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18344557	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149329	Cebpb<sup>tm1Vpo</sup>	is_implicated_in	DOID:934	viral infectious disease		MGI:2174941	Cebpb<sup>tm1Vpo</sup>/Cebpb<sup>tm1Vpo</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:7744000	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107286	Man2b1	is_implicated_in	DOID:3413	alpha-mannosidosis		MGI:3603566	Man2b1<sup>tm1Psa</sup>/Man2b1<sup>tm1Psa</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10400983	20051103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107286	Man2b1	is_implicated_in	DOID:3413	alpha-mannosidosis		MGI:3603566	Man2b1<sup>tm1Psa</sup>/Man2b1<sup>tm1Psa</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16014715	20051103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3800793	Efemp1<sup>tm1Eap</sup>/Efemp1<sup>tm1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17666404	20080808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3800794	Efemp1<sup>tm1Eap</sup>/Efemp1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17666404	20080808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3771020	Efemp1<sup>tm1Lmar</sup>/Efemp1<sup>tm1Lmar</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:17664227	20080808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3771021	Efemp1<sup>tm1Lmar</sup>/Efemp1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:17664227	20080808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3778526	Dnah5<sup>hlb612</sup>/Dnah5<sup>hlb612</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18037990	20101001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773048	Kit<sup>tm1Shta</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:3773052	Kit<sup>tm1Shta</sup>/Kit<sup>tm1Shta</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18098338	20080306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109589	Ocrl	is_not_implicated_in	DOID:1056	oculocerebrorenal syndrome		MGI:2668816	Ocrl<sup>tm1Nbm</sup>/Ocrl<sup>tm1Nbm</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:9593760	20120809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861103	Hfm	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:2181997	Hfm/Hfm<sup>+</sup>  [background:] involves: SWV-Mbp<sup>shi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7531669	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857735	Chuk<sup>tm1Aki</sup>	is_implicated_in	DOID:0060647	fetal encasement syndrome		MGI:3609425	Chuk<sup>tm1Aki</sup>/Chuk<sup>tm1Aki</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926388	Tg(Msx2)1Rem	is_implicated_in	DOID:2340	craniosynostosis		MGI:2174870	Tg(Msx2)1Rem/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:7597092	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88283	Serpinh1	is_implicated_in	DOID:0110346	osteogenesis imperfecta type 10		MGI:5505276	Serpinh1<sup>tm2Kzn</sup>/Serpinh1<sup>tm2Kzn</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22492985	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442330	Pten<sup>tm1.1Gle</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4442333	Pten<sup>tm1.1Gle</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20194734	20100504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:5788097	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Col2a1-cre/ERT2)1Dic/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23873233	20220608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857898	Cftr<sup>tm3Bay</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177541	Cftr<sup>tm3Bay</sup>/Cftr<sup>tm3Bay</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7482032	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6404636	Tardbp<sup>tm3.1Ckjs</sup>/Tardbp<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31964415	20220712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5563078	Tg(CAG-dsRed2/RNAi:Tardbp)6Zxu/0  [background:] involves: C57BL/6 * C57BL/6J * FVB/NJ * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24616503	20220712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6187717	Tardbp<sup>em1Rhbr</sup>/Tardbp<sup>em1Rhbr</sup>  [background:] C57BL/6J-Tardbp<sup>em1Rhbr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29556029	20220712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6405401	Tardbp<sup>tm2.1Neas</sup>/Tardbp<sup>tm2.1Neas</sup>  [background:] B6(C3)-Tardbp<sup>tm2.1Neas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30625319	20220712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:6405398	Tardbp<sup>tm1.1Neas</sup>/Tardbp<sup>tm1.1Neas</sup>  [background:] B6(C3)-Tardbp<sup>tm1.1Neas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30625319	20220712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:5513111	Mnx1<sup>tm4(cre)Tmj</sup>/Mnx1<sup>+</sup> Tardbp<sup>tm1.1Ckjs</sup>/Tardbp<sup>tm1.2Cjks</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22718760	20220712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:7311612	Tardbp<sup>tm1.1Sobue</sup>/Tardbp<sup>tm1.1Sobue</sup> Tg(SLC18A3-cre)Misa/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:23449777	20220712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856410	Hps6<sup>ru-6J</sup>	is_implicated_in	DOID:0060544	Hermansky-Pudlak syndrome 6		MGI:3805518	Hps6<sup>ru-6J</sup>/Hps6<sup>ru-6J</sup>  [background:] involves: C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:3614209	Wfs1<sup>tm1Perm</sup>/Wfs1<sup>tm1Perm</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:16215705	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:3044705	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15056606	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:3044706	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] B6.Cg-Wfs1<sup>tm1Yoka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15056606	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:5644332	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] B6J.129-Wfs1<sup>tm1Yoka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18343518	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:5643859	Wfs1<sup>tm1Koks</sup>/Wfs1<sup>tm1Koks</sup>  [background:] 129S6/SvEvTac-Wfs1<sup>tm1Koks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24710642	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:5643859	Wfs1<sup>tm1Koks</sup>/Wfs1<sup>tm1Koks</sup>  [background:] 129S6/SvEvTac-Wfs1<sup>tm1Koks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21031341	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856947	Tmem79<sup>ma</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5559357	Tmem79<sup>ma</sup>/Tmem79<sup>ma</sup>  [background:] B6.CBACaGr-Tmem79<sup>ma</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24084074	20140418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856947	Tmem79<sup>ma</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5559071	Tmem79<sup>ma</sup>/Tmem79<sup>ma</sup>  [background:] involves: C57BL/6JJcl * CBA/CaGr			ECO:0000033	author statement supported by traceable reference	PMID:24060273	20140418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	is_implicated_in	DOID:0060643	primary sclerosing cholangitis		MGI:5618431	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20921947	20150821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	is_implicated_in	DOID:0060643	primary sclerosing cholangitis		MGI:5659501	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] CAnNCrl.12P2(FVB)-Abcb4<sup>tm1Bor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25478810	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178443	Dll3<sup>tm1Rbe</sup>	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:2178677	Dll3<sup>tm1Rbe</sup>/Dll3<sup>tm1Rbe</sup>  [background:] involves: 129P2/Ola * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11923214	20070409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178321	Des<sup>tm1Cap</sup>	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:2178322	Des<sup>tm1Cap</sup>/Des<sup>tm1Cap</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8794866	20060523	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97492	Pax8	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:2651448	Pax8<sup>tm1(cre)Mbu</sup>/Pax8<sup>tm1(cre)Mbu</sup>  [background:] involves: 129P2/OlaHsd * C3H/He * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12435636	20151029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97492	Pax8	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5694079	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17932107	20151029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97492	Pax8	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3694004	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:14981357	20151029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97492	Pax8	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3694004	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9590297	20151029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174703	Pkd2<sup>tm1Som</sup>/Pkd2<sup>tm1Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9568711	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:3617451	Pkd2<sup>tm1Som</sup>/Pkd2<sup>tm2Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9568711	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174704	Pkd2<sup>tm1Som</sup>/Pkd2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9568711	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174705	Pkd2<sup>tm2Som</sup>/Pkd2<sup>tm2Som</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10615132	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2174706	Pkd2<sup>tm2Som</sup>/Pkd2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10615132	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:6317329	Pkd2<sup>tm3Som</sup>/Pkd2<sup>tm3Som</sup> Tg(Pkhd1-cre)1Igr/0  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2676553	Pkd2<sup>tm1Dwo</sup>/Pkd2<sup>tm1Dwo</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12062060	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1925044	Adamtsl2	is_implicated_in	DOID:0111725	geleophysic dysplasia 1		MGI:6378827	Adamtsl2<sup>tm1c(KOMP)Wtsi</sup>/Adamtsl2<sup>tm1c(KOMP)Wtsi</sup> Tg(Prrx1-cre)1Cjt/0  [background:] B6.Cg-Adamtsl2<sup>tm1c(KOMP)Wtsi</sup> Tg(Prrx1-cre)1Cjt			ECO:0000033	author statement supported by traceable reference	PMID:30738849	20200518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:6160427	Fat1<sup>tm1.1Nsib</sup>/Fat1<sup>tm1.1Nsib</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129/Sv * 129S4/SvJaeSor * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26905694	20180612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859638	Pqbp1	is_implicated_in	DOID:0060179	Renpenning syndrome		MGI:6474216	Pqbp1<sup>tm1.1Hiok</sup>/Y Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25070536	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352460	Nr0b1	is_implicated_in	DOID:0080156	X-linked adrenal hypoplasia congenita		MGI:2659009	Nr0b1<sup>tm1.1Lja</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9843206	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352460	Nr0b1	is_implicated_in	DOID:0080156	X-linked adrenal hypoplasia congenita		MGI:2659009	Nr0b1<sup>tm1.1Lja</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11564714	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	is_implicated_in	DOID:10825	essential hypertension		MGI:5707848	Gata5<sup>tm1.2Nemr</sup>/Gata5<sup>tm1.2Nemr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26617239	20160210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2177042	Twist1<sup>Pde</sup>/Twist1<sup>Pde</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11350121	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2177044	Twist1<sup>Pde</sup>/Twist1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11350121	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2667352	Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12221714	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2386978	Twist1<sup>tm1Bhr</sup>/Twist1<sup>tm1Bhr</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8988167	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2386979	Twist1<sup>tm1Bhr</sup>/Twist1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8988167	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2684461	Twist1<sup>Pas</sup>/Twist1<sup>+</sup>  [background:] involves: C57BL/6 * PDT/Pas			ECO:0000033	author statement supported by traceable reference	PMID:14724733	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2684458	Twist1<sup>Pas</sup>/Twist1<sup>Pas</sup>  [background:] involves: C57BL/6 * PDT/Pas			ECO:0000033	author statement supported by traceable reference	PMID:14724733	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857342	Crybb2<sup>Phil</sup>	is_implicated_in	DOID:0110269	cataract 3 multiple types		MGI:2183031	Crybb2<sup>Phil</sup>/Crybb2<sup>Phil</sup>  [background:] Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:1707874	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	is_implicated_in	DOID:12934	Kearns-Sayre syndrome		MGI:2177634	Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9916807	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	is_implicated_in	DOID:12934	Kearns-Sayre syndrome		MGI:2177637	Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup> Tg(Myhca-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10737799	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617533	Ciita<sup>tm1Ccum</sup>/Ciita<sup>tm1Ccum</sup>  [background:] NOD.129S2(B6)-Ciita<sup>tm1Ccum</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10201997	20060324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447196	Abcg2<sup>tm1Ahs</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:5698637	Abcg2<sup>tm1Ahs</sup>/Abcg2<sup>tm1Ahs</sup>  [background:] FVB.129P2-Abcg2<sup>tm1Ahs</sup>/Tac			ECO:0000033	author statement supported by traceable reference	PMID:22473008	20210319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861349	Tub<sup>tub</sup>	is_implicated_in	DOID:9970	obesity		MGI:2174793	Tub<sup>tub</sup>/Tub<sup>tub</sup>  [background:] B6(AU)-Tub<sup>tub</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8606774	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861349	Tub<sup>tub</sup>	is_implicated_in	DOID:9970	obesity		MGI:3715252	Tub<sup>tub</sup>/Tub<sup>tub</sup>  [background:] C57BL/6J-Tub<sup>tub</sup>			ECO:0000033	author statement supported by traceable reference	MGI:61951	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857079	Enpp1<sup>ttw</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:8055108	20060731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857079	Enpp1<sup>ttw</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:7344126	20060731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763909	Tg(HSA*LR)32aCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3763921	Tg(HSA*LR)32aCath/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447406	Sod2<sup>tm1Shs</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:5907992	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6CrSlc * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16959785	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447406	Sod2<sup>tm1Shs</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:5907999	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195081	20170901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5546509	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Msx2-rtTA)885Lma/0 Tg(tetO-cre)1Jaw/0  [background:] involves: 129 * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23928991	20140228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88278	Serpina6	is_implicated_in	DOID:0090030	corticosteroid-binding globulin deficiency		MGI:4833684	Serpina6<sup>tm1.1Mmp</sup>/Serpina6<sup>tm1.1Mmp</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22930537	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88278	Serpina6	is_implicated_in	DOID:0090030	corticosteroid-binding globulin deficiency		MGI:4833684	Serpina6<sup>tm1.1Mmp</sup>/Serpina6<sup>tm1.1Mmp</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20022933	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88278	Serpina6	is_implicated_in	DOID:0090030	corticosteroid-binding globulin deficiency		MGI:3710359	Serpina6<sup>tm1Tew</sup>/Serpina6<sup>tm1Tew</sup>  [background:] involves: 129/SvEmcTer * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:16980625	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419886	Hoga1<sup>tm2a(KOMP)Wtsi</sup>	is_implicated_in	DOID:2977	primary hyperoxaluria		MGI:5805971	Hoga1<sup>tm2a(KOMP)Wtsi</sup>/Hoga1<sup>tm2a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:26428388	20161102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856693	Bicc1<sup>jcpk-bpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8476712	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856693	Bicc1<sup>jcpk-bpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856693	Bicc1<sup>jcpk-bpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582929	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] involves: BALB/c * CAST/EiJ			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856693	Bicc1<sup>jcpk-bpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8341011	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3628446	Dnmt3b<sup>tm6Enl</sup>	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628830	Dnmt3b<sup>tm6Enl</sup>/Dnmt3b<sup>tm6Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3716137	Ins2<sup>tm1Jja</sup>/Ins2<sup>tm1Jja</sup>  [background:] NOD.129S2-Ins2<sup>tm1Jja</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12925730	20130927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5508894	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup>  [background:] C.B6N-Ins2<sup>Akita</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22297672	20130927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581452	Lama2<sup>dy-7J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3581453	Lama2<sup>dy-7J</sup>/Lama2<sup>dy-7J</sup>  [background:] C57BL/6J-Lama2<sup>dy-7J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18430779	20090626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102793	Fstl1	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:7256886	Fstl1<sup>tm1Ajn</sup>/Fstl1<sup>tm1Ajn</sup>  [background:] B6.Cg-Fstl1<sup>tm1Ajn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31834999	20220328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182402	Dmpk<sup>tm1Rdd</sup>	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3613697	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>tm1Rdd</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10021468	20060301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182402	Dmpk<sup>tm1Rdd</sup>	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3613741	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10021468	20060301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182402	Dmpk<sup>tm1Rdd</sup>	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3613697	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>tm1Rdd</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8673132	20060301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933758	Cdkn1c<sup>tm1Kat</sup>	is_not_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:2175766	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>tm1Kat</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10731669	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857793	Itga6<sup>tm1Egl</sup>	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:3583788	Itga6<sup>tm1Egl</sup>/Itga6<sup>tm1Egl</sup>  [background:] either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129S2/SvPas * C57BL/6 * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:8673141	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345146	Grk1	is_implicated_in	DOID:0110713	Oguchi disease-2		MGI:2668598	Grk1<sup>tm1Citb</sup>/Grk1<sup>tm1Citb</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10097103	20100707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97628	pma	is_implicated_in	DOID:0090124	neurogenic-type arthrogryposis multiplex congenita-2		MGI:3722144	pma/pma  [background:] involves: CF-1			ECO:0000033	author statement supported by traceable reference	PMID:3948960	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3529082	Slc17a5<sup>tm1Lex</sup>	is_implicated_in	DOID:3659	sialuria		MGI:4440830	Slc17a5<sup>tm1Lex</sup>/Slc17a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20007460	20100420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681515	Ghr<sup>tm1Arge</sup>	is_implicated_in	DOID:9521	Laron syndrome		MGI:2681520	Ghr<sup>tm1Arge</sup>/Ghr<sup>tm1Arge</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11133160	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347075	Nbea	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5495922	Nbea<sup>Tg(GH1)240BNec</sup>/Nbea<sup>+</sup>  [background:] B6JRj.Cg-Nbea<sup>Tg(GH1)240BNec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23153818	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87912	Acvr2b	is_implicated_in	DOID:0060856	right atrial isomerism		MGI:2654122	Acvr2b<sup>tm1Enl</sup>/Acvr2b<sup>tm1Enl</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9242489	20060424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	is_implicated_in	DOID:9245	Alagille syndrome		MGI:5447165	Jag1<sup>tm1Frad</sup>/Jag1<sup>tm1Frad</sup> Tg(Tagln-cre)1Her/0  [background:] B6.Cg-Jag1<sup>tm1Frad</sup> Tg(Tagln-cre)1Her			ECO:0000033	author statement supported by traceable reference	PMID:21062863	20190820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	is_implicated_in	DOID:9245	Alagille syndrome		MGI:6356371	Jag1<sup>Ndr</sup>/Jag1<sup>Ndr</sup>  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29162437	20190820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	is_implicated_in	DOID:9245	Alagille syndrome		MGI:5447166	Jag1<sup>tm1Frad</sup>/Jag1<sup>tm1Frad</sup> Tg(Cdh5-cre)7Mlia/0  [background:] B6.Cg-Jag1<sup>tm1Frad</sup> Tg(Cdh5-cre)7Mlia			ECO:0000033	author statement supported by traceable reference	PMID:23095891	20190820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	is_implicated_in	DOID:9245	Alagille syndrome		MGI:3717461	Jag1<sup>Mhdahtu</sup>/Jag1<sup>+</sup>  [background:] C3HeB/FeJ-Jag1<sup>Mhdahtu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11259677	20190820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	is_implicated_in	DOID:9245	Alagille syndrome		MGI:5318528	Jag1<sup>tm2Grid</sup>/Jag1<sup>tm2Grid</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22156581	20190820	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861626	Tcm	is_implicated_in	DOID:83	cataract		MGI:2174765	Tcm/Tcm<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934274	Prnp<sup>tm1Edin</sup>	is_not_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:2174710	Prnp<sup>tm1Edin</sup>/Prnp<sup>tm1Edin</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Edin</sup>/EdinH			ECO:0000033	author statement supported by traceable reference	PMID:10581259	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96789	Lipa	is_implicated_in	DOID:14497	Wolman disease		MGI:2451081	Lipa<sup>tm1Ggb</sup>/Lipa<sup>tm1Ggb</sup>  [background:] involves: 129P2/OlaHsd * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:9700186	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182739	G6pdx<sup>a-m1Neu</sup>	is_implicated_in	DOID:13628	favism		MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock			ECO:0000033	author statement supported by traceable reference	PMID:12777375	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182739	G6pdx<sup>a-m1Neu</sup>	is_implicated_in	DOID:13628	favism		MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock			ECO:0000033	author statement supported by traceable reference	PMID:14751857	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182739	G6pdx<sup>a-m1Neu</sup>	is_implicated_in	DOID:13628	favism		MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock			ECO:0000033	author statement supported by traceable reference	PMID:3377761	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397671	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] B6.129-Kcnq2<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397669	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397670	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397672	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] FVB.129-Kcnq2<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:2672848	Kcnq2<sup>tm1Hsa</sup>/Kcnq2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10854243	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153355	Fgfr1<sup>tm2.1Cxd</sup>	is_implicated_in	DOID:14705	Pfeiffer syndrome		MGI:5790247	Fgfr1<sup>tm2.1Cxd</sup>/Fgfr1<sup>+</sup>  [background:] D2.129S6(Cg)-Fgfr1<sup>tm2.1Cxd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21538817	20160831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3797603	Xlch	is_implicated_in	DOID:0110461	X-linked dilated cardiomyopathy		MGI:3797747	Xlch/Xlch<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18424640	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3797603	Xlch	is_implicated_in	DOID:0110461	X-linked dilated cardiomyopathy		MGI:3797627	Xlch/?  [background:] C57BL/6J-Xlch			ECO:0000033	author statement supported by traceable reference	PMID:18424640	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	is_implicated_in	DOID:2738	pseudoxanthoma elasticum		MGI:3605029	Abcc6<sup>tm1Jfk</sup>/Abcc6<sup>tm1Jfk</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16135817	20060307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	is_implicated_in	DOID:2738	pseudoxanthoma elasticum		MGI:3615174	Abcc6<sup>tm1Aabb</sup>/Abcc6<sup>tm1Aabb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15888484	20060307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859553	Dnaaf11	is_implicated_in	DOID:0110608	primary ciliary dyskinesia 19		MGI:6285740	Dnaaf11<sup>tm1.2Hmd</sup>/Dnaaf11<sup>tm1.2Hmd</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27353389	20190402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794030	Cdc73<sup>tm1Btt</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5925397	Cdc73<sup>tm1Btt</sup>/Cdc73<sup>tm1Btt</sup> Tg(PTH-cre)4167Slib/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794030	Cdc73<sup>tm1Btt</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5925396	Cdc73<sup>tm1Btt</sup>/Cdc73<sup>+</sup> Tg(PTH-cre)4167Slib/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857937	Pten<sup>tm1Mak</sup>	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome		MGI:2179030	Pten<sup>tm1Mak</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10910075	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110563	autosomal dominant nonsyndromic deafness 36		MGI:2177316	Tmc1<sup>Mhdabth</sup>/Tmc1<sup>+</sup>  [background:] C3HeB/FeJ-Tmc1<sup>Mhdabth</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	MGI:2681078	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110563	autosomal dominant nonsyndromic deafness 36		MGI:2177313	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] involves: STOCK Grhl3<sup>ct</sup> * M. m. molossinus			ECO:0000033	author statement supported by traceable reference	PMID:7719036	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110563	autosomal dominant nonsyndromic deafness 36		MGI:2177312	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] STOCK Grhl3<sup>ct</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:48774	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1306775	Sucla2	is_implicated_in	DOID:0080124	mitochondrial DNA depletion syndrome 5		MGI:5585621	Sucla2<sup>Gt(SAbetageo)1Bhg</sup>/Sucla2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24271779	20141003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:2226	myeloproliferative neoplasm		MGI:6356966	Jak2<sup>tm1.1Ble</sup>/Jak2<sup>+</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:29202466	20190826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98266	Sord	is_implicated_in	DOID:83	cataract		MGI:3836915	Sord<sup>C57BL/Lia</sup>/Sord<sup>C57BL/Lia</sup>  [background:] involves: C57BL/LiA			ECO:0000033	author statement supported by traceable reference	PMID:18760274	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388002	Mbd2<sup>tm1Bh</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:7276257	Mbd2<sup>tm1Bh</sup>/Mbd2<sup>tm1Bh</sup>  [background:] NOD.129P2(B6)-Mbd2<sup>tm1Bh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34420035	20220512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5442112	b2b1594Clo	is_implicated_in	DOID:11193	syndactyly		MGI:5442125	b2b1594Clo/b2b1594Clo  [background:] C57BL/6J-b2b1594Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88478	Cpa1	is_implicated_in	DOID:4989	pancreatitis		MGI:6501768	Cpa1<sup>tm1.1Satom</sup>/Cpa1<sup>tm1.1Satom</sup>  [background:] involves: C57BL/6NCrl * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:30045879	20210125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:2175043	Gja8<sup>No2</sup>/Gja8<sup>No2</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:1277597	20130610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:2175044	Gja8<sup>No2</sup>/Gja8<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:1277597	20130610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:2176492	Gja8<sup>tm1Paul</sup>/Gja8<sup>tm1Paul</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9813099	20130610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:5489760	Gja8<sup>R205G</sup>/Gja8<sup>R205G</sup>  [background:] B6.Cg-Gja8<sup>R205G</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23300808	20130610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933757	Cdkn1c<sup>tm1Bbd</sup>	is_not_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:2175762	Cdkn1c<sup>tm1Bbd</sup>/Cdkn1c<sup>tm1Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9136926	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353562	Cngb3	is_implicated_in	DOID:0110008	achromatopsia 3		MGI:4367994	Cngb3<sup>tm1Dgen</sup>/Cngb3<sup>tm1Dgen</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19767295	20190130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353562	Cngb3	is_implicated_in	DOID:0110008	achromatopsia 3		MGI:6275192	Cngb3<sup>cpfl10</sup>/Cngb3<sup>cpfl10</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30592498	20190130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:6154327	Scn1a<sup>tm1.1Kzy</sup>/Scn1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:29329111	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16921370	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5447490	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:22908258	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:6274702	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5523888	Scn1a<sup>tm2.1Kzy</sup>/Scn1a<sup>+</sup> Tg(Pvalb-cre)1Tama/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:23922229	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5523889	Scn1a<sup>tm2.1Kzy</sup>/Scn1a<sup>tm2.1Kzy</sup> Tg(Pvalb-cre)1Tama/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:23922229	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:3818175	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:17881658	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0080422	Dravet syndrome		MGI:5523996	Scn1a<sup>tm1Kea</sup>/Scn1a<sup>+</sup>  [background:] (C57BL/6J x 129S6/SvEvTac-Scn1a<sup>tm1Kea</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:24152123	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	is_implicated_in	DOID:10587	Krabbe disease		MGI:2183898	Psap<sup>tm2Suz</sup>/Psap<sup>tm2Suz</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11371512	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152603	Gnai2<sup>tm1Lbi</sup>	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047402	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7663509	20130417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152603	Gnai2<sup>tm1Lbi</sup>	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047403	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7663509	20130417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152603	Gnai2<sup>tm1Lbi</sup>	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047403	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8613481	20130417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152603	Gnai2<sup>tm1Lbi</sup>	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:4452344	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15219458	20130417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153817	Fgfr2<sup>tm2.3Dsn</sup>	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:2176483	Fgfr2<sup>tm2.3Dsn</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11274405	20080121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5572798	Tshr<sup>hyt-3J</sup>/Tshr<sup>hyt-3J</sup>  [background:] CXB10/HiAJ-Tshr<sup>hyt-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5571363	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5572808	Tshr<sup>hyt-3J</sup>/Tshr<sup>hyt-3J</sup>  [background:] CByJ;CXB10-Tshr<sup>hyt-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5571363	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3581208	Tshr<sup>hyt</sup>/Tshr<sup>hyt</sup>  [background:] CBy.RF-Tshr<sup>hyt</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10575115	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3766096	Tshr<sup>tm1Rmar</sup>/Tshr<sup>tm1Rmar</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12432094	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3581208	Tshr<sup>hyt</sup>/Tshr<sup>hyt</sup>  [background:] CBy.RF-Tshr<sup>hyt</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17932107	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857137	Bmp4<sup>tm1Blh</sup>	is_implicated_in	DOID:0110122	Axenfeld-Rieger syndrome type 3		MGI:3711773	Bmp4<sup>tm1Blh</sup>/Bmp4<sup>+</sup>  [background:] B6.129S2-Bmp4<sup>tm1Blh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11722794	20080318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4377985	Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>	is_implicated_in	DOID:0110764	hereditary spastic paraplegia 11		MGI:5790094	Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>/Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26284655	20160829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769404	Errfi1<sup>tm1Jwj</sup>	is_implicated_in	DOID:1380	endometrial cancer		MGI:3850221	Errfi1<sup>tm1Jwj</sup>/Errfi1<sup>tm1Jwj</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19439667	20090713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:5431996	Col1a1<sup>Aga2</sup>/Col1a1<sup>+</sup>  [background:] C3HeB/FeJ-Col1a1<sup>Aga2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22589248	20120822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522021	Ptpn11<sup>tm1Gsf</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:5788097	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Col2a1-cre/ERT2)1Dic/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23873233	20220608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856699	Sharpin<sup>cpdm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8362989	20070202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856699	Sharpin<sup>cpdm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8774148	20070202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856699	Sharpin<sup>cpdm</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16274458	20070202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:4942396	Tlr2<sup>tm1Aki</sup>/Tlr2<sup>tm1Aki</sup>  [background:] NOD.129P2-Tlr2<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17707128	20110329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	is_implicated_in	DOID:0090018	autosomal dominant familial periodic fever		MGI:4461160	Tnfrsf1a<sup>tm2.1Rsie</sup>/Tnfrsf1a<sup>+</sup>  [background:] B6.Cg-Tnfrsf1a<sup>tm2.1Rsie</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20457915	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	is_implicated_in	DOID:0090018	autosomal dominant familial periodic fever		MGI:4461165	Tnfrsf1a<sup>tm1Rsie</sup>/Tnfrsf1a<sup>+</sup>  [background:] B6.Cg-Tnfrsf1a<sup>tm1Rsie</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20457915	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	is_implicated_in	DOID:0090018	autosomal dominant familial periodic fever		MGI:2175019	Tnfrsf1a<sup>tm1Imx</sup>/Tnfrsf1a<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9551933	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177536	Cftr<sup>tm1Kth</sup>/Cftr<sup>tm1Kth</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7560099	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177542	Cftr<sup>tm1Hsc</sup>/Cftr<sup>tm1Hsc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8589719	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177531	Cftr<sup>tm1Hgu</sup>/Cftr<sup>tm1Hgu</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	PMID:1382232	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3689380	Cftr<sup>tm2Mrc</sup>/Cftr<sup>tm2Mrc</sup>  [background:] B6.129S6-Cftr<sup>tm2Mrc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3689381	Cftr<sup>tm3Mrc</sup>/Cftr<sup>tm3Mrc</sup>  [background:] B6.129S6-Cftr<sup>tm3Mrc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177529	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] B6.129P2-Cftr<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3689378	Cftr<sup>tm1Kth</sup>/Cftr<sup>tm1Kth</sup>  [background:] B6.129S7-Cftr<sup>tm1Kth</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:5445419	Cftr<sup>tm1Eur</sup>/Cftr<sup>tm1Eur</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:7556083	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3773702	Cftr<sup>tm1Hgu</sup>/Cftr<sup>tm1Hgu</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:7540910	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177436	Cftr<sup>tm1Cam</sup>/Cftr<sup>tm1Cam</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:1355249	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:7263380	Cftr<sup>tm1.1Sdw</sup>/Cftr<sup>tm1.1Sdw</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:35392567	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177530	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:1380723	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:6192451	Cftr<sup>em3Cwr</sup>/Cftr<sup>em3Cwr</sup>  [background:] C57BL/6J-Cftr<sup>em3Cwr</sup>/Cwr			ECO:0000033	author statement supported by traceable reference	PMID:29924856	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:5445420	Cftr<sup>tm1Eur</sup>/Cftr<sup>tm1Eur</sup>  [background:] B6.129P2-Cftr<sup>tm1Eur</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22711878	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177529	Cftr<sup>tm1Unc</sup>/Cftr<sup>tm1Unc</sup>  [background:] B6.129P2-Cftr<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10570187	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177534	Cftr<sup>tm2Cam</sup>/Cftr<sup>tm2Cam</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:7545494	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177541	Cftr<sup>tm3Bay</sup>/Cftr<sup>tm3Bay</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7482032	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177545	Cftr<sup>tm2Hgu</sup>/Cftr<sup>tm2Hgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11823443	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177543	Cftr<sup>tm3Hgu</sup>/Cftr<sup>tm3Hgu</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8605891	20220425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:3778526	Dnah5<sup>hlb612</sup>/Dnah5<sup>hlb612</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18037990	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5614980	Dnah5<sup>b2b2570Clo</sup>/Dnah5<sup>b2b2570Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2570Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5649319	Dnah5<sup>b2b3491Clo</sup>/Dnah5<sup>b2b3491Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b3491Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5430346	Dnah5<sup>b2b1565Clo</sup>/Dnah5<sup>b2b1565Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1565Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5314017	Dnah5<sup>b2b1154Clo</sup>/Dnah5<sup>b2b1154Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1154Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:3624520	Dnah5<sup>Tg1Htz</sup>/Dnah5<sup>Tg1Htz</sup>  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11912187	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4431064	Pld4<sup>thss</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4950056	Pld4<sup>thss</sup>/Pld4<sup>thss</sup>  [background:] BALB/cJ-Pld4<sup>thss</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:30679154	20190826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8177042	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3655811	Lepr<sup>tm1.2Chua</sup>/Lepr<sup>tm1.2Chua</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15207242	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:16113078	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:7545546	Lepr<sup>db-Nokl</sup>/Lepr<sup>db-Nokl</sup>  [background:] C57BL/6N-Lepr<sup>db-Nokl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:7545554	Lepr<sup>db</sup>/Lepr<sup>db-Nokl</sup>  [background:] B6NTac.Cg-Lepr<sup>db</sup> Lepr<sup>db-Nokl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:7545550	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6NTac.BKS(D)-Lepr<sup>db</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34390703	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3847120	Lepr<sup>brta</sup>/Lepr<sup>brta</sup>  [background:] C57BL/6JSfdAnu-Lepr<sup>brta</sup>/Anu			ECO:0000033	author statement supported by traceable reference	MGI:3611487	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:15685168	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3694548	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] BKS.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6991317	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3784993	Lepr<sup>Db-2Btlr</sup>/Lepr<sup>Db-2Btlr</sup>  [background:] C57BL/6J-Lepr<sup>Db-2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778962	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3655832	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] FVB.BKS-Lepr<sup>db</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12136396	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3511748	Lepr<sup>tm1.2Chua</sup>/Lepr<sup>tm1.2Chua</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15389315	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3511747	Lepr<sup>tm1.1Chua</sup>/Lepr<sup>tm1.1Chua</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15389315	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3511746	Lepr<sup>tm1Chua</sup>/Lepr<sup>tm1Chua</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15389315	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3784991	Lepr<sup>Db-Btlr</sup>/Lepr<sup>Db-Btlr</sup>  [background:] C57BL/6J-Lepr<sup>Db-Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778961	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3817475	Lepr<sup>m3Btlr</sup>/Lepr<sup>m3Btlr</sup>  [background:] C57BL/6J-Lepr<sup>m3Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3815208	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:2653295	Lepr<sup>tm1Mgmj</sup>/Lepr<sup>tm1Mgmj</sup>  [background:] B6.129-Lepr<sup>tm1Mgmj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12594516	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12885755	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3822317	Lepr<sup>tm1Yli</sup>/Lepr<sup>tm1Yli</sup>  [background:] B6.129-Lepr<sup>tm1Yli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19015522	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3822318	Lepr<sup>tm2Yli</sup>/Lepr<sup>tm2Yli</sup>  [background:] B6.129-Lepr<sup>tm2Yli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19015522	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:16443782	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3689720	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12590922	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9970	obesity		MGI:3586756	Lepr<sup>db-3J</sup>/Lepr<sup>db-3J</sup>  [background:] 129P3/J-Lepr<sup>db-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6993269	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3		MGI:2175787	Hps3<sup>coa-6J</sup>/Hps3<sup>coa-6J</sup>  [background:] C3H/HeJ-Hps3<sup>coa-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:1861465	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3		MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:3408670	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3		MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	is_implicated_in	DOID:674	cleft palate		MGI:7335182	Cdc42<sup>tm1.1Ayam</sup>/Cdc42<sup>tm1.1Ayam</sup> Tg(Mpz-cre)94Imeg/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28326341	20220909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182942	Gcdh<sup>tm1Dmk</sup>	is_implicated_in	DOID:0111254	glutaric acidemia I		MGI:6268336	Gcdh<sup>tm1Dmk</sup>/Gcdh<sup>tm1Dmk</sup>  [background:] involves: 129S4/SvJae * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28545977	20191122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182942	Gcdh<sup>tm1Dmk</sup>	is_implicated_in	DOID:0111254	glutaric acidemia I		MGI:2182958	Gcdh<sup>tm1Dmk</sup>/Gcdh<sup>tm1Dmk</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11854167	20191122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856144	Hps5<sup>ru2</sup>	is_implicated_in	DOID:0060543	Hermansky-Pudlak syndrome 5		MGI:4437300	Hps5<sup>ru2</sup>/Hps5<sup>ru2</sup>  [background:] involves: C57BL			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20181011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919570	Kifbp	is_implicated_in	DOID:0060481	Goldberg-Shprintzen syndrome		MGI:6154375	Kifbp<sup>em1Hmy</sup>/Kifbp<sup>em1Hmy</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29192291	20180503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919570	Kifbp	is_implicated_in	DOID:0060481	Goldberg-Shprintzen syndrome		MGI:6154376	Kifbp<sup>em2Hmy</sup>/Kifbp<sup>em2Hmy</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29192291	20180503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:5544331	Gnptab<sup>tm1Kkol</sup>/Gnptab<sup>tm1Kkol</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24127423	20161208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:4456351	Gnptab<sup>Gt(OST97730)Lex</sup>/Gnptab<sup>Gt(OST97730)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17962477	20161208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:5790646	Gnptab<sup>nym</sup>/Gnptab<sup>nym</sup>  [background:] involves: BALB/cAnNHsd * C3H/HeNHsd			ECO:0000033	author statement supported by traceable reference	PMID:25107912	20161208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:5811453	Gnptab<sup>tm1Dkji</sup>/Gnptab<sup>tm1Dkji</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26857995	20161208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3038633	Gad2<sup>tm1Miya</sup>/Gad2<sup>tm1Miya</sup>  [background:] NOD.129P2-Gad2<sup>tm1Miya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14676944	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685581	Ccn6	is_implicated_in	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood		MGI:5317004	Ccn6<sup>tm1(cre)Mawa</sup>/Ccn6<sup>tm1(cre)Mawa</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24040393	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685581	Ccn6	is_implicated_in	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood		MGI:5515356	Ccn6<sup>tm2Mawa</sup>/Ccn6<sup>tm2Mawa</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24040393	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685581	Ccn6	is_implicated_in	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood		MGI:3526050	Ccn6<sup>tm2Mawa</sup>/Ccn6<sup>tm2Mawa</sup>  [background:] 129S/SvEv-Ccn6<sup>tm2Mawa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15601861	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387409	Timp3<sup>tm1Rkho</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3056101	Timp3<sup>tm1Rkho</sup>/Timp3<sup>tm1Rkho</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16037568	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387409	Timp3<sup>tm1Rkho</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3056103	Timp3<sup>tm1Rkho</sup>/Timp3<sup>tm1Rkho</sup>  [background:] B6.129-Timp3<sup>tm1Rkho</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15262835	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153465	Bsnd	is_implicated_in	DOID:0110145	Bartter disease type 4a		MGI:3826852	Bsnd<sup>tm1Tjj</sup>/Bsnd<sup>tm1Tjj</sup> Tg(Sox10-cre)1Wdr/0  [background:] involves: 129/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18833191	20110913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153465	Bsnd	is_implicated_in	DOID:0110145	Bartter disease type 4a		MGI:5285220	Bsnd<sup>tm1.1Suc</sup>/Bsnd<sup>tm1.1Suc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21593186	20110913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690430	Gfap<sup>tm3Mes</sup>	is_implicated_in	DOID:4252	Alexander disease		MGI:3692743	Gfap<sup>tm3Mes</sup>/Gfap<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17065456	20070108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:2675319	Nbn<sup>tm1Xu</sup>/Nbn<sup>tm1Xu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11889050	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:2682001	Nbn<sup>tm1Zqw</sup>/Nbn<sup>tm1Zqw</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14612522	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:2682002	Nbn<sup>tm1Zqw</sup>/Nbn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14612522	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:3615834	Nbn<sup>tm1Jpt</sup>/Nbn<sup>tm1Jpt</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:11967151	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:3510438	Nbn<sup>tm1Md</sup>/Nbn<sup>tm1Zqw</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15333589	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:3510439	Nbn<sup>tm1.1Md</sup>/Nbn<sup>tm1.1Md</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15333589	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:3573788	Nbn<sup>tm1Nus</sup>/Nbn<sup>tm2Nus</sup> Tg(CD19-cre/ERT2)1Cgn/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15668392	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:2449173	Myo7a<sup>sh1-6J</sup>/Myo7a<sup>sh1-6J</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	MGI:65387	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:5312616	Myo7a<sup>sh1-11J</sup>/Myo7a<sup>sh1-11J</sup>  [background:] 129.B6-Myo7a<sup>sh1-11J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21447681	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:6405698	Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>/Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] B6J.Cg-Myo7a<sup>tm1b(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31824252	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3511901	Myo7a<sup>Hdb</sup>/Myo7a<sup>4626SB</sup>  [background:] involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:15389316	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3709041	Myo7a<sup>polka</sup>/Myo7a<sup>polka</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20016096	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587763	Myo7a<sup>816SB</sup>/Myo7a<sup>816SB</sup>  [background:] involves: BALB/cRl * 47BS/Rl			ECO:0000033	author statement supported by traceable reference	PMID:9435277	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:5566830	Myo7a<sup>sh1-13J</sup>/Myo7a<sup>sh1-13J</sup>  [background:] C.Cg-Myo7a<sup>sh1-13J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:2449164	Myo7a<sup>sh1</sup>/Myo7a<sup>sh1</sup>  [background:] involves: BALB			ECO:0000033	author statement supported by traceable reference	PMID:4187938	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587642	Myo7a<sup>sh1-9J</sup>/Myo7a<sup>sh1-9J</sup>  [background:] involves: C3.MRL-Fas<sup>lpr</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:1276604	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:2449164	Myo7a<sup>sh1</sup>/Myo7a<sup>sh1</sup>  [background:] involves: BALB			ECO:0000033	author statement supported by traceable reference	MGI:63673	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587744	Myo7a<sup>26SB</sup>/Myo7a<sup>26SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587759	Myo7a<sup>4494SB</sup>/Myo7a<sup>4494SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587760	Myo7a<sup>816SB</sup>/Myo7a<sup>816SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20200424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587758	Myo7a<sup>3336SB</sup>/Myo7a<sup>3336SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20200424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699162	Bckdk<sup>Gt(VICT48)710Lex</sup>	is_implicated_in	DOID:0090126	branched-chain keto acid dehydrogenase kinase deficiency		MGI:3699323	Bckdk<sup>Gt(VICT48)710Lex</sup>/Bckdk<sup>Gt(VICT48)710Lex</sup>  [background:] B6.129S5/SvEvBrd-Bckdk<sup>Gt(VICT48)710Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22956686	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3694813	Pparg<sup>tm1Avp</sup>	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3695903	Pparg<sup>tm1Avp</sup>/Pparg<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17003330	20070207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856915	Invs<sup>inv</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3622553	Invs<sup>inv</sup>/Invs<sup>inv</sup>  [background:] FVB/N-Invs<sup>inv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9664638	20101001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919638	Ripk4	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:2653681	Ripk4<sup>tm1Pmh</sup>/Ripk4<sup>tm1Pmh</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22197489	20130430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919638	Ripk4	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:2653681	Ripk4<sup>tm1Pmh</sup>/Ripk4<sup>tm1Pmh</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22197488	20130430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103264	Arhgef2	is_implicated_in	DOID:0080312	neurodevelopmental disorder with midbrain and hindbrain malformations		MGI:5576781	Arhgef2<sup>Gt(IST13976A8)Tigm</sup>/Arhgef2<sup>Gt(IST13976A8)Tigm</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28453519	20180725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856522	Pklr<sup>slc</sup>	is_implicated_in	DOID:0111077	pyruvate kinase deficiency of red cells		MGI:5433725	Pklr<sup>slc</sup>/Pklr<sup>slc</sup>  [background:] CBA/NSlc-Pklr<sup>slc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7579416	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3588490	Gdnf<sup>tm1Lmgd</sup>/Gdnf<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:11774071	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3588431	Gdnf<sup>tm1Lmgd</sup>/Gdnf<sup>tm1Lmgd</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S1/Sv * 129X1/SvJ)			ECO:0000033	author statement supported by traceable reference	PMID:8657307	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2675149	Gdnf<sup>tm1Rosl</sup>/Gdnf<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12668632	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	is_implicated_in	DOID:1920	hyperuricemia		MGI:5698637	Abcg2<sup>tm1Ahs</sup>/Abcg2<sup>tm1Ahs</sup>  [background:] FVB.129P2-Abcg2<sup>tm1Ahs</sup>/Tac			ECO:0000033	author statement supported by traceable reference	PMID:22473008	20210727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	is_implicated_in	DOID:1920	hyperuricemia		MGI:6726370	Abcg2<sup>em1Omw</sup>/Abcg2<sup>em1Omw</sup>  [background:] C57BL/6J-Abcg2<sup>em1Omw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32488095	20210727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809243	Tg(Gfap-GFAP*R239H)60TMIke	is_implicated_in	DOID:4252	Alexander disease		MGI:3809245	Tg(Gfap-GFAP*R239H)60TMIke/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17299771	20081002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809243	Tg(Gfap-GFAP*R239H)60TMIke	is_implicated_in	DOID:4252	Alexander disease		MGI:3809245	Tg(Gfap-GFAP*R239H)60TMIke/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18602179	20081002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927580	Bloc1s6	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8441253	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3652414	Fbn1<sup>tm3Rmz</sup>/Fbn1<sup>tm3Rmz</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16407178	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3619460	Fbn1<sup>tm2Rmz</sup>/Fbn1<sup>tm2Rmz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10097121	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3690327	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15546004	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:4880671	Fbn1<sup>tm1Lper</sup>/Fbn1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21152435	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:4880670	Fbn1<sup>tm1Lper</sup>/Fbn1<sup>+</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21152435	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3690327	Fbn1<sup>tm1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15254584	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3619415	Fbn1<sup>tm1Rmz</sup>/Fbn1<sup>tm1Rmz</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9326947	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9732288	20060725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3630163	Sgcg<sup>tm1Oza</sup>/Sgcg<sup>tm1Oza</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12609501	20060725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14982859	20060725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3037288	Sgcg<sup>tm1Mcn</sup>/Sgcg<sup>tm1Mcn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10485893	20060725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387154	Erbb2<sup>tm1Klee</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2654632	Erbb2<sup>tm1Klee</sup>/Erbb2<sup>tm1Klee</sup> Tg(Nes-cre)1Atp/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12526770	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:3758717	Gusb<sup>mps</sup>/Gusb<sup>mps</sup>  [background:] B6.C-H2-K<sup>bm1</sup>/ByBir-Gusb<sup>mps</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2495302	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:2451066	Gusb<sup>tm3Sly</sup>/Gusb<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:2451065	Gusb<sup>tm2Sly</sup>/Gusb<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:2451063	Gusb<sup>tm1Sly</sup>/Gusb<sup>tm1Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:2677921	Gusb<sup>mps-2J</sup>/Gusb<sup>mps-2J</sup>  [background:] C3H/HeOuJ-Gusb<sup>mps-2J</sup>/BrkJ			ECO:0000033	author statement supported by traceable reference	PMID:11228259	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:2661058	Gusb<sup>tm4Sly</sup>/Gusb<sup>tm4Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12700165	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:2677921	Gusb<sup>mps-2J</sup>/Gusb<sup>mps-2J</sup>  [background:] C3H/HeOuJ-Gusb<sup>mps-2J</sup>/BrkJ			ECO:0000033	author statement supported by traceable reference	PMID:9774663	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:3802703	Gusb<sup>mps-3J</sup>/Gusb<sup>mps-3J</sup>  [background:] C57BL/6J-Gusb<sup>mps-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3801433	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	is_implicated_in	DOID:12803	Sly syndrome		MGI:3784505	Gusb<sup>mps</sup>/Gusb<sup>mps</sup>  [background:] B6.Cg-Gusb<sup>mps</sup>/BrkJ			ECO:0000033	author statement supported by traceable reference	PMID:2111021	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	is_implicated_in	DOID:0050779	hydrolethalus syndrome		MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444169	Lmod3	is_implicated_in	DOID:0110931	nemaline myopathy 10		MGI:5819051	Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Lmod3<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26035871	20170125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444169	Lmod3	is_implicated_in	DOID:0110931	nemaline myopathy 10		MGI:5701349	Lmod3<sup>em1Eno</sup>/Lmod3<sup>em1Eno</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25774500	20170125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388032	Htt<sup>tm2Msl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698855	Htt<sup>tm2Msl</sup>/Htt<sup>tm2Msl</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12223581	20070306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388032	Htt<sup>tm2Msl</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698855	Htt<sup>tm2Msl</sup>/Htt<sup>tm2Msl</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10533044	20070306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3618869	Kcnq1<sup>tm1Kpfe</sup>/Kcnq1<sup>tm1Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11226272	20070116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3056757	Kcnq1<sup>tm2Kpfe</sup>/Kcnq1<sup>tm2Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15498462	20070116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3623773	Kcnq1<sup>tm1Apf</sup>/Kcnq1<sup>tm1Apf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15891643	20070116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336155	Lss	is_implicated_in	DOID:83	cataract		MGI:6849724	Lss<sup>em1Zhaol</sup>/Lss<sup>em1Zhaol</sup>  [background:] C57BL/6J-Lss<sup>em1Zhaol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34926465	20220106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451060	Gusb<sup>tm2Sly</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:2451065	Gusb<sup>tm2Sly</sup>/Gusb<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151208	Selenon	is_implicated_in	DOID:0110633	rigid spine muscular dystrophy 1		MGI:5298009	Selenon<sup>tm1.2Mred</sup>/Selenon<sup>tm1.2Mred</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21858002	20111212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349429	Arl2bp	is_implicated_in	DOID:0110419	retinitis pigmentosa with or without situs inversus		MGI:6376646	Arl2bp<sup>em1Visu</sup>/Arl2bp<sup>em1Visu</sup>  [background:] involves: 129S2/SvPasCrl * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29718757	20191114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2172351	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm1Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:10499585	20060522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2170195	Pitx2<sup>tm1Kki</sup>/Pitx2<sup>tm1Kki</sup>  [background:] involves: 129P2/OlaHsd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:10572050	20060522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3587787	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm2Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:14623826	20060522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2172351	Pitx2<sup>tm1Jfm</sup>/Pitx2<sup>tm1Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:14623826	20060522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3589210	Pitx2<sup>tm2Sac</sup>/Pitx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10498698	20060522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2170004	Pitx2<sup>tm1Sac</sup>/Pitx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10498698	20060522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3622905	Pitx2<sup>tm1Rsd</sup>/Pitx2<sup>tm1Rsd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10499586	20060522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856056	Hpd<sup>hty</sup>	is_implicated_in	DOID:0050727	tyrosinemia type III		MGI:3586712	Hpd<sup>hty</sup>/Hpd<sup>hty</sup>  [background:] ICRIII			ECO:0000033	author statement supported by traceable reference	MGI:62484	20050906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448554	Nbeal2	is_implicated_in	DOID:0111044	gray platelet syndrome		MGI:5527439	Nbeal2<sup>tm1Lex</sup>/Nbeal2<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23863626	20161103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448554	Nbeal2	is_implicated_in	DOID:0111044	gray platelet syndrome		MGI:5806080	Nbeal2<sup>gps</sup>/Nbeal2<sup>gps</sup>  [background:] 129S1/SvImJ-Nbeal2<sup>gps</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26950939	20161103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448554	Nbeal2	is_implicated_in	DOID:0111044	gray platelet syndrome		MGI:5608466	Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>/Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Nbeal2<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:25258341	20161103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95758	Slc2a4	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3586490	Slc2a4<sup>tm1Mch</sup>/Slc2a4<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9334720	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15979918	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:3587410	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9097952	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15111796	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:3587410	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9660052	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12576554	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:3839661	Idua<sup>tm1Clk</sup>/Idua<sup>tm1Clk</sup>  [background:] B6.129-Idua<sup>tm1Clk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18022143	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:4415196	Idua<sup>tm1.1Kmke</sup>/Idua<sup>tm1.1Kmke</sup>  [background:] B6.129-Idua<sup>tm1.1Kmke</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19751987	20100106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451172	Sox9<sup>tm2Crm</sup>/Sox9<sup>+</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451169	Sox9<sup>tm2Crm</sup>/Sox9<sup>+</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451173	Sox9<sup>tm2Crm</sup>/Sox9<sup>tm2Crm</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451170	Sox9<sup>tm2Crm</sup>/Sox9<sup>tm2Crm</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:3044095	Sox9<sup>tm1Crm</sup>/Sox9<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:11371614	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:3581014	Sox9<sup>tm1.1Gsr</sup>/Sox9<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11857796	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:7451325	Sox9<sup>tm1.2Ksec</sup>/Sox9<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:36343245	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:5659902	Sox9<sup>Bbfc</sup>/Sox9<sup>+</sup>  [background:] C57BL/6J-Sox9<sup>Bbfc</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26234751	20230407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:3817221	Sox9<sup>tm1Gsr</sup>/Sox9<sup>+</sup> Tg(Pdx1-cre)6Cvw/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18723011	20230407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653045	Ndn<sup>tm1Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653051	Ndn<sup>tm1Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10508517	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653045	Ndn<sup>tm1Stw</sup>	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653050	Ndn<sup>tm1Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10508517	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856886	Rabggta<sup>gm</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2679085	Rabggta<sup>gm</sup>/Rabggta<sup>gm</sup>  [background:] C57BL/6J-Rabggta<sup>gm</sup>			ECO:0000033	author statement supported by traceable reference	MGI:61612	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856886	Rabggta<sup>gm</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2679085	Rabggta<sup>gm</sup>/Rabggta<sup>gm</sup>  [background:] C57BL/6J-Rabggta<sup>gm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8490171	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	is_implicated_in	DOID:1727	retinal vein occlusion		MGI:5288598	Nrp1<sup>tm1.1Cruh</sup>/Nrp1<sup>tm1.1Cruh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21852397	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	is_implicated_in	DOID:12259	hemophilia B		MGI:3662691	F9<sup>tm1Dws</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9354664	20180830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	is_implicated_in	DOID:12259	hemophilia B		MGI:3662853	F9<sup>tm1Emg</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9639513	20180830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	is_implicated_in	DOID:12259	hemophilia B		MGI:6196105	F9<sup>em3Dlli</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26964564	20180830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	is_implicated_in	DOID:12259	hemophilia B		MGI:6196101	F9<sup>em1Dlli</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26964564	20180830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	is_implicated_in	DOID:12259	hemophilia B		MGI:2175873	F9<sup>tm1Ver</sup>/F9<sup>tm1Ver</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9326649	20180830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526444	Mkks<sup>tm1Vcs</sup>	is_implicated_in	DOID:9970	obesity		MGI:3582615	Mkks<sup>tm1Vcs</sup>/Mkks<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:15772095	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158345	Ccr2<sup>tm1Mae</sup>	is_implicated_in	DOID:10871	age related macular degeneration		MGI:3841005	Ccr2<sup>tm1Mae</sup>/Ccr2<sup>tm1Mae</sup>  [background:] B6.129P2-Ccr2<sup>tm1Mae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14566334	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3525053	Ppp1r13l	is_implicated_in	DOID:0050737	autosomal recessive disease		MGI:3836904	Ppp1r13l<sup>wa3-J</sup>/Ppp1r13l<sup>wa3-J</sup>  [background:] BALB/cJ-Ppp1r13l<sup>wa3-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28069640	20190702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	is_implicated_in	DOID:0110840	Usher syndrome type 2D		MGI:4462829	Whrn<sup>tm1Tili</sup>/Whrn<sup>tm1Tili</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20502675	20100803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3802571	Nfix<sup>tm1.1Rmg</sup>	is_implicated_in	DOID:0112102	Sotos syndrome 2		MGI:6467327	Nfix<sup>tm1.1Rmg</sup>/Nfix<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30503862	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857935	Ptch1<sup>tm1Zim</sup>	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:2679475	Ptch1<sup>tm1Zim</sup>/Ptch1<sup>+</sup>  [background:] either: (involves: 129 * C57BL/6) or (involves: 129 * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:9585239	20101104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	is_not_implicated_in	DOID:12638	hypertrophic pyloric stenosis		MGI:4366780	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10982771	20091111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677350	Slc7a9<sup>tm1Nune</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:2677400	Slc7a9<sup>tm1Nune</sup>/Slc7a9<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12915471	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677350	Slc7a9<sup>tm1Nune</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:2677399	Slc7a9<sup>tm1Nune</sup>/Slc7a9<sup>tm1Nune</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12915471	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386939	Tg(FGFR3-G380R)7Aya	is_implicated_in	DOID:4480	achondroplasia		MGI:6416492	Tg(FGFR3-G380R)7Aya/Tg(FGFR3-G380R)7Aya  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10607835	20200514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386939	Tg(FGFR3-G380R)7Aya	is_implicated_in	DOID:4480	achondroplasia		MGI:6416491	Tg(FGFR3-G380R)7Aya/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10607835	20200514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	is_implicated_in	DOID:12365	malaria		MGI:3766730	Icam1<sup>tm1Bay</sup>/Icam1<sup>tm1Bay</sup>  [background:] B6.129S7-Icam1<sup>tm1Bay</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12769195	20130314	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3639605	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/MpJ-Fas<sup>lpr</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17208228	20080806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7957574	20080806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1565490	20080806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3799268	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] C3.MRL-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1565490	20080806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8163351	20080806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913331	Sharpin	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8774148	20070202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913331	Sharpin	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16274458	20070202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913331	Sharpin	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3695413	Sharpin<sup>cpdm</sup>/Sharpin<sup>cpdm</sup>  [background:] C57BL/KaLawRij-Sharpin<sup>cpdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8362989	20070202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97495	Pbx1	is_implicated_in	DOID:0112359	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay		MGI:7264531	Pbx1<sup>em1Dunw</sup>/Pbx1<sup>em1Dunw</sup>  [background:] C57BL/6J-Pbx1<sup>em1Dunw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31625560	20220502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3801488	Mecp2<sup>tm1Pplt</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18557922	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3801487	Mecp2<sup>tm1Pplt</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18557922	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5310735	Mecp2<sup>tm1.1Joez</sup>/Y  [background:] B6.129-Mecp2<sup>tm1.1Joez</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22119903	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:4949888	Mecp2<sup>tm1Vnar</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:20163734	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5702941	Mecp2<sup>tm4.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26647311	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5702952	Mecp2<sup>tm6.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26647311	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5702951	Mecp2<sup>tm5.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26647311	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3817461	Mecp2<sup>tm1Bird</sup>/Y  [background:] (129S6.129P2-Mecp2<sup>tm1Bird</sup> x C57BL/6)F1			ECO:0000033	author statement supported by traceable reference	PMID:18321864	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3817462	Mecp2<sup>tm1Bird</sup>/Y  [background:] (129S6.129P2-Mecp2<sup>tm1Bird</sup> x FVB/N)F1			ECO:0000033	author statement supported by traceable reference	PMID:18321864	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266266	Mecp2<sup>tm1Nlnd</sup>/Y  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266284	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266261	Mecp2<sup>tm1Nlnd</sup>/Y  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:7266283	Mecp2<sup>tm1Nlnd</sup>/Mecp2<sup>+</sup>  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:30402709	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5529468	Mecp2<sup>tm2.1Meg</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:23770565	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624553	Mecp2<sup>tm1Hzo</sup>/Y  [background:] 129S7/SvEvBrd-Mecp2<sup>tm1Hzo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12160743	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624554	Mecp2<sup>tm1Hzo</sup>/Mecp2<sup>+</sup>  [background:] 129S7/SvEvBrd-Mecp2<sup>tm1Hzo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12160743	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624551	Mecp2<sup>tm1Hzo</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12160743	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624713	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20633611	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3817230	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:24735673	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5491051	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23452848	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3712286	Mecp2<sup>tm2Bird</sup>/Mecp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17289941	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5584025	Mecp2<sup>tm1.1Dhy</sup>/Y  [background:] C57BL/6N-Mecp2<sup>tm1.1Dhy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24352790	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5568994	Mecp2<sup>tm1.1Jtc</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24283265	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5568998	Mecp2<sup>tm1.1Jtc</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24283265	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5306241	Mecp2<sup>tm1.1Jae</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16446138	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624680	Mecp2<sup>tm1Jae</sup>/Y Tg(Nes-cre)1Atp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11242118	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624674	Mecp2<sup>tm1.1Jae</sup>/Y  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242118	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624685	Mecp2<sup>tm1Jae</sup>/Y Tg(Camk2a-cre)93Kln/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11242118	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624718	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624713	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624719	Mecp2<sup>tm1Bird</sup>/Y Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624717	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>tm1.1Bird</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242117	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5538526	Mecp2<sup>tm3Meg</sup>/Y  [background:] B6.129-Mecp2<sup>tm3Meg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23770587	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:3624676	Mecp2<sup>tm1.1Jae</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22302819	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5751716	Mecp2<sup>tm1.1Irsf</sup>/Mecp2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25634563	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:5751707	Mecp2<sup>tm1.1Irsf</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25634563	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:6472629	Mecp2<sup>em1Jlzn</sup>/Y  [background:] C57BL/6-Mecp2<sup>em1Jlzn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32469049	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098752	Mecp2<sup>tm1.1Bird</sup>/Y  [background:] B6.129P2(C)-Mecp2<sup>tm1.1Bird</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098754	Mecp2<sup>tm2Bird</sup>/Y  [background:] B6.129P2-Mecp2<sup>tm2Bird</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098756	Mecp2<sup>tm1Jae</sup>/Y Chat<sup>tm2(cre)Lowl</sup>/Chat<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	is_implicated_in	DOID:1206	Rett syndrome		MGI:6098753	Mecp2<sup>tm1.1Bird</sup>/Mecp2<sup>+</sup>  [background:] B6.129P2(C)-Mecp2<sup>tm1.1Bird</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28159985	20220503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	is_implicated_in	DOID:10825	essential hypertension		MGI:3618625	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11457755	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	is_implicated_in	DOID:10825	essential hypertension		MGI:3618724	Nos3<sup>tm1Gdk</sup>/Nos3<sup>tm1Gdk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9468189	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	is_implicated_in	DOID:10825	essential hypertension		MGI:2174979	Nos3<sup>tm1Plh</sup>/Nos3<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:7545787	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:0050471	Carney complex		MGI:4868217	Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20421483	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:0050471	Carney complex		MGI:3580533	Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15930266	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:0050471	Carney complex		MGI:3580534	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Tg(Tyr-cre)3Gfk/0  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15930266	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:0050471	Carney complex		MGI:3625140	Prkar1a<sup>tm1Gsm</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15371594	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419443	Tuft1<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:3390	palmoplantar keratosis		MGI:7532607	Tuft1<sup>tm1a(KOMP)Wtsi</sup>/Tuft1<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:37716648	20231003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195264	Slc3a1	is_implicated_in	DOID:9266	cystinuria		MGI:5707340	Slc3a1<sup>m1Crl</sup>/Slc3a1<sup>m1Crl</sup>  [background:] 129S2/SvPasCrl			ECO:0000033	author statement supported by traceable reference	PMID:25048459	20181015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195264	Slc3a1	is_implicated_in	DOID:9266	cystinuria		MGI:6202041	Slc3a1<sup>tm1Jat</sup>/Slc3a1<sup>tm1Jat</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19484501	20181015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195264	Slc3a1	is_implicated_in	DOID:9266	cystinuria		MGI:2677978	Slc3a1<sup>pbl</sup>/Slc3a1<sup>pbl</sup>  [background:] C3HeB/FeJ-Slc3a1<sup>pbl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12923163	20181015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195264	Slc3a1	is_implicated_in	DOID:9266	cystinuria		MGI:2677979	Slc3a1<sup>pbl</sup>/Slc3a1<sup>pbl</sup>  [background:] involves: C3HeB/FeJ * MRL/MpJ			ECO:0000033	author statement supported by traceable reference	PMID:12923163	20181015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195264	Slc3a1	is_implicated_in	DOID:9266	cystinuria		MGI:6202041	Slc3a1<sup>tm1Jat</sup>/Slc3a1<sup>tm1Jat</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28165480	20181015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104672	Tfap2b	is_implicated_in	DOID:13550	angle-closure glaucoma		MGI:6152756	Tfap2b<sup>tm1Rbu</sup>/Tfap2b<sup>tm2Will</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:27483349	20180423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818509	Coro1a<sup>koy</sup>	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818532	Coro1a<sup>koy</sup>/Coro1a<sup>koy</sup>  [background:] C57BL/6-Coro1a<sup>koy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3522251	vsd	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3522715	vsd/vsd<sup>+</sup>  [background:] C57BL/6J-vsd			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3522251	vsd	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3522714	vsd/vsd  [background:] C57BL/6J-vsd			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4431725	Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060230	basal ganglia calcification		MGI:5806601	Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>/Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6NTac-Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:23934451	20161110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4156922	Tmem218<sup>Gt(OST40451)Lex</sup>	is_implicated_in	DOID:0050576	Senior-Loken syndrome		MGI:5700364	Tmem218<sup>Gt(OST40451)Lex</sup>/Tmem218<sup>Gt(OST40451)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25161209	20160101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851135	Tg(Kera-PITX2*A)AHjal	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3851249	Tg(Kera-PITX2*A)AHjal/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15509533	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611911	Gan<sup>tm1Yany</sup>	is_implicated_in	DOID:0090068	giant axonal neuropathy 1		MGI:3616169	Gan<sup>tm1Yany</sup>/Gan<sup>tm1Yany</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16565160	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611911	Gan<sup>tm1Yany</sup>	is_implicated_in	DOID:0090068	giant axonal neuropathy 1		MGI:3616169	Gan<sup>tm1Yany</sup>/Gan<sup>tm1Yany</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16303566	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5438048	b2b1700Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856982	Bloc1s6<sup>pa</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8441253	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057181	Tg(TcrbAI4)1Dvs	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3618695	Tg(TcrbAI4)1Dvs/0  [background:] NOD-Tg(TcrbAI4)1Dvs			ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5314017	Dnah5<sup>b2b1154Clo</sup>/Dnah5<sup>b2b1154Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1154Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5649319	Dnah5<sup>b2b3491Clo</sup>/Dnah5<sup>b2b3491Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b3491Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5430346	Dnah5<sup>b2b1565Clo</sup>/Dnah5<sup>b2b1565Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1565Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5614980	Dnah5<sup>b2b2570Clo</sup>/Dnah5<sup>b2b2570Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2570Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	is_implicated_in	DOID:12388	neurohypophyseal diabetes insipidus		MGI:3843462	Avp<sup>tm1Lja</sup>/Avp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:14660745	20090508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	is_implicated_in	DOID:12388	neurohypophyseal diabetes insipidus		MGI:3843460	Avp<sup>tm1Hari</sup>/Avp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19297548	20090508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777968	Pnp<sup>f</sup>	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778899	Pnp<sup>f</sup>/Pnp<sup>f</sup>  [background:] involves: C3H/HeHa * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:2516826	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777968	Pnp<sup>f</sup>	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778900	Pnp<sup>f</sup>/Pnp<sup>f</sup>  [background:] C57BL/6J-Pnp<sup>f</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181791	Plec<sup>tm1Gwi</sup>	is_implicated_in	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy		MGI:3513191	Plec<sup>tm1Gwi</sup>/Plec<sup>tm1Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:2174989	Pparg<sup>tm1Rev</sup>/Pparg<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10675354	20070207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3695903	Pparg<sup>tm1Avp</sup>/Pparg<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17003330	20070207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3050152	Pparg<sup>tm1Mae</sup>/Pparg<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15254591	20070207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	is_not_implicated_in	DOID:0110586	autosomal dominant nonsyndromic deafness 65		MGI:6490525	Tbc1d24<sup>em4Tbf</sup>/Tbc1d24<sup>em4Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em4Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32987832	20210107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891427	Fgf23	is_implicated_in	DOID:0050948	autosomal dominant hypophosphatemic rickets		MGI:5305730	Fgf23<sup>tm1.1Kew</sup>/Fgf23<sup>tm1.1Kew</sup>  [background:] B6.129-Fgf23<sup>tm1.1Kew</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22006328	20120213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:7816342	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:4830506	Otc<sup>spf-J</sup>/Y  [background:] C57BL/6J-Otc<sup>spf-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25647322	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3851105	Otc<sup>spf</sup>/Y  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8750014	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8041507	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850111	Otc<sup>spf</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:3981356	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:2175223	Otc<sup>spf-ash</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:3162766	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850173	Otc<sup>spf</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1531355	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850111	Otc<sup>spf</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7707692	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:1575747	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:2175225	Otc<sup>spf</sup>/Otc<sup>spf</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:1575747	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3851332	Otc<sup>spf-ash</sup>/Y  [background:] B6EiC3Sn a/A-Otc<sup>spf-ash</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16497529	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894693	Galnt1	is_implicated_in	DOID:4079	heart valve disease		MGI:3769260	Galnt1<sup>tm1.1Jxm</sup>/Galnt1<sup>tm1.1Jxm</sup>  [background:] B6NHsd.Cg-Galnt1<sup>tm1.1Jxm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25615642	20190715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847119	Lepr<sup>brta</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3847120	Lepr<sup>brta</sup>/Lepr<sup>brta</sup>  [background:] C57BL/6JSfdAnu-Lepr<sup>brta</sup>/Anu			ECO:0000033	author statement supported by traceable reference	MGI:3611487	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155423	Myo7a<sup>816SB</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587760	Myo7a<sup>816SB</sup>/Myo7a<sup>816SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155423	Myo7a<sup>816SB</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587763	Myo7a<sup>816SB</sup>/Myo7a<sup>816SB</sup>  [background:] involves: BALB/cRl * 47BS/Rl			ECO:0000033	author statement supported by traceable reference	PMID:9435277	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629049	Stx1a<sup>tm1Tfuj</sup>	is_implicated_in	DOID:150	disease of mental health		MGI:5000258	Stx1a<sup>tm1Tfuj</sup>/Stx1a<sup>tm1Tfuj</sup>  [background:] B6.Cg-Stx1a<sup>tm1Tfuj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20576034	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629049	Stx1a<sup>tm1Tfuj</sup>	is_implicated_in	DOID:150	disease of mental health		MGI:5000259	Stx1a<sup>tm1Tfuj</sup>/Stx1a<sup>+</sup>  [background:] B6.Cg-Stx1a<sup>tm1Tfuj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20576034	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913647	Sar1b	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:7331486	Sar1b<sup>em1Emle</sup>/Sar1b<sup>+</sup>  [background:] C57BL/6N-Sar1b<sup>em1Emle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33964306	20220824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913647	Sar1b	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:7331489	Sar1b<sup>em2Emle</sup>/Sar1b<sup>+</sup>  [background:] C57BL/6N-Sar1b<sup>em2Emle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33964306	20220824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847803	Col2a1<sup>Lpk</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5441253	Col2a1<sup>Lpk</sup>/Col2a1<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22028304	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847803	Col2a1<sup>Lpk</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5441254	Col2a1<sup>Lpk</sup>/Col2a1<sup>+</sup>  [background:] C.B6(C3)-Col2a1<sup>Lpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22028304	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181008	Pex11b<sup>tm1Sjg</sup>	is_implicated_in	DOID:905	Zellweger syndrome		MGI:3042895	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>tm1Sjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12024045	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181008	Pex11b<sup>tm1Sjg</sup>	is_implicated_in	DOID:905	Zellweger syndrome		MGI:5307125	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>+</sup>  [background:] B6.129-Pex11b<sup>tm1Sjg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21954064	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181008	Pex11b<sup>tm1Sjg</sup>	is_implicated_in	DOID:905	Zellweger syndrome		MGI:5307126	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>tm1Sjg</sup>  [background:] B6.129-Pex11b<sup>tm1Sjg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21954064	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856876	Kcnn2<sup>fri</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3765154	Kcnn2<sup>fri</sup>/Kcnn2<sup>fri</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:11442353	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679886	Pten<sup>tm2.1Ppp</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:4838317	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk/0  [background:] 129S1.Cg-Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk			ECO:0000033	author statement supported by traceable reference	PMID:20676139	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181226	Serpinf2<sup>tm1Hrl</sup>	is_implicated_in	DOID:0060601	alpha-2-plasmin inhibitor deficiency		MGI:2672889	Serpinf2<sup>tm1Hrl</sup>/Serpinf2<sup>tm1Hrl</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10090937	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181226	Serpinf2<sup>tm1Hrl</sup>	is_implicated_in	DOID:0060601	alpha-2-plasmin inhibitor deficiency		MGI:2672889	Serpinf2<sup>tm1Hrl</sup>/Serpinf2<sup>tm1Hrl</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10318667	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927235	Mbtps1	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7281134	Mbtps1<sup>tm1Jdh</sup>/Mbtps1<sup>tm1Jdh</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:29437042	20220527	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3760264	Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] B6.129P2-Il2<sup>tm1Hor</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17207605	20170417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	is_implicated_in	DOID:0110144	Bartter disease type 3		MGI:6198300	Clcnkb<sup>em1Haca</sup>/Clcnkb<sup>em1Haca</sup>  [background:] C57BL/6-Clcnkb<sup>em1Haca</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27421685	20180917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6511077	Nexn<sup>em1Chen</sup>/Nexn<sup>em1Chen</sup>  [background:] C57BL/6J-Nexn<sup>em1Chen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32814711	20210405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6514898	Nexn<sup>tm1.1Chen</sup>/Nexn<sup>tm1.1Chen</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6514900	Nexn<sup>tm1Chen</sup>/Nexn<sup>tm1Chen</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	is_implicated_in	DOID:0110424	dilated cardiomyopathy 1CC		MGI:6514899	Nexn<sup>tm1Chen</sup>/Nexn<sup>tm1Chen</sup> Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: MF1			ECO:0000033	author statement supported by traceable reference	PMID:30982350	20210405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446595	Abcd1<sup>tm1Ymd</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:9126326	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446591	Abcd1<sup>tm1Ymd</sup>/Abcd1<sup>tm1Ymd</sup>  [background:] involves: 129S/SvEv * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:9126326	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446586	Abcd1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9418970	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446583	Abcd1<sup>tm1Kan</sup>/Abcd1<sup>tm1Kan</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9418970	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:3617307	Abcd1<sup>tm1Kds</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15489218	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2680904	Abcd1<sup>tm1Kds</sup>/Abcd1<sup>tm1Kds</sup>  [background:] involves: 129/Sv * 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11875044	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446589	Abcd1<sup>tm1Kds</sup>/Y  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9256488	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446588	Abcd1<sup>tm1Kds</sup>/Abcd1<sup>tm1Kds</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9256488	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:6255	growth hormone secreting pituitary adenoma		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511358	Pparg<sup>tm2(tTA)Yba</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:3784503	Pparg<sup>tm2(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929699	Arl3	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3625687	Arl3<sup>Gt(OST263303)Lex</sup>/Arl3<sup>Gt(OST263303)Lex</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16565502	20060627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	is_implicated_in	DOID:0110318	hypertrophic cardiomyopathy 12		MGI:4947966	Csrp3<sup>tm1.1Rkn</sup>/Csrp3<sup>tm1.1Rkn</sup>  [background:] either: (involves: Black Swiss) or (involves: C57BL/6N)			ECO:0000033	author statement supported by traceable reference	PMID:20044516	20110425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	is_implicated_in	DOID:2340	craniosynostosis		MGI:3580015	Axin2<sup>tm1Wbm</sup>/Axin2<sup>tm1Wbm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15790973	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915339	Arpc4	is_implicated_in	DOID:8893	psoriasis		MGI:6115481	Arpc4<sup>tm1c(EUCOMM)Wtsi</sup>/Arpc4<sup>tm1c(EUCOMM)Wtsi</sup> Krt14<sup>tm1(cre)Wbm</sup>/Krt14<sup>+</sup>  [background:] B6.Cg-Arpc4<sup>tm1c(EUCOMM)Wtsi</sup> Krt14<sup>tm1(cre)Wbm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29113991	20180209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	is_implicated_in	DOID:4194	glucose metabolism disease		MGI:6402419	Kcnh6<sup>em2Jkya</sup>/Kcnh6<sup>em2Jkya</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30590050	20200401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	is_implicated_in	DOID:4194	glucose metabolism disease		MGI:6402390	Kcnh6<sup>em1Jkya</sup>/Kcnh6<sup>em1Jkya</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30590050	20200401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351343	Grm6	is_implicated_in	DOID:0110865	congenital stationary night blindness 1B		MGI:5754843	Grm6<sup>nob7</sup>/Grm6<sup>nob7</sup>  [background:] C57BL/6J-Grm6<sup>nob7</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26241901	20170522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351343	Grm6	is_implicated_in	DOID:0110865	congenital stationary night blindness 1B		MGI:5897563	Grm6<sup>nob8</sup>/Grm6<sup>nob8</sup>  [background:] CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:28490646	20170522	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158670	Blm<sup>tm3Brd</sup>	is_implicated_in	DOID:2717	Bloom syndrome		MGI:2683906	Blm<sup>tm3Brd</sup>/Blm<sup>tm3Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11101838	20050714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861667	sar	is_implicated_in	DOID:0112307	sarcosinemia		MGI:7260274	sar/sar  [background:] BTBR-sar			ECO:0000033	author statement supported by traceable reference	PMID:1372986	20220411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135272	Vangl2	is_implicated_in	DOID:0080074	neural tube defect		MGI:3529938	Vangl2<sup>Lp</sup>/Vangl2<sup>Lp</sup>  [background:] involves: CBA/Ca * LPT/Le			ECO:0000033	author statement supported by traceable reference	PMID:9545534	20130429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855969	Lyst<sup>bg-J</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3581179	Lyst<sup>bg-J</sup>/Lyst<sup>bg-J</sup>  [background:] C57BL/6J-Lyst<sup>bg-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2450757	Ush1g	is_implicated_in	DOID:0110834	Usher syndrome type 1G		MGI:3662655	Ush1g<sup>js-2J</sup>/Ush1g<sup>js-2J</sup>  [background:] B6(Cg)-Ush1g<sup>js-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3662705	20120606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2450757	Ush1g	is_implicated_in	DOID:0110834	Usher syndrome type 1G		MGI:5320445	Ush1g<sup>js-3J</sup>/Ush1g<sup>js-3J</sup>  [background:] B6.Cg-Ush1g<sup>js-3J</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	MGI:5320439	20120606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2450757	Ush1g	is_implicated_in	DOID:0110834	Usher syndrome type 1G		MGI:3581211	Ush1g<sup>js</sup>/Ush1g<sup>js</sup>  [background:] B6.A-Ush1g<sup>js</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12588793	20120606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623523	B2m<sup>tm1Unc</sup>/B2m<sup>tm1Unc</sup>  [background:] NOD.129P2-B2m<sup>tm1Unc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8314025	20060531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_implicated_in	DOID:0111252	vestibular schwannomatosis		MGI:5619302	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Postn-cre)1Sjc/0  [background:] involves: 129P2/OlaHsd * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:25113746	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448372	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:14451913	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:3767061	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] either: (B6.C3-Spta1<sup>sph</sup> x WB.C3-Spta1<sup>sph</sup>)F1 or (WB.C3-Spta1<sup>sph</sup> x B6.C3-Spta1<sup>sph</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:7059672	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6234993	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6841965	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:63097	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:3615049	Spta1<sup>ihj</sup>/Spta1<sup>ihj</sup>  [background:] involves: HRS/J * LAH			ECO:0000033	author statement supported by traceable reference	PMID:20056793	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:78279	20101210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448951	Tlx2<sup>tm1Htno</sup>	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:3817243	Tlx2<sup>tm1Htno</sup>/Tlx2<sup>tm1Htno</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9259577	20081120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	is_implicated_in	DOID:0110919	hereditary spherocytosis type 4		MGI:3027982	Slc4a1<sup>wan</sup>/Slc4a1<sup>wan</sup>  [background:] C3H/HeJ-Slc4a1<sup>wan</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15070709	20100315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521669	Bbs2<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110124	Bardet-Biedl syndrome 2		MGI:3524999	Bbs2<sup>tm1Vcs</sup>/Bbs2<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:15539463	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183904	Nrp2<sup>tm1.2Mom</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4843917	Nrp2<sup>tm1.2Mom</sup>/Nrp2<sup>tm1.2Mom</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:18657176	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387358	Dag1<sup>tm2Kcam</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:2684281	Dag1<sup>tm2Kcam</sup>/Dag1<sup>tm2Kcam</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12140559	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153816	Strc	is_implicated_in	DOID:0110471	autosomal recessive nonsyndromic deafness 16		MGI:3818653	Strc<sup>tm1Ugds</sup>/Strc<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18849963	20081209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95790	Gnrhr	is_implicated_in	DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia		MGI:3574973	Gnrhr<sup>hh</sup>/Gnrhr<sup>hh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15625238	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	is_implicated_in	DOID:0110845	xeroderma pigmentosum group D		MGI:3696354	Ercc2<sup>tm3Jhjh</sup>/Ercc2<sup>tm3Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16904611	20070209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87868	Acads	is_implicated_in	DOID:0080154	short chain acyl-CoA dehydrogenase deficiency		MGI:3029782	Acads<sup>del-J</sup>/Acads<sup>del-J</sup>  [background:] involves: BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:2712823	20050822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4151115	Nme7<sup>Gt(OST31116)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:4950028	Nme7<sup>Gt(OST31116)Lex</sup>/Nme7<sup>Gt(OST31116)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98359	Sox11	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:5827939	Sox11<sup>tm1.1Gan</sup>/Sox11<sup>tm1.1Gan</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26826126	20170308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054788	Casr<sup>Nuf</sup>	is_implicated_in	DOID:0090107	autosomal dominant hypocalcemia 1		MGI:3603348	Casr<sup>Nuf</sup>/Casr<sup>+</sup>  [background:] either: (involves: 102/El * 102/H * C3H/He) or (involves: 102/El * C3H/He * C3H/HeH)			ECO:0000033	author statement supported by traceable reference	PMID:15347804	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054788	Casr<sup>Nuf</sup>	is_implicated_in	DOID:0090107	autosomal dominant hypocalcemia 1		MGI:3603347	Casr<sup>Nuf</sup>/Casr<sup>Nuf</sup>  [background:] involves: 102/El * C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:15347804	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy		MGI:5285183	Gnas<sup>tm1Gwa</sup>/Gnas<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:21747923	20170119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy		MGI:5818292	Gnas<sup>tm4Lsw</sup>/Gnas<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:26671181	20170119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036308	Ddb2<sup>tm1Linn</sup>	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3036310	Ddb2<sup>tm1Linn</sup>/Ddb2<sup>tm1Linn</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14769931	20070509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036308	Ddb2<sup>tm1Linn</sup>	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3036311	Ddb2<sup>tm1Linn</sup>/Ddb2<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14769931	20070509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180817	S1pr2<sup>tm1Ajml</sup>	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:3663255	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19903857	20170406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180817	S1pr2<sup>tm1Ajml</sup>	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5882507	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] 129S5/SvEvBrd-S1pr2<sup>tm1Ajml</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19903857	20170406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442252	Lrp4	is_implicated_in	DOID:0060757	sclerosteosis 2		MGI:5688562	Lrp4<sup>mdig-3J</sup>/Lrp4<sup>mdig-3J</sup>  [background:] B6.Cg-Lrp4<sup>mdig-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5688518	20200415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442252	Lrp4	is_implicated_in	DOID:0060757	sclerosteosis 2		MGI:6404118	Lrp4<sup>tm1.1Pg</sup>/Lrp4<sup>tm1.1Pg</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28477420	20200415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927248	Kcnj1	is_implicated_in	DOID:0110143	Bartter disease type 2		MGI:3041878	Kcnj1<sup>tm1Ges</sup>/Kcnj1<sup>tm1Ges</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12122007	20050913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87894	Chrne	is_implicated_in	DOID:0110679	congenital myasthenic syndrome 4C		MGI:2671994	Chrne<sup>tm1Vwi</sup>/Chrne<sup>tm1Vwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10998094	20090428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	is_implicated_in	DOID:8670	eating disorder		MGI:6441085	Hdac4<sup>em1Hcu</sup>/Hdac4<sup>em1Hcu</sup>  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:32153359	20200710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	is_implicated_in	DOID:8670	eating disorder		MGI:6441077	Hdac4<sup>em1Hcu</sup>/Hdac4<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:27884425	20200710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104671	Tfap2a	is_implicated_in	DOID:0050567	orofacial cleft		MGI:5647995	Tfap2a<sup>tm1Will</sup>/Tfap2a<sup>tm2.1Will</sup>  [background:] involves: 129S1/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:25381013	20150812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623589	Ctnna2<sup>tm1Mta</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3624367	Ctnna2<sup>tm1Mta</sup>/Ctnna2<sup>tm1Mta</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12750472	20060613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664604	Ercc2<sup>tm3Jhjh</sup>	is_implicated_in	DOID:0110845	xeroderma pigmentosum group D		MGI:3696354	Ercc2<sup>tm3Jhjh</sup>/Ercc2<sup>tm3Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16904611	20070209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3688892	Tg(Myh6-PRKAG2*R302Q)#Rro	is_implicated_in	DOID:384	Wolff-Parkinson-White syndrome		MGI:3689004	Tg(Myh6-PRKAG2*R302Q)#Rro/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:15611370	20061129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850079	Baz1b<sup>tm1Ska</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3850085	Baz1b<sup>tm1Ska</sup>/Baz1b<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19470456	20090710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850079	Baz1b<sup>tm1Ska</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3850084	Baz1b<sup>tm1Ska</sup>/Baz1b<sup>tm1Ska</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19470456	20090710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:5317923	Pla2g6<sup>m1J</sup>/Pla2g6<sup>m1J</sup>  [background:] C3H/HeJ-Pla2g6<sup>m1J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22442204	20120516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:4415286	Pla2g6<sup>m1Sein</sup>/Pla2g6<sup>m1Sein</sup>  [background:] C57BL/6JJcl-Pla2g6<sup>m1Sein</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19893029	20120516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3055190	Pla2g6<sup>tm1Turk</sup>/Pla2g6<sup>tm1Turk</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18202189	20120516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3777383	Pla2g6<sup>tm1Tsu</sup>/Pla2g6<sup>tm1Tsu</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21813701	20120516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861586	Krt71	is_implicated_in	DOID:0110710	hypotrichosis 13		MGI:5586979	Krt71<sup>Ca-19J</sup>/Krt71<sup>+</sup>  [background:] BALB/cJ-Krt71<sup>Ca-19J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5586973	20141009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196332	Arhgap6	is_implicated_in	DOID:10629	microphthalmia		MGI:3580093	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196332	Arhgap6	is_implicated_in	DOID:10629	microphthalmia		MGI:3580090	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196332	Arhgap6	is_implicated_in	DOID:10629	microphthalmia		MGI:3580089	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3623263	Cln3<sup>tm1Mkat</sup>/Cln3<sup>tm1Mkat</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10440905	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3759418	Cln3<sup>tm1Blda</sup>/Cln3<sup>tm1Blda</sup>  [background:] B6.129-Cln3<sup>tm1Blda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17855597	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:6474170	Cln3<sup>em1Dprc</sup>/Cln3<sup>em1Dprc</sup>  [background:] C57BL/6-Cln3<sup>em1Dprc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32601357	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3044770	Cln3<sup>tm1.1Mem</sup>/Cln3<sup>tm1.1Mem</sup>  [background:] involves: 129S/SvEv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12374761	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:2175783	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10527801	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:5788563	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27101989	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3715473	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] 129S6/SvEvTac-Cln3<sup>tm1Nbm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15326100	20201130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3040688	Slc7a14	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:5705137	Slc7a14<sup>em1Jqu</sup>/Slc7a14<sup>em1Jqu</sup>  [background:] C57BL/6-Slc7a14<sup>em1Jqu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3040688	Slc7a14	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:7277716	Slc7a14<sup>em1Jin</sup>/Slc7a14<sup>em1Jin</sup>  [background:] C57BL/6J-Slc7a14<sup>em1Jin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0110383	retinitis pigmentosa 7		MGI:3620587	Prph2<sup>Rd2</sup>/Prph2<sup>+</sup>  [background:] either: (involves: BALB/c * O20/A) or (involves: GR/A * O20/A) or (involves: O20/A * STS/A)			ECO:0000033	author statement supported by traceable reference	PMID:3830736	20090318	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0110383	retinitis pigmentosa 7		MGI:3836163	Prph2<sup>tm1Nmc</sup>/Prph2<sup>tm1Nmc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11978760	20090318	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0110383	retinitis pigmentosa 7		MGI:3836162	Prph2<sup>tm1Nmc</sup>/Prph2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11978760	20090318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158697	Men1<sup>tm1Ctre</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3843203	Men1<sup>tm1Ctre</sup>/Men1<sup>tm1Ctre</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19208834	20090507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671887	l11Jus16	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822146	l11Jus16/l11Jus16  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2681835	Nlgn2	is_implicated_in	DOID:5419	schizophrenia		MGI:6294898	Nlgn2<sup>tm1.1Gchn</sup>/Nlgn2<sup>tm1.1Gchn</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29859117	20190429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698276	Htt<sup>tm3Mem</sup>/Htt<sup>tm3Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698279	Htt<sup>tm2Mem</sup>/Htt<sup>tm2Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698001	Htt<sup>tm7Mem</sup>/Htt<sup>tm7Mem</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9398841	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698002	Htt<sup>tm3Mem</sup>/Htt<sup>tm3Mem</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9398841	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698007	Htt<sup>tm1Mem</sup>/Htt<sup>tm7Mem</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9398841	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2176436	Htt<sup>tm1Szi</sup>/Htt<sup>tm1Szi</sup>  [background:] either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * MF1)			ECO:0000033	author statement supported by traceable reference	PMID:7550343	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3586835	Htt<sup>tm1Hay</sup>/Htt<sup>tm1Hay</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7774020	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698408	Htt<sup>tm6Mem</sup>/Htt<sup>tm8Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11709539	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2176494	Htt<sup>tm1Mem</sup>/Htt<sup>tm1Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:7618107	20070302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442473	Rhbdf2	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome		MGI:2653142	Rhbdf2<sup>cub</sup>/Rhbdf2<sup>cub</sup>  [background:] B6.Cg-Rhbdf2<sup>cub</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29116018	20220516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442473	Rhbdf2	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome		MGI:6256982	Rhbdf2<sup>cub</sup>/Rhbdf2<sup>cub</sup>  [background:] MRL.Cg-Rhbdf2<sup>cub</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29116018	20220516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442473	Rhbdf2	is_implicated_in	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome		MGI:6256973	Rhbdf2<sup>em2Mvw</sup>/Rhbdf2<sup>em2Mvw</sup>  [background:] C57BL/6J-Rhbdf2<sup>em2Mvw</sup>/Mvw			ECO:0000033	author statement supported by traceable reference	PMID:28655741	20220516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857300	Mpv17	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	PMID:10233845	20070128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857300	Mpv17	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	PMID:1696177	20070128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924105	Slc17a5	is_implicated_in	DOID:3659	sialuria		MGI:4440830	Slc17a5<sup>tm1Lex</sup>/Slc17a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20007460	20100420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179728	Hap1<sup>tm1Hay</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2670622	Hap1<sup>tm1Hay</sup>/Hap1<sup>tm1Hay</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11971876	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	is_implicated_in	DOID:9296	cleft lip		MGI:6315241	Irf6<sup>tm1Bcsl</sup>/Irf6<sup>tm1Bcsl</sup> Pitx2<sup>tm4(cre)Jfm</sup>/Pitx2<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:27369589	20190626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158235	Atp2a2<sup>tm1Ges</sup>	is_implicated_in	DOID:2734	keratosis follicularis		MGI:2655642	Atp2a2<sup>tm1Ges</sup>/Atp2a2<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11389134	20130610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101909	Gpr12	is_implicated_in	DOID:9970	obesity		MGI:3664276	Gpr12<sup>tm1Dgen</sup>/Gpr12<sup>tm1Dgen</sup>  [background:] B6.129P2-Gpr12<sup>tm1Dgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16887097	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95813	Grid2	is_implicated_in	DOID:0080042	autosomal recessive spinocerebellar ataxia 18		MGI:4949279	Grid2<sup>tm1(cre)Mwa</sup>/Grid2<sup>tm1(cre)Mwa</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24078737	20150508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95813	Grid2	is_implicated_in	DOID:0080042	autosomal recessive spinocerebellar ataxia 18		MGI:5635067	Grid2<sup>ho-15J</sup>/Grid2<sup>ho-15J</sup>  [background:] involves: C3HeB/Fe			ECO:0000033	author statement supported by traceable reference	PMID:24078737	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574985	Umod<sup>tm1Kuma</sup>	is_implicated_in	DOID:0060062	familial juvenile hyperuricemic nephropathy		MGI:3575012	Umod<sup>tm1Kuma</sup>/Umod<sup>tm1Kuma</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:15522986	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584174	Tsc1<sup>tm1Chdl</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3587766	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Balb/cOlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15888477	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584174	Tsc1<sup>tm1Chdl</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3587768	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C3H/HeNHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15888477	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584174	Tsc1<sup>tm1Chdl</sup>	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3587764	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15888477	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2663064	Mitf<sup>Mi-wh</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686996	Mitf<sup>Mi-H</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:78359	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919276	Trmu	is_implicated_in	DOID:409	liver disease		MGI:6108884	Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup> Trmu<sup>tm1Tomik</sup>/Trmu<sup>tm1Tomik</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:27689697	20180112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385681	Myd88<sup>tm1Aki</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3577712	Myd88<sup>tm1Aki</sup>/Myd88<sup>tm1Aki</sup>  [background:] B6.129P2-Myd88<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531502	Vps13a<sup>tm1Asan</sup>	is_implicated_in	DOID:0050766	choreaacanthocytosis		MGI:3573789	Vps13a<sup>tm1Asan</sup>/Vps13a<sup>tm1Asan</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15686477	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0110965	brachydactyly type A2		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055440	Tg(Crh)227.1Pbl	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:3580003	Tg(Crh)227.1Pbl/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1597149	20171210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3573782	Dmd<sup>tm1.1Khan</sup>/Y  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15694376	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6438177	Dmd<sup>em4Eno</sup>/Dmd<sup>em4Eno</sup>  [background:] C57BL/6-Dmd<sup>em4Eno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30854433	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6438180	Dmd<sup>em4Eno</sup>/Y  [background:] C57BL/6-Dmd<sup>em4Eno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30854433	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5897011	Dmd<sup>tm1Kmf</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26365037	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798788	Dmd<sup>mdx-5Cv</sup>/Dmd<sup>mdx-5Cv</sup>  [background:] B6Ros.Cg-Dmd<sup>mdx-5Cv</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16857961	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798621	Dmd<sup>mdx-5Cv</sup>/Y  [background:] B6Ros.Cg-Dmd<sup>mdx-5Cv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21893021	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798607	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21893021	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6163637	Dmd<sup>em1Eno</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29187645	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:2176880	Dmd<sup>Gt(ROSABetageo)1Mpd</sup>/Y  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:9626497	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:4359195	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19535499	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798607	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19535499	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3722314	Dmd<sup>tm1Mok</sup>/Y  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:9299538	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5688354	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] D2.B10-Dmd<sup>mdx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20304955	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:6394025	Dmd<sup>em#Tve</sup>/Y  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:31028078	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3621491	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6583703	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3789123	Dmd<sup>mdx</sup>/Y  [background:] C57BL/10ScSn-Dmd<sup>mdx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6583703	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:5697652	Dmd<sup>mdx</sup>/Dmd<sup>mdx</sup>  [background:] D2.B10-Dmd<sup>mdx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26566673	20200709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:11723	Duchenne muscular dystrophy		MGI:3798606	Dmd<sup>mdx-3Cv</sup>/Y  [background:] involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus			ECO:0000033	author statement supported by traceable reference	PMID:7843915	20200709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856363	Glrb<sup>spa</sup>	is_implicated_in	DOID:0060697	hyperekplexia 2		MGI:3695037	Glrb<sup>spa</sup>/Glrb<sup>spa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8733750	20120514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179754	Ank2<sup>tm1Bnt</sup>	is_implicated_in	DOID:12849	autistic disorder		MGI:6790245	Ank2<sup>tm1Bnt</sup>/Ank2<sup>tm1Bnt</sup>  [background:] B6.129-Ank2<sup>tm1Bnt</sup>/Bnt			ECO:0000033	author statement supported by traceable reference	PMID:31285321	20211102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4338023	Zdhhc13<sup>Gt(AC0492)Wtsi</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:5466506	Zdhhc13<sup>Gt(AC0492)Wtsi</sup>/Zdhhc13<sup>Gt(AC0492)Wtsi</sup>  [background:] FVB.129P2-Zdhhc13<sup>Gt(AC0492)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23077216	20130227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182576	Gli3<sup>tm1Urt</sup>	is_implicated_in	DOID:9248	Pallister-Hall syndrome		MGI:3700824	Gli3<sup>tm1Urt</sup>/Gli3<sup>tm1Urt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11978771	20070324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98730	Tgm1	is_implicated_in	DOID:0060656	autosomal recessive congenital ichthyosis 1		MGI:3029167	Tgm1<sup>tm1Kfyn</sup>/Tgm1<sup>tm1Kfyn</sup>  [background:] involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11805136	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98730	Tgm1	is_implicated_in	DOID:0060656	autosomal recessive congenital ichthyosis 1		MGI:3029167	Tgm1<sup>tm1Kfyn</sup>/Tgm1<sup>tm1Kfyn</sup>  [background:] involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9448282	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716756	Ar<sup>tm1.1Jdz</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3717256	Ar<sup>tm1.1Jdz</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17317769	20081107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716756	Ar<sup>tm1.1Jdz</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3717244	Ar<sup>tm1.1Jdz</sup>/Y  [background:] B6.129X1-Ar<sup>tm1.1Jdz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16326839	20081107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:4836620	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21262837	20110409	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	is_implicated_in	DOID:0081060	X-linked nephrogenic diabetes insipidus		MGI:7282305	Avpr2<sup>tm2.1Jwe</sup>/Y Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19729836	20220606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775189	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24520391	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775294	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24520391	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:2669003	Eng<sup>tm1Mle</sup>/Eng<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10562296	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:3628821	Eng<sup>tm1Mle</sup>/Eng<sup>+</sup>  [background:] 129P2/OlaHsd-Eng<sup>tm1Mle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10562296	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775189	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:2177905	Eng<sup>tm1Dyl</sup>/Eng<sup>tm1Dyl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10348742	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:3623404	Eng<sup>tm1Hma</sup>/Eng<sup>+</sup>  [background:] 129P2/OlaHsd-Eng<sup>tm1Hma</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10625534	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349392	Macroh2a1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:6726548	Macroh2a1<sup>tm1.1Oxbo</sup>/Macroh2a1<sup>tm1.1Oxbo</sup>  [background:] B6.Cg-Macroh2a1<sup>tm1.1Oxbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31439048	20210728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924025	Slc10a7	is_implicated_in	DOID:225	syndrome		MGI:6199708	Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>/Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30082715	20180926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3613050	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm1Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11230174	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3613050	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm1Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:20670678	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:6690698	Dhcr7<sup>tm1.1Sbpa</sup>/Dhcr7<sup>tm1.1Sbpa</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] B6.Cg-Dhcr7<sup>tm1.1Sbpa</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33410752	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3621458	Dhcr7<sup>tm2Fdp</sup>/Dhcr7<sup>tm2Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:16446309	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3621459	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm2Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:16446309	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3620629	Dhcr7<sup>tm1Gst</sup>/Dhcr7<sup>tm1Gst</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11560960	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97373	Npr3	is_implicated_in	DOID:0080001	bone disease		MGI:6269453	Npr3<sup>kylb</sup>/Npr3<sup>kylb</sup>  [background:] involves: BALB/c * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27959934	20181227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18439426	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23977107	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622060	Tnf<sup>tm2Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685641	Frem3	is_not_implicated_in	DOID:0090001	Fraser syndrome		MGI:6455426	Frem3<sup>em1Osb</sup>/Frem3<sup>em1Osb</sup>  [background:] involves: C57BL/6NJcl * DBA/2NJcl			ECO:0000033	author statement supported by traceable reference	PMID:31554749	20200916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180306	Nfkb2<sup>tm2Brv</sup>	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:4352675	Nfkb2<sup>tm2Brv</sup>/Nfkb2<sup>tm2Brv</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4329496	Lrsam1<sup>Gt(RRK461)Byg</sup>	is_implicated_in	DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P		MGI:5496257	Lrsam1<sup>Gt(RRK461)Byg</sup>/Lrsam1<sup>Gt(RRK461)Byg</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:23519028	20130723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445723	Mmp14<sup>tm1Hbh</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3583010	Mmp14<sup>tm1Hbh</sup>/Mmp14<sup>tm1Hbh</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10520996	20050805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:0110910	leukocyte adhesion deficiency 1		MGI:2651618	Itgb2<sup>tm2Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9653089	20050808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:0110910	leukocyte adhesion deficiency 1		MGI:2651379	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8101543	20050808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:0110910	leukocyte adhesion deficiency 1		MGI:3583131	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8101543	20050808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98958	Wnt5a	is_implicated_in	DOID:0060254	Robinow syndrome		MGI:5648028	Wnt5a<sup>b2b3077.1Clo</sup>/Wnt5a<sup>b2b3077.1Clo</sup>  [background:] C57BL/6J-Wnt5a<sup>b2b3077.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857034	Foxp3<sup>sf</sup>	is_not_implicated_in	DOID:1700	X-linked ichthyosis		MGI:3589925	Foxp3<sup>sf</sup>/Y  [background:] either: 129Rl.Cg-Foxp3<sup>sf</sup> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)			ECO:0000033	author statement supported by traceable reference	PMID:2053595	20051019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857034	Foxp3<sup>sf</sup>	is_not_implicated_in	DOID:1700	X-linked ichthyosis		MGI:3589923	Foxp3<sup>sf</sup>/Y  [background:] involves: STOCK MR			ECO:0000033	author statement supported by traceable reference	MGI:62253	20051019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528558	Csmd1<sup>tm1Lex</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5574284	Csmd1<sup>tm1Lex</sup>/Csmd1<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:24244513	20140723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158807	Fkbp1a<sup>tm1Zuk</sup>	is_implicated_in	DOID:0050476	Barth syndrome		MGI:3622103	Fkbp1a<sup>tm1Zuk</sup>/Fkbp1a<sup>tm1Zuk</sup>  [background:] either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9461216	20060512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:7816342	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:2175225	Otc<sup>spf</sup>/Otc<sup>spf</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:1575747	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:1575747	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850173	Otc<sup>spf</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1531355	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3851105	Otc<sup>spf</sup>/Y  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8750014	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850182	Otc<sup>spf</sup>/Y  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8041507	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850111	Otc<sup>spf</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7707692	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856178	Otc<sup>spf</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3850111	Otc<sup>spf</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:3981356	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856157	Pax6<sup>Sey-Dey</sup>	is_not_implicated_in	DOID:14515	WAGR syndrome		MGI:2175204	Pax6<sup>Sey-Dey</sup>/Pax6<sup>+</sup>  [background:] C3H/HeJ-Pax6<sup>Sey-Dey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2173141	20071019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106594	Gk	is_implicated_in	DOID:0060363	glycerol kinase deficiency		MGI:3623584	Gk<sup>tm1Wjc</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16105550	20060531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106594	Gk	is_implicated_in	DOID:0060363	glycerol kinase deficiency		MGI:3623584	Gk<sup>tm1Wjc</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9302256	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180473	Tfap2b<sup>tm1Rbu</sup>	is_implicated_in	DOID:0060563	Char syndrome		MGI:5292663	Tfap2b<sup>tm1Rbu</sup>/Tfap2b<sup>tm1Rbu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21829553	20111020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154689	Col11a2<sup>tm1Mne</sup>	is_implicated_in	DOID:0110545	autosomal dominant nonsyndromic deafness 13		MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889844	Sumf1	is_implicated_in	DOID:0050441	mucosulfatidosis		MGI:3713764	Sumf1<sup>Gt(RST760)Byg</sup>/Sumf1<sup>Gt(RST760)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17360554	20070705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	is_implicated_in	DOID:3652	Leigh disease		MGI:4818648	Ndufs4<sup>tm1Rpa</sup>/Ndufs4<sup>tm1Rpa</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20534480	20130124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	is_implicated_in	DOID:3652	Leigh disease		MGI:5451011	Ndufs4<sup>tm1.1Rpa</sup>/Ndufs4<sup>tm1.1Rpa</sup>  [background:] B6.129S4-Ndufs4<sup>tm1.1Rpa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22653057	20130124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	is_implicated_in	DOID:3652	Leigh disease		MGI:5451025	Ndufs4<sup>tm1Rpa</sup>/Ndufs4<sup>tm1Rpa</sup> Tg(Nes-cre)1Kln/0  [background:] B6.Cg-Tg(Nes-cre)1Kln Ndufs4<sup>tm1Rpa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22653057	20130124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3815301	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Pax8-rtTA2S*M2)1Koes/0 Tg(tetO-cre)LC1Bjd/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18724376	20110502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857787	Morc1<sup>Tg(Tyr)1Az</sup>	is_implicated_in	DOID:1595	melancholic depression		MGI:5766068	Morc1<sup>Tg(Tyr)1Az</sup>/Morc1<sup>Tg(Tyr)1Az</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26275923	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794294	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] B6.Cg-Pmp22<sup>Tr-J</sup> Krt25<sup>Re</sup>/+ +/J			ECO:0000033	author statement supported by traceable reference	PMID:15363066	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794288	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15703401	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794294	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] B6.Cg-Pmp22<sup>Tr-J</sup> Krt25<sup>Re</sup>/+ +/J			ECO:0000033	author statement supported by traceable reference	PMID:1303281	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794288	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1303281	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687368	Txnip<sup>Hyplip1</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3719416	Txnip<sup>Hyplip1</sup>/Txnip<sup>Hyplip1</sup>  [background:] involves: CAST/Ei * HcB19/Dem			ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687368	Txnip<sup>Hyplip1</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3719414	Txnip<sup>Hyplip1</sup>/Txnip<sup>Hyplip1</sup>  [background:] HcB19/Dem-Txnip<sup>Hyplip1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687368	Txnip<sup>Hyplip1</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3719415	Txnip<sup>Hyplip1</sup>/Txnip<sup>+</sup>  [background:] involves: CAST/Ei * HcB19/Dem			ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3586912	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3586915	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3586914	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3587029	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>tm1Bem</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3850161	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15385444	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3619802	Tbx1<sup>tm2.1Bem</sup>/Tbx1<sup>tm2.2Bem</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129 * C57BL/6J * SJL * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:16600992	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3587028	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11239417	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510313	Tbx1<sup>tm1.1Dsr</sup>/Tbx1<sup>+</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510311	Tbx1<sup>tm1Dsr</sup>/Tbx1<sup>+</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510312	Tbx1<sup>tm1Dsr</sup>/Tbx1<sup>tm1Dsr</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510314	Tbx1<sup>tm1.1Dsr</sup>/Tbx1<sup>tm1.1Dsr</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3619802	Tbx1<sup>tm2.1Bem</sup>/Tbx1<sup>tm2.2Bem</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129 * C57BL/6J * SJL * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:16452092	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3610986	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242049	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3610987	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm1Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11242049	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046798	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046797	Tbx1<sup>tm2Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046803	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm3Bld</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046805	Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup> Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm3Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046796	Tbx1<sup>tm2Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20130130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046801	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm3Bld</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20130130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857881	plt	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4437582	plt/plt  [background:] either: B6.DDD-plt or C.DDD-plt			ECO:0000033	author statement supported by traceable reference	PMID:16473829	20100319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890619	Gan	is_implicated_in	DOID:0090068	giant axonal neuropathy 1		MGI:3616169	Gan<sup>tm1Yany</sup>/Gan<sup>tm1Yany</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16565160	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890619	Gan	is_implicated_in	DOID:0090068	giant axonal neuropathy 1		MGI:3812458	Gan<sup>tm1Jpj</sup>/Gan<sup>tm1Jpj</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18680552	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890619	Gan	is_implicated_in	DOID:0090068	giant axonal neuropathy 1		MGI:3616169	Gan<sup>tm1Yany</sup>/Gan<sup>tm1Yany</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16303566	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	is_implicated_in	DOID:674	cleft palate		MGI:7286375	Specc1l<sup>em3Kumc</sup>/Specc1l<sup>+</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	is_implicated_in	DOID:674	cleft palate		MGI:7286374	Specc1l<sup>em4Kumc</sup>/Specc1l<sup>+</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12818570	20210927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12142349	20210927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818340	Tdp1<sup>Gt(XD105)Byg</sup>	is_implicated_in	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1		MGI:3818341	Tdp1<sup>Gt(XD105)Byg</sup>/Tdp1<sup>Gt(XD105)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17914460	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442875	Adamts19	is_implicated_in	DOID:62	aortic valve disease		MGI:6437232	Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>/Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>  [background:] B6N(Cg)-Adamts19<sup>tm4b(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31844321	20210427	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442875	Adamts19	is_implicated_in	DOID:62	aortic valve disease		MGI:6695122	Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>/Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Adamts19<sup>tm4a(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31844321	20210427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3779035	Lyst<sup>bg-Btlr</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3779036	Lyst<sup>bg-Btlr</sup>/Lyst<sup>bg-Btlr</sup>  [background:] C57BL/6J-Lyst<sup>bg-Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778945	20080428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	is_implicated_in	DOID:13608	biliary atresia		MGI:6113926	Sox17<sup>tm1Ysk</sup>/Sox17<sup>+</sup>  [background:] B6.129S1-Sox17<sup>tm1Ysk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28432216	20180202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	is_implicated_in	DOID:13608	biliary atresia		MGI:6113926	Sox17<sup>tm1Ysk</sup>/Sox17<sup>+</sup>  [background:] B6.129S1-Sox17<sup>tm1Ysk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23293295	20180202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918112	Spata16	is_implicated_in	DOID:12336	male infertility		MGI:6162247	Spata16<sup>em2Osb</sup>/Spata16<sup>em2Osb</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:29065458	20180625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:9256	colorectal cancer		MGI:4358091	Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:22820288	20130110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913610	Bbip1	is_implicated_in	DOID:0110140	Bardet-Biedl syndrome 18		MGI:5563481	Bbip1<sup>tm1.1Gne</sup>/Bbip1<sup>tm1.1Gne</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24316073	20141028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:5617140	Fmr1<sup>tm1Usdn</sup>/Fmr1<sup>tm1Usdn</sup>  [background:] B6.129S6(Cg)-Fmr1<sup>tm1Usdn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22470123	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366442	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:16055059	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:2665401	Fmr1<sup>tm1Cgr</sup>/Fmr1<sup>tm1Cgr</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:16055059	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:3604219	Fmr1<sup>tm1.1Cidz</sup>/Fmr1<sup>tm1.1Cidz</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16055059	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366442	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8844056	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:2665400	Fmr1<sup>tm1Cgr</sup>/Fmr1<sup>tm1Cgr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8033209	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366351	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8033209	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4950076	Fmr1<sup>tm1Usdn</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21220020	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:6715340	Fmr1<sup>tm1.1Ics</sup>/Fmr1<sup>tm1.1Ics</sup>  [background:] C57BL/6-Fmr1<sup>tm1.1Ics</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33692361	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4366351	Fmr1<sup>tm1Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25153086	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4415714	Fmr1<sup>tm1Rbd</sup>/Y  [background:] B6.129-Fmr1<sup>tm1Rbd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20011099	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:14261	fragile X syndrome		MGI:5292357	Fmr1<sup>tm1.2Cidz</sup>/Y  [background:] involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19103683	20210614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667379	Trpv4<sup>tm1Msz</sup>	is_implicated_in	DOID:0110555	autosomal dominant nonsyndromic deafness 25		MGI:2669172	Trpv4<sup>tm1Msz</sup>/Trpv4<sup>tm1Msz</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15925108	20070112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712802	Eng<sup>tm2.1Hma</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775189	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712802	Eng<sup>tm2.1Hma</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775189	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24520391	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712802	Eng<sup>tm2.1Hma</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775294	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24520391	20160607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182312	Lat<sup>tm1.1Mal</sup>	is_implicated_in	DOID:0080356	IgG4-related disease		MGI:2385971	Lat<sup>tm1.1Mal</sup>/Lat<sup>tm1.1Mal</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:29902238	20191122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861634	Clock<sup>m1Jt</sup>	is_implicated_in	DOID:9351	diabetes mellitus		MGI:5576784	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20562852	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857441	Il1r1<sup>tm1Roml</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3622312	Il1r1<sup>tm1Roml</sup>/Il1r1<sup>tm1Roml</sup>  [background:] NOD.Cg-Il1r1<sup>tm1Roml</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14693705	20060531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3043224	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3043197	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>tm1.1Kry</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:5578346	Rps6ka3<sup>tm1.1Kry</sup>/Y  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15109498	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:5529680	Rps6ka3<sup>tm1.1Kry</sup>/Rps6ka3<sup>tm1.1Kry</sup>  [background:] B6.129X1(Cg)-Rps6ka3<sup>tm1.1Kry</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23742761	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:5578346	Rps6ka3<sup>tm1.1Kry</sup>/Y  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24416220	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3042280	Rps6ka3<sup>tm1Ljg</sup>/Y  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11113183	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3042280	Rps6ka3<sup>tm1Ljg</sup>/Y  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12765942	20140822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:3037831	Gjb6<sup>tm1Kwi</sup>/Gjb6<sup>tm1Kwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12490528	20101221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:4848186	Gjb6<sup>tm1.1Fama</sup>/Gjb6<sup>tm1.1Fama</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20858605	20101221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442760	Katnip	is_implicated_in	DOID:0110995	Joubert syndrome 26		MGI:5883451	Katnip<sup>Gt(RRG309)Byg</sup>/Katnip<sup>Gt(RRG309)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26714646	20170419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924290	Atg16l1	is_implicated_in	DOID:0110885	inflammatory bowel disease 10		MGI:3818604	Atg16l1<sup>Gt(XR0164)Wtsi</sup>/Atg16l1<sup>Gt(XR0164)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18849966	20081208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924290	Atg16l1	is_implicated_in	DOID:0110885	inflammatory bowel disease 10		MGI:3818603	Atg16l1<sup>Gt(BC0122)Wtsi</sup>/Atg16l1<sup>Gt(BC0122)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18849966	20081208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445442	Tg(GFAP-Hras1)2Agu	is_implicated_in	DOID:3069	malignant astrocytoma		MGI:5286097	Tg(GFAP-Hras1)2Agu/Tg(GFAP-Hras1)2Agu  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11325859	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934892	Hspg2<sup>tm1Ref</sup>	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12142349	20210927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934892	Hspg2<sup>tm1Ref</sup>	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12818570	20210927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2176762	Nf1<sup>tm1Cbr</sup>/Nf1<sup>tm1Cbr</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11279521	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:6275135	Nf1<sup>tm1.1Kest</sup>/Nf1<sup>tm1c(KOMP)Wtsi</sup> Tg(Dhh-cre)1Mejr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * C57BL/6NTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27482814	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:6275138	Nf1<sup>tm1c(KOMP)Wtsi</sup>/Nf1<sup>tm1c(KOMP)Wtsi</sup> Tg(Dhh-cre)1Mejr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27482814	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2175141	Nf1<sup>tm1Fcr</sup>/Nf1<sup>tm1Fcr</sup>  [background:] either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7926784	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3580056	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9054942	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2176767	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11297510	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:5493228	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:22868293	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:5492109	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:21478499	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:6283591	Nf1<sup>Mhdadsk9</sup>/Nf1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30571760	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3810648	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Fabp7-cre,-lacZ)3Gtm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18614544	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3710237	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3710235	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Mpz-cre)94Imeg/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:3710236	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Pax3-cre)1Joe/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12469121	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:4838320	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Fcr</sup> Tg(GFAP-cre)#Gtm/0  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20600672	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:10754	otitis media		MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105953	Hfm	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:2181997	Hfm/Hfm<sup>+</sup>  [background:] involves: SWV-Mbp<sup>shi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7531669	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	is_implicated_in	DOID:10871	age related macular degeneration		MGI:6389045	Ppargc1a<sup>tm1Brsp</sup>/Ppargc1a<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29925537	20200207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99913	Lamc2	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:4440827	Lamc2<sup>jeb</sup>/Lamc2<sup>jeb</sup>  [background:] 129X1/SvJ-Lamc2<sup>jeb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20336083	20100420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050956	spinocerebellar ataxia type 6		MGI:6278003	Cacna1a<sup>tm3Hzo</sup>/Cacna1a<sup>tm3Hzo</sup>  [background:] B6.129S7-Cacna1a<sup>tm3Hzo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26730403	20190213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050956	spinocerebellar ataxia type 6		MGI:5500085	Cacna1a<sup>smrl</sup>/Cacna1a<sup>smrl</sup>  [background:] CXB10/HiAJ-Cacna1a<sup>smrl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20190213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	is_implicated_in	DOID:0111077	pyruvate kinase deficiency of red cells		MGI:5433725	Pklr<sup>slc</sup>/Pklr<sup>slc</sup>  [background:] CBA/NSlc-Pklr<sup>slc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7579416	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	is_implicated_in	DOID:0111077	pyruvate kinase deficiency of red cells		MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14595440	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888773	Prnp<sup>tm1Cwe</sup>	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174709	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1373228	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928948	Scamp5	is_implicated_in	DOID:1826	epilepsy		MGI:6441509	Scamp5<sup>tm1Smoc</sup>/Scamp5<sup>tm1Smoc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32020363	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856982	Bloc1s6<sup>pa</sup>	is_implicated_in	DOID:0060547	Hermansky-Pudlak syndrome 9		MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25477496	20151231	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5824119	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25155956	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5641393	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] B6J.129S4-Tsc2<sup>tm1Tno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857708	Blm<sup>tm1Ches</sup>	is_implicated_in	DOID:2717	Bloom syndrome		MGI:2683844	Blm<sup>tm1Ches</sup>/Blm<sup>tm1Ches</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9808625	20050919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856987	Nphp3<sup>pcy</sup>	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3583125	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856987	Nphp3<sup>pcy</sup>	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3583121	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] KK-Nphp3<sup>pcy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3712587	20190712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856987	Nphp3<sup>pcy</sup>	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3583124	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] either: D2.KK-Nphp3<sup>pcy</sup> or (involves: DBA/2Fg * DBA/2J * KK)			ECO:0000033	author statement supported by traceable reference	PMID:1883968	20190712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926484	Itgb6<sup>tm1Des</sup>	is_implicated_in	DOID:2841	asthma		MGI:2175082	Itgb6<sup>tm1Des</sup>/Itgb6<sup>tm1Des</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8666675	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919019	Bbs10	is_implicated_in	DOID:0110132	Bardet-Biedl syndrome 10		MGI:5792863	Bbs10<sup>tm1.2Vmar</sup>/Bbs10<sup>tm1.2Vmar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26273430	20160922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926484	Itgb6<sup>tm1Des</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3581437	Itgb6<sup>tm1Des</sup>/Itgb6<sup>tm1Des</sup>  [background:] involves: 129T2/SvEms			ECO:0000033	author statement supported by traceable reference	PMID:12634787	20050712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5463439	b2b1456Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5463447	b2b1456Clo/b2b1456Clo  [background:] C57BL/6J-b2b1456Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857813	Edar<sup>Tg(OVE1B)Ove</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3717687	Edar<sup>Tg(OVE1B)Ove</sup>/Edar<sup>Tg(OVE1B)Ove</sup>  [background:] involves: C3H * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10431242	20070809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923810	Prss8	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3722899	Prss8<sup>tm1.1Hum</sup>/Prss8<sup>tm1.2Hum</sup> Tg(KRT14-cre)1Ipc/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16061697	20070927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154548	Cdh23<sup>v-2J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3581028	Cdh23<sup>v-2J</sup>/Cdh23<sup>v-2J</sup>  [background:] B6(V)-Cdh23<sup>v-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11138008	20090504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441787	Washc4	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:6783465	Washc4<sup>em1Ssod</sup>/Washc4<sup>em1Ssod</sup>  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:33749590	20211029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449789	Musk<sup>tm1Vwi</sup>	is_implicated_in	DOID:0110670	congenital myasthenic syndrome 9		MGI:3622117	Musk<sup>tm1Vwi</sup>/Musk<sup>tm1Vwi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16337809	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856197	Eda<sup>Ta</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3711694	Eda<sup>Ta</sup>/Y  [background:] involves: A * C57BL * CBA * RIII			ECO:0000033	author statement supported by traceable reference	PMID:2348861	20170104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856197	Eda<sup>Ta</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:4459458	Eda<sup>Ta</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:27590203	20170104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:3699817	Fgfr2<sup>tm1Schl</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:17132737	20161025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:3053579	Fgfr2<sup>tm4Lni</sup>/Fgfr2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25966306	20161025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:4461806	Fgfr2<sup>m1Sgg</sup>/Fgfr2<sup>m1Sgg</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20503384	20161025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:4461807	Fgfr2<sup>m1Sgg</sup>/Fgfr2<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20503384	20161025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:3053579	Fgfr2<sup>tm4Lni</sup>/Fgfr2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15316116	20161025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	is_implicated_in	DOID:2129	atypical teratoid rhabdoid tumor		MGI:3603677	Smarcb1<sup>tm1Gvk</sup>/Smarcb1<sup>tm1Gvk</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:16099835	20140205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	is_implicated_in	DOID:2129	atypical teratoid rhabdoid tumor		MGI:5538531	Smarcb1<sup>tm1Sho</sup>/Smarcb1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:17409406	20140205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:3513833	Gars1<sup>Nmf249</sup>/Gars1<sup>+</sup>  [background:] C57BL/6J-Gars1<sup>Nmf249</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16982418	20200305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:3849420	Gars1<sup>C201R</sup>/Gars1<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19470612	20200305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:3849420	Gars1<sup>C201R</sup>/Gars1<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22144914	20200305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:5308205	Gars1<sup>Nmf249</sup>/Gars1<sup>+</sup>  [background:] involves: C57BL/6J * CAST/Ei			ECO:0000033	author statement supported by traceable reference	PMID:22144914	20200305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	is_implicated_in	DOID:0110164	Charcot-Marie-Tooth disease type 2D		MGI:6393320	Gars1<sup>em1Rwb</sup>/Gars1<sup>em2Rwb</sup>  [background:] involves: C57BL/6NJ * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:31557132	20200305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102523	Pou4f3	is_not_implicated_in	DOID:0110546	autosomal dominant nonsyndromic deafness 15		MGI:3688923	Pou4f3<sup>tm1Rsd</sup>/Pou4f3<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10452377	20061129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96175	Hoxa3	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3033772	Hoxa3<sup>tm1Mrc</sup>/Hoxa3<sup>tm1Mrc</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:1673020	20050701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:14669	acrodysostosis		MGI:6682080	Prkar1a<sup>tm1.1Geno</sup>/Prkar1a<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27589370	20210409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604604	Lrp5<sup>tm1Dgen</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:4946082	Lrp5<sup>tm1Dgen</sup>/Lrp5<sup>tm1Dgen</sup>  [background:] B6.129P2-Lrp5<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27524797	20230428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604604	Lrp5<sup>tm1Dgen</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:3606583	Lrp5<sup>tm1Dgen</sup>/Lrp5<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96160	Hmga1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583951	Hmga1<sup>tm1Brun</sup>/Hmga1<sup>tm1Brun</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15924147	20050819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96160	Hmga1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583952	Hmga1<sup>tm1Brun</sup>/Hmga1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15924147	20050819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	is_implicated_in	DOID:0050681	Borjeson-Forssman-Lehmann syndrome		MGI:6295127	Phf6<sup>em1Azbi</sup>/Y  [background:] B6.Cg-Phf6<sup>em1Azbi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30403997	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	is_implicated_in	DOID:0050681	Borjeson-Forssman-Lehmann syndrome		MGI:6507205	Phf6<sup>tm1.2Avo</sup>/Y  [background:] involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:32994169	20210219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861705	Itgb2<sup>tm2Bay</sup>	is_implicated_in	DOID:0110910	leukocyte adhesion deficiency 1		MGI:2651618	Itgb2<sup>tm2Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9653089	20050808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177753	Htt<sup>tm2.1Pfs</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698754	Htt<sup>tm2.1Pfs</sup>/Htt<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10196365	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926439	Gfra1<sup>tm1Jmi</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2175040	Gfra1<sup>tm1Jmi</sup>/Gfra1<sup>tm1Jmi</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9728913	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	is_implicated_in	DOID:0111142	oligomeganephronia		MGI:2176707	Bcl2<sup>tm1Dlo</sup>/Bcl2<sup>tm1Dlo</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9794553	20180726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386969	Cps1<sup>tm1Mw</sup>	is_implicated_in	DOID:9280	carbamoyl phosphate synthetase I deficiency disease		MGI:3641098	Cps1<sup>tm1Mw</sup>/Cps1<sup>tm1Mw</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9862865	20060817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856226	Slc45a2<sup>uw-bls</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668607	Slc45a2<sup>uw-bls</sup>/Slc45a2<sup>uw-bls</sup>  [background:] wild Corsican mouse			ECO:0000033	author statement supported by traceable reference	MGI:61984	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856319	Ar<sup>Tfm</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:2665793	Ar<sup>Tfm</sup>/Y  [background:] STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>/+ +			ECO:0000033	author statement supported by traceable reference	PMID:5452809	20081118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856319	Ar<sup>Tfm</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3815199	Ar<sup>Tfm</sup>/Y  [background:] involves: NMRI * STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856319	Ar<sup>Tfm</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:2674328	Ar<sup>Tfm</sup>/Y  [background:] involves: STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107735	Myo9a	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6681843	Myo9a<sup>em1Atuf</sup>/Myo9a<sup>+</sup>  [background:] C57BL/6J-Myo9a<sup>em1Atuf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33412162	20210408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:8398	osteoarthritis		MGI:3758631	Gdf5<sup>Rgsc451</sup>/Gdf5<sup>Rgsc451</sup>  [background:] C57BL/6JJcl-Gdf5<sup>Rgsc451</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17656374	20071018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3771723	Rpe65<sup>tm1Lrcb</sup>	is_implicated_in	DOID:0110353	retinitis pigmentosa 20		MGI:3771806	Rpe65<sup>tm1Lrcb</sup>/Rpe65<sup>tm1Lrcb</sup>  [background:] 129S6/SvEvTac-Rpe65<sup>tm1Lrcb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17933883	20110509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667341	Ywhae<sup>tm1Awb</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2670755	Ywhae<sup>tm1Awb</sup>/Ywhae<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:12796778	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711057	Tg(HLA-A/H2-D/B2M)1Dvs	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3711108	Tg(HLA-A/H2-D/B2M)1Dvs/0  [background:] NOD/ShiLtDvs-Tg(HLA-A/H2-D/B2M)1Dvs			ECO:0000033	author statement supported by traceable reference	PMID:16493087	20070606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604561	Slc9a6<sup>tm1Dgen</sup>	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902076	Slc9a6<sup>tm1Dgen</sup>/Slc9a6<sup>+</sup>  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26515654	20181030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604561	Slc9a6<sup>tm1Dgen</sup>	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26515654	20181030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604561	Slc9a6<sup>tm1Dgen</sup>	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:29349289	20181030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604561	Slc9a6<sup>tm1Dgen</sup>	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21964919	20181030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604561	Slc9a6<sup>tm1Dgen</sup>	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902072	Slc9a6<sup>tm1Dgen</sup>/Slc9a6<sup>tm1Dgen</sup>  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21964919	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6256432	Nlrp3<sup>tm1Bhk</sup>/Nlrp3<sup>tm1Bhk</sup>  [background:] B6.129S6-Nlrp3<sup>tm1Bhk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28939830	20190117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88373	Cebpb	is_implicated_in	DOID:934	viral infectious disease		MGI:2174941	Cebpb<sup>tm1Vpo</sup>/Cebpb<sup>tm1Vpo</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:7744000	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933331	Elovl4	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3696675	Elovl4<sup>tm1Rayy</sup>/Elovl4<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17003453	20070613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933331	Elovl4	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3711534	Elovl4<sup>tm1Wked</sup>/Elovl4<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:17356513	20070613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528836	Trpm3<sup>tm1Lex</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:6727363	Trpm3<sup>tm1Lex</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:2166570	Ednra<sup>tm1Ywa</sup>/Ednra<sup>tm1Ywa</sup>  [background:] 129S/SvEv-Ednra<sup>tm1Ywa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9449664	20050622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2451311	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: 101 * C3H/He * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:9344762	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2168108	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2169285	Pax3<sup>Sp-2H</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2451350	Pax3<sup>Sp-d</sup>/Pax3<sup>+</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	is_implicated_in	DOID:0110184	Charcot-Marie-Tooth disease type 4J		MGI:3717180	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup>  [background:] involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17572665	20070806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028848	Tg(aP2-SREBF1c)9884Reh	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:3028851	Tg(aP2-SREBF1c)9884Reh/0  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9784493	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056564	Crebbp<sup>tm1.2Ltz</sup>	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:4941348	Crebbp<sup>tm1.2Ltz</sup>/Crebbp<sup>tm1.2Ltz</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: 129P2/OlaHsd * BALB/c * C57BL * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21289174	20110317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4123901	Eif4h<sup>Gt(Ex279)Byg</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5314953	Eif4h<sup>Gt(Ex279)Byg</sup>/Eif4h<sup>Gt(Ex279)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22234171	20120412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856089	Mitf<sup>mi-bw</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:5635983	Mitf<sup>mi-bw</sup>/Mitf<sup>mi-bw</sup> Tg(Dct-lacZ)A12Jkn/0  [background:] involves: C3H * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22563733	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	is_implicated_in	DOID:0060691	platelet-type bleeding disorder 16		MGI:2177829	Itgb3<sup>tm1Hyn</sup>/Itgb3<sup>tm1Hyn</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9916135	20070926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349429	Arl2bp	is_implicated_in	DOID:12336	male infertility		MGI:6377057	Arl2bp<sup>em1Visu</sup>/Arl2bp<sup>em1Visu</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31425546	20191115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861669	Ccw	is_implicated_in	DOID:83	cataract		MGI:2175749	Ccw/Ccw<sup>+</sup>  [background:] involves: unpedigreed stock			ECO:0000033	author statement supported by traceable reference	PMID:8812411	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861669	Ccw	is_implicated_in	DOID:83	cataract		MGI:2175749	Ccw/Ccw<sup>+</sup>  [background:] involves: unpedigreed stock			ECO:0000033	author statement supported by traceable reference	PMID:11062307	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179530	Cfc1<sup>tm1Mms</sup>	is_implicated_in	DOID:0060856	right atrial isomerism		MGI:3043046	Cfc1<sup>tm1Mms</sup>/Cfc1<sup>tm1Mms</sup>  [background:] either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10521397	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850496	Tg(Lck-Tslp)1Chea	is_implicated_in	DOID:2917	cryoglobulinemia		MGI:3850502	Tg(Lck-Tslp)1Chea/0  [background:] B6.Cg-Tg(Lck-Tslp)1Chea			ECO:0000033	author statement supported by traceable reference	PMID:11733384	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4457496	Sav1<sup>tm2.1Dlim</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4457497	Sav1<sup>tm2.1Dlim</sup>/Sav1<sup>tm2.1Dlim</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:26131558	20170208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276523	Ncoa1	is_implicated_in	DOID:9970	obesity		MGI:3664551	Ncoa1<sup>tm1.1Hkaw</sup>/Ncoa1<sup>tm1.1Hkaw</sup>  [background:] B6.Cg-Ncoa1<sup>tm1.1Hkaw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15312245	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435559	Porcn<sup>tm1Vdv</sup>/Porcn<sup>+</sup>  [background:] chimera involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435568	Porcn<sup>tm1.1Vdv</sup>/Y Tg(KRT14-cre)1Efu/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435562	Porcn<sup>tm1.1Vdv</sup>/Y Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435567	Porcn<sup>tm1.1Vdv</sup>/Y Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435565	Porcn<sup>tm1.1Vdv</sup>/Porcn<sup>+</sup> Hprt1<sup>tm1(CAG-cre)Mnn</sup>/Hprt1<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435560	Porcn<sup>tm1Vdv</sup>/Y  [background:] chimera involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5435561	Porcn<sup>tm1.1Vdv</sup>/Porcn<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22412863	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5049887	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>+</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21768372	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368182	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>tm1.2Lcm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368188	Porcn<sup>tm1.2Lcm</sup>/Porcn<sup>tm1.2Lcm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368183	Porcn<sup>tm1.1Lcm</sup>/Y Tg(rx3-icre)1Mjam/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368181	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>tm1.2Lcm</sup> Tg(Six3-cre)69Frty/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368185	Porcn<sup>tm1.1Lcm</sup>/Y H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368186	Porcn<sup>tm1.1Lcm</sup>/Y H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3054643	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9796923	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3054644	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] B6.129S2-Pdcd1<sup>tm1Hon</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10485649	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107932	Ndufs6	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:5428952	Ndufs6<sup>Gt(AR0138)Wtsi</sup>/Ndufs6<sup>Gt(AR0138)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22474353	20120726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3580298	Best3	is_implicated_in	DOID:0080685	aortic dissection		MGI:7536982	Best3<sup>tm1.1Zhoj</sup>/Best3<sup>tm1.1Zhoj</sup> Tg(Tagln-cre)1Her/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:37203562	20231005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	is_implicated_in	DOID:0111169	subcortical band heterotopia		MGI:6473560	Eml1<sup>tm1.2Ics</sup>/Eml1<sup>tm1.2Ics</sup>  [background:] C57BL/6N-Eml1<sup>tm1.2Ics</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31173351	20210418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	is_implicated_in	DOID:0111169	subcortical band heterotopia		MGI:6690862	Eml1<sup>tvrm360</sup>/Eml1<sup>tvrm360</sup>  [background:] C57BL/6J-Eml1<sup>tvrm360</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:32221352	20210418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4214000	Hspd1<sup>Gt(OST171441)Lex</sup>	is_implicated_in	DOID:0110766	hereditary spastic paraplegia 13		MGI:5516348	Hspd1<sup>Gt(OST171441)Lex</sup>/Hspd1<sup>+</sup>  [background:] B6.129S5-Hspd1<sup>Gt(OST171441)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23466696	20131106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849002	Fgfrl1<sup>tm1.1Ptew</sup>	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome		MGI:3849030	Fgfrl1<sup>tm1.1Ptew</sup>/Fgfrl1<sup>tm1.1Ptew</sup>  [background:] B6.129-Fgfrl1<sup>tm1.1Ptew</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19383940	20090626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:4412050	Nfkb2<sup>Lym1</sup>/Nfkb2<sup>Lym1</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:4412047	Nfkb2<sup>Lym1</sup>/Nfkb2<sup>+</sup>  [background:] BALB/c-Nfkb2<sup>Lym1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:4352675	Nfkb2<sup>tm2Brv</sup>/Nfkb2<sup>tm2Brv</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859635	Prickle3	is_implicated_in	DOID:0111754	Leber plus disease		MGI:6514802	Prickle3<sup>em1Mxg</sup>/Y  [background:] C57BL/6JSlacc-Prickle3<sup>em1Mxg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32516135	20210402	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859635	Prickle3	is_implicated_in	DOID:0111754	Leber plus disease		MGI:6514801	Prickle3<sup>em1Mxg</sup>/Prickle3<sup>em1Mxg</sup>  [background:] C57BL/6JSlacc-Prickle3<sup>em1Mxg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32516135	20210402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033462	Hfe<sup>tm3Sly</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033469	Hfe<sup>tm3Sly</sup>/Hfe<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447406	Sod2<sup>tm1Shs</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907999	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195081	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451328	Stat3<sup>tm1Flv</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2683230	Stat3<sup>tm1Flv</sup>/Stat3<sup>tm1Flv</sup> Tg(Tek-cre)1Xyfu/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14623907	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451328	Stat3<sup>tm1Flv</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3783296	Stat3<sup>tm1Flv</sup>/Stat3<sup>tm1Flv</sup> Tg(Tek-cre)12Flv/0  [background:] involves: 129 * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12571365	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1274784	Adgrv1	is_implicated_in	DOID:0110839	Usher syndrome type 2C		MGI:3527887	Adgrv1<sup>tm1Msat</sup>/Adgrv1<sup>tm1Msat</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17567809	20070821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1274784	Adgrv1	is_implicated_in	DOID:0110839	Usher syndrome type 2C		MGI:3046274	Adgrv1<sup>tm1Pwh</sup>/Adgrv1<sup>tm1Pwh</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16775142	20070821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:0110112	atrial heart septal defect 7		MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:0110112	atrial heart septal defect 7		MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714802	Lmx1b<sup>tm4.1Rjo</sup>	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3715141	Lmx1b<sup>tm4.1Rjo</sup>/Lmx1b<sup>tm4.1Rjo</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17316599	20070718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	is_implicated_in	DOID:0112061	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia		MGI:6473858	Rac2<sup>em1Shl</sup>/Rac2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30723080	20210909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96929	Mc3r	is_implicated_in	DOID:9970	obesity		MGI:3639355	Mc3r<sup>tm1Cone</sup>/Mc3r<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10965927	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96929	Mc3r	is_implicated_in	DOID:9970	obesity		MGI:3639354	Mc3r<sup>tm1Cone</sup>/Mc3r<sup>tm1Cone</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10965927	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5431571	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19805914	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5431572	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19805914	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:4398918	Acvrl1<sup>tm2Spo</sup>/Acvrl1<sup>tm2Spo</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17911384	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:3033418	Acvrl1<sup>tm1Enl</sup>/Acvrl1<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12588795	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:5775199	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup> Tg(Tal1-cre/ERT)1Jrg/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25082229	20160607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176441	Vhl<sup>tm1Wml</sup>/Vhl<sup>tm1Wml</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9286594	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3621460	Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16510575	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:4436912	Vhl<sup>tm1.1Wkr</sup>/Vhl<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19252526	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3844065	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19340311	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3844062	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Ins2-cre)25Mgn/0  [background:] either: (involves: 129X1/SvJ * C57BL/6 * DBA) or (involves: 129X1/SvJ * A/J * C57BL/6 * DBA)			ECO:0000033	author statement supported by traceable reference	PMID:19340311	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3844061	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1Lss</sup> Tg(Gcg-cre)1Slib/0  [background:] either: (involves: 129X1/SvJ * A/J) or (involves: 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:19340311	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2677759	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1.1Lss</sup> Tg(ACTB-cre)1Tes/0  [background:] involves: 129X1/SvJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14500363	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2677768	Vhl<sup>tm1.1Lss</sup>/Vhl<sup>+</sup>  [background:] involves: A/J			ECO:0000033	author statement supported by traceable reference	PMID:14500363	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2677767	Vhl<sup>tm1.1Lss</sup>/Vhl<sup>+</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:14500363	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2677761	Vhl<sup>tm1Lss</sup>/Vhl<sup>tm1.1Lss</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14500363	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176441	Vhl<sup>tm1Wml</sup>/Vhl<sup>tm1Wml</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14604887	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2174802	Vhl<sup>tm1.1Jae</sup>/Vhl<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11171994	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176966	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:11171994	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176966	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15798202	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3621460	Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15798202	20160502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154547	Cdh23<sup>v-6J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3714868	Cdh23<sup>v-6J</sup>/Cdh23<sup>v-6J</sup>  [background:] B10.A-H2<sup>h4</sup>/(4R)SgDvEgJ-Cdh23<sup>v-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11138008	20090504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5305254	Sirt1<sup>tm1.2Cxd</sup>/Sirt1<sup>tm1.2Cxd</sup> Tg(Alb1-cre)1Dlr/?  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21103071	20120209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5450851	Slc45a2<sup>uw-6J</sup>/Slc45a2<sup>uw-6J</sup>  [background:] CAST/EiJ-Slc45a2<sup>uw-6J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5449587	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668608	Slc45a2<sup>uw-d</sup>/Slc45a2<sup>uw-d</sup>  [background:] involves: TF/Le			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668609	Slc45a2<sup>Uw-dbr</sup>/Slc45a2<sup>Uw-dbr</sup>  [background:] B10.PL-H2<sup>u</sup>/(73NS)Sn			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668611	Slc45a2<sup>uw</sup>/Slc45a2<sup>uw</sup>  [background:] C57BL/6J-Slc45a2<sup>uw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668610	Slc45a2<sup>Uw-dbr</sup>/Slc45a2<sup>+</sup>  [background:] B10.PL-H2<sup>u</sup>/(73NS)Sn			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668607	Slc45a2<sup>uw-bls</sup>/Slc45a2<sup>uw-bls</sup>  [background:] wild Corsican mouse			ECO:0000033	author statement supported by traceable reference	MGI:61984	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5450850	Slc45a2<sup>uw-7J</sup>/Slc45a2<sup>uw-7J</sup>  [background:] C3H/HeJ-Slc45a2<sup>uw-7J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5449588	20130123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311027	b2b464Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5311117	b2b464Clo/b2b464Clo  [background:] C57BL/6J-b2b464Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355303	Galns	is_implicated_in	DOID:12804	mucopolysaccharidosis IV		MGI:2686939	Galns<sup>tm1Toma</sup>/Galns<sup>tm1Toma</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14583446	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:14755333	20090708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:18182166	20090708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3603013	Gck<sup>tm1.1Mgn</sup>/Gck<sup>tm1.1Mgn</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590686	Gck<sup>tm1.2Mgn</sup>/Gck<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590685	Gck<sup>tm1.2Mgn</sup>/Gck<sup>tm1.2Mgn</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3603003	Gck<sup>tm1.1Mgn</sup>/Gck<sup>tm1.1Mgn</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3603012	Gck<sup>tm1.1Mgn</sup>/Gck<sup>+</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:2176960	Gck<sup>tm1Efr</sup>/Gck<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7665557	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3618231	Gck<sup>tm1Hrt</sup>/Gck<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15569412	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:4820839	Gck<sup>m1Rge</sup>/Gck<sup>+</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:19952346	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:2176947	Gck<sup>tm1Ts</sup>/Gck<sup>tm1Ts</sup>  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J)			ECO:0000033	author statement supported by traceable reference	PMID:7553875	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:2176950	Gck<sup>tm1Ts</sup>/Gck<sup>+</sup>  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J)			ECO:0000033	author statement supported by traceable reference	PMID:7553875	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3618231	Gck<sup>tm1Hrt</sup>/Gck<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:24447392	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3713302	Gck<sup>tm2Mgn</sup>/Gck<sup>tm2Mgn</sup>  [background:] 129S6/SvEvTac-Gck<sup>tm2Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17353190	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3713294	Gck<sup>tm2Mgn</sup>/Gck<sup>+</sup>  [background:] 129S6/SvEvTac-Gck<sup>tm2Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17353190	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3583686	Gck<sup>tm1Tka</sup>/Gck<sup>+</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:8530440	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590140	Gck<sup>Rgsc735</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038221	Gck<sup>Rgsc702</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590141	Gck<sup>Rgsc552</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590142	Gck<sup>Rgsc149</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038214	Gck<sup>Rgsc272</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038219	Gck<sup>Rgsc392</sup>/Gck<sup>Rgsc392</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038222	Gck<sup>Rgsc702</sup>/Gck<sup>Rgsc702</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590138	Gck<sup>Rgsc236</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038212	Gck<sup>Rgsc210</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038220	Gck<sup>Rgsc475</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590139	Gck<sup>Rgsc553</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038218	Gck<sup>Rgsc392</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038213	Gck<sup>Rgsc210</sup>/Gck<sup>Rgsc210</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038216	Gck<sup>Rgsc341</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3044561	Gck<sup>Gena348</sup>/Gck<sup>Gena348</sup>  [background:] involves: BALB/c * C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:15161764	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3044560	Gck<sup>Gena348</sup>/Gck<sup>+</sup>  [background:] involves: BALB/c * C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:15161764	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5496284	Robo1<sup>b2b872Clo</sup>/Robo1<sup>b2b872Clo</sup>  [background:] C57BL/6J-Robo1<sup>b2b872Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:4367450	Ank1<sup>pale</sup>/Ank1<sup>pale</sup>  [background:] C57BL/6J-Ank1<sup>pale</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2449181	Ank1<sup>nb</sup>/Ank1<sup>nb</sup>  [background:] either: (involves: non-inbred stock) or (involves: C57BL/6) or (involves: WB/Re)			ECO:0000033	author statement supported by traceable reference	PMID:1716634	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:3844300	Ank1<sup>Rbc2</sup>/Ank1<sup>Rbc2</sup>  [background:] involves: 129S1/Sv * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:19179303	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:4948066	Ank1<sup>M1Wlst</sup>/Ank1<sup>M1Wlst</sup>  [background:] involves: 129S1/SvImJ * C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21193012	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525118	Tg(Dct-Grm1)ESzc	is_implicated_in	DOID:8923	skin melanoma		MGI:5432230	Tg(Dct-Grm1)ESzc/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12704387	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3835595	Elp1<sup>Gt(BGB184)Byg</sup>	is_implicated_in	DOID:0050120	hemophagocytic lymphohistiocytosis		MGI:3835654	Elp1<sup>Gt(BGB184)Byg</sup>/Elp1<sup>Gt(BGB184)Byg</sup>  [background:] B6.129P2-<sup>Gt(BGB184)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19015235	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764703	Ripply2<sup>tm1Asas</sup>	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:3764704	Ripply2<sup>tm1Asas</sup>/Ripply2<sup>tm1Asas</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17531978	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	is_implicated_in	DOID:0090145	dopamine beta-hydroxylase deficiency		MGI:2175826	Dbh<sup>tm1Rpa</sup>/Dbh<sup>tm1Rpa</sup>  [background:] either: (involves: 129S7/SvEvBrd * 129/SvCpj) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7715704	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920455	C9orf72	is_implicated_in	DOID:417	autoimmune disease		MGI:6278554	C9orf72<sup>tm1.1Eggn</sup>/C9orf72<sup>tm1.1Eggn</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920455	C9orf72	is_implicated_in	DOID:417	autoimmune disease		MGI:6278556	C9orf72<sup>em1Eggn</sup>/C9orf72<sup>em1Eggn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920455	C9orf72	is_implicated_in	DOID:417	autoimmune disease		MGI:6278552	C9orf72<sup>tm1Eggn</sup>/C9orf72<sup>tm1Eggn</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27412785	20190218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918771	Pds5a	is_implicated_in	DOID:11725	Cornelia de Lange syndrome		MGI:3847290	Pds5a<sup>Gt(RRM243)Byg</sup>/Pds5a<sup>Gt(RRM243)Byg</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19412548	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684302	F13a1<sup>tm1Gdi</sup>	is_implicated_in	DOID:2211	factor XIII deficiency		MGI:2684306	F13a1<sup>tm1Gdi</sup>/F13a1<sup>tm1Gdi</sup>  [background:] involves: 129P2/OlaHsd * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:12529747	20111107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684302	F13a1<sup>tm1Gdi</sup>	is_implicated_in	DOID:2211	factor XIII deficiency		MGI:2684307	F13a1<sup>tm1Gdi</sup>/F13a1<sup>tm1Gdi</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12933578	20111107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97311	Nfix	is_implicated_in	DOID:13300	Scheuermann's disease		MGI:3714196	Nfix<sup>tm1Aes</sup>/Nfix<sup>tm1Aes</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17353270	20070710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4589319	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3779043	Lyst<sup>bg-2Btlr</sup>/Lyst<sup>bg-2Btlr</sup>  [background:] C57BL/6J-Lyst<sup>bg-2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778946	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:6383409	Lyst<sup>bg-18J</sup>/Lyst<sup>bg-18J</sup>  [background:] B6.Cg-Lyst<sup>bg-18J</sup>/Boc			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3784690	Lyst<sup>bg-Lac</sup>/Lyst<sup>bg-Lac</sup>  [background:] CBA/CaLac-Lyst<sup>bg-Lac</sup>			ECO:0000033	author statement supported by traceable reference	MGI:77347	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4601767	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2672959	Lyst<sup>bg-14J</sup>/Lyst<sup>bg-14J</sup>  [background:] C3Fe;B6-Lyst<sup>bg-14J</sup>			ECO:0000033	author statement supported by traceable reference	MGI:2673072	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1523694	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3779036	Lyst<sup>bg-Btlr</sup>/Lyst<sup>bg-Btlr</sup>  [background:] C57BL/6J-Lyst<sup>bg-Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778945	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3588316	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7089489	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7366734	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1113502	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:408	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3620975	Lyst<sup>bg-grey</sup>/Lyst<sup>bg-grey</sup>  [background:] C57BL/6-Lyst<sup>bg-grey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16518687	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2661024	Lyst<sup>bg-slt</sup>/Lyst<sup>bg-slt</sup>  [background:] YZ57/Ch			ECO:0000033	author statement supported by traceable reference	PMID:13943454	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5590154	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2656344	Lyst<sup>bg</sup>/Lyst<sup>bg</sup>  [background:] B6.C3Rl-Lyst<sup>bg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4697831	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:9884	muscular dystrophy		MGI:6093458	Fkrp<sup>tvrm53</sup>/Fkrp<sup>tvrm53</sup>  [background:] C57BL/6J-Fkrp<sup>tvrm53</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680005	Stub1<sup>tm1Cpat</sup>	is_implicated_in	DOID:0080029	autosomal recessive spinocerebellar ataxia 16		MGI:2680011	Stub1<sup>tm1Cpat</sup>/Stub1<sup>tm1Cpat</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28593200	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664599	Coro1a<sup>tm1Achn</sup>	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818533	Coro1a<sup>tm1Achn</sup>/Coro1a<sup>tm1Achn</sup>  [background:] B6.129X1-Coro1a<sup>tm1Achn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	is_implicated_in	DOID:0070293	primary autosomal recessive microcephaly 2 with or without cortical malformations		MGI:6388425	Wdr62<sup>tm1.1Jfch</sup>/Wdr62<sup>tm1.1Jfch</sup>  [background:] involves: 129S1/SvImJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31197141	20200203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201673	Shox2	is_implicated_in	DOID:0060847	Leri-Weill dyschondrosteosis		MGI:3628806	Shox2<sup>tm1Ddu</sup>/Shox2<sup>tm1.1Ddu</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S2/SvPas * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:16537395	20060712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045305	Klhl31	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:6201559	Klhl31<sup>em1Eno</sup>/Klhl31<sup>em1Eno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28872460	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654430	Scarb2<sup>tm1Psa</sup>	is_implicated_in	DOID:891	progressive myoclonus epilepsy		MGI:5688743	Scarb2<sup>tm1Psa</sup>/Scarb2<sup>tm1Psa</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25316793	20151001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580100	Prkar1a<sup>tm1.1Lsk</sup>	is_implicated_in	DOID:0050471	Carney complex		MGI:4868217	Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20421483	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580100	Prkar1a<sup>tm1.1Lsk</sup>	is_implicated_in	DOID:0050471	Carney complex		MGI:3580533	Prkar1a<sup>tm1.1Lsk</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15930266	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7957574	20080806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3799268	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] C3.MRL-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1565490	20080806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1565490	20080806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8163351	20080806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3639605	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/MpJ-Fas<sup>lpr</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17208228	20080806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135676	Fgfr3<sup>tm4.1Cxd</sup>	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3640318	Fgfr3<sup>tm4.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10861287	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856885	Ostm1<sup>gl</sup>	is_implicated_in	DOID:0110939	autosomal recessive osteopetrosis 5		MGI:2655576	Ostm1<sup>gl</sup>/Ostm1<sup>gl</sup>  [background:] GL/Le Edar<sup>dl-J</sup> +/+ Ostm1<sup>gl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:1155801	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	is_implicated_in	DOID:3613	Canavan disease		MGI:3038607	Aspa<sup>tm1Mata</sup>/Aspa<sup>tm1Mata</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10894262	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	is_implicated_in	DOID:3613	Canavan disease		MGI:3027206	Aspa<sup>nur7</sup>/Aspa<sup>nur7</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18987190	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	is_implicated_in	DOID:3613	Canavan disease		MGI:3038607	Aspa<sup>tm1Mata</sup>/Aspa<sup>tm1Mata</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:14572139	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	is_implicated_in	DOID:3613	Canavan disease		MGI:3027206	Aspa<sup>nur7</sup>/Aspa<sup>nur7</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26511242	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	is_implicated_in	DOID:3613	Canavan disease		MGI:5008609	Aspa<sup>tm1a(EUCOMM)Wtsi</sup>/Aspa<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:21625469	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	is_implicated_in	DOID:3613	Canavan disease		MGI:5787605	Aspa<sup>deaf14</sup>/Aspa<sup>deaf14</sup>  [background:] BALB/c-Aspa<sup>deaf14</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24682784	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	is_implicated_in	DOID:9970	obesity		MGI:3821619	A<sup>iy</sup>/A<sup>iy</sup>  [background:] C3H/HeJ-A<sup>iy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5798139	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	is_implicated_in	DOID:9970	obesity		MGI:3821616	A<sup>iy</sup>/A  [background:] C3H/HeJ-A<sup>iy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5798139	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	is_implicated_in	DOID:9970	obesity		MGI:3772367	A<sup>vy</sup>/a  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14242032	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	is_implicated_in	DOID:9970	obesity		MGI:3772367	A<sup>vy</sup>/a  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17101998	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	is_implicated_in	DOID:9970	obesity		MGI:3773447	A<sup>y</sup>/A  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18172198	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712927	Otof<sup>deaf5Jcs</sup>	is_implicated_in	DOID:0110535	autosomal recessive nonsyndromic deafness 9		MGI:3760289	Otof<sup>deaf5Jcs</sup>/Otof<sup>deaf5Jcs</sup>  [background:] STOCK Otof<sup>deaf5Jcs</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	PMID:17967520	20071207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	is_implicated_in	DOID:0060873	isolated growth hormone deficiency type IA		MGI:3051589	Ghrh<sup>tm1Salv</sup>/Ghrh<sup>tm1Salv</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15155578	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	is_implicated_in	DOID:0090070	hypogonadotropic hypogonadism		MGI:2180104	Nr5a1<sup>tm2Klp</sup>/Nr5a1<sup>tm2.1Klp</sup> Tg(Cga-cre)3Sac/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11124111	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110958	Gaucher's disease type II		MGI:2177138	Gba1<sup>tm1Nsb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1594045	20071214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110958	Gaucher's disease type II		MGI:3764515	Gba1<sup>tm2Karl</sup>/Gba1<sup>tm2Karl</sup> Tg(KRT14-cre)8Brn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17954912	20071214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	is_implicated_in	DOID:0080169	tricuspid atresia		MGI:3620558	Zfpm2<sup>tm1Jml</sup>/Zfpm2<sup>tm1Jml</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10888889	20060427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148567	Ctnnb1<sup>tm2Kem</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5812797	Ctnnb1<sup>tm2Kem</sup>/Ctnnb1<sup>tm2Kem</sup> Pvalb<sup>tm1(cre)Arbr</sup>/Pvalb<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27131348	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	is_implicated_in	DOID:0110010	achromatopsia 4		MGI:6163747	Gnat2<sup>m1Erica</sup>/Gnat2<sup>m1Erica</sup>  [background:] C.Cg-Gnat2<sup>m1Erica</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23580486	20180629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	is_implicated_in	DOID:0110010	achromatopsia 4		MGI:3715214	Gnat2<sup>cpfl3</sup>/Gnat2<sup>cpfl3</sup>  [background:] ALS/LtJ			ECO:0000033	author statement supported by traceable reference	PMID:17065522	20180629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110473	autosomal recessive nonsyndromic deafness 18A		MGI:6359828	Ush1c<sup>dfcr-4J</sup>/Ush1c<sup>dfcr-4J</sup>  [background:] 129P3/J-Ush1c<sup>dfcr-4J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:6359814	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110473	autosomal recessive nonsyndromic deafness 18A		MGI:2676319	Ush1c<sup>dfcr</sup>/Ush1c<sup>dfcr</sup>  [background:] involves: BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110473	autosomal recessive nonsyndromic deafness 18A		MGI:2676317	Ush1c<sup>dfcr-2J</sup>/Ush1c<sup>dfcr-2J</sup>  [background:] B6;129S4			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20190913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687866	Aqp2<sup>tm1(AQP2)Suc</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3688527	Aqp2<sup>tm1(AQP2)Suc</sup>/Aqp2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16968783	20061122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3583125	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3583121	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] KK-Nphp3<sup>pcy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3712587	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3583124	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] either: D2.KK-Nphp3<sup>pcy</sup> or (involves: DBA/2Fg * DBA/2J * KK)			ECO:0000033	author statement supported by traceable reference	PMID:1883968	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:3527796	Lmna<sup>tm1Gbon</sup>/Lmna<sup>tm1Gbon</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15548545	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:10579712	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2450098	Fas<sup>tm1Osa</sup>/Fas<sup>tm1Osa</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8700897	20051011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2449985	Fas<sup>lpr-cg</sup>/Fas<sup>lpr-cg</sup>  [background:] CBA/KlJms-Fas<sup>lpr-cg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2406366	20051011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2449985	Fas<sup>lpr-cg</sup>/Fas<sup>lpr-cg</sup>  [background:] CBA/KlJms-Fas<sup>lpr-cg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2302830	20051011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76424	20051011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103285	Atp6v1b1	is_implicated_in	DOID:0050565	autosomal recessive nonsyndromic deafness		MGI:5910007	Atp6v1b1<sup>vtx</sup>/Atp6v1b1<sup>vtx</sup>  [background:] MRL/MpJ-Atp6v1b1<sup>vtx</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	PMID:28934385	20170920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671049	Igsf1<sup>tm1Zuk</sup>	is_implicated_in	DOID:0111140	IGSF1 deficiency syndrome		MGI:2671059	Igsf1<sup>tm1Zuk</sup>/Y  [background:] either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:23143598	20180725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412048	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4412052	Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz/0  [background:] C57BL/6-Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz			ECO:0000033	author statement supported by traceable reference	PMID:20615468	20101130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:6163608	Atp1a3<sup>tm1.1Tmklh</sup>/Atp1a3<sup>+</sup>  [background:] B6JRj.129S1-Atp1a3<sup>tm1.1Tmklh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27549929	20180907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26463346	20180907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:6162678	Atp1a3<sup>tm1Ute</sup>/Atp1a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25523819	20180907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	is_implicated_in	DOID:0050635	alternating hemiplegia of childhood		MGI:6197063	Atp1a3<sup>tm1Mika</sup>/Atp1a3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30071271	20180907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693226	Tg(tetO/CMV-KRAS*G12C)9.1Msmi	is_implicated_in	DOID:3683	lung benign neoplasm		MGI:3693291	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO/CMV-KRAS*G12C)9.1Msmi/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16051643	20171102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693226	Tg(tetO/CMV-KRAS*G12C)9.1Msmi	is_implicated_in	DOID:3683	lung benign neoplasm		MGI:3693292	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO/CMV-KRAS*G12C)9.1Msmi/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16051643	20171102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:2678248	Prkn<sup>tm1Roo</sup>/Prkn<sup>tm1Roo</sup>  [background:] either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12915482	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:3050555	Prkn<sup>tm1Tmd</sup>/Prkn<sup>tm1Tmd</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15249681	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:2681434	Prkn<sup>tm1Shn</sup>/Prkn<sup>tm1Shn</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:12930822	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:4939781	Prkn<sup>tm1Ccs</sup>/Prkn<sup>tm1Ccs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21212098	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:3757750	Prkn<sup>tm1Roo</sup>/Prkn<sup>tm1Roo</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:17623040	20110307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832877	Tg(Thy1-MAPT*V337M)1Godt	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:3832892	Tg(Thy1-MAPT*V337M)1Godt/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:17517691	20090223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3836258	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm1Maag</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19104150	20130526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3836256	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>tm3Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm3Maag</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19104150	20130526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:5487277	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>tm3Maag</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22144569	20130526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3836258	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] B6.129P2-Cacna1a<sup>tm1Maag</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22144569	20130526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:5487278	Cacna1a<sup>tm3Maag</sup>/Cacna1a<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22144569	20130526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0060178	familial hemiplegic migraine		MGI:3037958	Cacna1a<sup>tm1Maag</sup>/Cacna1a<sup>tm1Maag</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15003170	20130526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617390	Pkd1<sup>tm2.1Ggg</sup>/Pkd1<sup>tm2.1Ggg</sup>  [background:] involves: 129S4/SvJae * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15579506	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617392	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15579506	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3795669	Pkd1<sup>tm2Som</sup>/Pkd1<sup>tm2.1Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: C57BL/6 * ICR * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18263604	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3521730	Pkd1<sup>tm1Djmp</sup>/Pkd1<sup>tm1Djmp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15496422	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:6317327	Pkd1<sup>tm2Som</sup>/Pkd1<sup>tm2Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJae * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:6317334	Pkd1<sup>tm1.1Pcha</sup>/Pkd1<sup>tm2Som</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:28205547	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5476836	Pkd1<sup>tm1.1Pcha</sup>/Pkd1<sup>tm1.1Pcha</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23064367	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5476837	Pkd1<sup>tm1Shh</sup>/Pkd1<sup>tm1.1Pcha</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23064367	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:6188648	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Hoxb7-cre)13Amc/0  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21465620	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3811280	Pkd1<sup>tm3.1Jzh</sup>/Pkd1<sup>tm3.1Jzh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18385665	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3811282	Pkd1<sup>tm3Jzh</sup>/Pkd1<sup>tm3Jzh</sup> Tg(Ggt1-cre)M3Egn/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18385665	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3811281	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>tm2Jzh</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18385665	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617489	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>tm2Jzh</sup>  [background:] either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617490	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5430604	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Nes-cre)Wme/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20075061	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5471141	Pkd1<sup>tm1.1Fqi</sup>/Pkd1<sup>tm1.1Fqi</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23236168	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617386	Pkd1<sup>tm1Ggg</sup>/Pkd1<sup>tm1Ggg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12007403	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5445215	Pkd1<sup>b2b1585Clo</sup>/Pkd1<sup>b2b1585Clo</sup>  [background:] C57BL/6J-Pkd1<sup>b2b1585Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:5502373	Pkd1<sup>tm2Ggg</sup>/Pkd1<sup>tm2Ggg</sup> Tg(Col1a1-cre)1Bek/0  [background:] involves: 129S4/SvJae * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23029375	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3776498	Pkd1<sup>tm1Bdgz</sup>/Pkd1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17928412	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:4819716	Pkd1<sup>tm1Gztn</sup>/Pkd1<sup>tm1Gztn</sup> Gt(ROSA)26Sor<sup>tm9(cre/ESR1)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S/Sv * 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20562878	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:12514735	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:9326937	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:9326937	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:2173244	Pkd1<sup>tm1Rsa</sup>/Pkd1<sup>+</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:11593033	20190712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:9988265	20190712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036209	Junb<sup>tm3Wag</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4417904	Junb<sup>tm3Wag</sup>/Junb<sup>tm3Wag</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19918056	20100115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:5295754	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23690466	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23690466	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:5806144	Lmna<sup>tm12Lgf</sup>/Lmna<sup>tm12Lgf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26999604	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22030750	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:7518590	Lmna<sup>em1Fenz</sup>/Lmna<sup>+</sup>  [background:] C57BL/6-Lmna<sup>em1Fenz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36583724	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:2662910	Lmna<sup>tm2Stw</sup>/Lmna<sup>tm2Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12748643	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:4459466	Lmna<sup>Dhe</sup>/Lmna<sup>+</sup>  [background:] B6(D2)-Lmna<sup>Dhe</sup>/TyGrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:21464947	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:6423604	Lmna<sup>tm1Bliu</sup>/Lmna<sup>+</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:32128409	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:3817506	Lmna<sup>tm1Lgf</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16862216	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:7311569	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:29703891	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:7311570	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:29703891	20230816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:3911	progeria		MGI:5295749	Lmna<sup>tm1.1Otin</sup>/Lmna<sup>tm1.1Otin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21875900	20230816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148177	Mstn<sup>tm1Sjl</sup>	is_implicated_in	DOID:0111072	myostatin-related muscle hypertrophy		MGI:3714749	Mstn<sup>tm1Sjl</sup>/Mstn<sup>tm1Sjl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9139826	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587769	Atg7<sup>tm1Tchi</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5471365	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Slc6a3<sup>tm1(cre)Xz</sup>/Slc6a3<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23152632	20130402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587769	Atg7<sup>tm1Tchi</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5471363	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> En1<sup>tm2(cre)Wrst</sup>/En1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23152632	20130402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053095	Fgfr2<sup>tm4Lni</sup>	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:3053579	Fgfr2<sup>tm4Lni</sup>/Fgfr2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15316116	20161025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053095	Fgfr2<sup>tm4Lni</sup>	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:3053579	Fgfr2<sup>tm4Lni</sup>/Fgfr2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25966306	20161025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:3038120	Gata1<sup>tm1Mym</sup>/Gata1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9657742	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836986	Tg(Prnp*D177N*M128V)A21Rchi	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:3836993	Tg(Prnp*D177N*M128V)A21Rchi/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19038218	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836986	Tg(Prnp*D177N*M128V)A21Rchi	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:3836992	Tg(Prnp*D177N*M128V)A21Rchi/Tg(Prnp*D177N*M128V)A21Rchi  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19038218	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156985	Pax8<sup>tm1Pgr</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5694079	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17932107	20151029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156985	Pax8<sup>tm1Pgr</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3694004	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9590297	20151029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156985	Pax8<sup>tm1Pgr</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3694004	Pax8<sup>tm1Pgr</sup>/Pax8<sup>tm1Pgr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:14981357	20151029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	is_implicated_in	DOID:674	cleft palate		MGI:6151467	Golgb1<sup>em33Lanyu</sup>/Golgb1<sup>em33Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	is_implicated_in	DOID:674	cleft palate		MGI:6151460	Golgb1<sup>em33Lanyu</sup>/Golgb1<sup>m1Lanyu</sup>  [background:] involves: A/J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	is_implicated_in	DOID:674	cleft palate		MGI:6151466	Golgb1<sup>em8Lanyu</sup>/Golgb1<sup>em8Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	is_implicated_in	DOID:674	cleft palate		MGI:6151468	Golgb1<sup>em8Lanyu</sup>/Golgb1<sup>em33Lanyu</sup>  [background:] FVB/NJ-Golgb1<sup>em8Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	is_implicated_in	DOID:674	cleft palate		MGI:6151463	Golgb1<sup>m1Lanyu</sup>/Golgb1<sup>m1Lanyu</sup>  [background:] A/J-Golgb1<sup>m1Lanyu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27226319	20180419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043293	Mapt<sup>tm1(Mecp2)Jae</sup>	is_implicated_in	DOID:0060799	syndromic X-linked intellectual disability Lubs type		MGI:5318976	Mapt<sup>tm1(Mecp2)Jae</sup>/Mapt<sup>tm1(Mecp2)Jae</sup>  [background:] B6.Cg-Mapt<sup>tm1(Mecp2)Jae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22378884	20120522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050990	episodic ataxia type 2		MGI:3700746	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:25855180	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050990	episodic ataxia type 2		MGI:5707183	Cacna1a<sup>tm1.1Ehess</sup>/Cacna1a<sup>tm1.1Ehess</sup>  [background:] C57BL/6-Cacna1a<sup>tm1.1Ehess</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25109669	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050990	episodic ataxia type 2		MGI:6226089	Cacna1a<sup>tm1Lory</sup>/Cacna1a<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28688851	20181106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386324	Ikbkg<sup>tm1Mpa</sup>	is_implicated_in	DOID:12305	Bloch-Sulzberger syndrome		MGI:3844910	Ikbkg<sup>tm1Mpa</sup>/Ikbkg<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10911992	20090520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3522243	pta	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:3522704	pta/pta  [background:] C57BL/6J-pta			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20101008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653318	n-TUtca2<sup>tm1Dhat</sup>	is_implicated_in	DOID:65	connective tissue disease		MGI:4360984	n-TUtca2<sup>tm1Dhat</sup>/n-TUtca2<sup>tm1Dhat</sup> Tg(Col2a1-cre)1Bhr/0  [background:] B6.Cg-n-TUtca2<sup>tm1Dhat</sup> Tg(Col2a1-cre)1Bhr			ECO:0000033	author statement supported by traceable reference	PMID:19696890	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679336	Satb2	is_implicated_in	DOID:0110213	isolated cleft palate		MGI:3695610	Satb2<sup>tm1(cre)Vit</sup>/Satb2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16960803	20070205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10213384	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3044747	Runx2<sup>tm1Mjo</sup>/Runx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9182764	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10049712	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678410	Runx2<sup>tm1Kish</sup>/Runx2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9182763	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2678409	Runx2<sup>tm1Kish</sup>/Runx2<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9182763	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3829628	Runx2<sup>tm1Jals</sup>/Runx2<sup>tm1Jals</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19028669	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3044747	Runx2<sup>tm1Mjo</sup>/Runx2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204840	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	is_implicated_in	DOID:0111960	immunodeficiency 15A		MGI:6444681	Ikbkb<sup>em1Macc</sup>/Ikbkb<sup>+</sup>  [background:] involves: C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:30337470	20210120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	is_implicated_in	DOID:0111960	immunodeficiency 15A		MGI:6444680	Ikbkb<sup>em1Macc</sup>/Ikbkb<sup>em1Macc</sup>  [background:] involves: C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:30337470	20210120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347465	Foxh1	is_implicated_in	DOID:0060341	agnathia-otocephaly complex		MGI:5615273	Foxh1<sup>b2b2662Clo</sup>/Foxh1<sup>b2b2662Clo</sup>  [background:] C57BL/6J-Foxh1<sup>b2b2662Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5439657	Bap1<sup>tm1.1Geno</sup>/Bap1<sup>tm1.1Geno</sup> Gt(ROSA)26Sor<sup>tm9(cre/ESR1)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:22878500	20121026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180787	Comp<sup>tm1Aol</sup>	is_not_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:3037836	Comp<sup>tm1Aol</sup>/Comp<sup>tm1Aol</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12024046	20051007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5812797	Ctnnb1<sup>tm2Kem</sup>/Ctnnb1<sup>tm2Kem</sup> Pvalb<sup>tm1(cre)Arbr</sup>/Pvalb<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27131348	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861635	Crygs<sup>Opj</sup>	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584122	Crygs<sup>Opj</sup>/Crygs<sup>Opj</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8812411	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861635	Crygs<sup>Opj</sup>	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584120	Crygs<sup>Opj</sup>/Crygs<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8812411	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861635	Crygs<sup>Opj</sup>	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584120	Crygs<sup>Opj</sup>/Crygs<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:11121426	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861635	Crygs<sup>Opj</sup>	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584122	Crygs<sup>Opj</sup>/Crygs<sup>Opj</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:11121426	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107595	Sp4	is_implicated_in	DOID:5419	schizophrenia		MGI:3713111	Sp4<sup>tm3(Sp4)Krc</sup>/Sp4<sup>tm3(Sp4)Krc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:20634195	20140319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106299	Slx4	is_not_implicated_in	DOID:0111092	Fanconi anemia complementation group P		MGI:5559492	Slx4<sup>tm1.2Jrou</sup>/Slx4<sup>tm1.2Jrou</sup>  [background:] B6.129P2-Slx4<sup>tm1.2Jrou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24076219	20140421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:4887395	Ryr1<sup>tm2.1Alle</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17122579	20220408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:3620044	Ryr1<sup>tm1Slh</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16284304	20220408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:7260233	Ryr1<sup>em1Tmur</sup>/Ryr1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:34257294	20220408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:6515830	Ryr1<sup>tm3.1Alle</sup>/Ryr1<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30236258	20220408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:6515831	Ryr1<sup>tm3.1Alle</sup>/Ryr1<sup>tm3.1Alle</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30236258	20220408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397592	Kcnq2<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397669	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397592	Kcnq2<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397670	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397592	Kcnq2<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397672	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] FVB.129-Kcnq2<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397592	Kcnq2<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397671	Kcnq2<sup>tm1.1Naas</sup>/Kcnq2<sup>tm1.1Naas</sup>  [background:] B6.129-Kcnq2<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934905	Fbn1<sup>tm1Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3619415	Fbn1<sup>tm1Rmz</sup>/Fbn1<sup>tm1Rmz</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9326947	20060413	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:5924952	Rho<sup>Tvrm334</sup>/Rho<sup>+</sup>  [background:] B6.Cg-Rho<sup>Tvrm334</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4367272	Rho<sup>R3</sup>/Rho<sup>R3</sup>  [background:] C57BL/6J-Rho<sup>R3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19741247	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4367269	Rho<sup>R3</sup>/Rho<sup>+</sup>  [background:] C57BL/6J-Rho<sup>R3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19741247	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4367270	Rho<sup>R3</sup>/Rho<sup>tm1Jlem</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19741247	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4947235	Rho<sup>tm1.1Kpal</sup>/Rho<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21224384	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4455025	Rho<sup>Tvrm4</sup>/Rho<sup>+</sup>  [background:] B6.Cg-Rho<sup>Tvrm4</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:20207741	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4455026	Rho<sup>Tvrm1</sup>/Rho<sup>+</sup>  [background:] C57BL/6J-Rho<sup>Tvrm1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20207741	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:5566851	Rho<sup>tm1.1Eye</sup>/Rho<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22252712	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:3836169	Rho<sup>tm1Phm</sup>/Rho<sup>tm1Phm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9020854	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	is_implicated_in	DOID:9997	peripartum cardiomyopathy		MGI:5906908	Stat3<sup>tm1Vpo</sup>/Stat3<sup>tm1Vpo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17289576	20170814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	is_implicated_in	DOID:6000	congestive heart failure		MGI:7261455	Cxcr4<sup>tm2Yzo</sup>/Cxcr4<sup>tm2Yzo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31071921	20220418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182334	Cyp27b1<sup>tm1Star</sup>	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11416036	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182334	Cyp27b1<sup>tm1Star</sup>	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11415990	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182334	Cyp27b1<sup>tm1Star</sup>	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12689675	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182334	Cyp27b1<sup>tm1Star</sup>	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12674324	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182334	Cyp27b1<sup>tm1Star</sup>	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12205031	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4433295	Chd7<sup>tm2a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7492422	Chd7<sup>tm2a(EUCOMM)Wtsi</sup>/Chd7<sup>+</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:36232804	20230626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386105	Smarca4<sup>tm1Mag</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:5763438	Smarca4<sup>tm1Mag</sup>/Smarca4<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160427	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343184	Samd9l	is_not_implicated_in	DOID:0080170	normophosphatemic familial tumoral calcinosis		MGI:5694935	Samd9l<sup>tm1Homy</sup>/Samd9l<sup>tm1Homy</sup>  [background:] B6N.129P2-Samd9l<sup>tm1Homy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22716256	20151105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98812	Tpmt	is_implicated_in	DOID:0080172	thiopurine S-methyltransferase deficiency		MGI:3712780	Tpmt<sup>tm1Rlng</sup>/Tpmt<sup>tm1Rlng</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:17510427	20070626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98388	Sptbn1	is_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:4936861	Sptbn1<sup>tm1Mish</sup>/Sptbn1<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:20739274	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360790	Tg(RBP3-ELOVL4*)1Kzh	is_implicated_in	DOID:0050817	Stargardt disease		MGI:4360796	Tg(RBP3-ELOVL4*)1Kzh/0  [background:] C57BL/6-Tg(RBP3-ELOVL4*)1Kzh			ECO:0000033	author statement supported by traceable reference	PMID:15749821	20091008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4125284	Ppib<sup>Gt(RST139)Byg</sup>	is_implicated_in	DOID:0110349	osteogenesis imperfecta type 9		MGI:5698101	Ppib<sup>Gt(RST139)Byg</sup>/Ppib<sup>Gt(RST139)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24968150	20151207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662140	Mitf<sup>Mi-Crc</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154515	Pthlh<sup>tm1Hmk</sup>	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy		MGI:3583956	Pthlh<sup>tm1Hmk</sup>/Pthlh<sup>tm1Hmk</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8314082	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96399	Idc	is_implicated_in	DOID:83	cataract		MGI:2175077	Idc/Idc<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20675713	20190515	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:6303809	Fkrp<sup>tm1Scbr</sup>/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26306834	20190515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039664	Rpsa<sup>tp1</sup>	is_implicated_in	DOID:0110074	arrhythmogenic right ventricular dysplasia 5		MGI:3039683	Rpsa<sup>tp1</sup>/Rpsa<sup>tp1</sup>  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:14730304	20110420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:3842843	Ush1c<sup>dfcr-3J</sup>/Ush1c<sup>dfcr-3J</sup>  [background:] STOCK Ush1c<sup>dfcr-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3842839	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:3700039	Ush1c<sup>tm1Bkts</sup>/Ush1c<sup>tm1Bkts</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17174357	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:6359828	Ush1c<sup>dfcr-4J</sup>/Ush1c<sup>dfcr-4J</sup>  [background:] 129P3/J-Ush1c<sup>dfcr-4J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:6359814	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:2676319	Ush1c<sup>dfcr</sup>/Ush1c<sup>dfcr</sup>  [background:] involves: BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:2676317	Ush1c<sup>dfcr-2J</sup>/Ush1c<sup>dfcr-2J</sup>  [background:] B6;129S4			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:5751490	Ush1c<sup>tm1Xzl</sup>/Ush1c<sup>tm1Xzl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24725409	20190913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1862037	Slc12a5	is_implicated_in	DOID:1826	epilepsy		MGI:3686900	Slc12a5<sup>tm1Dlp</sup>/Slc12a5<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12000122	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657247	Pde6c<sup>cpfl1</sup>	is_implicated_in	DOID:13911	achromatopsia		MGI:2657248	Pde6c<sup>cpfl1</sup>/Pde6c<sup>cpfl1</sup>  [background:] involves: CXB1/ByJ			ECO:0000033	author statement supported by traceable reference	PMID:11853768	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657247	Pde6c<sup>cpfl1</sup>	is_implicated_in	DOID:13911	achromatopsia		MGI:4411994	Pde6c<sup>cpfl1</sup>/Pde6c<sup>cpfl1</sup>  [background:] B6.CXB1-Pde6c<sup>cpfl1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19887631	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_not_implicated_in	DOID:3911	progeria		MGI:4868583	Lmna<sup>tm8Lgf</sup>/Lmna<sup>tm8Lgf</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21088111	20110119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_not_implicated_in	DOID:3911	progeria		MGI:4457609	Lmna<sup>tm5Lgf</sup>/Lmna<sup>tm5Lgf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20421363	20110119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2175798	Cryaa<sup>lop18</sup>/Cryaa<sup>lop18</sup>  [background:] involves: CBA/CaGnLeJ			ECO:0000033	author statement supported by traceable reference	PMID:8812430	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2653233	Cryaa<sup>Aey7</sup>/Cryaa<sup>Aey7</sup>  [background:] C3HeB/FeJ-Cryaa<sup>Aey7</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:11687536	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2653234	Cryaa<sup>Aey7</sup>/Cryaa<sup>+</sup>  [background:] C3HeB/FeJ-Cryaa<sup>Aey7</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:11687536	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:3784582	Cryaa<sup>tm1.1Ady</sup>/Cryaa<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18056999	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:3784583	Cryaa<sup>tm1.1Ady</sup>/Cryaa<sup>tm1.1Ady</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18056999	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2175800	Cryaa<sup>tm1Wawr</sup>/Cryaa<sup>tm1Wawr</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9023351	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2175799	Cryaa<sup>tm1Wawr</sup>/Cryaa<sup>tm1Wawr</sup>  [background:] involves: 129/Sv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9023351	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:4437476	Cryaa<sup>tm1Ady</sup>/Cryaa<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:19619312	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:4437475	Cryaa<sup>tm1Ady</sup>/Cryaa<sup>tm1Ady</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:19619312	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822147	Mks1<sup>avc6</sup>/Mks1<sup>avc6</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351637	Peg12	is_not_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3530544	Peg12<sup>tm1Brn</sup>/Peg12<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15681612	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836281	Fgfr1<sup>Eask</sup>	is_implicated_in	DOID:10754	otitis media		MGI:5301811	Fgfr1<sup>Eask</sup>/Fgfr1<sup>+</sup>  [background:] BALB/cByJ-Fgfr1<sup>Eask</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384726	Tfr2<sup>tm1Slu</sup>	is_implicated_in	DOID:0111030	hemochromatosis type 3		MGI:2655464	Tfr2<sup>tm1Slu</sup>/Tfr2<sup>tm1Slu</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12134060	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	is_implicated_in	DOID:557	kidney disease		MGI:5905032	Col4a1<sup>tm1.1Ics</sup>/Col4a1<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26260163	20170719	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	is_implicated_in	DOID:557	kidney disease		MGI:5905035	Col4a1<sup>tm1.1Ics</sup>/Col4a1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26260163	20170719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586916	Fem1b<sup>tm1Jfma</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3590085	Fem1b<sup>tm1Jfma</sup>/Fem1b<sup>tm1Jfma</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16024793	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861609	Hps3<sup>coa-6J</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2175787	Hps3<sup>coa-6J</sup>/Hps3<sup>coa-6J</sup>  [background:] C3H/HeJ-Hps3<sup>coa-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:1861465	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3806790	Scn8a<sup>8J</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:3840657	Scn8a<sup>8J</sup>/Scn8a<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19254928	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3806790	Scn8a<sup>8J</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:3840657	Scn8a<sup>8J</sup>/Scn8a<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24657915	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:5501106	Acvrl1<sup>tm2.1Spo</sup>/Acvrl1<sup>tm2.1Spo</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:22571958	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146906	Ift140	is_implicated_in	DOID:0110097	short-rib thoracic dysplasia 9 with or without polydactyly		MGI:5560283	Ift140<sup>b2b1283Clo</sup>/Ift140<sup>b2b1283Clo</sup>  [background:] C57BL/6J-Ift140<sup>b2b1283Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606251	Cpt1a<sup>tm1Pwo</sup>	is_implicated_in	DOID:0090129	carnitine palmitoyltransferase I deficiency		MGI:3606425	Cpt1a<sup>tm1Pwo</sup>/Cpt1a<sup>+</sup>  [background:] either: 129S6/SvEvTac-Cpt1a<sup>tm1Pwo</sup> or (involves: 129S6/SvEvTac * C57BL/6NTac)			ECO:0000033	author statement supported by traceable reference	PMID:16169268	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450889	B4galt1<sup>tm1Yiw</sup>	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:6306320	B4galt1<sup>tm1Yiw</sup>/B4galt1<sup>tm1Yiw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17255313	20190530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105381	Rpsa	is_implicated_in	DOID:0110074	arrhythmogenic right ventricular dysplasia 5		MGI:3039683	Rpsa<sup>tp1</sup>/Rpsa<sup>tp1</sup>  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:14730304	20110420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857473	Ednra<sup>tm1Ywa</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:2166570	Ednra<sup>tm1Ywa</sup>/Ednra<sup>tm1Ywa</sup>  [background:] 129S/SvEv-Ednra<sup>tm1Ywa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9449664	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043588	Ercc5<sup>tm2Shm</sup>	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043596	Ercc5<sup>tm2Shm</sup>/Ercc5<sup>tm2Shm</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442111	Ppm1k	is_implicated_in	DOID:9269	maple syrup urine disease		MGI:3850972	Ppm1k<sup>tm1Yiwa</sup>/Ppm1k<sup>tm1Yiwa</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19411760	20090722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0111013	cone-rod dystrophy 3		MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0111013	cone-rod dystrophy 3		MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	is_implicated_in	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia		MGI:3762762	Kiss1<sup>tm1Rla</sup>/Kiss1<sup>tm1Rla</sup>  [background:] involves: 129S1/SvImJ			ECO:0000033	author statement supported by traceable reference	PMID:17595229	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	is_implicated_in	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia		MGI:3716929	Kiss1<sup>tm1Coll</sup>/Kiss1<sup>tm1Coll</sup>  [background:] involves: 129S/SvEv * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:17563351	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:3525574	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9697838	20120226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:5307127	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] 129S6/SvEvTac-Was<sup>tm1Sbs</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22079330	20120226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298216	Crygs	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584120	Crygs<sup>Opj</sup>/Crygs<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:11121426	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298216	Crygs	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584122	Crygs<sup>Opj</sup>/Crygs<sup>Opj</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:11121426	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298216	Crygs	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584122	Crygs<sup>Opj</sup>/Crygs<sup>Opj</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8812411	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298216	Crygs	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:3584120	Crygs<sup>Opj</sup>/Crygs<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8812411	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298216	Crygs	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:2181684	Crygs<sup>rncat</sup>/Crygs<sup>rncat</sup>  [background:] Kunming			ECO:0000033	author statement supported by traceable reference	PMID:12079281	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	is_implicated_in	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome		MGI:3581978	Chrm3<sup>tm1Mmt</sup>/Chrm3<sup>tm1Mmt</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10944224	20140525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:3804722	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1Plob</sup>  [background:] B6.129S1-Tpp1<sup>tm1Plob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18343701	20131017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:3804729	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1.1Plob</sup>  [background:] B6.129S1-Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1.1Plob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18343701	20131017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:5512911	Tpp1<sup>m1J</sup>/Tpp1<sup>m1J</sup>  [background:] STOCK Tpp1<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5511005	20131017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	is_implicated_in	DOID:0110726	neuronal ceroid lipofuscinosis 2		MGI:3522157	Tpp1<sup>tm1Plob</sup>/Tpp1<sup>tm1Plob</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15483130	20131017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3759225	Pkhd1<sup>tm1.1Ggg</sup>/Pkhd1<sup>tm1.1Ggg</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17575307	20130917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:4936857	Pkhd1<sup>tm1Gwu</sup>/Pkhd1<sup>tm1Gwu</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20875407	20130917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:5438332	Pkhd1<sup>tm2Cjwa</sup>/Pkhd1<sup>tm2Cjwa</sup>  [background:] either: B6.129(Cg)-Pkhd1<sup>tm2Cjwa</sup> or C.129(Cg)-Pkhd1<sup>tm2Cjwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22021705	20130917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:5430995	Pkhd1<sup>tm1Sswi</sup>/Pkhd1<sup>tm1Sswi</sup>  [background:] B6.Cg-Pkhd1<sup>tm1Sswi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18286309	20130917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3814175	Pkhd1<sup>tm1Cjwa</sup>/Pkhd1<sup>tm1Cjwa</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17519956	20130917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3826786	Pkhd1<sup>tm1Gwu</sup>/Pkhd1<sup>tm1Gwu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18235088	20130917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388706	Star<sup>tm1Klp</sup>	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9326645	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388706	Star<sup>tm1Klp</sup>	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:10976923	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388706	Star<sup>tm1Klp</sup>	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9888583	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6423338	Prph2<sup>tm1.1Itl</sup>/Prph2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25001182	20210115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6423341	Prph2<sup>tm1.1Itl</sup>/Prph2<sup>tm1.1Itl</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25001182	20210115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6492346	Prph2<sup>tm4.1Itl</sup>/Prph2<sup>tm4.1Itl</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:31914632	20210115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	is_implicated_in	DOID:0060866	patterned macular dystrophy 1		MGI:6492344	Prph2<sup>tm4.1Itl</sup>/Prph2<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:31914632	20210115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:4413583	Wt1<sup>tm1.1Lahe</sup>/Wt1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19797313	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3611443	Wt1<sup>tm2Hst</sup>/Wt1<sup>+</sup>  [background:] chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac			ECO:0000033	author statement supported by traceable reference	PMID:16245160	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3803665	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18040647	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3803666	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] 129P2/OlaHsd-Wt1<sup>tm1Mlh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18040647	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3803667	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * MF1			ECO:0000033	author statement supported by traceable reference	PMID:18040647	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3611443	Wt1<sup>tm2Hst</sup>/Wt1<sup>+</sup>  [background:] chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac			ECO:0000033	author statement supported by traceable reference	PMID:10077614	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3512883	Wt1<sup>tm1Vih</sup>/Wt1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * MF1			ECO:0000033	author statement supported by traceable reference	PMID:15509792	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3628757	Vegfa<sup>tm4Pec</sup>/Vegfa<sup>tm4Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12539040	20060711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3047228	Vegfa<sup>tm1Pec</sup>/Vegfa<sup>tm1Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12539040	20060711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177823	Eng<sup>tm1Dyl</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:2177905	Eng<sup>tm1Dyl</sup>/Eng<sup>tm1Dyl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10348742	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347001	Btd	is_implicated_in	DOID:856	biotinidase deficiency		MGI:4888512	Btd<sup>tm1Bwol</sup>/Btd<sup>tm1Bwol</sup>  [background:] B6.Cg-Btd<sup>tm1Bwol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21051254	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181780	Foxe1<sup>tm1Rdl</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9697704	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603561	Smarcb1<sup>tm1Gvk</sup>	is_implicated_in	DOID:2129	atypical teratoid rhabdoid tumor		MGI:3603677	Smarcb1<sup>tm1Gvk</sup>/Smarcb1<sup>tm1Gvk</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:16099835	20051107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856946	Dock7<sup>m</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3582588	Dock7<sup>m</sup>/Dock7<sup>m</sup>  [background:] B6.D(Cg)-Dock7<sup>m</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9475748	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	is_implicated_in	DOID:0110350	osteogenesis imperfecta type 6		MGI:5758948	Serpinf1<sup>tm1Craw</sup>/Serpinf1<sup>tm1Craw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:23413146	20160411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5446147	b2b1430Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5446380	b2b1430Clo/b2b1430Clo  [background:] C57BL/6J-b2b1430Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934258	Ihh<sup>tm1Amc</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3584475	Ihh<sup>tm1Amc</sup>/Ihh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:10821773	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3623411	Tgfbr2<sup>tm1Karl</sup>/Tgfbr2<sup>tm1Karl</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15741317	20060529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695884	Tg(SOD1*H46R*H48Q)58Dbo	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3833108	Tg(SOD1*H46R*H48Q)58Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12127151	20090223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:4438262	Amelx<sup>Rgsc888</sup>/Amelx<sup>Rgsc888</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:4438260	Amelx<sup>Rgsc888</sup>/Amelx<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:4438261	Amelx<sup>Rgsc888</sup>/Y  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:2177295	Amelx<sup>tm1Kul</sup>/Amelx<sup>tm1Kul</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11406633	20100331	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5495415	Kif7<sup>dda</sup>/Kif7<sup>dda</sup>  [background:] FVB.A-Kif7<sup>dda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23650387	20130717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2513	basal cell carcinoma		MGI:4452396	Ptch1<sup>tm1Hahn</sup>/Ptch1<sup>tm1Hahn</sup> Gt(ROSA)26Sor<sup>tm2(cre/ERT2)Brn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20233865	20181207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2513	basal cell carcinoma		MGI:6259595	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:10545995	20181207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2513	basal cell carcinoma		MGI:5925369	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(KRT14-cre)8Brn/0  [background:] involves: 129T2/SvEms * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23404854	20181207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931805	Crkl<sup>tm1Imo</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:2175797	Crkl<sup>tm1Imo</sup>/Crkl<sup>tm1Imo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11242111	20060607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177742	Hps4	is_implicated_in	DOID:0060542	Hermansky-Pudlak syndrome 4		MGI:3587187	Hps4<sup>le</sup>/Hps4<sup>le</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11836498	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711771	Braf<sup>tm1Mmcm</sup>	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5780077	Braf<sup>tm1Mmcm</sup>/Braf<sup>+</sup> Tg(Tg-cre/ERT2)#Mmcm/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21512141	20160708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5318689	Chrnb2<sup>tm1Jpc</sup>/Chrnb2<sup>tm1Jpc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12876201	20140122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038748	Frem1<sup>eyes2</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5473606	Frem1<sup>eyes2</sup>/Frem1<sup>eyes2</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23221805	20130410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889800	Myot	is_not_implicated_in	DOID:0080094	myofibrillar myopathy 3		MGI:3699229	Myot<sup>tm1.1Moza</sup>/Myot<sup>tm1.1Moza</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:17074808	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857159	Drd3<sup>tm1Dac</sup>	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:4839954	Drd3<sup>tm1Dac</sup>/Drd3<sup>tm1Dac</sup>  [background:] B6.129S4-Drd3<sup>tm1Dac</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15601940	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690299	Myh6<sup>tm1Ces</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3691280	Myh6<sup>tm1Ces</sup>/Myh6<sup>tm1Ces</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690299	Myh6<sup>tm1Ces</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3691279	Myh6<sup>tm1Ces</sup>/Myh6<sup>+</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856157	Pax6<sup>Sey-Dey</sup>	is_implicated_in	DOID:12271	aniridia		MGI:2175204	Pax6<sup>Sey-Dey</sup>/Pax6<sup>+</sup>  [background:] C3H/HeJ-Pax6<sup>Sey-Dey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2173141	20071019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311334	b2b227Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287976	Becn1<sup>tm1Ebr</sup>/Becn1<sup>tm1Ebr</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822311	Lepr<sup>tm1Yli</sup>	is_implicated_in	DOID:9970	obesity		MGI:3822317	Lepr<sup>tm1Yli</sup>/Lepr<sup>tm1Yli</sup>  [background:] B6.129-Lepr<sup>tm1Yli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19015522	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856703	cl	is_implicated_in	DOID:11836	clubfoot		MGI:2663270	cl/cl  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:48832	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758741	Comp<sup>tm1Mbri</sup>	is_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:3758814	Comp<sup>tm1Mbri</sup>/Comp<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17588960	20071022	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2651573	Tub	is_implicated_in	DOID:9970	obesity		MGI:3715252	Tub<sup>tub</sup>/Tub<sup>tub</sup>  [background:] C57BL/6J-Tub<sup>tub</sup>			ECO:0000033	author statement supported by traceable reference	MGI:61951	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2651573	Tub	is_implicated_in	DOID:9970	obesity		MGI:2174793	Tub<sup>tub</sup>/Tub<sup>tub</sup>  [background:] B6(AU)-Tub<sup>tub</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8606774	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347487	Foxm1	is_implicated_in	DOID:1324	lung cancer		MGI:3710341	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21199796	20110306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	is_implicated_in	DOID:0060485	Mowat-Wilson syndrome		MGI:3624726	Zeb2<sup>tm1.2Yhi</sup>/Zeb2<sup>tm1.2Yhi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12522767	20060619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99909	Lama3	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:3042129	Lama3<sup>tm1Crt</sup>/Lama3<sup>tm1Crt</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10366601	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:3510446	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8956999	20140416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:4452030	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] 129-Col4a3<sup>tm1Dec</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20197625	20140416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:2176903	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8947561	20140416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:2176903	Col4a3<sup>tm1Jhm</sup>/Col4a3<sup>tm1Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24262794	20140416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:3510458	Col4a3<sup>tm1Dec</sup>/Col4a3<sup>tm1Dec</sup>  [background:] 129X1/SvJ-Col4a3<sup>tm1Dec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9682811	20140416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5695364	Srsf2<sup>tm1.1Oaw</sup>/Srsf2<sup>+</sup> Tg(Mx1-cre)1Cgn/?  [background:] B6.Cg-Tg(Mx1-cre)1Cgn Srsf2<sup>tm1.1Oaw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25965569	20151110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3616090	Sord<sup>C57BL/Lia</sup>	is_implicated_in	DOID:83	cataract		MGI:3836915	Sord<sup>C57BL/Lia</sup>/Sord<sup>C57BL/Lia</sup>  [background:] involves: C57BL/LiA			ECO:0000033	author statement supported by traceable reference	PMID:18760274	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:5803721	Notch2<sup>tm1.1Ecan</sup>/Notch2<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26627824	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:6766538	Notch2<sup>tm1.1Hhtg</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28856714	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:6157651	Notch2<sup>tm2.1Ecan</sup>/Notch2<sup>tm2.1Ecan</sup> Tg(BGLAP-cre)1Clem/0  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:28592489	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	is_implicated_in	DOID:2736	Hajdu-Cheney syndrome		MGI:6157629	Notch2<sup>tm2.2Ecan</sup>/Notch2<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28592489	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:2678506	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>/Nphs1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12039988	20060221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:2678505	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>/Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12039988	20060221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3613052	Nphs1<sup>tm1Ktry</sup>/Nphs1<sup>tm1Ktry</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11136707	20060221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3587727	Nphs1<sup>tm1Rkl</sup>/Nphs1<sup>tm1Rkl</sup>  [background:] involves: 129S2/SvPasCrl			ECO:0000033	author statement supported by traceable reference	PMID:12039968	20060221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525361	Ccn6<sup>tm2Mawa</sup>	is_implicated_in	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood		MGI:3526050	Ccn6<sup>tm2Mawa</sup>/Ccn6<sup>tm2Mawa</sup>  [background:] 129S/SvEv-Ccn6<sup>tm2Mawa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15601861	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525361	Ccn6<sup>tm2Mawa</sup>	is_implicated_in	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood		MGI:5515356	Ccn6<sup>tm2Mawa</sup>/Ccn6<sup>tm2Mawa</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24040393	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106633	Phox2a	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3531404	Phox2a/Inppl1<sup>tm1Ssch</sup>/Phox2a/Inppl1<sup>tm1Ssch</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11343120	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106633	Phox2a	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3531409	Phox2a/Inppl1<sup>tm1Ssch</sup>/Phox2a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11343120	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	is_not_implicated_in	DOID:0111112	nephronophthisis 1		MGI:3813305	Nphp1<sup>tm1.1Hung</sup>/Nphp1<sup>tm1.1Hung</sup>  [background:] B6.Cg-Nphp1<sup>tm1.1Hung</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18684731	20081030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98817	Hsp90b1	is_implicated_in	DOID:0112312	male infertility due to globozoospermia		MGI:6885740	Hsp90b1<sup>tm1Zhli</sup>/Hsp90b1<sup>tm1.1Zhli</sup> Tg(Ddx4-cre)1Dcas/0  [background:] involves: 129S/SvEv * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21208614	20220302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	is_implicated_in	DOID:0060689	atrichia with papular lesions		MGI:3850354	Hr<sup>rh-8J</sup>/Hr<sup>rh-8J</sup>  [background:] B10.D2/nSnJ-Hr<sup>rh-8J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9799606	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	is_implicated_in	DOID:0060689	atrichia with papular lesions		MGI:3052308	Hr<sup>rhsl</sup>/Hr<sup>rhsl</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:15955095	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3841005	Ccr2<sup>tm1Mae</sup>/Ccr2<sup>tm1Mae</sup>  [background:] B6.129P2-Ccr2<sup>tm1Mae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028848	Tg(aP2-SREBF1c)9884Reh	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3028851	Tg(aP2-SREBF1c)9884Reh/0  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9784493	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3843203	Men1<sup>tm1Ctre</sup>/Men1<sup>tm1Ctre</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19208834	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:5461308	Men1<sup>tm1Rvt</sup>/Men1<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19620250	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3839791	Men1<sup>tm1Gfk</sup>/Men1<sup>tm1Gfk</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15060136	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3813539	Men1<sup>tm2.1Gfk</sup>/Men1<sup>+</sup>  [background:] involves: 129T2/SvEms * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17044021	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3813538	Men1<sup>tm1.1Gfk</sup>/Men1<sup>+</sup>  [background:] involves: 129T2/SvEms * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17044021	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:2675251	Men1<sup>tm1.2Zqw</sup>/Men1<sup>tm1.2Zqw</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:12941803	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies		MGI:3625035	Pmp22<sup>tm1Lnot</sup>/Pmp22<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16436605	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies		MGI:3794447	Pmp22<sup>tm1Ueli</sup>/Pmp22<sup>tm1Ueli</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:7581450	20131031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682061	Ext1<sup>tm1Yama</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5316488	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Tg(Camk2a-cre)2834Lusc/0  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22411800	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:4941778	Slc6a8<sup>tm1.2Clar</sup>/Y  [background:] involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21249153	20180910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:5825026	Slc6a8<sup>tm1.2Lbar</sup>/Y  [background:] involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27466184	20180910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:5825021	Slc6a8<sup>tm1.2Lbar</sup>/Y  [background:] involves: 129 * 129S1/Sv * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25485098	20180910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:6197218	Slc6a8<sup>tm1e(KOMP)Wtsi</sup>/Y  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30013483	20180910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:5448415	Slc6a8<sup>tm1.1Clar</sup>/Y Tg(Camk2a-cre)2Gsc/0  [background:] involves: C57BL/6 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22751104	20180910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386271	Tyrobp<sup>tm1.1Viv</sup>	is_implicated_in	DOID:0090112	Nasu-Hakola disease		MGI:3818484	Tyrobp<sup>tm1.1Viv</sup>/Tyrobp<sup>tm1.1Viv</sup>  [background:] B6.129P2-Tyrobp<sup>tm1.1Viv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15632019	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:4950068	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195751	20110514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575662	Asxl1<sup>tm1.1Iaai</sup>/Asxl1<sup>tm1.1Iaai</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24218140	20140731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575661	Asxl1<sup>tm1.1Iaai</sup>/Asxl1<sup>tm1.1Iaai</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S/SvEv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24218140	20140731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575759	Asxl1<sup>tm1.1Mjxu</sup>/Asxl1<sup>tm1.1Mjxu</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24255920	20140731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5575760	Asxl1<sup>tm1.1Mjxu</sup>/Asxl1<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24255920	20140731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587024	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] involves: MYA/Hu			ECO:0000033	author statement supported by traceable reference	MGI:1889019	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3521748	Hoxa13<sup>tm1Jwi</sup>/Hoxa13<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15385446	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3521745	Hoxa13<sup>tm1Jwi</sup>/Hoxa13<sup>tm1Jwi</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15385446	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587031	Hoxa13<sup>Hd</sup>/Hoxa13<sup>+</sup>  [background:] B6C3Fe-a/a Hoxa13<sup>Hd</sup> Mcoln3<sup>Va-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10210434	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587032	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] B6C3Fe-a/a Hoxa13<sup>Hd</sup> Mcoln3<sup>Va-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10569982	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587024	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] involves: MYA/Hu			ECO:0000033	author statement supported by traceable reference	PMID:5519671	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921258	Arsg	is_implicated_in	DOID:12798	mucopolysaccharidosis		MGI:5430642	Arsg<sup>tm1Tdi</sup>/Arsg<sup>tm1Tdi</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22689975	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3799277	Large1<sup>myd-3J</sup>	is_implicated_in	DOID:0110637	muscular dystrophy-dystroglycanopathy type B6		MGI:4454427	Large1<sup>myd-3J</sup>/Large1<sup>myd-3J</sup>  [background:] STOCK Large1<sup>myd-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:4454310	20100609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441950	Adgrl3	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5430804	Adgrl3<sup>Gt(S17-5H1)Sor</sup>/Adgrl3<sup>Gt(S17-5H1)Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27247960	20190718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183746	Tg(UcpDta)1Kz	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2385751	Tg(UcpDta)1Kz/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8264795	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	is_implicated_in	DOID:4644	epidermolysis bullosa simplex		MGI:3812462	Krt14<sup>tm1Efu</sup>/Krt14<sup>tm1Efu</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:7539810	20081029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	is_implicated_in	DOID:4644	epidermolysis bullosa simplex		MGI:2653129	Krt14<sup>tm1Der</sup>/Krt14<sup>tm1Der</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	is_implicated_in	DOID:12679	nephrocalcinosis		MGI:6368208	Brd4<sup>M1Rvt</sup>/Brd4<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:30830987	20211019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888378	Psap<sup>tm1Suz</sup>	is_implicated_in	DOID:0111330	combined saposin deficiency		MGI:3711319	Psap<sup>tm1Suz</sup>/Psap<sup>tm1Suz</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8776585	20200724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921325	Syce1	is_implicated_in	DOID:0080869	primary ovarian insufficiency 12		MGI:6760664	Syce1<sup>em1Rrca</sup>/Syce1<sup>em1Rrca</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32402064	20210920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	is_implicated_in	DOID:2527	nephrosis		MGI:2175097	Lamb2<sup>tm1Jrs</sup>/Lamb2<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:7670489	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437472	Cryaa<sup>tm1Ady</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:4437475	Cryaa<sup>tm1Ady</sup>/Cryaa<sup>tm1Ady</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:19619312	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437472	Cryaa<sup>tm1Ady</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:4437476	Cryaa<sup>tm1Ady</sup>/Cryaa<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:19619312	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857227	Nos1<sup>tm1Plh</sup>	is_not_implicated_in	DOID:12638	hypertrophic pyloric stenosis		MGI:4366780	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10982771	20091111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176405	Ppt2<sup>tm1Hof</sup>	is_implicated_in	DOID:14503	neuronal ceroid lipofuscinosis		MGI:2176416	Ppt2<sup>tm1Hof</sup>/Ppt2<sup>tm1Hof</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11717424	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:78359	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686996	Mitf<sup>Mi-H</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2663064	Mitf<sup>Mi-wh</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450310	Chat<sup>tm1Fhg</sup>	is_implicated_in	DOID:0110671	congenital myasthenic syndrome 6		MGI:2662570	Chat<sup>tm1Fhg</sup>/Chat<sup>tm1Fhg</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12533614	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95683	Gdf1	is_implicated_in	DOID:0060850	annular pancreas		MGI:3625848	Gdf1<sup>tm1Sjl</sup>/Gdf1<sup>tm1Sjl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10700179	20081215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384133	Mpz<sup>tm1Msch</sup>	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3		MGI:3576602	Mpz<sup>tm1Msch</sup>/Mpz<sup>tm1Msch</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7581451	20050511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343460	Gnpat	is_implicated_in	DOID:0110852	rhizomelic chondrodysplasia punctata type 2		MGI:2670462	Gnpat<sup>tm1Just</sup>/Gnpat<sup>tm1Just</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12874108	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11454988	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3029165	Smpd1<sup>tm1Wst</sup>/Smpd1<sup>tm1Wst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7600574	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7670466	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12594290	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8706124	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12213735	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3028763	Smpd1<sup>tm1Esc</sup>/Smpd1<sup>tm1Esc</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9382882	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813481	Tg(Ppp1r1b-HTT*)1Meeh	is_implicated_in	DOID:12858	Huntington's disease		MGI:3813482	Tg(Ppp1r1b-HTT*)1Meeh/0  [background:] C57BL/6J-Tg(Ppp1r1b-HTT*)1Meeh			ECO:0000033	author statement supported by traceable reference	PMID:18632688	20081103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	is_implicated_in	DOID:8398	osteoarthritis		MGI:6306137	Tg(Col2a1-cre/ERT2)1Dic/0 Tgfbr1<sup>tm1.1Karl</sup>/Tgfbr1<sup>tm1.1Karl</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28716756	20190529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926888	Crebbp<sup>tm1Dli</sup>	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10673499	20050926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916066	Ppil1	is_implicated_in	DOID:10907	microcephaly		MGI:6509640	Ppil1<sup>em4Jgg</sup>/Ppil1<sup>em4Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em4Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20211019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916066	Ppil1	is_implicated_in	DOID:10907	microcephaly		MGI:6509636	Ppil1<sup>em3Jgg</sup>/Ppil1<sup>em3Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em3Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20211019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:3785289	Cybb<sup>tm1Din</sup>/Cybb<sup>tm1Din</sup>  [background:] B6.129S-Cybb<sup>tm1Din</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19234224	20100414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:2449556	Cybb<sup>tm1Din</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7719350	20100414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	is_implicated_in	DOID:0110552	autosomal dominant nonsyndromic deafness 22		MGI:6431144	Myo6<sup>em1Bcgen</sup>/Myo6<sup>+</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:31103816	20200602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	is_implicated_in	DOID:0110552	autosomal dominant nonsyndromic deafness 22		MGI:3528185	Myo6<sup>sv</sup>/Myo6<sup>sv</sup>  [background:] involves: B10.HA/(33NX)Sn * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7493015	20200602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	is_implicated_in	DOID:0080547	metabolic dysfunction-associated steatohepatitis		MGI:7280898	Krt18<sup>tm1Tmm</sup>/Krt18<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27689336	20220526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3589477	Zfpm2<sup>lil</sup>/Zfpm2<sup>lil</sup>  [background:] involves: A/J			ECO:0000033	author statement supported by traceable reference	PMID:16103912	20051013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183399	Runx3<sup>tm1Yg</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:5689499	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861949	Stat1<sup>tm1Rds</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3771372	Stat1<sup>tm1Rds</sup>/Stat1<sup>tm1Rds</sup>  [background:] 129S6/SvEv-Stat1<sup>tm1Rds</sup>/Tac			ECO:0000033	author statement supported by traceable reference	PMID:22264274	20160425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2665504	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] C57BL/6J-Apc<sup>Min</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14522940	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:5521585	Apc<sup>tm2Tno</sup>/Apc<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14522940	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2175903	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] involves: AKR/J * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:1350108	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:5688288	Apc<sup>M1Tno</sup>/Apc<sup>+</sup>  [background:] either: B6JJcl.B6(D2JJcl)-Apc<sup>M1Tno</sup> or (involves: C57BL/6 * C57BL/6JJcl * DBA/2JJcl)			ECO:0000033	author statement supported by traceable reference	PMID:23551873	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2175907	Apc<sup>tm1Mmt</sup>/Apc<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7753829	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:3590232	Apc<sup>tm1Kk</sup>/Apc<sup>tm1Kk</sup> Tg(Lck-cre)1Cwi/?  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18077429	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2182592	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9311916	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:3513849	Apc<sup>tm1Cip</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15502862	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2175909	Apc<sup>tm1Rak</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8090754	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	is_not_implicated_in	DOID:2582	acatalasia		MGI:3615785	Cat<sup>b</sup>/Cat<sup>b</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6058079	20110725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:10283	prostate cancer		MGI:4358249	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21620777	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:10283	prostate cancer		MGI:4420974	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:14522255	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:10283	prostate cancer		MGI:5636613	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(KLK3-cre)13Saa/0  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24986896	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:10283	prostate cancer		MGI:5827768	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)20Fwan/?  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27345403	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:10283	prostate cancer		MGI:4358249	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22350410	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:3814579	Kmt2a<sup>tm1Saam</sup>/Kmt2a<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18977325	20100813	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:3527796	Lmna<sup>tm1Gbon</sup>/Lmna<sup>tm1Gbon</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22773734	20170810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:5906504	Lmna<sup>tm2.1Gbon</sup>/Lmna<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23575224	20170810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:3589459	Lmna<sup>tm3Stw</sup>/Lmna<sup>tm3Stw</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:15972724	20170810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:14755333	20170810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:18182166	20170810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856180	Spta1<sup>sph-2Bc</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6841965	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856180	Spta1<sup>sph-2Bc</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6234993	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:2663997	Kit<sup>tm2Bsm</sup>/Kit<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12754375	20121126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:3773052	Kit<sup>tm1Shta</sup>/Kit<sup>tm1Shta</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18098338	20121126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:3603337	Kit<sup>tm1Bpr</sup>/Kit<sup>tm1Bpr</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16061643	20121126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:3603339	Kit<sup>tm1Bpr</sup>/Kit<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16061643	20121126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:5442707	Kit<sup>tm4.1Bsm</sup>/Kit<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22652566	20121126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044768	Trak1<sup>hyrt</sup>	is_implicated_in	DOID:13366	Stiff-Person syndrome		MGI:3615358	Trak1<sup>hyrt</sup>/Trak1<sup>hyrt</sup>  [background:] involves: AKR * C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16380713	20060309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335088	Pstpip2	is_implicated_in	DOID:0060645	chronic recurrent multifocal osteomyelitis		MGI:3614947	Pstpip2<sup>cmo</sup>/Pstpip2<sup>cmo</sup>  [background:] C.Cg-Pstpip2<sup>cmo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16122996	20230119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335088	Pstpip2	is_implicated_in	DOID:0060645	chronic recurrent multifocal osteomyelitis		MGI:3614947	Pstpip2<sup>cmo</sup>/Pstpip2<sup>cmo</sup>  [background:] C.Cg-Pstpip2<sup>cmo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10678414	20230119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152564	Gusb<sup>mps-2J</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:2677921	Gusb<sup>mps-2J</sup>/Gusb<sup>mps-2J</sup>  [background:] C3H/HeOuJ-Gusb<sup>mps-2J</sup>/BrkJ			ECO:0000033	author statement supported by traceable reference	PMID:11228259	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152564	Gusb<sup>mps-2J</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:2677921	Gusb<sup>mps-2J</sup>/Gusb<sup>mps-2J</sup>  [background:] C3H/HeOuJ-Gusb<sup>mps-2J</sup>/BrkJ			ECO:0000033	author statement supported by traceable reference	PMID:9774663	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	is_implicated_in	DOID:1612	breast cancer		MGI:5469591	Pik3ca<sup>tm1Gne</sup>/Pik3ca<sup>+</sup> Tg(MMTV-cre)1Mam/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22370636	20160407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	is_implicated_in	DOID:1612	breast cancer		MGI:5755852	Pik3ca<sup>tm1.1Waph</sup>/Pik3ca<sup>+</sup> Tg(MMTV-cre)#Mam/0  [background:] involves: 129S1/Sv * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:22666336	20160407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3047689	Lum<sup>tm1Chak</sup>/Lum<sup>tm1Chak</sup>  [background:] involves: 129S/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9606218	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	is_implicated_in	DOID:0050634	alopecia universalis		MGI:3713665	Hr<sup>rh-Chr</sup>/Hr<sup>rh-Chr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9832318	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	is_implicated_in	DOID:0050634	alopecia universalis		MGI:3052308	Hr<sup>rhsl</sup>/Hr<sup>rhsl</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:15955095	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	is_implicated_in	DOID:0050634	alopecia universalis		MGI:3850354	Hr<sup>rh-8J</sup>/Hr<sup>rh-8J</sup>  [background:] B10.D2/nSnJ-Hr<sup>rh-8J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9799606	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	is_implicated_in	DOID:0110014	age related macular degeneration 1		MGI:5637298	Cryba1<sup>tm1.1Dbsa</sup>/Cryba1<sup>tm1.1Dbsa</sup> Tg(BEST1-cre)1Jdun/0  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25257511	20150525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109198	Eif4ebp2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3610950	Eif4ebp2<sup>tm1Klan</sup>/Eif4ebp2<sup>tm1Klan</sup>  [background:] B6.129S4(C)-Eif4ebp2<sup>tm1Klan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23172145	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:4429407	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: STOCK Mlph<sup>ln</sup> a Tgfa<sup>wa1</sup> Cdh23<sup>v</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24680679	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3777758	Crygb<sup>S11R</sup>/Crygb<sup>+</sup>  [background:] A/J-Crygb<sup>S11R</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18172107	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3777759	Crygb<sup>S11R</sup>/Crygb<sup>S11R</sup>  [background:] A/J-Crygb<sup>S11R</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18172107	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3603148	Crygb<sup>Clapper</sup>/Crygb<sup>+</sup>  [background:] C57BL/6J-Crygb<sup>Clapper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15878859	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3603147	Crygb<sup>Clapper</sup>/Crygb<sup>Clapper</sup>  [background:] C57BL/6J-Crygb<sup>Clapper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15878859	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:2175806	Crygb<sup>Nop</sup>/Crygb<sup>Nop</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6479248	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:2175807	Crygb<sup>Nop</sup>/Crygb<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6479248	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177814	Gpnmb<sup>R150X</sup>	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:2178291	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:10192392	20080310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177814	Gpnmb<sup>R150X</sup>	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:2178286	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:10192392	20080310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177814	Gpnmb<sup>R150X</sup>	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:3773274	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] B6.D2-Gpnmb<sup>R150X</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16827931	20080310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105956	Pde6c	is_implicated_in	DOID:13911	achromatopsia		MGI:4411994	Pde6c<sup>cpfl1</sup>/Pde6c<sup>cpfl1</sup>  [background:] B6.CXB1-Pde6c<sup>cpfl1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19887631	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105956	Pde6c	is_implicated_in	DOID:13911	achromatopsia		MGI:2657248	Pde6c<sup>cpfl1</sup>/Pde6c<sup>cpfl1</sup>  [background:] involves: CXB1/ByJ			ECO:0000033	author statement supported by traceable reference	PMID:11853768	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834461	Tg(Ly6a-BCR/ABL1)IS1AIsg	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3834481	Tg(Ly6a-BCR/ABL1)IS1AIsg/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19037256	20090305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	is_not_implicated_in	DOID:0060194	amyotrophic lateral sclerosis type 2		MGI:3807481	Als2<sup>tm1Garo</sup>/Als2<sup>tm1Garo</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:18558633	20080924	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	is_not_implicated_in	DOID:0060194	amyotrophic lateral sclerosis type 2		MGI:3616467	Als2<sup>tm1Jei</sup>/Als2<sup>tm1Jei</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16321985	20080924	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	is_not_implicated_in	DOID:0060194	amyotrophic lateral sclerosis type 2		MGI:3589591	Als2<sup>tm1Cai</sup>/Als2<sup>tm1Cai</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16107644	20080924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3709467	Tg(Camk2a-Bdnf)A9Stl	is_not_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5617753	Tg(Camk2a-Bdnf)A9Stl/0  [background:] C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J			ECO:0000033	author statement supported by traceable reference	PMID:24768643	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033229	Gck<sup>Rgsc236</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590138	Gck<sup>Rgsc236</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:3583142	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:8700894	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:2651381	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:8700894	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:2651381	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:14634077	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:3583142	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:3590414	Itgb2<sup>tm2Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:3590415	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] PL.129S7-Itgb2<sup>tm1Bay</sup> Itgb2<sup>tm2Bay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_implicated_in	DOID:8893	psoriasis		MGI:3590487	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154690	Cyp1b1<sup>tm1Gonz</sup>	is_implicated_in	DOID:11211	buphthalmos		MGI:3655821	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] 129X1.Cg-Cyp1b1<sup>tm1Gonz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154690	Cyp1b1<sup>tm1Gonz</sup>	is_implicated_in	DOID:11211	buphthalmos		MGI:3655819	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154690	Cyp1b1<sup>tm1Gonz</sup>	is_implicated_in	DOID:11211	buphthalmos		MGI:3655820	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] B6.Cg-Cyp1b1<sup>tm1Gonz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:3624438	Pomgnt1<sup>Gt(OST179231)Lex</sup>/Pomgnt1<sup>Gt(OST179231)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23454088	20130805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:3832643	Pomgnt1<sup>tm1Stk</sup>/Pomgnt1<sup>tm1Stk</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:19114101	20130805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:3624438	Pomgnt1<sup>Gt(OST179231)Lex</sup>/Pomgnt1<sup>Gt(OST179231)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16458488	20130805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:6407058	Fgfr2<sup>tm3.1Cxd</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18242159	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:4440856	Fgfr2<sup>tm2Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] B6.Cg-Fgfr2<sup>tm2Ewj</sup> Tg(EIIa-cre)C5379Lmgd			ECO:0000033	author statement supported by traceable reference	PMID:20175913	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:2176483	Fgfr2<sup>tm2.3Dsn</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11274405	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:3604078	Fgfr2<sup>tm2Cxd</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14499350	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:4430189	Fgfr2<sup>tm2Ewj</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20077479	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:3604025	Fgfr2<sup>tm1Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20077479	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:5790180	Fgfr2<sup>tm2Cxd</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21538817	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:6415627	Fgfr2<sup>tm3Cxd</sup>/Fgfr2<sup>+</sup> Tg(Col2a1-cre)1Xya/0  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28123344	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:12960	acrocephalosyndactylia		MGI:3604025	Fgfr2<sup>tm1Ewj</sup>/Fgfr2<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15975938	20200508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934892	Hspg2<sup>tm1Ref</sup>	is_implicated_in	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia		MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12814946	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3655816	Tg(YACW408A5)1952Ricc	is_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:3655962	Tg(YACW408A5)1952Ricc/0  [background:] involves: 129/Sv * SD7			ECO:0000033	author statement supported by traceable reference	PMID:15640248	20060927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5293439	Mapk1<sup>tm1.2Kuta</sup>/Mapk1<sup>tm1.2Kuta</sup> Tg(Nes-cre)1Kag/0  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21849556	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277124	Asah1	is_implicated_in	DOID:0050464	Farber lipogranulomatosis		MGI:2655551	Asah1<sup>tm1Esc</sup>/Asah1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11829492	20200325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277124	Asah1	is_implicated_in	DOID:0050464	Farber lipogranulomatosis		MGI:6401409	Asah1<sup>tm1.2Geno</sup>/Asah1<sup>tm1.2Geno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29908121	20200325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277124	Asah1	is_implicated_in	DOID:0050464	Farber lipogranulomatosis		MGI:5800675	Asah1<sup>tm1Medin</sup>/Asah1<sup>tm1Medin</sup>  [background:] involves: 129S6/SvEvTac * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23681708	20200325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777322	Agps<sup>bs2</sup>	is_implicated_in	DOID:0110853	rhizomelic chondrodysplasia punctata type 3		MGI:4949537	Agps<sup>bs2</sup>/Agps<sup>bs2</sup>  [background:] STOCK Agps<sup>bs2</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21353609	20120615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640614	Otof<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110535	autosomal recessive nonsyndromic deafness 9		MGI:3693849	Otof<sup>tm1Ugds</sup>/Otof<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17055430	20070116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441982	Aldh5a1	is_implicated_in	DOID:1826	epilepsy		MGI:2654880	Aldh5a1<sup>tm1Kmg</sup>/Aldh5a1<sup>tm1Kmg</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15262267	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385095	Lzts2	is_implicated_in	DOID:18	urinary system disease		MGI:5302224	Lzts2<sup>tm1.1Zsu</sup>/Lzts2<sup>tm1.1Zsu</sup>  [background:] B6.Cg-Lzts2<sup>tm1.1Zsu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21949185	20170619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858901	Fut8	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3608986	Fut8<sup>tm1Nta</sup>/Fut8<sup>tm1Nta</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16236725	20060104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6414873	Wnk4<sup>em1Cjc</sup>/Wnk4<sup>em1Cjc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30765526	20200505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174710	Prnp<sup>tm1Edin</sup>/Prnp<sup>tm1Edin</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Edin</sup>/EdinH			ECO:0000033	author statement supported by traceable reference	PMID:10581259	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174712	Prnp<sup>tm1Rcm</sup>/Prnp<sup>tm1Rcm</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Rcm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9462739	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174711	Prnp<sup>tm1Miy</sup>/Prnp<sup>tm1Miy</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7494265	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174709	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1373228	20050830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710095	Gt(ROSA)26Sor<sup>tm2(SS18)Mrc</sup>	is_implicated_in	DOID:5485	synovial sarcoma		MGI:3711005	Gt(ROSA)26Sor<sup>tm2(SS18)Mrc</sup>/Gt(ROSA)26Sor<sup>tm2(SS18)Mrc</sup> Myf5<sup>tm1(cre)Mrc</sup>/Myf5<sup>tm1(cre)Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17418413	20091223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3836962	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup> Tg(Atoh1-GFP)1Jejo/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19185848	20110922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:0050902	medulloblastoma		MGI:2675737	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19185848	20110922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3040327	Ptch1<sup>tm1Zim</sup>/Ptch1<sup>+</sup>  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12386820	20110922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5286071	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(Atoh1-cre/Esr1*)14Fsh/0  [background:] involves: 129T2/SvEms * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5286072	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129T2/SvEms * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5286070	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: 129T2/SvEms * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794650	Wt1<sup>tm1Mlh</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3803666	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] 129P2/OlaHsd-Wt1<sup>tm1Mlh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18040647	20080828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794650	Wt1<sup>tm1Mlh</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3803665	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18040647	20080828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794650	Wt1<sup>tm1Mlh</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3803667	Wt1<sup>tm1Mlh</sup>/Wt1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * MF1			ECO:0000033	author statement supported by traceable reference	PMID:18040647	20080828	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918882	Scn3b	is_implicated_in	DOID:0110224	Brugada syndrome 7		MGI:5294675	Scn3b<sup>tm1Clhh</sup>/Scn3b<sup>tm1Clhh</sup>  [background:] 129S/SvEv-Scn3b<sup>tm1Clhh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19351516	20111103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579991	Lmbr1<sup>tm1Kng</sup>	is_implicated_in	DOID:0050603	acheiropody		MGI:3580291	Lmbr1<sup>tm1Kng</sup>/Lmbr1<sup>tm1Kng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:11606546	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653915	Ppp1r3a<sup>tm1Ptwc</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2653988	Ppp1r3a<sup>tm1Ptwc</sup>/Ppp1r3a<sup>tm1Ptwc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12606498	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178319	Pde6b<sup>rd1-3H</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028388	Pde6b<sup>rd1-3H</sup>/Pde6b<sup>rd1-3H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156741	Pax6<sup>4Neu</sup>	is_implicated_in	DOID:0060673	Peters anomaly		MGI:3590308	Pax6<sup>4Neu</sup>/Pax6<sup>+</sup>  [background:] either: (involves: 102 * C3H) or (involves: C3H)			ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919163	Tmem79	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5559071	Tmem79<sup>ma</sup>/Tmem79<sup>ma</sup>  [background:] involves: C57BL/6JJcl * CBA/CaGr			ECO:0000033	author statement supported by traceable reference	PMID:24060273	20140418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919163	Tmem79	is_implicated_in	DOID:3310	atopic dermatitis		MGI:5559357	Tmem79<sup>ma</sup>/Tmem79<sup>ma</sup>  [background:] B6.CBACaGr-Tmem79<sup>ma</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24084074	20140418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105976	Myo5a	is_implicated_in	DOID:0060832	Griscelli syndrome type 1		MGI:3624435	Myo5a<sup>d-n</sup>/Myo5a<sup>d-n</sup>  [background:] B10.D2-H2<sup>d</sup>/nSnJ			ECO:0000033	author statement supported by traceable reference	PMID:21508232	20141222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105976	Myo5a	is_implicated_in	DOID:0060832	Griscelli syndrome type 1		MGI:5607614	Myo5a<sup>d-l34J</sup>/Myo5a<sup>d-l34J</sup>  [background:] BALB/cJ-Myo5a<sup>d-l34J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5607575	20141222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415595	Dnai1<sup>tm1.1Leo</sup>	is_implicated_in	DOID:0110594	primary ciliary dyskinesia 1		MGI:4415702	Dnai1<sup>tm1.1Leo</sup>/Dnai1<sup>tm1.1Leo</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19675306	20100823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2672943	Lyst<sup>bg-14J</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2672959	Lyst<sup>bg-14J</sup>/Lyst<sup>bg-14J</sup>  [background:] C3Fe;B6-Lyst<sup>bg-14J</sup>			ECO:0000033	author statement supported by traceable reference	MGI:2673072	20051103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685418	Gm572	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182645	Nbn<sup>tm1Xu</sup>	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:2675319	Nbn<sup>tm1Xu</sup>/Nbn<sup>tm1Xu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11889050	20060213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574586	Lmo4<sup>tm1.1Gng</sup>	is_implicated_in	DOID:0060668	anencephaly		MGI:3575660	Lmo4<sup>tm1.1Gng</sup>/Lmo4<sup>tm1.1Gng</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15691703	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:2174943	Clcnka<sup>tm1Suc</sup>/Clcnka<sup>tm1Suc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9916798	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4355871	Tg(tetO-Ifng)184Pop	is_implicated_in	DOID:0050902	medulloblastoma		MGI:4355902	Tg(GFAP-tTA)67Pop/0 Tg(tetO-Ifng)184Pop/0  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15537876	20090903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4355871	Tg(tetO-Ifng)184Pop	is_implicated_in	DOID:0050902	medulloblastoma		MGI:4355901	Tg(GFAP-tTA)67Pop/0 Tg(tetO-Ifng)184Pop/0  [background:] B6.Cg-Tg(GFAP-tTA)67Pop Tg(tetO-Ifng)184Pop			ECO:0000033	author statement supported by traceable reference	PMID:15537876	20090903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652342	App<sup>tm1Cep</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652361	App<sup>tm1Cep</sup>/App<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652342	App<sup>tm1Cep</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652360	App<sup>tm1Cep</sup>/App<sup>tm1Cep</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:2174790	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10096549	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5140838	Tg(Pcp2-cre)2Mpin/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.2Mjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21419848	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5140843	Tg(Pcp2-cre)2Mpin/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21419848	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:4358058	Tsc2<sup>tm2.2Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19357198	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5641393	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] B6J.129S4-Tsc2<sup>tm1Tno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:2174788	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10491404	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:4880715	Tg(GFAP-cre)8Gtm/0 Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup>  [background:] involves: 129X1/SvJ * 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21062901	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3811791	Tsc2<sup>tm1Djk</sup>/Tsc2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:18568033	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:3776560	Col1a1<sup>m1Btlr</sup>/Col1a1<sup>m1Btlr</sup>  [background:] C57BL/6J-Col1a1<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28916811	20190627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148889	Insl3<sup>tm1Par</sup>	is_implicated_in	DOID:11383	cryptorchidism		MGI:2661992	Insl3<sup>tm1Par</sup>/Insl3<sup>+</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10391220	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148889	Insl3<sup>tm1Par</sup>	is_implicated_in	DOID:11383	cryptorchidism		MGI:2661963	Insl3<sup>tm1Par</sup>/Insl3<sup>tm1Par</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10391220	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	is_implicated_in	DOID:1388	Tangier disease		MGI:3578113	Abca1<sup>tm1Jp</sup>/Abca1<sup>tm1Jp</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * B6.Cg-Tg(Alb-cre)21Mgn/J			ECO:0000033	author statement supported by traceable reference	PMID:15841208	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	is_implicated_in	DOID:1388	Tangier disease		MGI:3578115	Abca1<sup>tm1.1Jp</sup>/Abca1<sup>tm1.1Jp</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15841208	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	is_implicated_in	DOID:1388	Tangier disease		MGI:2450723	Abca1<sup>tm1Jdm</sup>/Abca1<sup>tm1Jdm</sup>  [background:] DBA/1LacJ-Abca1<sup>tm1Jdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10760292	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	is_implicated_in	DOID:1388	Tangier disease		MGI:3525153	Abca1<sup>tm1Blt</sup>/Abca1<sup>tm1Blt</sup>  [background:] C57BL/6-Abca1<sup>tm1Blt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15163665	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	is_implicated_in	DOID:1388	Tangier disease		MGI:2450673	Abca1<sup>tm1Wpfl</sup>/Abca1<sup>tm1Wpfl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10980140	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354721	Slc25a13	is_not_implicated_in	DOID:9273	citrullinemia		MGI:3852334	Slc25a13<sup>tm1Lct</sup>/Slc25a13<sup>tm1Lct</sup>  [background:] either: 129/Sv-Slc25a13<sup>tm1Lct</sup> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:14701727	20090807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	is_implicated_in	DOID:10908	hydrocephalus		MGI:3807202	Add1<sup>tm1Llp</sup>/Add1<sup>tm1Llp</sup>  [background:] involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18723693	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856581	Slc45a2<sup>uw</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668611	Slc45a2<sup>uw</sup>/Slc45a2<sup>uw</sup>  [background:] C57BL/6J-Slc45a2<sup>uw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5646601	b2b3077Clo	is_implicated_in	DOID:0060254	Robinow syndrome		MGI:5648026	b2b3077Clo/b2b3077Clo  [background:] C57BL/6J-b2b3077Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:4830462	Htr2c<sup>tm1.1Eme</sup>/Y  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20394819	20100923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	is_implicated_in	DOID:0060588	Noonan syndrome 10		MGI:6315869	Lztr1<sup>tm1a(EUCOMM)Wtsi</sup>/Lztr1<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30442762	20190702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4432946	Lztr1<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060588	Noonan syndrome 10		MGI:6315869	Lztr1<sup>tm1a(EUCOMM)Wtsi</sup>/Lztr1<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30442762	20190702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183742	Tg(Pmp22)My41Clh	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:5779417	Tg(Pmp22)My41Clh/0  [background:] involves: C57BL/6J * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:12090404	20160629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926728	Pdgfra<sup>tm2Sor</sup>	is_implicated_in	DOID:4297	scimitar syndrome		MGI:7545275	Pdgfra<sup>tm2Sor</sup>/Pdgfra<sup>tm2Sor</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:20071345	20231102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856372	Otc<sup>spf-J</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:4830506	Otc<sup>spf-J</sup>/Y  [background:] C57BL/6J-Otc<sup>spf-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25647322	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676825	Mir140	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:6423510	Mir140<sup>em1Tkob</sup>/Mir140<sup>em1Tkob</sup>  [background:] C57BL/6-Mir140<sup>em1Tkob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30804514	20200520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676825	Mir140	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:6423511	Mir140<sup>em1Tkob</sup>/Mir140<sup>+</sup>  [background:] C57BL/6-Mir140<sup>em1Tkob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30804514	20200520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179115	Tgm1<sup>tm1Kfyn</sup>	is_implicated_in	DOID:0060656	autosomal recessive congenital ichthyosis 1		MGI:3029167	Tgm1<sup>tm1Kfyn</sup>/Tgm1<sup>tm1Kfyn</sup>  [background:] involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11805136	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179115	Tgm1<sup>tm1Kfyn</sup>	is_implicated_in	DOID:0060656	autosomal recessive congenital ichthyosis 1		MGI:3029167	Tgm1<sup>tm1Kfyn</sup>/Tgm1<sup>tm1Kfyn</sup>  [background:] involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9448282	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353500	Foxe1	is_implicated_in	DOID:0050655	Bamforth-Lazarus syndrome		MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9697704	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353500	Foxe1	is_implicated_in	DOID:0050655	Bamforth-Lazarus syndrome		MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15367491	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:7467137	Lrp5<sup>em1Xjz</sup>/Lrp5<sup>em1Xjz</sup>  [background:] C57BL/6J-Lrp5<sup>em1Xjz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:3606583	Lrp5<sup>tm1Dgen</sup>/Lrp5<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:3806486	Lrp5<sup>r18</sup>/Lrp5<sup>r18</sup>  [background:] C57BL/6J-Lrp5<sup>r18</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18263894	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:4946082	Lrp5<sup>tm1Dgen</sup>/Lrp5<sup>tm1Dgen</sup>  [background:] B6.129P2-Lrp5<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27524797	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3522483	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10616210	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789197	Lama2<sup>tm1Stk</sup>/Lama2<sup>tm1Stk</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR			ECO:0000033	author statement supported by traceable reference	PMID:21084425	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3848948	Lama2<sup>dy-8J</sup>/Lama2<sup>dy-8J</sup>  [background:] C57BL/6J-Lama2<sup>dy-8J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:3848945	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3522485	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9710454	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:4947712	Lama2<sup>tm1Eeng</sup>/Lama2<sup>tm1Eeng</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:20876525	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789197	Lama2<sup>tm1Stk</sup>/Lama2<sup>tm1Stk</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9326364	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:6226150	Lama2<sup>dy-Pas</sup>/Lama2<sup>dy-Pas</sup>  [background:] involves: non-inbred stock			ECO:0000033	author statement supported by traceable reference	PMID:12609503	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3783638	Lama2<sup>dy</sup>/Lama2<sup>dy</sup>  [background:] involves: 129P1/Re			ECO:0000033	author statement supported by traceable reference	PMID:16589799	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789978	Lama2<sup>dy-6J</sup>/Lama2<sup>dy-6J</sup>  [background:] involves: C57BL/6JEi * DBA/2J			ECO:0000033	author statement supported by traceable reference	MGI:1342643	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3581453	Lama2<sup>dy-7J</sup>/Lama2<sup>dy-7J</sup>  [background:] C57BL/6J-Lama2<sup>dy-7J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18430779	20181106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789335	Lama2<sup>dy-2J</sup>/Lama2<sup>dy-2J</sup>  [background:] B6.WK-Lama2<sup>dy-2J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15823249	20181106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862004	Zic2<sup>Ku</sup>	is_implicated_in	DOID:0110878	holoprosencephaly 5		MGI:5827598	Zic2<sup>Ku</sup>/Zic2<sup>Ku</sup>  [background:] 129S.CAnNCrl(C3)-Zic2<sup>Ku</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27466203	20170303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862004	Zic2<sup>Ku</sup>	is_implicated_in	DOID:0110878	holoprosencephaly 5		MGI:3639581	Zic2<sup>Ku</sup>/Zic2<sup>Ku</sup>  [background:] C3.CAnNCrl-Zic2<sup>Ku</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18617531	20170303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840831	Rag1<sup>tm1Jsek</sup>	is_not_implicated_in	DOID:0060010	Omenn syndrome		MGI:3840832	Rag1<sup>tm1Jsek</sup>/Rag1<sup>tm1Jsek</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:19126872	20090422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856684	Tbc1d20<sup>bs</sup>	is_implicated_in	DOID:0110719	Warburg micro syndrome 4		MGI:4430075	Tbc1d20<sup>bs</sup>/Tbc1d20<sup>bs</sup>  [background:] 129S;AKR-Tbc1d20<sup>bs</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24239381	20140327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685815	Cfap58	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:6477412	Cfap58<sup>em1Fzh</sup>/Cfap58<sup>em1Fzh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32791035	20201203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311363	b2b954Clo	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5312912	b2b954Clo/b2b954Clo  [background:] C57BL/6J-b2b954Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914272	Acad9	is_implicated_in	DOID:0112072	nuclear type mitochondrial complex I deficiency 20		MGI:7378413	Acad9<sup>tm1c(KOMP)Wtsi</sup>/Acad9<sup>tm1c(KOMP)Wtsi</sup> Tg(ACTA1-cre)79Jme/0  [background:] involves: C57BL/6J * C57BL/6N * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:34556413	20221102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914272	Acad9	is_implicated_in	DOID:0112072	nuclear type mitochondrial complex I deficiency 20		MGI:7378415	Acad9<sup>tm1c(KOMP)Wtsi</sup>/Acad9<sup>tm1c(KOMP)Wtsi</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:34556413	20221102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894698	Sgca	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D		MGI:2176866	Sgca<sup>tm1Kcam</sup>/Sgca<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9744877	20220517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894698	Sgca	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D		MGI:7278768	Sgca<sup>tm2Kcam</sup>/Sgca<sup>tm2Kcam</sup>  [background:] B6.129S6-Sgca<sup>tm2Kcam</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28797108	20220517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894698	Sgca	is_implicated_in	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D		MGI:2656914	Sgca<sup>tm1Eeng</sup>/Sgca<sup>tm1Eeng</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12620894	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178315	Pde6b<sup>atrd2</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028001	Pde6b<sup>atrd2</sup>/Pde6b<sup>atrd2</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857018	Oat<sup>rhg</sup>	is_implicated_in	DOID:1415	gyrate atrophy		MGI:3838967	Oat<sup>rhg</sup>/Oat<sup>rhg</sup>  [background:] B6Ei;AKR-Oat<sup>rhg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25264521	20180626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	is_implicated_in	DOID:0110128	Bardet-Biedl syndrome 6		MGI:3582615	Mkks<sup>tm1Vcs</sup>/Mkks<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:15772095	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682826	Tg(Ins2-CD80)3B7Flv	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3757580	Tg(Ins2-CD80)3B7Flv/?  [background:] involves: C57BL/6 * CBA/Ca * NOD/Caj			ECO:0000033	author statement supported by traceable reference	PMID:7533734	20071009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385891	Zc3h12a	is_implicated_in	DOID:12236	primary biliary cholangitis		MGI:6717173	Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup>/Zc3h12a<sup>tm1c(EUCOMM)Hmgu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA			ECO:0000033	author statement supported by traceable reference	PMID:33513427	20210623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860083	Cd320	is_implicated_in	DOID:0060741	methylmalonic acidemia due to transcobalamin receptor defect		MGI:5512998	Cd320<sup>Gt(CC0426)Wtsi</sup>/Cd320<sup>Gt(CC0426)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23430977	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3811207	Hspg2<sup>tm1Soni</sup>/Hspg2<sup>tm1Soni</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18647752	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3811208	Hspg2<sup>tm1.1Soni</sup>/Hspg2<sup>tm1.1Soni</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18647752	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:5428882	Hspg2<sup>tm1Soni</sup>/Hspg2<sup>tm1Soni</sup>  [background:] involves: 129S/SvEv * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:22449950	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3713117	Hspg2<sup>tm1.1Rdgr</sup>/Hspg2<sup>tm1.1Rdgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17213231	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3713118	Hspg2<sup>tm1Rdgr</sup>/Hspg2<sup>tm1Rdgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17213231	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11802174	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20180601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20180601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0050817	Stargardt disease		MGI:6159288	Abca4<sup>tm1.1Rsmy</sup>/Abca4<sup>tm1.1Rsmy</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29145636	20180601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0050817	Stargardt disease		MGI:2653823	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10412977	20180601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:5440736	Ids<sup>tm1Eto</sup>/Ids<sup>tm1Eto</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22704483	20201201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:6476699	Ids<sup>tm1Dkji</sup>/Y  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22847837	20201201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:6474227	Ids<sup>tm1Dkji</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20652491	20201201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:6198013	Ids<sup>tm1Muen</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17876721	20201201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:3625957	Ids<sup>tm1Muen</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16505002	20201201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	is_implicated_in	DOID:12799	mucopolysaccharidosis II		MGI:3625957	Ids<sup>tm1Muen</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12572850	20201201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95586	Fst	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:3042286	Fst<sup>tm1Zuk</sup>/Fst<sup>tm1Zuk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7885475	20081113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95586	Fst	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:3042284	Fst<sup>tm1Zuk</sup>/Fst<sup>tm1Zuk</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7885475	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430086	Tg(Rho-GUCA1A*Y99C)L53Amd	is_implicated_in	DOID:0080314	cone-rod dystrophy 14		MGI:4430105	Tg(Rho-GUCA1A*Y99C)L53Amd/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22042849	20180725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612989	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:6110829	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>/Sclt1<sup>Tg(CAG-sb10)1Dla</sup>  [background:] FVB/N-Sclt1<sup>Tg(CAG-sb10)1Dla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28486600	20180118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4308701	Hpse2<sup>Gt(OST411605)Lex</sup>	is_implicated_in	DOID:0050816	urofacial syndrome		MGI:5694081	Hpse2<sup>Gt(OST411605)Lex</sup>/Hpse2<sup>Gt(OST411605)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25510506	20151030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6159715	Arid1b<sup>em1Hzhu</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Hzhu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28695822	20190404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6286096	Arid1b<sup>em1Iha</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Iha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28867767	20190404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350931	Tcirg1	is_implicated_in	DOID:11836	clubfoot		MGI:3770247	Tcirg1<sup>oc</sup>/Tcirg1<sup>oc</sup>  [background:] C57BL/6J-Vps33a<sup>bf</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76073	20110125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	is_implicated_in	DOID:0090019	sitosterolemia		MGI:3514172	Abcg8<sup>tm1Elk</sup>/Abcg8<sup>tm1Elk</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15040800	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159289	Scg5<sup>tm1Led</sup>	is_implicated_in	DOID:3946	pituitary-dependent Cushing's disease		MGI:3037127	Scg5<sup>tm1Led</sup>/Scg5<sup>tm1Led</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * FVB) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12021197	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652058	Ldb3<sup>tm1Chen</sup>	is_implicated_in	DOID:0081337	congenital myopathy		MGI:2652059	Ldb3<sup>tm1Chen</sup>/Ldb3<sup>tm1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11696561	20230605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3810987	Itm2b<sup>tm1.1Ldad</sup>	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4867887	Itm2b<sup>tm1.1Ldad</sup>/Itm2b<sup>tm1.1Ldad</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21048150	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3810987	Itm2b<sup>tm1.1Ldad</sup>	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4936846	Itm2b<sup>tm1.1Ldad</sup>/Itm2b<sup>+</sup>  [background:] B6.129-Itm2b<sup>tm1.1Ldad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21098268	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420979	Ift172<sup>tm1.1Rama</sup>	is_implicated_in	DOID:8466	retinal degeneration		MGI:6383402	Ift172<sup>tm1.1Rama</sup>/Ift172<sup>tm1.1Rama</sup> Tg(Rho-icre)1Ck/0  [background:] involves: 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29659833	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	is_implicated_in	DOID:2920	membranoproliferative glomerulonephritis		MGI:2662550	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12091909	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:6501951	Col4a4<sup>m1H</sup>/Col4a4<sup>m1H</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31892712	20210126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:5696196	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] D2.NON(NZO)-Col4a4<sup>bwk</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:24522496	20210126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:5696188	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] NON;NZO-Col4a4<sup>bwk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24522496	20210126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:5696200	Col4a4<sup>bwk</sup>/Col4a4<sup>bwk</sup>  [background:] 129S1.NON(NZO)-Col4a4<sup>bwk</sup>/PgnJ			ECO:0000033	author statement supported by traceable reference	PMID:24522496	20210126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:4838199	Col4a4<sup>m1Btlr</sup>/Col4a4<sup>m1Btlr</sup>  [background:] C57BL/6J-Col4a4<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21196518	20210126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:4838199	Col4a4<sup>m1Btlr</sup>/Col4a4<sup>m1Btlr</sup>  [background:] C57BL/6J-Col4a4<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:4440633	20210126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98347	Snrpn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3618139	Snrpn<sup>tm2Cbr</sup>/Snrpn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9590284	20070827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98347	Snrpn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3719120	Snrpn<sup>tm2Alb</sup>/Snrpn<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11431693	20070827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98347	Snrpn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3618137	Snrpn<sup>tm1Kaj</sup>/Snrpn<sup>+</sup>  [background:] either: 129S1-Snrpn<sup>tm1Kaj</sup> or (involves: 129S1/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:16368707	20070827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914682	Hoga1	is_implicated_in	DOID:2977	primary hyperoxaluria		MGI:5805971	Hoga1<sup>tm2a(KOMP)Wtsi</sup>/Hoga1<sup>tm2a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:26428388	20161102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5565512	Flt3<sup>tm1.1Dosm</sup>/Flt3<sup>+</sup>  [background:] B6.129(C)-Flt3<sup>tm1.1Dosm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24255108	20140529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5565510	Flt3<sup>tm2.1Dosm</sup>/Flt3<sup>+</sup>  [background:] B6.129(C)-Flt3<sup>tm2.1Dosm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24255108	20140529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96615	Itgb6	is_implicated_in	DOID:2841	asthma		MGI:2175082	Itgb6<sup>tm1Des</sup>/Itgb6<sup>tm1Des</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8666675	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	is_implicated_in	DOID:0110927	nemaline myopathy 3		MGI:5424992	Acta1<sup>tm1Hrd</sup>/Acta1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6JArc)			ECO:0000033	author statement supported by traceable reference	PMID:22067542	20120618	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809481	Dkc1<sup>tm1.1Pjma</sup>	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:5644816	Dkc1<sup>tm1.1Pjma</sup>/Y  [background:] B6.129X1(FVB)-Dkc1<sup>tm1.1Pjma</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21241452	20150723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429767	Phex<sup>Ska1</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:4450916	Phex<sup>Ska1</sup>/Phex<sup>+</sup>  [background:] C57BL/6-Phex<sup>Ska1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12414538	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429767	Phex<sup>Ska1</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:4450917	Phex<sup>Ska1</sup>/Y  [background:] C57BL/6-Phex<sup>Ska1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12414538	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857386	Dsg3<sup>bal-Pas</sup>	is_implicated_in	DOID:0060851	pemphigus vulgaris		MGI:2175832	Dsg3<sup>bal-Pas</sup>/Dsg3<sup>bal-Pas</sup>  [background:] 129S2.Cg-Dsg3<sup>bal-Pas</sup>			ECO:0000033	author statement supported by traceable reference	MGI:1202169	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	is_implicated_in	DOID:0050699	Dent disease		MGI:3510236	Clcn5<sup>tm1Gug</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11115837	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	is_implicated_in	DOID:0050699	Dent disease		MGI:3046533	Clcn5<sup>tm1Tjj</sup>/Y  [background:] B6.129-Clcn5<sup>tm1Tjj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11099045	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3581179	Lyst<sup>bg-J</sup>/Lyst<sup>bg-J</sup>  [background:] C57BL/6J-Lyst<sup>bg-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182950	Elk3<sup>tm1Wlyk</sup>	is_implicated_in	DOID:0060646	congenital chylothorax		MGI:3619005	Elk3<sup>tm1Wlyk</sup>/Elk3<sup>tm1Wlyk</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11566878	20060411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443337	Fscn2	is_implicated_in	DOID:2742	auditory system disease		MGI:6386243	Fscn2<sup>em1Fhan</sup>/Fscn2<sup>em1Fhan</sup>  [background:] C57BL/6J-Fscn2<sup>em1Fhan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30082328	20200124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:5897776	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NCr			ECO:0000033	author statement supported by traceable reference	PMID:22514108	20170622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888964	Chrna4<sup>tm1Dra</sup>	is_not_implicated_in	DOID:0060682	autosomal dominant nocturnal frontal lobe epilepsy 1		MGI:3587441	Chrna4<sup>tm1Dra</sup>/Chrna4<sup>tm1Dra</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12623222	20050914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888964	Chrna4<sup>tm1Dra</sup>	is_not_implicated_in	DOID:0060682	autosomal dominant nocturnal frontal lobe epilepsy 1		MGI:3587441	Chrna4<sup>tm1Dra</sup>/Chrna4<sup>tm1Dra</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964949	20050914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2156687	Slc2a10	is_not_implicated_in	DOID:0050645	arterial tortuosity syndrome		MGI:3814342	Slc2a10<sup>S150F</sup>/Slc2a10<sup>S150F</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:18693279	20081110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2156687	Slc2a10	is_not_implicated_in	DOID:0050645	arterial tortuosity syndrome		MGI:3814341	Slc2a10<sup>G128E</sup>/Slc2a10<sup>G128E</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:18693279	20081110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445168	Elmod3	is_implicated_in	DOID:0110533	autosomal recessive nonsyndromic deafness 88		MGI:6455517	Elmod3<sup>em1Jili</sup>/Elmod3<sup>em1Jili</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31628468	20200916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298218	Lrp6	is_implicated_in	DOID:0080074	neural tube defect		MGI:2661970	Lrp6<sup>Cd</sup>/Lrp6<sup>Cd</sup>  [background:] A-Lrp6<sup>Cd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10545599	20130104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298218	Lrp6	is_implicated_in	DOID:0080074	neural tube defect		MGI:2661970	Lrp6<sup>Cd</sup>/Lrp6<sup>Cd</sup>  [background:] A-Lrp6<sup>Cd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16126904	20130104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3605770	Htt<sup>tm1Szi</sup>/Htt<sup>tm2Szi</sup> Tg(Camk2a-cre)2Szi/0  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11062468	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3605769	Htt<sup>tm1Szi</sup>/Htt<sup>tm2Szi</sup> Tg(Camk2a-cre)1Szi/0  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11062468	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3586839	Htt<sup>tm1Hay</sup>/Htt<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7774020	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:6400710	Htt<sup>tm5Detl</sup>/Htt<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28927719	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:16697652	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:16697652	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:2675620	Htt<sup>tm1Mfc</sup>/Htt<sup>tm1Mfc</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12926013	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:7266814	Htt<sup>tm1Mem</sup>/Htt<sup>tm6Mem</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:27623015	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698041	Htt<sup>tm5Mem</sup>/Htt<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698040	Htt<sup>tm4Mem</sup>/Htt<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10699173	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3573928	Htt<sup>tm1Detl</sup>/Htt<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11152661	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3573927	Htt<sup>tm1Detl</sup>/Htt<sup>tm1Detl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11152661	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3043476	Htt<sup>tm2Detl</sup>/Htt<sup>tm2Detl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17715336	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:5698523	Htt<sup>tm2Detl</sup>/Htt<sup>+</sup>  [background:] B6J.129P2-Htt<sup>tm2Detl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25609071	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698042	Htt<sup>tm5Mem</sup>/Htt<sup>tm5Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698039	Htt<sup>tm4Mem</sup>/Htt<sup>tm4Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698752	Htt<sup>tm1.1Pfs</sup>/Htt<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10196365	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698754	Htt<sup>tm2.1Pfs</sup>/Htt<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10196365	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3699097	Htt<sup>tm1.1Tna</sup>/Htt<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11494364	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:3699093	Htt<sup>tm1.1Tna</sup>/Htt<sup>tm1.1Tna</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11494364	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	is_implicated_in	DOID:12858	Huntington's disease		MGI:2675620	Htt<sup>tm1Mfc</sup>/Htt<sup>tm1Mfc</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17239451	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	is_implicated_in	DOID:5419	schizophrenia		MGI:3606580	Avpr1a<sup>tm1Dgen</sup>/Avpr1a<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99422	Rapsn	is_implicated_in	DOID:0110675	congenital myasthenic syndrome 11		MGI:6389105	Rapsn<sup>em1Gan</sup>/Rapsn<sup>em1Gan</sup>  [background:] C57BL/6J-Rapsn<sup>em1Gan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31549961	20200210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928775	Crebbp<sup>Gt(U-San)112Imeg</sup>	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:2175792	Crebbp<sup>Gt(U-San)112Imeg</sup>/Crebbp<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9949198	20050929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859180	Nr2e3<sup>rd7</sup>	is_implicated_in	DOID:0090059	enhanced S-cone syndrome		MGI:2668613	Nr2e3<sup>rd7</sup>/Nr2e3<sup>rd7</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10805811	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859180	Nr2e3<sup>rd7</sup>	is_implicated_in	DOID:0090059	enhanced S-cone syndrome		MGI:3709293	Nr2e3<sup>rd7</sup>/Nr2e3<sup>rd7</sup>  [background:] B6.Cg-Nr2e3<sup>rd7</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16110338	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96909	Maf	is_implicated_in	DOID:0110256	cataract 21 multiple types		MGI:2654216	Maf<sup>Ofl</sup>/Maf<sup>+</sup>  [background:] either: 102/ElH or C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:12620964	20091016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603004	Kit<sup>tm1Bpr</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:3603339	Kit<sup>tm1Bpr</sup>/Kit<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16061643	20051031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603004	Kit<sup>tm1Bpr</sup>	is_implicated_in	DOID:9253	gastrointestinal stromal tumor		MGI:3603337	Kit<sup>tm1Bpr</sup>/Kit<sup>tm1Bpr</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16061643	20051031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158703	C3<sup>tm1Hrc</sup>	is_implicated_in	DOID:8354	complement component 3 deficiency		MGI:2449063	C3<sup>tm1Hrc</sup>/C3<sup>tm1Hrc</sup>  [background:] either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10408374	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926955	Nf2<sup>tm2Gth</sup>	is_implicated_in	DOID:4450	renal cell carcinoma		MGI:3850478	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19487675	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8952527	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583451	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] C3.FVB-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8191288	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8191288	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15580285	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583450	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] FVB/N-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11773599	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583453	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: C3H * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11773599	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583451	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] C3.FVB-Ift88<sup>Tg737Rpw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11773599	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3046284	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11062270	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3046284	Ift88<sup>Tg737Rpw</sup>/Ift88<sup>Tg737Rpw</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15226261	20050812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522468	Ppargc1a<sup>tm1Dpk</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6489606	Ppargc1a<sup>tm1Dpk</sup>/Ppargc1a<sup>tm1Dpk</sup>  [background:] B6.129X1-Ppargc1a<sup>tm1Dpk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:32439544	20210104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2180831	Zic3<sup>tm1Bca</sup>/Y  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3618630	Zic3<sup>tm1Bca</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3618631	Zic3<sup>tm1Bca</sup>/Zic3<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3618629	Zic3<sup>tm1Bca</sup>/Zic3<sup>tm1Bca</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10942421	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10942421	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	MGI:63130	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	MGI:63130	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10861288	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10861288	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:1018005	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:1018005	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:16589192	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:16589192	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832594	Tg(Amhr2-Pik3ca*,-GFP)#Lzh	is_not_implicated_in	DOID:2394	ovarian cancer		MGI:3832595	Tg(Amhr2-Pik3ca*,-GFP)#Lzh/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19172191	20090220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574787	Fgfr1<sup>Hspy</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3574963	Fgfr1<sup>Hspy</sup>/Fgfr1<sup>+</sup>  [background:] C3HeB/FeJ-Hspy			ECO:0000033	author statement supported by traceable reference	PMID:15630379	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96690	Krt16	is_implicated_in	DOID:0050449	pachyonychia congenita		MGI:5426823	Krt16<sup>tm1(KOMP)Vlcg</sup>/Krt16<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Krt16<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22336941	20140305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849590	Gpc3<sup>tm1Snd</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849593	Gpc3<sup>Gt(Ex136)Byg</sup>/Gpc3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849592	Gpc3<sup>Gt(Ex136)Byg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849591	Gpc3<sup>tm1Snd</sup>/Gpc3<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3530366	Gpc3<sup>tm1Fil</sup>/Gpc3<sup>+</sup>  [background:] B6.Cg-Gpc3<sup>tm1Fil</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10402475	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3530365	Gpc3<sup>tm1Fil</sup>/Y  [background:] B6.Cg-Gpc3<sup>tm1Fil</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10402475	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3629779	Gpc3<sup>tm1Arge</sup>/Y  [background:] either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11846487	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386183	Zfpm2<sup>tm1Sho</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2665413	Zfpm2<sup>tm1Sho</sup>/Zfpm2<sup>tm1Sho</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12223418	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386183	Zfpm2<sup>tm1Sho</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2665413	Zfpm2<sup>tm1Sho</sup>/Zfpm2<sup>tm1Sho</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:10892744	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	is_implicated_in	DOID:5419	schizophrenia		MGI:3819267	Chrna7<sup>tm1Bay</sup>/Chrna7<sup>tm1Bay</sup>  [background:] B6.129S7-Chrna7<sup>tm1Bay</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24983521	20141106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857191	Il2<sup>tm1Hor</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2450466	Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8402910	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528497	Notch3<sup>tm1Ul</sup>	is_not_implicated_in	DOID:0111035	CADASIL 1		MGI:3528982	Notch3<sup>tm1Ul</sup>/Notch3<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15645445	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528497	Notch3<sup>tm1Ul</sup>	is_not_implicated_in	DOID:0111035	CADASIL 1		MGI:3528980	Notch3<sup>tm1Ul</sup>/Notch3<sup>tm1Ul</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15645445	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:3525209	Aipl1<sup>tm1Mad</sup>/Aipl1<sup>tm1Mad</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15582159	20171114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:3054824	Aipl1<sup>tm1Visu</sup>/Aipl1<sup>tm1Visu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15365178	20171114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:5922030	Aipl1<sup>tvrm119</sup>/Aipl1<sup>tvrm119</sup>  [background:] C57BL/6J-Aipl1<sup>tvrm119</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:5922033	Aipl1<sup>tvrm127</sup>/Aipl1<sup>tvrm127</sup>  [background:] C57BL/6J-Aipl1<sup>tvrm127</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:3054803	Aipl1<sup>tm1Tili</sup>/Aipl1<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15365173	20171114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	is_not_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:3037836	Comp<sup>tm1Aol</sup>/Comp<sup>tm1Aol</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12024046	20051007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87930	Adk	is_implicated_in	DOID:9452	steatotic liver disease		MGI:2449928	Adk<sup>tm1Bois</sup>/Adk<sup>tm1Bois</sup>  [background:] involves: 129P3/JEmsJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11997462	20050526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856181	Spta1<sup>sph-ha</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:63097	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856181	Spta1<sup>sph-ha</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:78279	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105393	Dmc1	is_implicated_in	DOID:0050457	Sertoli cell-only syndrome		MGI:2177047	Dmc1<sup>Mei11</sup>/Dmc1<sup>Mei11</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10700192	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5086221	Shank3<sup>tm1.1Pfw</sup>/Shank3<sup>+</sup>  [background:] B6.129S6-Shank3<sup>tm1.1Pfw</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5499103	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4949761	Shank3<sup>tm2Gfng</sup>/Shank3<sup>tm2Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21423165	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6438116	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>tm3.2Cmpl</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6438117	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5776377	Shank3<sup>tm3.1Gfng</sup>/Shank3<sup>tm3.1Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26687841	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5285395	Shank3<sup>tm1.2Bux</sup>/Shank3<sup>+</sup>  [background:] C57BL/6-Shank3<sup>tm1.2Bux</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21167025	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5776354	Shank3<sup>tm5.1Gfng</sup>/Shank3<sup>tm5.1Gfng</sup>  [background:] involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26886798	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6437930	Shank3<sup>tm2Cmpl</sup>/Shank3<sup>tm2Cmpl</sup>  [background:] B6.129S6-Shank3<sup>tm2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27492494	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6437929	Shank3<sup>tm2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6-Shank3<sup>tm2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27492494	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5056404	Shank3<sup>tm1Yhj</sup>/Shank3<sup>tm1Yhj</sup>  [background:] B6.129S7-Shank3<sup>tm1Yhj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21558424	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6324047	Shank3<sup>tm2Gfng</sup>/Shank3<sup>+</sup>  [background:] B6.129-Shank3<sup>tm2Gfng</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27189882	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5883282	Shank3<sup>tm1Cmpl</sup>/Shank3<sup>tm1Cmpl</sup>  [background:] B6J.129S6-Shank3<sup>tm1Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26134648	20210614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6715314	Shank3<sup>em1Hzo</sup>/Shank3<sup>em1Hzo</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30610205	20210614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838184	Ethe1<sup>tm1.1Zev</sup>	is_implicated_in	DOID:0060640	ethylmalonic encephalopathy		MGI:3838185	Ethe1<sup>tm1.1Zev</sup>/Ethe1<sup>tm1.1Zev</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19136963	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0090107	autosomal dominant hypocalcemia 1		MGI:3603347	Casr<sup>Nuf</sup>/Casr<sup>Nuf</sup>  [background:] involves: 102/El * C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:15347804	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:0090107	autosomal dominant hypocalcemia 1		MGI:3603348	Casr<sup>Nuf</sup>/Casr<sup>+</sup>  [background:] either: (involves: 102/El * 102/H * C3H/He) or (involves: 102/El * C3H/He * C3H/HeH)			ECO:0000033	author statement supported by traceable reference	PMID:15347804	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043699	Ercc5<sup>tm1Shm</sup>/Ercc5<sup>tm1Shm</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10022922	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043597	Ercc5<sup>tm3Shm</sup>/Ercc5<sup>tm3Shm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043695	Ercc5<sup>tm4Shm</sup>/Ercc5<sup>tm4Shm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043596	Ercc5<sup>tm2Shm</sup>/Ercc5<sup>tm2Shm</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655714	Rpgrip1<sup>tm1Tili</sup>	is_implicated_in	DOID:0110329	Leber congenital amaurosis 6		MGI:2655715	Rpgrip1<sup>tm1Tili</sup>/Rpgrip1<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12651948	20110502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3587029	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>tm1Bem</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3587028	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11239417	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3771187	Tg(HIV)26Aln	is_implicated_in	DOID:635	acquired immunodeficiency syndrome		MGI:7263453	Tg(HIV)26Aln/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12861038	20220425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3697906	Htt<sup>tm7Mem</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698001	Htt<sup>tm7Mem</sup>/Htt<sup>tm7Mem</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9398841	20070227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2389173	Lrrtm1	is_implicated_in	DOID:5419	schizophrenia		MGI:5085920	Lrrtm1<sup>tm1.1Jaru</sup>/Lrrtm1<sup>tm1.1Jaru</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21818371	20110815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:3770518	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:3770517	Kras<sup>tm3Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:3770516	Kras<sup>tm3Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:3770515	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11323676	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:5528689	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24239348	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:5007794	Kras<sup>tm5Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21512139	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:3770518	Kras<sup>tm2Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:18493606	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:5508232	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21514245	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:4844190	Kras<sup>tm1Bbd</sup>/Kras<sup>tm2Bbd</sup> Polr2a<sup>tm1(cre/ERT2)Bbd</sup>/Polr2a<sup>tm1(cre/ERT2)Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20609353	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:4844193	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Polr2a<sup>tm1(cre/ERT2)Bbd</sup>/Polr2a<sup>tm1(cre/ERT2)Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20609353	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:1324	lung cancer		MGI:3716404	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:24430184	20171108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	is_implicated_in	DOID:11211	buphthalmos		MGI:3581209	Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6(Cg)-Tyr<sup>c-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856362	Glra1<sup>spd</sup>	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:3695040	Glra1<sup>spd</sup>/Glra1<sup>spd</sup>  [background:] involves: A/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:8733750	20070130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856646	Cdk5rap2<sup>an</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:4460825	Cdk5rap2<sup>an</sup>/Cdk5rap2<sup>an</sup>  [background:] B6.Cg-Cdk5rap2<sup>an</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20460369	20171027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261831	Hap1	is_implicated_in	DOID:1595	melancholic depression		MGI:5691394	Hap1<sup>tm2Xjl</sup>/Hap1<sup>tm2Xjl</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:25875952	20151015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261831	Hap1	is_implicated_in	DOID:1595	melancholic depression		MGI:5695752	Hap1<sup>tm2Xjl</sup>/Hap1<sup>tm2Xjl</sup> Tg(Camk2a-cre)159Kln/0  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25875952	20151015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105381	Rpsa	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:3804635	Rpsa<sup>tm1Ells</sup>/Rpsa<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3804630	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921303	Grip1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3035937	Grip1<sup>tm1Rha</sup>/Grip1<sup>tm1Rha</sup>  [background:] B6.129-Grip1<sup>tm1Rha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14730302	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921303	Grip1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665402	Grip1<sup>eb</sup>/Grip1<sup>eb</sup>  [background:] involves: ATEB/Le * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	is_implicated_in	DOID:5419	schizophrenia		MGI:4358724	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] DBA/2J-Dtnbp1<sup>sdy</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18984010	20151009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	is_implicated_in	DOID:5419	schizophrenia		MGI:5689331	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] B6J.D2-Dtnbp1<sup>sdy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23261874	20151009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	is_implicated_in	DOID:5419	schizophrenia		MGI:5689331	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] B6J.D2-Dtnbp1<sup>sdy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25677649	20151009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99569	S1pr2	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:3663255	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19903857	20170406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99569	S1pr2	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5882507	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] 129S5/SvEvBrd-S1pr2<sup>tm1Ajml</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19903857	20170406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	is_not_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:2446456	Abcc8<sup>tm1Jbry</sup>/Abcc8<sup>tm1Jbry</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10734066	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	is_not_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:2446508	Abcc8<sup>tm1.1Mgn</sup>/Abcc8<sup>tm1.1Mgn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12149271	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298218	Lrp6	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5694491	Lrp6<sup>tm1Arma</sup>/Lrp6<sup>tm1Arma</sup>  [background:] C57BL/6-Lrp6<sup>tm1Arma</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25917329	20151103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	is_implicated_in	DOID:9970	obesity		MGI:3055584	Bbs1<sup>Gt1Nk</sup>/Bbs1<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3619140	Gaa<sup>tm1Vdp</sup>/Gaa<sup>tm1Vdp</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)			ECO:0000033	author statement supported by traceable reference	PMID:9384603	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3624423	Gaa<sup>tm2Rabn</sup>/Gaa<sup>tm2Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3033756	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3624424	Gaa<sup>tm1.1Rabn</sup>/Gaa<sup>tm1.1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3033756	Gaa<sup>tm1Rabn</sup>/Gaa<sup>tm1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9668092	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3039785	Syngap1	is_implicated_in	DOID:5419	schizophrenia		MGI:5485349	Syngap1<sup>tm1Rlh</sup>/Syngap1<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19145222	20130516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924627	Kcnt1	is_not_implicated_in	DOID:0080439	developmental and epileptic encephalopathy 14		MGI:7442319	Kcnt1<sup>em1Pqt</sup>/Kcnt1<sup>+</sup>  [background:] C57BL/6J-Kcnt1<sup>em1Pqt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36173683	20230308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	is_implicated_in	DOID:1925	Coffin-Siris syndrome		MGI:5784730	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>tm1.1Mag</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26806701	20171117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	is_implicated_in	DOID:1925	Coffin-Siris syndrome		MGI:5784729	Arid1a<sup>tm1.1Mag</sup>/Arid1a<sup>+</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26806701	20171117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522021	Ptpn11<sup>tm1Gsf</sup>	is_implicated_in	DOID:0014667	disease of metabolism		MGI:5906203	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19001090	20170803	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7496044	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:21875659	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3616771	Chd7<sup>Whi</sup>/Chd7<sup>+</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:16207732	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7496091	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:36288662	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3708350	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17334657	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3708348	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>Gt(S20-7E1)Sor</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17334657	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7488670	Chd7<sup>Gt(XK403)Byg</sup>/Chd7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:29168327	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7339183	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:34732824	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7518241	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Neurod1-cre)RZ24Gsat/0  [background:] involves: C57BL/6J * C57BL/6N * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:34732824	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3589435	Chd7<sup>Whi</sup>/Chd7<sup>+</sup>  [background:] C3HeB/FeJ-Chd7<sup>Whi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36232804	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7492422	Chd7<sup>tm2a(EUCOMM)Wtsi</sup>/Chd7<sup>+</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:36232804	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493449	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: C57BL/6 * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28317875	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3719118	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6J) or (involves: 129S1/SvImJ * 129S4/SvJae C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17701983	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493591	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] 129S1.129S4(B6)-Chd7<sup>Gt(S20-7E1)Sor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21596839	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:6281675	Chd7<sup>Looper</sup>/Chd7<sup>+</sup>  [background:] BALB/c-Chd7<sup>Looper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24840056	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7496108	Chd7<sup>tm2c(EUCOMM)Wtsi</sup>/Chd7<sup>tm2c(EUCOMM)Wtsi</sup> Slc1a3<sup>tm1(cre/ERT2)Mgoe</sup>/Slc1a3<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25183173	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493591	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] 129S1.129S4(B6)-Chd7<sup>Gt(S20-7E1)Sor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19279158	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5774845	Chd7<sup>tm1.1Dmm</sup>/Chd7<sup>tm1.1Dmm</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:26670829	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5807347	Chd7<sup>Gt(S20-7E1)Sor</sup>/Chd7<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26670829	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5774943	Chd7<sup>tm1.1Dmm</sup>/Chd7<sup>+</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:26670829	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7493334	Chd7<sup>Trooper</sup>/Chd7<sup>+</sup>  [background:] BALB/c-Chd7<sup>Trooper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29615807	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5437367	Chd7<sup>Ome</sup>/Chd7<sup>+</sup>  [background:] involves: BALB/cByJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22539951	20230815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	is_implicated_in	DOID:5419	schizophrenia		MGI:5790635	Pdgfrb<sup>tm1Msas</sup>/Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu/0  [background:] B6J.Cg-Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu			ECO:0000033	author statement supported by traceable reference	PMID:25803852	20160902	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353656	Slc7a9	is_implicated_in	DOID:9266	cystinuria		MGI:2677400	Slc7a9<sup>tm1Nune</sup>/Slc7a9<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12915471	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353656	Slc7a9	is_implicated_in	DOID:9266	cystinuria		MGI:2677399	Slc7a9<sup>tm1Nune</sup>/Slc7a9<sup>tm1Nune</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12915471	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181718	Cfc1<sup>tm1Cbm</sup>	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10574770	20210927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104756	Itga9	is_implicated_in	DOID:0060646	congenital chylothorax		MGI:3583695	Itga9<sup>tm1Des</sup>/Itga9<sup>tm1Des</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10866676	20100302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664869	Men1<sup>tm1Zqw</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143886	Dot1l	is_implicated_in	DOID:0110425	dilated cardiomyopathy 1A		MGI:5424158	Dot1l<sup>tm1Tche</sup>/Dot1l<sup>tm1.1Tche</sup> Tg(Myhca-cre)1Abel/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21289070	20120613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:0060643	primary sclerosing cholangitis		MGI:5659501	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] CAnNCrl.12P2(FVB)-Abcb4<sup>tm1Bor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25478810	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:0060643	primary sclerosing cholangitis		MGI:5618431	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20921947	20150821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5473606	Frem1<sup>eyes2</sup>/Frem1<sup>eyes2</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23221805	20130410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5550384	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24163243	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3838721	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>tm1.1Sdie</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24163243	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5550383	Cacna1f<sup>tm1.1Sdie</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24163243	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3611756	Cacna1f<sup>tm1Ntbh</sup>/Cacna1f<sup>tm1Ntbh</sup>  [background:] B6.129-Cacna1f<sup>tm1Ntbh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16155113	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3611755	Cacna1f<sup>tm1Ntbh</sup>/Y  [background:] B6.129-Cacna1f<sup>tm1Ntbh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16155113	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3720002	Cacna1f<sup>nob2</sup>/Y  [background:] AXB6/PgnJ			ECO:0000033	author statement supported by traceable reference	PMID:16597347	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3720000	Cacna1f<sup>nob2</sup>/Cacna1f<sup>nob2</sup>  [background:] AXB6/PgnJ			ECO:0000033	author statement supported by traceable reference	PMID:16597347	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:6259768	Cacna1f<sup>nob9</sup>/Cacna1f<sup>nob9</sup>  [background:] B6(PWD)-Cacna1f<sup>nob9</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	PMID:30445045	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634274	Cacna1f<sup>tm1.2Sdie</sup>/Cacna1f<sup>tm1.2Sdie</sup>  [background:] B6.Cg-Cacna1f<sup>tm1.2Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634270	Cacna1f<sup>tm1.1Sdie</sup>/Y  [background:] B6.Cg-Cacna1f<sup>tm1.1Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634271	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>tm1.1Sdie</sup>  [background:] B6.Cg-Cacna1f<sup>tm1.1Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634279	Cacna1f<sup>tm1.2Sdie</sup>/Y  [background:] B6.Cg-Cacna1f<sup>tm1.2Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20181211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	is_implicated_in	DOID:0050711	aceruloplasminemia		MGI:3834850	Cp<sup>tm1Yos</sup>/Cp<sup>tm1Yos</sup>  [background:] C.129P2-Cp<sup>tm1Yos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18804145	20090309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	is_implicated_in	DOID:0050711	aceruloplasminemia		MGI:3044689	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11461924	20090309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	is_implicated_in	DOID:0050711	aceruloplasminemia		MGI:3044689	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10485908	20090309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096368	Ap1b1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:3832641	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm2(FCMD)Ttd</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:19017726	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5514353	Fktn<sup>tm3.1Ttd</sup>/Fktn<sup>tm3.1Ttd</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23562821	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5514355	Fktn<sup>tm3.1Ttd</sup>/Fktn<sup>tm3.1Ttd</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23562821	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459078	Pals1<sup>tm1Caw</sup>	is_implicated_in	DOID:14791	Leber congenital amaurosis		MGI:5428846	Pals1<sup>tm1Caw</sup>/Pals1<sup>tm1Caw</sup> Tg(rx3-icre)1Mjam/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22398208	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928729	Ebf1<sup>tm1Rug</sup>	is_implicated_in	DOID:811	lipodystrophy		MGI:3842704	Ebf1<sup>tm1Rug</sup>/Ebf1<sup>tm1Rug</sup>  [background:] involves: 129S2/SvPas * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19130908	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:7464299	mrs1	is_implicated_in	DOID:8465	retinoschisis		MGI:7465150	mrs1/Y  [background:] B6.Cg-mrs1/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:7464180	20230424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	is_not_implicated_in	DOID:0111035	CADASIL 1		MGI:5771891	Notch3<sup>tm1Grid</sup>/Notch3<sup>tm1Grid</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26563570	20160526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	is_not_implicated_in	DOID:0111035	CADASIL 1		MGI:3528980	Notch3<sup>tm1Ul</sup>/Notch3<sup>tm1Ul</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15645445	20160526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	is_not_implicated_in	DOID:0111035	CADASIL 1		MGI:3528982	Notch3<sup>tm1Ul</sup>/Notch3<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15645445	20160526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179955	Gaa<sup>tm1.1Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3624424	Gaa<sup>tm1.1Rabn</sup>/Gaa<sup>tm1.1Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2183924	Myo3a	is_implicated_in	DOID:0110489	autosomal recessive nonsyndromic deafness 30		MGI:4849847	Myo3a<sup>tm1.1Mckg</sup>/Myo3a<sup>tm1.1Mckg</sup>  [background:] C57BL/6-Myo3a<sup>tm1.1Mckg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21165622	20101230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:3046056	Rs1<sup>tm1Web</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11983912	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6383471	Rs1<sup>em1Fegu</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29379415	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6404946	Rs1<sup>tm2.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6404937	Rs1<sup>tm1.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:6404948	Rs1<sup>tm3.1Rom</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31174210	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:3056342	Rs1<sup>tm1Sie</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15326152	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:3056343	Rs1<sup>tm1Sie</sup>/Rs1<sup>tm1Sie</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15326152	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:2448896	Rs1<sup>tmgc1</sup>/Rs1<sup>tmgc1</sup>  [background:] involves: C3H/Rl * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16088326	20200421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:6512404	Pten<sup>tm1.2Mwst</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20194734	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4442333	Pten<sup>tm1.1Gle</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20194734	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4442335	Pten<sup>tm2.1Gle</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20194734	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:2179045	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9990064	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:5825461	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Nes-cre/ERT2,-ALPP)1Sbk/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27815386	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4836620	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17237784	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:3813525	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr/0  [background:] involves: 129S4/SvJae * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:18757421	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:3714016	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Gfap-cre)1Sbk/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11726926	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:5506904	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr/0  [background:] FVB.Cg-Pten<sup>tm1Hwu</sup> Tg(KRT14-cre)#Smr			ECO:0000033	author statement supported by traceable reference	PMID:23873941	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:2179030	Pten<sup>tm1Mak</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10910075	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4829793	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:12163417	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:6457	Cowden syndrome		MGI:2179025	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9697695	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96448	Ighm	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623426	Ighm<sup>tm1Cgn</sup>/Ighm<sup>+</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8920894	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3811187	Hspg2<sup>tm1Soni</sup>	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3811207	Hspg2<sup>tm1Soni</sup>/Hspg2<sup>tm1Soni</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18647752	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3811187	Hspg2<sup>tm1Soni</sup>	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:5428882	Hspg2<sup>tm1Soni</sup>/Hspg2<sup>tm1Soni</sup>  [background:] involves: 129S/SvEv * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:22449950	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88457	Col5a1	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3687258	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16492673	20220719	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88457	Col5a1	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:7314211	Col5a1<sup>em1Brle</sup>/Col5a1<sup>+</sup>  [background:] C57BL/6-Col5a1<sup>em1Brle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34740257	20220719	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88457	Col5a1	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3687258	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34740257	20220719	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88457	Col5a1	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3687246	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15383546	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930997	Csf2<sup>tm1Ard</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:2652689	Csf2<sup>tm1Ard</sup>/Csf2<sup>tm1Ard</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8202532	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	is_implicated_in	DOID:8466	retinal degeneration		MGI:5903076	Nmnat1<sup>tvrm113</sup>/Nmnat1<sup>tvrm113</sup>  [background:] C57BL/6J-Nmnat1<sup>tvrm113</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:27207593	20170623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916151	Adgrg6	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7266813	Adgrg6<sup>tm1Arte</sup>/Adgrg6<sup>tm1Arte</sup> Tg(Col2a1-cre)#Amc/0  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:25954032	20220506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916151	Adgrg6	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7266840	Adgrg6<sup>tm1Arte</sup>/Adgrg6<sup>tm1Arte</sup> Tg(Scx-GFP/cre)1Stzr/0  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:34318745	20220506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696404	Ass1<sup>fold</sup>	is_implicated_in	DOID:9273	citrullinemia		MGI:3697171	Ass1<sup>fold</sup>/Ass1<sup>fold</sup>  [background:] involves: C57BL/6JEiJ * P/J			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696404	Ass1<sup>fold</sup>	is_implicated_in	DOID:9273	citrullinemia		MGI:3707513	Ass1<sup>fold</sup>/Ass1<sup>fold</sup>  [background:] B6Ei.P-Ass1<sup>fold</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838156	Tg(ATXN3*)67.2Cce	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:3838164	Tg(ATXN3*)67.2Cce/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11978767	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329033	Agxt	is_implicated_in	DOID:0111670	primary hyperoxaluria type 1		MGI:6472964	Agxt<sup>tm1Ull</sup>/Agxt<sup>tm1Ull</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31821850	20201118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329033	Agxt	is_implicated_in	DOID:0111670	primary hyperoxaluria type 1		MGI:3717654	Agxt<sup>tm1Ull</sup>/Agxt<sup>tm1Ull</sup>  [background:] B6.129X1-Agxt<sup>tm1Ull</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17110443	20201118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814875	Six3<sup>tm4(cre/ERT2)Gco</sup>	is_implicated_in	DOID:0110872	holoprosencephaly 2		MGI:3814906	Six3<sup>tm4(cre/ERT2)Gco</sup>/Six3<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107928	Aldh1a2	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2451320	Aldh1a2<sup>tm1Dll</sup>/Aldh1a2<sup>tm1Ipc</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12563036	20060713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5440731	Nlgn3<sup>tm1Rhn</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22983708	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3758961	Nlgn3<sup>tm1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17823315	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4353654	Nlgn3<sup>tm1Bros</sup>/Nlgn3<sup>tm1Bros</sup>  [background:] B6.Cg-Nlgn3<sup>tm1Bros</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19243448	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5660857	Nlgn3<sup>tm2.1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24995986	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5660859	Nlgn3<sup>tm1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24995986	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720935	F12<sup>tm1Pbfd</sup>	is_implicated_in	DOID:2231	factor XII deficiency		MGI:3721103	F12<sup>tm1Pbfd</sup>/F12<sup>tm1Pbfd</sup>  [background:] B6.Cg-F12<sup>tm1Pbfd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16009717	20151122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2661061	Dsg4	is_implicated_in	DOID:0110703	hypotrichosis 6		MGI:2661074	Dsg4<sup>lah</sup>/Dsg4<sup>lah</sup>  [background:] LAH/Pas			ECO:0000033	author statement supported by traceable reference	PMID:8752833	20190422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2661061	Dsg4	is_implicated_in	DOID:0110703	hypotrichosis 6		MGI:2661068	Dsg4<sup>lah-J</sup>/Dsg4<sup>lah-J</sup>  [background:] involves: DBA/1LacJ			ECO:0000033	author statement supported by traceable reference	PMID:10839719	20190422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685011	Dchs1	is_implicated_in	DOID:988	mitral valve prolapse		MGI:5695318	Dchs1<sup>tm1.2Irv</sup>/Dchs1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26258302	20151110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652959	Kcnh2<sup>tm1Hjd</sup>	is_implicated_in	DOID:0050793	short QT syndrome		MGI:2652979	Kcnh2<sup>tm1Hjd</sup>/Kcnh2<sup>tm1Hjd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12612061	20060419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98961	Wnt7a	is_implicated_in	DOID:0090067	Fuhrmann syndrome		MGI:5440925	Wnt7a<sup>px-2J</sup>/Wnt7a<sup>px-2J</sup>  [background:] B6;C3Fe-Wnt7a<sup>px-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5440720	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654153	Maf<sup>Ofl</sup>	is_implicated_in	DOID:0110256	cataract 21 multiple types		MGI:2654216	Maf<sup>Ofl</sup>/Maf<sup>+</sup>  [background:] either: 102/ElH or C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:12620964	20091016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447990	Tns2<sup>nph</sup>	is_implicated_in	DOID:0060852	Pierson syndrome		MGI:3815328	Tns2<sup>nph</sup>/Tns2<sup>nph</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:16688531	20081119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148742	Cldn16	is_implicated_in	DOID:0060880	renal hypomagnesemia 3		MGI:4453304	Cldn16<sup>tm1.1Dmu</sup>/Cldn16<sup>tm1.1Dmu</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20147368	20151122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148742	Cldn16	is_implicated_in	DOID:0060880	renal hypomagnesemia 3		MGI:3822351	Tg(RNU6-RNAi:Cldn16)551Dago/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17442678	20151122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679732	Slc9a9	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6209392	Slc9a9<sup>tm1.1Yzj</sup>/Slc9a9<sup>tm1.1Yzj</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26755066	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679732	Slc9a9	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6201594	Slc9a9<sup>tm2c(KOMP)Wtsi</sup>/Slc9a9<sup>tm2c(KOMP)Wtsi</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29362376	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679732	Slc9a9	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6201596	Slc9a9<sup>tm2d(KOMP)Wtsi</sup>/Slc9a9<sup>tm2d(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29362376	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:762500	20081002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76424	20081002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12486097	20081002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:309911	20081002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921831	Sbf2	is_implicated_in	DOID:0110190	Charcot-Marie-Tooth disease type 4B2		MGI:3783887	Sbf2<sup>Gt(RRF511)Byg</sup>/Sbf2<sup>Gt(RRF511)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18349142	20080507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921831	Sbf2	is_implicated_in	DOID:0110190	Charcot-Marie-Tooth disease type 4B2		MGI:3784200	Sbf2<sup>Gt(XH212)Byg</sup>/Sbf2<sup>Gt(XH212)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:5955164	20080507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921622	Ulk4	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429215	Ulk4<sup>tm1Lex</sup>/Ulk4<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3068	glioblastoma		MGI:3849178	Trp53<sup>tm1Elee</sup>/Trp53<sup>tm1Tyj</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S2/SvPas * 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19477430	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3655101	Tg(KRT14-Vegfa)3Dtm	is_implicated_in	DOID:8893	psoriasis		MGI:3655625	Tg(KRT14-Vegfa)3Dtm/0  [background:] FVB/N-Tg(KRT14-Vegfa)3Dtm			ECO:0000033	author statement supported by traceable reference	PMID:15100155	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338049	Itsn2	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:6188890	Itsn2<sup>tm1Kure</sup>/Itsn2<sup>tm1Kure</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29773874	20180718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5560778	b2b2140Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561311	b2b2140Clo/b2b2140Clo  [background:] C57BL/6J-b2b2140Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:7339041	Tfrc<sup>tm3.1Nca</sup>/Tfrc<sup>tm3.1Nca</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:27362800	20220922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138334	Dgkd	is_implicated_in	DOID:0050561	Lennox-Gastaut syndrome		MGI:3763530	Dgkd<sup>Gt(RRT600)Byg</sup>/Dgkd<sup>Gt(RRT600)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17357084	20071210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4455649	Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:225	syndrome		MGI:6199708	Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>/Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Slc10a7<sup>tm1a(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30082715	20180926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3583907	Ins2<sup>Akita</sup>/Ins2<sup>+</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15914643	20060626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3583904	Ins2<sup>Akita</sup>/Ins2<sup>+</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9133560	20060626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_not_implicated_in	DOID:0110156	Charcot-Marie-Tooth disease type 2B1		MGI:7260355	Lmna<sup>tm1.1Vde</sup>/Lmna<sup>tm1.1Vde</sup>  [background:] B6.129(Cg)-Lmna<sup>tm1.1Vde</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22331516	20220411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1935122	Fbn2<sup>fp-2J</sup>	is_not_implicated_in	DOID:0050646	distal arthrogryposis		MGI:2451233	Fbn2<sup>fp-2J</sup>/Fbn2<sup>fp-2J</sup>  [background:] involves: C57BL/6J * C.B10-H2<sup>b</sup>/LiMcdJ			ECO:0000033	author statement supported by traceable reference	PMID:11285249	20050831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2657109	Mip<sup>Cat-Tohm</sup>/Mip<sup>Cat-Tohm</sup>  [background:] involves: DDI			ECO:0000033	author statement supported by traceable reference	PMID:12676560	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175114	Mip<sup>Hfi</sup>/Mip<sup>Hfi</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:62456	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175115	Mip<sup>Hfi</sup>/Mip<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:62456	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175113	Mip<sup>Cat-Lop</sup>/Mip<sup>+</sup>  [background:] involves: STOCK Rb(6.15)1Ald			ECO:0000033	author statement supported by traceable reference	PMID:8563764	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:2175110	Mip<sup>Cat-Fr</sup>/Mip<sup>Cat-Fr</sup>  [background:] involves: A/J			ECO:0000033	author statement supported by traceable reference	PMID:8563764	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:5487835	Mip<sup>Cts</sup>/Mip<sup>Cts</sup>  [background:] CTS/Shi			ECO:0000033	author statement supported by traceable reference	MGI:5487779	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:5487914	Mip<sup>Cts</sup>/Mip<sup>+</sup>  [background:] involves: C57BL/6J * CTS/Shi			ECO:0000033	author statement supported by traceable reference	MGI:5487779	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774275	Npr2<sup>slw</sup>	is_implicated_in	DOID:0080050	acromesomelic dysplasia, Maroteaux type		MGI:3806086	Npr2<sup>slw</sup>/Npr2<sup>slw</sup>  [background:] involves: C57BL/6 * DDY			ECO:0000033	author statement supported by traceable reference	PMID:17728275	20080916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491159	b2b2025Clo	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5555835	b2b2025Clo/b2b2025Clo  [background:] C57BL/6J-b2b2025Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20140407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847257	Pds5a<sup>Gt(RRM243)Byg</sup>	is_implicated_in	DOID:11725	Cornelia de Lange syndrome		MGI:3847290	Pds5a<sup>Gt(RRM243)Byg</sup>/Pds5a<sup>Gt(RRM243)Byg</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19412548	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442062	Sh3pxd2b	is_implicated_in	DOID:10754	otitis media		MGI:4365644	Sh3pxd2b<sup>nee</sup>/Sh3pxd2b<sup>nee</sup>  [background:] B10.Cg-H2<sup>h4</sup> Sh3pxd2b<sup>nee</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:19669234	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714028	Nfix<sup>tm1Aes</sup>	is_implicated_in	DOID:13300	Scheuermann's disease		MGI:3714196	Nfix<sup>tm1Aes</sup>/Nfix<sup>tm1Aes</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17353270	20070710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181746	Foxj1<sup>tm1Bph</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:2668968	Foxj1<sup>tm1Bph</sup>/Foxj1<sup>tm1Bph</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9739041	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2152938	Srgap3	is_implicated_in	DOID:5419	schizophrenia		MGI:5465282	Srgap3<sup>tm1.1Zi</sup>/Srgap3<sup>tm1.1Zi</sup>  [background:] B6.129(SJL)-Srgap3<sup>tm1.1Zi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22820399	20130221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4356167	Atp1a3<sup>Myk</sup>	is_implicated_in	DOID:3312	bipolar disorder		MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24342563	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4356167	Atp1a3<sup>Myk</sup>	is_implicated_in	DOID:3312	bipolar disorder		MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22025725	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657134	Gpc3<sup>tm1Arge</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3629779	Gpc3<sup>tm1Arge</sup>/Y  [background:] either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11846487	20060724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857187	Ighm<sup>tm1Cgn</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3793300	Ighm<sup>tm1Cgn</sup>/Ighm<sup>tm1Cgn</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>/DvsJ			ECO:0000033	author statement supported by traceable reference	PMID:12516557	20080611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857187	Ighm<sup>tm1Cgn</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623425	Ighm<sup>tm1Cgn</sup>/Ighm<sup>tm1Cgn</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8920894	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:3047228	Vegfa<sup>tm1Pec</sup>/Vegfa<sup>tm1Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12053176	20110217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807480	Als2<sup>tm1Garo</sup>	is_not_implicated_in	DOID:0060194	amyotrophic lateral sclerosis type 2		MGI:3807481	Als2<sup>tm1Garo</sup>/Als2<sup>tm1Garo</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:18558633	20080924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135666	Fgfr3<sup>tm1Cxd</sup>	is_not_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3586593	Fgfr3<sup>tm1Cxd</sup>/Fgfr3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9887329	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147627	Yars1	is_implicated_in	DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C		MGI:7258133	Yars1<sup>tm1.1Rwb</sup>/Yars1<sup>tm1.1Rwb</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:34516839	20220330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	is_implicated_in	DOID:5419	schizophrenia		MGI:5428133	Nrxn1<sup>tm1Sud</sup>/Nrxn1<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19822762	20120718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108114	Slc12a3	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:7495510	Slc12a3<sup>em3Gpt</sup>/Slc12a3<sup>em4Gpt</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:36370249	20230704	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108114	Slc12a3	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:3513541	Slc12a3<sup>tm1Ges</sup>/Slc12a3<sup>tm1Ges</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9786924	20230704	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796230	Cebpa<sup>tm8.1Nerl</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3809472	Cebpa<sup>tm8.1Nerl</sup>/Cebpa<sup>tm8.1Nerl</sup>  [background:] involves: 129P2/OlaHsd * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18394553	20081003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	MGI:63130	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	MGI:63130	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:1018005	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:1018005	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:16589192	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:16589192	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10942421	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10942421	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657283	Zic3<sup>Bn</sup>/Zic3<sup>Bn</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10861288	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856679	Zic3<sup>Bn</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2657281	Zic3<sup>Bn</sup>/Zic3<sup>+</sup>  [background:] BNT/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:10861288	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180638	Tgm2<sup>tm1Gml</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12205028	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180638	Tgm2<sup>tm1Gml</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12651621	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180638	Tgm2<sup>tm1Gml</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11883932	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906377	Ptger4<sup>tm1.1Matb</sup>/Ptger4<sup>tm1.1Matb</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20008274	20170809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5503965	Mks1<sup>tm1a(EUCOMM)Wtsi</sup>/Mks1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23454480	20130903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:4887579	Mks1<sup>hlb614</sup>/Mks1<sup>hlb614</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21045211	20130903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:4410618	Mks1<sup>krc</sup>/Mks1<sup>krc</sup>  [background:] involves: C3HeB/FeJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19776033	20130903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:5883288	Neb<sup>tm2Hgra</sup>/Neb<sup>tm2Hgra</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S6/SvEvTac * FVB			ECO:0000033	author statement supported by traceable reference	PMID:26123491	20200416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:6404227	Neb<sup>m1Anu</sup>/Neb<sup>m2Anu</sup>  [background:] C57BL/6J-Neb<sup>m1Anu</sup> Neb<sup>m2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32066503	20200416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:5553123	Neb<sup>tm1.1Hgra</sup>/Neb<sup>tm1.1Hgra</sup>  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23715096	20200416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:3706664	Neb<sup>tm1Slbt</sup>/Neb<sup>tm1Slbt</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:19346529	20200416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96071	Hesx1	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10626545	20090113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96071	Hesx1	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:3822779	Hesx1<sup>tm2Jpmb</sup>/Hesx1<sup>tm2Jpmb</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19093031	20090113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96071	Hesx1	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:3822781	Hesx1<sup>tm3Jpmb</sup>/Hesx1<sup>tm3Jpmb</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19093031	20090113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96071	Hesx1	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9620767	20090113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856395	Cpe<sup>fat</sup>	is_implicated_in	DOID:9970	obesity		MGI:3033164	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] involves: HRS/J			ECO:0000033	author statement supported by traceable reference	MGI:61833	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856395	Cpe<sup>fat</sup>	is_implicated_in	DOID:9970	obesity		MGI:3033165	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] BKSChpLt.HRS-Cpe<sup>fat</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2250094	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856395	Cpe<sup>fat</sup>	is_implicated_in	DOID:9970	obesity		MGI:3033164	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] involves: HRS/J			ECO:0000033	author statement supported by traceable reference	PMID:2250094	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:1380	endometrial cancer		MGI:3813633	Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18632614	20081103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3808026	Gja1<sup>tm3Gfi</sup>/Gja1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:18077386	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:4420313	Gja1<sup>tm1Dlg</sup>/Gja1<sup>tm1Dlg</sup> Tg(GFAP-cre)1Kdmc/0  [background:] involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17311295	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3807710	Gja1<sup>tm8Kwi</sup>/Gja1<sup>+</sup> Tg(Pgk1-cre)1Lni/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18003637	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3620827	Gja1<sup>M1Jrt</sup>/Gja1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16155213	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3620841	Gja1<sup>M1Jrt</sup>/Gja1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16155213	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:2179721	Lamb3<sup>IAP</sup>/Lamb3<sup>IAP</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9271670	20160218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:5749252	Lamb3<sup>tm1.1Hosc</sup>/Lamb3<sup>tm1.1Hosc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25350318	20160218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	is_implicated_in	DOID:11714	gestational diabetes		MGI:5504390	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22427375	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3691280	Myh6<sup>tm1Ces</sup>/Myh6<sup>tm1Ces</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3691279	Myh6<sup>tm1Ces</sup>/Myh6<sup>+</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437061	b2b1146Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387402	Stk11<sup>tm1.1Rdp</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814722	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(KRT14-cre)1Ipc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18172296	20081112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387402	Stk11<sup>tm1.1Rdp</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814590	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18227155	20081112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913266	Tk2	is_implicated_in	DOID:0080120	mitochondrial DNA depletion syndrome 2		MGI:3808758	Tk2<sup>tm1Mihi</sup>/Tk2<sup>tm1Mihi</sup>  [background:] involves: 129S6/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20940150	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913266	Tk2	is_implicated_in	DOID:0080120	mitochondrial DNA depletion syndrome 2		MGI:3808758	Tk2<sup>tm1Mihi</sup>/Tk2<sup>tm1Mihi</sup>  [background:] involves: 129S6/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18467430	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:3723301	Casq2<sup>tm1Jse</sup>/Casq2<sup>tm1Jse</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17607358	20090821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:3723302	Casq2<sup>tm2Jse</sup>/Casq2<sup>tm2Jse</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17607358	20090821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:4354215	Casq2<sup>tm1.1Sgp</sup>/Casq2<sup>tm1.1Sgp</sup>  [background:] involves: 129X1/SvJ * C57BL/6NCrL			ECO:0000033	author statement supported by traceable reference	PMID:18583715	20090821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:3691621	Casq2<sup>tm1Kpfe</sup>/Casq2<sup>tm1Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16932808	20090821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097692	Opn1mw	is_implicated_in	DOID:0050679	blue cone monochromacy		MGI:6259805	Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>/Opn1mw<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28751656	20181211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419159	Ildr1<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5691406	Ildr1<sup>tm1(KOMP)Wtsi</sup>/Ildr1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25217574	20151125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419159	Ildr1<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5691406	Ildr1<sup>tm1(KOMP)Wtsi</sup>/Ildr1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25822906	20151125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:7511685	Chd4<sup>em1Flc</sup>/Chd4<sup>em1Flc</sup>  [background:] C57BL/6J-Chd4<sup>em1Flc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37254794	20230804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617328	Notch2<sup>tm3Grid</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:5288006	Notch2<sup>tm3Grid</sup>/Notch2<sup>tm3Grid</sup> Tg(Tpbpa-cre,-EGFP)5Jcc/0  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:21693515	20111003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154553	Lama3<sup>tm1Crt</sup>	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:3042129	Lama3<sup>tm1Crt</sup>/Lama3<sup>tm1Crt</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10366601	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714171	Xylt2<sup>tm1Meh</sup>	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:3714838	Xylt2<sup>tm1Meh</sup>/Xylt2<sup>tm1Meh</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:17517600	20190924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038621	Gad2<sup>tm1Miya</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3038633	Gad2<sup>tm1Miya</sup>/Gad2<sup>tm1Miya</sup>  [background:] NOD.129P2-Gad2<sup>tm1Miya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14676944	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916625	Btbd9	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:6488227	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32446853	20201223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916625	Btbd9	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:5438092	Btbd9<sup>Gt(RRE078)Byg</sup>/Btbd9<sup>Gt(RRE078)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22678064	20201223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916625	Btbd9	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:6488233	Btbd9<sup>tm1c(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1c(EUCOMM)Wtsi</sup> Emx1<sup>tm1(cre)Yql</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31715135	20201223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916625	Btbd9	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:6488226	Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>/Btbd9<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31715135	20201223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I		MGI:5556062	Fkrp<sup>tm1Scbr</sup>/Fkrp<sup>tm1Scbr</sup> Sox1<sup>tm1(cre)Take</sup>/Sox1<sup>+</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:24234655	20200415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I		MGI:6404021	Fkrp<sup>tm1.1Pg</sup>/Fkrp<sup>tm1.1Pg</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26574668	20200415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I		MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20675713	20200415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	is_implicated_in	DOID:12336	male infertility		MGI:5629954	Bscl2<sup>tm1.1Gliu</sup>/Bscl2<sup>tm1.1Gliu</sup> Tg(Fabp4-cre)1Rev/0  [background:] involves: 129 * 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:24778225	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353569	Foxe3	is_implicated_in	DOID:11367	congenital aphakia		MGI:2175026	Foxe3<sup>dyl</sup>/Foxe3<sup>dyl</sup>  [background:] BALB/cLiA-Foxe3<sup>dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11980846	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353569	Foxe3	is_implicated_in	DOID:11367	congenital aphakia		MGI:2175026	Foxe3<sup>dyl</sup>/Foxe3<sup>dyl</sup>  [background:] BALB/cLiA-Foxe3<sup>dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10652278	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857352	Ap3b1<sup>pe-rim2</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3584030	Ap3b1<sup>pe-rim2</sup>/Ap3b1<sup>pe-rim2</sup>  [background:] involves: B10.A(R201) * C57BL/10Slc			ECO:0000033	author statement supported by traceable reference	PMID:9434937	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930136	Pmfbp1	is_implicated_in	DOID:12336	male infertility		MGI:6259651	Pmfbp1<sup>em1Wli</sup>/Pmfbp1<sup>em1Wli</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:30032984	20181210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861805	Cd86<sup>tm1Shr</sup>	is_implicated_in	DOID:12842	Guillain-Barre syndrome		MGI:3618096	Cd86<sup>tm1Shr</sup>/Cd86<sup>tm1Shr</sup>  [background:] NOD.129S4-Cd86<sup>tm1Shr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19050296	20090325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861805	Cd86<sup>tm1Shr</sup>	is_implicated_in	DOID:12842	Guillain-Barre syndrome		MGI:3618096	Cd86<sup>tm1Shr</sup>/Cd86<sup>tm1Shr</sup>  [background:] NOD.129S4-Cd86<sup>tm1Shr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11535635	20090325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12		MGI:5296512	Jup<sup>tm1.1Shou</sup>/Jup<sup>tm1.1Shou</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21880664	20111123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	is_implicated_in	DOID:0110083	arrhythmogenic right ventricular dysplasia 12		MGI:4947241	Jup<sup>tm1.1Glr</sup>/Jup<sup>tm1.1Glr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21245375	20111123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	is_implicated_in	DOID:0111072	myostatin-related muscle hypertrophy		MGI:3714749	Mstn<sup>tm1Sjl</sup>/Mstn<sup>tm1Sjl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9139826	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	is_implicated_in	DOID:0111072	myostatin-related muscle hypertrophy		MGI:5529108	Mstn<sup>Cmpt</sup>/Mstn<sup>+</sup>  [background:] either: HCI or HCR			ECO:0000033	author statement supported by traceable reference	PMID:9335610	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3841484	Ptprc<sup>tm1Weis</sup>/Ptprc<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11163182	20090428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3841485	Ptprc<sup>tm1Weis</sup>/Ptprc<sup>tm1Weis</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11163182	20090428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:6272035	Tnf<sup>Bpsm1</sup>/Tnf<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:6272036	Tnf<sup>Bpsm1</sup>/Tnf<sup>Bpsm1</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29618659	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3622062	Tnf<sup>tm1Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3622060	Tnf<sup>tm2Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678250	Hr<sup>rhsl</sup>	is_implicated_in	DOID:0050634	alopecia universalis		MGI:3052308	Hr<sup>rhsl</sup>/Hr<sup>rhsl</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:15955095	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6258771	Grin1<sup>tm1Bhk</sup>/Grin1<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22726567	20181203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923760	Trappc9	is_implicated_in	DOID:1059	intellectual disability		MGI:6715154	Trappc9<sup>em1Xyli</sup>/Trappc9<sup>em1Xyli</sup>  [background:] C57BL/6J-Trappc9<sup>em1Xyli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33208359	20210625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923760	Trappc9	is_implicated_in	DOID:1059	intellectual disability		MGI:6717362	Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>/Trappc9<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32877400	20210625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5438770	Bmpr2<sup>tm1Kmi</sup>/Bmpr2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16027259	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5827840	Bmpr2<sup>tm1Mmue</sup>/Bmpr2<sup>+</sup>  [background:] B6.129S1-Bmpr2<sup>tm1Mmue</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26076038	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5430750	Bmpr2<sup>tm1.1Enl</sup>/Bmpr2<sup>tm1.1Enl</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:18663089	20170307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	is_implicated_in	DOID:423	myopathy		MGI:6506379	Dnm2<sup>tm2.1Ics</sup>/Dnm2<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32129442	20210216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3032515	Nphp4<sup>nmf192</sup>	is_implicated_in	DOID:0111115	nephronophthisis 4		MGI:4868696	Nphp4<sup>nmf192</sup>/Nphp4<sup>nmf192</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21078623	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2674291	Ednrb<sup>WS4</sup>	is_implicated_in	DOID:0110953	Waardenburg syndrome type 4A		MGI:2675255	Ednrb<sup>WS4</sup>/Ednrb<sup>WS4</sup>  [background:] involves: BALB/c * MSM			ECO:0000033	author statement supported by traceable reference	PMID:11773966	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180202	Gba1<sup>tm1Rlp</sup>	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2651508	Gba1<sup>tm1Rlp</sup>/Gba1<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11994410	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:6198726	Phex<sup>Mhdabap024</sup>/Phex<sup>+</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29735309	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:6198725	Phex<sup>Mhdabap024</sup>/Y  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29735309	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3806979	Phex<sup>Pug</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17710565	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037642	Phex<sup>Hyp-Duk</sup>/Y  [background:] involves: BALB/cAnBomUrd			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764685	Phex<sup>Hyp</sup>/Phex<sup>+</sup>  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037638	Phex<sup>Hyp-2J</sup>/Y  [background:] C57BL/6-Phex<sup>Hyp-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037643	Phex<sup>Hyp-Duk</sup>/Phex<sup>+</sup>  [background:] involves: BALB/cAnBomUrd			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037641	Phex<sup>Hyp-2J</sup>/Phex<sup>+</sup>  [background:] C57BL/6-Phex<sup>Hyp-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3779061	Phex<sup>Hyp</sup>/?  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15976027	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:4450916	Phex<sup>Ska1</sup>/Phex<sup>+</sup>  [background:] C57BL/6-Phex<sup>Ska1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12414538	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:4450917	Phex<sup>Ska1</sup>/Y  [background:] C57BL/6-Phex<sup>Ska1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12414538	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9063736	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5492338	Phex<sup>m1Jrt</sup>/Phex<sup>+</sup>  [background:] B6.129S1-Phex<sup>M1Jrt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22573557	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5492341	Phex<sup>m1Jrt</sup>/Y  [background:] B6.129S1-Phex<sup>M1Jrt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22573557	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3764489	Phex<sup>Hyp</sup>/Y  [background:] B6.Cg-Phex<sup>Hyp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11159866	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5425687	Phex<sup>Mhdabap024</sup>/Phex<sup>Mhdabap024</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap024</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:5425546	Phex<sup>Mhdabap012</sup>/Phex<sup>Mhdabap012</sup>  [background:] C3HeB/FeJ-Phex<sup>Mhdabap012</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:3849173	Six1<sup>Cwe</sup>/Six1<sup>Cwe</sup>  [background:] C3HeB/FeJ-Six1<sup>Cwe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19389353	20090629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181791	Plec<sup>tm1Gwi</sup>	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:3513191	Plec<sup>tm1Gwi</sup>/Plec<sup>tm1Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180817	S1pr2<sup>tm1Ajml</sup>	is_implicated_in	DOID:0110519	autosomal recessive nonsyndromic deafness 68		MGI:3692665	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] either: (involves: 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:26805784	20170406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5430039	b2b243.1Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5430322	b2b243.1Clo/b2b243.1Clo  [background:] C57BL/6J-b2b243.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856377	Spta1<sup>sph</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448372	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:14451913	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9888583	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9326645	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:2661899	Star<sup>tm1Klp</sup>/Star<sup>tm1Klp</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:10976923	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	is_implicated_in	DOID:14756	vascular type Ehlers-Danlos syndrome		MGI:2664355	Col3a1<sup>tm1Jae</sup>/Col3a1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9050868	20120224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	is_implicated_in	DOID:14756	vascular type Ehlers-Danlos syndrome		MGI:5307019	Col3a1<sup>m1Lsmi</sup>/Col3a1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21071432	20120224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857336	Hoxa13<sup>Hd</sup>	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587032	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] B6C3Fe-a/a Hoxa13<sup>Hd</sup> Mcoln3<sup>Va-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10569982	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857336	Hoxa13<sup>Hd</sup>	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587024	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] involves: MYA/Hu			ECO:0000033	author statement supported by traceable reference	MGI:1889019	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857336	Hoxa13<sup>Hd</sup>	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587031	Hoxa13<sup>Hd</sup>/Hoxa13<sup>+</sup>  [background:] B6C3Fe-a/a Hoxa13<sup>Hd</sup> Mcoln3<sup>Va-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10210434	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857336	Hoxa13<sup>Hd</sup>	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3587024	Hoxa13<sup>Hd</sup>/Hoxa13<sup>Hd</sup>  [background:] involves: MYA/Hu			ECO:0000033	author statement supported by traceable reference	PMID:5519671	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5295223	Dlg4<sup>tm2.1Grnt</sup>/Dlg4<sup>tm2.1Grnt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20952458	20111108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5504442	Ins2<sup>Akita</sup>/?  [background:] involves: C57BL/6NSlc			ECO:0000033	author statement supported by traceable reference	PMID:17911348	20130905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3610389	Gt(ROSA)26Sor<sup>tm1(DTA)Jpmb</sup>	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:5432113	Gt(ROSA)26Sor<sup>tm1(DTA)Jpmb</sup>/Gt(ROSA)26Sor<sup>+</sup> Hcn4<sup>tm1(cre/ERT2)Anlu</sup>/Hcn4<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:21193513	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180880	Lrp1<sup>tm2Her</sup>	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:6102946	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24312398	20171219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861609	Hps3<sup>coa-6J</sup>	is_implicated_in	DOID:0060541	Hermansky-Pudlak syndrome 3		MGI:2175787	Hps3<sup>coa-6J</sup>/Hps3<sup>coa-6J</sup>  [background:] C3H/HeJ-Hps3<sup>coa-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:1861465	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:3513373	Plec<sup>tm2Gwi</sup>/Plec<sup>tm2Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20120321	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:3513191	Plec<sup>tm1Gwi</sup>/Plec<sup>tm1Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20120321	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:5311582	Plec<sup>tm7.1Gwi</sup>/Plec<sup>tm7.1Gwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22144912	20120321	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:5311585	Plec<sup>tm7.1Gwi</sup>/Plec<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22144912	20120321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856146	Hps5<sup>ru2-mr</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3805034	Hps5<sup>ru2-mr</sup>/Hps5<sup>ru2-mr</sup>  [background:] B6.Cg-Hps5<sup>ru2-mr</sup>/Re			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856146	Hps5<sup>ru2-mr</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2174727	Hps5<sup>ru2-mr</sup>/Hps5<sup>ru2-mr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807082	Hmx1<sup>mpe</sup>	is_implicated_in	DOID:0060482	oculoauricular syndrome		MGI:3838502	Hmx1<sup>mpe</sup>/Hmx1<sup>mpe</sup>  [background:] C3H/HeJ-Hmx1<sup>mpe</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:19379485	20090501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857300	Mpv17	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	MGI:1274824	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857140	Slc4a1<sup>tm1Llp</sup>	is_implicated_in	DOID:14219	renal tubular acidosis		MGI:2672144	Slc4a1<sup>tm1Llp</sup>/Slc4a1<sup>tm1Llp</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17409310	20090514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3579845	Tbx20<sup>tm1.1Rph</sup>/Tbx20<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15843414	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339754	Csf2ra	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:7261196	Csf2ra<sup>em1Szut</sup>/Csf2ra<sup>em1Szut</sup>  [background:] C57BL/6-Csf2ra<sup>em1Szut</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35043685	20220412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_not_implicated_in	DOID:0050771	pheochromocytoma		MGI:3583336	Ret<sup>tm1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6J * FVB/N * MF1			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:5911874	Sgcd<sup>tm1Ojml</sup>/Sgcd<sup>+</sup>  [background:] B6.129-Sgcd<sup>tm1Ojml</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23695275	20171026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:5911876	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] B6.129-Sgcd<sup>tm1Mcn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23695275	20171026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:3618464	Sgcd<sup>tm1Kcam</sup>/Sgcd<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10481911	20171026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:3618527	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10862711	20171026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358243	Tg(Pbsn-ERG*)1Vv	is_implicated_in	DOID:10283	prostate cancer		MGI:5705650	Tg(Pbsn-ERG*)1Vv/0  [background:] involves: 129S1/SvImJ * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26058078	20160128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98779	Tnnc1	is_implicated_in	DOID:0110319	hypertrophic cardiomyopathy 13		MGI:6304488	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26304555	20190522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98779	Tnnc1	is_implicated_in	DOID:0110319	hypertrophic cardiomyopathy 13		MGI:6304487	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>tm1.1Jrpi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26304555	20190522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98779	Tnnc1	is_implicated_in	DOID:0110319	hypertrophic cardiomyopathy 13		MGI:6304487	Tnnc1<sup>tm1.1Jrpi</sup>/Tnnc1<sup>tm1.1Jrpi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28235781	20190522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3712071	Aqp2<sup>tm1(cre)Blyg</sup>/Aqp2<sup>tm1(cre)Blyg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17229678	20070619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3639115	Aqp2<sup>cph</sup>/Aqp2<sup>cph</sup>  [background:] C57BL/6J-Aqp2<sup>cph</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16641094	20070619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3616879	Aqp2<sup>F204V</sup>/Aqp2<sup>F204V</sup>  [background:] C57BL/6-Aqp2<sup>F204V</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16121255	20070619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4441499	Chordc1<sup>tm1Mbra</sup>	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5644329	Chordc1<sup>tm1Mbra</sup>/Chordc1<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25678499	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3662903	Slc40a1<sup>ffe</sup>	is_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:3700665	Slc40a1<sup>ffe</sup>/Slc40a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17289807	20070322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861926	Gabrd<sup>tm1Geh</sup>	is_implicated_in	DOID:9478	postpartum depression		MGI:3713529	Gabrd<sup>tm1Geh</sup>/Gabrd<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18667149	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1888921	P3h1	is_implicated_in	DOID:0110336	osteogenesis imperfecta type 8		MGI:4830454	P3h1<sup>tm1Dgen</sup>/P3h1<sup>tm1Dgen</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20363744	20100923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5430041	b2b243.2Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5430324	b2b243.2Clo/b2b243.2Clo  [background:] C57BL/6J-b2b243.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:3040187	Ctsd<sup>tm1Cptr</sup>/Ctsd<sup>tm1Cptr</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd)			ECO:0000033	author statement supported by traceable reference	PMID:18498441	20160317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:5702327	Ctsd<sup>tm1.1Thre</sup>/Ctsd<sup>tm1.1Thre</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26232697	20160317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:5702324	Ctsd<sup>tm1.1Thre</sup>/Ctsd<sup>tm1.1Thre</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26232697	20160317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	is_implicated_in	DOID:0110725	neuronal ceroid lipofuscinosis 10		MGI:5752257	Ctsd<sup>m1J</sup>/Ctsd<sup>m1J</sup>  [background:] C3HeB/FeJ-Ctsd<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5751705	20160317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:5644542	Atm<sup>tm1Pmc</sup>/Atm<sup>tm1Pmc</sup>  [background:] B6.Cg-Atm<sup>tm1Pmc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25683718	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175703	Atm<sup>tm1Awb</sup>/Atm<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Atm<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:10449794	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175703	Atm<sup>tm1Awb</sup>/Atm<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Atm<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:8689683	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175706	Atm<sup>tm1Bal</sup>/Atm<sup>tm1Bal</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:8843193	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175707	Atm<sup>tm1Fwa</sup>/Atm<sup>tm1Fwa</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10716718	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175706	Atm<sup>tm1Bal</sup>/Atm<sup>tm1Bal</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9356511	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175708	Atm<sup>tm1Led</sup>/Atm<sup>tm1Led</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8917548	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2181774	Atm<sup>tm1Mfl</sup>/Atm<sup>tm1Mfl</sup>  [background:] involves: 129T2/SvEms * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11389091	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:6110012	Atm<sup>tm1.1Mmpl</sup>/Atm<sup>tm1.1Mmpl</sup>  [background:] involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26310626	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175710	Atm<sup>tm1Pmc</sup>/Atm<sup>tm1Pmc</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9582124	20180115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:3037431	Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] C3H/HeJ-Fasl<sup>gld</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6693832	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:3037431	Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] C3H/HeJ-Fasl<sup>gld</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:77345	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628914	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm6Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628828	Dnmt3b<sup>tm6Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628830	Dnmt3b<sup>tm6Enl</sup>/Dnmt3b<sup>tm6Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628826	Dnmt3b<sup>tm7Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628916	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3040301	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm1Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10555141	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	is_implicated_in	DOID:9281	phenylketonuria		MGI:6715269	Pah<sup>em1Skym</sup>/Pah<sup>em1Skym</sup>  [background:] C57BL/6J-Pah<sup>em1Skym</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33790381	20210611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	is_implicated_in	DOID:9281	phenylketonuria		MGI:3587815	Pah<sup>enu2</sup>/Pah<sup>enu2</sup>  [background:] involves: BTBR			ECO:0000033	author statement supported by traceable reference	PMID:9119379	20210611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	is_implicated_in	DOID:9281	phenylketonuria		MGI:5300789	Pah<sup>enu2</sup>/Pah<sup>enu2</sup>  [background:] BTBR-Pah<sup>enu2</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21640623	20210611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	is_implicated_in	DOID:9281	phenylketonuria		MGI:3587816	Pah<sup>enu3</sup>/Pah<sup>enu3</sup>  [background:] involves: BTBR			ECO:0000033	author statement supported by traceable reference	PMID:8375656	20210611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3802545	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1.1Djk</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18495876	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3587768	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C3H/HeNHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15888477	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3587764	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15888477	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3587766	Tsc1<sup>tm1Chdl</sup>/Tsc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Balb/cOlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15888477	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3708979	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11438694	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3588988	Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup> Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15601645	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3588773	Tsc1<sup>tm1.1Djk</sup>/Tsc1<sup>+</sup>  [background:] either: 129S4/SvJae-Tsc1<sup>tm1Djk</sup> or (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11875047	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:5641392	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] B6J.129S4-Tsc1<sup>tm1Hin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3802584	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(GFAP-cre)8Gtm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21062901	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:13515	tuberous sclerosis		MGI:3802584	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(GFAP-cre)8Gtm/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17714952	20150622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5538574	Oprm1<sup>tm1Kff</sup>/Oprm1<sup>tm1Kff</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20503133	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:1682	congenital heart disease		MGI:6286233	Nkx2-5<sup>tm1.1Burg</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S2/SvPasCrl * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:28302382	20190429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:1682	congenital heart disease		MGI:6294720	Nkx2-5<sup>tm1.1Hkas</sup>/Nkx2-5<sup>+</sup>  [background:] 129S2.Cg-Nkx2-5<sup>tm1.1Hkas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26226998	20190429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:1682	congenital heart disease		MGI:6294720	Nkx2-5<sup>tm1.1Hkas</sup>/Nkx2-5<sup>+</sup>  [background:] 129S2.Cg-Nkx2-5<sup>tm1.1Hkas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25028484	20190429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3716134	Ins1<sup>tm1Jja</sup>/Ins1<sup>tm1Jja</sup>  [background:] NOD.129S2-Ins1<sup>tm1Jja</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12925730	20070726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	is_implicated_in	DOID:0060589	Yunis-Varon syndrome		MGI:5554544	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup>  [background:] involves: 129P2/OlaHsd * C3H * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23623387	20140402	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384968	L2hgdh	is_implicated_in	DOID:0050574	L-2-hydroxyglutaric aciduria		MGI:5708062	L2hgdh<sup>Gt(DC0625)Wtsi</sup>/L2hgdh<sup>Gt(DC0625)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25763823	20160211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856174	Pax3<sup>Sp-d</sup>	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2451350	Pax3<sup>Sp-d</sup>/Pax3<sup>+</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856174	Pax3<sup>Sp-d</sup>	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	is_implicated_in	DOID:0110635	muscular dystrophy-dystroglycanopathy type B5		MGI:4834522	Fkrp<sup>tm1Itl</sup>/Fkrp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20675713	20101011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856587	Cat4<sup>Apcat1-3</sup>	is_implicated_in	DOID:83	cataract		MGI:3574974	Cat4<sup>Apcat1-3</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3784016	Nupr1<sup>tm1Jlio</sup>	is_implicated_in	DOID:0050457	Sertoli cell-only syndrome		MGI:3784866	Nupr1<sup>tm1Jlio</sup>/Nupr1<sup>tm1Jlio</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18495683	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	is_not_implicated_in	DOID:9821	choroideremia		MGI:3052952	Chm<sup>tm1Jvdh</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9175730	20051007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052066	Slc29a1<sup>tm1Msg</sup>	is_implicated_in	DOID:0050741	alcohol dependence		MGI:3052075	Slc29a1<sup>tm1Msg</sup>/Slc29a1<sup>tm1Msg</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15258586	20080206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777373	Pla2g6<sup>tm1Tsu</sup>	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3777383	Pla2g6<sup>tm1Tsu</sup>/Pla2g6<sup>tm1Tsu</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21813701	20110919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858204	Map3k14	is_implicated_in	DOID:12236	primary biliary cholangitis		MGI:3767418	Map3k14<sup>aly</sup>/Map3k14<sup>aly</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9620319	20091015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857832	Ebp<sup>Td</sup>	is_implicated_in	DOID:0060292	X-linked chondrodysplasia punctata 1		MGI:3587820	Ebp<sup>Td</sup>/Ebp<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10391218	20050916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861634	Clock<sup>m1Jt</sup>	is_implicated_in	DOID:3312	bipolar disorder		MGI:4867520	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: BALB/cJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21123577	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3628822	Unc13d<sup>Jinx</sup>	is_implicated_in	DOID:0110923	familial hemophagocytic lymphohistiocytosis 3		MGI:3628949	Unc13d<sup>Jinx</sup>/Unc13d<sup>Jinx</sup>  [background:] C57BL/6J-Unc13d<sup>Jinx</sup>/Mmucd			ECO:0000033	author statement supported by traceable reference	PMID:17420270	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040267	Tg(rTH-Tag)20Dmc	is_implicated_in	DOID:769	neuroblastoma		MGI:5442286	Tg(rTH-Tag)20Dmc/0  [background:] involves: C57BL/6NTac * DBA/2NTac			ECO:0000033	author statement supported by traceable reference	PMID:7680068	20121120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177709	Gck<sup>tm1.1Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3603012	Gck<sup>tm1.1Mgn</sup>/Gck<sup>+</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177709	Gck<sup>tm1.1Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3603013	Gck<sup>tm1.1Mgn</sup>/Gck<sup>tm1.1Mgn</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177709	Gck<sup>tm1.1Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3603003	Gck<sup>tm1.1Mgn</sup>/Gck<sup>tm1.1Mgn</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	is_implicated_in	DOID:0110671	congenital myasthenic syndrome 6		MGI:2662570	Chat<sup>tm1Fhg</sup>/Chat<sup>tm1Fhg</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12533614	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	is_implicated_in	DOID:0110671	congenital myasthenic syndrome 6		MGI:3046097	Chat<sup>tm1.1Jrs</sup>/Chat<sup>tm1.1Jrs</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12441053	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	is_implicated_in	DOID:12365	malaria		MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14595440	20130313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	is_implicated_in	DOID:12365	malaria		MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17466543	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155771	Psen1<sup>tm1Psgh</sup>	is_not_implicated_in	DOID:10652	Alzheimer's disease		MGI:2177097	Psen1<sup>tm1Psgh</sup>/Psen1<sup>tm1Psgh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10962005	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:3046553	Col18a1<sup>tm1Hms</sup>/Col18a1<sup>tm1Hms</sup>  [background:] B6.129S4-Col18a1<sup>tm1Hms</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12766032	20150601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	is_implicated_in	DOID:8466	retinal degeneration		MGI:6383402	Ift172<sup>tm1.1Rama</sup>/Ift172<sup>tm1.1Rama</sup> Tg(Rho-icre)1Ck/0  [background:] involves: 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29659833	20200106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916202	Tlcd3b	is_implicated_in	DOID:0050572	cone-rod dystrophy		MGI:7277808	Tlcd3b<sup>em1(IMPC)Bay</sup>/Tlcd3b<sup>em1(IMPC)Bay</sup>  [background:] C57BL/6NJ-Tlcd3b<sup>em1(IMPC)Bay</sup>/Mmnc			ECO:0000033	author statement supported by traceable reference	PMID:33077892	20220516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	is_implicated_in	DOID:3310	atopic dermatitis		MGI:6241552	Adam17<sup>tm1.2Bbl</sup>/Adam17<sup>tm1.2Bbl</sup> Sox9<sup>tm3(cre)Crm</sup>/Sox9<sup>+</sup>  [background:] B6.129(SJL)-Sox9<sup>tm3(cre)Crm</sup> Adam17<sup>tm1.2Bbl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25902485	20181112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0050453	lissencephaly		MGI:2664130	Pafah1b1<sup>tm2.2Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0050453	lissencephaly		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0050453	lissencephaly		MGI:2664093	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>tm2Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0050453	lissencephaly		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10541472	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0050453	lissencephaly		MGI:2664549	Pafah1b1<sup>tm1Or</sup>/Pafah1b1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11344260	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	is_implicated_in	DOID:0090111	PCWH syndrome		MGI:5648371	Sox10<sup>gt</sup>/Sox10<sup>gt</sup>  [background:] GT/Le			ECO:0000033	author statement supported by traceable reference	PMID:25399070	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:4836620	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21262837	20110409	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446166	Marveld2	is_implicated_in	DOID:0110506	autosomal recessive nonsyndromic deafness 49		MGI:5550096	Marveld2<sup>tm1.1Sria</sup>/Marveld2<sup>tm1.1Sria</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23979167	20180517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446166	Marveld2	is_implicated_in	DOID:0110506	autosomal recessive nonsyndromic deafness 49		MGI:6156912	Marveld2<sup>tm1Sats</sup>/Marveld2<sup>tm1Sats</sup>  [background:] B6.Cg-Marveld2<sup>tm1Sats</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26677943	20180517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2677633	Qrfpr	is_implicated_in	DOID:0080010	bone structure disease		MGI:3830477	Qrfpr<sup>tm1Lex</sup>/Qrfpr<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16382160	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857796	Shh<sup>tm1Chg</sup>	is_implicated_in	DOID:0110875	holoprosencephaly 3		MGI:3042793	Shh<sup>tm1Chg</sup>/Shh<sup>tm1Chg</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15105374	20050817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857796	Shh<sup>tm1Chg</sup>	is_implicated_in	DOID:0110875	holoprosencephaly 3		MGI:2173405	Shh<sup>tm1Chg</sup>/Shh<sup>tm1Chg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8837770	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298379	Matr3	is_implicated_in	DOID:0060212	amyotrophic lateral sclerosis type 21		MGI:6490343	Matr3<sup>em1Tcp</sup>/Matr3<sup>em1Tcp</sup>  [background:] C57BL/6J-Matr3<sup>em1Tcp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33082323	20210106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857029	Rasa3<sup>scat</sup>	is_implicated_in	DOID:12449	aplastic anemia		MGI:6378723	Rasa3<sup>scat</sup>/Rasa3<sup>scat</sup>  [background:] involves: BALB/cBy * BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:29922180	20191202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108398	Mlx	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7444296	Mlx<sup>tm1.2Rne</sup>/Mlx<sup>tm1.2Rne</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:34669700	20230315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3655853	Krt1<sup>Mhdadsk12</sup>	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:3655854	Krt1<sup>Mhdadsk12</sup>/Krt1<sup>+</sup>  [background:] C3HeB/FeJ-Krt1<sup>Mhdadsk12</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16528356	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157489	Twist1<sup>Pde</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2177044	Twist1<sup>Pde</sup>/Twist1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11350121	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157489	Twist1<sup>Pde</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2177042	Twist1<sup>Pde</sup>/Twist1<sup>Pde</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11350121	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916449	Armc2	is_implicated_in	DOID:12336	male infertility		MGI:6369630	Armc2<sup>em1Pfr</sup>/Armc2<sup>em1Pfr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30686508	20191105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678005	Apc<sup>tm2Tno</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:5521585	Apc<sup>tm2Tno</sup>/Apc<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14522940	20131206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857160	Edn3<sup>tm1Ywa</sup>	is_implicated_in	DOID:0110954	Waardenburg syndrome type 4B		MGI:2174947	Edn3<sup>tm1Ywa</sup>/Edn3<sup>tm1Ywa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8001160	20100316	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5829465	Slc7a5<sup>tm1.1Daca</sup>/Slc7a5<sup>tm1.1Daca</sup> Tg(Tek-cre)12Flv/0  [background:] B6J.Cg-Slc7a5<sup>tm1.1Daca</sup> Tg(Tek-cre)12Flv			ECO:0000033	author statement supported by traceable reference	PMID:27912058	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:0014667	disease of metabolism		MGI:5906203	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19001090	20170803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3604814	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B10.D2/(58N)Sn			ECO:0000033	author statement supported by traceable reference	PMID:7873879	20060417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6971670	20060417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3719582	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12382103	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:2676935	Thrb<sup>tm3Few</sup>/Thrb<sup>tm3Few</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12925699	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:5528981	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:15983791	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:2657251	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1Df</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8673137	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3588064	Thrb<sup>tm2Few</sup>/Thrb<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11274423	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3588063	Thrb<sup>tm2Few</sup>/Thrb<sup>tm2Few</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11274423	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3715607	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11069286	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3715602	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11069286	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:2657251	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1Df</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8670802	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3849881	Thrb<sup>tm6.1Few</sup>/Thrb<sup>tm6.1Few</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19439650	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3849882	Thrb<sup>tm6.1Few</sup>/Thrb<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19439650	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3522243	pta	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3522704	pta/pta  [background:] C57BL/6J-pta			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3640358	Fgfr3<sup>tm5.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11181569	20090415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3640323	Fgfr3<sup>tm4Cxd</sup>/Fgfr3<sup>+</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * NIH Black Swiss * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10861287	20090415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3640318	Fgfr3<sup>tm4.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10861287	20090415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3840080	Fgfr3<sup>tm1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19073250	20090415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3709989	Slc35c1<sup>tm1Cknr</sup>	is_implicated_in	DOID:0070255	congenital disorder of glycosylation type IIc		MGI:3711227	Slc35c1<sup>tm1Cknr</sup>/Slc35c1<sup>tm1Cknr</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17276979	20190516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:11717	neonatal diabetes		MGI:6478875	Ins2<sup>em#Arak</sup>/Ins2<sup>+</sup>  [background:] C.129-Rag2<sup>tm1Fwa</sup> Ins2<sup>em#Arak</sup> Jak3<sup>tm1Tks</sup>/Arak			ECO:0000033	author statement supported by traceable reference	PMID:32699230	20201210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5315439	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:2651696	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12575948	20180815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:3774850	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16494529	20180815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5315442	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>tm1Hzo</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:22002997	20180815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:5315439	Atxn7<sup>tm1Hzo</sup>/Atxn7<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:22002997	20180815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527173	Ndufs4<sup>tm1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:5451025	Ndufs4<sup>tm1Rpa</sup>/Ndufs4<sup>tm1Rpa</sup> Tg(Nes-cre)1Kln/0  [background:] B6.Cg-Tg(Nes-cre)1Kln Ndufs4<sup>tm1Rpa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22653057	20130124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527173	Ndufs4<sup>tm1Rpa</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:4818648	Ndufs4<sup>tm1Rpa</sup>/Ndufs4<sup>tm1Rpa</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20534480	20130124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:1909	melanoma		MGI:3843341	Braf<sup>tm1Cpri</sup>/Braf<sup>tm1Cpri</sup> Tg(Tyr-cre/ERT2)1Lru/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19345328	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857992	Hoxa3<sup>tm1Mrc</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3033772	Hoxa3<sup>tm1Mrc</sup>/Hoxa3<sup>tm1Mrc</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:1673020	20050701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98917	Uros	is_implicated_in	DOID:13271	cutaneous porphyria		MGI:3621357	Uros<sup>tm1Cged</sup>/Uros<sup>tm1Cged</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16314073	20080623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98917	Uros	is_implicated_in	DOID:13271	cutaneous porphyria		MGI:3777397	Uros<sup>tm3Rjde</sup>/Uros<sup>tm3Rjde</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16532394	20080623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98917	Uros	is_implicated_in	DOID:13271	cutaneous porphyria		MGI:3777399	Uros<sup>tm2Rjde</sup>/Uros<sup>tm3Rjde</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16532394	20080623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341818	Cnga3	is_implicated_in	DOID:0110007	achromatopsia 2		MGI:5796753	Cnga3<sup>cpfl5</sup>/Cnga3<sup>cpfl5</sup>  [background:] B6.RHJ-Cnga3<sup>cpfl5</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	PMID:22509403	20160909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341818	Cnga3	is_implicated_in	DOID:0110007	achromatopsia 2		MGI:4867912	Cnga3<sup>cpfl5</sup>/Cnga3<sup>cpfl5</sup>  [background:] involves: RHJ/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:22509403	20160909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341818	Cnga3	is_implicated_in	DOID:0110007	achromatopsia 2		MGI:2663832	Cnga3<sup>tm1Biel</sup>/Cnga3<sup>tm1Biel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10377453	20160909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2177705	Gck<sup>tm1Tka</sup>/Gck<sup>tm1Tka</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:8530440	20050816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2680668	Foxn1<sup>nu</sup>/Foxn1<sup>nu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:596425	20131203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833390	Tg(Thy1-SERPINI1*G392E)333Icka	is_implicated_in	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies		MGI:3833392	Tg(Thy1-SERPINI1*G392E)333Icka/0  [background:] involves: C57BL * CD-1 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18940798	20090224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833390	Tg(Thy1-SERPINI1*G392E)333Icka	is_implicated_in	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies		MGI:3833393	Tg(Thy1-SERPINI1*G392E)333Icka/Tg(Thy1-SERPINI1*G392E)333Icka  [background:] involves: C57BL * CD-1 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18940798	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100492	Nrp2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4843917	Nrp2<sup>tm1.2Mom</sup>/Nrp2<sup>tm1.2Mom</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:18657176	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346317	Nr2e3	is_implicated_in	DOID:0090059	enhanced S-cone syndrome		MGI:2668613	Nr2e3<sup>rd7</sup>/Nr2e3<sup>rd7</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10805811	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346317	Nr2e3	is_implicated_in	DOID:0090059	enhanced S-cone syndrome		MGI:3709293	Nr2e3<sup>rd7</sup>/Nr2e3<sup>rd7</sup>  [background:] B6.Cg-Nr2e3<sup>rd7</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16110338	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680042	Slc12a6<sup>tm1Tjj</sup>	is_implicated_in	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy		MGI:2680045	Slc12a6<sup>tm1Tjj</sup>/Slc12a6<sup>tm1Tjj</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14532115	20180617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181744	Kif3b<sup>tm1Noh</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6423106	Kif3b<sup>tm1Noh</sup>/Kif3b<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31746486	20200518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	is_implicated_in	DOID:0060574	von Willebrand's disease 2		MGI:6258654	Vwf<sup>tm1.1Geno</sup>/Vwf<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27212476	20181203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	is_implicated_in	DOID:0060574	von Willebrand's disease 2		MGI:6258657	Vwf<sup>tm1.1Geno</sup>/Vwf<sup>tm1.1Geno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27212476	20181203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934891	Hspg2<sup>tm1Nid</sup>	is_implicated_in	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia		MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11802174	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933758	Cdkn1c<sup>tm1Kat</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3838163	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12468647	20090401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933758	Cdkn1c<sup>tm1Kat</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3838162	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>tm1Kat</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12468647	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	is_implicated_in	DOID:2717	Bloom syndrome		MGI:3582673	Blm<sup>tm1Grdn</sup>/Blm<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12242442	20061024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	is_implicated_in	DOID:2717	Bloom syndrome		MGI:2683906	Blm<sup>tm3Brd</sup>/Blm<sup>tm3Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11101838	20061024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	is_implicated_in	DOID:2717	Bloom syndrome		MGI:2683845	Blm<sup>tm1Ches</sup>/Blm<sup>tm3Brd</sup>  [background:] involves: 129S/SvEv * C57BL/6 * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:14642567	20061024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	is_implicated_in	DOID:2717	Bloom syndrome		MGI:2683844	Blm<sup>tm1Ches</sup>/Blm<sup>tm1Ches</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9808625	20061024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	is_implicated_in	DOID:2717	Bloom syndrome		MGI:3664441	Blm<sup>tm1Ches</sup>/Blm<sup>tm4Ches</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16914751	20061024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	is_implicated_in	DOID:2717	Bloom syndrome		MGI:3664440	Blm<sup>tm1Ches</sup>/Blm<sup>tm4Ches</sup> Tg(LGB-cre)74Acl/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16914751	20061024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18728777	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17559418	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5763612	Itpr3<sup>tf</sup>/Itpr3<sup>tf</sup>  [background:] BTBR T<sup>+</sup> Itpr3<sup>tf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25879444	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777967	Pnp<sup>e</sup>	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778897	Pnp<sup>e</sup>/Pnp<sup>e</sup>  [background:] involves: C3H/HeHa * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:2516826	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777967	Pnp<sup>e</sup>	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778898	Pnp<sup>e</sup>/Pnp<sup>e</sup>  [background:] C57BL/6J-Pnp<sup>e</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_not_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3586593	Fgfr3<sup>tm1Cxd</sup>/Fgfr3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9887329	20050901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860885	Tlr4<sup>tm1Aki</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3706992	Tlr4<sup>tm1Aki</sup>/Tlr4<sup>tm1Aki</sup>  [background:] B6.129P2-Tlr4<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17053835	20091216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3654320	Pjvk<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110511	autosomal recessive nonsyndromic deafness 59		MGI:3654321	Pjvk<sup>tm1Ugds</sup>/Pjvk<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16804542	20060912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8341011	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8476712	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582952	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk</sup>  [background:] involves: 101 * C3H * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7723240	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582929	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] involves: BALB/c * CAST/EiJ			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582934	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] involves: 101 * BALB/c * C3H * C57BL/6J * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582933	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk</sup>  [background:] involves: 101 * C3H * C57BL/6J * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3037282	Bicc1<sup>jcpk-bpk</sup>/Bicc1<sup>jcpk-bpk</sup>  [background:] BALB/c-Bicc1<sup>jcpk-bpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3711062	Bicc1<sup>tm1Emdr</sup>/Bicc1<sup>tm1Emdr</sup>  [background:] B6SJL-Bicc1<sup>tm1Emdr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3710978	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437061	b2b1146Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	is_implicated_in	DOID:0080060	autosomal recessive spinocerebellar ataxia 12		MGI:7541130	Wwox<sup>em1Mald</sup>/Wwox<sup>em1Mald</sup>  [background:] FVB/N-Wwox<sup>em1Mald</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36828035	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10		MGI:5557989	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup>  [background:] involves: BXD24/TyJ			ECO:0000033	author statement supported by traceable reference	PMID:17898177	20140410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0110291	Leber congenital amaurosis 10		MGI:5557979	Cep290<sup>rd16</sup>/Cep290<sup>rd16</sup>  [background:] involves: BXD24/TyJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21245082	20140410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1		MGI:2654709	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25144618	20151001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3		MGI:3576602	Mpz<sup>tm1Msch</sup>/Mpz<sup>tm1Msch</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7581451	20050511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2674077	Cldn14<sup>tm1Tbf</sup>	is_implicated_in	DOID:0110487	autosomal recessive nonsyndromic deafness 29		MGI:2674081	Cldn14<sup>tm1Tbf</sup>/Cldn14<sup>tm1Tbf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12913076	20110613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96788	Lifr	is_implicated_in	DOID:0080205	CAKUT		MGI:6093713	Lifr<sup>tm1Imx</sup>/Lifr<sup>tm1Imx</sup>  [background:] B6;129S7-Lifr<sup>tm1Imx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28334964	20180725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842979	Ihh<sup>tm1.1Dcha</sup>	is_implicated_in	DOID:0110964	brachydactyly type A1		MGI:3842982	Ihh<sup>tm1.1Dcha</sup>/Ihh<sup>tm1.1Dcha</sup>  [background:] either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:19252479	20090505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921700	Pank2	is_not_implicated_in	DOID:3981	pantothenate kinase-associated neurodegeneration		MGI:3514129	Pank2<sup>tm1Jgt</sup>/Pank2<sup>tm1Jgt</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15525657	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3783594	Tg(Amelx-Ambn)1Mlp	is_implicated_in	DOID:2187	amelogenesis imperfecta		MGI:5140073	Tg(Amelx-Ambn)1Mlp/Tg(Amelx-Ambn)1Mlp  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12657627	20220426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584185	Man2b1<sup>tm1Psa</sup>	is_implicated_in	DOID:3413	alpha-mannosidosis		MGI:3603566	Man2b1<sup>tm1Psa</sup>/Man2b1<sup>tm1Psa</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10400983	20051103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584185	Man2b1<sup>tm1Psa</sup>	is_implicated_in	DOID:3413	alpha-mannosidosis		MGI:3603566	Man2b1<sup>tm1Psa</sup>/Man2b1<sup>tm1Psa</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16014715	20051103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	is_implicated_in	DOID:3755	antithrombin III deficiency		MGI:3696558	Serpinc1<sup>tm1Dwr</sup>/Serpinc1<sup>tm1Dwr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:14592998	20091123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054868	Rassf5<sup>tm1Kina</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4939894	Rassf5<sup>tm1Kina</sup>/Rassf5<sup>tm1Kina</sup>  [background:] B6.Cg-Rassf5<sup>tm1Kina</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21194982	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2150019	Spred2	is_implicated_in	DOID:4480	achondroplasia		MGI:3603325	Spred2<sup>Gt(XB228)Byg</sup>/Spred2<sup>Gt(XB228)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15946934	20051031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859929	Vdr<sup>tm1Ska</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:10746634	20061019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	is_implicated_in	DOID:5812	MHC class II deficiency		MGI:3617399	Ciita<sup>tm1Ccum</sup>/Ciita<sup>tm1Ccum</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8624807	20060323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	is_implicated_in	DOID:5812	MHC class II deficiency		MGI:3052466	Ciita<sup>tm2Wrth</sup>/Ciita<sup>tm2Wrth</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15322541	20060323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619379	Uros<sup>tm1Cged</sup>	is_implicated_in	DOID:13271	cutaneous porphyria		MGI:3621357	Uros<sup>tm1Cged</sup>/Uros<sup>tm1Cged</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16314073	20060504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056648	Kcnq1<sup>tm2Kpfe</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3056757	Kcnq1<sup>tm2Kpfe</sup>/Kcnq1<sup>tm2Kpfe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15498462	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	is_implicated_in	DOID:3614	Kallmann syndrome		MGI:3039429	Sox10<sup>tm1Weg</sup>/Sox10<sup>tm1Weg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:23643381	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201678	Cacna1g	is_implicated_in	DOID:0111742	cerebellar ataxia type 42		MGI:6400523	Cacna1g<sup>em1Ftan</sup>/Cacna1g<sup>em1Ftan</sup>  [background:] C57BL/6NCrSlc-Cacna1g<sup>em1Ftan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31229688	20200702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201678	Cacna1g	is_implicated_in	DOID:0111742	cerebellar ataxia type 42		MGI:6400524	Cacna1g<sup>em1Ftan</sup>/Cacna1g<sup>+</sup>  [background:] C57BL/6NCrSlc-Cacna1g<sup>em1Ftan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31229688	20200702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:3713297	Gck<sup>tm3Mgn</sup>/Gck<sup>+</sup>  [background:] B6.129S6-Gck<sup>tm3Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039266	Trp53<sup>tm3.1Tyj</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584470	Trp53<sup>tm3.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:78359	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686996	Mitf<sup>Mi-H</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2663064	Mitf<sup>Mi-wh</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:5635983	Mitf<sup>mi-bw</sup>/Mitf<sup>mi-bw</sup> Tg(Dct-lacZ)A12Jkn/0  [background:] involves: C3H * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22563733	20150514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146110	Washc5	is_not_implicated_in	DOID:0110823	hereditary spastic paraplegia 8		MGI:6256431	Washc5<sup>tm1.2Cbee</sup>/Washc5<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26572744	20181115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	is_implicated_in	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1		MGI:3603515	Ighmbp2<sup>nmd-2J</sup>/Ighmbp2<sup>nmd-2J</sup>  [background:] B6.BKS-Ighmbp2<sup>nmd-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15269181	20220720	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	is_implicated_in	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1		MGI:7314416	Ighmbp2<sup>em1Cll</sup>/Ighmbp2<sup>em1Cll</sup>  [background:] FVB/NJ-Ighmbp2<sup>em1Cll</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34726235	20220720	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:5523972	Pax3<sup>Sp-1Wli</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451311	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: 101 * C3H/He * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:9344762	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2169285	Pax3<sup>Sp-2H</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2168108	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2763211	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451350	Pax3<sup>Sp-d</sup>/Pax3<sup>+</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1101355	Ltbp3	is_implicated_in	DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome		MGI:2451201	Ltbp3<sup>tm1Bdvc</sup>/Ltbp3<sup>tm1Bdvc</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:25669657	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856996	pma	is_implicated_in	DOID:11836	clubfoot		MGI:3722144	pma/pma  [background:] involves: CF-1			ECO:0000033	author statement supported by traceable reference	PMID:3948960	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617905	Chm<sup>tm1.3Seab</sup>	is_implicated_in	DOID:9821	choroideremia		MGI:3620090	Chm<sup>tm1.3Seab</sup>/Chm<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584470	Trp53<sup>tm3.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584464	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm2.1Tyj</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584471	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm3.1Tyj</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584474	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584463	Trp53<sup>tm2.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584473	Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:2174783	Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7922305	20101019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3576493	Trp53<sup>tm3.1Glo</sup>/Trp53<sup>+</sup>  [background:] B6.129S7-Trp53<sup>tm3.1Glo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15607981	20101019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:5517709	Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Nkx2-1-cre)2Sand/0  [background:] B6.Cg-Pten<sup>tm1Hwu</sup> Tg(Nkx2-1-cre)2Sand			ECO:0000033	author statement supported by traceable reference	PMID:22167068	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445185	Klhl3	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6393411	Klhl3<sup>tm1.1Slin</sup>/Klhl3<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30148674	20200306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445185	Klhl3	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6393415	Klhl3<sup>tm1.1Slin</sup>/Klhl3<sup>tm1.1Slin</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30148674	20200306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445185	Klhl3	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6157462	Klhl3<sup>tm2.1Esoh</sup>/Klhl3<sup>tm2.1Esoh</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28052936	20200306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445185	Klhl3	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:5646380	Klhl3<sup>tm1.1Esoh</sup>/Klhl3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24821705	20200306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	is_implicated_in	DOID:0080462	developmental and epileptic encephalopathy 7		MGI:6488175	Kcnq2<sup>tm1.1Lvi</sup>/Kcnq2<sup>+</sup>  [background:] 129-Kcnq2<sup>tm1.1Lvi</sup>/Lvi			ECO:0000033	author statement supported by traceable reference	PMID:32239694	20201222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	is_implicated_in	DOID:0111454	SHORT syndrome		MGI:6275834	Pik3r1<sup>tm1.1Geno</sup>/Pik3r1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26974159	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96214	hph1	is_implicated_in	DOID:12638	hypertrophic pyloric stenosis		MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:15144277	20060726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387851	Tbx5<sup>tm1.1Jse</sup>	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3052529	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:15289437	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387851	Tbx5<sup>tm1.1Jse</sup>	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3052529	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:16870172	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387851	Tbx5<sup>tm1.1Jse</sup>	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3623769	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] involves: 129/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11572777	20150821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932397	Cryge<sup>Aey1</sup>	is_implicated_in	DOID:83	cataract		MGI:2175810	Cryge<sup>Aey1</sup>/Cryge<sup>+</sup>  [background:] C3HeB/FeJ-Cryge<sup>Aey1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10932192	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932397	Cryge<sup>Aey1</sup>	is_implicated_in	DOID:83	cataract		MGI:2175809	Cryge<sup>Aey1</sup>/Cryge<sup>Aey1</sup>  [background:] C3HeB/FeJ-Cryge<sup>Aey1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10932192	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856377	Spta1<sup>sph</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:3767061	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] either: (B6.C3-Spta1<sup>sph</sup> x WB.C3-Spta1<sup>sph</sup>)F1 or (WB.C3-Spta1<sup>sph</sup> x B6.C3-Spta1<sup>sph</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:7059672	20080110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856377	Spta1<sup>sph</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448372	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:14451913	20080110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445125	Timd4	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287981	Timd4<sup>tm1Kuch</sup>/Timd4<sup>tm1Kuch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105062	Amhr2	is_implicated_in	DOID:0050791	persistent Mullerian duct syndrome		MGI:3042182	Amhr2<sup>tm1Bhr</sup>/Amhr2<sup>tm1Bhr</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:21490063	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447874	Mmp20<sup>tm1Jdb</sup>	is_implicated_in	DOID:0110060	amelogenesis imperfecta hypomaturation type 2A2		MGI:2450776	Mmp20<sup>tm1Jdb</sup>/Mmp20<sup>tm1Jdb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12393861	20090121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699319	Gdf5<sup>Rgsc451</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3758631	Gdf5<sup>Rgsc451</sup>/Gdf5<sup>Rgsc451</sup>  [background:] C57BL/6JJcl-Gdf5<sup>Rgsc451</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17656374	20071018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856202	Eda<sup>Ta-6J</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3707523	Eda<sup>Ta-6J</sup>/Y  [background:] C57BL/6J A<sup>w-J</sup>-Eda<sup>Ta-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14506134	20070628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	is_implicated_in	DOID:2861	congenital nonspherocytic hemolytic anemia		MGI:2177287	Gpi1<sup>b-m1Neu</sup>/Gpi1<sup>b-m1Neu</sup>  [background:] C3.Cg-Gpi1<sup>b-m1Neu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8417789	20110309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	is_implicated_in	DOID:2861	congenital nonspherocytic hemolytic anemia		MGI:2177288	Gpi1<sup>b-m2Neu</sup>/Gpi1<sup>b-m2Neu</sup>  [background:] C3.Cg-Gpi1<sup>b-m2Neu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8417789	20110309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336209	Trappc10	is_implicated_in	DOID:0060341	agnathia-otocephaly complex		MGI:5561310	Trappc10<sup>b2b2416Clo</sup>/Trappc10<sup>b2b2416Clo</sup>  [background:] Trappc10<sup>b2b2416Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429386	Krt14<sup>tm1Efu</sup>	is_implicated_in	DOID:4644	epidermolysis bullosa simplex		MGI:3812462	Krt14<sup>tm1Efu</sup>/Krt14<sup>tm1Efu</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:7539810	20081029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3581193	Pde6b<sup>rd10</sup>/Pde6b<sup>rd10</sup>  [background:] B6.CXB1-Pde6b<sup>rd10</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17267005	20081103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	is_implicated_in	DOID:0110955	Waardenburg syndrome type 4C		MGI:5897680	Sox10<sup>Dom</sup>/Sox10<sup>+</sup>  [background:] C57BL/6J-Sox10<sup>Dom</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20739296	20170519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:5394	prolactinoma		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_not_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3821583	Hfe<sup>tm1Wsr</sup>/Hfe<sup>tm1Wsr</sup> Tg(Vil1-cre)997Gum/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17264297	20081230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3811188	Hspg2<sup>tm1.1Soni</sup>	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3811208	Hspg2<sup>tm1.1Soni</sup>/Hspg2<sup>tm1.1Soni</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18647752	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653028	Cryaa<sup>Aey7</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2653234	Cryaa<sup>Aey7</sup>/Cryaa<sup>+</sup>  [background:] C3HeB/FeJ-Cryaa<sup>Aey7</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:11687536	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653028	Cryaa<sup>Aey7</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2653233	Cryaa<sup>Aey7</sup>/Cryaa<sup>Aey7</sup>  [background:] C3HeB/FeJ-Cryaa<sup>Aey7</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:11687536	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	is_implicated_in	DOID:3144	cutis laxa		MGI:2681537	Fbln5<sup>tm1Krc</sup>/Fbln5<sup>tm1Krc</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11805835	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	is_implicated_in	DOID:3144	cutis laxa		MGI:2681526	Fbln5<sup>tm1Eno</sup>/Fbln5<sup>tm1Eno</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11805834	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309517	Itm2b	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4936846	Itm2b<sup>tm1.1Ldad</sup>/Itm2b<sup>+</sup>  [background:] B6.129-Itm2b<sup>tm1.1Ldad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21098268	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309517	Itm2b	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4867886	Itm2b<sup>tm3.1Ldad</sup>/Itm2b<sup>tm3.1Ldad</sup>  [background:] B6.129-Itm2b<sup>tm3.1Ldad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21048150	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309517	Itm2b	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4867887	Itm2b<sup>tm1.1Ldad</sup>/Itm2b<sup>tm1.1Ldad</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21048150	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856845	Tmc1<sup>dn</sup>	is_implicated_in	DOID:0110563	autosomal dominant nonsyndromic deafness 36		MGI:2177313	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] involves: STOCK Grhl3<sup>ct</sup> * M. m. molossinus			ECO:0000033	author statement supported by traceable reference	PMID:7719036	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856845	Tmc1<sup>dn</sup>	is_implicated_in	DOID:0110563	autosomal dominant nonsyndromic deafness 36		MGI:2177312	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] STOCK Grhl3<sup>ct</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:48774	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3711151	Plp1<sup>jp-msd</sup>/Y  [background:] involves: BALB/c * C3H * C57BL/6 * C57BL/10			ECO:0000033	author statement supported by traceable reference	PMID:17394578	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3711148	Plp1<sup>jp-rsh</sup>/Y  [background:] involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr			ECO:0000033	author statement supported by traceable reference	PMID:17394578	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3828308	Plp1<sup>tm1Frca</sup>/Y  [background:] B6.129-Plp1<sup>tm1Frca</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18835559	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3838180	Plp1<sup>tm1Kan</sup>/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11872612	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0110153	Charcot-Marie-Tooth disease type 1E		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0111074	progressive familial heart block type IA		MGI:3621905	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11972032	20060817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0111074	progressive familial heart block type IA		MGI:3641169	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:15809371	20060817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149065	Add2<sup>tm1Llp</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:3664740	Add2<sup>tm1Llp</sup>/Add2<sup>tm1Llp</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10485892	20061026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931858	Kcnq1<sup>tm1Apf</sup>	is_not_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:3623773	Kcnq1<sup>tm1Apf</sup>/Kcnq1<sup>tm1Apf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11120752	20060605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	is_implicated_in	DOID:13042	persistent fetal circulation syndrome		MGI:3618597	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] B6.129P2-Nos3<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15016731	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	is_implicated_in	DOID:0050676	Birt-Hogg-Dube syndrome		MGI:3829652	Flcn<sup>tm1Btt</sup>/Flcn<sup>tm1Btt</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18974783	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	is_implicated_in	DOID:0050676	Birt-Hogg-Dube syndrome		MGI:3776087	Flcn<sup>tm1Baba</sup>/Flcn<sup>tm1.1Lss</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: C57BL/6 * FVB/N * ICR * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18182616	20090130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136623	Vegfa<sup>tm2Pec</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3796444	Vegfa<sup>tm2Pec</sup>/Vegfa<sup>tm2Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11381259	20080709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1306784	Cited2	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2667200	Cited2<sup>tm1Ycy</sup>/Cited2<sup>tm1Ycy</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12149478	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10016	multiple endocrine neoplasia type 2B		MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10016	multiple endocrine neoplasia type 2B		MGI:3583335	Ret<sup>tm2.1Cos</sup>/Ret<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:5924963	Alms1<sup>tvrm102</sup>/Alms1<sup>tvrm102</sup>  [background:] C57BL/6J-Alms1<sup>tvrm102</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20180914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:6197905	Alms1<sup>m2Btlr</sup>/Alms1<sup>m2Btlr</sup>  [background:] C57BL/6J-Alms1<sup>m2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:6197902	20180914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:3622093	Alms1<sup>foz</sup>/Alms1<sup>foz</sup>  [background:] involves: NOD			ECO:0000033	author statement supported by traceable reference	PMID:16516152	20180914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:3700128	Alms1<sup>L2131X</sup>/Alms1<sup>L2131X</sup>  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:17206865	20180914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:6197910	Alms1<sup>m3Btlr</sup>/Alms1<sup>m3Btlr</sup>  [background:] C57BL/6J-Alms1<sup>m3Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:6197907	20180914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:3589409	Alms1<sup>Gt(XH152)Byg</sup>/Alms1<sup>Gt(XH152)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16000322	20180914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919682	Spink5	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:3575519	Spink5<sup>tm1Hov</sup>/Spink5<sup>tm1Hov</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15619623	20120525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919682	Spink5	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:5319225	Spink5<sup>m1Btlr</sup>/Spink5<sup>m1Btlr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:5319224	20120525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919682	Spink5	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:5288470	Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>/Spink5<sup>Tn(Pgk2-sb10,sb-Tyr)1498Ove</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15466487	20120525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919682	Spink5	is_implicated_in	DOID:0050474	Netherton syndrome		MGI:3527451	Spink5<sup>tm1Drh</sup>/Spink5<sup>tm1Drh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15590704	20120525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714781	Pkd1<sup>tm1Bdgz</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3776498	Pkd1<sup>tm1Bdgz</sup>/Pkd1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17928412	20110502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	is_implicated_in	DOID:3312	bipolar disorder		MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24342563	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	is_implicated_in	DOID:3312	bipolar disorder		MGI:4356170	Atp1a3<sup>Myk</sup>/Atp1a3<sup>+</sup>  [background:] B6NCr.129S1-Atp1a3<sup>Myk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22025725	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044282	Gamt<sup>tm1Isb</sup>	is_implicated_in	DOID:0050799	guanidinoacetate methyltransferase deficiency		MGI:3044676	Gamt<sup>tm1Isb</sup>/Gamt<sup>tm1Isb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15028668	20090512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818503	Coro1a<sup>ptcd</sup>	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818531	Coro1a<sup>ptcd</sup>/Coro1a<sup>ptcd</sup>  [background:] B6.CTS-Coro1a<sup>ptcd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856662	Acc	is_implicated_in	DOID:83	cataract		MGI:2175693	Acc/Acc<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442934	Minar2	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5756630	Minar2<sup>tm1b(KOMP)Wtsi</sup>/Minar2<sup>tm1b(KOMP)Wtsi</sup>  [background:] C57BL/6N-Minar2<sup>tm1b(KOMP)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:32954300	20210113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3806986	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:17567478	20160113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5702658	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15199412	20160113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3054645	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] C.129S2(B6)-Pdcd1<sup>tm1Hon</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11209085	20170802	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2664102	Cngb1	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3851599	Cngb1<sup>tm1Sjpi</sup>/Cngb1<sup>tm1Sjpi</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19339551	20100720	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2664102	Cngb1	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3528030	Cngb1<sup>tm1.1Biel</sup>/Cngb1<sup>tm1.1Biel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:15634774	20100720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857079	Enpp1<sup>ttw</sup>	is_implicated_in	DOID:0060887	ossification of the posterior longitudinal ligament of spine		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:9359030	20060731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857079	Enpp1<sup>ttw</sup>	is_implicated_in	DOID:0060887	ossification of the posterior longitudinal ligament of spine		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:9662402	20060731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	is_implicated_in	DOID:0110632	megaconial type congenital muscular dystrophy		MGI:3625276	Chkb<sup>rmd</sup>/Chkb<sup>rmd</sup>  [background:] involves: BALB/cByJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16371353	20120130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88547	Csnk2a2	is_implicated_in	DOID:12336	male infertility		MGI:2451166	Csnk2a2<sup>tm1Dcs</sup>/Csnk2a2<sup>tm1Dcs</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10471512	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722325	Megf8<sup>hlb611</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3839106	Megf8<sup>hlb611</sup>/Megf8<sup>hlb611</sup>  [background:] involves: C57BL/6J * C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:18043505	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670461	Gnpat<sup>tm1Just</sup>	is_implicated_in	DOID:150	disease of mental health		MGI:6423170	Gnpat<sup>tm1Just</sup>/Gnpat<sup>tm1Just</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:31412538	20200518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5476166	b2b1929Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5476437	b2b1929Clo/b2b1929Clo  [background:] C57BL/6J-b2b1929Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385657	Tg(Ela1-TAg)18Bri	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:3766076	Tg(Ela1-TAg)18Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1316086	20100816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834913	Ext1<sup>tm1Vcs</sup>	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:4437605	Ext1<sup>tm1Vcs</sup>/Ext1<sup>tm1Vcs</sup> Tg(Col2a1-rtTA,tetO-cre)22Pjro/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20080592	20171214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857131	Ass1<sup>tm1Bay</sup>	is_implicated_in	DOID:9273	citrullinemia		MGI:2653766	Ass1<sup>tm1Bay</sup>/Ass1<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8197477	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177964	Smarcad1<sup>tm1Gos</sup>	is_implicated_in	DOID:0050592	asphyxiating thoracic dystrophy		MGI:2178041	Smarcad1<sup>tm1Gos</sup>/Smarcad1<sup>tm1Gos</sup>  [background:] 129S2/SvPas-Smarcad1<sup>tm1Gos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22912419	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	is_implicated_in	DOID:0080141	mosaic variegated aneuploidy syndrome 1		MGI:6478931	Bub1b<sup>tm1Jvd</sup>/Bub1b<sup>tm3.1Jvd</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31738183	20201210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	is_implicated_in	DOID:0080141	mosaic variegated aneuploidy syndrome 1		MGI:5487831	Bub1b<sup>tm2.1Jvd</sup>/Bub1b<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23300461	20201210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2660913	Lyst<sup>bg-slt</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:2661024	Lyst<sup>bg-slt</sup>/Lyst<sup>bg-slt</sup>  [background:] YZ57/Ch			ECO:0000033	author statement supported by traceable reference	PMID:13943454	20051103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135636	Fgfr3<sup>tm2Wei</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3639744	Fgfr3<sup>tm2Wei</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * MF1			ECO:0000033	author statement supported by traceable reference	PMID:10200283	20060803	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685581	Ccn6	is_implicated_in	DOID:4680	breast metaplastic carcinoma		MGI:6093470	Ccn6<sup>tm1.1Cgkl</sup>/Ccn6<sup>tm1.1Cgkl</sup> Tg(MMTV-cre)1Mam/0  [background:] FVB/N-Ccn6<sup>tm1.1Cgkl</sup> Tg(MMTV-cre)1Mam			ECO:0000033	author statement supported by traceable reference	PMID:27819674	20171130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	is_implicated_in	DOID:5419	schizophrenia		MGI:5444462	Map2k7<sup>tm1Pngr</sup>/Map2k7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22899651	20121205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	is_implicated_in	DOID:14330	Parkinson's disease		MGI:2675764	Drd2<sup>tm1Ebo</sup>/Drd2<sup>tm1Ebo</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7566118	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857897	Cftr<sup>tm1Bay</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177533	Cftr<sup>tm1Bay</sup>/Cftr<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7505691	20050809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:5582068	Scn5a<sup>tm1Clhh</sup>/Scn5a<sup>+</sup>  [background:] involves: 129/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:22287583	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:3769904	Scn5a<sup>tm1Care</sup>/Scn5a<sup>+</sup>  [background:] FVB.129P2-Scn5a<sup>tm1Care</sup>/Care			ECO:0000033	author statement supported by traceable reference	PMID:17145985	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:6415595	Scn5a<sup>tm1.1Iba</sup>/Scn5a<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30144447	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:3622652	Scn5a<sup>tm1Pec</sup>/Scn5a<sup>+</sup>  [background:] involves: Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11533705	20200508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:6356709	Myh6<sup>tm1.1Jpsc</sup>/Myh6<sup>tm2Jse</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:6356705	Myh6<sup>tm2Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:6356707	Myh6<sup>tm3.1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3718111	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] 129S.129X1-Myh6<sup>tm1Jse</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16332958	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3531468	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15001446	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3664295	Myh6<sup>tm2Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:15001446	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3531468	Myh6<sup>tm1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8614836	20190823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:4837384	Myh6<sup>tm3.1Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20811150	20190823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053448	Plscr3<sup>tm1Sims</sup>	is_implicated_in	DOID:9970	obesity		MGI:3053798	Plscr3<sup>tm1Sims</sup>/Plscr3<sup>tm1Sims</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15328404	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386944	Tg(Tnfsf13b)1Fma	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:5300824	Tg(Tnfsf13b)1Fma/Tg(Tnfsf13b)1Fma  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21881212	20120109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14645205	20061031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3663751	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17029828	20061031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524957	Tg(APPswe,PSEN1dE9)85Dbo	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3665286	Tg(APPswe,PSEN1dE9)85Dbo/0  [background:] B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:16899370	20061031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926051	Ak7	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429553	Ak7<sup>Gt(OST434404)Lex</sup>/Ak7<sup>Gt(OST434404)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98813	Tpo	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3698432	Tpo<sup>R479C</sup>/Tpo<sup>R479C</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:16762971	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5316479	Tyr<sup>c-h</sup>/Tyr<sup>c-h</sup>  [background:] B6.Cg-Tyr<sup>c-h</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21968110	20120426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:3581209	Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6(Cg)-Tyr<sup>c-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21968110	20120426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183796	Nbn<sup>tm1Jpt</sup>	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:3615834	Nbn<sup>tm1Jpt</sup>/Nbn<sup>tm1Jpt</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:11967151	20060313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3663104	C4b<sup>tm1Crr</sup>/C4b<sup>tm1Crr</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11067882	20061009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574034	Cecr2<sup>Gt(pGT1)1Hemc</sup>	is_implicated_in	DOID:0060668	anencephaly		MGI:3574274	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574034	Cecr2<sup>Gt(pGT1)1Hemc</sup>	is_implicated_in	DOID:0060668	anencephaly		MGI:3574277	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] C.129P2-Cecr2<sup>Gt(pGT1)1Hemc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574034	Cecr2<sup>Gt(pGT1)1Hemc</sup>	is_implicated_in	DOID:0060668	anencephaly		MGI:3574278	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] 129P2(C)-Cecr2<sup>Gt(pGT1)1Hemc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4455365	Wdfy3<sup>tm1a(KOMP)Mbp</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5825304	Wdfy3<sup>tm1a(KOMP)Mbp</sup>/Wdfy3<sup>tm1a(KOMP)Mbp</sup>  [background:] C57BL/6N-Wdfy3<sup>tm1a(KOMP)Mbp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25198012	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708379	Cdh23<sup>sals</sup>	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12		MGI:3709038	Cdh23<sup>sals</sup>/Cdh23<sup>sals</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19270079	20090504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5430047	b2b1470Clo	is_implicated_in	DOID:674	cleft palate		MGI:5430328	b2b1470Clo/b2b1470Clo  [background:] C57BL/6J-b2b1470Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289258	Cfap43	is_implicated_in	DOID:0070170	spermatogenic failure 19		MGI:6258952	Cfap43<sup>em1Fzh</sup>/Cfap43<sup>em1Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289258	Cfap43	is_implicated_in	DOID:0070170	spermatogenic failure 19		MGI:6258953	Cfap43<sup>em2Fzh</sup>/Cfap43<sup>em2Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857749	En1<sup>tm2Alj</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5604280	En1<sup>tm2Alj</sup>/En1<sup>+</sup> Tg(Th-EGFP)6-7Okn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J * OF1			ECO:0000033	author statement supported by traceable reference	PMID:25281317	20141113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3587028	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11239417	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3587029	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>tm1Bem</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146574	Ildr1	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5695554	Ildr1<sup>Gt(D178D03)Wrst</sup>/Ildr1<sup>Gt(D178D03)Wrst</sup>  [background:] involves: 129S2/SvPas * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:25217574	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146574	Ildr1	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5691406	Ildr1<sup>tm1(KOMP)Wtsi</sup>/Ildr1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25217574	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146574	Ildr1	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5903891	Ildr1<sup>tm1.1Lwa</sup>/Ildr1<sup>tm1.1Lwa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25819842	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146574	Ildr1	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5691406	Ildr1<sup>tm1(KOMP)Wtsi</sup>/Ildr1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25822906	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675469	Traf6<sup>tm1Jino</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:2675470	Traf6<sup>tm1Jino</sup>/Traf6<sup>tm1Jino</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12060722	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	is_implicated_in	DOID:0111809	syndromic microphthalmia 2		MGI:7343893	Bcor<sup>tm1.1Vjba</sup>/Bcor<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/Tmem163<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:32692983	20221006	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343498	Edar	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3717687	Edar<sup>Tg(OVE1B)Ove</sup>/Edar<sup>Tg(OVE1B)Ove</sup>  [background:] involves: C3H * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10431242	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343498	Edar	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3693941	Edar<sup>dl</sup>/Edar<sup>dl</sup>  [background:] involves: A/H			ECO:0000033	author statement supported by traceable reference	PMID:17148670	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343498	Edar	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:4889103	Edar<sup>dl-J</sup>/Edar<sup>dl-J</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9799834	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861942	Gtf2ird1	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5428426	Gtf2ird1<sup>tm1Hrd</sup>/Gtf2ird1<sup>tm1Hrd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22198572	20120720	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861942	Gtf2ird1	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3831537	Gtf2ird1<sup>Gt(XE465)Byg</sup>/Gtf2ird1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19109438	20120720	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5295223	Dlg4<sup>tm2.1Grnt</sup>/Dlg4<sup>tm2.1Grnt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20952458	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612989	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>	is_implicated_in	DOID:0060340	ciliopathy		MGI:6110829	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>/Sclt1<sup>Tg(CAG-sb10)1Dla</sup>  [background:] FVB/N-Sclt1<sup>Tg(CAG-sb10)1Dla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28486600	20180118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95623	Gabrg2	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:6740192	Gabrg2<sup>tm1.2Rmac</sup>/Gabrg2<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:33582225	20210817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721900	Casq2<sup>tm1Jse</sup>	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:3723301	Casq2<sup>tm1Jse</sup>/Casq2<sup>tm1Jse</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17607358	20090821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180364	Cav1<sup>tm1Mls</sup>	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:2669401	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:14690422	20170920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033224	Gck<sup>Rgsc341</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038216	Gck<sup>Rgsc341</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927616	Trps1	is_implicated_in	DOID:14743	trichorhinophalangeal syndrome type I		MGI:3723222	Trps1<sup>tm1.1Shiv</sup>/Trps1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12446778	20071002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95786	gnd	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3616877	gnd/gnd  [background:] C3H/HeJ-gnd			ECO:0000033	author statement supported by traceable reference	PMID:1634998	20060317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178959	Mdk<sup>tm1Tmu</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3579532	Mdk<sup>tm1Tmu</sup>/Mdk<sup>tm1Tmu</sup>  [background:] B6.129S2-Mdk<sup>tm1Tmu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19217924	20090818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387407	Htr1a<sup>tm1Rhn</sup>	is_implicated_in	DOID:2030	anxiety disorder		MGI:4881537	Htr1a<sup>tm1Rhn</sup>/Htr1a<sup>tm1Rhn</sup>  [background:] involves: 129S/SvEv * 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:20152131	20110201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387407	Htr1a<sup>tm1Rhn</sup>	is_implicated_in	DOID:2030	anxiety disorder		MGI:3045711	Htr1a<sup>tm1Rhn</sup>/Htr1a<sup>tm1Rhn</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:9826725	20110201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:5762537	Des<sup>tm1.1Ccrs</sup>/Des<sup>tm1.1Ccrs</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25394388	20170823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:5762541	Des<sup>tm1.1Ccrs</sup>/Des<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25394388	20170823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:2178322	Des<sup>tm1Cap</sup>/Des<sup>tm1Cap</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8794866	20170823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587739	Nhs<sup>Xcat</sup>/Nhs<sup>+</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587737	Nhs<sup>Xcat</sup>/Y  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587738	Nhs<sup>Xcat</sup>/Nhs<sup>Xcat</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587738	Nhs<sup>Xcat</sup>/Nhs<sup>Xcat</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587739	Nhs<sup>Xcat</sup>/Nhs<sup>+</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587737	Nhs<sup>Xcat</sup>/Y  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	is_implicated_in	DOID:10609	rickets		MGI:3779048	Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15976027	20080428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	is_implicated_in	DOID:10609	rickets		MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:10746634	20080428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	is_implicated_in	DOID:10609	rickets		MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:9241280	20080428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	is_implicated_in	DOID:10609	rickets		MGI:3588584	Vdr<sup>tm1Mbd</sup>/Vdr<sup>tm1Mbd</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9275211	20080428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412046	Nfkb2<sup>Lym1</sup>	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:4412047	Nfkb2<sup>Lym1</sup>/Nfkb2<sup>+</sup>  [background:] BALB/c-Nfkb2<sup>Lym1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412046	Nfkb2<sup>Lym1</sup>	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:4412050	Nfkb2<sup>Lym1</sup>/Nfkb2<sup>Lym1</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:24140114	20140327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652058	Ldb3<sup>tm1Chen</sup>	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:2652059	Ldb3<sup>tm1Chen</sup>/Ldb3<sup>tm1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11696561	20060404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102570	Ndp	is_implicated_in	DOID:0060844	Norrie disease		MGI:3695277	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12040033	20070201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102570	Ndp	is_implicated_in	DOID:0060844	Norrie disease		MGI:2676253	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8789439	20070201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3790955	Stk11<sup>tm1Tpm</sup>/Stk11<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15480979	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814533	Stk11<sup>tm1.2Rdp</sup>/Stk11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12226664	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3616342	Stk11<sup>tm1.1Mlfr</sup>/Stk11<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16357136	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3790954	Stk11<sup>tm1Tpm</sup>/Stk11<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12218179	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814590	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18227155	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814722	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(KRT14-cre)1Ipc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18172296	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814533	Stk11<sup>tm1.2Rdp</sup>/Stk11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18172296	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:5440238	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Stk11<sup>tm1Rdp</sup>/Stk11<sup>tm1Rdp</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22791749	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:2676549	Stk11<sup>tm1.1Jish</sup>/Stk11<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12060709	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	is_implicated_in	DOID:5419	schizophrenia		MGI:5752786	Disc1<sup>m1H</sup>/Disc1<sup>m1H</sup>  [background:] B6N.C(C3H)-Disc1<sup>m1H</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26728762	20160322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	is_implicated_in	DOID:5419	schizophrenia		MGI:5660929	Disc1<sup>tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho</sup>/Disc1<sup>del</sup>  [background:] 129S2/SvPasCrl-Disc1<sup>del</sup> Disc1<sup>tm1(DISC1/DISC1FP1,DISC1FP1/DISC1,DISC1)Xzho</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24908665	20160322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	is_implicated_in	DOID:5419	schizophrenia		MGI:3707975	Disc1<sup>Rgsc1390</sup>/Disc1<sup>Rgsc1390</sup>  [background:] B6.Cg-Disc1<sup>Rgsc1390</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17481393	20160322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	is_implicated_in	DOID:5419	schizophrenia		MGI:3623286	Disc1<sup>tm1Kara</sup>/Disc1<sup>+</sup>  [background:] B6.129S6-Disc1<sup>tm1Kara</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16484369	20160322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	is_implicated_in	DOID:5419	schizophrenia		MGI:3623253	Disc1<sup>tm1Kara</sup>/Disc1<sup>tm1Kara</sup>  [background:] B6.129S6-Disc1<sup>tm1Kara</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16484369	20160322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438890	Tg(Thy1-APPDutch)#Jckr	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4819110	Tg(Thy1-APPDutch)#Jckr/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17596707	20100818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438890	Tg(Thy1-APPDutch)#Jckr	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4819110	Tg(Thy1-APPDutch)#Jckr/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15311281	20100818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183207	Smpd1<sup>tm1Wst</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3029165	Smpd1<sup>tm1Wst</sup>/Smpd1<sup>tm1Wst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7600574	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:13580	cholestasis		MGI:5526018	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] C.129P2-Abcb4<sup>tm1Bor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23545228	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96398	Id3	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5000526	Id3<sup>tm1Zhu</sup>/Id3<sup>tm1Zhu</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:15485632	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96398	Id3	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5009805	Id3<sup>tm2.1Zhu</sup>/Id3<sup>tm2.1Zhu</sup> Tg(Lck-cre)#Zhu/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:20932862	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159007	Gja1<sup>tm1Dlg</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:4420313	Gja1<sup>tm1Dlg</sup>/Gja1<sup>tm1Dlg</sup> Tg(GFAP-cre)1Kdmc/0  [background:] involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17311295	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	is_implicated_in	DOID:0111533	gnathodiaphyseal dysplasia		MGI:6489966	Ano5<sup>em1Huyi</sup>/Ano5<sup>em1Huyi</sup>  [background:] C57BL/6N-Ano5<sup>em1Huyi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30712070	20230622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	is_implicated_in	DOID:0111533	gnathodiaphyseal dysplasia		MGI:7492024	Ano5<sup>em2Huyi</sup>/Ano5<sup>em2Huyi</sup>  [background:] C57BL/6-Ano5<sup>em2Huyi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34841576	20230622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443258	Map3k20	is_implicated_in	DOID:0090020	split hand-foot malformation		MGI:5903753	Map3k20<sup>em2Smun</sup>/Map3k20<sup>em2Smun</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:26755636	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2664130	Pafah1b1<sup>tm2.2Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2664093	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>tm2Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2664549	Pafah1b1<sup>tm1Or</sup>/Pafah1b1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11344260	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10541472	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178612	Ubr1<sup>tm1Avar</sup>	is_implicated_in	DOID:14694	Johanson-Blizzard syndrome		MGI:3654648	Ubr1<sup>tm1Avar</sup>/Ubr1<sup>tm1Avar</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16311597	20100309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178542	Comt<sup>tm1Kara</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3697681	Comt<sup>tm1Kara</sup>/Comt<sup>tm1Kara</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:18469803	20111003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675708	Neu1<sup>tm1Adz</sup>	is_implicated_in	DOID:3343	glycoproteinosis		MGI:3719098	Neu1<sup>tm1Adz</sup>/Neu1<sup>tm1Adz</sup>  [background:] either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * NMRI)			ECO:0000033	author statement supported by traceable reference	PMID:12023988	20070824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614578	Agrn<sup>nmf380</sup>	is_implicated_in	DOID:0110657	congenital myasthenic syndrome 8		MGI:3614637	Agrn<sup>nmf380</sup>/Agrn<sup>nmf380</sup>  [background:] C57BL/6J-Agrn<sup>nmf380</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21890498	20150511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096381	Bmal1	is_implicated_in	DOID:9351	diabetes mellitus		MGI:5576883	Bmal1<sup>tm2Bra</sup>/Bmal1<sup>tm2Bra</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * CBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:20562852	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181017	Clcn5<sup>tm1Gug</sup>	is_implicated_in	DOID:0050699	Dent disease		MGI:3510236	Clcn5<sup>tm1Gug</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11115837	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia		MGI:2178957	Hspg2<sup>tm1Ref</sup>/Hspg2<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12814946	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia		MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11802174	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138346	Suco	is_implicated_in	DOID:0110344	osteogenesis imperfecta type 5		MGI:4818953	Suco<sup>Gt(KST050)Byg</sup>/Suco<sup>Gt(KST050)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:20440000	20100811	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:5578216	Scn8a<sup>em1Mm</sup>/Scn8a<sup>+</sup>  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24288358	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857673	Pax2<sup>tm1Pgr</sup>	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:3694692	Pax2<sup>tm1Pgr</sup>/Pax2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8951055	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857673	Pax2<sup>tm1Pgr</sup>	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:2677317	Pax2<sup>tm1Pgr</sup>/Pax2<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8951055	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857673	Pax2<sup>tm1Pgr</sup>	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:3694699	Pax2<sup>tm1Pgr</sup>/Pax2<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15242798	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	is_implicated_in	DOID:0110495	autosomal recessive nonsyndromic deafness 37		MGI:3528185	Myo6<sup>sv</sup>/Myo6<sup>sv</sup>  [background:] involves: B10.HA/(33NX)Sn * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7493015	20060201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665235	Frem1<sup>tm1Ksek</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665237	Frem1<sup>tm1Ksek</sup>/Frem1<sup>tm1Ksek</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:5532923	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6.129S1-Tor1a<sup>tm2Wtd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24121114	20160412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:5532923	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6.129S1-Tor1a<sup>tm2Wtd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21464304	20160412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:5759931	Tor1a<sup>tm1Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6;129-Tor1a<sup>tm1Wtd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26183317	20160412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:3624527	Tor1a<sup>tm2Wtd</sup>/Tor1a<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:23748075	20160412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101925	Krt13	is_implicated_in	DOID:0050448	white sponge nevus		MGI:6509651	Krt13<sup>em1Hcha</sup>/Krt13<sup>em1Hcha</sup>  [background:] C57BL/6-Krt13<sup>em1Hcha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32758484	20210311	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105386	Dbt	is_implicated_in	DOID:9269	maple syrup urine disease		MGI:3704912	Dbt<sup>tm1Geh</sup>/Dbt<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16579849	20070426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5318772	Slc6a3<sup>tm1Hhg</sup>/Slc6a3<sup>tm1Hhg</sup>  [background:] B6.129X1-Slc6a3<sup>tm1Hhg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22034972	20150709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:2654500	Slc6a3<sup>tm1Mca</sup>/Slc6a3<sup>tm1Mca</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9888856	20150709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:2654522	Slc6a3<sup>tm2Mca</sup>/Slc6a3<sup>tm2Mca</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11172062	20150709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5643944	Slc6a3<sup>tm1Rbl</sup>/Slc6a3<sup>tm1Rbl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25331903	20150709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1337120	Slc7a7	is_implicated_in	DOID:0060439	lysinuric protein intolerance		MGI:7380585	Slc7a7<sup>em1Lbu</sup>/Slc7a7<sup>em1Lbu</sup>  [background:] involves: 129/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32504080	20221109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1925255	Rrn3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6113543	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-icre)9190Gsc/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21228155	20180131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1925255	Rrn3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6113542	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-cre/ERT2)1Span/0  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21228155	20180131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1925255	Rrn3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6113542	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-cre/ERT2)1Span/0  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28360124	20180131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104627	Dst	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:5577168	Dst<sup>Tg4</sup>/Dst<sup>Tg4</sup>  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24381311	20140814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311334	b2b227Clo	is_implicated_in	DOID:114	heart disease		MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651471	Idua<sup>tm1Efn</sup>	is_implicated_in	DOID:10754	otitis media		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17101178	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613036	Txnip<sup>tm1Jjy</sup>	is_implicated_in	DOID:14525	Reye syndrome		MGI:3613200	Txnip<sup>tm1Jjy</sup>/Txnip<sup>tm1Jjy</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16254043	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:2175836	Dysf<sup>im</sup>/Dysf<sup>im</sup>  [background:] involves: SJL			ECO:0000033	author statement supported by traceable reference	PMID:10508505	20210415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:3055578	Dysf<sup>tm1Meho</sup>/Dysf<sup>tm1Meho</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20210415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:3055667	Dysf<sup>prmd</sup>/Dysf<sup>prmd</sup>  [background:] A/J			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20210415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:6690813	Dysf<sup>tm1.1Mdcb</sup>/Dysf<sup>tm1.1Mdcb</sup>  [background:] B6.129P2(Cg)-Dysf<sup>tm1.1Mdcb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30292141	20210415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:2661118	Dysf<sup>tm1Kcam</sup>/Dysf<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12736685	20210415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:9970	obesity		MGI:5447549	Lep<sup>m1Btlr</sup>/Lep<sup>m1Btlr</sup>  [background:] C57BL/6J-Lep<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5447547	20130104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:9970	obesity		MGI:3623749	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12885755	20130104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:9970	obesity		MGI:3623749	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16394172	20130104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:9970	obesity		MGI:3655835	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] D2.Cg-Lep<sup>ob</sup>/Chua			ECO:0000033	author statement supported by traceable reference	PMID:12136396	20130104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693645	Parl<sup>tm1.1Bdes</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:6280686	Parl<sup>tm1.1Bdes</sup>/Parl<sup>tm1.1Bdes</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:30578322	20190228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102764	Six3	is_implicated_in	DOID:0110872	holoprosencephaly 2		MGI:3036833	Six3<sup>tm1Gco</sup>/Six3<sup>tm1Gco</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12569128	20081113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102764	Six3	is_implicated_in	DOID:0110872	holoprosencephaly 2		MGI:3814903	Six3<sup>tm3Gco</sup>/Six3<sup>tm3Gco</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102764	Six3	is_implicated_in	DOID:0110872	holoprosencephaly 2		MGI:3814906	Six3<sup>tm4(cre/ERT2)Gco</sup>/Six3<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837569	Tg(CSNK1D*,-EGFP)816Yfu	is_implicated_in	DOID:0110012	advanced sleep phase syndrome 2		MGI:3837653	Tg(CSNK1D*,-EGFP)816Yfu/?  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15800623	20130513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195272	Eda	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:4459458	Eda<sup>Ta</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:27590203	20170104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195272	Eda	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3711694	Eda<sup>Ta</sup>/Y  [background:] involves: A * C57BL * CBA * RIII			ECO:0000033	author statement supported by traceable reference	PMID:2348861	20170104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195272	Eda	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3707523	Eda<sup>Ta-6J</sup>/Y  [background:] C57BL/6J A<sup>w-J</sup>-Eda<sup>Ta-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14506134	20170104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856276	Gli3<sup>Xt-J</sup>	is_implicated_in	DOID:14761	Greig cephalopolysyndactyly syndrome		MGI:2166944	Gli3<sup>Xt-J</sup>/Gli3<sup>Xt-J</sup>  [background:] involves: C3H * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8387379	20060322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858416	Stk39	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:6423629	Stk39<sup>tm1Pawe</sup>/Stk39<sup>tm1Pawe</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28442491	20200521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858416	Stk39	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:5804131	Stk39<sup>tm2.1Arte</sup>/Stk39<sup>tm2.1Arte</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25994507	20200521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858416	Stk39	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:4838433	Stk39<sup>tm1.2Slin</sup>/Stk39<sup>tm1.2Slin</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20813865	20200521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443778	Cfap69	is_implicated_in	DOID:0111929	spermatogenic failure 24		MGI:6431858	Cfap69<sup>em1Fzh</sup>/Cfap69<sup>em1Fzh</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30415212	20220209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443778	Cfap69	is_implicated_in	DOID:0111929	spermatogenic failure 24		MGI:6865772	Cfap69<sup>tm1b(KOMP)Wtsi</sup>/Cfap69<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29606301	20220209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932376	Cacng8	is_implicated_in	DOID:10939	antisocial personality disorder		MGI:7256634	Cacng8<sup>tm1Ran</sup>/Cacng8<sup>tm1Ran</sup>  [background:] C57BL/6-Cacng8<sup>tm1Ran</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34099816	20220324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932376	Cacng8	is_implicated_in	DOID:10939	antisocial personality disorder		MGI:7256635	Cacng8<sup>tm1Ran</sup>/Cacng8<sup>+</sup>  [background:] C57BL/6-Cacng8<sup>tm1Ran</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34099816	20220324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915751	Nsmce2	is_implicated_in	DOID:2717	Bloom syndrome		MGI:5906758	Nsmce2<sup>tm2.1Ofc</sup>/Nsmce2<sup>tm2.1Ofc</sup> Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/0  [background:] involves: 129S/SvEv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26443207	20170811	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335087	Fem1b	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3590085	Fem1b<sup>tm1Jfma</sup>/Fem1b<sup>tm1Jfma</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16024793	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	is_implicated_in	DOID:0111035	CADASIL 1		MGI:5462095	Notch3<sup>tm1.1Dwr</sup>/Notch3<sup>tm1.1Dwr</sup>  [background:] involves: 129S/SvEv * Swiss			ECO:0000033	author statement supported by traceable reference	PMID:21940951	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	is_implicated_in	DOID:0111035	CADASIL 1		MGI:5462096	Notch3<sup>tm1.1Dwr</sup>/Notch3<sup>+</sup>  [background:] involves: 129S/SvEv * Swiss			ECO:0000033	author statement supported by traceable reference	PMID:21940951	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	is_implicated_in	DOID:0111035	CADASIL 1		MGI:4430347	Notch3<sup>hpbk</sup>/Notch3<sup>hpbk</sup>  [background:] C57BL/6J-Notch3<sup>hpbk</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	is_not_implicated_in	DOID:0110532	autosomal recessive nonsyndromic deafness 86		MGI:6490523	Tbc1d24<sup>em3Tbf</sup>/Tbc1d24<sup>em3Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em3Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32987832	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3616876	Aqp2<sup>F204V</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3616879	Aqp2<sup>F204V</sup>/Aqp2<sup>F204V</sup>  [background:] C57BL/6-Aqp2<sup>F204V</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16121255	20060317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:4838317	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk/0  [background:] 129S1.Cg-Pten<sup>tm2.1Ppp</sup> Tg(TPO-cre)1Shk			ECO:0000033	author statement supported by traceable reference	PMID:20676139	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:5517709	Pten<sup>tm1Hwu</sup>/Pten<sup>+</sup> Tg(Nkx2-1-cre)2Sand/0  [background:] B6.Cg-Pten<sup>tm1Hwu</sup> Tg(Nkx2-1-cre)2Sand			ECO:0000033	author statement supported by traceable reference	PMID:22167068	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:4443207	Ryr2<sup>tm1.1Maya</sup>/Ryr2<sup>+</sup>  [background:] C57BL/6J-Ryr2<sup>tm1.1Maya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20224043	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5582593	Ryr2<sup>tm3.1Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22828895	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5582594	Ryr2<sup>tm4.1Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22828895	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5582595	Ryr2<sup>tm2Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:22828895	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:6278119	Ryr2<sup>tm1Slh</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27482086	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5583981	Ryr2<sup>tm2Hhv</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23152493	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:3653876	Ryr2<sup>tm1Sgp</sup>/Ryr2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15890976	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:3689179	Ryr2<sup>tm1Slh</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16873551	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:6104247	Ryr2<sup>tm3.1Hhv</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25775566	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5432115	Ryr2<sup>tm1.1Clhh</sup>/Ryr2<sup>tm1.1Clhh</sup>  [background:] 129S/SvEv-Ryr2<sup>tm1.1Clhh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18419777	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	is_implicated_in	DOID:8354	complement component 3 deficiency		MGI:2449062	C3<sup>tm1Pkna</sup>/C3<sup>tm1Pkna</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9467654	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	is_implicated_in	DOID:8354	complement component 3 deficiency		MGI:2449063	C3<sup>tm1Hrc</sup>/C3<sup>tm1Hrc</sup>  [background:] either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10408374	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	is_implicated_in	DOID:8354	complement component 3 deficiency		MGI:2429606	C3<sup>tm1Crr</sup>/C3<sup>tm1Crr</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8524789	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355323	Slc7a8	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:6323255	Slc7a8<sup>tm1Geno</sup>/Slc7a8<sup>tm1Geno</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29355479	20190716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446518	Slc6a3<sup>tm2Mca</sup>	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:2654522	Slc6a3<sup>tm2Mca</sup>/Slc6a3<sup>tm2Mca</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15710042	20111021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775521	Flnb<sup>Gt(RRF239)Byg</sup>	is_implicated_in	DOID:0090116	spondylocarpotarsal synostosis syndrome		MGI:3775522	Flnb<sup>Gt(RRF239)Byg</sup>/Flnb<sup>Gt(RRF239)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17635842	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	is_implicated_in	DOID:0112014	congenital megabladder		MGI:6450809	Myocd<sup>em1Blk</sup>/Myocd<sup>tm1.1Msp</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:31513549	20211027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157968	Tcf4<sup>tm1Hmb</sup>/Tcf4<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157970	Tcf4<sup>em2Bdph</sup>/?  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157969	Tcf4<sup>em1Bdph</sup>/?  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6157967	Tcf4<sup>tm1Hmb</sup>/Tcf4<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/Tmem163<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29222403	20201217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6479897	Tcf4<sup>tm1a(EUCOMM)Wtsi</sup>/Tcf4<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29588831	20201217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6479882	Tcf4<sup>tm1Zhu</sup>/Tcf4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27568567	20201217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4432284	B9d1<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5301335	B9d1<sup>tm1a(EUCOMM)Wtsi</sup>/B9d1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21763481	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99613	Zap70	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3698734	Zap70<sup>m1Saka</sup>/Zap70<sup>m1Saka</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:14647385	20070305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	is_implicated_in	DOID:0070068	autosomal dominant intellectual developmental disorder 38		MGI:7277684	Eef1a2<sup>em#Abb</sup>/Eef1a2<sup>+</sup>  [background:] C57BL/6JCrl-Eef1a2<sup>em#Abb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32160274	20220513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050835	generalized dystonia		MGI:5792057	Cacna1a<sup>tg</sup>/Cacna1a<sup>tm2.1Maag</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * DBA/2J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22850483	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050835	generalized dystonia		MGI:3700786	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] B6.D2-Cacna1a<sup>tg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22850483	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499734	Myh9<sup>tm1.1(MYH9*)Mjk</sup>/Myh9<sup>+</sup>  [background:] B6.Cg-Myh9<sup>tm1.1(MYH9*)Mjk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499740	Myh9<sup>tm7.1Rsad</sup>/Myh9<sup>tm7.1Rsad</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499738	Myh9<sup>tm7.1Rsad</sup>/Myh9<sup>+</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	is_implicated_in	DOID:0060651	MYH-9 related disease		MGI:5499736	Myh9<sup>tm1.1(MYH9*)Mjk</sup>/Myh9<sup>tm1.1(MYH9*)Mjk</sup>  [background:] B6.129-Myh9<sup>tm1.1(MYH9*)Mjk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21908426	20130806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916052	Mypn	is_implicated_in	DOID:0110933	nemaline myopathy 11		MGI:6283403	Mypn<sup>tm1.1Epu</sup>/Mypn<sup>tm1.1Epu</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:28017374	20190318	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921173	Tmco1	is_implicated_in	DOID:0081072	craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome		MGI:5823987	Tmco1<sup>em1Smoc</sup>/Tmco1<sup>em1Smoc</sup>  [background:] C57BL/6J-Tmco1<sup>em1Smoc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27212239	20220616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:2176972	Nr3c1<sup>tm2Gsc</sup>/Nr3c1<sup>tm2Gsc</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10471508	20171210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	is_implicated_in	DOID:0060692	platelet-type bleeding disorder 8		MGI:3723060	P2ry12<sup>tm1Cjf</sup>/P2ry12<sup>tm1Cjf</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:11413167	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	is_implicated_in	DOID:0060692	platelet-type bleeding disorder 8		MGI:2674087	P2ry12<sup>tm1Pcon</sup>/P2ry12<sup>tm1Pcon</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12897207	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94891	Dhh	is_implicated_in	DOID:14448	46,XY sex reversal		MGI:2659090	Dhh<sup>tm1Amc</sup>/Dhh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * C57BL/6J * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11090455	20050923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143994	Psme4	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437116	Psme4<sup>b2b1508Clo</sup>/Psme4<sup>b2b1508Clo</sup>  [background:] C57BL/6J-Psme4<sup>b2b1508Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640478	Tg(ACTA1-MYOT*T57I)71Mah	is_implicated_in	DOID:0080094	myofibrillar myopathy 3		MGI:3789953	Tg(ACTA1-MYOT*T57I)71Mah/?  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16801328	20080602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97887	Rdx	is_implicated_in	DOID:12308	Dubin-Johnson syndrome		MGI:2671154	Rdx<sup>tm1Sts</sup>/Rdx<sup>tm1Sts</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12068294	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445477	Tg(GFAP-SRC)2Aag	is_implicated_in	DOID:3069	malignant astrocytoma		MGI:5569737	Tg(GFAP-SRC)2Aag/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9160879	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772576	Gt(ROSA)26Sor<sup>tm1(HBEGF)Awai</sup>	is_implicated_in	DOID:0060870	isolated growth hormone deficiency		MGI:4943177	Gt(ROSA)26Sor<sup>tm1(HBEGF)Awai</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Gh1-cre)bKnmn/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21283519	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:5558028	Scn11a<sup>tm1.1Ikth</sup>/Scn11a<sup>+</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24036948	20140410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:5544056	Nf1<sup>tm1Par</sup>/Nf1<sup>tm1Par</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14982883	20140213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276534	Bcat2	is_implicated_in	DOID:9269	maple syrup urine disease		MGI:3028730	Bcat2<sup>m1Ytc</sup>/Bcat2<sup>m1Ytc</sup>  [background:] C57BL/6J-Bcat2<sup>m1Ytc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14755340	20050603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:10283	prostate cancer		MGI:3836579	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19117991	20090320	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98907	Uox	is_implicated_in	DOID:1920	hyperuricemia		MGI:3687865	Uox<sup>tm1Bay</sup>/Uox<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8290593	20210212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98907	Uox	is_implicated_in	DOID:1920	hyperuricemia		MGI:6506273	Uox<sup>em1Cli</sup>/Uox<sup>em1Cli</sup>  [background:] C57BL/6J-Uox<sup>em1Cli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28729031	20210212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4432303	Tcf4<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060488	Pitt-Hopkins syndrome		MGI:6479897	Tcf4<sup>tm1a(EUCOMM)Wtsi</sup>/Tcf4<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29588831	20201217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96448	Ighm	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623425	Ighm<sup>tm1Cgn</sup>/Ighm<sup>tm1Cgn</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8920894	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96448	Ighm	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3793300	Ighm<sup>tm1Cgn</sup>/Ighm<sup>tm1Cgn</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>/DvsJ			ECO:0000033	author statement supported by traceable reference	PMID:12516557	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178798	Vps54	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:3614946	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] multiple strains			ECO:0000033	author statement supported by traceable reference	PMID:7416238	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856595	Pstpip2<sup>cmo</sup>	is_implicated_in	DOID:0060645	chronic recurrent multifocal osteomyelitis		MGI:3614947	Pstpip2<sup>cmo</sup>/Pstpip2<sup>cmo</sup>  [background:] C.Cg-Pstpip2<sup>cmo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16122996	20230119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856595	Pstpip2<sup>cmo</sup>	is_implicated_in	DOID:0060645	chronic recurrent multifocal osteomyelitis		MGI:3614947	Pstpip2<sup>cmo</sup>/Pstpip2<sup>cmo</sup>  [background:] C.Cg-Pstpip2<sup>cmo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10678414	20230119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182616	Zfpm2<sup>tm1Jml</sup>	is_implicated_in	DOID:0080169	tricuspid atresia		MGI:3620558	Zfpm2<sup>tm1Jml</sup>/Zfpm2<sup>tm1Jml</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10888889	20060427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4399318	Adck2<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:699	mitochondrial myopathy		MGI:6377285	Adck2<sup>tm1(KOMP)Vlcg</sup>/Adck2<sup>+</sup>  [background:] C57BL/6-Adck2<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31480808	20191118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107735	Myo9a	is_implicated_in	DOID:14159	obstructive hydrocephalus		MGI:6120521	Myo9a<sup>tm1.2Bah</sup>/Myo9a<sup>tm1.2Bah</sup>  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19828736	20180309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179440	Sox17<sup>tm1Ysk</sup>	is_implicated_in	DOID:13608	biliary atresia		MGI:6113926	Sox17<sup>tm1Ysk</sup>/Sox17<sup>+</sup>  [background:] B6.129S1-Sox17<sup>tm1Ysk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28432216	20180202	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179440	Sox17<sup>tm1Ysk</sup>	is_implicated_in	DOID:13608	biliary atresia		MGI:6113926	Sox17<sup>tm1Ysk</sup>/Sox17<sup>+</sup>  [background:] B6.129S1-Sox17<sup>tm1Ysk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23293295	20180202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_not_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:2176527	Ptpn11<sup>tm1Rbn</sup>/Ptpn11<sup>tm1Rbn</sup>  [background:] involves: 129 * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8702915	20051017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_not_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:2176529	Ptpn11<sup>tm1Rbn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129 * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8702915	20051017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_not_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:2176525	Ptpn11<sup>tm1Paw</sup>/Ptpn11<sup>tm1Paw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9171349	20051017	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343460	Gnpat	is_implicated_in	DOID:150	disease of mental health		MGI:6423170	Gnpat<sup>tm1Just</sup>/Gnpat<sup>tm1Just</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:31412538	20200518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149438	Pik3r1<sup>tm1Dfr</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2174983	Pik3r1<sup>tm1Dfr</sup>/Pik3r1<sup>tm1Dfr</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11062485	20081222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149438	Pik3r1<sup>tm1Dfr</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2174983	Pik3r1<sup>tm1Dfr</sup>/Pik3r1<sup>tm1Dfr</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9888855	20081222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336205	Fkbp1b	is_implicated_in	DOID:0060674	catecholaminergic polymorphic ventricular tachycardia		MGI:3623679	Fkbp1b<sup>tm1Amks</sup>/Fkbp1b<sup>tm1Amks</sup>  [background:] DBA/1LacJ-Fkbp1b<sup>tm1Amks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12837242	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386677	Abcc8<sup>tm1Jbry</sup>	is_implicated_in	DOID:0060334	transient neonatal diabetes mellitus		MGI:2446456	Abcc8<sup>tm1Jbry</sup>/Abcc8<sup>tm1Jbry</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10734066	20130415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6034501	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12124769	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14098314	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5538400	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2175787	Hps3<sup>coa-6J</sup>/Hps3<sup>coa-6J</sup>  [background:] C3H/HeJ-Hps3<sup>coa-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:1861465	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:3408670	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:5767124	Gbe1<sup>tm2.1Hoa</sup>/Gbe1<sup>tm2.1Hoa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:26385640	20160511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:4868493	Gbe1<sup>m1Yty</sup>/Gbe1<sup>m1Yty</sup>  [background:] C3HeB/FeJ-Gbe1<sup>m1Yty</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21075835	20160511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:5293613	Gbe1<sup>tm1Hoa</sup>/Gbe1<sup>tm1Hoa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:21856731	20160511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	is_implicated_in	DOID:2750	glycogen storage disease IV		MGI:5293614	Gbe1<sup>tm1.1Hoa</sup>/Gbe1<sup>tm1.1Hoa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:21856731	20160511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2145264	Nhlrc1	is_implicated_in	DOID:3534	Lafora disease		MGI:4839642	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>/Nhlrc1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:20538597	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2145264	Nhlrc1	is_implicated_in	DOID:3534	Lafora disease		MGI:5312936	Nhlrc1<sup>tm1.2Geno</sup>/Nhlrc1<sup>tm1.2Geno</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22186026	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2145264	Nhlrc1	is_implicated_in	DOID:3534	Lafora disease		MGI:5313256	Nhlrc1<sup>tm1Bmin</sup>/Nhlrc1<sup>tm1Bmin</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:21077101	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2145264	Nhlrc1	is_implicated_in	DOID:3534	Lafora disease		MGI:4839642	Nhlrc1<sup>tm1(KOMP)Vlcg</sup>/Nhlrc1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:21882344	20190214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5441254	Col2a1<sup>Lpk</sup>/Col2a1<sup>+</sup>  [background:] C.B6(C3)-Col2a1<sup>Lpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22028304	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5441253	Col2a1<sup>Lpk</sup>/Col2a1<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22028304	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:2676332	Col2a1<sup>sedc</sup>/Col2a1<sup>sedc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12968670	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5553144	Col2a1<sup>M3J</sup>/Col2a1<sup>+</sup>  [background:] B6(Cg)-Col2a1<sup>M3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:5292535	Col2a1<sup>M2J</sup>/Col2a1<sup>+</sup>  [background:] B6;C3Fe-Col2a1<sup>M2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:2677039	Col2a1<sup>tm1Prc</sup>/Col2a1<sup>tm1Prc</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7590256	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	is_implicated_in	DOID:0060021	DNA ligase IV deficiency		MGI:4437271	Lig4<sup>tm2.1Fwa</sup>/Lig4<sup>tm2.1Fwa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:20133615	20100315	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	is_implicated_in	DOID:0060021	DNA ligase IV deficiency		MGI:3714853	Lig4<sup>tiny</sup>/Lig4<sup>tiny</sup>  [background:] C57BL/6-Lig4<sup>tiny</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17554302	20100315	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397678	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397677	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] FVB.129-Kcnq3<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397674	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397673	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397675	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] B6.129-Kcnq3<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429408	Pitx3<sup>eyl</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:4429423	Pitx3<sup>eyl</sup>/Pitx3<sup>eyl</sup>  [background:] involves: C3H/He * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20033184	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443664	Rreb1	is_implicated_in	DOID:0080690	RASopathy		MGI:7339281	Rreb1<sup>em1Rtpl</sup>/Rreb1<sup>+</sup>  [background:] C57BL/6J-Rreb1<sup>em1Rtpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32938917	20220926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913283	Dnase2b	is_implicated_in	DOID:83	cataract		MGI:2675506	Dnase2b<sup>tm1Osa</sup>/Dnase2b<sup>tm1Osa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12944971	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447813	Serac1	is_implicated_in	DOID:0110001	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome		MGI:7316678	Serac1<sup>em1Bcgen</sup>/Serac1<sup>em1Bcgen</sup>  [background:] C57BL/6N-Serac1<sup>em1Bcgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35235340	20220728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:4868120	Dicer1<sup>tm1Bdh</sup>/Dicer1<sup>tm1Bdh</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:21098571	20110117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183790	Timp3<sup>tm1Web</sup>	is_implicated_in	DOID:0090114	Sorsby's fundus dystrophy		MGI:3664350	Timp3<sup>tm1Web</sup>/Timp3<sup>tm1Web</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12147610	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183790	Timp3<sup>tm1Web</sup>	is_implicated_in	DOID:0090114	Sorsby's fundus dystrophy		MGI:3664346	Timp3<sup>tm1Web</sup>/Timp3<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12147610	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856018	Edar<sup>dl-J</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:4889103	Edar<sup>dl-J</sup>/Edar<sup>dl-J</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9799834	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	is_implicated_in	DOID:0060897	Parkinson's disease 17		MGI:7466182	Vps35<sup>tm1.1Hlw</sup>/Vps35<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33257649	20230425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	is_implicated_in	DOID:0060897	Parkinson's disease 17		MGI:5695247	Vps35<sup>Gt(RRK261)Byg</sup>/Vps35<sup>+</sup>  [background:] B6.129P2-Vps35<sup>Gt(RRK261)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26203154	20230425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573697	Tg(Ins2-NP)25-3Olds	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3618925	Tg(Ins2-NP)25-3Olds/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1901765	20060411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456699	Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0110722	neuronal ceroid lipofuscinosis 7		MGI:5604251	Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>/Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24423645	20141112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442071	Gprasp2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6287871	Gprasp2<sup>tm1.1Jpe</sup>/Y  [background:] B6.129(FVB)-Gprasp2<sup>tm1.1Jpe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30926797	20190418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914421	Dram2	is_implicated_in	DOID:0050572	cone-rod dystrophy		MGI:7564407	Dram2<sup>em1Jean</sup>/Dram2<sup>em1Jean</sup>  [background:] C57BL/6J-Dram2<sup>em1Jean</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37691820	20231208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412286	Gt(ROSA)26Sor<sup>tm7(CAG-mCherry,-EGFP/tetX)Dym</sup>	is_implicated_in	DOID:9007	sudden infant death syndrome		MGI:4412290	Gt(ROSA)26Sor<sup>tm7(CAG-mCherry,-EGFP/tetX)Dym</sup>/Gt(ROSA)26Sor<sup>+</sup> Tmem163<sup>Tg(ACTB-cre)2Mrt</sup>/0 Tg(Fev-flpe)1Dym/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27053202	20161101	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	is_implicated_in	DOID:0050469	Costello syndrome		MGI:3805200	Hras<sup>tm2Xbr</sup>/Hras<sup>tm2Xbr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18483625	20140429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	is_implicated_in	DOID:0050469	Costello syndrome		MGI:3845065	Hras<sup>tm1Jaf</sup>/Hras<sup>+</sup> Tg(CAG-cre)13Miya/0  [background:] involves: 129S6/SvEvTac * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24057668	20140429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:3032576	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Ptf1a<sup>tm1.1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:14706336	20130822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:3032575	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Pdx1-cre)6Tuv/?  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14706336	20130822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5502430	Kras<sup>tm1Bbd</sup>/Kras<sup>tm1Bbd</sup> Tg(Cela1-tTA)#Eps/? Tg(tetO-cre)3Jig/?  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17349585	20130822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929878	Smoc1	is_implicated_in	DOID:0060861	microphthalmia with limb anomalies		MGI:5056093	Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>/Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21750680	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929878	Smoc1	is_implicated_in	DOID:0060861	microphthalmia with limb anomalies		MGI:4941783	Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>/Smoc1<sup>Tn(sb-lacZ,GFP)IR3.PV384Jtak</sup>  [background:] involves: C3H * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:21194678	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641546	Tg(Myh6-Ppara)402-2Dpk	is_implicated_in	DOID:9351	diabetes mellitus		MGI:3652398	Tg(Myh6-Ppara)402-2Dpk/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11781357	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4377328	Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:5819194	Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>/Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26158450	20170127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686901	Mpl<sup>tm1Fjs</sup>	is_implicated_in	DOID:0090118	congenital amegakaryocytic thrombocytopenia		MGI:2686902	Mpl<sup>tm1Fjs</sup>/Mpl<sup>tm1Fjs</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10611229	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834378	Syne1<sup>tm1.1Mcn</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:3834398	Syne1<sup>tm1.1Mcn</sup>/Syne1<sup>tm1.1Mcn</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:19008300	20100611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97075	Mpi	is_not_implicated_in	DOID:0050570	congenital disorder of glycosylation type I		MGI:3629215	Mpi<sup>Gt(OST90588)Lex</sup>/Mpi<sup>Gt(OST90588)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16339137	20060717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16720837	20140912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14699048	20140912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3035835	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14966562	20140912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857231	Nppa<sup>tm1Unc</sup>	is_implicated_in	DOID:10763	hypertension		MGI:3525012	Nppa<sup>tm1Unc</sup>/Nppa<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7839143	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857231	Nppa<sup>tm1Unc</sup>	is_implicated_in	DOID:10763	hypertension		MGI:3525013	Nppa<sup>tm1Unc</sup>/Nppa<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7839143	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425673	Alpl<sup>Mhdabap32</sup>/Alpl<sup>Mhdabap32</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap32</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425669	Alpl<sup>Mhdabap020</sup>/Alpl<sup>Mhdabap020</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap020</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425671	Alpl<sup>Mhdabap26</sup>/Alpl<sup>Mhdabap26</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap26</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425670	Alpl<sup>BAP023</sup>/Alpl<sup>BAP023</sup>  [background:] C3HeB/FeJ-Alpl<sup>BAP023</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5425672	Alpl<sup>Mhdabap27</sup>/Alpl<sup>Mhdabap27</sup>  [background:] C3HeB/FeJ-Alpl<sup>Mhdabap27</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:5818893	Alpl<sup>tm2.1Jlm</sup>/Alpl<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25716980	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7550313	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:3722926	Alpl<sup>Hpp</sup>/Alpl<sup>Hpp</sup>  [background:] involves: BALB/cAnN * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:17539739	20170124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:3722925	Alpl<sup>Hpp</sup>/Alpl<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:17539739	20170124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822777	Phyh<sup>tm1Safe</sup>	is_implicated_in	DOID:10582	Refsum disease		MGI:3822800	Phyh<sup>tm1Safe</sup>/Phyh<sup>tm1Safe</sup>  [background:] involves: 129P2/OlaHsd * 129X1/SvJ * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19004801	20090112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	is_implicated_in	DOID:12531	von Willebrand's disease		MGI:6473965	Vwf<sup>tm1.1Vhf</sup>/Vwf<sup>tm1.1Vhf</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30565388	20201124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	is_implicated_in	DOID:12531	von Willebrand's disease		MGI:6473967	Vwf<sup>tm1.1Vhf</sup>/Vwf<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30565388	20201124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	is_implicated_in	DOID:12705	Friedreich ataxia		MGI:6220717	Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] B6.129-Gt(ROSA)26Sor<sup>tm1(H1/tetO-RNAi:Fxn)Dhg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29257745	20181102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	is_implicated_in	DOID:12705	Friedreich ataxia		MGI:6101473	Fxn<sup>tm1.1Pand</sup>/Fxn<sup>tm1Mkn</sup>  [background:] B6.Cg-Fxn<sup>tm1.1Pand</sup> Fxn<sup>tm1Mkn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28444186	20181102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	is_implicated_in	DOID:12705	Friedreich ataxia		MGI:3652375	Fxn<sup>tm1Mkn</sup>/Fxn<sup>tm1Pand</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25104852	20181102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	is_implicated_in	DOID:12705	Friedreich ataxia		MGI:2177207	Fxn<sup>tm2Mkn</sup>/Fxn<sup>tm2.1Mkn</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11175786	20181102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	is_implicated_in	DOID:12705	Friedreich ataxia		MGI:2177208	Fxn<sup>tm2Mkn</sup>/Fxn<sup>tm2.1Mkn</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11175786	20181102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352456	Nr4a2	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3619915	Nr4a2<sup>tm1Omc</sup>/Nr4a2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15589522	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856298	Ank1<sup>nb</sup>	is_implicated_in	DOID:12365	malaria		MGI:3766445	Ank1<sup>nb</sup>/Ank1<sup>nb</sup>  [background:] involves: C57BL/6J * WB/Re			ECO:0000033	author statement supported by traceable reference	PMID:1832936	20130313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	is_implicated_in	DOID:0050824	sinoatrial node disease		MGI:4830468	Ank2<sup>tm1Bnt</sup>/Ank2<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:20525877	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530047	Clcn3<sup>tm1Suc</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3574028	Clcn3<sup>tm1Suc</sup>/Clcn3<sup>tm1Suc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12059962	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97249	Myb	is_implicated_in	DOID:4971	myelofibrosis		MGI:4868118	Myb<sup>boo</sup>/Myb<sup>boo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20610815	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443198	Slitrk6	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:4941487	Slitrk6<sup>tm1.1Jaru</sup>/Slitrk6<sup>tm1.1Jaru</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21298075	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829005	Cavin1<sup>tm1Pfp</sup>	is_implicated_in	DOID:6432	pulmonary hypertension		MGI:5614325	Cavin1<sup>tm1Pfp</sup>/Cavin1<sup>tm1Pfp</sup>  [background:] B6.129S6-Cavin1<sup>tm1Pfp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24303100	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104541	Gcdh	is_implicated_in	DOID:0111254	glutaric acidemia I		MGI:2182958	Gcdh<sup>tm1Dmk</sup>/Gcdh<sup>tm1Dmk</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11854167	20191122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104541	Gcdh	is_implicated_in	DOID:0111254	glutaric acidemia I		MGI:6268336	Gcdh<sup>tm1Dmk</sup>/Gcdh<sup>tm1Dmk</sup>  [background:] involves: 129S4/SvJae * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28545977	20191122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096393	Snai2	is_implicated_in	DOID:9258	Waardenburg syndrome		MGI:2652604	Snai2<sup>tm2Grid</sup>/Snai2<sup>tm2Grid</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12444107	20230703	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194903	Tsga8	is_implicated_in	DOID:12336	male infertility		MGI:6727060	Tsga8<sup>em1Ohbo</sup>/Y  [background:] C57BL/6-Tsga8<sup>em1Ohbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33766931	20210729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194903	Tsga8	is_implicated_in	DOID:12336	male infertility		MGI:6727062	Tsga8<sup>em2Ohbo</sup>/Tsga8<sup>em2Ohbo</sup>  [background:] C57BL/6-Tsga8<sup>em2Ohbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33766931	20210729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612048	Crebbp<sup>tm2Pkb</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5766814	Crebbp<sup>tm2Pkb</sup>/Crebbp<sup>tm2Pkb</sup>  [background:] (B6.129P2-Crebbp<sup>tm2Pkb</sup>/Pkb x 129S2.129P2(B6)-Crebbp<sup>tm2Pkb</sup>/Pkb)F1			ECO:0000033	author statement supported by traceable reference	PMID:26730956	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338076	Hivep2	is_implicated_in	DOID:5419	schizophrenia		MGI:6189202	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] either: (involves: BALB/cA * C57BL/6NCrlj * CBA/JNCrlj) or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)			ECO:0000033	author statement supported by traceable reference	PMID:23389689	20190403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338076	Hivep2	is_implicated_in	DOID:5419	schizophrenia		MGI:6189180	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:29233179	20190403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1321395	Ltbp4	is_implicated_in	DOID:3144	cutis laxa		MGI:5641752	Ltbp4<sup>Gt(E301B04)Wrst</sup>/Ltbp4<sup>Gt(E301B04)Wrst</sup>  [background:] B6N.129P2-Ltbp4<sup>Gt(E301B04)Wrst</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25713297	20150625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589208	Dicer1<sup>tm1Bdh</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:4868120	Dicer1<sup>tm1Bdh</sup>/Dicer1<sup>tm1Bdh</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:21098571	20110117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:6295837	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Lhx2-cre)1Lcar/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28250050	20190929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861441	Rab27a	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3640189	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] involves: C3H/HeDiSn			ECO:0000033	author statement supported by traceable reference	PMID:10859366	20080515	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138281	Lbr	is_implicated_in	DOID:9631	Pelger-Huet anomaly		MGI:3829382	Lbr<sup>ic-J</sup>/Lbr<sup>ic-J</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17403717	20090129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800602	Chd2<sup>Gt(RRBO46)Byg</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5515353	Chd2<sup>Gt(RRBO46)Byg</sup>/Chd2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18386809	20140818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617002	Manba<sup>tm1Khf</sup>	is_implicated_in	DOID:3633	beta-mannosidosis		MGI:3617198	Manba<sup>tm1Khf</sup>/Manba<sup>tm1Khf</sup>  [background:] B6.129-Manba<sup>tm1Khf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16377659	20060321	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106096	Loxl1	is_implicated_in	DOID:13641	exfoliation syndrome		MGI:3033884	Loxl1<sup>tm1Tili</sup>/Loxl1<sup>tm1Tili</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24425853	20200506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612337	Fscn2<sup>tm1Sykk</sup>	is_implicated_in	DOID:0110406	retinitis pigmentosa 30		MGI:3612480	Fscn2<sup>tm1Sykk</sup>/Fscn2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16043865	20060210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4436910	Vhl<sup>tm1.1Wkr</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:4436912	Vhl<sup>tm1.1Wkr</sup>/Vhl<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19252526	20100310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511276	Med1<sup>tm2Jkr</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:5911329	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511276	Med1<sup>tm2Jkr</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:5911326	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448246	Sirt1<sup>tm1Mcby</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3783471	Sirt1<sup>tm1Mcby</sup>/Sirt1<sup>tm1Mcby</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:18687325	20100728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2683230	Stat3<sup>tm1Flv</sup>/Stat3<sup>tm1Flv</sup> Tg(Tek-cre)1Xyfu/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14623907	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:4429499	Stat3<sup>tm1Dlv</sup>/Stat3<sup>tm1Dlv</sup> Tg(Csf1r-icre)1Jwp/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20042677	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3783296	Stat3<sup>tm1Flv</sup>/Stat3<sup>tm1Flv</sup> Tg(Tek-cre)12Flv/0  [background:] involves: 129 * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12571365	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354724	Sacs	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia		MGI:5702409	Sacs<sup>tm2Bebr</sup>/Sacs<sup>tm2Bebr</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25260547	20190710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354724	Sacs	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia		MGI:6316985	Sacs<sup>tm1(NCOM)Mfgc</sup>/Sacs<sup>tm1(NCOM)Mfgc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22307627	20190710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	is_implicated_in	DOID:1826	epilepsy		MGI:3840657	Scn8a<sup>8J</sup>/Scn8a<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19254928	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	is_implicated_in	DOID:1826	epilepsy		MGI:3840657	Scn8a<sup>8J</sup>/Scn8a<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24657915	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443327	Fa2h	is_implicated_in	DOID:0110786	hereditary spastic paraplegia 35		MGI:4999603	Fa2h<sup>tm1.1Hama</sup>/Fa2h<sup>tm1.1Hama</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21491498	20110523	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924066	Sdccag8	is_implicated_in	DOID:0110138	Bardet-Biedl syndrome 16		MGI:7336110	Sdccag8<sup>em2Lji</sup>/Sdccag8<sup>em2Lji</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:35503560	20220914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924066	Sdccag8	is_implicated_in	DOID:0110138	Bardet-Biedl syndrome 16		MGI:7336104	Sdccag8<sup>em1Lji</sup>/Sdccag8<sup>em1Lji</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:35503560	20220914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:870	neuropathy		MGI:6273176	Mpz<sup>tm1.1Wra</sup>/Mpz<sup>+</sup>  [background:] FVB.129S2-Mpz<sup>tm1.1Wra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30239779	20190111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856691	Fras1<sup>bl</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:2657302	Fras1<sup>bl</sup>/Fras1<sup>bl</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:12766769	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388316	Ciita<sup>tm1Wrth</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:5788294	Ciita<sup>tm1Wrth</sup>/Ciita<sup>tm1Wrth</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24038328	20160809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4363147	Wdr72<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110061	amelogenesis imperfecta hypomaturation type 2A3		MGI:5659959	Wdr72<sup>tm1a(KOMP)Wtsi</sup>/Wdr72<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25008349	20150826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933976	Cln3<sup>tm1Nbm</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3715473	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] 129S6/SvEvTac-Cln3<sup>tm1Nbm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15326100	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933976	Cln3<sup>tm1Nbm</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:2175783	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10527801	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933976	Cln3<sup>tm1Nbm</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:5788563	Cln3<sup>tm1Nbm</sup>/Cln3<sup>tm1Nbm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27101989	20160812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641575	Tg(Myh6-Ppara)404-3Dpk	is_implicated_in	DOID:9351	diabetes mellitus		MGI:3652395	Tg(Myh6-Ppara)404-3Dpk/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11781357	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848226	Prmt1<sup>tm1Rchd</sup>	is_implicated_in	DOID:674	cleft palate		MGI:7378837	Prmt1<sup>tm1Rchd</sup>/Prmt1<sup>tm1Rchd</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:29986157	20221107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530029	Tg(Th-SNCA)5Eric	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6099056	Tg(Th-SNCA)5Eric/0  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15009131	20171211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530029	Tg(Th-SNCA)5Eric	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3815302	Tg(Th-SNCA)5Eric/Tg(Th-SNCA)5Eric  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17537546	20171211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351649	Prl3c1	is_implicated_in	DOID:11613	hyperandrogenism		MGI:6159252	Prl3c1<sup>tm1(KOMP)Vlcg</sup>/Prl3c1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28576872	20180601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:3617447	Fah<sup>tm1Mgo</sup>/Fah<sup>tm1Mgo</sup>  [background:] involves: 129S7/SvEvBrd * PT			ECO:0000033	author statement supported by traceable reference	PMID:10518553	20140414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:5558898	Fah<sup>tm1Mgo</sup>/Fah<sup>tm1Mgo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:7545495	20140414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:2655554	Fah<sup>2R</sup>/Fah<sup>2R</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:11209059	20140414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:2655553	Fah<sup>1R</sup>/Fah<sup>1R</sup>  [background:] involves: BALB/cRl * C3H/Rl * C57BL/10Rl			ECO:0000033	author statement supported by traceable reference	PMID:11209059	20140414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818739	Tg(Ins-Igf2)1Fbos	is_implicated_in	DOID:0110741	type 1 diabetes mellitus 2		MGI:3818740	Tg(Ins-Igf2)1Fbos/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10727441	20081208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818739	Tg(Ins-Igf2)1Fbos	is_implicated_in	DOID:0110741	type 1 diabetes mellitus 2		MGI:3818741	Tg(Ins-Igf2)1Fbos/0  [background:] involves: C57BL/6 * C57BLKs/J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10727441	20081208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857936	Pten<sup>tm1Ppp</sup>	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome		MGI:2179025	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9697695	20050708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3623394	Hnf1a<sup>tm1.1Ylee</sup>/Hnf1a<sup>tm1.1Ylee</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9566924	20060526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347464	Foxg1	is_implicated_in	DOID:1206	Rett syndrome		MGI:5806112	Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27001178	20161103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917285	Rab28	is_implicated_in	DOID:0111024	cone-rod dystrophy 18		MGI:6360454	Rab28<sup>tm1d(EUCOMM)Hmgu</sup>/Rab28<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30228185	20190919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917285	Rab28	is_implicated_in	DOID:0111024	cone-rod dystrophy 18		MGI:6360455	Rab28<sup>tm1d(EUCOMM)Wtsi</sup>/Rab28<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30228185	20190919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	is_implicated_in	DOID:0060352	Kleefstra syndrome 1		MGI:4461144	Ehmt1<sup>tm1Yshk</sup>/Ehmt1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:19896504	20130305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	is_implicated_in	DOID:0060352	Kleefstra syndrome 1		MGI:4418566	Ehmt1<sup>tm1.1Tara</sup>/Ehmt1<sup>tm1.1Tara</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20005824	20130305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	is_implicated_in	DOID:0060352	Kleefstra syndrome 1		MGI:4461144	Ehmt1<sup>tm1Yshk</sup>/Ehmt1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23175442	20130305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	is_implicated_in	DOID:0060695	hyperekplexia		MGI:6471172	Glra1<sup>m1Cpai</sup>/Glra1<sup>m1Cpai</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28724750	20201111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3590646	Crygb<sup>Clapper</sup>	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3603148	Crygb<sup>Clapper</sup>/Crygb<sup>+</sup>  [background:] C57BL/6J-Crygb<sup>Clapper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15878859	20130513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3590646	Crygb<sup>Clapper</sup>	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3603147	Crygb<sup>Clapper</sup>/Crygb<sup>Clapper</sup>  [background:] C57BL/6J-Crygb<sup>Clapper</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15878859	20130513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612978	Als2<sup>tm1Jei</sup>	is_not_implicated_in	DOID:0060194	amyotrophic lateral sclerosis type 2		MGI:3616467	Als2<sup>tm1Jei</sup>/Als2<sup>tm1Jei</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16321985	20060316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857456	Ciita<sup>tm1Ccum</sup>	is_implicated_in	DOID:5812	MHC class II deficiency		MGI:3617399	Ciita<sup>tm1Ccum</sup>/Ciita<sup>tm1Ccum</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8624807	20060323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261831	Hap1	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2670610	Hap1<sup>tm1Xjl</sup>/Hap1<sup>tm1Xjl</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12890790	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261831	Hap1	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2670622	Hap1<sup>tm1Hay</sup>/Hap1<sup>tm1Hay</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11971876	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347521	Ror2	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:3793282	Ror2<sup>tm1Anec</sup>/Ror2<sup>tm1Anec</sup>  [background:] B6.129S1-Ror2<sup>tm1Anec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18353862	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347521	Ror2	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:3038706	Ror2<sup>tm1Ymi</sup>/Ror2<sup>tm1Ymi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14745966	20080611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857468	Tnfrsf1a<sup>tm1Imx</sup>	is_implicated_in	DOID:0090018	autosomal dominant familial periodic fever		MGI:2175019	Tnfrsf1a<sup>tm1Imx</sup>/Tnfrsf1a<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9551933	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181718	Cfc1<sup>tm1Cbm</sup>	is_implicated_in	DOID:6406	double outlet right ventricle		MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10574770	20060503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	is_implicated_in	DOID:0111115	nephronophthisis 4		MGI:4868696	Nphp4<sup>nmf192</sup>/Nphp4<sup>nmf192</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21078623	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194883	Crx	is_implicated_in	DOID:0110333	Leber congenital amaurosis 7		MGI:5526862	Crx<sup>Rip</sup>/Crx<sup>+</sup>  [background:] C57BL/6J-Crx<sup>Rip</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24382353	20140106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194883	Crx	is_implicated_in	DOID:0110333	Leber congenital amaurosis 7		MGI:3697471	Crx<sup>tm1Clc</sup>/Crx<sup>tm1Clc</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10581037	20140106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579084	Id4<sup>tm1Fsky</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:4819227	Id4<sup>tm1Fsky</sup>/Id4<sup>tm1Fsky</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20628571	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	is_implicated_in	DOID:0060671	cerebral cavernous malformation 3		MGI:5002697	Pdcd10<sup>tm1Wami</sup>/Pdcd10<sup>tm1Wami</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21321212	20190220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	is_implicated_in	DOID:0060671	cerebral cavernous malformation 3		MGI:5052328	Pdcd10<sup>tm1Kwhi</sup>/Pdcd10<sup>tm1.1Kwhi</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21490399	20190220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856150	Bmp5<sup>se</sup>	is_implicated_in	DOID:0060306	Meier-Gorlin syndrome		MGI:3587431	Bmp5<sup>se</sup>/Bmp5<sup>se</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7710253	20180305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328350	Matn3	is_implicated_in	DOID:0070299	multiple epiphyseal dysplasia 5		MGI:3759051	Matn3<sup>tm1Mbri</sup>/Matn3<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17517694	20190807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917200	Rcbtb2	is_implicated_in	DOID:2570	malignant histiocytic disease		MGI:6431137	Rcbtb2<sup>tm1.1Xyw</sup>/Rcbtb2<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26291700	20200602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917200	Rcbtb2	is_implicated_in	DOID:2570	malignant histiocytic disease		MGI:6431136	Rcbtb2<sup>tm1.1Xyw</sup>/Rcbtb2<sup>tm1.1Xyw</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26291700	20200602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	is_implicated_in	DOID:3613	Canavan disease		MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311352	b2b1200Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3620917	Lmna<sup>tm1Stw</sup>/Lmna<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11855819	20060502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3620916	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11855819	20060502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107357	Inpp5d	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6376530	Cd79a<sup>tm1(cre)Reth</sup>/Cd79a<sup>+</sup> Inpp5d<sup>tm1Rav</sup>/Inpp5d<sup>tm1Rav</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22078222	20191113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:2386959	Cdk4<sup>tm1Bbd</sup>/Cdk4<sup>tm1Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:10319860	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:3841959	Cyp11b1<sup>tm1Chjk</sup>/Cyp11b1<sup>tm1Chjk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19029289	20151122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3588195	Adamts17	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:6466719	Adamts17<sup>tm1.2Taks</sup>/Adamts17<sup>tm1.2Taks</sup>  [background:] involves: C57BL * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:31201465	20201013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797839	Sost<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0080036	SOST-related sclerosing bone dysplasia		MGI:4882107	Sost<sup>tm1(KOMP)Vlcg</sup>/Sost<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:22886088	20121119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3622294	Tg(Myh6-Tmod1)65Msus	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3622299	Tg(Myh6-Tmod1)65Msus/Tg(Myh6-Tmod1)65Msus  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9421465	20170724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3622294	Tg(Myh6-Tmod1)65Msus	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3622305	Tg(Myh6-Tmod1)65Msus/Tg(Myh6-Tmod1)65Msus  [background:] FVB/N-Tg(Myh6-Tmod1)65Msus			ECO:0000033	author statement supported by traceable reference	PMID:10595939	20170724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349410	Triobp	is_implicated_in	DOID:0110486	autosomal recessive nonsyndromic deafness 28		MGI:4881776	Triobp<sup>tm1Tbf</sup>/Triobp<sup>tm1Tbf</sup>  [background:] C57BL/6-Triobp<sup>tm1Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20510926	20220308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:2684391	Scgb1a1<sup>tm1Abm</sup>/Scgb1a1<sup>tm1Abm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10470078	20190611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047406	Tg(KRT14-HPV16)wt1Dh	is_not_implicated_in	DOID:3151	skin squamous cell carcinoma		MGI:4849991	Tg(KRT14-HPV16)wt1Dh/0  [background:] C.Cg-Tg(KRT14-HPV16)wt1Dh			ECO:0000033	author statement supported by traceable reference	PMID:8952526	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047406	Tg(KRT14-HPV16)wt1Dh	is_not_implicated_in	DOID:3151	skin squamous cell carcinoma		MGI:4849990	Tg(KRT14-HPV16)wt1Dh/0  [background:] either: (involves: C57BL/6 * DBA/2) or (involves: C57BL/6 * DBA/2 * SENCAR * SSIN)			ECO:0000033	author statement supported by traceable reference	PMID:8952526	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:0060673	Peters anomaly		MGI:3590308	Pax6<sup>4Neu</sup>/Pax6<sup>+</sup>  [background:] either: (involves: 102 * C3H) or (involves: C3H)			ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:0060673	Peters anomaly		MGI:3613467	Pax6<sup>7Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:0060673	Peters anomaly		MGI:3590307	Pax6<sup>3Neu</sup>/Pax6<sup>+</sup>  [background:] either: (involves: 102 * C3H) or (involves: C3H)			ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:0060673	Peters anomaly		MGI:2680573	Pax6<sup>1Jrt</sup>/Pax6<sup>+</sup>  [background:] C3.B6-Pax6<sup>1Jrt</sup>			ECO:0000033	author statement supported by traceable reference	MGI:2680583	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:0060673	Peters anomaly		MGI:4821786	Pax6<sup>tm2Pgr</sup>/Pax6<sup>+</sup> Tg(Pax6-cre,GFP)1Pgr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20538882	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96968	Mest	is_implicated_in	DOID:0050476	Barth syndrome		MGI:2677273	Mest<sup>tm1Masu</sup>/Mest<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12242721	20181015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:4820803	Ret<sup>tm2.1Heno</sup>/Ret<sup>tm2.1Heno</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18414682	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:4820807	Ret<sup>tm1Cos</sup>/Ret<sup>tm2(RET)Jmi</sup>  [background:] involves: 129S/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18414682	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:4820806	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18414682	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2175009	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:7595168	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2175009	Ret<sup>tm1Cos</sup>/Ret<sup>tm1Cos</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:8114940	20100826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044352	Mnt<sup>tm1.1Awb</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:3044750	Mnt<sup>tm1.1Awb</sup>/Mnt<sup>tm1.1Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15028671	20150831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	is_implicated_in	DOID:0060484	EAST syndrome		MGI:5698063	Kcnj10<sup>tm1Lst</sup>/Kcnj10<sup>tm1Lst</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:19420365	20151204	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	is_implicated_in	DOID:0060484	EAST syndrome		MGI:3038919	Kcnj10<sup>tm1Lst</sup>/Kcnj10<sup>tm1Lst</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11466414	20151204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033231	Gck<sup>Rgsc553</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590139	Gck<sup>Rgsc553</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443583	Fermt1	is_implicated_in	DOID:0060472	Kindler syndrome		MGI:3828513	Fermt1<sup>tm1Ref</sup>/Fermt1<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19057668	20090123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855953	Clcn1<sup>adr-mto</sup>	is_implicated_in	DOID:2106	myotonia congenita		MGI:3581032	Clcn1<sup>adr-mto</sup>/Clcn1<sup>adr-mto</sup>  [background:] SWR/J-Clcn1<sup>adr-mto</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8119941	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445447	Tg(GFAP-TAg121)1Tvd	is_implicated_in	DOID:3069	malignant astrocytoma		MGI:5286087	Tg(GFAP-TAg121)1Tvd/0  [background:] involves: C57BL/6 * DBA/2 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12086874	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5431480	b2b904.1Clo	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5431511	b2b904.1Clo/b2b904.1Clo  [background:] C57BL/6J-b2b904.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:5314998	Tmc1<sup>nice</sup>/Tmc1<sup>nice</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:5315001	Tmc1<sup>baringo</sup>/Tmc1<sup>baringo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:5314999	Tmc1<sup>stitch</sup>/Tmc1<sup>stitch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22330676	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:2177312	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] STOCK Grhl3<sup>ct</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:48774	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:2177313	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] involves: STOCK Grhl3<sup>ct</sup> * M. m. molossinus			ECO:0000033	author statement supported by traceable reference	PMID:7719036	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:2177316	Tmc1<sup>Mhdabth</sup>/Tmc1<sup>+</sup>  [background:] C3HeB/FeJ-Tmc1<sup>Mhdabth</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	MGI:2681078	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135679	Hes7	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:6725725	Hes7<sup>M1Btlr</sup>/Hes7<sup>+</sup>  [background:] C57BL/6J-Hes7<sup>M1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706312	Dlg3<sup>tm1Grnt</sup>	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:5824730	Dlg3<sup>tm1Grnt</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27466188	20170221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2686271	Opa3	is_implicated_in	DOID:0110004	3-methylglutaconic aciduria type 3		MGI:5312681	Opa3<sup>m1Votr</sup>/Opa3<sup>m1Votr</sup>  [background:] involves: C3H * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:18222992	20121115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2686271	Opa3	is_implicated_in	DOID:0110004	3-methylglutaconic aciduria type 3		MGI:5312681	Opa3<sup>m1Votr</sup>/Opa3<sup>m1Votr</sup>  [background:] involves: C3H * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:22869679	20121115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351629	Pign	is_implicated_in	DOID:4621	holoprosencephaly		MGI:5437465	Pign<sup>m1Nisw</sup>/Pign<sup>m1Nisw</sup>  [background:] involves: 129S1/SvImJ * C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23213481	20190927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5555837	Ccdc39<sup>b2b2025.1Clo</sup>/Ccdc39<sup>b2b2025.1Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b2025.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0110598	primary ciliary dyskinesia 14		MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138281	Lbr	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5897270	Lbr<sup>ic-J</sup>/Lbr<sup>+</sup>  [background:] (NZW/LacJ x C57BL/6J-Lbr<sup>ic-J</sup>/J)F1			ECO:0000033	author statement supported by traceable reference	PMID:27483354	20170512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:3716631	Rpgrip1l<sup>tm1Urt</sup>/Rpgrip1l<sup>tm1Urt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17558409	20150903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	is_implicated_in	DOID:0111731	familial episodic pain syndrome 3		MGI:6392909	Scn11a<sup>em1Akoi</sup>/Scn11a<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27224030	20210120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858122	Nek1<sup>kat-2J</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3831388	Nek1<sup>kat-2J</sup>/Nek1<sup>kat-2J</sup>  [background:] C57BL/6J-Nek1<sup>kat-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9070925	20090212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891247	Otof	is_implicated_in	DOID:0110535	autosomal recessive nonsyndromic deafness 9		MGI:3693849	Otof<sup>tm1Ugds</sup>/Otof<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17055430	20071207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891247	Otof	is_implicated_in	DOID:0110535	autosomal recessive nonsyndromic deafness 9		MGI:3760289	Otof<sup>deaf5Jcs</sup>/Otof<sup>deaf5Jcs</sup>  [background:] STOCK Otof<sup>deaf5Jcs</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	PMID:17967520	20071207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923416	Cplane2	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561553	Cplane2<sup>b2b2827Clo</sup>/Cplane2<sup>b2b2827Clo</sup>  [background:] C57BL/6J-Cplane2<sup>b2b2827Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	is_implicated_in	DOID:10754	otitis media		MGI:3777760	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17712420	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88048	Apo	is_implicated_in	DOID:83	cataract		MGI:2175702	Apo/Apo<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922783	Nme5	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429549	Nme5<sup>tm1Lex</sup>/Nme5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277211	Tyrobp	is_implicated_in	DOID:0090112	Nasu-Hakola disease		MGI:3818484	Tyrobp<sup>tm1.1Viv</sup>/Tyrobp<sup>tm1.1Viv</sup>  [background:] B6.129P2-Tyrobp<sup>tm1.1Viv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15632019	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277211	Tyrobp	is_implicated_in	DOID:0090112	Nasu-Hakola disease		MGI:2450846	Tyrobp<sup>tm1Ttk</sup>/Tyrobp<sup>tm1Ttk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12569157	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3622060	Tnf<sup>tm2Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20180824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20180824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136645	Vhl<sup>tm1Jae</sup>	is_implicated_in	DOID:9007	sudden infant death syndrome		MGI:5304714	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22977222	20131101	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95278	Epha2	is_implicated_in	DOID:0110229	cataract 6 multiple types		MGI:3689377	Epha2<sup>Gt(KST085)Byg</sup>/Epha2<sup>Gt(KST085)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19649315	20130512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	is_implicated_in	DOID:0110841	Usher syndrome type 3A		MGI:5432139	Clrn1<sup>tm2.1Kuna</sup>/Clrn1<sup>tm2.1Kuna</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22787034	20201016	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	is_implicated_in	DOID:0110841	Usher syndrome type 3A		MGI:3850181	Clrn1<sup>tm1.1Kuna</sup>/Clrn1<sup>tm1.1Kuna</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19414487	20201016	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	is_implicated_in	DOID:0110841	Usher syndrome type 3A		MGI:6467338	Clrn1<sup>tm1.1Ugpa</sup>/Clrn1<sup>tm1.1Ugpa</sup> Myo15a<sup>tm1.1(cre)Ugds</sup>/Myo15a<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29985171	20201016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3819772	Uqcrfs1<sup>tm1Ctm</sup>	is_implicated_in	DOID:700	mitochondrial metabolism disease		MGI:5444471	Uqcrfs1<sup>tm1Ctm</sup>/Uqcrfs1<sup>tm1Ctm</sup> Tg(Camk2a-cre)#Szi/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22914734	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589207	Apc<sup>tm1Kk</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:3590232	Apc<sup>tm1Kk</sup>/Apc<sup>tm1Kk</sup> Tg(Lck-cre)1Cwi/?  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18077429	20141010	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3723649	Ndn<sup>tm1.1Mus</sup>/Ndn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11115855	20091026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2654656	Ndn<sup>tm2Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10508517	20091026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653050	Ndn<sup>tm1Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10508517	20091026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653051	Ndn<sup>tm1Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10508517	20091026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653055	Ndn<sup>tm2Stw</sup>/Ndn<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12629158	20091026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3607781	Ndn<sup>tm1Ky</sup>/Ndn<sup>+</sup>  [background:] involves: C57BL/6 * CBA * ICR/Slc			ECO:0000033	author statement supported by traceable reference	PMID:16049186	20091026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3773672	Ndn<sup>tm1.1Mus</sup>/Ndn<sup>+</sup>  [background:] B6.129S2-Ndn<sup>tm1.1Mus</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17116257	20091026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137330	Nr1h4<sup>tm1Gonz</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437134	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17283114	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137330	Nr1h4<sup>tm1Gonz</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437134	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137330	Nr1h4<sup>tm1Gonz</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:2175162	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137330	Nr1h4<sup>tm1Gonz</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:2175162	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:17183066	20121001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5779643	Braf<sup>tm1Cpri</sup>/Braf<sup>tm1Cpri</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129P2/OlaHsd * FVB/NCr			ECO:0000033	author statement supported by traceable reference	PMID:21220306	20160708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:3969	thyroid gland papillary carcinoma		MGI:5780077	Braf<sup>tm1Mmcm</sup>/Braf<sup>+</sup> Tg(Tg-cre/ERT2)#Mmcm/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21512141	20160708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927072	Ppp1r15a	is_implicated_in	DOID:10241	thalassemia		MGI:3622193	Ppp1r15a<sup>tm1.1Ajf</sup>/Ppp1r15a<sup>tm1.1Ajf</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16478986	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:6324231	Atp7a<sup>Mo-ml</sup>/Y  [background:] involves: C3Hf/He			ECO:0000033	author statement supported by traceable reference	PMID:1819648	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:4940051	Atp7a<sup>Mo-ms</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20831904	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:2175712	Atp7a<sup>Mo</sup>/Atp7a<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:13103353	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:3793780	Atp7a<sup>Mo-br</sup>/Y  [background:] involves: C57BL			ECO:0000033	author statement supported by traceable reference	PMID:4858102	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:3618244	Atp7a<sup>Mo-Tohm</sup>/Atp7a<sup>+</sup>  [background:] B6.Cg-Atp7a<sup>Mo-Tohm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16338116	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:6324210	Atp7a<sup>Mo-blo</sup>/Atp7a<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6685755	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:6324209	Atp7a<sup>Mo-blo</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6685755	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:3793729	Atp7a<sup>Mo-vbr</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10098864	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:5696621	Atp7a<sup>Mo-dp</sup>/Y  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:25456742	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:5696613	Atp7a<sup>Mo-dp</sup>/Atp7a<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:25456742	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:1838	Menkes disease		MGI:6324231	Atp7a<sup>Mo-ml</sup>/Y  [background:] involves: C3Hf/He			ECO:0000033	author statement supported by traceable reference	MGI:60964	20190723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793279	Ror2<sup>tm1Anec</sup>	is_not_implicated_in	DOID:0110969	brachydactyly type B1		MGI:3793283	Ror2<sup>tm1Anec</sup>/Ror2<sup>+</sup>  [background:] B6.129S1-Ror2<sup>tm1Anec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18353862	20080611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055139	Dysf<sup>tm1Meho</sup>	is_implicated_in	DOID:11720	distal myopathy		MGI:3055578	Dysf<sup>tm1Meho</sup>/Dysf<sup>tm1Meho</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	is_implicated_in	DOID:10754	otitis media		MGI:3574963	Fgfr1<sup>Hspy</sup>/Fgfr1<sup>+</sup>  [background:] C3HeB/FeJ-Hspy			ECO:0000033	author statement supported by traceable reference	PMID:15630379	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	is_implicated_in	DOID:10754	otitis media		MGI:5301811	Fgfr1<sup>Eask</sup>/Fgfr1<sup>+</sup>  [background:] BALB/cByJ-Fgfr1<sup>Eask</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794893	Slc17a8<sup>tm1Selm</sup>	is_implicated_in	DOID:0110555	autosomal dominant nonsyndromic deafness 25		MGI:3804682	Slc17a8<sup>tm1Selm</sup>/Slc17a8<sup>tm1Selm</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18674745	20090520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3615946	Gck<sup>tm1Hrt</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3618231	Gck<sup>tm1Hrt</sup>/Gck<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15569412	20190520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3615946	Gck<sup>tm1Hrt</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3618231	Gck<sup>tm1Hrt</sup>/Gck<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:24447392	20190520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433489	Tmem67<sup>b2b1163.1Clo</sup>/Tmem67<sup>b2b1163.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1163.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437111	Tmem67<sup>b2b1291.1Clo</sup>/Tmem67<sup>b2b1291.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1291.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:5795582	Psen1<sup>tm1Tak</sup>/Psen1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16377636	20160926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2174994	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9883847	20160926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3702925	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15207348	20160926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2174998	Psen1<sup>tm1Shn</sup>/Psen1<sup>tm1Shn</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9160754	20160926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2684657	Psen1<sup>tm1Vln</sup>/Psen1<sup>tm1Vln</sup> Tg(Thy1-cre)1Vln/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11978821	20160926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667194	Fras1<sup>tm1Chpk</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:2667203	Fras1<sup>tm1Chpk</sup>/Fras1<sup>tm1Chpk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10			ECO:0000033	author statement supported by traceable reference	PMID:12766770	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667194	Fras1<sup>tm1Chpk</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3833377	Fras1<sup>tm1Chpk</sup>/Fras1<sup>tm1Chpk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:15623520	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180787	Comp<sup>tm1Aol</sup>	is_not_implicated_in	DOID:12721	multiple epiphyseal dysplasia		MGI:3037836	Comp<sup>tm1Aol</sup>/Comp<sup>tm1Aol</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12024046	20051007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	is_implicated_in	DOID:2921	glomerulonephritis		MGI:7507073	Cfi<sup>em1Jiwe</sup>/Cfi<sup>em1Jiwe</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34149444	20230714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_not_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3702089	Pkhd1<sup>tm1Rbu</sup>/Pkhd1<sup>tm1Rbu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15830394	20070410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:2451017	Mtm1<sup>tm1.1Jman</sup>/Y  [background:] involves: 129T1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12391329	20120227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574034	Cecr2<sup>Gt(pGT1)1Hemc</sup>	is_not_implicated_in	DOID:0060668	anencephaly		MGI:3574279	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] FVB.129P2(C)-Cecr2<sup>Gt(pGT1)1Hemc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180364	Cav1<sup>tm1Mls</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5014041	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21203469	20110712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3763425	Flt3<sup>tm1Dgg</sup>/Flt3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17936561	20160111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3763424	Flt3<sup>tm1Dgg</sup>/Flt3<sup>tm1Dgg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17936561	20160111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:8534	gastroesophageal reflux disease		MGI:2174785	Trp63<sup>tm1Fmc</sup>/Trp63<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:21703447	20111007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785162	Enpp1<sup>asj</sup>	is_implicated_in	DOID:10754	otitis media		MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:27959908	20190917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106652	Ro60	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2670272	Ro60<sup>tm1Woln</sup>/Ro60<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106652	Ro60	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2670271	Ro60<sup>tm1Woln</sup>/Ro60<sup>tm1Woln</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106652	Ro60	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2670276	Ro60<sup>tm1Woln</sup>/Ro60<sup>tm1Woln</sup>  [background:] B6.129S1-Ro60<sup>tm1Woln</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7523551	20060510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4048170	20060510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6604585	20060510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6847727	20060510	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924859	Odad3	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5445974	Odad3<sup>b2b1885Clo</sup>/Odad3<sup>b2b1885Clo</sup>  [background:] C57BL/6J-Odad3<sup>b2b1885Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861947	Il2rg<sup>tm1Cgn</sup>	is_not_implicated_in	DOID:0060013	X-linked severe combined immunodeficiency		MGI:2179821	Il2rg<sup>tm1Cgn</sup>/Il2rg<sup>tm1Cgn</sup>  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861947	Il2rg<sup>tm1Cgn</sup>	is_not_implicated_in	DOID:0060013	X-linked severe combined immunodeficiency		MGI:2179823	Il2rg<sup>tm1Cgn</sup>/Y  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857248	Stat4<sup>tm1Gru</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617975	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup>  [background:] NOD.129S2-Stat4<sup>tm1Gru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15041039	20060526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:5465030	Foxn1<sup>nu-2J</sup>/Foxn1<sup>nu-2J</sup>  [background:] B6(SJL)-Foxn1<sup>nu-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:2175029	Foxn1<sup>nu-Y</sup>/Foxn1<sup>nu-Y</sup>  [background:] 101/HY-Foxn1<sup>nu-Y</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76644	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:2175031	Foxn1<sup>tm1Tbo</sup>/Foxn1<sup>tm1Tbo</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8629026	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:2680668	Foxn1<sup>nu</sup>/Foxn1<sup>nu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:4547146	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102778	Six2	is_implicated_in	DOID:674	cleft palate		MGI:6470640	Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>/Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>  [background:] involves: 129/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31765609	20221108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	is_implicated_in	DOID:1391	Norum disease		MGI:3530620	Lcat<sup>tm1Nsa</sup>/Lcat<sup>tm1Nsa</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9054454	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	is_implicated_in	DOID:1391	Norum disease		MGI:3530641	Lcat<sup>tm1Nsa</sup>/Lcat<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9054454	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_implicated_in	DOID:0050433	fatal familial insomnia		MGI:4412280	Prnp<sup>tm2Lnq</sup>/Prnp<sup>tm2Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:19709627	20140227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_implicated_in	DOID:0050433	fatal familial insomnia		MGI:4412280	Prnp<sup>tm2Lnq</sup>/Prnp<sup>tm2Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23959875	20140227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931028	Recql4	is_implicated_in	DOID:2732	Rothmund-Thomson syndrome		MGI:2677318	Recql4<sup>tm1Abe</sup>/Recql4<sup>tm1Abe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12915449	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931028	Recql4	is_implicated_in	DOID:2732	Rothmund-Thomson syndrome		MGI:3575579	Recql4<sup>tm1Glu</sup>/Recql4<sup>tm1Glu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15703196	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842842	Ush1c<sup>dfcr-3J</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:3842843	Ush1c<sup>dfcr-3J</sup>/Ush1c<sup>dfcr-3J</sup>  [background:] STOCK Ush1c<sup>dfcr-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3842839	20090505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038539	Aspa<sup>tm1Mata</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:3038607	Aspa<sup>tm1Mata</sup>/Aspa<sup>tm1Mata</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:14572139	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038539	Aspa<sup>tm1Mata</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:3038607	Aspa<sup>tm1Mata</sup>/Aspa<sup>tm1Mata</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10894262	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151173	Sox10<sup>tm1Weg</sup>	is_implicated_in	DOID:3614	Kallmann syndrome		MGI:3039429	Sox10<sup>tm1Weg</sup>/Sox10<sup>tm1Weg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:23643381	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	is_implicated_in	DOID:3911	progeria		MGI:3620988	Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] B6.129S4-Zmpste24<sup>tm1Sgy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16484451	20101008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	is_implicated_in	DOID:3911	progeria		MGI:4834358	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20805469	20101008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	is_implicated_in	DOID:3911	progeria		MGI:3620907	Zmpste24<sup>tm1Sgy</sup>/Zmpste24<sup>tm1Sgy</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15608054	20101008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98241	Stmn2	is_implicated_in	DOID:870	neuropathy		MGI:7523309	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>em1Jmi</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617975	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup>  [background:] NOD.129S2-Stat4<sup>tm1Gru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15041039	20060526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8456819	20130702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3789135	Htr2c<sup>tm1Jul</sup>/Y  [background:] B6.129S-Htr2c<sup>tm1Jul</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9771748	20100129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927144	Sav1	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4457497	Sav1<sup>tm2.1Dlim</sup>/Sav1<sup>tm2.1Dlim</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:26131558	20170208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861674	Gnasas1	is_implicated_in	DOID:4184	pseudohypoparathyroidism		MGI:4459500	Gnasas1<sup>tm1.1Hju</sup>/Gnasas1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:20427744	20120727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1935192	Abca1<sup>tm1Jdm</sup>	is_implicated_in	DOID:1388	Tangier disease		MGI:2450723	Abca1<sup>tm1Jdm</sup>/Abca1<sup>tm1Jdm</sup>  [background:] DBA/1LacJ-Abca1<sup>tm1Jdm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10760292	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429961	Aprt<sup>tm1Dwm</sup>	is_implicated_in	DOID:0060350	adenine phosphoribosyltransferase deficiency		MGI:2449123	Aprt<sup>tm1Dwm</sup>/Aprt<sup>tm1Dwm</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:8864750	20120924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858099	Tg(CAMalpha1b)7Wjk	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3800634	Tg(CAMalpha1b)7Wjk/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11454600	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716166	Tg(AMELX*P70T)2Gibs	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:5086116	Tg(AMELX*P70T)2Gibs/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17384027	20110816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920989	Cby1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19364920	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920989	Cby1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21049041	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3839772	Hfe<sup>tm1Gfn</sup>/Hfe<sup>tm1Gfn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10557317	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3839772	Hfe<sup>tm1Gfn</sup>/Hfe<sup>tm1Gfn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20976594	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3775649	Hfe<sup>tm1.1Wsr</sup>/Hfe<sup>tm1.1Wsr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17264297	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033465	Hfe<sup>tm1Sly</sup>/Hfe<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033467	Hfe<sup>tm2Sly</sup>/Hfe<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033466	Hfe<sup>tm2Sly</sup>/Hfe<sup>tm2Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033464	Hfe<sup>tm1Sly</sup>/Hfe<sup>tm1Sly</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3033469	Hfe<sup>tm3Sly</sup>/Hfe<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14673107	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3839782	Hfe<sup>tm1.1Gfn</sup>/Hfe<sup>tm1.1Gfn</sup>  [background:] B6.129P2-Hfe<sup>tm1.1Gfn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16491649	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655513	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655482	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655512	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655506	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10381492	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655482	Hfe<sup>tm2Nca</sup>/Hfe<sup>tm2Nca</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10791995	20180801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:2655503	Hfe<sup>tm1.1Nca</sup>/Hfe<sup>tm1.1Nca</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10791995	20180801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530566	Kiss1r<sup>tm1Coll</sup>	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:3530658	Kiss1r<sup>tm1Coll</sup>/Kiss1r<sup>tm1Coll</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14573733	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88450	Col17a1	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:3711939	Col17a1<sup>tm1Shzu</sup>/Col17a1<sup>tm1Shzu</sup>  [background:] B6.129S-Col17a1<sup>tm1Shzu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17322897	20090304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856681	Cdh23<sup>v-bus</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:5140950	Cdh23<sup>v-bus</sup>/Cdh23<sup>v-bus</sup>  [background:] involves: KYF/MsIdr			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	is_implicated_in	DOID:0111089	Fanconi anemia complementation group D1		MGI:3833153	Brca2<sup>tm1Kamc</sup>/Brca2<sup>tm1Kamc</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:16859999	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	is_implicated_in	DOID:2566	corneal dystrophy		MGI:6405015	Tgfbi<sup>em1Yaou</sup>/Tgfbi<sup>em1Yaou</sup>  [background:] involves: C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:32029872	20200422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856174	Pax3<sup>Sp-d</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856174	Pax3<sup>Sp-d</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451350	Pax3<sup>Sp-d</sup>/Pax3<sup>+</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14170406	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856174	Pax3<sup>Sp-d</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451349	Pax3<sup>Sp-d</sup>/Pax3<sup>Sp-d</sup>  [background:] C57BL/6J-Pax3<sup>Sp-d</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2763211	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921657	Odad4	is_implicated_in	DOID:0110620	primary ciliary dyskinesia 35		MGI:6110172	Odad4<sup>em#Omra</sup>/Odad4<sup>em#Omra</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27486780	20180116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276574	Nsd2	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome		MGI:3851517	Nsd2<sup>tm1Ykan</sup>/Nsd2<sup>tm1Ykan</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19483677	20090729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276574	Nsd2	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome		MGI:3851518	Nsd2<sup>tm1Ykan</sup>/Nsd2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19483677	20090729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:8997	polycythemia vera		MGI:5320790	Jak2<sup>tm1Mohi</sup>/Jak2<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22144185	20120608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:8997	polycythemia vera		MGI:5320791	Jak2<sup>tm1Mohi</sup>/Jak2<sup>tm1Mohi</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22144185	20120608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:8997	polycythemia vera		MGI:4818803	Jak2<sup>tm1.2Ble</sup>/Jak2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20541703	20120608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:8997	polycythemia vera		MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20472827	20120608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100513	Lmx1b	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3715141	Lmx1b<sup>tm4.1Rjo</sup>/Lmx1b<sup>tm4.1Rjo</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17316599	20070718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100513	Lmx1b	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:2677374	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9590288	20070718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100513	Lmx1b	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3052222	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15562281	20070718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100513	Lmx1b	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3716366	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15562281	20070718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3769724	Tomt	is_implicated_in	DOID:0110515	autosomal recessive nonsyndromic deafness 63		MGI:3805735	Tomt<sup>m1Btlr</sup>/Tomt<sup>m1Btlr</sup>  [background:] C57BL/6J-Tomt<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18794526	20081003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	is_implicated_in	DOID:0050557	congenital muscular dystrophy		MGI:5514360	Col6a3<sup>tm1Chu</sup>/Col6a3<sup>tm1Chu</sup>  [background:] B6.129-Col6a3<sup>tm1Chu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23564457	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926157	Atf6	is_implicated_in	DOID:0110009	achromatopsia 7		MGI:6883630	Atf6<sup>tm1.1Rjk</sup>/Atf6<sup>tm1.1Rjk</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26029869	20220225	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151233	Dph1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:5659969	Dph1<sup>tm2Bhr</sup>/Dph1<sup>tm2Bhr</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151233	Dph1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:5659970	Dph1<sup>tm1.1Cmch</sup>/Dph1<sup>tm1.1Cmch</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151233	Dph1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:5659973	Dph1<sup>tm1.1Cmch</sup>/Dph1<sup>tm1.1Cmch</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857442	Kcne1<sup>tm1Sfh</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:2181486	Kcne1<sup>tm1Sfh</sup>/Kcne1<sup>tm1Sfh</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:11223304	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857442	Kcne1<sup>tm1Sfh</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:2181486	Kcne1<sup>tm1Sfh</sup>/Kcne1<sup>tm1Sfh</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:11438691	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	is_implicated_in	DOID:0080074	neural tube defect		MGI:5523973	Pax3<sup>Sp-1Wli</sup>/Pax3<sup>Sp-1Wli</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	is_implicated_in	DOID:6000	congestive heart failure		MGI:5907992	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6CrSlc * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16959785	20170901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	is_implicated_in	DOID:6000	congestive heart failure		MGI:5907999	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195081	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:5544476	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3772702	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:18776951	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:10908	hydrocephalus		MGI:5056384	Ccdc39<sup>prh</sup>/Ccdc39<sup>prh</sup>  [background:] involves: A/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29317443	20180222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97772	Prox1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907122	Prox1<sup>tm2Gco</sup>/Prox1<sup>tm2Gco</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:24938781	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335106	Pikfyve	is_implicated_in	DOID:8778	Crohn's disease		MGI:5474983	Pikfyve<sup>tm2.1Tssk</sup>/Pikfyve<sup>tm2.1Tssk</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:23322734	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449121	Nme7	is_implicated_in	DOID:10908	hydrocephalus		MGI:4950028	Nme7<sup>Gt(OST31116)Lex</sup>/Nme7<sup>Gt(OST31116)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915509	Ift80	is_implicated_in	DOID:0110087	asphyxiating thoracic dystrophy 3		MGI:4942392	Ift80<sup>Gt(AN0245)Wtsi</sup>/Ift80<sup>Gt(AN0245)Wtsi</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21227999	20140216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583763	Irs2<sup>tm1Mfw</sup>/Irs2<sup>tm1Mfw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9495343	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583344	Irs2<sup>tm1Tka</sup>/Irs2<sup>tm1Tka</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11078455	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3510669	Irs2<sup>tm2Mfw</sup>/Irs2<sup>tm2Mfw</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15467829	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889576	Cntrl	is_implicated_in	DOID:12712	nephronophthisis		MGI:5442123	Cntrl<sup>b2b1468.1Clo</sup>/Cntrl<sup>b2b1468.1Clo</sup>  [background:] C57BL/6J-Cntrl<sup>b2b1468.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675250	Men1<sup>tm1.2Zqw</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:2675251	Men1<sup>tm1.2Zqw</sup>/Men1<sup>tm1.2Zqw</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:12941803	20091021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	is_implicated_in	DOID:0050591	tooth agenesis		MGI:2175120	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae-Msx1<sup>tm1Rilm</sup>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7914451	20110428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	is_implicated_in	DOID:0050591	tooth agenesis		MGI:3702323	Msx1<sup>tm1Bero</sup>/Msx1<sup>tm1Bero</sup>  [background:] B6.129P2-Msx1<sup>tm1Bero</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9256350	20110428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3583957	Wdr72	is_implicated_in	DOID:0110061	amelogenesis imperfecta hypomaturation type 2A3		MGI:5659959	Wdr72<sup>tm1a(KOMP)Wtsi</sup>/Wdr72<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25008349	20150826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:9164	achalasia		MGI:5754489	Lmna<sup>tm11Lgf</sup>/Lmna<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25652409	20160324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856959	Cln8<sup>mnd</sup>	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:2388398	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] B6.KB2/Rn-Cln8<sup>mnd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7683855	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856959	Cln8<sup>mnd</sup>	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:2388401	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] involves: AKR/J * B6.KB2			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856959	Cln8<sup>mnd</sup>	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:3588732	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] AK.B6(Cg)-Cln8<sup>mnd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856959	Cln8<sup>mnd</sup>	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:2388398	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] B6.KB2/Rn-Cln8<sup>mnd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856959	Cln8<sup>mnd</sup>	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:3588731	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] involves: B6.KB2 * C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3045547	Bbs4<sup>tm1Vcs</sup>/Bbs4<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15173597	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3055585	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:6370045	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] B6.129S7-Bbs4<sup>Gt1Nk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31479441	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3608977	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16794820	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	is_implicated_in	DOID:0110126	Bardet-Biedl syndrome 4		MGI:3525001	Bbs4<sup>tm1Vcs</sup>/Bbs4<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15539463	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:3589971	Foxp3<sup>sf</sup>/Y  [background:] involves: 101/H * C3H/HeH * STOCK MR			ECO:0000033	author statement supported by traceable reference	PMID:2320565	20051019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	is_implicated_in	DOID:0110847	xeroderma pigmentosum variant type		MGI:3615437	Polh<sup>tm1.1Rak</sup>/Polh<sup>tm1.1Rak</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16397220	20060310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	is_implicated_in	DOID:0110847	xeroderma pigmentosum variant type		MGI:3586812	Polh<sup>tm1Fmh</sup>/Polh<sup>tm1Fmh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15939880	20060310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	is_implicated_in	DOID:0110847	xeroderma pigmentosum variant type		MGI:3579244	Polh<sup>tm1Crey</sup>/Polh<sup>tm1Crey</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15824086	20060310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856845	Tmc1<sup>dn</sup>	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:2177313	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] involves: STOCK Grhl3<sup>ct</sup> * M. m. molossinus			ECO:0000033	author statement supported by traceable reference	PMID:7719036	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856845	Tmc1<sup>dn</sup>	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:2177312	Tmc1<sup>dn</sup>/Tmc1<sup>dn</sup>  [background:] STOCK Grhl3<sup>ct</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:48774	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333878	Xirp1	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:3656023	Xirp1<sup>tm1Jl</sup>/Xirp1<sup>tm1Jl</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:17766470	20170810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	is_implicated_in	DOID:0080046	Stickler syndrome		MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861928	Gad2<sup>tm1Bae</sup>	is_not_implicated_in	DOID:13366	Stiff-Person syndrome		MGI:2177574	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9391152	20060203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861928	Gad2<sup>tm1Bae</sup>	is_not_implicated_in	DOID:13366	Stiff-Person syndrome		MGI:2177575	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * NOD			ECO:0000033	author statement supported by traceable reference	PMID:9391152	20060203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3699203	Sall4<sup>tm1Ryn</sup>/Sall4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16790473	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3617910	Sall4<sup>Gt(XE027)Byg</sup>/Sall4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16380715	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3617909	Sall4<sup>Gt(XE027)Byg</sup>/Sall4<sup>+</sup>  [background:] B6;129P2-Sall4<sup>Gt(XE027)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16380715	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3698627	Sall4<sup>tm1Brd</sup>/Sall4<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17216607	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	is_implicated_in	DOID:0050795	cone dystrophy		MGI:6716878	Yap1<sup>tm1.1Hmc</sup>/Yap1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * BALB/c * C57BL/6 * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:32801350	20210622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3838162	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>tm1Kat</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12468647	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3838163	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12468647	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:2174710	Prnp<sup>tm1Edin</sup>/Prnp<sup>tm1Edin</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Edin</sup>/EdinH			ECO:0000033	author statement supported by traceable reference	PMID:10581259	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:2174709	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1373228	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:2174712	Prnp<sup>tm1Rcm</sup>/Prnp<sup>tm1Rcm</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Rcm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9462739	20050830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180364	Cav1<sup>tm1Mls</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3843497	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19342371	20090511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97830	Pygm	is_implicated_in	DOID:2746	glycogen storage disease V		MGI:5696978	Pygm<sup>tm1.1Adru</sup>/Pygm<sup>tm1.1Adru</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22730558	20151123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3690223	Serpine1<sup>tm1Mlg</sup>/Serpine1<sup>tm1Mlg</sup>  [background:] B6.129S2-Serpine1<sup>tm1Mlg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23919993	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	is_implicated_in	DOID:0080111	mitochondrial complex III deficiency nuclear type 1		MGI:6387277	Bcs1l<sup>tm1.1Levp</sup>/Bcs1l<sup>tm1.1Levp</sup>  [background:] B6.129-Bcs1l<sup>tm1.1Levp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28424480	20200131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3697681	Comt<sup>tm1Kara</sup>/Comt<sup>tm1Kara</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:18469803	20111003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	is_implicated_in	DOID:3762	cytochrome-c oxidase deficiency disease		MGI:5758892	Sco1<sup>tm1c(KOMP)Wtsi</sup>/Sco1<sup>tm1c(KOMP)Wtsi</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA			ECO:0000033	author statement supported by traceable reference	PMID:25683716	20160411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526691	Frem1<sup>bat</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665272	Frem1<sup>bat</sup>/Frem1<sup>bat</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712962	Hspg2<sup>tm1Rdgr</sup>	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3713118	Hspg2<sup>tm1Rdgr</sup>/Hspg2<sup>tm1Rdgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17213231	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044226	Foxl2<sup>tm1Gpil</sup>	is_implicated_in	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome		MGI:3044667	Foxl2<sup>tm1Gpil</sup>/Foxl2<sup>tm1Gpil</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)			ECO:0000033	author statement supported by traceable reference	PMID:15056605	20071022	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:5501040	Hps1<sup>ep-7J</sup>/Hps1<sup>ep-7J</sup>  [background:] CAST/EiJ-Hps1<sup>ep-7J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5499306	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:3586967	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6232310	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:3588311	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] B6.C3Fe-Hps1<sup>ep</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:7520358	Tafazzin<sup>em1Xfa</sup>/Y Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: C57BL/6NCrl * MF1			ECO:0000033	author statement supported by traceable reference	PMID:34129362	20230824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856596	Coc	is_implicated_in	DOID:83	cataract		MGI:2175789	Coc/Coc<sup>+</sup>  [background:] involves: 101 * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856596	Coc	is_implicated_in	DOID:83	cataract		MGI:2175788	Coc/Coc  [background:] involves: 101 * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3576479	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	is_implicated_in	DOID:14330	Parkinson's disease		MGI:7378801	Vps35<sup>tm1.1Mjff</sup>/Vps35<sup>tm1.1Mjff</sup>  [background:] B6.Cg-Vps35<sup>tm1.1Mjff</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33745227	20221107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156742	Pax6<sup>3Neu</sup>	is_implicated_in	DOID:0060673	Peters anomaly		MGI:3590307	Pax6<sup>3Neu</sup>/Pax6<sup>+</sup>  [background:] either: (involves: 102 * C3H) or (involves: C3H)			ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:11720	distal myopathy		MGI:2661118	Dysf<sup>tm1Kcam</sup>/Dysf<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12736685	20090630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:11720	distal myopathy		MGI:2175836	Dysf<sup>im</sup>/Dysf<sup>im</sup>  [background:] involves: SJL			ECO:0000033	author statement supported by traceable reference	PMID:10508505	20090630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:11720	distal myopathy		MGI:3055578	Dysf<sup>tm1Meho</sup>/Dysf<sup>tm1Meho</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20090630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	is_implicated_in	DOID:11720	distal myopathy		MGI:3055667	Dysf<sup>prmd</sup>/Dysf<sup>prmd</sup>  [background:] A/J			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20090630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96214	hph1	is_implicated_in	DOID:9281	phenylketonuria		MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:3360305	20060726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96214	hph1	is_implicated_in	DOID:9281	phenylketonuria		MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:15144277	20060726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:2669009	Wt1<sup>tm1Jae</sup>/Wt1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * MF1			ECO:0000033	author statement supported by traceable reference	PMID:17071579	20170216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5824267	Wt1<sup>tm1.1Ndha</sup>/Wt1<sup>tm1.1Ndha</sup> Tg(Gata4*G2-cre)#Roja/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27642710	20170216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104873	Aga	is_implicated_in	DOID:0050461	aspartylglucosaminuria		MGI:3043584	Aga<sup>tm1Pltn</sup>/Aga<sup>tm1Pltn</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9425233	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104873	Aga	is_implicated_in	DOID:0050461	aspartylglucosaminuria		MGI:3045972	Aga<sup>tm1Vk</sup>/Aga<sup>tm1Vk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8946839	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:3716639	Pink1<sup>tm1Shn</sup>/Pink1<sup>tm1Shn</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17563363	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:4941907	Pink1<sup>tm1Hbu</sup>/Pink1<sup>tm1Hbu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21249202	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:5436309	Pink1<sup>tm1.1Wrst</sup>/Pink1<sup>tm1.1Wrst</sup>  [background:] involves: 129S2/SvPas * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22265660	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:3850371	Pink1<sup>tm1Aub</sup>/Pink1<sup>tm1Aub</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:19492057	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101939	Hmgcs2	is_implicated_in	DOID:0081168	HMG-CoA synthase 2 deficiency		MGI:7329791	Hmgcs2<sup>em1(IMPC)Tcp</sup>/Hmgcs2<sup>em1(IMPC)Tcp</sup>  [background:] C57BL/6NCrl-Hmgcs2<sup>em1(IMPC)Tcp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35421611	20220921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101939	Hmgcs2	is_implicated_in	DOID:0081168	HMG-CoA synthase 2 deficiency		MGI:7329792	Hmgcs2<sup>em1(IMPC)Tcp</sup>/Hmgcs2<sup>+</sup>  [background:] C57BL/6NCrl-Hmgcs2<sup>em1(IMPC)Tcp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35421611	20220921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108050	Ext2	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:3608784	Ext2<sup>tm1Werb</sup>/Ext2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16236767	20051230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181200	Gata3<sup>tm1Gsv</sup>	is_implicated_in	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome		MGI:3693614	Gata3<sup>tm1Gsv</sup>/Gata3<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15207274	20070115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181200	Gata3<sup>tm1Gsv</sup>	is_implicated_in	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome		MGI:3693366	Gata3<sup>tm1Gsv</sup>/Gata3<sup>+</sup>  [background:] FVB.129(B6)-Gata3<sup>tm1Gsv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15994092	20070115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	is_implicated_in	DOID:0060590	XFE progeroid syndrome		MGI:3804449	Ercc1<sup>tm1Jhjh</sup>/Ercc1<sup>tm1Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17183314	20080904	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711021	Bicc1<sup>tm1Emdr</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3711062	Bicc1<sup>tm1Emdr</sup>/Bicc1<sup>tm1Emdr</sup>  [background:] B6SJL-Bicc1<sup>tm1Emdr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3710978	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	is_implicated_in	DOID:12305	Bloch-Sulzberger syndrome		MGI:3844910	Ikbkg<sup>tm1Mpa</sup>/Ikbkg<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10911992	20090520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	is_implicated_in	DOID:12305	Bloch-Sulzberger syndrome		MGI:3621818	Ikbkg<sup>tm1Mka</sup>/Ikbkg<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10911991	20090520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104627	Dst	is_implicated_in	DOID:0070151	hereditary sensory and autonomic neuropathy type 6		MGI:6160388	Dst<sup>dt-23Rbrc</sup>/Dst<sup>dt-23Rbrc</sup>  [background:] involves: C3H/HeN * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27693510	20180612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442949	Zfp804a	is_implicated_in	DOID:5419	schizophrenia		MGI:6828730	Zfp804a<sup>em1Yqd</sup>/Zfp804a<sup>em1Yqd</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:33303946	20211201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612537	Ar<sup>tm4(AR)Dmr</sup>	is_not_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3614453	Ar<sup>tm4(AR)Dmr</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16400023	20060303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	is_implicated_in	DOID:2106	myotonia congenita		MGI:6725721	Clcn1<sup>em1Btlr</sup>/Clcn1<sup>em1Btlr</sup>  [background:] C57BL/6J-Clcn1<sup>em1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	is_implicated_in	DOID:2106	myotonia congenita		MGI:6725719	Clcn1<sup>m1Btlr</sup>/Clcn1<sup>m1Btlr</sup>  [background:] C57BL/6J-Clcn1<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	is_implicated_in	DOID:2106	myotonia congenita		MGI:3581032	Clcn1<sup>adr-mto</sup>/Clcn1<sup>adr-mto</sup>  [background:] SWR/J-Clcn1<sup>adr-mto</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8119941	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	is_implicated_in	DOID:2106	myotonia congenita		MGI:4835907	Clcn1<sup>adr</sup>/Clcn1<sup>adr</sup>  [background:] A2G-Clcn1<sup>adr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1653899	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907999	Sod2<sup>tm1Shs</sup>/Sod2<sup>tm1Shs</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195081	20170901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857183	Icam1<sup>tm1Bay</sup>	is_implicated_in	DOID:12365	malaria		MGI:3766730	Icam1<sup>tm1Bay</sup>/Icam1<sup>tm1Bay</sup>  [background:] B6.129S7-Icam1<sup>tm1Bay</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12769195	20130314	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360669	Tg(Eno2-ATN1)3Tx	is_implicated_in	DOID:0060162	dentatorubral-pallidoluysian atrophy		MGI:4360690	Tg(Eno2-ATN1)3Tx/Tg(Eno2-ATN1)3Tx  [background:] B6.Cg-Tg(Eno2-ATN1)3Tx			ECO:0000033	author statement supported by traceable reference	PMID:16407196	20091007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918961	Mus81	is_implicated_in	DOID:0050645	arterial tortuosity syndrome		MGI:3794044	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17293478	20080617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3843174	Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup> Ep300<sup>tm2Reck</sup>/Ep300<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17513743	20090506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95401	Epb41	is_implicated_in	DOID:2373	hereditary elliptocytosis		MGI:2449959	Epb41<sup>tm1Cnby</sup>/Epb41<sup>tm1Cnby</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9927493	20080321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4441058	Tubb3<sup>tm1.1Ece</sup>	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:4441061	Tubb3<sup>tm1.1Ece</sup>/Tubb3<sup>tm1.1Ece</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20074521	20100423	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5431488	b2b1436Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5431539	b2b1436Clo/b2b1436Clo  [background:] C57BL/6J-b2b1436Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856649	Alm	is_implicated_in	DOID:83	cataract		MGI:2175695	Alm/Alm<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920963	Rbm20	is_implicated_in	DOID:0110447	dilated cardiomyopathy 1DD		MGI:6477029	Rbm20<sup>em1Hide</sup>/Rbm20<sup>em1Hide</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33110103	20220509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920963	Rbm20	is_implicated_in	DOID:0110447	dilated cardiomyopathy 1DD		MGI:7275231	Rbm20<sup>em1Hgra</sup>/Rbm20<sup>em1Hgra</sup>  [background:] C57BL/6-Rbm20<sup>em1Hgra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35041844	20220509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920963	Rbm20	is_implicated_in	DOID:0110447	dilated cardiomyopathy 1DD		MGI:7275232	Rbm20<sup>em1Hgra</sup>/Rbm20<sup>+</sup>  [background:] C57BL/6-Rbm20<sup>em1Hgra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35041844	20220509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:4834658	Ccn1<sup>tm1Lfl</sup>/Ccn1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17023674	20101013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050453	lissencephaly		MGI:4359205	Arx<sup>tm2Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22565167	20130716	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050453	lissencephaly		MGI:2451237	Arx<sup>tm1Kki</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:12379852	20130716	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	is_implicated_in	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		MGI:4881338	Foxp3<sup>sf</sup>/Y  [background:] B6.Cg-Foxp3<sup>sf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19661482	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	is_implicated_in	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		MGI:3589925	Foxp3<sup>sf</sup>/Y  [background:] either: 129Rl.Cg-Foxp3<sup>sf</sup> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)			ECO:0000033	author statement supported by traceable reference	PMID:11137992	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437240	Ext1<sup>tm1.1Vcs</sup>	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:4437608	Ext1<sup>tm1.1Vcs</sup>/Ext1<sup>tm1.1Vcs</sup> Tg(Col2a1-rtTA,tetO-cre)22Pjro/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20080592	20171214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437240	Ext1<sup>tm1.1Vcs</sup>	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:6101207	Ext1<sup>tm1.1Vcs</sup>/Ext1<sup>tm1.1Vcs</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28445472	20171214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157350	Chrd<sup>tm1Emdr</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:2676545	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup>  [background:] either: B6SJL.129-Chrd<sup>tm1Emdr</sup> or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)			ECO:0000033	author statement supported by traceable reference	PMID:12810603	20070104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857162	Klf1<sup>tm1Sho</sup>	is_implicated_in	DOID:12241	beta thalassemia		MGI:2181627	Klf1<sup>tm1Sho</sup>/Klf1<sup>tm1Sho</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7753195	20121113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452857	Il33<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5790841	Il33<sup>tm1(KOMP)Vlcg</sup>/Il33<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Il33<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28675392	20190405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153005	Itga7<sup>tm1Umr</sup>	is_implicated_in	DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency		MGI:3583813	Itga7<sup>tm1Umr</sup>/Itga7<sup>tm1Umr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12588796	20100614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:7276257	Mbd2<sup>tm1Bh</sup>/Mbd2<sup>tm1Bh</sup>  [background:] NOD.129P2(B6)-Mbd2<sup>tm1Bh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34420035	20220512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352749	Cabp2	is_implicated_in	DOID:0110537	autosomal recessive nonsyndromic deafness 93		MGI:6155766	Cabp2<sup>tm1b(KOMP)Mbp</sup>/Cabp2<sup>tm1b(KOMP)Mbp</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28183797	20180511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	is_implicated_in	DOID:8986	narcolepsy		MGI:3763455	Hcrt<sup>tm1Ywa</sup>/Hcrt<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10481909	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	is_implicated_in	DOID:8986	narcolepsy		MGI:4949137	Hcrt<sup>tm1Ywa</sup>/Hcrt<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:12797957	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:3688418	Gba1<sup>tm1Karl</sup>/Gba1<sup>tm1.1Karl</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16954197	20230524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:3688419	Gba1<sup>tm1.1Karl</sup>/Gba1<sup>tm1.1Karl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16954197	20230524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:7484465	Gba1<sup>tm1.1Smoc</sup>/Gba1<sup>tm1.1Smoc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:35711931	20230524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:4867689	Gba1<sup>tm1.1Pmis</sup>/Gba1<sup>tm1.2Pmis</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20962279	20230524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:4867688	Gba1<sup>tm1.1Pmis</sup>/Gba1<sup>tm1.1Pmis</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20962279	20230524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:3699178	Gba1<sup>tm1Clk</sup>/Gba1<sup>tm1.1Clk</sup> Tg(Tek-cre)12Flv/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17079175	20230524	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856085	Mitf<sup>Mi</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:78359	20060201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96062	Hdc	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:3620632	Hdc<sup>tm1Nagy</sup>/Hdc<sup>tm1Nagy</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24411733	20151130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96062	Hdc	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:5697374	Hdc<sup>tm1Nagy</sup>/Hdc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24411733	20151130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	is_implicated_in	DOID:1612	breast cancer		MGI:5565367	Met<sup>tm4Gvw</sup>/Met<sup>+</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19567831	20140527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158701	C1qa<sup>tm1Mjw</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:4452482	C1qa<sup>tm1Mjw</sup>/C1qa<sup>tm1Mjw</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:20375278	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856877	Smpd3<sup>fro</sup>	is_implicated_in	DOID:0110341	osteogenesis imperfecta type 2		MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8456819	20130702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:3832641	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm2(FCMD)Ttd</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:19017726	20121009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:5435675	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S/SvEv * FVB			ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:5435674	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Tg(CAG-cre/Esr1*)5Amc/?  [background:] involves: 129S/SvEv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:5435676	Fktn<sup>tm1Kcam</sup>/Fktn<sup>tm1Kcam</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:22922256	20121009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:3577900	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm1Ttd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15837576	20121009	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922300	Kif27	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429550	Kif27<sup>Gt(OST441915)Lex</sup>/Kif27<sup>Gt(OST441915)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	is_implicated_in	DOID:9250	acrocallosal syndrome		MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99402	Adora2a	is_implicated_in	DOID:11830	myopia		MGI:3622794	Adora2a<sup>tm1Jfc</sup>/Adora2a<sup>tm1Jfc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20484596	20101006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583991	Gt(ROSA)26Sor<sup>tm1(HD*103Q)Xwy</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3584454	Emx1<sup>tm1(cre)Ito</sup>/? Gt(ROSA)26Sor<sup>tm1(HD*103Q)Xwy</sup>/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15882643	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857556	Dbh<sup>tm1Rpa</sup>	is_implicated_in	DOID:0090145	dopamine beta-hydroxylase deficiency		MGI:2175826	Dbh<sup>tm1Rpa</sup>/Dbh<sup>tm1Rpa</sup>  [background:] either: (involves: 129S7/SvEvBrd * 129/SvCpj) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7715704	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:10923	sickle cell anemia		MGI:3766996	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] either: (B6.D1-Spta1<sup>sph-ha</sup> x WB.D1-Spta1<sup>sph-ha</sup>)F1 or (WB.D1-Spta1<sup>sph-ha</sup> x B6.D1-Spta1<sup>sph-ha</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:8355480	20080109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459094	Tg(Mbp-Pad2)28Fgm	is_implicated_in	DOID:2377	multiple sclerosis		MGI:4459095	Tg(Mbp-Pad2)28Fgm/Tg(Mbp-Pad2)28Fgm  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19093029	20100712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4459094	Tg(Mbp-Pad2)28Fgm	is_implicated_in	DOID:2377	multiple sclerosis		MGI:4459096	Tg(Mbp-Pad2)28Fgm/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19093029	20100712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443207	Plekhm1	is_implicated_in	DOID:0110945	autosomal recessive osteopetrosis 6		MGI:5896639	Plekhm1<sup>tm1.2Hzhao</sup>/Plekhm1<sup>tm1.2Hzhao</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27777970	20170712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443207	Plekhm1	is_implicated_in	DOID:0110945	autosomal recessive osteopetrosis 6		MGI:5896640	Ctsk<sup>tm1(cre)Ska</sup>/Ctsk<sup>+</sup> Plekhm1<sup>tm1.1Hzhao</sup>/Plekhm1<sup>tm1.1Hzhao</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:27777970	20170712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712802	Eng<sup>tm2.1Hma</sup>	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:5501108	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22571958	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890773	Actn4	is_implicated_in	DOID:0111128	focal segmental glomerulosclerosis 1		MGI:2669775	Actn4<sup>tm1Mrpk</sup>/Actn4<sup>tm1Mrpk</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12782671	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	is_implicated_in	DOID:0060253	scapuloperoneal myopathy		MGI:5706792	Fhl1<sup>tm1.1Mihi</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J * C57BL/6NJ			ECO:0000033	author statement supported by traceable reference	PMID:25274776	20170925	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	is_implicated_in	DOID:0080450	developmental and epileptic encephalopathy 17		MGI:5620503	Gnao1<sup>tm2.1Rneu</sup>/Gnao1<sup>+</sup>  [background:] B6.129S-Gnao1<sup>tm2.1Rneu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24700286	20190501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	is_implicated_in	DOID:0080450	developmental and epileptic encephalopathy 17		MGI:6295359	Gnao1<sup>tm2Rneu</sup>/Gnao1<sup>+</sup>  [background:] B6.129S1-Gnao1<sup>tm2Rneu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30682176	20190501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	is_implicated_in	DOID:0080450	developmental and epileptic encephalopathy 17		MGI:6295357	Gnao1<sup>em1Rneu</sup>/Gnao1<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:30682176	20190501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344352	Dido1	is_implicated_in	DOID:4972	myelodysplastic/myeloproliferative neoplasm		MGI:3604722	Dido1<sup>tm1Cmar</sup>/Dido1<sup>tm1Cmar</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16127461	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039264	Trp53<sup>tm2.1Tyj</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584463	Trp53<sup>tm2.1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851210	Tg(Scn1a*)RH9Aesc	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:3851211	Tg(Scn1a*)RH9Aesc/0  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:19409490	20090724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3723258	Tg(Prnp-SNCA*A53T)AAub	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3723272	Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21684039	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3723258	Tg(Prnp-SNCA*A53T)AAub	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5639272	Tg(Prnp-SNCA*A53T)AAub/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25297088	20150612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3723258	Tg(Prnp-SNCA*A53T)AAub	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3723272	Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22722052	20150612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:5464901	Ndufs4<sup>tm1Capt</sup>/Ndufs4<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:19460290	20130218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351617	Abca3	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3711224	Abca3<sup>tm1Nina</sup>/Abca3<sup>tm1Nina</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17267394	20070807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351617	Abca3	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3717470	Abca3<sup>tm1Holz</sup>/Abca3<sup>tm1Holz</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17577581	20070807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351617	Abca3	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3707163	Abca3<sup>tm1Frm</sup>/Abca3<sup>tm1Frm</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:17142808	20070807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	is_implicated_in	DOID:1686	glaucoma		MGI:6275112	Pitx2<sup>egl1</sup>/Pitx2<sup>egl1</sup>  [background:] C57BL/6J-Pitx2<sup>egl1</sup>/Boc			ECO:0000033	author statement supported by traceable reference	MGI:6275025	20190129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3620916	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11855819	20060502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3620917	Lmna<sup>tm1Stw</sup>/Lmna<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11855819	20060502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813487	Ppp1r13l<sup>wa3-J</sup>	is_implicated_in	DOID:0050737	autosomal recessive disease		MGI:3836904	Ppp1r13l<sup>wa3-J</sup>/Ppp1r13l<sup>wa3-J</sup>  [background:] BALB/cJ-Ppp1r13l<sup>wa3-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28069640	20190702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98640	Tcte1	is_implicated_in	DOID:12336	male infertility		MGI:6111404	Tcte1<sup>tm1a(KOMP)Wtsi</sup>/Tcte1<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Tcte1<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28630322	20180123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3576481	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] C.Cg-Aire<sup>tm1Mmat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3576479	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3576483	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] B6.Cg-Aire<sup>tm1Mmat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793701	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] NOD.129S2(B6)-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793702	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] C.129S2-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793703	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] SJL.129S2-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3793700	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] B6.129S2-Aire<sup>tm1.1Doi</sup>/Doi			ECO:0000033	author statement supported by traceable reference	PMID:16172259	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:2182941	Aire<sup>tm1Pltn</sup>/Aire<sup>tm1Pltn</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11854172	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:2661915	Aire<sup>tm1.1Doi</sup>/Aire<sup>tm1.1Doi</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12376594	20080616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106065	Ppm1g	is_implicated_in	DOID:5419	schizophrenia		MGI:3606460	Ppm1g<sup>tm1Dgen</sup>/Ppm1g<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:5140950	Cdh23<sup>v-bus</sup>/Cdh23<sup>v-bus</sup>  [background:] involves: KYF/MsIdr			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3581030	Cdh23<sup>v-7J</sup>/Cdh23<sup>v-7J</sup>  [background:] CByJ(Cg)-Cdh23<sup>v-7J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3778632	Cdh23<sup>v</sup>/Cdh23<sup>v</sup>  [background:] involves: fancier's stocks			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:5050420	Cdh23<sup>v-4J</sup>/Cdh23<sup>v-4J</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3722079	Cdh23<sup>v-3J</sup>/Cdh23<sup>+</sup>  [background:] C57BL/6J-Cdh23<sup>v-3J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3722083	Cdh23<sup>v-J</sup>/Cdh23<sup>v-J</sup>  [background:] B6.C-H2-K<sup>bm1</sup>/ByJ			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3722081	Cdh23<sup>v-5J</sup>/Cdh23<sup>v-5J</sup>  [background:] involves: SENCARA/PtJ			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3714862	Cdh23<sup>v-ngt</sup>/Cdh23<sup>v-ngt</sup>  [background:] involves: ICR * MSM			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:2654804	Cdh23<sup>v-Alb</sup>/Cdh23<sup>v-Alb</sup>  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11138008	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3581028	Cdh23<sup>v-2J</sup>/Cdh23<sup>v-2J</sup>  [background:] B6(V)-Cdh23<sup>v-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11138008	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3714868	Cdh23<sup>v-6J</sup>/Cdh23<sup>v-6J</sup>  [background:] B10.A-H2<sup>h4</sup>/(4R)SgDvEgJ-Cdh23<sup>v-6J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11138008	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:2174785	Trp63<sup>tm1Fmc</sup>/Trp63<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10227294	20201203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:3588183	Trp63<sup>tm1Brd</sup>/Trp63<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10227293	20201203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:3511141	Trp63<sup>tm2Brd</sup>/Trp63<sup>tm2Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10227293	20201203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:6477390	Trp63<sup>tm3Aam</sup>/Trp63<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:23775923	20201203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:3622113	Jup<sup>tm1Kem</sup>/Jup<sup>tm1Kem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8954745	20060512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388035	Htt<sup>tm1.1Tna</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3699097	Htt<sup>tm1.1Tna</sup>/Htt<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11494364	20070307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388035	Htt<sup>tm1.1Tna</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3699093	Htt<sup>tm1.1Tna</sup>/Htt<sup>tm1.1Tna</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11494364	20070307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920963	Rbm20	is_implicated_in	DOID:0060224	atrial fibrillation		MGI:6477029	Rbm20<sup>em1Hide</sup>/Rbm20<sup>em1Hide</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33110103	20201202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	is_implicated_in	DOID:12712	nephronophthisis		MGI:4367783	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>tm1Jgg</sup> Tg(TCF/Lef1-lacZ)34Efu/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19718039	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	is_implicated_in	DOID:0080050	acromesomelic dysplasia, Maroteaux type		MGI:3806086	Npr2<sup>slw</sup>/Npr2<sup>slw</sup>  [background:] involves: C57BL/6 * DDY			ECO:0000033	author statement supported by traceable reference	PMID:17728275	20080916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3347	osteosarcoma		MGI:5521544	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:3347	osteosarcoma		MGI:5521546	Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 Tg(tetO-RNAi:Trp53)ASlowe/0  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:23486187	20131205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055491	Bbs1<sup>Gt1Nk</sup>	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1		MGI:3055584	Bbs1<sup>Gt1Nk</sup>/Bbs1<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20050603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183508	Tg(Prnp-ATXN7*92Q)6076Als	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:3712499	Tg(Prnp-ATXN7*92Q)6076Als/0  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12077187	20180815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183508	Tg(Prnp-ATXN7*92Q)6076Als	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:3712499	Tg(Prnp-ATXN7*92Q)6076Als/0  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16936724	20180815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183508	Tg(Prnp-ATXN7*92Q)6076Als	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:3712499	Tg(Prnp-ATXN7*92Q)6076Als/0  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11580893	20180815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261791	Apba2	is_not_implicated_in	DOID:10652	Alzheimer's disease		MGI:3697817	Apba2<sup>tm1Tsuz</sup>/Apba2<sup>tm1Tsuz</sup>  [background:] C57BL/6-Apba2<sup>tm1Tsuz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19420255	20100122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926179	Polr3h	is_implicated_in	DOID:5426	primary ovarian insufficiency		MGI:6696394	Polr3h<sup>em2Cfe</sup>/Polr3h<sup>em2Cfe</sup>  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:30830215	20210506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662307	Ppp1r3c<sup>tm1Ars</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:4429442	Ppp1r3c<sup>tm1Ars</sup>/Ppp1r3c<sup>+</sup>  [background:] B6.129-Ppp1r3c<sup>tm1Ars</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12727934	20100218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	is_implicated_in	DOID:0080021	Schmid metaphyseal chondrodysplasia		MGI:4397575	Col10a1<sup>tm1.1Rpbh</sup>/Col10a1<sup>tm1.1Rpbh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19834559	20181213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	is_implicated_in	DOID:0080021	Schmid metaphyseal chondrodysplasia		MGI:6259994	Col10a1<sup>tm2.1Rpbh</sup>/Col10a1<sup>+</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:30010889	20181213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	is_implicated_in	DOID:0080021	Schmid metaphyseal chondrodysplasia		MGI:6259995	Col10a1<sup>tm2.1Rpbh</sup>/Col10a1<sup>tm2.1Rpbh</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:30010889	20181213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179968	F8<sup>tm2Kaz</sup>	is_implicated_in	DOID:12134	factor VIII deficiency		MGI:2449546	F8<sup>tm2Kaz</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7647782	20200113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721902	Casq2<sup>tm2Jse</sup>	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:3723302	Casq2<sup>tm2Jse</sup>/Casq2<sup>tm2Jse</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17607358	20090821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386595	Vegfa<sup>tm4Pec</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3628757	Vegfa<sup>tm4Pec</sup>/Vegfa<sup>tm4Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12539040	20060711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796583	Enam<sup>tm1.1Jcch</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:5708536	Enam<sup>tm1.1Jcch</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24603688	20160216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796583	Enam<sup>tm1.1Jcch</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:5708531	Enam<sup>tm1.1Jcch</sup>/Enam<sup>tm1.1Jcch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24603688	20160216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696673	Glra1<sup>tm1Betz</sup>	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:3698026	Glra1<sup>tm1Betz</sup>/Glra1<sup>tm1Betz</sup>  [background:] B6.129P2-Glra1<sup>tm1Betz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17114051	20070227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917176	Dnah17	is_implicated_in	DOID:0111926	spermatogenic failure 39		MGI:6695074	Dnah17<sup>em1Qsh</sup>/Dnah17<sup>em1Qsh</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:31658987	20210427	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:3695051	Irf6<sup>Gt(OST398253)Lex</sup>/Irf6<sup>Gt(OST398253)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17041601	20070326	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:3693809	Irf6<sup>tm1Mjd</sup>/Irf6<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17041603	20070326	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174990	Psen1<sup>tm1Bdes</sup>/Psen1<sup>tm1Bdes</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9450754	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174994	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Mpm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9883847	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2684657	Psen1<sup>tm1Vln</sup>/Psen1<sup>tm1Vln</sup> Tg(Thy1-cre)1Vln/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11978821	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3589555	Psen1<sup>tm1Tak</sup>/Psen1<sup>tm1Tak</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15908021	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174998	Psen1<sup>tm1Shn</sup>/Psen1<sup>tm1Shn</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9160754	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3702925	Psen1<sup>tm1Mpm</sup>/Psen1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15207348	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3045183	Psen1<sup>tm1Jzt</sup>/Psen1<sup>tm1Jzt</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11738035	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182068	Tg(NEFH)200Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2183672	Tg(NEFH)200Jpj/Tg(NEFH)200Jpj  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182068	Tg(NEFH)200Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2183678	Tg(NEFH)200Jpj/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5467352	b2b1963Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5467392	b2b1963Clo/b2b1963Clo  [background:] C57BL/6J-b2b1963Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448063	Lrrc10	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905195	Lrrc10<sup>tm1Sgt</sup>/Lrrc10<sup>tm1Sgt</sup>  [background:] B6.129P2-Lrrc10<sup>tm1Sgt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23236519	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:4970465	20190929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12655058	20190929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:3042029	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12702666	20190929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158381	Mecom<sup>Jbo</sup>	is_implicated_in	DOID:10754	otitis media		MGI:6102908	Mecom<sup>Jbo</sup>/Mecom<sup>+</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20057387	20171218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158381	Mecom<sup>Jbo</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3689583	Mecom<sup>Jbo</sup>/Mecom<sup>+</sup>  [background:] C3N.C-Mecom<sup>Jbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17029558	20171218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856179	Otc<sup>spf-ash</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:2175223	Otc<sup>spf-ash</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:3162766	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856179	Otc<sup>spf-ash</sup>	is_implicated_in	DOID:9271	ornithine carbamoyltransferase deficiency		MGI:3851332	Otc<sup>spf-ash</sup>/Y  [background:] B6EiC3Sn a/A-Otc<sup>spf-ash</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:16497529	20090727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:3586560	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:9150142	20151124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:5697073	Ercc6<sup>tm1Gvh</sup>/Ercc6<sup>tm1Gvh</sup>  [background:] B6J.129P2-Ercc6<sup>tm1Gvh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25762674	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180096	Adam9<sup>tm1Bbl</sup>	is_implicated_in	DOID:0111020	cone-rod dystrophy 9		MGI:4360909	Adam9<sup>tm1Bbl</sup>/Adam9<sup>tm1Bbl</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:19409519	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106299	Slx4	is_implicated_in	DOID:0090066	Fanconi-like syndrome		MGI:5559492	Slx4<sup>tm1.2Jrou</sup>/Slx4<sup>tm1.2Jrou</sup>  [background:] B6.129P2-Slx4<sup>tm1.2Jrou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24076219	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3028634	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm1Antc</sup>  [background:] 129-Nphs2<sup>tm1Antc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14701729	20190709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3028633	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm1Antc</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14701729	20190709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:6316681	Nphs2<sup>tm2.1Antc</sup>/Nphs2<sup>tm3.1Antc</sup> Tg(CAG-cre/Esr1*)86Lbgn/0  [background:] involves: 129S2/SvPas * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:29049388	20190709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:4847559	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm3.1Antc</sup> Tg(CAG-cre/Esr1*)86Lbgn/0  [background:] involves: 129 * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:19713307	20190709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2144765	Pld4	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4950056	Pld4<sup>thss</sup>/Pld4<sup>thss</sup>  [background:] BALB/cJ-Pld4<sup>thss</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:30679154	20190826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934258	Ihh<sup>tm1Amc</sup>	is_implicated_in	DOID:0060850	annular pancreas		MGI:3584475	Ihh<sup>tm1Amc</sup>/Ihh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:10821773	20081215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98533	Tcm	is_implicated_in	DOID:83	cataract		MGI:2174765	Tcm/Tcm<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386944	Tg(Tnfsf13b)1Fma	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3692945	Tg(Tnfsf13b)1Fma/0  [background:] B6.Cg-Tg(Tnfsf13b)1Fma			ECO:0000033	author statement supported by traceable reference	PMID:11781351	20070109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106613	Dvl2	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:2654555	Dvl2<sup>tm1Awb</sup>/Dvl2<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Dvl2<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14976138	20210927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931047	Vegfa<sup>tm1Pec</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3047228	Vegfa<sup>tm1Pec</sup>/Vegfa<sup>tm1Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12539040	20060711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345138	Spry2	is_implicated_in	DOID:9164	achalasia		MGI:3584494	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup>  [background:] B6.Cg-Spry2<sup>tm1Ayos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15937482	20050829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861923	Fas<sup>tm1Osa</sup>	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2450098	Fas<sup>tm1Osa</sup>/Fas<sup>tm1Osa</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8700897	20051011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5471728	Acvr1<sup>tm1Emsh</sup>/Acvr1<sup>+</sup>  [background:] chimera involves: BALB/c * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:22508565	20170330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5881966	Acvr1<sup>tm2.1Vlcg</sup>/Acvr1<sup>+</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: C57BL/6J * C57BL/6NTac * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:26896819	20170330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	is_implicated_in	DOID:13374	fibrodysplasia ossificans progressiva		MGI:5825038	Acvr1<sup>tm2.1Vlcg</sup>/Acvr1<sup>+</sup> Gt(ROSA)26Sor<sup>tm3.1(cre/ERT2)Vlcg</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26333933	20170330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856209	Cacna1a<sup>tg</sup>	is_implicated_in	DOID:0050835	generalized dystonia		MGI:3700786	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] B6.D2-Cacna1a<sup>tg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22850483	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384429	Hnf1a<sup>tm1.1Ylee</sup>	is_implicated_in	DOID:0111102	maturity-onset diabetes of the young type 3		MGI:3623394	Hnf1a<sup>tm1.1Ylee</sup>/Hnf1a<sup>tm1.1Ylee</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9566924	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	is_implicated_in	DOID:0050558	Ullrich congenital muscular dystrophy		MGI:6401817	Col6a1<sup>tm1Sngi</sup>/Col6a1<sup>tm1Sngi</sup>  [background:] B6.Cg-Col6a1<sup>tm1Sngi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28043812	20200327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857562	Pkd1<sup>tm1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:9326937	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857562	Pkd1<sup>tm1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:9326937	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857562	Pkd1<sup>tm1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:12514735	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857562	Pkd1<sup>tm1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857562	Pkd1<sup>tm1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531115	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>tm1Jzh</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857562	Pkd1<sup>tm1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3531216	Pkd1<sup>tm1Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:9988265	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:0060581	Noonan syndrome 3		MGI:5649287	Kras<sup>tm4.1Bbd</sup>/Kras<sup>tm4.1Bbd</sup>  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25359213	20150819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915281	Rnf146	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:6150914	Rnf146<sup>tm1.1Rtpl</sup>/Rnf146<sup>tm1.1Rtpl</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28581440	20221010	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	is_implicated_in	DOID:0110165	Charcot-Marie-Tooth disease type 2E		MGI:5751579	Nefl<sup>tm2.1Liem</sup>/Nefl<sup>+</sup>  [background:] B6.Cg-Nefl<sup>tm2.1Liem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25552649	20160310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829607	Runx2<sup>tm1Jals</sup>	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3829628	Runx2<sup>tm1Jals</sup>/Runx2<sup>tm1Jals</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19028669	20090130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857629	Phc1<sup>tm1Os</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3042302	Phc1<sup>tm1Os</sup>/Phc1<sup>tm1Os</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9367423	20101001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183903	Epb41<sup>tm1Cnby</sup>	is_implicated_in	DOID:2373	hereditary elliptocytosis		MGI:2449959	Epb41<sup>tm1Cnby</sup>/Epb41<sup>tm1Cnby</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9927493	20080321	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	is_implicated_in	DOID:450	myotonic disease		MGI:3052930	Mbnl1<sup>tm1Sws</sup>/Mbnl1<sup>tm1Sws</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14671308	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5505393	Ndst1<sup>b2b2230Clo</sup>/Ndst1<sup>b2b2230Clo</sup>  [background:] C57BL/6J-Ndst1<sup>b2b2230Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447068	Cst6<sup>ichq</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:4429796	Cst6<sup>ichq</sup>/Cst6<sup>+</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:15044380	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447068	Cst6<sup>ichq</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:4429796	Cst6<sup>ichq</sup>/Cst6<sup>+</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:9212754	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862017	Fbxo11<sup>Jf</sup>	is_implicated_in	DOID:10754	otitis media		MGI:6102909	Fbxo11<sup>Jf</sup>/Fbxo11<sup>+</sup>  [background:] involves: BALB/cAnNCrl			ECO:0000033	author statement supported by traceable reference	PMID:20057387	20171218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862017	Fbxo11<sup>Jf</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3693665	Fbxo11<sup>Jf</sup>/Fbxo11<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeN * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17035249	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342771	Klf1	is_implicated_in	DOID:12971	hereditary spherocytosis		MGI:4819280	Klf1<sup>Nan</sup>/Klf1<sup>+</sup>  [background:] either: B6.Cg-Klf1<sup>Nan</sup> or WB.Cg-Klf1<sup>Nan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19409822	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3612246	Tmprss9	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6393881	Tmprss9<sup>tm1.3Hzo</sup>/Tmprss9<sup>tm1.3Hzo</sup>  [background:] involves: 129S1/Sv * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31943016	20200311	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448730	Atcay	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia		MGI:3719706	Atcay<sup>ji-hes</sup>/Atcay<sup>ji-hes</sup>  [background:] C3H/HeJ-Atcay<sup>ji-hes</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448730	Atcay	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia		MGI:3719717	Atcay<sup>swd</sup>/Atcay<sup>swd</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448730	Atcay	is_implicated_in	DOID:0060694	Cayman type cerebellar ataxia		MGI:3719716	Atcay<sup>ji</sup>/Atcay<sup>ji</sup>  [background:] JIGR			ECO:0000033	author statement supported by traceable reference	PMID:14556008	20130606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	is_implicated_in	DOID:9883	Becker muscular dystrophy		MGI:3798606	Dmd<sup>mdx-3Cv</sup>/Y  [background:] involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus			ECO:0000033	author statement supported by traceable reference	PMID:7843915	20090929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5305070	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/c-Npc1<sup>m1N</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21303697	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2686745	Npc1<sup>nmf164</sup>/Npc1<sup>nmf164</sup>  [background:] C57BL/6J-Npc1<sup>nmf164</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22048958	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:12528192	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:4436744	Npc1<sup>m1N</sup>/Npc1<sup>tm1.2Apl</sup>  [background:] B6.Cg-Npc1<sup>m1N</sup>/Npc1<sup>tm1.2Apl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20007718	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:4436745	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] B6.C-Npc1<sup>m1N</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20007718	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5925342	Npc1<sup>m1N</sup>/Npc1<sup>tm1.1Apl</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] B6J.Cg-Npc1<sup>m1N</sup>/Npc1<sup>tm1.1Apl</sup> Tg(CAG-cre/Esr1*)5Amc			ECO:0000033	author statement supported by traceable reference	PMID:21856732	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5642030	Npc1<sup>tm1.1Dso</sup>/Npc1<sup>tm1.1Dso</sup>  [background:] B6.129-Npc1<sup>tm1.1Dso</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26019327	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3849202	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/cNctr-Npc1<sup>m1N</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22163015	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3846848	Npc1<sup>spm</sup>/Npc1<sup>spm</sup>  [background:] C57BLKS/J-Npc1<sup>spm</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7202025	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5442413	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c * C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22869680	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5293760	Npc1<sup>tm1Mbjg</sup>/Npc1<sup>tm1Mbjg</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21896731	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:6257302	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3849202	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] BALB/cNctr-Npc1<sup>m1N</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24391715	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3044831	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: 129S1/Sv * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15071184	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18160655	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:23843985	20171120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:2386738	Npc1<sup>m1N</sup>/Npc1<sup>m1N</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:9950794	20171120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412099	Prnp<sup>tm2Lnq</sup>	is_implicated_in	DOID:0050433	fatal familial insomnia		MGI:4412280	Prnp<sup>tm2Lnq</sup>/Prnp<sup>tm2Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23959875	20140227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412099	Prnp<sup>tm2Lnq</sup>	is_implicated_in	DOID:0050433	fatal familial insomnia		MGI:4412280	Prnp<sup>tm2Lnq</sup>/Prnp<sup>tm2Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:19709627	20140227	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:0060545	Hermansky-Pudlak syndrome 7		MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:1936982	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:0060545	Hermansky-Pudlak syndrome 7		MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:12923531	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443409	Gpr179	is_implicated_in	DOID:0110869	congenital stationary night blindness 1E		MGI:5431492	Gpr179<sup>nob5</sup>/Gpr179<sup>nob5</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:22325362	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316740	Morc1	is_implicated_in	DOID:1595	melancholic depression		MGI:5766068	Morc1<sup>Tg(Tyr)1Az</sup>/Morc1<sup>Tg(Tyr)1Az</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26275923	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	is_implicated_in	DOID:2352	hemochromatosis		MGI:3576233	B2m<sup>tm1Jae</sup>/B2m<sup>tm1Jae</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8013958	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667300	Tg(Amhr2-SV40TAg)1Dcco	is_implicated_in	DOID:2394	ovarian cancer		MGI:4839563	Tg(Amhr2-SV40TAg)1Dcco/0  [background:] (C57BL/6 x C3H)F1			ECO:0000033	author statement supported by traceable reference	PMID:12649204	20101128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361267	Tbx22<sup>tm1.1Sta</sup>	is_implicated_in	DOID:0060613	X-linked cleft palate with or without ankyloglossia		MGI:4361283	Tbx22<sup>tm1.1Sta</sup>/Tbx22<sup>tm1.1Sta</sup>  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19648291	20091013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361267	Tbx22<sup>tm1.1Sta</sup>	is_implicated_in	DOID:0060613	X-linked cleft palate with or without ankyloglossia		MGI:4361326	Tbx22<sup>tm1.1Sta</sup>/Y  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19648291	20091013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580102	Pparg<sup>tm1Lja</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:3580111	Pparg<sup>tm1Lja</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15716267	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	is_implicated_in	DOID:2352	hemochromatosis		MGI:2429787	Hmox1<sup>tm1Poss</sup>/Hmox1<sup>tm1Poss</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9380735	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934157	Cilk1	is_implicated_in	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome		MGI:6759479	Cilk1<sup>tm1.1Zfu</sup>/Cilk1<sup>tm1.1Zfu</sup>  [background:] B6.Cg-Cilk1<sup>tm1.1Zfu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28380258	20210917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934157	Cilk1	is_implicated_in	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome		MGI:5693602	Cilk1<sup>tm1a(KOMP)Mbp</sup>/Cilk1<sup>tm1a(KOMP)Mbp</sup>  [background:] C57BL/6N-Cilk1<sup>tm1a(KOMP)Mbp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24853502	20210917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934157	Cilk1	is_implicated_in	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome		MGI:6759479	Cilk1<sup>tm1.1Zfu</sup>/Cilk1<sup>tm1.1Zfu</sup>  [background:] B6.Cg-Cilk1<sup>tm1.1Zfu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29098359	20210917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5775312	Cc2d2a<sup>tm1Asw</sup>/Cc2d2a<sup>tm1Asw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24947469	20160608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385198	Usp1	is_implicated_in	DOID:13636	Fanconi anemia		MGI:3838389	Usp1<sup>tm1.1Ada</sup>/Usp1<sup>tm1.1Ada</sup>  [background:] C57BL/6-Usp1<sup>tm1.1Ada</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19217432	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2152936	Srgap1	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:7442509	Srgap1<sup>tm1a(KOMP)Wtsi</sup>/Srgap1<sup>tm1a(KOMP)Wtsi</sup> Six2<sup>tm1(tTA,tetO-EGFP/cre)Amc</sup>/Six2<sup>+</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33514561	20230309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95391	Enc	is_implicated_in	DOID:83	cataract		MGI:3583154	Enc/Enc<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920036	Tdp1	is_implicated_in	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1		MGI:3818341	Tdp1<sup>Gt(XD105)Byg</sup>/Tdp1<sup>Gt(XD105)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17914460	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447846	Tg(Pcp2-SCA7)P7EJman	is_implicated_in	DOID:0050958	spinocerebellar ataxia type 7		MGI:4398718	Tg(Pcp2-SCA7)P7EJman/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11030754	20190626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:6195853	Arx<sup>tm1.1Ics</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29659809	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:4353223	Arx<sup>tm1.1Jno</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19587282	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:4359207	Arx<sup>tm4Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22565167	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:6196032	Arx<sup>tm4Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6NHsd			ECO:0000033	author statement supported by traceable reference	PMID:28602636	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:6196031	Arx<sup>tm5Kki</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6NHsd			ECO:0000033	author statement supported by traceable reference	PMID:28602636	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:3844352	Arx<sup>tm1Gldn</sup>/Y Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129/Sv * C57BL/6 * CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19439424	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:3844353	Arx<sup>tm1Gldn</sup>/Arx<sup>+</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129/Sv * C57BL/6 * CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19439424	20180829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857751	Mitf<sup>mi-enu122</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857751	Mitf<sup>mi-enu122</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	is_implicated_in	DOID:9406	hypopituitarism		MGI:3575735	Smpd3<sup>tm1Wst</sup>/Smpd3<sup>tm1Wst</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:15764706	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522096	Irf6<sup>Gt(OST398253)Lex</sup>	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:3695051	Irf6<sup>Gt(OST398253)Lex</sup>/Irf6<sup>Gt(OST398253)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17041601	20070130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856316	Clcn1<sup>adr</sup>	is_implicated_in	DOID:2106	myotonia congenita		MGI:4835907	Clcn1<sup>adr</sup>/Clcn1<sup>adr</sup>  [background:] A2G-Clcn1<sup>adr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1653899	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5883306	Il2ra<sup>tm1Dw</sup>/Il2ra<sup>tm1Dw</sup>  [background:] B6.129S4-Il2ra<sup>tm1Dw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17207605	20170417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652346	App<sup>tm1.1Cep</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652362	App<sup>tm1.1Cep</sup>/App<sup>tm1.1Cep</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652346	App<sup>tm1.1Cep</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652363	App<sup>tm1.1Cep</sup>/App<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20050510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845222	Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>	is_implicated_in	DOID:674	cleft palate		MGI:6470640	Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>/Six2<sup>tm3(EGFP/cre/ERT2)Amc</sup>  [background:] involves: 129/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31765609	20221108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96073	Hexa	is_implicated_in	DOID:3320	Tay-Sachs disease		MGI:2177433	Hexa<sup>tm1Rlp</sup>/Hexa<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7937929	20050713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96073	Hexa	is_implicated_in	DOID:3320	Tay-Sachs disease		MGI:2668037	Hexa<sup>tm1Grv</sup>/Hexa<sup>tm1Grv</sup>  [background:] involves: 129P2/Ola * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8789434	20050713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96073	Hexa	is_implicated_in	DOID:3320	Tay-Sachs disease		MGI:3581542	Hexa<sup>tm1Cota</sup>/Hexa<sup>tm1Cota</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8747922	20050713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	is_implicated_in	DOID:0080026	otospondylomegaepiphyseal dysplasia, autosomal recessive		MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575405	Smpd3<sup>tm1Wst</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3575735	Smpd3<sup>tm1Wst</sup>/Smpd3<sup>tm1Wst</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:15764706	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384179	Cfh<sup>tm1Mbo</sup>	is_implicated_in	DOID:2920	membranoproliferative glomerulonephritis		MGI:2662550	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12091909	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856102	Atp7a<sup>Mo-vbr</sup>	is_not_implicated_in	DOID:890	mitochondrial encephalomyopathy		MGI:3793729	Atp7a<sup>Mo-vbr</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9342151	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	is_not_implicated_in	DOID:0050646	distal arthrogryposis		MGI:2451231	Fbn2<sup>fp</sup>/Fbn2<sup>fp</sup>  [background:] C3Fe(B6)-Fbn2<sup>fp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11285249	20050831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	is_not_implicated_in	DOID:0050646	distal arthrogryposis		MGI:2451233	Fbn2<sup>fp-2J</sup>/Fbn2<sup>fp-2J</sup>  [background:] involves: C57BL/6J * C.B10-H2<sup>b</sup>/LiMcdJ			ECO:0000033	author statement supported by traceable reference	PMID:11285249	20050831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	is_implicated_in	DOID:9649	congenital nystagmus		MGI:2657002	Ahr<sup>tm1Yfk</sup>/Ahr<sup>tm1Yfk</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23301081	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105061	Clcn2	is_implicated_in	DOID:10579	leukodystrophy		MGI:5925277	Clcn2<sup>nmf289</sup>/Clcn2<sup>nmf289</sup>  [background:] CByJ.Cg-Clcn2<sup>nmf289</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:418	systemic scleroderma		MGI:5558879	Fbn1<sup>tm2.1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24107997	20140414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:418	systemic scleroderma		MGI:5558880	Fbn1<sup>tm3.1Hcd</sup>/Fbn1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24107997	20140414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919227	Zdhhc13	is_implicated_in	DOID:12858	Huntington's disease		MGI:5466506	Zdhhc13<sup>Gt(AC0492)Wtsi</sup>/Zdhhc13<sup>Gt(AC0492)Wtsi</sup>  [background:] FVB.129P2-Zdhhc13<sup>Gt(AC0492)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23077216	20130227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103266	Fgl2	is_implicated_in	DOID:0040094	autoimmune glomerulonephritis		MGI:3583697	Fgl2<sup>tm1Pam</sup>/Fgl2<sup>tm1Pam</sup>  [background:] B6.129X1-Fgl2<sup>tm1Pam</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18097026	20220531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857467	Fst<sup>tm1Zuk</sup>	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:3042286	Fst<sup>tm1Zuk</sup>/Fst<sup>tm1Zuk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7885475	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857467	Fst<sup>tm1Zuk</sup>	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:3042284	Fst<sup>tm1Zuk</sup>/Fst<sup>tm1Zuk</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7885475	20081113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3762755	Kiss1<sup>tm1Rla</sup>	is_implicated_in	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia		MGI:3762762	Kiss1<sup>tm1Rla</sup>/Kiss1<sup>tm1Rla</sup>  [background:] involves: 129S1/SvImJ			ECO:0000033	author statement supported by traceable reference	PMID:17595229	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5300249	Prickle1<sup>b2b019Clo</sup>/Prickle1<sup>b2b019Clo</sup>  [background:] C57BL/6J-Prickle1<sup>b2b019Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:3527165	Sdhd<sup>tm1Jlob</sup>/Sdhd<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15572694	20130930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:3527164	Sdhd<sup>tm1Jlob</sup>/Sdhd<sup>tm1Jlob</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15572694	20130930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:4418214	Sdhd<sup>tm1Jpb</sup>/Sdhd<sup>+</sup>  [background:] either: 129P2/OlaHsd-Sdhd<sup>tm1Jpb</sup> or (involves: 129P2/OlaHsd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:19956719	20130930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920999	Ttc7	is_implicated_in	DOID:8893	psoriasis		MGI:4366162	Ttc7<sup>fsn</sup>/Ttc7<sup>fsn</sup>  [background:] involves: A/J * BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:8406628	20170928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95390	En2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3719798	En2<sup>tm1Alj</sup>/En2<sup>tm1Alj</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16935268	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	is_implicated_in	DOID:5419	schizophrenia		MGI:5800496	Ncstn<sup>tm1.1Sud</sup>/Ncstn<sup>tm1.1Sud</sup> Olig1<sup>tm1(cre)Rth</sup>/Olig1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:27008863	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3828498	Fermt1<sup>tm1Ref</sup>	is_implicated_in	DOID:0060472	Kindler syndrome		MGI:3828513	Fermt1<sup>tm1Ref</sup>/Fermt1<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19057668	20090123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857273	Pah<sup>enu3</sup>	is_implicated_in	DOID:9281	phenylketonuria		MGI:3587816	Pah<sup>enu3</sup>/Pah<sup>enu3</sup>  [background:] involves: BTBR			ECO:0000033	author statement supported by traceable reference	PMID:8375656	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:83	cataract		MGI:2175741	Pax6<sup>132-14Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104726	Cplx2	is_implicated_in	DOID:5419	schizophrenia		MGI:5285873	Cplx2<sup>tm1Bros</sup>/Cplx2<sup>tm1Bros</sup>  [background:] B6NCrl.Cg-Cplx2<sup>tm1Bros</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20412316	20110919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:4417895	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:19893033	20200218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:3809430	Col7a1<sup>tm1Lbt</sup>/Col7a1<sup>tm1Lbt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6Crl			ECO:0000033	author statement supported by traceable reference	PMID:18382769	20200218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:3037979	Col7a1<sup>tm1Uit</sup>/Col7a1<sup>tm1Uit</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10523500	20200218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:6390913	Col7a1<sup>em#Jtol</sup>/Col7a1<sup>em#Jtol</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/Ka * NOD			ECO:0000033	author statement supported by traceable reference	PMID:28892093	20200218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0111000	Joubert syndrome 5		MGI:5749256	Cep290<sup>Gt(CC0582)Wtsi</sup>/Cep290<sup>Gt(CC0582)Wtsi</sup>  [background:] 129P2/OlaHsd-Cep290<sup>Gt(CC0582)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26301811	20160505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0111000	Joubert syndrome 5		MGI:5007766	Cep290<sup>tm1.1Jgg</sup>/Cep290<sup>tm1.1Jgg</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21623382	20160505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0111000	Joubert syndrome 5		MGI:5749256	Cep290<sup>Gt(CC0582)Wtsi</sup>/Cep290<sup>Gt(CC0582)Wtsi</sup>  [background:] 129P2/OlaHsd-Cep290<sup>Gt(CC0582)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24946806	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429559	Slc26a7<sup>tm1Sole</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:4429560	Slc26a7<sup>tm1Sole</sup>/Slc26a7<sup>tm1Sole</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:30333321	20220614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4454654	Tg(CD4-CIITA)357Ccum	is_implicated_in	DOID:11476	osteoporosis		MGI:5788295	Tg(CD4-CIITA)357Ccum/?  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24038328	20160809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99459	Nr3c2	is_implicated_in	DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1		MGI:3041700	Nr3c2<sup>tm1Gsc</sup>/Nr3c2<sup>tm1Gsc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9689096	20050913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:9256	colorectal cancer		MGI:5432239	Apc<sup>tm2Rak</sup>/Apc<sup>tm2Rak</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20080688	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:9256	colorectal cancer		MGI:5702414	Apc<sup>tm2.1Cip</sup>/Apc<sup>+</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26214133	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:9256	colorectal cancer		MGI:3513849	Apc<sup>tm1Cip</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15502862	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:9256	colorectal cancer		MGI:3844311	Apc<sup>tm1Tno</sup>/Apc<sup>+</sup> Tg(CDX2-cre)101Erf/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17942902	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:9256	colorectal cancer		MGI:2665504	Apc<sup>Min</sup>/Apc<sup>+</sup>  [background:] C57BL/6J-Apc<sup>Min</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12941845	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:9256	colorectal cancer		MGI:4456428	Apc<sup>tm1Rsmi</sup>/Apc<sup>+</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20176656	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17641777	20150330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918961	Mus81	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3794044	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17293478	20080617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	is_implicated_in	DOID:0060856	right atrial isomerism		MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10574770	20060503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	is_implicated_in	DOID:0060856	right atrial isomerism		MGI:3043046	Cfc1<sup>tm1Mms</sup>/Cfc1<sup>tm1Mms</sup>  [background:] either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10521397	20060503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:6479076	Col4a5<sup>em1Keha</sup>/Y  [background:] C57BL/6J-Col4a5<sup>em1Keha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30582011	20201214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610503	Col4a5<sup>tm1Yseg</sup>/Y  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15153557	20201214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610502	Col4a5<sup>tm1Yseg</sup>/Col4a5<sup>+</sup>  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15153557	20201214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610502	Col4a5<sup>tm1Yseg</sup>/Col4a5<sup>+</sup>  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23707242	20201214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610503	Col4a5<sup>tm1Yseg</sup>/Y  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23707242	20201214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367596	Tg(tetO-HTR4*D100A)2Niss	is_implicated_in	DOID:1858	McCune Albright syndrome		MGI:5643856	Tg(Col1a1-tTA)139Niss/0 Tg(tetO-HTR4*D100A)2Niss/0  [background:] FVB/N-Tg(Col1a1-tTA)139Niss Tg(tetO-HTR4*D100A)2Niss			ECO:0000033	author statement supported by traceable reference	PMID:24788917	20150708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107846	Prmt1	is_implicated_in	DOID:674	cleft palate		MGI:7378837	Prmt1<sup>tm1Rchd</sup>/Prmt1<sup>tm1Rchd</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:29986157	20221107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444646	Hpdl	is_implicated_in	DOID:1289	neurodegenerative disease		MGI:7447442	Hpdl<sup>em1Jgg</sup>/Hpdl<sup>em1Jgg</sup>  [background:] C57BL/6-Hpdl<sup>em1Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33188300	20230327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158345	Ccr2<sup>tm1Mae</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3841005	Ccr2<sup>tm1Mae</sup>/Ccr2<sup>tm1Mae</sup>  [background:] B6.129P2-Ccr2<sup>tm1Mae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918993	Coasy	is_implicated_in	DOID:0110740	neurodegeneration with brain iron accumulation 6		MGI:6491890	Coasy<sup>tm1.1Vtr</sup>/Coasy<sup>tm1.1Vtr</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129 * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33352696	20210114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926955	Nf2<sup>tm2Gth</sup>	is_implicated_in	DOID:0111252	vestibular schwannomatosis		MGI:5619302	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Postn-cre)1Sjc/0  [background:] involves: 129P2/OlaHsd * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:25113746	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351651	Yme1l1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5805256	Yme1l1<sup>tm1Tlan</sup>/Yme1l1<sup>tm1Tlan</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: C57BL/6 * C57BL/6NCrl * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26785494	20170929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916330	Gmppa	is_implicated_in	DOID:0112321	alacrima, achalasia, and impaired intellectual development syndrome		MGI:6711469	Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>/Gmppa<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33755596	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0110354	retinitis pigmentosa 19		MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0110354	retinitis pigmentosa 19		MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311336	b2b386Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312335	b2b386Clo/b2b386Clo  [background:] C57BL/6J-b2b386Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918615	Pdss2	is_implicated_in	DOID:0050730	coenzyme Q10 deficiency disease		MGI:3611217	Pdss2<sup>kd</sup>/Pdss2<sup>kd</sup>  [background:] CBA/H-Pdss2<sup>kd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23150520	20130711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2138070	Lamb2<sup>tm1Jrs</sup>	is_implicated_in	DOID:2527	nephrosis		MGI:2175097	Lamb2<sup>tm1Jrs</sup>/Lamb2<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:7670489	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	is_implicated_in	DOID:0080092	myofibrillar myopathy 1		MGI:2652059	Ldb3<sup>tm1Chen</sup>/Ldb3<sup>tm1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11696561	20060404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	is_implicated_in	DOID:0090118	congenital amegakaryocytic thrombocytopenia		MGI:2686902	Mpl<sup>tm1Fjs</sup>/Mpl<sup>tm1Fjs</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10611229	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96702	Krt5	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:3582826	Krt5<sup>tm1Tmm</sup>/Krt5<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11408584	20050802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857090	Whrn<sup>wi</sup>	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5538400	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857090	Whrn<sup>wi</sup>	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14098314	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857090	Whrn<sup>wi</sup>	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6034501	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857090	Whrn<sup>wi</sup>	is_implicated_in	DOID:0110490	autosomal recessive nonsyndromic deafness 31		MGI:3036713	Whrn<sup>wi</sup>/Whrn<sup>wi</sup>  [background:] involves: C57BL/6J * STOCK a Tyrp1<sup>b</sup> Myo5a<sup>d</sup> Oca2<sup>p</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12124769	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:10283	prostate cancer		MGI:5566610	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17363566	20140602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856965	Large1<sup>myd</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:3605230	Large1<sup>myd</sup>/Large1<sup>myd</sup>  [background:] B6.Cg-Large1<sup>myd</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:16111892	20101116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856399	Col11a1<sup>cho</sup>	is_implicated_in	DOID:0080046	Stickler syndrome		MGI:2174906	Col11a1<sup>cho</sup>/Col11a1<sup>cho</sup>  [background:] involves: C57BL/6Fr			ECO:0000033	author statement supported by traceable reference	PMID:7859283	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:2388401	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] involves: AKR/J * B6.KB2			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:3588731	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] involves: B6.KB2 * C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:3588732	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] AK.B6(Cg)-Cln8<sup>mnd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:2388398	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] B6.KB2/Rn-Cln8<sup>mnd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10191135	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	is_implicated_in	DOID:0110723	neuronal ceroid lipofuscinosis 8		MGI:2388398	Cln8<sup>mnd</sup>/Cln8<sup>mnd</sup>  [background:] B6.KB2/Rn-Cln8<sup>mnd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7683855	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	is_implicated_in	DOID:2030	anxiety disorder		MGI:3045711	Htr1a<sup>tm1Rhn</sup>/Htr1a<sup>tm1Rhn</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:9826725	20110201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	is_implicated_in	DOID:2030	anxiety disorder		MGI:4881537	Htr1a<sup>tm1Rhn</sup>/Htr1a<sup>tm1Rhn</sup>  [background:] involves: 129S/SvEv * 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:20152131	20110201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3845396	Rho<sup>Tvrm1</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4455026	Rho<sup>Tvrm1</sup>/Rho<sup>+</sup>  [background:] C57BL/6J-Rho<sup>Tvrm1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20207741	20130619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202304	Gnmt	is_implicated_in	DOID:0111037	glycine N-methyltransferase deficiency		MGI:3842683	Gnmt<sup>tm1Ymac</sup>/Gnmt<sup>tm1Ymac</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17937387	20090504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202304	Gnmt	is_implicated_in	DOID:0111037	glycine N-methyltransferase deficiency		MGI:3640329	Gnmt<sup>tm1Cwa</sup>/Gnmt<sup>tm1Cwa</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16779654	20090504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95760	Slc6a9	is_implicated_in	DOID:9268	glycine encephalopathy		MGI:2682534	Slc6a9<sup>tm1Betz</sup>/Slc6a9<sup>tm1Betz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14622582	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096368	Ap1b1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104750	Nrcam	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4461155	Nrcam<sup>tm1Gmt</sup>/Nrcam<sup>tm1Gmt</sup>  [background:] involves: 129S6/SvEvTac * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:19540269	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3051587	Alpl<sup>Hpp</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:3722926	Alpl<sup>Hpp</sup>/Alpl<sup>Hpp</sup>  [background:] involves: BALB/cAnN * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:17539739	20120620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3051587	Alpl<sup>Hpp</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:3722925	Alpl<sup>Hpp</sup>/Alpl<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:17539739	20120620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	is_implicated_in	DOID:0060583	Noonan syndrome 5		MGI:5445966	Raf1<sup>tm2.1Ara</sup>/Raf1<sup>tm2.1Ara</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:22826437	20121214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	is_implicated_in	DOID:0060583	Noonan syndrome 5		MGI:5003451	Raf1<sup>tm1.1Bgn</sup>/Raf1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCr			ECO:0000033	author statement supported by traceable reference	PMID:21339642	20121214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856555	Myo6<sup>sv</sup>	is_implicated_in	DOID:0110495	autosomal recessive nonsyndromic deafness 37		MGI:3528185	Myo6<sup>sv</sup>/Myo6<sup>sv</sup>  [background:] involves: B10.HA/(33NX)Sn * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7493015	20060201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858225	Tuba8	is_not_implicated_in	DOID:0090132	complex cortical dysplasia with other brain malformations 7		MGI:6094276	Tuba8<sup>tm1.2Ctpd</sup>/Tuba8<sup>tm1.2Ctpd</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28388629	20171204	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914411	Sclt1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:6110829	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>/Sclt1<sup>Tg(CAG-sb10)1Dla</sup>  [background:] FVB/N-Sclt1<sup>Tg(CAG-sb10)1Dla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28486600	20180118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384063	Pafah1b1<sup>tm2.2Awb</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2664130	Pafah1b1<sup>tm2.2Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3616079	Dnaaf5	is_implicated_in	DOID:12336	male infertility		MGI:7569326	Dnaaf5<sup>em1Slb</sup>/Dnaaf5<sup>em1Slb</sup>  [background:] C57BL/6-Dnaaf5<sup>em1Slb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37104040	20231229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861803	Cd38<sup>tm1Lnd</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623958	Cd38<sup>tm1Lnd</sup>/Cd38<sup>tm1Lnd</sup>  [background:] NOD.129P2(B6)-Cd38<sup>tm1Lnd</sup>/LtJ			ECO:0000033	author statement supported by traceable reference	PMID:16585549	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096362	Nrxn2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5632308	Nrxn2<sup>tm1Sud</sup>/Nrxn2<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J * C57BL/6NClr			ECO:0000033	author statement supported by traceable reference	PMID:25423136	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5637428	Polg<sup>tm1Prol</sup>/Polg<sup>tm1Prol</sup>  [background:] B6J.129S7-Polg<sup>tm1Prol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19734452	20150527	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3033142	Mrgprd	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6275457	Mrgprd<sup>tm5Mjz</sup>/Mrgprd<sup>tm5Mjz</sup>  [background:] B6.129S1-Mrgprd<sup>tm5Mjz</sup>/Mmnc			ECO:0000033	author statement supported by traceable reference	PMID:30339496	20190131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918017	Prpf3	is_not_implicated_in	DOID:0110356	retinitis pigmentosa 18		MGI:3820247	Prpf3<sup>Gt(RRO284)Byg</sup>/Prpf3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18552388	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95789	Gnrh1	is_implicated_in	DOID:0090072	hypogonadotropic hypogonadism 12 with or without anosmia		MGI:2663794	Gnrh1<sup>hpg</sup>/Gnrh1<sup>hpg</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:198666	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	is_implicated_in	DOID:0080505	Cornelia de Lange syndrome 1		MGI:4367868	Nipbl<sup>Gt(RRS564)Byg</sup>/Nipbl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19763162	20230626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	is_implicated_in	DOID:0080505	Cornelia de Lange syndrome 1		MGI:7491942	Nipbl<sup>Gt(RRS564)Byg</sup>/Nipbl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:32800293	20230626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:7284280	Tardbp<sup>tm1.1Hiok</sup>/Tardbp<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:6187717	Tardbp<sup>em1Rhbr</sup>/Tardbp<sup>em1Rhbr</sup>  [background:] C57BL/6J-Tardbp<sup>em1Rhbr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29556029	20220608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome		MGI:2179030	Pten<sup>tm1Mak</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10910075	20050708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome		MGI:2179045	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9990064	20050708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome		MGI:2179025	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9697695	20050708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2663583	Epas1<sup>tm1Pec</sup>	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:2663596	Epas1<sup>tm1Pec</sup>/Epas1<sup>tm1Pec</sup>  [background:] involves: 129/Sv * Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12053176	20110217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3759844	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] B6.129P2-Il10<sup>tm1Cgn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17574631	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2665845	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8770874	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3759844	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] B6.129P2-Il10<sup>tm1Cgn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17617560	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2665845	Il10<sup>tm1Cgn</sup>/Il10<sup>tm1Cgn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8402911	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577723	Abca1<sup>tm1Jp</sup>	is_implicated_in	DOID:1388	Tangier disease		MGI:3578113	Abca1<sup>tm1Jp</sup>/Abca1<sup>tm1Jp</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * B6.Cg-Tg(Alb-cre)21Mgn/J			ECO:0000033	author statement supported by traceable reference	PMID:15841208	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:4442633	Pax2<sup>M1Bpb</sup>/Pax2<sup>+</sup>  [background:] C57BL/6-Pax2<sup>M1Bpb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20221250	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:4442635	Pax2<sup>M1Bpb</sup>/Pax2<sup>M1Bpb</sup>  [background:] C57BL/6-Pax2<sup>M1Bpb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20221250	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:3694692	Pax2<sup>tm1Pgr</sup>/Pax2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8951055	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:2677317	Pax2<sup>tm1Pgr</sup>/Pax2<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8951055	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:5442586	Pax2<sup>1Neu</sup>/Pax2<sup>+</sup>  [background:] involves: 102 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:17881463	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:3694699	Pax2<sup>tm1Pgr</sup>/Pax2<sup>tm1Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15242798	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915841	Mocos	is_implicated_in	DOID:0070453	xanthinuria type II		MGI:7495807	Mocos<sup>em2(IMPC)Ics</sup>/Mocos<sup>em2(IMPC)Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35372998	20230731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388890	Phex<sup>Hyp-Duk</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3037642	Phex<sup>Hyp-Duk</sup>/Y  [background:] involves: BALB/cAnBomUrd			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1197013	Rasa3	is_implicated_in	DOID:12449	aplastic anemia		MGI:6378723	Rasa3<sup>scat</sup>/Rasa3<sup>scat</sup>  [background:] involves: BALB/cBy * BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:29922180	20191202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	is_implicated_in	DOID:0090128	Carvajal syndrome		MGI:3574845	Dsp<sup>rul</sup>/Dsp<sup>rul</sup>  [background:] RB156Bnr/Ei-Dsp<sup>rul</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25659760	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180818	Maoa<sup>Tg(H2-K1-Ifnb1)8Seif</sup>	is_implicated_in	DOID:0060693	Brunner Syndrome		MGI:3620543	Maoa<sup>Tg(H2-K1-Ifnb1)8Seif</sup>/Y  [background:] involves: C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:7792602	20160801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5439184	Traf3ip2<sup>tm1.1Lix</sup>/Traf3ip2<sup>tm1.1Lix</sup>  [background:] C.129-Traf3ip2<sup>tm1.1Lix</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18624351	20121024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1889070	C4b<sup>tm1Crr</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3663104	C4b<sup>tm1Crr</sup>/C4b<sup>tm1Crr</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11067882	20061009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653126	Krt14<sup>tm1Der</sup>	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:3812201	Krt14<sup>tm1Der</sup>/Krt14<sup>+</sup> Tg(KRT5-cre/PGR)1Der/?  [background:] involves: 129X1/SvJ * FVB * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653126	Krt14<sup>tm1Der</sup>	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:3812200	Krt14<sup>tm1Der</sup>/Krt14<sup>+</sup> Tg(KRT14-cre/PGR)1Der/?  [background:] involves: 129X1/SvJ * FVB * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	is_implicated_in	DOID:1474	aggressive periodontitis		MGI:3629331	Postn<sup>tm1Sjc</sup>/Postn<sup>tm1Sjc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16314533	20060718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581892	Mafa<sup>tm1Staka</sup>	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3582680	Mafa<sup>tm1Staka</sup>/Mafa<sup>tm1Staka</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:15923615	20050729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	is_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:2175768	Cdkn1c<sup>tm1Sje</sup>/Cdkn1c<sup>tm1Sje</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9144284	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511172	Tg(Ela1-Myc)158Bri	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5432344	Tg(Ela1-Myc)158Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1986386	20120828	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	is_implicated_in	DOID:0050425	restless legs syndrome		MGI:4839954	Drd3<sup>tm1Dac</sup>/Drd3<sup>tm1Dac</sup>  [background:] B6.129S4-Drd3<sup>tm1Dac</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15601940	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3806986	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:17567478	20160113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4829790	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:20837017	20160113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5702658	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15199412	20160113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456368	Tg(KRT5-IKBKB)2Armz	is_implicated_in	DOID:2723	dermatitis		MGI:4456370	Tg(KRT5-IKBKB)2Armz/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20200541	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420947	Jag1<sup>Ndr</sup>	is_implicated_in	DOID:9245	Alagille syndrome		MGI:6356371	Jag1<sup>Ndr</sup>/Jag1<sup>Ndr</sup>  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29162437	20190820	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678250	Hr<sup>rhsl</sup>	is_implicated_in	DOID:0060689	atrichia with papular lesions		MGI:3052308	Hr<sup>rhsl</sup>/Hr<sup>rhsl</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:15955095	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934580	Trp63<sup>tm2Brd</sup>	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:3511141	Trp63<sup>tm2Brd</sup>/Trp63<sup>tm2Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10227293	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178429	Zfp366	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5645264	Zfp366<sup>b2b2834Clo</sup>/Zfp366<sup>b2b2834Clo</sup>  [background:] C57BL/6J-Zfp366<sup>b2b2834Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857235	Prf1<sup>tm1Sdz</sup>	is_implicated_in	DOID:2377	multiple sclerosis		MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9736651	20070509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	is_implicated_in	DOID:12842	Guillain-Barre syndrome		MGI:3618096	Cd86<sup>tm1Shr</sup>/Cd86<sup>tm1Shr</sup>  [background:] NOD.129S4-Cd86<sup>tm1Shr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11535635	20090325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	is_implicated_in	DOID:12842	Guillain-Barre syndrome		MGI:3618096	Cd86<sup>tm1Shr</sup>/Cd86<sup>tm1Shr</sup>  [background:] NOD.129S4-Cd86<sup>tm1Shr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19050296	20090325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891217	Zfp423	is_implicated_in	DOID:2786	cerebellar disease		MGI:3693287	Zfp423<sup>nur12</sup>/Zfp423<sup>nur12</sup>  [background:] involves: BALB/c * C57BL/6 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:17151198	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	is_implicated_in	DOID:3627	aortic aneurysm		MGI:4947945	Efemp2<sup>tm1.1Hiya</sup>/Efemp2<sup>tm1.2Hiya</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23636094	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:3580111	Pparg<sup>tm1Lja</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15716267	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579514	Glb1<sup>tm1Adz</sup>	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3581423	Glb1<sup>tm1Adz</sup>/Glb1<sup>tm1Adz</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15687347	20050712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579514	Glb1<sup>tm1Adz</sup>	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3581421	Glb1<sup>tm1Adz</sup>/Glb1<sup>tm1Adz</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9063740	20050712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857034	Foxp3<sup>sf</sup>	is_implicated_in	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		MGI:3589925	Foxp3<sup>sf</sup>/Y  [background:] either: 129Rl.Cg-Foxp3<sup>sf</sup> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)			ECO:0000033	author statement supported by traceable reference	PMID:11137992	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857034	Foxp3<sup>sf</sup>	is_implicated_in	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome		MGI:4881338	Foxp3<sup>sf</sup>/Y  [background:] B6.Cg-Foxp3<sup>sf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19661482	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685418	Gm572	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612338	Fscn2<sup>tm2Sykk</sup>	is_implicated_in	DOID:0110406	retinitis pigmentosa 30		MGI:3612482	Fscn2<sup>tm2Sykk</sup>/Fscn2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16043865	20060210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931805	Crkl<sup>tm1Imo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2175797	Crkl<sup>tm1Imo</sup>/Crkl<sup>tm1Imo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11242111	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	is_implicated_in	DOID:12241	beta thalassemia		MGI:5460885	Hbb-b1<sup>Rbc13</sup>/Hbb-b1<sup>Rbc13</sup>  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23040355	20130128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	is_implicated_in	DOID:12241	beta thalassemia		MGI:3821602	Hbb-b1<sup>MommeD7</sup>/Hbb-b1<sup>MommeD7</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23040355	20130128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856182	sy	is_not_implicated_in	DOID:0050646	distal arthrogryposis		MGI:2451235	sy/sy  [background:] B6C3Fe-a/a			ECO:0000033	author statement supported by traceable reference	PMID:11285249	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3826780	Pkhd1<sup>tm1Gwu</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:4936857	Pkhd1<sup>tm1Gwu</sup>/Pkhd1<sup>tm1Gwu</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20875407	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3826780	Pkhd1<sup>tm1Gwu</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3826786	Pkhd1<sup>tm1Gwu</sup>/Pkhd1<sup>tm1Gwu</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18235088	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386172	Ttpa<sup>tm1Hsz</sup>	is_implicated_in	DOID:0090028	familial isolated deficiency of vitamin E		MGI:2665559	Ttpa<sup>tm1Hsz</sup>/Ttpa<sup>tm1Hsz</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11076932	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181227	Tnfrsf11b<sup>tm1Khs</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:3653631	Tnfrsf11b<sup>tm1Khs</sup>/Tnfrsf11b<sup>tm1Khs</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9647741	20210421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5560781	b2b2459Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5561312	b2b2459Clo/b2b2459Clo  [background:] C57BL/6J-b2b2459Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927222	Diaph3	is_implicated_in	DOID:1338	congenital dyserythropoietic anemia		MGI:6456066	Diaph3<sup>tm1.1Pji</sup>/Diaph3<sup>tm1.1Pji</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26471482	20200918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154695	Col1a1<sup>tm1Jcm</sup>	is_implicated_in	DOID:0110341	osteogenesis imperfecta type 2		MGI:3623481	Col1a1<sup>tm1Jcm</sup>/Col1a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:10608859	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4369232	Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>	is_implicated_in	DOID:0110718	Warburg micro syndrome 3		MGI:5629933	Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>/Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24764192	20150416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677452	Sall1<sup>tm1Mrau</sup>	is_implicated_in	DOID:0050887	Townes-Brocks syndrome		MGI:2677456	Sall1<sup>tm1Mrau</sup>/Sall1<sup>+</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12915476	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677452	Sall1<sup>tm1Mrau</sup>	is_implicated_in	DOID:0050887	Townes-Brocks syndrome		MGI:2677455	Sall1<sup>tm1Mrau</sup>/Sall1<sup>tm1Mrau</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12915476	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857431	Col3a1<sup>tm1Jae</sup>	is_implicated_in	DOID:14756	vascular type Ehlers-Danlos syndrome		MGI:2664355	Col3a1<sup>tm1Jae</sup>/Col3a1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9050868	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679446	Slitrk1	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:3834579	Slitrk1<sup>tm1Jaru</sup>/Slitrk1<sup>tm1Jaru</sup>  [background:] B6.129P2-Slitrk1<sup>tm1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18794888	20090305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156484	Mbtps1<sup>tm1Jdh</sup>	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7281134	Mbtps1<sup>tm1Jdh</sup>/Mbtps1<sup>tm1Jdh</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:29437042	20220527	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:8466	retinal degeneration		MGI:7266500	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33539865	20220504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2150920	Fgfrl1	is_implicated_in	DOID:0050460	Wolf-Hirschhorn syndrome		MGI:3849030	Fgfrl1<sup>tm1.1Ptew</sup>/Fgfrl1<sup>tm1.1Ptew</sup>  [background:] B6.129-Fgfrl1<sup>tm1.1Ptew</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19383940	20090626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617325	Pkd1<sup>tm2.1Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617390	Pkd1<sup>tm2.1Ggg</sup>/Pkd1<sup>tm2.1Ggg</sup>  [background:] involves: 129S4/SvJae * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15579506	20060323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857289	Plau<sup>tm1Mlg</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2662716	Plau<sup>tm1Mlg</sup>/Plau<sup>tm1Mlg</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15615772	20070928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920832	Camkmt	is_implicated_in	DOID:0060858	hypotonia-cystinuria syndrome		MGI:5804652	Camkmt<sup>tm1Rpav</sup>/Camkmt<sup>tm1Rpav</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25548191	20161024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920832	Camkmt	is_implicated_in	DOID:0060858	hypotonia-cystinuria syndrome		MGI:5804654	Camkmt<sup>tm1Rpav</sup>/Camkmt<sup>tm1Rpav</sup>  [background:] B6.129S7-Camkmt<sup>tm1Rpav</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25548191	20161024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858213	Clpp	is_implicated_in	DOID:0050857	Perrault syndrome		MGI:5532580	Clpp<sup>Gt(IST13563G11)Tigm</sup>/Clpp<sup>Gt(IST13563G11)Tigm</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23851121	20140129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858213	Clpp	is_implicated_in	DOID:0050857	Perrault syndrome		MGI:5532579	Clpp<sup>Gt(IST11134F10)Tigm</sup>/Clpp<sup>Gt(IST11134F10)Tigm</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23851121	20140129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4410614	Mks1<sup>krc</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:4410618	Mks1<sup>krc</sup>/Mks1<sup>krc</sup>  [background:] involves: C3HeB/FeJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19776033	20091215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655214	Tbx3<sup>tm1Pa</sup>	is_implicated_in	DOID:0060614	ulnar-mammary syndrome		MGI:2655216	Tbx3<sup>tm1Pa</sup>/Tbx3<sup>tm1Pa</sup>  [background:] either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)			ECO:0000033	author statement supported by traceable reference	PMID:12668638	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346036	Pin1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5433612	Pin1<sup>tm1Tuc</sup>/Pin1<sup>tm1Tuc</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16554819	20120912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574072	Egr2<sup>tm1Jmi</sup>	is_implicated_in	DOID:0110195	Charcot-Marie-Tooth disease type 4E		MGI:3576120	Egr2<sup>tm1Jmi</sup>/Egr2<sup>tm1Jmi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15695336	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	is_implicated_in	DOID:0110953	Waardenburg syndrome type 4A		MGI:2174949	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15294878	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	is_implicated_in	DOID:0110953	Waardenburg syndrome type 4A		MGI:2675255	Ednrb<sup>WS4</sup>/Ednrb<sup>WS4</sup>  [background:] involves: BALB/c * MSM			ECO:0000033	author statement supported by traceable reference	PMID:11773966	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6390918	Chd8<sup>tm1.1Csbd</sup>/Chd8<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30104731	20221230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:7413047	Chd8<sup>tm1Kei</sup>/Chd8<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27602517	20221230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6189103	Chd8<sup>tm2.1Kei</sup>/Chd8<sup>+</sup>  [background:] B6J.129P2-Chd8<sup>tm2.1Kei</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27602517	20221230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	is_implicated_in	DOID:0110214	cleft soft palate		MGI:5300942	Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup> Tg(KRT14-cre)52Smr/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:24496627	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4363493	Slc6a8<sup>tm1e(KOMP)Wtsi</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:6197218	Slc6a8<sup>tm1e(KOMP)Wtsi</sup>/Y  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30013483	20180910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4345389	Aspm<sup>Gt(AJ0069)Wtsi</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:4834525	Aspm<sup>Gt(AJ0069)Wtsi</sup>/Aspm<sup>Gt(AJ0069)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20823249	20101011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388392	Abcc8<sup>tm1.1Mgn</sup>	is_not_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:2446508	Abcc8<sup>tm1.1Mgn</sup>/Abcc8<sup>tm1.1Mgn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12149271	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178353	Mitf<sup>Mi-H</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178353	Mitf<sup>Mi-H</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:5578736	Crh<sup>m1H</sup>/Crh<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24302625	20171210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97305	Neu1	is_implicated_in	DOID:3343	glycoproteinosis		MGI:3719077	Neu1<sup>a</sup>/Neu1<sup>a</sup>  [background:] SM/J			ECO:0000033	author statement supported by traceable reference	PMID:9425240	20070824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97305	Neu1	is_implicated_in	DOID:3343	glycoproteinosis		MGI:3719098	Neu1<sup>tm1Adz</sup>/Neu1<sup>tm1Adz</sup>  [background:] either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * NMRI)			ECO:0000033	author statement supported by traceable reference	PMID:12023988	20070824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4126968	Mcm9<sup>Gt(XG743)Byg</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5295418	Mcm9<sup>Gt(XG743)Byg</sup>/Mcm9<sup>Gt(XG743)Byg</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690014	Tg(Myh6-TNNI3*G203S)4Chs	is_implicated_in	DOID:0110313	hypertrophic cardiomyopathy 7		MGI:3690015	Tg(Myh6-TNNI3*G203S)4Chs/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16950368	20170818	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96170	Hoxa1	is_implicated_in	DOID:0050682	Athabaskan brainstem dysgenesis syndrome		MGI:3773293	Hoxa1<sup>tm3.1Mrc</sup>/Hoxa1<sup>tm3.1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21940751	20120408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:4414022	n-TUtca2	is_implicated_in	DOID:65	connective tissue disease		MGI:4360984	n-TUtca2<sup>tm1Dhat</sup>/n-TUtca2<sup>tm1Dhat</sup> Tg(Col2a1-cre)1Bhr/0  [background:] B6.Cg-n-TUtca2<sup>tm1Dhat</sup> Tg(Col2a1-cre)1Bhr			ECO:0000033	author statement supported by traceable reference	PMID:19696890	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2450135	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] MRL/Mp-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76424	20050527	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	is_implicated_in	DOID:1949	cholecystitis		MGI:3840644	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] FVB.129P2-Abcb4<sup>tm1Bor</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14752830	20150311	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8325377	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1996978	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8155735	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10100867	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3352223	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9837751	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	MGI:62459	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	is_implicated_in	DOID:14365	systemic primary carnitine deficiency disease		MGI:3032447	Slc22a5<sup>jvs</sup>/Slc22a5<sup>jvs</sup>  [background:] C3.OH-H2<sup>o2</sup> Slc22a5<sup>jvs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9140816	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103011	Ccr7	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4430601	Ccr7<sup>tm1Rfor</sup>/Ccr7<sup>tm1Rfor</sup>  [background:] B6.129P2-Ccr7<sup>tm1Rfor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16473829	20100319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96071	Hesx1	is_implicated_in	DOID:9406	hypopituitarism		MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9620767	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	is_implicated_in	DOID:0111182	familial hemiplegic migraine 2		MGI:6729923	Atp1a2<sup>tm1.1Gica</sup>/Atp1a2<sup>+</sup>  [background:] B6.Cg-Atp1a2<sup>tm1.1Gica</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21731499	20210810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	is_implicated_in	DOID:0111182	familial hemiplegic migraine 2		MGI:6314222	Atp1a2<sup>tm1.1Tmklh</sup>/Atp1a2<sup>+</sup>  [background:] B6.129S1(Cg)-Atp1a2<sup>tm1.1Tmklh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26911348	20210810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859648	Ftsj1	is_implicated_in	DOID:0112034	non-syndromic X-linked intellectual disability 9		MGI:7341464	Ftsj1<sup>tm1Tomik</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:33771871	20220928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714454	Cby1<sup>tm1Ktkm</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21049041	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714454	Cby1<sup>tm1Ktkm</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19364920	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341884	Hey2	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2673834	Hey2<sup>tm1Uts</sup>/Hey2<sup>tm1Uts</sup>  [background:] either: (involves: 129X1/SvJ) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12372254	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387106	Crygd<sup>Aey4</sup>	is_implicated_in	DOID:0110234	cataract 4 multiple types		MGI:2387110	Crygd<sup>Aey4</sup>/Crygd<sup>+</sup>  [background:] C3HeB/FeJ-Crygd<sup>Aey4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12226711	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387106	Crygd<sup>Aey4</sup>	is_implicated_in	DOID:0110234	cataract 4 multiple types		MGI:2387109	Crygd<sup>Aey4</sup>/Crygd<sup>Aey4</sup>  [background:] C3HeB/FeJ-Crygd<sup>Aey4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12226711	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:0050745	diffuse large B-cell lymphoma		MGI:5014832	Trp53<sup>tm1.2Awbr</sup>/Trp53<sup>tm1.2Awbr</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21411755	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054784	Aipl1<sup>tm1Tili</sup>	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:3054803	Aipl1<sup>tm1Tili</sup>/Aipl1<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15365173	20050531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139535	Tprn	is_implicated_in	DOID:0110526	autosomal recessive nonsyndromic deafness 79		MGI:5897821	Tprn<sup>em1Pghu</sup>/Tprn<sup>em1Pghu</sup>  [background:] B6.Cg-Tprn<sup>em1Pghu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27693694	20170712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:5546408	Prnp<sup>tm3Lnq</sup>/Prnp<sup>tm3Lnq</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23959875	20140227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99499	Dsg3	is_implicated_in	DOID:0060851	pemphigus vulgaris		MGI:2175834	Dsg3<sup>tm1Stan</sup>/Dsg3<sup>tm1Stan</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9166409	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99499	Dsg3	is_implicated_in	DOID:0060851	pemphigus vulgaris		MGI:2175833	Dsg3<sup>bal</sup>/Dsg3<sup>bal</sup>  [background:] C57BL/6J-Dsg3<sup>bal</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9284099	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99499	Dsg3	is_implicated_in	DOID:0060851	pemphigus vulgaris		MGI:2175832	Dsg3<sup>bal-Pas</sup>/Dsg3<sup>bal-Pas</sup>  [background:] 129S2.Cg-Dsg3<sup>bal-Pas</sup>			ECO:0000033	author statement supported by traceable reference	MGI:1202169	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385918	Rxra<sup>tm1Krc</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4939884	Rxra<sup>tm1Krc</sup>/Rxra<sup>tm1Krc</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21135166	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098827	Reep1	is_implicated_in	DOID:0110782	hereditary spastic paraplegia 31		MGI:6199190	Reep1<sup>Gt(OST398247)Tigm</sup>/Reep1<sup>Gt(OST398247)Tigm</sup>  [background:] B6J.Cg-Reep1<sup>Gt(OST398247)Tigm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27638887	20180924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851815	Hdac8<sup>tm1.2Eno</sup>	is_implicated_in	DOID:0080509	Cornelia de Lange syndrome 5		MGI:7491951	Hdac8<sup>tm1.2Eno</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32800293	20230622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150344	Avpr2<sup>tm1Jwe</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:2175713	Avpr2<sup>tm1Jwe</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:11104789	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150344	Avpr2<sup>tm1Jwe</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3047777	Avpr2<sup>tm1Jwe</sup>/Avpr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:11104789	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818574	Atg16l1<sup>Gt(BC0122)Wtsi</sup>	is_implicated_in	DOID:0110885	inflammatory bowel disease 10		MGI:3818603	Atg16l1<sup>Gt(BC0122)Wtsi</sup>/Atg16l1<sup>Gt(BC0122)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18849966	20081209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916380	Vps13b	is_implicated_in	DOID:0111590	Cohen syndrome		MGI:6468047	Vps13b<sup>tm1.2Ics</sup>/Vps13b<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32915983	20201021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336894	Mocs2	is_implicated_in	DOID:0111163	molybdenum cofactor deficiency type B		MGI:5904770	Mocs2<sup>tm1(KOMP)Vlcg</sup>/Mocs2<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:27138983	20230619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177703	Gck<sup>tm1Tka</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3583686	Gck<sup>tm1Tka</sup>/Gck<sup>+</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:8530440	20050816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97930	Rlbp1	is_implicated_in	DOID:0050683	Bothnia retinal dystrophy		MGI:3038948	Rlbp1<sup>tm1Jsa</sup>/Rlbp1<sup>tm1Jsa</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11301032	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106598	Myo5b	is_implicated_in	DOID:0060775	microvillus inclusion disease		MGI:5752734	Myo5b<sup>tm1a(KOMP)Wtsi</sup>/Myo5b<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Myo5b<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26201991	20160909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106598	Myo5b	is_implicated_in	DOID:0060775	microvillus inclusion disease		MGI:5790964	Myo5b<sup>tm1.1Cle</sup>/Myo5b<sup>tm1.1Cle</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26392529	20160909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	is_implicated_in	DOID:0060230	basal ganglia calcification		MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109196	Efnb3	is_implicated_in	DOID:480	movement disease		MGI:5474304	Efnb3<sup>m1Btlr</sup>/Efnb3<sup>m1Btlr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:5474302	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178675	Tlr2<sup>tm1Aki</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:4942396	Tlr2<sup>tm1Aki</sup>/Tlr2<sup>tm1Aki</sup>  [background:] NOD.129P2-Tlr2<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17707128	20110329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857181	Hexa<sup>tm1Rlp</sup>	is_implicated_in	DOID:3320	Tay-Sachs disease		MGI:2177433	Hexa<sup>tm1Rlp</sup>/Hexa<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7937929	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87926	Adh7	is_implicated_in	DOID:14330	Parkinson's disease		MGI:4936868	Adh7<sup>tm1Gdu</sup>/Adh7<sup>tm1Gdu</sup>  [background:] B6.129(Cg)-Adh7<sup>tm1Gdu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21075145	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102567	Nrl	is_implicated_in	DOID:0090059	enhanced S-cone syndrome		MGI:5806540	Nrl<sup>tm1Asw</sup>/Nrl<sup>tm1Asw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21659555	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924832	Mboat7	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429558	Mboat7<sup>tm1Lex</sup>/Mboat7<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606688	Acadvl<sup>tm1Vje</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:3607794	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15025677	20060927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606688	Acadvl<sup>tm1Vje</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:3607794	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12893739	20060927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606688	Acadvl<sup>tm1Vje</sup>	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:3655859	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16199475	20060927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4366152	Tg(SFTPC-env)1Yhch	is_implicated_in	DOID:3910	lung adenocarcinoma		MGI:4366153	Tg(SFTPC-env)1Yhch/0  [background:] FVB/N-Tg(SFTPC-env)1Yhch			ECO:0000033	author statement supported by traceable reference	PMID:28419107	20190115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102722	Pcnt	is_implicated_in	DOID:0060609	microcephalic osteodysplastic primordial dwarfism type II		MGI:5705622	Pcnt<sup>Gt(RRU388)Byg</sup>/Pcnt<sup>Gt(RRU388)Byg</sup>  [background:] B6.129P2-Pcnt<sup>Gt(RRU388)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25220058	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857194	Il4<sup>tm1Cgn</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3622411	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] NOD.129P2-Il4<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16413168	20060516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857194	Il4<sup>tm1Cgn</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3622418	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] NOD.Cg-H2<sup>b</sup> Il4<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16413168	20060516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311334	b2b227Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437107	b2b227Clo/b2b227Clo  [background:] C57BL/6J-b2b227Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856852	Grip1<sup>eb</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665402	Grip1<sup>eb</sup>/Grip1<sup>eb</sup>  [background:] involves: ATEB/Le * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338882	Pex11b	is_implicated_in	DOID:905	Zellweger syndrome		MGI:5307126	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>tm1Sjg</sup>  [background:] B6.129-Pex11b<sup>tm1Sjg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21954064	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338882	Pex11b	is_implicated_in	DOID:905	Zellweger syndrome		MGI:5307125	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>+</sup>  [background:] B6.129-Pex11b<sup>tm1Sjg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21954064	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338882	Pex11b	is_implicated_in	DOID:905	Zellweger syndrome		MGI:3042895	Pex11b<sup>tm1Sjg</sup>/Pex11b<sup>tm1Sjg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12024045	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107172	Ppp3r1	is_implicated_in	DOID:5419	schizophrenia		MGI:3530740	Ppp3r1<sup>tm1Stl</sup>/Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl/0  [background:] C57BL/6-Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl			ECO:0000033	author statement supported by traceable reference	PMID:11733061	20070514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107172	Ppp3r1	is_implicated_in	DOID:5419	schizophrenia		MGI:3530740	Ppp3r1<sup>tm1Stl</sup>/Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl/0  [background:] C57BL/6-Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl			ECO:0000033	author statement supported by traceable reference	PMID:12851457	20070514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines		MGI:5639083	Ptpn11<sup>tm1.1Ics</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25288766	20150610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:14291	Noonan syndrome with multiple lentigines		MGI:5004709	Ptpn11<sup>tm4.2Bgn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21339643	20150610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928768	Crebbp<sup>tm1Sis</sup>	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:2175796	Crebbp<sup>tm1Sis</sup>/Crebbp<sup>+</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:9294190	20050923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919241	Ercc8	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:2663252	Ercc8<sup>tm1Jhjh</sup>/Ercc8<sup>tm1Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12509261	20151124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919241	Ercc8	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:5697079	Ercc8<sup>tm1Jhjh</sup>/Ercc8<sup>tm1Jhjh</sup>  [background:] B6J.129P2-Ercc8<sup>tm1Jhjh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25762674	20151124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9843205	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10802658	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3513510	Rpe65<sup>rd12</sup>/Rpe65<sup>rd12</sup>  [background:] B6(A)-Rpe65<sup>rd12</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15823427	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:5501103	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18296659	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14517541	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11528395	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110016	Leber congenital amaurosis 2		MGI:3039514	Rpe65<sup>tm1Tmr</sup>/Rpe65<sup>tm1Tmr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12506090	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108427	Insl3	is_implicated_in	DOID:11383	cryptorchidism		MGI:2662000	Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108427	Insl3	is_implicated_in	DOID:11383	cryptorchidism		MGI:2662181	Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108427	Insl3	is_implicated_in	DOID:11383	cryptorchidism		MGI:2661963	Insl3<sup>tm1Par</sup>/Insl3<sup>tm1Par</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10391220	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108427	Insl3	is_implicated_in	DOID:11383	cryptorchidism		MGI:2661992	Insl3<sup>tm1Par</sup>/Insl3<sup>+</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10391220	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	is_implicated_in	DOID:0080089	tubular aggregate myopathy 1		MGI:7450790	Stim1<sup>tm1.1Pg</sup>/Stim1<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31666234	20230404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923442	Abhd12	is_implicated_in	DOID:0080181	PHARC syndrome		MGI:5487655	Abhd12<sup>tm1Crv</sup>/Abhd12<sup>tm1Crv</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23297193	20130529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682493	Slc6a9<sup>tm1Betz</sup>	is_implicated_in	DOID:9268	glycine encephalopathy		MGI:2682534	Slc6a9<sup>tm1Betz</sup>/Slc6a9<sup>tm1Betz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14622582	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3717256	Ar<sup>tm1.1Jdz</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17317769	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3717244	Ar<sup>tm1.1Jdz</sup>/Y  [background:] B6.129X1-Ar<sup>tm1.1Jdz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16326839	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3036124	Ar<sup>tm1.1Verh</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14745012	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:2674328	Ar<sup>Tfm</sup>/Y  [background:] involves: STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3815199	Ar<sup>Tfm</sup>/Y  [background:] involves: NMRI * STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18401008	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:2665793	Ar<sup>Tfm</sup>/Y  [background:] STOCK Eda<sup>Ta</sup> Atp7a<sup>Mo-blo</sup>/+ +			ECO:0000033	author statement supported by traceable reference	PMID:5452809	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:2681522	Ar<sup>tm1Ska</sup>/Y Tg(CMV-cre)1Ipc/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12943692	20081118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:8398	osteoarthritis		MGI:3793864	Atp7a<sup>Mo-blo</sup>/Y  [background:] B6.Cg-Atp7a<sup>Mo-blo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8895222	20190722	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	is_implicated_in	DOID:0080005	bone remodeling disease		MGI:5578156	Idh2<sup>tm1Jwpk</sup>/Idh2<sup>tm1Jwpk</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29527922	20220527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178357	Mitf<sup>Rorp</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178357	Mitf<sup>Rorp</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:10754	otitis media		MGI:3624520	Dnah5<sup>Tg1Htz</sup>/Dnah5<sup>Tg1Htz</sup>  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11912187	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690001	Grhl3<sup>tm1Bogi</sup>	is_implicated_in	DOID:0060239	Van der Woude syndrome		MGI:5697288	Grhl3<sup>tm1Bogi</sup>/Grhl3<sup>tm1Bogi</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24360809	20151125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438932	Tg(ACTB-Eif4e)#Ppp	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5510994	Tg(ACTB-Eif4e)#Ppp/?  [background:] B6.Cg-Tg(ACTB-Eif4e)#Ppp			ECO:0000033	author statement supported by traceable reference	PMID:23263185	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384197	Irak3<sup>tm1Flv</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:3584247	Irak3<sup>tm1Flv</sup>/Irak3<sup>tm1Flv</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15809356	20050825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857951	Apc<sup>tm1Rak</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2175909	Apc<sup>tm1Rak</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8090754	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838717	Cacna1f<sup>tm1.1Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5550383	Cacna1f<sup>tm1.1Sdie</sup>/Y  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24163243	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838717	Cacna1f<sup>tm1.1Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5550384	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24163243	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838717	Cacna1f<sup>tm1.1Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3838721	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>tm1.1Sdie</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24163243	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838717	Cacna1f<sup>tm1.1Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634271	Cacna1f<sup>tm1.1Sdie</sup>/Cacna1f<sup>tm1.1Sdie</sup>  [background:] B6.Cg-Cacna1f<sup>tm1.1Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838717	Cacna1f<sup>tm1.1Sdie</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:5634270	Cacna1f<sup>tm1.1Sdie</sup>/Y  [background:] B6.Cg-Cacna1f<sup>tm1.1Sdie</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24466230	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934348	Pax6<sup>tm2Pgr</sup>	is_implicated_in	DOID:1068	juvenile glaucoma		MGI:4821786	Pax6<sup>tm2Pgr</sup>/Pax6<sup>+</sup> Tg(Pax6-cre,GFP)1Pgr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20538882	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3615496	Cdkn1a<sup>tm1Led</sup>/Cdkn1a<sup>tm1Led</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856013	Lepr<sup>db-Pas</sup>	is_implicated_in	DOID:9970	obesity		MGI:2663736	Lepr<sup>db-Pas</sup>/Lepr<sup>db-Pas</sup>  [background:] involves: DW/Pas			ECO:0000033	author statement supported by traceable reference	MGI:78566	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	is_implicated_in	DOID:0110376	retinitis pigmentosa 41		MGI:3838535	Prom1<sup>tm1Pec</sup>/Prom1<sup>tm1Pec</sup>  [background:] B6.129-Prom1<sup>tm1Pec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19228982	20141205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	is_implicated_in	DOID:0110376	retinitis pigmentosa 41		MGI:5605714	Prom1<sup>rd19</sup>/Prom1<sup>rd19</sup>  [background:] B6.BXD83-Prom1<sup>rd19</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:5605698	20141205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3709991	Abca3<sup>tm1Nina</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3711224	Abca3<sup>tm1Nina</sup>/Abca3<sup>tm1Nina</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17267394	20070807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604509	Chst3<sup>tm1Dgen</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3606703	Chst3<sup>tm1Dgen</sup>/Chst3<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856842	Prop1<sup>df</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6194978	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856842	Prop1<sup>df</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7390396	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856842	Prop1<sup>df</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14173795	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856842	Prop1<sup>df</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8934515	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856842	Prop1<sup>df</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:590190	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856842	Prop1<sup>df</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:3521856	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15459176	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	is_implicated_in	DOID:10907	microcephaly		MGI:4438359	Mcph1<sup>Gt(RRO608)Byg</sup>/Mcph1<sup>Gt(RRO608)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20169082	20110428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179738	Kcnab2<sup>tm1Kmc</sup>	is_implicated_in	DOID:0060410	chromosome 1p36 deletion syndrome		MGI:3619238	Kcnab2<sup>tm1Kmc</sup>/Kcnab2<sup>tm1Kmc</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21209188	20110225	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685574	Dnai2	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5619081	Dnai2<sup>b2b3405Clo</sup>/Dnai2<sup>b2b3405Clo</sup>  [background:] C57BL/6J-Dnai2<sup>b2b3405Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	is_implicated_in	DOID:0110848	xeroderma pigmentosum group F		MGI:3028691	Ercc4<sup>tm1Fwa</sup>/Ercc4<sup>tm1Fwa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14729965	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451061	Gusb<sup>tm3Sly</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:2451066	Gusb<sup>tm3Sly</sup>/Gusb<sup>tm3Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	is_implicated_in	DOID:2452	thrombophilia		MGI:3712469	Thbd<sup>tm2Emc</sup>/Thbd<sup>tm2Emc</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12208873	20120305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923416	Cplane2	is_implicated_in	DOID:14679	VACTERL association		MGI:5616148	Cplane2<sup>b2b2804Clo</sup>/Cplane2<sup>b2b2804Clo</sup>  [background:] C57BL/6J-Cplane2<sup>b2b2804Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665449	Apob<sup>tm1Mae</sup>	is_implicated_in	DOID:0111061	familial hypobetalipoproteinemia 2		MGI:3688001	Apob<sup>tm1Mae</sup>/Apob<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8921909	20061117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665449	Apob<sup>tm1Mae</sup>	is_implicated_in	DOID:0111061	familial hypobetalipoproteinemia 2		MGI:3688000	Apob<sup>tm1Mae</sup>/Apob<sup>tm1Mae</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8921909	20061117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665449	Apob<sup>tm1Mae</sup>	is_implicated_in	DOID:0111061	familial hypobetalipoproteinemia 2		MGI:3688001	Apob<sup>tm1Mae</sup>/Apob<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10705993	20061117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195265	Per2	is_implicated_in	DOID:0110011	advanced sleep phase syndrome 1		MGI:5906447	Per2<sup>M1Btlr</sup>/Per2<sup>M1Btlr</sup>  [background:] C57BL/6J-Per2<sup>M1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:6197761	20180913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843671	Tg(ACTB-TNFRSF6B)754Jwu	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4361591	Tg(ACTB-TNFRSF6B)754Jwu/?  [background:] B6.Cg-Tg(Actb-TNFRSF6B)754Jwu			ECO:0000033	author statement supported by traceable reference	PMID:17968950	20091016	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927073	Slc29a1	is_implicated_in	DOID:6652	diffuse idiopathic skeletal hyperostosis		MGI:6256838	Slc29a1<sup>tm1Msg</sup>/Slc29a1<sup>tm1Msg</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27237608	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856586	Cat4<sup>Apcat1-2</sup>	is_implicated_in	DOID:83	cataract		MGI:2175743	Cat4<sup>Apcat1-2</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856586	Cat4<sup>Apcat1-2</sup>	is_implicated_in	DOID:83	cataract		MGI:2175743	Cat4<sup>Apcat1-2</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623214	Fkbp1b<sup>tm1Amks</sup>	is_implicated_in	DOID:0060674	catecholaminergic polymorphic ventricular tachycardia		MGI:3623679	Fkbp1b<sup>tm1Amks</sup>/Fkbp1b<sup>tm1Amks</sup>  [background:] DBA/1LacJ-Fkbp1b<sup>tm1Amks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12837242	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182621	Prph2<sup>tm1Nmc</sup>	is_implicated_in	DOID:0110383	retinitis pigmentosa 7		MGI:3836162	Prph2<sup>tm1Nmc</sup>/Prph2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11978760	20090317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182621	Prph2<sup>tm1Nmc</sup>	is_implicated_in	DOID:0110383	retinitis pigmentosa 7		MGI:3836163	Prph2<sup>tm1Nmc</sup>/Prph2<sup>tm1Nmc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11978760	20090317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913863	Pigk	is_not_implicated_in	DOID:0112202	developmental and epileptic encephalopathy		MGI:7511860	Pigk<sup>em2Linwu</sup>/Pigk<sup>em2Linwu</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33392778	20230727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913863	Pigk	is_not_implicated_in	DOID:0112202	developmental and epileptic encephalopathy		MGI:7511857	Pigk<sup>em1Linwu</sup>/Pigk<sup>em1Linwu</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33392778	20230727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861309	Lrp6<sup>Cd</sup>	is_implicated_in	DOID:0080074	neural tube defect		MGI:2661970	Lrp6<sup>Cd</sup>/Lrp6<sup>Cd</sup>  [background:] A-Lrp6<sup>Cd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16126904	20130104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861309	Lrp6<sup>Cd</sup>	is_implicated_in	DOID:0080074	neural tube defect		MGI:2661970	Lrp6<sup>Cd</sup>/Lrp6<sup>Cd</sup>  [background:] A-Lrp6<sup>Cd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10545599	20130104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5517669	Snca<sup>tm1.1Koks</sup>/Snca<sup>+</sup>  [background:] either: B6.129P2-Snca<sup>tm1.1Koks</sup> or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:18622040	20131114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3720759	Snca<sup>tm1Rosl</sup>/Snca<sup>tm1Rosl</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10707987	20131114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525100	Abca1<sup>tm1Blt</sup>	is_implicated_in	DOID:1388	Tangier disease		MGI:3525153	Abca1<sup>tm1Blt</sup>/Abca1<sup>tm1Blt</sup>  [background:] C57BL/6-Abca1<sup>tm1Blt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15163665	20050513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:4429423	Pitx3<sup>eyl</sup>/Pitx3<sup>eyl</sup>  [background:] involves: C3H/He * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20033184	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3712364	Pitx3<sup>ak</sup>/Pitx3<sup>ak</sup>  [background:] involves: 129S1/Sv * C57BL/6 * C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:15728853	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857175	Gba1<sup>tm1Nsb</sup>	is_implicated_in	DOID:0110958	Gaucher's disease type II		MGI:2177138	Gba1<sup>tm1Nsb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1594045	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856982	Bloc1s6<sup>pa</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105115	Ctf1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5294956	Ctf1<sup>tm1Msd</sup>/Ctf1<sup>tm1Msd</sup>  [background:] B6.Cg-Ctf1<sup>tm1Msd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21803294	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:5316427	Kiss1r<sup>tm1.1Lex</sup>/Kiss1r<sup>tm1.1Lex</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:22067321	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:3614439	Kiss1r<sup>tm1Gstn</sup>/Kiss1r<sup>tm1Gstn</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:14652023	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:3530658	Kiss1r<sup>tm1Coll</sup>/Kiss1r<sup>tm1Coll</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14573733	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:3762763	Kiss1r<sup>tm1Rla</sup>/Kiss1r<sup>tm1Rla</sup>  [background:] involves: 129S1/SvImJ			ECO:0000033	author statement supported by traceable reference	PMID:17595229	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917923	Prdm16	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:7314277	Prdm16<sup>tm1.1Brsp</sup>/Prdm16<sup>tm1.1Brsp</sup> Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: 129 * C57BL/6J * MF1			ECO:0000033	author statement supported by traceable reference	PMID:34915728	20220721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387976	Nrcam<sup>tm1Gmt</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4461155	Nrcam<sup>tm1Gmt</sup>/Nrcam<sup>tm1Gmt</sup>  [background:] involves: 129S6/SvEvTac * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:19540269	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933825	Jam3	is_not_implicated_in	DOID:0111723	Jacobsen Syndrome		MGI:6388692	Jam3<sup>tm1Lex</sup>/Jam3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19533782	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437134	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17283114	20121001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:2175162	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437134	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:2175162	Nr1h4<sup>tm1Gonz</sup>/Nr1h4<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:17183066	20121001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2183449	Spata20	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:6163706	Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] FVB/NJ-Spata20<sup>Tn(pb-Act-RFP)1.1Zhu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29247744	20190226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	is_not_implicated_in	DOID:13809	familial combined hyperlipidemia		MGI:2175020	Tnfrsf1b<sup>tm1Imx</sup>/Tnfrsf1b<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9551933	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:1123	spondyloarthropathy		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:7344126	20060731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387863	Zmynd10	is_implicated_in	DOID:0110597	primary ciliary dyskinesia 22		MGI:6163475	Zmynd10<sup>tm1(KOMP)Wtsi</sup>/Zmynd10<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29601588	20180628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809457	Tg(HLA-DRA*0101,HLA-DRB1*0101)1Dmz	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3809475	Tg(HLA-DRA*0101,HLA-DRB1*0101)1Dmz/Tg(HLA-DRA*0101,HLA-DRB1*0101)1Dmz  [background:] involves: C57BL/6 * C57BL/10Sn * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:9091584	20081003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341884	Hey2	is_implicated_in	DOID:62	aortic valve disease		MGI:3620804	Hey2<sup>tm1Kkb</sup>/Hey2<sup>tm1Kkb</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23288164	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720481	Esrrb<sup>tm1.1Nat</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905569	Esrrb<sup>tm1.1Nat</sup>/Esrrb<sup>tm1.1Nat</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28130335	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3810641	Men1<sup>tm2.1Gfk</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3813539	Men1<sup>tm2.1Gfk</sup>/Men1<sup>+</sup>  [background:] involves: 129T2/SvEms * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17044021	20081103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96951	Mdm1	is_implicated_in	DOID:10871	age related macular degeneration		MGI:3826270	Mdm1<sup>m1J</sup>/Mdm1<sup>m1J</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18805803	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387011	Ripk4<sup>tm1Pmh</sup>	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:2653681	Ripk4<sup>tm1Pmh</sup>/Ripk4<sup>tm1Pmh</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22197489	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387011	Ripk4<sup>tm1Pmh</sup>	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:2653681	Ripk4<sup>tm1Pmh</sup>/Ripk4<sup>tm1Pmh</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22197488	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3588650	Chd7<sup>Whi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3589435	Chd7<sup>Whi</sup>/Chd7<sup>+</sup>  [background:] C3HeB/FeJ-Chd7<sup>Whi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36232804	20230626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3588650	Chd7<sup>Whi</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:3616771	Chd7<sup>Whi</sup>/Chd7<sup>+</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:16207732	20230626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3621811	Ppp1r15a<sup>tm1.1Ajf</sup>	is_implicated_in	DOID:10241	thalassemia		MGI:3622193	Ppp1r15a<sup>tm1.1Ajf</sup>/Ppp1r15a<sup>tm1.1Ajf</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16478986	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345961	Coro1a	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818532	Coro1a<sup>koy</sup>/Coro1a<sup>koy</sup>  [background:] C57BL/6-Coro1a<sup>koy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345961	Coro1a	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818533	Coro1a<sup>tm1Achn</sup>/Coro1a<sup>tm1Achn</sup>  [background:] B6.129X1-Coro1a<sup>tm1Achn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345961	Coro1a	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818531	Coro1a<sup>ptcd</sup>/Coro1a<sup>ptcd</sup>  [background:] B6.CTS-Coro1a<sup>ptcd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345961	Coro1a	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3818534	Coro1a<sup>ptcd</sup>/Coro1a<sup>tm1Achn</sup>  [background:] B6.Cg-Coro1a<sup>ptcd</sup> Coro1a<sup>tm1Achn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18836449	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341155	Gldc	is_implicated_in	DOID:9268	glycine encephalopathy		MGI:5766287	Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>/Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>  [background:] B6.129P2-Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25736695	20160503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857287	Serpine1<sup>tm1Mlg</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3690223	Serpine1<sup>tm1Mlg</sup>/Serpine1<sup>tm1Mlg</sup>  [background:] B6.129S2-Serpine1<sup>tm1Mlg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23919993	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137696	Mme<sup>tm1Cge</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3577843	Mme<sup>tm1Cge</sup>/Mme<sup>tm1Cge</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11375493	20050524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	is_implicated_in	DOID:0090031	D-bifunctional protein deficiency		MGI:3606112	Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10748062	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	is_implicated_in	DOID:0090031	D-bifunctional protein deficiency		MGI:3606112	Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15769750	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445461	Pax8<sup>tm1(cre)Mbu</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:2651448	Pax8<sup>tm1(cre)Mbu</sup>/Pax8<sup>tm1(cre)Mbu</sup>  [background:] involves: 129P2/OlaHsd * C3H/He * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12435636	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856664	Hgd<sup>aku</sup>	is_implicated_in	DOID:9270	alkaptonuria		MGI:3617439	Hgd<sup>aku</sup>/Hgd<sup>aku</sup>  [background:] either: (involves: 129/Sv * BALB/cByJ * NB) or (involves: 129/Sv * C57BL/6J * NB)			ECO:0000033	author statement supported by traceable reference	PMID:8188247	20060323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679260	Crb2	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5466335	Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Chx10-EGFP/cre,-ALPP)2Clc/0  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23001562	20141007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679260	Crb2	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5586690	Crb2<sup>tm1.1Wij</sup>/Crb2<sup>tm1.1Wij</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24493795	20141007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:1612	breast cancer		MGI:5759821	Trp53<sup>tm3Tyj</sup>/Trp53<sup>+</sup> Tg(Wap-cre)11738Mam/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16166291	20160412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1309480	Rtf1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:7523000	Rtf1<sup>tm1c(KOMP)Wtsi</sup>/Rtf1<sup>tm1c(KOMP)Wtsi</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:37233188	20230831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511352	Ppargc1a<sup>tm1Brsp</sup>	is_implicated_in	DOID:10871	age related macular degeneration		MGI:6389045	Ppargc1a<sup>tm1Brsp</sup>/Ppargc1a<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29925537	20200207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3871767	Aebp2<sup>Gt(BC0681)Wtsi</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5296959	Aebp2<sup>Gt(BC0681)Wtsi</sup>/Aebp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21949878	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3524971	Aipl1<sup>tm1Mad</sup>	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:3525209	Aipl1<sup>tm1Mad</sup>/Aipl1<sup>tm1Mad</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15582159	20050531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176058	Ucp2<sup>tm1Lowl</sup>	is_implicated_in	DOID:0050770	polycystic liver disease		MGI:6285862	Ucp2<sup>tm1Lowl</sup>/Ucp2<sup>tm1Lowl</sup>  [background:] B6.129S4-Ucp2<sup>tm1Lowl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29154852	20190403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861705	Itgb2<sup>tm2Bay</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:3590414	Itgb2<sup>tm2Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] involves: 129S7/SvEvBrd * PL/J			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384818	Mtss1	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5141084	Mtss1<sup>Gt(CSC156)Byg</sup>/Mtss1<sup>Gt(CSC156)Byg</sup>  [background:] B6.129P2-Mtss1<sup>Gt(CSC156)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22081072	20120912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289258	Cfap43	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:6457570	Cfap43<sup>em1Sono</sup>/Cfap43<sup>em1Sono</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:31004071	20200925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888374	Ntrk1<sup>tm1Bbd</sup>	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:2175185	Ntrk1<sup>tm1Bbd</sup>/Ntrk1<sup>tm1Bbd</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8145823	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3706992	Tlr4<sup>tm1Aki</sup>/Tlr4<sup>tm1Aki</sup>  [background:] B6.129P2-Tlr4<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17053835	20091216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155420	Myo7a<sup>3336SB</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587758	Myo7a<sup>3336SB</sup>/Myo7a<sup>3336SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2674094	Fanca<sup>tm1Wong</sup>	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A		MGI:3047131	Fanca<sup>tm1Wong</sup>/Fanca<sup>tm1Wong</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12913077	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182793	Ercc5<sup>tm1Shm</sup>	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043699	Ercc5<sup>tm1Shm</sup>/Ercc5<sup>tm1Shm</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10022922	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	is_implicated_in	DOID:0050884	triosephosphate isomerase deficiency		MGI:6188637	Tpi1<sup>rbc19</sup>/Tpi1<sup>rbc19</sup>  [background:] SJL-Tpi1<sup>rbc19</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29720471	20180716	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934765	Gpnmb	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:3773274	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] B6.D2-Gpnmb<sup>R150X</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16827931	20080310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934765	Gpnmb	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:2178286	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:10192392	20080310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934765	Gpnmb	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:2178291	Gpnmb<sup>R150X</sup>/Gpnmb<sup>R150X</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:10192392	20080310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775614	Fkbp8<sup>Gt(OST287985)Lex</sup>	is_implicated_in	DOID:0080016	spina bifida		MGI:3775615	Fkbp8<sup>Gt(OST287985)Lex</sup>/Fkbp8<sup>Gt(OST287985)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18003640	20211231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604008	Tg(Plp1-SNCA)1Haa	is_implicated_in	DOID:4752	multiple system atrophy		MGI:5008644	Tg(Plp1-SNCA)1Haa/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:15743798	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	is_implicated_in	DOID:0090140	cortisone reductase deficiency 2		MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	PMID:9405715	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	is_implicated_in	DOID:0090140	cortisone reductase deficiency 2		MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	MGI:85353	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	is_implicated_in	DOID:0090140	cortisone reductase deficiency 2		MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	PMID:11546766	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456470	Gstm1<sup>tm1Gcw</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4456472	Gstm1<sup>tm1Gcw</sup>/Gstm1<sup>tm1Gcw</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20178820	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675769	Ctf1<sup>tm1Msd</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5294956	Ctf1<sup>tm1Msd</sup>/Ctf1<sup>tm1Msd</sup>  [background:] B6.Cg-Ctf1<sup>tm1Msd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21803294	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:3627	aortic aneurysm		MGI:3793728	Atp7a<sup>Mo-blo</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:3385878	20190722	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:3627	aortic aneurysm		MGI:3793784	Atp7a<sup>Mo-blo</sup>/Atp7a<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:1115218	20190722	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:3627	aortic aneurysm		MGI:3793728	Atp7a<sup>Mo-blo</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:1115218	20190722	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2686934	Zfhx2	is_implicated_in	DOID:0081075	Marsili syndrome		MGI:7329779	Zfhx2<sup>tm3Ymri</sup>/Zfhx2<sup>tm3Ymri</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29253101	20220816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443047	Ttll1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:4461790	Ttll1<sup>tm1Seto</sup>/Ttll1<sup>tm1Seto</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20498047	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176342	Pltp<sup>tm1Jia</sup>	is_implicated_in	DOID:10140	dry eye syndrome		MGI:2176343	Pltp<sup>tm1Jia</sup>/Pltp<sup>tm1Jia</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21514421	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856106	Bloc1s5<sup>mu</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le			ECO:0000033	author statement supported by traceable reference	PMID:11912185	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856106	Bloc1s5<sup>mu</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856106	Bloc1s5<sup>mu</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3587678	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] involves: STOCK t			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2389008	Adamtsl4	is_implicated_in	DOID:110	lens disease		MGI:5902990	Adamtsl4<sup>tvrm267</sup>/Adamtsl4<sup>tvrm267</sup>  [background:] C57BL/6J-Adamtsl4<sup>tvrm267</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26405179	20170620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918511	Poc1b	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7530054	Poc1b<sup>em1Xjzha</sup>/Poc1b<sup>em1Xjzha</sup>  [background:] C57BL/6J-Poc1b<sup>em1Xjzha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37070736	20230925	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100846	Med1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5911329	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100846	Med1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5911326	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829987	Ncor2<sup>tm1Rev</sup>	is_implicated_in	DOID:4971	myelofibrosis		MGI:3829994	Ncor2<sup>tm1Rev</sup>/Ncor2<sup>tm1Rev</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24191050	20140306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429562	Tg(Alb-E2F1)8Sst	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437484	Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20850540	20121003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429562	Tg(Alb-E2F1)8Sst	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437484	Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11042693	20121003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429562	Tg(Alb-E2F1)8Sst	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437484	Tg(Alb-E2F1)8Sst/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:15885355	20121003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856022	Cacna2d2<sup>du</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:4358337	Cacna2d2<sup>du</sup>/Cacna2d2<sup>du</sup>  [background:] TKDU/DnJ			ECO:0000033	author statement supported by traceable reference	PMID:11487633	20110707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	is_implicated_in	DOID:9521	Laron syndrome		MGI:3796418	Ghr<sup>tm1Jjk</sup>/Ghr<sup>tm1Jjk</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:19269870	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	is_implicated_in	DOID:9521	Laron syndrome		MGI:2681520	Ghr<sup>tm1Arge</sup>/Ghr<sup>tm1Arge</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11133160	20110127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	is_implicated_in	DOID:9521	Laron syndrome		MGI:3796418	Ghr<sup>tm1Jjk</sup>/Ghr<sup>tm1Jjk</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:9371826	20110127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576373	Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:6197798	Gli2<sup>tm1(cre/ERT2)Tipe</sup>/Gli2<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(Smo/EYFP)Amc</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:29999500	20180913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043843	Tg(Ins1-Cat,Tyr)25Pne	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3624036	Tg(Ins1-Cat,Tyr)25Pne/0  [background:] NOD.FVB-Tg(Ins1-Cat,Tyr)25Pne			ECO:0000033	author statement supported by traceable reference	PMID:16731821	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043843	Tg(Ins1-Cat,Tyr)25Pne	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623483	Tg(Ins1-Cat,Tyr)25Pne/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:10515587	20060607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923566	Dnaaf2	is_implicated_in	DOID:0110612	primary ciliary dyskinesia 10		MGI:6369967	Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>/Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>  [background:] B6N(Cg)-Dnaaf2<sup>tm1.1(KOMP)Vlcg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:31107948	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923566	Dnaaf2	is_implicated_in	DOID:0110612	primary ciliary dyskinesia 10		MGI:5526986	Dnaaf2<sup>tm1.1Mkis</sup>/Dnaaf2<sup>tm1.1Mkis</sup>  [background:] involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23525783	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929470	Tyk2	is_implicated_in	DOID:9970	obesity		MGI:5515728	Tyk2<sup>tm1Shmd</sup>/Tyk2<sup>tm1Shmd</sup>  [background:] either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:23217260	20131030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716208	Rpgrip1l<sup>tm1Urt</sup>	is_implicated_in	DOID:0111002	Joubert syndrome 7		MGI:3716631	Rpgrip1l<sup>tm1Urt</sup>/Rpgrip1l<sup>tm1Urt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17558409	20150903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914921	Rpl38	is_implicated_in	DOID:10754	otitis media		MGI:3795975	Rpl38<sup>Ts</sup>/Rpl38<sup>+</sup>  [background:] TSJ/Le			ECO:0000033	author statement supported by traceable reference	PMID:21062742	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94863	Dbf	is_implicated_in	DOID:11836	clubfoot		MGI:2170796	Dbf/Dbf<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:9062079	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415188	Idua<sup>tm1.1Kmke</sup>	is_implicated_in	DOID:12802	mucopolysaccharidosis I		MGI:4415196	Idua<sup>tm1.1Kmke</sup>/Idua<sup>tm1.1Kmke</sup>  [background:] B6.129-Idua<sup>tm1.1Kmke</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19751987	20100106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3987403	Clpp<sup>Gt(IST11134F10)Tigm</sup>	is_implicated_in	DOID:0050857	Perrault syndrome		MGI:5532579	Clpp<sup>Gt(IST11134F10)Tigm</sup>/Clpp<sup>Gt(IST11134F10)Tigm</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23851121	20140129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2668595	Grk1<sup>tm1Citb</sup>	is_implicated_in	DOID:0110713	Oguchi disease-2		MGI:2668598	Grk1<sup>tm1Citb</sup>/Grk1<sup>tm1Citb</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10097103	20100707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5446153	b2b1941Clo	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5487398	b2b1941Clo/b2b1941Clo  [background:] C57BL/6J-b2b1941Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685615	Ceacam16	is_implicated_in	DOID:0110573	autosomal dominant nonsyndromic deafness 4A		MGI:5437687	Ceacam16<sup>tm1Wzm</sup>/Ceacam16<sup>tm1Wzm</sup>  [background:] BALB/cJ-Ceacam16<sup>tm1Wzm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22544735	20121004	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385585	Tg(Tuba1-MAPT)14Vle	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5318527	Tg(Tuba1-MAPT)14Vle/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12165467	20120517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202304	Gnmt	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3842683	Gnmt<sup>tm1Ymac</sup>/Gnmt<sup>tm1Ymac</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19035462	20150807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914935	Dnaaf4	is_implicated_in	DOID:0060254	Robinow syndrome		MGI:5312334	Dnaaf4<sup>b2b811.1Clo</sup>/Dnaaf4<sup>b2b811.1Clo</sup>  [background:] C57BL/6J-Dnaaf4<sup>b2b811.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	is_implicated_in	DOID:5603	T-cell acute lymphoblastic leukemia		MGI:6771693	Nbn<sup>em7Jpt</sup>/Nbn<sup>tm2Zqw</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:31285322	20211015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526665	Fzd9<sup>tm1Uta</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:4946081	Fzd9<sup>tm1Uta</sup>/Fzd9<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21402791	20110411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888740	Chrm3<sup>tm1Mmt</sup>	is_implicated_in	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome		MGI:3581978	Chrm3<sup>tm1Mmt</sup>/Chrm3<sup>tm1Mmt</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10944224	20140525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:2394	ovarian cancer		MGI:5583019	Apc<sup>tm1Rsmi</sup>/Apc<sup>tm1Rsmi</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24474556	20140919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934018	Naglu<sup>tm1Efn</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3777760	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17712420	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386679	Hif1a<sup>tm3Rsjo</sup>	is_implicated_in	DOID:2746	glycogen storage disease V		MGI:3621470	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15328538	20060505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	is_implicated_in	DOID:10754	otitis media		MGI:3037642	Phex<sup>Hyp-Duk</sup>/Y  [background:] involves: BALB/cAnBomUrd			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338761	Colq	is_implicated_in	DOID:0110667	congenital myasthenic syndrome 5		MGI:2176897	Colq<sup>tm1Jrs</sup>/Colq<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10087275	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181718	Cfc1<sup>tm1Cbm</sup>	is_implicated_in	DOID:0060856	right atrial isomerism		MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10574770	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797607	Xlch	is_implicated_in	DOID:0110461	X-linked dilated cardiomyopathy		MGI:3797747	Xlch/Xlch<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18424640	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797607	Xlch	is_implicated_in	DOID:0110461	X-linked dilated cardiomyopathy		MGI:3797627	Xlch/?  [background:] C57BL/6J-Xlch			ECO:0000033	author statement supported by traceable reference	PMID:18424640	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914828	Patl2	is_implicated_in	DOID:1100	ovarian disease		MGI:6200082	Patl2<sup>tm1b(EUCOMM)Hmgu</sup>/Patl2<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29661911	20180927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712056	Tpmt<sup>tm1Rlng</sup>	is_implicated_in	DOID:0080172	thiopurine S-methyltransferase deficiency		MGI:3712780	Tpmt<sup>tm1Rlng</sup>/Tpmt<sup>tm1Rlng</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:17510427	20070626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3823246	Lama5<sup>tm3Jhm</sup>	is_implicated_in	DOID:2975	cystic kidney disease		MGI:3823250	Lama5<sup>tm3Jhm</sup>/Lama5<sup>tm3Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16790509	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706439	Tg(Ins2-Nos2)40Okam	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3706514	Tg(Ins2-Nos2)40Okam/0  [background:] involves: C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:8499320	20070502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706439	Tg(Ins2-Nos2)40Okam	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3706545	Tg(Ins2-Nos2)40Okam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16936199	20070502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522021	Ptpn11<sup>tm1Gsf</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906203	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19001090	20170803	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2175179	Ntf3<sup>tm1Par</sup>/Ntf3<sup>tm1Par</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8841198	20060426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	is_implicated_in	DOID:10140	dry eye syndrome		MGI:5295260	Muc5ac<sup>tm1.1Evns</sup>/Muc5ac<sup>tm1.1Evns</sup>  [background:] B6.129S1-Muc5ac<sup>tm1.1Evns</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23272068	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	is_implicated_in	DOID:0050580	hereditary lymphedema		MGI:3026664	Vegfc<sup>tm1Ali</sup>/Vegfc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:24590274	20140825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928654	Nkx3-1<sup>tm1Hha</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:2175150	Nkx3-1<sup>tm1Hha</sup>/Nkx3-1<sup>tm1Hha</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10906459	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1928654	Nkx3-1<sup>tm1Hha</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:2175151	Nkx3-1<sup>tm1Hha</sup>/Nkx3-1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10906459	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444289	Glis3	is_implicated_in	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism		MGI:3848057	Glis3<sup>tm1Amj</sup>/Glis3<sup>tm1Amj</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19273592	20090708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444289	Glis3	is_implicated_in	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism		MGI:3849867	Glis3<sup>tm1Hiha</sup>/Glis3<sup>tm1Hiha</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19481545	20090708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722326	Dnah5<sup>hlb612</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3778526	Dnah5<sup>hlb612</sup>/Dnah5<sup>hlb612</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18037990	20101001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387003	Stk11<sup>tm1Tpm</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3790955	Stk11<sup>tm1Tpm</sup>/Stk11<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15480979	20080610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387003	Stk11<sup>tm1Tpm</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3790954	Stk11<sup>tm1Tpm</sup>/Stk11<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12218179	20080610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861932	Gt(ROSA)26Sor<sup>tm1Sor</sup>	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6402037	Gt(ROSA)26Sor<sup>tm1Sor</sup>/Gt(ROSA)26Sor<sup>tm1Sor</sup> Tg(NPHS2-rtTA2*M2)1Jbk/Tg(NPHS2-rtTA2*M2)1Jbk Tg(tetO-cre)LC1Bjd/Tg(tetO-cre)LC1Bjd  [background:] involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31588799	20200329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:6259526	Clcn7<sup>tm1.1Mawa</sup>/Clcn7<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28942122	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563097	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>tm1.1Teti</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563101	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>tm1.1Teti</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563098	Clcn7<sup>tm1.1Teti</sup>/Clcn7<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563125	Clcn7<sup>tm1.1Mjec</sup>/Clcn7<sup>+</sup>  [background:] involves: 129 * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:5563141	Clcn7<sup>tm1.1Mjec</sup>/Clcn7<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:24185277	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110938	autosomal dominant osteopetrosis 2		MGI:6466741	Clcn7<sup>tm1.1Aros</sup>/Clcn7<sup>tm1.1Aros</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30865697	20201013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384063	Pafah1b1<sup>tm2.2Awb</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:2664130	Pafah1b1<sup>tm2.2Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	is_implicated_in	DOID:3890	acute intermittent porphyria		MGI:3841015	Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>  [background:] C57BL/6-Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30615115	20200312	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	is_implicated_in	DOID:3890	acute intermittent porphyria		MGI:6394002	Hmbs<sup>tm1.1Rjde</sup>/Hmbs<sup>tm1.1Rjde</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30615115	20200312	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	is_implicated_in	DOID:3890	acute intermittent porphyria		MGI:3841015	Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>  [background:] C57BL/6-Hmbs<sup>tm2Uam</sup>/Hmbs<sup>tm3Uam</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8563760	20200312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182720	Gadd45a<sup>tm1Ajf</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3618357	Gadd45a<sup>tm1Ajf</sup>/Gadd45a<sup>tm1Ajf</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	is_implicated_in	DOID:28	endocrine system disease		MGI:7279194	Pcsk1<sup>em2Irli</sup>/Pcsk1<sup>em2Irli</sup>  [background:] C57BL/6J-Pcsk1<sup>em2Irli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35245347	20220520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3691577	Slc6a4<sup>tm1(cre)Xz</sup>	is_implicated_in	DOID:9007	sudden infant death syndrome		MGI:4417856	Slc6a4<sup>tm1(cre)Xz</sup>/Slc6a4<sup>tm1(cre)Xz</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19646988	20100114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97169	Msx2	is_implicated_in	DOID:0060285	parietal foramina		MGI:2175121	Msx2<sup>tm1Rilm</sup>/Msx2<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10742104	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927339	Pals1	is_implicated_in	DOID:14791	Leber congenital amaurosis		MGI:5428846	Pals1<sup>tm1Caw</sup>/Pals1<sup>tm1Caw</sup> Tg(rx3-icre)1Mjam/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22398208	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107357	Inpp5d	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:5319308	Inpp5d<sup>tm1Rkh</sup>/Inpp5d<sup>tm1Rkh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12161749	20120525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449112	Adamts10	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:6783439	Adamts10<sup>em1Jku</sup>/Adamts10<sup>em1Jku</sup>  [background:] C57BL/6J-Adamts10<sup>em1Jku</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34424262	20211029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449112	Adamts10	is_implicated_in	DOID:0050475	Weill-Marchesani syndrome		MGI:6258769	Adamts10<sup>em1Cbal</sup>/Adamts10<sup>em1Cbal</sup>  [background:] involves: C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30060141	20211029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931595	Nfkbiz	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3526428	Nfkbiz<sup>tm1Mamo</sup>/Nfkbiz<sup>tm1Mamo</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15491998	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922754	Cfap276	is_implicated_in	DOID:0050543	Charcot-Marie-Tooth disease intermediate type		MGI:6473225	Cfap276<sup>em2.1Fuxi</sup>/Cfap276<sup>em2.1Fuxi</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32592472	20201119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922754	Cfap276	is_implicated_in	DOID:0050543	Charcot-Marie-Tooth disease intermediate type		MGI:6473224	Cfap276<sup>em2.1Fuxi</sup>/Cfap276<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32592472	20201119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109572	Tuft1	is_implicated_in	DOID:3390	palmoplantar keratosis		MGI:7532607	Tuft1<sup>tm1a(KOMP)Wtsi</sup>/Tuft1<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:37716648	20231003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712146	Plod1<sup>tm1Soin</sup>	is_implicated_in	DOID:13359	Ehlers-Danlos syndrome		MGI:3712759	Plod1<sup>tm1Soin</sup>/Plod1<sup>tm1Soin</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17197443	20121106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3616190	Nfkbia<sup>tm1Stw</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3700172	Nfkbia<sup>tm1Stw</sup>/Nfkbia<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8628301	20070318	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347465	Foxh1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5615273	Foxh1<sup>b2b2662Clo</sup>/Foxh1<sup>b2b2662Clo</sup>  [background:] C57BL/6J-Foxh1<sup>b2b2662Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	is_not_implicated_in	DOID:13366	Stiff-Person syndrome		MGI:2177574	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9391152	20060203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	is_not_implicated_in	DOID:13366	Stiff-Person syndrome		MGI:2177575	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * NOD			ECO:0000033	author statement supported by traceable reference	PMID:9391152	20060203	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675769	Ctf1<sup>tm1Msd</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5294956	Ctf1<sup>tm1Msd</sup>/Ctf1<sup>tm1Msd</sup>  [background:] B6.Cg-Ctf1<sup>tm1Msd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21803294	20111104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614339	Tg(MMTV-PyVT*Y250F)250-2Mul	is_implicated_in	DOID:1612	breast cancer		MGI:3614341	Tg(MMTV-PyVT*Y250F)250-2Mul/?  [background:] FVB/N-Tg(MMTV-PyVT*Y250F)250-2Mul			ECO:0000033	author statement supported by traceable reference	PMID:9528804	20101110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624862	Hk2<sup>tm1Laak</sup>	is_not_implicated_in	DOID:0110741	type 1 diabetes mellitus 2		MGI:3625100	Hk2<sup>tm1Laak</sup>/Hk2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * BALB/c * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10428828	20110711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180102	Adh7<sup>tm1Gdu</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:4936868	Adh7<sup>tm1Gdu</sup>/Adh7<sup>tm1Gdu</sup>  [background:] B6.129(Cg)-Adh7<sup>tm1Gdu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21075145	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	is_not_implicated_in	DOID:0060485	Mowat-Wilson syndrome		MGI:3624727	Zeb2<sup>tm1.2Yhi</sup>/Zeb2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12522767	20060619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:7261455	Cxcr4<sup>tm2Yzo</sup>/Cxcr4<sup>tm2Yzo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31071921	20220418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3032571	Tg<sup>cog</sup>/Tg<sup>cog</sup>  [background:] involves: AKR/J * C57BL/6By			ECO:0000033	author statement supported by traceable reference	PMID:3803305	20100125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88335	Cd4	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623373	Cd4<sup>tm1Knw</sup>/Cd4<sup>tm1Knw</sup>  [background:] NOD.Cg-Cd4<sup>tm1Knw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:2176410	Ppt1<sup>tm1Hof</sup>/Ppt1<sup>tm1Hof</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11717424	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	is_implicated_in	DOID:0050836	focal dystonia		MGI:6273760	Tor1a<sup>tm1Calak</sup>/Tor1a<sup>tm1Calak</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27168150	20190117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388038	Blm<sup>tm1Grdn</sup>	is_implicated_in	DOID:2717	Bloom syndrome		MGI:3582673	Blm<sup>tm1Grdn</sup>/Blm<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12242442	20050729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443511	Slc9a6	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:29349289	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443511	Slc9a6	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21964919	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443511	Slc9a6	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902072	Slc9a6<sup>tm1Dgen</sup>/Slc9a6<sup>tm1Dgen</sup>  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21964919	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443511	Slc9a6	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902076	Slc9a6<sup>tm1Dgen</sup>/Slc9a6<sup>+</sup>  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26515654	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443511	Slc9a6	is_implicated_in	DOID:0060825	Christianson syndrome		MGI:5902071	Slc9a6<sup>tm1Dgen</sup>/Y  [background:] B6.129P2-Slc9a6<sup>tm1Dgen</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26515654	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346349	Sh3bp2	is_implicated_in	DOID:1856	cherubism		MGI:5701638	Sh3bp2<sup>tm1.1Ics</sup>/Sh3bp2<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25705883	20160108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346349	Sh3bp2	is_implicated_in	DOID:1856	cherubism		MGI:3699094	Sh3bp2<sup>tm1Bjro</sup>/Sh3bp2<sup>tm1Bjro</sup>  [background:] involves: 129S4/SvJae * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17218256	20160108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2665413	Zfpm2<sup>tm1Sho</sup>/Zfpm2<sup>tm1Sho</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12223418	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2665413	Zfpm2<sup>tm1Sho</sup>/Zfpm2<sup>tm1Sho</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:10892744	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:6392094	Fancd2<sup>em1Tzh</sup>/Fancd2<sup>em1Tzh</sup>  [background:] C57BL/6-Fancd2<sup>em1Tzh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31078270	20200226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:2673460	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] 129S4/SvJae-Fancd2<sup>tm1Hou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12893777	20200226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:2673459	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] B6.129S4-Fancd2<sup>tm1Hou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12893777	20200226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:2673461	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12893777	20200226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3610364	Rbm24	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:7408196	Rbm24<sup>tm1.1Xixu</sup>/Rbm24<sup>tm1.1Xixu</sup> Tg(Myhc-cre)1Xya/0  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:30267374	20221215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	is_implicated_in	DOID:0110943	autosomal recessive osteopetrosis 2		MGI:3800941	Tnfsf11<sup>tm1Ywc</sup>/Tnfsf11<sup>tm1Ywc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22836362	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	is_implicated_in	DOID:0110943	autosomal recessive osteopetrosis 2		MGI:5307894	Tnfsf11<sup>tles</sup>/Tnfsf11<sup>tles</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22068587	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	is_implicated_in	DOID:0110943	autosomal recessive osteopetrosis 2		MGI:5691824	Tnfsf11<sup>gum</sup>/Tnfsf11<sup>gum</sup>  [background:] STOCK Tnfsf11<sup>gum</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26234751	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445096	Dhtkd1	is_implicated_in	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q		MGI:6260058	Dhtkd1<sup>tm1Zgwg</sup>/Dhtkd1<sup>tm1Zgwg</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29661920	20200715	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445096	Dhtkd1	is_implicated_in	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q		MGI:6441736	Dhtkd1<sup>tm1Mmgu</sup>/Dhtkd1<sup>tm1Mmgu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32169121	20200715	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931307	Slc19a3	is_implicated_in	DOID:0050659	biotin-responsive basal ganglia disease		MGI:6162647	Slc19a3<sup>tm1.1Nwak</sup>/Slc19a3<sup>tm1.1Nwak</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28665968	20180627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931307	Slc19a3	is_implicated_in	DOID:0050659	biotin-responsive basal ganglia disease		MGI:6162677	Slc19a3<sup>tm1Said</sup>/Slc19a3<sup>tm1Said</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28665968	20180627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	is_implicated_in	DOID:0112276	neurodevelopmental disorder with involuntary movements		MGI:6513140	Gnao1<sup>em2Rneu</sup>/Gnao1<sup>+</sup>  [background:] C57BL/6J-Gnao1<sup>em2Rneu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31907305	20210727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914275	Rpl11	is_implicated_in	DOID:0111878	Diamond-Blackfan anemia 7		MGI:6510523	Ndor1<sup>Tg(UBC-cre/ERT2)1Ejb</sup>/Ndor1<sup>+</sup> Rpl11<sup>tm1.1Srn</sup>/Rpl11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:26489471	20210316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624976	Tg(Ckm-LPL)LRze	is_implicated_in	DOID:423	myopathy		MGI:3624986	Tg(Ckm-LPL)LRze/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:7635990	20190806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858015	Csrp3<sup>tm1Crni</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:3037157	Csrp3<sup>tm1Crni</sup>/Csrp3<sup>tm1Crni</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11087268	20171222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	is_implicated_in	DOID:0110477	autosomal recessive nonsyndromic deafness 2		MGI:5487460	Myo7a<sup>dmbo2</sup>/Myo7a<sup>dmbo2</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23251483	20130529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:5305276	Col8a2<sup>tm1.1Asj</sup>/Col8a2<sup>tm1.1Asj</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22002996	20160929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:5796114	Col8a2<sup>tm2.1Asj</sup>/Col8a2<sup>tm2.1Asj</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:7698753	20160929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	is_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:5796117	Col8a2<sup>tm1.1Asj</sup>/Col8a2<sup>tm1.1Asj</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23422828	20160929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3640134	Glb1<sup>tm1Jmat</sup>/Glb1<sup>tm1Jmat</sup>  [background:] involves: C57BL/6 * CBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9071485	20060808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3581423	Glb1<sup>tm1Adz</sup>/Glb1<sup>tm1Adz</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15687347	20060808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3640134	Glb1<sup>tm1Jmat</sup>/Glb1<sup>tm1Jmat</sup>  [background:] involves: C57BL/6 * CBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9337086	20060808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3581421	Glb1<sup>tm1Adz</sup>/Glb1<sup>tm1Adz</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9063740	20060808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104779	Prkdc	is_implicated_in	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive		MGI:3760369	Prkdc<sup>scid</sup>/Prkdc<sup>scid</sup>  [background:] C.BKa-Prkdc<sup>scid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6823332	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856227	Slc45a2<sup>Uw-dbr</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668610	Slc45a2<sup>Uw-dbr</sup>/Slc45a2<sup>+</sup>  [background:] B10.PL-H2<sup>u</sup>/(73NS)Sn			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856227	Slc45a2<sup>Uw-dbr</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668609	Slc45a2<sup>Uw-dbr</sup>/Slc45a2<sup>Uw-dbr</sup>  [background:] B10.PL-H2<sup>u</sup>/(73NS)Sn			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	is_implicated_in	DOID:0080188	chronic myelomonocytic leukemia		MGI:6192375	Kdm6a<sup>tm1Cdcn</sup>/Y Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29479066	20180731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	is_implicated_in	DOID:0080188	chronic myelomonocytic leukemia		MGI:6192376	Kdm6a<sup>tm1Cdcn</sup>/Kdm6a<sup>tm1Cdcn</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29479066	20180731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355314	Ddb2	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3512004	Ddb2<sup>tm1Pra</sup>/Ddb2<sup>tm1Pra</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15558025	20070509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355314	Ddb2	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3512005	Ddb2<sup>tm1Pra</sup>/Ddb2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15558025	20070509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355314	Ddb2	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3036311	Ddb2<sup>tm1Linn</sup>/Ddb2<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14769931	20070509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1355314	Ddb2	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3036310	Ddb2<sup>tm1Linn</sup>/Ddb2<sup>tm1Linn</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14769931	20070509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3762250	Tg(Timp1-Msx2*P7H)1Rem	is_implicated_in	DOID:2340	craniosynostosis		MGI:3762252	Tg(Timp1-Msx2*P7H)1Rem/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:7597092	20071126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314635	Rasgrp1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2675118	Rasgrp1<sup>lag</sup>/Rasgrp1<sup>lag</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12932358	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99698	Clock	is_implicated_in	DOID:9351	diabetes mellitus		MGI:5576784	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20562852	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443733	Ssu2	is_implicated_in	DOID:701	dentin dysplasia		MGI:5908863	Ssu2<sup>tm1.1Xmx</sup>/Ssu2<sup>tm1.1Xmx</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27680507	20170913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443733	Ssu2	is_implicated_in	DOID:701	dentin dysplasia		MGI:5908862	Ssu2<sup>tm1.1Xmx</sup>/Ssu2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27680507	20170913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5429771	b2b1528Clo	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5429854	b2b1528Clo/b2b1528Clo  [background:] C57BL/6J-b2b1528Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891295	Ube3b	is_implicated_in	DOID:0111456	Kaufman oculocerebrofacial syndrome		MGI:6295856	Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>/Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6-Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30808755	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:4821001	Tacr1<sup>tm1Sph</sup>/Tacr1<sup>tm1Sph</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9748515	20140115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3578806	Jak3<sup>tm1Tks</sup>	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3579842	Jak3<sup>tm1Tks</sup>/Jak3<sup>tm1Tks</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8777722	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442832	Osbpl2	is_implicated_in	DOID:0110588	autosomal dominant nonsyndromic deafness 67		MGI:7331344	Osbpl2<sup>em1Cya</sup>/Osbpl2<sup>em1Cya</sup>  [background:] C57BL/6-Osbpl2<sup>em1Cya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35041619	20220823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:3050469	Ptpn11<sup>tm1Bgn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15273746	20171206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:6095197	Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup> Ptpn11<sup>tm6Bgn</sup>/Ptpn11<sup>+</sup>  [background:] B6.129S-Ptpn11<sup>tm6Bgn</sup> Emx1<sup>tm1(cre)Krj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28346493	20171206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182409	Dnmt3b<sup>tm1Enl</sup>	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3040301	Dnmt3b<sup>tm1Enl</sup>/Dnmt3b<sup>tm1Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10555141	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774541	Tph2<sup>tm1Mca</sup>	is_implicated_in	DOID:1595	melancholic depression		MGI:3801152	Tph2<sup>tm1Mca</sup>/Tph2<sup>tm1Mca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23467366	20130805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106903	Gucy2c	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5300906	Gucy2c<sup>tm1Gar</sup>/Gucy2c<sup>tm1Gar</sup>  [background:] B6.129S6-Gucy2c<sup>tm1Gar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21865642	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88523	Crygc	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:2176925	Crygc<sup>Chl3</sup>/Crygc<sup>+</sup>  [background:] involves: 102/El * C3H/El			ECO:0000033	author statement supported by traceable reference	PMID:11773036	20050923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88523	Crygc	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:2176927	Crygc<sup>Chl3</sup>/Crygc<sup>Chl3</sup>  [background:] involves: 102/El * C3H/El			ECO:0000033	author statement supported by traceable reference	PMID:11773036	20050923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055139	Dysf<sup>tm1Meho</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:3055578	Dysf<sup>tm1Meho</sup>/Dysf<sup>tm1Meho</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15254015	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676125	Lgmn<sup>tm1Ihn</sup>	is_implicated_in	DOID:75	lymphatic system disease		MGI:3836291	Lgmn<sup>tm1Ihn</sup>/Lgmn<sup>tm1Ihn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19106291	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	is_implicated_in	DOID:5425	ovarian hyperstimulation syndrome		MGI:4358795	Nr1h3<sup>tm1Djm</sup>/Nr1h3<sup>tm1Djm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19325005	20100511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3815541	Tg(MECP2)3Hzo	is_implicated_in	DOID:0060799	syndromic X-linked intellectual disability Lubs type		MGI:5314412	Tg(MECP2)3Hzo/0  [background:] either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1			ECO:0000033	author statement supported by traceable reference	PMID:22231481	20120408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	is_implicated_in	DOID:1852	intrahepatic cholestasis		MGI:3694478	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21292027	20150312	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	is_implicated_in	DOID:10534	stomach cancer		MGI:5433072	Tff1<sup>tm1Mrio</sup>/Tff1<sup>tm1Mrio</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:12768581	20120906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C		MGI:3832390	Ldb3<sup>tm4Chen</sup>/Ldb3<sup>tm4Chen</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19028670	20090218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	is_implicated_in	DOID:0110423	dilated cardiomyopathy 1C		MGI:3832389	Ldb3<sup>tm4Chen</sup>/Ldb3<sup>tm4Chen</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:19028670	20090218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	is_implicated_in	DOID:0090120	hereditary neutrophilia		MGI:2183034	Csf3r<sup>tm1Eur</sup>/Csf3r<sup>tm1Eur</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:9639496	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4434627	Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>	is_implicated_in	DOID:0111456	Kaufman oculocerebrofacial syndrome		MGI:6295856	Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>/Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6-Ube3b<sup>tm1a(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30808755	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913277	Crbn	is_implicated_in	DOID:0060308	autosomal recessive intellectual developmental disorder		MGI:5302203	Crbn<sup>tm1.1Jjh</sup>/Crbn<sup>tm1.1Jjh</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21995942	20190703	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913277	Crbn	is_implicated_in	DOID:0060308	autosomal recessive intellectual developmental disorder		MGI:5302204	Crbn<sup>tm1.2Jjh</sup>/Crbn<sup>tm1.2Jjh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29459374	20190703	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5810302	Ctsl<sup>tm1Cptr</sup>/Ctsl<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11972068	20170802	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138319	Trp53bp2	is_implicated_in	DOID:0060412	chromosome 1q41-q42 deletion syndrome		MGI:6191758	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] B6.129S6-Trp53bp2<sup>tm1Xlu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138319	Trp53bp2	is_implicated_in	DOID:0060412	chromosome 1q41-q42 deletion syndrome		MGI:4819168	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] C.129S6-Trp53bp2<sup>tm1Xlu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138319	Trp53bp2	is_implicated_in	DOID:0060412	chromosome 1q41-q42 deletion syndrome		MGI:3629203	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96078	Hgd	is_implicated_in	DOID:9270	alkaptonuria		MGI:6416345	Hgd<sup>tm1a(KOMP)Wtsi</sup>/Hgd<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31600782	20200513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96078	Hgd	is_implicated_in	DOID:9270	alkaptonuria		MGI:3617439	Hgd<sup>aku</sup>/Hgd<sup>aku</sup>  [background:] either: (involves: 129/Sv * BALB/cByJ * NB) or (involves: 129/Sv * C57BL/6J * NB)			ECO:0000033	author statement supported by traceable reference	PMID:8188247	20200513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:0050879	fragile X-associated tremor/ataxia syndrome		MGI:3815023	Fmr1<sup>tm2Cgr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15876460	20081114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684616	Psen1<sup>tm1Vln</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2684657	Psen1<sup>tm1Vln</sup>/Psen1<sup>tm1Vln</sup> Tg(Thy1-cre)1Vln/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11978821	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384332	Insr<sup>tm1Khn</sup>	is_implicated_in	DOID:8947	diabetic retinopathy		MGI:7327617	Insr<sup>tm1Khn</sup>/Insr<sup>tm1Khn</sup> Tg(Pdgfrb-cre)#Rha/0  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34460911	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4127244	Ankfy1<sup>Gt(RRE069)Byg</sup>	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia		MGI:6316069	Ankfy1<sup>Gt(RRE069)Byg</sup>/Ankfy1<sup>+</sup>  [background:] B6.129P2-Ankfy1<sup>Gt(RRE069)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28588446	20190705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856271	Atp8a2<sup>wl</sup>	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3838994	Atp8a2<sup>wl</sup>/Atp8a2<sup>wl</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856271	Atp8a2<sup>wl</sup>	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3838969	Atp8a2<sup>wl</sup>/Atp8a2<sup>wl</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103099	Cox6a1	is_implicated_in	DOID:0110203	Charcot-Marie-Tooth disease recessive intermediate D		MGI:5804696	Cox6a1<sup>tm1(KOMP)Wtsi</sup>/Cox6a1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6JJcl * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25152455	20161024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843457	Avp<sup>tm1Lja</sup>	is_implicated_in	DOID:12388	neurohypophyseal diabetes insipidus		MGI:3843462	Avp<sup>tm1Lja</sup>/Avp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:14660745	20090508	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:0050433	fatal familial insomnia		MGI:2174712	Prnp<sup>tm1Rcm</sup>/Prnp<sup>tm1Rcm</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Rcm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9462739	20060525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	is_not_implicated_in	DOID:0050433	fatal familial insomnia		MGI:2174710	Prnp<sup>tm1Edin</sup>/Prnp<sup>tm1Edin</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Edin</sup>/EdinH			ECO:0000033	author statement supported by traceable reference	PMID:10581259	20060525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4		MGI:3623489	Col1a1<sup>tm1.1Jcm</sup>/Col1a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:10608859	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4		MGI:5689511	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:24443344	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110340	osteogenesis imperfecta type 4		MGI:5791061	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26277094	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5604139	Smad4<sup>tm2.1Cxd</sup>/Smad4<sup>tm2.1Cxd</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24006258	20170531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415497	Jakmip1<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5750066	Jakmip1<sup>tm1(KOMP)Vlcg</sup>/Jakmip1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26627310	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0110354	retinitis pigmentosa 19		MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857860	Abca4<sup>tm1Ght</sup>	is_implicated_in	DOID:0110354	retinitis pigmentosa 19		MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329042	Sgce	is_implicated_in	DOID:0090034	myoclonic dystonia 11		MGI:5308942	Sgce<sup>tm1Ygl</sup>/Sgce<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:22040906	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329042	Sgce	is_implicated_in	DOID:0090034	myoclonic dystonia 11		MGI:3618238	Sgce<sup>tm1Ygl</sup>/Sgce<sup>tm1Ygl</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16099459	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3863997	Lca5<sup>Gt(AG0283)Wtsi</sup>	is_implicated_in	DOID:0110215	Leber congenital amaurosis 5		MGI:5086280	Lca5<sup>Gt(AG0283)Wtsi</sup>/Lca5<sup>Gt(AG0283)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21606596	20110816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	is_implicated_in	DOID:0111112	nephronophthisis 1		MGI:7280905	Nphp1<sup>em1Lisu</sup>/Nphp1<sup>em1Lisu</sup>  [background:] C57BL/6J-Nphp1<sup>em1Lisu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34415307	20220526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103577	Hand1	is_not_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6766587	Hand1<sup>tm5Abfi</sup>/Hand1<sup>+</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:29016838	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103577	Hand1	is_not_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6766589	Hand1<sup>tm5Abfi</sup>/Hand1<sup>+</sup> Tg(Mef2c-cre)2Blk/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:29016838	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103577	Hand1	is_not_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6766588	Hand1<sup>tm5Abfi</sup>/Hand1<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:29016838	20211012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97750	Ppib	is_implicated_in	DOID:0110349	osteogenesis imperfecta type 9		MGI:5698101	Ppib<sup>Gt(RST139)Byg</sup>/Ppib<sup>Gt(RST139)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24968150	20160815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97750	Ppib	is_implicated_in	DOID:0110349	osteogenesis imperfecta type 9		MGI:4462833	Ppib<sup>tm1.1Rjb</sup>/Ppib<sup>tm1.1Rjb</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:19997487	20160815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3513416	Apc<sup>tm1Cip</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:3513849	Apc<sup>tm1Cip</sup>/Apc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15502862	20170302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919580	Klhl40	is_implicated_in	DOID:0110930	nemaline myopathy 8		MGI:5774663	Klhl40<sup>tm1(KOMP)Vlcg</sup>/Klhl40<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Klhl40<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24960163	20160601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:2175797	Crkl<sup>tm1Imo</sup>/Crkl<sup>tm1Imo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11242111	20060607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97800	Pthlh	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy		MGI:3583956	Pthlh<sup>tm1Hmk</sup>/Pthlh<sup>tm1Hmk</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8314082	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052967	Ptger4<sup>tm1.1Matb</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906377	Ptger4<sup>tm1.1Matb</sup>/Ptger4<sup>tm1.1Matb</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20008274	20170809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891834	Nupr1	is_implicated_in	DOID:0050457	Sertoli cell-only syndrome		MGI:3784866	Nupr1<sup>tm1Jlio</sup>/Nupr1<sup>tm1Jlio</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18495683	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857124	Alpl<sup>tm1Sor</sup>	is_implicated_in	DOID:0110913	adult hypophosphatasia		MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351342	Grm5	is_implicated_in	DOID:5419	schizophrenia		MGI:6315641	Grm5<sup>tm1Rod</sup>/Grm5<sup>tm1Rod</sup>  [background:] B6.129-Grm5<sup>tm1Rod</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30401923	20190701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521802	Cln5<sup>tm1Pltn</sup>	is_implicated_in	DOID:0110728	neuronal ceroid lipofuscinosis 5		MGI:3522019	Cln5<sup>tm1Pltn</sup>/Cln5<sup>tm1Pltn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15459177	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107877	Prkcsh	is_implicated_in	DOID:0050770	polycystic liver disease		MGI:5442315	Prkcsh<sup>tm1Som</sup>/Prkcsh<sup>tm1Som</sup> Tg(CAG-cre/Esr1*)1Lbe/0  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21685914	20121120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354168	Ttpa	is_implicated_in	DOID:0090028	familial isolated deficiency of vitamin E		MGI:2665559	Ttpa<sup>tm1Hsz</sup>/Ttpa<sup>tm1Hsz</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11076932	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354168	Ttpa	is_implicated_in	DOID:0090028	familial isolated deficiency of vitamin E		MGI:2174792	Ttpa<sup>tm1Far</sup>/Ttpa<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11095717	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354168	Ttpa	is_implicated_in	DOID:0090028	familial isolated deficiency of vitamin E		MGI:2174791	Ttpa<sup>tm1Far</sup>/Ttpa<sup>tm1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11095717	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930965	Ifngr2<sup>tm1Pbro</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3603845	Ifngr2<sup>tm1Pbro</sup>/Ifngr2<sup>tm1Pbro</sup>  [background:] NOD.129S1-Ifngr2<sup>tm1Pbro</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11714835	20101101	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652360	App<sup>tm1Cep</sup>/App<sup>tm1Cep</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652362	App<sup>tm1.1Cep</sup>/App<sup>tm1.1Cep</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652363	App<sup>tm1.1Cep</sup>/App<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652361	App<sup>tm1Cep</sup>/App<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8798542	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3044184	App<sup>tm1Ini</sup>/App<sup>+</sup>  [background:] involves: C57BL/6 * CBA * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15147316	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174917	App<sup>tm1Dbo</sup>/App<sup>tm1Dbo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10188929	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5638672	App<sup>tm2.1Tcs</sup>/App<sup>tm2.1Tcs</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24728269	20150608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5638675	App<sup>tm3.1Tcs</sup>/App<sup>tm3.1Tcs</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24728269	20150608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574585	Gnrhr<sup>hh</sup>	is_implicated_in	DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia		MGI:3574973	Gnrhr<sup>hh</sup>/Gnrhr<sup>hh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15625238	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693208	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3693295	Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17021169	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856897	Frem1<sup>heb</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665277	Frem1<sup>heb</sup>/Frem1<sup>heb</sup>  [background:] involves: AKR/J			ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	is_implicated_in	DOID:83	cataract		MGI:6727361	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	is_implicated_in	DOID:83	cataract		MGI:6727359	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>em1Alsh</sup>  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682255	Egfr<sup>Mhdadsk5</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6403356	Egfr<sup>Mhdadsk5</sup>/Egfr<sup>+</sup>  [background:] involves: 129S1/SvImJ * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:28404843	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3577843	Mme<sup>tm1Cge</sup>/Mme<sup>tm1Cge</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11375493	20050524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:7531415	Nsf<sup>tm1Himat</sup>/Nsf<sup>+</sup>  [background:] C57BL/6N-Nsf<sup>tm1Himat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34745222	20230928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104555	Mafb	is_implicated_in	DOID:0111534	multicentric carpotarsal osteolysis syndrome		MGI:6401826	Mafb<sup>em1Staka</sup>/Mafb<sup>em1Staka</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30369533	20200327	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857184	Ifng<sup>tm1Ts</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623448	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] NOD.Cg-Ifng<sup>tm1Ts</sup> Prkdc<sup>scid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11714835	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857184	Ifng<sup>tm1Ts</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623449	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] NOD.129S7(B6)-Ifng<sup>tm1Ts</sup>/DvsJ			ECO:0000033	author statement supported by traceable reference	PMID:11714835	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3053604	Cat<sup>b</sup>	is_not_implicated_in	DOID:2582	acatalasia		MGI:3615785	Cat<sup>b</sup>/Cat<sup>b</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6058079	20110725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685847	Pjvk	is_implicated_in	DOID:0110511	autosomal recessive nonsyndromic deafness 59		MGI:3654321	Pjvk<sup>tm1Ugds</sup>/Pjvk<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16804542	20060912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	is_implicated_in	DOID:0111448	progressive myoclonus epilepsy 1B		MGI:6890374	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>+</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033931	Vsx1<sup>tm2Mci</sup>	is_not_implicated_in	DOID:10126	keratoconus		MGI:3033935	Vsx1<sup>tm2Mci</sup>/Vsx1<sup>tm2Mci</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14745032	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339984	Pak2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6294052	Pak2<sup>Gt(OST104058)Lex</sup>/Pak2<sup>+</sup>  [background:] B6;129S5-Pak2<sup>Gt(OST104058)Lex</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:30134165	20190423	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97526	Pde6g	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3814998	Pde6g<sup>tm1Goff</sup>/Pde6g<sup>tm1Goff</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6 * MF1  * Swiss Webster) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * MF1 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:8638127	20081114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99402	Adora2a	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5473699	Adora2a<sup>tm1Jfc</sup>/Adora2a<sup>tm1Jfc</sup>  [background:] B6.129S4-Adora2a<sup>tm1Jfc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20938208	20130410	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136645	Vhl<sup>tm1Jae</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176966	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:11171994	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136645	Vhl<sup>tm1Jae</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3621460	Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16510575	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136645	Vhl<sup>tm1Jae</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:3621460	Hprt1<sup>tm1(Pck1-cre)Vhh</sup>/Y Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15798202	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136645	Vhl<sup>tm1Jae</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176966	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15798202	20060505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315202	Slit3	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3053453	Slit3<sup>Gt(OST106158)Lex</sup>/Slit3<sup>Gt(OST106158)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14550534	20140507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315202	Slit3	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5562646	Slit3<sup>tm1.1Dor</sup>/Slit3<sup>tm1.1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24355925	20140507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315202	Slit3	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:2662356	Slit3<sup>tm1Dor</sup>/Slit3<sup>tm1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12702769	20140507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315202	Slit3	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:2662361	Slit3<sup>tm1.1Dor</sup>/Slit3<sup>tm1.1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12702769	20140507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138968	Clp1	is_implicated_in	DOID:0060279	pontocerebellar hypoplasia type 10		MGI:5554934	Clp1<sup>tm1.1Pngr</sup>/Clp1<sup>tm1.1Pngr</sup>  [background:] CBA.Cg-Clp1<sup>tm1.1Pngr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24766809	20211014	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138968	Clp1	is_implicated_in	DOID:0060279	pontocerebellar hypoplasia type 10		MGI:6771475	Clp1<sup>em1Slac</sup>/Clp1<sup>em1Slac</sup>  [background:] C57BL/6J-Clp1<sup>em1Slac</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:34548404	20211014	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138968	Clp1	is_implicated_in	DOID:0060279	pontocerebellar hypoplasia type 10		MGI:6771478	Clp1<sup>em1Slac</sup>/Clp1<sup>em2Slac</sup>  [background:] C57BL/6J-Clp1<sup>em1Slac</sup>/Clp1<sup>em2Slac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34548404	20211014	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107177	Hsd17b3	is_implicated_in	DOID:0112248	17-beta hydroxysteroid dehydrogenase 3 deficiency		MGI:6508693	Hsd17b3<sup>tm1.2Mpo</sup>/Hsd17b3<sup>tm1.2Mpo</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:32190925	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95621	Gabrb3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5908397	Gabrb3<sup>tm2.1Uru</sup>/Gabrb3<sup>tm2.1Uru</sup>  [background:] B6J.129S6(Cg)-Gabrb3<sup>tm2.1Uru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26627235	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95621	Gabrb3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:2175037	Gabrb3<sup>tm1Geh</sup>/Gabrb3<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17983671	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443337	Fscn2	is_implicated_in	DOID:8466	retinal degeneration		MGI:6386243	Fscn2<sup>em1Fhan</sup>/Fscn2<sup>em1Fhan</sup>  [background:] C57BL/6J-Fscn2<sup>em1Fhan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30082328	20200124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179132	Slc6a6<sup>tm1Dhau</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3029356	Slc6a6<sup>tm1Dhau</sup>/Slc6a6<sup>tm1Dhau</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11772953	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923032	Lca5	is_implicated_in	DOID:0110215	Leber congenital amaurosis 5		MGI:5086280	Lca5<sup>Gt(AG0283)Wtsi</sup>/Lca5<sup>Gt(AG0283)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21606596	20110816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2182465	Vrk3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6112031	Vrk3<sup>Gt(YTA189)Byg</sup>/Vrk3<sup>Gt(YTA189)Byg</sup>  [background:] B6.129P2-Vrk3<sup>Gt(YTA189)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28899869	20180126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577345	Polh<sup>tm1Crey</sup>	is_implicated_in	DOID:0110847	xeroderma pigmentosum variant type		MGI:3579244	Polh<sup>tm1Crey</sup>/Polh<sup>tm1Crey</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15824086	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442327	Pten<sup>tm1.2Mwst</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:6512404	Pten<sup>tm1.2Mwst</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20194734	20210326	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110914	infantile hypophosphatasia		MGI:2654850	Alpl<sup>tm1Jlm</sup>/Alpl<sup>tm1Jlm</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9056646	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110914	infantile hypophosphatasia		MGI:5787924	Alpl<sup>tm1Jlm</sup>/Alpl<sup>tm1Jlm</sup>  [background:] involves: 129S1/SvImJ * 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22991301	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110914	infantile hypophosphatasia		MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7550313	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5502687	Ar<sup>tm1Verh</sup>/Y Tg(Fabp4-cre)1Rev/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22415878	20130827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931124	Hesx1<sup>tm1Icar</sup>	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10626545	20060403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931124	Hesx1<sup>tm1Icar</sup>	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9620767	20060403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913944	Uqcrfs1	is_implicated_in	DOID:700	mitochondrial metabolism disease		MGI:5444471	Uqcrfs1<sup>tm1Ctm</sup>/Uqcrfs1<sup>tm1Ctm</sup> Tg(Camk2a-cre)#Szi/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22914734	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88442	Coc	is_implicated_in	DOID:83	cataract		MGI:2175788	Coc/Coc  [background:] involves: 101 * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88442	Coc	is_implicated_in	DOID:83	cataract		MGI:2175789	Coc/Coc<sup>+</sup>  [background:] involves: 101 * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850120	Smad9<sup>tm3Jfm</sup>	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:3850122	Smad9<sup>tm3Jfm</sup>/Smad9<sup>tm3Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:19419974	20090710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793279	Ror2<sup>tm1Anec</sup>	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:3793282	Ror2<sup>tm1Anec</sup>/Ror2<sup>tm1Anec</sup>  [background:] B6.129S1-Ror2<sup>tm1Anec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18353862	20080611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181491	Rlbp1<sup>tm1Jsa</sup>	is_implicated_in	DOID:0050683	Bothnia retinal dystrophy		MGI:3038948	Rlbp1<sup>tm1Jsa</sup>/Rlbp1<sup>tm1Jsa</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11301032	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859929	Vdr<sup>tm1Ska</sup>	is_implicated_in	DOID:10609	rickets		MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:9241280	20061019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859929	Vdr<sup>tm1Ska</sup>	is_implicated_in	DOID:10609	rickets		MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:10746634	20061019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3514143	Dgkd<sup>Gt(RRT600)Byg</sup>	is_implicated_in	DOID:0050561	Lennox-Gastaut syndrome		MGI:3763530	Dgkd<sup>Gt(RRT600)Byg</sup>/Dgkd<sup>Gt(RRT600)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17357084	20071210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055296	Tnnt2<sup>tm1Mmto</sup>	is_not_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:3821723	Tnnt2<sup>tm1Mmto</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:18671960	20081230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931521	Fgfr3<sup>tm1Dor</sup>	is_not_implicated_in	DOID:4480	achondroplasia		MGI:3589422	Fgfr3<sup>tm1Dor</sup>/Fgfr3<sup>tm1Dor</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8630492	20051012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107172	Ppp3r1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6490510	Ppp3r1<sup>tm1.1Jhon</sup>/Ppp3r1<sup>tm1.1Jhon</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:32882262	20210107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384592	Tg(Mpz)88.1Mfel	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6276667	Tg(Mpz)88.1Mfel/0  [background:] FVB/N-Tg(Mpz)88.1Mfel			ECO:0000033	author statement supported by traceable reference	PMID:11086005	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682061	Ext1<sup>tm1Yama</sup>	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:6101205	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Acan<sup>tm1(cre/ERT2)Crm</sup>/Acan<sup>+</sup>  [background:] involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:28445472	20171214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682061	Ext1<sup>tm1Yama</sup>	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:4818630	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S5/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20534475	20171214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3528396	Iqsec2	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:6392161	Iqsec2<sup>em1Csbg</sup>/Y  [background:] C57BL/6NHsd-Iqsec2<sup>em1Csbg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31439632	20200303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3528396	Iqsec2	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:6392615	Iqsec2<sup>em1Frk</sup>/Y  [background:] involves: C3HeB/FeJ * C57BL/6NJ			ECO:0000033	author statement supported by traceable reference	PMID:31978606	20200303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3614443	Ccr1<sup>tm1Gao</sup>/Ccr1<sup>tm1Gao</sup>  [background:] B6.129S4-Ccr1<sup>tm1Gao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605485	Tecta<sup>tm2Gpr</sup>	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:3605834	Tecta<sup>tm2Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15995703	20051129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927489	Pdlim5	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5284902	Pdlim5<sup>tm1.1Chen</sup>/Pdlim5<sup>tm1.1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:20538684	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927489	Pdlim5	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5284901	Pdlim5<sup>tm1Chen</sup>/Pdlim5<sup>tm1Chen</sup> Tg(Tnnt2-cre)5Blh/?  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20538684	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430527	Gt(ROSA)26Sor<sup>tm7(Pik3ca*,EGFP)Rsky</sup>	is_implicated_in	DOID:0080351	CLOVES syndrome		MGI:6197269	Gt(ROSA)26Sor<sup>tm7(Pik3ca*,EGFP)Rsky</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] B6.Cg-Gt(ROSA)26Sor<sup>tm7(Pik3ca*,EGFP)Rsky</sup> Tg(CAG-cre/Esr1*)5Amc			ECO:0000033	author statement supported by traceable reference	PMID:29899452	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181190	Bmp4<sup>tm3.1Blh</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:2679083	Bmp4<sup>tm3.1Blh</sup>/Bmp4<sup>tm3.1Blh</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12975322	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:4882033	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Tyr-cre)1Lru/0  [background:] B6.Cg-Pten<sup>tm1Hwu</sup> Tg(Tyr-cre)1Lru			ECO:0000033	author statement supported by traceable reference	PMID:19884655	20200621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108399	Tcf20	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6726265	Tcf20<sup>em1Jwji</sup>/Tcf20<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32510763	20210727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	is_implicated_in	DOID:5419	schizophrenia		MGI:2674288	Akt1<sup>tm1Mbb</sup>/Akt1<sup>tm1Mbb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14745448	20120726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	is_implicated_in	DOID:12365	malaria		MGI:2448997	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup>  [background:] C.129S4-Fcgr2b<sup>tm1Ttk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17435165	20130312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156983	Ppp3r1<sup>tm1Stl</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3530740	Ppp3r1<sup>tm1Stl</sup>/Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl/0  [background:] C57BL/6-Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl			ECO:0000033	author statement supported by traceable reference	PMID:11733061	20070514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156983	Ppp3r1<sup>tm1Stl</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3530740	Ppp3r1<sup>tm1Stl</sup>/Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl/0  [background:] C57BL/6-Ppp3r1<sup>tm1Stl</sup> Tg(Camk2a-cre)CW2Stl			ECO:0000033	author statement supported by traceable reference	PMID:12851457	20070514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347474	Foxj1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:2668968	Foxj1<sup>tm1Bph</sup>/Foxj1<sup>tm1Bph</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9739041	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347474	Foxj1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:2679917	Foxj1<sup>tm1Slb</sup>/Foxj1<sup>tm1Slb</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10873152	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	is_implicated_in	DOID:1612	breast cancer		MGI:3710355	Brca1<sup>tm1Aash</sup>/Brca1<sup>tm1Aash</sup> Tg(LGB-cre)74Acl/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17212342	20080910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	is_implicated_in	DOID:1612	breast cancer		MGI:3805032	Brca1<sup>tm1Arge</sup>/Brca1<sup>tm1Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	is_implicated_in	DOID:1612	breast cancer		MGI:3805033	Brca1<sup>tm1Thl</sup>/Brca1<sup>tm1Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102570	Ndp	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:2676253	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20159112	20100420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913150	Trem2	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5904595	Trem2<sup>em2Bwef</sup>/Trem2<sup>em2Bwef</sup>  [background:] involves: C57BL/6J * DBA/2J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28559417	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856397	Egfr<sup>wa2</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:2176568	Egfr<sup>wa2</sup>/Egfr<sup>wa2</sup>  [background:] STOCK Egfr<sup>wa2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10700187	20170726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856397	Egfr<sup>wa2</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:5905421	Egfr<sup>wa2</sup>/Egfr<sup>wa2</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25997932	20170726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914535	Cwc27	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:6342435	Cwc27<sup>em1Bay</sup>/Cwc27<sup>em1Bay</sup>  [background:] C57BL/6J-Cwc27<sup>em1Bay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28285769	20190807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:2677133	G6pc1<sup>tm1Jyc</sup>/G6pc1<sup>tm1Jyc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:8640227	20230711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:4418690	G6pc1<sup>tm2.2Jyc</sup>/G6pc1<sup>tm2.2Jyc</sup>  [background:] involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19548314	20230711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:7506311	G6pc1<sup>em1Jyc</sup>/G6pc1<sup>em1Jyc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33359667	20230711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:5478556	G6pc1<sup>tm1.1Ics</sup>/G6pc1<sup>tm1.1Ics</sup> Alb<sup>tm1(cre/ERT2)Mtz</sup>/Alb<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21109326	20230711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:5823404	G6pc1<sup>tm1.1Ics</sup>/G6pc1<sup>tm1.1Ics</sup> Tg(Kap-icre)29066/2Sig/0  [background:] involves: 129S2/SvPas * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24717294	20230711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:2664353	Col1a2<sup>oim</sup>/Col1a2<sup>oim</sup>  [background:] involves: C3H/HeJ * C57BL/6JLe			ECO:0000033	author statement supported by traceable reference	PMID:8446583	20070907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:3720802	Col1a2<sup>oim</sup>/Col1a2<sup>oim</sup>  [background:] B6C3Fe a/a-Col1a2<sup>oim</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8968022	20070907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332146	Mcph1<sup>Gt(RRO608)Byg</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:4438359	Mcph1<sup>Gt(RRO608)Byg</sup>/Mcph1<sup>Gt(RRO608)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20169082	20110428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5441538	Gata4<sup>tm1.2Wtp</sup>/Gata4<sup>+</sup>  [background:] B6.Cg-Gata4<sup>tm1.2Wtp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17069789	20160609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5775440	Gata4<sup>tm1.1Sad</sup>/Gata4<sup>tm1.2Sad</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:25807280	20160609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	is_implicated_in	DOID:0060473	Kabuki syndrome		MGI:5829566	Kmt2d<sup>Gt(RRT024)Byg</sup>/Kmt2d<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25273096	20220902	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	is_implicated_in	DOID:0060473	Kabuki syndrome		MGI:7333170	H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Kmt2d<sup>tm2.1Kaig</sup>/Kmt2d<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:32541010	20220902	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	is_implicated_in	DOID:0060473	Kabuki syndrome		MGI:6515623	Kmt2d<sup>Gt(RRT024)Byg</sup>/Kmt2d<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:33431871	20220902	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800691	Col2a1<sup>Rgsc413</sup>	is_implicated_in	DOID:0080027	spondyloepimetaphyseal dysplasia		MGI:6151404	Col2a1<sup>Rgsc413</sup>/Col2a1<sup>Rgsc413</sup>  [background:] involves: C57BL/6JJcl * DBA/2JJcl			ECO:0000033	author statement supported by traceable reference	PMID:26545783	20180419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95453	Smarcad1	is_implicated_in	DOID:0050592	asphyxiating thoracic dystrophy		MGI:2178041	Smarcad1<sup>tm1Gos</sup>/Smarcad1<sup>tm1Gos</sup>  [background:] 129S2/SvPas-Smarcad1<sup>tm1Gos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22912419	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183520	Hnf4a<sup>tm1.1Gonz</sup>	is_implicated_in	DOID:0111099	maturity-onset diabetes of the young type 1		MGI:3653173	Hnf4a<sup>tm1.1Gonz</sup>/Hnf4a<sup>tm1.1Gonz</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:16377800	20060830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2660809	Arg1<sup>tm1Rki</sup>	is_implicated_in	DOID:9278	hyperargininemia		MGI:2668857	Arg1<sup>tm1Rki</sup>/Arg1<sup>tm1Rki</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12052859	20050602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926609	Trp53inp1	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1		MGI:3701944	Trp53inp1<sup>tm1Acar</sup>/Trp53inp1<sup>tm1Acar</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25828351	20170411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604533	Ctsc<sup>tm1Dgen</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3606731	Ctsc<sup>tm1Dgen</sup>/Ctsc<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852756	Smpx<sup>em1Jgao</sup>/Y  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852762	Smpx<sup>em2Jgao</sup>/Smpx<sup>+</sup>  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852759	Smpx<sup>em1Jgao</sup>/Smpx<sup>em1Jgao</sup>  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852760	Smpx<sup>em2Jgao</sup>/Smpx<sup>em2Jgao</sup>  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852757	Smpx<sup>em2Jgao</sup>/Y  [background:] CBA/CaJ-Smpx<sup>em2Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	is_implicated_in	DOID:0111735	X-linked deafness 4		MGI:6852761	Smpx<sup>em1Jgao</sup>/Smpx<sup>+</sup>  [background:] CBA/CaJ-Smpx<sup>em1Jgao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34722533	20220114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582343	Fgl2<sup>tm1Pam</sup>	is_implicated_in	DOID:0040094	autoimmune glomerulonephritis		MGI:3583697	Fgl2<sup>tm1Pam</sup>/Fgl2<sup>tm1Pam</sup>  [background:] B6.129X1-Fgl2<sup>tm1Pam</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18097026	20220531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346328	Def6	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3628445	Def6<sup>Gt(OST307148)Lex</sup>/Def6<sup>Gt(OST307148)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16470246	20060707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934860	Lztfl1	is_implicated_in	DOID:0110139	Bardet-Biedl syndrome 17		MGI:7435338	Lztfl1<sup>tm1.3Zpl</sup>/Lztfl1<sup>tm1.3Zpl</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30423168	20230217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934860	Lztfl1	is_implicated_in	DOID:0110139	Bardet-Biedl syndrome 17		MGI:5811522	Lztfl1<sup>tm1e(KOMP)Wtsi</sup>/Lztfl1<sup>tm1e(KOMP)Wtsi</sup>  [background:] involves: 129S/SvEv * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:26216965	20230217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3783471	Sirt1<sup>tm1Mcby</sup>/Sirt1<sup>tm1Mcby</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:18687325	20100728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386960	Nphs1<sup>tm1Rkl</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3587727	Nphs1<sup>tm1Rkl</sup>/Nphs1<sup>tm1Rkl</sup>  [background:] involves: 129S2/SvPasCrl			ECO:0000033	author statement supported by traceable reference	PMID:12039968	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179716	Lamb3<sup>IAP</sup>	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:2179721	Lamb3<sup>IAP</sup>/Lamb3<sup>IAP</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9271670	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5774687	Gabra1<sup>tm1.1Mjga</sup>/Gabra1<sup>+</sup>  [background:] B6J.Cg-Gabra1<sup>tm1.1Mjga</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26054439	20160601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5433047	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] B6.129(Cg)-Gabra1<sup>tm1.1Geh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26054439	20160601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5433031	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] D2.129(Cg)-Gabra1<sup>tm1.1Geh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22812724	20160601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5433047	Gabra1<sup>tm1.1Geh</sup>/Gabra1<sup>+</sup>  [background:] B6.129(Cg)-Gabra1<sup>tm1.1Geh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22812724	20160601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685418	Gm572	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5431537	Gm572<sup>b2b1167Clo</sup>/Gm572<sup>b2b1167Clo</sup>  [background:] C57BL/6J-Gm572<sup>b2b1167Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934923	Ifitm5	is_not_implicated_in	DOID:0110344	osteogenesis imperfecta type 5		MGI:6195291	Ifitm5<sup>em1Pmof</sup>/Ifitm5<sup>+</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:29174564	20180822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914311	Dzip1	is_implicated_in	DOID:0112175	spermatogenic failure 47		MGI:7435649	Dzip1<sup>em1Yxc</sup>/Dzip1<sup>em1Yxc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32051257	20230220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510921	Tg(Myl2-FGF19)1Dfre	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437999	Tg(Myl2-FGF19)1Dfre/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:22615798	20121011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510921	Tg(Myl2-FGF19)1Dfre	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5437999	Tg(Myl2-FGF19)1Dfre/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:12057932	20121011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:2571	Langerhans-cell histiocytosis		MGI:6192274	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Cd207<sup>tm2.1(cre)Bjec</sup>/Cd207<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24638167	20180731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:2571	Langerhans-cell histiocytosis		MGI:6192275	Braf<sup>tm1Mmcm</sup>/Braf<sup>tm1Mmcm</sup> Tg(Itgax-cre)1-1Reiz/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24638167	20180731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837437	Tg(PER2*S662G)867Ljp	is_implicated_in	DOID:0110011	advanced sleep phase syndrome 1		MGI:3852102	Tg(PER2*S662G)867Ljp/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17218255	20090806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683249	Pepd<sup>dal</sup>	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5604775	Pepd<sup>dal</sup>/Pepd<sup>dal</sup>  [background:] involves: C3H/HeJ * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:21472842	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856064	Lbr<sup>ic-J</sup>	is_implicated_in	DOID:1702	ichthyosis vulgaris		MGI:3829382	Lbr<sup>ic-J</sup>/Lbr<sup>ic-J</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17403717	20090129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814577	Tg(MT1A-Dyrk1a)33Xest	is_implicated_in	DOID:14250	Down syndrome		MGI:3814580	Tg(MT1A-Dyrk1a)33Xest/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11555628	20081111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	is_implicated_in	DOID:10825	essential hypertension		MGI:3620001	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] B6.129-Eln<sup>tm1Dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14597767	20060418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2		MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23160464	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	is_implicated_in	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2		MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15069016	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88458	Col5a2	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:5817903	Col5a2<sup>tm1.2Dgr</sup>/Col5a2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:25987251	20170117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:3695040	Glra1<sup>spd</sup>/Glra1<sup>spd</sup>  [background:] involves: A/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:8733750	20160907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:5790702	Glra1<sup>spd-ot9J</sup>/Glra1<sup>spd-ot9J</sup>  [background:] B6.Cg-Glra1<sup>spd-ot9J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5790609	20160907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:2677020	Glra1<sup>tm1Rah</sup>/Glra1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12954867	20160907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:3698026	Glra1<sup>tm1Betz</sup>/Glra1<sup>tm1Betz</sup>  [background:] B6.129P2-Glra1<sup>tm1Betz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17114051	20160907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:0050644	arterial calcification of infancy		MGI:5607167	Enpp1<sup>asj-2J</sup>/Enpp1<sup>asj-2J</sup>  [background:] BALB/cJ-Enpp1<sup>asj-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25479107	20141215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:0050644	arterial calcification of infancy		MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:23798568	20141215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367449	Ank1<sup>pale</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:4367450	Ank1<sup>pale</sup>/Ank1<sup>pale</sup>  [background:] C57BL/6J-Ank1<sup>pale</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome		MGI:7485763	Adar<sup>em3Qwan</sup>/Adar<sup>em3Qwan</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:34332594	20230530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome		MGI:7281842	Adar<sup>em1Stsn</sup>/Adar<sup>tm1.1Phs</sup> Meox2<sup>tm1(cre)Sor</sup>/Meox2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34343497	20230530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome		MGI:7281832	Adar<sup>em1Stsn</sup>/Adar<sup>tm1Olds</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34343497	20230530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3762251	Tg(CMV-Msx2*P7H)1Rem	is_implicated_in	DOID:2340	craniosynostosis		MGI:3762253	Tg(CMV-Msx2*P7H)1Rem/0  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:7597092	20071126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105090	Slc6a5	is_implicated_in	DOID:0060698	hyperekplexia 3		MGI:5796931	Slc6a5<sup>trsl</sup>/Slc6a5<sup>trsl</sup>  [background:] C57BL/6J-Slc6a5<sup>trsl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5796923	20161007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105090	Slc6a5	is_implicated_in	DOID:0060698	hyperekplexia 3		MGI:2682556	Slc6a5<sup>tm1Betz</sup>/Slc6a5<sup>tm1Betz</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:14622583	20161007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448714	Pcdh15<sup>av-Jfb</sup>	is_implicated_in	DOID:0110832	Usher syndrome type 1F		MGI:3575018	Pcdh15<sup>av-Jfb</sup>/Pcdh15<sup>av-Jfb</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12782354	20090220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929988	Klf15	is_implicated_in	DOID:3627	aortic aneurysm		MGI:4888122	Klf15<sup>tm1Jain</sup>/Klf15<sup>tm1Jain</sup>  [background:] B6.129X1-Klf15<sup>tm1Jain</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20375365	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	is_implicated_in	DOID:0060852	Pierson syndrome		MGI:5578543	Lamb2<sup>npht</sup>/Lamb2<sup>npht</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24293254	20140826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	is_implicated_in	DOID:0060852	Pierson syndrome		MGI:2175097	Lamb2<sup>tm1Jrs</sup>/Lamb2<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16452099	20140826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	is_implicated_in	DOID:10140	dry eye syndrome		MGI:3820405	Sod1<sup>tm1Leb</sup>/Sod1<sup>tm1Leb</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25036096	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385355	Cited2<sup>tm1Ycy</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2667200	Cited2<sup>tm1Ycy</sup>/Cited2<sup>tm1Ycy</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12149478	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052223	Ciita<sup>tm2Wrth</sup>	is_implicated_in	DOID:5812	MHC class II deficiency		MGI:3052466	Ciita<sup>tm2Wrth</sup>/Ciita<sup>tm2Wrth</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15322541	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856506	Hr<sup>rh-8J</sup>	is_implicated_in	DOID:0050634	alopecia universalis		MGI:3850354	Hr<sup>rh-8J</sup>/Hr<sup>rh-8J</sup>  [background:] B10.D2/nSnJ-Hr<sup>rh-8J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9799606	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858235	Celsr2	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429557	Celsr2<sup>tm1Lex</sup>/Celsr2<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	is_implicated_in	DOID:0060255	rippling muscle disease 2		MGI:6114152	Cav3<sup>tm1Ncnp</sup>/Cav3<sup>tm1Ncnp</sup>  [background:] involves: 129S4/SvJae * C57BL/10			ECO:0000033	author statement supported by traceable reference	PMID:19535499	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	is_implicated_in	DOID:0060255	rippling muscle disease 2		MGI:2660653	Cav3<sup>tm1Mls</sup>/Cav3<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11259414	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4417930	Tg(KRT14-Fyn*)aJsey	is_implicated_in	DOID:3151	skin squamous cell carcinoma		MGI:4417941	Tg(KRT14-Fyn*)aJsey/0  [background:] involves: C57BL/6 * CBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19934324	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:5085321	Ccm2<sup>tm2.1Sbn</sup>/Ccm2<sup>tm2.1Sbn</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21596842	20190220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:6279212	Ccm2<sup>tm1Mlkn</sup>/Ccm2<sup>tm1Mlkn</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:27513872	20190220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:5052330	Ccm2<sup>tm1Kwhi</sup>/Ccm2<sup>tm1.1Kwhi</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21490399	20190220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	is_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:5297594	Ccm2<sup>tm1.1Etl</sup>/Ccm2<sup>tm1Etl</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21859843	20190220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J		MGI:4838324	Ttn<sup>tm1.1Isrd</sup>/Ttn<sup>tm1.1Isrd</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20855473	20101115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J		MGI:3041561	Ttn<sup>mdm</sup>/Ttn<sup>mdm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11829483	20101115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J		MGI:2651647	Ttn<sup>tm1Her</sup>/Ttn<sup>tm1Her</sup> Tg(Ckmm-cre)5Khn/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12464612	20101115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3041135	Met<sup>tm1Sst</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4950068	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195751	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:5501108	Eng<sup>tm2.1Hma</sup>/Eng<sup>tm2.1Hma</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22571958	20130814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182840	Pkd1<sup>tm2Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617490	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>+</sup>  [background:] either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20081020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182840	Pkd1<sup>tm2Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617489	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>tm2Jzh</sup>  [background:] either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11689485	20081020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182840	Pkd1<sup>tm2Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3811281	Pkd1<sup>tm2Jzh</sup>/Pkd1<sup>tm2Jzh</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18385665	20081020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931787	Scyl1	is_implicated_in	DOID:0050951	hereditary ataxia		MGI:3712360	Scyl1<sup>mdf</sup>/Scyl1<sup>mdf</sup>  [background:] B6C3Fe a/a-Scyl1<sup>mdf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17571074	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386464	Kif3a<sup>tm2Gsn</sup>	is_implicated_in	DOID:1934	dysostosis		MGI:4443124	Kif3a<sup>tm2Gsn</sup>/Kif3a<sup>tm2Gsn</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20106874	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622062	Tnf<sup>tm1Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622060	Tnf<sup>tm2Gkl</sup>/Tnf<sup>tm2Gkl</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10204494	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18439426	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3622061	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23977107	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5558947	Tnf<sup>tm2.1Gkl</sup>/Tnf<sup>tm2.1Gkl</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129S/SvEv * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23977323	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:3699155	Spast<sup>tm1.1Jme</sup>/Spast<sup>tm1.1Jme</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17101632	20200306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:3847312	Spast<sup>M1Gri</sup>/Spast<sup>M1Gri</sup>  [background:] B6.C-Spast<sup>M1Gri</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19453301	20200306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:6393456	Spast<sup>tm1.1Evre</sup>/Spast<sup>tm1.1Evre</sup>  [background:] C57BL/6-Spast<sup>tm1.1Evre</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27019090	20200306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4340776	Pcnt<sup>Gt(RRU388)Byg</sup>	is_implicated_in	DOID:0060609	microcephalic osteodysplastic primordial dwarfism type II		MGI:5705622	Pcnt<sup>Gt(RRU388)Byg</sup>/Pcnt<sup>Gt(RRU388)Byg</sup>  [background:] B6.129P2-Pcnt<sup>Gt(RRU388)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25220058	20160128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043446	Uaca<sup>tm1Kiy</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4430084	Uaca<sup>tm1Kiy</sup>/Uaca<sup>tm1Kiy</sup>  [background:] B6.129P2-Uaca<sup>tm1Kiy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19637241	20100224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:3619449	Sufu<sup>tm1Rto</sup>/Sufu<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16459298	20060413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758741	Comp<sup>tm1Mbri</sup>	is_implicated_in	DOID:12721	multiple epiphyseal dysplasia		MGI:4417874	Comp<sup>tm1Mbri</sup>/Comp<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19808781	20100115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526691	Frem1<sup>bat</sup>	is_implicated_in	DOID:0060732	chromosome 9p deletion syndrome		MGI:3665272	Frem1<sup>bat</sup>/Frem1<sup>bat</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21931569	20111118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526691	Frem1<sup>bat</sup>	is_implicated_in	DOID:0060732	chromosome 9p deletion syndrome		MGI:5295995	Frem1<sup>bat</sup>/Frem1<sup>+</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21931569	20111118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3621567	Erbb2<sup>tm1Cbm</sup>/Erbb2<sup>tm2Cbm</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:12072561	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652418	Zfp36<sup>tm1Pjb</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3037334	Zfp36<sup>tm1Pjb</sup>/Zfp36<sup>tm1Pjb</sup>  [background:] B6.Cg-Zfp36<sup>tm1Pjb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24727475	20141024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	is_not_implicated_in	DOID:1700	X-linked ichthyosis		MGI:3589923	Foxp3<sup>sf</sup>/Y  [background:] involves: STOCK MR			ECO:0000033	author statement supported by traceable reference	MGI:62253	20051019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	is_not_implicated_in	DOID:1700	X-linked ichthyosis		MGI:3589925	Foxp3<sup>sf</sup>/Y  [background:] either: 129Rl.Cg-Foxp3<sup>sf</sup> or (involves: 101/Rl * C3Hf/Rl * STOCK MR)			ECO:0000033	author statement supported by traceable reference	PMID:2053595	20051019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107689	Kif3a	is_implicated_in	DOID:1934	dysostosis		MGI:4443124	Kif3a<sup>tm2Gsn</sup>/Kif3a<sup>tm2Gsn</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20106874	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	is_implicated_in	DOID:14452	hypokalemic periodic paralysis		MGI:5301550	Scn4a<sup>tm1.1Cann</sup>/Scn4a<sup>tm1.1Cann</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21881211	20120116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437270	Lig4<sup>tm2.1Fwa</sup>	is_implicated_in	DOID:0060021	DNA ligase IV deficiency		MGI:4437271	Lig4<sup>tm2.1Fwa</sup>/Lig4<sup>tm2.1Fwa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:20133615	20100315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3610301	Wt1<sup>tm2Hst</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3611443	Wt1<sup>tm2Hst</sup>/Wt1<sup>+</sup>  [background:] chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac			ECO:0000033	author statement supported by traceable reference	PMID:10077614	20060130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3610301	Wt1<sup>tm2Hst</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3611443	Wt1<sup>tm2Hst</sup>/Wt1<sup>+</sup>  [background:] chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac			ECO:0000033	author statement supported by traceable reference	PMID:16245160	20060130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576273	Tg(Ins2*Y16A)3Ell	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3619409	Tg(Ins2*Y16A)3Ell/0  [background:] NOD-Tg(Ins2*Y16A)3Ell			ECO:0000033	author statement supported by traceable reference	PMID:15889095	20060606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934200	Pitx1<sup>tm1Rsd</sup>	is_implicated_in	DOID:11836	clubfoot		MGI:5294943	Pitx1<sup>tm1Rsd</sup>/Pitx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21775501	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	is_implicated_in	DOID:1380	endometrial cancer		MGI:4438263	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Sprr2f-cre)1Dcas/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20142330	20100331	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444274	Cfap65	is_implicated_in	DOID:0111918	spermatogenic failure 40		MGI:6451096	Cfap65<sup>em1Fzh</sup>/Cfap65<sup>em1Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31501240	20200821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151070	Ophn1	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:3758489	Ophn1<sup>tm1Bill</sup>/Y  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:17728457	20090714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429761	Slc19a2<sup>tm1Gelb</sup>	is_implicated_in	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome		MGI:3033364	Slc19a2<sup>tm1Gelb</sup>/Slc19a2<sup>tm1Gelb</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12393806	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794302	Frem2<sup>ne</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3796628	Frem2<sup>ne</sup>/Frem2<sup>ne</sup>  [background:] STOCK Frem2<sup>ne</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794302	Frem2<sup>ne</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3796628	Frem2<sup>ne</sup>/Frem2<sup>ne</sup>  [background:] STOCK Frem2<sup>ne</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5428032	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857873	Sod1<sup>tm1Leb</sup>	is_implicated_in	DOID:13544	low tension glaucoma		MGI:3580495	Sod1<sup>tm1Leb</sup>/Sod1<sup>tm1Leb</sup>  [background:] B6;129S-Sod1<sup>tm1Leb</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21421868	20120325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	is_implicated_in	DOID:14705	Pfeiffer syndrome		MGI:2174904	Fgfr1<sup>tm1Led</sup>/Fgfr1<sup>tm1Led</sup>  [background:] involves: 129S4/SvJae * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8001823	20160831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	is_implicated_in	DOID:14705	Pfeiffer syndrome		MGI:5790247	Fgfr1<sup>tm2.1Cxd</sup>/Fgfr1<sup>+</sup>  [background:] D2.129S6(Cg)-Fgfr1<sup>tm2.1Cxd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21538817	20160831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926024	Cfap61	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7448446	Cfap61<sup>em1Yqt</sup>/Cfap61<sup>em1Yqt</sup>  [background:] C57BL/6-Cfap61<sup>em1Yqt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35387802	20230328	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	is_implicated_in	DOID:10907	microcephaly		MGI:6119481	Tubb5<sup>tm2.1Dak</sup>/Tubb5<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26903504	20180305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	is_implicated_in	DOID:10907	microcephaly		MGI:6119480	Tubb5<sup>tm1.1Dak</sup>/Tubb5<sup>tm1.1Dak</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:26903504	20180305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920918	Ttc21b	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5587035	Ttc21b<sup>tm2c(KOMP)Wtsi</sup>/Ttc21b<sup>aln</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24700869	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:10754	otitis media		MGI:4459466	Lmna<sup>Dhe</sup>/Lmna<sup>+</sup>  [background:] B6(D2)-Lmna<sup>Dhe</sup>/TyGrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:22819531	20180206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	is_implicated_in	DOID:0110005	Leber congenital amaurosis 9		MGI:6272874	Nmnat1<sup>tm1Ruch</sup>/Nmnat1<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29674119	20190110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	is_implicated_in	DOID:0110005	Leber congenital amaurosis 9		MGI:5903761	Nmnat1<sup>imh</sup>/Nmnat1<sup>imh</sup>  [background:] B6J.C(C3H)-Nmnat1<sup>imh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27207593	20190110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:9452	steatotic liver disease		MGI:4829790	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:24802098	20160113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5702658	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15199412	20160113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448567	Chd2	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5515353	Chd2<sup>Gt(RRBO46)Byg</sup>/Chd2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18386809	20140818	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918673	Epg5	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:5505671	Epg5<sup>tm1Ygz</sup>/Epg5<sup>tm1Ygz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23479740	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3574621	Muc2<sup>tm1Avel</sup>/Muc2<sup>tm1Avel</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24945909	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3615592	Muc2<sup>wnn</sup>/Muc2<sup>wnn</sup>  [background:] C57BL/6-Muc2<sup>wnn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18318598	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5471480	Muc2<sup>eey</sup>/Muc2<sup>eey</sup>  [background:] C57BL/6-Muc2<sup>eey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18318598	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155417	Myo7a<sup>26SB</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587744	Myo7a<sup>26SB</sup>/Myo7a<sup>26SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652946	Bsn<sup>tm1Gund</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:2652947	Bsn<sup>tm1Gund</sup>/Bsn<sup>tm1Gund</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12628169	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914944	Ift74	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5311937	Ift74<sup>b2b796Clo</sup>/Ift74<sup>b2b796Clo</sup>  [background:] C57BL/6J-Ift74<sup>b2b796Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4443333	Best1<sup>tm1.1Amar</sup>	is_implicated_in	DOID:0050662	bestrophinopathy		MGI:4443335	Best1<sup>tm1.1Amar</sup>/Best1<sup>tm1.1Amar</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4443333	Best1<sup>tm1.1Amar</sup>	is_implicated_in	DOID:0050662	bestrophinopathy		MGI:4450918	Best1<sup>tm1.1Amar</sup>/Best1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451080	Lipa<sup>tm1Ggb</sup>	is_implicated_in	DOID:0080217	lysosomal acid lipase deficiency		MGI:2451081	Lipa<sup>tm1Ggb</sup>/Lipa<sup>tm1Ggb</sup>  [background:] involves: 129P2/OlaHsd * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:9700186	20190729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	is_not_implicated_in	DOID:0050470	Donohue syndrome		MGI:2174959	Insr<sup>tm1Dac</sup>/Insr<sup>tm1Dac</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8528241	20051024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	is_not_implicated_in	DOID:0050470	Donohue syndrome		MGI:2174961	Insr<sup>tm1Jja</sup>/Insr<sup>tm1Jja</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:8612577	20051024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_not_implicated_in	DOID:10016	multiple endocrine neoplasia type 2B		MGI:3583336	Ret<sup>tm1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * C57BL/6J * FVB/N * MF1			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	is_implicated_in	DOID:0110545	autosomal dominant nonsyndromic deafness 13		MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107361	Ctse	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3629084	Ctse<sup>tm1Kjy</sup>/Ctse<sup>tm1Kjy</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14769879	20140520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443373	Relt	is_implicated_in	DOID:0111722	amelogenesis imperfecta type 3C		MGI:6369622	Relt<sup>em1Jpsi</sup>/Relt<sup>em1Jpsi</sup>  [background:] C57BL/6-Relt<sup>em1Jpsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30506946	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429923	Glb1<sup>tm1Jmat</sup>	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3640134	Glb1<sup>tm1Jmat</sup>/Glb1<sup>tm1Jmat</sup>  [background:] involves: C57BL/6 * CBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9337086	20060808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429923	Glb1<sup>tm1Jmat</sup>	is_implicated_in	DOID:3322	GM1 gangliosidosis		MGI:3640134	Glb1<sup>tm1Jmat</sup>/Glb1<sup>tm1Jmat</sup>  [background:] involves: C57BL/6 * CBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:9071485	20060808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913563	Smurf2	is_implicated_in	DOID:0050745	diffuse large B-cell lymphoma		MGI:5446903	Smurf2<sup>Gt(RRA098)Byg</sup>/Smurf2<sup>Gt(RRA098)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28107482	20190709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	is_implicated_in	DOID:0050158	desquamative interstitial pneumonia		MGI:3037342	Sftpc<sup>tm1Swg</sup>/Sftpc<sup>tm1Swg</sup>  [background:] either: 129 or (involves: 129 * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:12519727	20080910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491160	b2b2059Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5555838	b2b2059Clo/b2b2059Clo  [background:] C57BL/6J-b2b2059Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180882	Krt10<sup>tm1Tmm</sup>	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:2672094	Krt10<sup>tm1Tmm</sup>/Krt10<sup>+</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8603923	20090224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180882	Krt10<sup>tm1Tmm</sup>	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:2672093	Krt10<sup>tm1Tmm</sup>/Krt10<sup>tm1Tmm</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8603923	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	is_implicated_in	DOID:0110403	retinitis pigmentosa 13		MGI:4950567	Prpf8<sup>tm1.1Eap</sup>/Prpf8<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	is_implicated_in	DOID:0110403	retinitis pigmentosa 13		MGI:4950566	Prpf8<sup>tm1.1Eap</sup>/Prpf8<sup>tm1.1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857729	Hapln1<sup>tm1Nid</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:3038695	Hapln1<sup>tm1Nid</sup>/Hapln1<sup>tm1Nid</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9988279	20051006	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88223	C1qa	is_implicated_in	DOID:1826	epilepsy		MGI:4452482	C1qa<sup>tm1Mjw</sup>/C1qa<sup>tm1Mjw</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:20375278	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3664332	plt	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4437582	plt/plt  [background:] either: B6.DDD-plt or C.DDD-plt			ECO:0000033	author statement supported by traceable reference	PMID:16473829	20100319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201690	Map6	is_implicated_in	DOID:5419	schizophrenia		MGI:5694660	Map6<sup>tm1Job</sup>/Map6<sup>tm1Job</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23002183	20151104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201690	Map6	is_implicated_in	DOID:5419	schizophrenia		MGI:5694657	Map6<sup>tm1Job</sup>/Map6<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23002183	20151104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201690	Map6	is_implicated_in	DOID:5419	schizophrenia		MGI:3041140	Map6<sup>tm1Job</sup>/Map6<sup>tm1Job</sup>  [background:] either: 129S2/SvPas or (involves: 129S2/SvPas * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:12231625	20151104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	is_not_implicated_in	DOID:10041	dysplastic nevus syndrome		MGI:2175771	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup>  [background:] involves: 129/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8620534	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4417931	Slitrk6<sup>tm1.1Jaru</sup>	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:4941487	Slitrk6<sup>tm1.1Jaru</sup>/Slitrk6<sup>tm1.1Jaru</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21298075	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583532	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] D2J.B6(Cg)-Cys1<sup>cpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:4032601	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583529	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/JUnc			ECO:0000033	author statement supported by traceable reference	PMID:6624875	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583531	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] C.B6(Cg)-Cys1<sup>cpk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11004214	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3583530	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] involves: C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8800407	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2175905	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7062441	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2175905	Cys1<sup>cpk</sup>/Cys1<sup>cpk</sup>  [background:] B6(Cg)-Cys1<sup>cpk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:3404974	20050812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:4850046	Fbn2<sup>tm1Rmz</sup>/Fbn2<sup>tm1Rmz</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:20729550	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:5574592	Fbn2<sup>fp-4J</sup>/Fbn2<sup>fp-4J</sup>  [background:] BALB/cByJ-Fbn2<sup>fp-4J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:4438065	Fbn2<sup>mz</sup>/Fbn2<sup>mz</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:20161761	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:3652413	Fbn2<sup>tm1Rmz</sup>/Fbn2<sup>tm1Rmz</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11470817	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	is_implicated_in	DOID:0110746	type 1 diabetes mellitus 7		MGI:2174973	Neurod1<sup>tm1Mjts</sup>/Neurod1<sup>tm1Mjts</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9308961	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419915	Cox6a1<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110203	Charcot-Marie-Tooth disease recessive intermediate D		MGI:5804696	Cox6a1<sup>tm1(KOMP)Wtsi</sup>/Cox6a1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6JJcl * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25152455	20161024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429387	Tg(Vav-BCL2)69Jad	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:3842939	Tg(Vav-BCL2)69Jad/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14630790	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857344	Sod2<sup>tm1Cje</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3584030	Ap3b1<sup>pe-rim2</sup>/Ap3b1<sup>pe-rim2</sup>  [background:] involves: B10.A(R201) * C57BL/10Slc			ECO:0000033	author statement supported by traceable reference	PMID:9434937	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12		MGI:5141009	Cdh23<sup>12J</sup>/Cdh23<sup>12J</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20644563	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12		MGI:3709038	Cdh23<sup>sals</sup>/Cdh23<sup>sals</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19270079	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	is_implicated_in	DOID:0110467	autosomal recessive nonsyndromic deafness 12		MGI:5140886	Cdh23<sup>Jera</sup>/Cdh23<sup>Jera</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685903	B3glct	is_implicated_in	DOID:0080201	Peters plus syndrome		MGI:6406868	B3glct<sup>tm1.2Nari</sup>/B3glct<sup>tm1.2Nari</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J * DBA/2 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:31600785	20200429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685903	B3glct	is_implicated_in	DOID:0080201	Peters plus syndrome		MGI:6406756	B3glct<sup>tm1b(KOMP)Wtsi</sup>/B3glct<sup>tm1b(KOMP)Wtsi</sup>  [background:] B6(Cg)-B3glct<sup>tm1b(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31600785	20200429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277977	Ubr1	is_implicated_in	DOID:14694	Johanson-Blizzard syndrome		MGI:3654648	Ubr1<sup>tm1Avar</sup>/Ubr1<sup>tm1Avar</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16311597	20100309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3047777	Avpr2<sup>tm1Jwe</sup>/Avpr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:11104789	20050602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:2175713	Avpr2<sup>tm1Jwe</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:11104789	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843052	Ep300<sup>tm2Reck</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3843174	Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup> Ep300<sup>tm2Reck</sup>/Ep300<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17513743	20090506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2383957	Sh2b3<sup>tm1Paw</sup>	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5296515	Sh2b3<sup>tm1Paw</sup>/Sh2b3<sup>tm1Paw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20458146	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100882	Phox2b	is_implicated_in	DOID:0060731	congenital central hypoventilation syndrome		MGI:3797591	Phox2b<sup>tm2Jbr</sup>/Phox2b<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18198276	20221205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100882	Phox2b	is_implicated_in	DOID:0060731	congenital central hypoventilation syndrome		MGI:7397263	Phox2b<sup>tm1Rth</sup>/Phox2b<sup>+</sup> Hprt1<sup>tm1(CAG-cre)Mnn</sup>/?  [background:] involves: 129 * 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25975378	20221205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95457	Mecom	is_implicated_in	DOID:10754	otitis media		MGI:6102908	Mecom<sup>Jbo</sup>/Mecom<sup>+</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20057387	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95457	Mecom	is_implicated_in	DOID:10754	otitis media		MGI:3689583	Mecom<sup>Jbo</sup>/Mecom<sup>+</sup>  [background:] C3N.C-Mecom<sup>Jbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17029558	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	is_implicated_in	DOID:2841	asthma		MGI:2680727	Il4ra<sup>tm1Tch</sup>/Il4ra<sup>tm1Tch</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:14557412	20091021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	is_implicated_in	DOID:2841	asthma		MGI:4361938	Il4ra<sup>tm2Tch</sup>/Il4ra<sup>tm2Tch</sup>  [background:] C.129X1-Il4ra<sup>tm2Tch</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19770271	20091021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334462	Copa	is_implicated_in	DOID:0081242	autoimmune interstitial lung, joint, and kidney disease		MGI:7336761	Copa<sup>tm1.1Shum</sup>/Copa<sup>+</sup>  [background:] B6(CBA)-Copa<sup>tm1.1Shum</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32198142	20230113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043589	Ercc5<sup>tm3Shm</sup>	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043597	Ercc5<sup>tm3Shm</sup>/Ercc5<sup>tm3Shm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889383	Ap1s2	is_implicated_in	DOID:0060800	syndromic X-linked intellectual disability 5		MGI:5661462	Ap1s2<sup>tm1Pschu</sup>/Ap1s2<sup>tm1Pschu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20203623	20150911	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916835	Hjv	is_implicated_in	DOID:0111027	hemochromatosis type 2A		MGI:3588420	Hjv<sup>tm1Nca</sup>/Hjv<sup>tm1Nca</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:16075059	20050929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916835	Hjv	is_implicated_in	DOID:0111027	hemochromatosis type 2A		MGI:3588579	Hjv<sup>tm1Arbr</sup>/Hjv<sup>tm1Arbr</sup>  [background:] involves: 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16075058	20050929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387466	Pank4	is_implicated_in	DOID:83	cataract		MGI:6508539	Pank4<sup>em1Nju</sup>/Pank4<sup>em1Nju</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30585370	20210303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919782	Sap130	is_implicated_in	DOID:1682	congenital heart disease		MGI:5906296	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919782	Sap130	is_implicated_in	DOID:1682	congenital heart disease		MGI:5906294	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup> Pcdha9<sup>b2b635.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181803	Mest<sup>tm1Masu</sup>	is_implicated_in	DOID:0050476	Barth syndrome		MGI:2677273	Mest<sup>tm1Masu</sup>/Mest<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12242721	20181015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856393	Gnrh1<sup>hpg</sup>	is_implicated_in	DOID:0090072	hypogonadotropic hypogonadism 12 with or without anosmia		MGI:2663794	Gnrh1<sup>hpg</sup>/Gnrh1<sup>hpg</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:198666	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:4418710	nad	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:4418721	nad/nad  [background:] C(D2)-nad			ECO:0000033	author statement supported by traceable reference	PMID:16542671	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437115	Cep290<sup>b2b1454Clo</sup>/Cep290<sup>b2b1454Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1454Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921303	Grip1	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:2654707	Grip1<sup>tm1Paw</sup>/Grip1<sup>tm1Paw</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11983858	20050719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838534	Prom1<sup>tm1Pec</sup>	is_implicated_in	DOID:0110376	retinitis pigmentosa 41		MGI:3838535	Prom1<sup>tm1Pec</sup>/Prom1<sup>tm1Pec</sup>  [background:] B6.129-Prom1<sup>tm1Pec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19228982	20090403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857768	Chuk<sup>tm1Mka</sup>	is_implicated_in	DOID:0060647	fetal encasement syndrome		MGI:3609030	Chuk<sup>tm1Mka</sup>/Chuk<sup>tm1Mka</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858026	Crygd<sup>Lop12</sup>	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:2175808	Crygd<sup>Lop12</sup>/Crygd<sup>+</sup>  [background:] involves: BALB/cJ * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:10704279	20050718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386677	Abcc8<sup>tm1Jbry</sup>	is_not_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:2446456	Abcc8<sup>tm1Jbry</sup>/Abcc8<sup>tm1Jbry</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10734066	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926381	Msx2<sup>tm1Rilm</sup>	is_implicated_in	DOID:0060285	parietal foramina		MGI:2175121	Msx2<sup>tm1Rilm</sup>/Msx2<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10742104	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856008	Myo5a<sup>d-n</sup>	is_implicated_in	DOID:0060832	Griscelli syndrome type 1		MGI:3624435	Myo5a<sup>d-n</sup>/Myo5a<sup>d-n</sup>  [background:] B10.D2-H2<sup>d</sup>/nSnJ			ECO:0000033	author statement supported by traceable reference	PMID:21508232	20110606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444628	Sh3rf2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6430624	Sh3rf2<sup>tm1Zhxu</sup>/Sh3rf2<sup>+</sup> Tg(Thy1-EGFP)MJrs/0  [background:] involves: C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:30540932	20200529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444628	Sh3rf2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6430623	Sh3rf2<sup>tm1Zhxu</sup>/Sh3rf2<sup>+</sup>  [background:] C57BL/6-Sh3rf2<sup>tm1Zhxu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30540932	20200529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710185	Ift88<sup>tm1Bky</sup>	is_implicated_in	DOID:61	mitral valve disease		MGI:6718510	Ift88<sup>tm1Bky</sup>/Ift88<sup>tm1Bky</sup> Nfatc1<sup>tm1.1(cre)Bz</sup>/Nfatc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398904	Acvrl1<sup>tm2Spo</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:4398918	Acvrl1<sup>tm2Spo</sup>/Acvrl1<sup>tm2Spo</sup> Tg(Acvrl1-cre)L1Spo/0  [background:] involves: 129 * 129S4/SvJae * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17911384	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	is_implicated_in	DOID:3323	Sandhoff disease		MGI:2668046	Hexb<sup>tm1Grv</sup>/Hexb<sup>tm1Grv</sup>  [background:] either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J)			ECO:0000033	author statement supported by traceable reference	PMID:8789434	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	is_implicated_in	DOID:3323	Sandhoff disease		MGI:2177468	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23028353	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	is_implicated_in	DOID:3323	Sandhoff disease		MGI:3579385	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14722612	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	is_implicated_in	DOID:3323	Sandhoff disease		MGI:6507051	Hexb<sup>lysd</sup>/Hexb<sup>lysd</sup>  [background:] B6.Cg-Hexb<sup>lysd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:31547903	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	is_implicated_in	DOID:3323	Sandhoff disease		MGI:2177468	Hexb<sup>tm1Rlp</sup>/Hexb<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7550345	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3525053	Ppp1r13l	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy		MGI:5910392	Ppp1r13l<sup>tm1.1Xlu</sup>/Ppp1r13l<sup>tm1.1Xlu</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25691752	20170926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822145	Dnah11<sup>avc4</sup>/Dnah11<sup>avc4</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_implicated_in	DOID:12270	coloboma		MGI:7261162	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:33075808	20220412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	is_implicated_in	DOID:11105	fundus albipunctatus		MGI:2386344	Mfrp<sup>rd6</sup>/Mfrp<sup>rd6</sup>  [background:] B6.C3-Mfrp<sup>rd6</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10967077	20050510	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97851	Slc20a2	is_implicated_in	DOID:0060230	basal ganglia calcification		MGI:5806601	Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>/Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6NTac-Slc20a2<sup>tm1a(EUCOMM)Wtsi</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:23934451	20161110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99461	Piga	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3758821	Piga<sup>tm1Tak</sup>/Y Tg(KRT5-cre)1Tak/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15304084	20190517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99461	Piga	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:6303984	Piga<sup>tm1Tak</sup>/Piga<sup>tm1Tak</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15304084	20190517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930996	Csf2<sup>tm1Mlg</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3606654	Csf2<sup>tm1Mlg</sup>/Csf2<sup>tm1Mlg</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8171324	20051207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2145645	Exoc5	is_implicated_in	DOID:0070314	obstructive nephropathy		MGI:5774940	Exoc5<sup>tm1c(KOMP)Mbp</sup>/Exoc5<sup>tm1c(KOMP)Mbp</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:27511831	20190705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2145645	Exoc5	is_implicated_in	DOID:0070314	obstructive nephropathy		MGI:5774940	Exoc5<sup>tm1c(KOMP)Mbp</sup>/Exoc5<sup>tm1c(KOMP)Mbp</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:26046524	20190705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:0090111	PCWH syndrome		MGI:3576603	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12616486	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:13359	Ehlers-Danlos syndrome		MGI:5689511	Col1a1<sup>M1Jrt</sup>/Col1a1<sup>+</sup>  [background:] involves: C3H/HeJ * C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:24443344	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916066	Ppil1	is_implicated_in	DOID:0112325	pontocerebellar hypoplasia type 14		MGI:6509640	Ppil1<sup>em4Jgg</sup>/Ppil1<sup>em4Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em4Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916066	Ppil1	is_implicated_in	DOID:0112325	pontocerebellar hypoplasia type 14		MGI:6509636	Ppil1<sup>em3Jgg</sup>/Ppil1<sup>em3Jgg</sup>  [background:] C57BL/6-Ppil1<sup>em3Jgg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33220177	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526416	Iqgap2<sup>tm1Vs</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5568837	Iqgap2<sup>tm1Vs</sup>/Iqgap2<sup>tm1Vs</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:23951254	20140619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2138030	Mapt<sup>tm1Noh</sup>	is_not_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174969	Mapt<sup>tm1Noh</sup>/Mapt<sup>tm1Noh</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:8202139	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	is_implicated_in	DOID:4480	achondroplasia		MGI:2183025	Npr2<sup>cn-2J</sup>/Npr2<sup>cn-2J</sup>  [background:] B6;CBACa-A<sup>w-J</sup>/A-Kcnj6<sup>wv</sup>/+			ECO:0000033	author statement supported by traceable reference	MGI:2152911	20180629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	is_implicated_in	DOID:4480	achondroplasia		MGI:3828048	Npr2<sup>cn</sup>/Npr2<sup>cn</sup>  [background:] involves: AKR/J			ECO:0000033	author statement supported by traceable reference	MGI:75337	20180629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	is_implicated_in	DOID:4480	achondroplasia		MGI:4947978	Npr2<sup>cn-3J</sup>/Npr2<sup>cn-3J</sup>  [background:] MRL/MpJ-Npr2<sup>cn-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:4947088	20180629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573699	Tg(Ins2-GP)34-20Olds	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3618987	Tg(Ins2-GP)34-20Olds/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7889411	20060411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1		MGI:5474570	Bbs1<sup>tm2Vcs</sup>/Bbs1<sup>tm2Vcs</sup> Tg(Pdgfra-cre)1Clc/0  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23160237	20130418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1		MGI:3055584	Bbs1<sup>Gt1Nk</sup>/Bbs1<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20130418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	is_implicated_in	DOID:0110123	Bardet-Biedl syndrome 1		MGI:3767679	Bbs1<sup>tm1Vcs</sup>/Bbs1<sup>tm1Vcs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18032602	20130418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	is_implicated_in	DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L		MGI:6149568	Ano5<sup>tm1Lrk</sup>/Ano5<sup>tm1Lrk</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26911675	20180405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88414	ckr	is_implicated_in	DOID:5419	schizophrenia		MGI:2663269	ckr/ckr  [background:] involves: C3H/HeRos * C57BL/10Ros			ECO:0000033	author statement supported by traceable reference	PMID:14709346	20081212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3578641	Frem2<sup>my-Ucl</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3579980	Frem2<sup>my-Ucl</sup>/Frem2<sup>my-Ucl</sup>  [background:] involves: NMRI			ECO:0000033	author statement supported by traceable reference	PMID:15838507	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653208	Dspp<sup>tm1Kul</sup>	is_implicated_in	DOID:4154	dentinogenesis imperfecta		MGI:2673970	Dspp<sup>tm1Kul</sup>/Dspp<sup>tm1Kul</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12721295	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	is_implicated_in	DOID:3883	Lynch syndrome		MGI:2663863	Mlh1<sup>tm1Rak</sup>/Mlh1<sup>tm1Rak</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10096563	20091216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347521	Ror2	is_not_implicated_in	DOID:0110969	brachydactyly type B1		MGI:3793283	Ror2<sup>tm1Anec</sup>/Ror2<sup>+</sup>  [background:] B6.129S1-Ror2<sup>tm1Anec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18353862	20080611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429736	Il2rg<sup>tm1Sug</sup>	is_not_implicated_in	DOID:0060013	X-linked severe combined immunodeficiency		MGI:2655194	Il2rg<sup>tm1Sug</sup>/Y  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8562967	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2448607	Nyx	is_implicated_in	DOID:0110870	congenital stationary night blindness 1A		MGI:3055970	Nyx<sup>nob</sup>/Nyx<sup>nob</sup>  [background:] BALB/c-Nyx<sup>nob</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9804152	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906203	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19001090	20170803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4156902	Sdccag8<sup>Gt(OST40418)Lex</sup>	is_implicated_in	DOID:12712	nephronophthisis		MGI:5705821	Sdccag8<sup>Gt(OST40418)Lex</sup>/Sdccag8<sup>Gt(OST40418)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24722439	20220915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917311	Sdr9c7	is_implicated_in	DOID:0080257	autosomal recessive congenital ichthyosis 13		MGI:6469470	Sdr9c7<sup>em1Maak</sup>/Sdr9c7<sup>em1Maak</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31671075	20201027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619530	Spi1<sup>tm1.3Dgt</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3714968	Spi1<sup>tm1.3Dgt</sup>/Spi1<sup>tm1.3Dgt</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15146183	20070717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861707	Was<sup>tm1Sbs</sup>	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:5307127	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] 129S6/SvEvTac-Was<sup>tm1Sbs</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22079330	20120226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052739	Pex7<sup>tm1Rjaw</sup>	is_implicated_in	DOID:0110851	rhizomelic chondrodysplasia punctata type 1		MGI:3052846	Pex7<sup>tm1Rjaw</sup>/Pex7<sup>tm1Rjaw</sup>  [background:] Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12915479	20050713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5646610	b2b3077.2Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5648030	b2b3077.2Clo/b2b3077.2Clo  [background:] C57BL/6J-b2b3077.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3044955	Impg2	is_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:6693692	Impg2<sup>em1Visu</sup>/Impg2<sup>em1Visu</sup>  [background:] involves: C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:32265257	20210420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444341	Phf8	is_implicated_in	DOID:0060812	syndromic X-linked intellectual disability Siderius type		MGI:6370003	Phf8<sup>tm1.1Cdcn</sup>/Y  [background:] B6.129S6(Cg)-Phf8<sup>tm1.1Cdcn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29317619	20191107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147790	Fermt3	is_implicated_in	DOID:0110912	leukocyte adhesion deficiency 3		MGI:3795785	Fermt3<sup>tm1Ref</sup>/Fermt3<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19234461	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339968	Cth	is_implicated_in	DOID:0090142	cystathioninuria		MGI:4840250	Cth<sup>tm1Iish</sup>/Cth<sup>tm1Iish</sup>  [background:] B6.129-Cth<sup>tm1Iish</sup>/Iish			ECO:0000033	author statement supported by traceable reference	PMID:20566639	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	is_implicated_in	DOID:13628	favism		MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock			ECO:0000033	author statement supported by traceable reference	PMID:12777375	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	is_implicated_in	DOID:13628	favism		MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock			ECO:0000033	author statement supported by traceable reference	PMID:14751857	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	is_implicated_in	DOID:13628	favism		MGI:3628913	G6pdx<sup>a-m1Neu</sup>/Y  [background:] involves: 102/El * C3H/El * T-stock			ECO:0000033	author statement supported by traceable reference	PMID:3377761	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276523	Ncoa1	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3527794	Ncoa1<sup>tm1Bwo</sup>/Ncoa1<sup>tm1Bwo</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10202153	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106582	Rfx3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5560505	Rfx3<sup>b2b1213Clo</sup>/Rfx3<sup>b2b1213Clo</sup>  [background:] C57BL/6J-Rfx3<sup>b2b1213Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3870362	Cep290<sup>Gt(CC0582)Wtsi</sup>	is_implicated_in	DOID:0111000	Joubert syndrome 5		MGI:5749256	Cep290<sup>Gt(CC0582)Wtsi</sup>/Cep290<sup>Gt(CC0582)Wtsi</sup>  [background:] 129P2/OlaHsd-Cep290<sup>Gt(CC0582)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24946806	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3870362	Cep290<sup>Gt(CC0582)Wtsi</sup>	is_implicated_in	DOID:0111000	Joubert syndrome 5		MGI:5749256	Cep290<sup>Gt(CC0582)Wtsi</sup>/Cep290<sup>Gt(CC0582)Wtsi</sup>  [background:] 129P2/OlaHsd-Cep290<sup>Gt(CC0582)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26301811	20160505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	is_implicated_in	DOID:14452	hypokalemic periodic paralysis		MGI:5474008	Cacna1s<sup>tm1.1Cann</sup>/Cacna1s<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:23187123	20130411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	is_implicated_in	DOID:14452	hypokalemic periodic paralysis		MGI:5474009	Cacna1s<sup>tm1.1Cann</sup>/Cacna1s<sup>tm1.1Cann</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:7962166	20130411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857061	Slc7a11<sup>sut</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2677961	Slc7a11<sup>sut</sup>/Slc7a11<sup>sut</sup>  [background:] C3H/HeSnJ-Slc7a11<sup>sut</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8699821	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929915	Ncoa6	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276351	Ncoa6<sup>tm1Jkr</sup>/Ncoa6<sup>tm1Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929915	Ncoa6	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276352	Ncoa6<sup>tm1Jkr</sup>/Ncoa6<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	is_implicated_in	DOID:0050477	Liddle syndrome		MGI:3796438	Scnn1b<sup>tm1.1Ipt</sup>/Scnn1b<sup>tm1.1Ipt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10589691	20080709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040264	Tg(RIR-Tag)87Dh	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5431967	Tg(RIR-Tag)87Dh/0  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:2986015	20120821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574015	Tg(SOD1*G37R)9Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3814059	Tg(SOD1*G37R)9Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7605627	20081106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88415	cl	is_implicated_in	DOID:11836	clubfoot		MGI:2663270	cl/cl  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:48832	20110125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	is_implicated_in	DOID:0070037	autosomal dominant intellectual developmental disorder 7		MGI:7264822	Dyrk1a<sup>em1Kzy</sup>/Dyrk1a<sup>+</sup>  [background:] C57BL/6J-Dyrk1a<sup>em1Kzy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29223763	20220428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3806463	Tg(H2-L-IL6)46Kish	is_implicated_in	DOID:9120	amyloidosis		MGI:5301598	Tg(H2-L-IL6)46Kish/Tg(H2-L-IL6)46Kish  [background:] C.B6-Tg(H2-L-IL6)46Kish			ECO:0000033	author statement supported by traceable reference	PMID:19149411	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441769	Dclre1c	is_implicated_in	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation		MGI:3576477	Dclre1c<sup>tm2Mcow</sup>/Dclre1c<sup>tm2Mcow</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15699179	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441769	Dclre1c	is_implicated_in	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation		MGI:3843211	Dclre1c<sup>tm1Jsek</sup>/Dclre1c<sup>tm1Jsek</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19349461	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857268	Wt1<sup>tm1Jae</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:2669009	Wt1<sup>tm1Jae</sup>/Wt1<sup>tm1Jae</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * MF1			ECO:0000033	author statement supported by traceable reference	PMID:17071579	20161003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665237	Frem1<sup>tm1Ksek</sup>/Frem1<sup>tm1Ksek</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665276	Frem1<sup>bfd</sup>/Frem1<sup>bfd</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665272	Frem1<sup>bat</sup>/Frem1<sup>bat</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665277	Frem1<sup>heb</sup>/Frem1<sup>heb</sup>  [background:] involves: AKR/J			ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2136853	Fam20c	is_implicated_in	DOID:10609	rickets		MGI:5428021	Fam20c<sup>tm1.1Cqi</sup>/Fam20c<sup>tm1.1Cqi</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22615579	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	is_implicated_in	DOID:0111102	maturity-onset diabetes of the young type 3		MGI:3623394	Hnf1a<sup>tm1.1Ylee</sup>/Hnf1a<sup>tm1.1Ylee</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9566924	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861947	Il2rg<sup>tm1Cgn</sup>	is_not_implicated_in	DOID:628	combined T cell and B cell immunodeficiency		MGI:2179821	Il2rg<sup>tm1Cgn</sup>/Il2rg<sup>tm1Cgn</sup>  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861947	Il2rg<sup>tm1Cgn</sup>	is_not_implicated_in	DOID:628	combined T cell and B cell immunodeficiency		MGI:2179823	Il2rg<sup>tm1Cgn</sup>/Y  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	is_implicated_in	DOID:14755	argininosuccinic aciduria		MGI:5308984	Asl<sup>tm1Brle</sup>/Asl<sup>tm1Brle</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:22541557	20130912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	is_implicated_in	DOID:14755	argininosuccinic aciduria		MGI:3605490	Asl<sup>tm1Wjc</sup>/Asl<sup>tm1Wjc</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12559843	20130912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	is_implicated_in	DOID:0110497	autosomal recessive nonsyndromic deafness 39		MGI:6446738	Hgf<sup>tm1.1Tbf</sup>/Hgf<sup>tm1.1Tbf</sup>  [background:] B6.Cg-Hgf<sup>tm1.1Tbf</sup>/Tbf			ECO:0000033	author statement supported by traceable reference	PMID:32152201	20200730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	is_implicated_in	DOID:0110497	autosomal recessive nonsyndromic deafness 39		MGI:6446736	Hgf<sup>tm1Tbf</sup>/Hgf<sup>tm1Tbf</sup>  [background:] B6.Cg-Hgf<sup>tm1Tbf</sup>/Tbf			ECO:0000033	author statement supported by traceable reference	PMID:32152201	20200730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:0050771	pheochromocytoma		MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7417782	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	is_implicated_in	DOID:10587	Krabbe disease		MGI:2652424	Galc<sup>tm1Wngr</sup>/Galc<sup>tm1Wngr</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:11461188	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20441793	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7437911	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	is_implicated_in	DOID:10587	Krabbe disease		MGI:6725727	Galc<sup>m4Btlr</sup>/Galc<sup>m4Btlr</sup>  [background:] C57BL/6J-Galc<sup>m4Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	is_implicated_in	DOID:10587	Krabbe disease		MGI:3581125	Galc<sup>twi</sup>/Galc<sup>twi</sup>  [background:] B6.CE-Galc<sup>twi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21389217	20220426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429651	Cd200<sup>tm1Jods</sup>	is_implicated_in	DOID:417	autoimmune disease		MGI:3576859	Cd200<sup>tm1Jods</sup>/Cd200<sup>tm1Jods</sup>  [background:] C57BL/6-Cd200<sup>tm1Jods</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11099416	20050516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109189	Fgf14	is_implicated_in	DOID:0050976	spinocerebellar ataxia type 27		MGI:3663129	Fgf14<sup>tm1Dor</sup>/Fgf14<sup>tm1Dor</sup>  [background:] B6.129S6-Fgf14<sup>tm1Dor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17236779	20150703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857194	Il4<sup>tm1Cgn</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3625060	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] either: NOD.129-Il4<sup>tm1Cgn</sup> or (involves: 129 * NOD)			ECO:0000033	author statement supported by traceable reference	PMID:9703318	20060622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178045	Krt18<sup>tm1Tmm</sup>	is_implicated_in	DOID:0080547	metabolic dysfunction-associated steatohepatitis		MGI:7280898	Krt18<sup>tm1Tmm</sup>/Krt18<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27689336	20220526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913302	Sdhc	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:6392337	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>/Sdhc<sup>tm1c(EUCOMM)Wtsi</sup> Gt(ROSA)26Sor<sup>tm1.1(rtTA,tetO-cre)Bkmn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31469588	20200302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3715267	Gfra1<sup>tm1Jmi</sup>/Gfra1<sup>tm2Jmi</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129/Sv * C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17507417	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2175040	Gfra1<sup>tm1Jmi</sup>/Gfra1<sup>tm1Jmi</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9728913	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920230	Wdr11	is_implicated_in	DOID:0060340	ciliopathy		MGI:6162486	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>/Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>  [background:] B6.Cg-Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29263200	20180626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	is_implicated_in	DOID:11589	Riley-Day syndrome		MGI:5558037	Elp1<sup>tm1c(KOMP)Wtsi</sup>/Elp1<sup>tm1c(KOMP)Wtsi</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * C57BL/6N * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:24173031	20140410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	is_implicated_in	DOID:11589	Riley-Day syndrome		MGI:5444635	Elp1<sup>tm1Id</sup>/Elp1<sup>tm1.1Id</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22922231	20140410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	is_implicated_in	DOID:11589	Riley-Day syndrome		MGI:5444514	Elp1<sup>tm1Id</sup>/Elp1<sup>tm1Id</sup> Tg(Hsp70-1-cre)6Arge/0  [background:] involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22922231	20140410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861691	Lgi1	is_implicated_in	DOID:0060748	familial temporal lobe epilepsy 1		MGI:4437122	Lgi1<sup>tm1Mafu</sup>/Lgi1<sup>tm1Mafu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20133599	20120502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861691	Lgi1	is_implicated_in	DOID:0060748	familial temporal lobe epilepsy 1		MGI:5317116	Lgi1<sup>tm1.1Ics</sup>/Lgi1<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20659958	20120502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847119	Lepr<sup>brta</sup>	is_implicated_in	DOID:9970	obesity		MGI:3847120	Lepr<sup>brta</sup>/Lepr<sup>brta</sup>  [background:] C57BL/6JSfdAnu-Lepr<sup>brta</sup>/Anu			ECO:0000033	author statement supported by traceable reference	MGI:3611487	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5431478	b2b904Clo	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5431510	b2b904Clo/b2b904Clo  [background:] C57BL/6J-b2b904Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657016	Lox<sup>tm1Ikh</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:2657020	Lox<sup>tm1Ikh</sup>/Lox<sup>tm1Ikh</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12473682	20060706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	is_implicated_in	DOID:10629	microphthalmia		MGI:6727363	Trpm3<sup>tm1Lex</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	is_implicated_in	DOID:10629	microphthalmia		MGI:6727361	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	is_implicated_in	DOID:10629	microphthalmia		MGI:6727359	Trpm3<sup>em1Alsh</sup>/Trpm3<sup>em1Alsh</sup>  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33484482	20210730	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97601	Prkcq	is_implicated_in	DOID:5327	retinal detachment		MGI:5817744	Prkcq<sup>rpea1</sup>/Prkcq<sup>rpea1</sup>  [background:] B6.ABJ-Prkcq<sup>rpea1</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	PMID:26978024	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97601	Prkcq	is_implicated_in	DOID:5327	retinal detachment		MGI:4843311	Prkcq<sup>tm1Litt</sup>/Prkcq<sup>tm1Litt</sup>  [background:] B6.129P2-Prkcq<sup>tm1Litt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26978024	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106683	Zic1	is_implicated_in	DOID:0050777	Joubert syndrome		MGI:3716303	Zic1<sup>tm1Jaru</sup>/Zic1<sup>+</sup>  [background:] B6.129S4-Zic1<sup>tm1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11699604	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109249	Adamts1	is_implicated_in	DOID:5200	urinary tract obstruction		MGI:2450509	Adamts1<sup>tm1Hku</sup>/Adamts1<sup>tm1Hku</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10811842	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:3588875	Gjb2<sup>tm1Ugds</sup>/Gjb2<sup>tm1Ugds</sup> Tg(Otog-cre)1Ugds/0  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12121617	20140702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:5571190	Gjb2<sup>tm1Ugds</sup>/Gjb2<sup>tm1Ugds</sup> Tg(Sox10-cre)1Wdr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24333301	20140702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:4480	achondroplasia		MGI:5551435	Fgfr3<sup>tm1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:23200862	20140317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:4480	achondroplasia		MGI:3639744	Fgfr3<sup>tm2Wei</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * MF1			ECO:0000033	author statement supported by traceable reference	PMID:10200283	20140317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:4480	achondroplasia		MGI:3640358	Fgfr3<sup>tm5.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11181569	20140317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:4480	achondroplasia		MGI:3640338	Fgfr3<sup>tm3.1Cxd</sup>/Fgfr3<sup>tm3.1Cxd</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10587515	20140317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:4480	achondroplasia		MGI:3640343	Fgfr3<sup>tm3.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10587515	20140317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:4480	achondroplasia		MGI:3586593	Fgfr3<sup>tm1Cxd</sup>/Fgfr3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9887329	20140317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156165	Bcl2<sup>tm1Dlo</sup>	is_implicated_in	DOID:0111142	oligomeganephronia		MGI:2176707	Bcl2<sup>tm1Dlo</sup>/Bcl2<sup>tm1Dlo</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9794553	20180726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:0060887	ossification of the posterior longitudinal ligament of spine		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:9662402	20200406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:0060887	ossification of the posterior longitudinal ligament of spine		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:9359030	20200406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:0060887	ossification of the posterior longitudinal ligament of spine		MGI:6402953	Enpp1<sup>ttw-Ham</sup>/Enpp1<sup>ttw-Ham</sup>  [background:] Jcl:ICR-Enpp1<sup>ttw-Ham</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24770645	20200406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843046	Dclre1c<sup>tm1Jsek</sup>	is_implicated_in	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation		MGI:3843211	Dclre1c<sup>tm1Jsek</sup>/Dclre1c<sup>tm1Jsek</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19349461	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429928	Gk<sup>tm1Wjc</sup>	is_implicated_in	DOID:0060363	glycerol kinase deficiency		MGI:3623584	Gk<sup>tm1Wjc</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9302256	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429928	Gk<sup>tm1Wjc</sup>	is_implicated_in	DOID:0060363	glycerol kinase deficiency		MGI:3623584	Gk<sup>tm1Wjc</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16105550	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677291	Slc3a1<sup>pbl</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:2677979	Slc3a1<sup>pbl</sup>/Slc3a1<sup>pbl</sup>  [background:] involves: C3HeB/FeJ * MRL/MpJ			ECO:0000033	author statement supported by traceable reference	PMID:12923163	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677291	Slc3a1<sup>pbl</sup>	is_implicated_in	DOID:9266	cystinuria		MGI:2677978	Slc3a1<sup>pbl</sup>/Slc3a1<sup>pbl</sup>  [background:] C3HeB/FeJ-Slc3a1<sup>pbl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12923163	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109618	Atp6v1b2	is_implicated_in	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy		MGI:6359427	Atp6v1b2<sup>tm1Yoyu</sup>/Atp6v1b2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31257146	20210120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109618	Atp6v1b2	is_implicated_in	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy		MGI:6359426	Atp6v1b2<sup>tm1Yoyu</sup>/Atp6v1b2<sup>tm1Yoyu</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31257146	20210120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676278	Muc19	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15593201	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676278	Muc19	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10793067	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676278	Muc19	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25447050	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676278	Muc19	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3619532	Muc19<sup>sld</sup>/Muc19<sup>sld</sup>  [background:] NFS/N-Muc19<sup>sld</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8077681	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353499	Baz1b	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3850085	Baz1b<sup>tm1Ska</sup>/Baz1b<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19470456	20090710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353499	Baz1b	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3850084	Baz1b<sup>tm1Ska</sup>/Baz1b<sup>tm1Ska</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19470456	20090710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353499	Baz1b	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3821613	Baz1b<sup>MommeD10</sup>/Baz1b<sup>MommeD10</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19099580	20090710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353499	Baz1b	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3821614	Baz1b<sup>MommeD10</sup>/Baz1b<sup>+</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19099580	20090710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857478	Nf1<sup>tm1Tyj</sup>	is_not_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2175144	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7920653	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2671601	skc3	is_implicated_in	DOID:11836	clubfoot		MGI:3027853	skc3/skc3  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12955145	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181679	Crygs<sup>rncat</sup>	is_implicated_in	DOID:0110240	cataract 20 multiple types		MGI:2181684	Crygs<sup>rncat</sup>/Crygs<sup>rncat</sup>  [background:] Kunming			ECO:0000033	author statement supported by traceable reference	PMID:12079281	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:2175870	Eya1<sup>bor</sup>/Eya1<sup>bor</sup>  [background:] C3HeB/FeJ-Eya1<sup>bor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10072433	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:3054666	Eya1<sup>tm1Rilm</sup>/Eya1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:3054668	Eya1<sup>tm1Rilm</sup>/Eya1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:2677316	Eya1<sup>tm1Rilm</sup>/Eya1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180033	Zmpste24<sup>tm1Otin</sup>	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3621007	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/Ola * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11923874	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1889939	Ndst1<sup>tm1Hgx</sup>	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:3587788	Ndst1<sup>tm1Hgx</sup>/Ndst1<sup>tm1Hgx</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10664446	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5433292	b2b1519Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433295	b2b1519Clo/b2b1519Clo  [background:] C57BL/6J-b2b1519Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857528	Myo7a<sup>sh1-9J</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587642	Myo7a<sup>sh1-9J</sup>/Myo7a<sup>sh1-9J</sup>  [background:] involves: C3.MRL-Fas<sup>lpr</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:1276604	20060307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914596	Daam1	is_implicated_in	DOID:0060036	intrinsic cardiomyopathy		MGI:6150918	Daam1<sup>tm1.1Tpy</sup>/Daam1<sup>tm1.1Tpy</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:26526197	20180417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:4928	intrahepatic cholangiocarcinoma		MGI:5428897	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:22266220	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385796	Hsd11b1<sup>tm1Yko</sup>	is_implicated_in	DOID:0090140	cortisone reductase deficiency 2		MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	PMID:11546766	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385796	Hsd11b1<sup>tm1Yko</sup>	is_implicated_in	DOID:0090140	cortisone reductase deficiency 2		MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	PMID:9405715	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385796	Hsd11b1<sup>tm1Yko</sup>	is_implicated_in	DOID:0090140	cortisone reductase deficiency 2		MGI:3606188	Hsd11b1<sup>tm1Yko</sup>/Hsd11b1<sup>tm1Yko</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	MGI:85353	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3689328	Sh3pxd2b<sup>nee</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:4365644	Sh3pxd2b<sup>nee</sup>/Sh3pxd2b<sup>nee</sup>  [background:] B10.Cg-H2<sup>h4</sup> Sh3pxd2b<sup>nee</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:21282566	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530578	Nod2<sup>tm1Mka</sup>	is_implicated_in	DOID:0110892	inflammatory bowel disease 1		MGI:3531186	Nod2<sup>tm1Mka</sup>/Nod2<sup>tm1Mka</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15692052	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0050736	autosomal dominant disease		MGI:3640198	Fgfr3<sup>tm1.1Iwa</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11406607	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3576010	hpld	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3576038	hpld/hpld  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351338	Grm1	is_implicated_in	DOID:0080062	autosomal recessive spinocerebellar ataxia 13		MGI:3664785	Grm1<sup>crv4</sup>/Grm1<sup>crv4</sup>  [background:] BALB/cPas-Grm1<sup>crv4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16964410	20151117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105061	Clcn2	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:6850120	Clcn2<sup>em1Uis</sup>/Clcn2<sup>+</sup>  [background:] C57BL/6N-Clcn2<sup>em1Uis</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31727896	20220110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449643	Bloc1s4<sup>cno</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3588317	Bloc1s4<sup>cno</sup>/Bloc1s4<sup>cno</sup>  [background:] involves: C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449643	Bloc1s4<sup>cno</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2663842	Bloc1s4<sup>cno</sup>/Bloc1s4<sup>cno</sup>  [background:] C3H/HeJ-Bloc1s4<sup>cno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11110696	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96613	Itgb4	is_implicated_in	DOID:0060733	junctional epidermolysis bullosa with pyloric atresia		MGI:3694660	Itgb4<sup>tm1Fgg</sup>/Itgb4<sup>tm1Fgg</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9670011	20090319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0110977	brachydactyly type A1C		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2673307	Mafa	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3582680	Mafa<sup>tm1Staka</sup>/Mafa<sup>tm1Staka</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:15923615	20050729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429574	Irs2<sup>tm1Tka</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583344	Irs2<sup>tm1Tka</sup>/Irs2<sup>tm1Tka</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:11078455	20050811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157350	Chrd<sup>tm1Emdr</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2676545	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup>  [background:] either: B6SJL.129-Chrd<sup>tm1Emdr</sup> or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)			ECO:0000033	author statement supported by traceable reference	PMID:12810603	20070104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930923	Slurp1	is_implicated_in	DOID:0060862	mal de Meleda		MGI:5629822	Slurp1<sup>tm1Lex</sup>/Slurp1<sup>tm1Lex</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24499735	20150416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930923	Slurp1	is_implicated_in	DOID:0060862	mal de Meleda		MGI:5629846	Slurp1<sup>tm1.1Sgy</sup>/Slurp1<sup>tm1.1Sgy</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24499735	20150416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769585	Col1a1<sup>Aga2</sup>	is_implicated_in	DOID:0110341	osteogenesis imperfecta type 2		MGI:3769907	Col1a1<sup>Aga2</sup>/Col1a1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18248096	20080229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857286	Ifngr1<sup>tm1Agt</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:4361526	Ifngr1<sup>tm1Agt</sup>/Ifngr1<sup>tm1Agt</sup>  [background:] B6.129S7-Ifngr1<sup>tm1Agt</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21308779	20170515	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2671987	Shank2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5437480	Shank2<sup>tm1Mgle</sup>/Shank2<sup>tm1Mgle</sup>  [background:] B6.129S4-Shank2<sup>tm1Mgle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27903723	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2671987	Shank2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5437480	Shank2<sup>tm1Mgle</sup>/Shank2<sup>tm1Mgle</sup>  [background:] B6.129S4-Shank2<sup>tm1Mgle</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22699620	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2671987	Shank2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5435702	Shank2<sup>tm1.1Tmb</sup>/Shank2<sup>tm1.1Tmb</sup>  [background:] B6.129-Shank2<sup>tm1.1Tmb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22699619	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386295	Scgb1a1<sup>tm1Abm</sup>	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:2684391	Scgb1a1<sup>tm1Abm</sup>/Scgb1a1<sup>tm1Abm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10470078	20190611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3511278	Foxi3	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:7493642	Foxi3<sup>em1Ybz</sup>/Foxi3<sup>em1Ybz</sup>  [background:] C57BL/6-Foxi3<sup>em1Ybz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37041148	20230628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2149946	Gopc	is_implicated_in	DOID:14227	azoospermia		MGI:3722133	Gopc<sup>tm1.1Tno</sup>/Gopc<sup>tm1.1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12149515	20070920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916732	Nup35	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:6154633	Nup35<sup>m1Apb</sup>/Nup35<sup>m1Apb</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27427419	20200621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511359	Pparg<sup>tm3(tTA)Yba</sup>	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:3784504	Pparg<sup>tm3(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681527	Fbln5<sup>tm1Krc</sup>	is_implicated_in	DOID:3144	cutis laxa		MGI:2681537	Fbln5<sup>tm1Krc</sup>/Fbln5<sup>tm1Krc</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11805835	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182914	Hivep2<sup>tm1Sis</sup>	is_implicated_in	DOID:1059	intellectual disability		MGI:6189180	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:29233179	20190403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181780	Foxe1<sup>tm1Rdl</sup>	is_implicated_in	DOID:0050655	Bamforth-Lazarus syndrome		MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15367491	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181780	Foxe1<sup>tm1Rdl</sup>	is_implicated_in	DOID:0050655	Bamforth-Lazarus syndrome		MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9697704	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861180	Enc	is_implicated_in	DOID:83	cataract		MGI:3583154	Enc/Enc<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178598	Bloc1s5	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178598	Bloc1s5	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3587678	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] involves: STOCK t			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178598	Bloc1s5	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le			ECO:0000033	author statement supported by traceable reference	PMID:11912185	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:3584030	Ap3b1<sup>pe-rim2</sup>/Ap3b1<sup>pe-rim2</sup>  [background:] involves: B10.A(R201) * C57BL/10Slc			ECO:0000033	author statement supported by traceable reference	PMID:9434937	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97740	Polb	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5427085	Polb<sup>tm1.1Jbsw</sup>/Polb<sup>tm1.1Jbsw</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24388753	20140715	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96217	Hprt1	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome		MGI:5637726	Hprt1<sup>b-m3</sup>/Hprt1<sup>b-m3</sup>  [background:] B6.129P2-Hprt1<sup>b-m3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7509865	20150529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96217	Hprt1	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome		MGI:3625335	Hprt1<sup>b-m3</sup>/Y  [background:] B6.129P2-Hprt1<sup>b-m3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7509865	20150529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96217	Hprt1	is_implicated_in	DOID:1919	Lesch-Nyhan syndrome		MGI:3625335	Hprt1<sup>b-m3</sup>/Y  [background:] B6.129P2-Hprt1<sup>b-m3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11297820	20150529	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438056	Fbn2<sup>mz</sup>	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:4438065	Fbn2<sup>mz</sup>/Fbn2<sup>mz</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:20161761	20100329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	is_implicated_in	DOID:2945	severe acute respiratory syndrome		MGI:3771372	Stat1<sup>tm1Rds</sup>/Stat1<sup>tm1Rds</sup>  [background:] 129S6/SvEv-Stat1<sup>tm1Rds</sup>/Tac			ECO:0000033	author statement supported by traceable reference	PMID:20386712	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052550	Tg(H2-Ea<sup>d</sup>)12Lt	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3618813	Tg(H2-Ea<sup>d</sup>)12Lt/0  [background:] NOD/ShiLt-Tg(H2-Ea<sup>d</sup>)12Lt			ECO:0000033	author statement supported by traceable reference	PMID:8757636	20060531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3576012	hpmd	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:3576039	hpmd/hpmd  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20050526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722138	Gusb<sup>mps-3J</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:3802703	Gusb<sup>mps-3J</sup>/Gusb<sup>mps-3J</sup>  [background:] C57BL/6J-Gusb<sup>mps-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3801433	20080819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682223	Nf1<sup>Mhdadsk9</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:6283591	Nf1<sup>Mhdadsk9</sup>/Nf1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30571760	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856920	Bicc1<sup>jcpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582933	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk</sup>  [background:] involves: 101 * C3H * C57BL/6J * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:8887273	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856920	Bicc1<sup>jcpk</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3582952	Bicc1<sup>jcpk</sup>/Bicc1<sup>jcpk</sup>  [background:] involves: 101 * C3H * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7723240	20050803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677504	Pde6g<sup>tm1Goff</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3814998	Pde6g<sup>tm1Goff</sup>/Pde6g<sup>tm1Goff</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6 * MF1  * Swiss Webster) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * MF1 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:8638127	20081114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3760281	A<sup>y</sup>/a  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:5468422	20071105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917780	Lrfn2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5904009	Lrfn2<sup>tm1.1Jaru</sup>/Lrfn2<sup>tm1.1Jaru</sup>  [background:] B6J.129P2-Lrfn2<sup>tm1.1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28604739	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526665	Fzd9<sup>tm1Uta</sup>	is_not_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3578414	Fzd9<sup>tm1Uta</sup>/Fzd9<sup>tm1Uta</sup>  [background:] involves: 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15572594	20050531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98742	Thra	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:6317178	Thra<sup>em1Ffla</sup>/Thra<sup>+</sup>  [background:] C57BL/6-Thra<sup>em1Ffla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29205102	20190711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98742	Thra	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:6317180	Thra<sup>em2Ffla</sup>/Thra<sup>+</sup>  [background:] C57BL/6-Thra<sup>em2Ffla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29205102	20190711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3828298	Plp1<sup>tm1Frca</sup>	is_implicated_in	DOID:3210	Pelizaeus-Merzbacher disease		MGI:3828308	Plp1<sup>tm1Frca</sup>/Y  [background:] B6.129-Plp1<sup>tm1Frca</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18835559	20090122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:3529	congenital myopathy 1A		MGI:4881413	Ryr1<sup>tm1.1Dhm</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S2/SvPasCrl * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:19959667	20160218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:3529	congenital myopathy 1A		MGI:5749228	Ryr1<sup>m1Nisw</sup>/Ryr1<sup>+</sup>  [background:] 129S1.B6-Ryr1<sup>m1Nisw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25564733	20160218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	is_implicated_in	DOID:3529	congenital myopathy 1A		MGI:3620609	Ryr1<sup>tm1Tno</sup>/Ryr1<sup>tm1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7515481	20160218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3051561	Ghrh<sup>tm1Salv</sup>	is_implicated_in	DOID:0060873	isolated growth hormone deficiency type IA		MGI:3051589	Ghrh<sup>tm1Salv</sup>/Ghrh<sup>tm1Salv</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15155578	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891468	Lgr4	is_implicated_in	DOID:1686	glaucoma		MGI:3797606	Lgr4<sup>Gt(LST020)Byg</sup>/Lgr4<sup>Gt(LST020)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18424556	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662346	Slit3<sup>tm1Dor</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:2662356	Slit3<sup>tm1Dor</sup>/Slit3<sup>tm1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12702769	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	is_implicated_in	DOID:0112247	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder		MGI:6451664	Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>/Cdk13<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31440507	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042719	Nrxn2<sup>tm1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5632308	Nrxn2<sup>tm1Sud</sup>/Nrxn2<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J * C57BL/6NClr			ECO:0000033	author statement supported by traceable reference	PMID:25423136	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098221	Gamt	is_implicated_in	DOID:0050799	guanidinoacetate methyltransferase deficiency		MGI:3044676	Gamt<sup>tm1Isb</sup>/Gamt<sup>tm1Isb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15028668	20090512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5554187	Drc1<sup>b2b2237Clo</sup>/Drc1<sup>b2b2237Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b2237Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88291	Ccd	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3583772	Ccd/Ccd<sup>+</sup>  [background:] B10Rl.101-Ccd			ECO:0000033	author statement supported by traceable reference	PMID:8270769	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88291	Ccd	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2660662	Ccd/Ccd<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:62184	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347344	Gla	is_implicated_in	DOID:14499	Fabry disease		MGI:2183938	Gla<sup>tm1Kul</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9122231	20121008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347344	Gla	is_implicated_in	DOID:14499	Fabry disease		MGI:2183938	Gla<sup>tm1Kul</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22574107	20121008	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859911	Trp73<sup>tm1Fmc</sup>	is_implicated_in	DOID:10754	otitis media		MGI:2174786	Trp73<sup>tm1Fmc</sup>/Trp73<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10716451	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776016	Sbf2<sup>Gt(XH212)Byg</sup>	is_implicated_in	DOID:0110190	Charcot-Marie-Tooth disease type 4B2		MGI:3784200	Sbf2<sup>Gt(XH212)Byg</sup>/Sbf2<sup>Gt(XH212)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:5955164	20080507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	is_implicated_in	DOID:1612	breast cancer		MGI:3814365	Brca2<sup>tm1Mbn</sup>/Brca2<sup>+</sup>  [background:] B6.Cg-Brca2<sup>tm1Mbn</sup> Apc<sup>Min</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11215675	20081111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	is_implicated_in	DOID:1612	breast cancer		MGI:2177239	Brca2<sup>tm2Arge</sup>/Brca2<sup>tm2Arge</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>tm1(cre)Arge</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11494122	20081111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	is_implicated_in	DOID:1612	breast cancer		MGI:2177237	Brca2<sup>tm1Arge</sup>/Brca2<sup>tm2Arge</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11494122	20081111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	is_implicated_in	DOID:1612	breast cancer		MGI:3055719	Brca2<sup>tm1Mhun</sup>/Brca2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14981540	20081111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	is_implicated_in	DOID:0090129	carnitine palmitoyltransferase I deficiency		MGI:3606425	Cpt1a<sup>tm1Pwo</sup>/Cpt1a<sup>+</sup>  [background:] either: 129S6/SvEvTac-Cpt1a<sup>tm1Pwo</sup> or (involves: 129S6/SvEvTac * C57BL/6NTac)			ECO:0000033	author statement supported by traceable reference	PMID:16169268	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104672	Tfap2b	is_implicated_in	DOID:0060563	Char syndrome		MGI:5292663	Tfap2b<sup>tm1Rbu</sup>/Tfap2b<sup>tm1Rbu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21829553	20111020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856903	hph1	is_implicated_in	DOID:12638	hypertrophic pyloric stenosis		MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:15144277	20060726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156882	Csf3r<sup>tm1Eur</sup>	is_implicated_in	DOID:0090120	hereditary neutrophilia		MGI:2183034	Csf3r<sup>tm1Eur</sup>/Csf3r<sup>tm1Eur</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:9639496	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:5911876	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] B6.129-Sgcd<sup>tm1Mcn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23695275	20171026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180193	Sgcd<sup>tm1Mcn</sup>	is_implicated_in	DOID:0110436	dilated cardiomyopathy 1L		MGI:3618527	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10862711	20171026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711982	Gjb3<sup>tm2.1Kwi</sup>	is_implicated_in	DOID:0050467	erythrokeratodermia variabilis		MGI:3712799	Gjb3<sup>tm2.1Kwi</sup>/Gjb3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17446259	20070626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:0111196	X-linked distal spinal muscular atrophy 3		MGI:6393655	Atp7a<sup>tm1.2Mlke</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27293072	20200310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_implicated_in	DOID:0111196	X-linked distal spinal muscular atrophy 3		MGI:6324372	Atp7a<sup>tm1.1Mjp</sup>/Y Mnx1<sup>tm4(cre)Tmj</sup>/Mnx1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25639447	20200310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800577	Arsb<sup>m1J</sup>	is_implicated_in	DOID:12800	mucopolysaccharidosis VI		MGI:3849442	Arsb<sup>m1J</sup>/Arsb<sup>m1J</sup>  [background:] C57BL/6J-Arsb<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:3849437	20090702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386579	Tg(Ins2-TCF1*P291)2Kya	is_implicated_in	DOID:0111102	maturity-onset diabetes of the young type 3		MGI:3603406	Tg(Ins2-TCF1*P291)2Kya/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11756330	20051101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4329141	Trim37<sup>Gt(RRO307)Byg</sup>	is_implicated_in	DOID:0050436	mulibrey nanism		MGI:5789948	Trim37<sup>Gt(RRO307)Byg</sup>/Trim37<sup>Gt(RRO307)Byg</sup>  [background:] B6J.129P2-Trim37<sup>Gt(RRO307)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27044324	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857776	Nsdhl<sup>Bpa-1H</sup>	is_implicated_in	DOID:0060292	X-linked chondrodysplasia punctata 1		MGI:3587801	Nsdhl<sup>Bpa-1H</sup>/Nsdhl<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:6682087	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915720	Bpnt2	is_implicated_in	DOID:0112224	chondrodysplasia with joint dislocations gPAPP type		MGI:6466738	Bpnt2<sup>tm1.2Aros</sup>/Bpnt2<sup>tm1.2Aros</sup>  [background:] B6(SJL)-Bpnt2<sup>tm1.2Aros</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30865697	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794557	Tg(HBV-HCV)Kko	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5578176	Tg(HBV-HCV)Kko/0  [background:] C57BL/6N-Tg(HBV-HCV)Kko			ECO:0000033	author statement supported by traceable reference	PMID:11389061	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388129	Rxfp2<sup>tm1Aia</sup>	is_implicated_in	DOID:11383	cryptorchidism		MGI:2388134	Rxfp2<sup>tm1Aia</sup>/Rxfp2<sup>tm1Aia</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12217959	20151207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890646	Nek8	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2429561	Nek8<sup>jck</sup>/Nek8<sup>jck</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8510385	20050805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923799	Cecr2	is_implicated_in	DOID:0060668	anencephaly		MGI:3574278	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] 129P2(C)-Cecr2<sup>Gt(pGT1)1Hemc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923799	Cecr2	is_implicated_in	DOID:0060668	anencephaly		MGI:3574277	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] C.129P2-Cecr2<sup>Gt(pGT1)1Hemc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923799	Cecr2	is_implicated_in	DOID:0060668	anencephaly		MGI:3574274	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4456472	Gstm1<sup>tm1Gcw</sup>/Gstm1<sup>tm1Gcw</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20178820	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:2181896	Pkd1<sup>m1Bei</sup>/Pkd1<sup>m1Bei</sup>  [background:] involves: A/J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20121115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100537	Mid1	is_implicated_in	DOID:0080697	Opitz GBBB syndrome		MGI:4437568	Mid1<sup>tm1Mero</sup>/Y  [background:] B6.Cg-Mid1<sup>tm1Mero</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20181585	20220608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98731	Tgm2	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12205028	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98731	Tgm2	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11883932	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98731	Tgm2	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3029267	Tgm2<sup>tm1Gml</sup>/Tgm2<sup>tm1Gml</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12651621	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1925230	Sbf1	is_implicated_in	DOID:0110194	Charcot-Marie-Tooth disease type 4B3		MGI:7316771	Sbf1<sup>em1Frobi</sup>/Sbf1<sup>em1Frobi</sup>  [background:] C57BL/6N-Sbf1<sup>em1Frobi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34718573	20220729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415606	Tg(Prnp-ITM2B*)1Ruvi	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:5525128	Tg(Prnp-ITM2B*)1Ruvi/Tg(Prnp-ITM2B*)1Ruvi  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23418567	20131226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415606	Tg(Prnp-ITM2B*)1Ruvi	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4415607	Tg(Prnp-ITM2B*)1Ruvi/?  [background:] B6.C3Fe-Tg(Prnp-ITM2B*)1Ruvi			ECO:0000033	author statement supported by traceable reference	PMID:18410407	20131226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2687010	Notch3<sup>tm1Grid</sup>	is_not_implicated_in	DOID:0111035	CADASIL 1		MGI:5771891	Notch3<sup>tm1Grid</sup>/Notch3<sup>tm1Grid</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26563570	20160526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2654632	Erbb2<sup>tm1Klee</sup>/Erbb2<sup>tm1Klee</sup> Tg(Nes-cre)1Atp/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12526770	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104611	Mdfic	is_implicated_in	DOID:0081030	central conducting lymphatic anomaly		MGI:7314827	Mdfic<sup>em#Nlh</sup>/Mdfic<sup>em#Nlh</sup>  [background:] C57BL/6J-Mdfic<sup>em#Nlh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35235341	20220722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857751	Mitf<sup>mi-enu122</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857751	Mitf<sup>mi-enu122</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2678724	Hlb228	is_implicated_in	DOID:9970	obesity		MGI:2680503	Hlb228/?  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:2656149	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808361	Cyp4v3<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:0050664	Bietti crystalline corneoretinal dystrophy		MGI:5804204	Cyp4v3<sup>tm1(KOMP)Vlcg</sup>/Cyp4v3<sup>tm1(KOMP)Vlcg</sup>  [background:] B6(Cg)-Cyp4v3<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25118264	20161020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667262	Nsd1<sup>tm1.1Pcn</sup>	is_not_implicated_in	DOID:14748	Sotos syndrome		MGI:2668882	Nsd1<sup>tm1.1Pcn</sup>/Nsd1<sup>tm1.1Pcn</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12805229	20110630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107404	Tbr1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5752313	Tbr1<sup>tm1Jlr</sup>/Tbr1<sup>+</sup>  [background:] B6.129X1-Tbr1<sup>tm1Jlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24441682	20200204	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107404	Tbr1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6388550	Tbr1<sup>tm1.1Csbd</sup>/Tbr1<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31680851	20200204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386263	Tnfsf11<sup>tm1Ywc</sup>	is_implicated_in	DOID:0110943	autosomal recessive osteopetrosis 2		MGI:3800941	Tnfsf11<sup>tm1Ywc</sup>/Tnfsf11<sup>tm1Ywc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22836362	20160804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	is_implicated_in	DOID:5419	schizophrenia		MGI:2654500	Slc6a3<sup>tm1Mca</sup>/Slc6a3<sup>tm1Mca</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8628395	20081006	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:3655859	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16199475	20060927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:3607794	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12893739	20060927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:2446598	Acadvl<sup>tm1Uab</sup>/Acadvl<sup>tm1Uab</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11590124	20060927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:3607794	Acadvl<sup>tm1Vje</sup>/Acadvl<sup>tm1Vje</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15025677	20060927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3621007	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/Ola * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11923874	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856929	Dsg4<sup>lah</sup>	is_implicated_in	DOID:0110703	hypotrichosis 6		MGI:2661074	Dsg4<sup>lah</sup>/Dsg4<sup>lah</sup>  [background:] LAH/Pas			ECO:0000033	author statement supported by traceable reference	PMID:8752833	20190422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914346	Mmachc	is_implicated_in	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC		MGI:6107640	Mmachc<sup>Gt(AZ0348)Wtsi</sup>/Mmachc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24889031	20180104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2142763	Cyp4v3	is_implicated_in	DOID:0050664	Bietti crystalline corneoretinal dystrophy		MGI:5804204	Cyp4v3<sup>tm1(KOMP)Vlcg</sup>/Cyp4v3<sup>tm1(KOMP)Vlcg</sup>  [background:] B6(Cg)-Cyp4v3<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25118264	20161020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684927	Cenpj	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:5509044	Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>/Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] B6Brd;B6N-Tyr<sup>c-Brd</sup> Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:23166506	20131001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920831	Stk36	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429551	Stk36<sup>tm1Lex</sup>/Stk36<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046186	Rho<sup>tm2(RHO/GFP)Jhw</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:3836175	Rho<sup>tm2(RHO/GFP)Jhw</sup>/Rho<sup>tm2(RHO/GFP)Jhw</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16979686	20130619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919847	Auts2	is_implicated_in	DOID:0070056	autosomal dominant intellectual developmental disorder 26		MGI:6156953	Auts2<sup>tm1Mhos</sup>/Auts2<sup>+</sup>  [background:] C57BL/6N-Auts2<sup>tm1Mhos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26717414	20180518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	is_implicated_in	DOID:0050787	juvenile polyposis syndrome		MGI:2182801	Smad4<sup>tm1Mmt</sup>/Smad4<sup>+</sup>  [background:] B6.129S2-Smad4<sup>tm1Mmt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10626800	20071105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106184	Npm1	is_not_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5478730	Npm1<sup>tm1Hft</sup>/Npm1<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:23226219	20130507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4315078	Ywhaz<sup>Gt(OST432062)Lex</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5762957	Ywhaz<sup>Gt(OST432062)Lex</sup>/Ywhaz<sup>Gt(OST432062)Lex</sup>  [background:] either: B6.129S5-Ywhaz<sup>Gt(OST432062)Lex</sup> or C.129S5-Ywhaz<sup>Gt(OST432062)Lex</sup> or (involves: 129S5/SvEvBrd * 129T2/SvEmsWehi))			ECO:0000033	author statement supported by traceable reference	PMID:22124272	20160422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	is_implicated_in	DOID:0110107	atrial heart septal defect 2		MGI:5427936	Gata4<sup>tm1Grg</sup>/Gata4<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22589735	20120716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3505575	Ccdc85c<sup>hhy</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:3510639	Ccdc85c<sup>hhy</sup>/Ccdc85c<sup>hhy</sup>  [background:] involves: BALB/cHeA * STS/A			ECO:0000033	author statement supported by traceable reference	PMID:15283996	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102708	Efnb1	is_implicated_in	DOID:14737	craniofrontonasal syndrome		MGI:3717637	Efnb1<sup>tm1.1Sor</sup>/Efnb1<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16968134	20070809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389582	Tyk2<sup>tm1Shmd</sup>	is_implicated_in	DOID:9970	obesity		MGI:5515728	Tyk2<sup>tm1Shmd</sup>/Tyk2<sup>tm1Shmd</sup>  [background:] either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:23217260	20131030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	is_implicated_in	DOID:0090125	brain small vessel disease 1		MGI:3579768	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] B6.129S-Col4a1<sup>deltaex40</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16598045	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861441	Rab27a	is_implicated_in	DOID:0050120	hemophagocytic lymphohistiocytosis		MGI:5476655	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] B6.C3Sn-Rab27a<sup>ash</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23160464	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050095	Pparg<sup>tm1Mae</sup>	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3050152	Pparg<sup>tm1Mae</sup>/Pparg<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15254591	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2174925	Tgfb1<sup>tm1Doe</sup>/Tgfb1<sup>tm1Doe</sup>  [background:] involves: 129S2/SvPas * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:1436033	20050711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97576	Phka1	is_implicated_in	DOID:0111040	glycogen storage disease IXd		MGI:4821261	Phka1<sup>I/FnLn</sup>/Phka1<sup>I/FnLn</sup>  [background:] I/FnLn			ECO:0000033	author statement supported by traceable reference	PMID:7874115	20100913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97576	Phka1	is_implicated_in	DOID:0111040	glycogen storage disease IXd		MGI:4821274	Phka1<sup>I/FnLn</sup>/Y  [background:] I/FnLn			ECO:0000033	author statement supported by traceable reference	PMID:7874115	20100913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97515	Pcsk5	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5430345	Pcsk5<sup>b2b1549Clo</sup>/Pcsk5<sup>b2b1549Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b1549Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:2661972	Ncf1<sup>m1J</sup>/Ncf1<sup>m1J</sup>  [background:] B6.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10670582	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:3590146	Ncf1<sup>tm1Hbd</sup>/Ncf1<sup>tm1Hbd</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:11733538	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:2175140	Ncf1<sup>tm1Shl</sup>/Ncf1<sup>tm1Shl</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7650482	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:4438111	Ncf1<sup>tm1Shl</sup>/Ncf1<sup>tm1Shl</sup>  [background:] B6.129S2-Ncf1<sup>tm1Shl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16843452	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:4461053	Abca12<sup>el12</sup>/Abca12<sup>el12</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18802465	20180713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:6188328	Abca12<sup>smsk</sup>/Abca12<sup>smsk</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27551807	20180713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3834263	Abca12<sup>tm1Lex</sup>/Abca12<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18957418	20180713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3809674	Abca12<sup>tm1Shzu</sup>/Abca12<sup>tm1Shzu</sup>  [background:] B6.129S-Abca12<sup>tm1Shzu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18632686	20180713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441738	Npsr1	is_implicated_in	DOID:535	sleep disorder		MGI:7284791	Npsr1<sup>em1Yfu</sup>/Npsr1<sup>+</sup>  [background:] C57BL/6J-Npsr1<sup>em1Yfu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31619542	20220610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3811233	Pkd1<sup>tm3Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3811282	Pkd1<sup>tm3Jzh</sup>/Pkd1<sup>tm3Jzh</sup> Tg(Ggt1-cre)M3Egn/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18385665	20081020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857966	Apc<sup>tm1Tno</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2182592	Apc<sup>tm1Tno</sup>/Apc<sup>tm1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9311916	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670461	Gnpat<sup>tm1Just</sup>	is_implicated_in	DOID:0110852	rhizomelic chondrodysplasia punctata type 2		MGI:2670462	Gnpat<sup>tm1Just</sup>/Gnpat<sup>tm1Just</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12874108	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5605721	b2b386.1Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5605970	b2b386.1Clo/b2b386.1Clo  [background:] C57BL/6J-b2b386.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	is_not_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174969	Mapt<sup>tm1Noh</sup>/Mapt<sup>tm1Noh</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:8202139	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2140175	Ldlrap1	is_implicated_in	DOID:0090105	autosomal recessive hypercholesterolemia		MGI:2670516	Ldlrap1<sup>tm1Her</sup>/Ldlrap1<sup>tm1Her</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:12746448	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2140175	Ldlrap1	is_implicated_in	DOID:0090105	autosomal recessive hypercholesterolemia		MGI:3611042	Ldlrap1<sup>Gt(OST149604)Lex</sup>/Ldlrap1<sup>Gt(OST149604)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15472122	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	is_implicated_in	DOID:0110555	autosomal dominant nonsyndromic deafness 25		MGI:2669172	Trpv4<sup>tm1Msz</sup>/Trpv4<sup>tm1Msz</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15925108	20070112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448247	Foxm1<sup>tm1Rhc</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3522660	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15082532	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438491	Tg(Thy1-TARDBP)6Singh	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:4438493	Tg(Thy1-TARDBP)6Singh/Tg(Thy1-TARDBP)6Singh  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20133711	20160504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300566	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (FVB/NJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300564	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (BALB/cByJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300563	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (A/J x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5300565	Col1a2<sup>tm1.1Mcbr</sup>/Col1a2<sup>+</sup>  [background:] (C3H/HeJ x B6.129-Col1a2<sup>tm1.1Mcbr</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:19594296	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:3720800	Col1a2<sup>oim</sup>/Col1a2<sup>+</sup>  [background:] B6C3Fe a/a-Col1a2<sup>oim</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8968022	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3703320	Neb<sup>tm1Slbt</sup>	is_implicated_in	DOID:0110928	nemaline myopathy 2		MGI:3706664	Neb<sup>tm1Slbt</sup>/Neb<sup>tm1Slbt</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:19346529	20090625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387092	Tg(Ggamma-T)15Cps	is_implicated_in	DOID:10283	prostate cancer		MGI:3819956	Tg(Ggamma-T)15Cps/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:9041192	20081215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387092	Tg(Ggamma-T)15Cps	is_implicated_in	DOID:10283	prostate cancer		MGI:3819955	Tg(Ggamma-T)15Cps/Tg(Ggamma-T)15Cps  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:9041192	20081215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	is_implicated_in	DOID:0080349	developmental and epileptic encephalopathy 39		MGI:3715869	Slc25a12<sup>Gt(OST123999)Lex</sup>/Slc25a12<sup>Gt(OST123999)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28429368	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693324	Irf6<sup>tm1Mjd</sup>	is_implicated_in	DOID:0060055	popliteal pterygium syndrome		MGI:3693809	Irf6<sup>tm1Mjd</sup>/Irf6<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17041603	20070326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447694	Tg(Mpz)80.2Wra	is_implicated_in	DOID:870	neuropathy		MGI:2653547	Tg(Mpz)80.2Wra/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10704451	20190211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156086	Pten<sup>tm1Hwu</sup>	is_implicated_in	DOID:13042	persistent fetal circulation syndrome		MGI:5503192	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Twist2<sup>tm1.1(cre)Dor</sup>/Twist2<sup>+</sup>  [background:] B6.129-Twist2<sup>tm1.1(cre)Dor</sup> Pten<sup>tm1Hwu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23023706	20130830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047089	Tg(MMTV-Erbb2)12Pjo	is_implicated_in	DOID:1612	breast cancer		MGI:5604891	Tg(MMTV-Erbb2)12Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3034098	Ar<sup>tm1Verh</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5502687	Ar<sup>tm1Verh</sup>/Y Tg(Fabp4-cre)1Rev/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22415878	20130827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856920	Bicc1<sup>jcpk</sup>	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3582953	Bicc1<sup>jcpk</sup>/Bicc1<sup>+</sup>  [background:] involves: 101 * C3H * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7723240	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	is_implicated_in	DOID:0060010	Omenn syndrome		MGI:3714069	Rag2<sup>tm1Avla</sup>/Rag2<sup>tm1Avla</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17476358	20070709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3628447	Dnmt3b<sup>tm7Enl</sup>	is_implicated_in	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1		MGI:3628826	Dnmt3b<sup>tm7Enl</sup>/Dnmt3b<sup>tm7Enl</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16501171	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033226	Gck<sup>Rgsc475</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038220	Gck<sup>Rgsc475</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443198	Slitrk6	is_implicated_in	DOID:0111628	high myopia-sensorineural deafness syndrome		MGI:4417932	Slitrk6<sup>tm1.1Jaru</sup>/Slitrk6<sup>tm1.1Jaru</sup>  [background:] B6.129P2-Slitrk6<sup>tm1.1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23543054	20221103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	is_implicated_in	DOID:0080074	neural tube defect		MGI:3574961	Mthfr<sup>tm1Rzn</sup>/Mthfr<sup>tm1Rzn</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11181567	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:2655609	Atf2<sup>tm1Glm</sup>/Atf2<sup>tm1Glm</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8538792	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	is_implicated_in	DOID:0110258	cataract 10 multiple types		MGI:2175802	Cryba1<sup>Po1</sup>/Cryba1<sup>+</sup>  [background:] C3HeB/FeJ-Cryba1<sup>Po1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10585769	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	is_implicated_in	DOID:0110258	cataract 10 multiple types		MGI:2175801	Cryba1<sup>Po1</sup>/Cryba1<sup>Po1</sup>  [background:] C3HeB/FeJ-Cryba1<sup>Po1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10585769	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609567	Sgcg<sup>tm1Oza</sup>	is_implicated_in	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C		MGI:3630163	Sgcg<sup>tm1Oza</sup>/Sgcg<sup>tm1Oza</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12609501	20060725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926728	Pdgfra<sup>tm2Sor</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:4818797	Pdgfra<sup>tm2Sor</sup>/Pdgfra<sup>tm2Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17568391	20100810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857974	Psen1<sup>tm1Shn</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174998	Psen1<sup>tm1Shn</sup>/Psen1<sup>tm1Shn</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9160754	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182816	Epb42<sup>tm1Llp</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2449964	Epb42<sup>tm1Llp</sup>/Epb42<sup>tm1Llp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10359562	20050622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_not_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2177097	Psen1<sup>tm1Psgh</sup>/Psen1<sup>tm1Psgh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10962005	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623448	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] NOD.Cg-Ifng<sup>tm1Ts</sup> Prkdc<sup>scid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11714835	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623449	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] NOD.129S7(B6)-Ifng<sup>tm1Ts</sup>/DvsJ			ECO:0000033	author statement supported by traceable reference	PMID:11714835	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:3804498	Tnnt2<sup>tm2Mmto</sup>/Tnnt2<sup>tm2Mmto</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17556660	20171002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:3804499	Tnnt2<sup>tm2Mmto</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17556660	20171002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	is_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:5910772	Tnnt2<sup>tm2.1Feah</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27936050	20171002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330812	Acox1	is_implicated_in	DOID:0050797	peroxisomal acyl-CoA oxidase deficiency		MGI:2652088	Acox1<sup>tm1Jkr</sup>/Acox1<sup>tm1Jkr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8798738	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	is_implicated_in	DOID:0080109	infantile myofibromatosis		MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:6279297	Grn<sup>tm1.1Aidi</sup>/Grn<sup>tm1.1Aidi</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30271659	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574429	Msmb<sup>tm1Xuan</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:3574653	Msmb<sup>tm1Xuan</sup>/Msmb<sup>tm1Xuan</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:15674347	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924291	Arsk	is_implicated_in	DOID:12798	mucopolysaccharidosis		MGI:5797380	Arsk<sup>tm1b(KOMP)Wtsi</sup>/Arsk<sup>tm1b(KOMP)Wtsi</sup>  [background:] B6N(Cg)-Arsk<sup>tm1b(KOMP)Wtsi</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:32856704	20210405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6438116	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>tm3.2Cmpl</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6438117	Shank3<sup>tm3.2Cmpl</sup>/Shank3<sup>+</sup>  [background:] B6.129S6(Cg)-Shank3<sup>tm3.2Cmpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26559786	20200708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6394127	Shank3<sup>tm2.1Bux</sup>/Shank3<sup>tm2.1Bux</sup>  [background:] B6(Cg)-Shank3<sup>tm2.1Bux</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30302388	20200708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6324047	Shank3<sup>tm2Gfng</sup>/Shank3<sup>+</sup>  [background:] B6.129-Shank3<sup>tm2Gfng</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27189882	20200708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531321	Phox2a/Inppl1<sup>tm1Ssch</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3531404	Phox2a/Inppl1<sup>tm1Ssch</sup>/Phox2a/Inppl1<sup>tm1Ssch</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11343120	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3531321	Phox2a/Inppl1<sup>tm1Ssch</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3531409	Phox2a/Inppl1<sup>tm1Ssch</sup>/Phox2a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11343120	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351636	Srr	is_implicated_in	DOID:5419	schizophrenia		MGI:4354165	Srr<sup>rgsc1872</sup>/Srr<sup>rgsc1872</sup>  [background:] C57BL/6JJcl-Srr<sup>rgsc1872</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19483194	20100407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351636	Srr	is_implicated_in	DOID:5419	schizophrenia		MGI:4438921	Srr<sup>tm1.2Jtc</sup>/Srr<sup>tm1.2Jtc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19065142	20100407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:5750594	Tg(CMV-cre)1Cgn/0 Trp53<sup>tm4Att</sup>/Trp53<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25119037	20160229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181380	Nr1h3<sup>tm1Djm</sup>	is_implicated_in	DOID:5425	ovarian hyperstimulation syndrome		MGI:4358795	Nr1h3<sup>tm1Djm</sup>/Nr1h3<sup>tm1Djm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19325005	20100511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:63097	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448372	Spta1<sup>sph</sup>/Spta1<sup>sph</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:14451913	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:78279	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6234993	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6841965	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158221	Foxj1<sup>tm1Slb</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:2679917	Foxj1<sup>tm1Slb</sup>/Foxj1<sup>tm1Slb</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10873152	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367773	Ahi1<sup>tm1Jgg</sup>	is_implicated_in	DOID:0110998	Joubert syndrome 3		MGI:5007765	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>tm1Jgg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21623382	20110616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926888	Crebbp<sup>tm1Dli</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10673499	20050926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3688831	Tg(Myh6-PRKAG2*R531G)22Dca	is_implicated_in	DOID:384	Wolff-Parkinson-White syndrome		MGI:3688834	Tg(Myh6-PRKAG2*R531G)22Dca/0  [background:] involves: C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:16339829	20061128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920177	Hepacam	is_implicated_in	DOID:0080315	megalencephalic leukoencephalopathy with subcortical cysts		MGI:6287231	Hepacam<sup>tm1Vlcg</sup>/Hepacam<sup>tm1Vlcg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28695146	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587769	Atg7<sup>tm1Tchi</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5295638	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6NCrlj * C57BL/10 * CBA/Ca * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:21339326	20111114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679321	Limk1<sup>tm1Zpj</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:2679324	Limk1<sup>tm1Zpj</sup>/Limk1<sup>tm1Zpj</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:12123613	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926078	Rhot1	is_implicated_in	DOID:231	motor neuron disease		MGI:5619354	Rhot1<sup>tm1.1Jmsu</sup>/Rhot1<sup>tm1.1Jmsu</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25136135	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919782	Sap130	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5906294	Sap130<sup>b2b635.2Clo</sup>/Sap130<sup>b2b635.2Clo</sup>  [background:] C57BL/6J-Sap130<sup>b2b635.2Clo</sup> Pcdha9<sup>b2b635.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28530678	20170808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856266	Kit<sup>W-v</sup>	is_implicated_in	DOID:2361	macrocytic anemia		MGI:3840691	Kit<sup>W-v</sup>/Kit<sup>W-v</sup>  [background:] C57BL/6J-Kit<sup>W-v</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	is_implicated_in	DOID:893	Wilson disease		MGI:3793274	Atp7b<sup>tx-J</sup>/Atp7b<sup>tx-J</sup>  [background:] C3H/HeJ-Atp7b<sup>tx-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17981064	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	is_implicated_in	DOID:893	Wilson disease		MGI:3793277	Atp7b<sup>tx</sup>/Atp7b<sup>tx</sup>  [background:] DL-Atp7b<sup>tx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8894697	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	is_implicated_in	DOID:893	Wilson disease		MGI:3043693	Atp7b<sup>tm1Tcg</sup>/Atp7b<sup>tm1Tcg</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:10441329	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:3698637	Zic3<sup>tm1Jwb</sup>/Zic3<sup>tm1Jwb</sup>  [background:] either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17127413	20070305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:3698642	Zic3<sup>tm1Jwb</sup>/Y  [background:] either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17127413	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4443333	Best1<sup>tm1.1Amar</sup>	is_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:4443335	Best1<sup>tm1.1Amar</sup>/Best1<sup>tm1.1Amar</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4443333	Best1<sup>tm1.1Amar</sup>	is_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:4450918	Best1<sup>tm1.1Amar</sup>/Best1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4432238	Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:5509044	Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>/Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] B6Brd;B6N-Tyr<sup>c-Brd</sup> Cenpj<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:23166506	20131001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437109	Odad2<sup>b2b227.1Clo</sup>/Odad2<sup>b2b227.1Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b227.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2179512	Il2ra<sup>tm1Dw</sup>/Il2ra<sup>tm1Dw</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7584142	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	is_implicated_in	DOID:6406	double outlet right ventricle		MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10574770	20060503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104841	Cpox	is_implicated_in	DOID:13269	hereditary coproporphyria		MGI:5488915	Cpox<sup>nct</sup>/Cpox<sup>nct</sup>  [background:] involves: BALB/cCrSlc			ECO:0000033	author statement supported by traceable reference	PMID:23631845	20180613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104841	Cpox	is_implicated_in	DOID:13269	hereditary coproporphyria		MGI:6160805	Cpox<sup>Rbc16</sup>/Cpox<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28600349	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641051	Dicer1<sup>tm1Smr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906349	Dicer1<sup>tm1Smr</sup>/Dicer1<sup>tm1Smr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S7/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18256189	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926345	Tsc2<sup>tm1Tno</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5641393	Tsc2<sup>tm1Tno</sup>/Tsc2<sup>+</sup>  [background:] B6J.129S4-Tsc2<sup>tm1Tno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888773	Prnp<sup>tm1Cwe</sup>	is_not_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:2174709	Prnp<sup>tm1Cwe</sup>/Prnp<sup>tm1Cwe</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1373228	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107822	Ebp	is_implicated_in	DOID:0060292	X-linked chondrodysplasia punctata 1		MGI:3587820	Ebp<sup>Td</sup>/Ebp<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10391218	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:6159581	Map2k1<sup>tm2.1Chrn</sup>/Map2k1<sup>tm2.1Chrn</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:29590634	20180605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3664791	Gja5<sup>tm1Paul</sup>/Gja5<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12842919	20061030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3664790	Gja5<sup>tm1Paul</sup>/Gja5<sup>tm1Paul</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12842919	20061030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97829	Pygl	is_implicated_in	DOID:2754	glycogen storage disease VI		MGI:6392248	Pygl<sup>tm1a(KOMP)Wtsi</sup>/Pygl<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Pygl<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31701076	20200228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98331	Snap25	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5774646	Snap25<sup>tm1Mcw</sup>/Snap25<sup>+</sup>  [background:] B6N.Cg-Snap25<sup>tm1Mcw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26300453	20161107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:5693885	Tbp<sup>tm1Xjl</sup>/Tbp<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/0  [background:] involves: 129S/SvEv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24462098	20151028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88524	Crygd	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:2175808	Crygd<sup>Lop12</sup>/Crygd<sup>+</sup>  [background:] involves: BALB/cJ * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:10704279	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	is_implicated_in	DOID:0110078	Leber congenital amaurosis 1		MGI:6274727	Gucy2e<sup>cpfl9</sup>/Gucy2e<sup>cpfl9</sup>  [background:] B6;129P2-Gucy2e<sup>cpfl9</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:6274742	20190125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6423102	Muc4<sup>tm1Unc</sup>/Muc4<sup>tm1Unc</sup>  [background:] B6NTac.129(FVB)-Muc4<sup>tm1Unc</sup>/Rand			ECO:0000033	author statement supported by traceable reference	MGI:6416514	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832386	Gt(ROSA)26Sor<sup>tm4(HIF2A*)Kael</sup>	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5304716	Gt(ROSA)26Sor<sup>tm4(HIF2A*)Kael</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20733101	20170814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889411	Tnfrsf13b	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3847256	Tnfrsf13b<sup>tm1Vmd</sup>/Tnfrsf13b<sup>tm1Vmd</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12594954	20090609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	is_implicated_in	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome		MGI:3693614	Gata3<sup>tm1Gsv</sup>/Gata3<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15207274	20070115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	is_implicated_in	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome		MGI:3693366	Gata3<sup>tm1Gsv</sup>/Gata3<sup>+</sup>  [background:] FVB.129(B6)-Gata3<sup>tm1Gsv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15994092	20070115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055135	Rasgrp2<sup>tm1Amg</sup>	is_implicated_in	DOID:0110912	leukocyte adhesion deficiency 3		MGI:3055194	Rasgrp2<sup>tm1Amg</sup>/Rasgrp2<sup>tm1Amg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17492052	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857437	Grm5<sup>tm1Rod</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:6315641	Grm5<sup>tm1Rod</sup>/Grm5<sup>tm1Rod</sup>  [background:] B6.129-Grm5<sup>tm1Rod</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30401923	20190701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397593	Kcnq3<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397678	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397593	Kcnq3<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397677	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] FVB.129-Kcnq3<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397593	Kcnq3<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397673	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397593	Kcnq3<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397674	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397593	Kcnq3<sup>tm1.1Naas</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:4397675	Kcnq3<sup>tm1.1Naas</sup>/Kcnq3<sup>tm1.1Naas</sup>  [background:] B6.129-Kcnq3<sup>tm1.1Naas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18483067	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855933	A<sup>iy</sup>	is_implicated_in	DOID:9970	obesity		MGI:3821619	A<sup>iy</sup>/A<sup>iy</sup>  [background:] C3H/HeJ-A<sup>iy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:5798139	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664783	Grm1<sup>crv4</sup>	is_implicated_in	DOID:0080062	autosomal recessive spinocerebellar ataxia 13		MGI:3664785	Grm1<sup>crv4</sup>/Grm1<sup>crv4</sup>  [background:] BALB/cPas-Grm1<sup>crv4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16964410	20151117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574428	Sf3b1<sup>tm1Hko</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:7279138	Sf3b1<sup>tm1Hko</sup>/Sf3b1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25481243	20220520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96189	Hoxb8	is_implicated_in	DOID:0050587	trichotillomania		MGI:2673421	Hoxb8<sup>tm1.1Mrc</sup>/Hoxb8<sup>tm1.1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11779477	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	is_implicated_in	DOID:4183	pseudopseudohypoparathyroidism		MGI:5285183	Gnas<sup>tm1Gwa</sup>/Gnas<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:21747923	20110913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448356	Syn1<sup>tm1Pggd</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5517482	Syn1<sup>tm1Pggd</sup>/Syn1<sup>tm1Pggd</sup>  [background:] B6.129P2-Syn1<sup>tm1Pggd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3522243	pta	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:3522704	pta/pta  [background:] C57BL/6J-pta			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429649	Sox9<sup>tm2Crm</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451173	Sox9<sup>tm2Crm</sup>/Sox9<sup>tm2Crm</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429649	Sox9<sup>tm2Crm</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451172	Sox9<sup>tm2Crm</sup>/Sox9<sup>+</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S7/SvEvBrd * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429649	Sox9<sup>tm2Crm</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451169	Sox9<sup>tm2Crm</sup>/Sox9<sup>+</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429649	Sox9<sup>tm2Crm</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:2451170	Sox9<sup>tm2Crm</sup>/Sox9<sup>tm2Crm</sup> Tg(Col2a1-cre)1Bhr/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12414734	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177010	Dmc1<sup>Mei11</sup>	is_implicated_in	DOID:0050457	Sertoli cell-only syndrome		MGI:2177047	Dmc1<sup>Mei11</sup>/Dmc1<sup>Mei11</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10700192	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388132	Ikzf3<sup>tm1Kge</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2653187	Ikzf3<sup>tm1Kge</sup>/Ikzf3<sup>tm1Kge</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9806640	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388132	Ikzf3<sup>tm1Kge</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2653187	Ikzf3<sup>tm1Kge</sup>/Ikzf3<sup>tm1Kge</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12574333	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	is_not_implicated_in	DOID:14330	Parkinson's disease		MGI:4429667	Drd2<sup>tm1Low</sup>/Drd2<sup>tm1Low</sup>  [background:] B6.129S2-Drd2<sup>tm1Low</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9547254	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856555	Myo6<sup>sv</sup>	is_implicated_in	DOID:0110552	autosomal dominant nonsyndromic deafness 22		MGI:3528185	Myo6<sup>sv</sup>/Myo6<sup>sv</sup>  [background:] involves: B10.HA/(33NX)Sn * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7493015	20060201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586504	Fzd9<sup>tm1Sjp</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3586704	Fzd9<sup>tm1Sjp</sup>/Fzd9<sup>tm1Sjp</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15930120	20050906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3622418	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] NOD.Cg-H2<sup>b</sup> Il4<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16413168	20060516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3622411	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] NOD.129P2-Il4<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16413168	20060516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3056103	Timp3<sup>tm1Rkho</sup>/Timp3<sup>tm1Rkho</sup>  [background:] B6.129-Timp3<sup>tm1Rkho</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15262835	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3056101	Timp3<sup>tm1Rkho</sup>/Timp3<sup>tm1Rkho</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16037568	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3767995	Lyn<sup>tm1Ard</sup>/Lyn<sup>tm1Ard</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20512127	20100729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:5287852	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1Jme</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15076752	20111003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:3721894	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1.1Jme</sup> Tg(ACTA1-cre)79Jme/0  [background:] involves: 129 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11238465	20111003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:4398737	Smn1<sup>tm1Msd</sup>/Smn1<sup>tm1Rako</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19497369	20111003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	is_implicated_in	DOID:13137	Werdnig-Hoffmann disease		MGI:3721431	Smn1<sup>tm1Jme</sup>/Smn1<sup>tm1.1Jme</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10749994	20111003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	is_implicated_in	DOID:5419	schizophrenia		MGI:5559028	Slc6a1<sup>tm1Mlit</sup>/Slc6a1<sup>tm1Mlit</sup>  [background:] B6.129S1-Slc6a1<sup>tm1Mlit</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23922840	20140415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:12271	aniridia		MGI:2175208	Pax6<sup>Sey-Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:12714618	20080218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:12271	aniridia		MGI:2175204	Pax6<sup>Sey-Dey</sup>/Pax6<sup>+</sup>  [background:] C3H/HeJ-Pax6<sup>Sey-Dey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2173141	20080218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818575	Atg16l1<sup>Gt(XR0164)Wtsi</sup>	is_implicated_in	DOID:0110885	inflammatory bowel disease 10		MGI:3818604	Atg16l1<sup>Gt(XR0164)Wtsi</sup>/Atg16l1<sup>Gt(XR0164)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18849966	20081208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776796	Slc24a5<sup>tm1Lex</sup>	is_implicated_in	DOID:0050633	ocular albinism 1		MGI:4421409	Slc24a5<sup>tm1Lex</sup>/Slc24a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18424845	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384729	Fech<sup>tm1Dab</sup>	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:2664560	Fech<sup>tm1Dab</sup>/Fech<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12149233	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3497903	Irs2<sup>tm2Mfw</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3510669	Irs2<sup>tm2Mfw</sup>/Irs2<sup>tm2Mfw</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15467829	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3781475	Cfap47	is_implicated_in	DOID:12336	male infertility		MGI:6727110	Cfap47<sup>em1Fzh</sup>/Y  [background:] C57BL/6-Cfap47<sup>em1Fzh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33472045	20210729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778898	Pnp<sup>e</sup>/Pnp<sup>e</sup>  [background:] C57BL/6J-Pnp<sup>e</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778900	Pnp<sup>f</sup>/Pnp<sup>f</sup>  [background:] C57BL/6J-Pnp<sup>f</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778902	Pnp<sup>g</sup>/Pnp<sup>g</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778897	Pnp<sup>e</sup>/Pnp<sup>e</sup>  [background:] involves: C3H/HeHa * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:2516826	20120928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778899	Pnp<sup>f</sup>/Pnp<sup>f</sup>  [background:] involves: C3H/HeHa * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:2516826	20120928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138281	Lbr	is_implicated_in	DOID:1702	ichthyosis vulgaris		MGI:3829382	Lbr<sup>ic-J</sup>/Lbr<sup>ic-J</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17403717	20090129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3844284	Ank1<sup>Rbc2</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:3844300	Ank1<sup>Rbc2</sup>/Ank1<sup>Rbc2</sup>  [background:] involves: 129S1/Sv * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:19179303	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154359	Hnf1a<sup>tm1Mya</sup>	is_implicated_in	DOID:9281	phenylketonuria		MGI:3610388	Hnf1a<sup>tm1Mya</sup>/Hnf1a<sup>tm1Mya</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8598044	20060119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2136886	Rtn4r	is_not_implicated_in	DOID:5419	schizophrenia		MGI:5293444	Rtn4r<sup>rgsc1836</sup>/Rtn4r<sup>rgsc1836</sup>  [background:] C57BL/6JJcl-Rtn4r<sup>rgsc1836</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21645550	20111026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2136886	Rtn4r	is_not_implicated_in	DOID:5419	schizophrenia		MGI:3806713	Rtn4r<sup>tm1Gogo</sup>/Rtn4r<sup>tm1Gogo</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18043741	20111026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684578	Cav3<sup>tm1Ncnp</sup>	is_implicated_in	DOID:0060255	rippling muscle disease 2		MGI:6114152	Cav3<sup>tm1Ncnp</sup>/Cav3<sup>tm1Ncnp</sup>  [background:] involves: 129S4/SvJae * C57BL/10			ECO:0000033	author statement supported by traceable reference	PMID:19535499	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:1214	tympanosclerosis		MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:27959908	20190917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858025	Cryaa<sup>tm1Wawr</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2175799	Cryaa<sup>tm1Wawr</sup>/Cryaa<sup>tm1Wawr</sup>  [background:] involves: 129/Sv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9023351	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858025	Cryaa<sup>tm1Wawr</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2175800	Cryaa<sup>tm1Wawr</sup>/Cryaa<sup>tm1Wawr</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9023351	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153817	Fgfr2<sup>tm2.3Dsn</sup>	is_implicated_in	DOID:14705	Pfeiffer syndrome		MGI:2176483	Fgfr2<sup>tm2.3Dsn</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11274405	20080121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926562	Gucy1a1	is_implicated_in	DOID:1070	primary open angle glaucoma		MGI:5516430	Gucy1a1<sup>tm1.1Brou</sup>/Gucy1a1<sup>tm1.1Brou</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:23527308	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818633	Strc<sup>tm1Ugds</sup>	is_implicated_in	DOID:0110471	autosomal recessive nonsyndromic deafness 16		MGI:3818653	Strc<sup>tm1Ugds</sup>/Strc<sup>tm1Ugds</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18849963	20081209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330223	Papss2	is_implicated_in	DOID:0050812	spondyloepimetaphyseal dysplasia, Pakistani type		MGI:3054675	Papss2<sup>bm</sup>/Papss2<sup>bm</sup>  [background:] LDJ/Le			ECO:0000033	author statement supported by traceable reference	PMID:5713631	20090819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1925349	Atrip	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:6505486	Atrip<sup>tm1.1Pof</sup>/Atrip<sup>tm1.1Pof</sup> Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32994318	20210208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3784988	Lepr<sup>Db-Btlr</sup>	is_implicated_in	DOID:9970	obesity		MGI:3784991	Lepr<sup>Db-Btlr</sup>/Lepr<sup>Db-Btlr</sup>  [background:] C57BL/6J-Lepr<sup>Db-Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778961	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	is_not_implicated_in	DOID:1926	Gaucher's disease		MGI:6444208	Psap<sup>tm1Suz</sup>/Psap<sup>tm2.1Juma</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20175216	20200724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	is_not_implicated_in	DOID:1926	Gaucher's disease		MGI:6444206	Psap<sup>tm2.1Juma</sup>/Psap<sup>tm2.1Juma</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20175216	20200724	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182005	Pten<sup>tm2Mak</sup>	is_implicated_in	DOID:0060867	macrocephaly-autism syndrome		MGI:5660888	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16675393	20150903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677314	Recql4<sup>tm1Abe</sup>	is_implicated_in	DOID:2732	Rothmund-Thomson syndrome		MGI:2677318	Recql4<sup>tm1Abe</sup>/Recql4<sup>tm1Abe</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12915449	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:2394	ovarian cancer		MGI:5432223	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:2394	ovarian cancer		MGI:5432228	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429385	Tg(Htt-ATXN3*148Q)3746Thsc	is_implicated_in	DOID:1440	Machado-Joseph disease		MGI:4429405	Tg(Htt-ATXN3*148Q)3746Thsc/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:19699305	20100218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3644668	Prlh	is_implicated_in	DOID:9970	obesity		MGI:3832410	Prlh<sup>tm1Taon</sup>/Prlh<sup>tm1Taon</sup>  [background:] B6N.129X1-Prlh<sup>tm1Taon</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19033670	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033230	Gck<sup>Rgsc552</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590141	Gck<sup>Rgsc552</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	is_implicated_in	DOID:0050729	Chanarin-Dorfman syndrome		MGI:5007482	Abhd5<sup>tm1.1Rze</sup>/Abhd5<sup>tm1.1Rze</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20023287	20110614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685397	Rc3h1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3582186	Rc3h1<sup>san</sup>/Rc3h1<sup>san</sup>  [background:] either: C57BL/6JSfdAnu-Rc3h1<sup>san</sup>/Anu or (involves: C57BL/6JSfdAnu * CBA/Ca)			ECO:0000033	author statement supported by traceable reference	PMID:15917799	20050721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	is_implicated_in	DOID:0050638	transthyretin amyloidosis		MGI:6194720	Ttr<sup>tm1.1Smoc</sup>/?  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29360446	20180816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916120	Ak8	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429555	Ak8<sup>Gt(OST16378)Lex</sup>/Ak8<sup>Gt(OST16378)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	is_implicated_in	DOID:14525	Reye syndrome		MGI:3613200	Txnip<sup>tm1Jjy</sup>/Txnip<sup>tm1Jjy</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16254043	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88061	Aprt	is_implicated_in	DOID:0060350	adenine phosphoribosyltransferase deficiency		MGI:2449114	Aprt<sup>tm1Jat</sup>/Aprt<sup>tm1Jat</sup>  [background:] involves: 129S2/SvPas * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8643571	20120924	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88061	Aprt	is_implicated_in	DOID:0060350	adenine phosphoribosyltransferase deficiency		MGI:2449115	Aprt<sup>tm1Jat</sup>/Aprt<sup>tm1Jat</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8643571	20120924	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88061	Aprt	is_implicated_in	DOID:0060350	adenine phosphoribosyltransferase deficiency		MGI:2449123	Aprt<sup>tm1Dwm</sup>/Aprt<sup>tm1Dwm</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:8864750	20120924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856181	Spta1<sup>sph-ha</sup>	is_implicated_in	DOID:10923	sickle cell anemia		MGI:3766996	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] either: (B6.D1-Spta1<sup>sph-ha</sup> x WB.D1-Spta1<sup>sph-ha</sup>)F1 or (WB.D1-Spta1<sup>sph-ha</sup> x B6.D1-Spta1<sup>sph-ha</sup>)F1			ECO:0000033	author statement supported by traceable reference	PMID:8355480	20080109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	is_not_implicated_in	DOID:0080119	mitochondrial DNA depletion syndrome 1		MGI:3699315	Tymp<sup>tm1Akiy</sup>/Tymp<sup>tm1Akiy</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12077348	20070309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329021	Msh5	is_implicated_in	DOID:0080870	primary ovarian insufficiency 13		MGI:7260343	Msh5<sup>em1Jzc</sup>/Msh5<sup>em1Jzc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28175301	20220411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832575	Gt(ROSA)26Sor<sup>tm1(Kcnj11*V59M)Fmas</sup>	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus		MGI:4819394	Gt(ROSA)26Sor<sup>tm1(Kcnj11*V59M)Fmas</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20595581	20100817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832575	Gt(ROSA)26Sor<sup>tm1(Kcnj11*V59M)Fmas</sup>	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus		MGI:3832577	Gt(ROSA)26Sor<sup>tm1(Kcnj11*V59M)Fmas</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19065048	20100817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339956	Cdyl	is_implicated_in	DOID:1826	epilepsy		MGI:6121112	Cdyl<sup>tm1.1Yuw</sup>/Cdyl<sup>tm1.1Yuw</sup> Emx1<sup>tm1(cre)Yql</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28076783	20180313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3795786	Pcsk5<sup>vcc</sup>	is_implicated_in	DOID:14679	VACTERL association		MGI:3797214	Pcsk5<sup>vcc</sup>/Pcsk5<sup>vcc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18519639	20150724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2387586	Tns2	is_implicated_in	DOID:0060852	Pierson syndrome		MGI:3815328	Tns2<sup>nph</sup>/Tns2<sup>nph</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:16688531	20081119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848931	Lama2<sup>dy-8J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3848948	Lama2<sup>dy-8J</sup>/Lama2<sup>dy-8J</sup>  [background:] C57BL/6J-Lama2<sup>dy-8J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:3848945	20090626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	is_implicated_in	DOID:0110449	dilated cardiomyopathy 1M		MGI:3037157	Csrp3<sup>tm1Crni</sup>/Csrp3<sup>tm1Crni</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9039266	20060518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857597	Crygb<sup>Nop</sup>	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:2175807	Crygb<sup>Nop</sup>/Crygb<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6479248	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857597	Crygb<sup>Nop</sup>	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:2175806	Crygb<sup>Nop</sup>/Crygb<sup>Nop</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6479248	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F		MGI:3618464	Sgcd<sup>tm1Kcam</sup>/Sgcd<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10481911	20220517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F		MGI:5911876	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] B6.129-Sgcd<sup>tm1Mcn</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28797108	20220517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F		MGI:3618527	Sgcd<sup>tm1Mcn</sup>/Sgcd<sup>tm1Mcn</sup>  [background:] involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10862711	20220517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797014	Phex<sup>Pug</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3806979	Phex<sup>Pug</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17710565	20120620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1		MGI:3527906	Ppt1<sup>tm1Aj</sup>/Ppt1<sup>tm1Aj</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15649713	20150701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1		MGI:5296508	Ppt1<sup>tm1Hof</sup>/Ppt1<sup>tm1Hof</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22031903	20150701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1		MGI:5585410	Ppt1<sup>tm1.1Dprc</sup>/Ppt1<sup>tm1.1Dprc</sup>  [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25205113	20150701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913689	Borcs7	is_implicated_in	DOID:2367	neuroaxonal dystrophy		MGI:6302764	Borcs7<sup>Q87X</sup>/Borcs7<sup>Q87X</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30067980	20190513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511358	Pparg<sup>tm2(tTA)Yba</sup>	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3784503	Pparg<sup>tm2(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891217	Zfp423	is_implicated_in	DOID:2785	Dandy-Walker syndrome		MGI:3693287	Zfp423<sup>nur12</sup>/Zfp423<sup>nur12</sup>  [background:] involves: BALB/c * C57BL/6 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:17151198	20070111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103013	Cacna1c	is_implicated_in	DOID:0060173	Timothy syndrome		MGI:5296910	Cacna1c<sup>tm2Itl</sup>/Cacna1c<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:21878566	20111201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921409	Acbd5	is_implicated_in	DOID:906	peroxisomal disease		MGI:6502847	Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>/Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-A<sup>tm1Brd</sup> Acbd5<sup>tm1a(EUCOMM)Wtsi</sup>/WtsiCnbc			ECO:0000033	author statement supported by traceable reference	PMID:33244184	20210129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5314147	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] B6.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21908517	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894695	Galnt3	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:4355581	Galnt3<sup>tm1Mjec</sup>/Galnt3<sup>tm1Mjec</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19213845	20121114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894695	Galnt3	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:5435288	Galnt3<sup>tcal</sup>/Galnt3<sup>tcal</sup>  [background:] involves: C3H * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22912827	20121114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624977	Tg(Ckm-LPL)MRze	is_implicated_in	DOID:423	myopathy		MGI:3624987	Tg(Ckm-LPL)MRze/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:7635990	20190806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857456	Ciita<sup>tm1Ccum</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617533	Ciita<sup>tm1Ccum</sup>/Ciita<sup>tm1Ccum</sup>  [background:] NOD.129S2(B6)-Ciita<sup>tm1Ccum</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10201997	20060324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857869	Foxc1<sup>tm1Blh</sup>	is_implicated_in	DOID:11211	buphthalmos		MGI:3655827	Foxc1<sup>tm1Blh</sup>/Foxc1<sup>+</sup>  [background:] B6.Cg-Foxc1<sup>tm1Blh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437430	Mid1<sup>tm1Mero</sup>	is_implicated_in	DOID:0080697	Opitz GBBB syndrome		MGI:4437568	Mid1<sup>tm1Mero</sup>/Y  [background:] B6.Cg-Mid1<sup>tm1Mero</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20181585	20220608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914285	Dnajb4	is_implicated_in	DOID:11720	distal myopathy		MGI:7444383	Dnajb4<sup>em1Sngi</sup>/Dnajb4<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:36512060	20230315	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914285	Dnajb4	is_implicated_in	DOID:11720	distal myopathy		MGI:7444385	Dnajb4<sup>em2Sngi</sup>/Dnajb4<sup>em2Sngi</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:36512060	20230315	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107799	Gadd45a	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3618357	Gadd45a<sup>tm1Ajf</sup>/Gadd45a<sup>tm1Ajf</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315195	Emg1	is_implicated_in	DOID:0050684	Bowen-Conradi syndrome		MGI:5787933	Emg1<sup>tm1.1Btr</sup>/Emg1<sup>tm1.1Btr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25708872	20160804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385463	Hnf4a<sup>tm1Sad</sup>	is_implicated_in	DOID:1062	Fanconi syndrome		MGI:6392256	Hnf4a<sup>tm1Sad</sup>/Hnf4a<sup>tm1Sad</sup> Six2<sup>tm1(tTA,tetO-EGFP/cre)Amc</sup>/Six2<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30046000	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3041135	Met<sup>tm1Sst</sup>	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:4950068	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195751	20110514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:1712	aortic valve stenosis		MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923097	Crppa	is_implicated_in	DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U		MGI:7279103	Crppa<sup>em2Mbp</sup>/Crppa<sup>em2Mbp</sup> Myf5<sup>tm3(cre)Sor</sup>/Myf5<sup>+</sup>  [background:] B6.Cg-Myf5<sup>tm3(cre)Sor</sup> Crppa<sup>em2Mbp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35422047	20220519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920024	Neil1	is_implicated_in	DOID:9970	obesity		MGI:3620067	Neil1<sup>tm1Rsld</sup>/Neil1<sup>+</sup>  [background:] either: B6.129S1-Neil1<sup>tm1Rsld</sup> or (involves: 129S1/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16446448	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106679	Zic2	is_implicated_in	DOID:0110878	holoprosencephaly 5		MGI:5827598	Zic2<sup>Ku</sup>/Zic2<sup>Ku</sup>  [background:] 129S.CAnNCrl(C3)-Zic2<sup>Ku</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27466203	20170303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106679	Zic2	is_implicated_in	DOID:0110878	holoprosencephaly 5		MGI:3639581	Zic2<sup>Ku</sup>/Zic2<sup>Ku</sup>  [background:] C3.CAnNCrl-Zic2<sup>Ku</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18617531	20170303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106679	Zic2	is_implicated_in	DOID:0110878	holoprosencephaly 5		MGI:2653209	Zic2<sup>tm1Jaru</sup>/Zic2<sup>tm1Jaru</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10677508	20170303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:3840340	Mmut<sup>tm1Cpv</sup>/Mmut<sup>tm1Cpv</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17937813	20180521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:6157364	Mmut<sup>tm1.1Mrb</sup>/Mmut<sup>tm1.1Mrb</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27519416	20180521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:6157365	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1.1Mrb</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27519416	20180521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	is_implicated_in	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency		MGI:3026845	Mmut<sup>tm1Pai</sup>/Mmut<sup>tm1Pai</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14555645	20180521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687967	Clcn6<sup>tm1Tjj</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3688436	Clcn6<sup>tm1Tjj</sup>/Clcn6<sup>tm1Tjj</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16950870	20061121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676546	Stk11<sup>tm1.1Jish</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:2676549	Stk11<sup>tm1.1Jish</sup>/Stk11<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12060709	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	is_implicated_in	DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K		MGI:5690112	Gdap1<sup>tm1.2Geno</sup>/Gdap1<sup>tm1.2Geno</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25860513	20151014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856704	ckr	is_implicated_in	DOID:5419	schizophrenia		MGI:2663269	ckr/ckr  [background:] involves: C3H/HeRos * C57BL/10Ros			ECO:0000033	author statement supported by traceable reference	PMID:14709346	20081212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096875	Wdfy3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5825287	Wdfy3<sup>disc</sup>/Wdfy3<sup>disc</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:25198012	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096875	Wdfy3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5825304	Wdfy3<sup>tm1a(KOMP)Mbp</sup>/Wdfy3<sup>tm1a(KOMP)Mbp</sup>  [background:] C57BL/6N-Wdfy3<sup>tm1a(KOMP)Mbp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25198012	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98488	Slc6a6	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3029356	Slc6a6<sup>tm1Dhau</sup>/Slc6a6<sup>tm1Dhau</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11772953	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914280	Fancl	is_implicated_in	DOID:14450	46 XX gonadal dysgenesis		MGI:2660751	Fancl<sup>gcd</sup>/Fancl<sup>gcd</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:8373945	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108072	Traf6	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:2675470	Traf6<sup>tm1Jino</sup>/Traf6<sup>tm1Jino</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12060722	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683318	Zap70<sup>m1Saka</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3698734	Zap70<sup>m1Saka</sup>/Zap70<sup>m1Saka</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:14647385	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4356541	Pfkm<sup>tm1Fbos</sup>	is_implicated_in	DOID:11721	glycogen storage disease VII		MGI:4356551	Pfkm<sup>tm1Fbos</sup>/Pfkm<sup>tm1Fbos</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19696889	20090911	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914703	Slc25a46	is_implicated_in	DOID:0080068	Charcot-Marie-Tooth disease type 6		MGI:6286393	Slc25a46<sup>atc</sup>/Slc25a46<sup>atc</sup>  [background:] B6.Cg-Slc25a46<sup>atc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28376086	20190408	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:6115249	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>/Y  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25422369	20180208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:6115250	Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>/Rp2<sup>Gt(EUCJ0183f04)Hmgu</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25422369	20180208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:5619363	Rp2<sup>tm1.2Asw</sup>/Rp2<sup>tm1.2Asw</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23745007	20180208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	is_implicated_in	DOID:0110415	retinitis pigmentosa 2		MGI:5620352	Rp2<sup>tm1.2Asw</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23745007	20180208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919834	Cul4b	is_implicated_in	DOID:1059	intellectual disability		MGI:5438241	Cul4b<sup>tm1Swl</sup>/Y Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] B6.Cg-Edil3<sup>Tg(Sox2-cre)1Amc</sup> Cul4b<sup>tm1Swl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22763239	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916703	Prss56	is_implicated_in	DOID:0060835	isolated microphthalmia 6		MGI:5444191	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] C57BL/6J-Prss56<sup>glcr4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916703	Prss56	is_implicated_in	DOID:0060835	isolated microphthalmia 6		MGI:5444190	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] involves: C3H/HeA * C57BL/6J * C57BL/LiA			ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916703	Prss56	is_implicated_in	DOID:0060835	isolated microphthalmia 6		MGI:5444192	Prss56<sup>glcr4</sup>/Prss56<sup>glcr4</sup>  [background:] C3A.Cg-Prss56<sup>glcr4</sup> Pde6b<sup>+</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21532570	20121203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:2387326	Aifm1<sup>Hq</sup>/Y  [background:] B6CBACa A<sup>w-J</sup>/A-Aifm1<sup>Hq</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18791645	20171031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:2387325	Aifm1<sup>Hq</sup>/Aifm1<sup>Hq</sup>  [background:] B6CBACa A<sup>w-J</sup>/A-Aifm1<sup>Hq</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18791645	20171031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	is_implicated_in	DOID:5419	schizophrenia		MGI:2175046	Grin1<sup>tm1Bhk</sup>/Grin1<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10481908	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822350	Tg(RNU6-RNAi:Cldn16)551Dago	is_implicated_in	DOID:0060880	renal hypomagnesemia 3		MGI:3822351	Tg(RNU6-RNAi:Cldn16)551Dago/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17442678	20090107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177929	Capn3<sup>tm1Jsb</sup>	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A		MGI:2659043	Capn3<sup>tm1Jsb</sup>/Capn3<sup>tm1Jsb</sup>  [background:] either: 129/Sv-Capn3<sup>tm1Jsb</sup> or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11134085	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336209	Trappc10	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5615097	Trappc10<sup>b2b2613Clo</sup>/Trappc10<sup>b2b2613Clo</sup>  [background:] C57BL/6J-Trappc10<sup>b2b2613Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107542	Ccw	is_implicated_in	DOID:83	cataract		MGI:2175749	Ccw/Ccw<sup>+</sup>  [background:] involves: unpedigreed stock			ECO:0000033	author statement supported by traceable reference	PMID:8812411	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107542	Ccw	is_implicated_in	DOID:83	cataract		MGI:2175749	Ccw/Ccw<sup>+</sup>  [background:] involves: unpedigreed stock			ECO:0000033	author statement supported by traceable reference	PMID:11062307	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929293	Cib2	is_not_implicated_in	DOID:0110836	Usher syndrome type 1J		MGI:6192643	Cib2<sup>tm1.1Aela</sup>/Cib2<sup>tm1.1Aela</sup>  [background:] involves: BALB/c * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29084757	20180803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817496	Sqstm1<sup>tm1Jjw</sup>	is_not_implicated_in	DOID:5408	Paget's disease of bone		MGI:3817497	Sqstm1<sup>tm1Jjw</sup>/Sqstm1<sup>tm1Jjw</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18765443	20081124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923275	Cant1	is_implicated_in	DOID:0060462	Desbuquois dysplasia		MGI:7264676	Cant1<sup>tm1.1Aros</sup>/Cant1<sup>tm1.1Aros</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30439444	20220427	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923275	Cant1	is_implicated_in	DOID:0060462	Desbuquois dysplasia		MGI:7264693	Cant1<sup>tm1.2Aros</sup>/Cant1<sup>tm1.2Aros</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30439444	20220427	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	is_implicated_in	DOID:3883	Lynch syndrome		MGI:4460268	Msh2<sup>tm1Rak</sup>/Msh2<sup>tm2.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19931261	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	is_implicated_in	DOID:3883	Lynch syndrome		MGI:4460267	Msh2<sup>tm2.1Rak</sup>/Msh2<sup>tm3.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * C57BL/6 * DBA/2 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19931261	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	is_implicated_in	DOID:3883	Lynch syndrome		MGI:4460266	Msh2<sup>tm2.1Rak</sup>/Msh2<sup>tm2.1Rak</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19931261	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	is_implicated_in	DOID:3883	Lynch syndrome		MGI:4429602	Msh2<sup>tm1Htr</sup>/Msh2<sup>tm1Htr</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9443401	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343139	Ikzf4	is_implicated_in	DOID:640	encephalomyelitis		MGI:6467272	Foxp3<sup>tm4(YFP/icre)Ayr</sup>/Foxp3<sup>tm4(YFP/icre)Ayr</sup> Ikzf4<sup>tm1Djr</sup>/Ikzf4<sup>tm1Djr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:31296356	20201015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851440	Tg(tetO-HTT*94Q,-lacZ)1Rhn	is_implicated_in	DOID:12858	Huntington's disease		MGI:3851446	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-HTT*94Q,-lacZ)1Rhn/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:10778856	20090729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	is_implicated_in	DOID:10871	age related macular degeneration		MGI:3815114	Ccl2<sup>tm1Rol</sup>/Ccl2<sup>tm1Rol</sup>  [background:] B6.129S4-Ccl2<sup>tm1Rol</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14566334	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358115	Npr2<sup>pwe</sup>	is_implicated_in	DOID:0080050	acromesomelic dysplasia, Maroteaux type		MGI:5443996	Npr2<sup>pwe</sup>/Npr2<sup>pwe</sup>  [background:] involves: C3H/HeJ * C57BL/6 * NAW/WI			ECO:0000033	author statement supported by traceable reference	PMID:23065701	20121130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052754	Trex1<sup>tm1Tld</sup>	is_implicated_in	DOID:0050169	cutaneous lupus erythematosus		MGI:5925413	Trex1<sup>tm1Tld</sup>/Trex1<sup>tm1Tld</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28351661	20171121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931595	Nfkbiz	is_implicated_in	DOID:0050426	Stevens-Johnson syndrome		MGI:3047105	Nfkbiz<sup>tm1Aki</sup>/Nfkbiz<sup>tm1Aki</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15671285	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931595	Nfkbiz	is_implicated_in	DOID:0050426	Stevens-Johnson syndrome		MGI:3819765	Nfkbiz<sup>tm1Aki</sup>/Nfkbiz<sup>tm1Aki</sup>  [background:] C.129P2-Nfkbiz<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18441309	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	is_implicated_in	DOID:12721	multiple epiphyseal dysplasia		MGI:4417874	Comp<sup>tm1Mbri</sup>/Comp<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19808781	20100115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2665102	Pde6b<sup>rd1-2J</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:2665106	Pde6b<sup>rd1-2J</sup>/Pde6b<sup>rd1-2J</sup>  [background:] C57BL/6J-Pde6b<sup>rd1-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:2651853	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934259	Dhh<sup>tm1Amc</sup>	is_implicated_in	DOID:14448	46,XY sex reversal		MGI:2659090	Dhh<sup>tm1Amc</sup>/Dhh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * C57BL/6J * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11090455	20050923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028629	Nphs2<sup>tm1Antc</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3028634	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm1Antc</sup>  [background:] 129-Nphs2<sup>tm1Antc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14701729	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028629	Nphs2<sup>tm1Antc</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3028633	Nphs2<sup>tm1Antc</sup>/Nphs2<sup>tm1Antc</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14701729	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803603	Rpsa<sup>tm1Ells</sup>	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:3804635	Rpsa<sup>tm1Ells</sup>/Rpsa<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3804630	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2152541	srt	is_implicated_in	DOID:0050592	asphyxiating thoracic dystrophy		MGI:2181881	srt/srt  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5906349	Dicer1<sup>tm1Smr</sup>/Dicer1<sup>tm1Smr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S7/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18256189	20170809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	is_implicated_in	DOID:0060614	ulnar-mammary syndrome		MGI:2655216	Tbx3<sup>tm1Pa</sup>/Tbx3<sup>tm1Pa</sup>  [background:] either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac)			ECO:0000033	author statement supported by traceable reference	PMID:12668638	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107689	Kif3a	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:5142310	Kif3a<sup>tm1Gsn</sup>/Kif3a<sup>tm2Gsn</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12672950	20210125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720652	Tg(DMD-APP*)7Neve	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720676	Tg(DMD-APP*)7Neve/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8744400	20070906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720652	Tg(DMD-APP*)7Neve	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720676	Tg(DMD-APP*)7Neve/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1438289	20070906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921004	Thap1	is_implicated_in	DOID:0090039	torsion dystonia 6		MGI:6107698	Thap1<sup>tm1.2Meeh</sup>/Thap1<sup>+</sup>  [background:] involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26376866	20180105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921004	Thap1	is_implicated_in	DOID:0090039	torsion dystonia 6		MGI:6107696	Thap1<sup>tm1.1Meeh</sup>/Thap1<sup>+</sup>  [background:] involves: 129S/SvEv * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26376866	20180105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829641	Flcn<sup>tm1Btt</sup>	is_implicated_in	DOID:0050676	Birt-Hogg-Dube syndrome		MGI:3829652	Flcn<sup>tm1Btt</sup>/Flcn<sup>tm1Btt</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18974783	20090130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311352	b2b1200Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105084	Satb1	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:7281769	Satb1<sup>tm2Kos</sup>/Satb1<sup>tm2Kos</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/10 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:29127143	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137383	Csmd1	is_not_implicated_in	DOID:5419	schizophrenia		MGI:5485273	Csmd1<sup>tm1Lex</sup>/Csmd1<sup>tm1Lex</sup>  [background:] B6;129S5-Csmd1<sup>tm1Lex</sup>/Mmucd			ECO:0000033	author statement supported by traceable reference	PMID:23284669	20130516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	is_implicated_in	DOID:0080449	developmental and epileptic encephalopathy 16		MGI:6306133	Tbc1d24<sup>em2Tbf</sup>/Tbc1d24<sup>em2Tbf</sup>  [background:] C57BL/6J-Tbc1d24<sup>em2Tbf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30602030	20190529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921932	Wdr35	is_implicated_in	DOID:0110090	short-rib thoracic dysplasia 7 with or without polydactyly		MGI:5501229	Wdr35<sup>yeti</sup>/Wdr35<sup>yeti</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21473986	20130815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387675	Clcn7<sup>tm1Tjj</sup>	is_implicated_in	DOID:0110944	autosomal recessive osteopetrosis 4		MGI:2680797	Clcn7<sup>tm1Tjj</sup>/Clcn7<sup>tm1Tjj</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11207362	20120117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156738	Pax6<sup>7Neu</sup>	is_implicated_in	DOID:0060673	Peters anomaly		MGI:3613467	Pax6<sup>7Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:11779807	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3841488	Tacr3<sup>tm1Jasi</sup>	is_implicated_in	DOID:0090071	hypogonadotropic hypogonadism 11 with or without anosmia		MGI:3841558	Tacr3<sup>tm1Jasi</sup>/Tacr3<sup>tm1Jasi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22253416	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582306	Gnas<sup>tm4Lsw</sup>	is_implicated_in	DOID:0080053	Albright's hereditary osteodystrophy		MGI:5818292	Gnas<sup>tm4Lsw</sup>/Gnas<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:26671181	20170119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437105	Slit2<sup>b2b1200.1Clo</sup>/Slit2<sup>b2b1200.1Clo</sup>  [background:] C57BL/6J-Slit2<sup>b2b1200.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892968	Tacr3	is_implicated_in	DOID:0090071	hypogonadotropic hypogonadism 11 with or without anosmia		MGI:3841558	Tacr3<sup>tm1Jasi</sup>/Tacr3<sup>tm1Jasi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22253416	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856905	Trf<sup>hpx</sup>	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037942	Trf<sup>hpx</sup>/Trf<sup>hpx</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3681112	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856905	Trf<sup>hpx</sup>	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037943	Trf<sup>hpx</sup>/Trf<sup>+</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3681112	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856905	Trf<sup>hpx</sup>	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037942	Trf<sup>hpx</sup>/Trf<sup>hpx</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	MGI:1889268	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856905	Trf<sup>hpx</sup>	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037943	Trf<sup>hpx</sup>/Trf<sup>+</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	MGI:1889268	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857439	Htr2c<sup>tm1Jul</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3789135	Htr2c<sup>tm1Jul</sup>/Y  [background:] B6.129S-Htr2c<sup>tm1Jul</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9771748	20100129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857133	B2m<sup>tm1Unc</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623523	B2m<sup>tm1Unc</sup>/B2m<sup>tm1Unc</sup>  [background:] NOD.129P2-B2m<sup>tm1Unc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8314025	20060531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3057279	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)			ECO:0000033	author statement supported by traceable reference	PMID:15514019	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	is_implicated_in	DOID:0110893	inflammatory bowel disease 13		MGI:5693947	Abcb1a<sup>tm1Bor</sup>/Abcb1a<sup>tm1Bor</sup>  [background:] FVB.129P2-Abcb1a<sup>tm1Bor</sup>/TacImx			ECO:0000033	author statement supported by traceable reference	PMID:9820555	20151029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857114	Pax2<sup>1Neu</sup>	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:5442586	Pax2<sup>1Neu</sup>/Pax2<sup>+</sup>  [background:] involves: 102 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:17881463	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0110970	brachydactyly type C		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	is_implicated_in	DOID:10754	otitis media		MGI:3776413	Eya4<sup>tm1Jse</sup>/Eya4<sup>tm1Jse</sup>  [background:] involves: 129S6/SvEvTac * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:18219393	20080624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809940	Lrrc10<sup>tm1Sgt</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905195	Lrrc10<sup>tm1Sgt</sup>/Lrrc10<sup>tm1Sgt</sup>  [background:] B6.129P2-Lrrc10<sup>tm1Sgt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23236519	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346523	Sgcb	is_not_implicated_in	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E		MGI:6323188	Sgcb<sup>em1Isrd</sup>/Sgcb<sup>em1Isrd</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29360879	20190716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776559	Col1a1<sup>m1Btlr</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:3776560	Col1a1<sup>m1Btlr</sup>/Col1a1<sup>m1Btlr</sup>  [background:] C57BL/6J-Col1a1<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28916811	20190627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:4941348	Crebbp<sup>tm1.2Ltz</sup>/Crebbp<sup>tm1.2Ltz</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: 129P2/OlaHsd * BALB/c * C57BL * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21289174	20110317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:2175796	Crebbp<sup>tm1Sis</sup>/Crebbp<sup>+</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:9294190	20110317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10673499	20110317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:1933	Rubinstein-Taybi syndrome		MGI:2175792	Crebbp<sup>Gt(U-San)112Imeg</sup>/Crebbp<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9949198	20110317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614822	Pmp22<sup>tm1Lnot</sup>	is_implicated_in	DOID:0060843	hereditary neuropathy with liability to pressure palsies		MGI:3625035	Pmp22<sup>tm1Lnot</sup>/Pmp22<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16436605	20060621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040182	Ticam2<sup>tm1Aki</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3040184	Ticam2<sup>tm1Aki</sup>/Ticam2<sup>tm1Aki</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28592648	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774128	Rtn4r<sup>tm1Gogo</sup>	is_not_implicated_in	DOID:5419	schizophrenia		MGI:3806713	Rtn4r<sup>tm1Gogo</sup>/Rtn4r<sup>tm1Gogo</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18043741	20080919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107576	Sipa1	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3575736	Sipa1<sup>tm1Nm</sup>/Sipa1<sup>tm1Nm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12892713	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107576	Sipa1	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3575737	Sipa1<sup>tm1Nm</sup>/Sipa1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12892713	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033228	Gck<sup>Rgsc149</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590142	Gck<sup>Rgsc149</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449938	Ly6a<sup>tm1Pmf</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:3815037	Ly6a<sup>tm1Pmf</sup>/Ly6a<sup>tm1Pmf</sup>  [background:] C.129P2-Ly6a<sup>tm1Pmf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12732718	20081114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2448998	Fcgr2b<sup>tm1Ttk</sup>/Fcgr2b<sup>tm1Ttk</sup>  [background:] B6.129S4-Fcgr2b<sup>tm1Ttk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10981970	20051011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	is_implicated_in	DOID:14679	VACTERL association		MGI:5290081	Ift172<sup>avc1</sup>/Ift172<sup>avc1</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21653639	20111011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930964	Thap11	is_implicated_in	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC		MGI:6860682	Thap11<sup>em1Poche</sup>/Thap11<sup>em1Poche</sup>  [background:] C57BL/6J-Thap11<sup>em1Poche</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35013307	20220131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159584	Des<sup>tm1Cba</sup>	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5912041	Des<sup>tm1Cba</sup>/Des<sup>tm1Cba</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11827695	20171030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	is_implicated_in	DOID:0090114	Sorsby's fundus dystrophy		MGI:3664346	Timp3<sup>tm1Web</sup>/Timp3<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12147610	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	is_implicated_in	DOID:0090114	Sorsby's fundus dystrophy		MGI:3664350	Timp3<sup>tm1Web</sup>/Timp3<sup>tm1Web</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12147610	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97166	Msmb	is_implicated_in	DOID:10283	prostate cancer		MGI:3574653	Msmb<sup>tm1Xuan</sup>/Msmb<sup>tm1Xuan</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:15674347	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98214	Rxra	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4939884	Rxra<sup>tm1Krc</sup>/Rxra<sup>tm1Krc</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21135166	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_not_implicated_in	DOID:4480	achondroplasia		MGI:3589422	Fgfr3<sup>tm1Dor</sup>/Fgfr3<sup>tm1Dor</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8630492	20051012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3622312	Il1r1<sup>tm1Roml</sup>/Il1r1<sup>tm1Roml</sup>  [background:] NOD.Cg-Il1r1<sup>tm1Roml</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14693705	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3796837	Ncstn<sup>tm1.1Sud</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5800496	Ncstn<sup>tm1.1Sud</sup>/Ncstn<sup>tm1.1Sud</sup> Olig1<sup>tm1(cre)Rth</sup>/Olig1<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:27008863	20161013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3590299	Spred2<sup>Gt(XB228)Byg</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3603325	Spred2<sup>Gt(XB228)Byg</sup>/Spred2<sup>Gt(XB228)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15946934	20051031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611799	Alms1<sup>bbb</sup>	is_implicated_in	DOID:9970	obesity		MGI:3611807	Alms1<sup>bbb</sup>/Alms1<sup>bbb</sup>  [background:] C57BL/6JSfdAnu-Alms1<sup>bbb</sup>/Anu			ECO:0000033	author statement supported by traceable reference	MGI:3611487	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443767	Aaas	is_not_implicated_in	DOID:0050602	triple-A syndrome		MGI:3622153	Aaas<sup>tm1Ahue</sup>/Aaas<sup>tm1Ahue</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16479006	20060512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664793	Elovl4<sup>tm1Sie</sup>	is_not_implicated_in	DOID:0050817	Stargardt disease		MGI:3664797	Elovl4<sup>tm1Sie</sup>/Elovl4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16877435	20061027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664793	Elovl4<sup>tm1Sie</sup>	is_not_implicated_in	DOID:0050817	Stargardt disease		MGI:3664796	Elovl4<sup>tm1Sie</sup>/Elovl4<sup>tm1Sie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16877435	20061027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352451	Nr2f1	is_implicated_in	DOID:0112226	Bosch-Boonstra-Schaaf optic atrophy syndrome		MGI:6434270	Nr2f1<sup>tm1Mjts</sup>/Nr2f1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:31600777	20220113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:5568494	Abcc8<sup>tm1.1Fmas</sup>/Abcc8<sup>tm1.1Fmas</sup>  [background:] B6.129S2(Cg)-Abcc8<sup>tm1.1Fmas</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23903354	20140616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	is_implicated_in	DOID:0110892	inflammatory bowel disease 1		MGI:3531186	Nod2<sup>tm1Mka</sup>/Nod2<sup>tm1Mka</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15692052	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655153	Tbx19<sup>tm1Jdr</sup>	is_implicated_in	DOID:0080150	adrenocorticotropic hormone deficiency		MGI:2655154	Tbx19<sup>tm1Jdr</sup>/Tbx19<sup>tm1Jdr</sup>  [background:] either: (involves: 129/Sv) or (involves: BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:12651888	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:2663596	Epas1<sup>tm1Pec</sup>/Epas1<sup>tm1Pec</sup>  [background:] involves: 129/Sv * Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12053176	20110217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914623	Prss3b	is_implicated_in	DOID:4989	pancreatitis		MGI:6307806	Prss3b<sup>tm1.1Satom</sup>/Prss3b<sup>+</sup>  [background:] B6(FVB)-Prss3b<sup>tm1.1Satom</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30487519	20190607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104783	Atxn1	is_implicated_in	DOID:0050954	spinocerebellar ataxia type 1		MGI:3774931	Atxn1<sup>tm1Hzo</sup>/Atxn1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12086639	20080325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386674	Rpgr<sup>tm1Tili</sup>	is_implicated_in	DOID:0111008	X-linked cone-rod dystrophy 1		MGI:3038416	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10725384	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773717	Myocd<sup>tm1Msp</sup>	is_implicated_in	DOID:13832	patent ductus arteriosus		MGI:3797650	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18188448	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773717	Myocd<sup>tm1Msp</sup>	is_implicated_in	DOID:13832	patent ductus arteriosus		MGI:3797716	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> Tg(Pax3-cre)1Joe/0  [background:] involves: 129/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18188448	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277186	Atg5	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287975	Atg5<sup>tm1Myok</sup>/Atg5<sup>tm1Myok</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	is_implicated_in	DOID:0070042	Coffin-Siris syndrome 1		MGI:6159715	Arid1b<sup>em1Hzhu</sup>/Arid1b<sup>+</sup>  [background:] C57BL/6J-Arid1b<sup>em1Hzhu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28695822	20180606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	is_implicated_in	DOID:0111061	familial hypobetalipoproteinemia 2		MGI:3688001	Apob<sup>tm1Mae</sup>/Apob<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10705993	20061117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	is_implicated_in	DOID:0111061	familial hypobetalipoproteinemia 2		MGI:3688001	Apob<sup>tm1Mae</sup>/Apob<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8921909	20061117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	is_implicated_in	DOID:0111061	familial hypobetalipoproteinemia 2		MGI:3688000	Apob<sup>tm1Mae</sup>/Apob<sup>tm1Mae</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8921909	20061117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3811234	Pkd1<sup>tm3.1Jzh</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3811280	Pkd1<sup>tm3.1Jzh</sup>/Pkd1<sup>tm3.1Jzh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18385665	20081020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683091	Ldlr<sup>Hlb301</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3622102	Ldlr<sup>Hlb301</sup>/Ldlr<sup>+</sup>  [background:] C57BL/6J-Ldlr<sup>Hlb301</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:2656149	20060511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683091	Ldlr<sup>Hlb301</sup>	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3622101	Ldlr<sup>Hlb301</sup>/Ldlr<sup>Hlb301</sup>  [background:] C57BL/6J-Ldlr<sup>Hlb301</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:2656149	20060511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384272	Stat3<sup>tm1Dlv</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:4429499	Stat3<sup>tm1Dlv</sup>/Stat3<sup>tm1Dlv</sup> Tg(Csf1r-icre)1Jwp/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20042677	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3843817	Il6st<sup>tm1Thir</sup>/Il6st<sup>tm1Thir</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12370259	20090512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome		MGI:3615357	Lrp5<sup>tm1Grw</sup>/Lrp5<sup>tm1Grw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome		MGI:3664613	Lrp5<sup>tm1Kry</sup>/Lrp5<sup>tm1Kry</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11956231	20150422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	is_implicated_in	DOID:0060849	osteoporosis-pseudoglioma syndrome		MGI:3664614	Lrp5<sup>tm1Kry</sup>/Lrp5<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11956231	20150422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107852	Gp1bb	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3512041	Gp1bb<sup>tm1Ware</sup>/Gp1bb<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15213102	20111110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107852	Gp1bb	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3512040	Gp1bb<sup>tm1Ware</sup>/Gp1bb<sup>tm1Ware</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15213102	20111110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107852	Gp1bb	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3805720	Gp1bb<sup>tm1Frla</sup>/Gp1bb<sup>tm1Frla</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17095718	20111110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3830475	Qrfpr<sup>tm1Lex</sup>	is_implicated_in	DOID:0080010	bone structure disease		MGI:3830477	Qrfpr<sup>tm1Lex</sup>/Qrfpr<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16382160	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88519	Crybb2	is_implicated_in	DOID:0110269	cataract 3 multiple types		MGI:2183031	Crybb2<sup>Phil</sup>/Crybb2<sup>Phil</sup>  [background:] Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:1707874	20120918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88519	Crybb2	is_implicated_in	DOID:0110269	cataract 3 multiple types		MGI:5435246	Crybb2<sup>Lop19</sup>/Crybb2<sup>+</sup>  [background:] SJL/J-Crybb2<sup>Lop19</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	MGI:5435169	20120918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88519	Crybb2	is_implicated_in	DOID:0110269	cataract 3 multiple types		MGI:2175803	Crybb2<sup>Aey2</sup>/Crybb2<sup>+</sup>  [background:] C3HeB/FeJ-Crybb2<sup>Aey2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11381063	20120918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88077	Arsa	is_implicated_in	DOID:10581	metachromatic leukodystrophy		MGI:2655526	Arsa<sup>tm1Gie</sup>/Arsa<sup>tm1Gie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8962139	20070823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88077	Arsa	is_implicated_in	DOID:10581	metachromatic leukodystrophy		MGI:2655526	Arsa<sup>tm1Gie</sup>/Arsa<sup>tm1Gie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9728336	20070823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443963	Cadps2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3711235	Cadps2<sup>tm1Tfr</sup>/Cadps2<sup>tm1Tfr</sup>  [background:] C57BL/6-Cadps2<sup>tm1Tfr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17380209	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330281	Cd2ap	is_implicated_in	DOID:783	end stage renal disease		MGI:6476763	Cd2ap<sup>em1Irgu</sup>/Cd2ap<sup>em1Irgu</sup>  [background:] C57BL/6-Cd2ap<sup>em1Irgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30612599	20201201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183502	Tgfbr2<sup>tm1Karl</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3623411	Tgfbr2<sup>tm1Karl</sup>/Tgfbr2<sup>tm1Karl</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15741317	20060529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106653	Epcam	is_implicated_in	DOID:0060776	congenital diarrhea 5 with tufting enteropathy		MGI:5476929	Epcam<sup>Gt(RST412)Byg</sup>/Epcam<sup>Gt(RST412)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23209569	20130502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96605	Itga6	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:3583788	Itga6<sup>tm1Egl</sup>/Itga6<sup>tm1Egl</sup>  [background:] either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129S2/SvPas * C57BL/6 * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:8673141	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5439421	E330023G01Rik	is_implicated_in	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome		MGI:5907679	E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/E330023G01Rik<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24565867	20170829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2386258	Card14	is_implicated_in	DOID:0080475	psoriasis 2		MGI:6314145	Card14<sup>em9Lutzy</sup>/Card14<sup>+</sup>  [background:] C57BL/6J-Card14<sup>em9Lutzy</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:29689250	20200713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2386258	Card14	is_implicated_in	DOID:0080475	psoriasis 2		MGI:6441186	Card14<sup>em2Tshu</sup>/Card14<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29980436	20200713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856096	Atp7a<sup>Mo</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:2175712	Atp7a<sup>Mo</sup>/Atp7a<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:13103353	20050926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154258	Cdh23<sup>v-7J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3581030	Cdh23<sup>v-7J</sup>/Cdh23<sup>v-7J</sup>  [background:] CByJ(Cg)-Cdh23<sup>v-7J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857227	Nos1<sup>tm1Plh</sup>	is_implicated_in	DOID:9164	achalasia		MGI:3618910	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11438492	20091111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96213	Hpd	is_implicated_in	DOID:0050727	tyrosinemia type III		MGI:3586712	Hpd<sup>hty</sup>/Hpd<sup>hty</sup>  [background:] ICRIII			ECO:0000033	author statement supported by traceable reference	MGI:62484	20050906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605782	Cox10<sup>tm1Ctm</sup>	is_implicated_in	DOID:699	mitochondrial myopathy		MGI:3609951	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Myl1<sup>tm1(cre)Sjb</sup>/Myl1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16103131	20060112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:891978	Phyh	is_implicated_in	DOID:10582	Refsum disease		MGI:3822800	Phyh<sup>tm1Safe</sup>/Phyh<sup>tm1Safe</sup>  [background:] involves: 129P2/OlaHsd * 129X1/SvJ * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19004801	20090112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3527191	Ppt1<sup>tm1Aj</sup>	is_implicated_in	DOID:0110721	neuronal ceroid lipofuscinosis 1		MGI:3527906	Ppt1<sup>tm1Aj</sup>/Ppt1<sup>tm1Aj</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15649713	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676917	Glra1<sup>tm1Rah</sup>	is_implicated_in	DOID:0060696	hyperekplexia 1		MGI:2677020	Glra1<sup>tm1Rah</sup>/Glra1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12954867	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178779	B4galt1<sup>tm1Shur</sup>	is_implicated_in	DOID:28	endocrine system disease		MGI:3664861	B4galt1<sup>tm1Shur</sup>/B4galt1<sup>tm1Shur</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9013935	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857263	Trp53<sup>tm1Tyj</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584473	Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857263	Trp53<sup>tm1Tyj</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:3584474	Trp53<sup>tm1Tyj</sup>/Trp53<sup>tm1Tyj</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15607980	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857263	Trp53<sup>tm1Tyj</sup>	is_implicated_in	DOID:3012	Li-Fraumeni syndrome		MGI:2174783	Trp53<sup>tm1Tyj</sup>/Trp53<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7922305	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389548	Cyp19a1<sup>tm1Sih</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2658880	Cyp19a1<sup>tm1Sih</sup>/Cyp19a1<sup>tm1Sih</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:25447050	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3644008	Ccdc85c	is_implicated_in	DOID:10908	hydrocephalus		MGI:3510639	Ccdc85c<sup>hhy</sup>/Ccdc85c<sup>hhy</sup>  [background:] involves: BALB/cHeA * STS/A			ECO:0000033	author statement supported by traceable reference	PMID:15283996	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418317	Ryr1<sup>tm1.1Dhm</sup>	is_implicated_in	DOID:3529	congenital myopathy 1A		MGI:4881413	Ryr1<sup>tm1.1Dhm</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S2/SvPasCrl * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:19959667	20110131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350935	Tlx2	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:3817243	Tlx2<sup>tm1Htno</sup>/Tlx2<sup>tm1Htno</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9259577	20081120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350935	Tlx2	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:2655191	Tlx2<sup>tm1Sjk</sup>/Tlx2<sup>tm1Sjk</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9176491	20081120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3040056	Ticam2	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3040184	Ticam2<sup>tm1Aki</sup>/Ticam2<sup>tm1Aki</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28592648	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384974	Flvcr2	is_implicated_in	DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome		MGI:6415690	Flvcr2<sup>tm1.2Tda</sup>/Flvcr2<sup>tm1.2Tda</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32369453	20200511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814567	Kmt2a<sup>tm1Saam</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:3814579	Kmt2a<sup>tm1Saam</sup>/Kmt2a<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18977325	20100813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2674084	P2ry12<sup>tm1Pcon</sup>	is_implicated_in	DOID:0060692	platelet-type bleeding disorder 8		MGI:2674087	P2ry12<sup>tm1Pcon</sup>/P2ry12<sup>tm1Pcon</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12897207	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576739	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11323694	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576740	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11323694	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576734	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] B6.129S4-Sh2d1a<sup>tm1Cpt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15774582	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576735	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] C.129S4-Sh2d1a<sup>tm1Cpt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15774582	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576734	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] B6.129S4-Sh2d1a<sup>tm1Cpt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15749842	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3036915	Sh2d1a<sup>tm1Pls</sup>/Sh2d1a<sup>tm1Pls</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11404475	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3575716	Sh2d1a<sup>tm1Lyin</sup>/Sh2d1a<sup>tm1Lyin</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:5515317	Sh2d1a<sup>tm1Lyin</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12966553	20131028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	is_not_implicated_in	DOID:628	combined T cell and B cell immunodeficiency		MGI:2655194	Il2rg<sup>tm1Sug</sup>/Y  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8562967	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	is_not_implicated_in	DOID:628	combined T cell and B cell immunodeficiency		MGI:2179821	Il2rg<sup>tm1Cgn</sup>/Il2rg<sup>tm1Cgn</sup>  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	is_not_implicated_in	DOID:628	combined T cell and B cell immunodeficiency		MGI:2179823	Il2rg<sup>tm1Cgn</sup>/Y  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857722	Htt<sup>tm1Szi</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2176436	Htt<sup>tm1Szi</sup>/Htt<sup>tm1Szi</sup>  [background:] either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * MF1)			ECO:0000033	author statement supported by traceable reference	PMID:7550343	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441908	Pianp	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6364110	Pianp<sup>tm1d(KOMP)Wtsi</sup>/Pianp<sup>tm1d(KOMP)Wtsi</sup>  [background:] involves: BALB/cJ * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:31511635	20210817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856334	Fas<sup>lpr</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3622771	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] NOD.MRL(B6)-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10946317	20060526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4421708	Tg(CAG-SYVN1)1Tn	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:4421709	Tg(CAG-SYVN1)1Tn/?  [background:] D1.Cg-Tg(CAG-SYVN1)1Tn			ECO:0000033	author statement supported by traceable reference	PMID:12975321	20100212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360673	Tg(Eno2-ATN1)14Tx	is_implicated_in	DOID:0060162	dentatorubral-pallidoluysian atrophy		MGI:4360692	Tg(Eno2-ATN1)14Tx/0  [background:] B6.Cg-Tg(Eno2-ATN1)14Tx			ECO:0000033	author statement supported by traceable reference	PMID:16407196	20091007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917619	Bag5	is_implicated_in	DOID:0081162	dilated cardiomyopathy 2F		MGI:7328939	Bag5<sup>em1Asay</sup>/Bag5<sup>em1Asay</sup>  [background:] C57BL/6JJcl-Bag5<sup>em1Asay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35044787	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577725	Abca1<sup>tm1.1Jp</sup>	is_implicated_in	DOID:1388	Tangier disease		MGI:3578115	Abca1<sup>tm1.1Jp</sup>/Abca1<sup>tm1.1Jp</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15841208	20050526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577101	inad	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3577344	inad/inad  [background:] C57BL/6-inad			ECO:0000033	author statement supported by traceable reference	PMID:15859351	20050519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345138	Spry2	is_implicated_in	DOID:0060340	ciliopathy		MGI:3702557	Spry2<sup>tm1.1Mrt</sup>/Spry2<sup>tm1.1Mrt</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:34423857	20220705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99150	Yy1	is_implicated_in	DOID:4769	pleuropulmonary blastoma		MGI:5902325	Yy1<sup>tm2.1Yshi</sup>/Yy1<sup>tm2.1Yshi</sup> Tg(Nkx2-1-cre)2Sand/0  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26329601	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818761	Tg(Psp-Rbbp4)1Yoha	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3818860	Tg(Psp-Rbbp4)1Yoha/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19015307	20081209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342771	Klf1	is_implicated_in	DOID:12241	beta thalassemia		MGI:2181627	Klf1<sup>tm1Sho</sup>/Klf1<sup>tm1Sho</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7753195	20121113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934891	Hspg2<sup>tm1Nid</sup>	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10545953	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149725	Slc2a4<sup>tm1Mch</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3586490	Slc2a4<sup>tm1Mch</sup>/Slc2a4<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9334720	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:13533	osteopetrosis		MGI:4356528	Mitf<sup>Mi-Or</sup>/Mitf<sup>Mi-Or</sup>  [background:] involves: 101/Rl * C3H/Rl			ECO:0000033	author statement supported by traceable reference	PMID:7495310	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3779040	Lyst<sup>bg-2Btlr</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3779043	Lyst<sup>bg-2Btlr</sup>/Lyst<sup>bg-2Btlr</sup>  [background:] C57BL/6J-Lyst<sup>bg-2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778946	20080428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3688435	Apc<sup>tm2Rak</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:5432239	Apc<sup>tm2Rak</sup>/Apc<sup>tm2Rak</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20080688	20120827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	is_implicated_in	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy		MGI:2680045	Slc12a6<sup>tm1Tjj</sup>/Slc12a6<sup>tm1Tjj</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14532115	20180617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	is_implicated_in	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy		MGI:2451348	Slc12a6<sup>tm1Dlp</sup>/Slc12a6<sup>tm1Dlp</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12368912	20180617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	is_implicated_in	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy		MGI:5318542	Slc12a6<sup>tm1Garo</sup>/Slc12a6<sup>tm1Garo</sup> Tg(Syn1-cre)671Jxm/0  [background:] involves: 129 * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22423107	20180617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276118	Bey	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:2656223	Bey/Bey<sup>+</sup>  [background:] 129S/SvEv-Bey			ECO:0000033	author statement supported by traceable reference	PMID:9626498	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109558	Terc	is_implicated_in	DOID:11476	osteoporosis		MGI:5695524	Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup>  [background:] B6J.Cg-Terc<sup>tm1Rdp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24626990	20151111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5313544	Lox<sup>b2b370.2Clo</sup>/Lox<sup>b2b370.2Clo</sup>  [background:] C57BL/6J-Lox<sup>b2b370.2Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109239	Kcnab2	is_implicated_in	DOID:0060410	chromosome 1p36 deletion syndrome		MGI:3619238	Kcnab2<sup>tm1Kmc</sup>/Kcnab2<sup>tm1Kmc</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21209188	20110225	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101785	Mybl2	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5518769	Mybl2<sup>tm1.1Jof</sup>/Mybl2<sup>+</sup> Tg(Zp3-cre)3Mrt/0  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22910183	20131120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934627	Flna<sup>Dilp2</sup>	is_implicated_in	DOID:0050454	periventricular nodular heterotopia		MGI:3688533	Flna<sup>Dilp2</sup>/Y  [background:] involves: BALB/cAnN * C3H/HeN * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16825286	20061124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849878	Thrb<sup>tm6.1Few</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3849882	Thrb<sup>tm6.1Few</sup>/Thrb<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19439650	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849878	Thrb<sup>tm6.1Few</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3849881	Thrb<sup>tm6.1Few</sup>/Thrb<sup>tm6.1Few</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19439650	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	is_implicated_in	DOID:0110081	arrhythmogenic right ventricular dysplasia 10		MGI:6501726	Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>/Dsg2<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27170944	20210125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3870680	Gas8<sup>Gt(CH0760)Wtsi</sup>	is_implicated_in	DOID:0110619	primary ciliary dyskinesia 33		MGI:5803879	Gas8<sup>Gt(CH0760)Wtsi</sup>/Gas8<sup>Gt(CH0760)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27472056	20161018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180363	Arsa<sup>tm1Gie</sup>	is_implicated_in	DOID:10581	metachromatic leukodystrophy		MGI:2655526	Arsa<sup>tm1Gie</sup>/Arsa<sup>tm1Gie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9728336	20070823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180363	Arsa<sup>tm1Gie</sup>	is_implicated_in	DOID:10581	metachromatic leukodystrophy		MGI:2655526	Arsa<sup>tm1Gie</sup>/Arsa<sup>tm1Gie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8962139	20070823	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97249	Myb	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:4868118	Myb<sup>boo</sup>/Myb<sup>boo</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20610815	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:2181486	Kcne1<sup>tm1Sfh</sup>/Kcne1<sup>tm1Sfh</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:11223304	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:2181486	Kcne1<sup>tm1Sfh</sup>/Kcne1<sup>tm1Sfh</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:11438691	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3623789	Kcne1<sup>pkr</sup>/Kcne1<sup>pkr</sup>  [background:] C57BL/10J-Kcne1<sup>pkr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11003695	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2655333	Grhl3	is_implicated_in	DOID:0060239	Van der Woude syndrome		MGI:5697288	Grhl3<sup>tm1Bogi</sup>/Grhl3<sup>tm1Bogi</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24360809	20151125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88275	Ctnna2	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3624367	Ctnna2<sup>tm1Mta</sup>/Ctnna2<sup>tm1Mta</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12750472	20060613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857780	Nsdhl<sup>Str-1H</sup>	is_implicated_in	DOID:12305	Bloch-Sulzberger syndrome		MGI:3590076	Nsdhl<sup>Str-1H</sup>/Nsdhl<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:11005611	20191224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104669	Man2a1	is_implicated_in	DOID:1338	congenital dyserythropoietic anemia		MGI:3850627	Man2a1<sup>tm1Jxm</sup>/Man2a1<sup>tm1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9230311	20100302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3621217	Dhcr7<sup>tm2Fdp</sup>	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3621458	Dhcr7<sup>tm2Fdp</sup>/Dhcr7<sup>tm2Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:16446309	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856064	Lbr<sup>ic-J</sup>	is_implicated_in	DOID:9631	Pelger-Huet anomaly		MGI:3829382	Lbr<sup>ic-J</sup>/Lbr<sup>ic-J</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17403717	20090129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447625	Dlx5/Dlx6<sup>tm1Levi</sup>	is_implicated_in	DOID:0090021	split hand-foot malformation 1		MGI:3703555	Dlx5/Dlx6<sup>tm1Levi</sup>/Dlx5/Dlx6<sup>tm1Levi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12112878	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177743	Htt<sup>tm1Hay</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3586835	Htt<sup>tm1Hay</sup>/Htt<sup>tm1Hay</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7774020	20050907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:2175186	Ntrk1<sup>tm1Par</sup>/Ntrk1<sup>tm1Par</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10681461	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:2175185	Ntrk1<sup>tm1Bbd</sup>/Ntrk1<sup>tm1Bbd</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8145823	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	is_implicated_in	DOID:0110358	retinitis pigmentosa 12		MGI:3697463	Crb1<sup>tm1Wij</sup>/Crb1<sup>tm2Wij</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17234588	20070222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	is_not_implicated_in	DOID:0110005	Leber congenital amaurosis 9		MGI:6272871	Nmnat1<sup>tm1Ruch</sup>/Nmnat1<sup>tm1Ruch</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:29674119	20190110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	is_implicated_in	DOID:0060280	primary pigmented nodular adrenocortical disease		MGI:4819186	Prkar1a<sup>tm1Lsk</sup>/Prkar1a<sup>tm1Lsk</sup> Tg(Akr1b7-cre)1Anm/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20548949	20100813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640130	Ush1g<sup>js-2J</sup>	is_implicated_in	DOID:0110834	Usher syndrome type 1G		MGI:3662655	Ush1g<sup>js-2J</sup>/Ush1g<sup>js-2J</sup>  [background:] B6(Cg)-Ush1g<sup>js-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3662705	20120606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	is_implicated_in	DOID:0110832	Usher syndrome type 1F		MGI:5704195	Pcdh15<sup>roda</sup>/Pcdh15<sup>roda</sup>  [background:] BALB/c-Pcdh15<sup>roda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24044941	20160226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	is_implicated_in	DOID:0110832	Usher syndrome type 1F		MGI:3581190	Pcdh15<sup>av-3J</sup>/Pcdh15<sup>av-3J</sup>  [background:] C57BL/6J-Pcdh15<sup>av-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15537665	20160226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	is_implicated_in	DOID:0110832	Usher syndrome type 1F		MGI:3575018	Pcdh15<sup>av-Jfb</sup>/Pcdh15<sup>av-Jfb</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12782354	20160226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4946226	Dag1<sup>tm2Kcam</sup>/Dag1<sup>tm2Kcam</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19797173	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	is_not_implicated_in	DOID:0060682	autosomal dominant nocturnal frontal lobe epilepsy 1		MGI:3587441	Chrna4<sup>tm1Dra</sup>/Chrna4<sup>tm1Dra</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12623222	20050914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	is_not_implicated_in	DOID:0060682	autosomal dominant nocturnal frontal lobe epilepsy 1		MGI:3587441	Chrna4<sup>tm1Dra</sup>/Chrna4<sup>tm1Dra</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964949	20050914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	is_implicated_in	DOID:0110915	childhood hypophosphatasia		MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3719582	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12382103	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:5528981	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:15983791	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3715607	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11069286	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137592	Thrb<sup>tm1.1Syc</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3715602	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11069286	20140116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856181	Spta1<sup>sph-ha</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:78279	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856181	Spta1<sup>sph-ha</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448446	Spta1<sup>sph-ha</sup>/Spta1<sup>sph-ha</sup>  [background:] involves: DBA/1J			ECO:0000033	author statement supported by traceable reference	MGI:63097	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:2176912	Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8790370	20100906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:2176915	Gjb1<sup>tm1Kwi</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8790370	20100906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:4821788	Gjb1<sup>tm1Kwi</sup>/Gjb1<sup>tm1Kwi</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9169515	20100906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	is_implicated_in	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1		MGI:4821790	Gjb1<sup>tm1Kwi</sup>/Y  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9169515	20100906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178798	Vps54	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5490471	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] involves: C57BL/6J * C57BL/Fa			ECO:0000033	author statement supported by traceable reference	PMID:20643756	20130614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178798	Vps54	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5490471	Vps54<sup>wr</sup>/Vps54<sup>wr</sup>  [background:] involves: C57BL/6J * C57BL/Fa			ECO:0000033	author statement supported by traceable reference	PMID:23539154	20130614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	is_implicated_in	DOID:13544	low tension glaucoma		MGI:7279070	Optn<sup>em1Hyua</sup>/Optn<sup>em1Hyua</sup>  [background:] C57BL/6J-Optn<sup>em1Hyua</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35436991	20231003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	is_implicated_in	DOID:13544	low tension glaucoma		MGI:7279070	Optn<sup>em1Hyua</sup>/Optn<sup>em1Hyua</sup>  [background:] C57BL/6J-Optn<sup>em1Hyua</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33723228	20231003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	is_implicated_in	DOID:0110076	arrhythmogenic right ventricular dysplasia 8		MGI:5660416	Dsp<sup>tm1Efu</sup>/Dsp<sup>tm1Efu</sup> Myl2<sup>tm1(cre)Krc</sup>/Myl2<sup>+</sup>  [background:] involves: 129 * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24108106	20150831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892003	Tcof1	is_implicated_in	DOID:2908	Treacher Collins syndrome		MGI:3513306	Tcof1<sup>tm1Mjd</sup>/Tcof1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/1			ECO:0000033	author statement supported by traceable reference	PMID:16938878	20190212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892003	Tcof1	is_implicated_in	DOID:2908	Treacher Collins syndrome		MGI:3029251	Tcof1<sup>tm1Mjd</sup>/Tcof1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10888597	20190212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107934	Mdm4	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3616711	Mdm4<sup>tm2Glo</sup>/Mdm4<sup>tm2.1Glo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17533180	20170817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4176423	Bckdk<sup>Gt(OST79912)Lex</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5829468	Bckdk<sup>Gt(OST79912)Lex</sup>/Bckdk<sup>Gt(OST79912)Lex</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:27912058	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3588207	Dnaaf3	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917633	Cox10	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5775427	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>/?  [background:] B6.Cg-Cox10<sup>tm1Ctm</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27038906	20160609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147913	Igsf1	is_implicated_in	DOID:0111140	IGSF1 deficiency syndrome		MGI:2671059	Igsf1<sup>tm1Zuk</sup>/Y  [background:] either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:23143598	20180725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923488	Grhpr	is_implicated_in	DOID:0111671	primary hyperoxaluria type 2		MGI:5314653	Grhpr<sup>Gt(OST383093)Lex</sup>/Grhpr<sup>Gt(OST383093)Lex</sup>  [background:] B6.129S5-Grhpr<sup>Gt(OST383093)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22189945	20201118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923488	Grhpr	is_implicated_in	DOID:0111671	primary hyperoxaluria type 2		MGI:6472965	Grhpr<sup>Gt(OST383093)Lex</sup>/Grhpr<sup>Gt(OST383093)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31821850	20201118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712279	Umod<sup>Urehd1</sup>	is_implicated_in	DOID:557	kidney disease		MGI:5571280	Umod<sup>Urehd1</sup>/Umod<sup>+</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:23748428	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712279	Umod<sup>Urehd1</sup>	is_implicated_in	DOID:557	kidney disease		MGI:5571287	Umod<sup>Urehd1</sup>/Umod<sup>Urehd1</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:23748428	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684789	Lrsam1	is_implicated_in	DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P		MGI:5496257	Lrsam1<sup>Gt(RRK461)Byg</sup>/Lrsam1<sup>Gt(RRK461)Byg</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:23519028	20130723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918480	Dym	is_implicated_in	DOID:0060247	Smith-McCort dysplasia		MGI:3817313	Dym<sup>Gt(GTR1.3)1Rul</sup>/Dym<sup>Gt(GTR1.3)1Rul</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:18852472	20081120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_not_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653069	Ndn<sup>tm1Alb</sup>/Ndn<sup>tm1Alb</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10319852	20090723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	is_not_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653070	Ndn<sup>tm1Alb</sup>/Ndn<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10319852	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605845	Cacna1f<sup>nob2</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3720002	Cacna1f<sup>nob2</sup>/Y  [background:] AXB6/PgnJ			ECO:0000033	author statement supported by traceable reference	PMID:16597347	20070830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605845	Cacna1f<sup>nob2</sup>	is_implicated_in	DOID:0110871	congenital stationary night blindness 2A		MGI:3720000	Cacna1f<sup>nob2</sup>/Cacna1f<sup>nob2</sup>  [background:] AXB6/PgnJ			ECO:0000033	author statement supported by traceable reference	PMID:16597347	20070830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3826849	Bsnd<sup>tm1Tjj</sup>	is_implicated_in	DOID:0110145	Bartter disease type 4a		MGI:3826852	Bsnd<sup>tm1Tjj</sup>/Bsnd<sup>tm1Tjj</sup> Tg(Sox10-cre)1Wdr/0  [background:] involves: 129/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18833191	20090119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3759415	Cln3<sup>tm1Blda</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3759418	Cln3<sup>tm1Blda</sup>/Cln3<sup>tm1Blda</sup>  [background:] B6.129-Cln3<sup>tm1Blda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17855597	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924836	Mthfd1l	is_implicated_in	DOID:0080074	neural tube defect		MGI:5470154	Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>/Mthfd1l<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23267094	20130327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	is_implicated_in	DOID:0080698	Teebi hypertelorism syndrome 1		MGI:7286353	Specc1l<sup>em4Kumc</sup>/Specc1l<sup>em4Kumc</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	is_implicated_in	DOID:0080698	Teebi hypertelorism syndrome 1		MGI:7286352	Specc1l<sup>em3Kumc</sup>/Specc1l<sup>em3Kumc</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:34302166	20220617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858224	Chst3	is_implicated_in	DOID:5419	schizophrenia		MGI:3606703	Chst3<sup>tm1Dgen</sup>/Chst3<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:4946647	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21383153	20180704	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:4946650	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] B6.129-Braf<sup>tm1Bbd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21383153	20180704	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:4946646	Braf<sup>tm1Bbd</sup>/Braf<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21383153	20180704	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:5902221	Braf<sup>tm1Tumg</sup>/Braf<sup>+</sup> Tg(CAG-cre)2Osb/0  [background:] involves: C57BL * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:25035421	20180704	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	is_implicated_in	DOID:0060233	cardiofaciocutaneous syndrome		MGI:6164161	Braf<sup>tm1Tumg</sup>/Braf<sup>+</sup> Tg(CAG-cre)2Osb/0  [background:] involves: C57BL * C57BL/6J * DBA * ICR			ECO:0000033	author statement supported by traceable reference	PMID:26472072	20180704	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927073	Slc29a1	is_implicated_in	DOID:0050741	alcohol dependence		MGI:3052075	Slc29a1<sup>tm1Msg</sup>/Slc29a1<sup>tm1Msg</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15258586	20080206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107474	Cd38	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623958	Cd38<sup>tm1Lnd</sup>/Cd38<sup>tm1Lnd</sup>  [background:] NOD.129P2(B6)-Cd38<sup>tm1Lnd</sup>/LtJ			ECO:0000033	author statement supported by traceable reference	PMID:16585549	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108084	Cep250	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:6357191	Cep250<sup>tm1Jzb</sup>/Cep250<sup>tm1Jzb</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30998843	20190827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	is_implicated_in	DOID:0080509	Cornelia de Lange syndrome 5		MGI:7491951	Hdac8<sup>tm1.2Eno</sup>/Y  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32800293	20230622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0110218	Brugada syndrome 1		MGI:3769904	Scn5a<sup>tm1Care</sup>/Scn5a<sup>+</sup>  [background:] FVB.129P2-Scn5a<sup>tm1Care</sup>/Care			ECO:0000033	author statement supported by traceable reference	PMID:17145985	20101221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:0110218	Brugada syndrome 1		MGI:3641169	Scn5a<sup>tm1Agrc</sup>/Scn5a<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21097662	20101221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343184	Samd9l	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5308655	Samd9l<sup>tm1Homy</sup>/Samd9l<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:24029230	20140701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929711	Anapc7	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:6887846	Anapc7<sup>tm1.1Azbi</sup>/Anapc7<sup>tm1.1Azbi</sup>  [background:] B6.129S6(CBA)-Anapc7<sup>tm1.1Azbi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34942119	20220310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149331	Cacna2d2<sup>du-2J</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:5632120	Cacna2d2<sup>du-2J</sup>/Cacna2d2<sup>du-2J</sup>  [background:] involves: C57BL/6 * C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:23732642	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680164	Tgfbr1<sup>tm1.1Karl</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:6306137	Tg(Col2a1-cre/ERT2)1Dic/0 Tgfbr1<sup>tm1.1Karl</sup>/Tgfbr1<sup>tm1.1Karl</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28716756	20190529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:6443692	Fras1<sup>rdf</sup>/Fras1<sup>rdf</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:26813283	20221116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3833377	Fras1<sup>tm1Chpk</sup>/Fras1<sup>tm1Chpk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:15623520	20221116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:2667203	Fras1<sup>tm1Chpk</sup>/Fras1<sup>tm1Chpk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/10			ECO:0000033	author statement supported by traceable reference	PMID:12766770	20221116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:5564953	Fras1<sup>bfb</sup>/Fras1<sup>bfb</sup>  [background:] involves: C57BL/6JAnu			ECO:0000033	author statement supported by traceable reference	PMID:24143185	20221116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:2657302	Fras1<sup>bl</sup>/Fras1<sup>bl</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:12766769	20221116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3622763	Prf1<sup>tm1Clrk</sup>/Prf1<sup>tm1Clrk</sup>  [background:] involves: 129S7/SvEvBrd * BALB/c * NOD			ECO:0000033	author statement supported by traceable reference	PMID:10946317	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4443125	Pex7<sup>tm1Nbra</sup>	is_implicated_in	DOID:0110851	rhizomelic chondrodysplasia punctata type 1		MGI:4443126	Pex7<sup>tm1Nbra</sup>/Pex7<sup>tm1Nbra</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20060764	20100512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924823	Vps33a	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3034088	Vps33a<sup>bf</sup>/Vps33a<sup>bf</sup>  [background:] C57BL/6J-Vps33a<sup>bf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9585243	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:1612	breast cancer		MGI:4360685	Apc<sup>tm2Rfo</sup>/Apc<sup>+</sup>  [background:] (C57BL/6J x 129P2/OlaHsd)F1			ECO:0000033	author statement supported by traceable reference	PMID:23955540	20140430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1889570	Kl<sup>kl</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:2181617	Kl<sup>kl</sup>/Kl<sup>kl</sup>  [background:] either: C.Cg-Kl<sup>kl</sup> or (involves: C3H/HeJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9363890	20060905	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:6355948	Hvf	is_implicated_in	DOID:0060249	scoliosis		MGI:6356523	Hvf/Hvf<sup>+</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30283900	20220518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850496	Tg(Lck-Tslp)1Chea	is_implicated_in	DOID:2920	membranoproliferative glomerulonephritis		MGI:3850502	Tg(Lck-Tslp)1Chea/0  [background:] B6.Cg-Tg(Lck-Tslp)1Chea			ECO:0000033	author statement supported by traceable reference	PMID:11733384	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4363232	Lztfl1<sup>tm1e(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110139	Bardet-Biedl syndrome 17		MGI:5811522	Lztfl1<sup>tm1e(KOMP)Wtsi</sup>/Lztfl1<sup>tm1e(KOMP)Wtsi</sup>  [background:] involves: 129S/SvEv * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:26216965	20161209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856064	Lbr<sup>ic-J</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5897270	Lbr<sup>ic-J</sup>/Lbr<sup>+</sup>  [background:] (NZW/LacJ x C57BL/6J-Lbr<sup>ic-J</sup>/J)F1			ECO:0000033	author statement supported by traceable reference	PMID:27483354	20170512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856384	Fasl<sup>gld</sup>	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:3037431	Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] C3H/HeJ-Fasl<sup>gld</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6693832	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856384	Fasl<sup>gld</sup>	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:3037431	Fasl<sup>gld</sup>/Fasl<sup>gld</sup>  [background:] C3H/HeJ-Fasl<sup>gld</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:77345	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103285	Atp6v1b1	is_implicated_in	DOID:0050332	enlarged vestibular aqueduct		MGI:5910007	Atp6v1b1<sup>vtx</sup>/Atp6v1b1<sup>vtx</sup>  [background:] MRL/MpJ-Atp6v1b1<sup>vtx</sup>/Kjn			ECO:0000033	author statement supported by traceable reference	PMID:28934385	20170920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611751	Postn<sup>tm1Sjc</sup>	is_implicated_in	DOID:0080010	bone structure disease		MGI:5511052	Postn<sup>tm1Sjc</sup>/Postn<sup>tm1Sjc</sup>  [background:] B6.Cg-Postn<sup>tm1Sjc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23505553	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	is_implicated_in	DOID:1064	cystinosis		MGI:2672886	Ctns<sup>tm1Antc</sup>/Ctns<sup>tm1Antc</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12370309	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:6102946	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(Tagln-cre)1Her/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24312398	20171219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449765	Lrp2<sup>tm1Tew</sup>	is_implicated_in	DOID:11829	degenerative myopia		MGI:6199478	Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup> Lrp2<sup>tm1Tew</sup>/Lrp2<sup>tm1Tew</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26107939	20180925	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277201	Col13a1	is_implicated_in	DOID:0110673	congenital myasthenic syndrome 19		MGI:6316981	Col13a1<sup>tm3.1Pih</sup>/Col13a1<sup>tm3.1Pih</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:28369367	20190710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033225	Gck<sup>Rgsc392</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038218	Gck<sup>Rgsc392</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033225	Gck<sup>Rgsc392</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038219	Gck<sup>Rgsc392</sup>/Gck<sup>Rgsc392</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	is_implicated_in	DOID:0110124	Bardet-Biedl syndrome 2		MGI:3524999	Bbs2<sup>tm1Vcs</sup>/Bbs2<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:15539463	20201113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	is_implicated_in	DOID:0110124	Bardet-Biedl syndrome 2		MGI:6471957	Bbs2<sup>tm1.1Huss</sup>/Bbs2<sup>tm1.1Huss</sup>  [background:] involves: 129S6/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32620959	20201113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3505770	Grid2<sup>ho-15J</sup>	is_implicated_in	DOID:0080042	autosomal recessive spinocerebellar ataxia 18		MGI:5635067	Grid2<sup>ho-15J</sup>/Grid2<sup>ho-15J</sup>  [background:] involves: C3HeB/Fe			ECO:0000033	author statement supported by traceable reference	PMID:24078737	20150508	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445476	Tg(GFAP-SRC)1Aag	is_implicated_in	DOID:3069	malignant astrocytoma		MGI:5569735	Tg(GFAP-SRC)1Aag/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9160879	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338038	Aebp2	is_implicated_in	DOID:9258	Waardenburg syndrome		MGI:5296959	Aebp2<sup>Gt(BC0681)Wtsi</sup>/Aebp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21949878	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046792	Tbx1<sup>tm2Bld</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046797	Tbx1<sup>tm2Bld</sup>/Tbx1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046792	Tbx1<sup>tm2Bld</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3046796	Tbx1<sup>tm2Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445110	Zdhhc17	is_implicated_in	DOID:12858	Huntington's disease		MGI:5292519	Zdhhc17<sup>Gt(RRJ233)Byg</sup>/Zdhhc17<sup>Gt(RRJ233)Byg</sup>  [background:] FVB.129P2-Zdhhc17<sup>Gt(RRJ233)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21775500	20111019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109246	Htr4	is_implicated_in	DOID:8689	anorexia nervosa		MGI:3027496	Htr4<sup>tm1Comp</sup>/Htr4<sup>tm1Comp</sup>  [background:] 129/Sv-Htr4<sup>tm1Comp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17913892	20180515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429639	Slc12a6<sup>tm1Dlp</sup>	is_implicated_in	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy		MGI:2451348	Slc12a6<sup>tm1Dlp</sup>/Slc12a6<sup>tm1Dlp</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12368912	20180617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3841177	Tg(Myh6/tetO-PRKAG2*N488I)1Chib	is_implicated_in	DOID:0090101	lethal congenital glycogen storage disease of heart		MGI:3841180	Tg(Myh6-tTA)55Rbns/0 Tg(Myh6/tetO-PRKAG2*N488I)1Chib/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18158359	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653208	Dspp<sup>tm1Kul</sup>	is_implicated_in	DOID:3388	periodontal disease		MGI:5911481	Dspp<sup>tm1Kul</sup>/Dspp<sup>tm1Kul</sup>  [background:] B6;129-Dspp<sup>tm1Kul</sup>/Mmnc			ECO:0000033	author statement supported by traceable reference	PMID:22934831	20171013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	is_not_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:3664794	Sbds<sup>tm1Jrom</sup>/Sbds<sup>tm1Jrom</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16914746	20061027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443639	Ccdc66	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5285951	Ccdc66<sup>Gt(E021F10)Wrst</sup>/Ccdc66<sup>Gt(E021F10)Wrst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:21680557	20110920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194488	Slc32a1	is_implicated_in	DOID:3328	temporal lobe epilepsy		MGI:6730293	Slc32a1<sup>tm2(cre)Lowl</sup>/Slc32a1<sup>tm2(cre)Lowl</sup>  [background:] either: B6J.129S6(FVB)-Slc32a1<sup>tm2(cre)Lowl</sup> or (involves: 129S6/SvEvTac * C57BL/6J * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:32954490	20210812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148050	Nexmif	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6468250	Nexmif<sup>tm1(KOMP)Wtsi</sup>/Y  [background:] B6J.B6N-Nexmif<sup>tm1(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31704787	20201022	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	is_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:3758814	Comp<sup>tm1Mbri</sup>/Comp<sup>tm1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17588960	20140314	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	is_implicated_in	DOID:0080047	pseudoachondroplasia		MGI:5550573	Comp<sup>tm2.1Mbri</sup>/Comp<sup>tm2.1Mbri</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:22006726	20140314	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2441730	Tbl1xr1	is_implicated_in	DOID:0081362	Pierpont syndrome		MGI:7469827	Tbl1xr1<sup>em2H</sup>/Tbl1xr1<sup>em2H</sup>  [background:] C57BL/6J-Tbl1xr1<sup>em2H</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35416977	20231020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	is_implicated_in	DOID:0110875	holoprosencephaly 3		MGI:2173405	Shh<sup>tm1Chg</sup>/Shh<sup>tm1Chg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:8837770	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	is_implicated_in	DOID:0110875	holoprosencephaly 3		MGI:3042793	Shh<sup>tm1Chg</sup>/Shh<sup>tm1Chg</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15105374	20050817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698290	Sall4<sup>tm1Brd</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3698627	Sall4<sup>tm1Brd</sup>/Sall4<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17216607	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793788	Tg(Eno2-Scn2a1*)Q54Mm	is_implicated_in	DOID:1826	epilepsy		MGI:3797753	Tg(Eno2-Scn2a1*)Q54Mm/0  [background:] B6.Cg-Tg(Eno2-Scn2a1*)Q54Mm			ECO:0000033	author statement supported by traceable reference	PMID:16464983	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6197548	Pnpla3<sup>tm2.1Hobb</sup>/Pnpla3<sup>tm2.1Hobb</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24917523	20180911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180017	Ltbp3<sup>tm1Bdvc</sup>	is_implicated_in	DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome		MGI:2451201	Ltbp3<sup>tm1Bdvc</sup>/Ltbp3<sup>tm1Bdvc</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:25669657	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180359	Gy	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037661	Gy/Y  [background:] involves: C3H/Sn * C57BL/6Ei			ECO:0000033	author statement supported by traceable reference	PMID:9063736	20100308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180359	Gy	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037661	Gy/Y  [background:] involves: C3H/Sn * C57BL/6Ei			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20100308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:2385830	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:11152663	20210118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:17299139	20210118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3712949	Slc26a4<sup>pdsm</sup>/Slc26a4<sup>pdsm</sup>  [background:] BXA7/PgnJ-Slc26a4<sup>pdsm</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:3712813	20210118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14690057	20210118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:6500763	Slc26a4<sup>em1Jgao</sup>/Slc26a4<sup>em1Jgao</sup>  [background:] involves: CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:31155292	20210118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3697081	Slc26a4<sup>tm1Egr</sup>/Slc26a4<sup>tm1Egr</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:15320950	20210118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3797048	Bmp4<sup>tm4Blh</sup>	is_implicated_in	DOID:0080015	physical disorder		MGI:5642272	Bmp4<sup>tm4Blh</sup>/Bmp4<sup>tm4Blh</sup> Isl1<sup>tm1(cre)Sev</sup>/Isl1<sup>+</sup>  [background:] involves: 129 * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23028455	20180605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12689675	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12674324	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11416036	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12205031	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	is_implicated_in	DOID:10609	rickets		MGI:3045592	Cyp27b1<sup>tm1Star</sup>/Cyp27b1<sup>tm1Star</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11415990	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	is_implicated_in	DOID:10609	rickets		MGI:2658930	Cyp27b1<sup>tm1Dgo</sup>/Cyp27b1<sup>tm1Dgo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11416220	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856335	Fas<sup>lpr-cg</sup>	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2449985	Fas<sup>lpr-cg</sup>/Fas<sup>lpr-cg</sup>  [background:] CBA/KlJms-Fas<sup>lpr-cg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2406366	20051011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856335	Fas<sup>lpr-cg</sup>	is_implicated_in	DOID:6688	autoimmune lymphoproliferative syndrome		MGI:2449985	Fas<sup>lpr-cg</sup>/Fas<sup>lpr-cg</sup>  [background:] CBA/KlJms-Fas<sup>lpr-cg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2302830	20051011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857515	Zeb1<sup>tm1Yhi</sup>	is_implicated_in	DOID:321	tropical spastic paraparesis		MGI:3812399	Zeb1<sup>tm1Yhi</sup>/Zeb1<sup>tm1Yhi</sup>  [background:] either: (involves: 129 * C3H * C57BL/6) or (involves: 129 * C57BL/6 * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:18467597	20081028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690078	Tg(tetO-EGFR*L858R)56Hev	is_implicated_in	DOID:1324	lung cancer		MGI:3690087	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)56Hev/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16705038	20150501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	is_implicated_in	DOID:0110195	Charcot-Marie-Tooth disease type 4E		MGI:3836731	Egr2<sup>tm2Jmi</sup>/Egr2<sup>tm2Jmi</sup>  [background:] B6.Cg-Egr2<sup>tm2Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19244508	20090323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	is_implicated_in	DOID:0110195	Charcot-Marie-Tooth disease type 4E		MGI:3576120	Egr2<sup>tm1Jmi</sup>/Egr2<sup>tm1Jmi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15695336	20090323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444681	Hhat	is_implicated_in	DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome		MGI:5447979	Hhat<sup>Tg(TFAP2A-cre)1Will</sup>/Hhat<sup>Tg(TFAP2A-cre)1Will</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24784881	20160519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97352	Nkx3-1	is_implicated_in	DOID:10283	prostate cancer		MGI:2175151	Nkx3-1<sup>tm1Hha</sup>/Nkx3-1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10906459	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97352	Nkx3-1	is_implicated_in	DOID:10283	prostate cancer		MGI:2175150	Nkx3-1<sup>tm1Hha</sup>/Nkx3-1<sup>tm1Hha</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10906459	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97352	Nkx3-1	is_implicated_in	DOID:10283	prostate cancer		MGI:2175153	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10215624	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97352	Nkx3-1	is_implicated_in	DOID:10283	prostate cancer		MGI:2175152	Nkx3-1<sup>tm1Mms</sup>/Nkx3-1<sup>tm1Mms</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ) or (involves: 129S1/Sv * 129S1/SvImJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:10215624	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437073	b2b1291Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437110	b2b1291Clo/b2b1291Clo  [background:] C57BL/6J-b2b1291Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836429	Ercc3<sup>tm2Jhjh</sup>	is_implicated_in	DOID:0110850	xeroderma pigmentosum group B		MGI:3836472	Ercc3<sup>tm2Jhjh</sup>/Ercc3<sup>tm2Jhjh</sup>  [background:] B6.129P2-Ercc3<sup>tm2Jhjh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19114557	20090320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4453886	Tg(Fabp4-LMNA*R482Q)11ACdl	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:4454331	Tg(Fabp4-LMNA*R482Q)11ACdl/0  [background:] FVB-Tg(Fabp4-LMNA*R482Q)11ACdl			ECO:0000033	author statement supported by traceable reference	PMID:19201734	20100608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857539	Jup<sup>tm1Kem</sup>	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:3622113	Jup<sup>tm1Kem</sup>/Jup<sup>tm1Kem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8954745	20060512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2389465	Tbx22	is_implicated_in	DOID:0060613	X-linked cleft palate with or without ankyloglossia		MGI:4361283	Tbx22<sup>tm1.1Sta</sup>/Tbx22<sup>tm1.1Sta</sup>  [background:] involves: 129 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19648291	20091013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2389465	Tbx22	is_implicated_in	DOID:0060613	X-linked cleft palate with or without ankyloglossia		MGI:4361326	Tbx22<sup>tm1.1Sta</sup>/Y  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19648291	20091013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	is_implicated_in	DOID:0110329	Leber congenital amaurosis 6		MGI:4367266	Rpgrip1<sup>nmf247</sup>/Rpgrip1<sup>nmf247</sup>  [background:] C57BL/6J-Rpgrip1<sup>nmf247</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	is_implicated_in	DOID:0110329	Leber congenital amaurosis 6		MGI:5924950	Rpgrip1<sup>tvrm111</sup>/Rpgrip1<sup>tvrm111</sup>  [background:] C57BL/6J-Rpgrip1<sup>tvrm111</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	is_implicated_in	DOID:0110329	Leber congenital amaurosis 6		MGI:2655715	Rpgrip1<sup>tm1Tili</sup>/Rpgrip1<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12651948	20171115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6971670	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11168809	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1576433	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6562869	20080811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857348	Fbn1<sup>Tsk</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3619520	Fbn1<sup>Tsk</sup>/Fbn1<sup>+</sup>  [background:] B6.Cg-Fbn1<sup>Tsk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7271067	20080811	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5285350	Bicc1<sup>b2b222Clo</sup>/Bicc1<sup>b2b222Clo</sup>  [background:] C57BL/6J-Bicc1<sup>b2b222Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109618	Atp6v1b2	is_implicated_in	DOID:1826	epilepsy		MGI:7567701	Atp6v1b2<sup>em1Pcamp</sup>/Atp6v1b2<sup>em1Pcamp</sup>  [background:] C57BL/6N-Atp6v1b2<sup>em1Pcamp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37628590	20231220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856502	Foxn1<sup>nu-Y</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:2175029	Foxn1<sup>nu-Y</sup>/Foxn1<sup>nu-Y</sup>  [background:] 101/HY-Foxn1<sup>nu-Y</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76644	20060201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028001	Pde6b<sup>atrd2</sup>/Pde6b<sup>atrd2</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028383	Pde6b<sup>rd1-4H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028389	Pde6b<sup>rd1-4H</sup>/Pde6b<sup>rd1-4H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028004	Pde6b<sup>atrd3</sup>/Pde6b<sup>atrd3</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028003	Pde6b<sup>atrd3</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028382	Pde6b<sup>rd1-3H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028000	Pde6b<sup>atrd1</sup>/Pde6b<sup>atrd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028388	Pde6b<sup>rd1-3H</sup>/Pde6b<sup>rd1-3H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028380	Pde6b<sup>rd1-1H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028002	Pde6b<sup>atrd2</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3027999	Pde6b<sup>atrd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028381	Pde6b<sup>rd1-2H</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:2178344	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16576828	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:2665106	Pde6b<sup>rd1-2J</sup>/Pde6b<sup>rd1-2J</sup>  [background:] C57BL/6J-Pde6b<sup>rd1-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:2651853	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87912	Acvr2b	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2654122	Acvr2b<sup>tm1Enl</sup>/Acvr2b<sup>tm1Enl</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9242489	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915451	Ccdc34	is_implicated_in	DOID:0111910	spermatogenic failure		MGI:7442184	Ccdc34<sup>em1Fzg</sup>/Ccdc34<sup>em1Fzg</sup>  [background:] C57BL/6-Ccdc34<sup>em1Fzg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34348960	20230308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2389008	Adamtsl4	is_implicated_in	DOID:0111149	autosomal recessive isolated ectopia lentis 2		MGI:5902990	Adamtsl4<sup>tvrm267</sup>/Adamtsl4<sup>tvrm267</sup>  [background:] C57BL/6J-Adamtsl4<sup>tvrm267</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26405179	20180306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	is_implicated_in	DOID:11252	microcytic anemia		MGI:7378853	Dnm2<sup>Rbc12</sup>/Dnm2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28466468	20221107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181792	Plec<sup>tm2Gwi</sup>	is_implicated_in	DOID:0060736	epidermolysis bullosa simplex Ogna type		MGI:3513373	Plec<sup>tm2Gwi</sup>/Plec<sup>tm2Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177540	Cftr<sup>tm3Hgu</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177543	Cftr<sup>tm3Hgu</sup>/Cftr<sup>tm3Hgu</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8605891	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857236	Abcb4<sup>tm1Bor</sup>	is_implicated_in	DOID:1949	cholecystitis		MGI:3840644	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] FVB.129P2-Abcb4<sup>tm1Bor</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14752830	20150311	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3844257	Tg(PTH-CCND1)PC2Anar	is_implicated_in	DOID:11202	primary hyperparathyroidism		MGI:3844276	Tg(PTH-CCND1)PC2Anar/0  [background:] FVB/N-Tg(PTH-CCND1)PC2Anar			ECO:0000033	author statement supported by traceable reference	PMID:11342573	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202386	Gas8	is_implicated_in	DOID:0110619	primary ciliary dyskinesia 33		MGI:5803880	Gas8<sup>Gt(CH0760)Wtsi</sup>/Gas8<sup>em1Bky</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27472056	20161018	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202386	Gas8	is_implicated_in	DOID:0110619	primary ciliary dyskinesia 33		MGI:5803879	Gas8<sup>Gt(CH0760)Wtsi</sup>/Gas8<sup>Gt(CH0760)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27472056	20161018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856147	Hps5<sup>ru2-J</sup>	is_implicated_in	DOID:0060543	Hermansky-Pudlak syndrome 5		MGI:2174726	Hps5<sup>ru2-J</sup>/Hps5<sup>ru2-J</sup>  [background:] C57BL/6J-Hps5<sup>ru2-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449557	Adk<sup>tm1Bois</sup>	is_implicated_in	DOID:9452	steatotic liver disease		MGI:2449928	Adk<sup>tm1Bois</sup>/Adk<sup>tm1Bois</sup>  [background:] involves: 129P3/JEmsJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11997462	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6489606	Ppargc1a<sup>tm1Dpk</sup>/Ppargc1a<sup>tm1Dpk</sup>  [background:] B6.129X1-Ppargc1a<sup>tm1Dpk</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:32439544	20210104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180716	Gy	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037661	Gy/Y  [background:] involves: C3H/Sn * C57BL/6Ei			ECO:0000033	author statement supported by traceable reference	PMID:9063736	20100308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180716	Gy	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037661	Gy/Y  [background:] involves: C3H/Sn * C57BL/6Ei			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20100308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448995	Ncoa6<sup>tm1Jkr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276351	Ncoa6<sup>tm1Jkr</sup>/Ncoa6<sup>tm1Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448995	Ncoa6<sup>tm1Jkr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:6276352	Ncoa6<sup>tm1Jkr</sup>/Ncoa6<sup>+</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25131203	20190207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182454	Ube3a<sup>tm1Jwf</sup>	is_implicated_in	DOID:1932	Angelman syndrome		MGI:3852128	Ube3a<sup>tm1Jwf</sup>/Ube3a<sup>+</sup>  [background:] B6.129S4-Ube3a<sup>tm1Jwf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11895368	20090806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617904	Chm<sup>tm1.2Seab</sup>	is_implicated_in	DOID:9821	choroideremia		MGI:3620089	Chm<sup>tm1.2Seab</sup>/Chm<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1888986	Dlg3	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:5824730	Dlg3<sup>tm1Grnt</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27466188	20170221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3588774	Atp7a<sup>Mo-Tohm</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:3618244	Atp7a<sup>Mo-Tohm</sup>/Atp7a<sup>+</sup>  [background:] B6.Cg-Atp7a<sup>Mo-Tohm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16338116	20060330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	is_implicated_in	DOID:13533	osteopetrosis		MGI:3610379	Csf1<sup>op</sup>/Csf1<sup>op</sup>  [background:] B6C3Fe a/a-Csf1<sup>op</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:1887865	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920970	Cst6	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:4429796	Cst6<sup>ichq</sup>/Cst6<sup>+</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:15044380	20181011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920970	Cst6	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:4429796	Cst6<sup>ichq</sup>/Cst6<sup>+</sup>  [background:] involves: BALB/cJ			ECO:0000033	author statement supported by traceable reference	PMID:9212754	20181011	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3582830	Kras<sup>tm1Bbd</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:3836577	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19117991	20090320	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97597	Prkcg	is_implicated_in	DOID:0050964	spinocerebellar ataxia type 14		MGI:6865691	Prkcg<sup>em1Jpka</sup>/Prkcg<sup>+</sup>  [background:] FVB/N-Prkcg<sup>em1Jpka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33478986	20220208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97597	Prkcg	is_implicated_in	DOID:0050964	spinocerebellar ataxia type 14		MGI:6865686	Prkcg<sup>em1Jpka</sup>/Prkcg<sup>em1Jpka</sup>  [background:] FVB/N-Prkcg<sup>em1Jpka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33478986	20220208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822474	Hesx1<sup>tm2Jpmb</sup>	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:3822779	Hesx1<sup>tm2Jpmb</sup>/Hesx1<sup>tm2Jpmb</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19093031	20090113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107654	Ifngr2	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3603845	Ifngr2<sup>tm1Pbro</sup>/Ifngr2<sup>tm1Pbro</sup>  [background:] NOD.129S1-Ifngr2<sup>tm1Pbro</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11714835	20101101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510784	Traf3ip2<sup>tm1.1Lix</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5440213	Traf3ip2<sup>tm1.1Lix</sup>/Traf3ip2<sup>tm1.1Lix</sup>  [background:] B6.129-Traf3ip2<sup>tm1.1Lix</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22585710	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102673	Lhx3	is_implicated_in	DOID:9406	hypopituitarism		MGI:4941332	Lhx3<sup>tm1.1Sjr</sup>/Lhx3<sup>tm1.1Sjr</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21149718	20110317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914608	1700093K21Rik	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5618826	1700093K21Rik<sup>b2b3025Clo</sup>/1700093K21Rik<sup>b2b3025Clo</sup>  [background:] C57BL/6J-1700093K21Rik<sup>b2b3025Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_not_implicated_in	DOID:14515	WAGR syndrome		MGI:2175204	Pax6<sup>Sey-Dey</sup>/Pax6<sup>+</sup>  [background:] C3H/HeJ-Pax6<sup>Sey-Dey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2173141	20071019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662152	Mitf<sup>mi-x</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387473	Rps6ka3<sup>tm1Ljg</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3042280	Rps6ka3<sup>tm1Ljg</sup>/Y  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12765942	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387473	Rps6ka3<sup>tm1Ljg</sup>	is_implicated_in	DOID:3783	Coffin-Lowry syndrome		MGI:3042280	Rps6ka3<sup>tm1Ljg</sup>/Y  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11113183	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446244	Setd1a	is_implicated_in	DOID:5419	schizophrenia		MGI:7378550	Setd1a<sup>em1Yzhg</sup>/Setd1a<sup>+</sup>  [background:] B6.Cg-Setd1a<sup>em1Yzhg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35245111	20221103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860299	Dnah10	is_implicated_in	DOID:0111910	spermatogenic failure		MGI:6780172	Dnah10<sup>em1Yxc</sup>/Dnah10<sup>em1Yxc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34237282	20211019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860299	Dnah10	is_implicated_in	DOID:0111910	spermatogenic failure		MGI:6780173	Dnah10<sup>em2Yxc</sup>/Dnah10<sup>em2Yxc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34237282	20211019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	is_implicated_in	DOID:2226	myeloproliferative neoplasm		MGI:5618622	Pdgfrb<sup>b2b2903Clo</sup>/Pdgfrb<sup>b2b2903Clo</sup>  [background:] C57BL/6J-Pdgfrb<sup>b2b2903Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88524	Crygd	is_implicated_in	DOID:0110234	cataract 4 multiple types		MGI:2387110	Crygd<sup>Aey4</sup>/Crygd<sup>+</sup>  [background:] C3HeB/FeJ-Crygd<sup>Aey4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12226711	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88524	Crygd	is_implicated_in	DOID:0110234	cataract 4 multiple types		MGI:2387109	Crygd<sup>Aey4</sup>/Crygd<sup>Aey4</sup>  [background:] C3HeB/FeJ-Crygd<sup>Aey4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12226711	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148811	Npnt	is_implicated_in	DOID:0080200	bilateral renal aplasia		MGI:6825769	Npnt<sup>em1Zhwe</sup>/Npnt<sup>em1Zhwe</sup>  [background:] C57BL/6-Npnt<sup>em1Zhwe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34049960	20211122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106679	Zic2	is_implicated_in	DOID:5419	schizophrenia		MGI:5085985	Zic2<sup>tm1Jaru</sup>/Zic2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22355535	20110815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154694	Sgcd<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F		MGI:3618464	Sgcd<sup>tm1Kcam</sup>/Sgcd<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10481911	20060404	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4366146	Scn4a<sup>tm1.1Ljh</sup>	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420396	Scn4a<sup>tm1.1Ljh</sup>/Scn4a<sup>+</sup>  [background:] B6.129S4-Scn4a<sup>tm1.1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4366146	Scn4a<sup>tm1.1Ljh</sup>	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420228	Scn4a<sup>tm1.1Ljh</sup>/Scn4a<sup>tm1.1Ljh</sup>  [background:] B6.129S4-Scn4a<sup>tm1.1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3613573	Arhgdia<sup>tm1Ytk</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3614391	Arhgdia<sup>tm1Ytk</sup>/Arhgdia<sup>tm1Ytk</sup>  [background:] involves: 129S/SvEv * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:10498891	20060302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429133	Porcn<sup>tm1.1Lcm</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:5049887	Porcn<sup>tm1.1Lcm</sup>/Porcn<sup>+</sup> Edil3<sup>Tg(Sox2-cre)1Amc</sup>/Edil3<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21768372	20191029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429133	Porcn<sup>tm1.1Lcm</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368185	Porcn<sup>tm1.1Lcm</sup>/Y H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429133	Porcn<sup>tm1.1Lcm</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368183	Porcn<sup>tm1.1Lcm</sup>/Y Tg(rx3-icre)1Mjam/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429133	Porcn<sup>tm1.1Lcm</sup>	is_implicated_in	DOID:2120	focal dermal hypoplasia		MGI:6368186	Porcn<sup>tm1.1Lcm</sup>/Y H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:25451153	20191029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837679	Eef1a1<sup>tm1(Kras*)Arge</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3837707	Eef1a1<sup>tm1(Kras*)Arge</sup>/Eef1a1<sup>+</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:19174523	20090330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690457	Tg(tetO-EGFR*delta19)11Hev	is_implicated_in	DOID:1324	lung cancer		MGI:3690458	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*delta19)11Hev/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16705038	20150501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	is_implicated_in	DOID:11211	buphthalmos		MGI:3655827	Foxc1<sup>tm1Blh</sup>/Foxc1<sup>+</sup>  [background:] B6.Cg-Foxc1<sup>tm1Blh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104555	Mafb	is_implicated_in	DOID:12557	Duane retraction syndrome		MGI:6278262	Mafb<sup>tm1.2Good</sup>/Mafb<sup>+</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27181683	20190215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104555	Mafb	is_implicated_in	DOID:12557	Duane retraction syndrome		MGI:6278261	Mafb<sup>tm1.2Good</sup>/Mafb<sup>tm1.2Good</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27181683	20190215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586566	Tg(Myh6-Tnf)1Brgi	is_implicated_in	DOID:6000	congestive heart failure		MGI:3586618	Tg(Myh6-Tnf)1Brgi/?  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9577949	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3608770	Cnga3<sup>cpfl5</sup>	is_implicated_in	DOID:0110007	achromatopsia 2		MGI:4867912	Cnga3<sup>cpfl5</sup>/Cnga3<sup>cpfl5</sup>  [background:] involves: RHJ/LeJ			ECO:0000033	author statement supported by traceable reference	PMID:22509403	20151122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3608770	Cnga3<sup>cpfl5</sup>	is_implicated_in	DOID:0110007	achromatopsia 2		MGI:5796753	Cnga3<sup>cpfl5</sup>/Cnga3<sup>cpfl5</sup>  [background:] B6.RHJ-Cnga3<sup>cpfl5</sup>/BocJ			ECO:0000033	author statement supported by traceable reference	PMID:22509403	20151122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106215	Aqp5	is_implicated_in	DOID:10140	dry eye syndrome		MGI:7310130	Aqp5<sup>em1Cya</sup>/Aqp5<sup>em1Cya</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33013441	20220706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:2653844	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB/N)			ECO:0000033	author statement supported by traceable reference	PMID:7977654	20100329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5471363	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> En1<sup>tm2(cre)Wrst</sup>/En1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23152632	20130402	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5471365	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Slc6a3<sup>tm1(cre)Xz</sup>/Slc6a3<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:23152632	20130402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447196	Abcg2<sup>tm1Ahs</sup>	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:3040915	Abcg2<sup>tm1Ahs</sup>/Abcg2<sup>tm1Ahs</sup>  [background:] either: (involves: 129P2/OlaHsd * FVB) or (involves: FVB)			ECO:0000033	author statement supported by traceable reference	PMID:12429862	20050913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387940	Hey2<sup>tm1Uts</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2673834	Hey2<sup>tm1Uts</sup>/Hey2<sup>tm1Uts</sup>  [background:] either: (involves: 129X1/SvJ) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12372254	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179754	Ank2<sup>tm1Bnt</sup>	is_implicated_in	DOID:0050824	sinoatrial node disease		MGI:4830468	Ank2<sup>tm1Bnt</sup>/Ank2<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:20525877	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137365	Nf1<sup>tm1Cbr</sup>	is_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2176762	Nf1<sup>tm1Cbr</sup>/Nf1<sup>tm1Cbr</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11279521	20231018	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857271	Pah<sup>enu1</sup>	is_not_implicated_in	DOID:9281	phenylketonuria		MGI:3587792	Pah<sup>enu1</sup>/Pah<sup>enu1</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9119379	20050916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857969	Cryba1<sup>Po1</sup>	is_implicated_in	DOID:0110258	cataract 10 multiple types		MGI:2175802	Cryba1<sup>Po1</sup>/Cryba1<sup>+</sup>  [background:] C3HeB/FeJ-Cryba1<sup>Po1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10585769	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857969	Cryba1<sup>Po1</sup>	is_implicated_in	DOID:0110258	cataract 10 multiple types		MGI:2175801	Cryba1<sup>Po1</sup>/Cryba1<sup>Po1</sup>  [background:] C3HeB/FeJ-Cryba1<sup>Po1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10585769	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313278	Fzd9	is_not_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3578414	Fzd9<sup>tm1Uta</sup>/Fzd9<sup>tm1Uta</sup>  [background:] involves: 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15572594	20050531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	is_implicated_in	DOID:0050663	Bethlem myopathy		MGI:3037904	Col6a1<sup>tm1Gmb</sup>/Col6a1<sup>tm1Gmb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14625552	20120117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	is_implicated_in	DOID:0050663	Bethlem myopathy		MGI:3037904	Col6a1<sup>tm1Gmb</sup>/Col6a1<sup>tm1Gmb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9817932	20120117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848928	Dlg4<sup>tm2.1Grnt</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5295223	Dlg4<sup>tm2.1Grnt</sup>/Dlg4<sup>tm2.1Grnt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20952458	20111108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	is_implicated_in	DOID:0050437	Danon disease		MGI:6259615	Lamp2<sup>tm1Psa</sup>/Lamp2<sup>tm1Psa</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:28526246	20220923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	is_implicated_in	DOID:0050437	Danon disease		MGI:7339154	Lamp2<sup>tm1.2Ces</sup>/Y  [background:] involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:34459252	20220923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	is_implicated_in	DOID:0050437	Danon disease		MGI:3042186	Lamp2<sup>tm1Psa</sup>/Lamp2<sup>tm1Psa</sup>  [background:] either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv)			ECO:0000033	author statement supported by traceable reference	PMID:10972293	20220923	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5433292	b2b1519Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5433295	b2b1519Clo/b2b1519Clo  [background:] C57BL/6J-b2b1519Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	is_implicated_in	DOID:0060850	annular pancreas		MGI:3584475	Ihh<sup>tm1Amc</sup>/Ihh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:10821773	20081215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589211	Ndst1<sup>tm1Je</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3589869	Ndst1<sup>tm1Je</sup>/Ndst1<sup>tm1Je</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24355925	20140507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450901	Six3<sup>tm1Gco</sup>	is_implicated_in	DOID:0110872	holoprosencephaly 2		MGI:3036833	Six3<sup>tm1Gco</sup>/Six3<sup>tm1Gco</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12569128	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583805	Hmga1<sup>tm1Brun</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583952	Hmga1<sup>tm1Brun</sup>/Hmga1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15924147	20050819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583805	Hmga1<sup>tm1Brun</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3583951	Hmga1<sup>tm1Brun</sup>/Hmga1<sup>tm1Brun</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15924147	20050819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:2999	granulosa cell tumor		MGI:5432228	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	is_implicated_in	DOID:0060316	orofaciodigital syndrome I		MGI:3620650	Ofd1<sup>tm2.1Bfra</sup>/Y Tg(CAG-cre)1Nagy/0  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16311594	20060428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	is_implicated_in	DOID:0060316	orofaciodigital syndrome I		MGI:3620649	Ofd1<sup>tm2.1Bfra</sup>/Ofd1<sup>+</sup> Tg(CAG-cre)1Nagy/0  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16311594	20060428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856707	Hps3<sup>coa</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3587102	Hps3<sup>coa</sup>/Hps3<sup>coa</sup>  [background:] involves: C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:3408670	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3618742	Mir199a-2	is_implicated_in	DOID:1206	Rett syndrome		MGI:6357214	Mir199a-2<sup>tm1Kinn</sup>/Mir199a-2<sup>tm1Kinn</sup>  [background:] involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:26344767	20190827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341105	Rp1	is_implicated_in	DOID:0110390	retinitis pigmentosa 1		MGI:5604912	Rp1<sup>m1Jdun</sup>/Rp1<sup>m1Jdun</sup>  [background:] C57BL/6-Rp1<sup>m1Jdun</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25088982	20141121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341105	Rp1	is_implicated_in	DOID:0110390	retinitis pigmentosa 1		MGI:3038333	Rp1<sup>tm1Jnz</sup>/Rp1<sup>tm1Jnz</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:11960024	20141121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587769	Atg7<sup>tm1Tchi</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287973	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857283	Atf2<sup>tm1Glm</sup>	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:2655609	Atf2<sup>tm1Glm</sup>/Atf2<sup>tm1Glm</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8538792	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153008	Lum<sup>tm1Chak</sup>	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3047689	Lum<sup>tm1Chak</sup>/Lum<sup>tm1Chak</sup>  [background:] involves: 129S/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9606218	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840232	Kdm3a<sup>tm1.1Yzha</sup>	is_implicated_in	DOID:9970	obesity		MGI:3840234	Kdm3a<sup>tm1.1Yzha</sup>/Kdm3a<sup>tm1.1Yzha</sup>  [background:] B6.129P2-Kdm3a<sup>tm1.1Yzha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19194461	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2152844	Slc2a9	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5760132	Slc2a9<sup>tm1Khm</sup>/Slc2a9<sup>tm1Khm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25100214	20210319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	is_implicated_in	DOID:9278	hyperargininemia		MGI:2668857	Arg1<sup>tm1Rki</sup>/Arg1<sup>tm1Rki</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12052859	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576051	Alms1<sup>Gt(XH152)Byg</sup>	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:3589409	Alms1<sup>Gt(XH152)Byg</sup>/Alms1<sup>Gt(XH152)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16000322	20051012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926494	Tg(ITGB1)0840Fmw	is_implicated_in	DOID:8893	psoriasis		MGI:3583560	Tg(ITGB1)0840Fmw/0  [background:] involves: C57BL/10 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	is_implicated_in	DOID:445	Bartter disease		MGI:6200350	Clcnkb<sup>tm1.1Doel</sup>/Clcnkb<sup>tm1.1Doel</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:27335120	20180928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87996	Alm	is_implicated_in	DOID:83	cataract		MGI:2175695	Alm/Alm<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695425	Satb2<sup>tm1(cre)Vit</sup>	is_implicated_in	DOID:0110213	isolated cleft palate		MGI:3695610	Satb2<sup>tm1(cre)Vit</sup>/Satb2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16960803	20070205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158937	Man2a1<sup>tm1Jxm</sup>	is_implicated_in	DOID:1338	congenital dyserythropoietic anemia		MGI:3850627	Man2a1<sup>tm1Jxm</sup>/Man2a1<sup>tm1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9230311	20100302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661723	Ace2<sup>tm1Pngr</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:2661730	Ace2<sup>tm1Pngr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17499227	20171101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384272	Stat3<sup>tm1Dlv</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:4429499	Stat3<sup>tm1Dlv</sup>/Stat3<sup>tm1Dlv</sup> Tg(Csf1r-icre)1Jwp/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20042677	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920989	Cby1	is_implicated_in	DOID:10754	otitis media		MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19364920	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857957	Apc<sup>tm1Mmt</sup>	is_implicated_in	DOID:0050424	familial adenomatous polyposis		MGI:2175907	Apc<sup>tm1Mmt</sup>/Apc<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7753829	20050822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774352	Sqstm1<sup>tm1Keta</sup>	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:6387275	Sqstm1<sup>tm1Keta</sup>/Sqstm1<sup>tm1Keta</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29555685	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934348	Pax6<sup>tm2Pgr</sup>	is_implicated_in	DOID:0060673	Peters anomaly		MGI:4821786	Pax6<sup>tm2Pgr</sup>/Pax6<sup>+</sup> Tg(Pax6-cre,GFP)1Pgr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20538882	20100906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	is_not_implicated_in	DOID:9281	phenylketonuria		MGI:3587792	Pah<sup>enu1</sup>/Pah<sup>enu1</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9119379	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	is_not_implicated_in	DOID:9281	phenylketonuria		MGI:3587793	Pah<sup>enu1</sup>/Pah<sup>enu2</sup>  [background:] involves: 101 * C3H * BTBR			ECO:0000033	author statement supported by traceable reference	PMID:10767173	20050916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856879	Ttc7<sup>fsn</sup>	is_implicated_in	DOID:8893	psoriasis		MGI:4366162	Ttc7<sup>fsn</sup>/Ttc7<sup>fsn</sup>  [background:] involves: A/J * BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:8406628	20170928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	is_implicated_in	DOID:1826	epilepsy		MGI:4833820	Kcna1<sup>tm1Tem</sup>/Kcna1<sup>tm1Tem</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:20392939	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842799	Tg(RP23-65I14)2Jno	is_implicated_in	DOID:1826	epilepsy		MGI:3842800	Tg(RP23-65I14)2Jno/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19211869	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3796628	Frem2<sup>ne</sup>/Frem2<sup>ne</sup>  [background:] STOCK Frem2<sup>ne</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5428032	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3796628	Frem2<sup>ne</sup>/Frem2<sup>ne</sup>  [background:] STOCK Frem2<sup>ne</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:5429856	Frem2<sup>b2b1562Clo</sup>/Frem2<sup>b2b1562Clo</sup>  [background:] C57BL/6J-Frem2<sup>b2b1562Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3842612	Frem2<sup>my</sup>/Frem2<sup>my</sup>  [background:] MY/HuLeJ			ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3579980	Frem2<sup>my-Ucl</sup>/Frem2<sup>my-Ucl</sup>  [background:] involves: NMRI			ECO:0000033	author statement supported by traceable reference	PMID:15838507	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3579982	Frem2<sup>Gt(KST252)Byg</sup>/Frem2<sup>my-Ucl</sup>  [background:] involves: 129P2/OlaHsd * CD-1 * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:15838507	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919277	Slc39a4	is_implicated_in	DOID:0050605	acrodermatitis enteropathica		MGI:5438021	Slc39a4<sup>tm2Gka</sup>/Slc39a4<sup>tm2Gka</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22737083	20121009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856273	Atp8a2<sup>wl-vmd</sup>	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3581212	Atp8a2<sup>wl-vmd</sup>/Atp8a2<sup>wl-vmd</sup>  [background:] C3H/HeSnJ-Atp8a2<sup>wl-vmd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146906	Ift140	is_implicated_in	DOID:0110085	asphyxiating thoracic dystrophy 1		MGI:5510810	Ift140<sup>cauli</sup>/Ift140<sup>cauli</sup>  [background:] involves: C3H/HeH * C57BL/6JAnu			ECO:0000033	author statement supported by traceable reference	PMID:24009529	20151209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	is_implicated_in	DOID:5723	optic atrophy		MGI:3712038	Opa1<sup>Q285X</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:21803037	20180718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	is_implicated_in	DOID:5723	optic atrophy		MGI:4412040	Opa1<sup>M1Bewi</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17314202	20180718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	is_implicated_in	DOID:5723	optic atrophy		MGI:3712038	Opa1<sup>Q285X</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6JCrl			ECO:0000033	author statement supported by traceable reference	PMID:17428816	20180718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	is_implicated_in	DOID:5723	optic atrophy		MGI:6188926	Opa1<sup>tm1.1Geno</sup>/Opa1<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:23250881	20180718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:4822359	Dnm1<sup>Ftfl</sup>/Dnm1<sup>Ftfl</sup>  [background:] C57BL/6J-Dnm1<sup>Ftfl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20700442	20161014	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:5800565	Dnm1<sup>Ftfl</sup>/Dnm1<sup>tm1.2Frk</sup>  [background:] involves: 129 * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:27363778	20161014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177211	Brca2<sup>tm2Arge</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:2177239	Brca2<sup>tm2Arge</sup>/Brca2<sup>tm2Arge</sup> Wap<sup>tm1(cre)Arge</sup>/Wap<sup>tm1(cre)Arge</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11494122	20060807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651858	Ush1c<sup>dfcr</sup>	is_implicated_in	DOID:0110473	autosomal recessive nonsyndromic deafness 18A		MGI:2676319	Ush1c<sup>dfcr</sup>/Ush1c<sup>dfcr</sup>  [background:] involves: BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609548	Prox1<sup>tm2Gco</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907122	Prox1<sup>tm2Gco</sup>/Prox1<sup>tm2Gco</sup> Nkx2-5<sup>tm1(cre)Rjs</sup>/Nkx2-5<sup>+</sup>  [background:] involves: 129S1/Sv * 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:24938781	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276121	Bckdk	is_implicated_in	DOID:0090126	branched-chain keto acid dehydrogenase kinase deficiency		MGI:3699323	Bckdk<sup>Gt(VICT48)710Lex</sup>/Bckdk<sup>Gt(VICT48)710Lex</sup>  [background:] B6.129S5/SvEvBrd-Bckdk<sup>Gt(VICT48)710Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22956686	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	is_implicated_in	DOID:12365	malaria		MGI:2429786	Hmox1<sup>tm1Mlee</sup>/Hmox1<sup>tm1Mlee</sup>  [background:] involves: 129S2/SvPas * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:19706490	20130313	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135646	Car2<sup>n</sup>	is_implicated_in	DOID:0110941	autosomal recessive osteopetrosis 3		MGI:2175729	Car2<sup>n</sup>/Car2<sup>n</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:3126501	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1337080	Ncor2	is_implicated_in	DOID:4971	myelofibrosis		MGI:3829994	Ncor2<sup>tm1Rev</sup>/Ncor2<sup>tm1Rev</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24191050	20140306	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102790	Rab18	is_implicated_in	DOID:0110718	Warburg micro syndrome 3		MGI:5629933	Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>/Rab18<sup>Gt(EUCE0233a03)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24764192	20151211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102790	Rab18	is_implicated_in	DOID:0110718	Warburg micro syndrome 3		MGI:5698703	Rab18<sup>m1Hongc</sup>/Rab18<sup>m1Hongc</sup>  [background:] C57BL/6J-Rab18<sup>m1Hongc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25779931	20151211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:5560742	Eml1<sup>heco</sup>/Eml1<sup>heco</sup>  [background:] involves: C57BL/6 * NOR			ECO:0000033	author statement supported by traceable reference	PMID:18562329	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:5560741	Eml1<sup>heco</sup>/Eml1<sup>heco</sup>  [background:] involves: NOR			ECO:0000033	author statement supported by traceable reference	PMID:18562329	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:5648122	Eml1<sup>heco</sup>/?  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24859200	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857213	Lifr<sup>tm1Imx</sup>	is_implicated_in	DOID:0080205	CAKUT		MGI:6093713	Lifr<sup>tm1Imx</sup>/Lifr<sup>tm1Imx</sup>  [background:] B6;129S7-Lifr<sup>tm1Imx</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:28334964	20180725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333849	Rasgrp2	is_implicated_in	DOID:0110912	leukocyte adhesion deficiency 3		MGI:3055194	Rasgrp2<sup>tm1Amg</sup>/Rasgrp2<sup>tm1Amg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:17492052	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353466	Mmp20	is_implicated_in	DOID:0110060	amelogenesis imperfecta hypomaturation type 2A2		MGI:2450776	Mmp20<sup>tm1Jdb</sup>/Mmp20<sup>tm1Jdb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12393861	20090121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039362	Cdkn1a<sup>tm1(HBsAg)Xya</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3046834	Cdkn1a<sup>tm1(HBsAg)Xya</sup>/Cdkn1a<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039362	Cdkn1a<sup>tm1(HBsAg)Xya</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3046807	Cdkn1a<sup>tm1(HBsAg)Xya</sup>/Cdkn1a<sup>tm1(HBsAg)Xya</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706986	Rab27b<sup>tm1.2Seab</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3711073	Rab27b<sup>tm1.2Seab</sup>/Rab27b<sup>tm1.2Seab</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17384153	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	is_implicated_in	DOID:0110130	Bardet-Biedl syndrome 8		MGI:5140726	Ttc8<sup>tm1Reed</sup>/Ttc8<sup>tm1Reed</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:21646512	20141028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449487	Btk<sup>tm1Gsv</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2449488	Btk<sup>tm1Gsv</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8890160	20081222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918836	Ifih1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5617219	Ifih1<sup>Rgsc422</sup>/Ifih1<sup>+</sup>  [background:] D2JJcl.B6JJcl-Ifih1<sup>Rgsc422</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24530055	20150302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918836	Ifih1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5617218	Ifih1<sup>Rgsc422</sup>/Ifih1<sup>Rgsc422</sup>  [background:] D2JJcl.B6JJcl-Ifih1<sup>Rgsc422</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24530055	20150302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	is_implicated_in	DOID:0060602	alpha-methylacyl-CoA racemase deficiency		MGI:3044685	Amacr<sup>tm1Jkh</sup>/Amacr<sup>tm1Jkh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15016763	20111031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88446	Col11a1	is_implicated_in	DOID:8398	osteoarthritis		MGI:5294332	Col11a1<sup>cho</sup>/Col11a1<sup>+</sup>  [background:] involves: C57BL/6Fr			ECO:0000033	author statement supported by traceable reference	PMID:13130470	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2386848	Cyb5r4	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3051529	Cyb5r4<sup>tm1Hfb</sup>/Cyb5r4<sup>tm1Hfb</sup>  [background:] involves: 129S4/SvJae * BALB/cAnN			ECO:0000033	author statement supported by traceable reference	PMID:15247412	20060320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3578417	Chkb<sup>rmd</sup>	is_implicated_in	DOID:0110632	megaconial type congenital muscular dystrophy		MGI:3625276	Chkb<sup>rmd</sup>/Chkb<sup>rmd</sup>  [background:] involves: BALB/cByJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16371353	20120130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848965	Tg(Prnp-FTL*)4Ruvi	is_implicated_in	DOID:0110737	neurodegeneration with brain iron accumulation 3		MGI:3848974	Tg(Prnp-FTL*)4Ruvi/Tg(Prnp-FTL*)4Ruvi  [background:] B6.C3Fe-Tg(Prnp-FTL*)4Ruvi			ECO:0000033	author statement supported by traceable reference	PMID:18171923	20090626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88075	Arsb	is_implicated_in	DOID:12800	mucopolysaccharidosis VI		MGI:2655540	Arsb<sup>tm1Cptr</sup>/Arsb<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8710849	20090702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88075	Arsb	is_implicated_in	DOID:12800	mucopolysaccharidosis VI		MGI:3849442	Arsb<sup>m1J</sup>/Arsb<sup>m1J</sup>  [background:] C57BL/6J-Arsb<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:3849437	20090702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88075	Arsb	is_implicated_in	DOID:12800	mucopolysaccharidosis VI		MGI:3712734	Arsb<sup>tm1Cptr</sup>/Arsb<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:12904606	20090702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384197	Irak3<sup>tm1Flv</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5800315	Irak3<sup>tm1Flv</sup>/Irak3<sup>tm1Flv</sup>  [background:] NOD.129S1(B6)-Irak3<sup>tm1Flv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24696448	20161011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921624	Clec16a	is_implicated_in	DOID:1289	neurodegenerative disease		MGI:5009333	Clec16a<sup>curt</sup>/Clec16a<sup>curt</sup>  [background:] SWR/J-Clec16a<sup>curt</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26987296	20191217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836060	Tg(MMTV-AURKA)#Cxd	is_implicated_in	DOID:1612	breast cancer		MGI:3836157	Tg(MMTV-AURKA)#Cxd/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16715125	20090317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5316396	Fmr1<sup>tm1Cgr</sup>/Y  [background:] B6.129P2-Fmr1<sup>tm1Cgr</sup>/Nwu			ECO:0000033	author statement supported by traceable reference	PMID:21364941	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1889298	Bey	is_implicated_in	DOID:2339	Crouzon syndrome		MGI:2656223	Bey/Bey<sup>+</sup>  [background:] 129S/SvEv-Bey			ECO:0000033	author statement supported by traceable reference	PMID:9626498	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100508	Kcnj8	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6389011	Kcnj8<sup>em1Nich</sup>/Kcnj8<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:30089727	20200207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	is_implicated_in	DOID:0110430	dilated cardiomyopathy 1G		MGI:4359814	Ttn<sup>tm1Brge</sup>/Ttn<sup>+</sup>  [background:] B6.Cg-Ttn<sup>tm1Brge</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19406126	20091001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	is_not_implicated_in	DOID:12721	multiple epiphyseal dysplasia		MGI:3037836	Comp<sup>tm1Aol</sup>/Comp<sup>tm1Aol</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12024046	20051007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135677	Fgfr3<sup>tm5.1Cxd</sup>	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3640358	Fgfr3<sup>tm5.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11181569	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039777	Tg(Mt1-RET)304Ina	is_implicated_in	DOID:1909	melanoma		MGI:5297714	Tg(Mt1-RET)304Ina/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20048069	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680557	Pax6<sup>1Jrt</sup>	is_implicated_in	DOID:0060673	Peters anomaly		MGI:2680573	Pax6<sup>1Jrt</sup>/Pax6<sup>+</sup>  [background:] C3.B6-Pax6<sup>1Jrt</sup>			ECO:0000033	author statement supported by traceable reference	MGI:2680583	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4417888	Tg(Krt14-Fyn)AJsey	is_implicated_in	DOID:37	skin disease		MGI:4417896	Tg(Krt14-Fyn)AJsey/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17046829	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	is_implicated_in	DOID:0060545	Hermansky-Pudlak syndrome 7		MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:12923531	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	is_implicated_in	DOID:0060545	Hermansky-Pudlak syndrome 7		MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:1936982	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661039	Dsg4<sup>lah-J</sup>	is_implicated_in	DOID:0110703	hypotrichosis 6		MGI:2661068	Dsg4<sup>lah-J</sup>/Dsg4<sup>lah-J</sup>  [background:] involves: DBA/1LacJ			ECO:0000033	author statement supported by traceable reference	PMID:10839719	20190422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5431478	b2b904Clo	is_implicated_in	DOID:114	heart disease		MGI:5431510	b2b904Clo/b2b904Clo  [background:] C57BL/6J-b2b904Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	is_implicated_in	DOID:0111011	cone-rod dystrophy 6		MGI:3693895	Gucy2e<sup>tm1Gar</sup>/Gucy2e<sup>tm1Gar</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10407028	20090604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891763	Ppp4c	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:7281440	Ppp4c<sup>em1Qys</sup>/Ppp4c<sup>em1Qys</sup> Tg(Stra8-icre)1Reb/0  [background:] involves: 129S/SvEv * C57BL/6 * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:33543287	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179757	Rs1<sup>tm1Web</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:3046056	Rs1<sup>tm1Web</sup>/Y  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11983912	20070912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:3263	piebaldism		MGI:5523971	Kit<sup>Wps</sup>/Kit<sup>Wps</sup>  [background:] involves: C57BL/6J * CBA/CaJ			ECO:0000033	author statement supported by traceable reference	PMID:20095975	20131217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3689328	Sh3pxd2b<sup>nee</sup>	is_implicated_in	DOID:10754	otitis media		MGI:4365644	Sh3pxd2b<sup>nee</sup>/Sh3pxd2b<sup>nee</sup>  [background:] B10.Cg-H2<sup>h4</sup> Sh3pxd2b<sup>nee</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:19669234	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194497	Tgif1	is_not_implicated_in	DOID:0110880	holoprosencephaly 4		MGI:3577403	Tgif1<sup>tm1.1Caw</sup>/Tgif1<sup>tm1.1Caw</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15831469	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2651833	Nmf15	is_implicated_in	DOID:9970	obesity		MGI:2651886	Nmf15/Nmf15<sup>+</sup>  [background:] C57BL/6J-Nmf15/J			ECO:0000033	author statement supported by traceable reference	MGI:2651853	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330805	Rab33b	is_implicated_in	DOID:0081271	Smith-McCort dysplasia 2		MGI:7517090	Rab33b<sup>em1Rmr</sup>/Rab33b<sup>em1Rmr</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:37359363	20230814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330805	Rab33b	is_implicated_in	DOID:0081271	Smith-McCort dysplasia 2		MGI:7517091	Rab33b<sup>em1Rmr</sup>/Rab33b<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:37359363	20230814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104968	Ppox	is_implicated_in	DOID:4346	variegate porphyria		MGI:5697205	Ppox<sup>tm1.1Had</sup>/Ppox<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11929050	20151125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104968	Ppox	is_implicated_in	DOID:4346	variegate porphyria		MGI:5697204	Ppox<sup>tm1Had</sup>/Ppox<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11929050	20151125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:4971	myelofibrosis		MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3588207	Dnaaf3	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98331	Snap25	is_implicated_in	DOID:9970	obesity		MGI:5766495	Snap25<sup>tm1.1Bark</sup>/Snap25<sup>tm1.1Bark</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26195742	20160504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_not_implicated_in	DOID:14323	Marfan syndrome		MGI:5313384	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_not_implicated_in	DOID:14323	Marfan syndrome		MGI:5313383	Fbn1<sup>tm3.2Lysa</sup>/Fbn1<sup>tm3.2Lysa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:22242013	20120328	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99698	Clock	is_implicated_in	DOID:3312	bipolar disorder		MGI:4867520	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: BALB/cJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21123577	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589247	Edn3<sup>tmgc48</sup>	is_implicated_in	DOID:0110954	Waardenburg syndrome type 4B		MGI:3589405	Edn3<sup>tmgc48</sup>/Edn3<sup>tmgc48</sup>  [background:] C57BL/6-19<sup>PWK</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17516928	20100330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3589247	Edn3<sup>tmgc48</sup>	is_implicated_in	DOID:0110954	Waardenburg syndrome type 4B		MGI:3802920	Edn3<sup>tmgc48</sup>/Edn3<sup>+</sup>  [background:] C57BL/6-19<sup>PWK</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17516928	20100330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033425	Dph1<sup>tm2Bhr</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:5659969	Dph1<sup>tm2Bhr</sup>/Dph1<sup>tm2Bhr</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24895408	20150827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347360	Cul3	is_not_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:5901736	Cul3<sup>tm2Suc</sup>/Cul3<sup>tm2Suc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26490675	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347360	Cul3	is_not_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:5901734	Cul3<sup>tm1Suc</sup>/Cul3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26490675	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4417931	Slitrk6<sup>tm1.1Jaru</sup>	is_implicated_in	DOID:0111628	high myopia-sensorineural deafness syndrome		MGI:4417932	Slitrk6<sup>tm1.1Jaru</sup>/Slitrk6<sup>tm1.1Jaru</sup>  [background:] B6.129P2-Slitrk6<sup>tm1.1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23543054	20221103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512112	Prkar1a<sup>tm1.2Lsk</sup>	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:5897776	Prkar1a<sup>tm1.2Lsk</sup>/Prkar1a<sup>tm1.2Lsk</sup> Tg(TPO-cre)1Shk/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/NCr			ECO:0000033	author statement supported by traceable reference	PMID:22514108	20170622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155738	Gjb3<sup>tm1Kwi</sup>	is_not_implicated_in	DOID:0110558	autosomal dominant nonsyndromic deafness 2A		MGI:3588971	Gjb3<sup>tm1Kwi</sup>/Gjb3<sup>tm1Kwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11237463	20051005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176390	Ppt1<sup>tm1Hof</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:2176410	Ppt1<sup>tm1Hof</sup>/Ppt1<sup>tm1Hof</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11717424	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:4821838	avc2	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:4822143	avc2/avc2  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20101008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	is_implicated_in	DOID:3310	atopic dermatitis		MGI:2384175	Trpv3<sup>Nh</sup>/Trpv3<sup>+</sup>  [background:] involves: DS			ECO:0000033	author statement supported by traceable reference	PMID:9250484	20060125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510459	Gp1bb<sup>tm1Ware</sup>	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3512040	Gp1bb<sup>tm1Ware</sup>/Gp1bb<sup>tm1Ware</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15213102	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510459	Gp1bb<sup>tm1Ware</sup>	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3512041	Gp1bb<sup>tm1Ware</sup>/Gp1bb<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:15213102	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5446426	Dnah11<sup>b2b1775Clo</sup>/Dnah11<sup>b2b1775Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1775Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5437114	Dnah11<sup>b2b1289Clo</sup>/Dnah11<sup>b2b1289Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1289Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5318339	Dnah11<sup>b2b1203Clo</sup>/Dnah11<sup>b2b1203Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1203Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5312336	Dnah11<sup>b2b598Clo</sup>/Dnah11<sup>b2b598Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b598Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:5317649	Dnah11<sup>b2b1279Clo</sup>/Dnah11<sup>b2b1279Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1279Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0110605	primary ciliary dyskinesia 7		MGI:2172625	Dnah11<sup>iv</sup>/Dnah11<sup>iv</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	MGI:48750	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927144	Sav1	is_implicated_in	DOID:5353	colonic disease		MGI:4838642	Sav1<sup>tm1.1Dupa</sup>/Sav1<sup>tm1.1Dupa</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21041407	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	is_implicated_in	DOID:289	endometriosis		MGI:6281662	Hdac3<sup>tm1.1Eno</sup>/Hdac3<sup>tm1.1Eno</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30626716	20190308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350931	Tcirg1	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1		MGI:2174761	Tcirg1<sup>oc</sup>/Tcirg1<sup>oc</sup>  [background:] B6C3Fe a/a-Tcirg1<sup>oc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10709991	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350931	Tcirg1	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1		MGI:2174763	Tcirg1<sup>tm1Ypl</sup>/Tcirg1<sup>tm1Ypl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10581033	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138741	Hnrnpf	is_implicated_in	DOID:9432	renal glycosuria		MGI:6392034	Hnrnpf<sup>tm1Jsdc</sup>/Hnrnpf<sup>tm1Jsdc</sup> Pax8<sup>tm1.1(cre)Mbu</sup>/Pax8<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31673025	20200226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109172	Dspp	is_implicated_in	DOID:4154	dentinogenesis imperfecta		MGI:2673970	Dspp<sup>tm1Kul</sup>/Dspp<sup>tm1Kul</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12721295	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3697454	Apba2<sup>tm1Tsuz</sup>	is_not_implicated_in	DOID:10652	Alzheimer's disease		MGI:3697817	Apba2<sup>tm1Tsuz</sup>/Apba2<sup>tm1Tsuz</sup>  [background:] C57BL/6-Apba2<sup>tm1Tsuz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19420255	20100122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98342	Snrpb	is_implicated_in	DOID:0111248	cerebrocostomandibular syndrome		MGI:7437965	E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup> Snrpb<sup>em1Lajm</sup>/Snrpb<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6J * CD1			ECO:0000033	author statement supported by traceable reference	PMID:35593225	20230224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046930	Nfkbiz<sup>tm1Aki</sup>	is_implicated_in	DOID:0050426	Stevens-Johnson syndrome		MGI:3819765	Nfkbiz<sup>tm1Aki</sup>/Nfkbiz<sup>tm1Aki</sup>  [background:] C.129P2-Nfkbiz<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18441309	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046930	Nfkbiz<sup>tm1Aki</sup>	is_implicated_in	DOID:0050426	Stevens-Johnson syndrome		MGI:3047105	Nfkbiz<sup>tm1Aki</sup>/Nfkbiz<sup>tm1Aki</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15671285	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	is_implicated_in	DOID:0111717	isolated cryptophthalmia		MGI:6389584	Frem2<sup>em1Hali</sup>/Frem2<sup>em2Hali</sup>  [background:] C57BL/6J-Frem2<sup>em1Hali</sup> Frem2<sup>em2Hali</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30802441	20200526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923799	Cecr2	is_not_implicated_in	DOID:0060668	anencephaly		MGI:3574279	Cecr2<sup>Gt(pGT1)1Hemc</sup>/Cecr2<sup>Gt(pGT1)1Hemc</sup>  [background:] FVB.129P2(C)-Cecr2<sup>Gt(pGT1)1Hemc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15640247	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915040	Rab39b	is_implicated_in	DOID:0112059	non-syndromic X-linked intellectual disability 72		MGI:7547388	Rab39b<sup>tm1Pdad</sup>/Y  [background:] B6N.Cg-Rab39b<sup>tm1Pdad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34761259	20231113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3709065	Tg(tetO-APPSwInd)18Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3709154	Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-APPSwInd)18Dbo/0  [background:] involves: C3H/HeJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16279840	20120824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3625060	Il4<sup>tm1Cgn</sup>/Il4<sup>tm1Cgn</sup>  [background:] either: NOD.129-Il4<sup>tm1Cgn</sup> or (involves: 129 * NOD)			ECO:0000033	author statement supported by traceable reference	PMID:9703318	20060622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934891	Hspg2<sup>tm1Nid</sup>	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11802174	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5428133	Nrxn1<sup>tm1Sud</sup>/Nrxn1<sup>tm1Sud</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19822762	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3579842	Jak3<sup>tm1Tks</sup>/Jak3<sup>tm1Tks</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8777722	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3769345	Jak3<sup>tm1Ljb</sup>/Jak3<sup>tm1Ljb</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11034372	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107734	Ap3d1	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:5559208	Ap3d1<sup>mh-4J</sup>/Ap3d1<sup>mh-4J</sup>  [background:] involves: 129P2/OlaHsd * BALB/cByJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:5558048	20140416	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442331	Pten<sup>tm2.1Gle</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:4442335	Pten<sup>tm2.1Gle</sup>/Pten<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20194734	20100504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97515	Pcsk5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5430345	Pcsk5<sup>b2b1549Clo</sup>/Pcsk5<sup>b2b1549Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b1549Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	is_implicated_in	DOID:0050453	lissencephaly		MGI:3698561	Tuba1a<sup>Jna</sup>/Tuba1a<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:17218254	20070305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928904	Mocs1	is_implicated_in	DOID:0111164	molybdenum cofactor deficiency type A		MGI:2659147	Mocs1<sup>tm1Jre</sup>/Mocs1<sup>tm1Jre</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12471057	20230619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856588	Cat4<sup>Apcat1-4</sup>	is_implicated_in	DOID:83	cataract		MGI:2175746	Cat4<sup>Apcat1-4</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:1511869	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:2178785	Hspg2<sup>tm1Nid</sup>/Hspg2<sup>tm1Nid</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10545953	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156822	Zic1<sup>tm1Jaru</sup>	is_implicated_in	DOID:0050777	Joubert syndrome		MGI:3716303	Zic1<sup>tm1Jaru</sup>/Zic1<sup>+</sup>  [background:] B6.129S4-Zic1<sup>tm1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11699604	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856688	Papss2<sup>bm</sup>	is_implicated_in	DOID:0050812	spondyloepimetaphyseal dysplasia, Pakistani type		MGI:3054675	Papss2<sup>bm</sup>/Papss2<sup>bm</sup>  [background:] LDJ/Le			ECO:0000033	author statement supported by traceable reference	PMID:5713631	20090819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	is_implicated_in	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type		MGI:6163736	Kdm5c<sup>tm1.2Yshi</sup>/Y  [background:] involves: 129 * 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26804915	20180629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914502	Cap2	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907446	Cap2<sup>tm1e(EUCOMM)Wtsi</sup>/Cap2<sup>tm1e(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Cap2<sup>tm1e(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22945801	20170825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056560	Hsf4<sup>ldis1</sup>	is_implicated_in	DOID:0110255	cataract 5 multiple types		MGI:5305581	Hsf4<sup>ldis1</sup>/Hsf4<sup>ldis1</sup>  [background:] involves: C57BL/6 * CAST/EiJ * RIIIS/J			ECO:0000033	author statement supported by traceable reference	PMID:22162625	20120210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891009	Noa	is_implicated_in	DOID:3310	atopic dermatitis		MGI:2667689	Noa/Noa<sup>+</sup>  [background:] NOA			ECO:0000033	author statement supported by traceable reference	MGI:1097454	20100208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6272014	Tnni2<sup>tm1Sgao</sup>/Tnni2<sup>tm1Sgao</sup>  [background:] involves: 129 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:25340332	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6272015	Tnni2<sup>tm1Sgao</sup>/Tnni2<sup>+</sup>  [background:] involves: 129 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:25340332	20190103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	is_implicated_in	DOID:9870	galactosemia		MGI:6191762	Galt<sup>Gt(E285B04)Wrst</sup>/Galt<sup>Gt(E285B04)Wrst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24549051	20180727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450834	Tyrobp<sup>tm1Ttk</sup>	is_implicated_in	DOID:0090112	Nasu-Hakola disease		MGI:2450846	Tyrobp<sup>tm1Ttk</sup>/Tyrobp<sup>tm1Ttk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12569157	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775648	Hfe<sup>tm1.1Wsr</sup>	is_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3775649	Hfe<sup>tm1.1Wsr</sup>/Hfe<sup>tm1.1Wsr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17264297	20081230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	is_implicated_in	DOID:707	B-cell lymphoma		MGI:6393679	Ezh2<sup>tm1.1Nesh</sup>/Ezh2<sup>+</sup> Cd19<sup>tm1(cre)Cgn</sup>/Cd19<sup>+</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27135738	20200310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856293	Pax3<sup>Sp-2H</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2168108	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20100907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856293	Pax3<sup>Sp-2H</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2169285	Pax3<sup>Sp-2H</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20100907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856293	Pax3<sup>Sp-2H</sup>	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2451311	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: 101 * C3H/He * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:9344762	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5804451	Ednrb<sup>tm1.1Nrd</sup>/Ednrb<sup>tm1.1Nrd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26240367	20161021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2174949	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15294878	20161021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5617944	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] B6;129-Ednrb<sup>tm1Ywa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24945437	20161021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3589108	Ednrb<sup>s-l</sup>/Ednrb<sup>s-l</sup>  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:5917257	20161021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	is_implicated_in	DOID:0110431	dilated cardiomyopathy 1I		MGI:2178322	Des<sup>tm1Cap</sup>/Des<sup>tm1Cap</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8794866	20060523	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3046463	Tafa3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6164125	Tafa3<sup>em1Hssh</sup>/Tafa3<sup>em1Hssh</sup>  [background:] C57BL/6NTac-Tafa3<sup>em1Hssh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29184127	20180704	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861928	Gad2<sup>tm1Bae</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:2177575	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * NOD			ECO:0000033	author statement supported by traceable reference	PMID:9391152	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043815	Atp8b1<sup>tm1Nbf</sup>	is_not_implicated_in	DOID:1852	intrahepatic cholestasis		MGI:3043817	Atp8b1<sup>tm1Nbf</sup>/Atp8b1<sup>tm1Nbf</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:14976163	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	is_implicated_in	DOID:0050476	Barth syndrome		MGI:4943692	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21068380	20230824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	is_implicated_in	DOID:0050476	Barth syndrome		MGI:5288490	Gt(ROSA)26Sor<sup>tm37(H1/tetO-RNAi:Tafazzin)Arte</sup>/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21091282	20230824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	is_implicated_in	DOID:0050476	Barth syndrome		MGI:7520358	Tafazzin<sup>em1Xfa</sup>/Y Tg(myl7.L-cre)1118Tmhn/0  [background:] involves: C57BL/6NCrl * MF1			ECO:0000033	author statement supported by traceable reference	PMID:34129362	20230824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4414643	Tspan12<sup>tm1Wye</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:4414647	Tspan12<sup>tm1Wye</sup>/Tspan12<sup>tm1Wye</sup>  [background:] either: B6.129S5-Tspan12<sup>tm1Wye</sup> or FVB.129S5-Tspan12<sup>tm1Wye</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20159112	20120326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178357	Mitf<sup>Rorp</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178357	Mitf<sup>Rorp</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926483	Nectin1	is_not_implicated_in	DOID:0060773	cleft lip-palate-ectodermal dysplasia syndrome		MGI:4838217	Nectin1<sup>tm1Ytk</sup>/Nectin1<sup>tm1Ytk</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21038445	20101111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98306	Sim1	is_implicated_in	DOID:9970	obesity		MGI:3036852	Sim1<sup>tm1Fan</sup>/Sim1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11448938	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3766134	Tg(Gfap-TNF*)K21Gkl	is_implicated_in	DOID:2377	multiple sclerosis		MGI:4461137	Tg(Gfap-TNF*)K21Gkl/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9736029	20100722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785405	Mus81<sup>tm1Esse</sup>	is_implicated_in	DOID:0050645	arterial tortuosity syndrome		MGI:3794044	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17293478	20080617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445096	Dhtkd1	is_implicated_in	DOID:0111453	2-aminoadipic 2-oxoadipic aciduria		MGI:6268326	Dhtkd1<sup>em1Hpr</sup>/Dhtkd1<sup>em1Hpr</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28545977	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:3040915	Abcg2<sup>tm1Ahs</sup>/Abcg2<sup>tm1Ahs</sup>  [background:] either: (involves: 129P2/OlaHsd * FVB) or (involves: FVB)			ECO:0000033	author statement supported by traceable reference	PMID:12429862	20050913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580071	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580093	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580071	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580089	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580071	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580090	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862000	Nog<sup>tm1Amc</sup>	is_implicated_in	DOID:0080171	esophageal atresia/tracheoesophageal fistula		MGI:3819135	Nog<sup>tm1Amc</sup>/Nog<sup>tm1Amc</sup>  [background:] either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1 * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:17260385	20081212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347487	Foxm1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5638149	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16556734	20150603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914672	Dhdds	is_implicated_in	DOID:0110352	retinitis pigmentosa 59		MGI:6693811	Dhdds<sup>tm1.1Sjpi</sup>/Dhdds<sup>tm1.1Sjpi</sup> Tg(BEST1-rtTA,tetO-cre)1Yzl/0  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:32245241	20210421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452356	Nbea<sup>Tg(GH1)240BNec</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5495922	Nbea<sup>Tg(GH1)240BNec</sup>/Nbea<sup>+</sup>  [background:] B6JRj.Cg-Nbea<sup>Tg(GH1)240BNec</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23153818	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:2178344	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16576828	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	is_implicated_in	DOID:11211	buphthalmos		MGI:3655820	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] B6.Cg-Cyp1b1<sup>tm1Gonz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	is_implicated_in	DOID:11211	buphthalmos		MGI:3655821	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] 129X1.Cg-Cyp1b1<sup>tm1Gonz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	is_implicated_in	DOID:11211	buphthalmos		MGI:3655819	Cyp1b1<sup>tm1Gonz</sup>/Cyp1b1<sup>tm1Gonz</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442819	Tshz3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:7261388	Tshz3<sup>tm2.1Lafa</sup>/Tshz3<sup>tm2.1Lafa</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31060802	20220414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438490	Tg(Thy1-TARDBP)4Singh	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:4438492	Tg(Thy1-TARDBP)4Singh/Tg(Thy1-TARDBP)4Singh  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:20133711	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438490	Tg(Thy1-TARDBP)4Singh	is_implicated_in	DOID:0060201	amyotrophic lateral sclerosis type 10		MGI:4438494	Tg(Thy1-TARDBP)4Singh/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:20133711	20160504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5641392	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] B6J.129S4-Tsc1<sup>tm1Hin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5641483	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22763451	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3626344	Kat6a<sup>tm1Avo</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3629227	Kat6a<sup>tm1Avo</sup>/Kat6a<sup>tm1Avo</sup>  [background:] involves: 129/Sv * BALB/c * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22921202	20121228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4128978	Katnip<sup>Gt(RRG309)Byg</sup>	is_implicated_in	DOID:0110995	Joubert syndrome 26		MGI:5883451	Katnip<sup>Gt(RRG309)Byg</sup>/Katnip<sup>Gt(RRG309)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26714646	20170419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653065	Ndn<sup>tm1Alb</sup>	is_not_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653069	Ndn<sup>tm1Alb</sup>/Ndn<sup>tm1Alb</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10319852	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653065	Ndn<sup>tm1Alb</sup>	is_not_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:2653070	Ndn<sup>tm1Alb</sup>/Ndn<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10319852	20090723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849300	Acp3<sup>tm1Pivi</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:5007486	Acp3<sup>tm1Pivi</sup>/Acp3<sup>tm1Pivi</sup>  [background:] B6.Cg-Acp3<sup>tm1Pivi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24039861	20140424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720593	Il4ra<sup>tm2Tch</sup>	is_implicated_in	DOID:2841	asthma		MGI:4361938	Il4ra<sup>tm2Tch</sup>/Il4ra<sup>tm2Tch</sup>  [background:] C.129X1-Il4ra<sup>tm2Tch</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19770271	20091021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695408	Krt4<sup>Bcc1</sup>	is_implicated_in	DOID:0050448	white sponge nevus		MGI:3695719	Krt4<sup>Bcc1</sup>/Krt4<sup>Bcc1</sup>  [background:] C3HeB/FeJ-Krt4<sup>Bcc1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16858417	20070206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695408	Krt4<sup>Bcc1</sup>	is_implicated_in	DOID:0050448	white sponge nevus		MGI:3695720	Krt4<sup>Bcc1</sup>/Krt4<sup>+</sup>  [background:] C3HeB/FeJ-Krt4<sup>Bcc1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16858417	20070206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome		MGI:3530074	Atrx<sup>tm1Rjg</sup>/Y Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15668733	20090309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome		MGI:3530076	Atrx<sup>tm1Rjg</sup>/Y Tg(Nes-cre)2472Pick/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15668733	20090309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	is_implicated_in	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome		MGI:3834848	Atrx<sup>tm1Rjg</sup>/Y Tg(Pax6-cre,GFP)2Pgr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19088125	20090309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88355	Cdh2	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:7434319	Cdh2<sup>em1Obir</sup>/Cdh2<sup>em1Obir</sup>  [background:] C57BL/6JRcc-Cdh2<sup>em1Obir</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34702855	20230214	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525073	Tg(CAG-WRN*K577M)5025Wcl	is_implicated_in	DOID:5688	Werner syndrome		MGI:3525190	Tg(CAG-WRN*K577M)5025Wcl/0  [background:] involves: C3H * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10628995	20081030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444417	Sh3tc2	is_implicated_in	DOID:0110183	Charcot-Marie-Tooth disease type 4C		MGI:4367049	Sh3tc2<sup>tm1.1Rchr</sup>/Sh3tc2<sup>tm1.1Rchr</sup>  [background:] involves: 129/Sv * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19805030	20091112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6825757	Abcc9<sup>em3Nich</sup>/Abcc9<sup>+</sup>  [background:] B6.Cg-Abcc9<sup>em3Nich</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33529173	20211122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6825756	Abcc9<sup>em3Nich</sup>/Abcc9<sup>em3Nich</sup>  [background:] B6.Cg-Abcc9<sup>em3Nich</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33529173	20211122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6389016	Abcc9<sup>em1Nich</sup>/Abcc9<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:30089727	20211122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	is_implicated_in	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type		MGI:6389024	Abcc9<sup>em1Nich</sup>/Abcc9<sup>em1Nich</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:30089727	20211122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587746	Hjv<sup>tm1Nca</sup>	is_implicated_in	DOID:0111027	hemochromatosis type 2A		MGI:3588420	Hjv<sup>tm1Nca</sup>/Hjv<sup>tm1Nca</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:16075059	20050927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2655574	Ostm1	is_implicated_in	DOID:0110939	autosomal recessive osteopetrosis 5		MGI:2655576	Ostm1<sup>gl</sup>/Ostm1<sup>gl</sup>  [background:] GL/Le Edar<sup>dl-J</sup> +/+ Ostm1<sup>gl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:1155801	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442827	Tbc1d32	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148258	Taar1	is_implicated_in	DOID:5419	schizophrenia		MGI:3818698	Taar1<sup>tm1Tdw</sup>/Taar1<sup>tm1Tdw</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17212650	20081208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	is_implicated_in	DOID:0050567	orofacial cleft		MGI:2175120	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae-Msx1<sup>tm1Rilm</sup>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7914451	20060803	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923221	Sugct	is_implicated_in	DOID:0112246	glutaric acidemia type 3		MGI:6456764	Sugct<sup>tm1.2Kald</sup>/Sugct<sup>tm1.2Kald</sup>  [background:] B6.Cg-Sugct<sup>tm1.2Kald</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31722069	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683665	Icos<sup>tm1Shr</sup>	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:2683669	Icos<sup>tm1Shr</sup>/Icos<sup>tm1Shr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11343122	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:8398	osteoarthritis		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:7344126	20060731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:8398	osteoarthritis		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:8055108	20060731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289196	Rnf213	is_not_implicated_in	DOID:13099	Moyamoya disease		MGI:5752779	Rnf213<sup>tm1.1Mfuji</sup>/Rnf213<sup>tm1.1Mfuji</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26315378	20160322	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858229	Ppp1r3c	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:4429442	Ppp1r3c<sup>tm1Ars</sup>/Ppp1r3c<sup>+</sup>  [background:] B6.129-Ppp1r3c<sup>tm1Ars</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12727934	20100218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97515	Pcsk5	is_implicated_in	DOID:14679	VACTERL association		MGI:3797214	Pcsk5<sup>vcc</sup>/Pcsk5<sup>vcc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18519639	20150724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97515	Pcsk5	is_implicated_in	DOID:14679	VACTERL association		MGI:5313813	Pcsk5<sup>b2b585Clo</sup>/Pcsk5<sup>b2b585Clo</sup>  [background:] C57BL/6J-Pcsk5<sup>b2b585Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20150724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3847120	Lepr<sup>brta</sup>/Lepr<sup>brta</sup>  [background:] C57BL/6JSfdAnu-Lepr<sup>brta</sup>/Anu			ECO:0000033	author statement supported by traceable reference	MGI:3611487	20181012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5620891	Lepr<sup>tm1Jke</sup>/Lepr<sup>tm1Jke</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:25157166	20181012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3694548	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] BKS.Cg-Dock7<sup>m</sup> +/+ Lepr<sup>db</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22609345	20181012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2654708	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:16113078	20181012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857702	Vhl<sup>tm1Wml</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176441	Vhl<sup>tm1Wml</sup>/Vhl<sup>tm1Wml</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9286594	20160502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857702	Vhl<sup>tm1Wml</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2176441	Vhl<sup>tm1Wml</sup>/Vhl<sup>tm1Wml</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14604887	20160502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919358	Ddhd2	is_implicated_in	DOID:0110806	hereditary spastic paraplegia 54		MGI:5662254	Ddhd2<sup>tm1Crv</sup>/Ddhd2<sup>tm1Crv</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25267624	20150921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1		MGI:2654709	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25144618	20151001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039067	Tg(C3-1-TAg)cJeg	is_implicated_in	DOID:10283	prostate cancer		MGI:3835423	Tg(C3-1-TAg)cJeg/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:7972041	20141204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926888	Crebbp<sup>tm1Dli</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22198154	20130222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043985	Nr4a2<sup>tm1Omc</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3619915	Nr4a2<sup>tm1Omc</sup>/Nr4a2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15589522	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919127	Efhc1	is_implicated_in	DOID:4890	juvenile myoclonic epilepsy		MGI:3836724	Efhc1<sup>tm1Kzy</sup>/Efhc1<sup>tm1Kzy</sup>  [background:] B6.129P2-Efhc1<sup>tm1Kzy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19147686	20090323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919127	Efhc1	is_implicated_in	DOID:4890	juvenile myoclonic epilepsy		MGI:3836725	Efhc1<sup>tm1Kzy</sup>/Efhc1<sup>+</sup>  [background:] B6.129P2-Efhc1<sup>tm1Kzy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19147686	20090323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926375	Rassf5	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4939894	Rassf5<sup>tm1Kina</sup>/Rassf5<sup>tm1Kina</sup>  [background:] B6.Cg-Rassf5<sup>tm1Kina</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21194982	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	is_implicated_in	DOID:5418	schizoaffective disorder		MGI:4888960	Gria1<sup>tm1Rsp</sup>/Gria1<sup>tm1Rsp</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20699120	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	is_implicated_in	DOID:5418	schizoaffective disorder		MGI:4888959	Gria1<sup>tm1Rsp</sup>/Gria1<sup>tm1Rsp</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20699120	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926332	Irf8<sup>tm1Hor</sup>	is_implicated_in	DOID:0060761	familial chronic myelocytic leukemia-like syndrome		MGI:2175074	Irf8<sup>tm1Hor</sup>/Irf8<sup>tm1Hor</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8861914	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926332	Irf8<sup>tm1Hor</sup>	is_implicated_in	DOID:0060761	familial chronic myelocytic leukemia-like syndrome		MGI:2175075	Irf8<sup>tm1Hor</sup>/Irf8<sup>+</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8861914	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:4997	Camurati-Engelmann disease		MGI:4455020	Mitf<sup>mi-ew</sup>/Mitf<sup>mi-ew</sup>  [background:] involves: C57BL/6Bn * NAW			ECO:0000033	author statement supported by traceable reference	PMID:11930005	20100615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386786	Slc34a1<sup>tm1Hten</sup>	is_implicated_in	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria		MGI:3029314	Slc34a1<sup>tm1Hten</sup>/Slc34a1<sup>tm1Hten</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9560283	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	is_implicated_in	DOID:3328	temporal lobe epilepsy		MGI:6285755	Glul<sup>tm1.1Ncd</sup>/Glul<sup>tm1.1Ncd</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] B6.Cg-Glul<sup>tm1.1Ncd</sup> Emx1<sup>tm1(cre)Krj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30053506	20190402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033929	Vsx1<sup>tm1Mci</sup>	is_not_implicated_in	DOID:10126	keratoconus		MGI:3033934	Vsx1<sup>tm1Mci</sup>/Vsx1<sup>tm1Mci</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14745032	20050718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777975	Pnp<sup>g</sup>	is_implicated_in	DOID:5813	purine nucleoside phosphorylase deficiency		MGI:3778902	Pnp<sup>g</sup>/Pnp<sup>g</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:9122228	20120928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772700	Tg(Prnp-TBP*)105Xjl	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:3772885	Tg(Prnp-TBP*)105Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)105Xjl			ECO:0000033	author statement supported by traceable reference	PMID:17994014	20080305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:4355020	Atr<sup>tm1Ofc</sup>/Atr<sup>tm1Ofc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:19620979	20090826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5486338	Cybb<sup>tm1Din</sup>/Cybb<sup>tm1Din</sup>  [background:] B6.129S-Cybb<sup>tm1Din</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856851	Foxe3<sup>dyl</sup>	is_implicated_in	DOID:11367	congenital aphakia		MGI:2175026	Foxe3<sup>dyl</sup>/Foxe3<sup>dyl</sup>  [background:] BALB/cLiA-Foxe3<sup>dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11980846	20170130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856851	Foxe3<sup>dyl</sup>	is_implicated_in	DOID:11367	congenital aphakia		MGI:2175026	Foxe3<sup>dyl</sup>/Foxe3<sup>dyl</sup>  [background:] BALB/cLiA-Foxe3<sup>dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10652278	20170130	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98907	Uox	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3687865	Uox<sup>tm1Bay</sup>/Uox<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11316859	20061116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	is_implicated_in	DOID:2219	Glanzmann's thrombasthenia		MGI:5688878	Itgb3<sup>tm1Hyn</sup>/Itgb3<sup>tm1.1Wlbcr</sup> Tg(Pf4-icre)Q3Rsko/0  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19933310	20151002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385656	Acsbg1	is_not_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:3851594	Acsbg1<sup>tm1Mld</sup>/Acsbg1<sup>tm1Mld</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19167491	20090730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055440	Tg(Crh)227.1Pbl	is_implicated_in	DOID:9970	obesity		MGI:3580003	Tg(Crh)227.1Pbl/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1597149	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:2675764	Drd2<sup>tm1Ebo</sup>/Drd2<sup>tm1Ebo</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9717839	20171210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341822	Eif4h	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5314953	Eif4h<sup>Gt(Ex279)Byg</sup>/Eif4h<sup>Gt(Ex279)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22234171	20120412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:936	brain disease		MGI:3714016	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Gfap-cre)1Sbk/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:19470613	20171116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3621812	Aaas<sup>tm1Ahue</sup>	is_not_implicated_in	DOID:0050602	triple-A syndrome		MGI:3622153	Aaas<sup>tm1Ahue</sup>/Aaas<sup>tm1Ahue</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16479006	20060512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679499	Slit3<sup>Gt(OST106158)Lex</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3053453	Slit3<sup>Gt(OST106158)Lex</sup>/Slit3<sup>Gt(OST106158)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14550534	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5560145	m12Anu	is_implicated_in	DOID:0050563	nonsyndromic deafness		MGI:5582638	m12Anu/m12Anu  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24086324	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696985	Casp8<sup>tm1Hed</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4888399	Casp8<sup>tm1Hed</sup>/Casp8<sup>tm1Hed</sup> Tg(KRT14-cre)1Efu/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21135236	20110217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664558	Adam33<sup>tm1.1Chch</sup>	is_not_implicated_in	DOID:2841	asthma		MGI:3664641	Adam33<sup>tm1.1Chch</sup>/Adam33<sup>tm1.1Chch</sup>  [background:] 129S4/SvJae-Adam33<sup>tm1.1Chch</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16943435	20061026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183212	Gucy2e<sup>tm1Gar</sup>	is_implicated_in	DOID:0111011	cone-rod dystrophy 6		MGI:3693895	Gucy2e<sup>tm1Gar</sup>/Gucy2e<sup>tm1Gar</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10407028	20090604	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831358	Tg(Prnp-ATN1)150Dbo	is_implicated_in	DOID:0060162	dentatorubral-pallidoluysian atrophy		MGI:5056394	Tg(Prnp-ATN1)150Dbo/?  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10677044	20110810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687966	Gba1<sup>tm1.1Karl</sup>	is_implicated_in	DOID:0110957	Gaucher's disease type I		MGI:3688419	Gba1<sup>tm1.1Karl</sup>/Gba1<sup>tm1.1Karl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16954197	20061121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341070	Fkbp8	is_implicated_in	DOID:0080016	spina bifida		MGI:3775615	Fkbp8<sup>Gt(OST287985)Lex</sup>/Fkbp8<sup>Gt(OST287985)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18003640	20211231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4434258	Aspa<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:3613	Canavan disease		MGI:5008609	Aspa<sup>tm1a(EUCOMM)Wtsi</sup>/Aspa<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:21625469	20170922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576262	Sh2d1a<sup>tm1Cpt</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576739	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11323694	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576262	Sh2d1a<sup>tm1Cpt</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576740	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11323694	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576262	Sh2d1a<sup>tm1Cpt</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576734	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] B6.129S4-Sh2d1a<sup>tm1Cpt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15749842	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576262	Sh2d1a<sup>tm1Cpt</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576734	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] B6.129S4-Sh2d1a<sup>tm1Cpt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15774582	20050513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576262	Sh2d1a<sup>tm1Cpt</sup>	is_implicated_in	DOID:0060705	X-linked lymphoproliferative syndrome 1		MGI:3576735	Sh2d1a<sup>tm1Cpt</sup>/Sh2d1a<sup>tm1Cpt</sup>  [background:] C.129S4-Sh2d1a<sup>tm1Cpt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15774582	20050513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	is_implicated_in	DOID:8946	severe nonproliferative diabetic retinopathy		MGI:5661928	Pdgfrb<sup>redeye</sup>/Pdgfrb<sup>redeye</sup>  [background:] C3N.C-Pdgfrb<sup>redeye</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23633653	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511276	Med1<sup>tm2Jkr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5911329	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511276	Med1<sup>tm2Jkr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5911326	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153588	Ppp1r3a	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2653988	Ppp1r3a<sup>tm1Ptwc</sup>/Ppp1r3a<sup>tm1Ptwc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12606498	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	is_implicated_in	DOID:62	aortic valve disease		MGI:3618597	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] B6.129P2-Nos3<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10821808	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	is_implicated_in	DOID:3328	temporal lobe epilepsy		MGI:3625870	Kcna1<sup>tm1Tem</sup>/Kcna1<sup>tm1Tem</sup>  [background:] C3Fe.129S7-Kcna1<sup>tm1Tem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24270080	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152755	Pdx1<sup>tm1Ted</sup>	is_implicated_in	DOID:0111103	maturity-onset diabetes of the young type 4		MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12697734	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857187	Ighm<sup>tm1Cgn</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623426	Ighm<sup>tm1Cgn</sup>/Ighm<sup>+</sup>  [background:] NOD.129S2-Ighm<sup>tm1Cgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8920894	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921123	Fam161a	is_implicated_in	DOID:0110365	retinitis pigmentosa 28		MGI:5609024	Fam161a<sup>Gt(462E7)Cmhd</sup>/Fam161a<sup>Gt(462E7)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24833722	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181191	Crx<sup>tm1Clc</sup>	is_implicated_in	DOID:0110333	Leber congenital amaurosis 7		MGI:3697471	Crx<sup>tm1Clc</sup>/Crx<sup>tm1Clc</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10581037	20110502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179992	Tg(tetO-Kras2)12Hev	is_implicated_in	DOID:3910	lung adenocarcinoma		MGI:5912341	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-Kras2)12Hev/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11751631	20171103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914407	Cfap418	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:6157954	Cfap418<sup>em3Jyang</sup>/Cfap418<sup>em3Jyang</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29440555	20180524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354161	Sirt6	is_implicated_in	DOID:3911	progeria		MGI:3686897	Sirt6<sup>tm1Fwa</sup>/Sirt6<sup>tm1Fwa</sup>  [background:] involves: 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16439206	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676325	Col2a1<sup>sedc</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:2676332	Col2a1<sup>sedc</sup>/Col2a1<sup>sedc</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12968670	20051006	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	is_implicated_in	DOID:13580	cholestasis		MGI:5526018	Abcb4<sup>tm1Bor</sup>/Abcb4<sup>tm1Bor</sup>  [background:] C.129P2-Abcb4<sup>tm1Bor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23545228	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889818	Tspan12	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:4414647	Tspan12<sup>tm1Wye</sup>/Tspan12<sup>tm1Wye</sup>  [background:] either: B6.129S5-Tspan12<sup>tm1Wye</sup> or FVB.129S5-Tspan12<sup>tm1Wye</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20159112	20120326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512766	Wt1<sup>tm1Vih</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:3512883	Wt1<sup>tm1Vih</sup>/Wt1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * MF1			ECO:0000033	author statement supported by traceable reference	PMID:15509792	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653126	Krt14<sup>tm1Der</sup>	is_implicated_in	DOID:4644	epidermolysis bullosa simplex		MGI:2653129	Krt14<sup>tm1Der</sup>/Krt14<sup>tm1Der</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081029	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341830	Eif2ak3	is_implicated_in	DOID:0090060	Wolcott-Rallison syndrome		MGI:3582643	Eif2ak3<sup>tm1Dron</sup>/Eif2ak3<sup>tm1Dron</sup>  [background:] involves: 129S6/SvEvTac * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11430819	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341830	Eif2ak3	is_implicated_in	DOID:0090060	Wolcott-Rallison syndrome		MGI:3618624	Eif2ak3<sup>tm1Drc</sup>/Eif2ak3<sup>tm1Drc</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11997520	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	is_implicated_in	DOID:0090123	aromatic L-amino acid decarboxylase deficiency		MGI:5495915	Ddc<sup>tm1.1Nwlh</sup>/Ddc<sup>tm1.1Nwlh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23275025	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4439280	Tg(CAG-lacZ,-SV40)#Bcv	is_implicated_in	DOID:2394	ovarian cancer		MGI:4439300	Tg(CAG-lacZ,-SV40)#Bcv/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20056833	20100412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4433029	Mks1<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5503965	Mks1<sup>tm1a(EUCOMM)Wtsi</sup>/Mks1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23454480	20130903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794028	Cdc73<sup>Gt(RRE190)Byg</sup>	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5925391	Cdc73<sup>Gt(RRE190)Byg</sup>/Cdc73<sup>+</sup>  [background:] B6.129P2-Cdc73<sup>Gt(RRE190)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491174	b2b2350Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664936	Kera<sup>tm1Cyl</sup>	is_implicated_in	DOID:0060287	cornea plana		MGI:2672991	Kera<sup>tm1Cyl</sup>/Kera<sup>tm1Cyl</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:12665512	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857191	Il2<sup>tm1Hor</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3760264	Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] B6.129P2-Il2<sup>tm1Hor</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17207605	20170417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651645	Ttn<sup>tm1Her</sup>	is_implicated_in	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J		MGI:2651647	Ttn<sup>tm1Her</sup>/Ttn<sup>tm1Her</sup> Tg(Ckmm-cre)5Khn/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12464612	20050919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921749	Sost	is_implicated_in	DOID:0060756	sclerosteosis 1		MGI:3850032	Sost<sup>tm1Paz</sup>/Sost<sup>tm1Paz</sup>  [background:] involves: 129/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	is_implicated_in	DOID:0050454	periventricular nodular heterotopia		MGI:3688533	Flna<sup>Dilp2</sup>/Y  [background:] involves: BALB/cAnN * C3H/HeN * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16825286	20061124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107374	Pitx1	is_implicated_in	DOID:11836	clubfoot		MGI:5294943	Pitx1<sup>tm1Rsd</sup>/Pitx1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21775501	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	is_implicated_in	DOID:0110596	primary ciliary dyskinesia 21		MGI:5445342	Drc1<sup>b2b1654Clo</sup>/Drc1<sup>b2b1654Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b1654Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	is_implicated_in	DOID:0110596	primary ciliary dyskinesia 21		MGI:5554187	Drc1<sup>b2b2237Clo</sup>/Drc1<sup>b2b2237Clo</sup>  [background:] C57BL/6J-Drc1<sup>b2b2237Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278313	Coch	is_implicated_in	DOID:0110593	autosomal dominant nonsyndromic deafness 9		MGI:3814540	Coch<sup>tm1Mrtn</sup>/Coch<sup>tm1Mrtn</sup>  [background:] CBACa.129S4-Coch<sup>tm1Mrtn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21073934	20110128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278313	Coch	is_implicated_in	DOID:0110593	autosomal dominant nonsyndromic deafness 9		MGI:3814540	Coch<sup>tm1Mrtn</sup>/Coch<sup>tm1Mrtn</sup>  [background:] CBACa.129S4-Coch<sup>tm1Mrtn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18697796	20110128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861228	Rpl38<sup>Ts</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3795975	Rpl38<sup>Ts</sup>/Rpl38<sup>+</sup>  [background:] TSJ/Le			ECO:0000033	author statement supported by traceable reference	PMID:21062742	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579503	Axin2<sup>tm1Wbm</sup>	is_implicated_in	DOID:2340	craniosynostosis		MGI:3580015	Axin2<sup>tm1Wbm</sup>/Axin2<sup>tm1Wbm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15790973	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447298	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580091	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Mid1<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447298	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580086	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447298	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580085	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384513	Tgfbr2<sup>tm1.2Hlm</sup>	is_implicated_in	DOID:0110214	cleft soft palate		MGI:5300942	Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup> Tg(KRT14-cre)52Smr/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:24496627	20140521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158741	Chrne<sup>tm1Vwi</sup>	is_implicated_in	DOID:0110679	congenital myasthenic syndrome 4C		MGI:2671994	Chrne<sup>tm1Vwi</sup>/Chrne<sup>tm1Vwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10998094	20090428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685267	Lrit3	is_implicated_in	DOID:0110864	congenital stationary night blindness 1F		MGI:5688660	Lrit3<sup>tm1Lex</sup>/Lrit3<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24598786	20151001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:4418655	Ccr5<sup>tm1Kuz</sup>/Ccr5<sup>tm1Kuz</sup>  [background:] B6.129P2-Ccr5<sup>tm1Kuz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98241	Stmn2	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:7523314	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>+</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98241	Stmn2	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:7523309	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>em1Jmi</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680393	Gba1<sup>tm2Ggb</sup>/Gba1<sup>tm2Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680502	Gba1<sup>tm3Ggb</sup>/Gba1<sup>tm3Ggb</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680399	Gba1<sup>tm2Ggb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680509	Gba1<sup>tm4Ggb</sup>/Gba1<sup>tm4Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680386	Gba1<sup>tm1Ggb</sup>/Gba1<sup>tm1Ggb</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680512	Gba1<sup>tm4Ggb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2680504	Gba1<sup>tm3Ggb</sup>/Gba1<sup>tm1Nsb</sup>  [background:] involves: 129S/SvEv * 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14578207	20181026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	is_implicated_in	DOID:1926	Gaucher's disease		MGI:2651508	Gba1<sup>tm1Rlp</sup>/Gba1<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11994410	20181026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834479	Tg(Ly6a-TK,-BCR/ABL1)IS9AIsg	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3834483	Tg(Ly6a-TK,-BCR/ABL1)IS9AIsg/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19037256	20090305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4457055	Irf6<sup>clft1</sup>	is_implicated_in	DOID:0060239	Van der Woude syndrome		MGI:4457064	Irf6<sup>clft1</sup>/Irf6<sup>clft1</sup>  [background:] involves: A/J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20196077	20100629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929813	Cacna2d2	is_implicated_in	DOID:1826	epilepsy		MGI:5632120	Cacna2d2<sup>du-2J</sup>/Cacna2d2<sup>du-2J</sup>  [background:] involves: C57BL/6 * C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:23732642	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857204	Insr<sup>tm1Dac</sup>	is_not_implicated_in	DOID:0050470	Donohue syndrome		MGI:2174959	Insr<sup>tm1Dac</sup>/Insr<sup>tm1Dac</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8528241	20051024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856293	Pax3<sup>Sp-2H</sup>	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2451311	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: 101 * C3H/He * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:9344762	20100907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856293	Pax3<sup>Sp-2H</sup>	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2169285	Pax3<sup>Sp-2H</sup>/Pax3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20100907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856293	Pax3<sup>Sp-2H</sup>	is_not_implicated_in	DOID:0110949	Waardenburg syndrome type 3		MGI:2168108	Pax3<sup>Sp-2H</sup>/Pax3<sup>Sp-2H</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:62273	20100907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:4882033	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Tg(Tyr-cre)1Lru/0  [background:] B6.Cg-Pten<sup>tm1Hwu</sup> Tg(Tyr-cre)1Lru			ECO:0000033	author statement supported by traceable reference	PMID:19884655	20200621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1321392	Pex7	is_implicated_in	DOID:0110851	rhizomelic chondrodysplasia punctata type 1		MGI:3052846	Pex7<sup>tm1Rjaw</sup>/Pex7<sup>tm1Rjaw</sup>  [background:] Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12915479	20100512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1321392	Pex7	is_implicated_in	DOID:0110851	rhizomelic chondrodysplasia punctata type 1		MGI:4443126	Pex7<sup>tm1Nbra</sup>/Pex7<sup>tm1Nbra</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20060764	20100512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384162	Tg(IghelMD4)4Ccg	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3793301	Tg(IghelMD4)4Ccg/Tg(IghelMD4)4Ccg  [background:] NOD.B6-Tg(IghelMD4)4Ccg/DvsJ			ECO:0000033	author statement supported by traceable reference	PMID:12516557	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102483	mt-Tk	is_implicated_in	DOID:700	mitochondrial metabolism disease		MGI:5606285	mt-Tk<sup>m1</sup>  [background:] involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:24510903	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654383	Tg(Myh6-Gnaq)40Gwd	is_implicated_in	DOID:6000	congestive heart failure		MGI:2654386	Tg(Myh6-Gnaq)40Gwd/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9223325	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857811	Acox1<sup>tm1Jkr</sup>	is_implicated_in	DOID:0050797	peroxisomal acyl-CoA oxidase deficiency		MGI:2652088	Acox1<sup>tm1Jkr</sup>/Acox1<sup>tm1Jkr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8798738	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A		MGI:2659043	Capn3<sup>tm1Jsb</sup>/Capn3<sup>tm1Jsb</sup>  [background:] either: 129/Sv-Capn3<sup>tm1Jsb</sup> or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11134085	20161220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A		MGI:4829971	Capn3<sup>tm1.1Hiso</sup>/Capn3<sup>tm1.1Hiso</sup>  [background:] B6.129P2-Capn3<sup>tm1.1Hiso</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20592470	20161220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	is_implicated_in	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A		MGI:3047138	Capn3<sup>Gt(OST141731)Lex</sup>/Capn3<sup>Gt(OST141731)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15138196	20161220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661042	Gusb<sup>tm4Sly</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:2661058	Gusb<sup>tm4Sly</sup>/Gusb<sup>tm4Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12700165	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924908	Ap5z1	is_implicated_in	DOID:0110800	hereditary spastic paraplegia 48		MGI:6458731	Ap5z1<sup>tm1(KOMP)Wtsi</sup>/Ap5z1<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30930081	20200930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	is_implicated_in	DOID:14693	Clouston syndrome		MGI:5607782	Gjb6<sup>tm2.2Kwi</sup>/Gjb6<sup>tm2.2Kwi</sup>  [background:] involves: 129P2/OlaHsd * BALB/c * C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24685692	20150106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	is_implicated_in	DOID:0050453	lissencephaly		MGI:3624851	Dcx<sup>tm1.2Ffr</sup>/Y  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16571605	20060620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526444	Mkks<sup>tm1Vcs</sup>	is_implicated_in	DOID:0110128	Bardet-Biedl syndrome 6		MGI:3582615	Mkks<sup>tm1Vcs</sup>/Mkks<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:15772095	20141028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:2683647	Icos<sup>tm1Flv</sup>/Icos<sup>tm1Flv</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11343121	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:2683669	Icos<sup>tm1Shr</sup>/Icos<sup>tm1Shr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11343122	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	is_implicated_in	DOID:5419	schizophrenia		MGI:5689835	Reln<sup>rl</sup>/Reln<sup>+</sup>  [background:] B6.Cg-Reln<sup>rl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25845740	20151012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	is_implicated_in	DOID:5419	schizophrenia		MGI:5661067	Reln<sup>rl</sup>/Reln<sup>+</sup>  [background:] B6C3Fe a/a-Reln<sup>rl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11982630	20151012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	is_implicated_in	DOID:13359	Ehlers-Danlos syndrome		MGI:3530609	Dcn<sup>tm1Ioz</sup>/Dcn<sup>tm1Ioz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9024701	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850370	Pink1<sup>tm1Aub</sup>	is_implicated_in	DOID:0060369	Parkinson's disease 6		MGI:3850371	Pink1<sup>tm1Aub</sup>/Pink1<sup>tm1Aub</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:19492057	20090714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778286	Tg(DRD1-ctxA)7Burt	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:3778393	Tg(DRD1-ctxA)7Burt/0  [background:] C.Cg-Tg(DRD1-ctxA)7Burt			ECO:0000033	author statement supported by traceable reference	PMID:12140785	20080423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778286	Tg(DRD1-ctxA)7Burt	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:3778393	Tg(DRD1-ctxA)7Burt/0  [background:] C.Cg-Tg(DRD1-ctxA)7Burt			ECO:0000033	author statement supported by traceable reference	PMID:10636303	20080423	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330838	Lgmn	is_implicated_in	DOID:75	lymphatic system disease		MGI:3836291	Lgmn<sup>tm1Ihn</sup>/Lgmn<sup>tm1Ihn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19106291	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4364947	Klhl41<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:3191	nemaline myopathy		MGI:6156408	Klhl41<sup>tm1a(KOMP)Wtsi</sup>/Klhl41<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6-Klhl41<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28826497	20180515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840003	Fgfr3<sup>tm1Llm</sup>	is_implicated_in	DOID:13481	thanatophoric dysplasia		MGI:3840080	Fgfr3<sup>tm1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19073250	20090415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:10283	prostate cancer		MGI:3836577	Kras<sup>tm1Bbd</sup>/Kras<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19117991	20090320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4362669	Pygl<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:2754	glycogen storage disease VI		MGI:6392248	Pygl<sup>tm1a(KOMP)Wtsi</sup>/Pygl<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6N-Pygl<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31701076	20200228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3771547	Slc40a1<sup>tm1Nca</sup>	is_not_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:3771550	Slc40a1<sup>tm1Nca</sup>/Slc40a1<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:16054062	20080222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033341	Dnm1<sup>Ftfl</sup>	is_implicated_in	DOID:1827	idiopathic generalized epilepsy		MGI:4822359	Dnm1<sup>Ftfl</sup>/Dnm1<sup>Ftfl</sup>  [background:] C57BL/6J-Dnm1<sup>Ftfl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20700442	20100910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88223	C1qa	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2384126	C1qa<sup>tm1Mjw</sup>/C1qa<sup>tm1Mjw</sup>  [background:] involves: 129P2/Ola * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9590289	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856710	Cftr<sup>tm1Hgu</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3773702	Cftr<sup>tm1Hgu</sup>/Cftr<sup>tm1Hgu</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:7540910	20080314	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856710	Cftr<sup>tm1Hgu</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177531	Cftr<sup>tm1Hgu</sup>/Cftr<sup>tm1Hgu</sup>  [background:] involves: 129P2/OlaHsd * MF1			ECO:0000033	author statement supported by traceable reference	PMID:1382232	20080314	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6324924	Camk2a<sup>em1Rjco</sup>/Camk2a<sup>em1Rjco</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:28130356	20190726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88465	Col9a1	is_implicated_in	DOID:8398	osteoarthritis		MGI:3699108	Col9a1<sup>tm1Jae</sup>/Col9a1<sup>tm1Jae</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:11680679	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	is_implicated_in	DOID:0050770	polycystic liver disease		MGI:6285862	Ucp2<sup>tm1Lowl</sup>/Ucp2<sup>tm1Lowl</sup>  [background:] B6.129S4-Ucp2<sup>tm1Lowl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29154852	20190403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693364	Tg(PSEN1H163R)G9Btla	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3693491	Tg(PSEN1H163R)G9Btla/0  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10412057	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5295638	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Commd10<sup>Tg(Vav1-icre)A2Kio</sup>/Commd10<sup>+</sup>  [background:] involves: C57BL/6NCrlj * C57BL/10 * CBA/Ca * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:21339326	20111114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056939	Tg(Igh-6/Igh-V281)3Jwt	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623591	Tg(Igh-6/Igh-V281)3Jwt/0  [background:] NOD.B6-Tg(Igh-6/Igh-V281)3Jwt			ECO:0000033	author statement supported by traceable reference	PMID:11698422	20060601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159356	Gpc3<sup>tm1Fil</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3530366	Gpc3<sup>tm1Fil</sup>/Gpc3<sup>+</sup>  [background:] B6.Cg-Gpc3<sup>tm1Fil</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10402475	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159356	Gpc3<sup>tm1Fil</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3530365	Gpc3<sup>tm1Fil</sup>/Y  [background:] B6.Cg-Gpc3<sup>tm1Fil</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10402475	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099438	Nsdhl	is_implicated_in	DOID:0060292	X-linked chondrodysplasia punctata 1		MGI:3587801	Nsdhl<sup>Bpa-1H</sup>/Nsdhl<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:6682087	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:3527229	Mybpc3<sup>tm1Rmos</sup>/Mybpc3<sup>tm1Rmos</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11909824	20170919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5909891	Mybpc3<sup>tm2.1Lcrr</sup>/Mybpc3<sup>+</sup>  [background:] involves: 129S2/SvPasCrl * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:22465693	20170919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:5909888	Mybpc3<sup>tm2.1Lcrr</sup>/Mybpc3<sup>tm2.1Lcrr</sup>  [background:] involves: 129S2/SvPasCrl * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:22465693	20170919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:3608495	Mybpc3<sup>tm1Lcrr</sup>/Mybpc3<sup>+</sup>  [background:] involves: 129S4/SvJae * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:15249187	20170919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:2654422	Mybpc3<sup>tm1.1Jse</sup>/Mybpc3<sup>tm1.1Jse</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10545522	20170919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:2654421	Mybpc3<sup>tm1Jse</sup>/Mybpc3<sup>tm1Jse</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10545522	20170919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921765	Cdkal1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5301577	Cdkal1<sup>tm1.1Tomik</sup>/Cdkal1<sup>tm1.1Tomik</sup> Tg(Ins2-cre)25Mgn/0  [background:] B6.Cg-Cdkal1<sup>tm1.1Tomik</sup> Tg(Ins2-cre)25Mgn			ECO:0000033	author statement supported by traceable reference	PMID:21841312	20130415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3589869	Ndst1<sup>tm1Je</sup>/Ndst1<sup>tm1Je</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:24355925	20140507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448148	Tg(Msmb-TAg)183-2Xuan	is_implicated_in	DOID:10283	prostate cancer		MGI:3574636	Tg(Msmb-TAg)183-2Xuan/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12424611	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386182	Nphs1<sup>tm1Ktry</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3613052	Nphs1<sup>tm1Ktry</sup>/Nphs1<sup>tm1Ktry</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11136707	20060221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180159	Aldh5a1<sup>tm1Kmg</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:2654880	Aldh5a1<sup>tm1Kmg</sup>/Aldh5a1<sup>tm1Kmg</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15262267	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920230	Wdr11	is_implicated_in	DOID:3614	Kallmann syndrome		MGI:6162486	Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>/Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>  [background:] B6.Cg-Wdr11<sup>Gt(Ayu21-KBW205)Imeg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29263200	20180626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862040	Lim2<sup>To3</sup>	is_implicated_in	DOID:0110263	cataract 19 multiple types		MGI:2175102	Lim2<sup>To3</sup>/Lim2<sup>To3</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:9238094	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1862040	Lim2<sup>To3</sup>	is_implicated_in	DOID:0110263	cataract 19 multiple types		MGI:2175103	Lim2<sup>To3</sup>/Lim2<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:9238094	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341826	St6galnac1	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:7488220	St6galnac1<sup>em1Len</sup>/St6galnac1<sup>em1Len</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:35303419	20230608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5316003	Ezh2<sup>tm2Sho</sup>/Ezh2<sup>tm2.1Sho</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22431509	20120422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5316002	Ezh2<sup>tm2Sho</sup>/Ezh2<sup>tm2Sho</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22431509	20120422	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576788	Ncf1<sup>tm1Hbd</sup>	is_implicated_in	DOID:3265	chronic granulomatous disease		MGI:3590146	Ncf1<sup>tm1Hbd</sup>/Ncf1<sup>tm1Hbd</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:11733538	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4433255	Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0110127	Bardet-Biedl syndrome 5		MGI:6741540	Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>/Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6-Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33560420	20210820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914724	Snap29	is_implicated_in	DOID:0060337	CEDNIK syndrome		MGI:5812299	Snap29<sup>tm1b(EUCOMM)Wtsi</sup>/Snap29<sup>tm1b(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26747696	20161216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914724	Snap29	is_implicated_in	DOID:0060337	CEDNIK syndrome		MGI:5812300	Snap29<sup>tm1c(EUCOMM)Wtsi</sup>/Snap29<sup>tm1c(EUCOMM)Wtsi</sup> Tg(KRT14-cre)1Cgn/0  [background:] involves: C57BL/6 * C57BL/6N * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26747696	20161216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774282	Lrp5<sup>r18</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:3806486	Lrp5<sup>r18</sup>/Lrp5<sup>r18</sup>  [background:] C57BL/6J-Lrp5<sup>r18</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18263894	20120326	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2674095	Fanca<sup>tm1.1Wong</sup>	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A		MGI:3047099	Fanca<sup>tm1.1Wong</sup>/Fanca<sup>tm1.1Wong</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12913077	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920428	Wasl	is_implicated_in	DOID:3310	atopic dermatitis		MGI:6295452	Wasl<sup>tm1.1Ttha</sup>/Wasl<sup>tm1.1Ttha</sup> Tg(KRT14-cre)1Amc/0  [background:] involves: C57BL/6 * C57BL/6N * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28779153	20190501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039531	Tg(MMTV-Erbb2)17Pjo	is_implicated_in	DOID:1612	breast cancer		MGI:5604892	Tg(MMTV-Erbb2)17Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158947	Ece1<sup>tm1Reh</sup>	is_implicated_in	DOID:6406	double outlet right ventricle		MGI:3815024	Ece1<sup>tm1Reh</sup>/Ece1<sup>tm1Reh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10811845	20110509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87961	Agrn	is_implicated_in	DOID:0110657	congenital myasthenic syndrome 8		MGI:3614637	Agrn<sup>nmf380</sup>/Agrn<sup>nmf380</sup>  [background:] C57BL/6J-Agrn<sup>nmf380</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21890498	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675033	Rasgrp1<sup>lag</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2675118	Rasgrp1<sup>lag</sup>/Rasgrp1<sup>lag</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12932358	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842797	Tg(RP23-65I14)1Jno	is_implicated_in	DOID:1826	epilepsy		MGI:3842801	Tg(RP23-65I14)1Jno/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:19211869	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367773	Ahi1<sup>tm1Jgg</sup>	is_implicated_in	DOID:12712	nephronophthisis		MGI:4367783	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>tm1Jgg</sup> Tg(TCF/Lef1-lacZ)34Efu/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19718039	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584035	Rrn3<sup>tm1.1Igt</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6113542	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-cre/ERT2)1Span/0  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28360124	20180131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584035	Rrn3<sup>tm1.1Igt</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6113543	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-icre)9190Gsc/0  [background:] involves: 129/Sv * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21228155	20180131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584035	Rrn3<sup>tm1.1Igt</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:6113542	Rrn3<sup>tm1.1Igt</sup>/Rrn3<sup>tm1.1Igt</sup> Tg(Slc6a3-cre/ERT2)1Span/0  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21228155	20180131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4345319	Aspm<sup>Gt(AA0137)Wtsi</sup>	is_implicated_in	DOID:10907	microcephaly		MGI:4834526	Aspm<sup>Gt(AA0137)Wtsi</sup>/Aspm<sup>Gt(AA0137)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20823249	20101011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196458	Scarb2	is_implicated_in	DOID:891	progressive myoclonus epilepsy		MGI:5688743	Scarb2<sup>tm1Psa</sup>/Scarb2<sup>tm1Psa</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:25316793	20151001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88436	Cnga1	is_implicated_in	DOID:0110377	retinitis pigmentosa 49		MGI:7434657	Cnga1<sup>m1Mhda</sup>/Cnga1<sup>m1Mhda</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:36115851	20230215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604807	Npm1<sup>tm1Ppp</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:3606861	Npm1<sup>tm1Ppp</sup>/Npm1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16007073	20171027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913746	Ppdpf	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6739868	Ppdpf<sup>tm1Nju</sup>/Ppdpf<sup>tm1Nju</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:34031390	20210816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103291	Rai1	is_implicated_in	DOID:0060768	Smith-Magenis syndrome		MGI:3577939	Rai1<sup>tm1Jrl</sup>/Rai1<sup>+</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15746153	20170113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103291	Rai1	is_implicated_in	DOID:0060768	Smith-Magenis syndrome		MGI:4835032	Rai1<sup>tm1Jrl</sup>/Rai1<sup>+</sup>  [background:] B6.129S7-Rai1<sup>tm1Jrl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20663924	20170113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103291	Rai1	is_implicated_in	DOID:0060768	Smith-Magenis syndrome		MGI:5817471	Rai1<sup>tm2.1Luo</sup>/Rai1<sup>tm2.1Luo</sup> Tg(Nes-cre)1Kln/?  [background:] either: (involves: 129S1/Sv * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)			ECO:0000033	author statement supported by traceable reference	PMID:27693255	20170113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341085	Epm2a	is_implicated_in	DOID:3534	Lafora disease		MGI:3054886	Epm2a<sup>tm1Kzy</sup>/Epm2a<sup>tm1Kzy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12019206	20110826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341085	Epm2a	is_implicated_in	DOID:3534	Lafora disease		MGI:3054886	Epm2a<sup>tm1Kzy</sup>/Epm2a<sup>tm1Kzy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21493628	20110826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3622771	Fas<sup>lpr</sup>/Fas<sup>lpr</sup>  [background:] NOD.MRL(B6)-Fas<sup>lpr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10946317	20060526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857278	Aprt<sup>tm1Jat</sup>	is_implicated_in	DOID:0060350	adenine phosphoribosyltransferase deficiency		MGI:2449114	Aprt<sup>tm1Jat</sup>/Aprt<sup>tm1Jat</sup>  [background:] involves: 129S2/SvPas * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8643571	20120924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857278	Aprt<sup>tm1Jat</sup>	is_implicated_in	DOID:0060350	adenine phosphoribosyltransferase deficiency		MGI:2449115	Aprt<sup>tm1Jat</sup>/Aprt<sup>tm1Jat</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8643571	20120924	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107714	Dnah8	is_implicated_in	DOID:0112164	spermatogenic failure 46		MGI:6473984	Dnah8<sup>em1Osb</sup>/Dnah8<sup>em1Osb</sup>  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:32619401	20210118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861959	Kcna1<sup>tm1Tem</sup>	is_implicated_in	DOID:3328	temporal lobe epilepsy		MGI:3625870	Kcna1<sup>tm1Tem</sup>/Kcna1<sup>tm1Tem</sup>  [background:] C3Fe.129S7-Kcna1<sup>tm1Tem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24270080	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609047	Col4a5<sup>tm1Yseg</sup>	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610502	Col4a5<sup>tm1Yseg</sup>/Col4a5<sup>+</sup>  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23707242	20140709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609047	Col4a5<sup>tm1Yseg</sup>	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610503	Col4a5<sup>tm1Yseg</sup>/Y  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23707242	20140709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609047	Col4a5<sup>tm1Yseg</sup>	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610502	Col4a5<sup>tm1Yseg</sup>/Col4a5<sup>+</sup>  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15153557	20140709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609047	Col4a5<sup>tm1Yseg</sup>	is_implicated_in	DOID:0110034	X-linked Alport syndrome		MGI:3610503	Col4a5<sup>tm1Yseg</sup>/Y  [background:] B6.Cg-Col4a5<sup>tm1Yseg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15153557	20140709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104572	Limk1	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:2679324	Limk1<sup>tm1Zpj</sup>/Limk1<sup>tm1Zpj</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:12123613	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3037820	Kcna10	is_implicated_in	DOID:3426	vestibular disease		MGI:5574086	Kcna10<sup>tm1Lex</sup>/Kcna10<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23528307	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	is_not_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:6378557	Best1<sup>tm2.1Web</sup>/Best1<sup>tm2.1Web</sup>  [background:] B6.129S1(Cg)-Best1<sup>tm2.1Web</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31201163	20191126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_implicated_in	DOID:2224	essential thrombocythemia		MGI:4836619	Jak2<sup>tm1(JAK2)Argr</sup>/Jak2<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20489053	20101028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3809668	Abca12<sup>tm1Shzu</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3809674	Abca12<sup>tm1Shzu</sup>/Abca12<sup>tm1Shzu</sup>  [background:] B6.129S-Abca12<sup>tm1Shzu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18632686	20081006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040254	Tg(OMP-SV40T)13Bse	is_implicated_in	DOID:769	neuroblastoma		MGI:5442284	Tg(OMP-SV40T)13Bse/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:7923140	20121120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:3715718	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15231697	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:3962	thyroid gland follicular carcinoma		MGI:3715723	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15231697	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103232	Grb10	is_not_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:2668444	Grb10<sup>Gt(Betageo)1Ward</sup>/Grb10<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12829789	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103232	Grb10	is_not_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:2668440	Grb10<sup>Gt(Betageo)1Ward</sup>/Grb10<sup>Gt(Betageo)1Ward</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12829789	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387402	Stk11<sup>tm1.1Rdp</sup>	is_implicated_in	DOID:1380	endometrial cancer		MGI:4438263	Stk11<sup>tm1.1Rdp</sup>/Stk11<sup>tm1.1Rdp</sup> Tg(Sprr2f-cre)1Dcas/0  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20142330	20100331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3688292	Cftr<sup>tm3Mrc</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3689381	Cftr<sup>tm3Mrc</sup>/Cftr<sup>tm3Mrc</sup>  [background:] B6.129S6-Cftr<sup>tm3Mrc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20061130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384029	Fgg<sup>tm1Fjc</sup>	is_implicated_in	DOID:2236	congenital afibrinogenemia		MGI:3662854	Fgg<sup>tm1Fjc</sup>/Fgg<sup>tm1Fjc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11891199	20061005	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6403356	Egfr<sup>Mhdadsk5</sup>/Egfr<sup>+</sup>  [background:] involves: 129S1/SvImJ * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:28404843	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2176849	Fgf8<sup>tm1.3Mrt</sup>/Fgf8<sup>tm1.4Mrt</sup> Tg(Msx2-cre)5Rem/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11101846	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183630	Itgb4<sup>tm1Efu</sup>	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:3836294	Itgb4<sup>tm1Efu</sup>/Itgb4<sup>tm1Efu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8707838	20090319	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667740	Mgat2<sup>tm1.1Jxm</sup>	is_implicated_in	DOID:0070253	congenital disorder of glycosylation type IIa		MGI:2667791	Mgat2<sup>tm1.1Jxm</sup>/Mgat2<sup>tm1.1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11805078	20190516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667740	Mgat2<sup>tm1.1Jxm</sup>	is_implicated_in	DOID:0070253	congenital disorder of glycosylation type IIa		MGI:2667777	Mgat2<sup>tm1.1Jxm</sup>/Mgat2<sup>tm1.1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11805078	20190516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87919	Add2	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:3664740	Add2<sup>tm1Llp</sup>/Add2<sup>tm1Llp</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10485892	20061026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181756	Atm<sup>tm1Mfl</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2181774	Atm<sup>tm1Mfl</sup>/Atm<sup>tm1Mfl</sup>  [background:] involves: 129T2/SvEms * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11389091	20050603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665236	Tpo<sup>R479C</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3698432	Tpo<sup>R479C</sup>/Tpo<sup>R479C</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:16762971	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97387	Nuca	is_implicated_in	DOID:83	cataract		MGI:2175193	Nuca/Nuca<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429760	Dvl2<sup>tm1Awb</sup>	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:2654555	Dvl2<sup>tm1Awb</sup>/Dvl2<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac-Dvl2<sup>tm1Awb</sup> or (involves: 129S6/SvEvTac * NIH Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14976138	20210927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99698	Clock	is_implicated_in	DOID:535	sleep disorder		MGI:4366720	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: C57BL/6 * C57BL/6J * Jcl:ICR			ECO:0000033	author statement supported by traceable reference	PMID:17445238	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690075	Tg(tetO-EGFR*L858R)57Hev	is_implicated_in	DOID:1324	lung cancer		MGI:3690090	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-EGFR*L858R)57Hev/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16705038	20150501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3610476	Mybl2<sup>tm1.1Jof</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:5518769	Mybl2<sup>tm1.1Jof</sup>/Mybl2<sup>+</sup> Tg(Zp3-cre)3Mrt/0  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22910183	20131120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	is_implicated_in	DOID:1595	melancholic depression		MGI:3707972	Disc1<sup>Rgsc1393</sup>/Disc1<sup>Rgsc1393</sup>  [background:] B6.Cg-Disc1<sup>Rgsc1393</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17481393	20070514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055492	Bbs4<sup>Gt1Nk</sup>	is_implicated_in	DOID:9970	obesity		MGI:3055585	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	is_implicated_in	DOID:1932	Angelman syndrome		MGI:3694359	Ube3a<sup>tm1Alb</sup>/Ube3a<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9808466	20160120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	is_implicated_in	DOID:1932	Angelman syndrome		MGI:3852128	Ube3a<sup>tm1Jwf</sup>/Ube3a<sup>+</sup>  [background:] B6.129S4-Ube3a<sup>tm1Jwf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11895368	20160120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	is_implicated_in	DOID:1932	Angelman syndrome		MGI:5704111	Ube3a<sup>tm1Yelg</sup>/Ube3a<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPasCrl			ECO:0000033	author statement supported by traceable reference	PMID:25866966	20160120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	is_implicated_in	DOID:1932	Angelman syndrome		MGI:5461654	Ube3a<sup>tm1Alb</sup>/Ube3a<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22916201	20160120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420970	Gadd45gip1<sup>tm2Kong</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5637560	Gadd45gip1<sup>tm2Kong</sup>/Gadd45gip1<sup>tm2Kong</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:25660120	20150528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934269	Trp63<sup>tm1Fmc</sup>	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:2174785	Trp63<sup>tm1Fmc</sup>/Trp63<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10227294	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196251	Casz1	is_implicated_in	DOID:0060410	chromosome 1p36 deletion syndrome		MGI:5904617	Casz1<sup>Gt(CJ0565)Wtsi</sup>/Casz1<sup>Gt(CJ0565)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25190801	20170714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653130	Krt14<sup>tm2Der</sup>	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:2653131	Krt14<sup>tm2Der</sup>/Krt14<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	is_implicated_in	DOID:0060242	synpolydactyly		MGI:2178096	Hoxd13<sup>tm1Ddu</sup>/Hoxd13<sup>tm1Ddu</sup>  [background:] either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8106170	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	is_implicated_in	DOID:0060242	synpolydactyly		MGI:3513188	Hoxd13<sup>tm1Mrc</sup>/Hoxd13<sup>tm1Mrc</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8620844	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	is_implicated_in	DOID:0060242	synpolydactyly		MGI:3587188	Hoxd13<sup>spdh</sup>/Hoxd13<sup>spdh</sup>  [background:] B6C3Fe a/a-Hoxd13<sup>spdh</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9580668	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	is_implicated_in	DOID:10754	otitis media		MGI:6102909	Fbxo11<sup>Jf</sup>/Fbxo11<sup>+</sup>  [background:] involves: BALB/cAnNCrl			ECO:0000033	author statement supported by traceable reference	PMID:20057387	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	is_implicated_in	DOID:10754	otitis media		MGI:3693665	Fbxo11<sup>Jf</sup>/Fbxo11<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeN * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17035249	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	is_implicated_in	DOID:10754	otitis media		MGI:3693680	Fbxo11<sup>Jf</sup>/Fbxo11<sup>Mutt</sup>  [background:] involves: BALB/c * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:17035249	20171218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814567	Kmt2a<sup>tm1Saam</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3814579	Kmt2a<sup>tm1Saam</sup>/Kmt2a<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18977325	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857942	Cdkn2a<sup>tm1Rdp</sup>	is_not_implicated_in	DOID:10041	dysplastic nevus syndrome		MGI:2175771	Cdkn2a<sup>tm1Rdp</sup>/Cdkn2a<sup>tm1Rdp</sup>  [background:] involves: 129/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8620534	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437562	Ush1c<sup>tm1Xzl</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:5751490	Ush1c<sup>tm1Xzl</sup>/Ush1c<sup>tm1Xzl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24725409	20160309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449180	Ercc8<sup>tm1Jhjh</sup>	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:5697079	Ercc8<sup>tm1Jhjh</sup>/Ercc8<sup>tm1Jhjh</sup>  [background:] B6J.129P2-Ercc8<sup>tm1Jhjh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25762674	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449180	Ercc8<sup>tm1Jhjh</sup>	is_implicated_in	DOID:2962	Cockayne syndrome		MGI:2663252	Ercc8<sup>tm1Jhjh</sup>/Ercc8<sup>tm1Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12509261	20151124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671844	skc3	is_implicated_in	DOID:11836	clubfoot		MGI:3027853	skc3/skc3  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12955145	20110125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178598	Bloc1s5	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178598	Bloc1s5	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3587678	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] involves: STOCK t			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	is_implicated_in	DOID:0110191	Charcot-Marie-Tooth disease type 4B1		MGI:3513600	Mtmr2<sup>tm1.1Abol</sup>/Mtmr2<sup>tm1.1Abol</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:15557122	20060224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	is_implicated_in	DOID:0110191	Charcot-Marie-Tooth disease type 4B1		MGI:3613518	Mtmr2<sup>tm1Ueli</sup>/Mtmr2<sup>tm1Ueli</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16249189	20060224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857310	Cdh23<sup>v-Alb</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:2654804	Cdh23<sup>v-Alb</sup>/Cdh23<sup>v-Alb</sup>  [background:] involves: C3H/HeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11138008	20090504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	is_implicated_in	DOID:3652	Leigh disease		MGI:6280686	Parl<sup>tm1.1Bdes</sup>/Parl<sup>tm1.1Bdes</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:30578322	20190228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	is_implicated_in	DOID:3652	Leigh disease		MGI:6280694	Parl<sup>tm1Bdes</sup>/Parl<sup>tm1Bdes</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:30578322	20190228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:4928	intrahepatic cholangiocarcinoma		MGI:5428897	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:22266220	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4457372	Tcap<sup>tm1Mkc</sup>	is_implicated_in	DOID:0110281	autosomal recessive limb-girdle muscular dystrophy type 2G		MGI:4457377	Tcap<sup>tm1Mkc</sup>/Tcap<sup>tm1Mkc</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20233748	20100701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3805034	Hps5<sup>ru2-mr</sup>/Hps5<sup>ru2-mr</sup>  [background:] B6.Cg-Hps5<sup>ru2-mr</sup>/Re			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2174727	Hps5<sup>ru2-mr</sup>/Hps5<sup>ru2-mr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	is_implicated_in	DOID:0050848	obstructive sleep apnea		MGI:6509439	Bmp7<sup>tm1.1Dgra</sup>/Bmp7<sup>tm1.1Dgra</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:33431521	20210310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152545	srt	is_implicated_in	DOID:0050592	asphyxiating thoracic dystrophy		MGI:2181881	srt/srt  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579432	Fkbp4<sup>tm1Dvds</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3583221	Fkbp4<sup>tm1Dvds</sup>/Fkbp4<sup>tm1Dvds</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15831525	20050809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	is_implicated_in	DOID:10591	pre-eclampsia		MGI:5823026	Ido1<sup>tm1.1Mkks</sup>/Ido1<sup>tm1.1Mkks</sup>  [background:] B6.Cg-Ido1<sup>tm1.1Mkks</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25602015	20170201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857344	Sod2<sup>tm1Cje</sup>	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929511	Ndufa1	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:6187936	Ndufa1<sup>tm1.1Nay</sup>/Ndufa1<sup>tm1.1Nay</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJaeSor * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:28506826	20180712	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	is_not_implicated_in	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type		MGI:6358542	Eftud2<sup>em1Lajm</sup>/Eftud2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31276534	20190906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	is_not_implicated_in	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type		MGI:6358540	Eftud2<sup>em2Lajm</sup>/Eftud2<sup>+</sup>  [background:] involves: CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31276534	20190906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107181	Slc26a3	is_implicated_in	DOID:0060296	congenital secretory chloride diarrhea 1		MGI:3697730	Slc26a3<sup>tm1Sole</sup>/Slc26a3<sup>tm1Sole</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17001077	20070226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97578	Phkb	is_implicated_in	DOID:0111041	glycogen storage disease IXb		MGI:6263156	Phkb<sup>em1(IMPC)J</sup>/Phkb<sup>+</sup>  [background:] C57BL/6NJ-Phkb<sup>em1(IMPC)J</sup>/Mmjax			ECO:0000033	author statement supported by traceable reference	PMID:36077341	20221108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4818928	Dnm1l<sup>Py</sup>/Dnm1l<sup>+</sup>  [background:] involves: BALB/cAnNCrl * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:20585624	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785744	Gt(ROSA)26Sor<sup>tm1(Tgfbr1*)Crm</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:3789306	Gt(ROSA)26Sor<sup>tm1(Tgfbr1*)Crm</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17195237	20080527	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182067	Tg(NFH)120Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2183662	Tg(NFH)120Jpj/Tg(NFH)120Jpj  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182067	Tg(NFH)120Jpj	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:2183668	Tg(NFH)120Jpj/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8462101	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277968	Cavin1	is_implicated_in	DOID:0111138	congenital generalized lipodystrophy type 4		MGI:3829009	Cavin1<sup>tm1Pfp</sup>/Cavin1<sup>tm1Pfp</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19546242	20100614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0111013	cone-rod dystrophy 3		MGI:3820396	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	is_implicated_in	DOID:0111013	cone-rod dystrophy 3		MGI:3697458	Abca4<sup>tm1Ght</sup>/Abca4<sup>tm1Ght</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:18515570	20081217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848928	Dlg4<sup>tm2.1Grnt</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5295223	Dlg4<sup>tm2.1Grnt</sup>/Dlg4<sup>tm2.1Grnt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20952458	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	is_not_implicated_in	DOID:10652	Alzheimer's disease		MGI:2177097	Psen1<sup>tm1Psgh</sup>/Psen1<sup>tm1Psgh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10962005	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857411	Rbpj<sup>tm1Kyo</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:6236251	Rbpj<sup>tm1Kyo</sup>/Rbpj<sup>+</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21493891	20181108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:4452344	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15219458	20130417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047403	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8613481	20130417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047402	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7663509	20130417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	is_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047403	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7663509	20130417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100511	Myt1l	is_implicated_in	DOID:0070069	autosomal dominant intellectual developmental disorder 39		MGI:7328859	Myt1l<sup>em1Mwer</sup>/Myt1l<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35538503	20220811	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100511	Myt1l	is_implicated_in	DOID:0070069	autosomal dominant intellectual developmental disorder 39		MGI:7265077	Myt1l<sup>em1Jdd</sup>/Myt1l<sup>+</sup>  [background:] C57BL/6-Myt1l<sup>em1Jdd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:34614421	20220811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814339	Slc2a10<sup>S150F</sup>	is_not_implicated_in	DOID:0050645	arterial tortuosity syndrome		MGI:3814342	Slc2a10<sup>S150F</sup>/Slc2a10<sup>S150F</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:18693279	20081110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	is_implicated_in	DOID:9970	obesity		MGI:3579026	Mc4r<sup>tm1Dhu</sup>/Mc4r<sup>tm1Dhu</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9019399	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603539	Dido1<sup>tm1Cmar</sup>	is_implicated_in	DOID:4972	myelodysplastic/myeloproliferative neoplasm		MGI:3604722	Dido1<sup>tm1Cmar</sup>/Dido1<sup>tm1Cmar</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16127461	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099809	Fgf10	is_implicated_in	DOID:0050331	lacrimoauriculodentodigital syndrome 1		MGI:5816495	Fgf10<sup>tm1Wss</sup>/Fgf10<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:27590203	20170104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861800	Pak2<sup>Gt(OST104058)Lex</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6294052	Pak2<sup>Gt(OST104058)Lex</sup>/Pak2<sup>+</sup>  [background:] B6;129S5-Pak2<sup>Gt(OST104058)Lex</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:30134165	20190423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178357	Mitf<sup>Rorp</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686997	Mitf<sup>Rorp</sup>/Mitf<sup>Rorp</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178357	Mitf<sup>Rorp</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2686998	Mitf<sup>Rorp</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604506	Avpr1a<sup>tm1Dgen</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3606580	Avpr1a<sup>tm1Dgen</sup>/Avpr1a<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857446	Plp1<sup>tm1Kan</sup>	is_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:3620242	Plp1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857446	Plp1<sup>tm1Kan</sup>	is_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:3620242	Plp1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9616125	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604206	Sgce<sup>tm1Ygl</sup>	is_implicated_in	DOID:0090034	myoclonic dystonia 11		MGI:3618238	Sgce<sup>tm1Ygl</sup>/Sgce<sup>tm1Ygl</sup>  [background:] involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16099459	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604206	Sgce<sup>tm1Ygl</sup>	is_implicated_in	DOID:0090034	myoclonic dystonia 11		MGI:5308942	Sgce<sup>tm1Ygl</sup>/Sgce<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:22040906	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617977	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup>  [background:] C.129S2-Stat4<sup>tm1Gru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15596856	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617976	Stat4<sup>tm1Gru</sup>/Stat4<sup>+</sup>  [background:] NOD.129S2-Stat4<sup>tm1Gru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15041039	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3800574	Tomt<sup>m1Btlr</sup>	is_implicated_in	DOID:0110515	autosomal recessive nonsyndromic deafness 63		MGI:3805735	Tomt<sup>m1Btlr</sup>/Tomt<sup>m1Btlr</sup>  [background:] C57BL/6J-Tomt<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18794526	20081003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612339	Pkd1<sup>tm1Ggg</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:3617386	Pkd1<sup>tm1Ggg</sup>/Pkd1<sup>tm1Ggg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12007403	20060323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652553	Plcb1<sup>tm1Hssh</sup>/Plcb1<sup>tm1Hssh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9305844	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180390	Sim1<sup>tm1Fan</sup>	is_implicated_in	DOID:9970	obesity		MGI:3036852	Sim1<sup>tm1Fan</sup>/Sim1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11448938	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	is_implicated_in	DOID:0060246	MASA syndrome		MGI:3624801	L1cam<sup>tm1Mtei</sup>/Y  [background:] either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)			ECO:0000033	author statement supported by traceable reference	PMID:9354804	20081114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861779	Acvr2a<sup>tm1Zuk</sup>	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:2450541	Acvr2a<sup>tm1Zuk</sup>/Acvr2a<sup>tm1Zuk</sup>  [background:] either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7885474	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712964	Hspg2<sup>tm1.1Rdgr</sup>	is_implicated_in	DOID:0090005	Schwartz-Jampel syndrome 1		MGI:3713117	Hspg2<sup>tm1.1Rdgr</sup>/Hspg2<sup>tm1.1Rdgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17213231	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98289	Scg5	is_implicated_in	DOID:3946	pituitary-dependent Cushing's disease		MGI:3037127	Scg5<sup>tm1Led</sup>/Scg5<sup>tm1Led</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * FVB) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12021197	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849832	Tg(Lck-Tnfsf14)24Yxf	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:3849839	Tg(Lck-Tnfsf14)24Yxf/?  [background:] C57BL/6-Tg(Lck-Tnfsf14)24Yxf			ECO:0000033	author statement supported by traceable reference	PMID:15067315	20190612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:289	endometriosis		MGI:4836591	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C3H/HeJ)			ECO:0000033	author statement supported by traceable reference	PMID:15619626	20101028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934273	Prnp<sup>tm1Rcm</sup>	is_not_implicated_in	DOID:0050433	fatal familial insomnia		MGI:2174712	Prnp<sup>tm1Rcm</sup>/Prnp<sup>tm1Rcm</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Rcm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9462739	20050711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	is_implicated_in	DOID:0111114	nephronophthisis 3		MGI:3809288	Nphp3<sup>pcy</sup>/Nphp3<sup>tm1Cbe</sup>  [background:] involves: C57BL/6 * CD-1 * KK/Upj			ECO:0000033	author statement supported by traceable reference	PMID:18371931	20081002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	is_implicated_in	DOID:0111114	nephronophthisis 3		MGI:3583125	Nphp3<sup>pcy</sup>/Nphp3<sup>pcy</sup>  [background:] involves: KK			ECO:0000033	author statement supported by traceable reference	PMID:12872122	20081002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817487	Tg(ACTA1-FRG1)medRotu	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:3817493	Tg(ACTA1-FRG1)medRotu/0  [background:] C57BL/6-Tg(ACTA1-FRG1)medRotu			ECO:0000033	author statement supported by traceable reference	PMID:16341202	20081124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609205	Cacng8<sup>tm1Ran</sup>	is_implicated_in	DOID:10939	antisocial personality disorder		MGI:7256634	Cacng8<sup>tm1Ran</sup>/Cacng8<sup>tm1Ran</sup>  [background:] C57BL/6-Cacng8<sup>tm1Ran</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34099816	20220324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609205	Cacng8<sup>tm1Ran</sup>	is_implicated_in	DOID:10939	antisocial personality disorder		MGI:7256635	Cacng8<sup>tm1Ran</sup>/Cacng8<sup>+</sup>  [background:] C57BL/6-Cacng8<sup>tm1Ran</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34099816	20220324	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388605	Gdi1<sup>tm1Toni</sup>	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:3833428	Gdi1<sup>tm1Toni</sup>/Y  [background:] B6N.129S7-Gdi1<sup>tm1Toni</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18829665	20131021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88525	Cryge	is_implicated_in	DOID:83	cataract		MGI:2175810	Cryge<sup>Aey1</sup>/Cryge<sup>+</sup>  [background:] C3HeB/FeJ-Cryge<sup>Aey1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10932192	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88525	Cryge	is_implicated_in	DOID:83	cataract		MGI:2175809	Cryge<sup>Aey1</sup>/Cryge<sup>Aey1</sup>  [background:] C3HeB/FeJ-Cryge<sup>Aey1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10932192	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446577	Ccn1<sup>tm1Lfl</sup>	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:4834658	Ccn1<sup>tm1Lfl</sup>/Ccn1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17023674	20101013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2181763	Hps6	is_implicated_in	DOID:0060544	Hermansky-Pudlak syndrome 6		MGI:3805518	Hps6<sup>ru-6J</sup>/Hps6<sup>ru-6J</sup>  [background:] involves: C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860087	Tnfrsf1b<sup>tm1Imx</sup>	is_not_implicated_in	DOID:13809	familial combined hyperlipidemia		MGI:2175020	Tnfrsf1b<sup>tm1Imx</sup>/Tnfrsf1b<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9551933	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	is_not_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:3623773	Kcnq1<sup>tm1Apf</sup>/Kcnq1<sup>tm1Apf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11120752	20060605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039783	Ctnnb1<sup>tm1(Nfkbia)Rsu</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3706574	Ctnnb1<sup>tm1(Nfkbia)Rsu</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11585809	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2451059	Gusb<sup>tm1Sly</sup>	is_implicated_in	DOID:12803	Sly syndrome		MGI:2451063	Gusb<sup>tm1Sly</sup>/Gusb<sup>tm1Sly</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12403825	20090805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4397569	Col10a1<sup>tm1.1Rpbh</sup>	is_implicated_in	DOID:0080021	Schmid metaphyseal chondrodysplasia		MGI:4397575	Col10a1<sup>tm1.1Rpbh</sup>/Col10a1<sup>tm1.1Rpbh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19834559	20091201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3870873	Casz1<sup>Gt(CJ0565)Wtsi</sup>	is_implicated_in	DOID:0060410	chromosome 1p36 deletion syndrome		MGI:5904617	Casz1<sup>Gt(CJ0565)Wtsi</sup>/Casz1<sup>Gt(CJ0565)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25190801	20170714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	is_implicated_in	DOID:0070241	primary coenzyme Q10 deficiency 4		MGI:6359449	Coq8a<sup>tm1.1Ics</sup>/Coq8a<sup>tm1.1Ics</sup>  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27499294	20190911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447146	Tg(Thy1-APP)3Somm	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:2652447	Tg(Thy1-APP)3Somm/0  [background:] involves: C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:11222652	20101005	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99907	Plod1	is_implicated_in	DOID:13359	Ehlers-Danlos syndrome		MGI:3712759	Plod1<sup>tm1Soin</sup>/Plod1<sup>tm1Soin</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17197443	20121106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856656	Rab27a<sup>ash</sup>	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:5505710	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] C3H/HeSn-Rab27a<sup>ash</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12070017	20130912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99569	S1pr2	is_implicated_in	DOID:0110519	autosomal recessive nonsyndromic deafness 68		MGI:6277930	S1pr2<sup>stdf</sup>/S1pr2<sup>stdf</sup>  [background:] involves: C57BL/6Brd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27383011	20190212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99569	S1pr2	is_implicated_in	DOID:0110519	autosomal recessive nonsyndromic deafness 68		MGI:3692665	S1pr2<sup>tm1Ajml</sup>/S1pr2<sup>tm1Ajml</sup>  [background:] either: (involves: 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:26805784	20190212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277968	Cavin1	is_implicated_in	DOID:6432	pulmonary hypertension		MGI:5614325	Cavin1<sup>tm1Pfp</sup>/Cavin1<sup>tm1Pfp</sup>  [background:] B6.129S6-Cavin1<sup>tm1Pfp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24303100	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857871	Hoxd13<sup>tm1Ddu</sup>	is_implicated_in	DOID:0060242	synpolydactyly		MGI:2178096	Hoxd13<sup>tm1Ddu</sup>/Hoxd13<sup>tm1Ddu</sup>  [background:] either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8106170	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387406	Dhcr7<sup>tm1Gst</sup>	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3620629	Dhcr7<sup>tm1Gst</sup>/Dhcr7<sup>tm1Gst</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11560960	20060428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773717	Myocd<sup>tm1Msp</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907042	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19850880	20170816	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773717	Myocd<sup>tm1Msp</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907041	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129/Sv * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19850880	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890596	Evc	is_implicated_in	DOID:12714	Ellis-Van Creveld syndrome		MGI:3721945	Evc<sup>tm1Jago</sup>/Evc<sup>tm1Jago</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17660199	20070918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105311	Efs	is_implicated_in	DOID:8778	Crohn's disease		MGI:3611467	Efs<sup>tm1Kale</sup>/Efs<sup>tm1Kale</sup>  [background:] either: (involves: 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:16314525	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856412	Cdh23<sup>v-J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3722083	Cdh23<sup>v-J</sup>/Cdh23<sup>v-J</sup>  [background:] B6.C-H2-K<sup>bm1</sup>/ByJ			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856099	Atp7a<sup>Mo-dp</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:5696613	Atp7a<sup>Mo-dp</sup>/Atp7a<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:25456742	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856099	Atp7a<sup>Mo-dp</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:5696621	Atp7a<sup>Mo-dp</sup>/Y  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:25456742	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87867	Acadm	is_implicated_in	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency		MGI:3693216	Acadm<sup>tm1Uab</sup>/Acadm<sup>tm1Uab</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16121256	20070111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857868	Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>	is_implicated_in	DOID:3490	Noonan syndrome		MGI:3588510	Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>/Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:9753320	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3610476	Mybl2<sup>tm1.1Jof</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5518769	Mybl2<sup>tm1.1Jof</sup>/Mybl2<sup>+</sup> Tg(Zp3-cre)3Mrt/0  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22910183	20131120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888983	Lepr<sup>Tg(Mth11)1Aig</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2175101	Lepr<sup>Tg(Mth11)1Aig</sup>/Lepr<sup>Tg(Mth11)1Aig</sup>  [background:] involves: Him:OF1			ECO:0000033	author statement supported by traceable reference	PMID:10708583	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354162	Srr<sup>rgsc1872</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:4354165	Srr<sup>rgsc1872</sup>/Srr<sup>rgsc1872</sup>  [background:] C57BL/6JJcl-Srr<sup>rgsc1872</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19483194	20090820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	is_implicated_in	DOID:1062	Fanconi syndrome		MGI:3790867	Lrp2<sup>tm1Her</sup>/Lrp2<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10514418	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9279	hyperhomocysteinemia		MGI:6448986	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15622513	20220602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857139	Cbs<sup>tm1Unc</sup>	is_implicated_in	DOID:9279	hyperhomocysteinemia		MGI:6448988	Cbs<sup>tm1Unc</sup>/Cbs<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15622513	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	is_implicated_in	DOID:10763	hypertension		MGI:3525012	Nppa<sup>tm1Unc</sup>/Nppa<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7839143	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	is_implicated_in	DOID:10763	hypertension		MGI:3525013	Nppa<sup>tm1Unc</sup>/Nppa<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7839143	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096368	Ap1b1	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5433329	Ap1b1<sup>b2b1660Clo</sup>/Ap1b1<sup>b2b1660Clo</sup>  [background:] C57BL/6J-Ap1b1<sup>b2b1660Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617352	Tuba1a<sup>Jna</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:3698561	Tuba1a<sup>Jna</sup>/Tuba1a<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:17218254	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181719	Gdf1<sup>tm1Sjl</sup>	is_implicated_in	DOID:0060850	annular pancreas		MGI:3625848	Gdf1<sup>tm1Sjl</sup>/Gdf1<sup>tm1Sjl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10700179	20081215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351648	Magel2	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:5781308	Magel2<sup>tm1Stw</sup>/Magel2<sup>tm1Stw</sup>  [background:] C57BL/6-Magel2<sup>tm1Stw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27436578	20160725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351648	Magel2	is_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3834842	Magel2<sup>tm1Stw</sup>/Magel2<sup>+</sup>  [background:] C57BL/6-Magel2<sup>tm1Stw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19172181	20160725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103156	Gabrg1	is_implicated_in	DOID:12098	trigeminal neuralgia		MGI:6506871	Gabrg1<sup>em1Ktka</sup>/Gabrg1<sup>em1Ktka</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33083721	20210217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388899	Nppc<sup>lbab</sup>	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:3707539	Nppc<sup>lbab</sup>/Nppc<sup>lbab</sup>  [background:] B6.PL-Nppc<sup>lbab</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:22271248	20220512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491159	b2b2025Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5555835	b2b2025Clo/b2b2025Clo  [background:] C57BL/6J-b2b2025Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	is_implicated_in	DOID:0110936	nemaline myopathy 5A		MGI:5697946	Tnnt1<sup>tm1.2Jin</sup>/Tnnt1<sup>tm1.2Jin</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24445317	20151203	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	is_implicated_in	DOID:0111330	combined saposin deficiency		MGI:3711319	Psap<sup>tm1Suz</sup>/Psap<sup>tm1Suz</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8776585	20200724	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4417904	Junb<sup>tm3Wag</sup>/Junb<sup>tm3Wag</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: 129/Sv * 129P2/OlaHsd * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19918056	20100115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662152	Mitf<sup>mi-x</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923457	Tmem98	is_not_implicated_in	DOID:0080634	nanophthalmos		MGI:7520868	Tmem98<sup>em1Siggs</sup>/Tmem98<sup>em1Siggs</sup>  [background:] C57BL/6J-Tmem98<sup>em1Siggs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37419942	20230828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657000	Ahr<sup>tm1Yfk</sup>	is_implicated_in	DOID:9649	congenital nystagmus		MGI:2657002	Ahr<sup>tm1Yfk</sup>/Ahr<sup>tm1Yfk</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23301081	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922941	Anks6	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5465103	Anks6<sup>b2b1801.1Clo</sup>/Anks6<sup>b2b1801.1Clo</sup>  [background:] C57BL/6J-Anks6<sup>b2b1801.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338783	Pts	is_implicated_in	DOID:0090106	BH4-deficient hyperphenylalaninemia A		MGI:2669893	Pts<sup>tm1Ich</sup>/Pts<sup>tm1Ich</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11517215	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338783	Pts	is_implicated_in	DOID:0090106	BH4-deficient hyperphenylalaninemia A		MGI:2672965	Pts<sup>tm1Thny</sup>/Pts<sup>tm1Thny</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12734191	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931011	Trp53<sup>tm1Brn</sup>	is_implicated_in	DOID:1380	endometrial cancer		MGI:5604728	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:24930886	20141118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919757	Dzip1l	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:6107228	Dzip1l<sup>warpy</sup>/Dzip1l<sup>warpy</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28530676	20180102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919757	Dzip1l	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:6107229	Dzip1l<sup>warpy</sup>/Dzip1l<sup>warpy</sup>  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28530676	20180102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome		MGI:5543899	Tgfbr2<sup>tm1.1Hcd</sup>/Tgfbr2<sup>+</sup>  [background:] 129S6(Cg)-Tgfbr2<sup>tm1.1Hcd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24355923	20140212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386272	Chuk<sup>tm1Ver</sup>	is_implicated_in	DOID:0060647	fetal encasement syndrome		MGI:3609426	Chuk<sup>tm1Ver</sup>/Chuk<sup>tm1Ver</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038126	nm3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3038236	nm3/nm3  [background:] involves: RIIIS/J			ECO:0000033	author statement supported by traceable reference	PMID:14966677	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676366	Crb1<sup>rd8</sup>	is_implicated_in	DOID:0110079	Leber congenital amaurosis 8		MGI:3581037	Crb1<sup>rd8</sup>/Crb1<sup>rd8</sup>  [background:] STOCK Crb1<sup>rd8</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20089206	20110520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3702932	Slc6a3<sup>tm1(cre)Lrsn</sup>/Slc6a3<sup>+</sup> Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17227870	20110624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180178	Snap25<sup>tm1Mcw</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5774646	Snap25<sup>tm1Mcw</sup>/Snap25<sup>+</sup>  [background:] B6N.Cg-Snap25<sup>tm1Mcw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26300453	20161107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	is_implicated_in	DOID:0110838	Usher syndrome type 2A		MGI:3702269	Ush2a<sup>tm1Tili</sup>/Ush2a<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17360538	20070409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3608690	Ext2<sup>tm1Werb</sup>	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:3608784	Ext2<sup>tm1Werb</sup>/Ext2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16236767	20051230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3766089	Tg(COL1A1)73Prc	is_implicated_in	DOID:0110334	osteogenesis imperfecta type 1		MGI:3838157	Tg(COL1A1)73Prc/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:8432871	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820834	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] AK.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820833	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] C.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820830	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820832	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] B6.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4820831	Traf3ip2<sup>adjm</sup>/Traf3ip2<sup>adjm</sup>  [background:] A.KOR-Traf3ip2<sup>adjm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20660351	20100826	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	is_implicated_in	DOID:1929	supravalvular aortic stenosis		MGI:3620001	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] B6.129-Eln<sup>tm1Dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14597767	20060418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	is_implicated_in	DOID:1929	supravalvular aortic stenosis		MGI:3619994	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9819363	20060418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3622101	Ldlr<sup>Hlb301</sup>/Ldlr<sup>Hlb301</sup>  [background:] C57BL/6J-Ldlr<sup>Hlb301</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:2656149	20120221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3622102	Ldlr<sup>Hlb301</sup>/Ldlr<sup>+</sup>  [background:] C57BL/6J-Ldlr<sup>Hlb301</sup>/J			ECO:0000033	author statement supported by traceable reference	MGI:2656149	20120221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3611043	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15472122	20120221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	is_implicated_in	DOID:13810	familial hypercholesterolemia		MGI:3691620	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12746448	20120221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:7390396	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8934515	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:590190	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6194978	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	is_implicated_in	DOID:9406	hypopituitarism		MGI:3042606	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] STOCK Prop1<sup>df</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14173795	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	is_implicated_in	DOID:9406	hypopituitarism		MGI:3521856	Prop1<sup>df</sup>/Prop1<sup>df</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15459176	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769258	Galnt1<sup>tm1.1Jxm</sup>	is_implicated_in	DOID:4079	heart valve disease		MGI:3769260	Galnt1<sup>tm1.1Jxm</sup>/Galnt1<sup>tm1.1Jxm</sup>  [background:] B6NHsd.Cg-Galnt1<sup>tm1.1Jxm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25615642	20190715	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270850	Slc6a2	is_implicated_in	DOID:10273	heart conduction disease		MGI:5516191	Slc6a2<sup>tm1.1Mkh</sup>/Slc6a2<sup>+</sup>  [background:] B6.129S6-Slc6a2<sup>tm1.1Mkh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23580201	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579521	Col4a1<sup>deltaex40</sup>	is_implicated_in	DOID:0060263	porencephaly		MGI:3579768	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] B6.129S-Col4a1<sup>deltaex40</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15905400	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097165	Nrg3	is_implicated_in	DOID:5419	schizophrenia		MGI:6283412	Nrg3<sup>tm1.1Plet</sup>/Nrg3<sup>tm1.1Plet</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27606322	20190318	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101932	Cpe	is_implicated_in	DOID:9970	obesity		MGI:3033164	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] involves: HRS/J			ECO:0000033	author statement supported by traceable reference	MGI:61833	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101932	Cpe	is_implicated_in	DOID:9970	obesity		MGI:3033164	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] involves: HRS/J			ECO:0000033	author statement supported by traceable reference	PMID:2250094	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101932	Cpe	is_implicated_in	DOID:9970	obesity		MGI:3033165	Cpe<sup>fat</sup>/Cpe<sup>fat</sup>  [background:] BKSChpLt.HRS-Cpe<sup>fat</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:2250094	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3579508	Park7<sup>tm1Shn</sup>/Park7<sup>tm1Shn</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15721235	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3576369	Park7<sup>tm1Dsp</sup>/Park7<sup>tm1Dsp</sup>  [background:] B6.129P2-Park7<sup>tm1Dsp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23019375	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3604390	Park7<sup>tm1Xz</sup>/Park7<sup>tm1Xz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15799973	20150303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3833851	Park7<sup>tm1Cai</sup>/Park7<sup>tm1Cai</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18187333	20150303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412026	Pla2g6<sup>m1J</sup>	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:5317923	Pla2g6<sup>m1J</sup>/Pla2g6<sup>m1J</sup>  [background:] C3H/HeJ-Pla2g6<sup>m1J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22442204	20120516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612427	Mtmr2<sup>tm1Ueli</sup>	is_implicated_in	DOID:0110191	Charcot-Marie-Tooth disease type 4B1		MGI:3613518	Mtmr2<sup>tm1Ueli</sup>/Mtmr2<sup>tm1Ueli</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16249189	20060224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919069	Kif23	is_not_implicated_in	DOID:0111399	congenital dyserythropoietic anemia type III		MGI:7522153	Kif23<sup>tm1.1Igo</sup>/Kif23<sup>tm1.1Igo</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:32818800	20230829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919069	Kif23	is_not_implicated_in	DOID:0111399	congenital dyserythropoietic anemia type III		MGI:7522155	Kif23<sup>tm1.1Igo</sup>/Kif23<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:32818800	20230829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330818	Qsox1	is_implicated_in	DOID:14679	VACTERL association		MGI:5615576	Qsox1<sup>b2b2673Clo</sup>/Qsox1<sup>b2b2673Clo</sup>  [background:] C57BL/6J-Qsox1<sup>b2b2673Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443480	Setx	is_implicated_in	DOID:0060196	amyotrophic lateral sclerosis type 4		MGI:6883565	Setx<sup>tm1.1Als</sup>/Setx<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29725819	20220225	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2662716	Plau<sup>tm1Mlg</sup>/Plau<sup>tm1Mlg</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15615772	20070928	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135672	Lmod2	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5796293	Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>/Lmod2<sup>Tn(pb-Act-RFP)1.1Zhu</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27274810	20170818	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437115	Cep290<sup>b2b1454Clo</sup>/Cep290<sup>b2b1454Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1454Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5442145	Cep290<sup>b2b1752Clo</sup>/Cep290<sup>b2b1752Clo</sup>  [background:] C57BL/6J-Cep290<sup>b2b1752Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338036	Bpifa1	is_implicated_in	DOID:10754	otitis media		MGI:5558082	Bpifa1<sup>m1Ingm</sup>/Bpifa1<sup>m1Ingm</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:25765466	20151216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3857614	Mmachc<sup>Gt(AZ0348)Wtsi</sup>	is_implicated_in	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC		MGI:6107640	Mmachc<sup>Gt(AZ0348)Wtsi</sup>/Mmachc<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24889031	20180104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580072	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580092	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Hccs<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580072	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580087	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580072	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>	is_implicated_in	DOID:10629	microphthalmia		MGI:3580088	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577049	Tgif1<sup>tm1.1Caw</sup>	is_implicated_in	DOID:10754	otitis media		MGI:5516484	Tgif1<sup>tm1.1Caw</sup>/Tgif1<sup>tm1.1Caw</sup>  [background:] B6.129S-Tgif1<sup>tm1.1Caw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23459932	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926361	Foxn1<sup>tm1Tbo</sup>	is_implicated_in	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy		MGI:2175031	Foxn1<sup>tm1Tbo</sup>/Foxn1<sup>tm1Tbo</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8629026	20050701	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:9007	sudden infant death syndrome		MGI:5304714	Vhl<sup>tm1Jae</sup>/Vhl<sup>tm1Jae</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22977222	20131101	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856421	Dst<sup>Tg4</sup>	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:5577168	Dst<sup>Tg4</sup>/Dst<sup>Tg4</sup>  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24381311	20140814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577993	Jag1<sup>tm1Frad</sup>	is_implicated_in	DOID:9245	Alagille syndrome		MGI:5447166	Jag1<sup>tm1Frad</sup>/Jag1<sup>tm1Frad</sup> Tg(Cdh5-cre)7Mlia/0  [background:] B6.Cg-Jag1<sup>tm1Frad</sup> Tg(Cdh5-cre)7Mlia			ECO:0000033	author statement supported by traceable reference	PMID:23095891	20121231	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577993	Jag1<sup>tm1Frad</sup>	is_implicated_in	DOID:9245	Alagille syndrome		MGI:5447165	Jag1<sup>tm1Frad</sup>/Jag1<sup>tm1Frad</sup> Tg(Tagln-cre)1Her/0  [background:] B6.Cg-Jag1<sup>tm1Frad</sup> Tg(Tagln-cre)1Her			ECO:0000033	author statement supported by traceable reference	PMID:21062863	20121231	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2142810	Ppip5k2	is_implicated_in	DOID:0050563	nonsyndromic deafness		MGI:6198763	Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>/Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29590114	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929512	Litaf	is_implicated_in	DOID:0110151	Charcot-Marie-Tooth disease type 1C		MGI:6887866	Litaf<sup>tm1.1Cwc</sup>/Litaf<sup>tm1.1Cwc</sup>  [background:] B6.Cg-Litaf<sup>tm1.1Cwc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23576546	20220310	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857545	Cftr<sup>tm1Hsc</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177542	Cftr<sup>tm1Hsc</sup>/Cftr<sup>tm1Hsc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8589719	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344313	Zeb1	is_implicated_in	DOID:321	tropical spastic paraparesis		MGI:3812399	Zeb1<sup>tm1Yhi</sup>/Zeb1<sup>tm1Yhi</sup>  [background:] either: (involves: 129 * C3H * C57BL/6) or (involves: 129 * C57BL/6 * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:18467597	20081028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96701	Krt4	is_implicated_in	DOID:0050448	white sponge nevus		MGI:3695719	Krt4<sup>Bcc1</sup>/Krt4<sup>Bcc1</sup>  [background:] C3HeB/FeJ-Krt4<sup>Bcc1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16858417	20070206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96701	Krt4	is_implicated_in	DOID:0050448	white sponge nevus		MGI:3695720	Krt4<sup>Bcc1</sup>/Krt4<sup>+</sup>  [background:] C3HeB/FeJ-Krt4<sup>Bcc1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16858417	20070206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926875	Atm<sup>tm1Led</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175708	Atm<sup>tm1Led</sup>/Atm<sup>tm1Led</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8917548	20050603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685968	Ripply2	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:3764704	Ripply2<sup>tm1Asas</sup>/Ripply2<sup>tm1Asas</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17531978	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922870	Kxd1	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:5466156	Kxd1<sup>tm1Wli</sup>/Kxd1<sup>tm1Wli</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22554196	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860075	Ppt2	is_implicated_in	DOID:14503	neuronal ceroid lipofuscinosis		MGI:2176416	Ppt2<sup>tm1Hof</sup>/Ppt2<sup>tm1Hof</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11717424	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850849	Tg(Acta2-RAC1*G12V)33Pjgc	is_implicated_in	DOID:8632	Kaposi's sarcoma		MGI:3851237	Tg(Acta2-RAC1*G12V)33Pjgc/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19429708	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850849	Tg(Acta2-RAC1*G12V)33Pjgc	is_implicated_in	DOID:8632	Kaposi's sarcoma		MGI:3851236	Tg(Acta2-RAC1*G12V)33Pjgc/Tg(Acta2-RAC1*G12V)33Pjgc  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19429708	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831364	Fgfr3<sup>tm1.1Aomw</sup>	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831377	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] 129S6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831364	Fgfr3<sup>tm1.1Aomw</sup>	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831373	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] B6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831364	Fgfr3<sup>tm1.1Aomw</sup>	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831374	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] B6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831364	Fgfr3<sup>tm1.1Aomw</sup>	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831375	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] CBACa.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831364	Fgfr3<sup>tm1.1Aomw</sup>	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831378	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] 129S6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831364	Fgfr3<sup>tm1.1Aomw</sup>	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831376	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] CBACa.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5637814	Lgals3<sup>tm1Ftl</sup>/Lgals3<sup>tm1Ftl</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:18637146	20150601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5637814	Lgals3<sup>tm1Ftl</sup>/Lgals3<sup>tm1Ftl</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:17029217	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456205	Abhd5<sup>tm1.1Rze</sup>	is_implicated_in	DOID:0050729	Chanarin-Dorfman syndrome		MGI:5007482	Abhd5<sup>tm1.1Rze</sup>/Abhd5<sup>tm1.1Rze</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20023287	20110614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3702286	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] B6.C3-Ap3b1<sup>pe</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856989	Ap3b1<sup>pe</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2655702	Ap3b1<sup>pe</sup>/Ap3b1<sup>pe</sup>  [background:] involves: C3H/He			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682554	Slc6a5<sup>tm1Betz</sup>	is_implicated_in	DOID:0060698	hyperekplexia 3		MGI:2682556	Slc6a5<sup>tm1Betz</sup>/Slc6a5<sup>tm1Betz</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:14622583	20120514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	is_implicated_in	DOID:0111001	Joubert syndrome 6		MGI:5292226	Tmem67<sup>tm1Dgen</sup>/Tmem67<sup>tm1Dgen</sup>  [background:] B6.129P2-Tmem67<sup>tm1Dgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23283079	20131104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:7280898	Krt18<sup>tm1Tmm</sup>/Krt18<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27689336	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712284	Umod<sup>urehr4</sup>	is_implicated_in	DOID:557	kidney disease		MGI:3712576	Umod<sup>urehr4</sup>/Umod<sup>urehr4</sup>  [background:] C3HeB/FeJ-Umod<sup>urehr4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19692485	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858023	Cryaa<sup>lop18</sup>	is_implicated_in	DOID:0110266	cataract 9 multiple types		MGI:2175798	Cryaa<sup>lop18</sup>/Cryaa<sup>lop18</sup>  [background:] involves: CBA/CaGnLeJ			ECO:0000033	author statement supported by traceable reference	PMID:8812430	20130528	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3583907	Ins2<sup>Akita</sup>/Ins2<sup>+</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15914643	20060626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3583904	Ins2<sup>Akita</sup>/Ins2<sup>+</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9133560	20060626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:2361	macrocytic anemia		MGI:5912375	Kit<sup>W</sup>/Kit<sup>W</sup>  [background:] B6.Cg-Kit<sup>W</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:2361	macrocytic anemia		MGI:3840691	Kit<sup>W-v</sup>/Kit<sup>W-v</sup>  [background:] C57BL/6J-Kit<sup>W-v</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	is_implicated_in	DOID:2361	macrocytic anemia		MGI:3771729	Kit<sup>W</sup>/Kit<sup>W-v</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581675	Rc3h1<sup>san</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3582186	Rc3h1<sup>san</sup>/Rc3h1<sup>san</sup>  [background:] either: C57BL/6JSfdAnu-Rc3h1<sup>san</sup>/Anu or (involves: C57BL/6JSfdAnu * CBA/Ca)			ECO:0000033	author statement supported by traceable reference	PMID:15917799	20050721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444393	Zdhhc9	is_implicated_in	DOID:0060824	syndromic X-linked intellectual disability Raymond type		MGI:6315636	Zdhhc9<sup>tm1Lex</sup>/Y  [background:] B6.129S5-Zdhhc9<sup>tm1Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29944857	20190701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4436769	Nfil3<sup>tm1Pbro</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5576251	Nfil3<sup>tm1Pbro</sup>/Nfil3<sup>tm1Pbro</sup>  [background:] B6.129S6-Nfil3<sup>tm1Pbro</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24442434	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843171	Hbb<sup>tm1.1(HBG1,HBB*)Ryan</sup>	is_implicated_in	DOID:12241	beta thalassemia		MGI:3843172	Hbb<sup>tm1.1(HBG1,HBB*)Ryan</sup>/Hbb<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19098001	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604466	Ppm1g<sup>tm1Dgen</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3606460	Ppm1g<sup>tm1Dgen</sup>/Ppm1g<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855979	Tyr<sup>c-h</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5316479	Tyr<sup>c-h</sup>/Tyr<sup>c-h</sup>  [background:] B6.Cg-Tyr<sup>c-h</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21968110	20120426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109553	Ctsc	is_implicated_in	DOID:5419	schizophrenia		MGI:3606731	Ctsc<sup>tm1Dgen</sup>/Ctsc<sup>tm1Dgen</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:3604450	20051207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0050790	fibular hypoplasia and complex brachydactyly		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5620178	b2b2696Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5620189	b2b2696Clo/b2b2696Clo  [background:] C57BL/6J-b2b2696Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861640	Fancl<sup>gcd</sup>	is_implicated_in	DOID:14450	46 XX gonadal dysgenesis		MGI:2660751	Fancl<sup>gcd</sup>/Fancl<sup>gcd</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:8373945	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856102	Atp7a<sup>Mo-vbr</sup>	is_implicated_in	DOID:1838	Menkes disease		MGI:3793729	Atp7a<sup>Mo-vbr</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10098864	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5427014	Bscl2<sup>tm1.1Lchan</sup>/Bscl2<sup>tm1.1Lchan</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24358199	20161206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5014340	Bscl2<sup>tm1.2Gliu</sup>/Bscl2<sup>tm1.2Gliu</sup>  [background:] involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:21551454	20161206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5014340	Bscl2<sup>tm1.2Gliu</sup>/Bscl2<sup>tm1.2Gliu</sup>  [background:] involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24778225	20161206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:5519974	Bscl2<sup>tm1Geno</sup>/Bscl2<sup>tm1Geno</sup>  [background:] B6.129P2-Bscl2<sup>tm1Geno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23680914	20161206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152964	Col9a1<sup>tm1Jae</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3699108	Col9a1<sup>tm1Jae</sup>/Col9a1<sup>tm1Jae</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:11680679	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95543	Fkbp4	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3710989	Fkbp4<sup>tm1Shou</sup>/Fkbp4<sup>tm1Shou</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:17142810	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95543	Fkbp4	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3583221	Fkbp4<sup>tm1Dvds</sup>/Fkbp4<sup>tm1Dvds</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15831525	20070605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699224	Alms1<sup>L2131X</sup>	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:3700128	Alms1<sup>L2131X</sup>/Alms1<sup>L2131X</sup>  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:17206865	20080111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3702742	Wwtr1<sup>tm1Whun</sup>	is_implicated_in	DOID:12712	nephronophthisis		MGI:3703807	Wwtr1<sup>tm1Whun</sup>/Wwtr1<sup>tm1Whun</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:17251353	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311352	b2b1200Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137511	Crybb2<sup>Aey2</sup>	is_implicated_in	DOID:0110269	cataract 3 multiple types		MGI:2175803	Crybb2<sup>Aey2</sup>/Crybb2<sup>+</sup>  [background:] C3HeB/FeJ-Crybb2<sup>Aey2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11381063	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891340	Lpin1	is_implicated_in	DOID:811	lipodystrophy		MGI:3839539	Lpin1<sup>fld-2J</sup>/Lpin1<sup>fld-2J</sup>  [background:] C3H/HeJ-Lpin1<sup>fld-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11138012	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693364	Tg(PSEN1H163R)G9Btla	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3693491	Tg(PSEN1H163R)G9Btla/0  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10412057	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858054	Mlh1<sup>tm1Rak</sup>	is_implicated_in	DOID:3883	Lynch syndrome		MGI:2663863	Mlh1<sup>tm1Rak</sup>/Mlh1<sup>tm1Rak</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10096563	20091216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328361	Bard1	is_implicated_in	DOID:1612	breast cancer		MGI:3805029	Bard1<sup>tm2Thl</sup>/Bard1<sup>tm2Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129/Sv * 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18443292	20130918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328361	Bard1	is_implicated_in	DOID:1612	breast cancer		MGI:3805024	Bard1<sup>tm1Thl</sup>/Bard1<sup>tm2Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18443292	20130918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	is_implicated_in	DOID:0060543	Hermansky-Pudlak syndrome 5		MGI:2174726	Hps5<sup>ru2-J</sup>/Hps5<sup>ru2-J</sup>  [background:] C57BL/6J-Hps5<sup>ru2-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	is_implicated_in	DOID:0060543	Hermansky-Pudlak syndrome 5		MGI:4437300	Hps5<sup>ru2</sup>/Hps5<sup>ru2</sup>  [background:] involves: C57BL			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	is_implicated_in	DOID:0060543	Hermansky-Pudlak syndrome 5		MGI:2174725	Hps5<sup>ru2-hz</sup>/Hps5<sup>ru2-hz</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619134	Cdc42<sup>tm1Brak</sup>	is_implicated_in	DOID:0060775	microvillus inclusion disease		MGI:5427868	Cdc42<sup>tm1Brak</sup>/Cdc42<sup>tm1Brak</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22354172	20120713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	is_implicated_in	DOID:10581	metachromatic leukodystrophy		MGI:3802581	Psap<sup>tm2Ggb</sup>/Psap<sup>tm2Ggb</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18480170	20080818	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2450466	Il2<sup>tm1Hor</sup>/Il2<sup>tm1Hor</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8402910	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443065	Agps	is_implicated_in	DOID:0110853	rhizomelic chondrodysplasia punctata type 3		MGI:4949537	Agps<sup>bs2</sup>/Agps<sup>bs2</sup>  [background:] STOCK Agps<sup>bs2</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21353609	20120615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2144877	Spata7	is_implicated_in	DOID:0110331	Leber congenital amaurosis 3		MGI:6386739	Spata7<sup>tm1Mrd</sup>/Spata7<sup>tm2Mrd</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:29100828	20200129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2144877	Spata7	is_implicated_in	DOID:0110331	Leber congenital amaurosis 3		MGI:5660492	Spata7<sup>tm1Mrd</sup>/Spata7<sup>tm1Mrd</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:25398945	20200129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:6197758	Pomt1<sup>tm1c(EUCOMM)Hmgu</sup>/Pomt1<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Crx-cre)1Tfur/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29867208	20180912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:10486	intestinal atresia		MGI:2173367	Fgfr2<sup>tm1.1Dsn</sup>/Fgfr2<sup>tm1.1Dsn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15234214	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:2679083	Bmp4<sup>tm3.1Blh</sup>/Bmp4<sup>tm3.1Blh</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12975322	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:2679084	Bmp4<sup>tm1Blh</sup>/Bmp4<sup>tm3.1Blh</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: 129S/Sv * Black Swiss * C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:12975322	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917976	Angptl6	is_implicated_in	DOID:9970	obesity		MGI:3577766	Angptl6<sup>tm1Yo</sup>/Angptl6<sup>tm1Yo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15778720	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	is_implicated_in	DOID:5419	schizophrenia		MGI:3530450	Nrg1<sup>tm2Zhou</sup>/Nrg1<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12145742	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822132	Tg(Myh7-Ptpn11*Q79R)11Rbns	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:3822143	Tg(Myh7-Ptpn11*Q79R)11Rbns/0  [background:] FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns			ECO:0000033	author statement supported by traceable reference	PMID:17641779	20090105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183579	Mc3r<sup>tm1Cone</sup>	is_implicated_in	DOID:9970	obesity		MGI:3639355	Mc3r<sup>tm1Cone</sup>/Mc3r<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10965927	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183579	Mc3r<sup>tm1Cone</sup>	is_implicated_in	DOID:9970	obesity		MGI:3639354	Mc3r<sup>tm1Cone</sup>/Mc3r<sup>tm1Cone</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10965927	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	is_implicated_in	DOID:10871	age related macular degeneration		MGI:5586971	Cd46<sup>tm1Atk</sup>/Cd46<sup>tm1Atk</sup>  [background:] B6.129-Cd46<sup>tm1Atk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27295359	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386184	Pdcd1<sup>tm1Hon</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3054644	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] B6.129S2-Pdcd1<sup>tm1Hon</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10485649	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386184	Pdcd1<sup>tm1Hon</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3054643	Pdcd1<sup>tm1Hon</sup>/Pdcd1<sup>tm1Hon</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9796923	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448640	Rs1<sup>tmgc1</sup>	is_implicated_in	DOID:0060763	X-linked juvenile retinoschisis 1		MGI:2448896	Rs1<sup>tmgc1</sup>/Rs1<sup>tmgc1</sup>  [background:] involves: C3H/Rl * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16088326	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:3620242	Plp1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9616125	20180613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:6160757	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>/Y Cnp<sup>tm1(cre)Kan</sup>/Cnp<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:3620242	Plp1<sup>tm1Kan</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857347	Slc4a1<sup>wan</sup>	is_implicated_in	DOID:0110919	hereditary spherocytosis type 4		MGI:3027982	Slc4a1<sup>wan</sup>/Slc4a1<sup>wan</sup>  [background:] C3H/HeJ-Slc4a1<sup>wan</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15070709	20100315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769902	Scn5a<sup>tm1Care</sup>	is_implicated_in	DOID:0110646	long QT syndrome 3		MGI:3769904	Scn5a<sup>tm1Care</sup>/Scn5a<sup>+</sup>  [background:] FVB.129P2-Scn5a<sup>tm1Care</sup>/Care			ECO:0000033	author statement supported by traceable reference	PMID:17145985	20080206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4353799	Tg(Ckm-GSN*D187N)AJewe	is_implicated_in	DOID:0050637	Finnish type amyloidosis		MGI:4353803	Tg(Ckm-GSN*D187N)AJewe/Tg(Ckm-GSN*D187N)AJewe  [background:] C57BL/6J-Tg(Ckm-GSN*D187N)AJewe			ECO:0000033	author statement supported by traceable reference	PMID:19549824	20090819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4353799	Tg(Ckm-GSN*D187N)AJewe	is_implicated_in	DOID:0050637	Finnish type amyloidosis		MGI:4353802	Tg(Ckm-GSN*D187N)AJewe/0  [background:] C57BL/6J-Tg(Ckm-GSN*D187N)AJewe			ECO:0000033	author statement supported by traceable reference	PMID:19549824	20090819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915181	Serpini2	is_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:3767713	Serpini2<sup>pq</sup>/Serpini2<sup>pq</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16184191	20080117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522333	vsd	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3522715	vsd/vsd<sup>+</sup>  [background:] C57BL/6J-vsd			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522333	vsd	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3522714	vsd/vsd  [background:] C57BL/6J-vsd			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437091	b2b1200.2Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437106	b2b1200.2Clo/b2b1200.2Clo  [background:] C57BL/6J-b2b1200.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	is_implicated_in	DOID:0090144	Donnai-Barrow syndrome		MGI:4847969	Lrp2<sup>m267Asp</sup>/Lrp2<sup>m267Asp</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20653565	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890498	Mcoln1	is_implicated_in	DOID:0080490	mucolipidosis type IV		MGI:3795387	Mcoln1<sup>tm1Sasl</sup>/Mcoln1<sup>tm1Sasl</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17924347	20210121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437073	b2b1291Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437110	b2b1291Clo/b2b1291Clo  [background:] C57BL/6J-b2b1291Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2665316	Gucy2c<sup>tm1Gar</sup>	is_implicated_in	DOID:9970	obesity		MGI:5300906	Gucy2c<sup>tm1Gar</sup>/Gucy2c<sup>tm1Gar</sup>  [background:] B6.129S6-Gucy2c<sup>tm1Gar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21865642	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919595	Amer1	is_implicated_in	DOID:0060886	osteopathia striata with cranial sclerosis		MGI:5086009	Amer1<sup>tm1.1Nbar</sup>/Y Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21571217	20110815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919595	Amer1	is_implicated_in	DOID:0060886	osteopathia striata with cranial sclerosis		MGI:5086005	Amer1<sup>tm1.2Nbar</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21571217	20110815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857880	Pitx2<sup>tm1Kki</sup>	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:2170195	Pitx2<sup>tm1Kki</sup>/Pitx2<sup>tm1Kki</sup>  [background:] involves: 129P2/OlaHsd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:10572050	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3046798	Tbx1<sup>tm1Bld</sup>/Tbx1<sup>tm2Bld</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15175244	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3586912	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3587030	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3587029	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>tm1Bem</sup>  [background:] FVB.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15190012	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3587028	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11239417	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857227	Nos1<sup>tm1Plh</sup>	is_implicated_in	DOID:12638	hypertrophic pyloric stenosis		MGI:2174975	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7505721	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3617850	Pnpla1	is_implicated_in	DOID:0060719	autosomal recessive congenital ichthyosis 10		MGI:6286487	Pnpla1<sup>tm1a(KOMP)Wtsi</sup>/Pnpla1<sup>tm1a(KOMP)Wtsi</sup>  [background:] B6NTac;B6N-A<sup>tm1Brd</sup> Pnpla1<sup>tm1a(KOMP)Wtsi</sup>/Ics			ECO:0000033	author statement supported by traceable reference	PMID:28369476	20190409	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924461	Rarres1	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:7311758	Rarres1<sup>tm1d(KOMP)Wtsi</sup>/Rarres1<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924461	Rarres1	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:7311738	Rarres1<sup>tm1.2Mhl</sup>/Rarres1<sup>tm1.2Mhl</sup>  [background:] involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924461	Rarres1	is_implicated_in	DOID:0050873	follicular lymphoma		MGI:7311756	Rarres1<sup>tm1.2Mhl</sup>/Rarres1<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:35541897	20220713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5318689	Chrnb2<sup>tm1Jpc</sup>/Chrnb2<sup>tm1Jpc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12876201	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576026	hpld	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3576038	hpld/hpld  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776022	Flvcr1<sup>tm1.1Jlab</sup>	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:3807528	Flvcr1<sup>tm1.1Jlab</sup>/Flvcr1<sup>tm1.1Jlab</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18258918	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341817	Lgr5	is_implicated_in	DOID:0060604	ankyloglossia		MGI:3512741	Lgr5<sup>tm1Ah</sup>/Lgr5<sup>tm1Ah</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15509778	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	is_implicated_in	DOID:2377	multiple sclerosis		MGI:3707399	Prf1<sup>tm1Sdz</sup>/Prf1<sup>tm1Sdz</sup>  [background:] C57BL/6-Prf1<sup>tm1Sdz</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9736651	20070509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860434	Thrb<sup>tm1Df</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:2657251	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1Df</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8673137	20070306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860434	Thrb<sup>tm1Df</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:2657251	Thrb<sup>tm1Df</sup>/Thrb<sup>tm1Df</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8670802	20070306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856903	hph1	is_implicated_in	DOID:9281	phenylketonuria		MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:3360305	20060726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856903	hph1	is_implicated_in	DOID:9281	phenylketonuria		MGI:3639091	hph1/hph1  [background:] involves: C57BL/6 * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:15144277	20060726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	is_implicated_in	DOID:8398	osteoarthritis		MGI:3760091	Smad3<sup>tm1Cxd</sup>/Smad3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11285272	20090225	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10673499	20050926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6890374	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>+</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6890373	Prickle1<sup>em1Yzou</sup>/Prickle1<sup>em1Yzou</sup>  [background:] C57BL/6-Prickle1<sup>em1Yzou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34597683	20220317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	is_implicated_in	DOID:0111046	platelet-type bleeding disorder 10		MGI:3587412	Cd36<sup>tm1Mfe</sup>/Cd36<sup>tm1Mfe</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10383407	20050913	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278336	Cdkl5	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2		MGI:5574073	Cdkl5<sup>tm1.2Cogr</sup>/Cdkl5<sup>tm1.2Cogr</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24838000	20201218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1278336	Cdkl5	is_implicated_in	DOID:0080467	developmental and epileptic encephalopathy 2		MGI:5574074	Cdkl5<sup>tm1.2Cogr</sup>/Y  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24838000	20201218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721910	Tg(CMV-IgkvaD11)BCat	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5581429	Tg(CMV-IgkvaD11)BCat/Tg(CMV-IgkvaD11)BCat  [background:] involves: 129 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22986780	20140901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721910	Tg(CMV-IgkvaD11)BCat	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5578629	Tg(CMV-IgkvaD11)BCat/Tg(CMV-IgkvaD11)BCat  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20182028	20140901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443390	Lrch1	is_implicated_in	DOID:2377	multiple sclerosis		MGI:6140058	Lrch1<sup>em1Hwa</sup>/Lrch1<sup>em1Hwa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28028151	20180316	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	is_implicated_in	DOID:4184	pseudohypoparathyroidism		MGI:5818291	Gnas<sup>tm5.1Lsw</sup>/Gnas<sup>tm5.1Lsw</sup> Tg(Slc5a2-cre)1Tauc/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26671181	20170119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	is_implicated_in	DOID:12376	juvenile spinal muscular atrophy		MGI:4836985	Smn1<sup>tm1.1Dscd</sup>/Smn1<sup>tm1.1Dscd</sup>  [background:] involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20705738	20101102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384791	Slc26a7	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:4429560	Slc26a7<sup>tm1Sole</sup>/Slc26a7<sup>tm1Sole</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:30333321	20220614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2142523	Crtc1	is_implicated_in	DOID:1470	major depressive disorder		MGI:6098717	Crtc1<sup>Gt(XK522)Byg</sup>/Crtc1<sup>Gt(XK522)Byg</sup>  [background:] B6N.129P2-Crtc1<sup>Gt(XK522)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22592058	20171208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152376	Nrl<sup>tm1Asw</sup>	is_implicated_in	DOID:0090059	enhanced S-cone syndrome		MGI:5806540	Nrl<sup>tm1Asw</sup>/Nrl<sup>tm1Asw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21659555	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919815	Uaca	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:4430084	Uaca<sup>tm1Kiy</sup>/Uaca<sup>tm1Kiy</sup>  [background:] B6.129P2-Uaca<sup>tm1Kiy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19637241	20100224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052066	Slc29a1<sup>tm1Msg</sup>	is_implicated_in	DOID:6652	diffuse idiopathic skeletal hyperostosis		MGI:6256838	Slc29a1<sup>tm1Msg</sup>/Slc29a1<sup>tm1Msg</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27237608	20181119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665249	Gt(ROSA)26Sor<sup>tm1(MAML1)Wsp</sup>	is_implicated_in	DOID:12895	keratoconjunctivitis sicca		MGI:5512988	Gt(ROSA)26Sor<sup>tm1(MAML1)Wsp</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-cre)1Jaw/0  [background:] involves: 129 * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23293291	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842320	Atf2<sup>tm1Sis</sup>	is_implicated_in	DOID:11049	meconium aspiration syndrome		MGI:3842387	Atf2<sup>tm1Sis</sup>/Atf2<sup>tm1Sis</sup>  [background:] either: (involves: C57BL/6 * CBA) or (involves: BALB/c * C57BL/6 * CBA) or (involves: C57BL/6 * CBA * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:10364225	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443342	Pgap1	is_implicated_in	DOID:4621	holoprosencephaly		MGI:5432254	Pgap1<sup>m1Nisw</sup>/Pgap1<sup>m1Nisw</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23213481	20190927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102495	mt-Nd6	is_implicated_in	DOID:705	Leber hereditary optic neuropathy		MGI:5469320	mt-Nd6<sup>m3Dwa</sup>  [background:] B6.129S-mt-Nd6<sup>m3Dwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23129651	20130320	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:2652689	Csf2<sup>tm1Ard</sup>/Csf2<sup>tm1Ard</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8202532	20051207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3606654	Csf2<sup>tm1Mlg</sup>/Csf2<sup>tm1Mlg</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8171324	20051207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817312	Dym<sup>Gt(GTR1.3)1Rul</sup>	is_implicated_in	DOID:0060247	Smith-McCort dysplasia		MGI:3817313	Dym<sup>Gt(GTR1.3)1Rul</sup>/Dym<sup>Gt(GTR1.3)1Rul</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:18852472	20081120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4450989	Ppp1r14c<sup>tm1Uhl</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6433773	Ppp1r14c<sup>tm1Uhl</sup>/Ppp1r14c<sup>tm1Uhl</sup>  [background:] B6;129S6-Ppp1r14c<sup>tm1Uhl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27663205	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445864	Slc27a4<sup>wrfr</sup>	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:2662270	Slc27a4<sup>wrfr</sup>/Slc27a4<sup>wrfr</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12697906	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625620	Tnf<sup>tm2.1Gkl</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5558947	Tnf<sup>tm2.1Gkl</sup>/Tnf<sup>tm2.1Gkl</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129S/SvEv * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23977323	20170621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	is_implicated_in	DOID:1324	lung cancer		MGI:3719290	Xpc<sup>tm1Ecf</sup>/Xpc<sup>tm1Ecf</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16141330	20070827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104698	Lim2	is_implicated_in	DOID:0110263	cataract 19 multiple types		MGI:2175102	Lim2<sup>To3</sup>/Lim2<sup>To3</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:9238094	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104698	Lim2	is_implicated_in	DOID:0110263	cataract 19 multiple types		MGI:2175103	Lim2<sup>To3</sup>/Lim2<sup>+</sup>  [background:] involves: 102 * C3H/He * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:9238094	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511284	Lepr<sup>tm1.1Chua</sup>	is_implicated_in	DOID:9970	obesity		MGI:3511747	Lepr<sup>tm1.1Chua</sup>/Lepr<sup>tm1.1Chua</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15389315	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641232	Fbn1<sup>tm3Rmz</sup>	is_implicated_in	DOID:114	heart disease		MGI:3652414	Fbn1<sup>tm3Rmz</sup>/Fbn1<sup>tm3Rmz</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16407178	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341799	Ndrg1	is_implicated_in	DOID:0110186	Charcot-Marie-Tooth disease type 4D		MGI:7366893	Ndrg1<sup>em1Lxli</sup>/Ndrg1<sup>em1Lxli</sup>  [background:] C57BL/6N-Ndrg1<sup>em1Lxli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35708320	20221025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341799	Ndrg1	is_implicated_in	DOID:0110186	Charcot-Marie-Tooth disease type 4D		MGI:3043397	Ndrg1<sup>tm1Myta</sup>/Ndrg1<sup>tm1Myta</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15082788	20221025	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110341	osteogenesis imperfecta type 2		MGI:3769907	Col1a1<sup>Aga2</sup>/Col1a1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18248096	20080229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110341	osteogenesis imperfecta type 2		MGI:3623481	Col1a1<sup>tm1Jcm</sup>/Col1a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:10608859	20080229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933331	Elovl4	is_not_implicated_in	DOID:0050817	Stargardt disease		MGI:3664797	Elovl4<sup>tm1Sie</sup>/Elovl4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16877435	20061027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933331	Elovl4	is_not_implicated_in	DOID:0050817	Stargardt disease		MGI:3664796	Elovl4<sup>tm1Sie</sup>/Elovl4<sup>tm1Sie</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16877435	20061027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5555837	Ccdc39<sup>b2b2025.1Clo</sup>/Ccdc39<sup>b2b2025.1Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b2025.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5316790	Ccdc39<sup>b2b1304Clo</sup>/Ccdc39<sup>b2b1304Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1304Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5445973	Ccdc39<sup>b2b1735Clo</sup>/Ccdc39<sup>b2b1735Clo</sup>  [background:] C57BL/6J-Ccdc39<sup>b2b1735Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044170	Trhr<sup>tm1Bau</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5637537	Trhr<sup>tm1Bau</sup>/Trhr<sup>tm1Bau</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25490146	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387895	Drd2<sup>tm1Ebo</sup>	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:2675764	Drd2<sup>tm1Ebo</sup>/Drd2<sup>tm1Ebo</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9717839	20171210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933766	Msx1<sup>tm1Bero</sup>	is_implicated_in	DOID:0050591	tooth agenesis		MGI:3702323	Msx1<sup>tm1Bero</sup>/Msx1<sup>tm1Bero</sup>  [background:] B6.129P2-Msx1<sup>tm1Bero</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9256350	20110428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856016	Edar<sup>dl</sup>	is_implicated_in	DOID:14793	hypohidrotic ectodermal dysplasia		MGI:3693941	Edar<sup>dl</sup>/Edar<sup>dl</sup>  [background:] involves: A/H			ECO:0000033	author statement supported by traceable reference	PMID:17148670	20070118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3608699	Fut8<sup>tm1Nta</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3608986	Fut8<sup>tm1Nta</sup>/Fut8<sup>tm1Nta</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:16236725	20060104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5438049	b2b1709Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5445972	b2b1709Clo/b2b1709Clo  [background:] C57BL/6J-b2b1709Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641232	Fbn1<sup>tm3Rmz</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3652414	Fbn1<sup>tm3Rmz</sup>/Fbn1<sup>tm3Rmz</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16407178	20060822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3577712	Myd88<sup>tm1Aki</sup>/Myd88<sup>tm1Aki</sup>  [background:] B6.129P2-Myd88<sup>tm1Aki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857229	Nos3<sup>tm1Unc</sup>	is_implicated_in	DOID:10825	essential hypertension		MGI:3618625	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11457755	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437096	b2b227.2Clo	is_implicated_in	DOID:114	heart disease		MGI:5437108	b2b227.2Clo/b2b227.2Clo  [background:] C57BL/6J-b2b227.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2673422	Fancd2<sup>tm1Hou</sup>	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:2673460	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] 129S4/SvJae-Fancd2<sup>tm1Hou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12893777	20110518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2673422	Fancd2<sup>tm1Hou</sup>	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:2673459	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] B6.129S4-Fancd2<sup>tm1Hou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12893777	20110518	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2673422	Fancd2<sup>tm1Hou</sup>	is_implicated_in	DOID:0111083	Fanconi anemia complementation group D2		MGI:2673461	Fancd2<sup>tm1Hou</sup>/Fancd2<sup>tm1Hou</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12893777	20110518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105980	Cntn1	is_implicated_in	DOID:0080101	Compton-North congenital myopathy		MGI:5523906	Cntn1<sup>usl</sup>/Cntn1<sup>usl</sup>  [background:] MRL/MpJ-Fas<sup>lpr</sup> Cntn1<sup>usl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105980	Cntn1	is_implicated_in	DOID:0080101	Compton-North congenital myopathy		MGI:5523900	Cntn1<sup>usl</sup>/Cntn1<sup>usl</sup>  [background:] B6.MRL-Cntn1<sup>usl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105980	Cntn1	is_implicated_in	DOID:0080101	Compton-North congenital myopathy		MGI:5300199	Cntn1<sup>m1J</sup>/Cntn1<sup>m1J</sup>  [background:] B6;C-Cntn1<sup>m1J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2159344	Vangl1	is_not_implicated_in	DOID:0080074	neural tube defect		MGI:3778823	Vangl1<sup>Gt(XL802)Byg</sup>/Vangl1<sup>Gt(XL802)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18296642	20080424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354710	Atp8a2	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3581212	Atp8a2<sup>wl-vmd</sup>/Atp8a2<sup>wl-vmd</sup>  [background:] C3H/HeSnJ-Atp8a2<sup>wl-vmd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354710	Atp8a2	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3838969	Atp8a2<sup>wl</sup>/Atp8a2<sup>wl</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354710	Atp8a2	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3838994	Atp8a2<sup>wl</sup>/Atp8a2<sup>wl</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354710	Atp8a2	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3839293	Atp8a2<sup>wl-3J</sup>/Atp8a2<sup>wl-3J</sup>  [background:] CBA/J-Atp8a2<sup>wl-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2146159	Alg10b	is_implicated_in	DOID:0050563	nonsyndromic deafness		MGI:5581451	Alg10b<sup>nse5</sup>/Alg10b<sup>nse5</sup>  [background:] 129S6.B6-Alg10b<sup>nse5</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24303013	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	is_implicated_in	DOID:0110448	dilated cardiomyopathy 1HH		MGI:6107910	Bag3<sup>tm1c(EUCOMM)Hmgu</sup>/Bag3<sup>tm1.1Chen</sup> Tg(Myhca-cre)1Abel/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28737513	20180109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	is_implicated_in	DOID:0110448	dilated cardiomyopathy 1HH		MGI:6107901	Bag3<sup>tm1c(EUCOMM)Hmgu</sup>/Bag3<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Myhca-cre)1Abel/0  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28737513	20180109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109484	Ywhaz	is_implicated_in	DOID:5419	schizophrenia		MGI:5762957	Ywhaz<sup>Gt(OST432062)Lex</sup>/Ywhaz<sup>Gt(OST432062)Lex</sup>  [background:] either: B6.129S5-Ywhaz<sup>Gt(OST432062)Lex</sup> or C.129S5-Ywhaz<sup>Gt(OST432062)Lex</sup> or (involves: 129S5/SvEvBrd * 129T2/SvEmsWehi))			ECO:0000033	author statement supported by traceable reference	PMID:22124272	20160422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5430037	b2b243Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5430325	b2b243Clo/b2b243Clo  [background:] C57BL/6J-b2b243Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921742	Kbtbd13	is_implicated_in	DOID:0110935	nemaline myopathy 6		MGI:6469361	Kbtbd13<sup>em1Coeo</sup>/Kbtbd13<sup>em1Coeo</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31671076	20201026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526219	Agxt<sup>tm1Ull</sup>	is_implicated_in	DOID:0111670	primary hyperoxaluria type 1		MGI:3717654	Agxt<sup>tm1Ull</sup>/Agxt<sup>tm1Ull</sup>  [background:] B6.129X1-Agxt<sup>tm1Ull</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17110443	20201118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526219	Agxt<sup>tm1Ull</sup>	is_implicated_in	DOID:0111670	primary hyperoxaluria type 1		MGI:6472964	Agxt<sup>tm1Ull</sup>/Agxt<sup>tm1Ull</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31821850	20201118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931862	Gpr143<sup>tm1Inc</sup>	is_implicated_in	DOID:0050633	ocular albinism 1		MGI:3587945	Gpr143<sup>tm1Inc</sup>/Y  [background:] either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11092754	20050919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857229	Nos3<sup>tm1Unc</sup>	is_implicated_in	DOID:13042	persistent fetal circulation syndrome		MGI:3618597	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] B6.129P2-Nos3<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15016731	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106683	Zic1	is_implicated_in	DOID:2785	Dandy-Walker syndrome		MGI:3511193	Zic1/Zic4<sup>tm1Kjmi</sup>/Zic1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15338008	20050830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:1380	endometrial cancer		MGI:5604728	Trp53<sup>tm1Brn</sup>/Trp53<sup>tm1Brn</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB/N * ICR			ECO:0000033	author statement supported by traceable reference	PMID:24930886	20141118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914762	Agpat2	is_implicated_in	DOID:0111135	congenital generalized lipodystrophy type 1		MGI:3838352	Agpat2<sup>tm1Garg</sup>/Agpat2<sup>tm1Garg</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:19187773	20090402	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	is_implicated_in	DOID:0060309	syndromic X-linked intellectual disability		MGI:6195853	Arx<sup>tm1.1Ics</sup>/Y  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29659809	20180829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:3054170	Vip<sup>tm1Clw</sup>/Vip<sup>tm1Clw</sup>  [background:] involves: 129S/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17309917	20130417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:3834398	Syne1<sup>tm1.1Mcn</sup>/Syne1<sup>tm1.1Mcn</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:19008300	20100611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028848	Tg(aP2-SREBF1c)9884Reh	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:3028851	Tg(aP2-SREBF1c)9884Reh/0  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:28490610	20181211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655223	Tg(Ela1-TAg)19Bri	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:4819252	Tg(Ela1-TAg)19Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1316086	20100816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2175797	Crkl<sup>tm1Imo</sup>/Crkl<sup>tm1Imo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11242111	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774133	Slc35d1<sup>tm1Hko</sup>	is_implicated_in	DOID:0050775	schneckenbecken dysplasia		MGI:3812126	Slc35d1<sup>tm1Hko</sup>/Slc35d1<sup>tm1Hko</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17952091	20081027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	is_implicated_in	DOID:440	neuromuscular disease		MGI:6850159	Nemf<sup>em8Cx</sup>/Nemf<sup>em8Cx</sup>  [background:] C57BL/6J-Nemf<sup>em8Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	is_implicated_in	DOID:440	neuromuscular disease		MGI:6718876	Nemf<sup>tvrm116</sup>/Nemf<sup>tvrm116</sup>  [background:] C57BL/6J-Nemf<sup>tvrm116</sup>/PjnCx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	is_implicated_in	DOID:440	neuromuscular disease		MGI:6719084	Nemf<sup>pdft</sup>/Nemf<sup>pdft</sup>  [background:] B6(C3)-Nemf<sup>pdft</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20220126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152826	Ryr1<sup>tm1Tno</sup>	is_implicated_in	DOID:3529	congenital myopathy 1A		MGI:3620609	Ryr1<sup>tm1Tno</sup>/Ryr1<sup>tm1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7515481	20060823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3686895	Slc12a5<sup>tm1Dlp</sup>	is_implicated_in	DOID:1826	epilepsy		MGI:3686900	Slc12a5<sup>tm1Dlp</sup>/Slc12a5<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12000122	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856877	Smpd3<sup>fro</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16025116	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387895	Drd2<sup>tm1Ebo</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:2675764	Drd2<sup>tm1Ebo</sup>/Drd2<sup>tm1Ebo</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7566118	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856085	Mitf<sup>Mi</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:78359	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855971	Lyst<sup>bg-Lac</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3784690	Lyst<sup>bg-Lac</sup>/Lyst<sup>bg-Lac</sup>  [background:] CBA/CaLac-Lyst<sup>bg-Lac</sup>			ECO:0000033	author statement supported by traceable reference	MGI:77347	20080512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3610389	Gt(ROSA)26Sor<sup>tm1(DTA)Jpmb</sup>	is_implicated_in	DOID:2377	multiple sclerosis		MGI:5796111	Gt(ROSA)26Sor<sup>tm1(DTA)Jpmb</sup>/Gt(ROSA)26Sor<sup>+</sup> Tg(Plp1-cre/ERT)3Pop/0  [background:] involves: 129S/SvEv * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26656646	20160929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	is_implicated_in	DOID:5419	schizophrenia		MGI:5776380	Shank3<sup>tm4.1Gfng</sup>/Shank3<sup>tm4.1Gfng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26687841	20160620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924859	Odad3	is_implicated_in	DOID:0110624	primary ciliary dyskinesia 30		MGI:6360703	Odad3<sup>tm1b(EUCOMM)Hmgu</sup>/Odad3<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Odad3<sup>tm1b(EUCOMM)Hmgu</sup>/Cnrm			ECO:0000033	author statement supported by traceable reference	PMID:31383820	20190924	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924859	Odad3	is_implicated_in	DOID:0110624	primary ciliary dyskinesia 30		MGI:5445974	Odad3<sup>b2b1885Clo</sup>/Odad3<sup>b2b1885Clo</sup>  [background:] C57BL/6J-Odad3<sup>b2b1885Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20190924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028639	Slc25a13<sup>tm1Lct</sup>	is_not_implicated_in	DOID:9273	citrullinemia		MGI:3852334	Slc25a13<sup>tm1Lct</sup>/Slc25a13<sup>tm1Lct</sup>  [background:] either: 129/Sv-Slc25a13<sup>tm1Lct</sup> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:14701727	20090807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351614	Gyg1	is_implicated_in	DOID:0050579	glycogen storage disease XV		MGI:6273835	Gyg1<sup>tm1a(KOMP)Wtsi</sup>/Gyg1<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33219378	20220318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934273	Prnp<sup>tm1Rcm</sup>	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174712	Prnp<sup>tm1Rcm</sup>/Prnp<sup>tm1Rcm</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Rcm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9462739	20050711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	is_implicated_in	DOID:1062	Fanconi syndrome		MGI:6392256	Hnf4a<sup>tm1Sad</sup>/Hnf4a<sup>tm1Sad</sup> Six2<sup>tm1(tTA,tetO-EGFP/cre)Amc</sup>/Six2<sup>+</sup>  [background:] involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30046000	20200228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94919	Dpp4	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400425	Dpp4<sup>em1Rba</sup>/Dpp4<sup>em1Rba</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31339932	20200615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94919	Dpp4	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400427	Dpp4<sup>em1Rba</sup>/Dpp4<sup>+</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27892925	20200615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94919	Dpp4	is_implicated_in	DOID:0080642	Middle East respiratory syndrome		MGI:6400425	Dpp4<sup>em1Rba</sup>/Dpp4<sup>em1Rba</sup>  [background:] C57BL/6J-Dpp4<sup>em1Rba</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27892925	20200615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:2664560	Fech<sup>tm1Dab</sup>/Fech<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12149233	20190726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:6324956	Fech<sup>m1Pas</sup>/Fech<sup>tm1.1(FECH*)Emi</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28093505	20190726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	is_implicated_in	DOID:13270	erythropoietic protoporphyria		MGI:2175882	Fech<sup>m1Pas</sup>/Fech<sup>m1Pas</sup>  [background:] involves: 129/Sv * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:1939658	20190726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5433489	Tmem67<sup>b2b1163.1Clo</sup>/Tmem67<sup>b2b1163.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1163.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437111	Tmem67<sup>b2b1291.1Clo</sup>/Tmem67<sup>b2b1291.1Clo</sup>  [background:] C57BL/6J-Tmem67<sup>b2b1291.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5320164	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:22302806	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5805821	Pten<sup>tm1Rps</sup>/Pten<sup>+</sup>  [background:] B6.129S1-Pten<sup>tm1Rps</sup>/Nci			ECO:0000033	author statement supported by traceable reference	PMID:25561290	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044175	Wfs1<sup>tm1Yoka</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:5644332	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] B6J.129-Wfs1<sup>tm1Yoka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18343518	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044175	Wfs1<sup>tm1Yoka</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:3044706	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] B6.Cg-Wfs1<sup>tm1Yoka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15056606	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044175	Wfs1<sup>tm1Yoka</sup>	is_implicated_in	DOID:0110629	Wolfram syndrome 1		MGI:3044705	Wfs1<sup>tm1Yoka</sup>/Wfs1<sup>tm1Yoka</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15056606	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	is_implicated_in	DOID:0050558	Ullrich congenital muscular dystrophy		MGI:5565211	Col6a3<sup>tm2.1Chu</sup>/Col6a3<sup>+</sup>  [background:] B6.129(Cg)-Col6a3<sup>tm2.1Chu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24563484	20140522	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442827	Tbc1d32	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182172	Tg(SOD1*G85R)74Dwc	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3832567	Tg(SOD1*G85R)74Dwc/?  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9052802	20090220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920024	Neil1	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:3620065	Neil1<sup>tm1Rsld</sup>/Neil1<sup>tm1Rsld</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16446448	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2148676	Clcnka<sup>tm1Suc</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:2174943	Clcnka<sup>tm1Suc</sup>/Clcnka<sup>tm1Suc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9916798	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419911	Nexmif<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6468250	Nexmif<sup>tm1(KOMP)Wtsi</sup>/Y  [background:] B6J.B6N-Nexmif<sup>tm1(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31704787	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3828146	Tg(Dspp-TGFB1)3Kul	is_implicated_in	DOID:701	dentin dysplasia		MGI:3835822	Tg(Dspp-TGFB1)3Kul/?  [background:] FVB/N-Tg(Dspp-TGFB1)3Kul			ECO:0000033	author statement supported by traceable reference	PMID:11116156	20090316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3810388	Cacna1a<sup>tm3Hzo</sup>	is_implicated_in	DOID:0050956	spinocerebellar ataxia type 6		MGI:6278003	Cacna1a<sup>tm3Hzo</sup>/Cacna1a<sup>tm3Hzo</sup>  [background:] B6.129S7-Cacna1a<sup>tm3Hzo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26730403	20190213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099438	Nsdhl	is_implicated_in	DOID:12305	Bloch-Sulzberger syndrome		MGI:3590076	Nsdhl<sup>Str-1H</sup>/Nsdhl<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:11005611	20191224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623134	Cln3<sup>tm1Mkat</sup>	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3623263	Cln3<sup>tm1Mkat</sup>/Cln3<sup>tm1Mkat</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10440905	20060525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525252	Nfkbiz<sup>tm1Mamo</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3526428	Nfkbiz<sup>tm1Mamo</sup>/Nfkbiz<sup>tm1Mamo</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15491998	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:4429407	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] involves: STOCK Mlph<sup>ln</sup> a Tgfa<sup>wa1</sup> Cdh23<sup>v</sup> Ednrb<sup>s</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24680679	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918382	Cabyr	is_implicated_in	DOID:12336	male infertility		MGI:6152755	Cabyr<sup>em1Osb</sup>/Cabyr<sup>em1Osb</sup>  [background:] involves: C57BL/6NJcl * DBA/2NJcl			ECO:0000033	author statement supported by traceable reference	PMID:27802166	20180423	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96522	Rbpj	is_implicated_in	DOID:62	aortic valve disease		MGI:6236251	Rbpj<sup>tm1Kyo</sup>/Rbpj<sup>+</sup>  [background:] involves: 129S2/SvPas * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21493891	20181108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	is_not_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047407	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] 129-Gnai2<sup>tm1Lbi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15219458	20081208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277955	Bsn	is_implicated_in	DOID:1826	epilepsy		MGI:2652947	Bsn<sup>tm1Gund</sup>/Bsn<sup>tm1Gund</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12628169	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107193	Gpr143	is_implicated_in	DOID:0050633	ocular albinism 1		MGI:3587945	Gpr143<sup>tm1Inc</sup>/Y  [background:] either: (involves: 129/Sv * 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11092754	20050919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158701	C1qa<sup>tm1Mjw</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2384126	C1qa<sup>tm1Mjw</sup>/C1qa<sup>tm1Mjw</sup>  [background:] involves: 129P2/Ola * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9590289	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5446153	b2b1941Clo	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5487398	b2b1941Clo/b2b1941Clo  [background:] C57BL/6J-b2b1941Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857300	Mpv17	is_implicated_in	DOID:0080121	mitochondrial DNA depletion syndrome 3		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	PMID:18818194	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385089	Zng1	is_implicated_in	DOID:0080205	CAKUT		MGI:7309153	Zng1<sup>em1Skan</sup>/Zng1<sup>em1Skan</sup>  [background:] C57BL/6N-Zng1<sup>em1Skan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31862704	20220705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385089	Zng1	is_implicated_in	DOID:0080205	CAKUT		MGI:7309156	Zng1<sup>em2Skan</sup>/Zng1<sup>em2Skan</sup>  [background:] C57BL/6N-Zng1<sup>em2Skan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31862704	20220705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916712	Slurp2	is_implicated_in	DOID:3390	palmoplantar keratosis		MGI:6159891	Slurp2<sup>tm1.1Sgy</sup>/Slurp2<sup>tm1.1Sgy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26967477	20180607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916712	Slurp2	is_implicated_in	DOID:3390	palmoplantar keratosis		MGI:6159890	Slurp2<sup>tm1Lex</sup>/Slurp2<sup>tm1Lex</sup>  [background:] involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26967477	20180607	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95714	Gja3	is_implicated_in	DOID:0110253	cataract 14 multiple types		MGI:5762599	Gja3<sup>tm1.1Vmb</sup>/Gja3<sup>tm1.1Vmb</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25103261	20160419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95714	Gja3	is_implicated_in	DOID:0110253	cataract 14 multiple types		MGI:5762600	Gja3<sup>tm1.1Vmb</sup>/Gja3<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25103261	20160419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670480	Ldlrap1<sup>tm1Her</sup>	is_implicated_in	DOID:0090105	autosomal recessive hypercholesterolemia		MGI:2670516	Ldlrap1<sup>tm1Her</sup>/Ldlrap1<sup>tm1Her</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:12746448	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429736	Il2rg<sup>tm1Sug</sup>	is_not_implicated_in	DOID:628	combined T cell and B cell immunodeficiency		MGI:2655194	Il2rg<sup>tm1Sug</sup>/Y  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8562967	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3700172	Nfkbia<sup>tm1Stw</sup>/Nfkbia<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8628301	20070318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604881	Asl<sup>tm1Wjc</sup>	is_implicated_in	DOID:14755	argininosuccinic aciduria		MGI:3605490	Asl<sup>tm1Wjc</sup>/Asl<sup>tm1Wjc</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12559843	20051122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443878	Slc4a7	is_implicated_in	DOID:0110839	Usher syndrome type 2C		MGI:2682644	Slc4a7<sup>tm1Krtz</sup>/Slc4a7<sup>tm1Krtz</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12808454	20061219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:2651494	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12576554	20080417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:3777760	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17712420	20080417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:2651509	Naglu<sup>tm1Efn</sup>/Naglu<sup>tm1Efn</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6) or (involves: C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10588735	20080417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180679	Ccr7<sup>tm1Rfor</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4430601	Ccr7<sup>tm1Rfor</sup>/Ccr7<sup>tm1Rfor</sup>  [background:] B6.129P2-Ccr7<sup>tm1Rfor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16473829	20100319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385321	Cchcr1	is_implicated_in	DOID:986	alopecia areata		MGI:6782396	Cchcr1<sup>em1Aoka</sup>/Cchcr1<sup>em1Aoka</sup>  [background:] C57BL/6NJcl-Cchcr1<sup>em1Aoka</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32580135	20211027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831374	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] B6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831378	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] 129S6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831375	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] CBACa.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831377	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>tm1.1Aomw</sup>  [background:] 129S6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831373	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] B6.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060703	Muenke Syndrome		MGI:3831376	Fgfr3<sup>tm1.1Aomw</sup>/Fgfr3<sup>+</sup>  [background:] CBACa.129P2-Fgfr3<sup>tm1.1Aomw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19086028	20090211	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88424	Cm	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:3717464	Cm/+  [background:] C3Sn.Cg-Cm/J			ECO:0000033	author statement supported by traceable reference	PMID:1613559	20090731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313509	Cc2d2a<sup>b2b1035Clo</sup>/Cc2d2a<sup>b2b1035Clo</sup>  [background:] C57BL/6J-Cc2d2a<sup>b2b1035Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	is_implicated_in	DOID:0060285	parietal foramina		MGI:5695543	Alx4<sup>Lst-2J</sup>/Alx4<sup>Lst-2J</sup>  [background:] C57BL/6J-Alx4<sup>Lst-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25673119	20151112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	is_not_implicated_in	DOID:10825	essential hypertension		MGI:2175020	Tnfrsf1b<sup>tm1Imx</sup>/Tnfrsf1b<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9551933	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857061	Slc7a11<sup>sut</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2677961	Slc7a11<sup>sut</sup>/Slc7a11<sup>sut</sup>  [background:] C3H/HeSnJ-Slc7a11<sup>sut</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8699821	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	is_implicated_in	DOID:12365	malaria		MGI:4946419	Aqp4<sup>tm1.1Lmno</sup>/Aqp4<sup>tm1.1Lmno</sup>  [background:] B6.Cg-Aqp4<sup>tm1.1Lmno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23277579	20131001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654881	Robo1<sup>tm1Phr</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3806464	Robo1<sup>tm1Phr</sup>/Robo1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15374951	20080917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5438046	b2b1639Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5442129	b2b1639Clo/b2b1639Clo  [background:] C57BL/6J-b2b1639Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110640	congenital muscular dystrophy due to LMNA mutation		MGI:5306920	Lmna<sup>tm2.1Gbon</sup>/Lmna<sup>tm2.1Gbon</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22090424	20120223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921569	Mettl23	is_implicated_in	DOID:1686	glaucoma		MGI:7388555	Mettl23<sup>em1Itwa</sup>/Mettl23<sup>em1Itwa</sup>  [background:] C57BL/6J-Mettl23<sup>em1Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921569	Mettl23	is_implicated_in	DOID:1686	glaucoma		MGI:7388557	Mettl23<sup>em2Itwa</sup>/Mettl23<sup>+</sup>  [background:] C57BL/6J-Mettl23<sup>em2Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921569	Mettl23	is_implicated_in	DOID:1686	glaucoma		MGI:7388554	Mettl23<sup>em1Itwa</sup>/Mettl23<sup>+</sup>  [background:] C57BL/6J-Mettl23<sup>em1Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921569	Mettl23	is_implicated_in	DOID:1686	glaucoma		MGI:7388558	Mettl23<sup>em2Itwa</sup>/Mettl23<sup>em2Itwa</sup>  [background:] C57BL/6J-Mettl23<sup>em2Itwa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36099048	20221202	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	is_implicated_in	DOID:0090062	familial cold autoinflammatory syndrome 1		MGI:3850052	Nlrp3<sup>tm2Hhf</sup>/Nlrp3<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/?  [background:] involves: 129/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19501000	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	is_implicated_in	DOID:0090062	familial cold autoinflammatory syndrome 1		MGI:3850048	Nlrp3<sup>tm2Hhf</sup>/Nlrp3<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19501000	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4431198	Tg(tetO-Notch4*)1Rwng	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:5502689	Tg(Tek-tTA)1Rwng/0 Tg(tetO-Notch4*)1Rwng/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18667694	20130827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5431482	b2b904.2Clo	is_implicated_in	DOID:114	heart disease		MGI:5431512	b2b904.2Clo/b2b904.2Clo  [background:] C57BL/6J-b2b904.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859993	Smad9	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:3850122	Smad9<sup>tm3Jfm</sup>/Smad9<sup>tm3Jfm</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:19419974	20090710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917700	Unc13d	is_implicated_in	DOID:0110923	familial hemophagocytic lymphohistiocytosis 3		MGI:3628949	Unc13d<sup>Jinx</sup>/Unc13d<sup>Jinx</sup>  [background:] C57BL/6J-Unc13d<sup>Jinx</sup>/Mmucd			ECO:0000033	author statement supported by traceable reference	PMID:17420270	20130430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5645239	Dnah5<sup>b2b2451Clo</sup>/Dnah5<sup>b2b2451Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2451Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95762	Gm2a	is_implicated_in	DOID:4795	GM2 gangliosidosis, AB variant		MGI:2176850	Gm2a<sup>tm1Rlp</sup>/Gm2a<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9223328	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	is_implicated_in	DOID:0090130	cortical dysplasia-focal epilepsy syndrome		MGI:5295268	Cntnap2<sup>tm1Pele</sup>/Cntnap2<sup>tm1Pele</sup>  [background:] B6.129-Cntnap2<sup>tm1Pele</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21962519	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772868	Tg(Prnp-TBP*)71-27Xjl	is_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:3772884	Tg(Prnp-TBP*)71-27Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)71-27Xjl			ECO:0000033	author statement supported by traceable reference	PMID:17994014	20080305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584497	Tg(Amelx)42Msnd	is_not_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:3584512	Tg(Amelx)42Msnd/Tg(Amelx)42Msnd  [background:] involves: C57BL/6J * CBA/J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:11243888	20050829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573749	Aire<sup>tm1Mmat</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3576481	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] C.Cg-Aire<sup>tm1Mmat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573749	Aire<sup>tm1Mmat</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3576479	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573749	Aire<sup>tm1Mmat</sup>	is_implicated_in	DOID:0050167	autoimmune polyendocrine syndrome type 1		MGI:3576483	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] B6.Cg-Aire<sup>tm1Mmat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044323	Tg(INS-MT2A,Tyr)1Pne	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3624037	Tg(INS-MT2A,Tyr)1Pne/0  [background:] NOD.FVB-Tg(INS-MT2A,Tyr)1Pne			ECO:0000033	author statement supported by traceable reference	PMID:16731821	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044323	Tg(INS-MT2A,Tyr)1Pne	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623677	Tg(INS-MT2A,Tyr)1Pne/0  [background:] FVB-Tg(INS-MT2A,Tyr)1Pne			ECO:0000033	author statement supported by traceable reference	PMID:9836515	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671151	Rdx<sup>tm1Sts</sup>	is_implicated_in	DOID:12308	Dubin-Johnson syndrome		MGI:2671154	Rdx<sup>tm1Sts</sup>/Rdx<sup>tm1Sts</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12068294	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	is_implicated_in	DOID:0060340	ciliopathy		MGI:5315749	Wdr19<sup>twto</sup>/Wdr19<sup>twto</sup>  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:22228095	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158221	Foxj1<sup>tm1Slb</sup>	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:2679917	Foxj1<sup>tm1Slb</sup>/Foxj1<sup>tm1Slb</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10873152	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385822	Hsd17b4<sup>tm1Baes</sup>	is_implicated_in	DOID:0090031	D-bifunctional protein deficiency		MGI:3606112	Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15769750	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385822	Hsd17b4<sup>tm1Baes</sup>	is_implicated_in	DOID:0090031	D-bifunctional protein deficiency		MGI:3606112	Hsd17b4<sup>tm1Baes</sup>/Hsd17b4<sup>tm1Baes</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10748062	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858746	Kat6b	is_implicated_in	DOID:3490	Noonan syndrome		MGI:2679734	Kat6b<sup>Gt(pKC199)1Pgr</sup>/Kat6b<sup>Gt(pKC199)1Pgr</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:21804188	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857890	Lama2<sup>dy-6J</sup>	is_implicated_in	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A		MGI:3789978	Lama2<sup>dy-6J</sup>/Lama2<sup>dy-6J</sup>  [background:] involves: C57BL/6JEi * DBA/2J			ECO:0000033	author statement supported by traceable reference	MGI:1342643	20080603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180558	Cav3<sup>tm1Mls</sup>	is_implicated_in	DOID:0060255	rippling muscle disease 2		MGI:2660653	Cav3<sup>tm1Mls</sup>/Cav3<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11259414	20190224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3640114	Slc6a4<sup>tm1Kpl</sup>/Slc6a4<sup>tm1Kpl</sup>  [background:] B6.129-Slc6a4<sup>tm1Kpl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23142422	20190708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6316332	Slc6a4<sup>tm2.1Rbl</sup>/Slc6a4<sup>tm2.1Rbl</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:22431635	20190708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6316332	Slc6a4<sup>tm2.1Rbl</sup>/Slc6a4<sup>tm2.1Rbl</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:27111230	20190708	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917579	Gon4l	is_implicated_in	DOID:8850	salivary gland cancer		MGI:4829639	Gon4l<sup>justy</sup>/Gon4l<sup>justy</sup>  [background:] C3HeB/FeJ-Gon4l<sup>justy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23608756	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99887	Pitpna	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:2676371	Pitpna<sup>Gt(OST1152)Lex</sup>/Pitpna<sup>Gt(OST1152)Lex</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12788952	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99887	Pitpna	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:2676370	Pitpna<sup>tm1Vab</sup>/Pitpna<sup>tm1Vab</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12788952	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus		MGI:3583906	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9593767	20050819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:7427405	Tnfrsf11a<sup>tm1.1Sral</sup>/Tnfrsf11a<sup>+</sup>  [background:] B6.129P2(Cg)-Tnfrsf11a<sup>tm1.1Sral</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33724536	20230117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329019	Dnase2a	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3692382	Dnase2a<sup>tm1Osa</sup>/Dnase2a<sup>tm2Osa</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:17066036	20070104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	is_implicated_in	DOID:9452	steatotic liver disease		MGI:3692534	Mc4r<sup>tm1Lowl</sup>/Mc4r<sup>tm1Lowl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21906580	20111123	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445420	Jun<sup>tm4Wag</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:5306592	Jun<sup>tm4Wag</sup>/Jun<sup>tm4Wag</sup> Tg(Sftpc-cre)1Blh/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22265050	20120220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667674	Noa	is_implicated_in	DOID:3310	atopic dermatitis		MGI:2667689	Noa/Noa<sup>+</sup>  [background:] NOA			ECO:0000033	author statement supported by traceable reference	MGI:1097454	20100208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	is_implicated_in	DOID:0111008	X-linked cone-rod dystrophy 1		MGI:3038416	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10725384	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333754	Agfg1	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:3609494	Agfg1<sup>tm1Jvd</sup>/Agfg1<sup>tm1Jvd</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15705627	20220127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	is_implicated_in	DOID:0060798	hypomyelinating leukodystrophy 6		MGI:6444908	Tubb4a<sup>em1Avan</sup>/Tubb4a<sup>em1Avan</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:32463361	20220316	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	is_implicated_in	DOID:0060798	hypomyelinating leukodystrophy 6		MGI:6888378	Tubb4a<sup>Jit</sup>/Tubb4a<sup>Jit</sup>  [background:] FVB.B6-Tubb4a<sup>Jit</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35171680	20220316	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	is_implicated_in	DOID:0060798	hypomyelinating leukodystrophy 6		MGI:6888382	Tubb4a<sup>Jit</sup>/Tubb4a<sup>+</sup>  [background:] FVB.B6-Tubb4a<sup>Jit</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35171680	20220316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684616	Psen1<sup>tm1Vln</sup>	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2684657	Psen1<sup>tm1Vln</sup>/Psen1<sup>tm1Vln</sup> Tg(Thy1-cre)1Vln/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11978821	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808000	Tnfrsf1a<sup>tm1Rsie</sup>	is_implicated_in	DOID:0090018	autosomal dominant familial periodic fever		MGI:4461165	Tnfrsf1a<sup>tm1Rsie</sup>/Tnfrsf1a<sup>+</sup>  [background:] B6.Cg-Tnfrsf1a<sup>tm1Rsie</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20457915	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3697318	Slc26a3<sup>tm1Sole</sup>	is_implicated_in	DOID:0060296	congenital secretory chloride diarrhea 1		MGI:3697730	Slc26a3<sup>tm1Sole</sup>/Slc26a3<sup>tm1Sole</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17001077	20070226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	is_implicated_in	DOID:10591	pre-eclampsia		MGI:5288006	Notch2<sup>tm3Grid</sup>/Notch2<sup>tm3Grid</sup> Tg(Tpbpa-cre,-EGFP)5Jcc/0  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:21693515	20111003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664379	Prkcq<sup>tm1Litt</sup>	is_implicated_in	DOID:5327	retinal detachment		MGI:4843311	Prkcq<sup>tm1Litt</sup>/Prkcq<sup>tm1Litt</sup>  [background:] B6.129P2-Prkcq<sup>tm1Litt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26978024	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914549	Dock7	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3582588	Dock7<sup>m</sup>/Dock7<sup>m</sup>  [background:] B6.D(Cg)-Dock7<sup>m</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9475748	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178353	Mitf<sup>Mi-H</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178353	Mitf<sup>Mi-H</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388715	Tnf<sup>tm2Gkl</sup>	is_implicated_in	DOID:1123	spondyloarthropathy		MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857034	Foxp3<sup>sf</sup>	is_implicated_in	DOID:9169	Wiskott-Aldrich syndrome		MGI:3589971	Foxp3<sup>sf</sup>/Y  [background:] involves: 101/H * C3H/HeH * STOCK MR			ECO:0000033	author statement supported by traceable reference	PMID:2320565	20051019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	is_implicated_in	DOID:10283	prostate cancer		MGI:5543401	Tgfbr2<sup>tm1.2Hlm</sup>/Tgfbr2<sup>tm1.2Hlm</sup> Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22904682	20140207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181752	Slc2a2<sup>tm1Thor</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3029380	Slc2a2<sup>tm1Thor</sup>/Slc2a2<sup>tm1Thor</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9354799	20061012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176466	Runx2<sup>tm1Kish</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:2678410	Runx2<sup>tm1Kish</sup>/Runx2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20375239	20170621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530790	Def6<sup>Gt(OST307148)Lex</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3628445	Def6<sup>Gt(OST307148)Lex</sup>/Def6<sup>Gt(OST307148)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16470246	20060707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	is_implicated_in	DOID:9256	colorectal cancer		MGI:4429499	Stat3<sup>tm1Dlv</sup>/Stat3<sup>tm1Dlv</sup> Tg(Csf1r-icre)1Jwp/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20042677	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	is_not_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:2175762	Cdkn1c<sup>tm1Bbd</sup>/Cdkn1c<sup>tm1Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9136926	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	is_not_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:2175766	Cdkn1c<sup>tm1Kat</sup>/Cdkn1c<sup>tm1Kat</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10731669	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	is_implicated_in	DOID:9279	hyperhomocysteinemia		MGI:6448988	Cbs<sup>tm1Unc</sup>/Cbs<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15622513	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	is_implicated_in	DOID:9279	hyperhomocysteinemia		MGI:6448986	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15622513	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5620178	b2b2696Clo	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5620189	b2b2696Clo/b2b2696Clo  [background:] C57BL/6J-b2b2696Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924627	Kcnt1	is_implicated_in	DOID:0080439	developmental and epileptic encephalopathy 14		MGI:7442320	Kcnt1<sup>em1Pqt</sup>/Kcnt1<sup>em1Pqt</sup>  [background:] C57BL/6J-Kcnt1<sup>em1Pqt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36173683	20230308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861441	Rab27a	is_implicated_in	DOID:0060539	Hermansky-Pudlak syndrome 1		MGI:5505710	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] C3H/HeSn-Rab27a<sup>ash</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12070017	20130912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360657	Apc<sup>tm2Rfo</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:4360685	Apc<sup>tm2Rfo</sup>/Apc<sup>+</sup>  [background:] (C57BL/6J x 129P2/OlaHsd)F1			ECO:0000033	author statement supported by traceable reference	PMID:23955540	20140430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	is_implicated_in	DOID:418	systemic scleroderma		MGI:2655257	Col3a1<sup>Tsk2</sup>/Col3a1<sup>+</sup>  [background:] C3H101H-Col3a1<sup>Tsk2</sup>/H			ECO:0000033	author statement supported by traceable reference	PMID:8849351	20160420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915509	Ift80	is_implicated_in	DOID:0110086	asphyxiating thoracic dystrophy 2		MGI:4942392	Ift80<sup>Gt(AN0245)Wtsi</sup>/Ift80<sup>Gt(AN0245)Wtsi</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21227999	20110329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	is_implicated_in	DOID:10754	otitis media		MGI:2174786	Trp73<sup>tm1Fmc</sup>/Trp73<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10716451	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136843	Gdnf<sup>tm1Rosl</sup>	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2675149	Gdnf<sup>tm1Rosl</sup>/Gdnf<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12668632	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775647	Hfe<sup>tm1Wsr</sup>	is_not_implicated_in	DOID:0111029	hemochromatosis type 1		MGI:3821583	Hfe<sup>tm1Wsr</sup>/Hfe<sup>tm1Wsr</sup> Tg(Vil1-cre)997Gum/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17264297	20081230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105057	Cdh5	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:7467143	Cdh5<sup>tm1Dvst</sup>/Cdh5<sup>tm1Dvst</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	is_implicated_in	DOID:0090132	complex cortical dysplasia with other brain malformations 7		MGI:5522833	Tubb2b<sup>brdp</sup>/Tubb2b<sup>brdp</sup>  [background:] involves: A/J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:23727838	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926192	E2f5<sup>tm1Dli</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:3582637	E2f5<sup>tm1Dli</sup>/E2f5<sup>tm1Dli</sup>  [background:] either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9553039	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:4818797	Pdgfra<sup>tm2Sor</sup>/Pdgfra<sup>tm2Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17568391	20100810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692385	Serpinc1<sup>tm1Dwr</sup>	is_implicated_in	DOID:3755	antithrombin III deficiency		MGI:3696558	Serpinc1<sup>tm1Dwr</sup>/Serpinc1<sup>tm1Dwr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:14592998	20091123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107201	Zic4	is_implicated_in	DOID:2785	Dandy-Walker syndrome		MGI:3511195	Zic1/Zic4<sup>tm1Kjmi</sup>/Zic4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15338008	20050830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3757945	Gnptab<sup>Gt(OST97730)Lex</sup>	is_implicated_in	DOID:0080070	mucolipidosis II alpha/beta		MGI:4456351	Gnptab<sup>Gt(OST97730)Lex</sup>/Gnptab<sup>Gt(OST97730)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17962477	20100623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851914	Hr<sup>Hp</sup>	is_implicated_in	DOID:0110701	hypotrichosis 4		MGI:3851927	Hr<sup>Hp</sup>/Hr<sup>Hp</sup>  [background:] BALB/cJ-Hr<sup>Hp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19513791	20090804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2657145	Cdh23<sup>v-3J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3722079	Cdh23<sup>v-3J</sup>/Cdh23<sup>+</sup>  [background:] C57BL/6J-Cdh23<sup>v-3J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182831	Per1<sup>tm1Drw</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5634972	Per1<sup>tm1Drw</sup>/Per1<sup>tm1Drw</sup>  [background:] B6.129-Per1<sup>tm1Drw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25673850	20150507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	is_implicated_in	DOID:12365	malaria		MGI:3766445	Ank1<sup>nb</sup>/Ank1<sup>nb</sup>  [background:] involves: C57BL/6J * WB/Re			ECO:0000033	author statement supported by traceable reference	PMID:1832936	20130313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	is_implicated_in	DOID:12365	malaria		MGI:5438702	Ank1<sup>MRI23420</sup>/Ank1<sup>MRI23420</sup>  [background:] SJL/J-Ank1<sup>MRI23420</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22723917	20130313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	is_not_implicated_in	DOID:2224	essential thrombocythemia		MGI:4829588	Jak2<sup>tm1.1Jlvl</sup>/Jak2<sup>tm1.1Jlvl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20472827	20100915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4365636	Tg(Vim*R113C)1Tmm	is_implicated_in	DOID:0110248	cataract 30		MGI:4365717	Tg(Vim*R113C)1Tmm/0  [background:] B6.CBA-Tg(Vim*R113C)1Tmm			ECO:0000033	author statement supported by traceable reference	PMID:18940912	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:5648857	Prickle1<sup>tm1Asw</sup>/Prickle1<sup>tm1.2Asw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25190059	20150818	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:5648842	Prickle1<sup>tm1Asw</sup>/Prickle1<sup>tm1Asw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25190059	20150818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3630275	Hr<sup>rh-Chr</sup>	is_implicated_in	DOID:0050634	alopecia universalis		MGI:3713665	Hr<sup>rh-Chr</sup>/Hr<sup>rh-Chr</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9832318	20070703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528440	Abca12<sup>tm1Lex</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3834263	Abca12<sup>tm1Lex</sup>/Abca12<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18957418	20090304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4247868	Pomk<sup>Gt(OST243203)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429556	Pomk<sup>Gt(OST243203)Lex</sup>/Pomk<sup>Gt(OST243203)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	is_implicated_in	DOID:0110766	hereditary spastic paraplegia 13		MGI:5516348	Hspd1<sup>Gt(OST171441)Lex</sup>/Hspd1<sup>+</sup>  [background:] B6.129S5-Hspd1<sup>Gt(OST171441)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23466696	20131106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107418	Ptprn2	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3051907	Ptprn2<sup>tm1Aln</sup>/Ptprn2<sup>tm1Aln</sup>  [background:] involves: 129S4/SvJae * C57BL/6N * NOD/LtJ			ECO:0000033	author statement supported by traceable reference	PMID:12535631	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99909	Lama3	is_implicated_in	DOID:3209	junctional epidermolysis bullosa		MGI:6277933	Lama3<sup>tm1Arte</sup>/Lama3<sup>tm1Arte</sup> Tg(KRT14-cre/ERT)20Efu/0  [background:] involves: C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:27729280	20190212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	is_implicated_in	DOID:0080015	physical disorder		MGI:5642272	Bmp4<sup>tm4Blh</sup>/Bmp4<sup>tm4Blh</sup> Isl1<sup>tm1(cre)Sev</sup>/Isl1<sup>+</sup>  [background:] involves: 129 * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23028455	20180605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338038	Aebp2	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:5296959	Aebp2<sup>Gt(BC0681)Wtsi</sup>/Aebp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21949878	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	is_implicated_in	DOID:0110954	Waardenburg syndrome type 4B		MGI:2174947	Edn3<sup>tm1Ywa</sup>/Edn3<sup>tm1Ywa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8001160	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	is_implicated_in	DOID:0110954	Waardenburg syndrome type 4B		MGI:3589405	Edn3<sup>tmgc48</sup>/Edn3<sup>tmgc48</sup>  [background:] C57BL/6-19<sup>PWK</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17516928	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	is_implicated_in	DOID:0110954	Waardenburg syndrome type 4B		MGI:3802920	Edn3<sup>tmgc48</sup>/Edn3<sup>+</sup>  [background:] C57BL/6-19<sup>PWK</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17516928	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313278	Fzd9	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3586704	Fzd9<sup>tm1Sjp</sup>/Fzd9<sup>tm1Sjp</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15930120	20110411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313278	Fzd9	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:4946081	Fzd9<sup>tm1Uta</sup>/Fzd9<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21402791	20110411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857352	Ap3b1<sup>pe-rim2</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:3584030	Ap3b1<sup>pe-rim2</sup>/Ap3b1<sup>pe-rim2</sup>  [background:] involves: B10.A(R201) * C57BL/10Slc			ECO:0000033	author statement supported by traceable reference	PMID:9434937	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	is_implicated_in	DOID:9164	achalasia		MGI:3618910	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11438492	20091111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3695128	Tg(Syn1-ADCY7)11004Btab	is_implicated_in	DOID:1595	melancholic depression		MGI:3695129	Tg(Syn1-ADCY7)11004Btab/0  [background:] B6.Cg-Tg(Syn1-ADCY7)11004Btab			ECO:0000033	author statement supported by traceable reference	PMID:17135423	20070130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857937	Pten<sup>tm1Mak</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:2179030	Pten<sup>tm1Mak</sup>/Pten<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10910075	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857981	Cp<sup>tm1Hrs</sup>	is_implicated_in	DOID:0050711	aceruloplasminemia		MGI:3044689	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10485908	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857981	Cp<sup>tm1Hrs</sup>	is_implicated_in	DOID:0050711	aceruloplasminemia		MGI:3044689	Cp<sup>tm1Hrs</sup>/Cp<sup>tm1Hrs</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11461924	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	is_implicated_in	DOID:0060775	microvillus inclusion disease		MGI:5427868	Cdc42<sup>tm1Brak</sup>/Cdc42<sup>tm1Brak</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22354172	20120713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386303	Slc6a3<sup>tm1Mca</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:2654500	Slc6a3<sup>tm1Mca</sup>/Slc6a3<sup>tm1Mca</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:8628395	20081006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785405	Mus81<sup>tm1Esse</sup>	is_implicated_in	DOID:14323	Marfan syndrome		MGI:3794044	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17293478	20080617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150426	Eya1<sup>tm1Rilm</sup>	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:3054668	Eya1<sup>tm1Rilm</sup>/Eya1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150426	Eya1<sup>tm1Rilm</sup>	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:3054666	Eya1<sup>tm1Rilm</sup>/Eya1<sup>+</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150426	Eya1<sup>tm1Rilm</sup>	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:2677316	Eya1<sup>tm1Rilm</sup>/Eya1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10471511	20050901	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103581	Musk	is_implicated_in	DOID:0110670	congenital myasthenic syndrome 9		MGI:3815537	Musk<sup>tm1.1Vwi</sup>/Musk<sup>tm2Vwi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:18718936	20150511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103581	Musk	is_implicated_in	DOID:0110670	congenital myasthenic syndrome 9		MGI:3622118	Musk<sup>tm1Vwi</sup>/Musk<sup>tm1.1Vwi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16337809	20150511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103581	Musk	is_implicated_in	DOID:0110670	congenital myasthenic syndrome 9		MGI:3622117	Musk<sup>tm1Vwi</sup>/Musk<sup>tm1Vwi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16337809	20150511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834439	Tg(tetO-PIK3CA*H1047R)13Lca	is_implicated_in	DOID:1324	lung cancer		MGI:3834442	Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-PIK3CA*H1047R)13Lca/0  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19029981	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861111	Nhs<sup>Xcat</sup>	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587737	Nhs<sup>Xcat</sup>/Y  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861111	Nhs<sup>Xcat</sup>	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587739	Nhs<sup>Xcat</sup>/Nhs<sup>+</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861111	Nhs<sup>Xcat</sup>	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587738	Nhs<sup>Xcat</sup>/Nhs<sup>Xcat</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7806224	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861111	Nhs<sup>Xcat</sup>	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587739	Nhs<sup>Xcat</sup>/Nhs<sup>+</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861111	Nhs<sup>Xcat</sup>	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587738	Nhs<sup>Xcat</sup>/Nhs<sup>Xcat</sup>  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861111	Nhs<sup>Xcat</sup>	is_implicated_in	DOID:0060599	Nance-Horan syndrome		MGI:3587737	Nhs<sup>Xcat</sup>/Y  [background:] involves: DBA/2 * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:15081118	20050915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438620	Prpf31<sup>tm1Bha</sup>	is_not_implicated_in	DOID:0110408	retinitis pigmentosa 11		MGI:4438627	Prpf31<sup>tm1Bha</sup>/Prpf31<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19578015	20100405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180365	Arsb<sup>tm1Cptr</sup>	is_implicated_in	DOID:12800	mucopolysaccharidosis VI		MGI:2655540	Arsb<sup>tm1Cptr</sup>/Arsb<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8710849	20070625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180365	Arsb<sup>tm1Cptr</sup>	is_implicated_in	DOID:12800	mucopolysaccharidosis VI		MGI:3712734	Arsb<sup>tm1Cptr</sup>/Arsb<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd * 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:12904606	20070625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351209	Tlx3	is_implicated_in	DOID:0060731	congenital central hypoventilation syndrome		MGI:2669096	Tlx3<sup>tm1Sjk</sup>/Tlx3<sup>tm1Sjk</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10700185	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347347	Slc27a4	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:2662270	Slc27a4<sup>wrfr</sup>/Slc27a4<sup>wrfr</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12697906	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347347	Slc27a4	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:2670851	Slc27a4<sup>tm1Wsr</sup>/Slc27a4<sup>tm1Wsr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12821645	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914345	Trak1	is_implicated_in	DOID:13366	Stiff-Person syndrome		MGI:3615358	Trak1<sup>hyrt</sup>/Trak1<sup>hyrt</sup>  [background:] involves: AKR * C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16380713	20060309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4939883	Pparg<sup>tm1.1Gonz</sup>/Pparg<sup>tm1.1Gonz</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21135166	20110307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861620	Idc	is_implicated_in	DOID:83	cataract		MGI:2175077	Idc/Idc<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3712362	Duox2<sup>thyd</sup>/Duox2<sup>thyd</sup>  [background:] B6(129)-Duox2<sup>thyd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17440044	20070622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98331	Snap25	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5766495	Snap25<sup>tm1.1Bark</sup>/Snap25<sup>tm1.1Bark</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26195742	20160504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712468	Thbd<sup>tm2Emc</sup>	is_implicated_in	DOID:2452	thrombophilia		MGI:3712469	Thbd<sup>tm2Emc</sup>/Thbd<sup>tm2Emc</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12208873	20120305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861097	Aifm1<sup>Hq</sup>	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:2387326	Aifm1<sup>Hq</sup>/Y  [background:] B6CBACa A<sup>w-J</sup>/A-Aifm1<sup>Hq</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18791645	20171031	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861097	Aifm1<sup>Hq</sup>	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:2387325	Aifm1<sup>Hq</sup>/Aifm1<sup>Hq</sup>  [background:] B6CBACa A<sup>w-J</sup>/A-Aifm1<sup>Hq</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18791645	20171031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921627	Hsf2bp	is_implicated_in	DOID:0112278	primary ovarian insufficiency 19		MGI:7282037	Hsf2bp<sup>em2Amp</sup>/Hsf2bp<sup>em2Amp</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:32845237	20220603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	is_implicated_in	DOID:4480	achondroplasia		MGI:3707539	Nppc<sup>lbab</sup>/Nppc<sup>lbab</sup>  [background:] B6.PL-Nppc<sup>lbab</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:17439653	20220512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	is_implicated_in	DOID:4480	achondroplasia		MGI:3522090	Nppc<sup>tm1Yog</sup>/Nppc<sup>tm1Yog</sup>  [background:] either: 129X1/SvJ or (involves: 129 * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:11259675	20220512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027491	Htr4<sup>tm1Comp</sup>	is_implicated_in	DOID:8689	anorexia nervosa		MGI:3027496	Htr4<sup>tm1Comp</sup>/Htr4<sup>tm1Comp</sup>  [background:] 129/Sv-Htr4<sup>tm1Comp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17913892	20180515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857883	Dysf<sup>im</sup>	is_implicated_in	DOID:11720	distal myopathy		MGI:2175836	Dysf<sup>im</sup>/Dysf<sup>im</sup>  [background:] involves: SJL			ECO:0000033	author statement supported by traceable reference	PMID:10508505	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918957	Ubiad1	is_implicated_in	DOID:0060456	Schnyder corneal dystrophy		MGI:6273247	Ubiad1<sup>em1Wwk</sup>/Ubiad1<sup>+</sup>  [background:] C57BL/6N-Ubiad1<sup>em1Wwk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29977031	20190111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918957	Ubiad1	is_implicated_in	DOID:0060456	Schnyder corneal dystrophy		MGI:6273246	Ubiad1<sup>em1Wwk</sup>/Ubiad1<sup>em1Wwk</sup>  [background:] C57BL/6N-Ubiad1<sup>em1Wwk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29977031	20190111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2450166	Arhgap32	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5811989	Arhgap32<sup>tm1Taki</sup>/Arhgap32<sup>tm1Taki</sup>  [background:] B6N.Cg-Arhgap32<sup>tm1Taki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26979507	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929237	Pus1	is_implicated_in	DOID:0080099	myopathy, lactic acidosis, and sideroblastic anemia		MGI:5811553	Pus1<sup>tm1.1Mdf</sup>/Pus1<sup>tm1.1Mdf</sup>  [background:] B6.129S7(C)-Pus1<sup>tm1.1Mdf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27197761	20161209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136646	Vhl<sup>tm1.1Jae</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2174802	Vhl<sup>tm1.1Jae</sup>/Vhl<sup>+</sup>  [background:] involves: 129S4/SvJae * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11171994	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5438050	b2b1714Clo	is_implicated_in	DOID:114	heart disease		MGI:5442137	b2b1714Clo/b2b1714Clo  [background:] C57BL/6J-b2b1714Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921272	Glyr1	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:7279300	Glyr1<sup>em1Dsr</sup>/Glyr1<sup>em1Dsr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:35182466	20220523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3620573	Lyst<sup>bg-grey</sup>	is_implicated_in	DOID:2935	Chediak-Higashi syndrome		MGI:3620975	Lyst<sup>bg-grey</sup>/Lyst<sup>bg-grey</sup>  [background:] C57BL/6-Lyst<sup>bg-grey</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16518687	20060503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95300	Eif2b4	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6160483	Eif2b4<sup>tm1.1Vdk</sup>/Eif2b4<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26974157	20180612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	is_implicated_in	DOID:3652	Leigh disease		MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	is_implicated_in	DOID:10754	otitis media		MGI:3698627	Sall4<sup>tm1Brd</sup>/Sall4<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17216607	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576223	Syngap1<sup>tm1Rlh</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5485349	Syngap1<sup>tm1Rlh</sup>/Syngap1<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19145222	20130516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526519	Rsc1a1<sup>tm1Koep</sup>	is_implicated_in	DOID:9970	obesity		MGI:3526863	Rsc1a1<sup>tm1Koep</sup>/Rsc1a1<sup>tm1Koep</sup>  [background:] B6.129-Rsc1a1<sup>tm1Koep</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15601832	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149414	Pik3r1<sup>tm1Tka</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2174985	Pik3r1<sup>tm1Tka</sup>/Pik3r1<sup>tm1Tka</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9888854	20081222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856424	Lep<sup>ob</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:5807153	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/JRj			ECO:0000033	author statement supported by traceable reference	PMID:22118645	20190821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2183747	Fgd4	is_implicated_in	DOID:0110192	Charcot-Marie-Tooth disease type 4H		MGI:5460859	Fgd4<sup>tm1.1Ics</sup>/Fgd4<sup>tm1.1Ics</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:23171661	20130128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:2179721	Lamb3<sup>IAP</sup>/Lamb3<sup>IAP</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9271670	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664197	Myh6<sup>tm2Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:6356705	Myh6<sup>tm2Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:24829265	20190823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664197	Myh6<sup>tm2Jse</sup>	is_implicated_in	DOID:0110320	hypertrophic cardiomyopathy 14		MGI:3664295	Myh6<sup>tm2Jse</sup>/Myh6<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:15001446	20190823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4301247	Grhpr<sup>Gt(OST383093)Lex</sup>	is_implicated_in	DOID:0111671	primary hyperoxaluria type 2		MGI:5314653	Grhpr<sup>Gt(OST383093)Lex</sup>/Grhpr<sup>Gt(OST383093)Lex</sup>  [background:] B6.129S5-Grhpr<sup>Gt(OST383093)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22189945	20201118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4301247	Grhpr<sup>Gt(OST383093)Lex</sup>	is_implicated_in	DOID:0111671	primary hyperoxaluria type 2		MGI:6472965	Grhpr<sup>Gt(OST383093)Lex</sup>/Grhpr<sup>Gt(OST383093)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31821850	20201118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181746	Foxj1<sup>tm1Bph</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:2668968	Foxj1<sup>tm1Bph</sup>/Foxj1<sup>tm1Bph</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9739041	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651806	Lpl<sup>tm1Bres</sup>/Lpl<sup>tm1Bres</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8675619	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651807	Lpl<sup>tm1Bres</sup>/Lpl<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8675619	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651821	Lpl<sup>tm1Sem</sup>/Lpl<sup>tm1Sem</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7759497	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651823	Lpl<sup>tm1Sem</sup>/Lpl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7759497	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261811	Myo15a	is_implicated_in	DOID:0110488	autosomal recessive nonsyndromic deafness 3		MGI:6192743	Myo15a<sup>tm1.1Jebd</sup>/Myo15a<sup>tm1.1Jebd</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26302205	20180806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261811	Myo15a	is_implicated_in	DOID:0110488	autosomal recessive nonsyndromic deafness 3		MGI:2175132	Myo15a<sup>sh2-2J</sup>/Myo15a<sup>sh2-2J</sup>  [background:] involves: STOCK Rb(16.17)7Bnr			ECO:0000033	author statement supported by traceable reference	MGI:2135933	20180806	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712283	Slc12a1<sup>urehr3</sup>	is_implicated_in	DOID:0110142	Bartter disease type 1		MGI:4457194	Slc12a1<sup>urehr3</sup>/Slc12a1<sup>urehr3</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:20219826	20100630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5296754	Dnah5<sup>b2b002Clo</sup>/Dnah5<sup>b2b002Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b002Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433327	Dnah5<sup>b2b1537Clo</sup>/Dnah5<sup>b2b1537Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1537Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5554212	Dnah5<sup>b2b2395Clo</sup>/Dnah5<sup>b2b2395Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2395Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5314016	Dnah5<sup>b2b1134Clo</sup>/Dnah5<sup>b2b1134Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1134Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5285617	Dnah5<sup>b2b016Clo</sup>/Dnah5<sup>b2b016Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b016Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313323	Dnah5<sup>b2b1003Clo</sup>/Dnah5<sup>b2b1003Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b1003Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5311158	Dnah5<sup>b2b601Clo</sup>/Dnah5<sup>b2b601Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b601Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5618819	Dnah5<sup>b2b2925Clo</sup>/Dnah5<sup>b2b2925Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2925Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5645239	Dnah5<sup>b2b2451Clo</sup>/Dnah5<sup>b2b2451Clo</sup>  [background:] C57BL/6J-Dnah5<sup>b2b2451Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712359	Duox2<sup>thyd</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3712362	Duox2<sup>thyd</sup>/Duox2<sup>thyd</sup>  [background:] B6(129)-Duox2<sup>thyd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17440044	20070622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:5902457	Mapk1<sup>tm1Gela</sup>/Mapk1<sup>tm1Gela</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26395480	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95705	B4galt1	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:6306320	B4galt1<sup>tm1Yiw</sup>/B4galt1<sup>tm1Yiw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17255313	20190530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96615	Itgb6	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:3581437	Itgb6<sup>tm1Des</sup>/Itgb6<sup>tm1Des</sup>  [background:] involves: 129T2/SvEms			ECO:0000033	author statement supported by traceable reference	PMID:12634787	20050712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606782	Tg(Lim2*G15V)1Rlc	is_implicated_in	DOID:0110263	cataract 19 multiple types		MGI:3606783	Tg(Lim2*G15V)1Rlc/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10851259	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606782	Tg(Lim2*G15V)1Rlc	is_implicated_in	DOID:0110263	cataract 19 multiple types		MGI:3606787	Tg(Lim2*G15V)1Rlc/Tg(Lim2*G15V)1Rlc  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10851259	20130617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442676	Cdc14a	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694867	Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442676	Cdc14a	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694869	Cdc14a<sup>em1Tbf</sup>/Cdc14a<sup>em1Tbf</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442676	Cdc14a	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694857	Cdc14a<sup>tm1a(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442676	Cdc14a	is_implicated_in	DOID:0110491	autosomal recessive nonsyndromic deafness 32		MGI:6694858	Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>/Cdc14a<sup>tm1b(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:29293958	20210426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339977	Agtrap	is_implicated_in	DOID:0060158	acquired metabolic disease		MGI:6511096	Agtrap<sup>tm1Tamk</sup>/Agtrap<sup>tm1Tamk</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23902639	20210318	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	is_implicated_in	DOID:62	aortic valve disease		MGI:5905421	Egfr<sup>wa2</sup>/Egfr<sup>wa2</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25997932	20170726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	is_implicated_in	DOID:62	aortic valve disease		MGI:2176568	Egfr<sup>wa2</sup>/Egfr<sup>wa2</sup>  [background:] STOCK Egfr<sup>wa2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10700187	20170726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95766	Gna11	is_implicated_in	DOID:0090108	autosomal dominant hypocalcemia 2		MGI:6376290	Gna11<sup>em1Mman</sup>/Gna11<sup>em1Mman</sup>  [background:] C57BL/6NCrl-Gna11<sup>em1Mman</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28194446	20191112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95766	Gna11	is_implicated_in	DOID:0090108	autosomal dominant hypocalcemia 2		MGI:6376303	Gna11<sup>em1Mman</sup>/Gna11<sup>+</sup>  [background:] C57BL/6NCrl-Gna11<sup>em1Mman</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28194446	20191112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:2654522	Slc6a3<sup>tm2Mca</sup>/Slc6a3<sup>tm2Mca</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15710042	20111021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856094	Mitf<sup>mi-ew</sup>	is_implicated_in	DOID:4997	Camurati-Engelmann disease		MGI:4455020	Mitf<sup>mi-ew</sup>/Mitf<sup>mi-ew</sup>  [background:] involves: C57BL/6Bn * NAW			ECO:0000033	author statement supported by traceable reference	PMID:11930005	20100615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	is_implicated_in	DOID:2960	photosensitive trichothiodystrophy		MGI:2386443	Ercc2<sup>tm1Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9651581	20050825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	is_implicated_in	DOID:2960	photosensitive trichothiodystrophy		MGI:2386444	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9651581	20050825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	is_implicated_in	DOID:2960	photosensitive trichothiodystrophy		MGI:2386444	Ercc2<sup>tm2(ERCC2)Jhjh</sup>/Ercc2<sup>tm2(ERCC2)Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11950998	20050825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640328	Gnmt<sup>tm1Cwa</sup>	is_implicated_in	DOID:0111037	glycine N-methyltransferase deficiency		MGI:3640329	Gnmt<sup>tm1Cwa</sup>/Gnmt<sup>tm1Cwa</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16779654	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388199	Pdlim3<sup>tm1Krc</sup>	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy		MGI:3621956	Pdlim3<sup>tm1Krc</sup>/Pdlim3<sup>tm1Krc</sup>  [background:] either: (involves: 129S) or (involves: C57BL/6) or (involves: Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:11329061	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3719836	Glis2<sup>tm1Tre</sup>	is_implicated_in	DOID:0111116	nephronophthisis 7		MGI:3720098	Glis2<sup>tm1Tre</sup>/Glis2<sup>tm1Tre</sup>  [background:] B6.129P2-Glis2<sup>tm1Tre</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17618285	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918972	Cic	is_implicated_in	DOID:150	disease of mental health		MGI:6275604	Cic<sup>tm1c(KOMP)Wtsi</sup>/Cic<sup>tm1c(KOMP)Wtsi</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28288114	20190201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:9452	steatotic liver disease		MGI:5807153	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/JRj			ECO:0000033	author statement supported by traceable reference	PMID:25621497	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832950	Tg(CMV-TOR1A*)1Nush	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:3832988	Tg(CMV-TOR1A*)1Nush/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15930383	20090223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	is_implicated_in	DOID:0110481	autosomal recessive nonsyndromic deafness 23		MGI:5704195	Pcdh15<sup>roda</sup>/Pcdh15<sup>roda</sup>  [background:] BALB/c-Pcdh15<sup>roda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24044941	20160226	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856083	Ap3d1<sup>mh</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3528946	Ap3d1<sup>mh</sup>/Ap3d1<sup>mh</sup>  [background:] B6.C3-Grxcr1<sup>pi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858055	Msh2<sup>tm1Htr</sup>	is_implicated_in	DOID:3883	Lynch syndrome		MGI:4429602	Msh2<sup>tm1Htr</sup>/Msh2<sup>tm1Htr</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9443401	20110923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822475	Hesx1<sup>tm3Jpmb</sup>	is_implicated_in	DOID:0060857	septooptic dysplasia		MGI:3822781	Hesx1<sup>tm3Jpmb</sup>/Hesx1<sup>tm3Jpmb</sup>  [background:] involves: 129S/SvEv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19093031	20090113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	is_implicated_in	DOID:9452	steatotic liver disease		MGI:3700375	Ikbkg<sup>tm1.1Mpa</sup>/Ikbkg<sup>tm1.1Mpa</sup> Tg(Alb1-cre)7Gsc/0  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17292824	20150601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927140	Git1	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5000121	Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>/Git1<sup>Gt(FHCRC-GT-S10-12C1)Sor</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21499268	20140115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101785	Mybl2	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5518769	Mybl2<sup>tm1.1Jof</sup>/Mybl2<sup>+</sup> Tg(Zp3-cre)3Mrt/0  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22910183	20131120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813493	Tg(H2-K-Fosl2,-EGFP)13Wag	is_implicated_in	DOID:0050156	idiopathic pulmonary fibrosis		MGI:3813506	Tg(H2-K-Fosl2,-EGFP)13Wag/0  [background:] either: 129.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag or B6.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag			ECO:0000033	author statement supported by traceable reference	PMID:18641127	20081103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3762756	Kiss1r<sup>tm1Rla</sup>	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:3762763	Kiss1r<sup>tm1Rla</sup>/Kiss1r<sup>tm1Rla</sup>  [background:] involves: 129S1/SvImJ			ECO:0000033	author statement supported by traceable reference	PMID:17595229	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101762	Elk3	is_implicated_in	DOID:0060646	congenital chylothorax		MGI:3619005	Elk3<sup>tm1Wlyk</sup>/Elk3<sup>tm1Wlyk</sup>  [background:] either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11566878	20060411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3688281	Cftr<sup>tm2Mrc</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:3689380	Cftr<sup>tm2Mrc</sup>/Cftr<sup>tm2Mrc</sup>  [background:] B6.129S6-Cftr<sup>tm2Mrc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15246977	20061130	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177710	Gck<sup>tm1.2Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590685	Gck<sup>tm1.2Mgn</sup>/Gck<sup>tm1.2Mgn</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177710	Gck<sup>tm1.2Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590686	Gck<sup>tm1.2Mgn</sup>/Gck<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9867845	20051026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	is_not_implicated_in	DOID:0111253	neurofibromatosis 1		MGI:2175144	Nf1<sup>tm1Tyj</sup>/Nf1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7920653	20231019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5560774	b2b2736Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561115	b2b2736Clo/b2b2736Clo  [background:] C57BL/6J-b2b2736Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:4079	heart valve disease		MGI:6272038	Tnf<sup>Bpsm1</sup>/Tnf<sup>+</sup>  [background:] C.Cg-Tnf<sup>Bpsm1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26195802	20190103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675356	Ptch1<sup>tm1Bjw</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5286071	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(Atoh1-cre/Esr1*)14Fsh/0  [background:] involves: 129T2/SvEms * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675356	Ptch1<sup>tm1Bjw</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5286070	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(Atoh1-cre)1Bfri/0  [background:] involves: 129T2/SvEms * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675356	Ptch1<sup>tm1Bjw</sup>	is_implicated_in	DOID:0050902	medulloblastoma		MGI:5286072	Ptch1<sup>tm1Bjw</sup>/Ptch1<sup>tm1Bjw</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129T2/SvEms * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18691548	20110922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921303	Grip1	is_implicated_in	DOID:11836	clubfoot		MGI:3665403	Grip1<sup>eb</sup>/Grip1<sup>eb</sup>  [background:] involves: hairless stock			ECO:0000033	author statement supported by traceable reference	MGI:61605	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716859	Prex1<sup>tm1Hcew</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3717173	Prex1<sup>tm1Hcew</sup>/Prex1<sup>tm1Hcew</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26621702	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449975	Iqgap2	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5568837	Iqgap2<sup>tm1Vs</sup>/Iqgap2<sup>tm1Vs</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:23951254	20140619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3798815	Mta2<sup>tm1.1Yzha</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3803013	Mta2<sup>tm1.1Yzha</sup>/Mta2<sup>tm1.1Yzha</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18353770	20080915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677579	Vhl<sup>tm1.1Lss</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2677768	Vhl<sup>tm1.1Lss</sup>/Vhl<sup>+</sup>  [background:] involves: A/J			ECO:0000033	author statement supported by traceable reference	PMID:14500363	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2677579	Vhl<sup>tm1.1Lss</sup>	is_implicated_in	DOID:14175	von Hippel-Lindau disease		MGI:2677767	Vhl<sup>tm1.1Lss</sup>/Vhl<sup>+</sup>  [background:] involves: BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:14500363	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851245	Tg(Kera-PITX2*A)BHjal	is_implicated_in	DOID:0110120	Axenfeld-Rieger syndrome type 1		MGI:3851250	Tg(Kera-PITX2*A)BHjal/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15509533	20090727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915443	Rpl24	is_implicated_in	DOID:5723	optic atrophy		MGI:2658856	Rpl24<sup>Bst</sup>/Rpl24<sup>+</sup>  [background:] involves: C57BLKS			ECO:0000033	author statement supported by traceable reference	PMID:8589526	20090814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	is_implicated_in	DOID:12638	hypertrophic pyloric stenosis		MGI:2174975	Nos1<sup>tm1Plh</sup>/Nos1<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7505721	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	is_implicated_in	DOID:0060647	fetal encasement syndrome		MGI:3609030	Chuk<sup>tm1Mka</sup>/Chuk<sup>tm1Mka</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	is_implicated_in	DOID:0060647	fetal encasement syndrome		MGI:3609426	Chuk<sup>tm1Ver</sup>/Chuk<sup>tm1Ver</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	is_implicated_in	DOID:0060647	fetal encasement syndrome		MGI:3609425	Chuk<sup>tm1Aki</sup>/Chuk<sup>tm1Aki</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20961246	20130501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6416112	Eif2b5<sup>tm1.1Sidr</sup>/Eif2b5<sup>tm1.1Sidr</sup>  [background:] B6(Cg)-Eif2b5<sup>tm1.1Sidr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30624206	20200512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:5752255	Eif2b5<sup>tm1Itl</sup>/Eif2b5<sup>tm1Itl</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:23056417	20200512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:6160484	Eif2b5<sup>tm1.1Vdk</sup>/Eif2b5<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26974157	20200512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	is_implicated_in	DOID:0060868	leukoencephalopathy with vanishing white matter		MGI:5306390	Eif2b5<sup>tm1Itl</sup>/Eif2b5<sup>tm1Itl</sup>  [background:] involves: 129S/SvEv * C57BL * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:20826436	20200512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919819	Bbs5	is_implicated_in	DOID:0110127	Bardet-Biedl syndrome 5		MGI:6741540	Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>/Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6-Bbs5<sup>tm1a(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33560420	20210820	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5009037	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(VAV1-cre)1Graf/0  [background:] involves: 129 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21562564	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5009036	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129 * C57BL/6 * CBA * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21562564	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444989	Spg11	is_implicated_in	DOID:0110764	hereditary spastic paraplegia 11		MGI:5790094	Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>/Spg11<sup>Gt(EUCE0085f05)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26284655	20160829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3606208	Mybpc3<sup>tm1Lcrr</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:3608495	Mybpc3<sup>tm1Lcrr</sup>/Mybpc3<sup>+</sup>  [background:] involves: 129S4/SvJae * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:15249187	20051227	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108186	Aldh7a1	is_implicated_in	DOID:0080768	pyridoxine-dependent epilepsy		MGI:6491217	Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>/Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>  [background:] B6(FVB)-Aldh7a1<sup>tm1d(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32969477	20210111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98457	sy	is_not_implicated_in	DOID:0050646	distal arthrogryposis		MGI:2451235	sy/sy  [background:] B6C3Fe-a/a			ECO:0000033	author statement supported by traceable reference	PMID:11285249	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934580	Trp63<sup>tm2Brd</sup>	is_implicated_in	DOID:0080174	bladder exstrophy		MGI:3511141	Trp63<sup>tm2Brd</sup>/Trp63<sup>tm2Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17079275	20121109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176524	Ptpn11<sup>tm1Paw</sup>	is_not_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:2176525	Ptpn11<sup>tm1Paw</sup>/Ptpn11<sup>tm1Paw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9171349	20051017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158463	Lmx1b<sup>tm1Rjo</sup>	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3052222	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15562281	20070727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158463	Lmx1b<sup>tm1Rjo</sup>	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3716366	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15562281	20070727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158463	Lmx1b<sup>tm1Rjo</sup>	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:2677374	Lmx1b<sup>tm1Rjo</sup>/Lmx1b<sup>tm1Rjo</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9590288	20070727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858008	Ctnnb1<sup>tm1Mmt</sup>	is_implicated_in	DOID:2394	ovarian cancer		MGI:5432223	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(CYP19A1-cre)1Jri/0  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858008	Ctnnb1<sup>tm1Mmt</sup>	is_implicated_in	DOID:2394	ovarian cancer		MGI:5432228	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21860425	20120827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98241	Stmn2	is_implicated_in	DOID:2477	motor peripheral neuropathy		MGI:7523313	Chat<sup>tm2(cre)Lowl</sup>/Chat<sup>+</sup> Stmn2<sup>em2Jmi</sup>/Stmn2<sup>em2Jmi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98241	Stmn2	is_implicated_in	DOID:2477	motor peripheral neuropathy		MGI:7523314	Stmn2<sup>em1Jmi</sup>/Stmn2<sup>+</sup>  [background:] C57BL/6N-Stmn2<sup>em1Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35767949	20230904	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	is_implicated_in	DOID:0110293	autosomal recessive limb-girdle muscular dystrophy type 2P		MGI:4940545	Dag1<sup>tm4.1Kcam</sup>/Dag1<sup>tm4.1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21388311	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	is_implicated_in	DOID:0111078	tibial muscular dystrophy		MGI:4838323	Ttn<sup>tm1.1Isrd</sup>/Ttn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20855473	20101115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0080041	hypochondroplasia		MGI:7517089	Fgfr3<sup>tm3.1Llm</sup>/Fgfr3<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:37345656	20230812	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586567	Tg(Myh6-Tnf)2Brgi	is_implicated_in	DOID:6000	congestive heart failure		MGI:3586619	Tg(Myh6-Tnf)2Brgi/?  [background:] involves: C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:9577949	20170830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894697	Rad54l	is_implicated_in	DOID:0060252	sclerocornea		MGI:6288687	Rad54l<sup>em1Murr</sup>/Rad54l<sup>+</sup>  [background:] C57BL/6N-Rad54l<sup>em1Murr</sup>/MurrJ			ECO:0000033	author statement supported by traceable reference	MGI:5576271	20200108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5906364	rd21	is_implicated_in	DOID:8466	retinal degeneration		MGI:5906382	rd21/rd21  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:5906378	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3662623	Ret<sup>tm1Kln</sup>	is_implicated_in	DOID:11836	clubfoot		MGI:3662906	Ret<sup>tm1Kln</sup>/Ret<sup>tm1Kln</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16600854	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388040	Map6<sup>tm1Job</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5694657	Map6<sup>tm1Job</sup>/Map6<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23002183	20151104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388040	Map6<sup>tm1Job</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5694660	Map6<sup>tm1Job</sup>/Map6<sup>tm1Job</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23002183	20151104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388040	Map6<sup>tm1Job</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3041140	Map6<sup>tm1Job</sup>/Map6<sup>tm1Job</sup>  [background:] either: 129S2/SvPas or (involves: 129S2/SvPas * BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:12231625	20151104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857258	Tgfb1<sup>tm1Doe</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2174925	Tgfb1<sup>tm1Doe</sup>/Tgfb1<sup>tm1Doe</sup>  [background:] involves: 129S2/SvPas * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:1436033	20050711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:9970	obesity		MGI:3589409	Alms1<sup>Gt(XH152)Byg</sup>/Alms1<sup>Gt(XH152)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16000322	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	is_implicated_in	DOID:9970	obesity		MGI:3611807	Alms1<sup>bbb</sup>/Alms1<sup>bbb</sup>  [background:] C57BL/6JSfdAnu-Alms1<sup>bbb</sup>/Anu			ECO:0000033	author statement supported by traceable reference	MGI:3611487	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918673	Epg5	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5505671	Epg5<sup>tm1Ygz</sup>/Epg5<sup>tm1Ygz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27715390	20200127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860443	Rabggta	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2679085	Rabggta<sup>gm</sup>/Rabggta<sup>gm</sup>  [background:] C57BL/6J-Rabggta<sup>gm</sup>			ECO:0000033	author statement supported by traceable reference	MGI:61612	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860443	Rabggta	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2679085	Rabggta<sup>gm</sup>/Rabggta<sup>gm</sup>  [background:] C57BL/6J-Rabggta<sup>gm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8490171	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	is_implicated_in	DOID:0050662	bestrophinopathy		MGI:4450918	Best1<sup>tm1.1Amar</sup>/Best1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	is_implicated_in	DOID:0050662	bestrophinopathy		MGI:4443335	Best1<sup>tm1.1Amar</sup>/Best1<sup>tm1.1Amar</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:2679475	Ptch1<sup>tm1Zim</sup>/Ptch1<sup>+</sup>  [background:] either: (involves: 129 * C57BL/6) or (involves: 129 * CD-1)			ECO:0000033	author statement supported by traceable reference	PMID:9585239	20140512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:5544602	Ptch1<sup>dl</sup>/Ptch1<sup>dl</sup>  [background:] involves: 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23897749	20140512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:3610455	Ptch1<sup>tm1Kmmt</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12542834	20140512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:2177702	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9262482	20140512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932535	Glis2	is_implicated_in	DOID:0111116	nephronophthisis 7		MGI:3720098	Glis2<sup>tm1Tre</sup>/Glis2<sup>tm1Tre</sup>  [background:] B6.129P2-Glis2<sup>tm1Tre</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17618285	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103012	E2f4	is_implicated_in	DOID:10754	otitis media		MGI:3582492	E2f4<sup>tm1Lees</sup>/E2f4<sup>tm1Lees</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10983976	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917887	Ankrd26	is_implicated_in	DOID:9970	obesity		MGI:3799316	Ankrd26<sup>Gt(XK525)Byg</sup>/Ankrd26<sup>Gt(XK525)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18162531	20100603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856083	Ap3d1<sup>mh</sup>	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:3528946	Ap3d1<sup>mh</sup>/Ap3d1<sup>mh</sup>  [background:] B6.C3-Grxcr1<sup>pi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:5807153	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] B6.Cg-Lep<sup>ob</sup>/JRj			ECO:0000033	author statement supported by traceable reference	PMID:22118645	20190821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180194	Tbx21<sup>tm1Glm</sup>	is_implicated_in	DOID:2841	asthma		MGI:2180790	Tbx21<sup>tm1Glm</sup>/Tbx21<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11786643	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180194	Tbx21<sup>tm1Glm</sup>	is_implicated_in	DOID:2841	asthma		MGI:2180789	Tbx21<sup>tm1Glm</sup>/Tbx21<sup>tm1Glm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11786643	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104698	Lim2	is_implicated_in	DOID:83	cataract		MGI:5304399	Lim2<sup>Aca47</sup>/Lim2<sup>Aca47</sup>  [background:] C57BL/6J-Lim2<sup>Aca47</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21617753	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831171	Tg(Pbsn-Ar*E231G)7353Ng	is_implicated_in	DOID:10283	prostate cancer		MGI:3831195	Tg(Pbsn-Ar*E231G)7353Ng/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15657128	20090210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	is_implicated_in	DOID:1059	intellectual disability		MGI:6754183	Elp2<sup>em2Bjw</sup>/Elp2<sup>em3Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	is_implicated_in	DOID:1059	intellectual disability		MGI:6754173	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	is_implicated_in	DOID:1059	intellectual disability		MGI:6754175	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803954	Mapk1<sup>tm1Gela</sup>	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:5902457	Mapk1<sup>tm1Gela</sup>/Mapk1<sup>tm1Gela</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:26395480	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3770755	Efemp1<sup>tm1Lmar</sup>	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3771020	Efemp1<sup>tm1Lmar</sup>/Efemp1<sup>tm1Lmar</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:17664227	20080215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3770755	Efemp1<sup>tm1Lmar</sup>	is_implicated_in	DOID:0060745	Doyne honeycomb retinal dystrophy		MGI:3771021	Efemp1<sup>tm1Lmar</sup>/Efemp1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:17664227	20080215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678809	Tg(Alb1HBV)44Bri	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5689882	Tg(Alb1HBV)44Bri/0  [background:] C57BL/6J-Tg(Alb1HBV)44Bri/J			ECO:0000033	author statement supported by traceable reference	PMID:26035378	20151013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110944	autosomal recessive osteopetrosis 4		MGI:2680800	Clcn7<sup>tm2Tjj</sup>/Clcn7<sup>tm2Tjj</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11207362	20120117	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	is_implicated_in	DOID:0110944	autosomal recessive osteopetrosis 4		MGI:2680797	Clcn7<sup>tm1Tjj</sup>/Clcn7<sup>tm1Tjj</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11207362	20120117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681980	Prnp<sup>tm1(PRNP)Tkit</sup>	is_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2681992	Prnp<sup>tm1(PRNP)Tkit</sup>/Prnp<sup>tm1(PRNP)Tkit</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:14633630	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	is_implicated_in	DOID:13482	Proteus syndrome		MGI:6460379	Akt1<sup>tm1.1Mjl</sup>/Akt1<sup>+</sup>  [background:] chimera involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31194862	20201008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	is_implicated_in	DOID:13482	Proteus syndrome		MGI:6460345	Akt1<sup>tm1Mjl</sup>/Akt1<sup>+</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31194862	20201008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3642370	Apela	is_implicated_in	DOID:10591	pre-eclampsia		MGI:6118197	Apela<sup>tm1.2Brre</sup>/Apela<sup>tm1.2Brre</sup>  [background:] B6(Cg)-Apela<sup>tm1.2Brre</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28663440	20180301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180367	Asah1<sup>tm1Esc</sup>	is_implicated_in	DOID:0050464	Farber lipogranulomatosis		MGI:2655551	Asah1<sup>tm1Esc</sup>/Asah1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11829492	20050602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803954	Mapk1<sup>tm1Gela</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5660194	Mapk1<sup>tm1Gela</sup>/Mapk1<sup>tm1Gela</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:18952847	20150827	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4201195	Nosip<sup>Gt(OST138992)Lex</sup>	is_implicated_in	DOID:4621	holoprosencephaly		MGI:6711274	Nosip<sup>Gt(OST138992)Lex</sup>/Nosip<sup>Gt(OST138992)Lex</sup>  [background:] B6.129S5-Nosip<sup>Gt(OST138992)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25546391	20210519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183244	Upk3a<sup>tm1Tsun</sup>	is_implicated_in	DOID:9620	vesicoureteral reflux		MGI:2654027	Upk3a<sup>tm1Tsun</sup>/Upk3a<sup>tm1Tsun</sup>  [background:] either: (involves: 129S/SvEv) or (involves: 129S/SvEv * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:11085999	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:2654712	Dkc1<sup>tm1Ppp</sup>/Dkc1<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12522253	20150723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:2661986	Dkc1<sup>tm1Ppp</sup>/Y  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12522253	20150723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:5644816	Dkc1<sup>tm1.1Pjma</sup>/Y  [background:] B6.129X1(FVB)-Dkc1<sup>tm1.1Pjma</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21241452	20150723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440439	Tg(CAG-VCP*R155H)55Jpat	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:4440449	Tg(CAG-VCP*R155H)55Jpat/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20147319	20100414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438491	Tg(Thy1-TARDBP)6Singh	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:4438493	Tg(Thy1-TARDBP)6Singh/Tg(Thy1-TARDBP)6Singh  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20133711	20100402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849082	Six1<sup>Cwe</sup>	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:3849173	Six1<sup>Cwe</sup>/Six1<sup>Cwe</sup>  [background:] C3HeB/FeJ-Six1<sup>Cwe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19389353	20090629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5526095	Jak1<sup>M1Mhda</sup>/Jak1<sup>+</sup>  [background:] C3HeB/FeJ-Jak1<sup>M1Mhda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23791841	20140103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3586448	Park7<sup>tm1Xz</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3604390	Park7<sup>tm1Xz</sup>/Park7<sup>tm1Xz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15799973	20051114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856097	Atp7a<sup>Mo-blo</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3793864	Atp7a<sup>Mo-blo</sup>/Y  [background:] B6.Cg-Atp7a<sup>Mo-blo</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8895222	20190722	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5790841	Il33<sup>tm1(KOMP)Vlcg</sup>/Il33<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Il33<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28675392	20190405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2664387	Mmp21	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313515	Mmp21<sup>b2b873Clo</sup>/Mmp21<sup>b2b873Clo</sup>  [background:] C57BL/6J-Mmp21<sup>b2b873Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2664387	Mmp21	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5555841	Mmp21<sup>b2b2458Clo</sup>/Mmp21<sup>b2b2458Clo</sup>  [background:] C57BL/6J-Mmp21<sup>b2b2458Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109514	Cstb	is_implicated_in	DOID:3535	Unverricht-Lundborg syndrome		MGI:3040574	Cstb<sup>tm1Rm</sup>/Cstb<sup>tm1Rm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:11555622	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109514	Cstb	is_implicated_in	DOID:3535	Unverricht-Lundborg syndrome		MGI:3040574	Cstb<sup>tm1Rm</sup>/Cstb<sup>tm1Rm</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9806543	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857404	Mstn<sup>Cmpt</sup>	is_implicated_in	DOID:0111072	myostatin-related muscle hypertrophy		MGI:5529108	Mstn<sup>Cmpt</sup>/Mstn<sup>+</sup>  [background:] either: HCI or HCR			ECO:0000033	author statement supported by traceable reference	PMID:9335610	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921273	Rd3	is_implicated_in	DOID:0110080	Leber congenital amaurosis 12		MGI:3715440	Rd3<sup>rd3</sup>/Rd3<sup>rd3</sup>  [background:] RBF/DnJ-Rd3<sup>rd3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23687432	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97524	Pde6a	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3828991	Pde6a<sup>nmf363</sup>/Pde6a<sup>nmf363</sup>  [background:] C57BL/6J-Pde6a<sup>nmf363</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18849587	20090126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97524	Pde6a	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3611315	Pde6a<sup>nmf282</sup>/Pde6a<sup>nmf282</sup>  [background:] A.B6 Tyr<sup>+</sup>-Pde6a<sup>nmf282</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18849587	20090126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676373	Pkd2<sup>tm1Dwo</sup>	is_implicated_in	DOID:0110859	polycystic kidney disease 2		MGI:2676553	Pkd2<sup>tm1Dwo</sup>/Pkd2<sup>tm1Dwo</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12062060	20091021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5925396	Cdc73<sup>tm1Btt</sup>/Cdc73<sup>+</sup> Tg(PTH-cre)4167Slib/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5925391	Cdc73<sup>Gt(RRE190)Byg</sup>/Cdc73<sup>+</sup>  [background:] B6.129P2-Cdc73<sup>Gt(RRE190)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5925397	Cdc73<sup>tm1Btt</sup>/Cdc73<sup>tm1Btt</sup> Tg(PTH-cre)4167Slib/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28288139	20171121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027491	Htr4<sup>tm1Comp</sup>	is_not_implicated_in	DOID:3083	chronic obstructive pulmonary disease		MGI:6156525	Htr4<sup>tm1Comp</sup>/Htr4<sup>tm1Comp</sup>  [background:] B6.129S1(129T)-Htr4<sup>tm1Comp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24183679	20180516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857713	Jag1<sup>tm1Grid</sup>	is_not_implicated_in	DOID:9245	Alagille syndrome		MGI:2384058	Jag1<sup>tm1Grid</sup>/Jag1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10196361	20050920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	is_implicated_in	DOID:0060340	ciliopathy		MGI:5498234	Kif7<sup>b2b2254Clo</sup>/Kif7<sup>b2b2254Clo</sup>  [background:] C57BL/6J-Kif7<sup>b2b2254Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	is_implicated_in	DOID:0110594	primary ciliary dyskinesia 1		MGI:5285345	Dnai1<sup>b2b284Clo</sup>/Dnai1<sup>b2b284Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	is_implicated_in	DOID:0110594	primary ciliary dyskinesia 1		MGI:5317636	Dnai1<sup>b2b1526Clo</sup>/Dnai1<sup>b2b1526Clo</sup>  [background:] C57BL/6J-Dnai1<sup>b2b1526Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	is_implicated_in	DOID:0110594	primary ciliary dyskinesia 1		MGI:4415702	Dnai1<sup>tm1.1Leo</sup>/Dnai1<sup>tm1.1Leo</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT)Nat</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19675306	20120807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	is_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:4443335	Best1<sup>tm1.1Amar</sup>/Best1<sup>tm1.1Amar</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	is_implicated_in	DOID:0050661	vitelliform macular dystrophy		MGI:4450918	Best1<sup>tm1.1Amar</sup>/Best1<sup>+</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:20053664	20100513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859274	Pdlim3	is_implicated_in	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy		MGI:3621956	Pdlim3<sup>tm1Krc</sup>/Pdlim3<sup>tm1Krc</sup>  [background:] either: (involves: 129S) or (involves: C57BL/6) or (involves: Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:11329061	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99414	Id4	is_implicated_in	DOID:11476	osteoporosis		MGI:4819227	Id4<sup>tm1Fsky</sup>/Id4<sup>tm1Fsky</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20628571	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491162	b2b2153Clo	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5516012	b2b2153Clo/b2b2153Clo  [background:] C57BL/6J-b2b2153Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859606	Wdr45	is_implicated_in	DOID:0110739	neurodegeneration with brain iron accumulation 5		MGI:6721006	Wdr45<sup>em1Wrst</sup>/Y  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:34043061	20210714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859606	Wdr45	is_implicated_in	DOID:0110739	neurodegeneration with brain iron accumulation 5		MGI:6721005	Wdr45<sup>em1Wrst</sup>/Wdr45<sup>em1Wrst</sup>  [background:] involves: C57BL/6N * FVB			ECO:0000033	author statement supported by traceable reference	PMID:34043061	20210714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662295	Adcy5<sup>tm1Yish</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:2662300	Adcy5<sup>tm1Yish</sup>/Adcy5<sup>tm1Yish</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12665504	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856830	Aqp2<sup>cph</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3639115	Aqp2<sup>cph</sup>/Aqp2<sup>cph</sup>  [background:] C57BL/6J-Aqp2<sup>cph</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16641094	20060727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856671	Col1a1<sup>Mov13</sup>	is_implicated_in	DOID:0110334	osteogenesis imperfecta type 1		MGI:3620112	Col1a1<sup>Mov13</sup>/Col1a1<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:2402497	20060421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107736	Dync2h1	is_implicated_in	DOID:0110087	asphyxiating thoracic dystrophy 3		MGI:5311880	Dync2h1<sup>b2b414Clo</sup>/Dync2h1<sup>b2b414Clo</sup>  [background:] C57BL/6J-Dync2h1<sup>b2b414Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183897	Psap<sup>tm2Suz</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:2183898	Psap<sup>tm2Suz</sup>/Psap<sup>tm2Suz</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11371512	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763906	Tg(HSA*LR)20aCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3763920	Tg(HSA*LR)20aCath/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386679	Hif1a<sup>tm3Rsjo</sup>	is_implicated_in	DOID:11721	glycogen storage disease VII		MGI:3621470	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15328538	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3810467	Tg(tetO-MET)23Rwng	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3810811	Tg(tetO-MET)23Rwng/0 Tg(Cebpb-tTA)5Bjd/0  [background:] involves: FVB/N * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:11381087	20090323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857803	Eya1<sup>bor</sup>	is_implicated_in	DOID:14702	branchiootorenal syndrome		MGI:2175870	Eya1<sup>bor</sup>/Eya1<sup>bor</sup>  [background:] C3HeB/FeJ-Eya1<sup>bor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10072433	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	is_not_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:5085318	Ccm2<sup>tm2.1Sbn</sup>/Ccm2<sup>tm2.1Sbn</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21596842	20110812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	is_not_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:3837691	Ccm2<sup>tm1Etl</sup>/Ccm2<sup>tm1Etl</sup> Tg(Nes-cre)1Kln/?  [background:] B6.Cg-Ccm2<sup>tm1Etl</sup> Tg(Nes-cre)1Kln			ECO:0000033	author statement supported by traceable reference	PMID:19259391	20110812	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924105	Slc17a5	is_implicated_in	DOID:3211	lysosomal storage disease		MGI:3609722	Slc17a5<sup>tm1Lex</sup>/Slc17a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:3609573	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914167	Chordc1	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:5644329	Chordc1<sup>tm1Mbra</sup>/Chordc1<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25678499	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312336	Dnah11<sup>b2b598Clo</sup>/Dnah11<sup>b2b598Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b598Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5317649	Dnah11<sup>b2b1279Clo</sup>/Dnah11<sup>b2b1279Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1279Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437114	Dnah11<sup>b2b1289Clo</sup>/Dnah11<sup>b2b1289Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1289Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5512643	Dnah11<sup>b2b2349Clo</sup>/Dnah11<sup>b2b2349Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b2349Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5446426	Dnah11<sup>b2b1775Clo</sup>/Dnah11<sup>b2b1775Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1775Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5318339	Dnah11<sup>b2b1203Clo</sup>/Dnah11<sup>b2b1203Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1203Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5437752	Dnah11<sup>b2b1727Clo</sup>/Dnah11<sup>b2b1727Clo</sup>  [background:] C57BL/6J-Dnah11<sup>b2b1727Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793297	Gp1bb<sup>tm2Frla</sup>	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3805721	Gp1bb<sup>tm2Frla</sup>/Gp1bb<sup>tm2Frla</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17095718	20111110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:6199038	Grn<sup>tm1.1Hiok</sup>/Grn<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29382817	20190613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:6314154	Grn<sup>tm2.1Far</sup>/Grn<sup>tm2.1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29511098	20190613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	is_implicated_in	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions		MGI:5444200	Grn<sup>tm1.1Far</sup>/Grn<sup>tm1.1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:25155018	20190613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4434291	Aff3<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0112383	KINSSHIP syndrome		MGI:5608405	Aff3<sup>tm1a(EUCOMM)Wtsi</sup>/Aff3<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Aff3<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:33961779	20220613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	is_implicated_in	DOID:8398	osteoarthritis		MGI:3578783	Bmpr1a<sup>tm2.1Bhr</sup>/Bmpr1a<sup>tm2.2Bhr</sup> Tg(Gdf5-cre,-ALPP)1Kng/0  [background:] involves: 129 * C57BL/6 * FVB/N-Tg(Gdf5-cre-ALPP)1Kng			ECO:0000033	author statement supported by traceable reference	PMID:15492776	20050603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155421	Myo7a<sup>4494SB</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3587759	Myo7a<sup>4494SB</sup>/Myo7a<sup>4494SB</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:9186010	20060307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849598	Dkc1<sup>tm2Pjma</sup>	is_not_implicated_in	DOID:2729	dyskeratosis congenita		MGI:3849602	Dkc1<sup>tm2Pjma</sup>/Y  [background:] chimera involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19391112	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154520	Cdk4<sup>tm1Bbd</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:2386959	Cdk4<sup>tm1Bbd</sup>/Cdk4<sup>tm1Bbd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:10319860	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153048	Sgcb<sup>tm1Kcam</sup>	is_implicated_in	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E		MGI:3626292	Sgcb<sup>tm1Kcam</sup>/Sgcb<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10678176	20060706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579836	Tbx20<sup>tm1.1Rph</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3579845	Tbx20<sup>tm1.1Rph</sup>/Tbx20<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15843414	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105382	Lama5	is_implicated_in	DOID:2975	cystic kidney disease		MGI:3823250	Lama5<sup>tm3Jhm</sup>/Lama5<sup>tm3Jhm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16790509	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97772	Prox1	is_implicated_in	DOID:9970	obesity		MGI:2669229	Prox1<sup>tm1Gco</sup>/Prox1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:16170315	20060127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932522	Foxg1<sup>tm1(cre)Skm</sup>	is_implicated_in	DOID:1206	Rett syndrome		MGI:5806112	Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27001178	20161103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915541	Mto1	is_implicated_in	DOID:0060286	combined oxidative phosphorylation deficiency		MGI:5659847	Mto1<sup>Gt(G019A03)Wrst</sup>/Mto1<sup>Gt(G019A03)Wrst</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25506927	20150825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	is_implicated_in	DOID:10907	microcephaly		MGI:5753081	Aspm<sup>tm1(cre)Mrc</sup>/Aspm<sup>tm1(cre)Mrc</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26581405	20160323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	is_implicated_in	DOID:10907	microcephaly		MGI:4834526	Aspm<sup>Gt(AA0137)Wtsi</sup>/Aspm<sup>Gt(AA0137)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20823249	20160323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	is_implicated_in	DOID:10907	microcephaly		MGI:4834525	Aspm<sup>Gt(AJ0069)Wtsi</sup>/Aspm<sup>Gt(AJ0069)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20823249	20160323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104511	Tnfsf4	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3640479	Tnfsf4<sup>tm1Shr</sup>/Tnfsf4<sup>tm1Shr</sup>  [background:] NOD.129S4-Tnfsf4<sup>tm1Shr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14662903	20060811	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3774583	Pdx1<sup>tm1Cvw</sup>/Pdx1<sup>tm4Cvw</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18155690	20080321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3817472	Lepr<sup>m3Btlr</sup>	is_implicated_in	DOID:9970	obesity		MGI:3817475	Lepr<sup>m3Btlr</sup>/Lepr<sup>m3Btlr</sup>  [background:] C57BL/6J-Lepr<sup>m3Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3815208	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94910	Dmp1	is_implicated_in	DOID:0050949	autosomal recessive hypophosphatemic rickets		MGI:5694692	Dmp1<sup>tm1Mis</sup>/Dmp1<sup>tm1Mis</sup>  [background:] involves: 129S7/SvEvBrd * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21542006	20151105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	is_implicated_in	DOID:0110414	retinitis pigmentosa 3		MGI:3720014	Rpgr<sup>Rd9</sup>/Y  [background:] C57BL/6-Rpgr<sup>Rd9</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22563472	20170111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	is_implicated_in	DOID:0110414	retinitis pigmentosa 3		MGI:3038416	Rpgr<sup>tm1Tili</sup>/Rpgr<sup>tm1Tili</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10725384	20170111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:5527171	Tecta<sup>tm3.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:5527173	Tecta<sup>tm4.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:5527175	Tecta<sup>tm5.1Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:24363064	20140108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	is_implicated_in	DOID:0110544	autosomal dominant nonsyndromic deafness 12		MGI:3605834	Tecta<sup>tm2Gpr</sup>/Tecta<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15995703	20140108	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583746	Npr2<sup>cn-3J</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:4947978	Npr2<sup>cn-3J</sup>/Npr2<sup>cn-3J</sup>  [background:] MRL/MpJ-Npr2<sup>cn-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:4947088	20110426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913529	Tmem218	is_implicated_in	DOID:0050576	Senior-Loken syndrome		MGI:5700364	Tmem218<sup>Gt(OST40451)Lex</sup>/Tmem218<sup>Gt(OST40451)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25161209	20160101	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:0080027	spondyloepimetaphyseal dysplasia		MGI:5007718	Col2a1<sup>Rgsc856</sup>/Col2a1<sup>Rgsc856</sup>  [background:] involves: C57BL/6JJcl * DBA/2JJcl			ECO:0000033	author statement supported by traceable reference	PMID:21538020	20180419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:0080027	spondyloepimetaphyseal dysplasia		MGI:6151404	Col2a1<sup>Rgsc413</sup>/Col2a1<sup>Rgsc413</sup>  [background:] involves: C57BL/6JJcl * DBA/2JJcl			ECO:0000033	author statement supported by traceable reference	PMID:26545783	20180419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438490	Tg(Thy1-TARDBP)4Singh	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:4438492	Tg(Thy1-TARDBP)4Singh/Tg(Thy1-TARDBP)4Singh  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:20133711	20100402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438490	Tg(Thy1-TARDBP)4Singh	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:4438494	Tg(Thy1-TARDBP)4Singh/0  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:20133711	20100402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054985	Klf15<sup>tm1Jain</sup>	is_implicated_in	DOID:3627	aortic aneurysm		MGI:4888122	Klf15<sup>tm1Jain</sup>/Klf15<sup>tm1Jain</sup>  [background:] B6.129X1-Klf15<sup>tm1Jain</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20375365	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99917	Slc1a3	is_implicated_in	DOID:13544	low tension glaucoma		MGI:4417921	Slc1a3<sup>tm1Kta</sup>/Slc1a3<sup>tm1Kta</sup>  [background:] B6.129P2-Slc1a3<sup>tm1Kta</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17607354	20100115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096877	Dll3	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:2178677	Dll3<sup>tm1Rbe</sup>/Dll3<sup>tm1Rbe</sup>  [background:] involves: 129P2/Ola * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11923214	20070409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3629669	Pcsk1<sup>N222D</sup>	is_implicated_in	DOID:9970	obesity		MGI:3629805	Pcsk1<sup>N222D</sup>/Pcsk1<sup>N222D</sup>  [background:] C57BL/6-Pcsk1<sup>N222D</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16644867	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135666	Fgfr3<sup>tm1Cxd</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3586593	Fgfr3<sup>tm1Cxd</sup>/Fgfr3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9887329	20050901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179190	Tbx1<sup>tm1Pa</sup>	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:3586912	Tbx1<sup>tm1Pa</sup>/Tbx1<sup>tm1Pa</sup>  [background:] either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:11242110	20050908	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445879	Lcat<sup>tm1Nsa</sup>	is_implicated_in	DOID:1391	Norum disease		MGI:3530641	Lcat<sup>tm1Nsa</sup>/Lcat<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9054454	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445879	Lcat<sup>tm1Nsa</sup>	is_implicated_in	DOID:1391	Norum disease		MGI:3530620	Lcat<sup>tm1Nsa</sup>/Lcat<sup>tm1Nsa</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9054454	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934274	Prnp<sup>tm1Edin</sup>	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174710	Prnp<sup>tm1Edin</sup>/Prnp<sup>tm1Edin</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Edin</sup>/EdinH			ECO:0000033	author statement supported by traceable reference	PMID:10581259	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	is_implicated_in	DOID:12842	Guillain-Barre syndrome		MGI:3803199	Aire<sup>tm1Mand</sup>/Aire<sup>+</sup>  [background:] NOD.129P2-Aire<sup>tm1Mand</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22490868	20130503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3721399	Evc<sup>tm1Jago</sup>	is_implicated_in	DOID:12714	Ellis-Van Creveld syndrome		MGI:3721945	Evc<sup>tm1Jago</sup>/Evc<sup>tm1Jago</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17660199	20070918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388062	Fgfr3<sup>tm1.1Iwa</sup>	is_implicated_in	DOID:0050736	autosomal dominant disease		MGI:3640198	Fgfr3<sup>tm1.1Iwa</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11406607	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	is_implicated_in	DOID:9263	homocystinuria		MGI:2660658	Cbs<sup>tm1Unc</sup>/Cbs<sup>tm1Unc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15386278	20141013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	is_implicated_in	DOID:9263	homocystinuria		MGI:3623008	Cbs<sup>tm1Unc</sup>/Cbs<sup>+</sup>  [background:] B6.129P2-Cbs<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25016930	20141013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3833917	Tg(Cd4-NPM/ALK)N1Ingh	is_implicated_in	DOID:9538	multiple myeloma		MGI:5805976	Tg(Cd4-NPM/ALK)N1Ingh/0  [background:] either: (involves: BALB/c * Swiss Webster) or (involves: C57BL/6 * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:12424201	20161102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4366527	Tg(Camk2a-App*,-Apbb1)25Spim	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4366531	Tg(Camk2a-App*,-Apbb1)25Spim/0  [background:] C57BL/6-Tg(Camk2a-App*,-Apbb1)25Spim			ECO:0000033	author statement supported by traceable reference	PMID:19837693	20091109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822312	Lepr<sup>tm2Yli</sup>	is_implicated_in	DOID:9970	obesity		MGI:3822318	Lepr<sup>tm2Yli</sup>/Lepr<sup>tm2Yli</sup>  [background:] B6.129-Lepr<sup>tm2Yli</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19015522	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913321	Ethe1	is_implicated_in	DOID:0060640	ethylmalonic encephalopathy		MGI:3838185	Ethe1<sup>tm1.1Zev</sup>/Ethe1<sup>tm1.1Zev</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19136963	20090401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	is_implicated_in	DOID:0050465	Muir-Torre syndrome		MGI:3029765	Fhit<sup>tm1Hbn</sup>/Fhit<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10758156	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178778	Casp3<sup>tm1Mak</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623576	Casp3<sup>tm1Mak</sup>/Casp3<sup>tm1Mak</sup>  [background:] B6.129P2-Casp3<sup>tm1Mak</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15831467	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611307	Pde6a<sup>nmf282</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3611315	Pde6a<sup>nmf282</sup>/Pde6a<sup>nmf282</sup>  [background:] A.B6 Tyr<sup>+</sup>-Pde6a<sup>nmf282</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18849587	20090126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:2669401	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:14690422	20170920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822142	Ift172<sup>avc1</sup>/Ift172<sup>avc1</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821597	Hbb-b1<sup>MommeD7</sup>	is_implicated_in	DOID:12241	beta thalassemia		MGI:3821602	Hbb-b1<sup>MommeD7</sup>/Hbb-b1<sup>MommeD7</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23040355	20130128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	is_implicated_in	DOID:0110116	autoimmune lymphoproliferative syndrome type 2B		MGI:2655731	Casp8<sup>tm1Raz</sup>/Casp8<sup>tm1Raz</sup> Tg(Lck-cre)548Jxm/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16157684	20060822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95402	Epb42	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2449964	Epb42<sup>tm1Llp</sup>/Epb42<sup>tm1Llp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10359562	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354204	Casq2<sup>tm1.1Sgp</sup>	is_implicated_in	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2		MGI:4354215	Casq2<sup>tm1.1Sgp</sup>/Casq2<sup>tm1.1Sgp</sup>  [background:] involves: 129X1/SvJ * C57BL/6NCrL			ECO:0000033	author statement supported by traceable reference	PMID:18583715	20090821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706347	Abca3<sup>tm1Frm</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3707163	Abca3<sup>tm1Frm</sup>/Abca3<sup>tm1Frm</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:17142808	20070807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857950	Tcirg1<sup>tm1Ypl</sup>	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1		MGI:2174763	Tcirg1<sup>tm1Ypl</sup>/Tcirg1<sup>tm1Ypl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10581033	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5311115	Sirt3<sup>tm1.1Fwa</sup>/Sirt3<sup>tm1.1Fwa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:21856199	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2673307	Mafa	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3582680	Mafa<sup>tm1Staka</sup>/Mafa<sup>tm1Staka</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:15923615	20050729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039290	Efnb1<sup>tm1.1Sor</sup>	is_implicated_in	DOID:14737	craniofrontonasal syndrome		MGI:3717637	Efnb1<sup>tm1.1Sor</sup>/Efnb1<sup>+</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16968134	20070809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916267	Prrt2	is_implicated_in	DOID:0090053	episodic kinesigenic dyskinesia 1		MGI:6502639	Prrt2<sup>tm1d(KOMP)Wtsi</sup>/Prrt2<sup>tm1d(KOMP)Wtsi</sup>  [background:] B6(Cg)-Prrt2<sup>tm1d(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32891704	20210128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916267	Prrt2	is_implicated_in	DOID:0090053	episodic kinesigenic dyskinesia 1		MGI:6502640	Prrt2<sup>tm1d(KOMP)Wtsi</sup>/Prrt2<sup>+</sup>  [background:] B6(Cg)-Prrt2<sup>tm1d(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32891704	20210128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4359454	Tg(Krt14-Angptl2)1Yo	is_implicated_in	DOID:10223	dermatomyositis		MGI:4359630	Tg(Krt14-Angptl2)1Yo/0  [background:] C.Cg-Tg(Krt14-Angptl2)1Yo			ECO:0000033	author statement supported by traceable reference	PMID:22281496	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347474	Foxj1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:2668968	Foxj1<sup>tm1Bph</sup>/Foxj1<sup>tm1Bph</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9739041	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347474	Foxj1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:2679917	Foxj1<sup>tm1Slb</sup>/Foxj1<sup>tm1Slb</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10873152	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856692	Dsg3<sup>bal</sup>	is_implicated_in	DOID:0060851	pemphigus vulgaris		MGI:2175833	Dsg3<sup>bal</sup>/Dsg3<sup>bal</sup>  [background:] C57BL/6J-Dsg3<sup>bal</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9284099	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:0050660	Beare-Stevenson cutis gyrata syndrome		MGI:5450965	Fgfr2<sup>tm3Ewj</sup>/Fgfr2<sup>+</sup>  [background:] B6.129-Fgfr2<sup>tm3Ewj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22585574	20130124	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681517	Fbln5<sup>tm1Eno</sup>	is_implicated_in	DOID:3144	cutis laxa		MGI:2681526	Fbln5<sup>tm1Eno</sup>/Fbln5<sup>tm1Eno</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11805834	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:5903776	Kl<sup>ecalc1</sup>/Kl<sup>ecalc1</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25860694	20170703	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:5903847	Kl<sup>ecalc2</sup>/Kl<sup>ecalc2</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25860694	20170703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3622478	Tg(Fabp4-Hsd11b1)7Jesf	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1		MGI:3622480	Tg(Fabp4-Hsd11b1)7Jesf/0  [background:] FVB-Tg(Fabp4-Hsd11b1)7Jesf			ECO:0000033	author statement supported by traceable reference	PMID:11739957	20150504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	is_implicated_in	DOID:1838	Menkes disease		MGI:2657020	Lox<sup>tm1Ikh</sup>/Lox<sup>tm1Ikh</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12473682	20060706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3772702	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:18776951	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3027999	Pde6b<sup>atrd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028000	Pde6b<sup>atrd1</sup>/Pde6b<sup>atrd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028002	Pde6b<sup>atrd2</sup>/Pde6b<sup>rd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028001	Pde6b<sup>atrd2</sup>/Pde6b<sup>atrd2</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:5544476	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028004	Pde6b<sup>atrd3</sup>/Pde6b<sup>atrd3</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:5544447	Pde6b<sup>atrd1</sup>/Pde6b<sup>tm1Eye</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23946405	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:5544446	Pde6b<sup>atrd1</sup>/Pde6b<sup>tm1Eye</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23946405	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338010	Hic1	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2672030	Hic1<sup>tm1Sbb</sup>/Hic1<sup>tm1Sbb</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10655551	20150831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:6387275	Sqstm1<sup>tm1Keta</sup>/Sqstm1<sup>tm1Keta</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29555685	20200131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:5056476	Sqstm1<sup>tm1.1Sral</sup>/Sqstm1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21515589	20200131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:5056475	Sqstm1<sup>tm1.1Sral</sup>/Sqstm1<sup>tm1.1Sral</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21515589	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661086	Adcy3<sup>tm1Drs</sup>	is_implicated_in	DOID:1470	major depressive disorder		MGI:7260147	Adcy3<sup>tm1Drs</sup>/Adcy3<sup>tm1Drs</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26868444	20220407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152880	Apoca	is_implicated_in	DOID:83	cataract		MGI:2655437	Apoca/Apoca<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857697	Smad4<sup>tm1Mmt</sup>	is_implicated_in	DOID:0050787	juvenile polyposis syndrome		MGI:2182801	Smad4<sup>tm1Mmt</sup>/Smad4<sup>+</sup>  [background:] B6.129S2-Smad4<sup>tm1Mmt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10626800	20071105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108520	Fzd4	is_implicated_in	DOID:0060844	Norrie disease		MGI:3622318	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15035989	20060515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177703	Gck<sup>tm1Tka</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2177705	Gck<sup>tm1Tka</sup>/Gck<sup>tm1Tka</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:8530440	20050816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	is_implicated_in	DOID:9821	choroideremia		MGI:3620089	Chm<sup>tm1.2Seab</sup>/Chm<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	is_implicated_in	DOID:9821	choroideremia		MGI:3620090	Chm<sup>tm1.3Seab</sup>/Chm<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	is_implicated_in	DOID:9821	choroideremia		MGI:3620093	Chm<sup>tm1.1Seab</sup>/Chm<sup>tm1.1Seab</sup> Tg(Six3-cre)69Frty/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	is_implicated_in	DOID:9821	choroideremia		MGI:3620094	Chm<sup>tm1.1Seab</sup>/Y Tg(Six3-cre)69Frty/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155985	Adora2a<sup>tm1Jfc</sup>	is_implicated_in	DOID:11830	myopia		MGI:3622794	Adora2a<sup>tm1Jfc</sup>/Adora2a<sup>tm1Jfc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20484596	20101006	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349390	Pclo	is_not_implicated_in	DOID:1595	melancholic depression		MGI:5819105	Pclo<sup>tm1.1Mver</sup>/Pclo<sup>tm1.1Mver</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26045179	20170126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4457607	Lmna<sup>tm5Lgf</sup>	is_not_implicated_in	DOID:3911	progeria		MGI:4457609	Lmna<sup>tm5Lgf</sup>/Lmna<sup>tm5Lgf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20421363	20100706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605782	Cox10<sup>tm1Ctm</sup>	is_implicated_in	DOID:3762	cytochrome-c oxidase deficiency disease		MGI:5444474	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Tg(Camk2a-cre)#Szi/0  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22914734	20130415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158495	Bmp4<sup>tm2Blh</sup>	is_implicated_in	DOID:18	urinary system disease		MGI:3811541	Bmp4<sup>tm2Blh</sup>/Bmp4<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10749566	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2137411	Gja8<sup>tm1Paul</sup>	is_implicated_in	DOID:0110231	cataract 1 multiple types		MGI:2176492	Gja8<sup>tm1Paul</sup>/Gja8<sup>tm1Paul</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9813099	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916192	Chmp2b	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:7284279	Chmp2b<sup>tm1.1Hiok</sup>/Chmp2b<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3858540	Cd320<sup>Gt(CC0426)Wtsi</sup>	is_implicated_in	DOID:0060741	methylmalonic acidemia due to transcobalamin receptor defect		MGI:5512998	Cd320<sup>Gt(CC0426)Wtsi</sup>/Cd320<sup>Gt(CC0426)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23430977	20151201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98443	Surf1	is_implicated_in	DOID:3652	Leigh disease		MGI:2651426	Surf1<sup>tm1Zev</sup>/Surf1<sup>tm1Zev</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12566387	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670227	Ro60<sup>tm1Woln</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2670276	Ro60<sup>tm1Woln</sup>/Ro60<sup>tm1Woln</sup>  [background:] B6.129S1-Ro60<sup>tm1Woln</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670227	Ro60<sup>tm1Woln</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2670271	Ro60<sup>tm1Woln</sup>/Ro60<sup>tm1Woln</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670227	Ro60<sup>tm1Woln</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2670272	Ro60<sup>tm1Woln</sup>/Ro60<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12788971	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448247	Foxm1<sup>tm1Rhc</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5638149	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16556734	20150603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857021	Bloc1s3<sup>rp</sup>	is_implicated_in	DOID:0060546	Hermansky-Pudlak syndrome 8		MGI:3588307	Bloc1s3<sup>rp</sup>/Bloc1s3<sup>rp</sup>  [background:] involves: C57BL/10ScSn * C57BL/Tb			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339759	Csf2rb	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3604114	Csf2rb<sup>tm1Mur</sup>/Csf2rb<sup>tm1Mur</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:7697542	20051110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339759	Csf2rb	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3604113	Csf2rb<sup>tm1Mur</sup>/Csf2rb<sup>tm1Mur</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8839836	20051110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	is_implicated_in	DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O		MGI:6198577	Dync1h1<sup>tm1.1Sjki</sup>/Dync1h1<sup>+</sup>  [background:] involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29379136	20180918	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	is_implicated_in	DOID:0050540	Charcot-Marie-Tooth disease type 3		MGI:5515892	Pmp22<sup>Tr-2J</sup>/Pmp22<sup>+</sup>  [background:] C57BL/6J-Pmp22<sup>Tr-2J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5515889	20131031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5575856	Srf<sup>tm1Zli</sup>/Srf<sup>tm1Zli</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16260633	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138865	Dlgap4	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6358593	Dlgap4<sup>Gt(XH723)Byg</sup>/Dlgap4<sup>Gt(XH723)Byg</sup>  [background:] B6.129P2-Dlgap4<sup>Gt(XH723)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30664629	20190906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:891999	Adarb1	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:4843114	Adarb1<sup>tm1.1Skwa</sup>/Adarb1<sup>tm1.1Skwa</sup> Tg(SLC18A3-cre)KMisa/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20826656	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831693	Hdac3<sup>tm1.1Eno</sup>	is_implicated_in	DOID:289	endometriosis		MGI:6281662	Hdac3<sup>tm1.1Eno</sup>/Hdac3<sup>tm1.1Eno</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30626716	20190308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4126344	Smurf2<sup>Gt(RRA098)Byg</sup>	is_implicated_in	DOID:0050745	diffuse large B-cell lymphoma		MGI:5446903	Smurf2<sup>Gt(RRA098)Byg</sup>/Smurf2<sup>Gt(RRA098)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28107482	20190709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681507	Ar<sup>tm1Ska</sup>	is_implicated_in	DOID:9970	obesity		MGI:2681522	Ar<sup>tm1Ska</sup>/Y Tg(CMV-cre)1Ipc/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12943692	20100603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856180	Spta1<sup>sph-2Bc</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6234993	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856180	Spta1<sup>sph-2Bc</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:2448454	Spta1<sup>sph-2Bc</sup>/Spta1<sup>sph-2Bc</sup>  [background:] involves: SELH			ECO:0000033	author statement supported by traceable reference	PMID:6841965	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5646601	b2b3077Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5648026	b2b3077Clo/b2b3077Clo  [background:] C57BL/6J-b2b3077Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584128	Spry2<sup>tm1Ayos</sup>	is_implicated_in	DOID:9164	achalasia		MGI:3584494	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup>  [background:] B6.Cg-Spry2<sup>tm1Ayos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15937482	20050829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888389	Tgfb2<sup>tm1Doe</sup>	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome		MGI:5444484	Tgfb2<sup>tm1Doe</sup>/Tgfb2<sup>+</sup>  [background:] STOCK Tgfb2<sup>tm1Doe</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22772368	20121205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	is_implicated_in	DOID:0110024	age related macular degeneration 12		MGI:3814728	Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] C.129-Cx3cr1<sup>tm1Zm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17909628	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	is_implicated_in	DOID:0110024	age related macular degeneration 12		MGI:3814729	Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17909628	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153182	Kcnn2	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3765154	Kcnn2<sup>fri</sup>/Kcnn2<sup>fri</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:11442353	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776021	Flvcr1<sup>tm1Jlab</sup>	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:3807529	Flvcr1<sup>tm1Jlab</sup>/Flvcr1<sup>tm1Jlab</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18258918	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2651673	Btk<sup>tm1Wk</sup>/Btk<sup>tm1Wk</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7552994	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687750	Btk<sup>xid</sup>/Y  [background:] CBA/HN-Btk<sup>xid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687752	Btk<sup>xid</sup>/Y  [background:] involves: CBA/HN * DBA/2N			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687751	Btk<sup>xid</sup>/Btk<sup>xid</sup>  [background:] involves: CBA/HN * DBA/2N			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687754	Btk<sup>xid</sup>/Btk<sup>xid</sup>  [background:] CBA/HN-Btk<sup>xid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2449488	Btk<sup>tm1Gsv</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8890160	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856964	Frem2<sup>my</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3842612	Frem2<sup>my</sup>/Frem2<sup>my</sup>  [background:] MY/HuLeJ			ECO:0000033	author statement supported by traceable reference	PMID:16880404	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	is_implicated_in	DOID:14731	Weaver syndrome		MGI:6275998	Ezh2<sup>em1Jbn</sup>/Ezh2<sup>+</sup>  [background:] C57BL/6J-Ezh2<sup>em1Jbn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29244146	20190205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	is_implicated_in	DOID:14731	Weaver syndrome		MGI:6275997	Ezh2<sup>em1Jbn</sup>/Ezh2<sup>em1Jbn</sup>  [background:] C57BL/6J-Ezh2<sup>em1Jbn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29244146	20190205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97800	Pthlh	is_implicated_in	DOID:4480	achondroplasia		MGI:3583956	Pthlh<sup>tm1Hmk</sup>/Pthlh<sup>tm1Hmk</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8314082	20050819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95705	B4galt1	is_implicated_in	DOID:28	endocrine system disease		MGI:3664861	B4galt1<sup>tm1Shur</sup>/B4galt1<sup>tm1Shur</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9013935	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446294	Megf8	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3839106	Megf8<sup>hlb611</sup>/Megf8<sup>hlb611</sup>  [background:] involves: C57BL/6J * C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:18043505	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446294	Megf8	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5311833	Megf8<sup>b2b288Clo</sup>/Megf8<sup>b2b288Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b288Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20231103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	is_implicated_in	DOID:0110644	long QT syndrome 1		MGI:3056760	Kcnq1<sup>tm3Kpfe</sup>/Kcnq1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15498462	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0050794	multiple synostoses syndrome		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	is_implicated_in	DOID:10871	age related macular degeneration		MGI:3841005	Ccr2<sup>tm1Mae</sup>/Ccr2<sup>tm1Mae</sup>  [background:] B6.129P2-Ccr2<sup>tm1Mae</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14566334	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653294	Lepr<sup>tm1Mgmj</sup>	is_implicated_in	DOID:9970	obesity		MGI:2653295	Lepr<sup>tm1Mgmj</sup>/Lepr<sup>tm1Mgmj</sup>  [background:] B6.129-Lepr<sup>tm1Mgmj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12594516	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180105	Tlx3<sup>tm1Sjk</sup>	is_implicated_in	DOID:0060731	congenital central hypoventilation syndrome		MGI:2669096	Tlx3<sup>tm1Sjk</sup>/Tlx3<sup>tm1Sjk</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10700185	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:14557	primary pulmonary hypertension		MGI:5444198	Pparg<sup>tm2Rev</sup>/Pparg<sup>tm2Rev</sup> Tg(Tagln-cre)1Her/?  [background:] involves: 129S4/SvJae * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18382765	20130416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2154244	Plxnd1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5476432	Plxnd1<sup>b2b1863Clo</sup>/Plxnd1<sup>b2b1863Clo</sup>  [background:] C57BL/6J-Plxnd1<sup>b2b1863Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2154244	Plxnd1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5648021	Plxnd1<sup>b2b3150Clo</sup>/Plxnd1<sup>b2b3150Clo</sup>  [background:] C57BL/6J-Plxnd1<sup>b2b3150Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20130429	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384875	Cdk5rap2	is_implicated_in	DOID:10907	microcephaly		MGI:4460825	Cdk5rap2<sup>an</sup>/Cdk5rap2<sup>an</sup>  [background:] B6.Cg-Cdk5rap2<sup>an</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20460369	20171027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1927183	B2m<sup>tm1Jae</sup>	is_implicated_in	DOID:2352	hemochromatosis		MGI:3576233	B2m<sup>tm1Jae</sup>/B2m<sup>tm1Jae</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8013958	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178555	Clec3b<sup>tm1Umw</sup>	is_implicated_in	DOID:13300	Scheuermann's disease		MGI:2656035	Clec3b<sup>tm1Umw</sup>/Clec3b<sup>tm1Umw</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11604516	20090128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98214	Rxra	is_implicated_in	DOID:1682	congenital heart disease		MGI:2176444	Rxra<sup>tm1Rev</sup>/Rxra<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8823298	20170713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933844	Ntf3<sup>tm1Par</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:2175179	Ntf3<sup>tm1Par</sup>/Ntf3<sup>tm1Par</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8841198	20060426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_not_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14699048	20140912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446294	Megf8	is_implicated_in	DOID:0060234	Carpenter syndrome		MGI:5437117	Megf8<sup>b2b1702.2Clo</sup>/Megf8<sup>b2b1702.2Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b1702.2Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446294	Megf8	is_implicated_in	DOID:0060234	Carpenter syndrome		MGI:5311833	Megf8<sup>b2b288Clo</sup>/Megf8<sup>b2b288Clo</sup>  [background:] C57BL/6J-Megf8<sup>b2b288Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107688	Kif3b	is_implicated_in	DOID:5419	schizophrenia		MGI:6423106	Kif3b<sup>tm1Noh</sup>/Kif3b<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31746486	20200518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	is_implicated_in	DOID:3310	atopic dermatitis		MGI:4888399	Casp8<sup>tm1Hed</sup>/Casp8<sup>tm1Hed</sup> Tg(KRT14-cre)1Efu/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21135236	20110217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3697714	Myot<sup>tm1.1Moza</sup>	is_not_implicated_in	DOID:0080094	myofibrillar myopathy 3		MGI:3699229	Myot<sup>tm1.1Moza</sup>/Myot<sup>tm1.1Moza</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:17074808	20190224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052865	Chm<sup>tm1Jvdh</sup>	is_not_implicated_in	DOID:9821	choroideremia		MGI:3052952	Chm<sup>tm1Jvdh</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9175730	20051007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4456367	Tg(KRT5-IKBKB)1Armz	is_implicated_in	DOID:2723	dermatitis		MGI:4456369	Tg(KRT5-IKBKB)1Armz/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:20200541	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	is_implicated_in	DOID:9280	carbamoyl phosphate synthetase I deficiency disease		MGI:3641098	Cps1<sup>tm1Mw</sup>/Cps1<sup>tm1Mw</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9862865	20060817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3035931	Grip1<sup>tm1Rha</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3035937	Grip1<sup>tm1Rha</sup>/Grip1<sup>tm1Rha</sup>  [background:] B6.129-Grip1<sup>tm1Rha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14730302	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96699	Krt2	is_implicated_in	DOID:0060877	bullous congenital ichthyosiform erythroderma		MGI:2682252	Krt2<sup>Mhdadsk2</sup>/Krt2<sup>+</sup>  [background:] C3HeB/FeJ-Krt2<sup>Mhdadsk2</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:12533510	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96699	Krt2	is_implicated_in	DOID:0060877	bullous congenital ichthyosiform erythroderma		MGI:2682251	Krt2<sup>Mhdadsk2</sup>/Krt2<sup>Mhdadsk2</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12533510	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579521	Col4a1<sup>deltaex40</sup>	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:5308056	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21625620	20120229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	is_implicated_in	DOID:0060227	Adams-Oliver syndrome		MGI:7545577	Dll4<sup>tm1Frad</sup>/Dll4<sup>+</sup> Isl1<sup>tm1(cre)Tmj</sup>/Isl1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:33899511	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438112	Tg(ACTB-APP*V717F)1Colm	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4438223	Tg(ACTB-APP*V717F)1Colm/0  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:20085783	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1888984	Tbx21	is_implicated_in	DOID:2841	asthma		MGI:2180790	Tbx21<sup>tm1Glm</sup>/Tbx21<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11786643	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1888984	Tbx21	is_implicated_in	DOID:2841	asthma		MGI:2180789	Tbx21<sup>tm1Glm</sup>/Tbx21<sup>tm1Glm</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11786643	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176919	Crygc<sup>Chl3</sup>	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:2176925	Crygc<sup>Chl3</sup>/Crygc<sup>+</sup>  [background:] involves: 102/El * C3H/El			ECO:0000033	author statement supported by traceable reference	PMID:11773036	20050923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176919	Crygc<sup>Chl3</sup>	is_implicated_in	DOID:0110235	cataract 2 multiple types		MGI:2176927	Crygc<sup>Chl3</sup>/Crygc<sup>Chl3</sup>  [background:] involves: 102/El * C3H/El			ECO:0000033	author statement supported by traceable reference	PMID:11773036	20050923	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856829	Tg<sup>cog</sup>	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3032571	Tg<sup>cog</sup>/Tg<sup>cog</sup>  [background:] involves: AKR/J * C57BL/6By			ECO:0000033	author statement supported by traceable reference	PMID:3803305	20100125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	is_implicated_in	DOID:0060556	Kufor-Rakeb syndrome		MGI:5642335	Atp13a2<sup>tm1.2Wtd</sup>/Atp13a2<sup>tm1.2Wtd</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25855184	20150702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	is_implicated_in	DOID:9248	Pallister-Hall syndrome		MGI:3700824	Gli3<sup>tm1Urt</sup>/Gli3<sup>tm1Urt</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11978771	20070324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	is_implicated_in	DOID:1561	cognitive disorder		MGI:3697681	Comt<sup>tm1Kara</sup>/Comt<sup>tm1Kara</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:9707588	20190411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857595	Cryga<sup>1Neu</sup>	is_implicated_in	DOID:83	cataract		MGI:2175805	Cryga<sup>1Neu</sup>/Cryga<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:6877261	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574394	Hey2<sup>tm1Kkb</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:3620804	Hey2<sup>tm1Kkb</sup>/Hey2<sup>tm1Kkb</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23288164	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3692774	Tbx5<sup>tm1Jse</sup>/Tbx5<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:16870172	20150821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3052529	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:16870172	20150821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3623769	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] involves: 129/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11572777	20150821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	is_implicated_in	DOID:0060468	Holt-Oram syndrome		MGI:3052529	Tbx5<sup>tm1.1Jse</sup>/Tbx5<sup>+</sup>  [background:] either: (involves: 129/Sv) or (involves: Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:15289437	20150821	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3629188	Akt2<sup>tm1.1Mbb</sup>/Akt2<sup>tm1.1Mbb</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11387480	20060717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917057	Trim32	is_implicated_in	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H		MGI:3837478	Trim32<sup>Gt(BGA355)Byg</sup>/Trim32<sup>Gt(BGA355)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19155210	20110930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917057	Trim32	is_implicated_in	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H		MGI:5287716	Trim32<sup>tm1Spc</sup>/Trim32<sup>tm1Spc</sup>  [background:] involves: 129S/SvEvBrd * BALB/cJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21775502	20110930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	is_implicated_in	DOID:10754	otitis media		MGI:2651485	Idua<sup>tm1Efn</sup>/Idua<sup>tm1Efn</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17101178	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785405	Mus81<sup>tm1Esse</sup>	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:5661527	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25255451	20150911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1889069	Gcm2<sup>tm1Kry</sup>	is_implicated_in	DOID:11199	hypoparathyroidism		MGI:3588582	Gcm2<sup>tm1Kry</sup>/Gcm2<sup>tm1Kry</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10910362	20050929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183602	Prkar1a<sup>tm1Gsm</sup>	is_implicated_in	DOID:0050471	Carney complex		MGI:3625140	Prkar1a<sup>tm1Gsm</sup>/Prkar1a<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15371594	20060622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931872	Slc1a3<sup>tm1Kta</sup>	is_implicated_in	DOID:13544	low tension glaucoma		MGI:4417921	Slc1a3<sup>tm1Kta</sup>/Slc1a3<sup>tm1Kta</sup>  [background:] B6.129P2-Slc1a3<sup>tm1Kta</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17607354	20100115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921405	Errfi1	is_implicated_in	DOID:8398	osteoarthritis		MGI:3603638	Errfi1<sup>tm1Gvw</sup>/Errfi1<sup>tm1Gvw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16087873	20051107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050753	cerebellar ataxia		MGI:5903412	Cacna1a<sup>tm2.1Maag</sup>/Cacna1a<sup>tm2.1Maag</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21870131	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3615021	Spta1<sup>ihj</sup>	is_implicated_in	DOID:0110918	hereditary spherocytosis type 3		MGI:3615049	Spta1<sup>ihj</sup>/Spta1<sup>ihj</sup>  [background:] involves: HRS/J * LAH			ECO:0000033	author statement supported by traceable reference	PMID:20056793	20101210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	is_implicated_in	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S		MGI:7495806	Ighmbp2<sup>em5Cx</sup>/Ighmbp2<sup>em5Cx</sup>  [background:] C57BL/6J-Ighmbp2<sup>em5Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:36413117	20230706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	is_implicated_in	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S		MGI:7495585	Ighmbp2<sup>em1Cx</sup>/Ighmbp2<sup>em1Cx</sup>  [background:] C57BL/6J-Ighmbp2<sup>em1Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:36413117	20230706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387813	Sftpc<sup>tm1Swg</sup>	is_implicated_in	DOID:0050158	desquamative interstitial pneumonia		MGI:3037342	Sftpc<sup>tm1Swg</sup>/Sftpc<sup>tm1Swg</sup>  [background:] either: 129 or (involves: 129 * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:12519727	20080910	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664869	Men1<sup>tm1Zqw</sup>	is_implicated_in	DOID:5394	prolactinoma		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438917	Srr<sup>tm1.2Jtc</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:4438921	Srr<sup>tm1.2Jtc</sup>/Srr<sup>tm1.2Jtc</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19065142	20100407	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676923	Thrb<sup>tm3Few</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:2676935	Thrb<sup>tm3Few</sup>/Thrb<sup>tm3Few</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12925699	20070611	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4366152	Tg(SFTPC-env)1Yhch	is_implicated_in	DOID:1324	lung cancer		MGI:4366153	Tg(SFTPC-env)1Yhch/0  [background:] FVB/N-Tg(SFTPC-env)1Yhch			ECO:0000033	author statement supported by traceable reference	PMID:19695657	20091103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138934	Mbd5	is_implicated_in	DOID:0060307	autosomal dominant intellectual developmental disorder		MGI:5617468	Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>/Mbd5<sup>+</sup>  [background:] B6.Cg-Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25001218	20150417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919425	Mfsd8	is_implicated_in	DOID:0110722	neuronal ceroid lipofuscinosis 7		MGI:5604251	Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>/Mfsd8<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24423645	20141112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100537	Mid1	is_implicated_in	DOID:10629	microphthalmia		MGI:3580085	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100537	Mid1	is_implicated_in	DOID:10629	microphthalmia		MGI:3580086	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100537	Mid1	is_implicated_in	DOID:10629	microphthalmia		MGI:3580091	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Mid1<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4441956	Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:5806128	Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>/Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:27491071	20161103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178316	Pde6b<sup>atrd3</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028004	Pde6b<sup>atrd3</sup>/Pde6b<sup>atrd3</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5634327	St14<sup>tm2Bug</sup>/St14<sup>tm3Bug</sup> Tg(MMTV-cre)4Mam/0  [background:] involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * N:Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:24551030	20150503	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	is_implicated_in	DOID:3310	atopic dermatitis		MGI:3588865	Relb<sup>tm1Brv</sup>/Relb<sup>tm1Brv</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: C57BL/6) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10940923	20140520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918817	Mcm9	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5295417	Mcm9<sup>Gt(AW0655)Wtsi</sup>/Mcm9<sup>Gt(AW0655)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918817	Mcm9	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5295418	Mcm9<sup>Gt(XG743)Byg</sup>/Mcm9<sup>Gt(XG743)Byg</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918817	Mcm9	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5295419	Mcm9<sup>Gt(AW0655)Wtsi</sup>/Mcm9<sup>Gt(XG743)Byg</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101926	Dlx5	is_implicated_in	DOID:0090021	split hand-foot malformation 1		MGI:2653534	Dlx5/Dlx6<sup>tm1Levi</sup>/Dlx5/Dlx6<sup>tm1Levi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12112878	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5431549	Daw1<sup>b2b1584Clo</sup>/Daw1<sup>b2b1584Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1584Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5313814	Daw1<sup>b2b1116Clo</sup>/Daw1<sup>b2b1116Clo</sup>  [background:] C57BL/6J-Daw1<sup>b2b1116Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055613	Brca2<sup>tm1Mhun</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3055719	Brca2<sup>tm1Mhun</sup>/Brca2<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14981540	20060807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388890	Phex<sup>Hyp-Duk</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037643	Phex<sup>Hyp-Duk</sup>/Phex<sup>+</sup>  [background:] involves: BALB/cAnBomUrd			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388890	Phex<sup>Hyp-Duk</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037642	Phex<sup>Hyp-Duk</sup>/Y  [background:] involves: BALB/cAnBomUrd			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	is_implicated_in	DOID:9273	citrullinemia		MGI:4838091	Ass1<sup>bar</sup>/Ass1<sup>fold</sup>  [background:] involves: C57BL/6Ei * C57BL/6J * OF1 * P/J			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	is_implicated_in	DOID:9273	citrullinemia		MGI:4838087	Ass1<sup>bar</sup>/Ass1<sup>bar</sup>  [background:] FVB.BAR-Ass1<sup>bar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	is_implicated_in	DOID:9273	citrullinemia		MGI:3697171	Ass1<sup>fold</sup>/Ass1<sup>fold</sup>  [background:] involves: C57BL/6JEiJ * P/J			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	is_implicated_in	DOID:9273	citrullinemia		MGI:4838089	Ass1<sup>bar</sup>/Ass1<sup>bar</sup>  [background:] B6.BAR-Ass1<sup>bar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	is_implicated_in	DOID:9273	citrullinemia		MGI:3707513	Ass1<sup>fold</sup>/Ass1<sup>fold</sup>  [background:] B6Ei.P-Ass1<sup>fold</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:20724589	20101109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	is_implicated_in	DOID:9273	citrullinemia		MGI:2653766	Ass1<sup>tm1Bay</sup>/Ass1<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8197477	20101109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856535	Agtpbp1<sup>pcd</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5446655	Agtpbp1<sup>pcd</sup>/Agtpbp1<sup>pcd</sup>  [background:] involves: C57BL/6J * C57BR/cdJ * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:21824473	20121219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88521	Cryga	is_implicated_in	DOID:83	cataract		MGI:2175805	Cryga<sup>1Neu</sup>/Cryga<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:6877261	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159003	Nos3<sup>tm1Gdk</sup>	is_implicated_in	DOID:10825	essential hypertension		MGI:3618724	Nos3<sup>tm1Gdk</sup>/Nos3<sup>tm1Gdk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9468189	20060406	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926033	Brpf1	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:5896655	Brpf1<sup>tm1c(EUCOMM)Wtsi</sup>/Brpf1<sup>tm1c(EUCOMM)Wtsi</sup> Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27939640	20170619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926033	Brpf1	is_implicated_in	DOID:0050888	syndromic intellectual disability		MGI:5902766	Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>/Brpf1<sup>tm1d(EUCOMM)Wtsi</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27939640	20170619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107690	Zfp462	is_implicated_in	DOID:14320	generalized anxiety disorder		MGI:6198752	Zfp462<sup>Tn(pb-Act-RFP)1.090115023-HRAZhu</sup>/Zfp462<sup>+</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27621227	20180920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385061	Pcare	is_implicated_in	DOID:0110364	retinitis pigmentosa 54		MGI:5755292	Pcare<sup>tm1Kpal</sup>/Pcare<sup>tm1Kpal</sup>  [background:] involves: C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:25616964	20160401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	is_implicated_in	DOID:5419	schizophrenia		MGI:4353812	Plcb1<sup>tm1Hssh</sup>/Plcb1<sup>tm1Hssh</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17667964	20090819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159321	Nr0b1<sup>tm1.1Lja</sup>	is_implicated_in	DOID:0080156	X-linked adrenal hypoplasia congenita		MGI:2659009	Nr0b1<sup>tm1.1Lja</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9843206	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159321	Nr0b1<sup>tm1.1Lja</sup>	is_implicated_in	DOID:0080156	X-linked adrenal hypoplasia congenita		MGI:2659009	Nr0b1<sup>tm1.1Lja</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11564714	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3700974	Trp53inp1<sup>tm1Acar</sup>	is_implicated_in	DOID:14221	abdominal obesity-metabolic syndrome 1		MGI:3701944	Trp53inp1<sup>tm1Acar</sup>/Trp53inp1<sup>tm1Acar</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25828351	20170411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916027	Tmem53	is_implicated_in	DOID:0112340	craniotubular dysplasia Ikegawa type		MGI:6854714	Tmem53<sup>em1Ikeg</sup>/Tmem53<sup>em1Ikeg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:33824347	20220921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050214	Lambert-Eaton myasthenic syndrome		MGI:3624868	Cacna1a<sup>tg-rol</sup>/Cacna1a<sup>tg-rol</sup>  [background:] involves: C57BL/6 * SIII			ECO:0000033	author statement supported by traceable reference	PMID:18653245	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107736	Dync2h1	is_implicated_in	DOID:14679	VACTERL association		MGI:5311880	Dync2h1<sup>b2b414Clo</sup>/Dync2h1<sup>b2b414Clo</sup>  [background:] C57BL/6J-Dync2h1<sup>b2b414Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20120612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	is_implicated_in	DOID:0110850	xeroderma pigmentosum group B		MGI:3836472	Ercc3<sup>tm2Jhjh</sup>/Ercc3<sup>tm2Jhjh</sup>  [background:] B6.129P2-Ercc3<sup>tm2Jhjh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19114557	20090320	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	is_not_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:3771550	Slc40a1<sup>tm1Nca</sup>/Slc40a1<sup>+</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:16054062	20080222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690020	Akt2<sup>tm1Hem</sup>	is_implicated_in	DOID:11612	polycystic ovary syndrome		MGI:5429853	Akt2<sup>tm1Hem</sup>/Akt2<sup>tm1Hem</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22275470	20120802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625686	Trp53bp2<sup>tm1Xlu</sup>	is_implicated_in	DOID:0060412	chromosome 1q41-q42 deletion syndrome		MGI:6191758	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] B6.129S6-Trp53bp2<sup>tm1Xlu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625686	Trp53bp2<sup>tm1Xlu</sup>	is_implicated_in	DOID:0060412	chromosome 1q41-q42 deletion syndrome		MGI:3629203	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3625686	Trp53bp2<sup>tm1Xlu</sup>	is_implicated_in	DOID:0060412	chromosome 1q41-q42 deletion syndrome		MGI:4819168	Trp53bp2<sup>tm1Xlu</sup>/Trp53bp2<sup>tm1Xlu</sup>  [background:] C.129S6-Trp53bp2<sup>tm1Xlu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27447114	20180726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:2174947	Edn3<sup>tm1Ywa</sup>/Edn3<sup>tm1Ywa</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8001160	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3589107	Edn3<sup>ls</sup>/Edn3<sup>ls</sup>  [background:] involves: C57BL			ECO:0000033	author statement supported by traceable reference	PMID:5917257	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511272	Dsp<sup>rul</sup>	is_implicated_in	DOID:0090128	Carvajal syndrome		MGI:3574845	Dsp<sup>rul</sup>/Dsp<sup>rul</sup>  [background:] RB156Bnr/Ei-Dsp<sup>rul</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25659760	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028726	Bcat2<sup>m1Ytc</sup>	is_implicated_in	DOID:9269	maple syrup urine disease		MGI:3028730	Bcat2<sup>m1Ytc</sup>/Bcat2<sup>m1Ytc</sup>  [background:] C57BL/6J-Bcat2<sup>m1Ytc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14755340	20050603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661116	Dysf<sup>tm1Kcam</sup>	is_implicated_in	DOID:11720	distal myopathy		MGI:2661118	Dysf<sup>tm1Kcam</sup>/Dysf<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12736685	20090630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:0070113	Niemann-Pick disease type C1		MGI:6359477	Npc1<sup>tm1Tacf</sup>/Npc1<sup>tm1Tacf</sup>  [background:] B6(Cg)-Npc1<sup>tm1Tacf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28167839	20190911	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	is_implicated_in	DOID:0070113	Niemann-Pick disease type C1		MGI:6359481	Npc1<sup>tm1Tacf</sup>/Npc1<sup>tm2Tacf</sup>  [background:] B6(Cg)-Npc1<sup>tm1Tacf</sup> Npc1<sup>tm2Tacf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28167839	20190911	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	is_implicated_in	DOID:0110154	Charcot-Marie-Tooth disease type 2A1		MGI:2387931	Kif1b<sup>tm1Noh</sup>/Kif1b<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11389829	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360793	Tg(RBP3-ELOVL4*)3Kzh	is_implicated_in	DOID:0050817	Stargardt disease		MGI:4360798	Tg(RBP3-ELOVL4*)3Kzh/0  [background:] C57BL/6-Tg(RBP3-ELOVL4*)3Kzh			ECO:0000033	author statement supported by traceable reference	PMID:15749821	20091008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924809	Agl	is_implicated_in	DOID:2748	glycogen storage disease III		MGI:5661390	Agl<sup>tm1Geno</sup>/Agl<sup>tm1Geno</sup>  [background:] C57BL/6J-Agl<sup>tm1Geno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25092169	20151110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924809	Agl	is_implicated_in	DOID:2748	glycogen storage disease III		MGI:5695480	Agl<sup>tm1a(EUCOMM)Wtsi</sup>/Agl<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24613482	20151110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915674	Chn1	is_implicated_in	DOID:12557	Duane retraction syndrome		MGI:6406385	Chn1<sup>tm1.1Ece</sup>/Chn1<sup>tm1.1Ece</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28346224	20200427	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183399	Runx3<sup>tm1Yg</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:3057279	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)			ECO:0000033	author statement supported by traceable reference	PMID:15514019	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605782	Cox10<sup>tm1Ctm</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5775427	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>/?  [background:] B6.Cg-Cox10<sup>tm1Ctm</sup> Slc6a3<sup>tm1.1(cre)Bkmn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27038906	20160609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861755	Nsmf	is_not_implicated_in	DOID:3614	Kallmann syndrome		MGI:6358417	Nsmf<sup>tm1.2Mrkr</sup>/Nsmf<sup>tm1.2Mrkr</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26977770	20190905	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	is_implicated_in	DOID:0110408	retinitis pigmentosa 11		MGI:4950568	Prpf31<sup>tm1.1Bha</sup>/Prpf31<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	is_implicated_in	DOID:1324	lung cancer		MGI:3806464	Robo1<sup>tm1Phr</sup>/Robo1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15374951	20080917	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	is_not_implicated_in	DOID:0110741	type 1 diabetes mellitus 2		MGI:3625100	Hk2<sup>tm1Laak</sup>/Hk2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * BALB/c * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10428828	20110711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927580	Bloc1s6	is_implicated_in	DOID:0060547	Hermansky-Pudlak syndrome 9		MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25477496	20151231	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928761	Slc19a2	is_implicated_in	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome		MGI:3033364	Slc19a2<sup>tm1Gelb</sup>/Slc19a2<sup>tm1Gelb</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12393806	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928761	Slc19a2	is_implicated_in	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome		MGI:3606089	Slc19a2<sup>tm1Ejn</sup>/Slc19a2<sup>tm1Ejn</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14567973	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4123936	Suco<sup>Gt(KST050)Byg</sup>	is_implicated_in	DOID:0110344	osteogenesis imperfecta type 5		MGI:4818953	Suco<sup>Gt(KST050)Byg</sup>/Suco<sup>Gt(KST050)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:20440000	20100811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528080	Tg(Lck-Tal1)4709Led	is_implicated_in	DOID:1037	lymphoid leukemia		MGI:3849439	Tg(Lck-Tal1)4709Led/0  [background:] FVB/N-Tg(Lck-Tal1)4709Led			ECO:0000033	author statement supported by traceable reference	PMID:8895560	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448149	Tg(Msmb-TAg)186-3Xuan	is_implicated_in	DOID:10283	prostate cancer		MGI:3574638	Tg(Msmb-TAg)186-3Xuan/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12424611	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386794	Gopc<sup>tm1.1Tno</sup>	is_implicated_in	DOID:14227	azoospermia		MGI:3722133	Gopc<sup>tm1.1Tno</sup>/Gopc<sup>tm1.1Tno</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12149515	20070920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	is_implicated_in	DOID:905	Zellweger syndrome		MGI:5571189	Pex1<sup>tm1.1Sjms</sup>/Pex1<sup>tm1.1Sjms</sup>  [background:] involves: 129 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24503136	20200217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	is_implicated_in	DOID:905	Zellweger syndrome		MGI:6390207	Pex1<sup>tm1.1Hrw</sup>/Pex1<sup>tm1.1Hrw</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:31207289	20200217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:7314952	Sdhb<sup>tm1c(EUCOMM)Hmgu</sup>/Sdhb<sup>tm1c(EUCOMM)Hmgu</sup> Tg(Ins2-cre)23Herr/0  [background:] involves: C57BL/6J * C57BL/6N * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:35472723	20220725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313268	Chrd	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:2676545	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup>  [background:] either: B6SJL.129-Chrd<sup>tm1Emdr</sup> or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)			ECO:0000033	author statement supported by traceable reference	PMID:12810603	20070104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037943	Trf<sup>hpx</sup>/Trf<sup>+</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3681112	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037942	Trf<sup>hpx</sup>/Trf<sup>hpx</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	PMID:3681112	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037943	Trf<sup>hpx</sup>/Trf<sup>+</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	MGI:1889268	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	is_implicated_in	DOID:0050649	atransferrinemia		MGI:3037942	Trf<sup>hpx</sup>/Trf<sup>hpx</sup>  [background:] BALB/cJ-Trf<sup>hpx</sup>			ECO:0000033	author statement supported by traceable reference	MGI:1889268	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419911	Nexmif<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0112044	non-syndromic X-linked intellectual disability 98		MGI:6468250	Nexmif<sup>tm1(KOMP)Wtsi</sup>/Y  [background:] B6J.B6N-Nexmif<sup>tm1(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31704787	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612540	Stk11<sup>tm1.1Mlfr</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3616342	Stk11<sup>tm1.1Mlfr</sup>/Stk11<sup>+</sup>  [background:] involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16357136	20060315	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135915	Myo15a<sup>sh2-2J</sup>	is_implicated_in	DOID:0110488	autosomal recessive nonsyndromic deafness 3		MGI:2175132	Myo15a<sup>sh2-2J</sup>/Myo15a<sup>sh2-2J</sup>  [background:] involves: STOCK Rb(16.17)7Bnr			ECO:0000033	author statement supported by traceable reference	MGI:2135933	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287973	Atg7<sup>tm1Tchi</sup>/Atg7<sup>tm1Tchi</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100508	Kcnj8	is_implicated_in	DOID:3393	coronary artery disease		MGI:3041531	Kcnj8<sup>tm1Sse</sup>/Kcnj8<sup>tm1Sse</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11984590	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856394	Pcdh15<sup>av-3J</sup>	is_implicated_in	DOID:0110832	Usher syndrome type 1F		MGI:3581190	Pcdh15<sup>av-3J</sup>/Pcdh15<sup>av-3J</sup>  [background:] C57BL/6J-Pcdh15<sup>av-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15537665	20090219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856298	Ank1<sup>nb</sup>	is_implicated_in	DOID:0110916	hereditary spherocytosis type 1		MGI:2449181	Ank1<sup>nb</sup>/Ank1<sup>nb</sup>  [background:] either: (involves: non-inbred stock) or (involves: C57BL/6) or (involves: WB/Re)			ECO:0000033	author statement supported by traceable reference	PMID:1716634	20050601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2429765	Dock1	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:5618862	Dock1<sup>b2b3190Clo</sup>/Dock1<sup>b2b3190Clo</sup>  [background:] C57BL/6J-Dock1<sup>b2b3190Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856687	Vps33a<sup>bf</sup>	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3034088	Vps33a<sup>bf</sup>/Vps33a<sup>bf</sup>  [background:] C57BL/6J-Vps33a<sup>bf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9585243	20170721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	is_implicated_in	DOID:11476	osteoporosis		MGI:4361526	Ifngr1<sup>tm1Agt</sup>/Ifngr1<sup>tm1Agt</sup>  [background:] B6.129S7-Ifngr1<sup>tm1Agt</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21308779	20170515	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	is_implicated_in	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy		MGI:3513373	Plec<sup>tm2Gwi</sup>/Plec<sup>tm2Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	is_implicated_in	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy		MGI:3513191	Plec<sup>tm1Gwi</sup>/Plec<sup>tm1Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3044955	Impg2	is_implicated_in	DOID:0110371	retinitis pigmentosa 56		MGI:6466735	Impg2<sup>em2Xjz</sup>/Impg2<sup>em2Xjz</sup>  [background:] C57BL/6J-Impg2<sup>em2Xjz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32242237	20201013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3044955	Impg2	is_implicated_in	DOID:0110371	retinitis pigmentosa 56		MGI:6466733	Impg2<sup>em1Xjz</sup>/Impg2<sup>em1Xjz</sup>  [background:] C57BL/6J-Impg2<sup>em1Xjz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32242237	20201013	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183367	Thrb<sup>tm2Few</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3588064	Thrb<sup>tm2Few</sup>/Thrb<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11274423	20050921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183367	Thrb<sup>tm2Few</sup>	is_implicated_in	DOID:11633	thyroid hormone resistance syndrome		MGI:3588063	Thrb<sup>tm2Few</sup>/Thrb<sup>tm2Few</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11274423	20050921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3709467	Tg(Camk2a-Bdnf)A9Stl	is_implicated_in	DOID:1826	epilepsy		MGI:5617753	Tg(Camk2a-Bdnf)A9Stl/0  [background:] C57BL/6-Tg(Camk2a-Bdnf)A9Stl/J			ECO:0000033	author statement supported by traceable reference	PMID:24768643	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039784	Ctnnb1<sup>tm2(Nfkbia)Rsu</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3706580	Ctnnb1<sup>tm2(Nfkbia)Rsu</sup>/Ctnnb1<sup>+</sup> Tg(CMV-cre)1Cgn/0  [background:] involves: 129P2/OlaHsd * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11585809	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888407	Chrna7<sup>tm1Bay</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3819267	Chrna7<sup>tm1Bay</sup>/Chrna7<sup>tm1Bay</sup>  [background:] B6.129S7-Chrna7<sup>tm1Bay</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24983521	20141106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3715520	Kiss1<sup>tm1Coll</sup>	is_implicated_in	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia		MGI:3716929	Kiss1<sup>tm1Coll</sup>/Kiss1<sup>tm1Coll</sup>  [background:] involves: 129S/SvEv * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:17563351	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176526	Ptpn11<sup>tm1Rbn</sup>	is_not_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:2176527	Ptpn11<sup>tm1Rbn</sup>/Ptpn11<sup>tm1Rbn</sup>  [background:] involves: 129 * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8702915	20051017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176526	Ptpn11<sup>tm1Rbn</sup>	is_not_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:2176529	Ptpn11<sup>tm1Rbn</sup>/Ptpn11<sup>+</sup>  [background:] involves: 129 * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8702915	20051017	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831350	Tg(Prnp-ATN1)124Dbo	is_implicated_in	DOID:0060162	dentatorubral-pallidoluysian atrophy		MGI:5056392	Tg(Prnp-ATN1)124Dbo/?  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10677044	20110810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107734	Ap3d1	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3528946	Ap3d1<sup>mh</sup>/Ap3d1<sup>mh</sup>  [background:] B6.C3-Grxcr1<sup>pi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386879	Hic1<sup>tm1Sbb</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2672030	Hic1<sup>tm1Sbb</sup>/Hic1<sup>tm1Sbb</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10655551	20150831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5428893	Lep<sup>ob</sup>/Lep<sup>ob</sup>  [background:] BTBR.Cg-Lep<sup>ob</sup>/WiscJ			ECO:0000033	author statement supported by traceable reference	PMID:16280642	20130926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619445	Tg(Pbsn-MYC)6Key	is_implicated_in	DOID:10283	prostate cancer		MGI:3620105	Tg(Pbsn-MYC)6Key/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:14522256	20060420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3778822	Vangl1<sup>Gt(XL802)Byg</sup>	is_not_implicated_in	DOID:0080074	neural tube defect		MGI:3778823	Vangl1<sup>Gt(XL802)Byg</sup>/Vangl1<sup>Gt(XL802)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18296642	20080424	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:0050868	hepatocellular adenoma		MGI:5009546	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:21575863	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149116	Psen1<sup>tm1Bdes</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2174990	Psen1<sup>tm1Bdes</sup>/Psen1<sup>tm1Bdes</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9450754	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701697	Gck<sup>tm2Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3713294	Gck<sup>tm2Mgn</sup>/Gck<sup>+</sup>  [background:] 129S6/SvEvTac-Gck<sup>tm2Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701697	Gck<sup>tm2Mgn</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3713302	Gck<sup>tm2Mgn</sup>/Gck<sup>tm2Mgn</sup>  [background:] 129S6/SvEvTac-Gck<sup>tm2Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579521	Col4a1<sup>deltaex40</sup>	is_implicated_in	DOID:0090125	brain small vessel disease 1		MGI:3579768	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] B6.129S-Col4a1<sup>deltaex40</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16598045	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:0060732	chromosome 9p deletion syndrome		MGI:5295995	Frem1<sup>bat</sup>/Frem1<sup>+</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21931569	20111118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	is_implicated_in	DOID:0060732	chromosome 9p deletion syndrome		MGI:3665272	Frem1<sup>bat</sup>/Frem1<sup>bat</sup>  [background:] C57BL/6J-Frem1<sup>bat</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21931569	20111118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88040	Cat4	is_implicated_in	DOID:83	cataract		MGI:2175743	Cat4<sup>Apcat1-2</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88040	Cat4	is_implicated_in	DOID:83	cataract		MGI:2175746	Cat4<sup>Apcat1-4</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:1511869	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88040	Cat4	is_implicated_in	DOID:83	cataract		MGI:3574974	Cat4<sup>Apcat1-3</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88040	Cat4	is_implicated_in	DOID:83	cataract		MGI:2175743	Cat4<sup>Apcat1-2</sup>/Cat4<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039363	Cdkn1a<sup>tm2(HBx)Xya</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3046808	Cdkn1a<sup>tm2(HBx)Xya</sup>/Cdkn1a<sup>tm2(HBx)Xya</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039363	Cdkn1a<sup>tm2(HBx)Xya</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3046835	Cdkn1a<sup>tm2(HBx)Xya</sup>/Cdkn1a<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5316756	b2b520Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5316792	b2b520Clo/b2b520Clo  [background:] C57BL/6J-b2b520Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3514037	Abcg8<sup>tm1Elk</sup>	is_implicated_in	DOID:0090019	sitosterolemia		MGI:3514172	Abcg8<sup>tm1Elk</sup>/Abcg8<sup>tm1Elk</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15040800	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686951	Hcn1<sup>tm2Kndl</sup>	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:5688197	Hcn1<sup>tm2Kndl</sup>/Hcn1<sup>tm2Kndl</sup>  [background:] involves: 129 * 129S/SvEv * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24218458	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328317	Trex1	is_implicated_in	DOID:0050629	Aicardi-Goutieres syndrome		MGI:3053060	Trex1<sup>tm1Tld</sup>/Trex1<sup>tm1Tld</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:18724932	20090702	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182135	Csnk2a2<sup>tm1Dcs</sup>	is_implicated_in	DOID:12336	male infertility		MGI:2451166	Csnk2a2<sup>tm1Dcs</sup>/Csnk2a2<sup>tm1Dcs</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10471512	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367025	Sh3tc2<sup>tm1.1Rchr</sup>	is_implicated_in	DOID:0110183	Charcot-Marie-Tooth disease type 4C		MGI:4367049	Sh3tc2<sup>tm1.1Rchr</sup>/Sh3tc2<sup>tm1.1Rchr</sup>  [background:] involves: 129/Sv * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19805030	20091112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109188	Kif21a	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:6241435	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>tm1.1Ece</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109188	Kif21a	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:6241436	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>tm1.1Ece</sup> Tg(Isl1-EGFP*)1Slp/0  [background:] involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109188	Kif21a	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:6241434	Kif21a<sup>tm1.1Ece</sup>/Kif21a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:24656932	20181109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855985	Tyr<sup>c-2J</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:3581209	Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6(Cg)-Tyr<sup>c-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21968110	20120426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929751	Asb4	is_implicated_in	DOID:10591	pre-eclampsia		MGI:5703970	Asb4<sup>tm1.2Cpat</sup>/Asb4<sup>tm1.2Cpat</sup>  [background:] involves: 129/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:27821757	20170317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349428	Foxl2	is_implicated_in	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome		MGI:3029674	Foxl2<sup>tm1Tre</sup>/Foxl2<sup>tm1Tre</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:14736745	20071022	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349428	Foxl2	is_implicated_in	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome		MGI:3044667	Foxl2<sup>tm1Gpil</sup>/Foxl2<sup>tm1Gpil</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC)			ECO:0000033	author statement supported by traceable reference	PMID:15056605	20071022	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915040	Rab39b	is_implicated_in	DOID:0060309	syndromic X-linked intellectual disability		MGI:6695982	Rab39b<sup>em1Jfch</sup>/Y  [background:] C57BL/6N-Rab39b<sup>em1Jfch</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32115408	20210503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043590	Ercc5<sup>tm4Shm</sup>	is_implicated_in	DOID:0110849	xeroderma pigmentosum group G		MGI:3043695	Ercc5<sup>tm4Shm</sup>/Ercc5<sup>tm4Shm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15082767	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	is_implicated_in	DOID:1612	breast cancer		MGI:5763438	Smarca4<sup>tm1Mag</sup>/Smarca4<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24220145	20160427	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5912041	Des<sup>tm1Cba</sup>/Des<sup>tm1Cba</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11827695	20171030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387403	Stk11<sup>tm1.2Rdp</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814533	Stk11<sup>tm1.2Rdp</sup>/Stk11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:12226664	20081112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387403	Stk11<sup>tm1.2Rdp</sup>	is_implicated_in	DOID:3852	Peutz-Jeghers syndrome		MGI:3814533	Stk11<sup>tm1.2Rdp</sup>/Stk11<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18172296	20081112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574666	Enam<sup>Rgsc514</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20160216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574667	Enam<sup>Rgsc521</sup>/Enam<sup>Rgsc521</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20160216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574665	Enam<sup>Rgsc395</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20160216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574668	Enam<sup>Rgsc521</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20160216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:5708536	Enam<sup>tm1.1Jcch</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24603688	20160216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:5708531	Enam<sup>tm1.1Jcch</sup>/Enam<sup>tm1.1Jcch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24603688	20160216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182322	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5461561	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:22652393	20130201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182322	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3820200	Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>/Gtf2ird1<sup>Tg(Alb1-Myc)166.8Sst</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:16293761	20130201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	is_implicated_in	DOID:0060249	scoliosis		MGI:6256787	Fgfr3<sup>tm1Dor</sup>/Fgfr3<sup>tm1Dor</sup>  [background:] C3.129S6(B6)-Fgfr3<sup>tm1Dor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25852647	20181116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2687035	Far2	is_implicated_in	DOID:987	alopecia		MGI:6267296	Far2<sup>tm2b(KOMP)Wtsi</sup>/Far2<sup>tm2b(KOMP)Wtsi</sup>  [background:] B6N(Cg)-Far2<sup>tm2b(KOMP)Wtsi</sup>/2J			ECO:0000033	author statement supported by traceable reference	PMID:30372477	20181219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685233	Ptchd1	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5792693	Ptchd1<sup>tm2.2Gfng</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27007844	20170712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651834	Nmf15	is_implicated_in	DOID:9970	obesity		MGI:2651886	Nmf15/Nmf15<sup>+</sup>  [background:] C57BL/6J-Nmf15/J			ECO:0000033	author statement supported by traceable reference	MGI:2651853	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1337124	Cmas	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:6402523	Cmas<sup>tm1.1Bwei</sup>/Cmas<sup>tm1.1Bwei</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:31040189	20200402	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040905	Tg(Utg-TAg)7593Fjd	is_implicated_in	DOID:1324	lung cancer		MGI:5547757	Tg(Utg-TAg)7593Fjd/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:9040936	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3819437	Tg(tetO-TAg,CMV-rtTA)123Yihu	is_implicated_in	DOID:0050902	medulloblastoma		MGI:3819453	Tg(tetO-TAg,CMV-rtTA)123Yihu/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18271920	20081211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526574	Parl<sup>tm1Bdes</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:6280694	Parl<sup>tm1Bdes</sup>/Parl<sup>tm1Bdes</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:30578322	20190228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856333	Csf1<sup>op</sup>	is_implicated_in	DOID:13533	osteopetrosis		MGI:3610379	Csf1<sup>op</sup>/Csf1<sup>op</sup>  [background:] B6C3Fe a/a-Csf1<sup>op</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:1887865	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4439298	p23-ST1	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:4439299	p23-ST1/p23-ST1  [background:] C57BL/6J-p23-ST1			ECO:0000033	author statement supported by traceable reference	PMID:19924295	20100412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95697	Gfap	is_implicated_in	DOID:4252	Alexander disease		MGI:3692745	Gfap<sup>tm2Mes</sup>/Gfap<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17065456	20070108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95697	Gfap	is_implicated_in	DOID:4252	Alexander disease		MGI:3692743	Gfap<sup>tm3Mes</sup>/Gfap<sup>+</sup>  [background:] involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17065456	20070108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	is_implicated_in	DOID:13832	patent ductus arteriosus		MGI:3797650	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18188448	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	is_implicated_in	DOID:13832	patent ductus arteriosus		MGI:3797716	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> Tg(Pax3-cre)1Joe/0  [background:] involves: 129/Sv * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18188448	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106184	Npm1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:3606861	Npm1<sup>tm1Ppp</sup>/Npm1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16007073	20171027	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623976	Parp1<sup>tm1Hsmm</sup>/Parp1<sup>tm1Hsmm</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10051636	20060606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2159437	Agtpbp1	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5446655	Agtpbp1<sup>pcd</sup>/Agtpbp1<sup>pcd</sup>  [background:] involves: C57BL/6J * C57BR/cdJ * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:21824473	20121219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96698	Krt1	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:3655854	Krt1<sup>Mhdadsk12</sup>/Krt1<sup>+</sup>  [background:] C3HeB/FeJ-Krt1<sup>Mhdadsk12</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16528356	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	is_implicated_in	DOID:0110964	brachydactyly type A1		MGI:3842982	Ihh<sup>tm1.1Dcha</sup>/Ihh<sup>tm1.1Dcha</sup>  [background:] either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:19252479	20090505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858008	Ctnnb1<sup>tm1Mmt</sup>	is_implicated_in	DOID:10283	prostate cancer		MGI:3836579	Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup> Tg(Pbsn-cre)4Prb/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19117991	20090320	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055154	Pla2g6<sup>tm1Turk</sup>	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3055190	Pla2g6<sup>tm1Turk</sup>/Pla2g6<sup>tm1Turk</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:18202189	20100219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3712063	Tsc2<sup>tm1.1Mjg</sup>	is_implicated_in	DOID:13223	uterine fibroid		MGI:5641710	Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:23820898	20150624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861793	Aga<sup>tm1Vk</sup>	is_implicated_in	DOID:0050461	aspartylglucosaminuria		MGI:3045972	Aga<sup>tm1Vk</sup>/Aga<sup>tm1Vk</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8946839	20050526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934274	Prnp<sup>tm1Edin</sup>	is_not_implicated_in	DOID:0050433	fatal familial insomnia		MGI:2174710	Prnp<sup>tm1Edin</sup>/Prnp<sup>tm1Edin</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Edin</sup>/EdinH			ECO:0000033	author statement supported by traceable reference	PMID:10581259	20060525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3828520	Pde6a<sup>nmf363</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3828991	Pde6a<sup>nmf363</sup>/Pde6a<sup>nmf363</sup>  [background:] C57BL/6J-Pde6a<sup>nmf363</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18849587	20090126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311352	b2b1200Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5437104	b2b1200Clo/b2b1200Clo  [background:] C57BL/6J-b2b1200Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88175	Manba	is_implicated_in	DOID:3633	beta-mannosidosis		MGI:3617198	Manba<sup>tm1Khf</sup>/Manba<sup>tm1Khf</sup>  [background:] B6.129-Manba<sup>tm1Khf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16377659	20060321	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3794202	Smn1<sup>tm5(Smn1/SMN2)Mrph</sup>	is_implicated_in	DOID:0050530	intermediate spinal muscular atrophy		MGI:5440978	Smn1<sup>tm5(Smn1/SMN2)Mrph</sup>/Smn1<sup>tm5(Smn1/SMN2)Mrph</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:22802075	20121108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99572	Gcgr	is_implicated_in	DOID:0112306	Mahvash Disease		MGI:6690506	Gcgr<sup>em2Smoc</sup>/Gcgr<sup>em2Smoc</sup>  [background:] C57BL/6J-Gcgr<sup>em2Smoc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32677665	20220301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106927	Aff3	is_implicated_in	DOID:0112383	KINSSHIP syndrome		MGI:5608405	Aff3<sup>tm1a(EUCOMM)Wtsi</sup>/Aff3<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Aff3<sup>tm1a(EUCOMM)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:33961779	20220613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97394	Oat	is_implicated_in	DOID:1415	gyrate atrophy		MGI:2174900	Oat<sup>tm1Dva</sup>/Oat<sup>tm1Dva</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7550347	20180626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97394	Oat	is_implicated_in	DOID:1415	gyrate atrophy		MGI:3838967	Oat<sup>rhg</sup>/Oat<sup>rhg</sup>  [background:] B6Ei;AKR-Oat<sup>rhg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25264521	20180626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97394	Oat	is_implicated_in	DOID:1415	gyrate atrophy		MGI:3719126	Oat<sup>tm1Dva</sup>/Oat<sup>tm1Dva</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10655512	20180626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858522	Map3k14<sup>aly</sup>	is_implicated_in	DOID:12236	primary biliary cholangitis		MGI:3767418	Map3k14<sup>aly</sup>/Map3k14<sup>aly</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9620319	20091015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180081	Dnah5<sup>Tg1Htz</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3624520	Dnah5<sup>Tg1Htz</sup>/Dnah5<sup>Tg1Htz</sup>  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11912187	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045345	Awat2	is_implicated_in	DOID:10140	dry eye syndrome		MGI:6729732	Awat2<sup>tm1.2Golc</sup>/Awat2<sup>tm1.2Golc</sup>  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32851726	20210809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045345	Awat2	is_implicated_in	DOID:10140	dry eye syndrome		MGI:6729736	Awat2<sup>tm1.2Golc</sup>/Y  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32851726	20210809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	is_not_implicated_in	DOID:0110773	hereditary spastic paraplegia 2		MGI:6160754	Plp1<sup>tm1c(EUCOMM)Wtsi</sup>/Y Neurod6<sup>tm1(cre)Kan</sup>/Neurod6<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28836307	20180613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3822861	Tg(Ly6a-SET/NUP214)2969Gcg	is_implicated_in	DOID:12603	acute leukemia		MGI:3822915	Tg(Ly6a-SET/NUP214)2969Gcg/0  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:17569777	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682000	Nbn<sup>tm1Zqw</sup>	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:2682001	Nbn<sup>tm1Zqw</sup>/Nbn<sup>tm1Zqw</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14612522	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682000	Nbn<sup>tm1Zqw</sup>	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:2682002	Nbn<sup>tm1Zqw</sup>/Nbn<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14612522	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4451568	Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6501754	Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>/Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33168096	20210317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:2678410	Runx2<sup>tm1Kish</sup>/Runx2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20375239	20170621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6274702	Scn1a<sup>tm2.1Wac</sup>/Scn1a<sup>+</sup> Tg(I12b-cre)1Jlr/0  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914311	Dzip1	is_implicated_in	DOID:988	mitral valve prolapse		MGI:6718509	Dzip1<sup>em1Sasl</sup>/Dzip1<sup>+</sup>  [background:] C57BL/6J-Dzip1<sup>em1Sasl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914311	Dzip1	is_implicated_in	DOID:988	mitral valve prolapse		MGI:6718507	Dzip1<sup>tm1Sasl</sup>/Dzip1<sup>tm1Sasl</sup> Nfatc1<sup>tm1.1(cre)Bz</sup>/Nfatc1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:4849542	Vcp<sup>tm1Itl</sup>/Vcp<sup>+</sup>  [background:] B6.129S-Vcp<sup>tm1Itl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19713307	20130808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	is_implicated_in	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia		MGI:5500068	Vcp<sup>tm1Itl</sup>/Vcp<sup>tm1Itl</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23029473	20130808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682236	Krt2<sup>Mhdadsk2</sup>	is_implicated_in	DOID:0060877	bullous congenital ichthyosiform erythroderma		MGI:2682252	Krt2<sup>Mhdadsk2</sup>/Krt2<sup>+</sup>  [background:] C3HeB/FeJ-Krt2<sup>Mhdadsk2</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	PMID:12533510	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682236	Krt2<sup>Mhdadsk2</sup>	is_implicated_in	DOID:0060877	bullous congenital ichthyosiform erythroderma		MGI:2682251	Krt2<sup>Mhdadsk2</sup>/Krt2<sup>Mhdadsk2</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12533510	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	is_implicated_in	DOID:3312	bipolar disorder		MGI:6189158	Camk2a<sup>tm1Sva</sup>/Camk2a<sup>+</sup>  [background:] B6.129P2-Camk2a<sup>tm1Sva</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27028761	20180723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330233	Tcap	is_implicated_in	DOID:0110281	autosomal recessive limb-girdle muscular dystrophy type 2G		MGI:4457377	Tcap<sup>tm1Mkc</sup>/Tcap<sup>tm1Mkc</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20233748	20100701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452377	Tg(CYP1A1-PPARD)#Jfoe	is_implicated_in	DOID:8893	psoriasis		MGI:4452388	Tg(CYP1A1-PPARD)#Jfoe/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20300524	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5442112	b2b1594Clo	is_implicated_in	DOID:674	cleft palate		MGI:5442125	b2b1594Clo/b2b1594Clo  [background:] C57BL/6J-b2b1594Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:2672029	Gp1ba<sup>tm1Ware</sup>/Gp1ba<sup>tm1Ware</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10706630	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	is_implicated_in	DOID:9452	steatotic liver disease		MGI:3611043	Ldlr<sup>tm1Her</sup>/Ldlr<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21690266	20111104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177742	Hps4	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3587187	Hps4<sup>le</sup>/Hps4<sup>le</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	is_implicated_in	DOID:2734	keratosis follicularis		MGI:2655642	Atp2a2<sup>tm1Ges</sup>/Atp2a2<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11389134	20130610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1195267	Ilk	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907206	Ilk<sup>tm1Star</sup>/Ilk<sup>tm1Star</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16951252	20170822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924983	Rnf170	is_implicated_in	DOID:0050951	hereditary ataxia		MGI:5907140	Rnf170<sup>Gt(OST104375)Lex</sup>/Rnf170<sup>Gt(OST104375)Lex</sup>  [background:] B6.129S-Rnf170<sup>Gt(OST104375)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26433933	20170817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384054	Pafah1b1<sup>tm1Awb</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384054	Pafah1b1<sup>tm1Awb</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10541472	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583919	Myc<sup>tm1Lbox</sup>	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3603014	Myc<sup>tm1Lbox</sup>/Myc<sup>tm1Lbox</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15687498	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583919	Myc<sup>tm1Lbox</sup>	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3603015	Myc<sup>tm1Lbox</sup>/Myc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15687498	20051026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676199	Ndp<sup>tm1Wbrg</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:2676253	Ndp<sup>tm1Wbrg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20159112	20100420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861149	Iac	is_implicated_in	DOID:83	cataract		MGI:2175073	Iac/Iac<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97311	Nfix	is_implicated_in	DOID:0112102	Sotos syndrome 2		MGI:6467327	Nfix<sup>tm1.1Rmg</sup>/Nfix<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30503862	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860700	Col3a1<sup>Tsk2</sup>	is_implicated_in	DOID:418	systemic scleroderma		MGI:2655257	Col3a1<sup>Tsk2</sup>/Col3a1<sup>+</sup>  [background:] C3H101H-Col3a1<sup>Tsk2</sup>/H			ECO:0000033	author statement supported by traceable reference	PMID:8849351	20160420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5528981	Thrb<sup>tm1.1Syc</sup>/Thrb<sup>tm1.1Syc</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:15983791	20140116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16025116	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858305	Pgrmc1	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6272838	Pgrmc1<sup>em1Ejho</sup>/Pgrmc1<sup>em1Ejho</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30356113	20190110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3910613	Galt<sup>Gt(E285B04)Wrst</sup>	is_implicated_in	DOID:9870	galactosemia		MGI:6191762	Galt<sup>Gt(E285B04)Wrst</sup>/Galt<sup>Gt(E285B04)Wrst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24549051	20180727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856852	Grip1<sup>eb</sup>	is_implicated_in	DOID:11836	clubfoot		MGI:3665403	Grip1<sup>eb</sup>/Grip1<sup>eb</sup>  [background:] involves: hairless stock			ECO:0000033	author statement supported by traceable reference	MGI:61605	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154611	Sgcb<sup>tm1Oza</sup>	is_implicated_in	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E		MGI:3850524	Sgcb<sup>tm1Oza</sup>/Sgcb<sup>tm1Oza</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10441321	20090716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384054	Pafah1b1<sup>tm1Awb</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10541472	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384054	Pafah1b1<sup>tm1Awb</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:3053446	Pafah1b1<sup>tm1Awb</sup>/Pafah1b1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9697693	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9637677	20051104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	is_implicated_in	DOID:0050524	maturity-onset diabetes of the young		MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12697734	20051104	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057174	Tg(HD)63Aron	is_implicated_in	DOID:12858	Huntington's disease		MGI:3723505	Tg(HD)63Aron/?  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11717344	20071004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385045	Lemd2	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:7444862	Lemd2<sup>em1Eno</sup>/Lemd2<sup>em1Eno</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:36377660	20230317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3577064	inad	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3577344	inad/inad  [background:] C57BL/6-inad			ECO:0000033	author statement supported by traceable reference	PMID:15859351	20050519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2181178	Mkrn3	is_implicated_in	DOID:0112309	central precocious puberty 2		MGI:6704951	Mkrn3<sup>em1Rhu</sup>/Mkrn3<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34692086	20220301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182467	Kcnj10<sup>tm1Lst</sup>	is_implicated_in	DOID:0060484	EAST syndrome		MGI:5698063	Kcnj10<sup>tm1Lst</sup>/Kcnj10<sup>tm1Lst</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:19420365	20151204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182467	Kcnj10<sup>tm1Lst</sup>	is_implicated_in	DOID:0060484	EAST syndrome		MGI:3038919	Kcnj10<sup>tm1Lst</sup>/Kcnj10<sup>tm1Lst</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11466414	20151204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437718	Tg(Pkd1)26Mtru	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:4437766	Tg(Pkd1)26Mtru/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:20053665	20100323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522333	vsd	is_implicated_in	DOID:11836	clubfoot		MGI:3522714	vsd/vsd  [background:] C57BL/6J-vsd			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814536	Coch<sup>tm1Mrtn</sup>	is_implicated_in	DOID:0110593	autosomal dominant nonsyndromic deafness 9		MGI:3814540	Coch<sup>tm1Mrtn</sup>/Coch<sup>tm1Mrtn</sup>  [background:] CBACa.129S4-Coch<sup>tm1Mrtn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18697796	20110128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814536	Coch<sup>tm1Mrtn</sup>	is_implicated_in	DOID:0110593	autosomal dominant nonsyndromic deafness 9		MGI:3814540	Coch<sup>tm1Mrtn</sup>/Coch<sup>tm1Mrtn</sup>  [background:] CBACa.129S4-Coch<sup>tm1Mrtn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21073934	20110128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95553	Flg	is_implicated_in	DOID:0110098	atopic dermatitis 2		MGI:5532944	Flg<sup>ft</sup>/Flg<sup>ft</sup>  [background:] STOCK a/a Tmem79<sup>ma</sup> Flg<sup>ft</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:23844115	20140131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108053	Rit1	is_implicated_in	DOID:0060586	Noonan syndrome 8		MGI:6356633	Rit1<sup>tm1.1Tumg</sup>/Rit1<sup>+</sup>  [background:] B6.Cg-Rit1<sup>tm1.1Tumg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30898653	20190822	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858030	Nek1<sup>kat</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3831332	Nek1<sup>kat</sup>/Nek1<sup>kat</sup>  [background:] involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn			ECO:0000033	author statement supported by traceable reference	PMID:9070925	20090212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856373	Pde6b<sup>rd1</sup>	is_implicated_in	DOID:8466	retinal degeneration		MGI:7266500	Pde6b<sup>rd1</sup>/Pde6b<sup>rd1</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33539865	20220504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098283	Per1	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5634972	Per1<sup>tm1Drw</sup>/Per1<sup>tm1Drw</sup>  [background:] B6.129-Per1<sup>tm1Drw</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25673850	20150507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0080052	acromesomelic dysplasia, Grebe type		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	is_implicated_in	DOID:0060758	immunodeficiency with hyper-IgM type 2		MGI:7511767	Aicda<sup>em1Jaych</sup>/Aicda<sup>em1Jaych</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:33098766	20230726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861107	Klf1<sup>Nan</sup>	is_implicated_in	DOID:12971	hereditary spherocytosis		MGI:4819280	Klf1<sup>Nan</sup>/Klf1<sup>+</sup>  [background:] either: B6.Cg-Klf1<sup>Nan</sup> or WB.Cg-Klf1<sup>Nan</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19409822	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452494	Tg(Utg-TAg)#Fjd	is_implicated_in	DOID:1324	lung cancer		MGI:5547756	Tg(Utg-TAg)#Fjd/?  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:9040936	20140304	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045984	Syn2<sup>tm1Pggd</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5517484	Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup>  [background:] B6.1129-Syn2<sup>tm1Pggd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	is_implicated_in	DOID:0080547	metabolic dysfunction-associated steatohepatitis		MGI:6405042	Mc4r<sup>tm1Matsu</sup>/Mc4r<sup>tm1Matsu</sup>  [background:] C57BL/6J-Mc4r<sup>tm1Matsu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31990961	20200422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97628	pma	is_implicated_in	DOID:11836	clubfoot		MGI:3722144	pma/pma  [background:] involves: CF-1			ECO:0000033	author statement supported by traceable reference	PMID:3948960	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2138070	Lamb2<sup>tm1Jrs</sup>	is_implicated_in	DOID:0060852	Pierson syndrome		MGI:2175097	Lamb2<sup>tm1Jrs</sup>/Lamb2<sup>tm1Jrs</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16452099	20061018	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	is_implicated_in	DOID:0111030	hemochromatosis type 3		MGI:2655464	Tfr2<sup>tm1Slu</sup>/Tfr2<sup>tm1Slu</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12134060	20100709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	is_implicated_in	DOID:0111030	hemochromatosis type 3		MGI:4458421	Tfr2<sup>tm1.1Anro</sup>/Tfr2<sup>tm1.1Anro</sup>  [background:] 129.Cg-Tfr2<sup>tm1.1Anro</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20179178	20100709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:0060564	spinal disease		MGI:7280953	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28523278	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856217	Pmp22<sup>Tr-J</sup>	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794294	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] B6.Cg-Pmp22<sup>Tr-J</sup> Krt25<sup>Re</sup>/+ +/J			ECO:0000033	author statement supported by traceable reference	PMID:15363066	20080818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856217	Pmp22<sup>Tr-J</sup>	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794288	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15703401	20080818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856217	Pmp22<sup>Tr-J</sup>	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794294	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] B6.Cg-Pmp22<sup>Tr-J</sup> Krt25<sup>Re</sup>/+ +/J			ECO:0000033	author statement supported by traceable reference	PMID:1303281	20080818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856217	Pmp22<sup>Tr-J</sup>	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794288	Pmp22<sup>Tr-J</sup>/Pmp22<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:1303281	20080818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4421705	Grn<sup>tm1.1Aidi</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:6279297	Grn<sup>tm1.1Aidi</sup>/Grn<sup>tm1.1Aidi</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30271659	20190221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832409	Prlh<sup>tm1Taon</sup>	is_implicated_in	DOID:9970	obesity		MGI:3832410	Prlh<sup>tm1Taon</sup>/Prlh<sup>tm1Taon</sup>  [background:] B6N.129X1-Prlh<sup>tm1Taon</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19033670	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623576	Casp3<sup>tm1Mak</sup>/Casp3<sup>tm1Mak</sup>  [background:] B6.129P2-Casp3<sup>tm1Mak</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15831467	20060531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858195	Hnrnpu	is_implicated_in	DOID:0080418	developmental and epileptic encephalopathy 54		MGI:7550770	Hnrnpu<sup>em1Frk</sup>/Hnrnpu<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:37782669	20231122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:7264454	Large1<sup>m1Btlr</sup>/Large1<sup>m1Btlr</sup>  [background:] C57BL/6J-Large1<sup>m1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34142127	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:3605225	Large1<sup>vls</sup>/Large1<sup>vls</sup>  [background:] B6.CAST(Cg)-Large1<sup>vls</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:16111892	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:3605230	Large1<sup>myd</sup>/Large1<sup>myd</sup>  [background:] B6.Cg-Large1<sup>myd</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:16111892	20220426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347049	Clcn6	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3688436	Clcn6<sup>tm1Tjj</sup>/Clcn6<sup>tm1Tjj</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16950870	20061121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152978	Col2a1<sup>tm1Prc</sup>	is_implicated_in	DOID:0080056	achondrogenesis type II		MGI:3590207	Col2a1<sup>tm1Prc</sup>/Col2a1<sup>tm1Prc</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:11680679	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	is_implicated_in	DOID:0050450	Gitelman syndrome		MGI:5427703	Wnk4<sup>tm1Pfi</sup>/Wnk4<sup>tm1Pfi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22550170	20120713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857248	Stat4<sup>tm1Gru</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617977	Stat4<sup>tm1Gru</sup>/Stat4<sup>tm1Gru</sup>  [background:] C.129S2-Stat4<sup>tm1Gru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15596856	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857248	Stat4<sup>tm1Gru</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3617976	Stat4<sup>tm1Gru</sup>/Stat4<sup>+</sup>  [background:] NOD.129S2-Stat4<sup>tm1Gru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15041039	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4364071	Gyg1<sup>tm1a(KOMP)Wtsi</sup>	is_implicated_in	DOID:0050579	glycogen storage disease XV		MGI:6273835	Gyg1<sup>tm1a(KOMP)Wtsi</sup>/Gyg1<sup>tm1a(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33219378	20220318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3799499	Add1<sup>tm1Llp</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:3807202	Add1<sup>tm1Llp</sup>/Add1<sup>tm1Llp</sup>  [background:] involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18723693	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814869	Six3<sup>tm3Gco</sup>	is_implicated_in	DOID:0110872	holoprosencephaly 2		MGI:3814903	Six3<sup>tm3Gco</sup>/Six3<sup>tm3Gco</sup> Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18694563	20081113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5440213	Traf3ip2<sup>tm1.1Lix</sup>/Traf3ip2<sup>tm1.1Lix</sup>  [background:] B6.129-Traf3ip2<sup>tm1.1Lix</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22585710	20121031	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347355	Slc7a11	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2677961	Slc7a11<sup>sut</sup>/Slc7a11<sup>sut</sup>  [background:] C3H/HeSnJ-Slc7a11<sup>sut</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8699821	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685397	Rc3h1	is_implicated_in	DOID:0050749	peripheral T-cell lymphoma		MGI:5445374	Rc3h1<sup>san</sup>/Rc3h1<sup>+</sup>  [background:] involves: C57BL/6JSfdAnu			ECO:0000033	author statement supported by traceable reference	PMID:22700722	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4127354	Sptbn2<sup>Gt(XK442)Byg</sup>	is_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:5300032	Sptbn2<sup>Gt(XK442)Byg</sup>/Sptbn2<sup>Gt(XK442)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20231455	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3050230	Prkn<sup>tm1Tmd</sup>	is_implicated_in	DOID:0060368	Parkinson's disease 2		MGI:3050555	Prkn<sup>tm1Tmd</sup>/Prkn<sup>tm1Tmd</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15249681	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860214	Nuca	is_implicated_in	DOID:83	cataract		MGI:2175193	Nuca/Nuca<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055586	Enam<sup>Rgsc514</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574666	Enam<sup>Rgsc514</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196990	Cd200	is_implicated_in	DOID:417	autoimmune disease		MGI:3576859	Cd200<sup>tm1Jods</sup>/Cd200<sup>tm1Jods</sup>  [background:] C57BL/6-Cd200<sup>tm1Jods</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11099416	20050516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526856	Gata4<sup>tm1.2Wtp</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5441538	Gata4<sup>tm1.2Wtp</sup>/Gata4<sup>+</sup>  [background:] B6.Cg-Gata4<sup>tm1.2Wtp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17069789	20121115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4358722	Tg(Prnp-TARDBP*A315T)95Balo	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:4361717	Tg(Prnp-TARDBP*A315T)95Balo/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19833869	20111207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443337	Fscn2	is_implicated_in	DOID:0110406	retinitis pigmentosa 30		MGI:3612482	Fscn2<sup>tm2Sykk</sup>/Fscn2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16043865	20060210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443337	Fscn2	is_implicated_in	DOID:0110406	retinitis pigmentosa 30		MGI:3612480	Fscn2<sup>tm1Sykk</sup>/Fscn2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16043865	20060210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861929	Gck<sup>tm1Efr</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:2176960	Gck<sup>tm1Efr</sup>/Gck<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7665557	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	is_implicated_in	DOID:1612	breast cancer		MGI:3843497	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] involves: 129/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19342371	20090511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696966	Cacna1a<sup>tm2.1Maag</sup>	is_implicated_in	DOID:0050753	cerebellar ataxia		MGI:5903412	Cacna1a<sup>tm2.1Maag</sup>/Cacna1a<sup>tm2.1Maag</sup> Tg(Pcp2-cre)2Mpin/0  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21870131	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446543	Tg(NEFL-APP)#Nalb	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5550547	Tg(NEFL-APP)#Nalb/0  [background:] involves: C57BL/6 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:23833557	20140314	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385468	Sox9<sup>tm1Gsr</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:3817221	Sox9<sup>tm1Gsr</sup>/Sox9<sup>+</sup> Tg(Pdx1-cre)6Cvw/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18723011	20081120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4432988	Agl<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:2748	glycogen storage disease III		MGI:5695480	Agl<sup>tm1a(EUCOMM)Wtsi</sup>/Agl<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24613482	20151110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446134	Sidt2	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:5532830	Sidt2<sup>tm1.1Hzha</sup>/Sidt2<sup>tm1.1Hzha</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27233614	20180921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859665	Atp8b1	is_not_implicated_in	DOID:1852	intrahepatic cholestasis		MGI:3043817	Atp8b1<sup>tm1Nbf</sup>/Atp8b1<sup>tm1Nbf</sup>  [background:] involves: 129S1/SvImJ * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:14976163	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574021	Dclre1c<sup>tm2Mcow</sup>	is_implicated_in	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation		MGI:3576477	Dclre1c<sup>tm2Mcow</sup>/Dclre1c<sup>tm2Mcow</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15699179	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418718	nad	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:4418721	nad/nad  [background:] C(D2)-nad			ECO:0000033	author statement supported by traceable reference	PMID:16542671	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4415610	Itm2b<sup>tm2.1Ldad</sup>	is_not_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4415612	Itm2b<sup>tm2.1Ldad</sup>/Itm2b<sup>tm2.1Ldad</sup>  [background:] B6.129-Itm2b<sup>tm2.1Ldad</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19924302	20100112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338820	Bmp10	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5616119	Bmp10<sup>b2b2711Clo</sup>/Bmp10<sup>b2b2711Clo</sup>  [background:] C57BL/6J-Bmp10<sup>b2b2711Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042795	Neu1<sup>a</sup>	is_implicated_in	DOID:3343	glycoproteinosis		MGI:3719077	Neu1<sup>a</sup>/Neu1<sup>a</sup>  [background:] SM/J			ECO:0000033	author statement supported by traceable reference	PMID:9425240	20070824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857642	Vangl2<sup>Lp</sup>	is_implicated_in	DOID:0080074	neural tube defect		MGI:3529938	Vangl2<sup>Lp</sup>/Vangl2<sup>Lp</sup>  [background:] involves: CBA/Ca * LPT/Le			ECO:0000033	author statement supported by traceable reference	PMID:9545534	20130429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609165	Gnas<sup>tm5.1Lsw</sup>	is_implicated_in	DOID:4184	pseudohypoparathyroidism		MGI:5818291	Gnas<sup>tm5.1Lsw</sup>/Gnas<sup>tm5.1Lsw</sup> Tg(Slc5a2-cre)1Tauc/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26671181	20170119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443301	Slc35c1	is_implicated_in	DOID:0070255	congenital disorder of glycosylation type IIc		MGI:3711227	Slc35c1<sup>tm1Cknr</sup>/Slc35c1<sup>tm1Cknr</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17276979	20190516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	is_implicated_in	DOID:10534	stomach cancer		MGI:3837032	Il6st<sup>tm1Ern</sup>/Il6st<sup>tm1Ern</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14699500	20130521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	is_implicated_in	DOID:0050704	childhood electroclinical syndrome		MGI:3700786	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] B6.D2-Cacna1a<sup>tg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:572084	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442253	Cln5	is_implicated_in	DOID:0110728	neuronal ceroid lipofuscinosis 5		MGI:3522019	Cln5<sup>tm1Pltn</sup>/Cln5<sup>tm1Pltn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15459177	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860092	Myo7a<sup>sh1-6J</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:2449173	Myo7a<sup>sh1-6J</sup>/Myo7a<sup>sh1-6J</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	MGI:65387	20060307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3814579	Kmt2a<sup>tm1Saam</sup>/Kmt2a<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18977325	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777160	Fkbp8<sup>tm1Kei</sup>	is_implicated_in	DOID:11836	clubfoot		MGI:3819790	Fkbp8<sup>tm1Kei</sup>/Fkbp8<sup>tm1Kei</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18459960	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2446577	Ccn1<sup>tm1Lfl</sup>	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:3040322	Ccn1<sup>tm1Lfl</sup>/Ccn1<sup>tm1Lfl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17023674	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848037	Lmna<sup>Dhe</sup>	is_implicated_in	DOID:3911	progeria		MGI:4459466	Lmna<sup>Dhe</sup>/Lmna<sup>+</sup>  [background:] B6(D2)-Lmna<sup>Dhe</sup>/TyGrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:21464947	20110606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341070	Fkbp8	is_implicated_in	DOID:11836	clubfoot		MGI:3819790	Fkbp8<sup>tm1Kei</sup>/Fkbp8<sup>tm1Kei</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18459960	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857229	Nos3<sup>tm1Unc</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:3618597	Nos3<sup>tm1Unc</sup>/Nos3<sup>tm1Unc</sup>  [background:] B6.129P2-Nos3<sup>tm1Unc</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:10821808	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3719416	Txnip<sup>Hyplip1</sup>/Txnip<sup>Hyplip1</sup>  [background:] involves: CAST/Ei * HcB19/Dem			ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3719415	Txnip<sup>Hyplip1</sup>/Txnip<sup>+</sup>  [background:] involves: CAST/Ei * HcB19/Dem			ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3719414	Txnip<sup>Hyplip1</sup>/Txnip<sup>Hyplip1</sup>  [background:] HcB19/Dem-Txnip<sup>Hyplip1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16607285	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039435	Sell<sup>tm1Flv</sup>/Sell<sup>tm1Flv</sup>  [background:] NOD.Cg-Sell<sup>tm1Flv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039428	Sell<sup>tm1Flv</sup>/Sell<sup>tm1Flv</sup>  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039434	Sell<sup>tm1Flv</sup>/Sell<sup>+</sup>  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039437	Sell<sup>tm1Flv</sup>/Sell<sup>+</sup>  [background:] NOD.Cg-Sell<sup>tm1Flv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4433621	Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0050563	nonsyndromic deafness		MGI:6198763	Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>/Ppip5k2<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29590114	20180920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857584	Lpin1<sup>fld-2J</sup>	is_implicated_in	DOID:811	lipodystrophy		MGI:3839539	Lpin1<sup>fld-2J</sup>/Lpin1<sup>fld-2J</sup>  [background:] C3H/HeJ-Lpin1<sup>fld-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11138012	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5646288	b2b2966Clo	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:5646375	b2b2966Clo/b2b2966Clo  [background:] C57BL/6J-b2b2966Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3046835	Cdkn1a<sup>tm2(HBx)Xya</sup>/Cdkn1a<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3046808	Cdkn1a<sup>tm2(HBx)Xya</sup>/Cdkn1a<sup>tm2(HBx)Xya</sup>  [background:] either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14767984	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386266	C3<sup>tm1Pkna</sup>	is_implicated_in	DOID:8354	complement component 3 deficiency		MGI:2449062	C3<sup>tm1Pkna</sup>/C3<sup>tm1Pkna</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9467654	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857469	Gck<sup>tm1Ts</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:2176950	Gck<sup>tm1Ts</sup>/Gck<sup>+</sup>  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J)			ECO:0000033	author statement supported by traceable reference	PMID:7553875	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857469	Gck<sup>tm1Ts</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:2176947	Gck<sup>tm1Ts</sup>/Gck<sup>tm1Ts</sup>  [background:] either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J)			ECO:0000033	author statement supported by traceable reference	PMID:7553875	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617903	Chm<sup>tm1.1Seab</sup>	is_implicated_in	DOID:9821	choroideremia		MGI:3620093	Chm<sup>tm1.1Seab</sup>/Chm<sup>tm1.1Seab</sup> Tg(Six3-cre)69Frty/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617903	Chm<sup>tm1.1Seab</sup>	is_implicated_in	DOID:9821	choroideremia		MGI:3620094	Chm<sup>tm1.1Seab</sup>/Y Tg(Six3-cre)69Frty/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:16410831	20060420	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	is_implicated_in	DOID:2211	factor XIII deficiency		MGI:2684307	F13a1<sup>tm1Gdi</sup>/F13a1<sup>tm1Gdi</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12933578	20111107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	is_implicated_in	DOID:2211	factor XIII deficiency		MGI:2684306	F13a1<sup>tm1Gdi</sup>/F13a1<sup>tm1Gdi</sup>  [background:] involves: 129P2/OlaHsd * CBA/Ca			ECO:0000033	author statement supported by traceable reference	PMID:12529747	20111107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848479	Apc<sup>tm1Rsmi</sup>	is_implicated_in	DOID:2394	ovarian cancer		MGI:5583019	Apc<sup>tm1Rsmi</sup>/Apc<sup>tm1Rsmi</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24474556	20140919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149629	Insr<sup>tm1Jja</sup>	is_not_implicated_in	DOID:0050470	Donohue syndrome		MGI:2174961	Insr<sup>tm1Jja</sup>/Insr<sup>tm1Jja</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:8612577	20051024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3054793	Aipl1<sup>tm1Visu</sup>	is_implicated_in	DOID:0110332	Leber congenital amaurosis 4		MGI:3054824	Aipl1<sup>tm1Visu</sup>/Aipl1<sup>tm1Visu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15365178	20050531	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328350	Matn3	is_implicated_in	DOID:8398	osteoarthritis		MGI:3687322	Matn3<sup>tm1Brd</sup>/Matn3<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16877353	20061113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2687035	Far2	is_implicated_in	DOID:10140	dry eye syndrome		MGI:7355994	Far2<sup>em1Akih</sup>/Far2<sup>em1Akih</sup>  [background:] C57BL/6J-Far2<sup>em1Akih</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35238077	20221018	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96949	Mdk	is_implicated_in	DOID:5419	schizophrenia		MGI:3579532	Mdk<sup>tm1Tmu</sup>/Mdk<sup>tm1Tmu</sup>  [background:] B6.129S2-Mdk<sup>tm1Tmu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19217924	20090818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158403	Prf1<sup>tm1Clrk</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3622763	Prf1<sup>tm1Clrk</sup>/Prf1<sup>tm1Clrk</sup>  [background:] involves: 129S7/SvEvBrd * BALB/c * NOD			ECO:0000033	author statement supported by traceable reference	PMID:10946317	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785162	Enpp1<sup>asj</sup>	is_implicated_in	DOID:1214	tympanosclerosis		MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:27959908	20190917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027066	Pklr<sup>char4</sup>	is_implicated_in	DOID:0111077	pyruvate kinase deficiency of red cells		MGI:3027071	Pklr<sup>char4</sup>/Pklr<sup>char4</sup>  [background:] involves: A/J * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14595440	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856966	Cpox<sup>nct</sup>	is_implicated_in	DOID:13269	hereditary coproporphyria		MGI:5488915	Cpox<sup>nct</sup>/Cpox<sup>nct</sup>  [background:] involves: BALB/cCrSlc			ECO:0000033	author statement supported by traceable reference	PMID:23631845	20130606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856492	Cat2<sup>no2</sup>	is_implicated_in	DOID:83	cataract		MGI:2175730	Cat2<sup>no2</sup>/Cat2<sup>+</sup>  [background:] DBA/2-Cat2<sup>no2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2072972	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	is_implicated_in	DOID:0060650	dicarboxylic aminoaciduria		MGI:2655192	Slc1a1<sup>tm1Wst</sup>/Slc1a1<sup>tm1Wst</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9233792	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803178	Arx<sup>tm1Gldn</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:3844352	Arx<sup>tm1Gldn</sup>/Y Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129/Sv * C57BL/6 * CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19439424	20090515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3803178	Arx<sup>tm1Gldn</sup>	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:3844353	Arx<sup>tm1Gldn</sup>/Arx<sup>+</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129/Sv * C57BL/6 * CD-1 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19439424	20090515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3653501	Nisch<sup>edsn</sup>	is_implicated_in	DOID:10754	otitis media		MGI:6101180	Nisch<sup>edsn</sup>/Nisch<sup>edsn</sup>  [background:] C3H.B6-Nisch<sup>edsn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28806779	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95721	Gjb3	is_not_implicated_in	DOID:0110558	autosomal dominant nonsyndromic deafness 2A		MGI:3588971	Gjb3<sup>tm1Kwi</sup>/Gjb3<sup>tm1Kwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11237463	20051005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437105	Lgi1<sup>tm1Mafu</sup>	is_implicated_in	DOID:0060748	familial temporal lobe epilepsy 1		MGI:4437122	Lgi1<sup>tm1Mafu</sup>/Lgi1<sup>tm1Mafu</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20133599	20100312	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522476	Als2<sup>tm1Cai</sup>	is_not_implicated_in	DOID:0060194	amyotrophic lateral sclerosis type 2		MGI:3589591	Als2<sup>tm1Cai</sup>/Als2<sup>tm1Cai</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16107644	20051014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510641	Large1<sup>vls</sup>	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:3605225	Large1<sup>vls</sup>/Large1<sup>vls</sup>  [background:] B6.CAST(Cg)-Large1<sup>vls</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:16111892	20101116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888705	Mfrp<sup>rd6</sup>	is_implicated_in	DOID:11105	fundus albipunctatus		MGI:2386344	Mfrp<sup>rd6</sup>/Mfrp<sup>rd6</sup>  [background:] B6.C3-Mfrp<sup>rd6</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10967077	20050510	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153480	Atp6v0a4	is_implicated_in	DOID:14219	renal tubular acidosis		MGI:5441585	Atp6v0a4<sup>tm1.1Fekf</sup>/Atp6v0a4<sup>tm1.1Fekf</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22872862	20121115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	is_implicated_in	DOID:0050453	lissencephaly		MGI:2684281	Dag1<sup>tm2Kcam</sup>/Dag1<sup>tm2Kcam</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12140559	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	is_implicated_in	DOID:0050453	lissencephaly		MGI:2684282	Dag1<sup>tm1Kcam</sup>/Dag1<sup>tm2Kcam</sup> Tg(GFAP-cre)25Mes/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12140559	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387337	Brca2<sup>tm1Mbn</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3814365	Brca2<sup>tm1Mbn</sup>/Brca2<sup>+</sup>  [background:] B6.Cg-Brca2<sup>tm1Mbn</sup> Apc<sup>Min</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11215675	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763903	Tg(HSA*LR)41Cath	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3763919	Tg(HSA*LR)41Cath/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511283	Lepr<sup>tm1Chua</sup>	is_implicated_in	DOID:9970	obesity		MGI:3511746	Lepr<sup>tm1Chua</sup>/Lepr<sup>tm1Chua</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15389315	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388899	Nppc<sup>lbab</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3707539	Nppc<sup>lbab</sup>/Nppc<sup>lbab</sup>  [background:] B6.PL-Nppc<sup>lbab</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:17439653	20220512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932559	Ttpa<sup>tm1Far</sup>	is_implicated_in	DOID:0090028	familial isolated deficiency of vitamin E		MGI:2174791	Ttpa<sup>tm1Far</sup>/Ttpa<sup>tm1Far</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11095717	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932559	Ttpa<sup>tm1Far</sup>	is_implicated_in	DOID:0090028	familial isolated deficiency of vitamin E		MGI:2174792	Ttpa<sup>tm1Far</sup>/Ttpa<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11095717	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5438048	b2b1700Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3522251	vsd	is_implicated_in	DOID:11836	clubfoot		MGI:3522714	vsd/vsd  [background:] C57BL/6J-vsd			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447176	Snai2<sup>tm2Grid</sup>	is_implicated_in	DOID:9258	Waardenburg syndrome		MGI:2652604	Snai2<sup>tm2Grid</sup>/Snai2<sup>tm2Grid</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12444107	20230703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152603	Gnai2<sup>tm1Lbi</sup>	is_not_implicated_in	DOID:0110887	inflammatory bowel disease 12		MGI:3047407	Gnai2<sup>tm1Lbi</sup>/Gnai2<sup>tm1Lbi</sup>  [background:] 129-Gnai2<sup>tm1Lbi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15219458	20081208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858522	Map3k14<sup>aly</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3767418	Map3k14<sup>aly</sup>/Map3k14<sup>aly</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9010048	20091015	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88272	Cat2	is_implicated_in	DOID:83	cataract		MGI:2175730	Cat2<sup>no2</sup>/Cat2<sup>+</sup>  [background:] DBA/2-Cat2<sup>no2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:2072972	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	is_implicated_in	DOID:0080010	bone structure disease		MGI:5511052	Postn<sup>tm1Sjc</sup>/Postn<sup>tm1Sjc</sup>  [background:] B6.Cg-Postn<sup>tm1Sjc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23505553	20170707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332250	Nipbl<sup>Gt(RRS564)Byg</sup>	is_implicated_in	DOID:0080505	Cornelia de Lange syndrome 1		MGI:7491942	Nipbl<sup>Gt(RRS564)Byg</sup>/Nipbl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:32800293	20230626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4332250	Nipbl<sup>Gt(RRS564)Byg</sup>	is_implicated_in	DOID:0080505	Cornelia de Lange syndrome 1		MGI:4367868	Nipbl<sup>Gt(RRS564)Byg</sup>/Nipbl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:19763162	20230626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040514	Pomc<sup>tm1Sora</sup>	is_implicated_in	DOID:9970	obesity		MGI:3041643	Pomc<sup>tm1Sora</sup>/Pomc<sup>tm1Sora</sup>  [background:] involves: 129S2/SvHsd * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:15070780	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3586967	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3588311	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] B6.C3Fe-Hps1<sup>ep</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2158505	Otud7a	is_implicated_in	DOID:0060394	chromosome 15q13.3 microdeletion syndrome		MGI:6115021	Otud7a<sup>em1Cpsc</sup>/Otud7a<sup>em1Cpsc</sup>  [background:] C57BL/6J-Otud7a<sup>em1Cpsc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29395075	20180418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857180	Htt<sup>tm1Mem</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2176494	Htt<sup>tm1Mem</sup>/Htt<sup>tm1Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:7618107	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347487	Foxm1	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3522660	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15082532	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2152844	Slc2a9	is_implicated_in	DOID:1920	hyperuricemia		MGI:5760132	Slc2a9<sup>tm1Khm</sup>/Slc2a9<sup>tm1Khm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129 * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25100214	20210319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	is_implicated_in	DOID:0080143	congenital fibrosis of the extraocular muscles		MGI:4441061	Tubb3<sup>tm1.1Ece</sup>/Tubb3<sup>tm1.1Ece</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20074521	20100423	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429485	Tg(tetO-Ppargc1a)1Dpk	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:4429501	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Ppargc1a)1Dpk/0  [background:] involves: FVB/N * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:14726475	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829005	Cavin1<sup>tm1Pfp</sup>	is_implicated_in	DOID:0111138	congenital generalized lipodystrophy type 4		MGI:3829009	Cavin1<sup>tm1Pfp</sup>/Cavin1<sup>tm1Pfp</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19546242	20100614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888950	Cdkn1a<sup>tm1Led</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3615496	Cdkn1a<sup>tm1Led</sup>/Cdkn1a<sup>tm1Led</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11970874	20060403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	is_implicated_in	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria		MGI:3029314	Slc34a1<sup>tm1Hten</sup>/Slc34a1<sup>tm1Hten</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9560283	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861949	Stat1<sup>tm1Rds</sup>	is_implicated_in	DOID:2945	severe acute respiratory syndrome		MGI:3771372	Stat1<sup>tm1Rds</sup>/Stat1<sup>tm1Rds</sup>  [background:] 129S6/SvEv-Stat1<sup>tm1Rds</sup>/Tac			ECO:0000033	author statement supported by traceable reference	PMID:20386712	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387833	Clip2<sup>tm1.1Gal</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3620031	Clip2<sup>tm1.1Gal</sup>/Clip2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12195424	20060419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891259	Lrat	is_implicated_in	DOID:0110188	Leber congenital amaurosis 14		MGI:3039274	Lrat<sup>tm1Kpal</sup>/Lrat<sup>tm1Kpal</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:18296659	20130814	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202722	Gtf2i	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3831546	Gtf2i<sup>Gt(XE029)Byg</sup>/Gtf2i<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19109438	20140127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202722	Gtf2i	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5532293	Gtf2i<sup>tm1Vcam</sup>/Gtf2i<sup>tm1Vcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:20403157	20140127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5779426	Ncstn<sup>tm1.1Akli</sup>/Ncstn<sup>tm1.1Akli</sup> Tg(Upk2-cre,-EGFP)#Akli/0  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:25194568	20160629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808759	Col2a1<sup>Rgsc856</sup>	is_implicated_in	DOID:0080027	spondyloepimetaphyseal dysplasia		MGI:5007718	Col2a1<sup>Rgsc856</sup>/Col2a1<sup>Rgsc856</sup>  [background:] involves: C57BL/6JJcl * DBA/2JJcl			ECO:0000033	author statement supported by traceable reference	PMID:21538020	20180419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152589	Pkd1<sup>tm1Rsa</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:2173244	Pkd1<sup>tm1Rsa</sup>/Pkd1<sup>+</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:11593033	20050530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3514020	Pank2<sup>tm1Jgt</sup>	is_not_implicated_in	DOID:3981	pantothenate kinase-associated neurodegeneration		MGI:3514129	Pank2<sup>tm1Jgt</sup>/Pank2<sup>tm1Jgt</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15525657	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2142227	Lrrk1	is_implicated_in	DOID:13533	osteopetrosis		MGI:5568131	Lrrk1<sup>tm1.1Smo</sup>/Lrrk1<sup>tm1.1Smo</sup>  [background:] involves: 129S/Sv			ECO:0000033	author statement supported by traceable reference	PMID:23526378	20180730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856085	Mitf<sup>Mi</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:3513118	Mitf<sup>Mi</sup>/Mitf<sup>Mi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	MGI:78359	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158699	Npy1r<sup>tm1Tped</sup>	is_implicated_in	DOID:9970	obesity		MGI:3639781	Npy1r<sup>tm1Tped</sup>/Npy1r<sup>tm1Tped</sup>  [background:] B6.129P2-Npy1r<sup>tm1Tped</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14525913	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	is_implicated_in	DOID:0111087	Fanconi anemia complementation group C		MGI:2450132	Fancc<sup>tm1Mgo</sup>/Fancc<sup>tm1Mgo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8704201	20110518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	is_implicated_in	DOID:0111087	Fanconi anemia complementation group C		MGI:2450130	Fancc<sup>tm1Mab</sup>/Fancc<sup>tm1Mab</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8630504	20110518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	is_implicated_in	DOID:13641	exfoliation syndrome		MGI:3581179	Lyst<sup>bg-J</sup>/Lyst<sup>bg-J</sup>  [background:] C57BL/6J-Lyst<sup>bg-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:19029039	20110715	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2656240	Tsc1<sup>tm1Djk</sup>	is_implicated_in	DOID:0060648	anterior segment dysgenesis		MGI:6295837	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Lhx2-cre)1Lcar/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:28250050	20190929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4318693	Kif27<sup>Gt(OST441915)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429550	Kif27<sup>Gt(OST441915)Lex</sup>/Kif27<sup>Gt(OST441915)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813500	Tg(Thy1-MAPT*)1Avil	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5529794	Tg(Thy1-MAPT*)1Avil/Tg(Thy1-MAPT*)1Avil  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:23774255	20140123	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	is_implicated_in	DOID:2231	factor XII deficiency		MGI:3721103	F12<sup>tm1Pbfd</sup>/F12<sup>tm1Pbfd</sup>  [background:] B6.Cg-F12<sup>tm1Pbfd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16009717	20151122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:3812200	Krt14<sup>tm1Der</sup>/Krt14<sup>+</sup> Tg(KRT14-cre/PGR)1Der/?  [background:] involves: 129X1/SvJ * FVB * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:2653131	Krt14<sup>tm2Der</sup>/Krt14<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:3812201	Krt14<sup>tm1Der</sup>/Krt14<sup>+</sup> Tg(KRT5-cre/PGR)1Der/?  [background:] involves: 129X1/SvJ * FVB * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11157990	20081028	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603462	Slc25a12<sup>Gt(OST123999)Lex</sup>	is_implicated_in	DOID:0080349	developmental and epileptic encephalopathy 39		MGI:3715869	Slc25a12<sup>Gt(OST123999)Lex</sup>/Slc25a12<sup>Gt(OST123999)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28429368	20181221	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	is_implicated_in	DOID:0060365	mandibulofacial dysostosis with alopecia		MGI:5817760	Ednra<sup>m1Mhda</sup>/Ednra<sup>+</sup>  [background:] C3HeB/FeJ-Ednra<sup>m1Mhda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27671791	20170116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	is_implicated_in	DOID:0060365	mandibulofacial dysostosis with alopecia		MGI:5817772	Ednra<sup>m1Mhda</sup>/Ednra<sup>m1Mhda</sup>  [background:] C3HeB/FeJ-Ednra<sup>m1Mhda</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27671791	20170116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5750217	Cntnap2<sup>tm2Pele</sup>/Cntnap2<sup>tm2Pele</sup>  [background:] B6.129(Cg)-Cntnap2<sup>tm2Pele</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26647347	20220526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5295268	Cntnap2<sup>tm1Pele</sup>/Cntnap2<sup>tm1Pele</sup>  [background:] B6.129-Cntnap2<sup>tm1Pele</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21962519	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183586	Mc4r<sup>tm1Dhu</sup>	is_implicated_in	DOID:9970	obesity		MGI:3579026	Mc4r<sup>tm1Dhu</sup>/Mc4r<sup>tm1Dhu</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9019399	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98970	Xbp1	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5441532	Xbp1<sup>tm2Glm</sup>/Xbp1<sup>tm2Glm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18775308	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763891	Scn4a<sup>tm1Ljh</sup>	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420395	Scn4a<sup>tm1Ljh</sup>/Scn4a<sup>+</sup>  [background:] B6.129S4-Scn4a<sup>tm1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763891	Scn4a<sup>tm1Ljh</sup>	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420394	Scn4a<sup>tm1Ljh</sup>/Scn4a<sup>tm1Ljh</sup>  [background:] B6.129S4-Scn4a<sup>tm1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856691	Fras1<sup>bl</sup>	is_implicated_in	DOID:11836	clubfoot		MGI:2657302	Fras1<sup>bl</sup>/Fras1<sup>bl</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:12766769	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438230	Tg(HTT*)1Xwy	is_implicated_in	DOID:12858	Huntington's disease		MGI:4438241	Tg(HTT*)1Xwy/0  [background:] FVB-Tg(HTT*)1Xwy			ECO:0000033	author statement supported by traceable reference	PMID:20064390	20100330	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458412	Ift140<sup>cauli</sup>	is_implicated_in	DOID:0110085	asphyxiating thoracic dystrophy 1		MGI:5510810	Ift140<sup>cauli</sup>/Ift140<sup>cauli</sup>  [background:] involves: C3H/HeH * C57BL/6JAnu			ECO:0000033	author statement supported by traceable reference	PMID:24009529	20151209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056651	Kcnq1<sup>tm3Kpfe</sup>	is_implicated_in	DOID:0110644	long QT syndrome 1		MGI:3056760	Kcnq1<sup>tm3Kpfe</sup>/Kcnq1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15498462	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:6251480	Pkd2<sup>tm1.1Gwu</sup>/Pkd2<sup>tm1.1Gwu</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:28244683	20181114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774017	Xbp1<sup>tm2Glm</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5441532	Xbp1<sup>tm2Glm</sup>/Xbp1<sup>tm2Glm</sup> Tg(Vil1-cre)997Gum/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18775308	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3710233	Slc16a2<sup>tm1Dgen</sup>	is_implicated_in	DOID:0050631	Allan-Herndon-Dudley syndrome		MGI:3710595	Slc16a2<sup>tm1Dgen</sup>/Y  [background:] either: (involves: C57BL/6N) or (involves: NMRI)			ECO:0000033	author statement supported by traceable reference	PMID:17318265	20070531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386393	Smad4<sup>tm2.1Cxd</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:5604139	Smad4<sup>tm2.1Cxd</sup>/Smad4<sup>tm2.1Cxd</sup> Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24006258	20170531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181641	Dhcr7<sup>tm1Fdp</sup>	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3613050	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm1Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:20670678	20101102	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181641	Dhcr7<sup>tm1Fdp</sup>	is_implicated_in	DOID:14692	Smith-Lemli-Opitz syndrome		MGI:3613050	Dhcr7<sup>tm1Fdp</sup>/Dhcr7<sup>tm1Fdp</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11230174	20101102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	is_implicated_in	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive		MGI:2174910	Rag2<sup>tm1Fwa</sup>/Rag2<sup>tm1Fwa</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:1547487	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663272	Matn3<sup>tm1Brd</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3687322	Matn3<sup>tm1Brd</sup>/Matn3<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16877353	20061113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	is_implicated_in	DOID:0111032	hemochromatosis type 2B		MGI:3702021	Hamp<sup>tm1Svl</sup>/Hamp<sup>tm1Svl</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16574947	20100330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915164	Coq9	is_implicated_in	DOID:0050730	coenzyme Q10 deficiency disease		MGI:5473683	Coq9<sup>tm1.1Lcl</sup>/Coq9<sup>tm1.1Lcl</sup>  [background:] involves: C57BL/6 * C57BL/6NTac * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23255162	20130410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859183	Smarcal1	is_implicated_in	DOID:0060490	Schimke immuno-osseous dysplasia		MGI:5425315	Smarcal1<sup>tm1.1Cfbo</sup>/Smarcal1<sup>tm1.1Cfbo</sup>  [background:] either: B6.129-Smarcal1<sup>tm1.1Cfbo</sup> or (involves: 129 * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:22378147	20120620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888952	E2f4<sup>tm1Lees</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3582492	E2f4<sup>tm1Lees</sup>/E2f4<sup>tm1Lees</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10983976	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437121	Pkd1<sup>tm1Gztn</sup>	is_implicated_in	DOID:0110858	polycystic kidney disease 1		MGI:4819716	Pkd1<sup>tm1Gztn</sup>/Pkd1<sup>tm1Gztn</sup> Gt(ROSA)26Sor<sup>tm9(cre/ESR1)Arte</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S/Sv * 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20562878	20110502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352456	Nr4a2	is_implicated_in	DOID:5419	schizophrenia		MGI:3841583	Nr4a2<sup>tm1Tpe</sup>/Nr4a2<sup>+</sup>  [background:] B6.129P2-Nr4a2<sup>tm1Tpe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17457314	20090428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857276	Jak3<sup>tm1Ljb</sup>	is_implicated_in	DOID:0090014	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive		MGI:3769345	Jak3<sup>tm1Ljb</sup>/Jak3<sup>tm1Ljb</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:11034372	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661997	Insl3<sup>tm1Imad</sup>	is_implicated_in	DOID:11383	cryptorchidism		MGI:2662181	Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2661997	Insl3<sup>tm1Imad</sup>	is_implicated_in	DOID:11383	cryptorchidism		MGI:2662000	Insl3<sup>tm1Imad</sup>/Insl3<sup>tm1Imad</sup>  [background:] involves: 129/Sv * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:10319319	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4450947	Tg(Myh6-Tnf)1.6Amf	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:4450976	Tg(Myh6-Tnf)1.6Amf/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:15923312	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4437299	Tg(GFAP-HTT*160Q)31Xjl	is_implicated_in	DOID:12858	Huntington's disease		MGI:4437302	Tg(GFAP-HTT*160Q)31Xjl/0  [background:] either: (involves: FVB/NCrl) or (involves: C3H * C57BL/6 * FVB/NCrl)			ECO:0000033	author statement supported by traceable reference	PMID:20018729	20100316	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	is_implicated_in	DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3		MGI:5789945	Chrnb2<sup>tm1.1Cont</sup>/Chrnb2<sup>tm1.1Cont</sup>  [background:] B6.129-Chrnb2<sup>tm1.1Cont</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20603624	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609560	Ptch1<sup>tm1Kmmt</sup>	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:3610455	Ptch1<sup>tm1Kmmt</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12542834	20060118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655190	Slc1a1<sup>tm1Wst</sup>	is_implicated_in	DOID:0060650	dicarboxylic aminoaciduria		MGI:2655192	Slc1a1<sup>tm1Wst</sup>/Slc1a1<sup>tm1Wst</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9233792	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	is_implicated_in	DOID:62	aortic valve disease		MGI:5428443	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22265892	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183225	Ror2<sup>tm1Ymi</sup>	is_implicated_in	DOID:0060764	autosomal recessive Robinow syndrome		MGI:3038706	Ror2<sup>tm1Ymi</sup>/Ror2<sup>tm1Ymi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14745966	20060517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890816	Vsx1	is_not_implicated_in	DOID:10126	keratoconus		MGI:3033934	Vsx1<sup>tm1Mci</sup>/Vsx1<sup>tm1Mci</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14745032	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890816	Vsx1	is_not_implicated_in	DOID:10126	keratoconus		MGI:3033935	Vsx1<sup>tm2Mci</sup>/Vsx1<sup>tm2Mci</sup>  [background:] either: (involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:14745032	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2445054	Senp1	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5707775	Senp1<sup>tm1Wami</sup>/Senp1<sup>tm1Wami</sup> Tg(Fabp4-cre)#Abel/0  [background:] B6.Cg-Senp1<sup>tm1Wami</sup> Tg(Fabp4-cre)#Abel			ECO:0000033	author statement supported by traceable reference	PMID:26596471	20160210	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384622	Men1<sup>tm1.1Gfk</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3813538	Men1<sup>tm1.1Gfk</sup>/Men1<sup>+</sup>  [background:] involves: 129T2/SvEms * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17044021	20081103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180015	Kcnj8<sup>tm1Sse</sup>	is_implicated_in	DOID:3393	coronary artery disease		MGI:3041531	Kcnj8<sup>tm1Sse</sup>/Kcnj8<sup>tm1Sse</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11984590	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98347	Snrpn	is_implicated_in	DOID:1932	Angelman syndrome		MGI:3618137	Snrpn<sup>tm1Kaj</sup>/Snrpn<sup>+</sup>  [background:] either: 129S1-Snrpn<sup>tm1Kaj</sup> or (involves: 129S1/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:16368707	20060329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	is_implicated_in	DOID:0060770	dextro-looped transposition of the great arteries		MGI:3043036	Cfc1<sup>tm1Cbm</sup>/Cfc1<sup>tm1Cbm</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10574770	20210927	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847797	Bmp7<sup>tm1.1Dgra</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:5642218	Bmp7<sup>tm1.1Dgra</sup>/Bmp7<sup>tm1.1Dgra</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:25889639	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1099809	Fgf10	is_implicated_in	DOID:10486	intestinal atresia		MGI:2175884	Fgf10<sup>tm1Ska</sup>/Fgf10<sup>tm1Ska</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15234214	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:7284974	Tlr7<sup>em2Anu</sup>/Tlr7<sup>+</sup>  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:7284986	Tlr7<sup>em2Anu</sup>/Y  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:7284944	Tlr7<sup>em2Anu</sup>/Tlr7<sup>em2Anu</sup>  [background:] C57BL/6NCrl-Tlr7<sup>em2Anu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35477763	20220613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857672	Rxra<sup>tm1Rev</sup>	is_implicated_in	DOID:1682	congenital heart disease		MGI:2176444	Rxra<sup>tm1Rev</sup>/Rxra<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8823298	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1349216	Abcd3	is_implicated_in	DOID:0111066	congenital bile acid synthesis defect 5		MGI:5695549	Abcd3<sup>tm1Safe</sup>/Abcd3<sup>tm1Safe</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25168382	20151111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6191699	Mpz<sup>tm3.1Wra</sup>/Mpz<sup>+</sup>  [background:] FVB.129S2(Cg)-Mpz<sup>tm3.1Wra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22689911	20180725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6191698	Mpz<sup>tm3.1Wra</sup>/Mpz<sup>tm3.1Wra</sup>  [background:] FVB.129S2(Cg)-Mpz<sup>tm1.1Wra</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22689911	20180725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:3576602	Mpz<sup>tm1Msch</sup>/Mpz<sup>tm1Msch</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7581451	20180725	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:3576605	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:7581451	20180725	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849599	Dkc1<sup>tm3Pjma</sup>	is_not_implicated_in	DOID:2729	dyskeratosis congenita		MGI:3849601	Dkc1<sup>tm3Pjma</sup>/Dkc1<sup>tm3Pjma</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19391112	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3849599	Dkc1<sup>tm3Pjma</sup>	is_not_implicated_in	DOID:2729	dyskeratosis congenita		MGI:3849600	Dkc1<sup>tm3Pjma</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19391112	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313268	Chrd	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:2676545	Chrd<sup>tm1Emdr</sup>/Chrd<sup>tm1Emdr</sup>  [background:] either: B6SJL.129-Chrd<sup>tm1Emdr</sup> or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)			ECO:0000033	author statement supported by traceable reference	PMID:12810603	20070104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97493	Pax9	is_implicated_in	DOID:0050591	tooth agenesis		MGI:3612954	Pax9<sup>tm1Hpt</sup>/Pax9<sup>tm1Hpt</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16236760	20060216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97493	Pax9	is_implicated_in	DOID:0050591	tooth agenesis		MGI:3612955	Pax9<sup>tm1Hpt</sup>/Pax9<sup>tm1Rbal</sup>  [background:] involves: 129 * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:16236760	20060216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:7467133	Ctnnb1<sup>em1V</sup>/Ctnnb1<sup>em1V</sup> Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0  [background:] involves: C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:4821394	Egr1<sup>tm1Jmi</sup>/Egr1<sup>tm1Jmi</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17420284	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425918	Casr<sup>BCH002</sup>/Casr<sup>BCH002</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH002</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425920	Casr<sup>BCH004</sup>/Casr<sup>BCH004</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH004</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425923	Casr<sup>BCH013</sup>/Casr<sup>BCH013</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH013</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425921	Casr<sup>BCH007</sup>/Casr<sup>BCH007</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH007</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425919	Casr<sup>BCH003</sup>/Casr<sup>BCH003</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH003</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	is_implicated_in	DOID:13543	hyperparathyroidism		MGI:5425922	Casr<sup>BCH011</sup>/Casr<sup>BCH011</sup>  [background:] C3HeB/FeJ-Casr<sup>BCH011</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22527485	20120625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3706438	Tg(Ins2-Nos2)31Okam	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3706513	Tg(Ins2-Nos2)31Okam/0  [background:] involves: C57BL/6 * CD-1 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9446547	20070501	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2669828	Pts<sup>tm1Thny</sup>	is_implicated_in	DOID:0090106	BH4-deficient hyperphenylalaninemia A		MGI:2672965	Pts<sup>tm1Thny</sup>/Pts<sup>tm1Thny</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12734191	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	is_implicated_in	DOID:0050977	spinocerebellar ataxia type 28		MGI:5696777	Afg3l2<sup>Emv66</sup>/Afg3l2<sup>+</sup>  [background:] involves: MEV/2Ty			ECO:0000033	author statement supported by traceable reference	PMID:19625515	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840596	Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:4353816	Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup>/Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup> 7630403G23Rik<sup>Tg(Th-cre)1Tmd</sup>/7630403G23Rik<sup>+</sup>  [background:] involves: 129 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19630976	20101129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840596	Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup>	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3851906	Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup>/Gt(ROSA)26Sor<sup>tm2(SNCA*119)Djmo</sup> 7630403G23Rik<sup>Tg(Th-cre)1Tmd</sup>/7630403G23Rik<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19630976	20101129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182573	Efna5<sup>tm1Ddmo</sup>	is_implicated_in	DOID:0060668	anencephaly		MGI:3575317	Efna5<sup>tm1Ddmo</sup>/Efna5<sup>tm1Ddmo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11089974	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438451	Col8a2<sup>Aca23</sup>	is_not_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:4438459	Col8a2<sup>Aca23</sup>/Col8a2<sup>+</sup>  [background:] C57BL/6J-Col8a2<sup>Aca23</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19578028	20100401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438451	Col8a2<sup>Aca23</sup>	is_not_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:4438460	Col8a2<sup>Aca23</sup>/Col8a2<sup>Aca23</sup>  [background:] C57BL/6J-Col8a2<sup>Aca23</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19578028	20100401	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510038	Tbx1<sup>tm1Dsr</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510311	Tbx1<sup>tm1Dsr</sup>/Tbx1<sup>+</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510038	Tbx1<sup>tm1Dsr</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510312	Tbx1<sup>tm1Dsr</sup>/Tbx1<sup>tm1Dsr</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98914	Upk3a	is_implicated_in	DOID:9620	vesicoureteral reflux		MGI:2654027	Upk3a<sup>tm1Tsun</sup>/Upk3a<sup>tm1Tsun</sup>  [background:] either: (involves: 129S/SvEv) or (involves: 129S/SvEv * Swiss Webster)			ECO:0000033	author statement supported by traceable reference	PMID:11085999	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3529082	Slc17a5<sup>tm1Lex</sup>	is_implicated_in	DOID:3211	lysosomal storage disease		MGI:3609722	Slc17a5<sup>tm1Lex</sup>/Slc17a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	MGI:3609573	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2149209	Otoa	is_implicated_in	DOID:0110480	autosomal recessive nonsyndromic deafness 22		MGI:5469422	Otoa<sup>tm1Gpr</sup>/Otoa<sup>tm1Gpr</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:23129639	20130329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	is_implicated_in	DOID:0050794	multiple synostoses syndrome		MGI:6161223	Fgf9<sup>tm1Zgwg</sup>/Fgf9<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:28169396	20180615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	is_implicated_in	DOID:0050794	multiple synostoses syndrome		MGI:6161224	Fgf9<sup>tm1Zgwg</sup>/Fgf9<sup>tm1Zgwg</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:28169396	20180615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:5306592	Jun<sup>tm4Wag</sup>/Jun<sup>tm4Wag</sup> Tg(Sftpc-cre)1Blh/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:22265050	20120220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442062	Sh3pxd2b	is_implicated_in	DOID:1686	glaucoma		MGI:4365644	Sh3pxd2b<sup>nee</sup>/Sh3pxd2b<sup>nee</sup>  [background:] B10.Cg-H2<sup>h4</sup> Sh3pxd2b<sup>nee</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:21282566	20190222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722326	Dnah5<sup>hlb612</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:3778526	Dnah5<sup>hlb612</sup>/Dnah5<sup>hlb612</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18037990	20081219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856996	pma	is_implicated_in	DOID:0090124	neurogenic-type arthrogryposis multiplex congenita-2		MGI:3722144	pma/pma  [background:] involves: CF-1			ECO:0000033	author statement supported by traceable reference	PMID:3948960	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858556	Rag2<sup>tm1Fwa</sup>	is_implicated_in	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive		MGI:2174910	Rag2<sup>tm1Fwa</sup>/Rag2<sup>tm1Fwa</sup>  [background:] involves: 129S/SvEv * MF1			ECO:0000033	author statement supported by traceable reference	PMID:1547487	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851598	Cngb1<sup>tm1Sjpi</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:3851599	Cngb1<sup>tm1Sjpi</sup>/Cngb1<sup>tm1Sjpi</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19339551	20100720	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929293	Cib2	is_implicated_in	DOID:0110505	autosomal recessive nonsyndromic deafness 48		MGI:6192643	Cib2<sup>tm1.1Aela</sup>/Cib2<sup>tm1.1Aela</sup>  [background:] involves: BALB/c * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29084757	20180803	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	is_implicated_in	DOID:0060239	Van der Woude syndrome		MGI:4457064	Irf6<sup>clft1</sup>/Irf6<sup>clft1</sup>  [background:] involves: A/J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20196077	20100629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3875890	Mtss1<sup>Gt(CSC156)Byg</sup>	is_implicated_in	DOID:0060060	non-Hodgkin lymphoma		MGI:5141084	Mtss1<sup>Gt(CSC156)Byg</sup>/Mtss1<sup>Gt(CSC156)Byg</sup>  [background:] B6.129P2-Mtss1<sup>Gt(CSC156)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22081072	20120912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926955	Nf2<sup>tm2Gth</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3850389	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)2Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926955	Nf2<sup>tm2Gth</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3850388	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)1Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711456	Aqp2<sup>tm1(cre)Blyg</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3712071	Aqp2<sup>tm1(cre)Blyg</sup>/Aqp2<sup>tm1(cre)Blyg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17229678	20070619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522330	pta	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3522704	pta/pta  [background:] C57BL/6J-pta			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	is_not_implicated_in	DOID:0060010	Omenn syndrome		MGI:3840832	Rag1<sup>tm1Jsek</sup>/Rag1<sup>tm1Jsek</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:19126872	20090422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1336213	Mybpc1	is_implicated_in	DOID:0081337	congenital myopathy		MGI:7258345	Mybpc1<sup>em1Lbmc</sup>/Mybpc1<sup>+</sup>  [background:] C57BL/6NTac-Mybpc1<sup>em1Lbmc</sup>/Lmcb			ECO:0000033	author statement supported by traceable reference	MGI:7256878	20230605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385566	Tg(Prnp-MAPT)43Vle	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:3663447	Tg(Prnp-MAPT)43Vle/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:10595524	20120502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177743	Htt<sup>tm1Hay</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3586839	Htt<sup>tm1Hay</sup>/Htt<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7774020	20050907	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447624	Dlx5/Dlx6<sup>tm1Levi</sup>	is_implicated_in	DOID:0090021	split hand-foot malformation 1		MGI:2653534	Dlx5/Dlx6<sup>tm1Levi</sup>/Dlx5/Dlx6<sup>tm1Levi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12112878	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655791	Mefv<sup>tm1Chae</sup>	is_implicated_in	DOID:2987	familial mediterranean fever		MGI:2655804	Mefv<sup>tm1Chae</sup>/Mefv<sup>tm1Chae</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12667444	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933844	Ntf3<sup>tm1Par</sup>	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:2175179	Ntf3<sup>tm1Par</sup>/Ntf3<sup>tm1Par</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8841198	20060426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510040	Tbx1<sup>tm1.1Dsr</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510314	Tbx1<sup>tm1.1Dsr</sup>/Tbx1<sup>tm1.1Dsr</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510040	Tbx1<sup>tm1.1Dsr</sup>	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3510313	Tbx1<sup>tm1.1Dsr</sup>/Tbx1<sup>+</sup>  [background:] either: 129/Sv or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15469978	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:1712	aortic valve stenosis		MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662358	Slit3<sup>tm1.1Dor</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5562646	Slit3<sup>tm1.1Dor</sup>/Slit3<sup>tm1.1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24355925	20140507	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662358	Slit3<sup>tm1.1Dor</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:2662361	Slit3<sup>tm1.1Dor</sup>/Slit3<sup>tm1.1Dor</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12702769	20140507	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442827	Tbc1d32	is_implicated_in	DOID:14679	VACTERL association		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20150727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3583010	Mmp14<sup>tm1Hbh</sup>/Mmp14<sup>tm1Hbh</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:10520996	20050805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107246	Tinf2	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:5556400	Tinf2<sup>tm2.2Tdl</sup>/Tinf2<sup>+</sup>  [background:] involves: BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24449270	20140415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840248	Ptpn11<sup>tm6Bgn</sup>	is_implicated_in	DOID:0060578	Noonan syndrome 1		MGI:6095197	Emx1<sup>tm1(cre)Krj</sup>/Emx1<sup>+</sup> Ptpn11<sup>tm6Bgn</sup>/Ptpn11<sup>+</sup>  [background:] B6.129S-Ptpn11<sup>tm6Bgn</sup> Emx1<sup>tm1(cre)Krj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28346493	20171206	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311343	b2b942Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5313520	b2b942Clo/b2b942Clo  [background:] C57BL/6J-b2b942Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624978	Tg(Ckm-LPL)HRze	is_implicated_in	DOID:423	myopathy		MGI:3624988	Tg(Ckm-LPL)HRze/0  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:7635990	20190806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924066	Sdccag8	is_implicated_in	DOID:12712	nephronophthisis		MGI:5705821	Sdccag8<sup>Gt(OST40418)Lex</sup>/Sdccag8<sup>Gt(OST40418)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:24722439	20220915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154689	Col11a2<sup>tm1Mne</sup>	is_implicated_in	DOID:0080026	otospondylomegaepiphyseal dysplasia, autosomal recessive		MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418685	G6pc1<sup>tm2.2Jyc</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:4418690	G6pc1<sup>tm2.2Jyc</sup>/G6pc1<sup>tm2.2Jyc</sup>  [background:] involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19548314	20100126	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614340	Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul	is_implicated_in	DOID:1612	breast cancer		MGI:3614342	Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul/?  [background:] FVB/N-Tg(MMTV-PyVT*Y315F*Y322F)Db-1Mul			ECO:0000033	author statement supported by traceable reference	PMID:9528804	20101110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	is_implicated_in	DOID:61	mitral valve disease		MGI:6718510	Ift88<sup>tm1Bky</sup>/Ift88<sup>tm1Bky</sup> Nfatc1<sup>tm1.1(cre)Bz</sup>/Nfatc1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:31118289	20210630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2678952	Bloc1s3	is_implicated_in	DOID:0060546	Hermansky-Pudlak syndrome 8		MGI:3588307	Bloc1s3<sup>rp</sup>/Bloc1s3<sup>rp</sup>  [background:] involves: C57BL/10ScSn * C57BL/Tb			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651859	Ush1c<sup>dfcr-2J</sup>	is_implicated_in	DOID:0110830	Usher syndrome type 1C		MGI:2676317	Ush1c<sup>dfcr-2J</sup>/Ush1c<sup>dfcr-2J</sup>  [background:] B6;129S4			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181018	Clcn5<sup>tm1Tjj</sup>	is_implicated_in	DOID:0050699	Dent disease		MGI:3046533	Clcn5<sup>tm1Tjj</sup>/Y  [background:] B6.129-Clcn5<sup>tm1Tjj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11099045	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104757	Ephb4	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5614941	Ephb4<sup>b2b2412Clo</sup>/Ephb4<sup>b2b2412Clo</sup>  [background:] C57BL/6J-Ephb4<sup>b2b2412Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	is_implicated_in	DOID:0111020	cone-rod dystrophy 9		MGI:4360909	Adam9<sup>tm1Bbl</sup>/Adam9<sup>tm1Bbl</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:19409519	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861438	Gcm2	is_implicated_in	DOID:11199	hypoparathyroidism		MGI:3588582	Gcm2<sup>tm1Kry</sup>/Gcm2<sup>tm1Kry</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10910362	20050929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384433	Egr1<sup>tm1Jmi</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:4821394	Egr1<sup>tm1Jmi</sup>/Egr1<sup>tm1Jmi</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17420284	20170616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387029	Dnase1<sup>tm1Tmo</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3639668	Dnase1<sup>tm1Tmo</sup>/Dnase1<sup>tm1Tmo</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10835632	20060802	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917925	Vcpip1	is_implicated_in	DOID:3911	progeria		MGI:6515750	Vcpip1<sup>em1Zlou</sup>/Vcpip1<sup>em1Zlou</sup>  [background:] C57BL/6NHsd-Vcpip1<sup>em1Zlou</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32649882	20210407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	is_implicated_in	DOID:0080051	acromesomelic dysplasia, Hunter-Thompson type		MGI:5509382	Gdf5<sup>Bp-5J</sup>/Gdf5<sup>+</sup>  [background:] C57BL/6J-Gdf5<sup>Bp-5J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5509308	20131004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442415	Kat6a	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3629227	Kat6a<sup>tm1Avo</sup>/Kat6a<sup>tm1Avo</sup>  [background:] involves: 129/Sv * BALB/c * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:22921202	20121228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916380	Vps13b	is_implicated_in	DOID:83	cataract		MGI:6468047	Vps13b<sup>tm1.2Ics</sup>/Vps13b<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:32915983	20201021	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891221	Crtap	is_implicated_in	DOID:0110337	osteogenesis imperfecta type 7		MGI:3693839	Crtap<sup>tm1Brle</sup>/Crtap<sup>tm1Brle</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:17055431	20070116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181691	Gp1ba<sup>tm1Ware</sup>	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:2672029	Gp1ba<sup>tm1Ware</sup>/Gp1ba<sup>tm1Ware</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10706630	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581820	Tg(GFAP)7Mes	is_implicated_in	DOID:4252	Alexander disease		MGI:3581823	Tg(GFAP)7Mes/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:9466565	20050718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437061	b2b1146Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437113	b2b1146Clo/b2b1146Clo  [background:] C57BL/6J-b2b1146Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3584128	Spry2<sup>tm1Ayos</sup>	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:3584494	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup>  [background:] B6.Cg-Spry2<sup>tm1Ayos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15937482	20050829	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	is_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:5607258	Slc40a1<sup>tm1.1Mmfe</sup>/Slc40a1<sup>tm1.1Mmfe</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25100063	20141216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	is_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:5607261	Slc40a1<sup>tm1.1Mmfe</sup>/Slc40a1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25100063	20141216	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	is_implicated_in	DOID:0111028	hemochromatosis type 4		MGI:3700665	Slc40a1<sup>ffe</sup>/Slc40a1<sup>+</sup>  [background:] either: (involves: 129X1/SvJ * C57BL/6J) or (involves: C3H/HeJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17289807	20141216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3784954	Flnb<sup>Gt(XD076)Byg</sup>	is_implicated_in	DOID:0090116	spondylocarpotarsal synostosis syndrome		MGI:3785077	Flnb<sup>Gt(XD076)Byg</sup>/Flnb<sup>Gt(XD076)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17606870	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678400	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:2678505	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>/Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12039988	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2678400	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:2678506	Nphs1<sup>Gt(pT1Betageo)1Ruiz</sup>/Nphs1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12039988	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5620180	b2b2696.1Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5620190	b2b2696.1Clo/b2b2696.1Clo  [background:] C57BL/6J-b2b2696.1Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664598	Col5a1<sup>tm1Rjw</sup>	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3687258	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:34740257	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664598	Col5a1<sup>tm1Rjw</sup>	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3687258	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16492673	20220719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664598	Col5a1<sup>tm1Rjw</sup>	is_implicated_in	DOID:14720	Ehlers-Danlos syndrome classic type 1		MGI:3687246	Col5a1<sup>tm1Rjw</sup>/Col5a1<sup>+</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:15383546	20220719	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	is_implicated_in	DOID:2746	glycogen storage disease V		MGI:3621470	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15328538	20060505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2152879	Apoca	is_implicated_in	DOID:83	cataract		MGI:2655437	Apoca/Apoca<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316714	Cox7a1	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5465105	Cox7a1<sup>tm1Hutt</sup>/Cox7a1<sup>tm1Hutt</sup>  [background:] B6.129-Cox7a1<sup>tm1Hutt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22119795	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4124012	Fat1<sup>Gt(KST249)Byg</sup>	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:5524134	Fat1<sup>Gt(KST249)Byg</sup>/Fat1<sup>Gt(KST249)Byg</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311361	b2b370Clo	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5313541	b2b370Clo/b2b370Clo  [background:] C57BL/6J-b2b370Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707260	Drd1<sup>tm2Jcd</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3709758	Drd1<sup>tm2Jcd</sup>/Drd1<sup>+</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17360497	20110805	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930136	Pmfbp1	is_implicated_in	DOID:0111922	spermatogenic failure 31		MGI:6681929	Pmfbp1<sup>em#Jfw</sup>/Pmfbp1<sup>em#Jfw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:30298696	20210408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3840615	Fmr1<sup>tm1Rbd</sup>	is_implicated_in	DOID:14261	fragile X syndrome		MGI:4415714	Fmr1<sup>tm1Rbd</sup>/Y  [background:] B6.129-Fmr1<sup>tm1Rbd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20011099	20100112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	is_implicated_in	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome		MGI:4867484	Gjb2<sup>tm2.2Kwi</sup>/Gjb2<sup>+</sup> Tg(Pgk1-cre)1Lni/0  [background:] involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20926451	20110111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105115	Ctf1	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5294956	Ctf1<sup>tm1Msd</sup>/Ctf1<sup>tm1Msd</sup>  [background:] B6.Cg-Ctf1<sup>tm1Msd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21803294	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623141	Arl3<sup>Gt(OST263303)Lex</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3625687	Arl3<sup>Gt(OST263303)Lex</sup>/Arl3<sup>Gt(OST263303)Lex</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:16565502	20060627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102674	Umod	is_implicated_in	DOID:557	kidney disease		MGI:3712576	Umod<sup>urehr4</sup>/Umod<sup>urehr4</sup>  [background:] C3HeB/FeJ-Umod<sup>urehr4</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19692485	20180627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102674	Umod	is_implicated_in	DOID:557	kidney disease		MGI:5571280	Umod<sup>Urehd1</sup>/Umod<sup>+</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:23748428	20180627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102674	Umod	is_implicated_in	DOID:557	kidney disease		MGI:5571287	Umod<sup>Urehd1</sup>/Umod<sup>Urehd1</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:23748428	20180627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102674	Umod	is_implicated_in	DOID:557	kidney disease		MGI:6162682	Umod<sup>em1Duf</sup>/Umod<sup>+</sup>  [background:] C57BL/6J-Umod<sup>em1Duf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28990932	20180627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921164	Irak3	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5800315	Irak3<sup>tm1Flv</sup>/Irak3<sup>tm1Flv</sup>  [background:] NOD.129S1(B6)-Irak3<sup>tm1Flv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24696448	20161011	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202398	Kera	is_implicated_in	DOID:0060287	cornea plana		MGI:2672991	Kera<sup>tm1Cyl</sup>/Kera<sup>tm1Cyl</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:12665512	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179134	Col18a1<sup>tm1Hms</sup>	is_implicated_in	DOID:0060680	pigment dispersion syndrome		MGI:3046553	Col18a1<sup>tm1Hms</sup>/Col18a1<sup>tm1Hms</sup>  [background:] B6.129S4-Col18a1<sup>tm1Hms</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12766032	20150601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3696473	Tg(Prnp-App/APPswe)E1-2Dbo	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3696576	Tg(Prnp-App/APPswe)E1-2Dbo/0  [background:] B6.C3-Tg(Prnp-App/APPswe)E1-2Dbo			ECO:0000033	author statement supported by traceable reference	PMID:12742740	20071026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:3040322	Ccn1<sup>tm1Lfl</sup>/Ccn1<sup>tm1Lfl</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17023674	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156825	Zic2<sup>tm1Jaru</sup>	is_implicated_in	DOID:0110878	holoprosencephaly 5		MGI:2653209	Zic2<sup>tm1Jaru</sup>/Zic2<sup>tm1Jaru</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10677508	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	is_implicated_in	DOID:6000	congestive heart failure		MGI:3037157	Csrp3<sup>tm1Crni</sup>/Csrp3<sup>tm1Crni</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11087268	20171222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931850	Ccr1<sup>tm1Gao</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:3614443	Ccr1<sup>tm1Gao</sup>/Ccr1<sup>tm1Gao</sup>  [background:] B6.129S4-Ccr1<sup>tm1Gao</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3808306	Prl3c1<sup>tm1(KOMP)Vlcg</sup>	is_implicated_in	DOID:11613	hyperandrogenism		MGI:6159252	Prl3c1<sup>tm1(KOMP)Vlcg</sup>/Prl3c1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:28576872	20180601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	is_implicated_in	DOID:11044	gastroschisis		MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3686893	Sirt6<sup>tm1Fwa</sup>	is_implicated_in	DOID:3911	progeria		MGI:3686897	Sirt6<sup>tm1Fwa</sup>/Sirt6<sup>tm1Fwa</sup>  [background:] involves: 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16439206	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3759215	Pkhd1<sup>tm1.1Ggg</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3759225	Pkhd1<sup>tm1.1Ggg</sup>/Pkhd1<sup>tm1.1Ggg</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17575307	20071025	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180720	Zic3<sup>tm1Bca</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3618631	Zic3<sup>tm1Bca</sup>/Zic3<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180720	Zic3<sup>tm1Bca</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3618629	Zic3<sup>tm1Bca</sup>/Zic3<sup>tm1Bca</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180720	Zic3<sup>tm1Bca</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:3618630	Zic3<sup>tm1Bca</sup>/Y  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180720	Zic3<sup>tm1Bca</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2180831	Zic3<sup>tm1Bca</sup>/Y  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:11959836	20060406	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793296	Gp1bb<sup>tm1Frla</sup>	is_implicated_in	DOID:2217	Bernard-Soulier syndrome		MGI:3805720	Gp1bb<sup>tm1Frla</sup>/Gp1bb<sup>tm1Frla</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17095718	20111110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921982	Stx11	is_implicated_in	DOID:0110924	familial hemophagocytic lymphohistiocytosis 4		MGI:5476653	Stx11<sup>tm1.2Ics</sup>/Stx11<sup>tm1.2Ics</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:23160464	20130430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860962	Tfam<sup>tm1Lrsn</sup>	is_implicated_in	DOID:12934	Kearns-Sayre syndrome		MGI:2177637	Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup> Tg(Myhca-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10737799	20060111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860962	Tfam<sup>tm1Lrsn</sup>	is_implicated_in	DOID:12934	Kearns-Sayre syndrome		MGI:2177634	Tfam<sup>tm1Lrsn</sup>/Tfam<sup>tm1Lrsn</sup> Tg(Ckmm-cre)1Lrsn/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9916807	20060111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2389007	Hydin	is_implicated_in	DOID:10908	hydrocephalus		MGI:3605005	Hydin<sup>hy3</sup>/Hydin<sup>hy3</sup>  [background:] involves: CBA			ECO:0000033	author statement supported by traceable reference	PMID:4784576	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	is_implicated_in	DOID:0050387	nonpapillary renal cell carcinoma		MGI:3829652	Flcn<sup>tm1Btt</sup>/Flcn<sup>tm1Btt</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18974783	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4419323	Zmynd10<sup>tm1(KOMP)Wtsi</sup>	is_implicated_in	DOID:0110597	primary ciliary dyskinesia 22		MGI:6163475	Zmynd10<sup>tm1(KOMP)Wtsi</sup>/Zmynd10<sup>tm1(KOMP)Wtsi</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29601588	20180628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	is_implicated_in	DOID:0111455	GRACILE syndrome		MGI:5446806	Bcs1l<sup>tm1.1Levp</sup>/Bcs1l<sup>tm1.1Levp</sup>  [background:] involves: 129 * 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21274865	20200131	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181877	Ins1<sup>tm1Jja</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3716134	Ins1<sup>tm1Jja</sup>/Ins1<sup>tm1Jja</sup>  [background:] NOD.129S2-Ins1<sup>tm1Jja</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12925730	20070726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3758960	Nlgn3<sup>tm2.1Sud</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5660857	Nlgn3<sup>tm2.1Sud</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:24995986	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921749	Sost	is_implicated_in	DOID:0080036	SOST-related sclerosing bone dysplasia		MGI:4882107	Sost<sup>tm1(KOMP)Vlcg</sup>/Sost<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:22886088	20121119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313261	Sptbn2	is_not_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:5426692	Sptbn2<sup>tm1Mjac</sup>/Sptbn2<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:20603325	20120702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861901	Mast1	is_implicated_in	DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations		MGI:6358832	Mast1<sup>em1Dak</sup>/Mast1<sup>+</sup>  [background:] B6.Cg-Mast1<sup>em1Dak</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30449657	20200518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_not_implicated_in	DOID:0050547	familial medullary thyroid carcinoma		MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_not_implicated_in	DOID:0050547	familial medullary thyroid carcinoma		MGI:3583335	Ret<sup>tm2.1Cos</sup>/Ret<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814338	Slc2a10<sup>G128E</sup>	is_not_implicated_in	DOID:0050645	arterial tortuosity syndrome		MGI:3814341	Slc2a10<sup>G128E</sup>/Slc2a10<sup>G128E</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:18693279	20081110	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87866	Acadl	is_implicated_in	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency		MGI:2448162	Acadl<sup>tm1Uab</sup>/Acadl<sup>tm1Uab</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:9861014	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	is_implicated_in	DOID:0060761	familial chronic myelocytic leukemia-like syndrome		MGI:2175074	Irf8<sup>tm1Hor</sup>/Irf8<sup>tm1Hor</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8861914	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	is_implicated_in	DOID:0060761	familial chronic myelocytic leukemia-like syndrome		MGI:2175075	Irf8<sup>tm1Hor</sup>/Irf8<sup>+</sup>  [background:] either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8861914	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429538	Tg(Notch3*R169C)88Bbb	is_implicated_in	DOID:2316	brain ischemia		MGI:4429555	Tg(Notch3*R169C)88Bbb/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20071773	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690994	Tg(KRT5-TGFB1)F2020Xjw	is_implicated_in	DOID:8893	psoriasis		MGI:4430068	Tg(KRT5-TGFB1)F2020Xjw/0  [background:] involves: C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:15057277	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384321	Pparg<sup>tm1.1Gonz</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:4939883	Pparg<sup>tm1.1Gonz</sup>/Pparg<sup>tm1.1Gonz</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21135166	20110307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4431709	Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>	is_implicated_in	DOID:0060861	microphthalmia with limb anomalies		MGI:5056093	Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>/Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] C57BL/6N-Smoc1<sup>tm1a(EUCOMM)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21750680	20110808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2174983	Pik3r1<sup>tm1Dfr</sup>/Pik3r1<sup>tm1Dfr</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11062485	20081222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2174983	Pik3r1<sup>tm1Dfr</sup>/Pik3r1<sup>tm1Dfr</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9888855	20081222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2174985	Pik3r1<sup>tm1Tka</sup>/Pik3r1<sup>tm1Tka</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9888854	20081222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2157910	Mlc1	is_implicated_in	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1		MGI:6105933	Mlc1<sup>tm1.1Vdk</sup>/Mlc1<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25382142	20190412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2157910	Mlc1	is_implicated_in	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1		MGI:6105933	Mlc1<sup>tm1.1Vdk</sup>/Mlc1<sup>tm1.1Vdk</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28695146	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155425	Fah<sup>2R</sup>	is_implicated_in	DOID:0050726	tyrosinemia type I		MGI:2655554	Fah<sup>2R</sup>/Fah<sup>2R</sup>  [background:] involves: BALB/cRl			ECO:0000033	author statement supported by traceable reference	PMID:11209059	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:6415731	Scn5a<sup>em1Coop</sup>/Scn5a<sup>+</sup>  [background:] involves: FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:30371314	20200511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:6415732	Scn5a<sup>em1Coop</sup>/Scn5a<sup>em1Coop</sup>  [background:] involves: C57BL/6NJ * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:30371314	20200511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043362	Ndrg1<sup>tm1Myta</sup>	is_implicated_in	DOID:0110186	Charcot-Marie-Tooth disease type 4D		MGI:3043397	Ndrg1<sup>tm1Myta</sup>/Ndrg1<sup>tm1Myta</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15082788	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3038234	nm3	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3038236	nm3/nm3  [background:] involves: RIIIS/J			ECO:0000033	author statement supported by traceable reference	PMID:14966677	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914325	Magt1	is_implicated_in	DOID:612	primary immunodeficiency disease		MGI:6155603	Magt1<sup>Gt(IST13422E1)Tigm</sup>/Y  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29581357	20180510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857497	Gpi1<sup>b-m1Neu</sup>	is_implicated_in	DOID:2861	congenital nonspherocytic hemolytic anemia		MGI:2177287	Gpi1<sup>b-m1Neu</sup>/Gpi1<sup>b-m1Neu</sup>  [background:] C3.Cg-Gpi1<sup>b-m1Neu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8417789	20110309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99180	Zfp36	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3037334	Zfp36<sup>tm1Pjb</sup>/Zfp36<sup>tm1Pjb</sup>  [background:] B6.Cg-Zfp36<sup>tm1Pjb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24727475	20141024	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95657	Gas2	is_implicated_in	DOID:10003	sensorineural hearing loss		MGI:7282200	Gas2<sup>tm1a(EUCOMM)Hmgu</sup>/Gas2<sup>tm1a(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-Gas2<sup>tm1a(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33964205	20220606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790742	Bard1<sup>tm2Thl</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3805029	Bard1<sup>tm2Thl</sup>/Bard1<sup>tm2Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129/Sv * 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18443292	20130918	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3869865	L2hgdh<sup>Gt(DC0625)Wtsi</sup>	is_implicated_in	DOID:0050574	L-2-hydroxyglutaric aciduria		MGI:5708062	L2hgdh<sup>Gt(DC0625)Wtsi</sup>/L2hgdh<sup>Gt(DC0625)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25763823	20160211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857695	Smad3<sup>tm1Cxd</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3760091	Smad3<sup>tm1Cxd</sup>/Smad3<sup>tm1Cxd</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11285272	20090225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3708382	Myo7a<sup>polka</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:3709041	Myo7a<sup>polka</sup>/Myo7a<sup>polka</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20016096	20100312	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102806	Acvr2a	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:2450541	Acvr2a<sup>tm1Zuk</sup>/Acvr2a<sup>tm1Zuk</sup>  [background:] either: 129 or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7885474	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384429	Hnf1a<sup>tm1.1Ylee</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3623394	Hnf1a<sup>tm1.1Ylee</sup>/Hnf1a<sup>tm1.1Ylee</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9566924	20060526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:3721424	Cdk5r1<sup>tm1Lht</sup>/Cdk5r1<sup>tm1Lht</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:20832057	20150225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3795718	Tg(Myh6-Cryab*R120G)708Rbns	is_implicated_in	DOID:0080093	myofibrillar myopathy 2		MGI:5907293	Tg(Myh6-Cryab*R120G)708Rbns/0  [background:] FVB/N-Tg(Myh6-Cryab*R120G)708Rbns			ECO:0000033	author statement supported by traceable reference	PMID:11440982	20170823	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698161	Zic3<sup>tm1Jwb</sup>	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:3698637	Zic3<sup>tm1Jwb</sup>/Zic3<sup>tm1Jwb</sup>  [background:] either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17127413	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698161	Zic3<sup>tm1Jwb</sup>	is_implicated_in	DOID:2907	Goldenhar syndrome		MGI:3698642	Zic3<sup>tm1Jwb</sup>/Y  [background:] either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:17127413	20070305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1196297	Hgsnat	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:5806128	Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>/Hgsnat<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:27491071	20161103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	is_implicated_in	DOID:6406	double outlet right ventricle		MGI:3815024	Ece1<sup>tm1Reh</sup>/Ece1<sup>tm1Reh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10811845	20110509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448247	Foxm1<sup>tm1Rhc</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3710341	Foxm1<sup>tm1Rhc</sup>/Foxm1<sup>tm1Rhc</sup> Tg(Tek-cre)1Ywa/0  [background:] involves: 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21199796	20110306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834463	Tg(Ly6a-BCR/ABL1)IS1BIsg	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3834482	Tg(Ly6a-BCR/ABL1)IS1BIsg/0  [background:] involves: C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19037256	20090305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330281	Cd2ap	is_implicated_in	DOID:0112245	focal segmental glomerulosclerosis 3		MGI:6476763	Cd2ap<sup>em1Irgu</sup>/Cd2ap<sup>em1Irgu</sup>  [background:] C57BL/6-Cd2ap<sup>em1Irgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30612599	20210727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919847	Auts2	is_implicated_in	DOID:0060307	autosomal dominant intellectual developmental disorder		MGI:5697531	Auts2<sup>tm1.1Dare</sup>/Auts2<sup>tm1.1Dare</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:25519132	20151201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667328	Slc27a4<sup>tm1Wsr</sup>	is_implicated_in	DOID:0060762	restrictive dermopathy		MGI:2670851	Slc27a4<sup>tm1Wsr</sup>/Slc27a4<sup>tm1Wsr</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12821645	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510918	Tg(CMV-EGFP,Rnu6-siAbca1)#Wcyy	is_implicated_in	DOID:1388	Tangier disease		MGI:3510920	Tg(ALB-cre,CMV-rtTA)#Wcyy/0 Tg(CMV-EGFP,Rnu6-siAbca1)#Wcyy/0  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:15509524	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3047079	Tg(MMTV-Erbb2)9Pjo	is_implicated_in	DOID:1612	breast cancer		MGI:5604887	Tg(MMTV-Erbb2)9Pjo/0  [background:] involves: BALB/c * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:2567634	20141120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154536	Cyp19a1<sup>tm1Esi</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450128	Cyp19a1<sup>tm1Esi</sup>/Cyp19a1<sup>tm1Esi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15314222	20150603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926253	Chrnb2<sup>tm1Jpc</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5318689	Chrnb2<sup>tm1Jpc</sup>/Chrnb2<sup>tm1Jpc</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12876201	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1932244	F9<sup>tm1Emg</sup>	is_implicated_in	DOID:12259	hemophilia B		MGI:3662853	F9<sup>tm1Emg</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9639513	20061005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3044413	Mitf<sup>Mi-wh</sup>/Mitf<sup>Mi-wh</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856088	Mitf<sup>Mi-wh</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:3044414	Mitf<sup>Mi-wh</sup>/Mitf<sup>+</sup>  [background:] involves: C57BL * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18902556	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491174	b2b2350Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929230	Bloc1s4	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2663842	Bloc1s4<sup>cno</sup>/Bloc1s4<sup>cno</sup>  [background:] C3H/HeJ-Bloc1s4<sup>cno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11110696	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929230	Bloc1s4	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:3588317	Bloc1s4<sup>cno</sup>/Bloc1s4<sup>cno</sup>  [background:] involves: C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:12445206	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:2177702	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9262482	20060118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701764	Gck<sup>tm3Mgn</sup>	is_implicated_in	DOID:13317	hyperinsulinemic hypoglycemia		MGI:3713297	Gck<sup>tm3Mgn</sup>/Gck<sup>+</sup>  [background:] B6.129S6-Gck<sup>tm3Mgn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17353190	20070629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576027	hpmd	is_implicated_in	DOID:4258	Weissenbacher-Zweymuller syndrome		MGI:3576039	hpmd/hpmd  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11818962	20050526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5445215	Pkd1<sup>b2b1585Clo</sup>/Pkd1<sup>b2b1585Clo</sup>  [background:] C57BL/6J-Pkd1<sup>b2b1585Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914797	Slc39a8	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:6360946	Slc39a8<sup>tm1.2Mrl</sup>/Slc39a8<sup>tm1.2Mrl</sup>  [background:] B6(Cg)-Slc39a8<sup>tm1.2Mrl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29337306	20190925	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3851593	Acsbg1<sup>tm1Mld</sup>	is_not_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:3851594	Acsbg1<sup>tm1Mld</sup>/Acsbg1<sup>tm1Mld</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19167491	20090730	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605162	Slc19a2<sup>tm1Ejn</sup>	is_implicated_in	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome		MGI:3606089	Slc19a2<sup>tm1Ejn</sup>/Slc19a2<sup>tm1Ejn</sup>  [background:] involves: 129S4/SvJae * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14567973	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	is_implicated_in	DOID:0050763	ARC syndrome		MGI:5770121	Vps33b<sup>tm1.1Arte</sup>/Vps33b<sup>tm1.1Arte</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25947942	20170112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102495	mt-Nd6	is_implicated_in	DOID:3650	lactic acidosis		MGI:4834214	mt-Nd6<sup>m2Jiha</sup>  [background:] involves: C3H/An * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:20674568	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521822	Apc<sup>tm2.1Cip</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:5702414	Apc<sup>tm2.1Cip</sup>/Apc<sup>+</sup> Tg(Vil1-cre/ERT2)23Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26214133	20160111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857751	Mitf<sup>mi-enu122</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3587636	Mitf<sup>mi-enu122</sup>/Mitf<sup>+</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20050914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857751	Mitf<sup>mi-enu122</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:3587635	Mitf<sup>mi-enu122</sup>/Mitf<sup>mi-enu122</sup>  [background:] involves: 102 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:9501313	20050914	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2175913	Itgb3<sup>tm1Hyn</sup>	is_implicated_in	DOID:0060691	platelet-type bleeding disorder 16		MGI:2177829	Itgb3<sup>tm1Hyn</sup>/Itgb3<sup>tm1Hyn</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9916135	20070926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4398963	Fancf<sup>tm1Nki</sup>	is_implicated_in	DOID:5426	primary ovarian insufficiency		MGI:6103876	Fancf<sup>tm1Nki</sup>/Fancf<sup>tm1Nki</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21915857	20171220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	is_implicated_in	DOID:0110017	age related macular degeneration 4		MGI:5546609	Cfh<sup>tm1Mbo</sup>/Cfh<sup>tm1Mbo</sup>  [background:] B6.129-Cfh<sup>tm1Mbo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23799019	20140228	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623147	Ppard<sup>tm1Dsvg</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5695740	Ppard<sup>tm1Dsvg</sup>/Ppard<sup>tm1Dsvg</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25279796	20151112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577652	Fktn<sup>tm1Ttd</sup>	is_implicated_in	DOID:0050559	Fukuyama congenital muscular dystrophy		MGI:3577900	Fktn<sup>tm1Ttd</sup>/Fktn<sup>tm1Ttd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15837576	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587949	Sall4<sup>Gt(XE027)Byg</sup>	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3617910	Sall4<sup>Gt(XE027)Byg</sup>/Sall4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16380715	20060328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587949	Sall4<sup>Gt(XE027)Byg</sup>	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3617909	Sall4<sup>Gt(XE027)Byg</sup>/Sall4<sup>+</sup>  [background:] B6;129P2-Sall4<sup>Gt(XE027)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16380715	20060328	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856931	Hps4<sup>le</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3587187	Hps4<sup>le</sup>/Hps4<sup>le</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856145	Hps5<sup>ru2-hz</sup>	is_implicated_in	DOID:0060543	Hermansky-Pudlak syndrome 5		MGI:2174725	Hps5<sup>ru2-hz</sup>/Hps5<sup>ru2-hz</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:12548288	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351471	B9d1	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5301335	B9d1<sup>tm1a(EUCOMM)Wtsi</sup>/B9d1<sup>tm1a(EUCOMM)Wtsi</sup>  [background:] involves: C57BL/6N * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:21763481	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156555	Amhr2<sup>tm1Bhr</sup>	is_implicated_in	DOID:0050791	persistent Mullerian duct syndrome		MGI:3042182	Amhr2<sup>tm1Bhr</sup>/Amhr2<sup>tm1Bhr</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:21490063	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3620964	Tg(MT2A-TGFBR2)4Rser	is_implicated_in	DOID:8398	osteoarthritis		MGI:5907609	Tg(MT2A-TGFBR2)4Rser/0  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:9334355	20170828	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	is_implicated_in	DOID:7442	monoclonal gammopathy of uncertain significance		MGI:7281484	Ighg1<sup>tm1(cre)Cgn</sup>/Ighg1<sup>+</sup> Myd88<sup>em1.1Rsky</sup>/Myd88<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:33343574	20220601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	is_implicated_in	DOID:7442	monoclonal gammopathy of uncertain significance		MGI:7281485	Cd19<sup>tm1(cre/ERT2)Rsky</sup>/Cd19<sup>+</sup> Myd88<sup>em1.1Rsky</sup>/Myd88<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:33343574	20220601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384620	Men1<sup>tm1Gfk</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:3839791	Men1<sup>tm1Gfk</sup>/Men1<sup>tm1Gfk</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:15060136	20170324	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:7279138	Sf3b1<sup>tm1Hko</sup>/Sf3b1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25481243	20220520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:4950068	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(mI56i-cre,EGFP)1Kc/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21195751	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429406	Tg(MMTV-TGFBR2)7Hlm	is_implicated_in	DOID:1612	breast cancer		MGI:3794972	Tg(MMTV-TGFBR2)7Hlm/Tg(MMTV-TGFBR2)7Hlm  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:14507660	20080624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3893035	Ildr1<sup>Gt(D178D03)Wrst</sup>	is_implicated_in	DOID:0110500	autosomal recessive nonsyndromic deafness 42		MGI:5695554	Ildr1<sup>Gt(D178D03)Wrst</sup>/Ildr1<sup>Gt(D178D03)Wrst</sup>  [background:] involves: 129S2/SvPas * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:25217574	20151111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923392	Ppp1r14c	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:6433773	Ppp1r14c<sup>tm1Uhl</sup>/Ppp1r14c<sup>tm1Uhl</sup>  [background:] B6;129S6-Ppp1r14c<sup>tm1Uhl</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27663205	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3843695	Tg(tetO-Chrnb2*V287L)H3Gica	is_implicated_in	DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3		MGI:3843698	Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-Chrnb2*V287L)H3Gica/0  [background:] involves: 129S7/SvEvBrd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:19153075	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	is_implicated_in	DOID:11612	polycystic ovary syndrome		MGI:5429853	Akt2<sup>tm1Hem</sup>/Akt2<sup>tm1Hem</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:22275470	20120802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3628756	Mpi<sup>Gt(OST90588)Lex</sup>	is_not_implicated_in	DOID:0050570	congenital disorder of glycosylation type I		MGI:3629215	Mpi<sup>Gt(OST90588)Lex</sup>/Mpi<sup>Gt(OST90588)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16339137	20060717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	is_implicated_in	DOID:114	heart disease		MGI:6682030	Ryr2<sup>em1Swch</sup>/Ryr2<sup>+</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33536282	20210409	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177943	Pin1<sup>tm1Tuc</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5433612	Pin1<sup>tm1Tuc</sup>/Pin1<sup>tm1Tuc</sup>  [background:] involves: 129 * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16554819	20120912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057179	Tg(TcraAI4)1Dvs	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3618697	Tg(TcraAI4)1Dvs/0  [background:] NOD-Tg(TcraAI4)1Dvs			ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060526	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385906	Spg7	is_implicated_in	DOID:0110816	hereditary spastic paraplegia 7		MGI:3028926	Spg7<sup>tm1Eir</sup>/Spg7<sup>tm1Eir</sup>  [background:] either: 129/Sv-Spg7<sup>tm1Eir</sup> or (involves: 129/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:14722615	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2677271	Slc24a5	is_implicated_in	DOID:0050633	ocular albinism 1		MGI:4421409	Slc24a5<sup>tm1Lex</sup>/Slc24a5<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18424845	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:2181617	Kl<sup>kl</sup>/Kl<sup>kl</sup>  [background:] either: C.Cg-Kl<sup>kl</sup> or (involves: C3H/HeJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9363890	20060905	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2686209	Cfap57	is_implicated_in	DOID:12336	male infertility		MGI:7529045	Cfap57<sup>em1Qsh</sup>/Cfap57<sup>em1Qsh</sup>  [background:] C57BL/6-Cfap57<sup>em1Qsh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36752199	20230920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3620011	Neil1<sup>tm1Rsld</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:3620065	Neil1<sup>tm1Rsld</sup>/Neil1<sup>tm1Rsld</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16446448	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861634	Clock<sup>m1Jt</sup>	is_implicated_in	DOID:535	sleep disorder		MGI:4366720	Clock<sup>m1Jt</sup>/Clock<sup>m1Jt</sup>  [background:] involves: C57BL/6 * C57BL/6J * Jcl:ICR			ECO:0000033	author statement supported by traceable reference	PMID:17445238	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109150	Mnt	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:3044750	Mnt<sup>tm1.1Awb</sup>/Mnt<sup>tm1.1Awb</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15028671	20150831	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	is_implicated_in	DOID:0110353	retinitis pigmentosa 20		MGI:3771806	Rpe65<sup>tm1Lrcb</sup>/Rpe65<sup>tm1Lrcb</sup>  [background:] 129S6/SvEvTac-Rpe65<sup>tm1Lrcb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17933883	20110509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6783448	Scn2a<sup>em1Gsp</sup>/Scn2a<sup>+</sup>  [background:] involves: C57BL/6J * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:34156984	20211029	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3040284	Tg(Pbsn-Tag)12T10Rjm	is_implicated_in	DOID:2526	prostate adenocarcinoma		MGI:5566661	Tg(Pbsn-Tag)12T10Rjm/0  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:11280793	20180207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928478	Brinp1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5770244	Brinp1<sup>tm1.1Pib</sup>/Brinp1<sup>tm1.1Pib</sup>  [background:] involves: BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27042284	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676298	Pitpna<sup>tm1Vab</sup>	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:2676370	Pitpna<sup>tm1Vab</sup>/Pitpna<sup>tm1Vab</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12788952	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445466	Gja5<sup>tm1Paul</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3664791	Gja5<sup>tm1Paul</sup>/Gja5<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12842919	20061030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445466	Gja5<sup>tm1Paul</sup>	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3664790	Gja5<sup>tm1Paul</sup>/Gja5<sup>tm1Paul</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12842919	20061030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	is_implicated_in	DOID:0080301	atypical hemolytic-uremic syndrome		MGI:6314805	Cfh<sup>tm1.1Song</sup>/Cfh<sup>tm1.1Song</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28057640	20190625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511285	Lepr<sup>tm1.2Chua</sup>	is_implicated_in	DOID:9970	obesity		MGI:3655811	Lepr<sup>tm1.2Chua</sup>/Lepr<sup>tm1.2Chua</sup>  [background:] involves: 129 * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15207242	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511285	Lepr<sup>tm1.2Chua</sup>	is_implicated_in	DOID:9970	obesity		MGI:3511748	Lepr<sup>tm1.2Chua</sup>/Lepr<sup>tm1.2Chua</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15389315	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664869	Men1<sup>tm1Zqw</sup>	is_implicated_in	DOID:10017	multiple endocrine neoplasia type 1		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20110629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156622	Wrn<sup>tm1Led</sup>	is_implicated_in	DOID:5688	Werner syndrome		MGI:3665480	Wrn<sup>tm1Led</sup>/Wrn<sup>tm1Led</sup>  [background:] B6.129S6(BKSW)-Wrn<sup>tm1Led</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16330174	20061103	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3584043	Dok7	is_implicated_in	DOID:0110668	congenital myasthenic syndrome 10		MGI:5636739	Dok7<sup>tm2Yyam</sup>/Dok7<sup>tm2Yyam</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25237101	20150521	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	is_implicated_in	DOID:12849	autistic disorder		MGI:6790238	Ank2<sup>em1Bnt</sup>/Ank2<sup>em1Bnt</sup>  [background:] C57BL/6J-Ank2<sup>em1Bnt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31285321	20211102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	is_implicated_in	DOID:12849	autistic disorder		MGI:6790245	Ank2<sup>tm1Bnt</sup>/Ank2<sup>tm1Bnt</sup>  [background:] B6.129-Ank2<sup>tm1Bnt</sup>/Bnt			ECO:0000033	author statement supported by traceable reference	PMID:31285321	20211102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome		MGI:5444484	Tgfb2<sup>tm1Doe</sup>/Tgfb2<sup>+</sup>  [background:] STOCK Tgfb2<sup>tm1Doe</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22772368	20121205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194506	Serpini1	is_implicated_in	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies		MGI:2669541	Serpini1<sup>tm1Dpw</sup>/Serpini1<sup>tm1Dpw</sup>  [background:] involves: 129/Sv * C57BL/6JBom			ECO:0000033	author statement supported by traceable reference	PMID:12837630	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2665170	P2rx2	is_implicated_in	DOID:0110567	autosomal dominant nonsyndromic deafness 41		MGI:6886231	P2rx2<sup>em1Xzl</sup>/P2rx2<sup>+</sup>  [background:] CBA/J-P2rx2<sup>em1Xzl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33791800	20220307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914407	Cfap418	is_implicated_in	DOID:0111022	cone-rod dystrophy 16		MGI:6157954	Cfap418<sup>em3Jyang</sup>/Cfap418<sup>em3Jyang</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:29440555	20180524	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919232	Snx10	is_implicated_in	DOID:0110940	autosomal recessive osteopetrosis 8		MGI:6441471	Snx10<sup>em2Ael</sup>/Snx10<sup>em2Ael</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:32278070	20200714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919232	Snx10	is_implicated_in	DOID:0110940	autosomal recessive osteopetrosis 8		MGI:6441464	Snx10<sup>em1Ael</sup>/Snx10<sup>em1Ael</sup>  [background:] involves: 129 * C57BL/6J * C57BL/6JOlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:32278070	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888706	Ndst1<sup>tm1Ekf</sup>	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:3587786	Ndst1<sup>tm1Ekf</sup>/Ndst1<sup>tm1Ekf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10852901	20050916	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773691	Phox2b<sup>tm2Jbr</sup>	is_implicated_in	DOID:0060731	congenital central hypoventilation syndrome		MGI:3797591	Phox2b<sup>tm2Jbr</sup>/Phox2b<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18198276	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045900	Chat<sup>tm1.1Jrs</sup>	is_implicated_in	DOID:0110671	congenital myasthenic syndrome 6		MGI:3046097	Chat<sup>tm1.1Jrs</sup>/Chat<sup>tm1.1Jrs</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12441053	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1930206	Tg(K6ODCtr)55Tgo	is_implicated_in	DOID:0060689	atrichia with papular lesions		MGI:3799519	Tg(K6ODCtr)55Tgo/0  [background:] C57BL/6-Tg(K6ODCtr)55Tgo/J			ECO:0000033	author statement supported by traceable reference	PMID:10772389	20080731	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386099	Epor<sup>tm1.4Jtp</sup>	is_implicated_in	DOID:0060652	familial erythrocytosis 1		MGI:2386210	Epor<sup>tm1.4Jtp</sup>/Epor<sup>tm1.4Jtp</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11158582	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386099	Epor<sup>tm1.4Jtp</sup>	is_implicated_in	DOID:0060652	familial erythrocytosis 1		MGI:2386211	Epor<sup>tm1.4Jtp</sup>/Epor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11158582	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95593	Fuca1	is_implicated_in	DOID:14500	fucosidosis		MGI:6188994	Fuca1<sup>tm1Tlub</sup>/Fuca1<sup>tm1Tlub</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27491075	20180719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926386	Msx1<sup>tm1Rilm</sup>	is_implicated_in	DOID:0050567	orofacial cleft		MGI:2175120	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae-Msx1<sup>tm1Rilm</sup>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7914451	20060803	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3837678	Ccm2<sup>tm1Etl</sup>	is_not_implicated_in	DOID:0060670	cerebral cavernous malformation 2		MGI:3837691	Ccm2<sup>tm1Etl</sup>/Ccm2<sup>tm1Etl</sup> Tg(Nes-cre)1Kln/?  [background:] B6.Cg-Ccm2<sup>tm1Etl</sup> Tg(Nes-cre)1Kln			ECO:0000033	author statement supported by traceable reference	PMID:19259391	20090330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	is_implicated_in	DOID:0060872	isolated growth hormone deficiency type II		MGI:3042292	Gh<sup>Sma1</sup>/Gh<sup>+</sup>  [background:] C3HeB/FeJ-Gh<sup>Sma1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14726450	20051003	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	is_implicated_in	DOID:0060872	isolated growth hormone deficiency type II		MGI:3042272	Gh<sup>Sma1</sup>/Gh<sup>Sma1</sup>  [background:] C3HeB/FeJ-Gh<sup>Sma1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14726450	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857540	Slc45a2<sup>uw-d</sup>	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:2668608	Slc45a2<sup>uw-d</sup>/Slc45a2<sup>uw-d</sup>  [background:] involves: TF/Le			ECO:0000033	author statement supported by traceable reference	PMID:9864865	20050624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6754173	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6754183	Elp2<sup>em2Bjw</sup>/Elp2<sup>em3Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6754175	Elp2<sup>em2Bjw</sup>/Elp2<sup>em2Bjw</sup>  [background:] involves: C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:33976153	20210830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813522	Spast<sup>M1Gri</sup>	is_implicated_in	DOID:0110792	hereditary spastic paraplegia 4		MGI:3847312	Spast<sup>M1Gri</sup>/Spast<sup>M1Gri</sup>  [background:] B6.C-Spast<sup>M1Gri</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19453301	20090609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:4821841	avc3	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822144	avc3/avc3  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3856827	Ift80<sup>Gt(AN0245)Wtsi</sup>	is_implicated_in	DOID:0110087	asphyxiating thoracic dystrophy 3		MGI:4942392	Ift80<sup>Gt(AN0245)Wtsi</sup>/Ift80<sup>Gt(AN0245)Wtsi</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21227999	20140216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3923358	Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>	is_implicated_in	DOID:0060307	autosomal dominant intellectual developmental disorder		MGI:5617468	Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>/Mbd5<sup>+</sup>  [background:] B6.Cg-Mbd5<sup>Gt(Ayu21-B205)Imeg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25001218	20150417	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	is_not_implicated_in	DOID:0110426	dilated cardiomyopathy 1D		MGI:3821723	Tnnt2<sup>tm1Mmto</sup>/Tnnt2<sup>+</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:18671960	20081230	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859214	Pmm2	is_implicated_in	DOID:0050570	congenital disorder of glycosylation type I		MGI:5811784	Pmm2<sup>tm1.1Jins</sup>/Pmm2<sup>tm2.1Jins</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7884320	20161213	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3838373	Usp1<sup>tm1.1Ada</sup>	is_implicated_in	DOID:13636	Fanconi anemia		MGI:3838389	Usp1<sup>tm1.1Ada</sup>/Usp1<sup>tm1.1Ada</sup>  [background:] C57BL/6-Usp1<sup>tm1.1Ada</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19217432	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662152	Mitf<sup>mi-x</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2663063	Mitf<sup>mi-x</sup>/Mitf<sup>mi-x</sup>  [background:] involves: NZB/Mac			ECO:0000033	author statement supported by traceable reference	MGI:2662103	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664792	Sbds<sup>tm1Jrom</sup>	is_not_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:3664794	Sbds<sup>tm1Jrom</sup>/Sbds<sup>tm1Jrom</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16914746	20061027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528977	Spr<sup>tm1Lex</sup>	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3774594	Spr<sup>tm1Lex</sup>/Spr<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18201550	20110629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153007	Eln<sup>tm1Dyl</sup>	is_implicated_in	DOID:10825	essential hypertension		MGI:3620001	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] B6.129-Eln<sup>tm1Dyl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14597767	20060418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914935	Dnaaf4	is_implicated_in	DOID:0110615	primary ciliary dyskinesia 25		MGI:5547595	Dnaaf4<sup>tm1.2Jjlo</sup>/Dnaaf4<sup>tm1.2Jjlo</sup>  [background:] involves: 129S1/Sv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23872636	20140304	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921903	Pomk	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429556	Pomk<sup>Gt(OST243203)Lex</sup>/Pomk<sup>Gt(OST243203)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3793476	Tg(Myh6-TNNT2*I79N)8Jdp	is_implicated_in	DOID:0110308	hypertrophic cardiomyopathy 2		MGI:5910053	Tg(Myh6-TNNT2*I79N)8Jdp/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23532597	20170922	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2651811	Tph2	is_implicated_in	DOID:1595	melancholic depression		MGI:3801152	Tph2<sup>tm1Mca</sup>/Tph2<sup>tm1Mca</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:23467366	20130805	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038080	Gata1<sup>tm1Mym</sup>	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:3038120	Gata1<sup>tm1Mym</sup>/Gata1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:9657742	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103157	Dnase1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6400352	Dnase1<sup>tm2092.1Arte</sup>/Dnase1<sup>tm2092.1Arte</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:30758851	20200317	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1354947	Polg2	is_implicated_in	DOID:12679	nephrocalcinosis		MGI:6368626	Polg2<sup>M1Rvt</sup>/Polg2<sup>+</sup>  [background:] involves: BALB/c * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:30395686	20211019	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99675	Adcy3	is_implicated_in	DOID:1470	major depressive disorder		MGI:7260147	Adcy3<sup>tm1Drs</sup>/Adcy3<sup>tm1Drs</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26868444	20220407	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	is_implicated_in	DOID:0111103	maturity-onset diabetes of the young type 4		MGI:3531547	Pdx1<sup>tm1Ted</sup>/Pdx1<sup>+</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12697734	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931859	Lrp2<sup>tm1Her</sup>	is_implicated_in	DOID:1062	Fanconi syndrome		MGI:3790867	Lrp2<sup>tm1Her</sup>/Lrp2<sup>tm1Her</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:10514418	20170621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	is_implicated_in	DOID:0110781	hereditary spastic paraplegia 30		MGI:5752905	Kif1a<sup>lgdg</sup>/Kif1a<sup>lgdg</sup>  [background:] C3.Cg-Kif1a<sup>lgdg</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:5752885	20160323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	is_implicated_in	DOID:0110781	hereditary spastic paraplegia 30		MGI:5752897	Kif1a<sup>lgdg-2J</sup>/Kif1a<sup>lgdg-2J</sup>  [background:] C57BL/6J-Kif1a<sup>lgdg-2J</sup>/CxJ			ECO:0000033	author statement supported by traceable reference	MGI:5752885	20160323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652485	Plcb1<sup>tm1Hssh</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:4353812	Plcb1<sup>tm1Hssh</sup>/Plcb1<sup>tm1Hssh</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17667964	20090819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386949	Jag1<sup>Mhdahtu</sup>	is_implicated_in	DOID:9245	Alagille syndrome		MGI:3717461	Jag1<sup>Mhdahtu</sup>/Jag1<sup>+</sup>  [background:] C3HeB/FeJ-Jag1<sup>Mhdahtu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11259677	20070807	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:3587788	Ndst1<sup>tm1Hgx</sup>/Ndst1<sup>tm1Hgx</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10664446	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:3587786	Ndst1<sup>tm1Ekf</sup>/Ndst1<sup>tm1Ekf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10852901	20050916	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109542	Sycp3	is_implicated_in	DOID:14227	azoospermia		MGI:2664131	Sycp3<sup>tm1Hoog</sup>/Sycp3<sup>tm1Hoog</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10678170	20050909	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4127559	Chd7<sup>Gt(XK403)Byg</sup>	is_implicated_in	DOID:0050834	CHARGE syndrome		MGI:7488670	Chd7<sup>Gt(XK403)Byg</sup>/Chd7<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:29168327	20230612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3761163	Tg(MMTV-neu/OT-I/OT-II)CBnel	is_implicated_in	DOID:1612	breast cancer		MGI:3761174	Tg(MMTV-neu/OT-I/OT-II)CBnel/?  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17616705	20080617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861186	Shh<sup>Dsh</sup>	is_implicated_in	DOID:0110964	brachydactyly type A1		MGI:3583764	Shh<sup>Dsh</sup>/Shh<sup>+</sup>  [background:] B10Rl.Cg-Shh<sup>Dsh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15841179	20050818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777015	Crygb<sup>S11R</sup>	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3777758	Crygb<sup>S11R</sup>/Crygb<sup>+</sup>  [background:] A/J-Crygb<sup>S11R</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18172107	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3777015	Crygb<sup>S11R</sup>	is_implicated_in	DOID:0110236	cataract 39 multiple types		MGI:3777759	Crygb<sup>S11R</sup>/Crygb<sup>S11R</sup>  [background:] A/J-Crygb<sup>S11R</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18172107	20130528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388138	Gpr132<sup>tm1Witt</sup>	is_implicated_in	DOID:417	autoimmune disease		MGI:3639677	Gpr132<sup>tm1Witt</sup>/Gpr132<sup>tm1Witt</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11371358	20060802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857014	Rd3<sup>rd3</sup>	is_implicated_in	DOID:0110080	Leber congenital amaurosis 12		MGI:3715440	Rd3<sup>rd3</sup>/Rd3<sup>rd3</sup>  [background:] RBF/DnJ-Rd3<sup>rd3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23687432	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3857270	Mcm9<sup>Gt(AW0655)Wtsi</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:5295417	Mcm9<sup>Gt(AW0655)Wtsi</sup>/Mcm9<sup>Gt(AW0655)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:21987787	20111109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442555	Dis3l2	is_implicated_in	DOID:0060476	Perlman syndrome		MGI:6286061	Dis3l2<sup>em3Jtm</sup>/Dis3l2<sup>em3Jtm</sup>  [background:] C57BL/6J-Dis3l2<sup>em3Jtm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29950491	20190404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442555	Dis3l2	is_implicated_in	DOID:0060476	Perlman syndrome		MGI:6286056	Dis3l2<sup>em1Jtm</sup>/Dis3l2<sup>em1Jtm</sup>  [background:] C57BL/6J-Dis3l2<sup>em1Jtm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29950491	20190404	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0060867	macrocephaly-autism syndrome		MGI:5629811	Pten<sup>tm1Engc</sup>/Pten<sup>tm1Engc</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:24470394	20150903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:0060867	macrocephaly-autism syndrome		MGI:5660888	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Eno2-cre)39Jme/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16675393	20150903	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107680	sar	is_implicated_in	DOID:0112307	sarcosinemia		MGI:7260274	sar/sar  [background:] BTBR-sar			ECO:0000033	author statement supported by traceable reference	PMID:1372986	20220411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2135677	Fgfr3<sup>tm5.1Cxd</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3640358	Fgfr3<sup>tm5.1Cxd</sup>/Fgfr3<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11181569	20060810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857572	Ins2<sup>Akita</sup>	is_implicated_in	DOID:0060639	permanent neonatal diabetes mellitus		MGI:3583906	Ins2<sup>Akita</sup>/Ins2<sup>Akita</sup>  [background:] C57BL/6-Ins2<sup>Akita</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9593767	20050819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857113	Prkdc<sup>scid</sup>	is_implicated_in	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive		MGI:3760369	Prkdc<sup>scid</sup>/Prkdc<sup>scid</sup>  [background:] C.BKa-Prkdc<sup>scid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:6823332	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807977	Amelx<sup>Rgsc888</sup>	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:4438262	Amelx<sup>Rgsc888</sup>/Amelx<sup>Rgsc888</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807977	Amelx<sup>Rgsc888</sup>	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:4438261	Amelx<sup>Rgsc888</sup>/Y  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3807977	Amelx<sup>Rgsc888</sup>	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:4438260	Amelx<sup>Rgsc888</sup>/Amelx<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:20067920	20100331	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039777	Tg(Mt1-RET)304Ina	is_implicated_in	DOID:8923	skin melanoma		MGI:4418371	Tg(Mt1-RET)304Ina/0  [background:] B6.C-Tg(Mt1-RET)304Ina			ECO:0000033	author statement supported by traceable reference	PMID:9778055	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95459	Zfp521	is_implicated_in	DOID:5419	schizophrenia		MGI:5699086	Zfp521<sup>tm1Nohk</sup>/Zfp521<sup>tm1Nohk</sup>  [background:] B6J.Cg-Zfp521<sup>tm1Nohk</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24676388	20151215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856506	Hr<sup>rh-8J</sup>	is_implicated_in	DOID:0060689	atrichia with papular lesions		MGI:3850354	Hr<sup>rh-8J</sup>/Hr<sup>rh-8J</sup>  [background:] B10.D2/nSnJ-Hr<sup>rh-8J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9799606	20090714	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312921	Cfc1<sup>b2b970Clo</sup>/Cfc1<sup>b2b970Clo</sup>  [background:] C57BL/6J-Cfc1<sup>b2b970Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5561116	Cfc1<sup>b2b2736.1Clo</sup>/Cfc1<sup>b2b2736.1Clo</sup>  [background:] C57BL/6J-Cfc1<sup>b2b2736.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154515	Pthlh<sup>tm1Hmk</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3583956	Pthlh<sup>tm1Hmk</sup>/Pthlh<sup>tm1Hmk</sup>  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8314082	20050819	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313136	Clip2	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3620031	Clip2<sup>tm1.1Gal</sup>/Clip2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12195424	20060419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	is_implicated_in	DOID:11198	DiGeorge syndrome		MGI:3037863	Fgf8<sup>tm1.3Mrt</sup>/Fgf8<sup>tm1.4Mrt</sup> Tg(Tbx1-cre)1Joe/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:14975726	20050622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	is_implicated_in	DOID:0050778	Meckel syndrome		MGI:5292226	Tmem67<sup>tm1Dgen</sup>/Tmem67<sup>tm1Dgen</sup>  [background:] B6.129P2-Tmem67<sup>tm1Dgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23283079	20131104	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	is_implicated_in	DOID:0050458	juvenile myelomonocytic leukemia		MGI:3845014	Ptpn11<sup>tm6Bgn</sup>/Ptpn11<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19179468	20090521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449094	Grip1<sup>tm1Paw</sup>	is_implicated_in	DOID:0060642	recessive dystrophic epidermolysis bullosa		MGI:2654707	Grip1<sup>tm1Paw</sup>/Grip1<sup>tm1Paw</sup>  [background:] involves: 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11983858	20050719	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97303	Nek1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3831332	Nek1<sup>kat</sup>/Nek1<sup>kat</sup>  [background:] involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn			ECO:0000033	author statement supported by traceable reference	PMID:9070925	20090212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97303	Nek1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3831388	Nek1<sup>kat-2J</sup>/Nek1<sup>kat-2J</sup>  [background:] C57BL/6J-Nek1<sup>kat-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:9070925	20090212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	is_implicated_in	DOID:0080121	mitochondrial DNA depletion syndrome 3		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	PMID:18818194	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	is_not_implicated_in	DOID:890	mitochondrial encephalomyopathy		MGI:3793729	Atp7a<sup>Mo-vbr</sup>/Y  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9342151	20190723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3603015	Myc<sup>tm1Lbox</sup>/Myc<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15687498	20051026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3603014	Myc<sup>tm1Lbox</sup>/Myc<sup>tm1Lbox</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15687498	20051026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342542	Ikzf3	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2653187	Ikzf3<sup>tm1Kge</sup>/Ikzf3<sup>tm1Kge</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12574333	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342542	Ikzf3	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:2653187	Ikzf3<sup>tm1Kge</sup>/Ikzf3<sup>tm1Kge</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9806640	20050608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	is_implicated_in	DOID:0110660	congenital myasthenic syndrome 12		MGI:6277926	Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup>/Gfpt1<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Ckmm-cre)5Khn/0  [background:] involves: C57BL/6J * C57BL/6N * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:29905857	20190212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	is_implicated_in	DOID:9970	obesity		MGI:3629805	Pcsk1<sup>N222D</sup>/Pcsk1<sup>N222D</sup>  [background:] C57BL/6-Pcsk1<sup>N222D</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16644867	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181812	Rho<sup>tm1Phm</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:3836169	Rho<sup>tm1Phm</sup>/Rho<sup>tm1Phm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9020854	20130619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491174	b2b2350Clo	is_implicated_in	DOID:0050144	Kartagener syndrome		MGI:5549965	b2b2350Clo/b2b2350Clo  [background:] C57BL/6J-b2b2350Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763908	Tg(HSA*LR)21Cath	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3763924	Tg(HSA*LR)21Cath/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848479	Apc<sup>tm1Rsmi</sup>	is_implicated_in	DOID:9256	colorectal cancer		MGI:4456428	Apc<sup>tm1Rsmi</sup>/Apc<sup>+</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20176656	20100625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042267	Gh<sup>Sma1</sup>	is_implicated_in	DOID:0060872	isolated growth hormone deficiency type II		MGI:3042272	Gh<sup>Sma1</sup>/Gh<sup>Sma1</sup>  [background:] C3HeB/FeJ-Gh<sup>Sma1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14726450	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3042267	Gh<sup>Sma1</sup>	is_implicated_in	DOID:0060872	isolated growth hormone deficiency type II		MGI:3042292	Gh<sup>Sma1</sup>/Gh<sup>+</sup>  [background:] C3HeB/FeJ-Gh<sup>Sma1</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14726450	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2389416	Tg(Nell1)1Ting	is_implicated_in	DOID:2340	craniosynostosis		MGI:6270159	Tg(Nell1)1Ting/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12235118	20181231	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109495	Nfil3	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:5576251	Nfil3<sup>tm1Pbro</sup>/Nfil3<sup>tm1Pbro</sup>  [background:] B6.129S6-Nfil3<sup>tm1Pbro</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24442434	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:0080174	bladder exstrophy		MGI:3511141	Trp63<sup>tm2Brd</sup>/Trp63<sup>tm2Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17079275	20121109	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3620102	Ikbkg<sup>tm1Mka</sup>	is_implicated_in	DOID:12305	Bloch-Sulzberger syndrome		MGI:3621818	Ikbkg<sup>tm1Mka</sup>/Ikbkg<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10911991	20060509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154549	Cdh23<sup>v-ngt</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3714862	Cdh23<sup>v-ngt</sup>/Cdh23<sup>v-ngt</sup>  [background:] involves: ICR * MSM			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110824	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785479	Fermt3<sup>tm1Ref</sup>	is_implicated_in	DOID:0110912	leukocyte adhesion deficiency 3		MGI:3795785	Fermt3<sup>tm1Ref</sup>/Fermt3<sup>tm1Ref</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19234461	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3579117	Nr2f2<sup>tm2.1Tsa</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3579773	Nkx3-2<sup>tm1(cre)Tsa</sup>/Nkx3-2<sup>+</sup> Nr2f2<sup>tm2.1Tsa</sup>/Nr2f2<sup>tm2.1Tsa</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16251273	20100614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:898	autosomal dominant polycystic kidney disease		MGI:3582953	Bicc1<sup>jcpk</sup>/Bicc1<sup>+</sup>  [background:] involves: 101 * C3H * T STOCK			ECO:0000033	author statement supported by traceable reference	PMID:7723240	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	is_implicated_in	DOID:9281	phenylketonuria		MGI:3610388	Hnf1a<sup>tm1Mya</sup>/Hnf1a<sup>tm1Mya</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:8598044	20060119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	is_implicated_in	DOID:6000	congestive heart failure		MGI:2661730	Ace2<sup>tm1Pngr</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17499227	20171101	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94906	Dmpk	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3613697	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>tm1Rdd</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8673132	20060301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94906	Dmpk	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3613697	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>tm1Rdd</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10021468	20060301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:94906	Dmpk	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3613741	Dmpk<sup>tm1Rdd</sup>/Dmpk<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10021468	20060301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339795	Smc3	is_implicated_in	DOID:0080507	Cornelia de Lange syndrome 3		MGI:7489810	Smc3<sup>tm1.2Toshi</sup>/Smc3<sup>+</sup>  [background:] B6.Cg-Smc3<sup>tm1.2Toshi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28408410	20230615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857709	Acvr2b<sup>tm1Enl</sup>	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:2654122	Acvr2b<sup>tm1Enl</sup>/Acvr2b<sup>tm1Enl</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9242489	20110307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0080212	polycystic kidney disease 4		MGI:6388658	Pkhd1<sup>em1Mrug</sup>/Pkhd1<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30600684	20200205	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	is_implicated_in	DOID:0080212	polycystic kidney disease 4		MGI:6388659	Pkhd1<sup>em1Mrug</sup>/Pkhd1<sup>em1Mrug</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30600684	20200205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663376	Gpr12<sup>tm1Dgen</sup>	is_implicated_in	DOID:9970	obesity		MGI:3664276	Gpr12<sup>tm1Dgen</sup>/Gpr12<sup>tm1Dgen</sup>  [background:] B6.129P2-Gpr12<sup>tm1Dgen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16887097	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109360	Lmo4	is_implicated_in	DOID:0060668	anencephaly		MGI:3575660	Lmo4<sup>tm1.1Gng</sup>/Lmo4<sup>tm1.1Gng</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15691703	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	is_implicated_in	DOID:3144	cutis laxa		MGI:5660617	Efemp2<sup>tm1.1Chu</sup>/Efemp2<sup>tm1.1Chu</sup>  [background:] B6(SJL)-Efemp2<sup>tm1.1Chu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26178373	20150901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2388322	Hmox1<sup>tm1Poss</sup>	is_implicated_in	DOID:2352	hemochromatosis		MGI:2429787	Hmox1<sup>tm1Poss</sup>/Hmox1<sup>tm1Poss</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9380735	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98369	Sox7	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:5437224	Sox7<sup>tm1.1Dsco</sup>/Sox7<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22723016	20121001	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385783	Galc<sup>tm1Wngr</sup>	is_implicated_in	DOID:10587	Krabbe disease		MGI:2652424	Galc<sup>tm1Wngr</sup>/Galc<sup>tm1Wngr</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:11461188	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525214	Cxcr4<sup>tm2Yzo</sup>	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:7261455	Cxcr4<sup>tm2Yzo</sup>/Cxcr4<sup>tm2Yzo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31071921	20220418	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158937	Man2a1<sup>tm1Jxm</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3850627	Man2a1<sup>tm1Jxm</sup>/Man2a1<sup>tm1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11158608	20100302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2429765	Dock1	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:5618862	Dock1<sup>b2b3190Clo</sup>/Dock1<sup>b2b3190Clo</sup>  [background:] C57BL/6J-Dock1<sup>b2b3190Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98460	Syn1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5517482	Syn1<sup>tm1Pggd</sup>/Syn1<sup>tm1Pggd</sup>  [background:] B6.129P2-Syn1<sup>tm1Pggd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664107	Ncoa1<sup>tm1.1Hkaw</sup>	is_implicated_in	DOID:9970	obesity		MGI:3664551	Ncoa1<sup>tm1.1Hkaw</sup>/Ncoa1<sup>tm1.1Hkaw</sup>  [background:] B6.Cg-Ncoa1<sup>tm1.1Hkaw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15312245	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107527	Ly6a	is_implicated_in	DOID:11476	osteoporosis		MGI:3815037	Ly6a<sup>tm1Pmf</sup>/Ly6a<sup>tm1Pmf</sup>  [background:] C.129P2-Ly6a<sup>tm1Pmf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12732718	20081114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4943741	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: 129S7/SvEvBrd * BALB/c * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:21159977	20110405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:7435429	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:32552404	20230217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:7435433	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Slco1c1-icre/ERT2)1Mrks/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:32552404	20230217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690300	Myh6<sup>tm2Ces</sup>	is_implicated_in	DOID:0110453	dilated cardiomyopathy 1EE		MGI:3691282	Myh6<sup>tm2Ces</sup>/Myh6<sup>+</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690300	Myh6<sup>tm2Ces</sup>	is_implicated_in	DOID:0110453	dilated cardiomyopathy 1EE		MGI:3691281	Myh6<sup>tm2Ces</sup>/Myh6<sup>tm2Ces</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3603195	Errfi1<sup>tm1Gvw</sup>	is_implicated_in	DOID:8398	osteoarthritis		MGI:3603638	Errfi1<sup>tm1Gvw</sup>/Errfi1<sup>tm1Gvw</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16087873	20051107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3621814	E2f1<sup>tm1Meg</sup>/E2f1<sup>tm1Meg</sup>  [background:] NOD.Cg-E2f1<sup>tm1Meg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15470032	20060509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_not_implicated_in	DOID:9119	acute myeloid leukemia		MGI:5582314	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:14699048	20140912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95275	Ebf1	is_implicated_in	DOID:811	lipodystrophy		MGI:3842704	Ebf1<sup>tm1Rug</sup>/Ebf1<sup>tm1Rug</sup>  [background:] involves: 129S2/SvPas * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19130908	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	is_implicated_in	DOID:5688	Werner syndrome		MGI:3665480	Wrn<sup>tm1Led</sup>/Wrn<sup>tm1Led</sup>  [background:] B6.129S6(BKSW)-Wrn<sup>tm1Led</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16330174	20061103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575291	Sipa1<sup>tm1Nm</sup>	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3575736	Sipa1<sup>tm1Nm</sup>/Sipa1<sup>tm1Nm</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12892713	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3575291	Sipa1<sup>tm1Nm</sup>	is_implicated_in	DOID:8552	chronic myeloid leukemia		MGI:3575737	Sipa1<sup>tm1Nm</sup>/Sipa1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12892713	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662140	Mitf<sup>Mi-Crc</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662140	Mitf<sup>Mi-Crc</sup>	is_implicated_in	DOID:0090002	Tietz syndrome		MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933963	Ntrk1<sup>tm1Par</sup>	is_implicated_in	DOID:0050548	hereditary sensory neuropathy		MGI:2175186	Ntrk1<sup>tm1Par</sup>/Ntrk1<sup>tm1Par</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10681461	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341813	Adam33	is_not_implicated_in	DOID:2841	asthma		MGI:3664641	Adam33<sup>tm1.1Chch</sup>/Adam33<sup>tm1.1Chch</sup>  [background:] 129S4/SvJae-Adam33<sup>tm1.1Chch</sup>			ECO:0000033	author statement supported by traceable reference	PMID:16943435	20061026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	is_implicated_in	DOID:13544	low tension glaucoma		MGI:3580495	Sod1<sup>tm1Leb</sup>/Sod1<sup>tm1Leb</sup>  [background:] B6;129S-Sod1<sup>tm1Leb</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:21421868	20120325	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624537	Dcx<sup>tm1.2Ffr</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:3624851	Dcx<sup>tm1.2Ffr</sup>/Y  [background:] either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16571605	20060620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	is_implicated_in	DOID:0060691	platelet-type bleeding disorder 16		MGI:2677136	Itga2b<sup>tm1Tlr</sup>/Itga2b<sup>tm1Tlr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10942384	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773697	Tg(tetO-Prkar1a*x2as)1Stra	is_implicated_in	DOID:0060280	primary pigmented nodular adrenocortical disease		MGI:5897214	Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0  [background:] involves: C57BL/6 * NMRI * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15591278	20170511	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813493	Tg(H2-K-Fosl2,-EGFP)13Wag	is_implicated_in	DOID:418	systemic scleroderma		MGI:5927436	Tg(H2-K-Fosl2,-EGFP)13Wag/0  [background:] B6.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag			ECO:0000033	author statement supported by traceable reference	PMID:27864286	20171122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926492	Tg(ITGB1)0869Fmw	is_implicated_in	DOID:8893	psoriasis		MGI:3583561	Tg(ITGB1)0869Fmw/0  [background:] involves: C57BL/10 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4452483	Tg(Prnp-ITM2B*)7Jckr	is_implicated_in	DOID:9246	cerebral amyloid angiopathy		MGI:4452488	Tg(Prnp-ITM2B*)7Jckr/0  [background:] C57BL/6-Tg(Prnp-ITM2B*)7Jckr			ECO:0000033	author statement supported by traceable reference	PMID:20385796	20100520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448678	Tg(APOB)1102Sgy	is_implicated_in	DOID:0110014	age related macular degeneration 1		MGI:5571628	Tg(APOB)1102Sgy/?  [background:] B6.Cg-Tg(APOB)1102Sgy			ECO:0000033	author statement supported by traceable reference	PMID:19450445	20140709	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5491160	b2b2059Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5555838	b2b2059Clo/b2b2059Clo  [background:] C57BL/6J-b2b2059Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385955	Defb19	is_implicated_in	DOID:229	female reproductive system disease		MGI:7427684	Defb19<sup>em1Cya</sup>/Defb19<sup>em1Cya</sup>  [background:] C57BL/6-Defb19<sup>em1Cya</sup>			ECO:0000033	author statement supported by traceable reference	PMID:36513070	20230120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343461	Ecel1	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6160055	Ecel1<sup>tm1Hiki</sup>/Ecel1<sup>tm1Hiki</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26951213	20180608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1343461	Ecel1	is_implicated_in	DOID:0050646	distal arthrogryposis		MGI:6160009	Ecel1<sup>em1Hiki</sup>/Ecel1<sup>em1Hiki</sup> Tg(Hlxb9-GFP)1Tmj/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:26951213	20180608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	is_implicated_in	DOID:11836	clubfoot		MGI:2657302	Fras1<sup>bl</sup>/Fras1<sup>bl</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:12766769	20110125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95541	Fkbp1a	is_implicated_in	DOID:0050476	Barth syndrome		MGI:3622103	Fkbp1a<sup>tm1Zuk</sup>/Fkbp1a<sup>tm1Zuk</sup>  [background:] either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9461216	20060512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104669	Man2a1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3850627	Man2a1<sup>tm1Jxm</sup>/Man2a1<sup>tm1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11158608	20100302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5766814	Crebbp<sup>tm2Pkb</sup>/Crebbp<sup>tm2Pkb</sup>  [background:] (B6.129P2-Crebbp<sup>tm2Pkb</sup>/Pkb x 129S2.129P2(B6)-Crebbp<sup>tm2Pkb</sup>/Pkb)F1			ECO:0000033	author statement supported by traceable reference	PMID:26730956	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:3784504	Pparg<sup>tm3(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:0111136	congenital generalized lipodystrophy type 2		MGI:3784503	Pparg<sup>tm2(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3663625	Atg5<sup>tm1Myok</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287975	Atg5<sup>tm1Myok</sup>/Atg5<sup>tm1Myok</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856873	fm	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5619656	fm/fm  [background:] involves: CBA/H			ECO:0000033	author statement supported by traceable reference	PMID:970440	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3621814	E2f1<sup>tm1Meg</sup>/E2f1<sup>tm1Meg</sup>  [background:] NOD.Cg-E2f1<sup>tm1Meg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15470032	20060509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3818697	Taar1<sup>tm1Tdw</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:3818698	Taar1<sup>tm1Tdw</sup>/Taar1<sup>tm1Tdw</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17212650	20081208	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	is_implicated_in	DOID:9970	obesity		MGI:2681522	Ar<sup>tm1Ska</sup>/Y Tg(CMV-cre)1Ipc/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12943692	20100603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521922	Serpini2<sup>pq</sup>	is_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:3767713	Serpini2<sup>pq</sup>/Serpini2<sup>pq</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16184191	20080117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387343	G6pc1<sup>tm1Jyc</sup>	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:2677133	G6pc1<sup>tm1Jyc</sup>/G6pc1<sup>tm1Jyc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:8640227	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511359	Pparg<sup>tm3(tTA)Yba</sup>	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3784504	Pparg<sup>tm3(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931858	Kcnq1<sup>tm1Apf</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3623773	Kcnq1<sup>tm1Apf</sup>/Kcnq1<sup>tm1Apf</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15891643	20070116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576237	Ptgs1<sup>tm1Fun</sup>	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3576657	Ptgs1<sup>tm1Fun</sup>/Ptgs1<sup>tm1Fun</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15776109	20050512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581892	Mafa<sup>tm1Staka</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3582680	Mafa<sup>tm1Staka</sup>/Mafa<sup>tm1Staka</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:15923615	20050729	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1339656	Pak3	is_implicated_in	DOID:0112051	non-syndromic X-linked intellectual disability 30		MGI:6466594	Pak3<sup>tm1.1Rpo</sup>/Y  [background:] B6.129S2(Cg)-Pak3<sup>tm1.1Rpo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31943058	20201012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033223	Gck<sup>Rgsc272</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038214	Gck<sup>Rgsc272</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150145	Nos3<sup>tm1Plh</sup>	is_implicated_in	DOID:10825	essential hypertension		MGI:2174979	Nos3<sup>tm1Plh</sup>/Nos3<sup>tm1Plh</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:7545787	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	is_not_implicated_in	DOID:2729	dyskeratosis congenita		MGI:3849601	Dkc1<sup>tm3Pjma</sup>/Dkc1<sup>tm3Pjma</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19391112	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	is_not_implicated_in	DOID:2729	dyskeratosis congenita		MGI:3849602	Dkc1<sup>tm2Pjma</sup>/Y  [background:] chimera involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19391112	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	is_not_implicated_in	DOID:2729	dyskeratosis congenita		MGI:3849600	Dkc1<sup>tm3Pjma</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19391112	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850013	Nlrp3<sup>tm2Hhf</sup>	is_implicated_in	DOID:0090062	familial cold autoinflammatory syndrome 1		MGI:3850052	Nlrp3<sup>tm2Hhf</sup>/Nlrp3<sup>+</sup> Tg(CAG-cre/Esr1*)5Amc/?  [background:] involves: 129/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:19501000	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850013	Nlrp3<sup>tm2Hhf</sup>	is_implicated_in	DOID:0090062	familial cold autoinflammatory syndrome 1		MGI:3850048	Nlrp3<sup>tm2Hhf</sup>/Nlrp3<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19501000	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384170	Trpv3<sup>Nh</sup>	is_implicated_in	DOID:3310	atopic dermatitis		MGI:2384175	Trpv3<sup>Nh</sup>/Trpv3<sup>+</sup>  [background:] involves: DS			ECO:0000033	author statement supported by traceable reference	PMID:9250484	20060125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3038358	Hhat<sup>Tg(TFAP2A-cre)1Will</sup>	is_implicated_in	DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome		MGI:5447979	Hhat<sup>Tg(TFAP2A-cre)1Will</sup>/Hhat<sup>Tg(TFAP2A-cre)1Will</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24784881	20160519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2149838	Pparg<sup>tm1Rev</sup>	is_not_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:2174989	Pparg<sup>tm1Rev</sup>/Pparg<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10675354	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	is_implicated_in	DOID:9970	obesity		MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17641777	20150330	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	is_implicated_in	DOID:1123	spondyloarthropathy		MGI:3629514	Tnf<sup>tm2Gkl</sup>/Tnf<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:29618659	20180824	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98247	Scn1b	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:4830676	Scn1b<sup>tm1.1Bion</sup>/Scn1b<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20628201	20100927	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	is_implicated_in	DOID:0050989	episodic ataxia type 1		MGI:2655695	Kcna1<sup>tm1Jmay</sup>/Kcna1<sup>+</sup>  [background:] B6.129S4-Kcna1<sup>tm1Jmay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12612586	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	is_implicated_in	DOID:0112225	BH4-deficient hyperphenylalaninemia B		MGI:6474005	Gch1<sup>em1Ypt</sup>/Gch1<sup>em1Ypt</sup>  [background:] C57BL/6-Gch1<sup>em1Ypt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30742839	20210727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	is_implicated_in	DOID:2841	asthma		MGI:3057279	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)			ECO:0000033	author statement supported by traceable reference	PMID:16027362	20060825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4315923	Ak7<sup>Gt(OST434404)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:5429553	Ak7<sup>Gt(OST434404)Lex</sup>/Ak7<sup>Gt(OST434404)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3856827	Ift80<sup>Gt(AN0245)Wtsi</sup>	is_implicated_in	DOID:0110086	asphyxiating thoracic dystrophy 2		MGI:4942392	Ift80<sup>Gt(AN0245)Wtsi</sup>/Ift80<sup>Gt(AN0245)Wtsi</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:21227999	20110329	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3880442	Vrk3<sup>Gt(YTA189)Byg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6112031	Vrk3<sup>Gt(YTA189)Byg</sup>/Vrk3<sup>Gt(YTA189)Byg</sup>  [background:] B6.129P2-Vrk3<sup>Gt(YTA189)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28899869	20180126	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98282	Spi1	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3714968	Spi1<sup>tm1.3Dgt</sup>/Spi1<sup>tm1.3Dgt</sup>  [background:] involves: 129 * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15146183	20070717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769585	Col1a1<sup>Aga2</sup>	is_implicated_in	DOID:0110339	osteogenesis imperfecta type 3		MGI:5431996	Col1a1<sup>Aga2</sup>/Col1a1<sup>+</sup>  [background:] C3HeB/FeJ-Col1a1<sup>Aga2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22589248	20120822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351645	Prmt5	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7277815	Prmt5<sup>tm2c(EUCOMM)Wtsi</sup>/Prmt5<sup>tm2c(EUCOMM)Wtsi</sup> Tg(Col2a1-cre)#Amc/0  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31848143	20220516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3763910	Tg(HSA*LR)32bCath	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3763922	Tg(HSA*LR)32bCath/?  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10976074	20121112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177263	Tmc1<sup>Mhdabth</sup>	is_implicated_in	DOID:0110520	autosomal recessive nonsyndromic deafness 7		MGI:2177316	Tmc1<sup>Mhdabth</sup>/Tmc1<sup>+</sup>  [background:] C3HeB/FeJ-Tmc1<sup>Mhdabth</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	MGI:2681078	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931047	Vegfa<sup>tm1Pec</sup>	is_implicated_in	DOID:12716	newborn respiratory distress syndrome		MGI:3047228	Vegfa<sup>tm1Pec</sup>/Vegfa<sup>tm1Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12053176	20110217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927580	Bloc1s6	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3588035	Bloc1s6<sup>pa</sup>/Bloc1s6<sup>pa</sup>  [background:] B6.Cg-Bloc1s6<sup>pa</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444453	Arhgef10	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6287207	Arhgef10<sup>tm1.1Ssfg</sup>/Arhgef10<sup>tm1.1Ssfg</sup>  [background:] B6.129S1-Arhgef10<sup>tm1.1Ssfg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:29456827	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178311	Pde6b<sup>atrd1</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028000	Pde6b<sup>atrd1</sup>/Pde6b<sup>atrd1</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050617	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:4439296	p23-ST1	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:4439299	p23-ST1/p23-ST1  [background:] C57BL/6J-p23-ST1			ECO:0000033	author statement supported by traceable reference	PMID:19924295	20100412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1861746	Lmbr1	is_implicated_in	DOID:0050603	acheiropody		MGI:3580291	Lmbr1<sup>tm1Kng</sup>/Lmbr1<sup>tm1Kng</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:11606546	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	is_implicated_in	DOID:13544	low tension glaucoma		MGI:4417919	Slc1a1<sup>tm1Wst</sup>/Slc1a1<sup>tm1Wst</sup>  [background:] B6.129-Slc1a1<sup>tm1Wst</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17607354	20100115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2667341	Ywhae<sup>tm1Awb</sup>	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:5512772	Ywhae<sup>tm1Awb</sup>/Ywhae<sup>tm1Awb</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23071090	20131016	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277238	Cfap44	is_implicated_in	DOID:0070166	spermatogenic failure 20		MGI:6258951	Cfap44<sup>em1Fzh</sup>/Cfap44<sup>em1Fzh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28552195	20181204	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857266	Uox<sup>tm1Bay</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:3687865	Uox<sup>tm1Bay</sup>/Uox<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11316859	20061116	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5442113	b2b1723Clo	is_implicated_in	DOID:114	heart disease		MGI:5442140	b2b1723Clo/b2b1723Clo  [background:] C57BL/6J-b2b1723Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342293	Lat	is_implicated_in	DOID:0080356	IgG4-related disease		MGI:2385971	Lat<sup>tm1.1Mal</sup>/Lat<sup>tm1.1Mal</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:29902238	20191122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5615582	Pomgnt1<sup>tm1.1Cfg</sup>/Pomgnt1<sup>tm1.1Cfg</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26306834	20190515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3785090	Tg(Thy1-SOD1*G93A)T3Hgrd	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3785390	Tg(Thy1-SOD1*G93A)T3Hgrd/Tg(Thy1-SOD1*G93A)T3Hgrd  [background:] involves: C57BL/6 * CBA * FVB			ECO:0000033	author statement supported by traceable reference	PMID:18305242	20080516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152744	Gnas<sup>tm1Gwa</sup>	is_implicated_in	DOID:4183	pseudopseudohypoparathyroidism		MGI:5285183	Gnas<sup>tm1Gwa</sup>/Gnas<sup>+</sup>  [background:] involves: 129S/SvEv * 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:21747923	20110913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3836632	Egr2<sup>tm2Jmi</sup>	is_implicated_in	DOID:0110195	Charcot-Marie-Tooth disease type 4E		MGI:3836731	Egr2<sup>tm2Jmi</sup>/Egr2<sup>tm2Jmi</sup>  [background:] B6.Cg-Egr2<sup>tm2Jmi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19244508	20090323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442827	Tbc1d32	is_implicated_in	DOID:1935	Bardet-Biedl syndrome		MGI:5512641	Tbc1d32<sup>b2b2284Clo</sup>/Tbc1d32<sup>b2b2284Clo</sup>  [background:] C57BL/6J-Tbc1d32<sup>b2b2284Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335082	Invs	is_implicated_in	DOID:0111113	nephronophthisis 2		MGI:2654613	Invs<sup>inv</sup>/Invs<sup>inv</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15213262	20120926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4346527	Ndufs6<sup>Gt(AR0138)Wtsi</sup>	is_implicated_in	DOID:0060536	mitochondrial complex I deficiency		MGI:5428952	Ndufs6<sup>Gt(AR0138)Wtsi</sup>/Ndufs6<sup>Gt(AR0138)Wtsi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22474353	20120726	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3621366	Tg(MT2A-TGFBR2)#Rser	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907611	Tg(MT2A-TGFBR2)#Rser/0  [background:] involves: C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:19933419	20170828	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109178	Fgf13	is_implicated_in	DOID:1059	intellectual disability		MGI:6729187	Fgf13<sup>em1Xuzh</sup>/Y  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34184986	20210806	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96690	Krt16	is_implicated_in	DOID:0050428	nonepidermolytic palmoplantar keratoderma		MGI:5426823	Krt16<sup>tm1(KOMP)Vlcg</sup>/Krt16<sup>tm1(KOMP)Vlcg</sup>  [background:] C57BL/6-Krt16<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22336941	20120703	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039697	Tg(tetO-MYC)36aBop	is_implicated_in	DOID:2975	cystic kidney disease		MGI:3815300	Tg(Pax8-rtTA2S*M2)1Koes/0 Tg(tetO-MYC)36aBop/0  [background:] involves: C57BL/6 * DBA * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18724376	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180081	Dnah5<sup>Tg1Htz</sup>	is_implicated_in	DOID:0110599	primary ciliary dyskinesia 3		MGI:3624520	Dnah5<sup>Tg1Htz</sup>/Dnah5<sup>Tg1Htz</sup>  [background:] involves: C57BL/6 * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:11912187	20060615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107444	Efna5	is_implicated_in	DOID:0060668	anencephaly		MGI:3575317	Efna5<sup>tm1Ddmo</sup>/Efna5<sup>tm1Ddmo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11089974	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3051779	Ptprn2<sup>tm1Aln</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3051907	Ptprn2<sup>tm1Aln</sup>/Ptprn2<sup>tm1Aln</sup>  [background:] involves: 129S4/SvJae * C57BL/6N * NOD/LtJ			ECO:0000033	author statement supported by traceable reference	PMID:12535631	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156980	Aga<sup>tm1Pltn</sup>	is_implicated_in	DOID:0050461	aspartylglucosaminuria		MGI:3043584	Aga<sup>tm1Pltn</sup>/Aga<sup>tm1Pltn</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9425233	20050526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680501	Hlb228	is_implicated_in	DOID:9970	obesity		MGI:2680503	Hlb228/?  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	MGI:2656149	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	is_implicated_in	DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency		MGI:3583813	Itga7<sup>tm1Umr</sup>/Itga7<sup>tm1Umr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12588796	20100614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1202064	Otog	is_implicated_in	DOID:0110474	autosomal recessive nonsyndromic deafness 18B		MGI:5883223	Otog<sup>vbd</sup>/Otog<sup>vbd</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26636018	20170414	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934272	Prnp<sup>tm1Miy</sup>	is_not_implicated_in	DOID:11949	Creutzfeldt-Jakob disease		MGI:2174711	Prnp<sup>tm1Miy</sup>/Prnp<sup>tm1Miy</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7494265	20050711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	is_not_implicated_in	DOID:0060013	X-linked severe combined immunodeficiency		MGI:2655194	Il2rg<sup>tm1Sug</sup>/Y  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8562967	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	is_not_implicated_in	DOID:0060013	X-linked severe combined immunodeficiency		MGI:2179823	Il2rg<sup>tm1Cgn</sup>/Y  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	is_not_implicated_in	DOID:0060013	X-linked severe combined immunodeficiency		MGI:2179821	Il2rg<sup>tm1Cgn</sup>/Il2rg<sup>tm1Cgn</sup>  [background:] involves: 129 * CB20			ECO:0000033	author statement supported by traceable reference	PMID:7831294	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	is_implicated_in	DOID:0111700	ankyrin-B-related cardiac arrhythmia		MGI:7514498	Ank2<sup>em1Melr</sup>/Ank2<sup>em1Melr</sup>  [background:] B6.Cg-Ank2<sup>em1Melr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37182735	20230804	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3528558	Csmd1<sup>tm1Lex</sup>	is_not_implicated_in	DOID:5419	schizophrenia		MGI:5485273	Csmd1<sup>tm1Lex</sup>/Csmd1<sup>tm1Lex</sup>  [background:] B6;129S5-Csmd1<sup>tm1Lex</sup>/Mmucd			ECO:0000033	author statement supported by traceable reference	PMID:23284669	20130516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861187	Ccd	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:3583772	Ccd/Ccd<sup>+</sup>  [background:] B10Rl.101-Ccd			ECO:0000033	author statement supported by traceable reference	PMID:8270769	20050817	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861187	Ccd	is_implicated_in	DOID:13994	cleidocranial dysplasia		MGI:2660662	Ccd/Ccd<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	MGI:62184	20050817	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	is_implicated_in	DOID:0110250	cataract 16 multiple types		MGI:5571860	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>tm1.1Ady</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23872361	20140710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:7464550	Got2<sup>em3Pcamp</sup>/Got2<sup>em3Pcamp</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31422819	20230421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	is_implicated_in	DOID:0050709	early infantile epileptic encephalopathy		MGI:7464549	Got2<sup>em2Pcamp</sup>/Got2<sup>em2Pcamp</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:31422819	20230421	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917633	Cox10	is_implicated_in	DOID:699	mitochondrial myopathy		MGI:3609951	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Myl1<sup>tm1(cre)Sjb</sup>/Myl1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16103131	20060112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3799273	Lrp2<sup>m267Asp</sup>	is_implicated_in	DOID:0090144	Donnai-Barrow syndrome		MGI:4847969	Lrp2<sup>m267Asp</sup>/Lrp2<sup>m267Asp</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20653565	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2652485	Plcb1<sup>tm1Hssh</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:2652553	Plcb1<sup>tm1Hssh</sup>/Plcb1<sup>tm1Hssh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:9305844	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2448634	Foxi1<sup>tm1Sven</sup>	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3056282	Foxi1<sup>tm1Sven</sup>/Foxi1<sup>tm1Sven</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12706902	20050622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	is_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:5446328	Sbds<sup>tm1Jrom</sup>/Sbds<sup>tm3.1Jrom</sup> Ptf1a<sup>tm1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:22510201	20230609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	is_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:5446326	Sbds<sup>tm2.1Jrom</sup>/Sbds<sup>tm3.1Jrom</sup> Ptf1a<sup>tm1(cre)Cvw</sup>/Ptf1a<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:22510201	20230609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	is_implicated_in	DOID:0060479	Shwachman-Diamond syndrome		MGI:7485960	Sbds<sup>em1(SBDS*)Dbau</sup>/Sbds<sup>em1(SBDS*)Dbau</sup>  [background:] C57BL/6J-Sbds<sup>em1(SBDS*)Dbau</sup>/Dbau			ECO:0000033	author statement supported by traceable reference	MGI:7485797	20230609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444797	Xylt2	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:3714838	Xylt2<sup>tm1Meh</sup>/Xylt2<sup>tm1Meh</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:17517600	20190924	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3766101	Tg(Tnf)6074Gkl	is_implicated_in	DOID:2377	multiple sclerosis		MGI:4461136	Tg(Tnf)6074Gkl/0  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:9736029	20100722	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857520	Cdh23<sup>v-5J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:3722081	Cdh23<sup>v-5J</sup>/Cdh23<sup>v-5J</sup>  [background:] involves: SENCARA/PtJ			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679626	Cplx2<sup>tm1Bros</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5285873	Cplx2<sup>tm1Bros</sup>/Cplx2<sup>tm1Bros</sup>  [background:] B6NCrl.Cg-Cplx2<sup>tm1Bros</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20412316	20110919	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1935193	Abca1<sup>tm1Wpfl</sup>	is_implicated_in	DOID:1388	Tangier disease		MGI:2450673	Abca1<sup>tm1Wpfl</sup>/Abca1<sup>tm1Wpfl</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10980140	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525180	Tg(INS-SOD2)3Pne	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3624038	Tg(INS-SOD2)3Pne/0  [background:] NOD.FVB-Tg(INS-SOD2)3Pne			ECO:0000033	author statement supported by traceable reference	PMID:16731821	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683635	Icos<sup>tm1Flv</sup>	is_implicated_in	DOID:12177	common variable immunodeficiency		MGI:2683647	Icos<sup>tm1Flv</sup>/Icos<sup>tm1Flv</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11343121	20050706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576787	Angptl6<sup>tm1Yo</sup>	is_implicated_in	DOID:9970	obesity		MGI:3577766	Angptl6<sup>tm1Yo</sup>/Angptl6<sup>tm1Yo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15778720	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108520	Fzd4	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:3622318	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108520	Fzd4	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:4412191	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20159112	20230428	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5445348	b2b1432Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5445971	b2b1432Clo/b2b1432Clo  [background:] C57BL/6J-b2b1432Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:7509544	Csrp3<sup>tm1.1Kage</sup>/Csrp3<sup>tm1.1Kage</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:30048712	20230719	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832387	Slc6a1<sup>tm1Mlit</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5559028	Slc6a1<sup>tm1Mlit</sup>/Slc6a1<sup>tm1Mlit</sup>  [background:] B6.129S1-Slc6a1<sup>tm1Mlit</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23922840	20140415	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3617823	Snrpn<sup>tm1Kaj</sup>	is_implicated_in	DOID:1932	Angelman syndrome		MGI:3618137	Snrpn<sup>tm1Kaj</sup>/Snrpn<sup>+</sup>  [background:] either: 129S1-Snrpn<sup>tm1Kaj</sup> or (involves: 129S1/Sv * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:16368707	20060329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106911	Hccs	is_implicated_in	DOID:10629	microphthalmia		MGI:3580087	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106911	Hccs	is_implicated_in	DOID:10629	microphthalmia		MGI:3580088	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Y Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106911	Hccs	is_implicated_in	DOID:10629	microphthalmia		MGI:3580092	Arhgap6/Hccs/Mid1<sup>tm1Hzo</sup>/Hccs<sup>+</sup> Tg(EIIa-cre)C5379Lmgd/?  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:12444108	20050623	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	is_implicated_in	DOID:11476	osteoporosis		MGI:3653631	Tnfrsf11b<sup>tm1Khs</sup>/Tnfrsf11b<sup>tm1Khs</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9647741	20210421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857138	Btk<sup>tm1Wk</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:2651673	Btk<sup>tm1Wk</sup>/Btk<sup>tm1Wk</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7552994	20081222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102674	Umod	is_implicated_in	DOID:0060062	familial juvenile hyperuricemic nephropathy		MGI:3575012	Umod<sup>tm1Kuma</sup>/Umod<sup>tm1Kuma</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:15522986	20050609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108399	Tcf20	is_implicated_in	DOID:0080354	Phelan-McDermid syndrome		MGI:6726265	Tcf20<sup>em1Jwji</sup>/Tcf20<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:32510763	20210727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858008	Ctnnb1<sup>tm1Mmt</sup>	is_implicated_in	DOID:2999	granulosa cell tumor		MGI:5432228	Amhr2<sup>tm3(cre)Bhr</sup>/Amhr2<sup>+</sup> Ctnnb1<sup>tm1Mmt</sup>/Ctnnb1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21860425	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856327	Col1a2<sup>oim</sup>	is_implicated_in	DOID:12347	osteogenesis imperfecta		MGI:3720800	Col1a2<sup>oim</sup>/Col1a2<sup>+</sup>  [background:] B6C3Fe a/a-Col1a2<sup>oim</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8968022	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045421	Ank	is_implicated_in	DOID:0080033	craniometaphyseal dysplasia		MGI:4889220	Ank<sup>tm1.1Ejr</sup>/Ank<sup>tm1.1Ejr</sup>  [background:] B6.129-Ank<sup>tm1.1Ejr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19257826	20110223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914481	Tbc1d20	is_implicated_in	DOID:0110719	Warburg micro syndrome 4		MGI:4430075	Tbc1d20<sup>bs</sup>/Tbc1d20<sup>bs</sup>  [background:] 129S;AKR-Tbc1d20<sup>bs</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:24239381	20140327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	is_implicated_in	DOID:11476	osteoporosis		MGI:5788294	Ciita<sup>tm1Wrth</sup>/Ciita<sup>tm1Wrth</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24038328	20160809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	is_implicated_in	DOID:0060327	omphalocele		MGI:5437118	Lrp1<sup>b2b1554Clo</sup>/Lrp1<sup>b2b1554Clo</sup>  [background:] C57BL/6J-Lrp1<sup>b2b1554Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20121002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1333777	Aqp3	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:2174933	Aqp3<sup>tm1Ask</sup>/Aqp3<sup>tm1Ask</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10737773	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346093	Psmc4	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:5470095	Psmc4<sup>tm1.1Ryot</sup>/Psmc4<sup>tm1.2Ryot</sup> Tg(SLC18A3-cre)KMisa/0  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:23095749	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109571	Tulp1	is_implicated_in	DOID:0110381	retinitis pigmentosa 14		MGI:2654886	Tulp1<sup>tm1Pjn</sup>/Tulp1<sup>tm1Pjn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10607826	20090429	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387667	Fzd4<sup>tm1Nat</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:4412191	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20159112	20230428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387667	Fzd4<sup>tm1Nat</sup>	is_implicated_in	DOID:0050535	exudative vitreoretinopathy		MGI:3622318	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:33497368	20230428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385580	Tg(Prnp-MAPT)7Vle	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:5569760	Tg(Prnp-MAPT)7Vle/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10595524	20140626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3584475	Ihh<sup>tm1Amc</sup>/Ihh<sup>tm1Amc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:10821773	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	is_implicated_in	DOID:0060474	familial erythrocytosis 2		MGI:3811151	Vhl<sup>tm1Mcs</sup>/Vhl<sup>tm1Mcs</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17992257	20081020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183755	Tg(Pmp22)247Ueli	is_implicated_in	DOID:0110148	Charcot-Marie-Tooth disease type 1A		MGI:3794450	Tg(Pmp22)247Ueli/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15755691	20080620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894689	Ywhae	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2670755	Ywhae<sup>tm1Awb</sup>/Ywhae<sup>tm1Awb</sup>  [background:] either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:12796778	20050608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587421	Myo7a<sup>sh1-11J</sup>	is_implicated_in	DOID:0110826	Usher syndrome type 1		MGI:5312616	Myo7a<sup>sh1-11J</sup>/Myo7a<sup>sh1-11J</sup>  [background:] 129.B6-Myo7a<sup>sh1-11J</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21447681	20120325	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:1380	endometrial cancer		MGI:3813633	Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup> Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup>  [background:] involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18632614	20081103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857266	Uox<sup>tm1Bay</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:3687865	Uox<sup>tm1Bay</sup>/Uox<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8290593	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857930	Terc<sup>tm1Rdp</sup>	is_implicated_in	DOID:11476	osteoporosis		MGI:5695524	Terc<sup>tm1Rdp</sup>/Terc<sup>tm1Rdp</sup>  [background:] B6J.Cg-Terc<sup>tm1Rdp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24626990	20151111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	is_implicated_in	DOID:11836	clubfoot		MGI:3662906	Ret<sup>tm1Kln</sup>/Ret<sup>tm1Kln</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:16600854	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856232	Kit<sup>W</sup>	is_implicated_in	DOID:2361	macrocytic anemia		MGI:5912375	Kit<sup>W</sup>/Kit<sup>W</sup>  [background:] B6.Cg-Kit<sup>W</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:14869351	20171103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4440514	Tg(Thy1-Sncg)HvP36Putt	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5431238	Tg(Thy1-Sncg)HvP36Putt/?  [background:] C57BL/6-Tg(Thy1-Sncg)HvP36Putt			ECO:0000033	author statement supported by traceable reference	PMID:22750530	20120815	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104672	Tfap2b	is_implicated_in	DOID:13832	patent ductus arteriosus		MGI:6393314	Tfap2b<sup>em1Fenli</sup>/Tfap2b<sup>em1Fenli</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29804851	20200305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922862	Gns	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:6105949	Gns<sup>tm1e(EUCOMM)Hmgu</sup>/Gns<sup>tm1e(EUCOMM)Hmgu</sup>  [background:] C57BL/6N-A<sup>tm1Brd</sup> Gns<sup>tm1e(EUCOMM)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28334745	20171222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918961	Mus81	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:5661527	Mus81<sup>tm1Esse</sup>/Mus81<sup>tm1Esse</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25255451	20150911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926493	Tg(ITGB1)0870Fmw	is_implicated_in	DOID:8893	psoriasis		MGI:3583562	Tg(ITGB1)0870Fmw/0  [background:] involves: C57BL/10 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8521519	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2686794	Tg(Rho)1Wbae	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:2686810	Tg(Rho)1Wbae/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8516292	20130619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2658880	Cyp19a1<sup>tm1Sih</sup>/Cyp19a1<sup>tm1Sih</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:25447050	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:2450128	Cyp19a1<sup>tm1Esi</sup>/Cyp19a1<sup>tm1Esi</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15314222	20150604	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924393	Trip11	is_implicated_in	DOID:0080054	achondrogenesis type IA		MGI:4829609	Trip11<sup>m1Mawa</sup>/Trip11<sup>m1Mawa</sup>  [background:] C57BL/6J-Trip11<sup>m1Mawa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20089971	20100915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526521	Sdhd<sup>tm1Jlob</sup>	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:3527165	Sdhd<sup>tm1Jlob</sup>/Sdhd<sup>+</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15572694	20130930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526521	Sdhd<sup>tm1Jlob</sup>	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:3527164	Sdhd<sup>tm1Jlob</sup>/Sdhd<sup>tm1Jlob</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:15572694	20130930	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033227	Gck<sup>Rgsc702</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038221	Gck<sup>Rgsc702</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033227	Gck<sup>Rgsc702</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038222	Gck<sup>Rgsc702</sup>/Gck<sup>Rgsc702</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856106	Bloc1s5<sup>mu</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3587678	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] involves: STOCK t			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856106	Bloc1s5<sup>mu</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3795672	Bloc1s5<sup>mu</sup>/Bloc1s5<sup>mu</sup>  [background:] CHMU/Le			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714803	Ldb1<sup>tm1Witz</sup>	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3715142	Ldb1<sup>tm1Witz</sup>/Ldb1<sup>tm1Witz</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17316599	20070718	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386991	Il6st<sup>tm1Thir</sup>	is_implicated_in	DOID:7148	rheumatoid arthritis		MGI:3843817	Il6st<sup>tm1Thir</sup>/Il6st<sup>tm1Thir</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12370259	20090512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	is_implicated_in	DOID:0060591	WHIM syndrome		MGI:5301555	Cxcr4<sup>tm1.1Bala</sup>/Cxcr4<sup>+</sup>  [background:] B6.129S2-Cxcr4<sup>tm1.1Bala</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22438253	20121004	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1345138	Spry2	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:3584494	Spry2<sup>tm1Ayos</sup>/Spry2<sup>tm1Ayos</sup>  [background:] B6.Cg-Spry2<sup>tm1Ayos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15937482	20050829	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856952	Scyl1<sup>mdf</sup>	is_implicated_in	DOID:0050951	hereditary ataxia		MGI:3712360	Scyl1<sup>mdf</sup>/Scyl1<sup>mdf</sup>  [background:] B6C3Fe a/a-Scyl1<sup>mdf</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17571074	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1351334	Syn3	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5517485	Syn3<sup>tm1Pggd</sup>/Syn3<sup>tm1Pggd</sup>  [background:] B6.129X1-Syn3<sup>tm1Jfe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3029768	Acads<sup>del-J</sup>	is_implicated_in	DOID:0080154	short chain acyl-CoA dehydrogenase deficiency		MGI:3029782	Acads<sup>del-J</sup>/Acads<sup>del-J</sup>  [background:] involves: BALB/cByJ			ECO:0000033	author statement supported by traceable reference	PMID:2712823	20050822	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104960	Tnfaip2	is_implicated_in	DOID:1312	focal segmental glomerulosclerosis		MGI:7564569	Tnfaip2<sup>tm1.1Ohno</sup>/Tnfaip2<sup>tm1.1Ohno</sup>  [background:] C.Cg-Tnfaip2<sup>tm1.1Ohno</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33722931	20231211	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3694810	Arhgap32<sup>tm1Taki</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5811989	Arhgap32<sup>tm1Taki</sup>/Arhgap32<sup>tm1Taki</sup>  [background:] B6N.Cg-Arhgap32<sup>tm1Taki</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26979507	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848053	Glis3<sup>tm1Amj</sup>	is_implicated_in	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism		MGI:3848057	Glis3<sup>tm1Amj</sup>/Glis3<sup>tm1Amj</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19273592	20090616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3586967	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856712	Hps1<sup>ep</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3588311	Hps1<sup>ep</sup>/Hps1<sup>ep</sup>  [background:] B6.C3Fe-Hps1<sup>ep</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6696991	20090608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2144805	Vipas39	is_implicated_in	DOID:0050763	ARC syndrome		MGI:5817425	Vipas39<sup>tm1c(KOMP)Mbp</sup>/Vipas39<sup>tm1c(KOMP)Mbp</sup> Gt(ROSA)26Sor<sup>tm1(cre/ERT2)Tyj</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27435297	20170112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894689	Ywhae	is_implicated_in	DOID:0060480	left ventricular noncompaction		MGI:5512772	Ywhae<sup>tm1Awb</sup>/Ywhae<sup>tm1Awb</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:23071090	20131016	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	is_implicated_in	DOID:0060693	Brunner Syndrome		MGI:3798179	Maoa<sup>K284stop</sup>/Y  [background:] 129S6/SvEvTac-Maoa<sup>K284stop</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18418249	20160801	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	is_implicated_in	DOID:0060693	Brunner Syndrome		MGI:3620543	Maoa<sup>Tg(H2-K1-Ifnb1)8Seif</sup>/Y  [background:] involves: C3H/HeJ			ECO:0000033	author statement supported by traceable reference	PMID:7792602	20160801	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522482	Park7<sup>tm1Cai</sup>	is_implicated_in	DOID:0060370	Parkinson's disease 7		MGI:3833851	Park7<sup>tm1Cai</sup>/Park7<sup>tm1Cai</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18187333	20090226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_not_implicated_in	DOID:4586	familial meningioma		MGI:2447459	Nf2<sup>tm1Tyj</sup>/Nf2<sup>+</sup>  [background:] either: (involves: 129S2/SvPas * 129S4/SvJae * C57BL/6) or (involves: 129S2/SvPas * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9553042	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525214	Cxcr4<sup>tm2Yzo</sup>	is_implicated_in	DOID:6000	congestive heart failure		MGI:7261455	Cxcr4<sup>tm2Yzo</sup>/Cxcr4<sup>tm2Yzo</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:31071921	20220418	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102854	Rpl5	is_implicated_in	DOID:0111879	Diamond-Blackfan anemia 6		MGI:7367115	Rpl5<sup>Skax23-Jus</sup>/Rpl5<sup>+</sup>  [background:] 129S6.B6-Rpl5<sup>Skax23-Jus</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34464976	20221026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033222	Gck<sup>Rgsc210</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038213	Gck<sup>Rgsc210</sup>/Gck<sup>Rgsc210</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033222	Gck<sup>Rgsc210</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3038212	Gck<sup>Rgsc210</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95563	fm	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:5619656	fm/fm  [background:] involves: CBA/H			ECO:0000033	author statement supported by traceable reference	PMID:970440	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5498329	Dnm2<sup>b2b2159Clo</sup>/Dnm2<sup>b2b2159Clo</sup>  [background:] C57BL/6J-Dnm2<sup>b2b2159Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641430	Pdgfrb<sup>tm1Msas</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5790635	Pdgfrb<sup>tm1Msas</sup>/Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu/0  [background:] B6J.Cg-Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu			ECO:0000033	author statement supported by traceable reference	PMID:25803852	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97548	Pfkm	is_implicated_in	DOID:11721	glycogen storage disease VII		MGI:4356551	Pfkm<sup>tm1Fbos</sup>/Pfkm<sup>tm1Fbos</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19696889	20090911	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429945	Abcd1<sup>tm1Ymd</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446591	Abcd1<sup>tm1Ymd</sup>/Abcd1<sup>tm1Ymd</sup>  [background:] involves: 129S/SvEv * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:9126326	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429945	Abcd1<sup>tm1Ymd</sup>	is_implicated_in	DOID:10588	adrenoleukodystrophy		MGI:2446595	Abcd1<sup>tm1Ymd</sup>/Y  [background:] involves: 129S/SvEv * C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:9126326	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385793	Itga2b<sup>tm1Tlr</sup>	is_implicated_in	DOID:0060691	platelet-type bleeding disorder 16		MGI:2677136	Itga2b<sup>tm1Tlr</sup>/Itga2b<sup>tm1Tlr</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:10942384	20050705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137383	Csmd1	is_implicated_in	DOID:5419	schizophrenia		MGI:5574284	Csmd1<sup>tm1Lex</sup>/Csmd1<sup>tm1Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:24244513	20140723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	is_implicated_in	DOID:8947	diabetic retinopathy		MGI:7327617	Insr<sup>tm1Khn</sup>/Insr<sup>tm1Khn</sup> Tg(Pdgfrb-cre)#Rha/0  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:34460911	20220808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856893	Sox10<sup>gt</sup>	is_implicated_in	DOID:0090111	PCWH syndrome		MGI:5648371	Sox10<sup>gt</sup>/Sox10<sup>gt</sup>  [background:] GT/Le			ECO:0000033	author statement supported by traceable reference	PMID:25399070	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101927	Dlx6	is_implicated_in	DOID:0090021	split hand-foot malformation 1		MGI:3703555	Dlx5/Dlx6<sup>tm1Levi</sup>/Dlx5/Dlx6<sup>tm1Levi</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12112878	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97499	Pcca	is_implicated_in	DOID:14701	propionic acidemia		MGI:3052741	Pcca<sup>tm1Tmiy</sup>/Pcca<sup>tm1Tmiy</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11461925	20200414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110453	dilated cardiomyopathy 1EE		MGI:3691281	Myh6<sup>tm2Ces</sup>/Myh6<sup>tm2Ces</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	is_implicated_in	DOID:0110453	dilated cardiomyopathy 1EE		MGI:3691282	Myh6<sup>tm2Ces</sup>/Myh6<sup>+</sup>  [background:] involves: 129S/SvEv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16983074	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180562	Tg(Ckmm-Cav3)1Ysu	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5286560	Tg(Ckmm-Cav3)1Ysu/0  [background:] involves: C57BL/Slc * DBA/Slc			ECO:0000033	author statement supported by traceable reference	PMID:14645200	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857344	Sod2<sup>tm1Cje</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:3639891	Sod2<sup>tm1Cje</sup>/Sod2<sup>tm1Cje</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9462746	20060804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915160	Rubcn	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:6287978	Rubcn<sup>em1Dgre</sup>/Rubcn<sup>em1Dgre</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931521	Fgfr3<sup>tm1Dor</sup>	is_implicated_in	DOID:0060249	scoliosis		MGI:6256787	Fgfr3<sup>tm1Dor</sup>/Fgfr3<sup>tm1Dor</sup>  [background:] C3.129S6(B6)-Fgfr3<sup>tm1Dor</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25852647	20181116	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850971	Ppm1k<sup>tm1Yiwa</sup>	is_implicated_in	DOID:9269	maple syrup urine disease		MGI:3850972	Ppm1k<sup>tm1Yiwa</sup>/Ppm1k<sup>tm1Yiwa</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19411760	20090722	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:6161435	b2b3183Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:6161438	b2b3183Clo/b2b3183Clo  [background:] C57BL/6J-b2b3183Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20180618	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:5308056	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21625620	20120229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857941	Nf2<sup>tm1Tyj</sup>	is_not_implicated_in	DOID:4586	familial meningioma		MGI:2447459	Nf2<sup>tm1Tyj</sup>/Nf2<sup>+</sup>  [background:] either: (involves: 129S2/SvPas * 129S4/SvJae * C57BL/6) or (involves: 129S2/SvPas * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9553042	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511481	Rpgr<sup>Rd9</sup>	is_implicated_in	DOID:0110414	retinitis pigmentosa 3		MGI:3720014	Rpgr<sup>Rd9</sup>/Y  [background:] C57BL/6-Rpgr<sup>Rd9</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22563472	20170111	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	is_implicated_in	DOID:11721	glycogen storage disease VII		MGI:3621470	Hif1a<sup>tm3Rsjo</sup>/Hif1a<sup>tm3Rsjo</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15328538	20060505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159735	Hoxb8<sup>tm1.1Mrc</sup>	is_implicated_in	DOID:0050587	trichotillomania		MGI:2673421	Hoxb8<sup>tm1.1Mrc</sup>/Hoxb8<sup>tm1.1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11779477	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178542	Comt<sup>tm1Kara</sup>	is_implicated_in	DOID:1561	cognitive disorder		MGI:3697681	Comt<sup>tm1Kara</sup>/Comt<sup>tm1Kara</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:9707588	20190411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1		MGI:3664199	Scnn1g<sup>tm1Bhk</sup>/Scnn1g<sup>tm1Bhk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:9788978	20100302	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3802531	Psap<sup>tm2Ggb</sup>	is_implicated_in	DOID:10581	metachromatic leukodystrophy		MGI:3802581	Psap<sup>tm2Ggb</sup>/Psap<sup>tm2Ggb</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18480170	20080818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3604623	Itpr2<sup>tm1Kmik</sup>	is_implicated_in	DOID:0060603	isolated anhidrosis with normal sweat glands		MGI:5630054	Itpr2<sup>tm1Kmik</sup>/Itpr2<sup>tm1Kmik</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:25329695	20150417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856656	Rab27a<sup>ash</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3640189	Rab27a<sup>ash</sup>/Rab27a<sup>ash</sup>  [background:] involves: C3H/HeDiSn			ECO:0000033	author statement supported by traceable reference	PMID:10859366	20080515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052922	Mbnl1<sup>tm1Sws</sup>	is_implicated_in	DOID:450	myotonic disease		MGI:3052930	Mbnl1<sup>tm1Sws</sup>/Mbnl1<sup>tm1Sws</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:14671308	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157909	Uox<sup>in</sup>	is_implicated_in	DOID:557	kidney disease		MGI:3687954	Uox<sup>in</sup>/Uox<sup>in</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:11474184	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	is_implicated_in	DOID:3490	Noonan syndrome		MGI:3588510	Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>/Apaf1<sup>Gt(IRESBetageo)XIX18Pgr</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:9753320	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	is_implicated_in	DOID:4297	scimitar syndrome		MGI:7545275	Pdgfra<sup>tm2Sor</sup>/Pdgfra<sup>tm2Sor</sup>  [background:] involves: 129S4/SvJaeSor			ECO:0000033	author statement supported by traceable reference	PMID:20071345	20231102	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	is_implicated_in	DOID:0110555	autosomal dominant nonsyndromic deafness 25		MGI:3804682	Slc17a8<sup>tm1Selm</sup>/Slc17a8<sup>tm1Selm</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18674745	20090520	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1316650	Slc37a4	is_implicated_in	DOID:2749	glycogen storage disease Ia		MGI:3046092	Slc37a4<sup>tm1Jyc</sup>/Slc37a4<sup>tm1Jyc</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12925567	20050614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:6101207	Ext1<sup>tm1.1Vcs</sup>/Ext1<sup>tm1.1Vcs</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28445472	20171214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:6101205	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Acan<sup>tm1(cre/ERT2)Crm</sup>/Acan<sup>+</sup>  [background:] involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:28445472	20171214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:4437608	Ext1<sup>tm1.1Vcs</sup>/Ext1<sup>tm1.1Vcs</sup> Tg(Col2a1-rtTA,tetO-cre)22Pjro/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20080592	20171214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:4437605	Ext1<sup>tm1Vcs</sup>/Ext1<sup>tm1Vcs</sup> Tg(Col2a1-rtTA,tetO-cre)22Pjro/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20080592	20171214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	is_implicated_in	DOID:206	hereditary multiple exostoses		MGI:4818630	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S5/SvEvBrd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20534475	20171214	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918017	Prpf3	is_implicated_in	DOID:0110356	retinitis pigmentosa 18		MGI:4950565	Prpf3<sup>tm1.1Eap</sup>/Prpf3<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918017	Prpf3	is_implicated_in	DOID:0110356	retinitis pigmentosa 18		MGI:4950564	Prpf3<sup>tm1.1Eap</sup>/Prpf3<sup>tm1.1Eap</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103150	Slc12a1	is_implicated_in	DOID:0110142	Bartter disease type 1		MGI:4457194	Slc12a1<sup>urehr3</sup>/Slc12a1<sup>urehr3</sup>  [background:] involves: C3HeB/FeJ			ECO:0000033	author statement supported by traceable reference	PMID:20219826	20131223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103150	Slc12a1	is_implicated_in	DOID:0110142	Bartter disease type 1		MGI:3036453	Slc12a1<sup>tm1Tkh</sup>/Slc12a1<sup>tm1Tkh</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:10779555	20131223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104621	Alx1	is_implicated_in	DOID:0081047	frontonasal dysplasia 3		MGI:7336692	Alx1<sup>em1Jian</sup>/Alx1<sup>em1Jian</sup>  [background:] C57BL/6N-Alx1<sup>em1Jian</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35127681	20220920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3529295	Ldlrap1<sup>Gt(OST149604)Lex</sup>	is_implicated_in	DOID:0090105	autosomal recessive hypercholesterolemia		MGI:3611042	Ldlrap1<sup>Gt(OST149604)Lex</sup>/Ldlrap1<sup>Gt(OST149604)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15472122	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2149543	Ubap1	is_implicated_in	DOID:0112341	hereditary spastic paraplegia 80		MGI:7414333	Ubap1<sup>em1Yta</sup>/Ubap1<sup>+</sup>  [background:] involves: C57BL/6 * C57BL/6N * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:35962060	20230106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3046775	Rpl5<sup>Skax23-Jus</sup>	is_implicated_in	DOID:0111879	Diamond-Blackfan anemia 6		MGI:7367115	Rpl5<sup>Skax23-Jus</sup>/Rpl5<sup>+</sup>  [background:] 129S6.B6-Rpl5<sup>Skax23-Jus</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34464976	20221026	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95751	Glrb	is_implicated_in	DOID:0060697	hyperekplexia 2		MGI:3695037	Glrb<sup>spa</sup>/Glrb<sup>spa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8733750	20120514	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857644	Dbf	is_implicated_in	DOID:11836	clubfoot		MGI:2170796	Dbf/Dbf<sup>+</sup>  [background:] involves: 101/H * C3H/HeH			ECO:0000033	author statement supported by traceable reference	PMID:9062079	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3692750	Elovl4<sup>tm1Rayy</sup>	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3696675	Elovl4<sup>tm1Rayy</sup>/Elovl4<sup>+</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17003453	20070213	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	is_not_implicated_in	DOID:5408	Paget's disease of bone		MGI:3817497	Sqstm1<sup>tm1Jjw</sup>/Sqstm1<sup>tm1Jjw</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18765443	20081124	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5504442	Ins2<sup>Akita</sup>/?  [background:] involves: C57BL/6NSlc			ECO:0000033	author statement supported by traceable reference	PMID:17911348	20130905	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4353109	Senp1<sup>tm1Wami</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:5707775	Senp1<sup>tm1Wami</sup>/Senp1<sup>tm1Wami</sup> Tg(Fabp4-cre)#Abel/0  [background:] B6.Cg-Senp1<sup>tm1Wami</sup> Tg(Fabp4-cre)#Abel			ECO:0000033	author statement supported by traceable reference	PMID:26596471	20160210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99421	Nfe2l1	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3575312	Nfe2l1<sup>tm1Jefc</sup>/Nfe2l1<sup>tm1Ywk</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15738389	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180848	Cebpb<sup>tm1Kish</sup>	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:2656637	Cebpb<sup>tm1Kish</sup>/Cebpb<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:24885110	20221010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829369	Alx4<sup>Lst-2J</sup>	is_implicated_in	DOID:0060285	parietal foramina		MGI:5695543	Alx4<sup>Lst-2J</sup>/Alx4<sup>Lst-2J</sup>  [background:] C57BL/6J-Alx4<sup>Lst-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25673119	20151112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913689	Borcs7	is_implicated_in	DOID:2476	hereditary spastic paraplegia		MGI:6302764	Borcs7<sup>Q87X</sup>/Borcs7<sup>Q87X</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30067980	20190513	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856628	Dtnbp1<sup>sdy</sup>	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:1936982	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2658730	Hyal1<sup>tm1Stn</sup>	is_implicated_in	DOID:0050809	mucopolysaccharidosis IX		MGI:3797579	Hyal1<sup>tm1Stn</sup>/Hyal1<sup>tm1Stn</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18344557	20080717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857424	E2f1<sup>tm1Meg</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3621814	E2f1<sup>tm1Meg</sup>/E2f1<sup>tm1Meg</sup>  [background:] NOD.Cg-E2f1<sup>tm1Meg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15470032	20060509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924407	Dpcd	is_implicated_in	DOID:10908	hydrocephalus		MGI:4950027	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>/Dpcd/Poll<sup>Gt(OST280355)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857124	Alpl<sup>tm1Sor</sup>	is_implicated_in	DOID:0110914	infantile hypophosphatasia		MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856585	Pax6<sup>132-14Neu</sup>	is_implicated_in	DOID:83	cataract		MGI:2175741	Pax6<sup>132-14Neu</sup>/Pax6<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:7035547	20170609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522330	pta	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:3522704	pta/pta  [background:] C57BL/6J-pta			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180033	Zmpste24<sup>tm1Otin</sup>	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:3621007	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/Ola * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11923874	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776013	Gja1<sup>tm8Kwi</sup>	is_implicated_in	DOID:0060291	oculodentodigital dysplasia		MGI:3807710	Gja1<sup>tm8Kwi</sup>/Gja1<sup>+</sup> Tg(Pgk1-cre)1Lni/0  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18003637	20080926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714454	Cby1<sup>tm1Ktkm</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3841093	Cby1<sup>tm1Ktkm</sup>/Cby1<sup>tm1Ktkm</sup>  [background:] B6.129-Cby1<sup>tm1Ktkm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19364920	20110303	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1855985	Tyr<sup>c-2J</sup>	is_implicated_in	DOID:11211	buphthalmos		MGI:3581209	Tyr<sup>c-2J</sup>/Tyr<sup>c-2J</sup>  [background:] B6(Cg)-Tyr<sup>c-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:12624268	20060926	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150650	Fgfr1<sup>tm1Led</sup>	is_implicated_in	DOID:14705	Pfeiffer syndrome		MGI:2174904	Fgfr1<sup>tm1Led</sup>/Fgfr1<sup>tm1Led</sup>  [background:] involves: 129S4/SvJae * NIH Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:8001823	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857284	Cybb<sup>tm1Din</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5486338	Cybb<sup>tm1Din</sup>/Cybb<sup>tm1Din</sup>  [background:] B6.129S-Cybb<sup>tm1Din</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27096368	20190419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:0060564	spinal disease		MGI:7280953	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Col2a1-cre/ERT)KA3Smac/0  [background:] involves: 129S4/SvJae * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28523278	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3036575	Tg(Wap-Hgf)402Mig	is_implicated_in	DOID:1612	breast cancer		MGI:5576517	Tg(Wap-Hgf)402Mig/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:14627990	20140808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99913	Lamc2	is_implicated_in	DOID:0060737	junctional epidermolysis bullosa Herlitz type		MGI:2679609	Lamc2<sup>tm1Uit</sup>/Lamc2<sup>tm1Uit</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14632187	20050707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:6507151	Tuba1a<sup>em1Rstot</sup>/Tuba1a<sup>em1Rstot</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:6507152	Tuba1a<sup>em2Rstot</sup>/Tuba1a<sup>em2Rstot</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	is_implicated_in	DOID:2490	congenital nervous system abnormality		MGI:6507156	Tuba1a<sup>em1Rstot</sup>/Tuba1a<sup>quas</sup>  [background:] involves: C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31386652	20210219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3722875	Atp2c1<sup>tm1Ges</sup>	is_not_implicated_in	DOID:0050429	Hailey-Hailey disease		MGI:3723214	Atp2c1<sup>tm1Ges</sup>/Atp2c1<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:17597066	20071002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347058	Hsf4	is_implicated_in	DOID:0110255	cataract 5 multiple types		MGI:5305581	Hsf4<sup>ldis1</sup>/Hsf4<sup>ldis1</sup>  [background:] involves: C57BL/6 * CAST/EiJ * RIIIS/J			ECO:0000033	author statement supported by traceable reference	PMID:22162625	20120210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	is_implicated_in	DOID:1826	epilepsy		MGI:2177575	Gad2<sup>tm1Bae</sup>/Gad2<sup>tm1Bae</sup>  [background:] involves: 129X1/SvJ * NOD			ECO:0000033	author statement supported by traceable reference	PMID:9391152	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181792	Plec<sup>tm2Gwi</sup>	is_implicated_in	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy		MGI:3513373	Plec<sup>tm2Gwi</sup>/Plec<sup>tm2Gwi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9389647	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776889	Uros<sup>tm3Rjde</sup>	is_implicated_in	DOID:13271	cutaneous porphyria		MGI:3777397	Uros<sup>tm3Rjde</sup>/Uros<sup>tm3Rjde</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16532394	20080623	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176758	Casr<sup>tm1Ces</sup>	is_implicated_in	DOID:0060700	familial hypocalciuric hypercalcemia 1		MGI:2176761	Casr<sup>tm1Ces</sup>/Casr<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:7493018	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4130266	Vps35<sup>Gt(RRK261)Byg</sup>	is_implicated_in	DOID:0060897	Parkinson's disease 17		MGI:5695247	Vps35<sup>Gt(RRK261)Byg</sup>/Vps35<sup>+</sup>  [background:] B6.129P2-Vps35<sup>Gt(RRK261)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:26203154	20151109	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	is_implicated_in	DOID:14761	Greig cephalopolysyndactyly syndrome		MGI:2166944	Gli3<sup>Xt-J</sup>/Gli3<sup>Xt-J</sup>  [background:] involves: C3H * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:8387379	20060322	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155980	Acvrl1<sup>tm1Enl</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:3033418	Acvrl1<sup>tm1Enl</sup>/Acvrl1<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12588795	20050525	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857447	Ptch1<sup>tm1Mps</sup>	is_implicated_in	DOID:2513	basal cell carcinoma		MGI:6259595	Ptch1<sup>tm1Mps</sup>/Ptch1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:10545995	20181207	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583662	Psen1<sup>tm1Tak</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3589555	Psen1<sup>tm1Tak</sup>/Psen1<sup>tm1Tak</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15908021	20051014	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790741	Brca1<sup>tm1Thl</sup>	is_implicated_in	DOID:1612	breast cancer		MGI:3805033	Brca1<sup>tm1Thl</sup>/Brca1<sup>tm1Thl</sup> Wap<sup>tm1(cre)Arge</sup>/0  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18443292	20080910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917560	Plscr3	is_implicated_in	DOID:9970	obesity		MGI:3053798	Plscr3<sup>tm1Sims</sup>/Plscr3<sup>tm1Sims</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15328404	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4354143	Gucy1a1<sup>tm1.1Brou</sup>	is_implicated_in	DOID:1070	primary open angle glaucoma		MGI:5516430	Gucy1a1<sup>tm1.1Brou</sup>/Gucy1a1<sup>tm1.1Brou</sup>  [background:] involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:23527308	20131107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857192	Il2ra<sup>tm1Dw</sup>	is_implicated_in	DOID:0050589	inflammatory bowel disease		MGI:2179512	Il2ra<sup>tm1Dw</sup>/Il2ra<sup>tm1Dw</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7584142	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179041	Sycp3<sup>tm1Hoog</sup>	is_implicated_in	DOID:14227	azoospermia		MGI:2664131	Sycp3<sup>tm1Hoog</sup>/Sycp3<sup>tm1Hoog</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10678170	20050909	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:3522324	Apc<sup>tm2.1Cip</sup>/Apc<sup>tm2.1Cip</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:15563600	20080717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	is_implicated_in	DOID:9007	sudden infant death syndrome		MGI:4417856	Slc6a4<sup>tm1(cre)Xz</sup>/Slc6a4<sup>tm1(cre)Xz</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19646988	20100114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3037816	Cerkl	is_implicated_in	DOID:0110368	retinitis pigmentosa 26		MGI:6758644	Cerkl<sup>em1Gmar</sup>/Cerkl<sup>tm1.1Geno</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:32658961	20210910	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444672	Madd	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5789257	Madd<sup>tm1Bpra</sup>/Madd<sup>tm1Bpra</sup> Tg(Ins2-cre/ERT)1Dam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:24379354	20160818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861703	Htt<sup>tm2Mem</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698279	Htt<sup>tm2Mem</sup>/Htt<sup>tm2Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5316765	b2b913Clo	is_implicated_in	DOID:1682	congenital heart disease		MGI:5316796	b2b913Clo/b2b913Clo  [background:] C57BL/6J-b2b913Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919762	Sting1	is_implicated_in	DOID:0111457	STING-associated vasculopathy with onset in infancy		MGI:6302788	Sting1<sup>em1Jmin</sup>/Sting1<sup>+</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28951494	20220209	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2665316	Gucy2c<sup>tm1Gar</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5300906	Gucy2c<sup>tm1Gar</sup>/Gucy2c<sup>tm1Gar</sup>  [background:] B6.129S6-Gucy2c<sup>tm1Gar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21865642	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850088	Tg(Myh6-BRUNOL4*)10Coop	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5426837	Tg(Myh6-BRUNOL4*)10Coop/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:15988035	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98331	Snap25	is_implicated_in	DOID:5419	schizophrenia		MGI:5428448	Snap25<sup>Bdr</sup>/Snap25<sup>+</sup>  [background:] involves: BALB/cAnNCrl			ECO:0000033	author statement supported by traceable reference	PMID:17283335	20120720	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2676301	Pitpna<sup>Gt(OST1152)Lex</sup>	is_implicated_in	DOID:0060357	chylomicron retention disease		MGI:2676371	Pitpna<sup>Gt(OST1152)Lex</sup>/Pitpna<sup>Gt(OST1152)Lex</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:12788952	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	is_implicated_in	DOID:0110701	hypotrichosis 4		MGI:3851927	Hr<sup>Hp</sup>/Hr<sup>Hp</sup>  [background:] BALB/cJ-Hr<sup>Hp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19513791	20090804	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96685	Krt10	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:2672094	Krt10<sup>tm1Tmm</sup>/Krt10<sup>+</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8603923	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96685	Krt10	is_implicated_in	DOID:4603	epidermolytic hyperkeratosis		MGI:2672093	Krt10<sup>tm1Tmm</sup>/Krt10<sup>tm1Tmm</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:8603923	20090224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96789	Lipa	is_implicated_in	DOID:0080217	lysosomal acid lipase deficiency		MGI:2451081	Lipa<sup>tm1Ggb</sup>/Lipa<sup>tm1Ggb</sup>  [background:] involves: 129P2/OlaHsd * CF-1			ECO:0000033	author statement supported by traceable reference	PMID:9700186	20190729	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3846404	Cisd2<sup>tm1Tfts</sup>	is_implicated_in	DOID:0110630	Wolfram syndrome 2		MGI:3846426	Cisd2<sup>tm1Tfts</sup>/Cisd2<sup>tm1Tfts</sup>  [background:] B6.129S7-Cisd2<sup>tm1Tfts</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19451219	20090602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4361456	Thbs1<sup>tm1Hyn</sup>/Thbs1<sup>tm1Hyn</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19700744	20091014	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:5014041	Cav1<sup>tm1Mls</sup>/Cav1<sup>tm1Mls</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:21203469	20110712	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386120	Piga<sup>tm1Tak</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:6303984	Piga<sup>tm1Tak</sup>/Piga<sup>tm1Tak</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15304084	20190517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386120	Piga<sup>tm1Tak</sup>	is_implicated_in	DOID:0060713	autosomal recessive congenital ichthyosis 4B		MGI:3758821	Piga<sup>tm1Tak</sup>/Y Tg(KRT5-cre)1Tak/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15304084	20190517	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153060	Gjc2	is_implicated_in	DOID:0060787	hypomyelinating leukodystrophy 2		MGI:5140117	Gjc2<sup>tm2.1Kwi</sup>/Gjc2<sup>tm2.1Kwi</sup>  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21750683	20110818	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2683854	Klhl41	is_implicated_in	DOID:3191	nemaline myopathy		MGI:6156408	Klhl41<sup>tm1a(KOMP)Wtsi</sup>/Klhl41<sup>tm1a(KOMP)Wtsi</sup>  [background:] C57BL/6-Klhl41<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28826497	20180515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178315	Pde6b<sup>atrd2</sup>	is_implicated_in	DOID:0110375	retinitis pigmentosa 40		MGI:3028001	Pde6b<sup>atrd2</sup>/Pde6b<sup>atrd2</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:16123450	20140219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3644953	Iigp1c	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:7439142	Iigp1c<sup>M1Btlr</sup>/Iigp1c<sup>M1Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>M1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3644953	Iigp1c	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:7439145	Iigp1c<sup>M2Btlr</sup>/Iigp1c<sup>M2Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>M2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3644953	Iigp1c	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:7439148	Iigp1c<sup>em1Btlr</sup>/Iigp1c<sup>em1Btlr</sup>  [background:] C57BL/6J-Iigp1c<sup>em1Btlr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35842425	20230228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	is_implicated_in	DOID:14687	diastrophic dysplasia		MGI:3575650	Slc26a2<sup>tm1Aros</sup>/Slc26a2<sup>tm1Aros</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15703192	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	is_implicated_in	DOID:0060198	amyotrophic lateral sclerosis type 6		MGI:6101467	Fus<sup>tm1.1Emcf</sup>/Fus<sup>+</sup>  [background:] involves: C3H * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:29053787	20171215	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	is_implicated_in	DOID:83	cataract		MGI:5475286	Gclc<sup>tm1c(EUCOMM)Wtsi</sup>/Gclc<sup>tm1c(EUCOMM)Wtsi</sup> Tg(Cryaa-cre)10Mlr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:23226398	20130425	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346523	Sgcb	is_implicated_in	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E		MGI:3850524	Sgcb<sup>tm1Oza</sup>/Sgcb<sup>tm1Oza</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10441321	20090716	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346523	Sgcb	is_implicated_in	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E		MGI:3626292	Sgcb<sup>tm1Kcam</sup>/Sgcb<sup>tm1Kcam</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:10678176	20090716	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2683777	Tnfsf4<sup>tm1Shr</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3640479	Tnfsf4<sup>tm1Shr</sup>/Tnfsf4<sup>tm1Shr</sup>  [background:] NOD.129S4-Tnfsf4<sup>tm1Shr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14662903	20060811	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	is_implicated_in	DOID:0111099	maturity-onset diabetes of the young type 1		MGI:3653173	Hnf4a<sup>tm1.1Gonz</sup>/Hnf4a<sup>tm1.1Gonz</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129X1/SvJ * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:16377800	20060830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136896	Ret<sup>tm2.1Cos</sup>	is_implicated_in	DOID:0050771	pheochromocytoma		MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2139806	Spart	is_implicated_in	DOID:0050886	Troyer syndrome		MGI:5430992	Spart<sup>tm1.1Xen</sup>/Spart<sup>tm1.1Xen</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22619377	20120813	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178320	Pde6b<sup>rd1-4H</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028389	Pde6b<sup>rd1-4H</sup>/Pde6b<sup>rd1-4H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913644	Nosip	is_implicated_in	DOID:4621	holoprosencephaly		MGI:6711274	Nosip<sup>Gt(OST138992)Lex</sup>/Nosip<sup>Gt(OST138992)Lex</sup>  [background:] B6.129S5-Nosip<sup>Gt(OST138992)Lex</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25546391	20210519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931883	Xpc<sup>tm1Brd</sup>	is_implicated_in	DOID:0110844	xeroderma pigmentosum group C		MGI:3665144	Xpc<sup>tm1Brd</sup>/Xpc<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:7675084	20061030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3588845	Gnat2<sup>cpfl3</sup>	is_implicated_in	DOID:0110010	achromatopsia 4		MGI:3715214	Gnat2<sup>cpfl3</sup>/Gnat2<sup>cpfl3</sup>  [background:] ALS/LtJ			ECO:0000033	author statement supported by traceable reference	PMID:17065522	20110519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920942	Cplane1	is_implicated_in	DOID:0110986	Joubert syndrome 17		MGI:5309129	Cplane1<sup>b2b012Clo</sup>/Cplane1<sup>b2b012Clo</sup>  [background:] C57BL/6J-Cplane1<sup>b2b012Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25877302	20160609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	is_implicated_in	DOID:2986	IgA glomerulonephritis		MGI:5307127	Was<sup>tm1Sbs</sup>/Was<sup>tm1Sbs</sup>  [background:] 129S6/SvEvTac-Was<sup>tm1Sbs</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:22079330	20120226	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	is_implicated_in	DOID:14717	centronuclear myopathy		MGI:4848149	Dnm2<sup>tm1.1Ics</sup>/Dnm2<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27870637	20170105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103248	Phc1	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3042302	Phc1<sup>tm1Os</sup>/Phc1<sup>tm1Os</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9367423	20101001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917585	Reep6	is_implicated_in	DOID:0080350	retinitis pigmentosa 77		MGI:6189553	Reep6<sup>em1Ruch</sup>/Reep6<sup>em1Ruch</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27889058	20181221	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385930	Nr2f1<sup>tm1Mjts</sup>	is_implicated_in	DOID:0112226	Bosch-Boonstra-Schaaf optic atrophy syndrome		MGI:6434270	Nr2f1<sup>tm1Mjts</sup>/Nr2f1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:31600777	20220113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3783290	Sbf2<sup>Gt(RRF511)Byg</sup>	is_implicated_in	DOID:0110190	Charcot-Marie-Tooth disease type 4B2		MGI:3783887	Sbf2<sup>Gt(RRF511)Byg</sup>/Sbf2<sup>Gt(RRF511)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18349142	20080506	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177751	Htt<sup>tm1.1Pfs</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3698752	Htt<sup>tm1.1Pfs</sup>/Htt<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10196365	20070305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347474	Foxj1	is_implicated_in	DOID:1682	congenital heart disease		MGI:7545539	Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>  [background:] STOCK Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:37158461	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857124	Alpl<sup>tm1Sor</sup>	is_implicated_in	DOID:0110915	childhood hypophosphatasia		MGI:2174902	Alpl<sup>tm1Sor</sup>/Alpl<sup>tm1Sor</sup>  [background:] either: (involves: 129S7/SvEvBrd-Alpl<sup>tm1Sor</sup>) or (involves: 129S7/SvEvBrd * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:7550313	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856209	Cacna1a<sup>tg</sup>	is_implicated_in	DOID:0050990	episodic ataxia type 2		MGI:3700746	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:25855180	20150702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:4829879	Nfkbia<sup>tm1.1Pjc</sup>/Nfkbia<sup>tm1.1Pjc</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20696914	20100917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619253	Ryr1<sup>tm1Slh</sup>	is_implicated_in	DOID:8545	malignant hyperthermia		MGI:3620044	Ryr1<sup>tm1Slh</sup>/Ryr1<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16284304	20060419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:5689499	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7281829	Runx3<sup>tm3Yg</sup>/Runx3<sup>tm3Yg</sup> Tg(Pou4f1-cre/ERT2)2Jiz/0  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	is_implicated_in	DOID:0060250	idiopathic scoliosis		MGI:7281828	Runx3<sup>tm3Yg</sup>/Runx3<sup>tm3Yg</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:28829946	20220602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	is_implicated_in	DOID:10754	otitis media		MGI:5141438	Enpp1<sup>asj</sup>/Enpp1<sup>asj</sup>  [background:] C57BL/6J-Enpp1<sup>asj</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:27959908	20190917	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3842652	Gnmt<sup>tm1Ymac</sup>	is_implicated_in	DOID:0111037	glycine N-methyltransferase deficiency		MGI:3842683	Gnmt<sup>tm1Ymac</sup>/Gnmt<sup>tm1Ymac</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17937387	20090504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178353	Mitf<sup>Mi-H</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686994	Mitf<sup>Mi-H</sup>/Mitf<sup>Mi-H</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178353	Mitf<sup>Mi-H</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2686995	Mitf<sup>Mi-H</sup>/Mitf<sup>+</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530465	Peg12<sup>tm1Brn</sup>	is_not_implicated_in	DOID:11983	Prader-Willi syndrome		MGI:3530544	Peg12<sup>tm1Brn</sup>/Peg12<sup>tm1Brn</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:15681612	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5446150	b2b1801Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5465102	b2b1801Clo/b2b1801Clo  [background:] C57BL/6J-b2b1801Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103151	Pltp	is_implicated_in	DOID:10140	dry eye syndrome		MGI:2176343	Pltp<sup>tm1Jia</sup>/Pltp<sup>tm1Jia</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21514421	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3573749	Aire<sup>tm1Mmat</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3576479	Aire<sup>tm1Mmat</sup>/Aire<sup>tm1Mmat</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15699112	20050509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444131	Cwh43	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:7437706	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>+</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444131	Cwh43	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:7437702	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em1Mdj</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444131	Cwh43	is_implicated_in	DOID:1572	normal pressure hydrocephalus		MGI:7437708	Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em2Mdj</sup>  [background:] C57BL/6-Cwh43<sup>em1Mdj</sup>/Cwh43<sup>em2Mdj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33459505	20230222	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	is_implicated_in	DOID:13911	achromatopsia		MGI:6798143	Gnat2<sup>cpfl3-2J</sup>/Gnat2<sup>cpfl3-2J</sup>  [background:] B6.Cg-Gnat2<sup>cpfl3-2J</sup>/Boc			ECO:0000033	author statement supported by traceable reference	MGI:6798134	20211110	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934269	Trp63<sup>tm1Fmc</sup>	is_implicated_in	DOID:8534	gastroesophageal reflux disease		MGI:2174785	Trp63<sup>tm1Fmc</sup>/Trp63<sup>tm1Fmc</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:21703447	20111007	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88269	Car2	is_implicated_in	DOID:0110941	autosomal recessive osteopetrosis 3		MGI:2175729	Car2<sup>n</sup>/Car2<sup>n</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:3126501	20050614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3772701	Tg(Prnp-TBP*)13Xjl	is_not_implicated_in	DOID:0050967	spinocerebellar ataxia type 17		MGI:3772886	Tg(Prnp-TBP*)13Xjl/0  [background:] FVB/N-Tg(Prnp-TBP*)13Xjl			ECO:0000033	author statement supported by traceable reference	PMID:17994014	20080305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3790207	Lgr4<sup>Gt(LST020)Byg</sup>	is_implicated_in	DOID:1686	glaucoma		MGI:3797606	Lgr4<sup>Gt(LST020)Byg</sup>/Lgr4<sup>Gt(LST020)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18424556	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511348	Rpgrip1<sup>nmf247</sup>	is_implicated_in	DOID:0110329	Leber congenital amaurosis 6		MGI:4367266	Rpgrip1<sup>nmf247</sup>/Rpgrip1<sup>nmf247</sup>  [background:] C57BL/6J-Rpgrip1<sup>nmf247</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28859131	20171115	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	is_implicated_in	DOID:0110079	Leber congenital amaurosis 8		MGI:3581037	Crb1<sup>rd8</sup>/Crb1<sup>rd8</sup>  [background:] STOCK Crb1<sup>rd8</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:20089206	20110520	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664470	Serpina6<sup>tm1Tew</sup>	is_implicated_in	DOID:0090030	corticosteroid-binding globulin deficiency		MGI:3710359	Serpina6<sup>tm1Tew</sup>/Serpina6<sup>tm1Tew</sup>  [background:] involves: 129/SvEmcTer * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:16980625	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2680765	Hcrtr2	is_implicated_in	DOID:8986	narcolepsy		MGI:4949134	Hcrtr2<sup>tm1Tesc</sup>/Hcrtr2<sup>tm1Tesc</sup>  [background:] B6.Cg-Hcrtr2<sup>tm1Tesc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21368172	20151120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2680765	Hcrtr2	is_implicated_in	DOID:8986	narcolepsy		MGI:2669895	Hcrtr2<sup>tm1Ywa</sup>/Hcrtr2<sup>tm1Ywa</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:12797957	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857936	Pten<sup>tm1Ppp</sup>	is_implicated_in	DOID:6457	Cowden syndrome		MGI:2179025	Pten<sup>tm1Ppp</sup>/Pten<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9697695	20050708	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367268	Rho<sup>R3</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4367272	Rho<sup>R3</sup>/Rho<sup>R3</sup>  [background:] C57BL/6J-Rho<sup>R3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19741247	20130619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4367268	Rho<sup>R3</sup>	is_implicated_in	DOID:0110372	retinitis pigmentosa 4		MGI:4367269	Rho<sup>R3</sup>/Rho<sup>+</sup>  [background:] C57BL/6J-Rho<sup>R3</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19741247	20130619	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5438048	b2b1700Clo	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5442135	b2b1700Clo/b2b1700Clo  [background:] C57BL/6J-b2b1700Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3698290	Sall4<sup>tm1Brd</sup>	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3698627	Sall4<sup>tm1Brd</sup>/Sall4<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17216607	20070305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856209	Cacna1a<sup>tg</sup>	is_implicated_in	DOID:0050704	childhood electroclinical syndrome		MGI:3700786	Cacna1a<sup>tg</sup>/Cacna1a<sup>tg</sup>  [background:] B6.D2-Cacna1a<sup>tg</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:572084	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1277223	Atxn2	is_implicated_in	DOID:0050955	spinocerebellar ataxia type 2		MGI:5467984	Atxn2<sup>tm2.1Aub</sup>/Atxn2<sup>tm2.1Aub</sup>  [background:] B6.129S2-Atxn2<sup>tm2.1Aub</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22956915	20130307	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3784992	Lepr<sup>Db-2Btlr</sup>	is_implicated_in	DOID:9970	obesity		MGI:3784993	Lepr<sup>Db-2Btlr</sup>/Lepr<sup>Db-2Btlr</sup>  [background:] C57BL/6J-Lepr<sup>Db-2Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:3778962	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	is_implicated_in	DOID:0110637	muscular dystrophy-dystroglycanopathy type B6		MGI:4454427	Large1<sup>myd-3J</sup>/Large1<sup>myd-3J</sup>  [background:] STOCK Large1<sup>myd-3J</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	MGI:4454310	20100609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103555	Clcn3	is_implicated_in	DOID:0110731	neuronal ceroid lipofuscinosis 3		MGI:3574028	Clcn3<sup>tm1Suc</sup>/Clcn3<sup>tm1Suc</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12059962	20050615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159355	Gpc3<sup>tm1Snd</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849590	Gpc3<sup>tm1Snd</sup>/Y  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159355	Gpc3<sup>tm1Snd</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849591	Gpc3<sup>tm1Snd</sup>/Gpc3<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894762	Ldb1	is_implicated_in	DOID:9467	nail-patella syndrome		MGI:3715142	Ldb1<sup>tm1Witz</sup>/Ldb1<sup>tm1Witz</sup> Tg(NPHS2-cre)295Lbh/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:17316599	20070718	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685574	Dnai2	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5619081	Dnai2<sup>b2b3405Clo</sup>/Dnai2<sup>b2b3405Clo</sup>  [background:] C57BL/6J-Dnai2<sup>b2b3405Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3041135	Met<sup>tm1Sst</sup>	is_implicated_in	DOID:11714	gestational diabetes		MGI:5504390	Met<sup>tm1Sst</sup>/Met<sup>tm1Sst</sup> Tg(Pdx1-cre)89.1Dam/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22427375	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1888377	Prlr<sup>tm1Cnp</sup>	is_implicated_in	DOID:0050547	familial medullary thyroid carcinoma		MGI:4431029	Prlr<sup>tm1Cnp</sup>/Prlr<sup>tm1Cnp</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:16166330	20100305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	is_implicated_in	DOID:13884	sick sinus syndrome		MGI:5688197	Hcn1<sup>tm2Kndl</sup>/Hcn1<sup>tm2Kndl</sup>  [background:] involves: 129 * 129S/SvEv * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:24218458	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860087	Tnfrsf1b<sup>tm1Imx</sup>	is_not_implicated_in	DOID:10825	essential hypertension		MGI:2175020	Tnfrsf1b<sup>tm1Imx</sup>/Tnfrsf1b<sup>tm1Imx</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9551933	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182612	Krt5<sup>tm1Tmm</sup>	is_implicated_in	DOID:0060735	epidermolysis bullosa simplex Dowling-Meara type		MGI:3582826	Krt5<sup>tm1Tmm</sup>/Krt5<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11408584	20050802	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1335082	Invs	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:3622553	Invs<sup>inv</sup>/Invs<sup>inv</sup>  [background:] FVB/N-Invs<sup>inv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9664638	20101001	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385958	C1qtnf5	is_implicated_in	DOID:0060869	late-onset retinal degeneration		MGI:4949225	C1qtnf5<sup>tm1.1Itl</sup>/C1qtnf5<sup>+</sup>  [background:] C57BL/6-C1qtnf5<sup>tm1.1Itl</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21349921	20110506	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	is_implicated_in	DOID:0110609	primary ciliary dyskinesia 23		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23850584	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	is_implicated_in	DOID:0110609	primary ciliary dyskinesia 23		MGI:5312338	Odad2<sup>b2b643Clo</sup>/Odad2<sup>b2b643Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b643Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	is_implicated_in	DOID:0110609	primary ciliary dyskinesia 23		MGI:5437109	Odad2<sup>b2b227.1Clo</sup>/Odad2<sup>b2b227.1Clo</sup>  [background:] C57BL/6J-Odad2<sup>b2b227.1Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856087	Mitf<sup>Mi-Or</sup>	is_implicated_in	DOID:13533	osteopetrosis		MGI:4356528	Mitf<sup>Mi-Or</sup>/Mitf<sup>Mi-Or</sup>  [background:] involves: 101/Rl * C3H/Rl			ECO:0000033	author statement supported by traceable reference	PMID:7495310	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	is_not_implicated_in	DOID:0060852	Pierson syndrome		MGI:6378620	Lamb2<sup>em1Jhm</sup>/Lamb2<sup>em1Jhm</sup>  [background:] involves: C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:29263159	20191127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716838	Fig4<sup>plt1</sup>	is_implicated_in	DOID:0060589	Yunis-Varon syndrome		MGI:5554544	Fig4<sup>plt1</sup>/Fig4<sup>plt1</sup>  [background:] involves: 129P2/OlaHsd * C3H * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23623387	20140402	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3796444	Vegfa<sup>tm2Pec</sup>/Vegfa<sup>tm2Pec</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:11381259	20080709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675502	Dnase2b<sup>tm1Osa</sup>	is_implicated_in	DOID:83	cataract		MGI:2675506	Dnase2b<sup>tm1Osa</sup>/Dnase2b<sup>tm1Osa</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12944971	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930618	Krit1	is_implicated_in	DOID:0060669	cerebral cavernous malformation		MGI:6279211	Krit1<sup>tm1Kwhi</sup>/Krit1<sup>tm1Kwhi</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27027284	20190220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1930618	Krit1	is_implicated_in	DOID:0060669	cerebral cavernous malformation		MGI:6279211	Krit1<sup>tm1Kwhi</sup>/Krit1<sup>tm1Kwhi</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S6/SvEvTac * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:27513872	20190220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2668495	Serpini1<sup>tm1Dpw</sup>	is_implicated_in	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies		MGI:2669541	Serpini1<sup>tm1Dpw</sup>/Serpini1<sup>tm1Dpw</sup>  [background:] involves: 129/Sv * C57BL/6JBom			ECO:0000033	author statement supported by traceable reference	PMID:12837630	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	is_implicated_in	DOID:10487	Hirschsprung's disease		MGI:3624521	Itgb1<sup>tm1Lscd</sup>/Itgb1<sup>tm1Ref</sup> Tg(PLAT-cre)116Sdu/0  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16571628	20170608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385760	Tg(Ins2-Fasl)24Ach	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3581611	Tg(Ins2-Fasl)24Ach/0  [background:] NOD-Tg(Ins2-Fasl)24Ach/J			ECO:0000033	author statement supported by traceable reference	PMID:9094710	20061006	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346340	Mta2	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3803013	Mta2<sup>tm1.1Yzha</sup>/Mta2<sup>tm1.1Yzha</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:18353770	20080915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183399	Runx3<sup>tm1Yg</sup>	is_implicated_in	DOID:2841	asthma		MGI:3057279	Runx3<sup>tm1Yg</sup>/Runx3<sup>tm1Yg</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)			ECO:0000033	author statement supported by traceable reference	PMID:16027362	20060825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	is_implicated_in	DOID:384	Wolff-Parkinson-White syndrome		MGI:3663711	Bmpr1a<sup>tm1Bhr</sup>/Bmpr1a<sup>tm2.1Bhr</sup> Tg(GATA6-cre)#Jbeb/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16037571	20061016	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	is_implicated_in	DOID:2987	familial mediterranean fever		MGI:2655804	Mefv<sup>tm1Chae</sup>/Mefv<sup>tm1Chae</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:12667444	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3699175	Sall4<sup>tm1Ryn</sup>	is_implicated_in	DOID:0060747	Duane-radial ray syndrome		MGI:3699203	Sall4<sup>tm1Ryn</sup>/Sall4<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16790473	20070308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	is_implicated_in	DOID:0080171	esophageal atresia/tracheoesophageal fistula		MGI:3819135	Nog<sup>tm1Amc</sup>/Nog<sup>tm1Amc</sup>  [background:] either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1 * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:17260385	20081212	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:5749248	Sod1<sup>m1H</sup>/Sod1<sup>m1H</sup>  [background:] involves: C3H/HeH * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:25468678	20160218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384133	Mpz<sup>tm1Msch</sup>	is_implicated_in	DOID:0090111	PCWH syndrome		MGI:3576603	Mpz<sup>tm1Msch</sup>/Mpz<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12616486	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814576	Tg(MT1A-Dyrk1a)9Xest	is_implicated_in	DOID:14250	Down syndrome		MGI:3814588	Tg(MT1A-Dyrk1a)9Xest/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:18940310	20081111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385652	Tg(Rbp3-SV40)IT-2Jjw	is_implicated_in	DOID:768	retinoblastoma		MGI:5009542	Tg(Rbp3-SV40)IT-2Jjw/?  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8112979	20110701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857883	Dysf<sup>im</sup>	is_implicated_in	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B		MGI:2175836	Dysf<sup>im</sup>/Dysf<sup>im</sup>  [background:] involves: SJL			ECO:0000033	author statement supported by traceable reference	PMID:10508505	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3581540	Hexa<sup>tm1Cota</sup>	is_implicated_in	DOID:3320	Tay-Sachs disease		MGI:3581542	Hexa<sup>tm1Cota</sup>/Hexa<sup>tm1Cota</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8747922	20050713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2158560	Cep63	is_implicated_in	DOID:0050569	Seckel syndrome		MGI:5819194	Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>/Cep63<sup>Gt(EUCE0251h11)Hmgu</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26158450	20170127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2174965	Irs1<sup>tm1Tka</sup>/Irs1<sup>tm1Tka</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7969452	20050811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183829	Eif2ak3<sup>tm1Drc</sup>	is_implicated_in	DOID:0090060	Wolcott-Rallison syndrome		MGI:3618624	Eif2ak3<sup>tm1Drc</sup>/Eif2ak3<sup>tm1Drc</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:11997520	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	is_implicated_in	DOID:0060601	alpha-2-plasmin inhibitor deficiency		MGI:2672889	Serpinf2<sup>tm1Hrl</sup>/Serpinf2<sup>tm1Hrl</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10090937	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	is_implicated_in	DOID:0060601	alpha-2-plasmin inhibitor deficiency		MGI:2672889	Serpinf2<sup>tm1Hrl</sup>/Serpinf2<sup>tm1Hrl</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10318667	20050610	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386336	Prox1<sup>tm1Gco</sup>	is_implicated_in	DOID:9970	obesity		MGI:2669229	Prox1<sup>tm1Gco</sup>/Prox1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * NMRI			ECO:0000033	author statement supported by traceable reference	PMID:16170315	20060127	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4262238	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:4950027	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>/Dpcd/Poll<sup>Gt(OST280355)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd			ECO:0000033	author statement supported by traceable reference	PMID:21746835	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857875	Drd2<sup>tm1Low</sup>	is_not_implicated_in	DOID:14330	Parkinson's disease		MGI:4429667	Drd2<sup>tm1Low</sup>/Drd2<sup>tm1Low</sup>  [background:] B6.129S2-Drd2<sup>tm1Low</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9547254	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907041	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129/Sv * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19850880	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5907042	Myocd<sup>tm1Msp</sup>/Myocd<sup>tm1Msp</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19850880	20170816	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:5524023	Trp53<sup>tm1.1Tldo</sup>/Trp53<sup>tm1.1Tldo</sup>  [background:] involves: 129S2/SvPas * BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23770245	20131220	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88181	Bmp5	is_implicated_in	DOID:0060306	Meier-Gorlin syndrome		MGI:3587431	Bmp5<sup>se</sup>/Bmp5<sup>se</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7710253	20180305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3045113	Recql4<sup>tm1Glu</sup>	is_implicated_in	DOID:2732	Rothmund-Thomson syndrome		MGI:3575579	Recql4<sup>tm1Glu</sup>/Recql4<sup>tm1Glu</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15703196	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3828266	Dll4<sup>tm1Frad</sup>	is_implicated_in	DOID:0060227	Adams-Oliver syndrome		MGI:7545577	Dll4<sup>tm1Frad</sup>/Dll4<sup>+</sup> Isl1<sup>tm1(cre)Tmj</sup>/Isl1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:33899511	20231103	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583991	Gt(ROSA)26Sor<sup>tm1(HD*103Q)Xwy</sup>	is_implicated_in	DOID:12858	Huntington's disease		MGI:3584455	Gt(ROSA)26Sor<sup>tm1(HD*103Q)Xwy</sup>/? Tg(Nes-cre)1Kln/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15882643	20050826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857424	E2f1<sup>tm1Meg</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3621814	E2f1<sup>tm1Meg</sup>/E2f1<sup>tm1Meg</sup>  [background:] NOD.Cg-E2f1<sup>tm1Meg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15470032	20060509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890220	Gpr132	is_implicated_in	DOID:417	autoimmune disease		MGI:3639677	Gpr132<sup>tm1Witt</sup>/Gpr132<sup>tm1Witt</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11371358	20060802	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889008	Atp2c1	is_not_implicated_in	DOID:0050429	Hailey-Hailey disease		MGI:3723214	Atp2c1<sup>tm1Ges</sup>/Atp2c1<sup>+</sup>  [background:] involves: 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:17597066	20071002	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	is_implicated_in	DOID:114	heart disease		MGI:3652414	Fbn1<sup>tm3Rmz</sup>/Fbn1<sup>tm3Rmz</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16407178	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	is_implicated_in	DOID:0090119	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome		MGI:5468673	Trp63<sup>tm1Cmis</sup>/Trp63<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23108156	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386963	Kcnq2<sup>tm1Hsa</sup>	is_implicated_in	DOID:14264	benign neonatal seizures		MGI:2672848	Kcnq2<sup>tm1Hsa</sup>/Kcnq2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10854243	20050913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3769234	Sirt3<sup>tm1.1Fwa</sup>	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:5311115	Sirt3<sup>tm1.1Fwa</sup>/Sirt3<sup>tm1.1Fwa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:21856199	20170614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	is_implicated_in	DOID:12583	velocardiofacial syndrome		MGI:5660194	Mapk1<sup>tm1Gela</sup>/Mapk1<sup>tm1Gela</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:18952847	20150827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2679449	Slitrk2	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:7547513	Slitrk2<sup>tm1.1Jwum</sup>/Y Tg(Nes-cre)1Atp/0  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:35840571	20231113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3723526	Atf6<sup>tm1.1Rjk</sup>	is_implicated_in	DOID:0110009	achromatopsia 7		MGI:6883630	Atf6<sup>tm1.1Rjk</sup>/Atf6<sup>tm1.1Rjk</sup>  [background:] involves: C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26029869	20220225	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3707232	Sumf1<sup>Gt(RST760)Byg</sup>	is_implicated_in	DOID:0050441	mucosulfatidosis		MGI:3713764	Sumf1<sup>Gt(RST760)Byg</sup>/Sumf1<sup>Gt(RST760)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17360554	20070705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107178	Hmx1	is_implicated_in	DOID:0060482	oculoauricular syndrome		MGI:3838401	Hmx1<sup>dmbo</sup>/Hmx1<sup>dmbo</sup>  [background:] involves: C3HeB/FeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19379485	20090501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107178	Hmx1	is_implicated_in	DOID:0060482	oculoauricular syndrome		MGI:3838502	Hmx1<sup>mpe</sup>/Hmx1<sup>mpe</sup>  [background:] C3H/HeJ-Hmx1<sup>mpe</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:19379485	20090501	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353500	Foxe1	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:3587185	Foxe1<sup>tm1Rdl</sup>/Foxe1<sup>tm1Rdl</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9697704	20050912	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	is_implicated_in	DOID:2477	motor peripheral neuropathy		MGI:6157847	Slc12a6<sup>em1Dlp</sup>/Slc12a6<sup>em1Dlp</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27485015	20180523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640522	Tg(APCS-Ifng)5Imeg	is_implicated_in	DOID:0050700	cardiomyopathy		MGI:5906283	Tg(APCS-Ifng)5Imeg/0  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:17556594	20170808	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:5515634	Prdm1<sup>tm1Clme</sup>/Prdm1<sup>tm1Clme</sup> Tg(Itgax-cre)1-1Reiz/0  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:21948081	20131030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3847797	Bmp7<sup>tm1.1Dgra</sup>	is_implicated_in	DOID:0050848	obstructive sleep apnea		MGI:6509439	Bmp7<sup>tm1.1Dgra</sup>/Bmp7<sup>tm1.1Dgra</sup> H2az2<sup>Tg(Wnt1-cre)11Rth</sup>/H2az2<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:33431521	20210310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97763	Prlr	is_implicated_in	DOID:0050547	familial medullary thyroid carcinoma		MGI:4431029	Prlr<sup>tm1Cnp</sup>/Prlr<sup>tm1Cnp</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:16166330	20100305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856915	Invs<sup>inv</sup>	is_implicated_in	DOID:0111113	nephronophthisis 2		MGI:2654613	Invs<sup>inv</sup>/Invs<sup>inv</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15213262	20120926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:2673003	Dtnbp1<sup>sdy</sup>/Dtnbp1<sup>sdy</sup>  [background:] involves: DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:1936982	20090608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4453303	Cldn16<sup>tm1.1Dmu</sup>	is_implicated_in	DOID:0060880	renal hypomagnesemia 3		MGI:4453304	Cldn16<sup>tm1.1Dmu</sup>/Cldn16<sup>tm1.1Dmu</sup>  [background:] involves: 129 * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:20147368	20151122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857709	Acvr2b<sup>tm1Enl</sup>	is_implicated_in	DOID:0060856	right atrial isomerism		MGI:2654122	Acvr2b<sup>tm1Enl</sup>/Acvr2b<sup>tm1Enl</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:9242489	20060424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614412	Polh<sup>tm1.1Rak</sup>	is_implicated_in	DOID:0110847	xeroderma pigmentosum variant type		MGI:3615437	Polh<sup>tm1.1Rak</sup>/Polh<sup>tm1.1Rak</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16397220	20060310	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924767	Zfyve26	is_implicated_in	DOID:0110768	hereditary spastic paraplegia 15		MGI:5749268	Zfyve26<sup>tm1.1Cahb</sup>/Zfyve26<sup>tm1.1Cahb</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24367272	20160219	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924337	Ankrd11	is_implicated_in	DOID:14780	KBG syndrome		MGI:6885557	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>/Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup> E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33996804	20220921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924337	Ankrd11	is_implicated_in	DOID:14780	KBG syndrome		MGI:7336829	Ankrd11<sup>tm1c(EUCOMM)Wtsi</sup>/Ankrd11<sup>+</sup> E2f1<sup>Tg(Wnt1-cre)2Sor</sup>/E2f1<sup>+</sup>  [background:] involves: C3H * C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33996804	20220921	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	is_implicated_in	DOID:0060864	patterned macular dystrophy 2		MGI:5699377	Ctnna1<sup>Tvrm5</sup>/Ctnna1<sup>+</sup>  [background:] C57BL/6J-Ctnna1<sup>Tvrm5</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26691986	20161209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	is_implicated_in	DOID:0060864	patterned macular dystrophy 2		MGI:5699376	Ctnna1<sup>Tvrm5</sup>/Ctnna1<sup>Tvrm5</sup>  [background:] C57BL/6J-Ctnna1<sup>Tvrm5</sup>/Pjn			ECO:0000033	author statement supported by traceable reference	PMID:26691986	20161209	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1337006	Hapln1	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:3038695	Hapln1<sup>tm1Nid</sup>/Hapln1<sup>tm1Nid</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:9988279	20051006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3714783	Lig4<sup>tiny</sup>	is_implicated_in	DOID:0060021	DNA ligase IV deficiency		MGI:3714853	Lig4<sup>tiny</sup>/Lig4<sup>tiny</sup>  [background:] C57BL/6-Lig4<sup>tiny</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17554302	20090727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182087	Tg(SOD1*G37R)106Dpr	is_implicated_in	DOID:0060193	amyotrophic lateral sclerosis type 1		MGI:3814056	Tg(SOD1*G37R)106Dpr/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7605627	20081106	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2150021	Aqp3<sup>tm1Ask</sup>	is_implicated_in	DOID:12387	nephrogenic diabetes insipidus		MGI:2174933	Aqp3<sup>tm1Ask</sup>/Aqp3<sup>tm1Ask</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10737773	20060926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347470	Foxf1	is_implicated_in	DOID:13042	persistent fetal circulation syndrome		MGI:6470789	Foxf1<sup>em1Vvk</sup>/Foxf1<sup>+</sup>  [background:] involves: C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:31199666	20201105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101884	Ppard	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5695740	Ppard<sup>tm1Dsvg</sup>/Ppard<sup>tm1Dsvg</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25279796	20151112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685814	Hpse2	is_implicated_in	DOID:0050816	urofacial syndrome		MGI:5694081	Hpse2<sup>Gt(OST411605)Lex</sup>/Hpse2<sup>Gt(OST411605)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25510506	20151030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447334	Tg(APP695)3Dbo	is_implicated_in	DOID:0110040	Alzheimer's disease 4		MGI:3696575	Tg(APP695)3Dbo/0  [background:] B6.C3-Tg(APP695)3Dbo			ECO:0000033	author statement supported by traceable reference	PMID:12742740	20071026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2159611	Ocrl<sup>tm1Nbm</sup>	is_not_implicated_in	DOID:1056	oculocerebrorenal syndrome		MGI:2668816	Ocrl<sup>tm1Nbm</sup>/Ocrl<sup>tm1Nbm</sup>  [background:] either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss)			ECO:0000033	author statement supported by traceable reference	PMID:9593760	20120809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3526693	Frem1<sup>bfd</sup>	is_implicated_in	DOID:0090001	Fraser syndrome		MGI:3665276	Frem1<sup>bfd</sup>/Frem1<sup>bfd</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15345741	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3775095	Eya4<sup>tm1Jse</sup>	is_implicated_in	DOID:10754	otitis media		MGI:3776413	Eya4<sup>tm1Jse</sup>/Eya4<sup>tm1Jse</sup>  [background:] involves: 129S6/SvEvTac * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:18219393	20080624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	is_implicated_in	DOID:0050580	hereditary lymphedema		MGI:3620108	Flt4<sup>Chy</sup>/Flt4<sup>+</sup>  [background:] involves: C3H			ECO:0000033	author statement supported by traceable reference	PMID:11592985	20060420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3831526	Gtf2ird1<sup>Gt(XE465)Byg</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3831537	Gtf2ird1<sup>Gt(XE465)Byg</sup>/Gtf2ird1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:19109438	20090212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181735	L1cam<sup>tm1Mtei</sup>	is_implicated_in	DOID:0060246	MASA syndrome		MGI:3624801	L1cam<sup>tm1Mtei</sup>/Y  [background:] either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv)			ECO:0000033	author statement supported by traceable reference	PMID:9354804	20081114	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	is_implicated_in	DOID:12449	aplastic anemia		MGI:5792659	Ifng<sup>tm1.1Hayg</sup>/Ifng<sup>tm1.1Hayg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:25342713	20160919	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	is_implicated_in	DOID:0110948	Waardenburg syndrome type 1		MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4458417	Tfr2<sup>tm1.1Anro</sup>	is_implicated_in	DOID:0111030	hemochromatosis type 3		MGI:4458421	Tfr2<sup>tm1.1Anro</sup>/Tfr2<sup>tm1.1Anro</sup>  [background:] 129.Cg-Tfr2<sup>tm1.1Anro</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20179178	20100709	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:7435429	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Cdh5-cre/ERT2)1Rha/0  [background:] involves: 129S4/SvJae * FVB			ECO:0000033	author statement supported by traceable reference	PMID:32552404	20230217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429948	Kras<sup>tm4Tyj</sup>	is_implicated_in	DOID:0060688	arteriovenous malformations of the brain		MGI:7435433	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup> Tg(Slco1c1-icre/ERT2)1Mrks/0  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:32552404	20230217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	is_implicated_in	DOID:4971	myelofibrosis		MGI:4417827	Gata1<sup>tm2Sho</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12149188	20130723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	is_implicated_in	DOID:4971	myelofibrosis		MGI:2653501	Gata1<sup>tm2Sho</sup>/Gata1<sup>tm2Sho</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12149188	20130723	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2385958	C1qtnf5	is_not_implicated_in	DOID:0060869	late-onset retinal degeneration		MGI:5309011	C1qtnf5<sup>tm1.1Geno</sup>/C1qtnf5<sup>tm1.1Geno</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22110650	20120312	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921405	Errfi1	is_implicated_in	DOID:1380	endometrial cancer		MGI:3850221	Errfi1<sup>tm1Jwj</sup>/Errfi1<sup>tm1Jwj</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:19439667	20090713	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4361203	Pla2g6<sup>m1Sein</sup>	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:4415286	Pla2g6<sup>m1Sein</sup>/Pla2g6<sup>m1Sein</sup>  [background:] C57BL/6JJcl-Pla2g6<sup>m1Sein</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19893029	20100108	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:3707539	Nppc<sup>lbab</sup>/Nppc<sup>lbab</sup>  [background:] B6.PL-Nppc<sup>lbab</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:22271248	20220512	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1096329	Foxi1	is_implicated_in	DOID:0060744	Pendred Syndrome		MGI:3056282	Foxi1<sup>tm1Sven</sup>/Foxi1<sup>tm1Sven</sup>  [background:] involves: CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12706902	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511173	Tg(Ela1-Myc)160Bri	is_implicated_in	DOID:4905	pancreatic carcinoma		MGI:5432346	Tg(Ela1-Myc)160Bri/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:1986386	20120828	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3802940	Ryr2<sup>tm2Amks</sup>	is_implicated_in	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1		MGI:5582595	Ryr2<sup>tm2Amks</sup>/Ryr2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:22828895	20140915	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2445936	P2ry12<sup>tm1Cjf</sup>	is_implicated_in	DOID:0060692	platelet-type bleeding disorder 8		MGI:3723060	P2ry12<sup>tm1Cjf</sup>/P2ry12<sup>tm1Cjf</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:11413167	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3814174	Pkhd1<sup>tm1Cjwa</sup>	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3814175	Pkhd1<sup>tm1Cjwa</sup>/Pkhd1<sup>tm1Cjwa</sup>  [background:] involves: 129S6/SvEvTac * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17519956	20081107	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177294	Amelx<sup>tm1Kul</sup>	is_implicated_in	DOID:0110058	amelogenesis imperfecta type 1E		MGI:2177295	Amelx<sup>tm1Kul</sup>/Amelx<sup>tm1Kul</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11406633	20050601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156825	Zic2<sup>tm1Jaru</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5085985	Zic2<sup>tm1Jaru</sup>/Zic2<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:22355535	20110815	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055587	Enam<sup>Rgsc521</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574667	Enam<sup>Rgsc521</sup>/Enam<sup>Rgsc521</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055587	Enam<sup>Rgsc521</sup>	is_implicated_in	DOID:0110052	amelogenesis imperfecta type 1B		MGI:3574668	Enam<sup>Rgsc521</sup>/Enam<sup>+</sup>  [background:] involves: C57BL/6JJcl * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15649948	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442602	Pax2<sup>M1Bpb</sup>	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:4442635	Pax2<sup>M1Bpb</sup>/Pax2<sup>M1Bpb</sup>  [background:] C57BL/6-Pax2<sup>M1Bpb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20221250	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4442602	Pax2<sup>M1Bpb</sup>	is_implicated_in	DOID:0090006	renal coloboma syndrome		MGI:4442633	Pax2<sup>M1Bpb</sup>/Pax2<sup>+</sup>  [background:] C57BL/6-Pax2<sup>M1Bpb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20221250	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	is_implicated_in	DOID:0110844	xeroderma pigmentosum group C		MGI:3665144	Xpc<sup>tm1Brd</sup>/Xpc<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:7675084	20061030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813273	Nphp1<sup>tm1.1Hung</sup>	is_not_implicated_in	DOID:0111112	nephronophthisis 1		MGI:3813305	Nphp1<sup>tm1.1Hung</sup>/Nphp1<sup>tm1.1Hung</sup>  [background:] B6.Cg-Nphp1<sup>tm1.1Hung</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18684731	20081030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856973	Tcirg1<sup>oc</sup>	is_implicated_in	DOID:11836	clubfoot		MGI:3770247	Tcirg1<sup>oc</sup>/Tcirg1<sup>oc</sup>  [background:] C57BL/6J-Vps33a<sup>bf</sup>			ECO:0000033	author statement supported by traceable reference	MGI:76073	20110125	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521795	Xirp1<sup>tm1Jl</sup>	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:3656023	Xirp1<sup>tm1Jl</sup>/Xirp1<sup>tm1Jl</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:17766470	20170810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679886	Pten<sup>tm2.1Ppp</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5320164	Pten<sup>tm2.1Ppp</sup>/Pten<sup>tm2.1Ppp</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:22302806	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857519	Cdh23<sup>v-4J</sup>	is_implicated_in	DOID:0110831	Usher syndrome type 1D		MGI:5050420	Cdh23<sup>v-4J</sup>/Cdh23<sup>v-4J</sup>  [background:] involves: C57BLKS/J			ECO:0000033	author statement supported by traceable reference	PMID:21689626	20110825	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671810	Alg10b<sup>nse5</sup>	is_implicated_in	DOID:0050563	nonsyndromic deafness		MGI:5581451	Alg10b<sup>nse5</sup>/Alg10b<sup>nse5</sup>  [background:] 129S6.B6-Alg10b<sup>nse5</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24303013	20170608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	is_implicated_in	DOID:0110326	hypertrophic cardiomyopathy 20		MGI:5780987	Nexn<sup>tm1.1Zhh</sup>/Nexn<sup>tm1.1Zhh</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26659360	20160721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	is_implicated_in	DOID:0110341	osteogenesis imperfecta type 2		MGI:4437913	Smpd3<sup>fro</sup>/Smpd3<sup>fro</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:8456819	20130702	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:3607259	Large1<sup>myd</sup>/Large1<sup>myd</sup>  [background:] B6C3Fe a/a-Large1<sup>myd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7602333	20051215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3512420	Lgr5<sup>tm1Ah</sup>	is_implicated_in	DOID:0060604	ankyloglossia		MGI:3512741	Lgr5<sup>tm1Ah</sup>/Lgr5<sup>tm1Ah</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15509778	20050629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338076	Hivep2	is_implicated_in	DOID:1059	intellectual disability		MGI:6189180	Hivep2<sup>tm1Sis</sup>/Hivep2<sup>tm1Sis</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:29233179	20190403	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1860425	Cldn14	is_implicated_in	DOID:0110487	autosomal recessive nonsyndromic deafness 29		MGI:2674081	Cldn14<sup>tm1Tbf</sup>/Cldn14<sup>tm1Tbf</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12913076	20110613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1933748	Atm<sup>tm1Fwa</sup>	is_implicated_in	DOID:12704	ataxia telangiectasia		MGI:2175707	Atm<sup>tm1Fwa</sup>/Atm<sup>tm1Fwa</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10716718	20050603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1194497	Tgif1	is_implicated_in	DOID:10754	otitis media		MGI:5516484	Tgif1<sup>tm1.1Caw</sup>/Tgif1<sup>tm1.1Caw</sup>  [background:] B6.129S-Tgif1<sup>tm1.1Caw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23459932	20131107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1913302	Sdhc	is_implicated_in	DOID:3652	Leigh disease		MGI:6392337	Sdhc<sup>tm1c(EUCOMM)Wtsi</sup>/Sdhc<sup>tm1c(EUCOMM)Wtsi</sup> Gt(ROSA)26Sor<sup>tm1.1(rtTA,tetO-cre)Bkmn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:31469588	20200302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313261	Sptbn2	is_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:5300032	Sptbn2<sup>Gt(XK442)Byg</sup>/Sptbn2<sup>Gt(XK442)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20231455	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313261	Sptbn2	is_implicated_in	DOID:0050882	spinocerebellar ataxia type 5		MGI:4821985	Sptbn2<sup>tm1Mjac</sup>/Sptbn2<sup>tm1Mjac</sup>  [background:] B6.129P2-Sptbn2<sup>tm1Mjac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20371805	20151118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3033232	Gck<sup>Rgsc735</sup>	is_implicated_in	DOID:0111100	maturity-onset diabetes of the young type 2		MGI:3590140	Gck<sup>Rgsc735</sup>/Gck<sup>+</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:15102714	20051020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	is_implicated_in	DOID:14289	Ebstein anomaly		MGI:3663711	Bmpr1a<sup>tm1Bhr</sup>/Bmpr1a<sup>tm2.1Bhr</sup> Tg(GATA6-cre)#Jbeb/0  [background:] involves: 129S7/SvEvBrd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:16037571	20061016	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3764517	Ptch1<sup>tm1Hahn</sup>	is_implicated_in	DOID:2513	basal cell carcinoma		MGI:4452396	Ptch1<sup>tm1Hahn</sup>/Ptch1<sup>tm1Hahn</sup> Gt(ROSA)26Sor<sup>tm2(cre/ERT2)Brn</sup>/Gt(ROSA)26Sor<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:20233865	20100519	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	is_implicated_in	DOID:0110014	age related macular degeneration 1		MGI:3797222	Vldlr<sup>tm1Her</sup>/Vldlr<sup>tm1Her</sup>  [background:] B6;129S7-Vldlr<sup>tm1Her</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:18172119	20080715	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	is_implicated_in	DOID:0060603	isolated anhidrosis with normal sweat glands		MGI:5630054	Itpr2<sup>tm1Kmik</sup>/Itpr2<sup>tm1Kmik</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:25329695	20150417	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651805	Lpl<sup>tm1Bres</sup>	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651807	Lpl<sup>tm1Bres</sup>/Lpl<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8675619	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651805	Lpl<sup>tm1Bres</sup>	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651806	Lpl<sup>tm1Bres</sup>/Lpl<sup>tm1Bres</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8675619	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931124	Hesx1<sup>tm1Icar</sup>	is_implicated_in	DOID:9406	hypopituitarism		MGI:2175062	Hesx1<sup>tm1Icar</sup>/Hesx1<sup>tm1Icar</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9620767	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387783	Pafah1b1<sup>tm1Or</sup>	is_implicated_in	DOID:0060469	Miller-Dieker lissencephaly syndrome		MGI:2664549	Pafah1b1<sup>tm1Or</sup>/Pafah1b1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11344260	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136896	Ret<sup>tm2.1Cos</sup>	is_implicated_in	DOID:10016	multiple endocrine neoplasia type 2B		MGI:3583335	Ret<sup>tm2.1Cos</sup>/Ret<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136896	Ret<sup>tm2.1Cos</sup>	is_implicated_in	DOID:10016	multiple endocrine neoplasia type 2B		MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	is_implicated_in	DOID:9970	obesity		MGI:3582615	Mkks<sup>tm1Vcs</sup>/Mkks<sup>tm1Vcs</sup>  [background:] either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:15772095	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3701943	Kmt2a<sup>tm1.1(Sh3gl1)Lcc</sup>	is_implicated_in	DOID:1240	leukemia		MGI:5559577	Kmt2a<sup>tm1.1(Sh3gl1)Lcc</sup>/Kmt2a<sup>+</sup> Lyz2<sup>tm1(cre)Ifo</sup>/Lyz2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24122813	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3578633	Spry2<sup>tm1.1Mrt</sup>	is_implicated_in	DOID:0060340	ciliopathy		MGI:3702557	Spry2<sup>tm1.1Mrt</sup>/Spry2<sup>tm1.1Mrt</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:34423857	20220705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:0110910	leukocyte adhesion deficiency 1		MGI:3583131	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8101543	20050808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857208	Itgb2<sup>tm1Bay</sup>	is_implicated_in	DOID:0110910	leukocyte adhesion deficiency 1		MGI:2651379	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm1Bay</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8101543	20050808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179960	Gaa<sup>tm2Rabn</sup>	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3624423	Gaa<sup>tm2Rabn</sup>/Gaa<sup>tm2Rabn</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10838256	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4454324	Tg(Fabp4-LMNA*R482Q)17CCdl	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:5008441	Tg(Fabp4-LMNA*R482Q)17CCdl/0  [background:] FVB/N-Tg(Fabp4-LMNA*R482Q)17CCdl			ECO:0000033	author statement supported by traceable reference	PMID:19201734	20110622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857079	Enpp1<sup>ttw</sup>	is_implicated_in	DOID:1123	spondyloarthropathy		MGI:3606141	Enpp1<sup>ttw</sup>/Enpp1<sup>ttw</sup>  [background:] involves: ICR			ECO:0000033	author statement supported by traceable reference	PMID:7344126	20060731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3784503	Pparg<sup>tm2(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	is_implicated_in	DOID:0050440	familial partial lipodystrophy		MGI:3784504	Pparg<sup>tm3(tTA)Yba</sup>/Pparg<sup>+</sup>  [background:] involves: 129S1/SvImJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17921248	20080509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420395	Scn4a<sup>tm1Ljh</sup>/Scn4a<sup>+</sup>  [background:] B6.129S4-Scn4a<sup>tm1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420394	Scn4a<sup>tm1Ljh</sup>/Scn4a<sup>tm1Ljh</sup>  [background:] B6.129S4-Scn4a<sup>tm1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420396	Scn4a<sup>tm1.1Ljh</sup>/Scn4a<sup>+</sup>  [background:] B6.129S4-Scn4a<sup>tm1.1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	is_implicated_in	DOID:14451	hyperkalemic periodic paralysis		MGI:4420228	Scn4a<sup>tm1.1Ljh</sup>/Scn4a<sup>tm1.1Ljh</sup>  [background:] B6.129S4-Scn4a<sup>tm1.1Ljh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18317596	20100201	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2651859	Ush1c<sup>dfcr-2J</sup>	is_implicated_in	DOID:0110473	autosomal recessive nonsyndromic deafness 18A		MGI:2676317	Ush1c<sup>dfcr-2J</sup>/Ush1c<sup>dfcr-2J</sup>  [background:] B6;129S4			ECO:0000033	author statement supported by traceable reference	PMID:14519688	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153811	Fgfr2<sup>tm1.1Dsn</sup>	is_implicated_in	DOID:10486	intestinal atresia		MGI:2173367	Fgfr2<sup>tm1.1Dsn</sup>/Fgfr2<sup>tm1.1Dsn</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15234214	20170710	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418503	Notch3<sup>hpbk</sup>	is_implicated_in	DOID:0111035	CADASIL 1		MGI:4430347	Notch3<sup>hpbk</sup>/Notch3<sup>hpbk</sup>  [background:] C57BL/6J-Notch3<sup>hpbk</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:101850	Usp45	is_implicated_in	DOID:0081169	Leber congenital amaurosis 19		MGI:7329919	Usp45<sup>em1Qzha</sup>/Usp45<sup>em1Qzha</sup>  [background:] C57BL/6J-Usp45<sup>em1Qzha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30573563	20220921	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3034099	Ar<sup>tm1.1Verh</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:3036124	Ar<sup>tm1.1Verh</sup>/Y  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:14745012	20081106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	is_implicated_in	DOID:0111002	Joubert syndrome 7		MGI:3716631	Rpgrip1l<sup>tm1Urt</sup>/Rpgrip1l<sup>tm1Urt</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17558409	20150903	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2653132	Cdon<sup>tm2Rsk</sup>	is_implicated_in	DOID:0110877	holoprosencephaly 11		MGI:2653135	Cdon<sup>tm2Rsk</sup>/Cdon<sup>tm2Rsk</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12620190	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105091	E2f5	is_implicated_in	DOID:10908	hydrocephalus		MGI:3582637	E2f5<sup>tm1Dli</sup>/E2f5<sup>tm1Dli</sup>  [background:] either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:9553039	20170711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4127340	Epcam<sup>Gt(RST412)Byg</sup>	is_implicated_in	DOID:0060776	congenital diarrhea 5 with tufting enteropathy		MGI:5476929	Epcam<sup>Gt(RST412)Byg</sup>/Epcam<sup>Gt(RST412)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23209569	20130502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926386	Msx1<sup>tm1Rilm</sup>	is_implicated_in	DOID:0050591	tooth agenesis		MGI:2175120	Msx1<sup>tm1Rilm</sup>/Msx1<sup>tm1Rilm</sup>  [background:] either: (involves: 129S4/SvJae-Msx1<sup>tm1Rilm</sup>) or (involves: 129S4/SvJae * BALB/c) or (involves: 129X1/SvJae * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:7914451	20050624	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151805	Hoxd13<sup>tm1Mrc</sup>	is_implicated_in	DOID:0060242	synpolydactyly		MGI:3513188	Hoxd13<sup>tm1Mrc</sup>/Hoxd13<sup>tm1Mrc</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:8620844	20050912	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4380899	Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>	is_implicated_in	DOID:9268	glycine encephalopathy		MGI:5766287	Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>/Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>  [background:] B6.129P2-Gldc<sup>Gt(EUCG0001d02)Hmgu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25736695	20160503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4412032	Opa1<sup>M1Bewi</sup>	is_implicated_in	DOID:5723	optic atrophy		MGI:4412040	Opa1<sup>M1Bewi</sup>/Opa1<sup>+</sup>  [background:] involves: C3HeB/FeJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17314202	20091217	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177539	Cftr<sup>tm2Hgu</sup>	is_implicated_in	DOID:1485	cystic fibrosis		MGI:2177545	Cftr<sup>tm2Hgu</sup>/Cftr<sup>tm2Hgu</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11823443	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444576	Kif20b	is_implicated_in	DOID:10907	microcephaly		MGI:6095619	Kif20b<sup>magoo</sup>/Kif20b<sup>magoo</sup>  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28359322	20171207	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	is_implicated_in	DOID:0060263	porencephaly		MGI:3579768	Col4a1<sup>deltaex40</sup>/Col4a1<sup>+</sup>  [background:] B6.129S-Col4a1<sup>deltaex40</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15905400	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	is_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3815301	Tsc1<sup>tm1Djk</sup>/Tsc1<sup>tm1Djk</sup> Tg(Pax8-rtTA2S*M2)1Koes/0 Tg(tetO-cre)LC1Bjd/0  [background:] involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:18724376	20110502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103170	Gfi1	is_implicated_in	DOID:0050590	severe congenital neutropenia		MGI:5318525	Gfi1<sup>Gen</sup>/Gfi1<sup>+</sup>  [background:] C57BL/6J-Gfi1<sup>Gen</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22393124	20121114	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684436	Twist1<sup>Pas</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2684458	Twist1<sup>Pas</sup>/Twist1<sup>Pas</sup>  [background:] involves: C57BL/6 * PDT/Pas			ECO:0000033	author statement supported by traceable reference	PMID:14724733	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2684436	Twist1<sup>Pas</sup>	is_implicated_in	DOID:14768	Saethre-Chotzen syndrome		MGI:2684461	Twist1<sup>Pas</sup>/Twist1<sup>+</sup>  [background:] involves: C57BL/6 * PDT/Pas			ECO:0000033	author statement supported by traceable reference	PMID:14724733	20050609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387676	Clcn7<sup>tm2Tjj</sup>	is_implicated_in	DOID:0110944	autosomal recessive osteopetrosis 4		MGI:2680800	Clcn7<sup>tm2Tjj</sup>/Clcn7<sup>tm2Tjj</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11207362	20120117	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176611	Fhit<sup>tm1Hbn</sup>	is_implicated_in	DOID:0050465	Muir-Torre syndrome		MGI:3029765	Fhit<sup>tm1Hbn</sup>/Fhit<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10758156	20050622	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	is_implicated_in	DOID:5117	dermoid cyst of ovary		MGI:4949205	Foxo3<sup>mommeR1</sup>/Foxo3<sup>mommeR1</sup> Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew  [background:] FVB/NJ-Foxo3<sup>mommeR1</sup> Tg(HBA1-Gfp)1Ew			ECO:0000033	author statement supported by traceable reference	PMID:21347845	20110505	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	is_implicated_in	DOID:10591	pre-eclampsia		MGI:3576657	Ptgs1<sup>tm1Fun</sup>/Ptgs1<sup>tm1Fun</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15776109	20050512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3580679	Cox7a1<sup>tm1Hutt</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5465105	Cox7a1<sup>tm1Hutt</sup>/Cox7a1<sup>tm1Hutt</sup>  [background:] B6.129-Cox7a1<sup>tm1Hutt</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22119795	20170809	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3057337	Maoa<sup>K284stop</sup>	is_implicated_in	DOID:0060693	Brunner Syndrome		MGI:3798179	Maoa<sup>K284stop</sup>/Y  [background:] 129S6/SvEvTac-Maoa<sup>K284stop</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18418249	20080721	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	is_implicated_in	DOID:0050793	short QT syndrome		MGI:2652979	Kcnh2<sup>tm1Hjd</sup>/Kcnh2<sup>tm1Hjd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12612061	20060419	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915349	Cibar1	is_implicated_in	DOID:1148	polydactyly		MGI:5797530	Cibar1<sup>tm1b(KOMP)Wtsi</sup>/Cibar1<sup>tm1b(KOMP)Wtsi</sup>  [background:] C57BL/6N-Cibar1<sup>tm1b(KOMP)Wtsi</sup>/Wtsi			ECO:0000033	author statement supported by traceable reference	PMID:30395363	20190523	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1328317	Trex1	is_implicated_in	DOID:0050169	cutaneous lupus erythematosus		MGI:5925413	Trex1<sup>tm1Tld</sup>/Trex1<sup>tm1Tld</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28351661	20171121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	is_implicated_in	DOID:0080096	myofibrillar myopathy 5		MGI:5907165	Flnc<sup>tm1.1Rsdf</sup>/Flnc<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26472074	20170818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3848037	Lmna<sup>Dhe</sup>	is_implicated_in	DOID:10754	otitis media		MGI:4459466	Lmna<sup>Dhe</sup>/Lmna<sup>+</sup>  [background:] B6(D2)-Lmna<sup>Dhe</sup>/TyGrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:22819531	20180206	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153007	Eln<sup>tm1Dyl</sup>	is_implicated_in	DOID:62	aortic valve disease		MGI:5428443	Eln<sup>tm1Dyl</sup>/Eln<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22265892	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	is_implicated_in	DOID:11829	degenerative myopia		MGI:6199478	Foxg1<sup>tm1(cre)Skm</sup>/Foxg1<sup>+</sup> Lrp2<sup>tm1Tew</sup>/Lrp2<sup>tm1Tew</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26107939	20180925	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6400998	Nlgn1<sup>em1Taku</sup>/Nlgn1<sup>em1Taku</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28841651	20200323	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6400995	Nlgn1<sup>em1Taku</sup>/Nlgn1<sup>+</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28841651	20200323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3806463	Tg(H2-L-IL6)46Kish	is_implicated_in	DOID:3721	plasmacytoma		MGI:5301598	Tg(H2-L-IL6)46Kish/Tg(H2-L-IL6)46Kish  [background:] C.B6-Tg(H2-L-IL6)46Kish			ECO:0000033	author statement supported by traceable reference	PMID:11805288	20170728	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926387	Cdon	is_implicated_in	DOID:0110877	holoprosencephaly 11		MGI:2653134	Cdon<sup>tm1Rsk</sup>/Cdon<sup>tm1Rsk</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12620190	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1926387	Cdon	is_implicated_in	DOID:0110877	holoprosencephaly 11		MGI:2653135	Cdon<sup>tm2Rsk</sup>/Cdon<sup>tm2Rsk</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12620190	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:5911896	Src<sup>inl</sup>/Src<sup>inl</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:26464974	20171026	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3716562	Abca3<sup>tm1Holz</sup>	is_implicated_in	DOID:12120	pulmonary alveolar proteinosis		MGI:3717470	Abca3<sup>tm1Holz</sup>/Abca3<sup>tm1Holz</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17577581	20070807	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511965	Ddb2<sup>tm1Pra</sup>	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3512004	Ddb2<sup>tm1Pra</sup>/Ddb2<sup>tm1Pra</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15558025	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3511965	Ddb2<sup>tm1Pra</sup>	is_implicated_in	DOID:0110846	xeroderma pigmentosum group E		MGI:3512005	Ddb2<sup>tm1Pra</sup>/Ddb2<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15558025	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	is_implicated_in	DOID:9970	obesity		MGI:3639781	Npy1r<sup>tm1Tped</sup>/Npy1r<sup>tm1Tped</sup>  [background:] B6.129P2-Npy1r<sup>tm1Tped</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14525913	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720795	Tg(Ckm-APPSw)A2Lfa	is_implicated_in	DOID:3429	inclusion body myositis		MGI:3720803	Tg(Ckm-APPSw)A2Lfa/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:11972038	20070914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3040696	Prex1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3717173	Prex1<sup>tm1Hcew</sup>/Prex1<sup>tm1Hcew</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26621702	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	is_implicated_in	DOID:3762	cytochrome-c oxidase deficiency disease		MGI:4413664	Sco2<sup>tm1.1Easc</sup>/Sco2<sup>tm2.1Easc</sup>  [background:] 129X1/SvJ-Sco2<sup>tm1.1Easc</sup>/Sco2<sup>tm2.1Easc</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19837698	20091229	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3850014	Sost<sup>tm1Paz</sup>	is_implicated_in	DOID:0060756	sclerosteosis 1		MGI:3850032	Sost<sup>tm1Paz</sup>/Sost<sup>tm1Paz</sup>  [background:] involves: 129/Sv * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:24225945	20150422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045266	Fan1	is_implicated_in	DOID:0060911	karyomegalic interstitial nephritis		MGI:5897864	Fan1<sup>tm1d(KOMP)Wtsi</sup>/Fan1<sup>tm1d(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26980189	20190307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045266	Fan1	is_implicated_in	DOID:0060911	karyomegalic interstitial nephritis		MGI:6281646	Fan1<sup>tm1a(KOMP)Wtsi</sup>/Fan1<sup>tm1a(KOMP)Wtsi</sup>  [background:] 129S1.B6-Fan1<sup>tm1a(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27026368	20190307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3045266	Fan1	is_implicated_in	DOID:0060911	karyomegalic interstitial nephritis		MGI:5897798	Fan1<sup>tm1.1Jrou</sup>/Fan1<sup>tm1.1Jrou</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:26980188	20190307	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915220	Slx1b	is_implicated_in	DOID:0090066	Fanconi-like syndrome		MGI:5559491	Slx1b<sup>tm1.1Jrou</sup>/Slx1b<sup>tm1.1Jrou</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24076219	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346542	Bace1	is_implicated_in	DOID:5419	schizophrenia		MGI:3720943	Bace1<sup>tm1Pcw</sup>/Bace1<sup>tm1Pcw</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18385378	20161101	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1353609	Zbtb18	is_implicated_in	DOID:0060307	autosomal dominant intellectual developmental disorder		MGI:5425229	Zbtb18<sup>tm1.1Nda</sup>/Zbtb18<sup>tm1.1Nda</sup> Tg(Nes-cre)1Kln/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:22095278	20120620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	is_implicated_in	DOID:4480	achondroplasia		MGI:3694235	Acan<sup>cmd</sup>/Acan<sup>cmd</sup>  [background:] involves: STOCK T t<sup>low</sup> Itpr3<sup>tf</sup>			ECO:0000033	author statement supported by traceable reference	PMID:632744	20070122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	is_implicated_in	DOID:4480	achondroplasia		MGI:3694235	Acan<sup>cmd</sup>/Acan<sup>cmd</sup>  [background:] involves: STOCK T t<sup>low</sup> Itpr3<sup>tf</sup>			ECO:0000033	author statement supported by traceable reference	MGI:78375	20070122	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:108074	Sptlc2	is_implicated_in	DOID:8893	psoriasis		MGI:5563659	Sptlc2<sup>tm1Yhir</sup>/Sptlc2<sup>tm1Yhir</sup> Tg(KRT5-cre)1Tak/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23633022	20140515	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276121	Bckdk	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5829468	Bckdk<sup>Gt(OST79912)Lex</sup>/Bckdk<sup>Gt(OST79912)Lex</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:27912058	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106403	Spg21	is_implicated_in	DOID:0060245	Mast syndrome		MGI:6508400	Spg21<sup>tm1Mchan</sup>/Spg21<sup>tm1Mchan</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:20661613	20210302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:105942	Hcfc1	is_implicated_in	DOID:0111814	methylmalonic acidemia and homocysteinemia cblX type		MGI:6860681	Hcfc1<sup>em1Poche</sup>/Y  [background:] C57BL/6J-Hcfc1<sup>em1Poche</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35013307	20220131	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	is_implicated_in	DOID:0060900	Parkinson's disease 14		MGI:6849976	Pla2g6<sup>tm1.1Hlw</sup>/Pla2g6<sup>tm1.1Hlw</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:30088174	20220107	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97742	Pomc	is_implicated_in	DOID:9970	obesity		MGI:3041643	Pomc<sup>tm1Sora</sup>/Pomc<sup>tm1Sora</sup>  [background:] involves: 129S2/SvHsd * 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:15070780	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039283	Sell<sup>tm1Flv</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039437	Sell<sup>tm1Flv</sup>/Sell<sup>+</sup>  [background:] NOD.Cg-Sell<sup>tm1Flv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039283	Sell<sup>tm1Flv</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039435	Sell<sup>tm1Flv</sup>/Sell<sup>tm1Flv</sup>  [background:] NOD.Cg-Sell<sup>tm1Flv</sup>			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039283	Sell<sup>tm1Flv</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039428	Sell<sup>tm1Flv</sup>/Sell<sup>tm1Flv</sup>  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3039283	Sell<sup>tm1Flv</sup>	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3039434	Sell<sup>tm1Flv</sup>/Sell<sup>+</sup>  [background:] involves: C57BL/6 * NOD			ECO:0000033	author statement supported by traceable reference	PMID:14734611	20060530	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3871767	Aebp2<sup>Gt(BC0681)Wtsi</sup>	is_implicated_in	DOID:9258	Waardenburg syndrome		MGI:5296959	Aebp2<sup>Gt(BC0681)Wtsi</sup>/Aebp2<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21949878	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5829832	Nkx2-5<sup>tm2.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm2.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5882084	Nkx2-5<sup>tm3.1Mwc</sup>/Nkx2-5<sup>+</sup>  [background:] B6J.Cg-Nkx2-5<sup>tm3.1Mwc</sup>/Mwc			ECO:0000033	author statement supported by traceable reference	PMID:28352650	20170329	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	is_implicated_in	DOID:0060854	autosomal recessive pseudohypoaldosteronism type 1		MGI:2181800	Scnn1b<sup>tm1Wsh</sup>/Scnn1b<sup>tm1Wsh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9990092	20060201	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95622	Gabrd	is_implicated_in	DOID:9478	postpartum depression		MGI:3713529	Gabrd<sup>tm1Geh</sup>/Gabrd<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18667149	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	is_implicated_in	DOID:0060334	transient neonatal diabetes mellitus		MGI:2446456	Abcc8<sup>tm1Jbry</sup>/Abcc8<sup>tm1Jbry</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10734066	20130415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2140361	Slc35d1	is_implicated_in	DOID:0050775	schneckenbecken dysplasia		MGI:3812126	Slc35d1<sup>tm1Hko</sup>/Slc35d1<sup>tm1Hko</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:17952091	20081027	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2655186	Tlx2<sup>tm1Sjk</sup>	is_implicated_in	DOID:0080072	intestinal pseudo-obstruction		MGI:2655191	Tlx2<sup>tm1Sjk</sup>/Tlx2<sup>tm1Sjk</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9176491	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	is_implicated_in	DOID:0110334	osteogenesis imperfecta type 1		MGI:3620112	Col1a1<sup>Mov13</sup>/Col1a1<sup>+</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:2402497	20060421	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4430585	Fa2h<sup>tm1.1Hama</sup>	is_implicated_in	DOID:0110786	hereditary spastic paraplegia 35		MGI:4999603	Fa2h<sup>tm1.1Hama</sup>/Fa2h<sup>tm1.1Hama</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21491498	20110523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662140	Mitf<sup>Mi-Crc</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662140	Mitf<sup>Mi-Crc</sup>	is_implicated_in	DOID:0090100	ocular albinism with sensorineural deafness		MGI:2662973	Mitf<sup>Mi-Crc</sup>/Mitf<sup>+</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2176270	Pou4f3<sup>tm1Rsd</sup>	is_not_implicated_in	DOID:0110546	autosomal dominant nonsyndromic deafness 15		MGI:3688923	Pou4f3<sup>tm1Rsd</sup>/Pou4f3<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10452377	20061129	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2684868	Zfp469	is_implicated_in	DOID:14775	brittle cornea syndrome 1		MGI:6765943	Zfp469<sup>em1Chms</sup>/Zfp469<sup>em1Chms</sup>  [background:] C57BL/6J-Zfp469<sup>em1Chms</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34368841	20211007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857765	Parp1<sup>tm1Hsmm</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623976	Parp1<sup>tm1Hsmm</sup>/Parp1<sup>tm1Hsmm</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:10051636	20060606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	is_implicated_in	DOID:8398	osteoarthritis		MGI:5642218	Bmp7<sup>tm1.1Dgra</sup>/Bmp7<sup>tm1.1Dgra</sup> Tg(Prrx1-cre)1Cjt/0  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * SJL/J			ECO:0000033	author statement supported by traceable reference	PMID:25889639	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156168	Adamts1<sup>tm1Hku</sup>	is_implicated_in	DOID:5200	urinary tract obstruction		MGI:2450509	Adamts1<sup>tm1Hku</sup>/Adamts1<sup>tm1Hku</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10811842	20170614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861699	Htt<sup>tm3Mem</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698276	Htt<sup>tm3Mem</sup>/Htt<sup>tm3Mem</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15935052	20070301	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861699	Htt<sup>tm3Mem</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:3698002	Htt<sup>tm3Mem</sup>/Htt<sup>tm3Mem</sup>  [background:] involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:9398841	20070301	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	is_implicated_in	DOID:9778	irritable bowel syndrome		MGI:6297092	Mlxipl<sup>tm1Kuy</sup>/Mlxipl<sup>tm1Kuy</sup>  [background:] B6.129S6-Mlxipl<sup>tm1Kuy</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:29669261	20190510	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3525118	Tg(Dct-Grm1)ESzc	is_implicated_in	DOID:6039	uveal melanoma		MGI:5803980	Tg(Dct-Grm1)ESzc/0  [background:] C57BL/6J-Tg(Dct-Grm1)ESzc			ECO:0000033	author statement supported by traceable reference	PMID:25051141	20161018	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924407	Dpcd	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:4950027	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>/Dpcd/Poll<sup>Gt(OST280355)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd			ECO:0000033	author statement supported by traceable reference	PMID:20080492	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3055491	Bbs1<sup>Gt1Nk</sup>	is_implicated_in	DOID:9970	obesity		MGI:3055584	Bbs1<sup>Gt1Nk</sup>/Bbs1<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20100603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916142	Urah	is_implicated_in	DOID:1920	hyperuricemia		MGI:4836356	Urah<sup>plt2</sup>/Urah<sup>plt2</sup>  [background:] C57BL/6-Urah<sup>plt2</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30383838	20220415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384871	Slc24a1	is_implicated_in	DOID:0110868	congenital stationary night blindness 1D		MGI:5766543	Slc24a1<sup>tm1Xen</sup>/Slc24a1<sup>tm1Xen</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26246500	20160505	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387667	Fzd4<sup>tm1Nat</sup>	is_implicated_in	DOID:0060844	Norrie disease		MGI:3622318	Fzd4<sup>tm1Nat</sup>/Fzd4<sup>tm1Nat</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15035989	20060515	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3043871	Mlxipl<sup>tm1Kuy</sup>	is_implicated_in	DOID:9778	irritable bowel syndrome		MGI:6297092	Mlxipl<sup>tm1Kuy</sup>/Mlxipl<sup>tm1Kuy</sup>  [background:] B6.129S6-Mlxipl<sup>tm1Kuy</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:29669261	20190510	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99673	Adcy5	is_implicated_in	DOID:14330	Parkinson's disease		MGI:2662300	Adcy5<sup>tm1Yish</sup>/Adcy5<sup>tm1Yish</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12665504	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449175	Dkc1<sup>tm1Ppp</sup>	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:2661986	Dkc1<sup>tm1Ppp</sup>/Y  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12522253	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449175	Dkc1<sup>tm1Ppp</sup>	is_implicated_in	DOID:2729	dyskeratosis congenita		MGI:2654712	Dkc1<sup>tm1Ppp</sup>/Dkc1<sup>+</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:12522253	20050616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444354	Arid4a	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3817454	Arid4a<sup>tm1Alb</sup>/Arid4a<sup>tm1Alb</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:18728284	20081121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3609880	Lamc2<sup>jeb</sup>	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:4440827	Lamc2<sup>jeb</sup>/Lamc2<sup>jeb</sup>  [background:] 129X1/SvJ-Lamc2<sup>jeb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20336083	20100420	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385823	Mthfr<sup>tm1Rzn</sup>	is_implicated_in	DOID:0080074	neural tube defect		MGI:3574961	Mthfr<sup>tm1Rzn</sup>/Mthfr<sup>tm1Rzn</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11181567	20050627	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2153072	Trim37	is_implicated_in	DOID:0050436	mulibrey nanism		MGI:5789948	Trim37<sup>Gt(RRO307)Byg</sup>/Trim37<sup>Gt(RRO307)Byg</sup>  [background:] B6J.129P2-Trim37<sup>Gt(RRO307)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27044324	20160826	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3640602	Tg(Myh6-Pfkfb3)7Pne	is_implicated_in	DOID:3978	extrinsic cardiomyopathy		MGI:3640608	Tg(Myh6-Pfkfb3)7Pne/0  [background:] FVB-Tg(Myh6-Pfkfb3)7Pne			ECO:0000033	author statement supported by traceable reference	PMID:15331593	20170602	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522021	Ptpn11<sup>tm1Gsf</sup>	is_implicated_in	DOID:0050868	hepatocellular adenoma		MGI:5009546	Ptpn11<sup>tm1Gsf</sup>/Ptpn11<sup>tm1Gsf</sup> Speer6-ps1<sup>Tg(Alb-cre)21Mgn</sup>/Speer6-ps1<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:21575863	20170626	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95389	En1	is_implicated_in	DOID:14330	Parkinson's disease		MGI:5604280	En1<sup>tm2Alj</sup>/En1<sup>+</sup> Tg(Th-EGFP)6-7Okn/?  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J * OF1			ECO:0000033	author statement supported by traceable reference	PMID:25281317	20141113	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183944	Ercc1<sup>tm1Jhjh</sup>	is_implicated_in	DOID:0060590	XFE progeroid syndrome		MGI:3804449	Ercc1<sup>tm1Jhjh</sup>/Ercc1<sup>tm1Jhjh</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17183314	20080904	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	is_implicated_in	DOID:6419	tetralogy of Fallot		MGI:4822147	Mks1<sup>avc6</sup>/Mks1<sup>avc6</sup>  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20101008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915775	Evc2	is_implicated_in	DOID:12714	Ellis-Van Creveld syndrome		MGI:5697977	Evc2<sup>tm1.1Mis</sup>/Evc2<sup>tm1.1Mis</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:26219237	20151204	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	is_implicated_in	DOID:0081337	congenital myopathy		MGI:2652059	Ldb3<sup>tm1Chen</sup>/Ldb3<sup>tm1Chen</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:11696561	20230605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	is_implicated_in	DOID:12134	factor VIII deficiency		MGI:2449544	F8<sup>tm1Kaz</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7647782	20200113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	is_implicated_in	DOID:12134	factor VIII deficiency		MGI:2449546	F8<sup>tm2Kaz</sup>/Y  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7647782	20200113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	is_implicated_in	DOID:14705	Pfeiffer syndrome		MGI:2176483	Fgfr2<sup>tm2.3Dsn</sup>/Fgfr2<sup>+</sup>  [background:] involves: 129 * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:11274405	20080121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97542	Pepd	is_implicated_in	DOID:11984	hypertrophic cardiomyopathy		MGI:5604775	Pepd<sup>dal</sup>/Pepd<sup>dal</sup>  [background:] involves: C3H/HeJ * CBA/J			ECO:0000033	author statement supported by traceable reference	PMID:21472842	20170711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1350341	Sgsh	is_implicated_in	DOID:12801	mucopolysaccharidosis III		MGI:3037061	Sgsh<sup>mps3a</sup>/Sgsh<sup>mps3a</sup>  [background:] involves: 129X1/SvJ * CD-1 * C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10561464	20050610	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96305	Iac	is_implicated_in	DOID:83	cataract		MGI:2175073	Iac/Iac<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3588207	Dnaaf3	is_implicated_in	DOID:0110626	primary ciliary dyskinesia 2		MGI:5442143	Dnaaf3<sup>b2b1739Clo</sup>/Dnaaf3<sup>b2b1739Clo</sup>  [background:] C57BL/6J-Dnaaf3<sup>b2b1739Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20141212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2664869	Men1<sup>tm1Zqw</sup>	is_implicated_in	DOID:6255	growth hormone secreting pituitary adenoma		MGI:5009321	Men1<sup>tm1Zqw</sup>/Men1<sup>+</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:12819299	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2153002	Dcn<sup>tm1Ioz</sup>	is_implicated_in	DOID:13359	Ehlers-Danlos syndrome		MGI:3530609	Dcn<sup>tm1Ioz</sup>/Dcn<sup>tm1Ioz</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:9024701	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	is_implicated_in	DOID:13223	uterine fibroid		MGI:5641710	Tsc2<sup>tm1.1Mjg</sup>/Tsc2<sup>tm1.1Mjg</sup> Pgr<sup>tm2(cre)Lyd</sup>/Pgr<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:23820898	20150624	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095438	Slc2a2	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:3029380	Slc2a2<sup>tm1Thor</sup>/Slc2a2<sup>tm1Thor</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9354799	20061012	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821974	Snap25<sup>tm1.1Bark</sup>	is_implicated_in	DOID:9970	obesity		MGI:5766495	Snap25<sup>tm1.1Bark</sup>/Snap25<sup>tm1.1Bark</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26195742	20160504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1889336	Adck2	is_implicated_in	DOID:699	mitochondrial myopathy		MGI:6377285	Adck2<sup>tm1(KOMP)Vlcg</sup>/Adck2<sup>+</sup>  [background:] C57BL/6-Adck2<sup>tm1(KOMP)Vlcg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31480808	20191118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	is_not_implicated_in	DOID:0110408	retinitis pigmentosa 11		MGI:4438627	Prpf31<sup>tm1Bha</sup>/Prpf31<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19578015	20100405	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	is_implicated_in	DOID:11049	meconium aspiration syndrome		MGI:3842387	Atf2<sup>tm1Sis</sup>/Atf2<sup>tm1Sis</sup>  [background:] either: (involves: C57BL/6 * CBA) or (involves: BALB/c * C57BL/6 * CBA) or (involves: C57BL/6 * CBA * ICR)			ECO:0000033	author statement supported by traceable reference	PMID:10364225	20170616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1916052	Mypn	is_implicated_in	DOID:397	restrictive cardiomyopathy		MGI:5910329	Mypn<sup>tm1.1Epu</sup>/Mypn<sup>+</sup>  [background:] either: (involves: 129S6/SvEv) or (involves: 129S6/SvEv * C57BL/6NCrl)			ECO:0000033	author statement supported by traceable reference	PMID:25541130	20170926	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:11054	urinary bladder cancer		MGI:5004866	Pten<sup>tm2Mak</sup>/Pten<sup>tm2Mak</sup> Tg(Fabp1-cre)1Jig/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:16951148	20110608	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3664756	Pkhd1<sup>tm1Rbu</sup>	is_not_implicated_in	DOID:0110861	autosomal recessive polycystic kidney disease		MGI:3702089	Pkhd1<sup>tm1Rbu</sup>/Pkhd1<sup>tm1Rbu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15830394	20070410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	is_implicated_in	DOID:5419	schizophrenia		MGI:6810192	Ppara<sup>em1Tyrb</sup>/Ppara<sup>em1Tyrb</sup>  [background:] C57BL/6J-Ppara<sup>em1Tyrb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:33279456	20211115	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931327	Nr3c1<sup>tm2Gsc</sup>	is_implicated_in	DOID:446	primary hyperaldosteronism		MGI:2176972	Nr3c1<sup>tm2Gsc</sup>/Nr3c1<sup>tm2Gsc</sup> Tg(Nes-cre)1Kln/0  [background:] involves: 129P2/OlaHsd * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:10471508	20171210	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	is_implicated_in	DOID:9970	obesity		MGI:3055585	Bbs4<sup>Gt1Nk</sup>/Bbs4<sup>Gt1Nk</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15322545	20100603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158398	Apoe<sup>tm3(APOE*4)Mae</sup>	is_implicated_in	DOID:0110014	age related macular degeneration 1		MGI:4355227	Apoe<sup>tm3(APOE*4)Mae</sup>/Apoe<sup>tm3(APOE*4)Mae</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16079201	20110906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155916	Abcc9<sup>tm1Cfb</sup>	is_implicated_in	DOID:3393	coronary artery disease		MGI:3622096	Abcc9<sup>tm1Cfb</sup>/Abcc9<sup>tm1Cfb</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:12122112	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136643	Irs1<sup>tm1Tka</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:2174965	Irs1<sup>tm1Tka</sup>/Irs1<sup>tm1Tka</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:7969452	20050811	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3583930	Polh<sup>tm1Fmh</sup>	is_implicated_in	DOID:0110847	xeroderma pigmentosum variant type		MGI:3586812	Polh<sup>tm1Fmh</sup>/Polh<sup>tm1Fmh</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15939880	20050907	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	is_implicated_in	DOID:0080093	myofibrillar myopathy 2		MGI:4999584	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21445271	20110523	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	is_implicated_in	DOID:0080093	myofibrillar myopathy 2		MGI:4999583	Cryab<sup>tm1.1Ady</sup>/Cryab<sup>tm1.1Ady</sup>  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21445271	20110523	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671784	Zfp423<sup>nur12</sup>	is_implicated_in	DOID:2786	cerebellar disease		MGI:3693287	Zfp423<sup>nur12</sup>/Zfp423<sup>nur12</sup>  [background:] involves: BALB/c * C57BL/6 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:17151198	20170705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2442071	Gprasp2	is_implicated_in	DOID:1059	intellectual disability		MGI:6287871	Gprasp2<sup>tm1.1Jpe</sup>/Y  [background:] B6.129(FVB)-Gprasp2<sup>tm1.1Jpe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30926797	20190419	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387573	Kif1b<sup>tm1Noh</sup>	is_implicated_in	DOID:0110154	Charcot-Marie-Tooth disease type 2A1		MGI:2387931	Kif1b<sup>tm1Noh</sup>/Kif1b<sup>+</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11389829	20050706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5433393	b2b1163Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5433487	b2b1163Clo/b2b1163Clo  [background:] C57BL/6J-b2b1163Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	is_implicated_in	DOID:0060582	Noonan syndrome 4		MGI:5000309	Sos1<sup>tm1.2Rak</sup>/Sos1<sup>tm1.2Rak</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21041952	20130308	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	is_implicated_in	DOID:0060582	Noonan syndrome 4		MGI:5000310	Sos1<sup>tm1.2Rak</sup>/Sos1<sup>+</sup>  [background:] involves: 129S/Sv * C57BL/6 * FVB/N * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21041952	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387501	Zeb2<sup>tm1.2Yhi</sup>	is_not_implicated_in	DOID:0060485	Mowat-Wilson syndrome		MGI:3624727	Zeb2<sup>tm1.2Yhi</sup>/Zeb2<sup>+</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12522767	20060619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2447863	Gjb6<sup>tm1Kwi</sup>	is_implicated_in	DOID:0110475	autosomal recessive nonsyndromic deafness 1A		MGI:3037831	Gjb6<sup>tm1Kwi</sup>/Gjb6<sup>tm1Kwi</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12490528	20051005	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	is_not_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:4438459	Col8a2<sup>Aca23</sup>/Col8a2<sup>+</sup>  [background:] C57BL/6J-Col8a2<sup>Aca23</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19578028	20100401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	is_not_implicated_in	DOID:11555	Fuchs' endothelial dystrophy		MGI:4438460	Col8a2<sup>Aca23</sup>/Col8a2<sup>Aca23</sup>  [background:] C57BL/6J-Col8a2<sup>Aca23</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19578028	20100401	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2671284	l11Jus16	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:4822146	l11Jus16/l11Jus16  [background:] involves: C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20511334	20110808	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3621984	Alms1<sup>foz</sup>	is_implicated_in	DOID:0050473	Alstrom syndrome		MGI:3622093	Alms1<sup>foz</sup>/Alms1<sup>foz</sup>  [background:] involves: NOD			ECO:0000033	author statement supported by traceable reference	PMID:16516152	20060606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861930	Gm2a<sup>tm1Rlp</sup>	is_implicated_in	DOID:4795	GM2 gangliosidosis, AB variant		MGI:2176850	Gm2a<sup>tm1Rlp</sup>/Gm2a<sup>tm1Rlp</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9223328	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	is_implicated_in	DOID:12712	nephronophthisis		MGI:3703807	Wwtr1<sup>tm1Whun</sup>/Wwtr1<sup>tm1Whun</sup>  [background:] either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:17251353	20170707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1919680	B4gat1	is_implicated_in	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1		MGI:5471464	B4gat1<sup>m1Ddg</sup>/B4gat1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C3H/He * C57BL/6 * C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:23217742	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4420297	Hepacam<sup>tm1Vlcg</sup>	is_implicated_in	DOID:0080315	megalencephalic leukoencephalopathy with subcortical cysts		MGI:6287231	Hepacam<sup>tm1Vlcg</sup>/Hepacam<sup>tm1Vlcg</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:28695146	20190412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522330	pta	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:3522704	pta/pta  [background:] C57BL/6J-pta			ECO:0000033	author statement supported by traceable reference	PMID:15548583	20101008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914947	Gadd45gip1	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5637560	Gadd45gip1<sup>tm2Kong</sup>/Gadd45gip1<sup>tm2Kong</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:25660120	20150528	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3576051	Alms1<sup>Gt(XH152)Byg</sup>	is_implicated_in	DOID:9970	obesity		MGI:3589409	Alms1<sup>Gt(XH152)Byg</sup>/Alms1<sup>Gt(XH152)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16000322	20100603	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183547	Tymp<sup>tm1Akiy</sup>	is_not_implicated_in	DOID:0080119	mitochondrial DNA depletion syndrome 1		MGI:3699315	Tymp<sup>tm1Akiy</sup>/Tymp<sup>tm1Akiy</sup>  [background:] involves: 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12077348	20070309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2151686	Hoxa1<sup>tm3.1Mrc</sup>	is_implicated_in	DOID:0050682	Athabaskan brainstem dysgenesis syndrome		MGI:3773293	Hoxa1<sup>tm3.1Mrc</sup>/Hoxa1<sup>tm3.1Mrc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21940751	20120408	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856330	Dmd<sup>mdx-3Cv</sup>	is_implicated_in	DOID:9883	Becker muscular dystrophy		MGI:3798606	Dmd<sup>mdx-3Cv</sup>/Y  [background:] involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus			ECO:0000033	author statement supported by traceable reference	PMID:7843915	20090929	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4329457	Prpf3<sup>Gt(RRO284)Byg</sup>	is_not_implicated_in	DOID:0110356	retinitis pigmentosa 18		MGI:3820247	Prpf3<sup>Gt(RRO284)Byg</sup>/Prpf3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18552388	20081217	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5285350	Bicc1<sup>b2b222Clo</sup>/Bicc1<sup>b2b222Clo</sup>  [background:] C57BL/6J-Bicc1<sup>b2b222Clo</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	is_implicated_in	DOID:14219	renal tubular acidosis		MGI:2672144	Slc4a1<sup>tm1Llp</sup>/Slc4a1<sup>tm1Llp</sup>  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17409310	20090514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	is_implicated_in	DOID:9970	obesity		MGI:3840234	Kdm3a<sup>tm1.1Yzha</sup>/Kdm3a<sup>tm1.1Yzha</sup>  [background:] B6.129P2-Kdm3a<sup>tm1.1Yzha</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19194461	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3574400	Igh<sup>tm1(Myc)Janz</sup>	is_implicated_in	DOID:8584	Burkitt lymphoma		MGI:3575899	Igh<sup>tm1(Myc)Janz</sup>/Igh<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15735016	20050525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98824	Trhr	is_implicated_in	DOID:0050328	congenital hypothyroidism		MGI:5637537	Trhr<sup>tm1Bau</sup>/Trhr<sup>tm1Bau</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:25490146	20170627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3690009	Tg(Myh6-TNNI3*G203S)1Chs	is_implicated_in	DOID:0110313	hypertrophic cardiomyopathy 7		MGI:3690017	Tg(Myh6-TNNI3*G203S)1Chs/0  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:16950368	20170818	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387501	Zeb2<sup>tm1.2Yhi</sup>	is_implicated_in	DOID:0060485	Mowat-Wilson syndrome		MGI:3624726	Zeb2<sup>tm1.2Yhi</sup>/Zeb2<sup>tm1.2Yhi</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:12522767	20060619	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182323	Cyp27b1<sup>tm1Dgo</sup>	is_implicated_in	DOID:10609	rickets		MGI:2658930	Cyp27b1<sup>tm1Dgo</sup>/Cyp27b1<sup>tm1Dgo</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:11416220	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3056186	Tg(Myh6-Ppp3ca)37Eno	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:3056188	Tg(Myh6-Ppp3ca)37Eno/0  [background:] involves: FVB			ECO:0000033	author statement supported by traceable reference	PMID:9568714	20170731	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2178103	Arhgdia	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3614391	Arhgdia<sup>tm1Ytk</sup>/Arhgdia<sup>tm1Ytk</sup>  [background:] involves: 129S/SvEv * C57BL/6 * DBA			ECO:0000033	author statement supported by traceable reference	PMID:10498891	20060302	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1931295	Rab27b	is_implicated_in	DOID:2223	platelet storage pool deficiency		MGI:3711073	Rab27b<sup>tm1.2Seab</sup>/Rab27b<sup>tm1.2Seab</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17384153	20070605	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2135756	Hspb8	is_implicated_in	DOID:0111208	obsolete distal hereditary motor neuronopathy type 2A		MGI:6392628	Hspb8<sup>tm1Vti</sup>/Hspb8<sup>tm1Vti</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl			ECO:0000033	author statement supported by traceable reference	PMID:28780615	20200303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1347355	Slc7a11	is_implicated_in	DOID:3753	Hermansky-Pudlak syndrome		MGI:2677961	Slc7a11<sup>sut</sup>/Slc7a11<sup>sut</sup>  [background:] C3H/HeSnJ-Slc7a11<sup>sut</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:8699821	20170705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429315	Lpl<sup>tm1Sem</sup>	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651821	Lpl<sup>tm1Sem</sup>/Lpl<sup>tm1Sem</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7759497	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429315	Lpl<sup>tm1Sem</sup>	is_implicated_in	DOID:14118	familial lipoprotein lipase deficiency		MGI:2651823	Lpl<sup>tm1Sem</sup>/Lpl<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:7759497	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385806	Tg(Cyp19)C2-3Rrte	is_implicated_in	DOID:0090122	aromatase excess syndrome		MGI:3587647	Tg(Cyp19)C2-3Rrte/0  [background:] involves: BALB/c * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11358670	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3040688	Slc7a14	is_implicated_in	DOID:1432	blindness		MGI:7277716	Slc7a14<sup>em1Jin</sup>/Slc7a14<sup>em1Jin</sup>  [background:] C57BL/6J-Slc7a14<sup>em1Jin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:35394837	20220513	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109172	Dspp	is_implicated_in	DOID:3388	periodontal disease		MGI:5911481	Dspp<sup>tm1Kul</sup>/Dspp<sup>tm1Kul</sup>  [background:] B6;129-Dspp<sup>tm1Kul</sup>/Mmnc			ECO:0000033	author statement supported by traceable reference	PMID:22934831	20171013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:5524134	Fat1<sup>Gt(KST249)Byg</sup>/Fat1<sup>Gt(KST249)Byg</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:5524136	Fat1<sup>tm1Fhel</sup>/Fat1<sup>tm1Fhel</sup> Pax3<sup>tm1(cre)Joe</sup>/Pax3<sup>+</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	is_implicated_in	DOID:11727	facioscapulohumeral muscular dystrophy		MGI:5524138	Fat1<sup>tm1.2Fhel</sup>/Fat1<sup>tm1.2Fhel</sup> Tg(Myl1-lacZ)1Ibdml/0  [background:] involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:23785297	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384015	F11<sup>tm1Gjb</sup>	is_implicated_in	DOID:2229	factor XI deficiency		MGI:3665566	F11<sup>tm1Gjb</sup>/F11<sup>tm1Gjb</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9518045	20151119	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	is_implicated_in	DOID:0050120	hemophagocytic lymphohistiocytosis		MGI:3835654	Elp1<sup>Gt(BGB184)Byg</sup>/Elp1<sup>Gt(BGB184)Byg</sup>  [background:] B6.129P2-<sup>Gt(BGB184)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19015235	20170601	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3893603	Ccdc66<sup>Gt(E021F10)Wrst</sup>	is_implicated_in	DOID:10584	retinitis pigmentosa		MGI:5285951	Ccdc66<sup>Gt(E021F10)Wrst</sup>/Ccdc66<sup>Gt(E021F10)Wrst</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:21680557	20110920	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931885	Cdk5r1<sup>tm1Lht</sup>	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:3721424	Cdk5r1<sup>tm1Lht</sup>/Cdk5r1<sup>tm1Lht</sup>  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:20832057	20150225	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928323	Nisch	is_implicated_in	DOID:10754	otitis media		MGI:6101180	Nisch<sup>edsn</sup>/Nisch<sup>edsn</sup>  [background:] C3H.B6-Nisch<sup>edsn</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28806779	20171218	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858416	Stk39	is_implicated_in	DOID:4479	pseudohypoaldosteronism		MGI:6423631	Stk39<sup>tm1Pawe</sup>/Stk39<sup>tm1Pawe</sup> Pvalb<sup>tm1(cre)Arbr</sup>/Pvalb<sup>+</sup>  [background:] B6.129-Stk39<sup>tm1Pawe</sup> Pvalb<sup>tm1(cre)Arbr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28442491	20200521	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821884	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis	is_implicated_in	DOID:674	cleft palate		MGI:7461096	Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0 Tg(KRT14-cre)1Amc/0  [background:] involves: C57BL/6 * CBA * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:26116174	20230411	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3052548	Tg(H2-Ea<sup>d</sup>)5Lt	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3618814	Tg(H2-Ea<sup>d</sup>)5Lt/0  [background:] NOD/ShiLt-Tg(H2-Ea<sup>d</sup>)5Lt			ECO:0000033	author statement supported by traceable reference	PMID:8757636	20060526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3029503	Foxl2<sup>tm1Tre</sup>	is_implicated_in	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome		MGI:3029674	Foxl2<sup>tm1Tre</sup>/Foxl2<sup>tm1Tre</sup>  [background:] involves: 129P2/OlaHsd * Black Swiss * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:14736745	20071022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2682641	Slc4a7<sup>tm1Krtz</sup>	is_implicated_in	DOID:0110839	Usher syndrome type 2C		MGI:2682644	Slc4a7<sup>tm1Krtz</sup>/Slc4a7<sup>tm1Krtz</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12808454	20061219	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3812434	Gan<sup>tm1Jpj</sup>	is_implicated_in	DOID:0090068	giant axonal neuropathy 1		MGI:3812458	Gan<sup>tm1Jpj</sup>/Gan<sup>tm1Jpj</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18680552	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2654419	Mybpc3<sup>tm1Jse</sup>	is_implicated_in	DOID:0110310	hypertrophic cardiomyopathy 4		MGI:2654421	Mybpc3<sup>tm1Jse</sup>/Mybpc3<sup>tm1Jse</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10545522	20060609	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	is_implicated_in	DOID:289	endometriosis		MGI:4836591	Kras<sup>tm4Tyj</sup>/Kras<sup>+</sup>  [background:] either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C3H/HeJ)			ECO:0000033	author statement supported by traceable reference	PMID:15619626	20101028	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313302	Cenpf	is_not_implicated_in	DOID:0110595	Stromme syndrome		MGI:6287445	Cenpf<sup>em3Bko</sup>/Cenpf<sup>em3Bko</sup>  [background:] involves: C57BL/6 * C57BL/6NTac * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:30856164	20190415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917488	Rnf168	is_implicated_in	DOID:0090113	RIDDLE syndrome		MGI:5505901	Rnf168<sup>Gt(405F11)Cmhd</sup>/Rnf168<sup>Gt(405F11)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21552324	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917488	Rnf168	is_implicated_in	DOID:0090113	RIDDLE syndrome		MGI:5505899	Rnf168<sup>Gt(156B6)Cmhd</sup>/Rnf168<sup>Gt(156B6)Cmhd</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21552324	20170630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	is_implicated_in	DOID:1612	breast cancer		MGI:3771372	Stat1<sup>tm1Rds</sup>/Stat1<sup>tm1Rds</sup>  [background:] 129S6/SvEv-Stat1<sup>tm1Rds</sup>/Tac			ECO:0000033	author statement supported by traceable reference	PMID:22264274	20160425	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612971	Galns<sup>tm2(GALNS)Toma</sup>	is_implicated_in	DOID:12804	mucopolysaccharidosis IV		MGI:3616632	Galns<sup>tm2(GALNS)Toma</sup>/Galns<sup>tm2(GALNS)Toma</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16219627	20060316	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3813454	Tg(DMPK/tetO-EGFP/DMPK)5-313Masm	is_implicated_in	DOID:11722	myotonic dystrophy type 1		MGI:3813458	Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:24039817	20140424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136896	Ret<sup>tm2.1Cos</sup>	is_not_implicated_in	DOID:0050547	familial medullary thyroid carcinoma		MGI:3583331	Ret<sup>tm2.1Cos</sup>/Ret<sup>tm2.1Cos</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136896	Ret<sup>tm2.1Cos</sup>	is_not_implicated_in	DOID:0050547	familial medullary thyroid carcinoma		MGI:3583335	Ret<sup>tm2.1Cos</sup>/Ret<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6J * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10675330	20050810	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88253	Car8	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:5766909	Car8<sup>wdl</sup>/Car8<sup>wdl</sup>  [background:] C57BLKS/J-Car8<sup>wdl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26586559	20160509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95554	Fli1	is_implicated_in	DOID:418	systemic scleroderma		MGI:4441385	Fli1<sup>tm1Matr</sup>/Fli1<sup>tm1Matr</sup> Tg(Tek-cre)12Flv/0  [background:] B6.Cg-Fli1<sup>tm1Matr</sup> Tg(Tek-cre)12Flv			ECO:0000033	author statement supported by traceable reference	PMID:20228226	20100428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856702	Npr2<sup>cn</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:3828048	Npr2<sup>cn</sup>/Npr2<sup>cn</sup>  [background:] involves: AKR/J			ECO:0000033	author statement supported by traceable reference	MGI:75337	20180629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182823	Tnfrsf13b<sup>tm1Vmd</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3847256	Tnfrsf13b<sup>tm1Vmd</sup>/Tnfrsf13b<sup>tm1Vmd</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12594954	20090609	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2183146	Tsc1<sup>tm1Hin</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5641392	Tsc1<sup>tm1Hin</sup>/Tsc1<sup>+</sup>  [background:] B6J.129S4-Tsc1<sup>tm1Hin</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23250422	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2182772	Agfg1<sup>tm1Jvd</sup>	is_implicated_in	DOID:0070311	oligoasthenoteratozoospermia		MGI:3609494	Agfg1<sup>tm1Jvd</sup>/Agfg1<sup>tm1Jvd</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15705627	20220127	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	is_not_implicated_in	DOID:0060744	Pendred Syndrome		MGI:5529274	Slc26a4<sup>tm2.1Dontu</sup>/Slc26a4<sup>tm2.1Dontu</sup>  [background:] B6.129-Slc26a4<sup>tm2.1Dontu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23755160	20140120	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_implicated_in	DOID:10754	otitis media		MGI:3850388	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)1Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_implicated_in	DOID:10754	otitis media		MGI:3850389	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)2Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_implicated_in	DOID:10754	otitis media		MGI:3850394	Nf2<sup>tm1Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Mpz-cre)2Brn/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:10887156	20110303	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1924287	Mrap	is_implicated_in	DOID:9553	adrenal gland disease		MGI:6363217	Mrap<sup>tm1.2Geno</sup>/Mrap<sup>tm1.2Geno</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:29879378	20191010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857025	Tbx6<sup>rv</sup>	is_implicated_in	DOID:0050568	spondylocostal dysostosis		MGI:3700984	Tbx6<sup>rv</sup>/Tbx6<sup>rv</sup>  [background:] involves: C57BL/J * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:4073528	20070327	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	is_implicated_in	DOID:0050766	choreaacanthocytosis		MGI:3573789	Vps13a<sup>tm1Asan</sup>/Vps13a<sup>tm1Asan</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:15686477	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3829641	Flcn<sup>tm1Btt</sup>	is_implicated_in	DOID:0050387	nonpapillary renal cell carcinoma		MGI:3829652	Flcn<sup>tm1Btt</sup>/Flcn<sup>tm1Btt</sup> Tg(Cdh16-cre)91Igr/0  [background:] involves: 129S4/SvJaeSor * C57BL/6 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:18974783	20151120	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156194	Gpc3<sup>Gt(Ex136)Byg</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849592	Gpc3<sup>Gt(Ex136)Byg</sup>/Y  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2156194	Gpc3<sup>Gt(Ex136)Byg</sup>	is_implicated_in	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1		MGI:3849593	Gpc3<sup>Gt(Ex136)Byg</sup>/Gpc3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10964473	20090706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	is_implicated_in	DOID:13042	persistent fetal circulation syndrome		MGI:5503192	Pten<sup>tm1Hwu</sup>/Pten<sup>tm1Hwu</sup> Twist2<sup>tm1.1(cre)Dor</sup>/Twist2<sup>+</sup>  [background:] B6.129-Twist2<sup>tm1.1(cre)Dor</sup> Pten<sup>tm1Hwu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23023706	20130830	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2449205	Nr1d2	is_implicated_in	DOID:0050651	atrioventricular septal defect		MGI:5804180	Nr1d2<sup>tm1Dgen</sup>/Nr1d2<sup>tm1Dgen</sup>  [background:] B6;129P2-Nr1d2<sup>tm1Dgen</sup>/H			ECO:0000033	author statement supported by traceable reference	PMID:27058611	20161020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	is_implicated_in	DOID:0060611	abdominal obesity-metabolic syndrome		MGI:3721145	Prkci<sup>tm1Rfar</sup>/Prkci<sup>+</sup> Tg(Ckmm-cre)5Khn/?  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:17641777	20170626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2662140	Mitf<sup>Mi-Crc</sup>	is_implicated_in	DOID:0110950	Waardenburg syndrome type 2A		MGI:2662939	Mitf<sup>Mi-Crc</sup>/Mitf<sup>Mi-Crc</sup>  [background:] involves: CBA/CaCrc			ECO:0000033	author statement supported by traceable reference	MGI:2662101	20050627	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1858041	Fancc<sup>tm1Mgo</sup>	is_implicated_in	DOID:0111087	Fanconi anemia complementation group C		MGI:2450132	Fancc<sup>tm1Mgo</sup>/Fancc<sup>tm1Mgo</sup>  [background:] involves: 129S4/SvJaeSor * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8704201	20110518	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2159324	Cln6	is_implicated_in	DOID:0110729	neuronal ceroid lipofuscinosis 6A		MGI:2182596	Cln6<sup>nclf</sup>/Cln6<sup>nclf</sup>  [background:] involves: C57BL/6J * C57BL/10J * C3HeB/FeJLe			ECO:0000033	author statement supported by traceable reference	PMID:11791207	20081009	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2675750	Syn3<sup>tm1Pggd</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5517485	Syn3<sup>tm1Pggd</sup>/Syn3<sup>tm1Pggd</sup>  [background:] B6.129X1-Syn3<sup>tm1Jfe</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2686379	Frmd7	is_implicated_in	DOID:0111790	congenital nystagmus 1		MGI:6491489	Frmd7<sup>tm1b(KOMP)Wtsi</sup>/Frmd7<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33007925	20210112	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2686379	Frmd7	is_implicated_in	DOID:0111790	congenital nystagmus 1		MGI:6491490	Frmd7<sup>tm1b(KOMP)Wtsi</sup>/Y  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33007925	20210112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856413	Atp8a2<sup>wl-3J</sup>	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:3839293	Atp8a2<sup>wl-3J</sup>/Atp8a2<sup>wl-3J</sup>  [background:] CBA/J-Atp8a2<sup>wl-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:25917818	20150717	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857184	Ifng<sup>tm1Ts</sup>	is_implicated_in	DOID:12365	malaria		MGI:3587743	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22723523	20130313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270153	Zfp106	is_implicated_in	DOID:332	amyotrophic lateral sclerosis		MGI:6150431	Zfp106<sup>tm1b(KOMP)Wtsi</sup>/Zfp106<sup>tm1b(KOMP)Wtsi</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28072389	20180411	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	is_implicated_in	DOID:0050632	oculocutaneous albinism		MGI:5607163	Oca2<sup>p-6Btlr</sup>/Oca2<sup>p-6Btlr</sup>  [background:] C57BL/6J-Oca2<sup>p-6Btlr</sup>			ECO:0000033	author statement supported by traceable reference	MGI:5607140	20141215	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3614434	Kiss1r<sup>tm1Gstn</sup>	is_implicated_in	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia		MGI:3614439	Kiss1r<sup>tm1Gstn</sup>/Kiss1r<sup>tm1Gstn</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:14652023	20170629	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	is_implicated_in	DOID:0050466	Loeys-Dietz syndrome		MGI:5543898	Tgfbr1<sup>tm1.1Hcd</sup>/Tgfbr1<sup>+</sup>  [background:] 129S6(Cg)-Tgfbr1<sup>tm1.1Hcd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24355923	20140212	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861713	Trp63<sup>tm1Brd</sup>	is_implicated_in	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3		MGI:3588183	Trp63<sup>tm1Brd</sup>/Trp63<sup>tm1Brd</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10227293	20050922	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857274	Gpi1<sup>b-m2Neu</sup>	is_implicated_in	DOID:2861	congenital nonspherocytic hemolytic anemia		MGI:2177288	Gpi1<sup>b-m2Neu</sup>/Gpi1<sup>b-m2Neu</sup>  [background:] C3.Cg-Gpi1<sup>b-m2Neu</sup>			ECO:0000033	author statement supported by traceable reference	PMID:8417789	20110309	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103020	Syn2	is_implicated_in	DOID:1826	epilepsy		MGI:3045985	Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:24009558	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1203732	Slc16a2	is_implicated_in	DOID:0050631	Allan-Herndon-Dudley syndrome		MGI:3710595	Slc16a2<sup>tm1Dgen</sup>/Y  [background:] either: (involves: C57BL/6N) or (involves: NMRI)			ECO:0000033	author statement supported by traceable reference	PMID:17318265	20070531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832953	Tg(CMV-TOR1A*)2Nush	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:3832989	Tg(CMV-TOR1A*)2Nush/0  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15930383	20090223	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5430037	b2b243Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5430325	b2b243Clo/b2b243Clo  [background:] C57BL/6J-b2b243Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4355571	Galnt3<sup>tm1Mjec</sup>	is_implicated_in	DOID:0111063	hyperphosphatemic familial tumoral calcinosis		MGI:4355581	Galnt3<sup>tm1Mjec</sup>/Galnt3<sup>tm1Mjec</sup>  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19213845	20090901	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429698	Hexa<sup>tm1Grv</sup>	is_implicated_in	DOID:3320	Tay-Sachs disease		MGI:2668037	Hexa<sup>tm1Grv</sup>/Hexa<sup>tm1Grv</sup>  [background:] involves: 129P2/Ola * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:8789434	20050613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	is_implicated_in	DOID:2236	congenital afibrinogenemia		MGI:3662854	Fgg<sup>tm1Fjc</sup>/Fgg<sup>tm1Fjc</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11891199	20061005	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2429641	Cp<sup>tm1Yos</sup>	is_implicated_in	DOID:0050711	aceruloplasminemia		MGI:3834850	Cp<sup>tm1Yos</sup>/Cp<sup>tm1Yos</sup>  [background:] C.129P2-Cp<sup>tm1Yos</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18804145	20090309	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3665322	Scn1a<sup>tm1Wac</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3690093	Scn1a<sup>tm1Wac</sup>/Scn1a<sup>+</sup>  [background:] B6.129-Scn1a<sup>tm1Wac</sup>			ECO:0000033	author statement supported by traceable reference	PMID:22914087	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3522510	Slc6a8<sup>tm1.2Clar</sup>	is_implicated_in	DOID:0050800	cerebral creatine deficiency syndrome 1		MGI:4941778	Slc6a8<sup>tm1.2Clar</sup>/Y  [background:] involves: BALB/cJ * C57BL/6 * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:21249153	20110323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856317	Btk<sup>xid</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687751	Btk<sup>xid</sup>/Btk<sup>xid</sup>  [background:] involves: CBA/HN * DBA/2N			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856317	Btk<sup>xid</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687752	Btk<sup>xid</sup>/Y  [background:] involves: CBA/HN * DBA/2N			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856317	Btk<sup>xid</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687754	Btk<sup>xid</sup>/Btk<sup>xid</sup>  [background:] CBA/HN-Btk<sup>xid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856317	Btk<sup>xid</sup>	is_implicated_in	DOID:14179	X-linked agammaglobulinemia		MGI:3687750	Btk<sup>xid</sup>/Y  [background:] CBA/HN-Btk<sup>xid</sup>			ECO:0000033	author statement supported by traceable reference	PMID:805203	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	is_implicated_in	DOID:0110106	atrial heart septal defect 1		MGI:2175179	Ntf3<sup>tm1Par</sup>/Ntf3<sup>tm1Par</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:8841198	20060426	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	PMID:1696177	20070128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	is_implicated_in	DOID:1184	nephrotic syndrome		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	PMID:10233845	20070128	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3704091	Dbt<sup>tm1Geh</sup>	is_implicated_in	DOID:9269	maple syrup urine disease		MGI:3704912	Dbt<sup>tm1Geh</sup>/Dbt<sup>tm1Geh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:16579849	20070426	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3608773	Cx3cr1<sup>tm1Zm</sup>	is_implicated_in	DOID:0110024	age related macular degeneration 12		MGI:3814729	Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17909628	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3608773	Cx3cr1<sup>tm1Zm</sup>	is_implicated_in	DOID:0110024	age related macular degeneration 12		MGI:3814728	Cx3cr1<sup>tm1Zm</sup>/Cx3cr1<sup>tm1Zm</sup>  [background:] C.129-Cx3cr1<sup>tm1Zm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:17909628	20110519	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4438621	Prpf31<sup>tm1.1Bha</sup>	is_implicated_in	DOID:0110408	retinitis pigmentosa 11		MGI:4950568	Prpf31<sup>tm1.1Bha</sup>/Prpf31<sup>+</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:20811066	20110517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152978	Col2a1<sup>tm1Prc</sup>	is_implicated_in	DOID:14789	spondyloepiphyseal dysplasia congenita		MGI:2677039	Col2a1<sup>tm1Prc</sup>/Col2a1<sup>tm1Prc</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:7590256	20051006	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834570	Tg(ATN1*)Q129Stsu	is_implicated_in	DOID:0060162	dentatorubral-pallidoluysian atrophy		MGI:3834589	Tg(ATN1*)Q129Stsu/0  [background:] involves: 129S/SvEv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19039037	20090305	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3693359	Tg(APPSwLon)96Btla	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3693440	Tg(APPSwLon)96Btla/0  [background:] involves: 129S4/SvJae			ECO:0000033	author statement supported by traceable reference	PMID:9285791	20070112	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2180880	Lrp1<sup>tm2Her</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:4943741	Lrp1<sup>tm2Her</sup>/Lrp1<sup>tm2Her</sup> Tg(Camk2a-cre)T29-1Stl/0  [background:] involves: 129S7/SvEvBrd * BALB/c * C57BL			ECO:0000033	author statement supported by traceable reference	PMID:21159977	20110405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1931790	Cd36<sup>tm1Mfe</sup>	is_implicated_in	DOID:0111046	platelet-type bleeding disorder 10		MGI:3587412	Cd36<sup>tm1Mfe</sup>/Cd36<sup>tm1Mfe</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:10383407	20050913	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857143	Cd4<sup>tm1Knw</sup>	is_not_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3623373	Cd4<sup>tm1Knw</sup>/Cd4<sup>tm1Knw</sup>  [background:] NOD.Cg-Cd4<sup>tm1Knw</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10725754	20060606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027340	Ptprc<sup>tm1Weis</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3841485	Ptprc<sup>tm1Weis</sup>/Ptprc<sup>tm1Weis</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11163182	20090428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3027340	Ptprc<sup>tm1Weis</sup>	is_implicated_in	DOID:9074	systemic lupus erythematosus		MGI:3841484	Ptprc<sup>tm1Weis</sup>/Ptprc<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11163182	20090428	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774032	Efhc1<sup>tm1Kzy</sup>	is_implicated_in	DOID:4890	juvenile myoclonic epilepsy		MGI:3836724	Efhc1<sup>tm1Kzy</sup>/Efhc1<sup>tm1Kzy</sup>  [background:] B6.129P2-Efhc1<sup>tm1Kzy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19147686	20090323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3774032	Efhc1<sup>tm1Kzy</sup>	is_implicated_in	DOID:4890	juvenile myoclonic epilepsy		MGI:3836725	Efhc1<sup>tm1Kzy</sup>/Efhc1<sup>+</sup>  [background:] B6.129P2-Efhc1<sup>tm1Kzy</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19147686	20090323	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3757756	Tg(Th-SNCA*)1702Yosh	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:3757843	Tg(Th-SNCA*)1702Yosh/0  [background:] involves: C3H * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:17174013	20101129	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3577049	Tgif1<sup>tm1.1Caw</sup>	is_not_implicated_in	DOID:0110880	holoprosencephaly 4		MGI:3577403	Tgif1<sup>tm1.1Caw</sup>/Tgif1<sup>tm1.1Caw</sup>  [background:] involves: C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:15831469	20140825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1923321	Jakmip1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5750066	Jakmip1<sup>tm1(KOMP)Vlcg</sup>/Jakmip1<sup>tm1(KOMP)Vlcg</sup>  [background:] involves: C57BL/6NTac			ECO:0000033	author statement supported by traceable reference	PMID:26627310	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3510784	Traf3ip2<sup>tm1.1Lix</sup>	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:5439184	Traf3ip2<sup>tm1.1Lix</sup>/Traf3ip2<sup>tm1.1Lix</sup>  [background:] C.129-Traf3ip2<sup>tm1.1Lix</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18624351	20121024	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2385469	Sox9<sup>tm1.1Gsr</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:3581014	Sox9<sup>tm1.1Gsr</sup>/Sox9<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11857796	20060614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87872	Acc	is_implicated_in	DOID:83	cataract		MGI:2175693	Acc/Acc<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170721	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2668436	Grb10<sup>Gt(Betageo)1Ward</sup>	is_not_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:2668440	Grb10<sup>Gt(Betageo)1Ward</sup>/Grb10<sup>Gt(Betageo)1Ward</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12829789	20050630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2668436	Grb10<sup>Gt(Betageo)1Ward</sup>	is_not_implicated_in	DOID:14681	Silver-Russell syndrome		MGI:2668444	Grb10<sup>Gt(Betageo)1Ward</sup>/Grb10<sup>+</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12829789	20050630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	is_implicated_in	DOID:12365	malaria		MGI:3587743	Ifng<sup>tm1Ts</sup>/Ifng<sup>tm1Ts</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22723523	20130313	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	is_implicated_in	DOID:4450	renal cell carcinoma		MGI:3850478	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(Vil1-cre)20Syr/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:19487675	20170613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3832592	Pomgnt1<sup>tm1Stk</sup>	is_implicated_in	DOID:0050560	Walker-Warburg syndrome		MGI:3832643	Pomgnt1<sup>tm1Stk</sup>/Pomgnt1<sup>tm1Stk</sup>  [background:] involves: 129S/SvEv			ECO:0000033	author statement supported by traceable reference	PMID:19114101	20090416	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	is_implicated_in	DOID:0080056	achondrogenesis type II		MGI:3590207	Col2a1<sup>tm1Prc</sup>/Col2a1<sup>tm1Prc</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:11680679	20070308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2679726	Kat6b<sup>Gt(pKC199)1Pgr</sup>	is_implicated_in	DOID:3490	Noonan syndrome		MGI:2679734	Kat6b<sup>Gt(pKC199)1Pgr</sup>/Kat6b<sup>Gt(pKC199)1Pgr</sup>  [background:] involves: 129S2/SvPas			ECO:0000033	author statement supported by traceable reference	PMID:21804188	20170706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	is_not_implicated_in	DOID:9245	Alagille syndrome		MGI:2384058	Jag1<sup>tm1Grid</sup>/Jag1<sup>+</sup>  [background:] involves: 129S1/Sv * C57BL/6 * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10196361	20050920	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104540	Clec3b	is_implicated_in	DOID:13300	Scheuermann's disease		MGI:2656035	Clec3b<sup>tm1Umw</sup>/Clec3b<sup>tm1Umw</sup>  [background:] involves: 129S1/Sv * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11604516	20090128	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99481	F11	is_implicated_in	DOID:2229	factor XI deficiency		MGI:3665566	F11<sup>tm1Gjb</sup>/F11<sup>tm1Gjb</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9518045	20151119	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4413579	Wt1<sup>tm1.1Lahe</sup>	is_implicated_in	DOID:3764	Denys-Drash syndrome		MGI:4413583	Wt1<sup>tm1.1Lahe</sup>/Wt1<sup>+</sup>  [background:] involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL			ECO:0000033	author statement supported by traceable reference	PMID:19797313	20091229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	is_not_implicated_in	DOID:14748	Sotos syndrome		MGI:2668882	Nsd1<sup>tm1.1Pcn</sup>/Nsd1<sup>tm1.1Pcn</sup>  [background:] involves: 129/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12805229	20110630	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	is_implicated_in	DOID:11476	osteoporosis		MGI:2174799	Vdr<sup>tm1Ska</sup>/Vdr<sup>tm1Ska</sup>  [background:] involves: C57BL/6NCrlj * CBA/JNCrlj			ECO:0000033	author statement supported by traceable reference	PMID:10746634	20061019	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3720650	Tg(DMD-APP*)18Neve	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3720677	Tg(DMD-APP*)18Neve/0  [background:] involves: C57BL/6 * SJL			ECO:0000033	author statement supported by traceable reference	PMID:8744400	20070906	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	is_implicated_in	DOID:9255	frontotemporal dementia		MGI:7284278	Vcp<sup>tm1.1Hiok</sup>/Vcp<sup>+</sup>  [background:] B6(Cg)-Vcp<sup>tm1.1Hiok</sup>			ECO:0000033	author statement supported by traceable reference	PMID:34130995	20220608	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098726	Emp2	is_implicated_in	DOID:3891	placental insufficiency		MGI:5925411	Emp2<sup>tm1.1Tac</sup>/Emp2<sup>tm1.1Tac</sup> Tg(Zp3-cre)93Knw/0  [background:] involves: C57BL/6 * C57BL/6J * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:28295343	20171121	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:106903	Gucy2c	is_implicated_in	DOID:9970	obesity		MGI:5300906	Gucy2c<sup>tm1Gar</sup>/Gucy2c<sup>tm1Gar</sup>  [background:] B6.129S6-Gucy2c<sup>tm1Gar</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21865642	20170727	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2681507	Ar<sup>tm1Ska</sup>	is_implicated_in	DOID:4674	androgen insensitivity syndrome		MGI:2681522	Ar<sup>tm1Ska</sup>/Y Tg(CMV-cre)1Ipc/?  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:12943692	20081106	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5790635	Pdgfrb<sup>tm1Msas</sup>/Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu/0  [background:] B6J.Cg-Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu			ECO:0000033	author statement supported by traceable reference	PMID:25803852	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4126537	Dlgap4<sup>Gt(XH723)Byg</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:6358593	Dlgap4<sup>Gt(XH723)Byg</sup>/Dlgap4<sup>Gt(XH723)Byg</sup>  [background:] B6.129P2-Dlgap4<sup>Gt(XH723)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:30664629	20190906	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2680722	Il4ra<sup>tm1Tch</sup>	is_implicated_in	DOID:2841	asthma		MGI:2680727	Il4ra<sup>tm1Tch</sup>/Il4ra<sup>tm1Tch</sup>  [background:] involves: 129X1/SvJ * BALB/c			ECO:0000033	author statement supported by traceable reference	PMID:14557412	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856012	Lepr<sup>db-3J</sup>	is_implicated_in	DOID:9970	obesity		MGI:3586756	Lepr<sup>db-3J</sup>/Lepr<sup>db-3J</sup>  [background:] 129P3/J-Lepr<sup>db-3J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:6993269	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1914411	Sclt1	is_implicated_in	DOID:0060340	ciliopathy		MGI:6110829	Sclt1<sup>Tg(CAG-sb10)1Dla</sup>/Sclt1<sup>Tg(CAG-sb10)1Dla</sup>  [background:] FVB/N-Sclt1<sup>Tg(CAG-sb10)1Dla</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28486600	20180118	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859840	Xpc<sup>tm1Ecf</sup>	is_implicated_in	DOID:1324	lung cancer		MGI:3719290	Xpc<sup>tm1Ecf</sup>/Xpc<sup>tm1Ecf</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16141330	20070827	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927555	Slc4a4	is_implicated_in	DOID:14219	renal tubular acidosis		MGI:5433858	Slc4a4<sup>tm1.1Slin</sup>/Slc4a4<sup>tm1.1Slin</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21228764	20120914	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3689889	Fancf	is_implicated_in	DOID:5426	primary ovarian insufficiency		MGI:6103876	Fancf<sup>tm1Nki</sup>/Fancf<sup>tm1Nki</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:21915857	20171220	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3620011	Neil1<sup>tm1Rsld</sup>	is_implicated_in	DOID:9970	obesity		MGI:3620067	Neil1<sup>tm1Rsld</sup>/Neil1<sup>+</sup>  [background:] either: B6.129S1-Neil1<sup>tm1Rsld</sup> or (involves: 129S1/Sv * C57BL/6)			ECO:0000033	author statement supported by traceable reference	PMID:16446448	20091105	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3618599	Tg(PSEN1dE9)S9Dbo	is_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:3618601	Tg(PSEN1dE9)S9Dbo/0  [background:] involves: C3H/HeJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9212102	20060405	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521726	Hoxa13<sup>tm1Jwi</sup>	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3521745	Hoxa13<sup>tm1Jwi</sup>/Hoxa13<sup>tm1Jwi</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15385446	20050701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3521726	Hoxa13<sup>tm1Jwi</sup>	is_implicated_in	DOID:0060739	hand-foot-genital syndrome		MGI:3521748	Hoxa13<sup>tm1Jwi</sup>/Hoxa13<sup>+</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15385446	20050701	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429148	Tg(GFAP-HTT*160Q)1Xjl	is_implicated_in	DOID:12858	Huntington's disease		MGI:4429156	Tg(GFAP-HTT*160Q)1Xjl/0  [background:] either: (involves: FVB/NCrl) or (involves: C3H * C57BL/6 * FVB/NCrl)			ECO:0000033	author statement supported by traceable reference	PMID:20018729	20100218	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450327	Sptbn1<sup>tm1Mish</sup>	is_implicated_in	DOID:5572	Beckwith-Wiedemann syndrome		MGI:4936861	Sptbn1<sup>tm1Mish</sup>/Sptbn1<sup>+</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:20739274	20110224	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A		MGI:3618892	Fanca<sup>tm1Faw</sup>/Fanca<sup>tm1Faw</sup>  [background:] involves: 129P2/OlaHsd * FVB			ECO:0000033	author statement supported by traceable reference	PMID:10915769	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A		MGI:3047131	Fanca<sup>tm1Wong</sup>/Fanca<sup>tm1Wong</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12913077	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	is_implicated_in	DOID:0111095	Fanconi anemia complementation group A		MGI:3047099	Fanca<sup>tm1.1Wong</sup>/Fanca<sup>tm1.1Wong</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:12913077	20060410	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5437077	b2b1291.2Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5437112	b2b1291.2Clo/b2b1291.2Clo  [background:] C57BL/6J-b2b1291.2Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95721	Gjb3	is_implicated_in	DOID:0050467	erythrokeratodermia variabilis		MGI:3712799	Gjb3<sup>tm2.1Kwi</sup>/Gjb3<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:17446259	20070626	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857051	Npc1<sup>spm</sup>	is_implicated_in	DOID:14504	Niemann-Pick disease		MGI:3846848	Npc1<sup>spm</sup>/Npc1<sup>spm</sup>  [background:] C57BLKS/J-Npc1<sup>spm</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:7202025	20111205	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2671784	Zfp423<sup>nur12</sup>	is_implicated_in	DOID:2785	Dandy-Walker syndrome		MGI:3693287	Zfp423<sup>nur12</sup>/Zfp423<sup>nur12</sup>  [background:] involves: BALB/c * C57BL/6 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:17151198	20070111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3768388	Tg(THY1-SNCA*A53T)M53Sud	is_implicated_in	DOID:0060367	Parkinson's disease 1		MGI:5632508	Tg(THY1-SNCA*A53T)M53Sud/0  [background:] B6.Cg-Tg(THY1-SNCA*A53T)M53Sud/J			ECO:0000033	author statement supported by traceable reference	PMID:24325796	20150424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821601	Baz1b<sup>MommeD10</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3821614	Baz1b<sup>MommeD10</sup>/Baz1b<sup>+</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19099580	20081230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821601	Baz1b<sup>MommeD10</sup>	is_implicated_in	DOID:1928	Williams-Beuren syndrome		MGI:3821613	Baz1b<sup>MommeD10</sup>/Baz1b<sup>MommeD10</sup>  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19099580	20081230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3530648	Chd8<sup>tm1Kei</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:7413047	Chd8<sup>tm1Kei</sup>/Chd8<sup>+</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:27602517	20221230	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1926955	Nf2<sup>tm2Gth</sup>	is_implicated_in	DOID:12270	coloboma		MGI:7261162	Nf2<sup>tm2Gth</sup>/Nf2<sup>tm2Gth</sup> Tg(rx3-icre)1Mjam/0  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:33075808	20220412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	is_implicated_in	DOID:0110156	Charcot-Marie-Tooth disease type 2B1		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:11799477	20060502	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	is_implicated_in	DOID:0110998	Joubert syndrome 3		MGI:5007765	Ahi1<sup>tm1Jgg</sup>/Ahi1<sup>tm1Jgg</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:21623382	20110616	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	is_implicated_in	DOID:0110125	Bardet-Biedl syndrome 3		MGI:7449243	Arl6<sup>tm2Vcs</sup>/Arl6<sup>tm2Vcs</sup>  [background:] B6.129-Arl6<sup>tm2Vcs</sup>			ECO:0000033	author statement supported by traceable reference	PMID:27170093	20230403	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2449035	Car8<sup>wdl</sup>	is_implicated_in	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome		MGI:5766909	Car8<sup>wdl</sup>/Car8<sup>wdl</sup>  [background:] C57BLKS/J-Car8<sup>wdl</sup>/GrsrJ			ECO:0000033	author statement supported by traceable reference	PMID:26586559	20160509	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	is_implicated_in	DOID:0110033	autosomal recessive Alport syndrome		MGI:3624035	Mpv17/Mpv17  [background:] CFW-Mpv17/J			ECO:0000033	author statement supported by traceable reference	MGI:1274824	20060607	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2669870	Pts<sup>tm1Ich</sup>	is_implicated_in	DOID:0090106	BH4-deficient hyperphenylalaninemia A		MGI:2669893	Pts<sup>tm1Ich</sup>/Pts<sup>tm1Ich</sup>  [background:] involves: 129X1/SvJ * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:11517215	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856927	Pdss2<sup>kd</sup>	is_implicated_in	DOID:0050730	coenzyme Q10 deficiency disease		MGI:3611217	Pdss2<sup>kd</sup>/Pdss2<sup>kd</sup>  [background:] CBA/H-Pdss2<sup>kd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23150520	20130711	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444881	Flvcr1	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:3807528	Flvcr1<sup>tm1.1Jlab</sup>/Flvcr1<sup>tm1.1Jlab</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:18258918	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444881	Flvcr1	is_implicated_in	DOID:1339	Diamond-Blackfan anemia		MGI:3807529	Flvcr1<sup>tm1Jlab</sup>/Flvcr1<sup>tm1Jlab</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S4/SvJae * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:18258918	20170710	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384966	Mgat2	is_implicated_in	DOID:0070253	congenital disorder of glycosylation type IIa		MGI:2667777	Mgat2<sup>tm1.1Jxm</sup>/Mgat2<sup>tm1.1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11805078	20190516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2384966	Mgat2	is_implicated_in	DOID:0070253	congenital disorder of glycosylation type IIa		MGI:2667791	Mgat2<sup>tm1.1Jxm</sup>/Mgat2<sup>tm1.1Jxm</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * ICR			ECO:0000033	author statement supported by traceable reference	PMID:11805078	20190516	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5433393	b2b1163Clo	is_implicated_in	DOID:2975	cystic kidney disease		MGI:5433487	b2b1163Clo/b2b1163Clo  [background:] C57BL/6J-b2b1163Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181653	Phex<sup>Hyp-2J</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037638	Phex<sup>Hyp-2J</sup>/Y  [background:] C57BL/6-Phex<sup>Hyp-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181653	Phex<sup>Hyp-2J</sup>	is_implicated_in	DOID:0050445	X-linked dominant hypophosphatemic rickets		MGI:3037641	Phex<sup>Hyp-2J</sup>/Phex<sup>+</sup>  [background:] C57BL/6-Phex<sup>Hyp-2J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:15029877	20050620	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921164	Irak3	is_implicated_in	DOID:11476	osteoporosis		MGI:3584247	Irak3<sup>tm1Flv</sup>/Irak3<sup>tm1Flv</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:15809356	20050825	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	is_implicated_in	DOID:18	urinary system disease		MGI:3811541	Bmp4<sup>tm2Blh</sup>/Bmp4<sup>+</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:10749566	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	is_implicated_in	DOID:870	neuropathy		MGI:6850159	Nemf<sup>em8Cx</sup>/Nemf<sup>em8Cx</sup>  [background:] C57BL/6J-Nemf<sup>em8Cx</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	is_implicated_in	DOID:870	neuropathy		MGI:6719084	Nemf<sup>pdft</sup>/Nemf<sup>pdft</sup>  [background:] B6(C3)-Nemf<sup>pdft</sup>/Cx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	is_implicated_in	DOID:870	neuropathy		MGI:6718876	Nemf<sup>tvrm116</sup>/Nemf<sup>tvrm116</sup>  [background:] C57BL/6J-Nemf<sup>tvrm116</sup>/PjnCx			ECO:0000033	author statement supported by traceable reference	PMID:32934225	20210707	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1329045	Tulp3	is_implicated_in	DOID:0080322	polycystic kidney disease		MGI:6392266	Tulp3<sup>m1Kflj</sup>/Tulp3<sup>m1Kflj</sup>  [background:] involves: C57BL/6J * FVB/NJ			ECO:0000033	author statement supported by traceable reference	PMID:30799240	20200228	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	is_implicated_in	DOID:0080600	COVID-19		MGI:6431340	Ace2<sup>em1(ACE2)Yowa</sup>/Ace2<sup>em1(ACE2)Yowa</sup>  [background:] C57BL/6-Ace2<sup>em1(ACE2)Yowa</sup>			ECO:0000033	author statement supported by traceable reference	PMID:32485164	20200603	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928480	Acp3	is_implicated_in	DOID:10283	prostate cancer		MGI:5007486	Acp3<sup>tm1Pivi</sup>/Acp3<sup>tm1Pivi</sup>  [background:] B6.Cg-Acp3<sup>tm1Pivi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24039861	20140424	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179716	Lamb3<sup>IAP</sup>	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:2179721	Lamb3<sup>IAP</sup>/Lamb3<sup>IAP</sup>  [background:] involves: C3H * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9271670	20050707	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857279	Camk2a<sup>tm1Sva</sup>	is_implicated_in	DOID:3312	bipolar disorder		MGI:6189158	Camk2a<sup>tm1Sva</sup>/Camk2a<sup>+</sup>  [background:] B6.129P2-Camk2a<sup>tm1Sva</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:27028761	20180723	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179961	Gaa<sup>tm1Vdp</sup>	is_implicated_in	DOID:2752	glycogen storage disease II		MGI:3619140	Gaa<sup>tm1Vdp</sup>/Gaa<sup>tm1Vdp</sup>  [background:] either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)			ECO:0000033	author statement supported by traceable reference	PMID:9384603	20060412	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4262238	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:4950027	Dpcd/Poll<sup>Gt(OST280355)Lex</sup>/Dpcd/Poll<sup>Gt(OST280355)Lex</sup>  [background:] involves: 129S5/SvEvBrd * C57BL/6Brd			ECO:0000033	author statement supported by traceable reference	PMID:20080492	20170615	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587747	Hjv<sup>tm1Arbr</sup>	is_implicated_in	DOID:0111027	hemochromatosis type 2A		MGI:3588579	Hjv<sup>tm1Arbr</sup>/Hjv<sup>tm1Arbr</sup>  [background:] involves: 129S4/SvJae * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:16075058	20050929	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443727	Spef2	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5295270	Spef2<sup>bgh</sup>/Spef2<sup>bgh</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:21715716	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443727	Spef2	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:5295269	Spef2<sup>bgh</sup>/Spef2<sup>bgh</sup>  [background:] involves: C57BL/6J * C57BL/10J			ECO:0000033	author statement supported by traceable reference	PMID:21715716	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103078	Spr	is_implicated_in	DOID:14330	Parkinson's disease		MGI:3774594	Spr<sup>tm1Lex</sup>/Spr<sup>tm1Lex</sup>  [background:] involves: 129S/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:18201550	20110629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3641430	Pdgfrb<sup>tm1Msas</sup>	is_implicated_in	DOID:5419	schizophrenia		MGI:5790635	Pdgfrb<sup>tm1Msas</sup>/Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu/0  [background:] B6J.Cg-Pdgfrb<sup>tm1Msas</sup> Tg(Nes-cre)1Nogu			ECO:0000033	author statement supported by traceable reference	PMID:25803852	20160902	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88446	Col11a1	is_implicated_in	DOID:0080046	Stickler syndrome		MGI:2174906	Col11a1<sup>cho</sup>/Col11a1<sup>cho</sup>  [background:] involves: C57BL/6Fr			ECO:0000033	author statement supported by traceable reference	PMID:7859283	20051003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178045	Krt18<sup>tm1Tmm</sup>	is_implicated_in	DOID:684	hepatocellular carcinoma		MGI:7280898	Krt18<sup>tm1Tmm</sup>/Krt18<sup>tm1Tmm</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:27689336	20220526	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2384593	Tg(Mpz)88.2Mfel	is_implicated_in	DOID:0110152	Charcot-Marie-Tooth disease type 1B		MGI:6276669	Tg(Mpz)88.2Mfel/0  [background:] FVB/N-Tg(Mpz)88.2Mfel			ECO:0000033	author statement supported by traceable reference	PMID:11086005	20190208	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3611072	Efs<sup>tm1Kale</sup>	is_implicated_in	DOID:8778	Crohn's disease		MGI:3611467	Efs<sup>tm1Kale</sup>/Efs<sup>tm1Kale</sup>  [background:] either: (involves: 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:16314525	20170615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1921588	Slc6a19	is_implicated_in	DOID:1060	Hartnup disease		MGI:5289692	Slc6a19<sup>tm1Dgen</sup>/Slc6a19<sup>tm1Dgen</sup>  [background:] involves: 129 * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:21636576	20111007	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1857161	Ednrb<sup>tm1Ywa</sup>	is_implicated_in	DOID:0110953	Waardenburg syndrome type 4A		MGI:2174949	Ednrb<sup>tm1Ywa</sup>/Ednrb<sup>tm1Ywa</sup>  [background:] involves: 129S5/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:15294878	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3028660	Ercc4<sup>tm1Fwa</sup>	is_implicated_in	DOID:0110848	xeroderma pigmentosum group F		MGI:3028691	Ercc4<sup>tm1Fwa</sup>/Ercc4<sup>tm1Fwa</sup>  [background:] involves: 129S6/SvEvTac			ECO:0000033	author statement supported by traceable reference	PMID:14729965	20050621	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3776030	Vhl<sup>tm1Mcs</sup>	is_implicated_in	DOID:0060474	familial erythrocytosis 2		MGI:3811151	Vhl<sup>tm1Mcs</sup>/Vhl<sup>tm1Mcs</sup>  [background:] involves: 129S4/SvJae * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:17992257	20081020	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3616079	Dnaaf5	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:7569326	Dnaaf5<sup>em1Slb</sup>/Dnaaf5<sup>em1Slb</sup>  [background:] C57BL/6-Dnaaf5<sup>em1Slb</sup>			ECO:0000033	author statement supported by traceable reference	PMID:37104040	20231229	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1858204	Map3k14	is_implicated_in	DOID:12894	Sjogren's syndrome		MGI:3767418	Map3k14<sup>aly</sup>/Map3k14<sup>aly</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:9010048	20091015	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3688255	Epha2<sup>Gt(KST085)Byg</sup>	is_implicated_in	DOID:0110229	cataract 6 multiple types		MGI:3689377	Epha2<sup>Gt(KST085)Byg</sup>/Epha2<sup>Gt(KST085)Byg</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19649315	20130512	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4360887	Tg(tetO-PLAGL2)P3Ysy	is_implicated_in	DOID:9675	pulmonary emphysema		MGI:4360917	Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-PLAGL2)P3Ysy/0  [background:] involves: FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:19574421	20091008	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311345	b2b997Clo	is_implicated_in	DOID:0050545	visceral heterotaxy		MGI:5312933	b2b997Clo/b2b997Clo  [background:] C57BL/6J-b2b997Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170602	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	is_implicated_in	DOID:0110122	Axenfeld-Rieger syndrome type 3		MGI:3711773	Bmp4<sup>tm1Blh</sup>/Bmp4<sup>+</sup>  [background:] B6.129S2-Bmp4<sup>tm1Blh</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11722794	20080318	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2158693	Sox9<sup>tm1Crm</sup>	is_implicated_in	DOID:0050463	campomelic dysplasia		MGI:3044095	Sox9<sup>tm1Crm</sup>/Sox9<sup>+</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6 * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:11371614	20060614	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1889639	Kcne1<sup>pkr</sup>	is_implicated_in	DOID:2842	Jervell-Lange Nielsen syndrome		MGI:3623789	Kcne1<sup>pkr</sup>/Kcne1<sup>pkr</sup>  [background:] C57BL/10J-Kcne1<sup>pkr</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11003695	20130308	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2136432	Ctsl<sup>tm1Cptr</sup>	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5810302	Ctsl<sup>tm1Cptr</sup>/Ctsl<sup>tm1Cptr</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:11972068	20170802	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1934273	Prnp<sup>tm1Rcm</sup>	is_not_implicated_in	DOID:4249	Gerstmann-Straussler-Scheinker syndrome		MGI:2174712	Prnp<sup>tm1Rcm</sup>/Prnp<sup>tm1Rcm</sup>  [background:] 129P2/OlaHsd-Prnp<sup>tm1Rcm</sup>			ECO:0000033	author statement supported by traceable reference	PMID:9462739	20050711	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2179191	Tbx1<sup>tm1Bem</sup>	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5314147	Tbx1<sup>tm1Bem</sup>/Tbx1<sup>+</sup>  [background:] B6.Cg-Tbx1<sup>tm1Bem</sup>			ECO:0000033	author statement supported by traceable reference	PMID:21908517	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1935123	Fbn2<sup>fp</sup>	is_not_implicated_in	DOID:0050646	distal arthrogryposis		MGI:2451231	Fbn2<sup>fp</sup>/Fbn2<sup>fp</sup>  [background:] C3Fe(B6)-Fbn2<sup>fp</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:11285249	20050831	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3821974	Snap25<sup>tm1.1Bark</sup>	is_implicated_in	DOID:9352	type 2 diabetes mellitus		MGI:5766495	Snap25<sup>tm1.1Bark</sup>/Snap25<sup>tm1.1Bark</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:26195742	20160504	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	is_implicated_in	DOID:1068	juvenile glaucoma		MGI:4821786	Pax6<sup>tm2Pgr</sup>/Pax6<sup>+</sup> Tg(Pax6-cre,GFP)1Pgr/0  [background:] involves: 129S1/Sv * 129X1/SvJ * FVB			ECO:0000033	author statement supported by traceable reference	PMID:20538882	20170728	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2178316	Pde6b<sup>atrd3</sup>	is_implicated_in	DOID:0110863	congenital stationary night blindness autosomal dominant 2		MGI:3028004	Pde6b<sup>atrd3</sup>/Pde6b<sup>atrd3</sup>  [background:] involves: BALB/cAnN * C3H/HeN			ECO:0000033	author statement supported by traceable reference	PMID:11929848	20050628	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1337008	Ankfy1	is_implicated_in	DOID:0050946	Charlevoix-Saguenay spastic ataxia		MGI:6316069	Ankfy1<sup>Gt(RRE069)Byg</sup>/Ankfy1<sup>+</sup>  [background:] B6.129P2-Ankfy1<sup>Gt(RRE069)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:28588446	20190705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	is_implicated_in	DOID:11726	Emery-Dreifuss muscular dystrophy		MGI:3621007	Zmpste24<sup>tm1Otin</sup>/Zmpste24<sup>tm1Otin</sup>  [background:] involves: 129P2/Ola * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:11923874	20060503	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3612401	Pax9<sup>tm1Hpt</sup>	is_implicated_in	DOID:0050591	tooth agenesis		MGI:3612954	Pax9<sup>tm1Hpt</sup>/Pax9<sup>tm1Hpt</sup>  [background:] involves: 129S2/SvPas * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16236760	20060216	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3623421	Tor1a<sup>tm1Wtd</sup>	is_implicated_in	DOID:0060730	torsion dystonia 1		MGI:5759931	Tor1a<sup>tm1Wtd</sup>/Tor1a<sup>+</sup>  [background:] B6;129-Tor1a<sup>tm1Wtd</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:26183317	20160412	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	is_not_implicated_in	DOID:8893	psoriasis		MGI:3590494	Itgb2<sup>tm1Bay</sup>/Itgb2<sup>tm2Bay</sup>  [background:] B6.129S7-Itgb2<sup>tm1Bay</sup> Itgb2<sup>tm2Bay</sup>			ECO:0000033	author statement supported by traceable reference	PMID:12819024	20170727	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1917633	Cox10	is_implicated_in	DOID:3762	cytochrome-c oxidase deficiency disease		MGI:5444474	Cox10<sup>tm1Ctm</sup>/Cox10<sup>tm1Ctm</sup> Tg(Camk2a-cre)#Szi/0  [background:] involves: 129X1/SvJ * C57BL/6 * C57BL/6J * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22914734	20130415	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:4458390	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20100831	20110514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	is_implicated_in	DOID:0060170	generalized epilepsy with febrile seizures plus		MGI:4458389	Scn1a<sup>tm1.1Aesc</sup>/Scn1a<sup>tm1.1Aesc</sup>  [background:] involves: 129X1/SvJ * C57BL/6J * SJL			ECO:0000033	author statement supported by traceable reference	PMID:20100831	20110514	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:95415	Erg	is_implicated_in	DOID:8398	osteoarthritis		MGI:5910547	Erg<sup>tm1.1Iwamo</sup>/Erg<sup>tm1.1Iwamo</sup> Tg(Gdf5-cre,-ALPP)1Kng/?  [background:] involves: 129S4/SvJaeSor * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:26097038	20170928	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177263	Tmc1<sup>Mhdabth</sup>	is_implicated_in	DOID:0110563	autosomal dominant nonsyndromic deafness 36		MGI:2177316	Tmc1<sup>Mhdabth</sup>/Tmc1<sup>+</sup>  [background:] C3HeB/FeJ-Tmc1<sup>Mhdabth</sup>/Ieg			ECO:0000033	author statement supported by traceable reference	MGI:2681078	20050622	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834680	Tg(SFTPC-EML4/ALK)502-4Hima	is_implicated_in	DOID:1324	lung cancer		MGI:3834683	Tg(SFTPC-EML4/ALK)502-4Hima/0  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19064915	20090306	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2152891	Npr2<sup>cn-2J</sup>	is_implicated_in	DOID:4480	achondroplasia		MGI:2183025	Npr2<sup>cn-2J</sup>/Npr2<sup>cn-2J</sup>  [background:] B6;CBACa-A<sup>w-J</sup>/A-Kcnj6<sup>wv</sup>/+			ECO:0000033	author statement supported by traceable reference	MGI:2152911	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99480	Cebpa	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3809472	Cebpa<sup>tm8.1Nerl</sup>/Cebpa<sup>tm8.1Nerl</sup>  [background:] involves: 129P2/OlaHsd * BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:18394553	20081003	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177822	Eng<sup>tm1Hma</sup>	is_implicated_in	DOID:1270	hereditary hemorrhagic telangiectasia		MGI:3623404	Eng<sup>tm1Hma</sup>/Eng<sup>+</sup>  [background:] 129P2/OlaHsd-Eng<sup>tm1Hma</sup>			ECO:0000033	author statement supported by traceable reference	PMID:10625534	20060529	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2148050	Nexmif	is_implicated_in	DOID:0112044	non-syndromic X-linked intellectual disability 98		MGI:6468250	Nexmif<sup>tm1(KOMP)Wtsi</sup>/Y  [background:] B6J.B6N-Nexmif<sup>tm1(KOMP)Wtsi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:31704787	20201022	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856913	Hydin<sup>hy3</sup>	is_implicated_in	DOID:10908	hydrocephalus		MGI:3605005	Hydin<sup>hy3</sup>/Hydin<sup>hy3</sup>  [background:] involves: CBA			ECO:0000033	author statement supported by traceable reference	PMID:4784576	20170606	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3652048	Gas2l2	is_implicated_in	DOID:9562	primary ciliary dyskinesia		MGI:6343406	Gas2l2<sup>tm1c(KOMP)Wtsi</sup>/Gas2l2<sup>tm1c(KOMP)Wtsi</sup> Foxj1<sup>tm1.1(cre/ERT2/GFP)Htg</sup>/Foxj1<sup>+</sup>  [background:] involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:30665704	20190814	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860482	Mip<sup>Cts</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:5487914	Mip<sup>Cts</sup>/Mip<sup>+</sup>  [background:] involves: C57BL/6J * CTS/Shi			ECO:0000033	author statement supported by traceable reference	MGI:5487779	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1860482	Mip<sup>Cts</sup>	is_implicated_in	DOID:0110251	cataract 15 multiple types		MGI:5487835	Mip<sup>Cts</sup>/Mip<sup>Cts</sup>  [background:] CTS/Shi			ECO:0000033	author statement supported by traceable reference	MGI:5487779	20130617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3605480	Nectin1<sup>tm1Ytk</sup>	is_not_implicated_in	DOID:0060773	cleft lip-palate-ectodermal dysplasia syndrome		MGI:4838217	Nectin1<sup>tm1Ytk</sup>/Nectin1<sup>tm1Ytk</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:21038445	20101111	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2155771	Psen1<sup>tm1Psgh</sup>	is_not_implicated_in	DOID:0110042	Alzheimer's disease 3		MGI:2177097	Psen1<sup>tm1Psgh</sup>/Psen1<sup>tm1Psgh</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:10962005	20050629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3823217	Ezh2<sup>tm2Sho</sup>	is_implicated_in	DOID:9952	acute lymphoblastic leukemia		MGI:5316002	Ezh2<sup>tm2Sho</sup>/Ezh2<sup>tm2Sho</sup> Tg(Mx1-cre)1Cgn/0  [background:] involves: 129S1/Sv * C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:22431509	20120422	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3526447	Rsc1a1	is_implicated_in	DOID:9970	obesity		MGI:3526863	Rsc1a1<sup>tm1Koep</sup>/Rsc1a1<sup>tm1Koep</sup>  [background:] B6.129-Rsc1a1<sup>tm1Koep</sup>			ECO:0000033	author statement supported by traceable reference	PMID:15601832	20091105	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2443538	Msrb3	is_implicated_in	DOID:0110523	autosomal recessive nonsyndromic deafness 74		MGI:5569513	Msrb3<sup>tm1Hyk</sup>/Msrb3<sup>tm1Hyk</sup>  [background:] involves: 129 * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:24191262	20140625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4352296	Ltbp4<sup>Gt(E301B04)Wrst</sup>	is_implicated_in	DOID:3144	cutis laxa		MGI:5641752	Ltbp4<sup>Gt(E301B04)Wrst</sup>/Ltbp4<sup>Gt(E301B04)Wrst</sup>  [background:] B6N.129P2-Ltbp4<sup>Gt(E301B04)Wrst</sup>			ECO:0000033	author statement supported by traceable reference	PMID:25713297	20150625	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3834477	Slitrk1<sup>tm1Jaru</sup>	is_implicated_in	DOID:11119	Gilles de la Tourette syndrome		MGI:3834579	Slitrk1<sup>tm1Jaru</sup>/Slitrk1<sup>tm1Jaru</sup>  [background:] B6.129P2-Slitrk1<sup>tm1Jaru</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18794888	20090305	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1915841	Mocos	is_implicated_in	DOID:0070314	obstructive nephropathy		MGI:7495807	Mocos<sup>em2(IMPC)Ics</sup>/Mocos<sup>em2(IMPC)Ics</sup>  [background:] involves: C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:35372998	20230706	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1352452	Nr2f2	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3579773	Nkx3-2<sup>tm1(cre)Tsa</sup>/Nkx3-2<sup>+</sup> Nr2f2<sup>tm2.1Tsa</sup>/Nr2f2<sup>tm2.1Tsa</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16251273	20100614	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:5311362	b2b635Clo	is_implicated_in	DOID:9955	hypoplastic left heart syndrome		MGI:5312337	b2b635Clo/b2b635Clo  [background:] C57BL/6J-b2b635Clo			ECO:0000033	author statement supported by traceable reference	MGI:5284969	20170613	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5316488	Ext1<sup>tm1Yama</sup>/Ext1<sup>tm1Yama</sup> Tg(Camk2a-cre)2834Lusc/0  [background:] involves: 129S5/SvEvBrd * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22411800	20190430	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891158	Tbx19	is_implicated_in	DOID:0080150	adrenocorticotropic hormone deficiency		MGI:2655154	Tbx19<sup>tm1Jdr</sup>/Tbx19<sup>tm1Jdr</sup>  [background:] either: (involves: 129/Sv) or (involves: BALB/c)			ECO:0000033	author statement supported by traceable reference	PMID:12651888	20050621	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	is_implicated_in	DOID:0050908	myelodysplastic syndrome		MGI:2175794	Crebbp<sup>tm1Dli</sup>/Crebbp<sup>+</sup>  [background:] involves: 129S6/SvEvTac * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:22198154	20130222	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856221	Atp7b<sup>tx-J</sup>	is_implicated_in	DOID:893	Wilson disease		MGI:3793274	Atp7b<sup>tx-J</sup>/Atp7b<sup>tx-J</sup>  [background:] C3H/HeJ-Atp7b<sup>tx-J</sup>/J			ECO:0000033	author statement supported by traceable reference	PMID:17981064	20080611	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1313302	Cenpf	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5467575	Cenpf<sup>tm1Dbdr</sup>/Cenpf<sup>tm1Dbdr</sup> Tg(Tnnt2-cre)5Blh/0  [background:] involves: C57BL/6 * DBA/2 * ICR			ECO:0000033	author statement supported by traceable reference	PMID:22563055	20170809	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99846	Gdi1	is_implicated_in	DOID:0050776	non-syndromic X-linked intellectual disability		MGI:3833428	Gdi1<sup>tm1Toni</sup>/Y  [background:] B6N.129S7-Gdi1<sup>tm1Toni</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18829665	20131021	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3619046	Sufu<sup>tm1Rto</sup>	is_implicated_in	DOID:2512	nevoid basal cell carcinoma syndrome		MGI:3619449	Sufu<sup>tm1Rto</sup>/Sufu<sup>+</sup>  [background:] involves: 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:16459298	20060413	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4429485	Tg(tetO-Ppargc1a)1Dpk	is_implicated_in	DOID:6000	congestive heart failure		MGI:4429501	Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Ppargc1a)1Dpk/0  [background:] involves: FVB/N * FVB/NTac			ECO:0000033	author statement supported by traceable reference	PMID:14726475	20170830	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3687004	Arid4a<sup>tm1Alb</sup>	is_implicated_in	DOID:9119	acute myeloid leukemia		MGI:3817454	Arid4a<sup>tm1Alb</sup>/Arid4a<sup>tm1Alb</sup>  [background:] involves: 129S7/SvEvBrd			ECO:0000033	author statement supported by traceable reference	PMID:18728284	20081121	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2450930	Surf1<sup>tm1Zev</sup>	is_implicated_in	DOID:3652	Leigh disease		MGI:2651426	Surf1<sup>tm1Zev</sup>/Surf1<sup>tm1Zev</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:12566387	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1928478	Brinp1	is_implicated_in	DOID:1094	attention deficit hyperactivity disorder		MGI:5770244	Brinp1<sup>tm1.1Pib</sup>/Brinp1<sup>tm1.1Pib</sup>  [background:] involves: BALB/cJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:27042284	20160517	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177930	Lmna<sup>tm1Stw</sup>	is_implicated_in	DOID:0110156	Charcot-Marie-Tooth disease type 2B1		MGI:2177931	Lmna<sup>tm1Stw</sup>/Lmna<sup>tm1Stw</sup>  [background:] involves: 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:11799477	20060502	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3044176	App<sup>tm1Ini</sup>	is_implicated_in	DOID:10652	Alzheimer's disease		MGI:3044184	App<sup>tm1Ini</sup>/App<sup>+</sup>  [background:] involves: C57BL/6 * CBA * CD-1			ECO:0000033	author statement supported by traceable reference	PMID:15147316	20050601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109355	Stx1a	is_implicated_in	DOID:150	disease of mental health		MGI:5000258	Stx1a<sup>tm1Tfuj</sup>/Stx1a<sup>tm1Tfuj</sup>  [background:] B6.Cg-Stx1a<sup>tm1Tfuj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20576034	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109355	Stx1a	is_implicated_in	DOID:150	disease of mental health		MGI:5000259	Stx1a<sup>tm1Tfuj</sup>/Stx1a<sup>+</sup>  [background:] B6.Cg-Stx1a<sup>tm1Tfuj</sup>			ECO:0000033	author statement supported by traceable reference	PMID:20576034	20170713	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2685163	Ccdc154	is_implicated_in	DOID:0110942	autosomal recessive osteopetrosis 1		MGI:5702613	Ccdc154<sup>ntl</sup>/Ccdc154<sup>ntl</sup>  [background:] involves: 129S7/SvEvBrd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:20121924	20160113	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	is_implicated_in	DOID:0070216	familial hyperinsulinemic hypoglycemia 3		MGI:6690664	Gck<sup>tm1Ydor</sup>/Gck<sup>+</sup> Tg(Ins2-cre)25Mgn/0  [background:] involves: C57BL/6 * C57BL/6J * DBA			ECO:0000033	author statement supported by traceable reference	PMID:33558985	20210414	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99135	Xpa	is_implicated_in	DOID:0110843	xeroderma pigmentosum group A		MGI:4361117	Xpa<sup>tm1Tnka</sup>/Xpa<sup>tm1Tnka</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:8751968	20190819	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861911	Ccr5<sup>tm1Kuz</sup>	is_implicated_in	DOID:0080599	Coronavirus infectious disease		MGI:4418655	Ccr5<sup>tm1Kuz</sup>/Ccr5<sup>tm1Kuz</sup>  [background:] B6.129P2-Ccr5<sup>tm1Kuz</sup>			ECO:0000033	author statement supported by traceable reference	PMID:19079579	20200714	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3505757	Nbn<sup>tm1.1Md</sup>	is_implicated_in	DOID:7400	Nijmegen breakage syndrome		MGI:3510439	Nbn<sup>tm1.1Md</sup>/Nbn<sup>tm1.1Md</sup>  [background:] involves: 129/Sv * 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:15333589	20050617	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2154689	Col11a2<sup>tm1Mne</sup>	is_implicated_in	DOID:0080046	Stickler syndrome		MGI:2664326	Col11a2<sup>tm1Mne</sup>/Col11a2<sup>tm1Mne</sup>  [background:] FVB.129-Col11a2<sup>tm1Mne</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11668593	20050615	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:103020	Syn2	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:5517484	Syn2<sup>tm1Pggd</sup>/Syn2<sup>tm1Pggd</sup>  [background:] B6.1129-Syn2<sup>tm1Pggd</sup>			ECO:0000033	author statement supported by traceable reference	PMID:23280234	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418563	Ehmt1<sup>tm1.1Tara</sup>	is_implicated_in	DOID:0060352	Kleefstra syndrome 1		MGI:4418566	Ehmt1<sup>tm1.1Tara</sup>/Ehmt1<sup>tm1.1Tara</sup> Tg(Camk2a-cre)2Gsc/0  [background:] involves: 129P2/OlaHsd * C57BL/6 * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:20005824	20100125	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2138987	Slc4a11	is_implicated_in	DOID:0060649	congenital hereditary endothelial dystrophy of cornea		MGI:5524271	Slc4a11<sup>tm1.1Jrcy</sup>/Slc4a11<sup>tm1.1Jrcy</sup>  [background:] involves: C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:23942972	20150515	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:96613	Itgb4	is_implicated_in	DOID:0060738	junctional epidermolysis bullosa non-Herlitz type		MGI:3836294	Itgb4<sup>tm1Efu</sup>/Itgb4<sup>tm1Efu</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8707838	20090319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1346832	Esrrb	is_implicated_in	DOID:12930	dilated cardiomyopathy		MGI:5905569	Esrrb<sup>tm1.1Nat</sup>/Esrrb<sup>tm1.1Nat</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:28130335	20170726	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2444680	Aldh1l2	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6501754	Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>/Aldh1l2<sup>tm2e(KOMP)Wtsi</sup>  [background:] involves: C57BL/6 * C57BL/6N			ECO:0000033	author statement supported by traceable reference	PMID:33168096	20210317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856605	gnd	is_implicated_in	DOID:0110735	neurodegeneration with brain iron accumulation 2a		MGI:3616877	gnd/gnd  [background:] C3H/HeJ-gnd			ECO:0000033	author statement supported by traceable reference	PMID:1634998	20060317	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2387783	Pafah1b1<sup>tm1Or</sup>	is_implicated_in	DOID:0050453	lissencephaly		MGI:2664549	Pafah1b1<sup>tm1Or</sup>/Pafah1b1<sup>+</sup>  [background:] Not Specified			ECO:0000033	author statement supported by traceable reference	PMID:11344260	20050616	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856931	Hps4<sup>le</sup>	is_implicated_in	DOID:0060542	Hermansky-Pudlak syndrome 4		MGI:3587187	Hps4<sup>le</sup>/Hps4<sup>le</sup>  [background:] B6.C3-Pde6b<sup>rd1</sup> Hps4<sup>le</sup>			ECO:0000033	author statement supported by traceable reference	PMID:11836498	20110705	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:3775191	Nlgn4l	is_implicated_in	DOID:0060041	autism spectrum disorder		MGI:3783593	Nlgn4l<sup>Gt(XST093)Byg</sup>/Nlgn4l<sup>Gt(XST093)Byg</sup>  [background:] B6.129P2-Nlgn4x<sup>Gt(XST093)Byg</sup>			ECO:0000033	author statement supported by traceable reference	PMID:18227507	20190430	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3841929	Cyp11b1<sup>tm1Chjk</sup>	is_implicated_in	DOID:0050811	congenital adrenal hyperplasia		MGI:3841959	Cyp11b1<sup>tm1Chjk</sup>/Cyp11b1<sup>tm1Chjk</sup>  [background:] involves: 129P2/OlaHsd * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:19029289	20151122	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1856666	Apo	is_implicated_in	DOID:83	cataract		MGI:2175702	Apo/Apo<sup>+</sup>  [background:] involves: 101 * C3H			ECO:0000033	author statement supported by traceable reference	PMID:3209064	20170612	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3590216	Tg(H2-Ea-Ins2)1Wehi	is_implicated_in	DOID:9744	type 1 diabetes mellitus		MGI:3590228	Tg(H2-Ea-Ins2)1Wehi/0  [background:] NOD/ShiLtJWehi-Tg(H2-Ea-Ins2)1Wehi			ECO:0000033	author statement supported by traceable reference	PMID:9836515	20060531	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2157909	Uox<sup>in</sup>	is_implicated_in	DOID:1920	hyperuricemia		MGI:3687954	Uox<sup>in</sup>/Uox<sup>in</sup>  [background:] involves: C57BL/6J * DBA/2J			ECO:0000033	author statement supported by traceable reference	PMID:11474184	20170601	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	is_implicated_in	DOID:0080208	metabolic dysfunction-associated steatotic liver disease		MGI:6356398	Lepr<sup>db</sup>/Lepr<sup>db</sup>  [background:] B6.BKS(D)-Lepr<sup>db</sup>/JOrlRj			ECO:0000033	author statement supported by traceable reference	PMID:22118645	20190821	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3711216	Elovl4<sup>tm1Wked</sup>	is_implicated_in	DOID:0050817	Stargardt disease		MGI:3711534	Elovl4<sup>tm1Wked</sup>/Elovl4<sup>+</sup>  [background:] involves: 129S/SvEv * 129S1/Sv			ECO:0000033	author statement supported by traceable reference	PMID:17356513	20070613	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2177666	Eif2ak3<sup>tm1Dron</sup>	is_implicated_in	DOID:0090060	Wolcott-Rallison syndrome		MGI:3582643	Eif2ak3<sup>tm1Dron</sup>/Eif2ak3<sup>tm1Dron</sup>  [background:] involves: 129S6/SvEvTac * Swiss Webster			ECO:0000033	author statement supported by traceable reference	PMID:11430819	20170629	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1859647	Fgf10<sup>tm1Ska</sup>	is_implicated_in	DOID:10486	intestinal atresia		MGI:2175884	Fgf10<sup>tm1Ska</sup>/Fgf10<sup>tm1Ska</sup>  [background:] involves: C57BL/6 * CBA			ECO:0000033	author statement supported by traceable reference	PMID:15234214	20170606	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3624790	Yy1<sup>tm2.1Yshi</sup>	is_implicated_in	DOID:4769	pleuropulmonary blastoma		MGI:5902325	Yy1<sup>tm2.1Yshi</sup>/Yy1<sup>tm2.1Yshi</sup> Tg(Nkx2-1-cre)2Sand/0  [background:] involves: 129S4/SvJae * C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:26329601	20170612	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	is_implicated_in	DOID:0090029	CINCA Syndrome		MGI:5517789	Nlrp3<sup>tm3.1Hhf</sup>/Nlrp3<sup>+</sup>  [background:] involves: 129			ECO:0000033	author statement supported by traceable reference	PMID:22558291	20170630	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3587413	Zfpm2<sup>lil</sup>	is_implicated_in	DOID:3827	congenital diaphragmatic hernia		MGI:3589477	Zfpm2<sup>lil</sup>/Zfpm2<sup>lil</sup>  [background:] involves: A/J			ECO:0000033	author statement supported by traceable reference	PMID:16103912	20051013	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1891731	Stub1	is_implicated_in	DOID:0080029	autosomal recessive spinocerebellar ataxia 16		MGI:2680011	Stub1<sup>tm1Cpat</sup>/Stub1<sup>tm1Cpat</sup>  [background:] involves: 129S/SvEv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:28593200	20180504	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2670598	Hap1<sup>tm1Xjl</sup>	is_not_implicated_in	DOID:12858	Huntington's disease		MGI:2670610	Hap1<sup>tm1Xjl</sup>/Hap1<sup>tm1Xjl</sup>  [background:] involves: 129S6/SvEvTac * Black Swiss			ECO:0000033	author statement supported by traceable reference	PMID:12890790	20050705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:1861799	C3<sup>tm1Crr</sup>	is_implicated_in	DOID:8354	complement component 3 deficiency		MGI:2429606	C3<sup>tm1Crr</sup>/C3<sup>tm1Crr</sup>  [background:] involves: 129S4/SvJae * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:8524789	20151118	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:88373	Cebpb	is_implicated_in	DOID:2256	osteochondrodysplasia		MGI:2656637	Cebpb<sup>tm1Kish</sup>/Cebpb<sup>tm1Kish</sup>  [background:] involves: 129P2/OlaHsd			ECO:0000033	author statement supported by traceable reference	PMID:24885110	20221010	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:4418212	Sdhd<sup>tm1Jpb</sup>	is_not_implicated_in	DOID:0050773	paraganglioma		MGI:4418214	Sdhd<sup>tm1Jpb</sup>/Sdhd<sup>+</sup>  [background:] either: 129P2/OlaHsd-Sdhd<sup>tm1Jpb</sup> or (involves: 129P2/OlaHsd * C57BL/6J)			ECO:0000033	author statement supported by traceable reference	PMID:19956719	20130930	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:109246	Htr4	is_not_implicated_in	DOID:3083	chronic obstructive pulmonary disease		MGI:6156525	Htr4<sup>tm1Comp</sup>/Htr4<sup>tm1Comp</sup>  [background:] B6.129S1(129T)-Htr4<sup>tm1Comp</sup>			ECO:0000033	author statement supported by traceable reference	PMID:24183679	20180516	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2386884	Inpp5d<sup>tm1Rkh</sup>	is_implicated_in	DOID:5408	Paget's disease of bone		MGI:5319308	Inpp5d<sup>tm1Rkh</sup>/Inpp5d<sup>tm1Rkh</sup>  [background:] involves: 129S1/Sv * 129X1/SvJ			ECO:0000033	author statement supported by traceable reference	PMID:12161749	20120525	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100846	Med1	is_implicated_in	DOID:6000	congestive heart failure		MGI:5911326	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> Tg(Myh6-cre)2182Mds/0  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:1100846	Med1	is_implicated_in	DOID:6000	congestive heart failure		MGI:5911329	Med1<sup>tm2Jkr</sup>/Med1<sup>tm2Jkr</sup> A1cf<sup>Tg(Myh6-cre/Esr1*)1Jmk</sup>/A1cf<sup>+</sup>  [background:] involves: 129P2/OlaHsd * FVB/N			ECO:0000033	author statement supported by traceable reference	PMID:27548259	20171012	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2681836	Polr3a	is_not_implicated_in	DOID:0060794	hypomyelinating leukodystrophy 7		MGI:6209828	Polr3a<sup>tm1.1Bebr</sup>/Polr3a<sup>tm1.1Bebr</sup>  [background:] involves: C57BL/6J			ECO:0000033	author statement supported by traceable reference	PMID:28407788	20181030	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:2681836	Polr3a	is_not_implicated_in	DOID:0060794	hypomyelinating leukodystrophy 7		MGI:6214847	Polr3a<sup>Gt(LG04)Osb</sup>/Polr3a<sup>tm1Bebr</sup>  [background:] involves: C57BL/6 * C57BL/6J * DBA/2			ECO:0000033	author statement supported by traceable reference	PMID:28407788	20181030	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:2181069	Itgb4<sup>tm1Fgg</sup>	is_implicated_in	DOID:0060733	junctional epidermolysis bullosa with pyloric atresia		MGI:3694660	Itgb4<sup>tm1Fgg</sup>/Itgb4<sup>tm1Fgg</sup>  [background:] involves: 129S1/Sv * C57BL/6			ECO:0000033	author statement supported by traceable reference	PMID:9670011	20090319	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:107734	Ap3d1	is_implicated_in	DOID:0060540	Hermansky-Pudlak syndrome 2		MGI:3528946	Ap3d1<sup>mh</sup>/Ap3d1<sup>mh</sup>  [background:] B6.C3-Grxcr1<sup>pi</sup>			ECO:0000033	author statement supported by traceable reference	PMID:1912584	20110705	MGI
NCBITaxon:10090	Mus musculus	allele	MGI:3773697	Tg(tetO-Prkar1a*x2as)1Stra	is_implicated_in	DOID:0050471	Carney complex		MGI:5897214	Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0  [background:] involves: C57BL/6 * NMRI * SJL			ECO:0000033	author statement supported by traceable reference	PMID:15591278	20170511	MGI
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913892	Ctnnbl1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913388	Bud23	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923051	4930447C04Rik	implicated_via_orthology	DOID:0112270	spermatogenic failure 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:0110026	age related macular degeneration 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097161	Bak1	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923810	Prss8	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:0070042	Coffin-Siris syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99495	Brd2	implicated_via_orthology	DOID:3159	photosensitivity disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87995	Aldob	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:0050606	acrokeratosis verruciformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	implicated_via_orthology	DOID:0112189	thyroid dyshormonogenesis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313302	Cenpf	implicated_via_orthology	DOID:0110595	Stromme syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347095	Adgre5	implicated_via_orthology	DOID:1554	vibratory urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0080122	Alpers-Huttenlocher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0111243	acromicric dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:4488	sarcomatoid mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442120	Bank1	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107508	Ereg	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913765	Cul7	implicated_via_orthology	DOID:0060241	3-M syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103301	Cacnb4	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679260	Crb2	implicated_via_orthology	DOID:0111134	focal segmental glomerulosclerosis 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345150	Cdc6	implicated_via_orthology	DOID:0080516	Meier-Gorlin syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:3025	acinar cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931001	Edaradd	implicated_via_orthology	DOID:14793	hypohidrotic ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106197	Stfa2	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97245	Mxi1	implicated_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	implicated_via_orthology	DOID:9273	citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108100	Dvl3	implicated_via_orthology	DOID:0060767	autosomal dominant Robinow syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859665	Atp8b1	implicated_via_orthology	DOID:0070226	progressive familial intrahepatic cholestasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443552	Themis	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	implicated_via_orthology	DOID:0111455	GRACILE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330841	Bcl2l10	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:9883	Becker muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448558	Fancb	implicated_via_orthology	DOID:0111098	Fanconi anemia complementation group B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	implicated_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891414	Cep41	implicated_via_orthology	DOID:0110984	Joubert syndrome 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	implicated_via_orthology	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88269	Car2	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:0080626	corticosterone methyloxidase deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148202	Ces1d	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929913	Bcl11b	implicated_via_orthology	DOID:0111979	immunodeficiency 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	implicated_via_orthology	DOID:0110231	cataract 1 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104725	Atn1	implicated_via_orthology	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347001	Btd	implicated_via_orthology	DOID:856	biotinidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142808	Cog4	implicated_via_orthology	DOID:0111673	Saul-Wilson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	implicated_via_orthology	DOID:0112000	immunodeficiency 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:2855	hyperthyroxinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685581	Ccn6	implicated_via_orthology	DOID:0090004	progressive pseudorheumatoid arthropathy of childhood						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918552	Arhgap26	implicated_via_orthology	DOID:0081082	acute myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107187	Bcl6	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0060655	autosomal recessive congenital ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446632	Ago2	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:8354	complement component 3 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661175	Cnksr2	implicated_via_orthology	DOID:0080242	syndromic X-linked mental retardation Hough type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:10024	migraine with aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913277	Crbn	implicated_via_orthology	DOID:0081178	autosomal recessive intellectual developmental disorder 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:0110849	xeroderma pigmentosum group G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104684	Eps8	implicated_via_orthology	DOID:0110463	autosomal recessive nonsyndromic deafness 102						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306784	Cited2	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3033992	Cldn19	implicated_via_orthology	DOID:0060881	renal hypomagnesemia 5 with ocular involvement						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442232	Gimap5	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924020	Csta2	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138968	Clp1	implicated_via_orthology	DOID:0060279	pontocerebellar hypoplasia type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923442	Abhd12	implicated_via_orthology	DOID:0080181	PHARC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890596	Evc	implicated_via_orthology	DOID:0111571	Weyers acrofacial dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892995	Dnajc5	implicated_via_orthology	DOID:0110720	neuronal ceroid lipofuscinosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	implicated_via_orthology	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104627	Dst	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	implicated_via_orthology	DOID:0080419	developmental and epileptic encephalopathy 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913945	Aspn	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443065	Agps	implicated_via_orthology	DOID:0110853	rhizomelic chondrodysplasia punctata type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346328	Def6	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:0110021	age related macular degeneration 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278313	Coch	implicated_via_orthology	DOID:0111644	autosomal recessive nonsyndromic deafness 110						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685369	Fat2	implicated_via_orthology	DOID:0080287	spinocerebellar ataxia 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	implicated_via_orthology	DOID:363	uterine cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:0111223	centronuclear myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919439	Bag6	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88526	Crygf	implicated_via_orthology	DOID:0110234	cataract 4 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861630	Espn	implicated_via_orthology	DOID:0110494	autosomal recessive nonsyndromic deafness 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	implicated_via_orthology	DOID:0110599	primary ciliary dyskinesia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0050864	non-arteritic anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:0060365	mandibulofacial dysostosis with alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347062	Creb3l1	implicated_via_orthology	DOID:0110345	osteogenesis imperfecta type 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338073	Cdc45	implicated_via_orthology	DOID:0080518	Meier-Gorlin syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3696883	Cstdc5	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644563	Acp4	implicated_via_orthology	DOID:0080953	amelogenesis imperfecta type 1J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137336	Baiap2	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99431	Arf1	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:0081339	congenital myopathy 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95402	Epb42	implicated_via_orthology	DOID:0110920	hereditary spherocytosis type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145890	Ano6	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261856	Ankle2	implicated_via_orthology	DOID:0070289	primary autosomal recessive microcephaly 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321398	F11r	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890646	Nek8	implicated_via_orthology	DOID:0111120	nephronophthisis 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277223	Atxn2	implicated_via_orthology	DOID:0050955	spinocerebellar ataxia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276121	Bckdk	implicated_via_orthology	DOID:0090126	branched-chain keto acid dehydrogenase kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919834	Cul4b	implicated_via_orthology	DOID:0060822	syndromic X-linked intellectual disability Cabezas type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917205	Fars2	implicated_via_orthology	DOID:0110822	hereditary spastic paraplegia 77						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107734	Ap3d1	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	implicated_via_orthology	DOID:0060602	alpha-methylacyl-CoA racemase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349431	Eif2s3x	implicated_via_orthology	DOID:0060801	MEHMO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447763	Dnd1	implicated_via_orthology	DOID:3305	teratocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919120	Cfap45	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:0050921	pharynx squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661061	Dsg4	implicated_via_orthology	DOID:0110703	hypotrichosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098230	Cenpe	implicated_via_orthology	DOID:0070283	primary autosomal recessive microcephaly 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:0050450	Gitelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923691	Daam2	implicated_via_orthology	DOID:2590	familial nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:10041	dysplastic nevus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443290	Cntrob	implicated_via_orthology	DOID:0112311	male infertility due to acephalic spermatozoa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88436	Cnga1	implicated_via_orthology	DOID:0110377	retinitis pigmentosa 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:0090084	hypogonadotropic hypogonadism 5 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921703	Cfap53	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88108	Atp1b1	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890773	Actn4	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858196	Mybph	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0111561	stiff skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:0080594	hyper IgE recurrent infection syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339972	Bhmt	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316660	Cacng2	implicated_via_orthology	DOID:0070040	autosomal dominant intellectual developmental disorder 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442402	Cnot1	implicated_via_orthology	DOID:0081398	holoprosencephaly 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:0081046	frontonasal dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916469	Ddah1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914427	Cdt1	implicated_via_orthology	DOID:0080515	Meier-Gorlin syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918816	Clmp	implicated_via_orthology	DOID:10605	short bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88450	Col17a1	implicated_via_orthology	DOID:0070337	epithelial recurrent erosion dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919847	Auts2	implicated_via_orthology	DOID:0070056	autosomal dominant intellectual developmental disorder 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387613	Erlin1	implicated_via_orthology	DOID:0110813	hereditary spastic paraplegia 62						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	implicated_via_orthology	DOID:0110821	hereditary spastic paraplegia 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340046	Adam22	implicated_via_orthology	DOID:0080434	developmental and epileptic encephalopathy 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3513977	Apcdd1	implicated_via_orthology	DOID:0110698	hypotrichosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104978	Cyp7b1	implicated_via_orthology	DOID:0111070	congenital bile acid synthesis defect 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179947	Catsper1	implicated_via_orthology	DOID:0070173	spermatogenic failure 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106653	Epcam	implicated_via_orthology	DOID:0070270	hereditary nonpolyposis colorectal cancer type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3524944	Stfa2l1	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859568	Cd164	implicated_via_orthology	DOID:0110587	autosomal dominant nonsyndromic deafness 66						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195272	Eda	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924298	Cep83	implicated_via_orthology	DOID:0111125	nephronophthisis 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94941	Dvl1	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:0070049	autosomal dominant intellectual developmental disorder 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95714	Gja3	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924290	Atg16l1	implicated_via_orthology	DOID:0110885	inflammatory bowel disease 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	implicated_via_orthology	DOID:0081060	X-linked nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	implicated_via_orthology	DOID:0070199	Miyoshi muscular dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88513	Cr1l	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104574	Ptprj	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	implicated_via_orthology	DOID:0110451	dilated cardiomyopathy 1O						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388633	Cltc	implicated_via_orthology	DOID:0080226	autosomal dominant intellectual developmental disorder 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891221	Crtap	implicated_via_orthology	DOID:0110337	osteogenesis imperfecta type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	implicated_via_orthology	DOID:3495	extrahepatic bile duct adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919683	Rab38	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444031	Alg6	implicated_via_orthology	DOID:0080555	congenital disorder of glycosylation Ic						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108117	Emd	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	implicated_via_orthology	DOID:0060889	prune belly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923097	Crppa	implicated_via_orthology	DOID:0111234	congenital muscular dystrophy-dystroglycanopathy A7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94921	Dpp6	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	implicated_via_orthology	DOID:0110965	brachydactyly type A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443778	Cfap69	implicated_via_orthology	DOID:0111929	spermatogenic failure 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924134	Cyfip2	implicated_via_orthology	DOID:0080430	developmental and epileptic encephalopathy 65						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	implicated_via_orthology	DOID:0110831	Usher syndrome type 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:5381	bile duct adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860083	Cd320	implicated_via_orthology	DOID:0060741	methylmalonic acidemia due to transcobalamin receptor defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919127	Efhc1	implicated_via_orthology	DOID:4890	juvenile myoclonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106198	Stfa1	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098282	C9	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444630	Dmxl2	implicated_via_orthology	DOID:0112217	developmental and epileptic encephalopathy 81						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:0060255	rippling muscle disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107822	Ebp	implicated_via_orthology	DOID:0080352	X-linked chondrodysplasia punctata 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274782	Alox12b	implicated_via_orthology	DOID:0060710	autosomal recessive congenital ichthyosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096877	Dll3	implicated_via_orthology	DOID:1934	dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894644	Cacnb2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385848	Bcas3	implicated_via_orthology	DOID:0070408	Hengel-Maroofian-Schols syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028576	Dhx37	implicated_via_orthology	DOID:14448	46,XY sex reversal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:10485	esophageal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104841	Cpox	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103286	Atp6v0a1	implicated_via_orthology	DOID:0070390	developmental and epileptic encephalopathy 104						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:0081138	agammaglobulinemia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103222	Zbtb16	implicated_via_orthology	DOID:1148	polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448715	Cxcr1	implicated_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919683	Rab38	implicated_via_orthology	DOID:2223	platelet storage pool deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:14415	Legg-Calve-Perthes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103249	Calm3	implicated_via_orthology	DOID:0060674	catecholaminergic polymorphic ventricular tachycardia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686394	Nckap5	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779470	Ces1b	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350933	Bcap31	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:0110307	hypertrophic cardiomyopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:3275	thymoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97371	Npr1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354737	Kdm2b	implicated_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:718	autoimmune hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:0111866	trichothiodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345140	Aloxe3	implicated_via_orthology	DOID:0060656	autosomal recessive congenital ichthyosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:559	acute pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:13774	Addison's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103249	Calm3	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99480	Cebpa	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646230	Clrn2	implicated_via_orthology	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661061	Dsg4	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919595	Amer1	implicated_via_orthology	DOID:0060886	osteopathia striata with cranial sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104965	Zp3r	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87921	Adh1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	implicated_via_orthology	DOID:1405	primary angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2668347	C8a	implicated_via_orthology	DOID:0060301	type I complement component 8 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926471	Fancg	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858496	Deaf1	implicated_via_orthology	DOID:0070054	Vulto-van Silfout-de Vries syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88035	Aox1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0110341	osteogenesis imperfecta type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95415	Erg	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097717	Ankrd1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916918	Ccdc115	implicated_via_orthology	DOID:0070267	congenital disorder of glycosylation type IIo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931001	Edaradd	implicated_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:0060875	isolated growth hormone deficiency type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3639762	Dnah7c	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:1849	cannabis dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	implicated_via_orthology	DOID:0111421	familial apolipoprotein A5 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151233	Dph1	implicated_via_orthology	DOID:0070477	diphthamide deficiency syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152695	Col4a6	implicated_via_orthology	DOID:0111740	X-linked deafness 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97722	Pnlip	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097689	Ackr1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298398	Mcm7	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442232	Gimap5	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349717	Ncor1	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:0080840	optic atrophy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919129	Acsl5	implicated_via_orthology	DOID:0060774	congenital diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:10933	obsessive-compulsive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661061	Dsg4	implicated_via_orthology	DOID:4535	hypotrichosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146430	Cblb	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	implicated_via_orthology	DOID:0080228	autosomal dominant intellectual developmental disorder 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442306	Fancm	implicated_via_orthology	DOID:0080872	primary ovarian insufficiency 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929699	Arl3	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	implicated_via_orthology	DOID:0080224	autosomal dominant dystrophic epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105313	Cit	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652818	Dcdc2a	implicated_via_orthology	DOID:0110517	autosomal recessive nonsyndromic deafness 66						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104725	Atn1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858500	Diaph2	implicated_via_orthology	DOID:0080858	primary ovarian insufficiency 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:12387	nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88448	Col12a1	implicated_via_orthology	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95710	Ghrhr	implicated_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	implicated_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921527	Chic2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:0111866	trichothiodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	implicated_via_orthology	DOID:0110913	adult hypophosphatasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:12399	pathological gambling						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343051	Actl7a	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096355	S1pr1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95478	Fabp2	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388707	Abca13	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:2697	renal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685615	Ceacam16	implicated_via_orthology	DOID:0111636	autosomal recessive nonsyndromic deafness 113						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387643	B9d2	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3613666	Ano3	implicated_via_orthology	DOID:0090052	dystonia 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045421	Ank	implicated_via_orthology	DOID:1156	chondrocalcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0112281	spondyloepiphyseal dysplasia Stanescu type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442253	Cln5	implicated_via_orthology	DOID:0110728	neuronal ceroid lipofuscinosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	implicated_via_orthology	DOID:0111030	hemochromatosis type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95618	Gabra6	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:3125	multiple endocrine neoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106442	Vkorc1	implicated_via_orthology	DOID:0080666	warfarin sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930088	Clcf1	implicated_via_orthology	DOID:0080330	cold-induced sweating syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	implicated_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88524	Crygd	implicated_via_orthology	DOID:0110234	cataract 4 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:10939	antisocial personality disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107508	Ereg	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341149	Akap3	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685784	Ccdc78	implicated_via_orthology	DOID:0111224	centronuclear myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:0060585	Noonan syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:0110456	dilated cardiomyopathy 1R						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351659	Abcg5	implicated_via_orthology	DOID:0090019	sitosterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:0050572	cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354713	Acsl4	implicated_via_orthology	DOID:0112050	non-syndromic X-linked intellectual disability 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355272	Csnk1d	implicated_via_orthology	DOID:0110012	advanced sleep phase syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0112195	spondyloperipheral dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916990	Dph5	implicated_via_orthology	DOID:0070479	neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:0060297	complement component 4a deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661061	Dsg4	implicated_via_orthology	DOID:4535	hypotrichosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922941	Anks6	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384790	Fanci	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102504	mt-Co1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:3145	hyperlipoproteinemia type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95278	Epha2	implicated_via_orthology	DOID:0110229	cataract 6 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919439	Bag6	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448730	Atcay	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098757	Coa3	implicated_via_orthology	DOID:0070499	mitochondrial complex IV deficiency nuclear type 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202294	Aff2	implicated_via_orthology	DOID:0080984	X-linked intellectual developmental disorder 109						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:0110116	autoimmune lymphoproliferative syndrome type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913838	Cmpk1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443767	Aaas	implicated_via_orthology	DOID:0050602	triple-A syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923582	Cog2	implicated_via_orthology	DOID:0070269	congenital disorder of glycosylation type IIq						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927617	Dhx38	implicated_via_orthology	DOID:0112141	retinitis pigmentosa 84						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096340	E2f3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197012	Aebp1	implicated_via_orthology	DOID:0080732	Ehlers-Danlos syndrome classic-like 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	implicated_via_orthology	DOID:0110944	autosomal recessive osteopetrosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:11372	megacolon						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88378	Ces1g	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97295	Casp2	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:12030	panuveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644688	Csta3	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104873	Aga	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442875	Adamts19	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	implicated_via_orthology	DOID:0070136	autosomal dominant cutis laxa 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97245	Mxi1	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	implicated_via_orthology	DOID:0081350	congenital myopathy 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338822	Celf2	implicated_via_orthology	DOID:0070383	developmental and epileptic encephalopathy 97						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340030	Crlf1	implicated_via_orthology	DOID:0080329	cold-induced sweating syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95432	Ces1e	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915270	Coa8	implicated_via_orthology	DOID:0070502	mitochondrial complex IV deficiency nuclear type 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	implicated_via_orthology	DOID:9258	Waardenburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:1283	enterocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918963	Cdc40	implicated_via_orthology	DOID:0112326	pontocerebellar hypoplasia type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918742	Bbs7	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105378	Adam12	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894701	Mgat5	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107822	Ebp	implicated_via_orthology	DOID:2581	chondrodysplasia punctata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88346	Cd8a	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894679	Bach2	implicated_via_orthology	DOID:0111954	immunodeficiency 60						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88610	Cyp3a13	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861586	Krt71	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914672	Dhdds	implicated_via_orthology	DOID:0110352	retinitis pigmentosa 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916978	Card11	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916978	Card11	implicated_via_orthology	DOID:0111958	immunodeficiency 11B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99476	Abhd16a	implicated_via_orthology	DOID:0112342	hereditary spastic paraplegia 86						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353627	Angptl3	implicated_via_orthology	DOID:0111061	familial hypobetalipoproteinemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	implicated_via_orthology	DOID:4797	SM-AHNMD						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914731	Alg2	implicated_via_orthology	DOID:0080561	congenital disorder of glycosylation Ii						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0110028	age related macular degeneration 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338758	Adnp	implicated_via_orthology	DOID:0070058	Helsmoortel-Van Der Aa Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:0050450	Gitelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443598	Cfap91	implicated_via_orthology	DOID:0112273	spermatogenic failure 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:12030	panuveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914217	Edem3	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346017	Clpx	implicated_via_orthology	DOID:13270	erythropoietic protoporphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343142	Arpc1b	implicated_via_orthology	DOID:0112004	immunodeficiency 71						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94941	Dvl1	implicated_via_orthology	DOID:0060765	autosomal dominant Robinow syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343461	Ecel1	implicated_via_orthology	DOID:0111594	distal arthrogryposis type 5D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855697	Atp5f1e	implicated_via_orthology	DOID:0060332	mitochondrial complex V (ATP synthase) deficiency nuclear type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87885	Chrna1	implicated_via_orthology	DOID:0110662	congenital myasthenic syndrome 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037816	Cerkl	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858500	Diaph2	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:14184	polyneuropathy due to drug						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88525	Cryge	implicated_via_orthology	DOID:0110234	cataract 4 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88233	C6	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443893	Ccdc40	implicated_via_orthology	DOID:0110623	primary ciliary dyskinesia 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919214	Atad3a	implicated_via_orthology	DOID:0081395	Harel-Yoon syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88229	C4bp	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106215	Aqp5	implicated_via_orthology	DOID:0111707	Bothnian type palmoplantar keratoderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99150	Yy1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309489	Cask	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921624	Clec16a	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:0111700	ankyrin-B-related cardiac arrhythmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924122	Ccdc116	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0060025	immunoglobulin alpha deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88226	C2	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917745	Atp6ap2	implicated_via_orthology	DOID:0112105	X-linked parkinsonism-spasticity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:0110032	autosomal dominant Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:686	liver carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97829	Pygl	implicated_via_orthology	DOID:3650	lactic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919164	Antxr2	implicated_via_orthology	DOID:0050871	fibroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889295	Eral1	implicated_via_orthology	DOID:0080256	Perrault syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445168	Elmod3	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:0090122	aromatase excess syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87870	Acat1	implicated_via_orthology	DOID:2978	carbohydrate metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:0080526	bronchiectasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922954	Ces1h	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88116	Atp6v0c	implicated_via_orthology	DOID:0070472	early-onset epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894686	Col9a3	implicated_via_orthology	DOID:0080046	Stickler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88223	C1qa	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922941	Anks6	implicated_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99538	Acsm3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	implicated_via_orthology	DOID:0080597	Kleefstra syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88466	Col9a2	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139083	Cep152	implicated_via_orthology	DOID:0070012	Seckel syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:0111370	apolipoprotein C-III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441769	Dclre1c	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918039	Kynu	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098592	Alg3	implicated_via_orthology	DOID:0080556	congenital disorder of glycosylation Id						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98181	Rrm2	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141101	Depdc5	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88421	Clps	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330281	Cd2ap	implicated_via_orthology	DOID:0112245	focal segmental glomerulosclerosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685838	Dnah7a	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920942	Cplane1	implicated_via_orthology	DOID:0110986	Joubert syndrome 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154263	Bicra	implicated_via_orthology	DOID:0112370	Coffin-Siris syndrome 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94921	Dpp6	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916197	Chst8	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	implicated_via_orthology	DOID:0111371	isolated hyperchlorhidrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88474	Cox5a	implicated_via_orthology	DOID:0070505	mitochondrial complex IV deficiency nuclear type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685062	Catip	implicated_via_orthology	DOID:0112335	spermatogenic failure 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337994	Bcl10	implicated_via_orthology	DOID:0111939	immunodeficiency 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141969	Efl1	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681869	Cep135	implicated_via_orthology	DOID:0070282	primary autosomal recessive microcephaly 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3524930	Csta1	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643681	Bhmt1b	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915838	Cthrc1	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914824	Alg13	implicated_via_orthology	DOID:0080470	developmental and epileptic encephalopathy 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:4990	essential tremor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0111007	X-linked cone-rod dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922941	Anks6	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:7575	pancreatic intraductal papillary-mucinous neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889383	Ap1s2	implicated_via_orthology	DOID:0060800	syndromic X-linked intellectual disability 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341265	Camk2d	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913498	Alg5	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87929	Adh5	implicated_via_orthology	DOID:0080952	AMED syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918993	Coasy	implicated_via_orthology	DOID:0112327	pontocerebellar hypoplasia type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	implicated_via_orthology	DOID:2935	Chediak-Higashi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:1962	fallopian tube disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916211	Phkg2	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	implicated_via_orthology	DOID:3613	Canavan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354962	Copb2	implicated_via_orthology	DOID:0070281	primary autosomal recessive microcephaly 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142166	C2cd3	implicated_via_orthology	DOID:4501	orofaciodigital syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	implicated_via_orthology	DOID:0060445	congenital stromal corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88355	Cdh2	implicated_via_orthology	DOID:0080948	agenesis of corpus callosum, cardiac, ocular, and genital syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105313	Cit	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102706	Fdft1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	implicated_via_orthology	DOID:0090129	carnitine palmitoyltransferase I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:4606	bile duct cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345634	Amfr	implicated_via_orthology	DOID:0070458	hereditary spastic paraplegia 89						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88233	C6	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892013	Agrp	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96965	Mertk	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920243	Appl1	implicated_via_orthology	DOID:0111111	maturity-onset diabetes of the young type 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3781475	Cfap47	implicated_via_orthology	DOID:0112274	X-linked spermatogenic failure 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88497	Crhbp	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919191	Cars2	implicated_via_orthology	DOID:0111489	combined oxidative phosphorylation deficiency 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924161	Brd1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137336	Baiap2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87893	Chrnd	implicated_via_orthology	DOID:0110665	congenital myasthenic syndrome 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:0111191	distal myopathy Tateyama type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353431	Pcsk1n	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648404	Cstdc3	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0070117	Meckel syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:13078	eumycotic mycetoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104855	Atp6v0a2	implicated_via_orthology	DOID:0112171	wrinkly skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138828	Eps8l2	implicated_via_orthology	DOID:0080261	autosomal recessive nonsyndromic deafness 106						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648919	Ces1a	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:620	blood protein disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	implicated_via_orthology	DOID:0060758	immunodeficiency with hyper-IgM type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915589	Ccdc88c	implicated_via_orthology	DOID:0050986	spinocerebellar ataxia type 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920004	Arhgef10l	implicated_via_orthology	DOID:6212	ovarian endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918552	Arhgap26	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88466	Col9a2	implicated_via_orthology	DOID:0080046	Stickler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328361	Bard1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88446	Col11a1	implicated_via_orthology	DOID:0080675	Stickler syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351331	Chaf1a	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97577	Phka2	implicated_via_orthology	DOID:0111042	glycogen storage disease IXa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919410	Tmem163	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355314	Ddb2	implicated_via_orthology	DOID:0110846	xeroderma pigmentosum group E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195966	Ctnnd2	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:12995	conduct disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277124	Asah1	implicated_via_orthology	DOID:1927	sphingolipidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:0060214	frontotemporal dementia and/or amyotrophic lateral sclerosis-2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88393	Chd1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141861	Ap2s1	implicated_via_orthology	DOID:0060702	familial hypocalciuric hypercalcemia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:10939	antisocial personality disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915142	Coa6	implicated_via_orthology	DOID:0080360	mitochondrial complex IV deficiency nuclear type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277124	Asah1	implicated_via_orthology	DOID:0111527	spinal muscular atrophy with progressive myoclonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:1573	communicating hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136853	Fam20c	implicated_via_orthology	DOID:2187	amelogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103222	Zbtb16	implicated_via_orthology	DOID:0080700	caudal regression syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146001	Ccdc65	implicated_via_orthology	DOID:0110611	primary ciliary dyskinesia 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:11759	hypochromic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97829	Pygl	implicated_via_orthology	DOID:2754	glycogen storage disease VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107474	Cd38	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338761	Colq	implicated_via_orthology	DOID:0110667	congenital myasthenic syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926045	Armc9	implicated_via_orthology	DOID:0080275	Joubert syndrome 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921765	Cdkal1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137706	Actn1	implicated_via_orthology	DOID:0111053	platelet-type bleeding disorder 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645124	Cstdc4	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337063	Ap4m1	implicated_via_orthology	DOID:0110802	hereditary spastic paraplegia 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351646	Abca7	implicated_via_orthology	DOID:0111364	Alzheimer's disease 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274784	Adgrv1	implicated_via_orthology	DOID:0110839	Usher syndrome type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919683	Rab38	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	implicated_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105313	Cit	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	implicated_via_orthology	DOID:0110915	childhood hypophosphatasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3505689	Cdsn	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919494	1600014C10Rik	implicated_via_orthology	DOID:0110795	hereditary spastic paraplegia 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:3234	central nervous system lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88331	Cd3d	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448730	Atcay	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	implicated_via_orthology	DOID:0060352	Kleefstra syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341818	Cnga3	implicated_via_orthology	DOID:0110007	achromatopsia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142687	Ces1f	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351615	Add3	implicated_via_orthology	DOID:0081361	spastic quadriplegic cerebral palsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:3829	pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931825	Chst5	implicated_via_orthology	DOID:2565	macular corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145517	B3galnt2	implicated_via_orthology	DOID:0111230	congenital muscular dystrophy-dystroglycanopathy type A11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201780	Atp6v1a	implicated_via_orthology	DOID:0070129	autosomal recessive cutis laxa type IID						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88016	Ampd2	implicated_via_orthology	DOID:0110814	hereditary spastic paraplegia 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	implicated_via_orthology	DOID:0110266	cataract 9 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:0110545	autosomal dominant nonsyndromic deafness 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261811	Myo15a	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101926	Dlx5	implicated_via_orthology	DOID:0090024	split hand-foot malformation 1 with sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276121	Bckdk	implicated_via_orthology	DOID:14228	oligospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:0050548	hereditary sensory neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	implicated_via_orthology	DOID:0081336	Thomsen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88589	Cyp1a2	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351471	B9d1	implicated_via_orthology	DOID:0110996	Joubert syndrome 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88075	Arsb	implicated_via_orthology	DOID:12800	mucopolysaccharidosis VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	implicated_via_orthology	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	implicated_via_orthology	DOID:3151	skin squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:0060297	complement component 4a deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87917	Adcy6	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106906	Eif4a2	implicated_via_orthology	DOID:0070512	neurodevelopmental disorder with hypotonia and speech delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445210	Cyp4f39	implicated_via_orthology	DOID:0060714	autosomal recessive congenital ichthyosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0110334	osteogenesis imperfecta type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88269	Car2	implicated_via_orthology	DOID:0110941	autosomal recessive osteopetrosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351660	Csnk1e	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88460	Col6a2	implicated_via_orthology	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103010	Epb41l1	implicated_via_orthology	DOID:0070041	autosomal dominant intellectual developmental disorder 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108405	Apbb2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179942	Adamts14	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3696881	Cstdc6	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611575	Cfhr2	implicated_via_orthology	DOID:0110014	age related macular degeneration 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:9383	iridocyclitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	implicated_via_orthology	DOID:1540	parathyroid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	implicated_via_orthology	DOID:0111407	Fraser syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108100	Dvl3	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921624	Clec16a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928896	Arpc1a	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:0080626	corticosterone methyloxidase deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94891	Dhh	implicated_via_orthology	DOID:14448	46,XY sex reversal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152539	Creld1	implicated_via_orthology	DOID:1681	heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:0110035	Alzheimer's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3027157	Kng2	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341877	Cyp46a1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914272	Acad9	implicated_via_orthology	DOID:0112072	nuclear type mitochondrial complex I deficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:8970	subacute sclerosing panencephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103301	Cacnb4	implicated_via_orthology	DOID:0050993	episodic ataxia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106196	Stfa3	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102676	Abcc1	implicated_via_orthology	DOID:0112168	autosomal dominant nonsyndromic deafness 77						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	implicated_via_orthology	DOID:0050489	multinodular goiter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384878	Cep164	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306784	Cited2	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98917	Uros	implicated_via_orthology	DOID:13271	cutaneous porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	implicated_via_orthology	DOID:0070303	multiple epiphyseal dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:3317	hepatic angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925064	Dstyk	implicated_via_orthology	DOID:0110774	hereditary spastic paraplegia 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681008	Cers3	implicated_via_orthology	DOID:0060718	autosomal recessive congenital ichthyosis 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913658	Aptx	implicated_via_orthology	DOID:14784	olivopontocerebellar atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	implicated_via_orthology	DOID:0110373	retinitis pigmentosa 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929293	Cib2	implicated_via_orthology	DOID:0110836	Usher syndrome type 1J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932723	Gimap3	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:1387	hypolipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:4189	mutism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	implicated_via_orthology	DOID:0080047	pseudoachondroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099442	Atxn3	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890651	Brwd1	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889276	Dgke	implicated_via_orthology	DOID:0080388	nephrotic syndrome type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:0112339	Tatton-Brown-Rahman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135956	Prlhr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:0110965	brachydactyly type A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915551	Cep57	implicated_via_orthology	DOID:0080142	mosaic variegated aneuploidy syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888986	Dlg3	implicated_via_orthology	DOID:0112041	non-syndromic X-linked intellectual disability 90						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932723	Gimap3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894289	Ebf3	implicated_via_orthology	DOID:0081176	hypotonia, ataxia, and delayed development syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	implicated_via_orthology	DOID:9280	carbamoyl phosphate synthetase I deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137612	Fkbp6	implicated_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95420	Ces1c	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87919	Add2	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685748	Mrs2	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:0081113	Baraitser-Winter syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:1849	cannabis dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330812	Acox1	implicated_via_orthology	DOID:0070516	Mitchell syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107731	Dnah2	implicated_via_orthology	DOID:0112163	spermatogenic failure 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341830	Eif2ak3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109618	Atp6v1b2	implicated_via_orthology	DOID:0080720	autosomal dominant congenital deafness with onychodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316745	Bmp15	implicated_via_orthology	DOID:0080494	ovarian dysgenesis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:0060882	renal hypomagnesemia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:3482	plague						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:0112238	X-linked lissencephaly 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:12574	posterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:0070131	autosomal dominant cutis laxa 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149842	Sdf2l1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684953	Dnah7b	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97599	Prkce	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351602	Dguok	implicated_via_orthology	DOID:0080121	mitochondrial DNA depletion syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3026886	Cdin1	implicated_via_orthology	DOID:0111397	congenital dyserythropoietic anemia type Ib						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102774	Aimp1	implicated_via_orthology	DOID:0060790	hypomyelinating leukodystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917317	Ermard	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919127	Efhc1	implicated_via_orthology	DOID:0111324	juvenile absence epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	implicated_via_orthology	DOID:0112153	hypomyelinating leukodystrophy 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201780	Atp6v1a	implicated_via_orthology	DOID:0112275	developmental and epileptic encephalopathy 93						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107721	Dnah1	implicated_via_orthology	DOID:0070165	spermatogenic failure 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917173	Agk	implicated_via_orthology	DOID:0080132	Sengers syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917130	Cfap74	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337065	Ap4s1	implicated_via_orthology	DOID:0110804	hereditary spastic paraplegia 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	implicated_via_orthology	DOID:0070133	autosomal recessive cutis laxa type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442833	Bbs9	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:13884	sick sinus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138169	Cfhr1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347077	Bdp1	implicated_via_orthology	DOID:0111637	autosomal recessive nonsyndromic deafness 112						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87894	Chrne	implicated_via_orthology	DOID:0110677	congenital myasthenic syndrome 4B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	implicated_via_orthology	DOID:2187	amelogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88446	Col11a1	implicated_via_orthology	DOID:0111510	Marshall syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153480	Atp6v0a4	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096360	Cd151	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	implicated_via_orthology	DOID:4769	pleuropulmonary blastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0110871	congenital stationary night blindness 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918673	Epg5	implicated_via_orthology	DOID:0060356	Vici syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102518	Adam3	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643524	Cdc5lrt5	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:10211	cholelithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098266	Chl1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:0080832	mild cognitive impairment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:0112231	lissencephaly 7 with cerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388266	Fam20a	implicated_via_orthology	DOID:0110066	amelogenesis imperfecta type 1G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178217	Akap9	implicated_via_orthology	DOID:0110652	long QT syndrome 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100883	Celsr1	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450151	Cog3	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920159	Chmp1a	implicated_via_orthology	DOID:0060277	pontocerebellar hypoplasia type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140224	Cyp2j11	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:12678	hypercalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717097	Cyp2j12	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925584	Cdk19	implicated_via_orthology	DOID:0112221	developmental and epileptic encephalopathy 87						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153465	Bsnd	implicated_via_orthology	DOID:0110145	Bartter disease type 4a						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88326	Cd27	implicated_via_orthology	DOID:0060708	lymphoproliferative syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277238	Cfap44	implicated_via_orthology	DOID:0070166	spermatogenic failure 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:13365	reading disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:12308	Dubin-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913335	Eif3f	implicated_via_orthology	DOID:0081228	autosomal recessive intellectual developmental disorder 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347049	Clcn6	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:0112263	hypoinsulinemic hypoglycemia with hemihypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109514	Cstb	implicated_via_orthology	DOID:3535	Unverricht-Lundborg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924408	Coq6	implicated_via_orthology	DOID:0070243	primary coenzyme Q10 deficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337994	Bcl10	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915251	Cfap298	implicated_via_orthology	DOID:0110627	primary ciliary dyskinesia 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:1614	male breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	implicated_via_orthology	DOID:0090123	aromatic L-amino acid decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684927	Cenpj	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098282	C9	implicated_via_orthology	DOID:0060303	complement component 9 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384959	Cybc1	implicated_via_orthology	DOID:0070368	autosomal recessive chronic granulomatous disease 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91842	D1Pas1	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108117	Emd	implicated_via_orthology	DOID:0070246	X-linked Emery-Dreifuss muscular dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:2033	communication disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:0050432	Asperger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106100	Etfdh	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94903	Dlx3	implicated_via_orthology	DOID:0111565	trichodontoosseous syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354710	Atp8a2	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102806	Acvr2a	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341085	Epm2a	implicated_via_orthology	DOID:891	progressive myoclonus epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107571	Cav2	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:0070229	intrahepatic cholestasis of pregnancy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:13258	typhoid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:0110953	Waardenburg syndrome type 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685431	Carmil2	implicated_via_orthology	DOID:0111984	immunodeficiency 58						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919819	Bbs5	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914792	Cog6	implicated_via_orthology	DOID:0070264	congenital disorder of glycosylation type IIl						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:14080	glucocorticoid-remediable aldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928842	Cacna1h	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88610	Cyp3a13	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94859	Dao	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	implicated_via_orthology	DOID:1171	hyperlipoproteinemia type V						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339972	Bhmt	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	implicated_via_orthology	DOID:14452	hypokalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858224	Chst3	implicated_via_orthology	DOID:0050813	spondyloepiphyseal dysplasia with congenital joint dislocations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351662	Akr1c13	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917745	Atp6ap2	implicated_via_orthology	DOID:0060806	syndromic X-linked intellectual disability Hedera type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	implicated_via_orthology	DOID:0112008	pituitary adenoma 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333798	Avil	implicated_via_orthology	DOID:0112267	nephrotic syndrome type 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148742	Cldn16	implicated_via_orthology	DOID:0060880	renal hypomagnesemia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606001	Apol9a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3583895	Ermardl2	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354949	Dlc1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95585	Cidec	implicated_via_orthology	DOID:0070203	familial partial lipodystrophy type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	implicated_via_orthology	DOID:0070027	CST3-related cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918952	Cdc5l	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88331	Cd3d	implicated_via_orthology	DOID:0111972	immunodeficiency 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:4988	alcoholic pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:4661	multiple chemical sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289258	Cfap43	implicated_via_orthology	DOID:0070170	spermatogenic failure 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913493	C1galt1c1	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920112	Cox15	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	implicated_via_orthology	DOID:1923	disorder of sexual development						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:0070396	progressive leukoencephalopathy with ovarian failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104540	Clec3b	implicated_via_orthology	DOID:0070441	retinal macular dystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94921	Dpp6	implicated_via_orthology	DOID:0070063	autosomal dominant intellectual developmental disorder 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913514	Ccdc28b	implicated_via_orthology	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448730	Atcay	implicated_via_orthology	DOID:0060694	Cayman type cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915589	Ccdc88c	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923428	Coa5	implicated_via_orthology	DOID:0080359	mitochondrial complex IV deficiency nuclear type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0080908	Cockayne syndrome B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917052	Cox11	implicated_via_orthology	DOID:0070485	mitochondrial complex IV deficiency nuclear type 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916192	Chmp2b	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104728	Caml	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106039	Dtna	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100510	Bub1	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096877	Dll3	implicated_via_orthology	DOID:0112365	spondylocostal dysostosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097717	Ankrd1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:0111460	cardiofaciocutaneous syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	implicated_via_orthology	DOID:0081063	DICER1 syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647146	Cdc5lrt7	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385197	Cyp2j13	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0080046	Stickler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442120	Bank1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:0111039	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:0110146	Bartter disease type 4b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	implicated_via_orthology	DOID:0081061	nephrogenic diabetes insipidus type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:0060873	isolated growth hormone deficiency type IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	implicated_via_orthology	DOID:0110841	Usher syndrome type 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924348	Colgalt1	implicated_via_orthology	DOID:0112315	brain small vessel disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045315	Bpi	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933403	Erap1	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:4661	multiple chemical sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923731	Eif4a3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914285	Dnajb4	implicated_via_orthology	DOID:0081353	congenital myopathy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:0080887	vitamin D-dependent rickets type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202403	Chrna9	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919680	B4gat1	implicated_via_orthology	DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343498	Edar	implicated_via_orthology	DOID:0111665	ectodermal dysplasia 10B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:0070044	Coffin-Siris syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913833	Exosc1	implicated_via_orthology	DOID:0112331	pontocerebellar hypoplasia type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316745	Bmp15	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919935	Dnajc6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333873	Cog1	implicated_via_orthology	DOID:0070259	congenital disorder of glycosylation type IIg						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:1969	cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045256	Fat4	implicated_via_orthology	DOID:0080586	Van Maldergem syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:11836	clubfoot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:11589	Riley-Day syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584043	Dok7	implicated_via_orthology	DOID:0111376	fetal akinesia deformation sequence syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444274	Cfap65	implicated_via_orthology	DOID:0111918	spermatogenic failure 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152819	B3galt6	implicated_via_orthology	DOID:0050802	Ehlers-Danlos syndrome spondylodysplastic type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929597	Bean1	implicated_via_orthology	DOID:0050980	spinocerebellar ataxia type 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101926	Dlx5	implicated_via_orthology	DOID:0090021	split hand-foot malformation 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:0110110	atrial heart septal defect 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179942	Adamts14	implicated_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270149	Cyp2j5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87886	Chrna2	implicated_via_orthology	DOID:0081119	benign familial infantile seizures 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444218	Ahdc1	implicated_via_orthology	DOID:0070055	Xia-Gibbs Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178103	Arhgdia	implicated_via_orthology	DOID:0080389	nephrotic syndrome type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109622	Aip	implicated_via_orthology	DOID:0112009	pituitary adenoma 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95402	Epb42	implicated_via_orthology	DOID:12971	hereditary spherocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:0050117	disease by infectious agent						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:0080940	hereditary angioedema type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:4423	sea-blue histiocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	implicated_via_orthology	DOID:10772	thrombotic thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135874	Cpn1	implicated_via_orthology	DOID:0111583	carboxypeptidase N deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915268	Cert1	implicated_via_orthology	DOID:0070064	autosomal dominant intellectual developmental disorder 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449817	Cyp2j8	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442306	Fancm	implicated_via_orthology	DOID:0111916	spermatogenic failure 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0070043	autosomal dominant intellectual developmental disorder 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913843	Diablo	implicated_via_orthology	DOID:0110585	autosomal dominant nonsyndromic deafness 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444103	Ankrd27	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913612	Exosc3	implicated_via_orthology	DOID:0060266	pontocerebellar hypoplasia type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	implicated_via_orthology	DOID:0050791	persistent Mullerian duct syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860206	Ammecr1	implicated_via_orthology	DOID:0111859	midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:999	hypereosinophilic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141959	Alg8	implicated_via_orthology	DOID:0080560	congenital disorder of glycosylation Ih						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931520	Dbr1	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389008	Adamtsl4	implicated_via_orthology	DOID:0111648	ectopia lentis with ectopia of pupil						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916192	Chmp2b	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913392	Cox7b	implicated_via_orthology	DOID:0111877	linear skin defects with multiple congenital anomalies 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915667	Ccdc17	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917887	Ankrd26	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931256	Cubn	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:5810	adenosine deaminase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3616079	Dnaaf5	implicated_via_orthology	DOID:0110604	primary ciliary dyskinesia 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141959	Alg8	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704456	Apol7e	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384878	Cep164	implicated_via_orthology	DOID:0111123	nephronophthisis 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87895	Chrng	implicated_via_orthology	DOID:0080110	contractures, pterygia, and spondylocarpotarsal fusion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:0070241	primary coenzyme Q10 deficiency 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:0080550	Noonan syndrome with multiple lentigines 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914667	Ears2	implicated_via_orthology	DOID:0111493	combined oxidative phosphorylation deficiency 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88236	C8b	implicated_via_orthology	DOID:0060302	type II complement component 8 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88251	Calm1	implicated_via_orthology	DOID:0060678	catecholaminergic polymorphic ventricular tachycardia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:0050699	Dent disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:0080437	developmental and epileptic encephalopathy 31A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446526	Cpt1c	implicated_via_orthology	DOID:0110818	hereditary spastic paraplegia 73						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917619	Bag5	implicated_via_orthology	DOID:0081162	dilated cardiomyopathy 2F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87935	Adra2b	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347353	Atp2b3	implicated_via_orthology	DOID:0111829	X-linked spinocerebellar ataxia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	implicated_via_orthology	DOID:0110856	posterior polymorphous corneal dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	implicated_via_orthology	DOID:0111438	optic atrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384875	Cdk5rap2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861431	Clec7a	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891304	Ap1s3	implicated_via_orthology	DOID:0111281	psoriasis 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:12399	pathological gambling						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919311	Aopep	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183158	Ash1l	implicated_via_orthology	DOID:0080231	autosomal dominant intellectual developmental disorder 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:161	keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350933	Bcap31	implicated_via_orthology	DOID:0112123	deafness, dystonia, and cerebral hypomyelination						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915520	Dnaaf1	implicated_via_orthology	DOID:0110618	primary ciliary dyskinesia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	implicated_via_orthology	DOID:0110916	hereditary spherocytosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	implicated_via_orthology	DOID:1798	pancreatic endocrine carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:0111062	familial hypobetalipoproteinemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351626	Fam50a	implicated_via_orthology	DOID:0050764	Armfield syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	implicated_via_orthology	DOID:0080086	nonsyndromic congenital nail disorder 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:0111511	melanoma and neural system tumor syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5591876	Cdc5lrt1	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:3144	cutis laxa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922869	Fastkd2	implicated_via_orthology	DOID:0070424	combined oxidative phosphorylation deficiency 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178598	Bloc1s5	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:0111338	isolated elevated serum creatine phosphokinase levels						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	implicated_via_orthology	DOID:0070461	mitochondrial complex V (ATP synthase) deficiency nuclear type 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330812	Acox1	implicated_via_orthology	DOID:0050797	peroxisomal acyl-CoA oxidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87893	Chrnd	implicated_via_orthology	DOID:0110664	congenital myasthenic syndrome 3C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643681	Bhmt1b	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921409	Acbd5	implicated_via_orthology	DOID:0080946	retinal dystrophy with leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	implicated_via_orthology	DOID:0110076	arrhythmogenic right ventricular dysplasia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933331	Elovl4	implicated_via_orthology	DOID:2566	corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347010	Avpr1b	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:0090107	autosomal dominant hypocalcemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347356	Adamts2	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278336	Cdkl5	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687282	Cep104	implicated_via_orthology	DOID:0110994	Joubert syndrome 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	implicated_via_orthology	DOID:0050663	Bethlem myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354735	Atp11a	implicated_via_orthology	DOID:0070406	hypomyelinating leukodystrophy 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442632	Cacna2d4	implicated_via_orthology	DOID:0081023	retinal cone dystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339968	Cth	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:0080523	adult-onset leukoencephalopathy with axonal spheroids and pigmented glia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88355	Cdh2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449569	Adamts15	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	implicated_via_orthology	DOID:0110978	brachydactyly type A1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926024	Cfap61	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913293	Atp5f1d	implicated_via_orthology	DOID:0070463	mitochondrial complex V (ATP synthase) deficiency nuclear type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88176	Bmp1	implicated_via_orthology	DOID:0110342	osteogenesis imperfecta type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685903	B3glct	implicated_via_orthology	DOID:0080201	Peters plus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920025	Fance	implicated_via_orthology	DOID:0111084	Fanconi anemia complementation group E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646594	Eif4a3l2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443455	Dse	implicated_via_orthology	DOID:0080737	Ehlers-Danlos syndrome musculocontractural type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684845	Bmal2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344381	Dnajb6	implicated_via_orthology	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444662	Dpy19l2	implicated_via_orthology	DOID:0111156	spermatogenic failure 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351602	Dguok	implicated_via_orthology	DOID:0111516	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	implicated_via_orthology	DOID:0112121	nephrogenic syndrome of inappropriate antidiuresis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341813	Adam33	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196398	Champ1	implicated_via_orthology	DOID:0070070	autosomal dominant intellectual developmental disorder 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103013	Cacna1c	implicated_via_orthology	DOID:0060173	Timothy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:0112151	corpus callosum agenesis-abnormal genitalia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340051	Adgrg1	implicated_via_orthology	DOID:0080924	bilateral perisylvian polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915134	Cfap410	implicated_via_orthology	DOID:0112299	axial spondylometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99851	Cbfb	implicated_via_orthology	DOID:0081082	acute myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443767	Aaas	implicated_via_orthology	DOID:9164	achalasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389490	B3gat2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341822	Eif4h	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913493	C1galt1c1	implicated_via_orthology	DOID:0080520	Tn polyagglutination syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097161	Bak1	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445168	Elmod3	implicated_via_orthology	DOID:0110533	autosomal recessive nonsyndromic deafness 88						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644226	Eif4a3l1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442120	Bank1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859293	Atxn10	implicated_via_orthology	DOID:0050960	spinocerebellar ataxia type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88519	Crybb2	implicated_via_orthology	DOID:0110269	cataract 3 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891374	Brdt	implicated_via_orthology	DOID:0070163	spermatogenic failure 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88253	Car8	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647148	Cdc5lrt6	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387215	Erlin2	implicated_via_orthology	DOID:0110771	hereditary spastic paraplegia 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933331	Elovl4	implicated_via_orthology	DOID:0050981	spinocerebellar ataxia type 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442402	Cnot1	implicated_via_orthology	DOID:0081397	Vissers-Bodmer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384784	Eif4g1	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917745	Atp6ap2	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859665	Atp8b1	implicated_via_orthology	DOID:0070228	intrahepatic cholestasis of pregnancy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195966	Ctnnd2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109620	Arvcf	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309468	Casq1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921123	Fam161a	implicated_via_orthology	DOID:0110365	retinitis pigmentosa 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919935	Dnajc6	implicated_via_orthology	DOID:0060891	Parkinson's disease 19A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914853	Dusp6	implicated_via_orthology	DOID:0090090	hypogonadotropic hypogonadism 19 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915021	Arpc5	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442833	Bbs9	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926952	Cyb5a	implicated_via_orthology	DOID:0112316	methemoglobinemia and ambiguous genitalia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107721	Dnah1	implicated_via_orthology	DOID:0080266	primary ciliary dyskinesia 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95389	En1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333879	Ap3b1	implicated_via_orthology	DOID:0060540	Hermansky-Pudlak syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644216	Cdc5lrt10	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929699	Arl3	implicated_via_orthology	DOID:0112140	retinitis pigmentosa 83						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096574	Car4	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919819	Bbs5	implicated_via_orthology	DOID:0110127	Bardet-Biedl syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:10211	cholelithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:1390	hypobetalipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	implicated_via_orthology	DOID:0060713	autosomal recessive congenital ichthyosis 4B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859661	Atp11c	implicated_via_orthology	DOID:0111846	X-linked congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647143	Cdc5lrt8	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923089	Daw1	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88355	Cdh2	implicated_via_orthology	DOID:0080959	arrhythmogenic right ventricular dysplasia 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	implicated_via_orthology	DOID:0110212	Charcot-Marie-Tooth disease X-linked recessive 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	implicated_via_orthology	DOID:0090125	brain small vessel disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88589	Cyp1a2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:0110440	dilated cardiomyopathy 1J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5591961	Cdc5lrt4	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924587	Akr1c21	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	implicated_via_orthology	DOID:0070284	primary autosomal recessive microcephaly 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914935	Dnaaf4	implicated_via_orthology	DOID:0110615	primary ciliary dyskinesia 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:4607	biliary tract cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:0080500	ovarian dysgenesis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106341	Atp5po	implicated_via_orthology	DOID:0070464	mitochondrial complex V (ATP synthase) deficiency nuclear type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	implicated_via_orthology	DOID:0060647	fetal encasement syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:0060244	specific language impairment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449816	Cyp2j7	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0080404	orofacial cleft 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99217	Cdh11	implicated_via_orthology	DOID:0081074	Teebi hypertelorism syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445085	Dync2i1	implicated_via_orthology	DOID:0110094	short-rib thoracic dysplasia 8 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097711	Degs1	implicated_via_orthology	DOID:0070399	hypomyelinating leukodystrophy 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446854	Adgrg2	implicated_via_orthology	DOID:0111863	X-linked congenital bilateral absence of vas deferens						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	implicated_via_orthology	DOID:10871	age related macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149010	Dock2	implicated_via_orthology	DOID:0111951	immunodeficiency 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88591	Cyp21a1	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298216	Crygs	implicated_via_orthology	DOID:0110240	cataract 20 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333828	Bfsp2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351661	Akr1c12	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3029414	Brwd3	implicated_via_orthology	DOID:0112045	non-syndromic X-linked intellectual disability 93						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349216	Abcd3	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:9286	priapism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926157	Atf6	implicated_via_orthology	DOID:0110009	achromatopsia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88335	Cd4	implicated_via_orthology	DOID:0112277	immunodeficiency 79						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:0112196	spondylometaepiphyseal dysplasia, short limb-hand type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442035	Atp5mc3	implicated_via_orthology	DOID:0070445	early-onset dystonia and/or spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88458	Col5a2	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927222	Diaph3	implicated_via_orthology	DOID:0060690	autosomal dominant auditory neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:0070384	developmental and epileptic encephalopathy 98						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106642	Baat	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	implicated_via_orthology	DOID:0112142	retinitis pigmentosa 85						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	implicated_via_orthology	DOID:0110081	arrhythmogenic right ventricular dysplasia 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894686	Col9a3	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137858	Cadm3	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107736	Dync2h1	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:14731	Weaver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95478	Fabp2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915720	Bpnt2	implicated_via_orthology	DOID:0112224	chondrodysplasia with joint dislocations gPAPP type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206582	Cacng1	implicated_via_orthology	DOID:8545	malignant hyperthermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103012	E2f4	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	implicated_via_orthology	DOID:0111682	diffuse cystic renal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919386	Chst14	implicated_via_orthology	DOID:0080736	Ehlers-Danlos syndrome musculocontractural type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87984	Akp3	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915433	Bcas2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921769	Cyp2j9	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104855	Atp6v0a2	implicated_via_orthology	DOID:0070134	autosomal recessive cutis laxa type IIA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894326	Atp6v1e1	implicated_via_orthology	DOID:0070140	autosomal recessive cutis laxa type IIC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105100	Ctnnd1	implicated_via_orthology	DOID:0080346	blepharocheilodontic syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:0080728	Ehlers-Danlos syndrome arthrochalasia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924294	Arid2	implicated_via_orthology	DOID:0080297	Coffin-Siris syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108009	Alppl2	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:0080886	vitamin D-dependent rickets type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922941	Anks6	implicated_via_orthology	DOID:0111124	nephronophthisis 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685013	Cog7	implicated_via_orthology	DOID:0070257	congenital disorder of glycosylation type IIe						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94893	Cyb5r3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921462	Dnal1	implicated_via_orthology	DOID:0110613	primary ciliary dyskinesia 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	implicated_via_orthology	DOID:0110023	age related macular degeneration 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195458	Abce1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:0050440	familial partial lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336168	Cradd	implicated_via_orthology	DOID:0081200	autosomal recessive intellectual developmental disorder 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858201	Cntnap1	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:0110275	autosomal recessive limb-girdle muscular dystrophy type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036238	Apol10a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	implicated_via_orthology	DOID:0081224	autosomal recessive intellectual developmental disorder 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	implicated_via_orthology	DOID:14757	Ehlers-Danlos syndrome hypermobility type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859168	Cacng6	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145890	Ano6	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346013	Bves	implicated_via_orthology	DOID:0110290	autosomal recessive limb-girdle muscular dystrophy type 2X						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3050566	Akap6	implicated_via_orthology	DOID:8689	anorexia nervosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108186	Aldh7a1	implicated_via_orthology	DOID:0080768	pyridoxine-dependent epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102708	Efnb1	implicated_via_orthology	DOID:1934	dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:0111196	X-linked distal spinal muscular atrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	implicated_via_orthology	DOID:0110258	cataract 10 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914731	Alg2	implicated_via_orthology	DOID:0110669	congenital myasthenic syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930124	Apom	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858943	Arl6ip1	implicated_via_orthology	DOID:0110812	hereditary spastic paraplegia 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	implicated_via_orthology	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	implicated_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102675	Crym	implicated_via_orthology	DOID:0110566	autosomal dominant nonsyndromic deafness 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446630	Ago1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:0070068	autosomal dominant intellectual developmental disorder 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:0110146	Bartter disease type 4b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	implicated_via_orthology	DOID:0081237	acromesomelic dysplasia-3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036248	Apol11b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88589	Cyp1a2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99677	Adcy1	implicated_via_orthology	DOID:0110501	autosomal recessive nonsyndromic deafness 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:0111046	platelet-type bleeding disorder 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925903	Bola3	implicated_via_orthology	DOID:0080134	multiple mitochondrial dysfunctions syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:12129	bulimia nervosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107714	Dnah8	implicated_via_orthology	DOID:0112164	spermatogenic failure 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	implicated_via_orthology	DOID:0060712	autosomal recessive congenital ichthyosis 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330281	Cd2ap	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152819	B3galt6	implicated_via_orthology	DOID:0112198	spondyloepimetaphyseal dysplasia with joint laxity type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346832	Esrrb	implicated_via_orthology	DOID:0110493	autosomal recessive nonsyndromic deafness 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:0111093	Fanconi anemia complementation group Q						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920912	Apol7c	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	implicated_via_orthology	DOID:0112314	brain small vessel disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340051	Adgrg1	implicated_via_orthology	DOID:0080922	bilateral frontoparietal polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97838	Eprs1	implicated_via_orthology	DOID:0070398	hypomyelinating leukodystrophy 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606482	Colec10	implicated_via_orthology	DOID:0060577	3MC syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:0080345	blepharocheilodontic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924755	Dnhd1	implicated_via_orthology	DOID:0112354	spermatogenic failure 65						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341098	Chil4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	implicated_via_orthology	DOID:0080093	myofibrillar myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384831	Cc2d1a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681120	Chsy1	implicated_via_orthology	DOID:0050814	temtamy preaxial brachydactyly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914311	Dzip1	implicated_via_orthology	DOID:0112175	spermatogenic failure 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	implicated_via_orthology	DOID:0080111	mitochondrial complex III deficiency nuclear type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353562	Cngb3	implicated_via_orthology	DOID:13399	color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933548	Actl6b	implicated_via_orthology	DOID:0112212	developmental and epileptic encephalopathy 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924161	Brd1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:0111504	Li-Fraumeni syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934157	Cilk1	implicated_via_orthology	DOID:0060641	endocrine-cerebro-osteodysplasia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685960	Cenatac	implicated_via_orthology	DOID:0080688	mosaic variegated aneuploidy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	implicated_via_orthology	DOID:0110332	Leber congenital amaurosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:0060590	XFE progeroid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	implicated_via_orthology	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109637	Erf	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139083	Cep152	implicated_via_orthology	DOID:0070292	primary autosomal recessive microcephaly 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109529	Dpf2	implicated_via_orthology	DOID:0112369	Coffin-Siris syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	implicated_via_orthology	DOID:0110914	infantile hypophosphatasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0112158	De Sanctis-Cacchione syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:0111039	hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:5812	MHC class II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919977	B3gat3	implicated_via_orthology	DOID:0080575	Larsen-like syndrome B3GAT3 type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:11212	hydrophthalmos						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88610	Cyp3a13	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:0070158	hereditary sensory neuropathy type 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142951	Edc3	implicated_via_orthology	DOID:0081213	autosomal recessive intellectual developmental disorder 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442833	Bbs9	implicated_via_orthology	DOID:0110131	Bardet-Biedl syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:631	fibromyalgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88464	Col8a2	implicated_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921354	Abcb6	implicated_via_orthology	DOID:0060304	dyschromatosis universalis hereditaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103064	Ddx3x	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676649	Chil5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109553	Ctsc	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	implicated_via_orthology	DOID:0110058	amelogenesis imperfecta type 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3810125	Ermardl1	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309489	Cask	implicated_via_orthology	DOID:14711	FG syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891740	Dact1	implicated_via_orthology	DOID:0050887	Townes-Brocks syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:0111029	hemochromatosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646469	Agbl1	implicated_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153465	Bsnd	implicated_via_orthology	DOID:445	Bartter disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684927	Cenpj	implicated_via_orthology	DOID:0070290	primary autosomal recessive microcephaly 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	implicated_via_orthology	DOID:0050677	Bjornstad syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:3443	mammary Paget's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	implicated_via_orthology	DOID:0050662	bestrophinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584043	Dok7	implicated_via_orthology	DOID:0110668	congenital myasthenic syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929293	Cib2	implicated_via_orthology	DOID:0110505	autosomal recessive nonsyndromic deafness 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:0111815	low molecular weight proteinuria with hypercalciuric nephrocalcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	implicated_via_orthology	DOID:0060681	autosomal dominant nocturnal frontal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:0070132	autosomal recessive cutis laxa type IIIA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682303	Chil6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:2582	acatalasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918495	Cfap251	implicated_via_orthology	DOID:0111915	spermatogenic failure 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136690	Cers1	implicated_via_orthology	DOID:0111451	progressive myoclonus epilepsy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	implicated_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931001	Edaradd	implicated_via_orthology	DOID:0111654	ectodermal dysplasia 11B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:0110825	hereditary spastic paraplegia 9B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913892	Ctnnbl1	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	implicated_via_orthology	DOID:0070025	X-linked dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919148	Apol9b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384774	Alg1	implicated_via_orthology	DOID:0080563	congenital disorder of glycosylation Ik						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914280	Fancl	implicated_via_orthology	DOID:0111082	Fanconi anemia complementation group L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894644	Cacnb2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146430	Cblb	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277124	Asah1	implicated_via_orthology	DOID:0050464	Farber lipogranulomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:0060879	primary hypomagnesemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889642	Elp2	implicated_via_orthology	DOID:0081220	autosomal recessive intellectual developmental disorder 58						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444151	Clec1a	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:0111869	photosensitive trichothiodystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195273	Cd70	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:0070085	schizophrenia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653678	Akr1c19	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588207	Dnaaf3	implicated_via_orthology	DOID:0110626	primary ciliary dyskinesia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277201	Col13a1	implicated_via_orthology	DOID:0110673	congenital myasthenic syndrome 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	implicated_via_orthology	DOID:0110396	retinitis pigmentosa 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:0110015	age related macular degeneration 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277223	Atxn2	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	implicated_via_orthology	DOID:0110448	dilated cardiomyopathy 1HH						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	implicated_via_orthology	DOID:0050636	familial visceral amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:10933	obsessive-compulsive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87890	Chrnb1	implicated_via_orthology	DOID:0110680	congenital myasthenic syndrome 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101763	Cfl2	implicated_via_orthology	DOID:0110934	nemaline myopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201678	Cacna1g	implicated_via_orthology	DOID:0111742	cerebellar ataxia type 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345961	Coro1a	implicated_via_orthology	DOID:0060019	coronin-1A deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103301	Cacnb4	implicated_via_orthology	DOID:0111323	idiopathic generalized epilepsy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	implicated_via_orthology	DOID:2477	motor peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924587	Akr1c21	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915229	Atad1	implicated_via_orthology	DOID:0080581	hyperekplexia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917205	Fars2	implicated_via_orthology	DOID:0111477	combined oxidative phosphorylation deficiency 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2451097	Cndp1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	implicated_via_orthology	DOID:12971	hereditary spherocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3505689	Cdsn	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105313	Cit	implicated_via_orthology	DOID:0070288	primary autosomal recessive microcephaly 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	implicated_via_orthology	DOID:13042	persistent fetal circulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88258	Camk4	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351490	Dok3	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:0070223	progressive familial intrahepatic cholestasis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918480	Dym	implicated_via_orthology	DOID:0111167	Dyggve-Melchior-Clausen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87930	Adk	implicated_via_orthology	DOID:0111038	hypermethioninemia due to adenosine kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913610	Bbip1	implicated_via_orthology	DOID:0110140	Bardet-Biedl syndrome 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159324	Cln6	implicated_via_orthology	DOID:0110730	neuronal ceroid lipofuscinosis 6B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87867	Acadm	implicated_via_orthology	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917336	Cysltr2	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88465	Col9a1	implicated_via_orthology	DOID:0080046	Stickler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94904	Dlx4	implicated_via_orthology	DOID:0080408	orofacial cleft 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109192	Actn2	implicated_via_orthology	DOID:0110428	dilated cardiomyopathy 1AA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:0111907	thrombophilia due to thrombin defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922858	Chmp4b	implicated_via_orthology	DOID:0110265	cataract 31 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	implicated_via_orthology	DOID:0110725	neuronal ceroid lipofuscinosis 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	implicated_via_orthology	DOID:0111502	combined oxidative phosphorylation deficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355314	Ddb2	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101932	Cpe	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445096	Dhtkd1	implicated_via_orthology	DOID:0111453	2-aminoadipic 2-oxoadipic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0111873	photosensitive trichothiodystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	implicated_via_orthology	DOID:1799	islet cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107321	Cux2	implicated_via_orthology	DOID:0112203	developmental and epileptic encephalopathy 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913945	Aspn	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343142	Arpc1b	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:0081164	dilated cardiomyopathy 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918993	Coasy	implicated_via_orthology	DOID:12801	mucopolysaccharidosis III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676368	Dnajc13	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:0060591	WHIM syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913522	Cox16	implicated_via_orthology	DOID:0070507	mitochondrial complex IV deficiency nuclear type 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685574	Dnai2	implicated_via_orthology	DOID:0110622	primary ciliary dyskinesia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934157	Cilk1	implicated_via_orthology	DOID:0111325	juvenile myoclonic epilepsy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	implicated_via_orthology	DOID:0070367	leukoencephalopathy with vanishing white matter 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684996	Ccdc62	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:0111089	Fanconi anemia complementation group D1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88465	Col9a1	implicated_via_orthology	DOID:0070301	multiple epiphyseal dysplasia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108481	Anxa11	implicated_via_orthology	DOID:0081121	inclusion body myopathy and brain white matter abnormalities						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861722	Aldh1a3	implicated_via_orthology	DOID:0060841	isolated microphthalmia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140230	Camta1	implicated_via_orthology	DOID:0050998	nonprogressive cerebellar ataxia with mental retardation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0111508	Torrance type platyspondylic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444507	Cilp	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	implicated_via_orthology	DOID:0050644	arterial calcification of infancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:216	dental caries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3043522	Apol10b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441982	Aldh5a1	implicated_via_orthology	DOID:0060175	succinic semialdehyde dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:1496	echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	implicated_via_orthology	DOID:0081202	autosomal recessive intellectual developmental disorder 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156057	Dclre1b	implicated_via_orthology	DOID:2729	dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915164	Coq9	implicated_via_orthology	DOID:0070242	primary coenzyme Q10 deficiency 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	implicated_via_orthology	DOID:0110056	amelogenesis imperfecta type 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913996	Dync2li1	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354735	Atp11a	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94869	Dcc	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	implicated_via_orthology	DOID:0080097	myofibrillar myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916788	Antxr1	implicated_via_orthology	DOID:0112249	GAPO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:3181	oligodendroglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	implicated_via_orthology	DOID:1405	primary angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337994	Bcl10	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	implicated_via_orthology	DOID:0112239	X-linked lissencephaly 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	implicated_via_orthology	DOID:0060670	cerebral cavernous malformation 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385311	Dlat	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:628	combined T cell and B cell immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107718	Dnah5	implicated_via_orthology	DOID:0050144	Kartagener syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329033	Agxt	implicated_via_orthology	DOID:0111670	primary hyperoxaluria type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443883	Aldh4a1	implicated_via_orthology	DOID:0080543	hyperprolinemia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	implicated_via_orthology	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914708	Ergic1	implicated_via_orthology	DOID:0090124	neurogenic-type arthrogryposis multiplex congenita-2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:0111442	optic atrophy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0110751	type 1 diabetes mellitus 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:3304	germinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448715	Cxcr1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103099	Cox6a1	implicated_via_orthology	DOID:0110203	Charcot-Marie-Tooth disease recessive intermediate D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87929	Adh5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926471	Fancg	implicated_via_orthology	DOID:0111086	Fanconi anemia complementation group G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:0050600	ABCD syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:0110927	nemaline myopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270845	Cidea	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921160	Arhgap18	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919214	Atad3a	implicated_via_orthology	DOID:0081396	neonatal lethal pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924018	Alpi	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:0060285	parietal foramina						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:0110136	Bardet-Biedl syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	implicated_via_orthology	DOID:0110123	Bardet-Biedl syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859165	Cacng3	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924291	Arsk	implicated_via_orthology	DOID:12798	mucopolysaccharidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914672	Dhdds	implicated_via_orthology	DOID:0080473	developmental delay and seizures with or without movement abnormalities						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87977	Ak1	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096337	Ephb1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	implicated_via_orthology	DOID:1172	hyperlipoproteinemia type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:0111322	idiopathic generalized epilepsy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444921	Apol8	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146012	Card10	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150302	Ddhd1	implicated_via_orthology	DOID:0110779	hereditary spastic paraplegia 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88275	Ctnna2	implicated_via_orthology	DOID:0090131	complex cortical dysplasia with other brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0080045	Kniest dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206591	Bik	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:657	adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:0060161	Kennedy's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:0110824	hereditary spastic paraplegia 9A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045256	Fat4	implicated_via_orthology	DOID:0060366	Hennekam syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95305	Eif4e	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915816	Caly	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891374	Brdt	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:4661	multiple chemical sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109501	Crat	implicated_via_orthology	DOID:0110734	neurodegeneration with brain iron accumulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:0050644	arterial calcification of infancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	implicated_via_orthology	DOID:0070051	autosomal dominant intellectual developmental disorder 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:0111137	congenital generalized lipodystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914751	Ccdc50	implicated_via_orthology	DOID:0110569	autosomal dominant nonsyndromic deafness 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330239	Dpm1	implicated_via_orthology	DOID:0080557	congenital disorder of glycosylation Ie						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335092	Casp14	implicated_via_orthology	DOID:0060655	autosomal recessive congenital ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:4661	multiple chemical sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859169	Azin1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:1558	angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923011	Apol7a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:0050864	non-arteritic anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442233	Arhgef9	implicated_via_orthology	DOID:0080215	developmental and epileptic encephalopathy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88075	Arsb	implicated_via_orthology	DOID:12800	mucopolysaccharidosis VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:0110146	Bartter disease type 4b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	implicated_via_orthology	DOID:0110605	primary ciliary dyskinesia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87921	Adh1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	implicated_via_orthology	DOID:0111068	congenital bile acid synthesis defect 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:14080	glucocorticoid-remediable aldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858213	Clpp	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:8619	recurrent hypersomnia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0050990	episodic ataxia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921506	Cyld	implicated_via_orthology	DOID:0050693	Brooke-Spiegler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87978	Ak2	implicated_via_orthology	DOID:0060020	reticular dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3689889	Fancf	implicated_via_orthology	DOID:0111088	Fanconi anemia complementation group F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	implicated_via_orthology	DOID:0110050	Alzheimer's disease 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3583950	Apol7b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922004	Dhcr24	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:0111519	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915024	Borcs5	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916469	Ddah1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103107	F10	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140364	Adprs	implicated_via_orthology	DOID:0070352	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:0060806	syndromic X-linked intellectual disability Hedera type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	implicated_via_orthology	DOID:0050546	congenital adrenal insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:0070037	autosomal dominant intellectual developmental disorder 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918480	Dym	implicated_via_orthology	DOID:0081270	Smith-McCort dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277097	Alx3	implicated_via_orthology	DOID:0081045	frontonasal dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921357	Cep55	implicated_via_orthology	DOID:0080327	multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87912	Acvr2b	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107460	Cox6b1	implicated_via_orthology	DOID:0070494	mitochondrial complex IV deficiency nuclear type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3642684	Cep85l	implicated_via_orthology	DOID:0112229	lissencephaly 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894291	Acsl6	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	implicated_via_orthology	DOID:0111347	epidermolysis bullosa with congenital localized absence of skin and deformity of nails						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:0111272	occipital horn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346052	Apc2	implicated_via_orthology	DOID:0112104	Sotos syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923097	Crppa	implicated_via_orthology	DOID:0110295	autosomal recessive limb-girdle muscular dystrophy type 2U						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104336	Cryba2	implicated_via_orthology	DOID:0110237	cataract 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0060240	UV-sensitive syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442555	Dis3l2	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915451	Ccdc34	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920942	Cplane1	implicated_via_orthology	DOID:0060376	Joubert syndrome with orofaciodigital defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:0080914	cerebrooculofacioskeletal syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:0111551	neurogenic scapuloperoneal syndrome Kaeser type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923164	Exoc6b	implicated_via_orthology	DOID:0112200	spondyloepimetaphyseal dysplasia with joint laxity type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88061	Aprt	implicated_via_orthology	DOID:0060350	adenine phosphoribosyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0080454	developmental and epileptic encephalopathy 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107928	Aldh1a2	implicated_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	implicated_via_orthology	DOID:0111773	46,XY sex reversal 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928953	Ccl24	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88323	Cd24a	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926944	Calcrl	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353427	Eif2ak4	implicated_via_orthology	DOID:0081269	pulmonary venoocclusive disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	implicated_via_orthology	DOID:0110250	cataract 16 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:4079	heart valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:0081356	spinal muscular atrophy, Jokela type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861434	Ctsf	implicated_via_orthology	DOID:0110727	neuronal ceroid lipofuscinosis 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0112129	severe congenital neutropenia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858304	Ctps1	implicated_via_orthology	DOID:0111938	immunodeficiency 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644213	Cdc5lrt9	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146159	Alg10b	implicated_via_orthology	DOID:0110645	long QT syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588271	Degs1l	implicated_via_orthology	DOID:0070399	hypomyelinating leukodystrophy 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278336	Cdkl5	implicated_via_orthology	DOID:1206	Rett syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:0060560	lethal congenital contracture syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:11702	dysgammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858224	Chst3	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914189	Aagab	implicated_via_orthology	DOID:0080214	punctate palmoplantar keratoderma type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88374	Cel	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442676	Cdc14a	implicated_via_orthology	DOID:0110491	autosomal recessive nonsyndromic deafness 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	implicated_via_orthology	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923707	Ccdc134	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87921	Adh1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0111805	syndromic microphthalmia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87894	Chrne	implicated_via_orthology	DOID:0110678	congenital myasthenic syndrome 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859165	Cacng3	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88523	Crygc	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:4606	bile duct cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914670	Far1	implicated_via_orthology	DOID:0081243	rhizomelic chondrodysplasia punctate type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88465	Col9a1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:0060210	amyotrophic lateral sclerosis type 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045346	Cfap300	implicated_via_orthology	DOID:0111852	primary ciliary dyskinesia 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88053	Apoc1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921241	Atl1	implicated_via_orthology	DOID:0110791	hereditary spastic paraplegia 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99240	Ddx39b	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925044	Adamtsl2	implicated_via_orthology	DOID:0111725	geleophysic dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:0110146	Bartter disease type 4b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385186	Clcc1	implicated_via_orthology	DOID:0110355	retinitis pigmentosa 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:12732	intermediate uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106653	Epcam	implicated_via_orthology	DOID:0060776	congenital diarrhea 5 with tufting enteropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932052	Chia1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108117	Emd	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916192	Chmp2b	implicated_via_orthology	DOID:0111227	chromosome 3-linked frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:4661	multiple chemical sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917716	Ckap2l	implicated_via_orthology	DOID:0112194	Filippi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106217	Cacna1e	implicated_via_orthology	DOID:0112205	developmental and epileptic encephalopathy 69						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88436	Cnga1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151114	Dgcr8	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88158	Bgn	implicated_via_orthology	DOID:0112150	X-linked spondyloepimetaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100864	Dnah11	implicated_via_orthology	DOID:0050144	Kartagener syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2677836	Dolk	implicated_via_orthology	DOID:0080565	congenital disorder of glycosylation Im						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890410	Acss2	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145118	Eif2b2	implicated_via_orthology	DOID:0070373	leukoencephalopathy with vanishing white matter 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97545	Cfp	implicated_via_orthology	DOID:0111768	X-linked properdin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87884	Acr	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384790	Fanci	implicated_via_orthology	DOID:0111091	Fanconi anemia complementation group I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108405	Apbb2	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159617	Arr3	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337130	Ap4b1	implicated_via_orthology	DOID:0110799	hereditary spastic paraplegia 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913695	Cyc1	implicated_via_orthology	DOID:0080115	mitochondrial complex III deficiency nuclear type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915508	Fam111a	implicated_via_orthology	DOID:0080723	Kenny-Caffey syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202394	Cblif	implicated_via_orthology	DOID:0050734	congenital intrinsic factor deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107736	Dync2h1	implicated_via_orthology	DOID:0110087	asphyxiating thoracic dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95478	Fabp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202384	Ddb1	implicated_via_orthology	DOID:2033	communication disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346342	Clca1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097680	C3ar1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0111150	autosomal dominant isolated ectopia lentis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355553	Atoh7	implicated_via_orthology	DOID:0060282	persistent hyperplastic primary vitreous						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333828	Bfsp2	implicated_via_orthology	DOID:0110239	cataract 12 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920174	Anln	implicated_via_orthology	DOID:0111133	focal segmental glomerulosclerosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141669	Eogt	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:6132	bronchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	implicated_via_orthology	DOID:0050975	spinocerebellar ataxia type 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88460	Col6a2	implicated_via_orthology	DOID:0050663	Bethlem myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	implicated_via_orthology	DOID:0081109	keratosis palmoplantaris striata 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:0050635	alternating hemiplegia of childhood						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	implicated_via_orthology	DOID:0050885	IMAGe syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:2216	factor V deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919110	Cfap52	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	implicated_via_orthology	DOID:178	vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	implicated_via_orthology	DOID:0050661	vitelliform macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276112	Cldn5	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109172	Dspp	implicated_via_orthology	DOID:4154	dentinogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914762	Agpat2	implicated_via_orthology	DOID:0111135	congenital generalized lipodystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330860	Chil3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333772	Enam	implicated_via_orthology	DOID:0110052	amelogenesis imperfecta type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	implicated_via_orthology	DOID:0070120	Meckel syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106927	Aff3	implicated_via_orthology	DOID:0112383	KINSSHIP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	implicated_via_orthology	DOID:0111981	immunodeficiency 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919494	1600014C10Rik	implicated_via_orthology	DOID:0110738	neurodegeneration with brain iron accumulation 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717143	Cyp4a29	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:0111541	pigmented paravenous chorioretinal atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:5374	pilomatrixoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353510	Arhgef1	implicated_via_orthology	DOID:0111991	immunodeficiency 62						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:0050968	autosomal dominant cerebellar ataxia, deafness and narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045348	Cpa6	implicated_via_orthology	DOID:0060752	familial temporal lobe epilepsy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142885	Cog8	implicated_via_orthology	DOID:0070260	congenital disorder of glycosylation type IIh						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913311	Dynlt2b	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045421	Ank	implicated_via_orthology	DOID:0080801	autosomal dominant craniometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	implicated_via_orthology	DOID:0110124	Bardet-Biedl syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107187	Bcl6	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915088	Dnajb11	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385237	Aimp2	implicated_via_orthology	DOID:0070404	hypomyelinating leukodystrophy 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138169	Cfhr1	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3709029	Dnajc19-ps	implicated_via_orthology	DOID:0110000	3-methylglutaconic aciduria type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	implicated_via_orthology	DOID:0111097	Fanconi anemia complementation group J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	implicated_via_orthology	DOID:0090019	sitosterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109629	Atp6ap1	implicated_via_orthology	DOID:0112002	immunodeficiency 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385958	C1qtnf5	implicated_via_orthology	DOID:0060869	late-onset retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:9775	diastolic heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916731	Actl9	implicated_via_orthology	DOID:0112279	spermatogenic failure 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914935	Dnaaf4	implicated_via_orthology	DOID:4428	dyslexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276121	Bckdk	implicated_via_orthology	DOID:0090126	branched-chain keto acid dehydrogenase kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:0080092	myofibrillar myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0080868	primary ovarian insufficiency 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:13399	color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104727	Cplx1	implicated_via_orthology	DOID:0080426	developmental and epileptic encephalopathy 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	implicated_via_orthology	DOID:0111187	distal myopathy with anterior tibial onset						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923051	4930447C04Rik	implicated_via_orthology	DOID:0112269	primary ovarian insufficiency 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:0111349	hereditary desmoid disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687282	Cep104	implicated_via_orthology	DOID:0081236	autosomal recessive intellectual developmental disorder 77						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88446	Col11a1	implicated_via_orthology	DOID:0080672	fibrochondrogenesis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	implicated_via_orthology	DOID:0111569	autosomal dominant vitreoretinochoroidopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384987	B4galt7	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915385	Eif3h	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:14264	benign neonatal seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:11257	social phobia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339968	Cth	implicated_via_orthology	DOID:0090142	cystathioninuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045301	Ankk1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	implicated_via_orthology	DOID:12259	hemophilia B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:0110017	age related macular degeneration 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:4852	pleomorphic xanthoastrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94869	Dcc	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930124	Apom	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103157	Dnase1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:0110033	autosomal recessive Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	implicated_via_orthology	DOID:0080839	X-linked warfarin sensitivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917352	Dnmbp	implicated_via_orthology	DOID:0070354	cataract 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:0070118	Meckel syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:5742	pancreatic acinar cell adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94869	Dcc	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:4154	dentinogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88332	Cd3e	implicated_via_orthology	DOID:0111971	immunodeficiency 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	implicated_via_orthology	DOID:8158	complement component 5 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0110845	xeroderma pigmentosum group D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:0110542	autosomal dominant nonsyndromic deafness 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861431	Clec7a	implicated_via_orthology	DOID:2058	chronic mucocutaneous candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441769	Dclre1c	implicated_via_orthology	DOID:0090012	severe combined immunodeficiency with sensitivity to ionizing radiation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349451	Corin	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923275	Cant1	implicated_via_orthology	DOID:0070302	multiple epiphyseal dysplasia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	implicated_via_orthology	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	implicated_via_orthology	DOID:0070347	encephalopathy due to defective mitochondrial and peroxisomal fission 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:2959	hyperimmunoglobulin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932286	Egln1	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916115	Arv1	implicated_via_orthology	DOID:0080417	developmental and epileptic encephalopathy 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	implicated_via_orthology	DOID:14040	autoimmune polyendocrine syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914549	Dock7	implicated_via_orthology	DOID:0080415	developmental and epileptic encephalopathy 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649942	Chchd2-ps	implicated_via_orthology	DOID:0080504	Parkinson's disease 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	implicated_via_orthology	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94941	Dvl1	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:0050636	familial visceral amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88259	Camk2g	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99481	F11	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652818	Dcdc2a	implicated_via_orthology	DOID:14268	sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278313	Coch	implicated_via_orthology	DOID:0110593	autosomal dominant nonsyndromic deafness 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:0060022	CD40 ligand deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88522	Crygb	implicated_via_orthology	DOID:0110236	cataract 39 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88396	Chrm1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145118	Eif2b2	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914762	Agpat2	implicated_via_orthology	DOID:811	lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443910	Bcorl1	implicated_via_orthology	DOID:0111841	Shukla-Vernon syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	implicated_via_orthology	DOID:0081268	pulmonary venoocclusive disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684927	Cenpj	implicated_via_orthology	DOID:0070010	Seckel syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	implicated_via_orthology	DOID:14213	hypophosphatasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448567	Chd2	implicated_via_orthology	DOID:0081325	developmental and epileptic encephalopathy 94						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914043	Clxn	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685581	Ccn6	implicated_via_orthology	DOID:381	arthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917173	Agk	implicated_via_orthology	DOID:0110245	cataract 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91860	Dcaf8	implicated_via_orthology	DOID:0090069	giant axonal neuropathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151060	Cnnm4	implicated_via_orthology	DOID:0111404	Jalili syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442120	Bank1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	implicated_via_orthology	DOID:0060200	amyotrophic lateral sclerosis type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88226	C2	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104649	Cox6a2	implicated_via_orthology	DOID:0070503	mitochondrial complex IV deficiency nuclear type 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353562	Cngb3	implicated_via_orthology	DOID:0110008	achromatopsia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646700	Amt	implicated_via_orthology	DOID:9268	glycine encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918671	Amtn	implicated_via_orthology	DOID:0080243	amelogenesis imperfecta type 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88016	Ampd2	implicated_via_orthology	DOID:0060278	pontocerebellar hypoplasia type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445053	Ccbe1	implicated_via_orthology	DOID:0060366	Hennekam syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	implicated_via_orthology	DOID:0070201	Miyoshi muscular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109176	Cpt2	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:0090145	dopamine beta-hydroxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88594	Cyp27a1	implicated_via_orthology	DOID:4810	cerebrotendinous xanthomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:0060023	immunodeficiency with hyper IgM type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914127	Crnkl1	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717148	Cyp4a32	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347010	Avpr1b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351602	Dguok	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:1394	urinary schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102806	Acvr2a	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859608	Ccdc22	implicated_via_orthology	DOID:0060572	Ritscher-Schinzel syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313286	Eif2b3	implicated_via_orthology	DOID:0070372	leukoencephalopathy with vanishing white matter 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:0080290	familial erythrocytosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	implicated_via_orthology	DOID:0111741	X-linked deafness 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88526	Crygf	implicated_via_orthology	DOID:0110260	cataract 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926387	Cdon	implicated_via_orthology	DOID:0110877	holoprosencephaly 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:0060656	autosomal recessive congenital ichthyosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88226	C2	implicated_via_orthology	DOID:0110026	age related macular degeneration 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444008	Bptf	implicated_via_orthology	DOID:0070514	neurodevelopmental disorder with dysmorphic facies and distal limb anomalies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:0050663	Bethlem myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:0110461	X-linked dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346342	Clca1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913836	Crls1	implicated_via_orthology	DOID:0070430	combined oxidative phosphorylation deficiency 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100517	Clpb	implicated_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652818	Dcdc2a	implicated_via_orthology	DOID:0111126	nephronophthisis 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:10024	migraine with aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103264	Arhgef2	implicated_via_orthology	DOID:0080312	neurodevelopmental disorder with midbrain and hindbrain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351659	Abcg5	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664358	Dsg1c	implicated_via_orthology	DOID:0081108	keratosis palmoplantaris striata 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	implicated_via_orthology	DOID:0060063	sideroblastic anemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	implicated_via_orthology	DOID:1681	heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921624	Clec16a	implicated_via_orthology	DOID:13774	Addison's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107675	Cd1d2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921769	Cyp2j9	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95316	Cela2a	implicated_via_orthology	DOID:0080945	abdominal obesity-metabolic syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274784	Adgrv1	implicated_via_orthology	DOID:0111305	familial febrile seizures 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:0110273	autosomal dominant limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:7442	monoclonal gammopathy of uncertain significance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341818	Cnga3	implicated_via_orthology	DOID:13399	color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87961	Agrn	implicated_via_orthology	DOID:0110657	congenital myasthenic syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919070	Dync2i2	implicated_via_orthology	DOID:0110095	short-rib thoracic dysplasia 11 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104992	Crybb1	implicated_via_orthology	DOID:0110270	cataract 17 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860299	Dnah10	implicated_via_orthology	DOID:0112336	spermatogenic failure 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	implicated_via_orthology	DOID:0080988	pretibial dystrophic epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195966	Ctnnd2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352749	Cabp2	implicated_via_orthology	DOID:0110537	autosomal recessive nonsyndromic deafness 93						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679260	Crb2	implicated_via_orthology	DOID:0111625	ventriculomegaly - cystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88610	Cyp3a13	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202065	Chek1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612184	Ccdc8	implicated_via_orthology	DOID:0060241	3-M syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:0111798	X-linked nephrolithiasis type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94896	Dio1	implicated_via_orthology	DOID:50	thyroid gland disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0080187	chronic neutrophilic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917336	Cysltr2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926051	Ak7	implicated_via_orthology	DOID:0111928	spermatogenic failure 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140224	Cyp2j11	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915568	Aph1c	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	implicated_via_orthology	DOID:0050645	arterial tortuosity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:9258	Waardenburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101774	Cd79a	implicated_via_orthology	DOID:0081137	agammaglobulinemia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339760	Csf2rb2	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913364	Dnajc30	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:13316	exocrine pancreatic insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109609	Faah	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:0060174	GABA aminotransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:0112125	alpha-thalassemia myelodysplasia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99698	Clock	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:9828	neonatal abstinence syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	implicated_via_orthology	DOID:0110938	autosomal dominant osteopetrosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443327	Fa2h	implicated_via_orthology	DOID:0110786	hereditary spastic paraplegia 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88137	Bckdhb	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894644	Cacnb2	implicated_via_orthology	DOID:0110221	Brugada syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916889	Exosc8	implicated_via_orthology	DOID:0112334	pontocerebellar hypoplasia type 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:0080264	exudative vitreoretinopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385197	Cyp2j13	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106210	Dmbt1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99402	Adora2a	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:0110893	inflammatory bowel disease 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105058	Atp2a1	implicated_via_orthology	DOID:0050692	Brody myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278336	Cdkl5	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180561	Atpaf2	implicated_via_orthology	DOID:0050768	mitochondrial complex V (ATP synthase) deficiency nuclear type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913629	Cox14	implicated_via_orthology	DOID:0070496	mitochondrial complex IV deficiency nuclear type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914311	Dzip1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860440	Bace2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	implicated_via_orthology	DOID:0110370	retinitis pigmentosa 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99217	Cdh11	implicated_via_orthology	DOID:0080631	Elsahy-Waters syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098826	Coq4	implicated_via_orthology	DOID:0070244	primary coenzyme Q10 deficiency 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334462	Copa	implicated_via_orthology	DOID:0081242	autoimmune interstitial lung, joint, and kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913128	Bet1l	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	implicated_via_orthology	DOID:0050473	Alstrom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142763	Cyp4v3	implicated_via_orthology	DOID:0050664	Bietti crystalline corneoretinal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685906	Drc1	implicated_via_orthology	DOID:0110596	primary ciliary dyskinesia 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151224	Alpk3	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0080028	spondyloepimetaphyseal dysplasia, Strudwick type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196396	Dpagt1	implicated_via_orthology	DOID:0080562	congenital disorder of glycosylation Ij						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	implicated_via_orthology	DOID:0110025	age related macular degeneration 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:4667	kyphosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	implicated_via_orthology	DOID:0112247	congenital heart defects, dysmorphic facial features, and intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:2583	agammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:0110017	age related macular degeneration 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:9540	vascular skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:0070219	familial hyperinsulinemic hypoglycemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:0110317	hypertrophic cardiomyopathy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104992	Crybb1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88333	Cd3g	implicated_via_orthology	DOID:0111973	immunodeficiency 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87870	Acat1	implicated_via_orthology	DOID:14723	beta-ketothiolase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:3144	cutis laxa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:3507	dermatofibrosarcoma protuberans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	implicated_via_orthology	DOID:4959	epidermolysis bullosa dystrophica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87935	Adra2b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448715	Cxcr1	implicated_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349216	Abcd3	implicated_via_orthology	DOID:0111066	congenital bile acid synthesis defect 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924145	Bicd2	implicated_via_orthology	DOID:0070350	spinal muscular atrophy with lower extremity predominant 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109533	Abcb7	implicated_via_orthology	DOID:0050554	X-linked sideroblastic anemia with ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:0070007	Seckel syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860425	Cldn14	implicated_via_orthology	DOID:0110487	autosomal recessive nonsyndromic deafness 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104518	Cntn2	implicated_via_orthology	DOID:0111691	familial adult myoclonic epilepsy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685013	Cog7	implicated_via_orthology	DOID:630	genetic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889008	Atp2c1	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277968	Cavin1	implicated_via_orthology	DOID:0111138	congenital generalized lipodystrophy type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	implicated_via_orthology	DOID:0110318	hypertrophic cardiomyopathy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916188	Aspscr1	implicated_via_orthology	DOID:4239	alveolar soft part sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351617	Abca3	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107701	Bckdha	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:0070009	Seckel syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:0080677	otospondylomegaepiphyseal dysplasia, autosomal dominant						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:0080913	cerebrooculofacioskeletal syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915130	Dcxr	implicated_via_orthology	DOID:0111258	pentosuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	implicated_via_orthology	DOID:0111004	Joubert syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:4927	Klatskin's tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	implicated_via_orthology	DOID:0070135	autosomal recessive cutis laxa type IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:5381	bile duct adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:0050635	alternating hemiplegia of childhood						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918972	Cic	implicated_via_orthology	DOID:0080236	autosomal dominant intellectual developmental disorder 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330302	Dyrk1b	implicated_via_orthology	DOID:0060612	abdominal obesity-metabolic syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:0110079	Leber congenital amaurosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0080727	Ehlers-Danlos syndrome arthrochalasia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036242	Camsap1	implicated_via_orthology	DOID:0090131	complex cortical dysplasia with other brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:0090109	autosomal dominant hypocalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94891	Dhh	implicated_via_orthology	DOID:0111774	46,XY sex reversal 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103285	Atp6v1b1	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:12549	hepatitis A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920004	Arhgef10l	implicated_via_orthology	DOID:0050933	ovarian serous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:13884	sick sinus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:2366	West Nile fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924337	Ankrd11	implicated_via_orthology	DOID:14780	KBG syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142567	Arhgef18	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	implicated_via_orthology	DOID:0080141	mosaic variegated aneuploidy syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443248	Exph5	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:10322	berylliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:1387	hypolipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:11664	nephrosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:0111095	Fanconi anemia complementation group A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0111348	multiple epiphyseal dysplasia with myopia and deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444630	Dmxl2	implicated_via_orthology	DOID:0080267	autosomal dominant nonsyndromic deafness 71						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	implicated_via_orthology	DOID:0060684	autosomal dominant nocturnal frontal lobe epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152539	Creld1	implicated_via_orthology	DOID:0050651	atrioventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88523	Crygc	implicated_via_orthology	DOID:0110235	cataract 2 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443967	Dpp9	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:0111013	cone-rod dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443333	Brinp2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:2320	obstructive lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:10322	berylliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:0111907	thrombophilia due to thrombin defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	implicated_via_orthology	DOID:0111020	cone-rod dystrophy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685011	Dchs1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109176	Cpt2	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0080846	latent autoimmune diabetes in adults						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934368	Cd96	implicated_via_orthology	DOID:0111581	C syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142632	Alg11	implicated_via_orthology	DOID:0080567	congenital disorder of glycosylation Ip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:14179	X-linked agammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	implicated_via_orthology	DOID:0111423	branchiootorenal syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:12574	posterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	implicated_via_orthology	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934852	Acox2	implicated_via_orthology	DOID:0111067	congenital bile acid synthesis defect 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333825	Dgat1	implicated_via_orthology	DOID:0060778	congenital diarrhea 7 with exudative enteropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:0110759	type 1 diabetes mellitus 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890596	Evc	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105061	Clcn2	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2678952	Bloc1s3	implicated_via_orthology	DOID:0060546	Hermansky-Pudlak syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:0050856	oppositional defiant disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919164	Antxr2	implicated_via_orthology	DOID:0111669	hyaline fibromatosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652818	Dcdc2a	implicated_via_orthology	DOID:4428	dyslexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99439	Btc	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99960	Ewsr1	implicated_via_orthology	DOID:3369	Ewing sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330824	Csrp3	implicated_via_orthology	DOID:0110449	dilated cardiomyopathy 1M						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920480	Bmper	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	implicated_via_orthology	DOID:0110150	Charcot-Marie-Tooth disease type 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:0081340	congenital myopathy 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	implicated_via_orthology	DOID:0070195	X-linked chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925064	Dstyk	implicated_via_orthology	DOID:0080206	CAKUT1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:12388	neurohypophyseal diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	implicated_via_orthology	DOID:0060545	Hermansky-Pudlak syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:0110341	osteogenesis imperfecta type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915385	Eif3h	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914502	Cap2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923920	Cfap70	implicated_via_orthology	DOID:0111912	spermatogenic failure 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915396	Arl13b	implicated_via_orthology	DOID:0111003	Joubert syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106039	Dtna	implicated_via_orthology	DOID:0060480	left ventricular noncompaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2657115	Fam151a	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261428	Chchd2	implicated_via_orthology	DOID:0080504	Parkinson's disease 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	implicated_via_orthology	DOID:0111418	familial apolipoprotein C-II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646735	Cyp2b23	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915674	Chn1	implicated_via_orthology	DOID:12557	Duane retraction syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:0110509	autosomal recessive nonsyndromic deafness 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923275	Cant1	implicated_via_orthology	DOID:0060462	Desbuquois dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:0080764	hereditary diffuse gastric cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717145	Cyp4a30b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914963	Dnajc19	implicated_via_orthology	DOID:0110000	3-methylglutaconic aciduria type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923566	Dnaaf2	implicated_via_orthology	DOID:0110612	primary ciliary dyskinesia 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098643	Coq5	implicated_via_orthology	DOID:0112138	primary coenzyme Q10 deficiency 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97748	Ctsa	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96878	Blnk	implicated_via_orthology	DOID:2583	agammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333857	Arhgap31	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87883	Acp5	implicated_via_orthology	DOID:0112295	spondylometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87936	Adra2c	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679722	Cpsf1	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919241	Ercc8	implicated_via_orthology	DOID:0080907	Cockayne syndrome A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88077	Arsa	implicated_via_orthology	DOID:10581	metachromatic leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	implicated_via_orthology	DOID:0050419	complement factor I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88525	Cryge	implicated_via_orthology	DOID:0110260	cataract 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:0111109	maturity-onset diabetes of the young type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	implicated_via_orthology	DOID:5363	myxoid liposarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109553	Ctsc	implicated_via_orthology	DOID:3389	Papillon-Lefevre disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779804	C1rb	implicated_via_orthology	DOID:0080986	Ehlers-Danlos syndrome periodontal type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:0080315	megalencephalic leukoencephalopathy with subcortical cysts						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88489	Cr2	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588195	Adamts17	implicated_via_orthology	DOID:0050475	Weill-Marchesani syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917633	Cox10	implicated_via_orthology	DOID:0070492	mitochondrial complex IV deficiency nuclear type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	implicated_via_orthology	DOID:11240	appendiceal neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445096	Dhtkd1	implicated_via_orthology	DOID:0110170	Charcot-Marie-Tooth disease axonal type 2Q						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924270	Atl3	implicated_via_orthology	DOID:0070154	hereditary sensory neuropathy type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88293	Cacna1d	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449816	Cyp2j7	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384987	B4galt7	implicated_via_orthology	DOID:0080738	Ehlers-Danlos syndrome spondylodysplastic type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:2044	drug-induced hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345140	Aloxe3	implicated_via_orthology	DOID:0060711	autosomal recessive congenital ichthyosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685011	Dchs1	implicated_via_orthology	DOID:0080585	Van Maldergem syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88141	Bcr	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384875	Cdk5rap2	implicated_via_orthology	DOID:0050569	Seckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105368	Atp2b2	implicated_via_orthology	DOID:0110467	autosomal recessive nonsyndromic deafness 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	implicated_via_orthology	DOID:0111338	isolated elevated serum creatine phosphokinase levels						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354713	Acsl4	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:0111087	Fanconi anemia complementation group C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108047	Bag1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:11512	Budd-Chiari syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441769	Dclre1c	implicated_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036261	Afg2b	implicated_via_orthology	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0080205	CAKUT						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88289	Cbx2	implicated_via_orthology	DOID:0111776	46,XY sex reversal 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88610	Cyp3a13	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100859	Capn5	implicated_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916359	Ccnq	implicated_via_orthology	DOID:0111931	syndactyly-telecanthus-anogenital and renal malformations syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:0070222	progressive familial intrahepatic cholestasis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	implicated_via_orthology	DOID:529	blepharospasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913609	Cox20	implicated_via_orthology	DOID:0070497	mitochondrial complex IV deficiency nuclear type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3145	hyperlipoproteinemia type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108092	Bin1	implicated_via_orthology	DOID:0111220	centronuclear myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:0070028	APP-related cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:0110019	age related macular degeneration 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664102	Cngb1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	implicated_via_orthology	DOID:0060263	porencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88589	Cyp1a2	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:0111809	syndromic microphthalmia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928842	Cacna1h	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920970	Cst6	implicated_via_orthology	DOID:0111651	ectodermal dysplasia 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:0050944	spastic ataxia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:0060673	Peters anomaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277186	Atg5	implicated_via_orthology	DOID:0080259	autosomal recessive spinocerebellar ataxia 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	implicated_via_orthology	DOID:0111169	subcortical band heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94869	Dcc	implicated_via_orthology	DOID:0111153	congenital mirror movement disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351352	Atic	implicated_via_orthology	DOID:653	purine-pyrimidine metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101913	Chml	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	implicated_via_orthology	DOID:0070238	primary coenzyme Q10 deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109192	Actn2	implicated_via_orthology	DOID:0081342	congenital myopathy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2677061	Dagla	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88524	Crygd	implicated_via_orthology	DOID:0110260	cataract 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919752	Cwf19l1	implicated_via_orthology	DOID:0080064	autosomal recessive spinocerebellar ataxia 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:0110893	inflammatory bowel disease 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717097	Cyp2j12	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	implicated_via_orthology	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:0110042	Alzheimer's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196224	Cdk8	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926952	Cyb5a	implicated_via_orthology	DOID:10783	methemoglobinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:9828	neonatal abstinence syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355319	Exosc9	implicated_via_orthology	DOID:0112323	pontocerebellar hypoplasia type 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916218	Cdan1	implicated_via_orthology	DOID:1338	congenital dyserythropoietic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:0111428	essential tremor 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	implicated_via_orthology	DOID:0111899	X-linked thrombophilia due to factor IX defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	implicated_via_orthology	DOID:8545	malignant hyperthermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	implicated_via_orthology	DOID:811	lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139354	Arfgef2	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920112	Cox15	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342057	B4galnt1	implicated_via_orthology	DOID:0110777	hereditary spastic paraplegia 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:2569	retinal drusen						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917912	Clic5	implicated_via_orthology	DOID:0110464	autosomal recessive nonsyndromic deafness 103						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921241	Atl1	implicated_via_orthology	DOID:0070156	hereditary sensory neuropathy type 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88457	Col5a1	implicated_via_orthology	DOID:14720	Ehlers-Danlos syndrome classic type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859553	Dnaaf11	implicated_via_orthology	DOID:0110608	primary ciliary dyskinesia 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611747	Cyp4a12b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270841	Cry1	implicated_via_orthology	DOID:0111141	delayed sleep phase syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:12574	posterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919595	Amer1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664357	Dsg1b	implicated_via_orthology	DOID:0081108	keratosis palmoplantaris striata 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	implicated_via_orthology	DOID:0060200	amyotrophic lateral sclerosis type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:9263	homocystinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87934	Adra2a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107822	Ebp	implicated_via_orthology	DOID:0111865	MEND syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045301	Ankk1	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:14744	Partington syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:0111202	autosomal dominant distal hereditary motor neuronopathy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107823	Ctsk	implicated_via_orthology	DOID:0080038	pycnodysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915039	Dalrd3	implicated_via_orthology	DOID:0112220	developmental and epileptic encephalopathy 86						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	implicated_via_orthology	DOID:2959	hyperimmunoglobulin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:0090008	immunodeficiency-centromeric instability-facial anomalies syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:0080730	Ehlers-Danlos syndrome cardiac valvular type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100517	Clpb	implicated_via_orthology	DOID:0081134	3-methylglutaconic aciduria type 7b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:3262	phagocyte bactericidal dysfunction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104655	Ambn	implicated_via_orthology	DOID:0110065	amelogenesis imperfecta type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87885	Chrna1	implicated_via_orthology	DOID:0110663	congenital myasthenic syndrome 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441769	Dclre1c	implicated_via_orthology	DOID:0060010	Omenn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676312	Abca12	implicated_via_orthology	DOID:0060656	autosomal recessive congenital ichthyosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919757	Dzip1l	implicated_via_orthology	DOID:0080273	polycystic kidney disease 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159324	Cln6	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	implicated_via_orthology	DOID:0111533	gnathodiaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:0081357	isolated mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928378	Dhodh	implicated_via_orthology	DOID:0111259	postaxial acrofacial dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919558	Brf1	implicated_via_orthology	DOID:0080898	cerebellofaciodental syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894291	Acsl6	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924145	Bicd2	implicated_via_orthology	DOID:0070349	spinal muscular atrophy with lower extremity predominant 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104654	Atoh1	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88257	Camk2b	implicated_via_orthology	DOID:0080230	autosomal dominant intellectual developmental disorder 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:0080026	otospondylomegaepiphyseal dysplasia, autosomal recessive						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:9828	neonatal abstinence syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920112	Cox15	implicated_via_orthology	DOID:0080358	mitochondrial complex IV deficiency nuclear type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441745	Agbl5	implicated_via_orthology	DOID:0110361	retinitis pigmentosa 75						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:0080391	nephrotic syndrome type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:0111479	combined oxidative phosphorylation deficiency 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	implicated_via_orthology	DOID:0050144	Kartagener syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:10609	rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:0112021	non-syndromic X-linked intellectual disability ARX-related						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889842	Fam13a	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	implicated_via_orthology	DOID:0060200	amyotrophic lateral sclerosis type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	implicated_via_orthology	DOID:0111418	familial apolipoprotein C-II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	implicated_via_orthology	DOID:0111686	hereditary mixed polyposis syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888908	Aldh18a1	implicated_via_orthology	DOID:0070143	autosomal recessive cutis laxa type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88612	Cyp4a12a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914407	Cfap418	implicated_via_orthology	DOID:0111022	cone-rod dystrophy 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661445	Ctnna3	implicated_via_orthology	DOID:0110084	arrhythmogenic right ventricular dysplasia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:1929	supravalvular aortic stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104540	Clec3b	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	implicated_via_orthology	DOID:0080628	alopecia-mental retardation syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914978	Dph2	implicated_via_orthology	DOID:0070478	diphthamide deficiency syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:0090050	dystonia 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109192	Actn2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:0110024	age related macular degeneration 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442833	Bbs9	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88356	Cdh3	implicated_via_orthology	DOID:0110711	congenital hypotrichosis with juvenile macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:0080353	X-linked recessive hypophosphatemic rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107508	Ereg	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449817	Cyp2j8	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384586	Armc5	implicated_via_orthology	DOID:0111624	ACTH-independent macronodular adrenal hyperplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389008	Adamtsl4	implicated_via_orthology	DOID:0111149	autosomal recessive isolated ectopia lentis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2158560	Cep63	implicated_via_orthology	DOID:0070006	Seckel syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0060887	ossification of the posterior longitudinal ligament of spine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153465	Bsnd	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913364	Dnajc30	implicated_via_orthology	DOID:0112065	nuclear type mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109336	Etv6	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:0111902	thrombophilia due to activated protein C resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88356	Cdh3	implicated_via_orthology	DOID:0111649	ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87995	Aldob	implicated_via_orthology	DOID:9869	hereditary fructose intolerance syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87886	Chrna2	implicated_via_orthology	DOID:0060685	autosomal dominant nocturnal frontal lobe epilepsy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94930	Dsg1a	implicated_via_orthology	DOID:0081108	keratosis palmoplantaris striata 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277964	Ehhadh	implicated_via_orthology	DOID:0080759	Fanconi renotubular syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913845	Aste1	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101950	Calcr	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098282	C9	implicated_via_orthology	DOID:0110027	age related macular degeneration 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859665	Atp8b1	implicated_via_orthology	DOID:0070231	benign recurrent intrahepatic cholestasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99495	Brd2	implicated_via_orthology	DOID:4890	juvenile myoclonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355313	C1ra	implicated_via_orthology	DOID:0080986	Ehlers-Danlos syndrome periodontal type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932286	Egln1	implicated_via_orthology	DOID:0080338	familial erythrocytosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	implicated_via_orthology	DOID:0110401	retinitis pigmentosa 74						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88599	Cyp2b13	implicated_via_orthology	DOID:9828	neonatal abstinence syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351471	B9d1	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	implicated_via_orthology	DOID:0110671	congenital myasthenic syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920185	Ddx41	implicated_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88350	Cdc25c	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928679	Dpys	implicated_via_orthology	DOID:653	purine-pyrimidine metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104621	Alx1	implicated_via_orthology	DOID:0081047	frontonasal dysplasia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102805	Entpd1	implicated_via_orthology	DOID:0110815	hereditary spastic paraplegia 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329040	Dkk1	implicated_via_orthology	DOID:13714	anodontia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028580	Cyp4a31	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890219	Cdh23	implicated_via_orthology	DOID:0110467	autosomal recessive nonsyndromic deafness 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:0070130	autosomal dominant cutis laxa 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920591	Arhgef6	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685628	Card9	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	implicated_via_orthology	DOID:0070462	mitochondrial complex V (ATP synthase) deficiency nuclear type 4B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444921	Apol8	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3522097	Aph1b	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108481	Anxa11	implicated_via_orthology	DOID:0080225	amyotrophic lateral sclerosis type 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384848	BC016579	implicated_via_orthology	DOID:4535	hypotrichosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386848	Cyb5r4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88334	Cd247	implicated_via_orthology	DOID:0111942	immunodeficiency 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:0070232	benign recurrent intrahepatic cholestasis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:0111365	benign familial hematuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	implicated_via_orthology	DOID:0110598	primary ciliary dyskinesia 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:0112348	hereditary spastic paraplegia 78						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106098	Etfb	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:2679	dysembryoplastic neuroepithelial tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194508	Ddost	implicated_via_orthology	DOID:0080569	congenital disorder of glycosylation Ir						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104653	Atp2b1	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:14069	cerebral malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:6688	autoimmune lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336993	Ap4e1	implicated_via_orthology	DOID:0060243	stuttering						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105062	Amhr2	implicated_via_orthology	DOID:0050791	persistent Mullerian duct syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:0110354	retinitis pigmentosa 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:8886	chorioretinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921958	Dnaaf6rt	implicated_via_orthology	DOID:0111850	primary ciliary dyskinesia 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94903	Dlx3	implicated_via_orthology	DOID:0110053	amelogenesis imperfecta type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106092	Etfa	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344418	Cib1	implicated_via_orthology	DOID:13777	epidermodysplasia verruciformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:0081002	Cowden syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920897	Capn9	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:11211	buphthalmos						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924908	Ap5z1	implicated_via_orthology	DOID:0110800	hereditary spastic paraplegia 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	implicated_via_orthology	DOID:0060200	amyotrophic lateral sclerosis type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442120	Bank1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102518	Adam3	implicated_via_orthology	DOID:1748	conjunctival squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385025	Alg12	implicated_via_orthology	DOID:0080559	congenital disorder of glycosylation Ig						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914407	Cfap418	implicated_via_orthology	DOID:0081010	Bardet-Biedl syndrome 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442409	Dpp10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916637	Dnajb13	implicated_via_orthology	DOID:0110610	primary ciliary dyskinesia 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386258	Card14	implicated_via_orthology	DOID:9212	pityriasis rubra pilaris						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:0050883	infantile cerebellar-retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:4428	dyslexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95478	Fabp2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384802	Eif2b1	implicated_via_orthology	DOID:0070374	leukoencephalopathy with vanishing white matter 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	implicated_via_orthology	DOID:0060682	autosomal dominant nocturnal frontal lobe epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179942	Adamts14	implicated_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95284	Edn2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147298	Cep120	implicated_via_orthology	DOID:0110093	short-rib thoracic dysplasia 13 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:0110850	xeroderma pigmentosum group B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919238	Esco2	implicated_via_orthology	DOID:5325	Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	implicated_via_orthology	DOID:0110195	Charcot-Marie-Tooth disease type 4E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88374	Cel	implicated_via_orthology	DOID:0111105	maturity-onset diabetes of the young type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914789	Dock6	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87921	Adh1	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	implicated_via_orthology	DOID:0111547	retinal arterial tortuosity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88462	Col7a1	implicated_via_orthology	DOID:0111345	transient bullous dermolysis of the newborn						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:14184	polyneuropathy due to drug						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664102	Cngb1	implicated_via_orthology	DOID:0110402	retinitis pigmentosa 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045354	Ccser1	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916151	Adgrg6	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346330	Banf1	implicated_via_orthology	DOID:0081334	Nestor-Guillermo progeria syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194505	C1qbp	implicated_via_orthology	DOID:0111495	combined oxidative phosphorylation deficiency 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	implicated_via_orthology	DOID:12387	nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934943	Amn	implicated_via_orthology	DOID:13382	megaloblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098242	Bpgm	implicated_via_orthology	DOID:0111630	familial erythrocytosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	implicated_via_orthology	DOID:0111169	subcortical band heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338833	Dio2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107765	Apbb1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384790	Fanci	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201681	Dennd5a	implicated_via_orthology	DOID:0080441	developmental and epileptic encephalopathy 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:0110144	Bartter disease type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88600	Cyp2b9	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	implicated_via_orthology	DOID:0060200	amyotrophic lateral sclerosis type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891435	Atp5mk	implicated_via_orthology	DOID:0111749	mitochondrial complex V (ATP synthase) deficiency nuclear type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928679	Dpys	implicated_via_orthology	DOID:0111629	dihydropyrimidinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:12678	hypercalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	implicated_via_orthology	DOID:0060200	amyotrophic lateral sclerosis type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141101	Depdc5	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100869	Ap3b2	implicated_via_orthology	DOID:0080448	developmental and epileptic encephalopathy 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924344	Adat3	implicated_via_orthology	DOID:0081099	neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88374	Cel	implicated_via_orthology	DOID:3153	lipomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	implicated_via_orthology	DOID:0070412	autosomal recessive spinocerebellar ataxia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	implicated_via_orthology	DOID:0080615	nephroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:2569	retinal drusen						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139743	Eps8l3	implicated_via_orthology	DOID:0110702	hypotrichosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107303	Cyp2b19	implicated_via_orthology	DOID:9828	neonatal abstinence syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859217	Dnal4	implicated_via_orthology	DOID:0111153	congenital mirror movement disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339759	Csf2rb	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144423	Arhgap44	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916340	Ascc1	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:11044	gastroschisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:0111799	syndromic microphthalmia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109176	Cpt2	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890496	Elac2	implicated_via_orthology	DOID:0111496	combined oxidative phosphorylation deficiency 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94866	Dbp	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88295	Cacna2d1	implicated_via_orthology	DOID:0070395	developmental and epileptic encephalopathy 110						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097164	Bnc1	implicated_via_orthology	DOID:0080873	primary ovarian insufficiency 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919019	Bbs10	implicated_via_orthology	DOID:0110132	Bardet-Biedl syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333857	Arhgap31	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105959	Cox8a	implicated_via_orthology	DOID:0070500	mitochondrial complex IV deficiency nuclear type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87873	Acd	implicated_via_orthology	DOID:0070023	autosomal dominant dyskeratosis congenita 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:4079	heart valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0090120	hereditary neutrophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103250	Calm2	implicated_via_orthology	DOID:0110656	long QT syndrome 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918769	Cyp2u1	implicated_via_orthology	DOID:0110808	hereditary spastic paraplegia 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:3304	germinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	implicated_via_orthology	DOID:0110034	X-linked Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:4674	androgen insensitivity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321119	Aurkc	implicated_via_orthology	DOID:0070183	spermatogenic failure 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919358	Ddhd2	implicated_via_orthology	DOID:0110806	hereditary spastic paraplegia 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449112	Adamts10	implicated_via_orthology	DOID:0050475	Weill-Marchesani syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	implicated_via_orthology	DOID:0111558	Charcot-Marie-Tooth disease type 2DD						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108554	Dab1	implicated_via_orthology	DOID:0050984	spinocerebellar ataxia type 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914256	Cisd2	implicated_via_orthology	DOID:0110630	Wolfram syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097689	Ackr1	implicated_via_orthology	DOID:12978	Plasmodium vivax malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685615	Ceacam16	implicated_via_orthology	DOID:0110574	autosomal dominant nonsyndromic deafness 4B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336993	Ap4e1	implicated_via_orthology	DOID:0110803	hereditary spastic paraplegia 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	implicated_via_orthology	DOID:0110770	hereditary spastic paraplegia 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157782	Cdhr1	implicated_via_orthology	DOID:0111021	cone-rod dystrophy 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926170	Dlst	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107571	Cav2	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:0110848	xeroderma pigmentosum group F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:61	mitral valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99675	Adcy3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88226	C2	implicated_via_orthology	DOID:0060295	complement component 2 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289258	Cfap43	implicated_via_orthology	DOID:1572	normal pressure hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:0050952	spastic ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	implicated_via_orthology	DOID:9278	hyperargininemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921624	Clec16a	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103013	Cacna1c	implicated_via_orthology	DOID:0110220	Brugada syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:0080958	primary hypoalphalipoproteinemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914061	Duoxa2	implicated_via_orthology	DOID:0112184	thyroid dyshormonogenesis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88226	C2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:0110144	Bartter disease type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:0060700	familial hypocalciuric hypercalcemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916051	Elovl5	implicated_via_orthology	DOID:0050985	spinocerebellar ataxia type 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328365	Aanat	implicated_via_orthology	DOID:0050628	advanced sleep phase syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891374	Brdt	implicated_via_orthology	DOID:14228	oligospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	implicated_via_orthology	DOID:0110723	neuronal ceroid lipofuscinosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88158	Bgn	implicated_via_orthology	DOID:0111861	Meester-Loeys syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159324	Cln6	implicated_via_orthology	DOID:0110729	neuronal ceroid lipofuscinosis 6A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88458	Col5a2	implicated_via_orthology	DOID:0080726	Ehlers-Danlos syndrome classic type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919279	Cnpy3	implicated_via_orthology	DOID:0080432	developmental and epileptic encephalopathy 60						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195272	Eda	implicated_via_orthology	DOID:0111664	ectodermal dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	implicated_via_orthology	DOID:0110125	Bardet-Biedl syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270149	Cyp2j5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:5750	endometrial serous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88457	Col5a1	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859549	Btnl2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918480	Dym	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87935	Adra2b	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341085	Epm2a	implicated_via_orthology	DOID:3534	Lafora disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	implicated_via_orthology	DOID:0050711	aceruloplasminemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	implicated_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346091	Fbln5	implicated_via_orthology	DOID:3144	cutis laxa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	implicated_via_orthology	DOID:0080155	very long chain acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88611	Cyp4a10	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	implicated_via_orthology	DOID:0110450	dilated cardiomyopathy 1II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88015	Ampd1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151054	Cnnm2	implicated_via_orthology	DOID:0060884	renal hypomagnesemia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	implicated_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346052	Apc2	implicated_via_orthology	DOID:0090131	complex cortical dysplasia with other brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87893	Chrnd	implicated_via_orthology	DOID:0110666	congenital myasthenic syndrome 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	implicated_via_orthology	DOID:0060194	amyotrophic lateral sclerosis type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0110340	osteogenesis imperfecta type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103202	Adsl	implicated_via_orthology	DOID:0050762	adenylosuccinase lyase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87894	Chrne	implicated_via_orthology	DOID:0110679	congenital myasthenic syndrome 4C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	implicated_via_orthology	DOID:0050726	tyrosinemia type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917143	Coa7	implicated_via_orthology	DOID:0070465	spinocerebellar ataxia with axonal neuropathy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096550	Cyp4a14	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:0080137	multiple endocrine neoplasia type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442555	Dis3l2	implicated_via_orthology	DOID:0060476	Perlman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109609	Faah	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:0110014	age related macular degeneration 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107674	Cd1d1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88251	Calm1	implicated_via_orthology	DOID:0110655	long QT syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923013	Dcaf17	implicated_via_orthology	DOID:0112264	Woodhouse-Sakati syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	implicated_via_orthology	DOID:14218	dihydropyrimidine dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102676	Abcc1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355312	C1s1	implicated_via_orthology	DOID:0080987	Ehlers-Danlos syndrome periodontal type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921258	Arsg	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045266	Fan1	implicated_via_orthology	DOID:0060911	karyomegalic interstitial nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:4257	Caffey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3505689	Cdsn	implicated_via_orthology	DOID:0110699	hypotrichosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915775	Evc2	implicated_via_orthology	DOID:12714	Ellis-Van Creveld syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339754	Csf2ra	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:37	skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88235	C7	implicated_via_orthology	DOID:0060300	complement component 7 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	implicated_via_orthology	DOID:0111498	combined oxidative phosphorylation deficiency 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0080912	cerebrooculofacioskeletal syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644269	C1s2	implicated_via_orthology	DOID:0080987	Ehlers-Danlos syndrome periodontal type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:0080463	developmental and epileptic encephalopathy 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:8501	fundus dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915385	Eif3h	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0111181	familial hemiplegic migraine 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87919	Add2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920455	C9orf72	implicated_via_orthology	DOID:0060213	frontotemporal dementia and/or amyotrophic lateral sclerosis-1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194490	Diaph1	implicated_via_orthology	DOID:0110541	autosomal dominant nonsyndromic deafness 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109294	Cd244a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446132	Bms1	implicated_via_orthology	DOID:0080661	nonsyndromic aplasia cutis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:13839	extrapyramidal and movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913845	Aste1	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103572	Cebpe	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:0070193	autosomal recessive chronic granulomatous disease 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917176	Dnah17	implicated_via_orthology	DOID:0111926	spermatogenic failure 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3607720	Dnaaf6	implicated_via_orthology	DOID:0111850	primary ciliary dyskinesia 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338076	Hivep2	implicated_via_orthology	DOID:0070073	autosomal dominant intellectual developmental disorder 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88233	C6	implicated_via_orthology	DOID:0060299	complement component 6 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181178	Mkrn3	implicated_via_orthology	DOID:0112309	central precocious puberty 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:13714	anodontia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	implicated_via_orthology	DOID:0080608	anterior segment dysgenesis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915247	Ddx59	implicated_via_orthology	DOID:0060375	orofaciodigital syndrome V						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95623	Gabrg2	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652818	Dcdc2a	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928953	Ccl24	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95852	Gss	implicated_via_orthology	DOID:0081034	glutatione synthetase deficiency with 5-oxoprolinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96540	Il12b	implicated_via_orthology	DOID:0060859	salmonellosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:0110293	autosomal recessive limb-girdle muscular dystrophy type 2P						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	implicated_via_orthology	DOID:0060754	familial temporal lobe epilepsy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	implicated_via_orthology	DOID:0090145	dopamine beta-hydroxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96448	Ighm	implicated_via_orthology	DOID:0081136	agammaglobulinemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932535	Glis2	implicated_via_orthology	DOID:0111116	nephronophthisis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107654	Ifngr2	implicated_via_orthology	DOID:0111995	immunodeficiency 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429763	Dock3	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915813	Dpm3	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111788	Melnick-Needles syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:0040086	Polyomavirus-associated nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95455	Ets1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96236	Hsd3b4	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388029	Liph	implicated_via_orthology	DOID:0110704	hypotrichosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0112149	terminal osseous dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0050956	spinocerebellar ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104978	Cyp7b1	implicated_via_orthology	DOID:0110810	hereditary spastic paraplegia 5A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99439	Btc	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:2215	factor VII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0111337	Jackson-Weiss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096398	Cd81	implicated_via_orthology	DOID:0081149	common variable immunodeficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927185	Chp1	implicated_via_orthology	DOID:0050952	spastic ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	implicated_via_orthology	DOID:5353	colonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	implicated_via_orthology	DOID:2729	dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	implicated_via_orthology	DOID:0110998	Joubert syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95285	Edn3	implicated_via_orthology	DOID:0110954	Waardenburg syndrome type 4B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95478	Fabp2	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	implicated_via_orthology	DOID:0111392	mucopolysaccharidosis type IVB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330238	Dpm2	implicated_via_orthology	DOID:0080571	congenital disorder of glycosylation Iu						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:0111366	familial hepatic adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178051	Cacna1i	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894686	Col9a3	implicated_via_orthology	DOID:0070304	multiple epiphyseal dysplasia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:0110564	autosomal dominant nonsyndromic deafness 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098244	Ap1s1	implicated_via_orthology	DOID:0060483	MEDNIK syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	implicated_via_orthology	DOID:0080021	Schmid metaphyseal chondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96709	Ky	implicated_via_orthology	DOID:0080098	myofibrillar myopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106925	Cldn11	implicated_via_orthology	DOID:0070402	hypomyelinating leukodystrophy 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930124	Apom	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88319	Cd19	implicated_via_orthology	DOID:0081146	common variable immunodeficiency 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442934	Minar2	implicated_via_orthology	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333768	Krt6b	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:0070280	primary autosomal recessive microcephaly 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914682	Hoga1	implicated_via_orthology	DOID:0111672	primary hyperoxaluria type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:4961	bone marrow disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87871	Acat2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99481	F11	implicated_via_orthology	DOID:2229	factor XI deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	implicated_via_orthology	DOID:0090005	Schwartz-Jampel syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	implicated_via_orthology	DOID:0111816	syndactyly type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147577	Ffar4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306784	Cited2	implicated_via_orthology	DOID:0110113	atrial heart septal defect 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145130	Cog5	implicated_via_orthology	DOID:0070261	congenital disorder of glycosylation type IIi						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153182	Kcnn2	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108092	Bin1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103159	Cish	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	implicated_via_orthology	DOID:0111785	frontometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103060	Ecm1	implicated_via_orthology	DOID:14498	lipoid proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109374	Fut2	implicated_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109424	Abca4	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96539	Il12a	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:10933	obsessive-compulsive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146574	Ildr1	implicated_via_orthology	DOID:0110500	autosomal recessive nonsyndromic deafness 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351659	Abcg5	implicated_via_orthology	DOID:0090019	sitosterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913658	Aptx	implicated_via_orthology	DOID:0050754	ataxia with oculomotor apraxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921727	4933427D14Rik	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100845	Krt6a	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	implicated_via_orthology	DOID:1064	cystinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444681	Hhat	implicated_via_orthology	DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	implicated_via_orthology	DOID:0110157	Charcot-Marie-Tooth disease type 2J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	implicated_via_orthology	DOID:0090128	Carvajal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95619	Gabrb1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	implicated_via_orthology	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1586	rheumatic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107277	Fyco1	implicated_via_orthology	DOID:0110238	cataract 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:11656	cicatricial pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:0110291	Leber congenital amaurosis 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444631	Bltp1	implicated_via_orthology	DOID:0111555	Alkuraya-Kucinskas syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:0060573	von Willebrand's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353569	Foxe3	implicated_via_orthology	DOID:0080607	anterior segment dysgenesis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104841	Cpox	implicated_via_orthology	DOID:13269	hereditary coproporphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:0090056	dystonia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:0090140	cortisone reductase deficiency 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921765	Cdkal1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	implicated_via_orthology	DOID:0111049	platelet-type bleeding disorder 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921727	4933427D14Rik	implicated_via_orthology	DOID:4501	orofaciodigital syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:4186	articulation disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95705	B4galt1	implicated_via_orthology	DOID:0070256	congenital disorder of glycosylation type IId						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:11695	portal vein thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147298	Cep120	implicated_via_orthology	DOID:0080277	Joubert syndrome 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	implicated_via_orthology	DOID:0080634	nanophthalmos						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	implicated_via_orthology	DOID:0110458	dilated cardiomyopathy 1BB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107207	Coq7	implicated_via_orthology	DOID:0070245	primary coenzyme Q10 deficiency 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103159	Cish	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0111158	SADDAN						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88071	Arnt	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387217	Ift52	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143103	Ano10	implicated_via_orthology	DOID:0050999	autosomal recessive spinocerebellar ataxia 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196453	Klhl7	implicated_via_orthology	DOID:0080331	cold-induced sweating syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104581	Gnb4	implicated_via_orthology	DOID:0110206	Charcot-Marie-Tooth disease dominant intermediate F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:0080218	primary spontaneous pneumothorax						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782634	Hsd3b9	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927344	Gmnn	implicated_via_orthology	DOID:0080517	Meier-Gorlin syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442120	Bank1	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890619	Gan	implicated_via_orthology	DOID:0090068	giant axonal neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855694	Isg15	implicated_via_orthology	DOID:0111934	immunodeficiency 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913945	Aspn	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88469	Comp	implicated_via_orthology	DOID:0070467	carpal tunnel syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:13482	Proteus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104756	Itga9	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914203	Cdca7	implicated_via_orthology	DOID:0090010	immunodeficiency-centromeric instability-facial anomalies syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389007	Hydin	implicated_via_orthology	DOID:0110617	primary ciliary dyskinesia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0080056	achondrogenesis type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664111	Fsip2	implicated_via_orthology	DOID:0111911	spermatogenic failure 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:2734	keratosis follicularis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890596	Evc	implicated_via_orthology	DOID:12714	Ellis-Van Creveld syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891495	Jph1	implicated_via_orthology	DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336155	Lss	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:0080451	developmental and epileptic encephalopathy 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95614	Gabra2	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333768	Krt6b	implicated_via_orthology	DOID:0111710	focal or diffuse nonepidermolytic palmoplantar keratoderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921579	Inava	implicated_via_orthology	DOID:0112155	inflammatory bowel disease 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861746	Lmbr1	implicated_via_orthology	DOID:0111564	hypoplastic or aplastic tibia with polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:5339	cyclic hematopoiesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104627	Dst	implicated_via_orthology	DOID:0070151	hereditary sensory and autonomic neuropathy type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95742	Glo1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913884	Mcm8	implicated_via_orthology	DOID:0080867	primary ovarian insufficiency 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	implicated_via_orthology	DOID:206	hereditary multiple exostoses						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	implicated_via_orthology	DOID:14766	renal agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928893	Sec1	implicated_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:0110431	dilated cardiomyopathy 1I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660880	Gmppb	implicated_via_orthology	DOID:0111233	congenital muscular dystrophy-dystroglycanopathy A14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87935	Adra2b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349481	Ing1	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347360	Cul3	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95390	En2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:0111000	Joubert syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94893	Cyb5r3	implicated_via_orthology	DOID:10783	methemoglobinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926170	Dlst	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87868	Acads	implicated_via_orthology	DOID:0080154	short chain acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914917	Alkbh8	implicated_via_orthology	DOID:0081232	autosomal recessive intellectual developmental disorder 71						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917004	Fbxo7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144423	Arhgap44	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916172	Dnai1	implicated_via_orthology	DOID:0110594	primary ciliary dyskinesia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346332	Best1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660880	Gmppb	implicated_via_orthology	DOID:0110294	autosomal recessive limb-girdle muscular dystrophy type 2T						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:216	dental caries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924268	Col25a1	implicated_via_orthology	DOID:0081020	congenital fibrosis of the extraocular muscles 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915403	Gtf2e2	implicated_via_orthology	DOID:0111872	nonphotosensitive trichothiodystrophy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145567	Fam149b	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	implicated_via_orthology	DOID:0060676	catecholaminergic polymorphic ventricular tachycardia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576497	Greb1l	implicated_via_orthology	DOID:14766	renal agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685815	Cfap58	implicated_via_orthology	DOID:0112271	spermatogenic failure 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921437	Katnb1	implicated_via_orthology	DOID:0112236	lissencephaly 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96529	Igll1	implicated_via_orthology	DOID:0081135	agammaglobulinemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145890	Ano6	implicated_via_orthology	DOID:0111052	Scott syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87934	Adra2a	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384785	Akr1d1	implicated_via_orthology	DOID:0111069	congenital bile acid synthesis defect 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037816	Cerkl	implicated_via_orthology	DOID:0110368	retinitis pigmentosa 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95762	Gm2a	implicated_via_orthology	DOID:3321	GM2 gangliosidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3577767	Grxcr1	implicated_via_orthology	DOID:0110483	autosomal recessive nonsyndromic deafness 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:2235	prothrombin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344367	Grem2	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:0080746	Sweet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0111584	dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96702	Krt5	implicated_via_orthology	DOID:0111346	epidermolysis bullosa simplex with mottled pigmentation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351338	Grm1	implicated_via_orthology	DOID:0080286	spinocerebellar ataxia 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96234	Hsd3b2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922780	Lyrm7	implicated_via_orthology	DOID:0080117	mitochondrial complex III deficiency nuclear type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88446	Col11a1	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611575	Cfhr2	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443583	Fermt1	implicated_via_orthology	DOID:1272	telangiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87914	Aspa	implicated_via_orthology	DOID:3613	Canavan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	implicated_via_orthology	DOID:5572	Beckwith-Wiedemann syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:0050977	spinocerebellar ataxia type 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916978	Card11	implicated_via_orthology	DOID:0111957	immunodeficiency 11A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443752	Intu	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050168	autoimmune polyendocrine syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918993	Coasy	implicated_via_orthology	DOID:0110740	neurodegeneration with brain iron accumulation 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442232	Gimap5	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:8632	Kaposi's sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924627	Kcnt1	implicated_via_orthology	DOID:0060686	autosomal dominant nocturnal frontal lobe epilepsy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108390	Kif2a	implicated_via_orthology	DOID:0090134	complex cortical dysplasia with other brain malformations 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	implicated_via_orthology	DOID:9821	choroideremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914421	Dram2	implicated_via_orthology	DOID:0050572	cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94906	Dmpk	implicated_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	implicated_via_orthology	DOID:0080431	developmental and epileptic encephalopathy 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104783	Atxn1	implicated_via_orthology	DOID:0050954	spinocerebellar ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107933	Mns1	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443696	Emc1	implicated_via_orthology	DOID:0081276	cerebellar atrophy, visual impairment, and psychomotor retardation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	implicated_via_orthology	DOID:0080502	GM1 gangliosidosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104781	Kcnj6	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917004	Fbxo7	implicated_via_orthology	DOID:0060372	Parkinson's disease 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345633	Mars1	implicated_via_orthology	DOID:0111866	trichothiodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:2231	factor XII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87977	Ak1	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109182	Acat3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	implicated_via_orthology	DOID:14756	vascular type Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109598	Hsd3b6	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96912	Mag	implicated_via_orthology	DOID:0110820	hereditary spastic paraplegia 75						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919540	Lsm11	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0070351	spinal muscular atrophy with lower extremity predominant 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:10772	thrombotic thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98658	Cripto	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104571	Clcn4	implicated_via_orthology	DOID:0112060	Raynaud-Claes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103221	Dsc2	implicated_via_orthology	DOID:0110082	arrhythmogenic right ventricular dysplasia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99538	Acsm3	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:3687	MELAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	implicated_via_orthology	DOID:0111136	congenital generalized lipodystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96613	Itgb4	implicated_via_orthology	DOID:0060733	junctional epidermolysis bullosa with pyloric atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103107	F10	implicated_via_orthology	DOID:2222	factor X deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934754	Kars1	implicated_via_orthology	DOID:0110534	autosomal recessive nonsyndromic deafness 89						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:2211	factor XIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349428	Foxl2	implicated_via_orthology	DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338011	Auh	implicated_via_orthology	DOID:0110002	3-methylglutaconic aciduria type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917115	A1cf	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892013	Agrp	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100496	Fmo3	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95623	Gabrg2	implicated_via_orthology	DOID:0111298	familial febrile seizures 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95751	Glrb	implicated_via_orthology	DOID:0060697	hyperekplexia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931001	Edaradd	implicated_via_orthology	DOID:0111653	ectodermal dysplasia 11A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:8927	learning disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859665	Atp8b1	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298405	Ap2m1	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045353	Adamts3	implicated_via_orthology	DOID:0060366	Hennekam syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	implicated_via_orthology	DOID:0080309	fatal infantile hypertonic myofibrillar myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	implicated_via_orthology	DOID:0090086	hypogonadotropic hypogonadism 6 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351330	Cartpt	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349481	Ing1	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	implicated_via_orthology	DOID:0050793	short QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298209	Hcn4	implicated_via_orthology	DOID:13884	sick sinus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0060581	Noonan syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100510	Bub1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681832	Cspp1	implicated_via_orthology	DOID:0110990	Joubert syndrome 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:4183	pseudopseudohypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:0070376	developmental and epileptic encephalopathy 31B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918686	Flrt3	implicated_via_orthology	DOID:0090093	hypogonadotropic hypogonadism 21 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88450	Col17a1	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341813	Adam33	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:0111241	congenital muscular dystrophy-dystroglycanopathy type A5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3586824	Epha10	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:4465	papillary renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145534	Ccno	implicated_via_orthology	DOID:0110600	primary ciliary dyskinesia 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109152	Lig3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915813	Dpm3	implicated_via_orthology	DOID:0112376	muscular dystrophy-dystroglycanopathy type B15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:0112262	leucine-sensitive hypoglycemia of infancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	implicated_via_orthology	DOID:0070340	classic citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926252	Gipc1	implicated_via_orthology	DOID:0081298	oculopharyngodistal myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145900	Fam83h	implicated_via_orthology	DOID:0110055	amelogenesis imperfecta type 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042378	Frmpd4	implicated_via_orthology	DOID:0112018	non-syndromic X-linked intellectual disability 104						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0111530	linear nevus sebaceous syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:14040	autoimmune polyendocrine syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:0060746	basal laminar drusen						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	implicated_via_orthology	DOID:2935	Chediak-Higashi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660880	Gmppb	implicated_via_orthology	DOID:0112374	muscular dystrophy-dystroglycanopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88448	Col12a1	implicated_via_orthology	DOID:0050663	Bethlem myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923673	Cep112	implicated_via_orthology	DOID:0112109	spermatogenic failure 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	implicated_via_orthology	DOID:0110209	Charcot-Marie-Tooth disease X-linked dominant 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104744	Kcnj2	implicated_via_orthology	DOID:1029	familial periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:4961	bone marrow disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	implicated_via_orthology	DOID:0090002	Tietz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670981	Kcnv2	implicated_via_orthology	DOID:0081022	retinal cone dystrophy 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	implicated_via_orthology	DOID:0060258	reticulate acropigmentation of Kitamura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194883	Crx	implicated_via_orthology	DOID:0111005	cone-rod dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923032	Lca5	implicated_via_orthology	DOID:0110215	Leber congenital amaurosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109183	Fgf12	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138169	Cfhr1	implicated_via_orthology	DOID:0110014	age related macular degeneration 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105980	Cntn1	implicated_via_orthology	DOID:0080101	Compton-North congenital myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102716	Cryba4	implicated_via_orthology	DOID:0110271	cataract 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101770	Bfsp1	implicated_via_orthology	DOID:0110264	cataract 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925016	Elp4	implicated_via_orthology	DOID:12271	aniridia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917458	Med23	implicated_via_orthology	DOID:0081190	autosomal recessive intellectual developmental disorder 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919519	Cda	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:1798	pancreatic endocrine carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145349	Cdk20	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104645	Hsd3b5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646318	Gm5478	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:0111697	cleft palate, cardiac defects, and intellectual disabillity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0110937	autosomal dominant osteopetrosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109514	Cstb	implicated_via_orthology	DOID:0111452	progressive myoclonus epilepsy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	implicated_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:0080982	X-linked mental retardation-hypotonic facies syndrome-1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:12190	descending colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929772	Dpysl5	implicated_via_orthology	DOID:0060565	Ritscher-Schinzel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102495	mt-Nd6	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104873	Aga	implicated_via_orthology	DOID:0050461	aspartylglucosaminuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0050748	marginal zone lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106378	Mbd6	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916218	Cdan1	implicated_via_orthology	DOID:0111398	congenital dyserythropoietic anemia type Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924908	Ap5z1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338011	Auh	implicated_via_orthology	DOID:447	renal tubular transport disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	implicated_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:150	disease of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157910	Mlc1	implicated_via_orthology	DOID:0080316	megalencephalic leukoencephalopathy with subcortical cysts 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	implicated_via_orthology	DOID:2717	Bloom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107450	Dld	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	implicated_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99846	Gdi1	implicated_via_orthology	DOID:0112058	non-syndromic X-linked intellectual disability 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347356	Adamts2	implicated_via_orthology	DOID:0080733	Ehlers-Danlos syndrome dermatosparaxis type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646939	Gm5414	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:0050437	Danon disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921765	Cdkal1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347010	Avpr1b	implicated_via_orthology	DOID:3324	mood disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916449	Armc2	implicated_via_orthology	DOID:0111919	spermatogenic failure 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:0080827	human cytomegalovirus infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95766	Gna11	implicated_via_orthology	DOID:0090108	autosomal dominant hypocalcemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:0112006	immunodeficiency 69						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351338	Grm1	implicated_via_orthology	DOID:0080062	autosomal recessive spinocerebellar ataxia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108030	Hyou1	implicated_via_orthology	DOID:0111974	immunodeficiency 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:0060746	basal laminar drusen						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:0080957	primary hypoalphalipoproteinemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88004	Amd1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	implicated_via_orthology	DOID:0060814	Wilson-Turner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923714	Knl1	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3711284	Hsd3b8	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333111	Amd2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:9828	neonatal abstinence syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337994	Bcl10	implicated_via_orthology	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94890	Dhfr	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88466	Col9a2	implicated_via_orthology	DOID:0070298	multiple epiphyseal dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	implicated_via_orthology	DOID:0111985	immunodeficiency 32B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	implicated_via_orthology	DOID:13271	cutaneous porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96659	Kcna2	implicated_via_orthology	DOID:0080416	developmental and epileptic encephalopathy 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102708	Efnb1	implicated_via_orthology	DOID:14737	craniofrontonasal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0050475	Weill-Marchesani syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	implicated_via_orthology	DOID:0060652	familial erythrocytosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341857	Mad1l1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:0110358	retinitis pigmentosa 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2669829	D630045J12Rik	implicated_via_orthology	DOID:0112143	retinitis pigmentosa 86						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:0110650	long QT syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:12995	conduct disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921265	Fcho1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922813	Dnali1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:0110177	Charcot-Marie-Tooth disease axonal type 2N						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919241	Ercc8	implicated_via_orthology	DOID:0060240	UV-sensitive syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140356	H6pd	implicated_via_orthology	DOID:0090141	cortisone reductase deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646318	Gm5478	implicated_via_orthology	DOID:0111710	focal or diffuse nonepidermolytic palmoplantar keratoderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:0080332	bicuspid aortic valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96691	Krt17	implicated_via_orthology	DOID:0111556	steatocystoma multiplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315201	Grcc10	implicated_via_orthology	DOID:0111621	Temtamy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	implicated_via_orthology	DOID:0080596	hyper IgE recurrent infection syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194490	Diaph1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96930	Mcc	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196297	Hgsnat	implicated_via_orthology	DOID:0111393	mucopolysaccharidosis type IIIC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:0060789	hypomyelinating leukodystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102849	Klkb1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917550	Fuz	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96235	Hsd3b3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96878	Blnk	implicated_via_orthology	DOID:0060027	agammaglobulinemia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106672	Cdh15	implicated_via_orthology	DOID:0070033	autosomal dominant intellectual developmental disorder 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386258	Card14	implicated_via_orthology	DOID:0080475	psoriasis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	implicated_via_orthology	DOID:14283	primary hypertrophic osteoarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	implicated_via_orthology	DOID:10611	protein-losing enteropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:0080827	human cytomegalovirus infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146921	Cyp4f15	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196378	Habp2	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	implicated_via_orthology	DOID:0060864	patterned macular dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343498	Edar	implicated_via_orthology	DOID:0111663	ectodermal dysplasia 10A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107193	Gpr143	implicated_via_orthology	DOID:0111795	congenital nystagmus 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104808	Lcp1	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	implicated_via_orthology	DOID:11847	coronary thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:2058	chronic mucocutaneous candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923035	Klhl24	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914039	Alg14	implicated_via_orthology	DOID:0110658	congenital myasthenic syndrome 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:686	liver carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:10024	migraine with aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0080911	cerebrooculofacioskeletal syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146052	Agxt2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87935	Adra2b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	implicated_via_orthology	DOID:0111255	McKusick-Kaufman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932723	Gimap3	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278336	Cdkl5	implicated_via_orthology	DOID:0080467	developmental and epileptic encephalopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98257	Msr1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917274	Mcm10	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	implicated_via_orthology	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107893	D6Wsu163e	implicated_via_orthology	DOID:0081227	autosomal recessive intellectual developmental disorder 66						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142808	Cog4	implicated_via_orthology	DOID:0070262	congenital disorder of glycosylation type IIj						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96550	Il2rb	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102498	mt-Nd4	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920717	1700066M21Rik	implicated_via_orthology	DOID:0070426	combined oxidative phosphorylation deficiency 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098726	Emp2	implicated_via_orthology	DOID:0080386	nephrotic syndrome type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333842	Grap2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:0110632	megaconial type congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105115	Ctf1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928739	Dnajb2	implicated_via_orthology	DOID:0111214	autosomal recessive distal hereditary motor neuronopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109152	Lig3	implicated_via_orthology	DOID:0070451	mitochondrial DNA depletion syndrome 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926876	Impg1	implicated_via_orthology	DOID:0050661	vitelliform macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:0050524	maturity-onset diabetes of the young						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917611	Lman1	implicated_via_orthology	DOID:2216	factor V deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	implicated_via_orthology	DOID:13270	erythropoietic protoporphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:0111864	autosomal recessive congenital bilateral absence of vas deferens						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913100	Cldn9	implicated_via_orthology	DOID:0112162	autosomal recessive nonsyndromic deafness 116						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349421	Figla	implicated_via_orthology	DOID:0080863	primary ovarian insufficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927669	Cyp4f14	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916790	Klk10	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0060532	latex allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88473	Cox4i1	implicated_via_orthology	DOID:0070501	mitochondrial complex IV deficiency nuclear type 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95705	B4galt1	implicated_via_orthology	DOID:5212	congenital disorder of glycosylation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0080068	Charcot-Marie-Tooth disease type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	implicated_via_orthology	DOID:11613	hyperandrogenism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0111461	cardiofaciocutaneous syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:3138	acanthosis nigricans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8691	mycosis fungoides						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891123	Kcne2	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:13963	nuclear senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329021	Msh5	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	implicated_via_orthology	DOID:0050637	Finnish type amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97748	Ctsa	implicated_via_orthology	DOID:0080540	galactosialidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95774	Gnal	implicated_via_orthology	DOID:0090055	dystonia 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196396	Dpagt1	implicated_via_orthology	DOID:0110676	congenital myasthenic syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	implicated_via_orthology	DOID:0111011	cone-rod dystrophy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920713	C2cd6	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104757	Ephb4	implicated_via_orthology	DOID:0081030	central conducting lymphatic anomaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:0060836	isolated microphthalmia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384831	Cc2d1a	implicated_via_orthology	DOID:0081179	autosomal recessive intellectual developmental disorder 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686651	Bbs12	implicated_via_orthology	DOID:0110134	Bardet-Biedl syndrome 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137612	Fkbp6	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101761	Hmga2	implicated_via_orthology	DOID:14681	Silver-Russell syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929242	Ivd	implicated_via_orthology	DOID:14753	isovaleric acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107178	Hmx1	implicated_via_orthology	DOID:0060482	oculoauricular syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891259	Lrat	implicated_via_orthology	DOID:0110188	Leber congenital amaurosis 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860077	Msh4	implicated_via_orthology	DOID:0070164	spermatogenic failure 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915760	Ints1	implicated_via_orthology	DOID:0070346	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0080207	CAKUT2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341823	Fanca	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:0110766	hereditary spastic paraplegia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95880	Gypa	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	implicated_via_orthology	DOID:1388	Tangier disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918836	Ifih1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918742	Bbs7	implicated_via_orthology	DOID:0110129	Bardet-Biedl syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:13258	typhoid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96687	Krt12	implicated_via_orthology	DOID:2566	corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96605	Itga6	implicated_via_orthology	DOID:0060733	junctional epidermolysis bullosa with pyloric atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444491	Heatr3	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0111359	large congenital melanocytic nevus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:0111189	distal myopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:0111232	congenital muscular dystrophy-dystroglycanopathy type A9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103301	Cacnb4	implicated_via_orthology	DOID:963	episodic ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:0080776	partial androgen insensitivity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915651	G6pc3	implicated_via_orthology	DOID:0112136	severe congenital neutropenia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	implicated_via_orthology	DOID:0060693	Brunner Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	implicated_via_orthology	DOID:0080071	mucolipidosis III alpha/beta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96540	Il12b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443258	Map3k20	implicated_via_orthology	DOID:0111221	centronuclear myopathy 6 with fiber-type disproportion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137336	Baiap2	implicated_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924809	Agl	implicated_via_orthology	DOID:2748	glycogen storage disease III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346500	Igbp1	implicated_via_orthology	DOID:0060816	corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:0040086	Polyomavirus-associated nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349447	Cln8	implicated_via_orthology	DOID:0110724	neuronal ceroid lipofuscinosis 8 northern epilepsy variant						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104756	Itga9	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	implicated_via_orthology	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917326	Esrp1	implicated_via_orthology	DOID:0111639	autosomal recessive nonsyndromic deafness 109						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	implicated_via_orthology	DOID:14755	argininosuccinic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:12574	posterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194883	Crx	implicated_via_orthology	DOID:0110333	Leber congenital amaurosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917609	Gtpbp3	implicated_via_orthology	DOID:0111500	combined oxidative phosphorylation deficiency 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926876	Impg1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:0080409	familial adenomatous polyposis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918943	Colec11	implicated_via_orthology	DOID:0060576	3MC syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919885	Lins1	implicated_via_orthology	DOID:0081193	autosomal recessive intellectual developmental disorder 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619440	Mir96	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915464	Gsto2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315195	Emg1	implicated_via_orthology	DOID:0050684	Bowen-Conradi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88489	Cr2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102717	Crybb3	implicated_via_orthology	DOID:0110268	cataract 22 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916885	Dapk1	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105368	Atp2b2	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	implicated_via_orthology	DOID:0111207	autosomal dominant distal hereditary motor neuronopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889272	Cadm1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95957	H2-T23	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349429	Arl2bp	implicated_via_orthology	DOID:0110419	retinitis pigmentosa with or without situs inversus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:0060918	facioscapulohumeral muscular dystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:0080339	familial erythrocytosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88141	Bcr	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:4186	articulation disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353452	Aldh3a2	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99614	Mst1r	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921566	Isca2	implicated_via_orthology	DOID:0080136	multiple mitochondrial dysfunctions syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349451	Corin	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138209	D2hgdh	implicated_via_orthology	DOID:0111351	D-2-hydroxyglutaric aciduria 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96062	Hdc	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109233	Kif22	implicated_via_orthology	DOID:0112199	spondyloepimetaphyseal dysplasia with joint laxity type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916469	Ddah1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:9563	bronchiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96974	Kitl	implicated_via_orthology	DOID:9258	Waardenburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576659	Ano5	implicated_via_orthology	DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12148	alveolar echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:0070385	developmental and epileptic encephalopathy 99						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576497	Greb1l	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100863	Kpna3	implicated_via_orthology	DOID:0070457	hereditary spastic paraplegia 88						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345633	Mars1	implicated_via_orthology	DOID:0110173	Charcot-Marie-Tooth disease axonal type 2U						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441849	Lpp	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135756	Hspb8	implicated_via_orthology	DOID:0111208	obsolete distal hereditary motor neuronopathy type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916950	Col22a1	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95778	Gnat1	implicated_via_orthology	DOID:0110714	congenital stationary night blindness 1G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	implicated_via_orthology	DOID:628	combined T cell and B cell immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102563	Dct	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0050660	Beare-Stevenson cutis gyrata syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890473	Il20	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	implicated_via_orthology	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109151	Ltbp1	implicated_via_orthology	DOID:3144	cutis laxa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145977	Dip2b	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914292	Ift27	implicated_via_orthology	DOID:0110141	Bardet-Biedl syndrome 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95781	Gnb1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:4961	bone marrow disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95530	Fh1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921765	Cdkal1	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289279	Dnah9	implicated_via_orthology	DOID:0111853	primary ciliary dyskinesia 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146430	Cblb	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353573	Aass	implicated_via_orthology	DOID:9274	hyperlysinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924937	Kcnq5	implicated_via_orthology	DOID:0080237	autosomal dominant intellectual developmental disorder 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919241	Ercc8	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045348	Cpa6	implicated_via_orthology	DOID:0111308	familial febrile seizures 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923824	Mfsd2a	implicated_via_orthology	DOID:0070277	primary autosomal recessive microcephaly 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149839	Hycc1	implicated_via_orthology	DOID:0060793	hypomyelinating leukodystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	implicated_via_orthology	DOID:12119	hemosiderosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3050566	Akap6	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442557	Frmd5	implicated_via_orthology	DOID:0081275	neurodevelopmental disorder with eye movement abnormalities and ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:0080468	developmental and epileptic encephalopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328361	Bard1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353592	Hacd1	implicated_via_orthology	DOID:0081337	congenital myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104579	Il12rb1	implicated_via_orthology	DOID:0111990	immunodeficiency 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341813	Adam33	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924753	Alg9	implicated_via_orthology	DOID:0080564	congenital disorder of glycosylation Il						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:0111182	familial hemiplegic migraine 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	implicated_via_orthology	DOID:0070251	X-linked Emery-Dreifuss muscular dystrophy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342540	Ikzf1	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646939	Gm5414	implicated_via_orthology	DOID:0111710	focal or diffuse nonepidermolytic palmoplantar keratoderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:3385	bacterial vaginosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182591	Acsf3	implicated_via_orthology	DOID:0111263	combined malonic and methylmalonic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:0060887	ossification of the posterior longitudinal ligament of spine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:0060486	Perry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917587	Iyd	implicated_via_orthology	DOID:0112188	thyroid dyshormonogenesis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298375	Cabin1	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443590	Ddx11	implicated_via_orthology	DOID:0060535	Warsaw breakage syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443583	Fermt1	implicated_via_orthology	DOID:2731	vesiculobullous skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:8689	anorexia nervosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0111286	psoriasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923776	Gatc	implicated_via_orthology	DOID:0112118	combined oxidative phosphorylation deficiency 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349472	Adh4	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100517	Clpb	implicated_via_orthology	DOID:0081133	3-methylglutaconic aciduria type 7a						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140726	Guf1	implicated_via_orthology	DOID:0080427	developmental and epileptic encephalopathy 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95457	Mecom	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913321	Ethe1	implicated_via_orthology	DOID:0060640	ethylmalonic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931627	Fgf16	implicated_via_orthology	DOID:0111813	syndactyly type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341803	Lipg	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321133	Hint1	implicated_via_orthology	DOID:0050526	Gamstorp-Wohlfart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341830	Eif2ak3	implicated_via_orthology	DOID:0090060	Wolcott-Rallison syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87890	Chrnb1	implicated_via_orthology	DOID:0110681	congenital myasthenic syndrome 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384875	Cdk5rap2	implicated_via_orthology	DOID:0070286	primary autosomal recessive microcephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88489	Cr2	implicated_via_orthology	DOID:0081150	common variable immunodeficiency 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	implicated_via_orthology	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:0080679	neuronal intestinal dysplasia type A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:12783	migraine without aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:0080611	anterior segment dysgenesis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95300	Eif2b4	implicated_via_orthology	DOID:0070371	leukoencephalopathy with vanishing white matter 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:0112003	immunodeficiency 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:3234	central nervous system lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95621	Gabrb3	implicated_via_orthology	DOID:0080447	developmental and epileptic encephalopathy 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98320	C4a	implicated_via_orthology	DOID:0060298	complement component 4b deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95686	Gdf3	implicated_via_orthology	DOID:0080591	Klippel-Feil syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915775	Evc2	implicated_via_orthology	DOID:0111571	Weyers acrofacial dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	implicated_via_orthology	DOID:12387	nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921396	Dock8	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88447	Col11a2	implicated_via_orthology	DOID:0080673	fibrochondrogenesis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96782	Lhb	implicated_via_orthology	DOID:0090091	hypogonadotropic hypogonadism 23 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153183	Kcnn3	implicated_via_orthology	DOID:1229	paranoid schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104995	Gclm	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3500	gallbladder adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	implicated_via_orthology	DOID:0110126	Bardet-Biedl syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921569	Mettl23	implicated_via_orthology	DOID:0081208	autosomal recessive intellectual developmental disorder 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88431	Cnbp	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	implicated_via_orthology	DOID:0080715	developmental and epileptic encephalopathy 82						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183747	Fgd4	implicated_via_orthology	DOID:0110192	Charcot-Marie-Tooth disease type 4H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:0090130	cortical dysplasia-focal epilepsy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922263	Ct55	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0060532	latex allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928379	Get3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:10646	schizotypal personality disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88519	Crybb2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050840	cervical dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:4961	bone marrow disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103097	Anapc1	implicated_via_orthology	DOID:2732	Rothmund-Thomson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684845	Bmal2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:0080625	severe congenital neutropenia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890773	Actn4	implicated_via_orthology	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103221	Dsc2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102495	mt-Nd6	implicated_via_orthology	DOID:0070350	spinal muscular atrophy with lower extremity predominant 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98505	Hnf1b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385133	Exosc2	implicated_via_orthology	DOID:0081175	short stature, hearing loss, retinitis pigmentosa, and distinctive facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100856	Mras	implicated_via_orthology	DOID:0112169	Noonan syndrome 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:0050636	familial visceral amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	implicated_via_orthology	DOID:0111365	benign familial hematuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	implicated_via_orthology	DOID:10611	protein-losing enteropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444484	Manea	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88015	Ampd1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96974	Kitl	implicated_via_orthology	DOID:0110590	autosomal dominant nonsyndromic deafness 69						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0080160	Cytomegalovirus retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105386	Dbt	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917542	Afap1	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96170	Hoxa1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148742	Cldn16	implicated_via_orthology	DOID:447	renal tubular transport disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309464	Mapk8ip1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:0050598	extrapulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:0111959	immunodeficiency 15B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:2862	glucosephosphate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	implicated_via_orthology	DOID:870	neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96666	Kcnb1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:0111862	congenital bilateral absence of vas deferens						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	implicated_via_orthology	DOID:0110054	amelogenesis imperfecta type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	implicated_via_orthology	DOID:0112282	spondyloepiphyseal dysplasia Kimberley type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685175	Asxl3	implicated_via_orthology	DOID:0080893	Bainbridge-Ropers syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099442	Atxn3	implicated_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:3875	thrombophlebitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096329	Foxi1	implicated_via_orthology	DOID:0110498	autosomal recessive nonsyndromic deafness 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12148	alveolar echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913514	Ccdc28b	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	implicated_via_orthology	DOID:0050749	peripheral T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920543	Ccdc103	implicated_via_orthology	DOID:0110621	primary ciliary dyskinesia 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	implicated_via_orthology	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927580	Bloc1s6	implicated_via_orthology	DOID:0060547	Hermansky-Pudlak syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0050331	lacrimoauriculodentodigital syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:0080676	Stickler syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	implicated_via_orthology	DOID:0060257	dyschromatosis symmetrica hereditaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0050630	Aland Island eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87894	Chrne	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109178	Fgf13	implicated_via_orthology	DOID:0070381	developmental and epileptic encephalopathy 90						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861586	Krt71	implicated_via_orthology	DOID:0110710	hypotrichosis 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	implicated_via_orthology	DOID:0080090	reducing body myopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105061	Clcn2	implicated_via_orthology	DOID:0111312	idiopathic generalized epilepsy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88228	C4b	implicated_via_orthology	DOID:0060298	complement component 4b deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346542	Bace1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	implicated_via_orthology	DOID:2468	psychotic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100845	Krt6a	implicated_via_orthology	DOID:0111710	focal or diffuse nonepidermolytic palmoplantar keratoderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196378	Habp2	implicated_via_orthology	DOID:0111907	thrombophilia due to thrombin defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104860	Fxr1	implicated_via_orthology	DOID:0081343	congenital myopathy 9A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:10024	migraine with aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913892	Ctnnbl1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88393	Chd1	implicated_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142227	Lrrk1	implicated_via_orthology	DOID:0081111	osteosclerotic metaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342771	Klf1	implicated_via_orthology	DOID:0111400	congenital dyserythropoietic anemia type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:0080444	developmental and epileptic encephalopathy 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321402	Lcp2	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:0110539	autosomal recessive nonsyndromic deafness 97						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	implicated_via_orthology	DOID:12803	Sly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196250	Klrk1	implicated_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:0060588	Noonan syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:0080802	autosomal recessive craniometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95722	Gjb4	implicated_via_orthology	DOID:0080248	erythrokeratodermia variabilis et progressiva 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861746	Lmbr1	implicated_via_orthology	DOID:0111818	syndactyly type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:0081320	multiple synostoses syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687319	Il1rapl1	implicated_via_orthology	DOID:0112022	non-syndromic X-linked intellectual disability 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916835	Hjv	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135672	Lmod2	implicated_via_orthology	DOID:0081163	dilated cardiomyopathy 2G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	implicated_via_orthology	DOID:3322	GM1 gangliosidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342540	Ikzf1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097667	Ganab	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95519	Fgf5	implicated_via_orthology	DOID:0111566	familial isolated trichomegaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4845848	Gon7	implicated_via_orthology	DOID:0080694	Galloway-Mowat syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919580	Klhl40	implicated_via_orthology	DOID:0110930	nemaline myopathy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354695	Fbxw7	implicated_via_orthology	DOID:0070420	developmental delay, hypotonia, and impaired language						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95762	Gm2a	implicated_via_orthology	DOID:4795	GM2 gangliosidosis, AB variant						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098597	Ift81	implicated_via_orthology	DOID:0080295	short-rib thoracic dysplasia 19 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0111450	progressive myoclonus epilepsy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444639	Fbxo38	implicated_via_orthology	DOID:0111210	autosomal dominant distal hereditary motor neuronopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0111244	palmoplantar keratoderma and congenital alopecia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147790	Fermt3	implicated_via_orthology	DOID:0110912	leukocyte adhesion deficiency 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106911	Hccs	implicated_via_orthology	DOID:0111808	linear skin defects with multiple congenital anomalies 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892032	Frzb	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	implicated_via_orthology	DOID:0060543	Hermansky-Pudlak syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923883	Lrmda	implicated_via_orthology	DOID:0070100	oculocutaneous albinism type VII						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:0050472	monilethrix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:0050472	monilethrix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107978	Klc1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141180	Glmn	implicated_via_orthology	DOID:2436	glomangioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298210	Hcn2	implicated_via_orthology	DOID:0111310	familial febrile seizures 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:350	mastocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95495	Ms4a2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384966	Mgat2	implicated_via_orthology	DOID:0070253	congenital disorder of glycosylation type IIa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443225	Gatad2b	implicated_via_orthology	DOID:0070048	GAND syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653368	Klf11	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	implicated_via_orthology	DOID:440	neuromuscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0080037	Worth syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96027	Hbb-y	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95615	Gabra3	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104744	Kcnj2	implicated_via_orthology	DOID:0050434	Andersen-Tawil syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96829	Lrpap1	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861438	Gcm2	implicated_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	implicated_via_orthology	DOID:2750	glycogen storage disease IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913558	Mplkip	implicated_via_orthology	DOID:0050528	nonphotosensitive trichothiodystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96539	Il12a	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:0111968	immunodeficiency 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3769724	Tomt	implicated_via_orthology	DOID:0110515	autosomal recessive nonsyndromic deafness 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96538	Il10ra	implicated_via_orthology	DOID:0110899	inflammatory bowel disease 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:3326	purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341803	Lipg	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890380	Kptn	implicated_via_orthology	DOID:0081206	autosomal recessive intellectual developmental disorder 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103197	Mcm5	implicated_via_orthology	DOID:0080255	Meier-Gorlin syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349441	Mecr	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:0111960	immunodeficiency 15A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107658	Ifnar1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:14040	autoimmune polyendocrine syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0060202	amyotrophic lateral sclerosis type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96829	Lrpap1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923661	Ift43	implicated_via_orthology	DOID:0080292	retinitis pigmentosa 81						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1340	pure red-cell aplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153089	Mrps2	implicated_via_orthology	DOID:0111482	combined oxidative phosphorylation deficiency 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097705	Kng1	implicated_via_orthology	DOID:0111676	high molecular weight kininogen deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96690	Krt16	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:1586	rheumatic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:14040	autoimmune polyendocrine syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:13774	Addison's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858195	Hnrnpu	implicated_via_orthology	DOID:0080418	developmental and epileptic encephalopathy 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0050168	autoimmune polyendocrine syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95492	Fbp1	implicated_via_orthology	DOID:5204	fructose-1,6-bisphosphatase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	implicated_via_orthology	DOID:8736	smallpox						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351614	Gyg1	implicated_via_orthology	DOID:0050579	glycogen storage disease XV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:0080096	myofibrillar myopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:0081226	autosomal recessive intellectual developmental disorder 65						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177742	Hps4	implicated_via_orthology	DOID:0060542	Hermansky-Pudlak syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96699	Krt2	implicated_via_orthology	DOID:0060877	bullous congenital ichthyosiform erythroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	implicated_via_orthology	DOID:0111044	gray platelet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928137	Mrps22	implicated_via_orthology	DOID:0111473	combined oxidative phosphorylation deficiency 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196620	Hpn	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915841	Mocos	implicated_via_orthology	DOID:0070453	xanthinuria type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0050790	fibular hypoplasia and complex brachydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917802	Lrrc56	implicated_via_orthology	DOID:0111854	primary ciliary dyskinesia 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917728	Mipep	implicated_via_orthology	DOID:0111488	combined oxidative phosphorylation deficiency 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353455	Mlh3	implicated_via_orthology	DOID:0070276	hereditary nonpolyposis colorectal cancer type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:0110971	brachydactyly type D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346022	Mab21l2	implicated_via_orthology	DOID:0111802	syndromic microphthalmia 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	implicated_via_orthology	DOID:11193	syndactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95622	Gabrd	implicated_via_orthology	DOID:0111292	idiopathic generalized epilepsy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261890	Fbxo28	implicated_via_orthology	DOID:0070386	developmental and epileptic encephalopathy 100						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926262	Irgm2	implicated_via_orthology	DOID:0110890	inflammatory bowel disease 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:3382	liposarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:0050864	non-arteritic anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102770	Guca1a	implicated_via_orthology	DOID:0080314	cone-rod dystrophy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	implicated_via_orthology	DOID:0111257	gamma-glutamyl transpeptidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353500	Foxe1	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347058	Hsf4	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0090116	spondylocarpotarsal synostosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96602	Itga3	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102482	mt-Tl1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309517	Itm2b	implicated_via_orthology	DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861438	Gcm2	implicated_via_orthology	DOID:0111387	familial isolated hypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385045	Lemd2	implicated_via_orthology	DOID:0110243	cataract 46 juvenile-onset						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:0070216	familial hyperinsulinemic hypoglycemia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96698	Krt1	implicated_via_orthology	DOID:0050428	nonepidermolytic palmoplantar keratoderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95742	Glo1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	implicated_via_orthology	DOID:0111595	congenital contractural arachnodactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:0060211	amyotrophic lateral sclerosis type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648735	Mplkipl1	implicated_via_orthology	DOID:0050528	nonphotosensitive trichothiodystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:0060827	X-linked intellectual disability-psychosis-macroorchidism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	implicated_via_orthology	DOID:0111032	hemochromatosis type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96909	Maf	implicated_via_orthology	DOID:0111688	Ayme-Gripp syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444506	Mbtps2	implicated_via_orthology	DOID:0111821	ichthyosis follicularis-alopecia-photophobia syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924082	Hyls1	implicated_via_orthology	DOID:0111355	hydrolethalus syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	implicated_via_orthology	DOID:14264	benign neonatal seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95815	Grik2	implicated_via_orthology	DOID:0081182	autosomal recessive intellectual developmental disorder 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:0111036	CADASIL 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0050467	erythrokeratodermia variabilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:0110160	Charcot-Marie-Tooth disease axonal type 2T						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923786	Mmadhc	implicated_via_orthology	DOID:0050716	methylmalonic aciduria and homocystinuria type cblD						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354367	Mrps7	implicated_via_orthology	DOID:0111497	combined oxidative phosphorylation deficiency 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333787	Inppl1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:0111631	familial erythrocytosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386030	Gabbr2	implicated_via_orthology	DOID:0080291	developmental and epileptic encephalopathy 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914241	Khdc3	implicated_via_orthology	DOID:3590	gestational trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147707	Kank1	implicated_via_orthology	DOID:0081360	spastic quadriplegic cerebral palsy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:93	language disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333850	Mbd4	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100845	Krt6a	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109362	Krt86	implicated_via_orthology	DOID:0050472	monilethrix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891124	Kcne3	implicated_via_orthology	DOID:14452	hypokalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338883	Gfpt2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:161	keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:421	hair disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:401	multidrug-resistant tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683854	Klhl41	implicated_via_orthology	DOID:0110929	nemaline myopathy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96613	Itgb4	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:0111932	severe congenital encephalopathy due to MECP2 mutation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:9123	eczema herpeticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333871	Hsd17b10	implicated_via_orthology	DOID:0060810	syndromic X-linked intellectual disability type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098243	Ifnar2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932386	Ift122	implicated_via_orthology	DOID:0080803	cranioectodermal dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934860	Lztfl1	implicated_via_orthology	DOID:0110139	Bardet-Biedl syndrome 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926262	Irgm2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646318	Gm5478	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153060	Gjc2	implicated_via_orthology	DOID:4977	lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96668	Kcnc2	implicated_via_orthology	DOID:0070389	developmental and epileptic encephalopathy 103						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102849	Klkb1	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	implicated_via_orthology	DOID:0080462	developmental and epileptic encephalopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	implicated_via_orthology	DOID:0080696	Winchester syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	implicated_via_orthology	DOID:14681	Silver-Russell syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289298	Knstrn	implicated_via_orthology	DOID:8866	actinic keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927248	Kcnj1	implicated_via_orthology	DOID:0110143	Bartter disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	implicated_via_orthology	DOID:0111544	Guttmacher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914393	Ikzf5	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:7235	pancreatic mucinous cystadenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101805	Gys1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137612	Fkbp6	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341851	Msl3	implicated_via_orthology	DOID:0111838	Basilicata-Akhtar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95626	Gabrr2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335082	Invs	implicated_via_orthology	DOID:0111113	nephronophthisis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442496	Gatb	implicated_via_orthology	DOID:0112119	combined oxidative phosphorylation deficiency 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96615	Itgb6	implicated_via_orthology	DOID:0110064	amelogenesis imperfecta type 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	implicated_via_orthology	DOID:13714	anodontia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3652048	Gas2l2	implicated_via_orthology	DOID:0111858	primary ciliary dyskinesia 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95776	Gnaq	implicated_via_orthology	DOID:0111529	familial multiple nevi flammei						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:530	eyelid disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:216	dental caries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443157	Mib1	implicated_via_orthology	DOID:0060480	left ventricular noncompaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385254	Gys2	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104645	Hsd3b5	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921303	Grip1	implicated_via_orthology	DOID:0111406	Fraser syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107729	Igtp	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918041	Hars2	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:0111577	dehydrated hereditary stomatocytosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	implicated_via_orthology	DOID:0050686	organ system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:0050581	brachydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261813	Mn1	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96231	Hspa1l	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108427	Insl3	implicated_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917416	Lipn	implicated_via_orthology	DOID:0060717	autosomal recessive congenital ichthyosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:4377	egg allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050748	marginal zone lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96235	Hsd3b3	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:0060081	triple-receptor negative breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96158	Hmgcl	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309517	Itm2b	implicated_via_orthology	DOID:0070030	ITM2B-related cerebral amyloid angiopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629975	Krt74	implicated_via_orthology	DOID:0110700	hypotrichosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:5016	hepatocellular clear cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:0111108	maturity-onset diabetes of the young type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104755	Kcnj5	implicated_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445077	Lacc1	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261831	Hap1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104744	Kcnj2	implicated_via_orthology	DOID:0050793	short QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347354	Homer2	implicated_via_orthology	DOID:0110589	autosomal dominant nonsyndromic deafness 68						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447810	Ltv1	implicated_via_orthology	DOID:0070510	inflammatory poikiloderma with hair abnormalities and acral keratoses						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	implicated_via_orthology	DOID:0111986	immunodeficiency 32A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96024	Hbb-bh1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96213	Hpd	implicated_via_orthology	DOID:0111362	hawkinsinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346322	Gpc6	implicated_via_orthology	DOID:0080844	omodysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	implicated_via_orthology	DOID:0090133	complex cortical dysplasia with other brain malformations 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96829	Lrpap1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	implicated_via_orthology	DOID:0111032	hemochromatosis type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:0110967	brachydactyly type A4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442463	Irf2bpl	implicated_via_orthology	DOID:0081327	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95683	Gdf1	implicated_via_orthology	DOID:0060772	multiple types of congenital heart defects 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102496	mt-Nd5	implicated_via_orthology	DOID:3687	MELAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3711284	Hsd3b8	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109519	Msh3	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:0060691	platelet-type bleeding disorder 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920094	Kctd17	implicated_via_orthology	DOID:0090036	myoclonic dystonia 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:0070272	hereditary nonpolyposis colorectal cancer type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:5577	gastrinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:161	keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:9663	aphthous stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98505	Hnf1b	implicated_via_orthology	DOID:0111101	maturity-onset diabetes of the young type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:0050472	monilethrix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153183	Kcnn3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261813	Mn1	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:4398	pustulosis of palm and sole						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917611	Lman1	implicated_via_orthology	DOID:2211	factor XIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95619	Gabrb1	implicated_via_orthology	DOID:0080428	developmental and epileptic encephalopathy 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444668	Fnip1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	implicated_via_orthology	DOID:0110010	achromatopsia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915522	Lingo1	implicated_via_orthology	DOID:0081225	autosomal recessive intellectual developmental disorder 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342273	Gsto1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	implicated_via_orthology	DOID:0060055	popliteal pterygium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888513	Fzd2	implicated_via_orthology	DOID:0080845	omodysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922862	Gns	implicated_via_orthology	DOID:12801	mucopolysaccharidosis III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923380	Las1l	implicated_via_orthology	DOID:0060814	Wilson-Turner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0110296	autosomal recessive limb-girdle muscular dystrophy type 2M						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	implicated_via_orthology	DOID:14686	Axenfeld-Rieger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915382	Lhfpl5	implicated_via_orthology	DOID:0110518	autosomal recessive nonsyndromic deafness 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95728	Gli2	implicated_via_orthology	DOID:0110873	holoprosencephaly 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	implicated_via_orthology	DOID:0110182	Charcot-Marie-Tooth disease axonal type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180197	Lgi4	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928858	Krt81	implicated_via_orthology	DOID:0050472	monilethrix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99926	mt-Atp8	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104541	Gcdh	implicated_via_orthology	DOID:0111254	glutaric acidemia I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105052	Il13ra1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181067	Klhl10	implicated_via_orthology	DOID:0070180	spermatogenic failure 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96909	Maf	implicated_via_orthology	DOID:0110256	cataract 21 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95742	Glo1	implicated_via_orthology	DOID:178	vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:12030	panuveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914325	Magt1	implicated_via_orthology	DOID:0111839	congenital disorder of glycosylation Icc						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:9383	iridocyclitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:0110083	arrhythmogenic right ventricular dysplasia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684762	Lzts1	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915415	Fdx2	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914609	Loxhd1	implicated_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341857	Mad1l1	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918836	Ifih1	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:0111334	congenital leptin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:0112225	BH4-deficient hyperphenylalaninemia B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103170	Gfi1	implicated_via_orthology	DOID:0112131	severe congenital neutropenia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384968	L2hgdh	implicated_via_orthology	DOID:0050573	2-hydroxyglutaric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108474	Fzd6	implicated_via_orthology	DOID:0080079	nonsyndromic congenital nail disorder 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918000	Kdsr	implicated_via_orthology	DOID:0080250	erythrokeratodermia variabilis et progressiva 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3574096	AK157302	implicated_via_orthology	DOID:0080274	multiple mitochondrial dysfunctions syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96540	Il12b	implicated_via_orthology	DOID:0111950	immunodeficiency 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:1742	drug psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	implicated_via_orthology	DOID:0111342	dermatopathia pigmentosa reticularis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:1827	idiopathic generalized epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	implicated_via_orthology	DOID:0112259	Leydig cell hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925517	Klhdc8b	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:8549	chronic ulcer of skin						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104756	Itga9	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	implicated_via_orthology	DOID:0081153	common variable immunodeficiency 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104698	Lim2	implicated_via_orthology	DOID:0110263	cataract 19 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342273	Gsto1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919289	Mccc1	implicated_via_orthology	DOID:0080579	3-Methylcrotonyl-CoA carboxylase 1 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95778	Gnat1	implicated_via_orthology	DOID:0110715	congenital stationary night blindness autosomal dominant 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443010	Lman2l	implicated_via_orthology	DOID:0081215	autosomal recessive intellectual developmental disorder 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96705	Krt8	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180756	Mchr1	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96691	Krt17	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149728	Impa2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:4006	bladder urothelial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10485	esophageal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328350	Matn3	implicated_via_orthology	DOID:0070299	multiple epiphyseal dysplasia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664387	Mmp21	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097667	Ganab	implicated_via_orthology	DOID:0110860	polycystic kidney disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:14768	Saethre-Chotzen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345633	Mars1	implicated_via_orthology	DOID:0070454	hereditary spastic paraplegia 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96234	Hsd3b2	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:0050933	ovarian serous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	implicated_via_orthology	DOID:0110645	long QT syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:0060473	Kabuki syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96605	Itga6	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95810	Gria3	implicated_via_orthology	DOID:0060823	syndromic X-linked intellectual disability 94						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096345	Gckr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441763	Gpr68	implicated_via_orthology	DOID:0080960	amelogenesis imperfecta type 2A6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97075	Mpi	implicated_via_orthology	DOID:2978	carbohydrate metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96236	Hsd3b4	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:0111631	familial erythrocytosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444783	Gfm2	implicated_via_orthology	DOID:0111475	combined oxidative phosphorylation deficiency 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894694	Galnt2	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685627	Kcnk18	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95683	Gdf1	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143163	Mapkapk3	implicated_via_orthology	DOID:0060865	patterned macular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924947	Mmab	implicated_via_orthology	DOID:0060743	methylmalonic acidemia cblB type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329038	Mllt10	implicated_via_orthology	DOID:8864	acute monocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101355	Ltbp3	implicated_via_orthology	DOID:0090143	brachyolmia-amelogenesis imperfecta syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:1926	Gaucher's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:0110217	Leber congenital amaurosis 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	implicated_via_orthology	DOID:0060739	hand-foot-genital syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1395	schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99456	Mc1r	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928138	Mrps23	implicated_via_orthology	DOID:0112115	combined oxidative phosphorylation deficiency 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107567	Irgm1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96743	Lamb1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95915	H2-M3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:12559	idiopathic juvenile osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:0050651	atrioventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:4927	Klatskin's tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109362	Krt86	implicated_via_orthology	DOID:421	hair disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98257	Msr1	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916608	Lrrc51	implicated_via_orthology	DOID:0110515	autosomal recessive nonsyndromic deafness 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926479	Lat2	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:11836	clubfoot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444646	Hpdl	implicated_via_orthology	DOID:0112346	hereditary spastic paraplegia 83						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926212	Med12	implicated_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102501	mt-Cytb	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	implicated_via_orthology	DOID:0111072	myostatin-related muscle hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:0110972	brachydactyly type E1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922862	Gns	implicated_via_orthology	DOID:0111402	mucopolysaccharidosis type IIID						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0050648	atelosteogenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	implicated_via_orthology	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	implicated_via_orthology	DOID:0111947	immunodeficiency 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050185	erythema multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915509	Ift80	implicated_via_orthology	DOID:0110086	asphyxiating thoracic dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3044955	Impg2	implicated_via_orthology	DOID:0110371	retinitis pigmentosa 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96009	Hadh	implicated_via_orthology	DOID:0070215	familial hyperinsulinemic hypoglycemia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99909	Lama3	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109178	Fgf13	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95617	Gabra5	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137379	Med15	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385067	Lims2	implicated_via_orthology	DOID:0110288	autosomal recessive limb-girdle muscular dystrophy type 2W						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:0111745	cerebellar ataxia type 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103220	Meox1	implicated_via_orthology	DOID:0080590	Klippel-Feil syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	implicated_via_orthology	DOID:0060239	Van der Woude syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159727	Il17rd	implicated_via_orthology	DOID:0090076	hypogonadotropic hypogonadism 18 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1395	schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923035	Klhl24	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	implicated_via_orthology	DOID:0111528	Naegeli-Franceschetti-Jadassohn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107567	Irgm1	implicated_via_orthology	DOID:0110890	inflammatory bowel disease 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354387	Mfap5	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684762	Lzts1	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101789	Lig1	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:0080763	diffuse gastric cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:14764	Larsen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0110640	congenital muscular dystrophy due to LMNA mutation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:0090110	immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181763	Hps6	implicated_via_orthology	DOID:0060544	Hermansky-Pudlak syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101848	Gnb5	implicated_via_orthology	DOID:0081008	intellectual developmental disorder with cardiac arrhythmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933158	Impa1	implicated_via_orthology	DOID:0081221	autosomal recessive intellectual developmental disorder 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384495	Mrtfa	implicated_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914854	Get4	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:0060574	von Willebrand's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96974	Kitl	implicated_via_orthology	DOID:0111373	familial progressive hyperpigmentation with or without hypopigmentation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0050168	autoimmune polyendocrine syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444506	Mbtps2	implicated_via_orthology	DOID:0112012	X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	implicated_via_orthology	DOID:0111835	congenital nongoitrous hypothyroidism 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099809	Fgf10	implicated_via_orthology	DOID:0081372	lacrimoauriculodentodigital syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:1417	choroid disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934923	Ifitm5	implicated_via_orthology	DOID:0110344	osteogenesis imperfecta type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147006	Gnptg	implicated_via_orthology	DOID:3343	glycoproteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	implicated_via_orthology	DOID:0060769	T-cell immunodeficiency, congenital alopecia, and nail dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111784	otopalatodigital syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	implicated_via_orthology	DOID:0080545	hyper IgE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	implicated_via_orthology	DOID:0110251	cataract 15 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:10632	Wolfram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0080006	bone development disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923714	Knl1	implicated_via_orthology	DOID:0070291	primary autosomal recessive microcephaly 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442415	Kat6a	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140175	Ldlrap1	implicated_via_orthology	DOID:0090105	autosomal recessive hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	implicated_via_orthology	DOID:0090073	hypogonadotropic hypogonadism 13 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10485	esophageal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:11162	respiratory failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97435	Mog	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99458	Mef2c	implicated_via_orthology	DOID:0070050	neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:0111623	ACTH-independent macronodular adrenal hyperplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914460	Gatad1	implicated_via_orthology	DOID:0110441	dilated cardiomyopathy 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107193	Gpr143	implicated_via_orthology	DOID:0050633	ocular albinism 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96699	Krt2	implicated_via_orthology	DOID:1697	ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108087	Hars1	implicated_via_orthology	DOID:0110162	Charcot-Marie-Tooth disease, axonal type 2W						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889850	Gsdme	implicated_via_orthology	DOID:0110575	autosomal dominant nonsyndromic deafness 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0080802	autosomal recessive craniometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	implicated_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	implicated_via_orthology	DOID:14766	renal agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890498	Mcoln1	implicated_via_orthology	DOID:3343	glycoproteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0060851	pemphigus vulgaris						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443764	Iqcb1	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96062	Hdc	implicated_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88321	Ms4a1	implicated_via_orthology	DOID:0081148	common variable immunodeficiency 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858193	Folh1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:0111941	immunodeficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0110117	autoimmune lymphoproliferative syndrome type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:11712	lipoatrophic diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858746	Kat6b	implicated_via_orthology	DOID:0060290	blepharophimosis-intellectual disability syndrome, SBBYS type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:8437	intestinal obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0080681	X-linked chronic idiopathic intestinal pseudo-obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102673	Lhx3	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0110184	Charcot-Marie-Tooth disease type 4J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:12399	pathological gambling						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443752	Intu	implicated_via_orthology	DOID:0080289	orofaciodigital syndrome XVII						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95617	Gabra5	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3027157	Kng2	implicated_via_orthology	DOID:0111676	high molecular weight kininogen deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933988	Kremen1	implicated_via_orthology	DOID:0111650	ectodermal dysplasia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915017	Jagn1	implicated_via_orthology	DOID:0112134	severe congenital neutropenia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195260	Fxyd2	implicated_via_orthology	DOID:0060885	renal hypomagnesemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349441	Mecr	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:0111631	familial erythrocytosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445087	Hid1	implicated_via_orthology	DOID:0070391	developmental and epileptic encephalopathy 105						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:0112156	X-linked dyserythropoietic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	implicated_via_orthology	DOID:0110637	muscular dystrophy-dystroglycanopathy type B6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3690448	Krt83	implicated_via_orthology	DOID:0050472	monilethrix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861901	Mast1	implicated_via_orthology	DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138934	Mbd5	implicated_via_orthology	DOID:0070031	autosomal dominant intellectual developmental disorder 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442252	Lrp4	implicated_via_orthology	DOID:0090015	Cenani-Lenz syndactyly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926212	Med12	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:4376	milk allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353569	Foxe3	implicated_via_orthology	DOID:0110230	cataract 34 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96202	Hoxd10	implicated_via_orthology	DOID:0111568	congenital vertical talus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	implicated_via_orthology	DOID:0070000	3-methylglutaconic aciduria type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351614	Gyg1	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10485	esophageal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347058	Hsf4	implicated_via_orthology	DOID:0110255	cataract 5 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95776	Gnaq	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144199	Mief2	implicated_via_orthology	DOID:0112110	combined oxidative phosphorylation deficiency 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142973	Lars2	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933820	Jam2	implicated_via_orthology	DOID:0060230	basal ganglia calcification						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:0050470	Donohue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:0080760	Fanconi renotubular syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924217	2700049A03Rik	implicated_via_orthology	DOID:0110096	short-rib thoracic dysplasia 14 with polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3029632	Med13	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931526	H1f2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107688	Kif3b	implicated_via_orthology	DOID:0112146	retinitis pigmentosa 89						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:0110741	type 1 diabetes mellitus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	implicated_via_orthology	DOID:0112276	neurodevelopmental disorder with involuntary movements						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859325	Il36rn	implicated_via_orthology	DOID:0080474	pustular psoriasis 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:0111204	obsolete distal hereditary motor neuronopathy type 5A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914163	Kdelr2	implicated_via_orthology	DOID:0112201	osteogenesis imperfecta type 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96550	Il2rb	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:480	movement disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445027	Malt1	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109519	Msh3	implicated_via_orthology	DOID:0080412	familial adenomatous polyposis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:0112313	brain small vessel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914944	Ift74	implicated_via_orthology	DOID:0081011	Bardet-Biedl syndrome 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333768	Krt6b	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101355	Ltbp3	implicated_via_orthology	DOID:0111727	geleophysic dysplasia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:3362	coronary aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096324	Lst1	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:161	keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194489	Guca1b	implicated_via_orthology	DOID:0110382	retinitis pigmentosa 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0050820	atrioventricular block						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177742	Hps4	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914418	Lpar6	implicated_via_orthology	DOID:0110705	hypotrichosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913442	Lage3	implicated_via_orthology	DOID:0080244	Galloway-Mowat syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101776	Lhx4	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0110958	Gaucher's disease type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	implicated_via_orthology	DOID:0060645	chronic recurrent multifocal osteomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646939	Gm5414	implicated_via_orthology	DOID:0050449	pachyonychia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919666	Lrpprc	implicated_via_orthology	DOID:0111180	French Canadian Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99456	Mc1r	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891346	Fgf20	implicated_via_orthology	DOID:14766	renal agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96789	Lipa	implicated_via_orthology	DOID:14502	cholesterol ester storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0110964	brachydactyly type A1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891112	Gmds	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140356	H6pd	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135593	Hadha	implicated_via_orthology	DOID:0111277	mitochondrial trifunctional protein deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782634	Hsd3b9	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:0060652	familial erythrocytosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676631	Il17f	implicated_via_orthology	DOID:2058	chronic mucocutaneous candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924287	Mrap	implicated_via_orthology	DOID:0080620	familial glucocorticoid deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919140	Mad2l2	implicated_via_orthology	DOID:0111080	Fanconi anemia complementation group V						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388361	Gldn	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107286	Man2b1	implicated_via_orthology	DOID:3413	alpha-mannosidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	implicated_via_orthology	DOID:2749	glycogen storage disease Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:13336	congenital toxoplasmosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	implicated_via_orthology	DOID:6678	tooth and nail syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96172	Hoxa11	implicated_via_orthology	DOID:9827	radioulnar synostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95554	Fli1	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708784	Iqcn	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141180	Glmn	implicated_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95924	H2-Oa	implicated_via_orthology	DOID:0080820	occupational asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100509	Kcnk3	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341865	Mark3	implicated_via_orthology	DOID:0070356	visual impairment and progressive phthisis bulbi						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104781	Kcnj6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891496	Jph2	implicated_via_orthology	DOID:0110323	hypertrophic cardiomyopathy 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146906	Ift140	implicated_via_orthology	DOID:0110097	short-rib thoracic dysplasia 9 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107729	Igtp	implicated_via_orthology	DOID:0110890	inflammatory bowel disease 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927596	Gprc5b	implicated_via_orthology	DOID:0080315	megalencephalic leukoencephalopathy with subcortical cysts						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890358	Igf2bp2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:0080249	erythrokeratodermia variabilis et progressiva 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:161	keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891468	Lgr4	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96698	Krt1	implicated_via_orthology	DOID:0081110	keratosis palmoplantaris striata 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88492	Masp1	implicated_via_orthology	DOID:0060575	3MC syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95776	Gnaq	implicated_via_orthology	DOID:0111563	Sturge-Weber syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	implicated_via_orthology	DOID:0112298	spondylometaphyseal dysplasia Sedaghatian type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111786	frontometaphyseal dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102499	mt-Nd3	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353455	Mlh3	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	implicated_via_orthology	DOID:4367	apparent mineralocorticoid excess syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449313	Gemin4	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:4441	dysgerminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:0111937	immunodeficiency 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349428	Foxl2	implicated_via_orthology	DOID:0080860	primary ovarian insufficiency 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934765	Gpnmb	implicated_via_orthology	DOID:0080932	primary localized cutaneous amyloidosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:11563	retinal vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924832	Mboat7	implicated_via_orthology	DOID:0081219	autosomal recessive intellectual developmental disorder 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050012	chikungunya						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891123	Kcne2	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:0050978	spinocerebellar ataxia type 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95730	Galk1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109598	Hsd3b6	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925847	Fhod3	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0080249	erythrokeratodermia variabilis et progressiva 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:419	scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:0111108	maturity-onset diabetes of the young type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335082	Invs	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933162	Lrba	implicated_via_orthology	DOID:0081151	common variable immunodeficiency 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444506	Mbtps2	implicated_via_orthology	DOID:0111847	osteogenesis imperfecta type 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045303	Mamld1	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:4184	pseudohypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687329	Kash5	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153060	Gjc2	implicated_via_orthology	DOID:0070208	hereditary lymphedema IC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	implicated_via_orthology	DOID:0111356	hydrolethalus syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916296	Isca1	implicated_via_orthology	DOID:0080274	multiple mitochondrial dysfunctions syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:591	phobic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355299	Hnrnpdl	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0050117	disease by infectious agent						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99502	Ltbp2	implicated_via_orthology	DOID:0050475	Weill-Marchesani syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99572	Gcgr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96913	Mak	implicated_via_orthology	DOID:0110380	retinitis pigmentosa 62						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138934	Mbd5	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	implicated_via_orthology	DOID:0110078	Leber congenital amaurosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95692	Gdf9	implicated_via_orthology	DOID:0080871	primary ovarian insufficiency 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925288	Mccc2	implicated_via_orthology	DOID:0080580	3-Methylcrotonyl-CoA carboxylase 2 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	implicated_via_orthology	DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10485	esophageal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1579	respiratory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:0111244	palmoplantar keratoderma and congenital alopecia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:9383	iridocyclitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:0111631	familial erythrocytosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146020	Mief1	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913480	Mrps28	implicated_via_orthology	DOID:0112114	combined oxidative phosphorylation deficiency 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	implicated_via_orthology	DOID:0110950	Waardenburg syndrome type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	implicated_via_orthology	DOID:0080489	GM1 gangliosidosis type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890498	Mcoln1	implicated_via_orthology	DOID:0080490	mucolipidosis type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914371	Mastl	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930618	Krit1	implicated_via_orthology	DOID:0080491	cerebral cavernous malformation 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930188	Mrps34	implicated_via_orthology	DOID:0111492	combined oxidative phosphorylation deficiency 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96789	Lipa	implicated_via_orthology	DOID:0080217	lysosomal acid lipase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:0050467	erythrokeratodermia variabilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920296	Glrx5	implicated_via_orthology	DOID:0080343	autosomal recessive pyridoxine-refractory sideroblastic anemia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12859	choreatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:1564	fungal infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	implicated_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:0050661	vitelliform macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141879	Hsd3b7	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0110444	dilated cardiomyopathy 1X						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99572	Gcgr	implicated_via_orthology	DOID:0112306	Mahvash Disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0110977	brachydactyly type A1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95697	Gfap	implicated_via_orthology	DOID:4252	Alexander disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861691	Lgi1	implicated_via_orthology	DOID:0060748	familial temporal lobe epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95742	Glo1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109321	Lama4	implicated_via_orthology	DOID:0110438	dilated cardiomyopathy 1JJ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0081290	Antley-Bixler syndrome without disordered steroidogenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12859	choreatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182543	Grhl2	implicated_via_orthology	DOID:0080669	posterior polymorphous corneal dystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:0111331	intellectual disability-severe speech delay-mild dysmorphism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180511	Il31ra	implicated_via_orthology	DOID:0080931	primary localized cutaneous amyloidosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443718	Lrig2	implicated_via_orthology	DOID:0050816	urofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181461	Ggn	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96071	Hesx1	implicated_via_orthology	DOID:0060857	septooptic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914346	Mmachc	implicated_via_orthology	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95781	Gnb1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12987	agranulocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:0111218	Friedreich ataxia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344333	Mid2	implicated_via_orthology	DOID:0112048	non-syndromic X-linked intellectual disability 101						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336155	Lss	implicated_via_orthology	DOID:0080950	alopecia-mental retardation syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104867	Lbx1	implicated_via_orthology	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629975	Krt74	implicated_via_orthology	DOID:0111573	autosomal dominant woolly hair						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098270	Jag2	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:0110741	type 1 diabetes mellitus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:0111733	pancreatic hypoplasia-diabetes-congenital heart disease syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96990	Mip	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353500	Foxe1	implicated_via_orthology	DOID:0050655	Bamforth-Lazarus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96204	Hoxd12	implicated_via_orthology	DOID:11836	clubfoot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:14040	autoimmune polyendocrine syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442420	Galm	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:2703	synovitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927204	Gosr2	implicated_via_orthology	DOID:0111449	progressive myoclonus epilepsy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0111160	camptodactyly-tall stature-scoliosis-hearing loss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338027	Gdf11	implicated_via_orthology	DOID:0070418	vertebral hypersegmentation and orofacial anomalies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97075	Mpi	implicated_via_orthology	DOID:0080554	congenital disorder of glycosylation Ib						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0050680	Boomerang dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	implicated_via_orthology	DOID:8670	eating disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:0110107	atrial heart septal defect 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070248	autosomal recessive Emery-Dreifuss muscular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95495	Ms4a2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444136	Mars2	implicated_via_orthology	DOID:0050942	spastic ataxia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891497	Jph3	implicated_via_orthology	DOID:0090104	Huntington's disease-like 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:0110497	autosomal recessive nonsyndromic deafness 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:11336	rhinoscleroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100870	Gcnt2	implicated_via_orthology	DOID:0110242	cataract 13 with adult i phenotype						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96231	Hspa1l	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96298	Hyal1	implicated_via_orthology	DOID:12798	mucopolysaccharidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0112379	muscular dystrophy-dystroglycanopathy type B4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135593	Hadha	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107953	Klc2	implicated_via_orthology	DOID:0060491	SPOAN syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:0111819	syndactyly type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:2860	hemoglobinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12859	choreatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:2862	glucosephosphate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96073	Hexa	implicated_via_orthology	DOID:3320	Tay-Sachs disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108088	Gab1	implicated_via_orthology	DOID:0110484	autosomal recessive nonsyndromic deafness 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	implicated_via_orthology	DOID:0111717	isolated cryptophthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919069	Kif23	implicated_via_orthology	DOID:0111399	congenital dyserythropoietic anemia type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95686	Gdf3	implicated_via_orthology	DOID:0060838	isolated microphthalmia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442071	Gprasp2	implicated_via_orthology	DOID:0111738	X-linked deafness 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921166	Ift57	implicated_via_orthology	DOID:4501	orofaciodigital syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704339	Gsta5	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333850	Mbd4	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861674	Gnasas1	implicated_via_orthology	DOID:0080222	pseudohypoparathyroidism type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:4253	melorheostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	implicated_via_orthology	DOID:0110200	Charcot-Marie-Tooth disease dominant intermediate D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929872	Mogs	implicated_via_orthology	DOID:0070254	congenital disorder of glycosylation type IIb						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	implicated_via_orthology	DOID:0060335	autosomal dominant sideroblastic anemia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859212	Irf7	implicated_via_orthology	DOID:0111969	immunodeficiency 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0060564	spinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96062	Hdc	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	implicated_via_orthology	DOID:0111056	platelet-type bleeding disorder 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95583	Fshr	implicated_via_orthology	DOID:0080493	ovarian dysgenesis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	implicated_via_orthology	DOID:0060573	von Willebrand's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97169	Msx2	implicated_via_orthology	DOID:0060285	parietal foramina						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:0110866	congenital stationary night blindness 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098226	Kif14	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	implicated_via_orthology	DOID:0070210	hereditary lymphedema IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619440	Mir96	implicated_via_orthology	DOID:0110576	autosomal dominant nonsyndromic deafness 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443132	Lrp12	implicated_via_orthology	DOID:0081382	amyotrophic lateral sclerosis type 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97051	Mdh1	implicated_via_orthology	DOID:0112222	developmental and epileptic encephalopathy 88						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:0110196	Charcot-Marie-Tooth disease type 4G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434102	Ftl1-ps2	implicated_via_orthology	DOID:0111256	hyperferritinemia-cataract syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:13481	thanatophoric dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	implicated_via_orthology	DOID:0110158	Charcot-Marie-Tooth disease type 2I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:0111982	immunodeficiency 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	implicated_via_orthology	DOID:0110128	Bardet-Biedl syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	implicated_via_orthology	DOID:0060603	isolated anhidrosis with normal sweat glands						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108476	Fzd3	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095413	Lfng	implicated_via_orthology	DOID:0112361	spondylocostal dysostosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96231	Hspa1l	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0050144	Kartagener syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:0070271	Lynch syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921627	Hsf2bp	implicated_via_orthology	DOID:0112278	primary ovarian insufficiency 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:0050465	Muir-Torre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	implicated_via_orthology	DOID:0110167	Charcot-Marie-Tooth disease axonal type 2K						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926158	Igsf3	implicated_via_orthology	DOID:13929	lacrimal duct obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387639	Fkbp14	implicated_via_orthology	DOID:0080735	Ehlers-Danlos syndrome kyphoscoliotic type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341803	Lipg	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	implicated_via_orthology	DOID:10587	Krabbe disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917685	Inf2	implicated_via_orthology	DOID:0110205	Charcot-Marie-Tooth disease dominant intermediate E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109189	Fgf14	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336155	Lss	implicated_via_orthology	DOID:0110267	cataract 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923400	Klhl15	implicated_via_orthology	DOID:0112020	non-syndromic X-linked intellectual disability 103						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918000	Kdsr	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	implicated_via_orthology	DOID:0081319	multiple synostoses syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	implicated_via_orthology	DOID:0110498	autosomal recessive nonsyndromic deafness 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10241	thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329021	Msh5	implicated_via_orthology	DOID:0080870	primary ovarian insufficiency 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96691	Krt17	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109602	Gphn	implicated_via_orthology	DOID:0111166	molybdenum cofactor deficiency type C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342540	Ikzf1	implicated_via_orthology	DOID:0081155	common variable immunodeficiency 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922428	Meiob	implicated_via_orthology	DOID:0070177	spermatogenic failure 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:11678	onchocerciasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95589	Ftl1	implicated_via_orthology	DOID:679	basal ganglia disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95590	Ftl2-ps	implicated_via_orthology	DOID:0110737	neurodegeneration with brain iron accumulation 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	implicated_via_orthology	DOID:0111384	inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444289	Glis3	implicated_via_orthology	DOID:0060638	neonatal diabetes mellitus with congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	implicated_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99456	Mc1r	implicated_via_orthology	DOID:0070096	oculocutaneous albinism type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:3390	palmoplantar keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:0111273	NARP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	implicated_via_orthology	DOID:0112148	Uruguay faciocardiomusculoskeletal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	implicated_via_orthology	DOID:6683	X-linked Aarskog syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:0050658	Bart-Pumphrey syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	implicated_via_orthology	DOID:0060691	platelet-type bleeding disorder 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9383	iridocyclitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340044	Lrp8	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:2320	obstructive lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434102	Ftl1-ps2	implicated_via_orthology	DOID:0110737	neurodegeneration with brain iron accumulation 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102502	mt-Co3	implicated_via_orthology	DOID:3687	MELAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95590	Ftl2-ps	implicated_via_orthology	DOID:0111256	hyperferritinemia-cataract syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105380	Mcm2	implicated_via_orthology	DOID:0110592	autosomal dominant nonsyndromic deafness 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95781	Gnb1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926212	Med12	implicated_via_orthology	DOID:591	phobic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108476	Fzd3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926790	Fzr1	implicated_via_orthology	DOID:0070378	developmental and epileptic encephalopathy 109						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96685	Krt10	implicated_via_orthology	DOID:0081359	epidermolytic hyperkeratosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	implicated_via_orthology	DOID:2277	gonadal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8483	retinal artery occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:12010	anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921772	Morc2a	implicated_via_orthology	DOID:0110181	Charcot-Marie-Tooth disease axonal type 2Z						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	implicated_via_orthology	DOID:0112313	brain small vessel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:9155	mucocutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070202	familial partial lipodystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914325	Magt1	implicated_via_orthology	DOID:0080319	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95590	Ftl2-ps	implicated_via_orthology	DOID:679	basal ganglia disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920177	Hepacam	implicated_via_orthology	DOID:0080317	megalencephalic leukoencephalopathy with subcortical cysts 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95614	Gabra2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109160	Mnx1	implicated_via_orthology	DOID:0111546	Currarino syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96024	Hbb-bh1	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346319	Hax1	implicated_via_orthology	DOID:0112133	severe congenital neutropenia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:37	skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927753	Inpp5e	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648807	Mcidas	implicated_via_orthology	DOID:0111855	primary ciliary dyskinesia 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104611	Mdfic	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	implicated_via_orthology	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13774	Addison's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	implicated_via_orthology	DOID:0111389	mucopolysaccharidosis Ih/s						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:0060872	isolated growth hormone deficiency type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660880	Gmppb	implicated_via_orthology	DOID:0112377	muscular dystrophy-dystroglycanopathy type B14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:0112223	developmental and epileptic encephalopathy 89						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	implicated_via_orthology	DOID:0112297	spondylometaphyseal dysplasia corner fracture type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447072	Kif26a	implicated_via_orthology	DOID:0090131	complex cortical dysplasia with other brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892970	Mal	implicated_via_orthology	DOID:10581	metachromatic leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96667	Kcnc1	implicated_via_orthology	DOID:0111447	progressive myoclonus epilepsy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:2860	hemoglobinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182585	Med17	implicated_via_orthology	DOID:0111262	infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104902	Gpc4	implicated_via_orthology	DOID:0111842	Keipert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202386	Gas8	implicated_via_orthology	DOID:0110619	primary ciliary dyskinesia 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891396	Kirrel1	implicated_via_orthology	DOID:0112266	nephrotic syndrome type 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861899	Htr3b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443132	Lrp12	implicated_via_orthology	DOID:0081297	oculopharyngodistal myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202401	Fgf17	implicated_via_orthology	DOID:0090082	hypogonadotropic hypogonadism 20 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	implicated_via_orthology	DOID:0080509	Cornelia de Lange syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:13714	anodontia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	implicated_via_orthology	DOID:14693	Clouston syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	implicated_via_orthology	DOID:0111787	frontometaphyseal dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387006	Gipc3	implicated_via_orthology	DOID:0110470	autosomal recessive nonsyndromic deafness 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	implicated_via_orthology	DOID:0090032	Silverman-Handmaker type dyssegmental dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:0081078	ectodermal dysplasia and immunodeficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444508	Fitm2	implicated_via_orthology	DOID:0081273	Siddiqi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	implicated_via_orthology	DOID:3323	Sandhoff disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:10316	pneumoconiosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96274	Htr1b	implicated_via_orthology	DOID:12995	conduct disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0081371	lacrimoauriculodentodigital syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351648	Magel2	implicated_via_orthology	DOID:0111715	Schaaf-Yang syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:350	mastocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:1206	Rett syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99913	Lamc2	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107852	Gp1bb	implicated_via_orthology	DOID:2217	Bernard-Soulier syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	implicated_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101789	Lig1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891421	Mesd	implicated_via_orthology	DOID:0111849	osteogenesis imperfecta type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861746	Lmbr1	implicated_via_orthology	DOID:0050603	acheiropody						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444506	Mbtps2	implicated_via_orthology	DOID:0080754	X-linked keratosis follicularis spinulosa decalvans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102497	mt-Nd4l	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384909	Micu1	implicated_via_orthology	DOID:0111335	myopathy with extrapyramidal signs						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95617	Gabra5	implicated_via_orthology	DOID:0112215	developmental and epileptic encephalopathy 79						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95583	Fshr	implicated_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:4372	intracranial embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443337	Fscn2	implicated_via_orthology	DOID:0110406	retinitis pigmentosa 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920177	Hepacam	implicated_via_orthology	DOID:0080318	megalencephalic leukoencephalopathy with subcortical cysts 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	implicated_via_orthology	DOID:0081235	autosomal recessive intellectual developmental disorder 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95863	Gsta2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342542	Ikzf3	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:0080770	autosomal dominant  beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:11336	rhinoscleroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858204	Map3k14	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95589	Ftl1	implicated_via_orthology	DOID:0110737	neurodegeneration with brain iron accumulation 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444664	Galnt12	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:0080770	autosomal dominant  beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:0112010	pituitary adenoma 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:0080095	myofibrillar myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442704	Frrs1l	implicated_via_orthology	DOID:0080435	developmental and epileptic encephalopathy 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:0060874	isolated growth hormone deficiency type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:4959	epidermolysis bullosa dystrophica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928141	Mrps14	implicated_via_orthology	DOID:0111466	combined oxidative phosphorylation deficiency 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444169	Lmod3	implicated_via_orthology	DOID:0110931	nemaline myopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	implicated_via_orthology	DOID:14021	Tietze's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96567	Impdh1	implicated_via_orthology	DOID:0110388	retinitis pigmentosa 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98505	Hnf1b	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0060849	osteoporosis-pseudoglioma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924825	Kmt2e	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0110965	brachydactyly type A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4906	small intestine adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:0080770	autosomal dominant  beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100496	Fmo3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0060703	Muenke Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	implicated_via_orthology	DOID:0060484	EAST syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:1884	viral hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13258	typhoid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443538	Msrb3	implicated_via_orthology	DOID:0110523	autosomal recessive nonsyndromic deafness 74						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	implicated_via_orthology	DOID:0050634	alopecia universalis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922672	Mettl5	implicated_via_orthology	DOID:0080765	autosomal recessive intellectual developmental disorder 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685814	Hpse2	implicated_via_orthology	DOID:0050816	urofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:4166	syphilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:4166	syphilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914152	Mtap	implicated_via_orthology	DOID:0080664	diaphyseal medullary stenosis with malignant fibrous histiocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96160	Hmga1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298398	Mcm7	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346863	Mapk10	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0111817	syndactyly type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100537	Mid1	implicated_via_orthology	DOID:0080697	Opitz GBBB syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107227	Gtf2h5	implicated_via_orthology	DOID:0111871	photosensitive trichothiodystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95589	Ftl1	implicated_via_orthology	DOID:0111256	hyperferritinemia-cataract syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891259	Lrat	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	implicated_via_orthology	DOID:0060696	hyperekplexia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95789	Gnrh1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4906	small intestine adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	implicated_via_orthology	DOID:0110639	congenital muscular dystrophy due to integrin alpha-7 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:12835	quadriplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444085	Glyctk	implicated_via_orthology	DOID:0111626	D-glyceric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339962	Ftcd	implicated_via_orthology	DOID:0111679	glutamate formiminotransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153839	Hps3	implicated_via_orthology	DOID:0060541	Hermansky-Pudlak syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109380	Il10rb	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891384	Mov10l1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333850	Mbd4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95588	Fth1	implicated_via_orthology	DOID:0111031	hemochromatosis type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927753	Inpp5e	implicated_via_orthology	DOID:0110980	Joubert syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	implicated_via_orthology	DOID:0110154	Charcot-Marie-Tooth disease type 2A1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923488	Grhpr	implicated_via_orthology	DOID:0111671	primary hyperoxaluria type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347470	Foxf1	implicated_via_orthology	DOID:13042	persistent fetal circulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859211	Irf6	implicated_via_orthology	DOID:0080593	orofacial cleft 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:10933	obsessive-compulsive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921496	Gale	implicated_via_orthology	DOID:0111458	galactose epimerase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:3390	palmoplantar keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95715	Gja4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354959	Hs6st2	implicated_via_orthology	DOID:0111843	Paganini-Miozzo syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	implicated_via_orthology	DOID:13399	color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95789	Gnrh1	implicated_via_orthology	DOID:0090072	hypogonadotropic hypogonadism 12 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:12305	Bloch-Sulzberger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104888	Fdps	implicated_via_orthology	DOID:3805	porokeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:2860	hemoglobinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685211	Gpr101	implicated_via_orthology	DOID:0112007	growth hormone secreting pituitary adenoma 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:0111578	Gillespie syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	implicated_via_orthology	DOID:13271	cutaneous porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3781032	Kcnj13	implicated_via_orthology	DOID:0111570	snowflake vitreoretinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341857	Mad1l1	implicated_via_orthology	DOID:0080688	mosaic variegated aneuploidy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0080125	mitochondrial DNA depletion syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95582	Fshb	implicated_via_orthology	DOID:13938	amenorrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:14116	multiple symmetric lipomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1586	rheumatic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:0080770	autosomal dominant  beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:0060873	isolated growth hormone deficiency type IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333850	Mbd4	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96170	Hoxa1	implicated_via_orthology	DOID:0050682	Athabaskan brainstem dysgenesis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:8566	herpes simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	implicated_via_orthology	DOID:0081009	Bardet-Biedl syndrome 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:0110423	dilated cardiomyopathy 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:11656	cicatricial pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343460	Gnpat	implicated_via_orthology	DOID:0110852	rhizomelic chondrodysplasia punctata type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4441431	Mir2861	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107658	Ifnar1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345146	Grk1	implicated_via_orthology	DOID:8499	night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685697	Grxcr2	implicated_via_orthology	DOID:0110462	autosomal recessive nonsyndromic deafness 101						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928479	Hspb3	implicated_via_orthology	DOID:0111209	autosomal dominant distal hereditary motor neuronopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109155	Kcnab1	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135679	Hes7	implicated_via_orthology	DOID:0112364	spondylocostal dysostosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	implicated_via_orthology	DOID:1391	Norum disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859179	Irf3	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685177	Megf10	implicated_via_orthology	DOID:0081345	congenital myopathy 10B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	implicated_via_orthology	DOID:0060837	isolated microphthalmia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354953	Magi2	implicated_via_orthology	DOID:0080271	nephrotic syndrome type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1340	pure red-cell aplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924217	2700049A03Rik	implicated_via_orthology	DOID:0110992	Joubert syndrome 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96687	Krt12	implicated_via_orthology	DOID:0080670	Meesmann corneal dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:1587	thrombocytopenia due to platelet alloimmunization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858746	Kat6b	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:0111505	palmoplantar keratoderma-deafness syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0110959	Gaucher's disease type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12859	choreatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	implicated_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:3390	palmoplantar keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	implicated_via_orthology	DOID:0111057	platelet-type bleeding disorder 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:2860	hemoglobinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96701	Krt4	implicated_via_orthology	DOID:0081287	white sponge nevus 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:11165	common wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96907	Marcks	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138271	Gorab	implicated_via_orthology	DOID:0111266	geroderma osteodysplasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136381	Hadhb	implicated_via_orthology	DOID:0111277	mitochondrial trifunctional protein deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95593	Fuca1	implicated_via_orthology	DOID:14500	fucosidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	implicated_via_orthology	DOID:0110363	retinitis pigmentosa 71						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:11656	cicatricial pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098243	Ifnar2	implicated_via_orthology	DOID:0111994	immunodeficiency 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888519	Lmx1a	implicated_via_orthology	DOID:0110591	autosomal dominant nonsyndromic deafness 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202398	Kera	implicated_via_orthology	DOID:11342	arcus senilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:0080251	erythrokeratodermia variabilis et progressiva 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:11836	clubfoot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107657	Ifnb1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:3181	oligodendroglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0081289	Antley-Bixler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858746	Kat6b	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921662	Gle1	implicated_via_orthology	DOID:0060559	lethal congenital contracture syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926884	Huwe1	implicated_via_orthology	DOID:0060811	syndromic X-linked intellectual disability Turner type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96690	Krt16	implicated_via_orthology	DOID:0111709	focal nonepidermolytic palmoplantar keratoderma 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96567	Impdh1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:0111817	syndactyly type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	implicated_via_orthology	DOID:0080450	developmental and epileptic encephalopathy 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384968	L2hgdh	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434102	Ftl1-ps2	implicated_via_orthology	DOID:679	basal ganglia disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:2320	obstructive lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96698	Krt1	implicated_via_orthology	DOID:0081358	epidermolytic hyperkeratosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:0111273	NARP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676665	Lrrc7	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916413	Mrpl44	implicated_via_orthology	DOID:0111469	combined oxidative phosphorylation deficiency 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096325	Mesp2	implicated_via_orthology	DOID:0112362	spondylocostal dysostosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176380	Mlph	implicated_via_orthology	DOID:0060834	Griscelli syndrome type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95781	Gnb1	implicated_via_orthology	DOID:0070072	autosomal dominant intellectual developmental disorder 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923661	Ift43	implicated_via_orthology	DOID:0080293	short-rib thoracic dysplasia 18 with polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:0060371	Parkinson's disease 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13258	typhoid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194899	Inpp5k	implicated_via_orthology	DOID:0080197	congenital muscular dystrophy with cataracts and intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652847	Lrrc8a	implicated_via_orthology	DOID:2583	agammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:13945	CADASIL						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95623	Gabrg2	implicated_via_orthology	DOID:0112210	developmental and epileptic encephalopathy 74						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346022	Mab21l2	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384910	Hkdc1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3826440	Gsta13	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107587	Irf9	implicated_via_orthology	DOID:0111978	immunodeficiency 65						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:0081384	ataxia-telangiectasia-like disorder-1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182543	Grhl2	implicated_via_orthology	DOID:0110557	autosomal dominant nonsyndromic deafness 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:0110031	hemoglobin H disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0112250	Gaucher's disease type IIIC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:0110031	hemoglobin H disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445185	Klhl3	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353569	Foxe3	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347469	Foxl1	implicated_via_orthology	DOID:0060928	otosclerosis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309998	Marco	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99846	Gdi1	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	implicated_via_orthology	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685385	Kalrn	implicated_via_orthology	DOID:12720	cerebral atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923733	Lmf1	implicated_via_orthology	DOID:0111422	familial lipase maturation factor 1 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104576	Lct	implicated_via_orthology	DOID:0111646	congenital lactase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928485	Mlycd	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926803	Kcnq4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353455	Mlh3	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097667	Ganab	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684960	Kiz	implicated_via_orthology	DOID:0110410	retinitis pigmentosa 69						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:2366	West Nile fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:0081042	T-cell prolymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153060	Gjc2	implicated_via_orthology	DOID:0110796	hereditary spastic paraplegia 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109519	Msh3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0080923	bilateral parasagittal parieto-occipital polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	implicated_via_orthology	DOID:8566	herpes simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96023	Hbb-bh0	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99913	Lamc2	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916520	Gins1	implicated_via_orthology	DOID:0111993	immunodeficiency 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95568	Folr1	implicated_via_orthology	DOID:0050719	cerebral folate receptor alpha deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384968	L2hgdh	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347476	Foxa2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96550	Il2rb	implicated_via_orthology	DOID:0111997	immunodeficiency 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111765	X-linked cardiac valvular dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919666	Lrpprc	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443010	Lman2l	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	implicated_via_orthology	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859268	Krt85	implicated_via_orthology	DOID:0111658	ectodermal dysplasia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584508	Kcnh5	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933382	Ifitm2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:0050465	Muir-Torre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	implicated_via_orthology	DOID:0111681	glutamate-cysteine ligase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136405	Glce	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	implicated_via_orthology	DOID:0060025	immunoglobulin alpha deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95554	Fli1	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925288	Mccc2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96027	Hbb-y	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96539	Il12a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:12960	acrocephalosyndactylia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	implicated_via_orthology	DOID:0081214	autosomal recessive intellectual developmental disorder 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915464	Gsto2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861379	Klk4	implicated_via_orthology	DOID:0110057	amelogenesis imperfecta type 2A1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	implicated_via_orthology	DOID:0060248	Simpson-Golabi-Behmel syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:8791	breast carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104555	Mafb	implicated_via_orthology	DOID:0111534	multicentric carpotarsal osteolysis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915267	Mrm2	implicated_via_orthology	DOID:0070448	mitochondrial DNA depletion syndrome 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384968	L2hgdh	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:0080770	autosomal dominant  beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0080788	proximal symphalangism 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95582	Fshb	implicated_via_orthology	DOID:0090088	hypogonadotropic hypogonadism 24 without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	implicated_via_orthology	DOID:0080429	developmental and epileptic encephalopathy 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:9164	achalasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4906	small intestine adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95653	Gapdhs	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321394	Gdf2	implicated_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3044955	Impg2	implicated_via_orthology	DOID:0050661	vitelliform macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	implicated_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340044	Lrp8	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0050440	familial partial lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137204	Mrpl3	implicated_via_orthology	DOID:0111472	combined oxidative phosphorylation deficiency 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341721	Kcnh1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919207	Ints11	implicated_via_orthology	DOID:0081387	neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180197	Lgi4	implicated_via_orthology	DOID:0080978	arthrogryposis multiplex congenita-1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:5577	gastrinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	implicated_via_orthology	DOID:0111390	mucopolysaccharidosis Ih						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96788	Lifr	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101761	Hmga2	implicated_via_orthology	DOID:3315	lipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913391	Ifitm3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197515	Irx1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354951	Gne	implicated_via_orthology	DOID:3659	sialuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444484	Manea	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	implicated_via_orthology	DOID:0080399	orofacial cleft 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	implicated_via_orthology	DOID:0060222	Scheie syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99953	Gja8	implicated_via_orthology	DOID:0110231	cataract 1 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	implicated_via_orthology	DOID:0050864	non-arteritic anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0111162	epidermal nevus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10241	thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96666	Kcnb1	implicated_via_orthology	DOID:0080461	developmental and epileptic encephalopathy 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95710	Ghrhr	implicated_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891123	Kcne2	implicated_via_orthology	DOID:0110648	long QT syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347473	Foxd3	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333743	Mpeg1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:0060496	respiratory allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:0110883	inflammatory bowel disease 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99909	Lama3	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95586	Fst	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96010	Hal	implicated_via_orthology	DOID:0060168	histidinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340044	Lrp8	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159336	Il17rc	implicated_via_orthology	DOID:2058	chronic mucocutaneous candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442554	Itpkc	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:2219	Glanzmann's thrombasthenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859648	Ftsj1	implicated_via_orthology	DOID:0112034	non-syndromic X-linked intellectual disability 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306778	Map1b	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96161	Hmga1b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914944	Ift74	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	implicated_via_orthology	DOID:0111955	immunodeficiency 27A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:252	alcoholic psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136405	Glce	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0080041	hypochondroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99926	mt-Atp8	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894646	Hlcs	implicated_via_orthology	DOID:859	holocarboxylase synthetase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336159	Minpp1	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918770	Grap	implicated_via_orthology	DOID:0111642	autosomal recessive nonsyndromic deafness 114						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102496	mt-Nd5	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104555	Mafb	implicated_via_orthology	DOID:12557	Duane retraction syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95614	Gabra2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159682	Havcr2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926053	Fbxo43	implicated_via_orthology	DOID:0112353	spermatogenic failure 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346318	Klf6	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177742	Hps4	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95748	Glra2	implicated_via_orthology	DOID:0070422	syndromic X-linked intellectual disability Pilorge type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:4977	lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108087	Hars1	implicated_via_orthology	DOID:0110842	Usher syndrome type 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860137	Gp9	implicated_via_orthology	DOID:2217	Bernard-Soulier syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915240	Mpc1	implicated_via_orthology	DOID:0080363	mitochondrial pyruvate carrier deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	implicated_via_orthology	DOID:0111110	maturity-onset diabetes of the young type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	implicated_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096353	Khk	implicated_via_orthology	DOID:0111680	essential fructosuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	implicated_via_orthology	DOID:12804	mucopolysaccharidosis IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96916	Maob	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528396	Iqsec2	implicated_via_orthology	DOID:0112038	non-syndromic X-linked intellectual disability 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861901	Mast1	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	implicated_via_orthology	DOID:0110781	hereditary spastic paraplegia 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0111161	Crouzon syndrome-acanthosis nigricans syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:0080589	Klippel-Feil syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0111726	geleophysic dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629975	Krt74	implicated_via_orthology	DOID:0111660	ectodermal dysplasia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353466	Mmp20	implicated_via_orthology	DOID:0110060	amelogenesis imperfecta hypomaturation type 2A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891123	Kcne2	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	implicated_via_orthology	DOID:0080380	nephrotic syndrome type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345146	Grk1	implicated_via_orthology	DOID:0110713	Oguchi disease-2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914609	Loxhd1	implicated_via_orthology	DOID:0110525	autosomal recessive nonsyndromic deafness 77						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95730	Galk1	implicated_via_orthology	DOID:14695	galactokinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	implicated_via_orthology	DOID:0112310	central precocious puberty 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3690448	Krt83	implicated_via_orthology	DOID:0080251	erythrokeratodermia variabilis et progressiva 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100870	Gcnt2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321395	Ltbp4	implicated_via_orthology	DOID:0070139	autosomal recessive cutis laxa type IC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1019	osteomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618739	Mir196a-2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0081318	multiple synostoses syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95852	Gss	implicated_via_orthology	DOID:0112252	glutathione synthetase deficiency of erythrocytes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96921	Max	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927235	Mbtps1	implicated_via_orthology	DOID:0112283	spondyloepiphyseal dysplasia Kondo-Fu type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860266	Pfpl	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687319	Il1rapl1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	implicated_via_orthology	DOID:0111059	Bernard-Soulier syndrome type A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098221	Gamt	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:0060580	Noonan syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	implicated_via_orthology	DOID:0080687	reducing body myopathy 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96965	Mertk	implicated_via_orthology	DOID:0110367	retinitis pigmentosa 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098231	Kif11	implicated_via_orthology	DOID:0060349	microcephaly with or without chorioretinopathy, lymphedema, or mental retardation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95615	Gabra3	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891704	Hbs1l	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934604	Lias	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	implicated_via_orthology	DOID:0111545	familial male-limited precocious puberty						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:0070036	autosomal dominant intellectual developmental disorder 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861899	Htr3b	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96909	Maf	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96023	Hbb-bh0	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108511	Mobp	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0090083	hypogonadotropic hypogonadism 2 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922984	Mff	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	implicated_via_orthology	DOID:0060852	Pierson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443337	Fscn2	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104698	Lim2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918817	Mcm9	implicated_via_orthology	DOID:0080496	ovarian dysgenesis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:2219	Glanzmann's thrombasthenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88175	Manba	implicated_via_orthology	DOID:3633	beta-mannosidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	implicated_via_orthology	DOID:0110660	congenital myasthenic syndrome 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136381	Hadhb	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:57	aortic valve insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0060025	immunoglobulin alpha deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105382	Lama5	implicated_via_orthology	DOID:2590	familial nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1340	pure red-cell aplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921164	Irak3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913808	Lars1	implicated_via_orthology	DOID:0080717	infantile liver failure syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102498	mt-Nd4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95811	Gria4	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913492	Mrps16	implicated_via_orthology	DOID:0111483	combined oxidative phosphorylation deficiency 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	implicated_via_orthology	DOID:0081144	common variable immunodeficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4906	small intestine adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97054	Mov10	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	implicated_via_orthology	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0080159	Cryptococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:10887	lepromatous leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	implicated_via_orthology	DOID:0111459	classic galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914944	Ift74	implicated_via_orthology	DOID:0112352	spermatogenic failure 58						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3609239	Mrap2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385368	Fras1	implicated_via_orthology	DOID:0111405	Fraser syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685267	Lrit3	implicated_via_orthology	DOID:0110864	congenital stationary night blindness 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102497	mt-Nd4l	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95823	Grin2d	implicated_via_orthology	DOID:0080456	developmental and epileptic encephalopathy 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445214	Lrif1	implicated_via_orthology	DOID:0060917	facioscapulohumeral muscular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	implicated_via_orthology	DOID:0110476	autosomal recessive nonsyndromic deafness 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0111532	osteoglophonic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99456	Mc1r	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:4959	epidermolysis bullosa dystrophica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:0070220	familial hyperinsulinemic hypoglycemia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:7959	duodenal gastrinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96217	Hprt1	implicated_via_orthology	DOID:0112127	HRPT-related hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444557	Kmt5b	implicated_via_orthology	DOID:0080232	autosomal dominant intellectual developmental disorder 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333811	Mbd1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:77	gastrointestinal system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861305	Fntb	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449311	Gemin5	implicated_via_orthology	DOID:0070443	neurodevelopmental disorder with cerebellar atrophy and motor dysfunction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919570	Kifbp	implicated_via_orthology	DOID:0060481	Goldberg-Shprintzen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9663	aphthous stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96024	Hbb-bh1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	implicated_via_orthology	DOID:0111314	idiopathic generalized epilepsy 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341155	Gldc	implicated_via_orthology	DOID:9268	glycine encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	implicated_via_orthology	DOID:13042	persistent fetal circulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107177	Hsd17b3	implicated_via_orthology	DOID:1923	disorder of sexual development						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96669	Kcnc3	implicated_via_orthology	DOID:0050963	spinocerebellar ataxia type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070370	restrictive dermopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1586	rheumatic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098232	Kif12	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195267	Ilk	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:0050965	spinocerebellar ataxia type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934754	Kars1	implicated_via_orthology	DOID:0110204	Charcot-Marie-Tooth disease recessive intermediate B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	implicated_via_orthology	DOID:0050744	anaplastic large cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923969	Kansl1	implicated_via_orthology	DOID:0050880	Koolen de Vries syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	implicated_via_orthology	DOID:0080662	atrial standstill 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928743	Kcnd3	implicated_via_orthology	DOID:0110226	Brugada syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96558	Il5ra	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:2862	glucosephosphate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10241	thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95722	Gjb4	implicated_via_orthology	DOID:0050467	erythrokeratodermia variabilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88151	Glb1	implicated_via_orthology	DOID:0080501	GM1 gangliosidosis type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095417	Gsta1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0080299	partial lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915703	Gpihbp1	implicated_via_orthology	DOID:0111420	familial GPIHBP1 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146636	Hrg	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861746	Lmbr1	implicated_via_orthology	DOID:0111350	Laurin-Sandrow syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:9733	renal tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	implicated_via_orthology	DOID:13714	anodontia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:2366	West Nile fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914609	Loxhd1	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070247	autosomal dominant Emery-Dreifuss muscular dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:0111767	X-linked thrombocytopenia with beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921732	Ifitm7	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923661	Ift43	implicated_via_orthology	DOID:0080805	cranioectodermal dysplasia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685054	Gpr161	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107339	Gfm1	implicated_via_orthology	DOID:0111474	combined oxidative phosphorylation deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96023	Hbb-bh0	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442114	Itga11	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104755	Kcnj5	implicated_via_orthology	DOID:0110654	long QT syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99778	Gpd2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:0080458	developmental and epileptic encephalopathy 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891990	Gykl1	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96436	Igfbp1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96027	Hbb-y	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12029	sympathetic ophthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96024	Hbb-bh1	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:0111102	maturity-onset diabetes of the young type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041174	Iba57	implicated_via_orthology	DOID:0080135	multiple mitochondrial dysfunctions syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333850	Mbd4	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	implicated_via_orthology	DOID:9258	Waardenburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446166	Marveld2	implicated_via_orthology	DOID:0110506	autosomal recessive nonsyndromic deafness 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	implicated_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347004	Mapkbp1	implicated_via_orthology	DOID:0111127	nephronophthisis 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13774	Addison's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	implicated_via_orthology	DOID:2752	glycogen storage disease II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12029	sympathetic ophthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261813	Mn1	implicated_via_orthology	DOID:4586	familial meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:0080551	Naxos disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928268	Ireb2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97050	Mdh2	implicated_via_orthology	DOID:0080433	developmental and epileptic encephalopathy 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:0080857	primary ovarian insufficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684954	Man1b1	implicated_via_orthology	DOID:0081097	Rafiq syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	implicated_via_orthology	DOID:0111956	immunodeficiency 27B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045293	Morc2b	implicated_via_orthology	DOID:0110181	Charcot-Marie-Tooth disease axonal type 2Z						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915671	Lmbrd1	implicated_via_orthology	DOID:0050717	methylmalonic aciduria and homocystinuria type cblF						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:0110135	Bardet-Biedl syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108520	Fzd4	implicated_via_orthology	DOID:0111412	exudative vitreoretinopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:0070442	paroxysmal nonkinesigenic dyskinesia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384568	Kank2	implicated_via_orthology	DOID:0080272	nephrotic syndrome type 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336200	Hpca	implicated_via_orthology	DOID:0090038	torsion dystonia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104860	Fxr1	implicated_via_orthology	DOID:0081344	congenital myopathy 9B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921778	Mgme1	implicated_via_orthology	DOID:0080129	mitochondrial DNA depletion syndrome 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:2860	hemoglobinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96690	Krt16	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098260	Kif1c	implicated_via_orthology	DOID:0050941	spastic ataxia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202398	Kera	implicated_via_orthology	DOID:0060287	cornea plana						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95614	Gabra2	implicated_via_orthology	DOID:0112214	developmental and epileptic encephalopathy 78						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	implicated_via_orthology	DOID:0080751	keratosis pilaris atrophicans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106271	Mapre2	implicated_via_orthology	DOID:0112243	congenital symmetric circumferential skin creases 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:12287	Crimean-Congo hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921392	Lonp1	implicated_via_orthology	DOID:0111274	CODAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	implicated_via_orthology	DOID:0050433	fatal familial insomnia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10241	thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	implicated_via_orthology	DOID:0070217	familial hyperinsulinemic hypoglycemia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	implicated_via_orthology	DOID:0070387	developmental and epileptic encephalopathy 101						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146636	Hrg	implicated_via_orthology	DOID:0111903	thrombophilia due to HRG deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:0110114	atrial heart septal defect 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:0111279	psoriasis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333787	Inppl1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:525	central nervous system vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442773	Marchf6	implicated_via_orthology	DOID:0111695	familial adult myoclonic epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147790	Fermt3	implicated_via_orthology	DOID:0110910	leukocyte adhesion deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106594	Gk	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860077	Msh4	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306778	Map1b	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:401	multidrug-resistant tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99560	Hoxc13	implicated_via_orthology	DOID:0111656	ectodermal dysplasia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916052	Mypn	implicated_via_orthology	DOID:0110933	nemaline myopathy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	implicated_via_orthology	DOID:14264	benign neonatal seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:4586	familial meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106923	Tll1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915084	Idh3a	implicated_via_orthology	DOID:0112147	retinitis pigmentosa 90						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098219	Hmgb3	implicated_via_orthology	DOID:0111811	syndromic microphthalmia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:2272	vulvovaginal candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3826440	Gsta13	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298407	Tspan7	implicated_via_orthology	DOID:0112024	non-syndromic X-linked intellectual disability 58						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201412	Rdh5	implicated_via_orthology	DOID:11105	fundus albipunctatus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:811	lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654325	Gba2	implicated_via_orthology	DOID:0110798	hereditary spastic paraplegia 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96078	Hgd	implicated_via_orthology	DOID:9270	alkaptonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:4378	peanut allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0111183	familial hemiplegic migraine 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445027	Malt1	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	implicated_via_orthology	DOID:0110910	leukocyte adhesion deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104815	Ier2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448526	Gmps	implicated_via_orthology	DOID:0081082	acute myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141135	Hscb	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0050168	autoimmune polyendocrine syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342270	Large1	implicated_via_orthology	DOID:0111242	congenital muscular dystrophy-dystroglycanopathy type A6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109497	Gata5	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:0110635	muscular dystrophy-dystroglycanopathy type B5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347344	Gla	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103170	Gfi1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928858	Krt81	implicated_via_orthology	DOID:421	hair disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:0070481	schwannomatosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96698	Krt1	implicated_via_orthology	DOID:4603	epidermolytic hyperkeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	implicated_via_orthology	DOID:0060021	DNA ligase IV deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96540	Il12b	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704359	Pam16l	implicated_via_orthology	DOID:0112304	spondylometaphyseal dysplasia Megarbane-Dagher-Melike type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	implicated_via_orthology	DOID:6612	leukocyte adhesion deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:0110031	hemoglobin H disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0060589	Yunis-Varon syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:11695	portal vein thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96685	Krt10	implicated_via_orthology	DOID:4603	epidermolytic hyperkeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924627	Kcnt1	implicated_via_orthology	DOID:0080439	developmental and epileptic encephalopathy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:2339	Crouzon syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0110957	Gaucher's disease type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95530	Fh1	implicated_via_orthology	DOID:0111261	fumarase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343489	Mpdz	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95778	Gnat1	implicated_via_orthology	DOID:8499	night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927468	Samhd1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108011	Nobox	implicated_via_orthology	DOID:0080862	primary ovarian insufficiency 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138281	Lbr	implicated_via_orthology	DOID:0111588	Greenberg dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101939	Hmgcs2	implicated_via_orthology	DOID:0081168	HMG-CoA synthase 2 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179326	Oxr1	implicated_via_orthology	DOID:0070339	cerebellar hyplasia/atrophy, epilepsy, and global developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97555	Pgk1	implicated_via_orthology	DOID:0111933	phosphoglycerate kinase 1 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0040091	autoimmune pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	implicated_via_orthology	DOID:9521	Laron syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95715	Gja4	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434102	Ftl1-ps2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:4441	dysgerminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315200	M1ap	implicated_via_orthology	DOID:0112176	spermatogenic failure 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:0060871	autosomal dominant keratitis-ichthyosis-deafness syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96622	Itpa	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1098	fetal erythroblastosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685177	Megf10	implicated_via_orthology	DOID:0111333	early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:11512	Budd-Chiari syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:2236	congenital afibrinogenemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921742	Kbtbd13	implicated_via_orthology	DOID:0110935	nemaline myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104709	Wbp2	implicated_via_orthology	DOID:0080262	autosomal recessive nonsyndromic deafness 107						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442174	Micos13	implicated_via_orthology	DOID:0111499	combined oxidative phosphorylation deficiency 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95818	Grik5	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159682	Havcr2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97887	Rdx	implicated_via_orthology	DOID:0110482	autosomal recessive nonsyndromic deafness 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099443	Nnmt	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3521816	Kcnk9	implicated_via_orthology	DOID:0050675	Birk-Barel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028579	Rasgrp3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355303	Galns	implicated_via_orthology	DOID:0111391	mucopolysaccharidosis IVA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434255	Gapdh-ps15	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:161	keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442535	Slc6a17	implicated_via_orthology	DOID:0081212	autosomal recessive intellectual developmental disorder 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3027157	Kng2	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861607	Gbf1	implicated_via_orthology	DOID:0110202	Charcot-Marie-Tooth disease dominant intermediate A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914342	Gatm	implicated_via_orthology	DOID:0080757	Fanconi renotubular syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102498	mt-Nd4	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	implicated_via_orthology	DOID:0111509	lymphedema-distichiasis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96282	Htr3a	implicated_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	implicated_via_orthology	DOID:12799	mucopolysaccharidosis II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670178	Med13l	implicated_via_orthology	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:0110292	autosomal recessive limb-girdle muscular dystrophy type 2O						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96621	Itk	implicated_via_orthology	DOID:0060707	lymphoproliferative syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:0080179	haemophilus meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933158	Impa1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:3204	schwannomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277956	Pycr2	implicated_via_orthology	DOID:0060788	hypomyelinating leukodystrophy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97489	Pax5	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685385	Kalrn	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95742	Glo1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:10871	age related macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:4927	Klatskin's tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102495	mt-Nd6	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:76	stomach disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	implicated_via_orthology	DOID:0110152	Charcot-Marie-Tooth disease type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676825	Mir140	implicated_via_orthology	DOID:0112288	spondyloepiphyseal dysplasia Nishimura type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384418	Rgs9bp	implicated_via_orthology	DOID:0070364	bradyopsia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0060496	respiratory allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	implicated_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104995	Gclm	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921173	Tmco1	implicated_via_orthology	DOID:0081124	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351343	Grm6	implicated_via_orthology	DOID:0110865	congenital stationary night blindness 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916835	Hjv	implicated_via_orthology	DOID:0111027	hemochromatosis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345622	Slc35a1	implicated_via_orthology	DOID:0070258	congenital disorder of glycosylation type IIf						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98505	Hnf1b	implicated_via_orthology	DOID:26	pancreas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196297	Hgsnat	implicated_via_orthology	DOID:0110389	retinitis pigmentosa 73						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:0111099	maturity-onset diabetes of the young type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:2383	neonatal jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918269	Kctd1	implicated_via_orthology	DOID:0111550	scalp-ear-nipple syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	implicated_via_orthology	DOID:0110163	Charcot-Marie-Tooth disease axonal type 2F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353569	Foxe3	implicated_via_orthology	DOID:0060648	anterior segment dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95616	Gabra4	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:0060473	Kabuki syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105123	Gucy2e	implicated_via_orthology	DOID:980	choroidal sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	implicated_via_orthology	DOID:3890	acute intermittent porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141879	Hsd3b7	implicated_via_orthology	DOID:0111071	congenital bile acid synthesis defect 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100496	Fmo3	implicated_via_orthology	DOID:0080361	trimethylaminuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346040	Mpdu1	implicated_via_orthology	DOID:0080558	congenital disorder of glycosylation If						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103199	Mcm4	implicated_via_orthology	DOID:0111967	immunodeficiency 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645678	Flg2	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95813	Grid2	implicated_via_orthology	DOID:0080042	autosomal recessive spinocerebellar ataxia 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923714	Knl1	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704339	Gsta5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289257	Gpd1l	implicated_via_orthology	DOID:0110219	Brugada syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106096	Loxl1	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097692	Opn1mw	implicated_via_orthology	DOID:0050679	blue cone monochromacy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684789	Lrsam1	implicated_via_orthology	DOID:0110169	Charcot-Marie-Tooth disease axonal type 2P						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	implicated_via_orthology	DOID:0070206	familial partial lipodystrophy type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	implicated_via_orthology	DOID:0110201	Charcot-Marie-Tooth disease recessive intermediate A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:13628	favism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:0111260	phosphoribosylpyrophosphate synthetase superactivity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340044	Lrp8	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96921	Max	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97243	Mx1	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96928	Mc2r	implicated_via_orthology	DOID:0050562	West syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101925	Krt13	implicated_via_orthology	DOID:0081288	white sponge nevus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2669037	Tmc8	implicated_via_orthology	DOID:13777	epidermodysplasia verruciformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104769	Fkbp10	implicated_via_orthology	DOID:0110351	osteogenesis imperfecta type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926212	Med12	implicated_via_orthology	DOID:14711	FG syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106096	Loxl1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:4428	dyslexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933391	Maged2	implicated_via_orthology	DOID:0110147	Bartter disease type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	implicated_via_orthology	DOID:0110895	inflammatory bowel disease 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	implicated_via_orthology	DOID:3209	junctional epidermolysis bullosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334203	Kcnmb1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96561	Il7	implicated_via_orthology	DOID:13777	epidermodysplasia verruciformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036243	Nlrc4	implicated_via_orthology	DOID:0090065	familial cold autoinflammatory syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	implicated_via_orthology	DOID:0080836	growth hormone insensitivity syndrome with immune dysregulation 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	implicated_via_orthology	DOID:13270	erythropoietic protoporphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:14705	Pfeiffer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0110443	dilated cardiomyopathy 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	implicated_via_orthology	DOID:0090144	Donnai-Barrow syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106209	Hells	implicated_via_orthology	DOID:0090011	immunodeficiency-centromeric instability-facial anomalies syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95714	Gja3	implicated_via_orthology	DOID:0110253	cataract 14 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	implicated_via_orthology	DOID:0112124	X-linked retinitis pigmentosa and sinorespiratory infections						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	implicated_via_orthology	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289160	Mpzl2	implicated_via_orthology	DOID:0111640	autosomal recessive nonsyndromic deafness 111						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328350	Matn3	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929242	Ivd	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	implicated_via_orthology	DOID:0110479	autosomal recessive nonsyndromic deafness 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098221	Gamt	implicated_via_orthology	DOID:0050799	guanidinoacetate methyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109602	Gphn	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:2236	congenital afibrinogenemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95915	H2-M3	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:0110031	hemoglobin H disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443138	Mphosph9	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354958	Hs6st1	implicated_via_orthology	DOID:0090075	hypogonadotropic hypogonadism 15 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	implicated_via_orthology	DOID:0110565	autosomal dominant nonsyndromic deafness 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95766	Gna11	implicated_via_orthology	DOID:0060701	familial hypocalciuric hypercalcemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:0050651	atrioventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103234	Herc2	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443143	Wdr3	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652847	Lrrc8a	implicated_via_orthology	DOID:0080588	agammaglobulinemia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102499	mt-Nd3	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:0111632	familial erythrocytosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	implicated_via_orthology	DOID:0070233	Loeys-Dietz syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:0080598	Kleefstra syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683541	Mast3	implicated_via_orthology	DOID:0070394	developmental and epileptic encephalopathy 108						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	implicated_via_orthology	DOID:0070285	primary autosomal recessive microcephaly 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:853	polymyalgia rheumatica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:0070274	hereditary nonpolyposis colorectal cancer type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915419	Ndnf	implicated_via_orthology	DOID:0090070	hypogonadotropic hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336155	Lss	implicated_via_orthology	DOID:0080582	hypotrichosis 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13404	uveoparotid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924968	Slf2	implicated_via_orthology	DOID:0080688	mosaic variegated aneuploidy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	implicated_via_orthology	DOID:0060740	methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:0080179	haemophilus meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95815	Grik2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106903	Gucy2c	implicated_via_orthology	DOID:0060780	congenital diarrhea 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:0080205	CAKUT						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:853	polymyalgia rheumatica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95683	Gdf1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:0111100	maturity-onset diabetes of the young type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201779	Hnrnph2	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329021	Msh5	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103234	Herc2	implicated_via_orthology	DOID:0081203	autosomal recessive intellectual developmental disorder 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921749	Sost	implicated_via_orthology	DOID:0060756	sclerosteosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0081317	multiple synostoses syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	implicated_via_orthology	DOID:0070380	developmental and epileptic encephalopathy 85						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	implicated_via_orthology	DOID:0060878	hypoparathyroidism-deafness-renal disease syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	implicated_via_orthology	DOID:0111463	cardiofaciocutaneous syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96897	Lyz2	implicated_via_orthology	DOID:0050636	familial visceral amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860433	Pigp	implicated_via_orthology	DOID:0080283	developmental and epileptic encephalopathy 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:0080053	Albright's hereditary osteodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	implicated_via_orthology	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88017	Mat1a	implicated_via_orthology	DOID:0050544	hypermethioninemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0070483	Watson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923396	Stx16	implicated_via_orthology	DOID:0080222	pseudohypoparathyroidism type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919028	Klhl5	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106096	Loxl1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95728	Gli2	implicated_via_orthology	DOID:0080328	Culler-Jones syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	implicated_via_orthology	DOID:2217	Bernard-Soulier syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:0110997	Joubert syndrome 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445027	Malt1	implicated_via_orthology	DOID:0111988	immunodeficiency 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3577015	Otulin	implicated_via_orthology	DOID:0080163	otulipenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919686	Tbcd	implicated_via_orthology	DOID:0070423	early onset progressive encephalopathy with brain atrophy and thin corpus callosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138584	Gigyf2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:0110019	age related macular degeneration 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:8927	learning disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196627	Htr6	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329038	Mllt10	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:0111632	familial erythrocytosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444136	Mars2	implicated_via_orthology	DOID:0111468	combined oxidative phosphorylation deficiency 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:0080325	tuberous sclerosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099809	Fgf10	implicated_via_orthology	DOID:0111549	aplasia of lacrimal and salivary glands						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102499	mt-Nd3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99502	Ltbp2	implicated_via_orthology	DOID:0060305	megalocornea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298209	Hcn4	implicated_via_orthology	DOID:1827	idiopathic generalized epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202398	Kera	implicated_via_orthology	DOID:2566	corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	implicated_via_orthology	DOID:11193	syndactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109519	Msh3	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:10887	lepromatous leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926273	Mrpl12	implicated_via_orthology	DOID:0112113	combined oxidative phosphorylation deficiency 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036246	Hfm1	implicated_via_orthology	DOID:0080866	primary ovarian insufficiency 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	implicated_via_orthology	DOID:2236	congenital afibrinogenemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	implicated_via_orthology	DOID:4990	essential tremor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0111162	epidermal nevus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0060785	adult-onset autosomal dominant demyelinating leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201682	Kif20a	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152389	Ivns1abp	implicated_via_orthology	DOID:0112005	immunodeficiency 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1098	fetal erythroblastosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0111337	Jackson-Weiss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891427	Fgf23	implicated_via_orthology	DOID:0050948	autosomal dominant hypophosphatemic rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337004	Loxl3	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929512	Litaf	implicated_via_orthology	DOID:0110151	Charcot-Marie-Tooth disease type 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147006	Gnptg	implicated_via_orthology	DOID:0080678	mucolipidosis III gamma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:4677	keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384495	Mrtfa	implicated_via_orthology	DOID:0111998	immunodeficiency 66						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:4249	Gerstmann-Straussler-Scheinker syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:1586	rheumatic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96217	Hprt1	implicated_via_orthology	DOID:1919	Lesch-Nyhan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101761	Hmga2	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:13258	typhoid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:6406	double outlet right ventricle						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:11963	esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111783	otopalatodigital syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107978	Klc1	implicated_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097705	Kng1	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036273	Kcnt2	implicated_via_orthology	DOID:0080284	developmental and epileptic encephalopathy 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196356	Iqsec1	implicated_via_orthology	DOID:0111674	intellectual developmental disorder with short stature and behavioral abnormalities						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182474	Irak4	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:2859	hemoglobin C disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:5016	hepatocellular clear cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916330	Gmppa	implicated_via_orthology	DOID:0112321	alacrima, achalasia, and impaired intellectual development syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	implicated_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351620	Mrpl39	implicated_via_orthology	DOID:0060286	combined oxidative phosphorylation deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:0080798	myeloid leukemia associated with Down Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146906	Ift140	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202304	Gnmt	implicated_via_orthology	DOID:0111037	glycine N-methyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:2859	hemoglobin C disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918060	Krt25	implicated_via_orthology	DOID:0111574	autosomal recessive woolly hair 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916323	Kdf1	implicated_via_orthology	DOID:0111652	ectodermal dysplasia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:4927	Klatskin's tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346327	Fyb1	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138281	Lbr	implicated_via_orthology	DOID:9631	Pelger-Huet anomaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95801	Grk4	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:2247	spondylosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347474	Foxj1	implicated_via_orthology	DOID:0111856	primary ciliary dyskinesia 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102949	Foxn1	implicated_via_orthology	DOID:4123	nail disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923805	Mmaa	implicated_via_orthology	DOID:0060742	methylmalonic acidemia cblA type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	implicated_via_orthology	DOID:9250	acrocallosal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	implicated_via_orthology	DOID:0090031	D-bifunctional protein deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105052	Il13ra1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	implicated_via_orthology	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95721	Gjb3	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99542	Usf1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105942	Hcfc1	implicated_via_orthology	DOID:0111814	methylmalonic acidemia and homocysteinemia cblX type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105383	Il18r1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914342	Gatm	implicated_via_orthology	DOID:0050712	AGAT deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:1229	paranoid schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	implicated_via_orthology	DOID:0110910	leukocyte adhesion deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	implicated_via_orthology	DOID:0110964	brachydactyly type A1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:0111431	essential tremor 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96974	Kitl	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102498	mt-Nd4	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:0111339	Vohwinkel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:1742	drug psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446294	Megf8	implicated_via_orthology	DOID:0060234	Carpenter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0080052	acromesomelic dysplasia, Grebe type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	implicated_via_orthology	DOID:0110091	short-rib thoracic dysplasia 10 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342540	Ikzf1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106911	Hccs	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354708	Fbxo31	implicated_via_orthology	DOID:0081209	autosomal recessive intellectual developmental disorder 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95790	Gnrhr	implicated_via_orthology	DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0111411	exudative vitreoretinopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653880	Gpr156	implicated_via_orthology	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:13628	favism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:0111632	familial erythrocytosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2158650	Idh3b	implicated_via_orthology	DOID:0110409	retinitis pigmentosa 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108559	Macf1	implicated_via_orthology	DOID:0112228	lissencephaly 9 with complex brainstem malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928904	Mocs1	implicated_via_orthology	DOID:0111164	molybdenum cofactor deficiency type A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:0080077	hypophosphatemic nephrolithiasis/osteoporosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	implicated_via_orthology	DOID:2219	Glanzmann's thrombasthenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104813	Jarid2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930618	Krit1	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13404	uveoparotid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0081128	mandibuloacral dysplasia type A lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915464	Gsto2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95814	Grik1	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96743	Lamb1	implicated_via_orthology	DOID:0112230	lissencephaly 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95721	Gjb3	implicated_via_orthology	DOID:0050467	erythrokeratodermia variabilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930923	Slurp1	implicated_via_orthology	DOID:3390	palmoplantar keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928140	Mrps25	implicated_via_orthology	DOID:0112111	combined oxidative phosphorylation deficiency 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095417	Gsta1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653368	Klf11	implicated_via_orthology	DOID:0111106	maturity-onset diabetes of the young type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389465	Tbx22	implicated_via_orthology	DOID:0111826	Abruzzo-Erickson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928137	Mrps22	implicated_via_orthology	DOID:0080499	ovarian dysgenesis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:2383	neonatal jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685047	Hmcn1	implicated_via_orthology	DOID:0110014	age related macular degeneration 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352738	Nkx6-2	implicated_via_orthology	DOID:0080252	spastic ataxia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:12960	acrocephalosyndactylia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928743	Kcnd3	implicated_via_orthology	DOID:0050970	spinocerebellar ataxia type 19/22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	implicated_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108398	Mlx	implicated_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109380	Il10rb	implicated_via_orthology	DOID:0110909	inflammatory bowel disease 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:0090043	dystonia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:0111632	familial erythrocytosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926483	Nectin1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:0110327	hypertrophic cardiomyopathy 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687329	Kash5	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:0110732	neuronal ceroid lipofuscinosis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0060233	cardiofaciocutaneous syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196453	Klhl7	implicated_via_orthology	DOID:0110386	retinitis pigmentosa 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927140	Git1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95852	Gss	implicated_via_orthology	DOID:0080699	glutathione synthetase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:401	multidrug-resistant tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098226	Kif14	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	implicated_via_orthology	DOID:12802	mucopolysaccharidosis I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:4480	achondroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147913	Igsf1	implicated_via_orthology	DOID:0111140	IGSF1 deficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97311	Nfix	implicated_via_orthology	DOID:0050858	Marshall-Smith syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924647	Lyz3	implicated_via_orthology	DOID:0050636	familial visceral amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:0060863	patterned macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580487	Hs3st6	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96702	Krt5	implicated_via_orthology	DOID:0060256	Dowling-Degos disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	implicated_via_orthology	DOID:11199	hypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442265	Kctd7	implicated_via_orthology	DOID:0111446	progressive myoclonus epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384968	L2hgdh	implicated_via_orthology	DOID:0050574	L-2-hydroxyglutaric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107177	Hsd17b3	implicated_via_orthology	DOID:0112248	17-beta hydroxysteroid dehydrogenase 3 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181763	Hps6	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	implicated_via_orthology	DOID:0060539	Hermansky-Pudlak syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:0080205	CAKUT						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336159	Minpp1	implicated_via_orthology	DOID:0112333	pontocerebellar hypoplasia type 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923488	Grhpr	implicated_via_orthology	DOID:2977	primary hyperoxaluria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	implicated_via_orthology	DOID:0080773	delta beta-thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111782	otopalatodigital syndrome spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	implicated_via_orthology	DOID:0110122	Axenfeld-Rieger syndrome type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108389	Kif4	implicated_via_orthology	DOID:0112040	non-syndromic X-linked intellectual disability 100						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926855	Kcnq1ot1	implicated_via_orthology	DOID:5572	Beckwith-Wiedemann syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	implicated_via_orthology	DOID:14761	Greig cephalopolysyndactyly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:0090139	cortisone reductase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0111559	Charcot-Marie-Tooth disease type 2EE						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920918	Ttc21b	implicated_via_orthology	DOID:0111119	nephronophthisis 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98295	Shbg	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149960	Rasa2	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	implicated_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:0060799	syndromic X-linked intellectual disability Lubs type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891124	Kcne3	implicated_via_orthology	DOID:0110223	Brugada syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:11829	degenerative myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384974	Flvcr2	implicated_via_orthology	DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0111530	linear nevus sebaceous syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135671	Lmod1	implicated_via_orthology	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104667	Hmmr	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444465	Frem2	implicated_via_orthology	DOID:0111407	Fraser syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95621	Gabrb3	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	implicated_via_orthology	DOID:6612	leukocyte adhesion deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858193	Folh1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95590	Ftl2-ps	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444210	Nr1d1	implicated_via_orthology	DOID:0112313	brain small vessel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	implicated_via_orthology	DOID:0050604	acrocapitofemoral dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388651	Mcat	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3712328	Pnp2	implicated_via_orthology	DOID:653	purine-pyrimidine metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96550	Il2rb	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96902	Lyz1	implicated_via_orthology	DOID:0050636	familial visceral amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96829	Lrpap1	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109188	Kif21a	implicated_via_orthology	DOID:0081015	congenital fibrosis of the extraocular muscles 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341847	Hhip	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	implicated_via_orthology	DOID:0110647	long QT syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:4511	breast angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0111705	oculoectodermal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	implicated_via_orthology	DOID:0060639	permanent neonatal diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	implicated_via_orthology	DOID:9248	Pallister-Hall syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580376	Lemd3	implicated_via_orthology	DOID:0111536	Buschke-Ollendorff syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104744	Kcnj2	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443573	Lefty2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298218	Lrp6	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:0111462	cardiofaciocutaneous syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96567	Impdh1	implicated_via_orthology	DOID:0110216	Leber congenital amaurosis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333752	Hdac6	implicated_via_orthology	DOID:0112106	chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924947	Mmab	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157166	Rp9	implicated_via_orthology	DOID:0110387	retinitis pigmentosa 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:8483	retinal artery occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041174	Iba57	implicated_via_orthology	DOID:0110819	hereditary spastic paraplegia 74						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	implicated_via_orthology	DOID:0070039	NESCAV syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685385	Kalrn	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:0050793	short QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889850	Gsdme	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3582693	Tor1aip1	implicated_via_orthology	DOID:0110289	autosomal recessive limb-girdle muscular dystrophy type 2Y						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619329	Mir30e	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:0110960	Gaucher's disease perinatal lethal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	implicated_via_orthology	DOID:0050548	hereditary sensory neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917685	Inf2	implicated_via_orthology	DOID:0111130	focal segmental glomerulosclerosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444484	Manea	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3605986	Rad54b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920441	Fezf1	implicated_via_orthology	DOID:0090081	hypogonadotropic hypogonadism 22 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	implicated_via_orthology	DOID:0060291	oculodentodigital dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	implicated_via_orthology	DOID:0112159	autosomal dominant nonsyndromic deafness 78						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	implicated_via_orthology	DOID:0080354	Phelan-McDermid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96702	Krt5	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	implicated_via_orthology	DOID:0111296	generalized epilepsy with febrile seizures plus 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336894	Mocs2	implicated_via_orthology	DOID:0111163	molybdenum cofactor deficiency type B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:0110763	hereditary spastic paraplegia 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916703	Prss56	implicated_via_orthology	DOID:0060835	isolated microphthalmia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0050469	Costello syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449313	Gemin4	implicated_via_orthology	DOID:0081263	neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10128	venous insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:0111386	inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:0090103	Huntington's disease-like 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0080051	acromesomelic dysplasia, Hunter-Thompson type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:0111190	distal myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98505	Hnf1b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929938	Perp	implicated_via_orthology	DOID:0112011	mutilating palmoplantar keratoderma with periorificial keratotic plaques						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:0111352	D-2-hydroxyglutaric aciduria 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342293	Lat	implicated_via_orthology	DOID:0111983	immunodeficiency 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334458	Pex19	implicated_via_orthology	DOID:0080486	peroxisome biogenesis disorder 12A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442415	Kat6a	implicated_via_orthology	DOID:0070062	Arboleda-Tham syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442647	Mpzl3	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	implicated_via_orthology	DOID:0111769	46,XY sex reversal 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:8505	dermatitis herpetiformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298209	Hcn4	implicated_via_orthology	DOID:0110225	Brugada syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	implicated_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95620	Gabrb2	implicated_via_orthology	DOID:0080471	developmental and epileptic encephalopathy 92						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328350	Matn3	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109380	Il10rb	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355324	Grb14	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149728	Impa2	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:12148	alveolar echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386030	Gabbr2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443921	Irf2bp2	implicated_via_orthology	DOID:0081156	common variable immunodeficiency 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442252	Lrp4	implicated_via_orthology	DOID:0110674	congenital myasthenic syndrome 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:0080030	spondyloepimetaphyseal dysplasia, Missouri type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	implicated_via_orthology	DOID:0080837	growth hormone insensitivity syndrome with immune dysregulation 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96051	Serpind1	implicated_via_orthology	DOID:0111901	heparin cofactor II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928858	Krt81	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934704	Rnf31	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0111557	Charcot-Marie-Tooth disease type 2A2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916047	Pdgfrl	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926212	Med12	implicated_via_orthology	DOID:0080985	syndromic X-linked intellectual disorder Lujan-Fryns-type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:3165	skin benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	implicated_via_orthology	DOID:9245	Alagille syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:0110749	type 1 diabetes mellitus 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	implicated_via_orthology	DOID:0080222	pseudohypoparathyroidism type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:3263	piebaldism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	implicated_via_orthology	DOID:0110475	autosomal recessive nonsyndromic deafness 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109519	Msh3	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442760	Katnip	implicated_via_orthology	DOID:0110995	Joubert syndrome 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95805	Grb2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	implicated_via_orthology	DOID:0060013	X-linked severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:895068	Lgals2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102496	mt-Nd5	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921426	Tgm5	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:0080334	aortic valve disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927655	Ggcx	implicated_via_orthology	DOID:0112173	combined deficiency of vitamin K-dependent clotting factors 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:0060532	latex allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890505	Plin1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141180	Glmn	implicated_via_orthology	DOID:2431	glomus tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386030	Gabbr2	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915383	Gcsh	implicated_via_orthology	DOID:0070330	multiple mitochondrial dysfunctions syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028590	Mei1	implicated_via_orthology	DOID:3590	gestational trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683538	Lyrm4	implicated_via_orthology	DOID:0111476	combined oxidative phosphorylation deficiency 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444886	Miat	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135756	Hspb8	implicated_via_orthology	DOID:0110174	Charcot-Marie-Tooth disease axonal type 2L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95785	Gnb3	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443583	Fermt1	implicated_via_orthology	DOID:0060472	Kindler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95789	Gnrh1	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99456	Mc1r	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102501	mt-Cytb	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	implicated_via_orthology	DOID:0050884	triosephosphate isomerase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333787	Inppl1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95589	Ftl1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859396	Mefv	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100513	Lmx1b	implicated_via_orthology	DOID:9467	nail-patella syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97275	Myod1	implicated_via_orthology	DOID:0081349	congenital myopathy 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95583	Fshr	implicated_via_orthology	DOID:14450	46 XX gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	implicated_via_orthology	DOID:2859	hemoglobin C disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104670	Fkbp5	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97169	Msx2	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443377	Unc45b	implicated_via_orthology	DOID:0081338	myofibrillar myopathy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859252	Fmn2	implicated_via_orthology	DOID:0081211	autosomal recessive intellectual developmental disorder 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	implicated_via_orthology	DOID:0070218	familial hyperinsulinemic hypoglycemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96231	Hspa1l	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:14705	Pfeiffer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	implicated_via_orthology	DOID:0111029	hemochromatosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95620	Gabrb2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442252	Lrp4	implicated_via_orthology	DOID:0060757	sclerosteosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:0081379	amyotrophic lateral sclerosis type 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443764	Iqcb1	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:0110644	long QT syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0060291	oculodentodigital dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	implicated_via_orthology	DOID:0070038	autosomal dominant intellectual developmental disorder 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353455	Mlh3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858746	Kat6b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446262	Foxred1	implicated_via_orthology	DOID:0112085	nuclear type mitochondrial complex I deficiency 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098566	Gypc	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	implicated_via_orthology	DOID:1148	polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	implicated_via_orthology	DOID:653	purine-pyrimidine metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194506	Serpini1	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340044	Lrp8	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96891	Lyl1	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	implicated_via_orthology	DOID:0112074	nuclear type mitochondrial complex I deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3781032	Kcnj13	implicated_via_orthology	DOID:0110118	Leber congenital amaurosis 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686379	Frmd7	implicated_via_orthology	DOID:0111790	congenital nystagmus 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926803	Kcnq4	implicated_via_orthology	DOID:0110558	autosomal dominant nonsyndromic deafness 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927126	Slc5a7	implicated_via_orthology	DOID:0110661	congenital myasthenic syndrome 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88401	Vsx2	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:0110970	brachydactyly type C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:0070115	Meckel syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96738	Hikeshi	implicated_via_orthology	DOID:0060795	hypomyelinating leukodystrophy 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922945	Rilpl1	implicated_via_orthology	DOID:0081300	oculopharyngodistal myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:9164	achalasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:0050879	fragile X-associated tremor/ataxia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338001	Gdap2	implicated_via_orthology	DOID:0111616	autosomal recessive spinocerebellar ataxia 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:0050647	Arts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96298	Hyal1	implicated_via_orthology	DOID:0050809	mucopolysaccharidosis IX						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	implicated_via_orthology	DOID:2859	hemoglobin C disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109573	Tep1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917585	Reep6	implicated_via_orthology	DOID:0080350	retinitis pigmentosa 77						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923373	Gpsm2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:0112161	Noonan syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96929	Mc3r	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289298	Knstrn	implicated_via_orthology	DOID:3151	skin squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443409	Gpr179	implicated_via_orthology	DOID:0110869	congenital stationary night blindness 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:0110757	type 1 diabetes mellitus 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861441	Rab27a	implicated_via_orthology	DOID:0060833	Griscelli syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	implicated_via_orthology	DOID:0070147	hereditary sensory neuropathy type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	implicated_via_orthology	DOID:0080527	bronchiectasis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96274	Htr1b	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3665486	Krt87	implicated_via_orthology	DOID:421	hair disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389216	Slc17a3	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:1733	cryptosporidiosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921727	4933427D14Rik	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913699	Pam16	implicated_via_orthology	DOID:0112304	spondylometaphyseal dysplasia Megarbane-Dagher-Melike type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619329	Mir30e	implicated_via_orthology	DOID:11202	primary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298379	Matr3	implicated_via_orthology	DOID:0060212	amyotrophic lateral sclerosis type 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	implicated_via_orthology	DOID:2859	hemoglobin C disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:0111275	speech-language disorder-1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336205	Fkbp1b	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	implicated_via_orthology	DOID:0050689	brachydactyly-syndactyly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96789	Lipa	implicated_via_orthology	DOID:14497	Wolman disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96928	Mc2r	implicated_via_orthology	DOID:0080621	glucocorticoid deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926562	Gucy1a1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140367	Fbxl4	implicated_via_orthology	DOID:0080131	mitochondrial DNA depletion syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:0110299	autosomal recessive limb-girdle muscular dystrophy type 2I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	implicated_via_orthology	DOID:0060689	atrichia with papular lesions						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354951	Gne	implicated_via_orthology	DOID:0080718	GNE myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95880	Gypa	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:0060888	transient myeloproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	implicated_via_orthology	DOID:0110185	Charcot-Marie-Tooth disease type 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96231	Hspa1l	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95863	Gsta2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443764	Iqcb1	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96213	Hpd	implicated_via_orthology	DOID:0050727	tyrosinemia type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0110156	Charcot-Marie-Tooth disease type 2B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891496	Jph2	implicated_via_orthology	DOID:0081161	dilated cardiomyopathy 2E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346318	Klf6	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342286	Flii	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	implicated_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153060	Gjc2	implicated_via_orthology	DOID:0060787	hypomyelinating leukodystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140356	H6pd	implicated_via_orthology	DOID:0090139	cortisone reductase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95752	Gls	implicated_via_orthology	DOID:0112207	developmental and epileptic encephalopathy 71						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	implicated_via_orthology	DOID:0111632	familial erythrocytosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918039	Kynu	implicated_via_orthology	DOID:0112257	hydroxykynureninuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107399	Il17ra	implicated_via_orthology	DOID:0111996	immunodeficiency 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101884	Ppard	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919425	Mfsd8	implicated_via_orthology	DOID:0110722	neuronal ceroid lipofuscinosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97167	Msn	implicated_via_orthology	DOID:0112001	immunodeficiency 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	implicated_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147032	Ticam1	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916264	Tnik	implicated_via_orthology	DOID:0081216	autosomal recessive intellectual developmental disorder 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354961	Synj1	implicated_via_orthology	DOID:0080464	developmental and epileptic encephalopathy 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107252	Nsun2	implicated_via_orthology	DOID:0081181	autosomal recessive intellectual developmental disorder 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101894	Pou3f4	implicated_via_orthology	DOID:0111737	X-linked deafness 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:0110548	autosomal dominant nonsyndromic deafness 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:0110859	polycystic kidney disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914701	Pkp2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859709	Rgs14	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332235	Nrf1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98881	Tyrp1	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933154	Slc26a5	implicated_via_orthology	DOID:0110513	autosomal recessive nonsyndromic deafness 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914638	Rab5if	implicated_via_orthology	DOID:0081125	craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:0050581	brachydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178759	Rtn4ip1	implicated_via_orthology	DOID:0111434	optic atrophy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143854	Nup107	implicated_via_orthology	DOID:0080694	Galloway-Mowat syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650385	Ssxb15	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:0050877	pancreatic agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:0060181	ischemic colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97930	Rlbp1	implicated_via_orthology	DOID:0111015	Newfoundland cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261422	Naga	implicated_via_orthology	DOID:0112319	Kanzaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927126	Slc5a7	implicated_via_orthology	DOID:0111201	obsolete distal hereditary motor neuronopathy type 7A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100511	Myt1l	implicated_via_orthology	DOID:0070069	autosomal dominant intellectual developmental disorder 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861452	Pigo	implicated_via_orthology	DOID:0070434	hyperphosphatasia with impaired intellectual development syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98366	Sox4	implicated_via_orthology	DOID:0112371	Coffin-Siris syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929481	Slc22a21	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	implicated_via_orthology	DOID:0110178	Charcot-Marie-Tooth disease axonal type 2V						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:0111344	myeloproliferative disorder with eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100881	Prss12	implicated_via_orthology	DOID:0081177	autosomal recessive intellectual developmental disorder 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88557	Pcyt1a	implicated_via_orthology	DOID:0112300	spondylometaphyseal dysplasia with cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150380	Srd5a2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:10811	nasal cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101934	Tfdp1	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111599	distal arthrogryposis type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914403	Rnaseh2b	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385316	Slc22a26	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101759	Rnf2	implicated_via_orthology	DOID:0070416	Luo-Schoch-Yamamoto syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:0080954	arthrogryposis multiplex congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:0060496	respiratory allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:0111908	thrombophilia due to thrombomodulin defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:0080538	Sweeney-Cox syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918615	Pdss2	implicated_via_orthology	DOID:0070240	primary coenzyme Q10 deficiency 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387466	Pank4	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3642927	Ssxb16	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	implicated_via_orthology	DOID:0070336	arthrogryposis multiplex congenita-6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913802	Sppl2a	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	implicated_via_orthology	DOID:0050887	Townes-Brocks syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700014	Sorbs1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202882	Rhd	implicated_via_orthology	DOID:4175	Rh isoimmunization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916221	Tamm41	implicated_via_orthology	DOID:0070429	combined oxidative phosphorylation deficiency 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926227	Nup160	implicated_via_orthology	DOID:0080394	nephrotic syndrome type 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98180	Rrm1	implicated_via_orthology	DOID:12558	chronic progressive external ophthalmoplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922667	Rspo2	implicated_via_orthology	DOID:0112193	tetraamelia syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98779	Tnnc1	implicated_via_orthology	DOID:0110434	dilated cardiomyopathy 1Z						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	implicated_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915235	Ssxb1	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920036	Tdp1	implicated_via_orthology	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:0112062	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108014	Polr1b	implicated_via_orthology	DOID:0080792	Treacher Collins syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685063	Tsga10	implicated_via_orthology	DOID:0111924	spermatogenic failure 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313274	Usp9y	implicated_via_orthology	DOID:0070187	Y-linked spermatogenic failure 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	implicated_via_orthology	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99515	Syk	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:0111970	immunodeficiency 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	implicated_via_orthology	DOID:3701	cervical mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338824	Rgs9	implicated_via_orthology	DOID:0070363	bradyopsia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	implicated_via_orthology	DOID:0081140	agammaglobulinemia 8A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	implicated_via_orthology	DOID:0110120	Axenfeld-Rieger syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1862037	Slc12a5	implicated_via_orthology	DOID:0080460	developmental and epileptic encephalopathy 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	implicated_via_orthology	DOID:0110439	dilated cardiomyopathy 1P						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:0080325	tuberous sclerosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354168	Ttpa	implicated_via_orthology	DOID:0090028	familial isolated deficiency of vitamin E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104513	Nqo2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346344	Nr0b2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9406	hypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97891	Rfc1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095438	Slc2a2	implicated_via_orthology	DOID:1062	Fanconi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096349	Ptprq	implicated_via_orthology	DOID:0110529	autosomal recessive nonsyndromic deafness 84A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109577	Taf1b	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446774	Ssxb5	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109433	Oaz1	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:0111618	autosomal recessive spinocerebellar ataxia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289288	Slc52a2	implicated_via_orthology	DOID:0080786	Brown-Vialetto-Van Laere syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	implicated_via_orthology	DOID:0081363	distal myopathy with rimmed vacuoles						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349163	Sdc3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97555	Pgk1	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:11151	cholecystolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	implicated_via_orthology	DOID:0111104	maturity-onset diabetes of the young type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107624	Mvk	implicated_via_orthology	DOID:0050452	mevalonic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	implicated_via_orthology	DOID:0070146	hereditary sensory neuropathy type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648526	Ndufs6b	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3783243	Sp110-ps1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448506	Pi4ka	implicated_via_orthology	DOID:0112347	hereditary spastic paraplegia 84						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316650	Slc37a4	implicated_via_orthology	DOID:0081331	glycogen storage disease Ic						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641889	Prss3l	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927616	Trps1	implicated_via_orthology	DOID:14743	trichorhinophalangeal syndrome type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102966	Ptgdr	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	implicated_via_orthology	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98742	Thra	implicated_via_orthology	DOID:0070128	congenital nongoitrous hypothyroidism 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	implicated_via_orthology	DOID:0110016	Leber congenital amaurosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97566	Pgm3	implicated_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917853	Mutyh	implicated_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	implicated_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913787	Pomp	implicated_via_orthology	DOID:0060914	proteosome-associated autoinflammatory syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99459	Nr3c2	implicated_via_orthology	DOID:0060855	autosomal dominant pseudohypoaldosteronism type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106442	Vkorc1	implicated_via_orthology	DOID:0080665	warfarin resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446777	Ssxb8	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:0081101	nonautoimmune hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:9649	congenital nystagmus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346523	Sgcb	implicated_via_orthology	DOID:0110279	autosomal recessive limb-girdle muscular dystrophy type 2E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929285	Orc6	implicated_via_orthology	DOID:0080514	Meier-Gorlin syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894657	Serpinb8	implicated_via_orthology	DOID:0060283	peeling skin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684944	Myrf	implicated_via_orthology	DOID:1405	primary angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97572	Phb1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	implicated_via_orthology	DOID:0050967	spinocerebellar ataxia type 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98331	Snap25	implicated_via_orthology	DOID:0110683	congenital myasthenic syndrome 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:0111194	autosomal dominant adult-onset proximal spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336173	Prkaa2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915853	Pmvk	implicated_via_orthology	DOID:3805	porokeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102643	Myh11	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277134	Per3	implicated_via_orthology	DOID:0050628	advanced sleep phase syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:0070095	oculocutaneous albinism type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0111359	large congenital melanocytic nevus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3046173	Nup85	implicated_via_orthology	DOID:0080392	nephrotic syndrome type 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	implicated_via_orthology	DOID:6195	conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914172	Rras2	implicated_via_orthology	DOID:0112170	Noonan syndrome 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446779	Ssxb10	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927347	Smarce1	implicated_via_orthology	DOID:0112368	Coffin-Siris syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446775	Ssxb6	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155865	Rrm2b	implicated_via_orthology	DOID:0070331	mitochondrial DNA depletion syndrome 8b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149633	Oas1c	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141625	Nup205	implicated_via_orthology	DOID:0080381	nephrotic syndrome type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203732	Slc16a2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916211	Phkg2	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150020	Rad51c	implicated_via_orthology	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914298	Vma21	implicated_via_orthology	DOID:0050760	X-linked myopathy with excessive autophagy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:0111252	vestibular schwannomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98780	Tnnc2	implicated_via_orthology	DOID:0081347	congenital myopathy 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108417	Nrtn	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928738	Slc25a20	implicated_via_orthology	DOID:0111585	carnitine-acylcarnitine translocase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916043	Rab3gap2	implicated_via_orthology	DOID:0111586	Martsolf syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261811	Myo15a	implicated_via_orthology	DOID:0110488	autosomal recessive nonsyndromic deafness 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	implicated_via_orthology	DOID:0110553	autosomal dominant nonsyndromic deafness 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448530	Vps13d	implicated_via_orthology	DOID:0111611	autosomal recessive spinocerebellar ataxia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700010	Sh3gl1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927234	Suclg1	implicated_via_orthology	DOID:0080128	mitochondrial DNA depletion syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097152	Ptpro	implicated_via_orthology	DOID:0080384	nephrotic syndrome type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442062	Sh3pxd2b	implicated_via_orthology	DOID:0111789	Frank-Ter Haar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931028	Recql4	implicated_via_orthology	DOID:0050774	rapadilino syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0080401	orofacial cleft 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102756	Try5	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446772	Ssxb3	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	implicated_via_orthology	DOID:0080212	polycystic kidney disease 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97464	P4hb	implicated_via_orthology	DOID:0060438	Cole-Carpenter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	implicated_via_orthology	DOID:0060751	familial temporal lobe epilepsy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104630	Wars1	implicated_via_orthology	DOID:0111212	autosomal dominant distal hereditary motor neuronopathy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921651	Terb2	implicated_via_orthology	DOID:0112357	spermatogenic failure 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:0111818	syndactyly type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3605624	Slc22a29	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350341	Sgsh	implicated_via_orthology	DOID:0111395	mucopolysaccharidosis type IIIA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858259	Tomm40	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:4398	pustulosis of palm and sole						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321152	Ptprt	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13258	typhoid fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351613	Txnl4a	implicated_via_orthology	DOID:0080695	Burn-McKeown syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443480	Setx	implicated_via_orthology	DOID:0060196	amyotrophic lateral sclerosis type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108403	Polr1d	implicated_via_orthology	DOID:0080790	Treacher Collins syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915235	Ssxb1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:0110455	dilated cardiomyopathy 1U						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929511	Ndufa1	implicated_via_orthology	DOID:0112099	nuclear type mitochondrial complex I deficiency 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	implicated_via_orthology	DOID:0070236	Loeys-Dietz syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:0111380	solitary median maxillary central incisor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0111539	parastremmatic dwarfism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646222	Prss1l	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	implicated_via_orthology	DOID:0070377	developmental and epileptic encephalopathy 96						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685806	Top6bl	implicated_via_orthology	DOID:3590	gestational trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180557	Rhobtb2	implicated_via_orthology	DOID:0070375	developmental and epileptic encephalopathy 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915599	Ndufs3	implicated_via_orthology	DOID:0112081	nuclear type mitochondrial complex I deficiency 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333876	Ppp1r17	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921984	Rhoh	implicated_via_orthology	DOID:13777	epidermodysplasia verruciformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920145	Setd5	implicated_via_orthology	DOID:0070053	autosomal dominant intellectual developmental disorder 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315213	Nrip1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:0111711	focal nonepidermolytic palmoplantar keratoderma 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:0111454	SHORT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913878	Thg1l	implicated_via_orthology	DOID:0070409	autosomal recessive spinocerebellar ataxia 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0081322	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109292	Rad50	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:0060573	von Willebrand's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341872	Tjp2	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921657	Odad4	implicated_via_orthology	DOID:0110620	primary ciliary dyskinesia 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650385	Ssxb15	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914780	Uqcrb	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333780	Rps19	implicated_via_orthology	DOID:0111895	Diamond-Blackfan anemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98813	Tpo	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098257	Psmb4	implicated_via_orthology	DOID:0060916	proteasome-associated autoinflammatory syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914780	Uqcrb	implicated_via_orthology	DOID:0080112	mitochondrial complex III deficiency nuclear type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97878	Rbp3	implicated_via_orthology	DOID:0110393	retinitis pigmentosa 66						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146634	Slc51a	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338026	Tom1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98660	Sry	implicated_via_orthology	DOID:0111778	46,XY sex reversal 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103078	Spr	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:0070490	infantile parkinsonism-dystonia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102809	Sars1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104900	Nup88	implicated_via_orthology	DOID:0111379	fetal akinesia deformation sequence syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3687012	Try10	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346087	Srp54a	implicated_via_orthology	DOID:0112135	severe congenital neutropenia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443999	Pde8b	implicated_via_orthology	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921831	Sbf2	implicated_via_orthology	DOID:0110190	Charcot-Marie-Tooth disease type 4B2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914902	Spaca1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914533	Slc25a19	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920230	Wdr11	implicated_via_orthology	DOID:0090087	hypogonadotropic hypogonadism 14 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261847	Vrk1	implicated_via_orthology	DOID:0060265	pontocerebellar hypoplasia type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913887	Tsen15	implicated_via_orthology	DOID:0112329	pontocerebellar hypoplasia type 2F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917678	Polr3b	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97357	Mycn	implicated_via_orthology	DOID:0060464	Feingold syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685542	Slc9a5	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446773	Ssxb13	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443511	Slc9a6	implicated_via_orthology	DOID:0060825	Christianson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	implicated_via_orthology	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97451	Otx2	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351629	Pign	implicated_via_orthology	DOID:0080138	multiple congenital anomalies-hypotonia-seizures syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180853	Oas1h	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891978	Phyh	implicated_via_orthology	DOID:10582	Refsum disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859993	Smad9	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098547	Nhp2	implicated_via_orthology	DOID:0070017	autosomal recessive dyskeratosis congenita 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918767	Vps35l	implicated_via_orthology	DOID:0060565	Ritscher-Schinzel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679446	Slitrk1	implicated_via_orthology	DOID:0050587	trichotillomania						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	implicated_via_orthology	DOID:0080944	familial Behcet-like autoinflammatory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:9663	aphthous stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	implicated_via_orthology	DOID:9649	congenital nystagmus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929096	Thsd1	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:7400	Nijmegen breakage syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0110426	dilated cardiomyopathy 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:12376	juvenile spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	implicated_via_orthology	DOID:0110555	autosomal dominant nonsyndromic deafness 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:0060496	respiratory allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109359	Nek2	implicated_via_orthology	DOID:0110359	retinitis pigmentosa 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	implicated_via_orthology	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:0111129	focal segmental glomerulosclerosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892010	Sfrp4	implicated_via_orthology	DOID:0080019	metaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443241	Ndufs1	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147319	Svil	implicated_via_orthology	DOID:0112108	myofibrillar myopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098733	Slc46a1	implicated_via_orthology	DOID:0111678	hereditary folate malabsorption						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97801	Pth1r	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917678	Polr3b	implicated_via_orthology	DOID:0060797	hypomyelinating leukodystrophy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	implicated_via_orthology	DOID:0080285	developmental and epileptic encephalopathy 58						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922960	Rbm12	implicated_via_orthology	DOID:0080281	schizophrenia 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444989	Spg11	implicated_via_orthology	DOID:0060197	amyotrophic lateral sclerosis type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921456	Sipa1l3	implicated_via_orthology	DOID:0110262	cataract 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	implicated_via_orthology	DOID:0110153	Charcot-Marie-Tooth disease type 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314635	Rasgrp1	implicated_via_orthology	DOID:0111980	immunodeficiency 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349387	Spag1	implicated_via_orthology	DOID:0110607	primary ciliary dyskinesia 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859183	Smarcal1	implicated_via_orthology	DOID:0060490	Schimke immuno-osseous dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913322	Sdhaf2	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0081321	contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105064	Slc9a3	implicated_via_orthology	DOID:0060777	congenital secretory sodium diarrhea 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929878	Smoc1	implicated_via_orthology	DOID:0060861	microphthalmia with limb anomalies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108176	Prx	implicated_via_orthology	DOID:0110193	Charcot-Marie-Tooth disease type 4F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917057	Trim32	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97860	Rasa1	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97567	Pgr	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99917	Slc1a3	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97243	Mx1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333865	Rfxank	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107560	Sema4a	implicated_via_orthology	DOID:0111017	cone-rod dystrophy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:0070249	autosomal dominant Emery-Dreifuss muscular dystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153207	Pofut1	implicated_via_orthology	DOID:0060256	Dowling-Degos disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	implicated_via_orthology	DOID:0060259	renal-hepatic-pancreatic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353497	Slc25a10	implicated_via_orthology	DOID:0070450	mitochondrial DNA depletion syndrome 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914255	Polr3k	implicated_via_orthology	DOID:0070407	hypomyelinating leukodystrophy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913679	Ufsp2	implicated_via_orthology	DOID:0070392	developmental and epileptic encephalopathy 106						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704336	Rpl10-ps3	implicated_via_orthology	DOID:0080241	syndromic X-linked mental retardation 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102758	Prss3	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095405	Ptch2	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927347	Smarce1	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448554	Nbeal2	implicated_via_orthology	DOID:0111044	gray platelet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	implicated_via_orthology	DOID:10457	Legionnaires' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916974	Rnaseh2a	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913511	Tm4sf20	implicated_via_orthology	DOID:0060244	specific language impairment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341872	Tjp2	implicated_via_orthology	DOID:0070224	progressive familial intrahepatic cholestasis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107181	Slc26a3	implicated_via_orthology	DOID:0060296	congenital secretory chloride diarrhea 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930153	Popdc3	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109186	Ncf4	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915040	Rab39b	implicated_via_orthology	DOID:0112059	non-syndromic X-linked intellectual disability 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98227	Sag	implicated_via_orthology	DOID:0110369	retinitis pigmentosa 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891698	Pnkp	implicated_via_orthology	DOID:0110179	Charcot-Marie-Tooth disease type 2B2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444588	Ttc12	implicated_via_orthology	DOID:0111857	primary ciliary dyskinesia 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446782	Ssxa1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914703	Slc25a46	implicated_via_orthology	DOID:0112330	pontocerebellar hypoplasia type 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107932	Ndufs6	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780170	Rpl35rt	implicated_via_orthology	DOID:0111886	Diamond-Blackfan anemia 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	implicated_via_orthology	DOID:0050476	Barth syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97397	Opcml	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0050563	nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108212	Ripk1	implicated_via_orthology	DOID:0111952	immunodeficiency 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926164	Nadsyn1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927259	Trpv6	implicated_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336213	Mybpc1	implicated_via_orthology	DOID:0081348	congenital myopathy 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:5585	Ferguson-Smith tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443665	Numa1	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920831	Stk36	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	implicated_via_orthology	DOID:0050432	Asperger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313276	Vamp1	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042283	Slc22a27	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922815	Sgf29	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108067	Nkx2-1	implicated_via_orthology	DOID:12859	choreatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930705	Stx1b	implicated_via_orthology	DOID:0111301	generalized epilepsy with febrile seizures plus 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915255	Naa10	implicated_via_orthology	DOID:0050781	Ogden syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0111521	autosomal dominant progressive external ophthalmoplegia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	implicated_via_orthology	DOID:0080006	bone development disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932040	Sil1	implicated_via_orthology	DOID:9277	primary cerebellar degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:2975	cystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685870	Pdp1	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99666	Syt2	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97794	Ptger2	implicated_via_orthology	DOID:0111579	asthma, nasal polyps, and aspirin intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	implicated_via_orthology	DOID:77	gastrointestinal system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97303	Nek1	implicated_via_orthology	DOID:0110092	short-rib thoracic dysplasia 6 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107486	Pex2	implicated_via_orthology	DOID:0080480	peroxisome biogenesis disorder 5A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860476	Nmu	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	implicated_via_orthology	DOID:5408	Paget's disease of bone						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3617850	Pnpla1	implicated_via_orthology	DOID:0060719	autosomal recessive congenital ichthyosis 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679449	Slitrk2	implicated_via_orthology	DOID:0060929	non-syndromic X-linked intellectual developmental disorder 111						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441738	Npsr1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:0110975	brachydactyly type B2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354947	Polg2	implicated_via_orthology	DOID:0070446	mitochondrial DNA depletion syndrome 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352460	Nr0b1	implicated_via_orthology	DOID:0111777	46,XY sex reversal 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:10322	berylliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0110136	Bardet-Biedl syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98476	Tac2	implicated_via_orthology	DOID:0090089	hypogonadotropic hypogonadism 10 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921305	Plce1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350925	Sec23b	implicated_via_orthology	DOID:0111401	congenital dyserythropoietic anemia type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914674	Myo1h	implicated_via_orthology	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676395	Pyroxd1	implicated_via_orthology	DOID:0080308	myofibrillar myopathy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	implicated_via_orthology	DOID:0111394	mucopolysaccharidosis type IIIB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3705601	Sms-ps	implicated_via_orthology	DOID:0060802	syndromic X-linked intellectual disability Snyder type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916047	Pdgfrl	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920150	Ndufv2	implicated_via_orthology	DOID:0112092	nuclear type mitochondrial complex I deficiency 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	implicated_via_orthology	DOID:0050647	Arts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2671932	Tspear	implicated_via_orthology	DOID:0111662	ectodermal dysplasia 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917285	Rab28	implicated_via_orthology	DOID:0111024	cone-rod dystrophy 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913520	Retreg1	implicated_via_orthology	DOID:0070150	hereditary sensory and autonomic neuropathy type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0110298	autosomal recessive limb-girdle muscular dystrophy type 2N						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277163	Vax1	implicated_via_orthology	DOID:0111804	syndromic microphthalmia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	implicated_via_orthology	DOID:0111600	distal arthrogryposis type 2B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	implicated_via_orthology	DOID:0110918	hereditary spherocytosis type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928761	Slc19a2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:0050430	multiple endocrine neoplasia type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	implicated_via_orthology	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917233	Sis	implicated_via_orthology	DOID:0111633	congenital sucrase-isomaltase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:520	aortic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101772	Snta1	implicated_via_orthology	DOID:0110653	long QT syndrome 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98511	Tfe3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916749	Tsr2	implicated_via_orthology	DOID:0111897	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924007	Trdn	implicated_via_orthology	DOID:0060674	catecholaminergic polymorphic ventricular tachycardia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098718	Tmem38b	implicated_via_orthology	DOID:0110343	osteogenesis imperfecta type 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:10533	viral pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104685	Twist2	implicated_via_orthology	DOID:0060549	Barber-Say syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915228	Tctn2	implicated_via_orthology	DOID:0070122	Meckel syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152936	Srgap1	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354961	Synj1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97565	Pgm1	implicated_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384789	Tmem63a	implicated_via_orthology	DOID:0070400	hypomyelinating leukodystrophy 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105108	Nin	implicated_via_orthology	DOID:0070011	Seckel syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918511	Poc1b	implicated_via_orthology	DOID:0111026	cone-rod dystrophy 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0070197	distal myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	implicated_via_orthology	DOID:0060897	Parkinson's disease 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889507	Pidd1	implicated_via_orthology	DOID:0081234	autosomal recessive intellectual developmental disorder 75						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98247	Scn1b	implicated_via_orthology	DOID:0111302	generalized epilepsy with febrile seizures plus 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446782	Ssxa1	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270850	Slc6a2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	implicated_via_orthology	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890149	Tpm3	implicated_via_orthology	DOID:0110926	nemaline myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913302	Sdhc	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685128	Nek10	implicated_via_orthology	DOID:0111851	primary ciliary dyskinesia 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328312	Ptf1a	implicated_via_orthology	DOID:0050877	pancreatic agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0060370	Parkinson's disease 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108029	Scn10a	implicated_via_orthology	DOID:0111730	familial episodic pain syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350341	Sgsh	implicated_via_orthology	DOID:12801	mucopolysaccharidosis III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:4330	non-Langerhans-cell histiocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353433	Timm8a1	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929915	Ncoa6	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:0110350	osteogenesis imperfecta type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	implicated_via_orthology	DOID:0080342	Simpson-Golabi-Behmel syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645714	Slc22a28	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923515	Tsen54	implicated_via_orthology	DOID:0060267	pontocerebellar hypoplasia type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	implicated_via_orthology	DOID:0081375	nemaline myopathy 5C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922814	Rsph9	implicated_via_orthology	DOID:0110601	primary ciliary dyskinesia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446773	Ssxb13	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683547	Plch1	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341799	Ndrg1	implicated_via_orthology	DOID:0110186	Charcot-Marie-Tooth disease type 4D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:0080758	Fanconi renotubular syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183447	Ugp2	implicated_via_orthology	DOID:0112218	developmental and epileptic encephalopathy 83						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442750	Slc22a30	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913518	Pigyl	implicated_via_orthology	DOID:0070437	hyperphosphatasia with impaired intellectual development syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929742	Timm22	implicated_via_orthology	DOID:0112116	combined oxidative phosphorylation deficiency 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352500	Tpk1	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	implicated_via_orthology	DOID:0111780	TARP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929237	Pus1	implicated_via_orthology	DOID:0111185	myopathy, lactic acidosis, and sideroblastic anemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917311	Sdr9c7	implicated_via_orthology	DOID:0080257	autosomal recessive congenital ichthyosis 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647600	Otogl	implicated_via_orthology	DOID:0110530	autosomal recessive nonsyndromic deafness 84B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921325	Syce1	implicated_via_orthology	DOID:0070172	spermatogenic failure 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143854	Nup107	implicated_via_orthology	DOID:0080498	ovarian dysgenesis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919232	Snx10	implicated_via_orthology	DOID:0110940	autosomal recessive osteopetrosis 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914724	Snap29	implicated_via_orthology	DOID:0060337	CEDNIK syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918781	Piezo2	implicated_via_orthology	DOID:0111607	distal arthrogryposis type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914475	Rnpc3	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	implicated_via_orthology	DOID:0111764	46,XX sex reversal 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140770	Oas1d	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0110168	Charcot-Marie-Tooth disease type 2Y						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921588	Slc6a19	implicated_via_orthology	DOID:1060	Hartnup disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144877	Spata7	implicated_via_orthology	DOID:0110331	Leber congenital amaurosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444879	Ripor2	implicated_via_orthology	DOID:0110465	autosomal recessive nonsyndromic deafness 104						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3642927	Ssxb16	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:0110042	Alzheimer's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	implicated_via_orthology	DOID:0112128	X-linked severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	implicated_via_orthology	DOID:0110272	cataract 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	implicated_via_orthology	DOID:0080526	bronchiectasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97324	Nhlh2	implicated_via_orthology	DOID:0090070	hypogonadotropic hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:0110460	dilated cardiomyopathy 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914701	Pkp2	implicated_via_orthology	DOID:0110077	arrhythmogenic right ventricular dysplasia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109589	Ocrl	implicated_via_orthology	DOID:1056	oculocerebrorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107898	Selenoi	implicated_via_orthology	DOID:0112349	hereditary spastic paraplegia 81						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:14400	capillary leak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442832	Osbpl2	implicated_via_orthology	DOID:0110588	autosomal dominant nonsyndromic deafness 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	implicated_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332226	Soat2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338829	Pex16	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98487	Tat	implicated_via_orthology	DOID:9275	tyrosinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913913	Uba5	implicated_via_orthology	DOID:0080424	developmental and epileptic encephalopathy 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	implicated_via_orthology	DOID:0080506	Cornelia de Lange syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095438	Slc2a2	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104685	Twist2	implicated_via_orthology	DOID:0060550	ablepharon macrostomia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446778	Ssxb9	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:3181	oligodendroglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	implicated_via_orthology	DOID:0090114	Sorsby's fundus dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:0060131	alexithymia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139535	Tprn	implicated_via_orthology	DOID:0110526	autosomal recessive nonsyndromic deafness 79						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97290	Ndn	implicated_via_orthology	DOID:11983	Prader-Willi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0080449	developmental and epileptic encephalopathy 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	implicated_via_orthology	DOID:0110424	dilated cardiomyopathy 1CC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919682	Spink5	implicated_via_orthology	DOID:0050474	Netherton syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096349	Ptprq	implicated_via_orthology	DOID:0080269	autosomal dominant nonsyndromic deafness 73						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0110360	retinitis pigmentosa 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195265	Per2	implicated_via_orthology	DOID:0050628	advanced sleep phase syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103288	Polr1c	implicated_via_orthology	DOID:0080791	Treacher Collins syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:0110313	hypertrophic cardiomyopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183441	Psat1	implicated_via_orthology	DOID:0050723	PSAT deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913300	Trappc2b	implicated_via_orthology	DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3630308	Rsph3b	implicated_via_orthology	DOID:0110603	primary ciliary dyskinesia 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	implicated_via_orthology	DOID:0110520	autosomal recessive nonsyndromic deafness 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446774	Ssxb5	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	implicated_via_orthology	DOID:0111797	autosomal recessive congenital nystagmus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97998	Rom1	implicated_via_orthology	DOID:0110383	retinitis pigmentosa 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:0110427	dilated cardiomyopathy 1V						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99422	Rapsn	implicated_via_orthology	DOID:0110675	congenital myasthenic syndrome 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929481	Slc22a21	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	implicated_via_orthology	DOID:0050638	transthyretin amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	implicated_via_orthology	DOID:0110698	hypotrichosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97373	Npr3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914275	Rpl11	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385292	Tnrc6a	implicated_via_orthology	DOID:0111696	familial adult myoclonic epilepsy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:0080130	mitochondrial DNA depletion syndrome 12a						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97524	Pde6a	implicated_via_orthology	DOID:0110379	retinitis pigmentosa 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97812	Ptprd	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183924	Myo3a	implicated_via_orthology	DOID:0110489	autosomal recessive nonsyndromic deafness 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921305	Plce1	implicated_via_orthology	DOID:0080379	nephrotic syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	implicated_via_orthology	DOID:0070237	Loeys-Dietz syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919336	Slc39a5	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103306	Tiam1	implicated_via_orthology	DOID:0070444	neurodevelopmental disorder with language delay and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3712328	Pnp2	implicated_via_orthology	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	implicated_via_orthology	DOID:12176	goiter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97488	Pax4	implicated_via_orthology	DOID:0111107	maturity-onset diabetes of the young type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109352	Ung	implicated_via_orthology	DOID:0060759	immunodeficiency with hyper IgM type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336883	Smad6	implicated_via_orthology	DOID:0080334	aortic valve disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102523	Pou4f3	implicated_via_orthology	DOID:0110546	autosomal dominant nonsyndromic deafness 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98839	Prss1	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	implicated_via_orthology	DOID:12176	goiter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:0080939	hereditary angioedema type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194909	Rsph1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	implicated_via_orthology	DOID:0070455	hereditary spastic paraplegia 79A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	implicated_via_orthology	DOID:8499	night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	implicated_via_orthology	DOID:14669	acrodysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102959	Ube2a	implicated_via_orthology	DOID:0060820	syndromic X-linked intellectual disability Nascimento type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932137	Tnxb	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:0110403	retinitis pigmentosa 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914384	Nop56	implicated_via_orthology	DOID:0050983	spinocerebellar ataxia type 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861441	Rab27a	implicated_via_orthology	DOID:4330	non-Langerhans-cell histiocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916052	Mypn	implicated_via_orthology	DOID:0110445	dilated cardiomyopathy 1KK						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270850	Slc6a2	implicated_via_orthology	DOID:11569	neurocirculatory asthenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102539	Tbx6	implicated_via_orthology	DOID:0112363	spondylocostal dysostosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102570	Ndp	implicated_via_orthology	DOID:0060844	Norrie disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313261	Sptbn2	implicated_via_orthology	DOID:0080058	autosomal recessive spinocerebellar ataxia 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443219	Tmem260	implicated_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332242	Mycs	implicated_via_orthology	DOID:0060464	Feingold syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675603	Trpm6	implicated_via_orthology	DOID:896	metal metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645767	Rnf212	implicated_via_orthology	DOID:0112351	spermatogenic failure 62						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890212	Porcn	implicated_via_orthology	DOID:2120	focal dermal hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926342	Sult2b1	implicated_via_orthology	DOID:0080258	autosomal recessive congenital ichthyosis 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	implicated_via_orthology	DOID:0110862	congenital stationary night blindness autosomal dominant 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:0111271	Oliver-McFarlane syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384782	Slc25a38	implicated_via_orthology	DOID:0060065	autosomal recessive pyridoxine-refractory sideroblastic anemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98353	Son	implicated_via_orthology	DOID:0112359	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	implicated_via_orthology	DOID:0050466	Loeys-Dietz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:13100	intracranial vasospasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930009	Ppp2r3c	implicated_via_orthology	DOID:0111921	spermatogenic failure 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0060584	Noonan syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99555	Pde4d	implicated_via_orthology	DOID:14669	acrodysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298388	Umps	implicated_via_orthology	DOID:653	purine-pyrimidine metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97774	Prph	implicated_via_orthology	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913590	Psenen	implicated_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919399	Strada	implicated_via_orthology	DOID:0070511	polyhydramnios, megalencephaly, and symptomatic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:0070113	Niemann-Pick disease type C1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:0090045	childhood onset GLUT1 deficiency syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106220	Six5	implicated_via_orthology	DOID:0111424	branchiootorenal syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447063	Tenm4	implicated_via_orthology	DOID:0111432	essential tremor 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923221	Sugct	implicated_via_orthology	DOID:0112246	glutaric acidemia type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919276	Trmu	implicated_via_orthology	DOID:0080778	transient infantile liver failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98003	Rpl18	implicated_via_orthology	DOID:0111896	Diamond-Blackfan anemia 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	implicated_via_orthology	DOID:0081158	dilated cardiomyopathy 1MM						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913276	Ngly1	implicated_via_orthology	DOID:0060728	NGLY1-deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684944	Myrf	implicated_via_orthology	DOID:9834	hyperopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917979	Nos1ap	implicated_via_orthology	DOID:0112268	nephrotic syndrome type 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139090	Stard7	implicated_via_orthology	DOID:0111692	familial adult myoclonic epilepsy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147553	Uqcc3	implicated_via_orthology	DOID:0080118	mitochondrial complex III deficiency nuclear type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913944	Uqcrfs1	implicated_via_orthology	DOID:0111139	mitochondrial complex III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	implicated_via_orthology	DOID:0060763	X-linked juvenile retinoschisis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102854	Rpl5	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915526	Toe1	implicated_via_orthology	DOID:0060276	pontocerebellar hypoplasia type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97267	Myl4	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	implicated_via_orthology	DOID:0080609	anterior segment dysgenesis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	implicated_via_orthology	DOID:0110398	retinitis pigmentosa 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355330	Phgdh	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922670	Secisbp2	implicated_via_orthology	DOID:50	thyroid gland disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342274	Slc25a15	implicated_via_orthology	DOID:0050720	ornithine translocase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150380	Srd5a2	implicated_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916211	Phkg2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918351	Uvssa	implicated_via_orthology	DOID:0060240	UV-sensitive syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0080173	bladder exstrophy-epispadias-cloacal exstrophy complex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0050563	nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888984	Tbx21	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98894	Ucp1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137410	Twnk	implicated_via_orthology	DOID:12558	chronic progressive external ophthalmoplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99540	Tal2	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104897	Rest	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914154	Pccb	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:13774	Addison's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0111162	epidermal nevus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180855	Oas1f	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97588	Pou1f1	implicated_via_orthology	DOID:53	pituitary gland disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346023	Tlk2	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338039	Ovol2	implicated_via_orthology	DOID:0110855	posterior polymorphous corneal dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385079	Ndufs8	implicated_via_orthology	DOID:0112083	nuclear type mitochondrial complex I deficiency 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855692	Nono	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921932	Wdr35	implicated_via_orthology	DOID:12714	Ellis-Van Creveld syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916027	Tmem53	implicated_via_orthology	DOID:0112340	craniotubular dysplasia Ikegawa type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108543	Tfpi2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104513	Nqo2	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261910	Pibf1	implicated_via_orthology	DOID:0080279	Joubert syndrome 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107374	Pitx1	implicated_via_orthology	DOID:11836	clubfoot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921261	Slc25a27	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913389	Mymk	implicated_via_orthology	DOID:0080194	Carey-Fineman-Ziter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183102	Sardh	implicated_via_orthology	DOID:0112307	sarcosinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444989	Spg11	implicated_via_orthology	DOID:0110176	Charcot-Marie-Tooth disease axonal type 2X						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915800	Tefm	implicated_via_orthology	DOID:0060286	combined oxidative phosphorylation deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647394	Ssxb14	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339795	Smc3	implicated_via_orthology	DOID:0080507	Cornelia de Lange syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926483	Nectin1	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107246	Tinf2	implicated_via_orthology	DOID:0070026	Revesz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97430	Oas1b	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	implicated_via_orthology	DOID:0090006	renal coloboma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97269	Myl1	implicated_via_orthology	DOID:0081346	congenital myopathy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3603204	Piezo1	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442413	Thoc2	implicated_via_orthology	DOID:0112056	X-linked intellectual disability-short stature-overweight syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:12376	juvenile spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	implicated_via_orthology	DOID:0110698	hypotrichosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351627	Pdhx	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99461	Piga	implicated_via_orthology	DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336213	Mybpc1	implicated_via_orthology	DOID:0060654	lethal congenital contracture syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338829	Pex16	implicated_via_orthology	DOID:0080483	peroxisome biogenesis disorder 8A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194909	Rsph1	implicated_via_orthology	DOID:0110628	primary ciliary dyskinesia 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444036	Srcap	implicated_via_orthology	DOID:0111358	Floating-Harbor syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298231	Tpst1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202302	Pms1	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102724	Tpp2	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	implicated_via_orthology	DOID:0070316	Miura type epiphyseal chondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108067	Nkx2-1	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916233	Rint1	implicated_via_orthology	DOID:0080716	infantile liver failure syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97365	Pnp	implicated_via_orthology	DOID:5813	purine nucleoside phosphorylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97860	Rasa1	implicated_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685726	Pitpnm3	implicated_via_orthology	DOID:0111010	cone-rod dystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2671932	Tspear	implicated_via_orthology	DOID:0110540	autosomal recessive nonsyndromic deafness 98						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:0111936	immunodeficiency 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:0112206	developmental and epileptic encephalopathy 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446777	Ssxb8	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99879	Prkd1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	implicated_via_orthology	DOID:0070438	retinal macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150020	Rad51c	implicated_via_orthology	DOID:0111096	Fanconi anemia complementation group O						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446772	Ssxb3	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:0080979	arthrogryposis multiplex congenita-3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5295678	Pet117	implicated_via_orthology	DOID:0070504	mitochondrial complex IV deficiency nuclear type 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922820	Nhej1	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444879	Ripor2	implicated_via_orthology	DOID:0110551	autosomal dominant nonsyndromic deafness 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:0050820	atrioventricular block						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0111530	linear nevus sebaceous syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098791	Sepsecs	implicated_via_orthology	DOID:0060270	pontocerebellar hypoplasia type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:3450	cutaneous Paget's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	implicated_via_orthology	DOID:0110180	Charcot-Marie-Tooth disease axonal type 2CC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:0111425	restrictive cardiomyopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:0060230	basal ganglia calcification						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927230	Trio	implicated_via_orthology	DOID:0070074	autosomal dominant intellectual developmental disorder 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925230	Sbf1	implicated_via_orthology	DOID:0110194	Charcot-Marie-Tooth disease type 4B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277977	Ubr1	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927468	Samhd1	implicated_via_orthology	DOID:0060386	Chilblain lupus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	implicated_via_orthology	DOID:0081368	Paget's disease of bone 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142810	Ppip5k2	implicated_via_orthology	DOID:0111638	autosomal recessive nonsyndromic deafness 100						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:0070204	familial partial lipodystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336878	Taf1	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921605	Smchd1	implicated_via_orthology	DOID:0111193	facioscapulohumeral muscular dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12732	intermediate uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98779	Tnnc1	implicated_via_orthology	DOID:0110319	hypertrophic cardiomyopathy 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298395	Tspyl1	implicated_via_orthology	DOID:9007	sudden infant death syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139434	Mylk2	implicated_via_orthology	DOID:0110307	hypertrophic cardiomyopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917583	Polr1g	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3605986	Rad54b	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0111268	autosomal recessive hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97576	Phka1	implicated_via_orthology	DOID:0111040	glycogen storage disease IXd						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	implicated_via_orthology	DOID:0110353	retinitis pigmentosa 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681836	Polr3a	implicated_via_orthology	DOID:0081333	Wiedemann-Rautenstrauch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	implicated_via_orthology	DOID:0081374	nemaline myopathy 5B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	implicated_via_orthology	DOID:0081210	autosomal recessive intellectual developmental disorder 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921372	Tmem43	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107755	Neurod2	implicated_via_orthology	DOID:0112208	developmental and epileptic encephalopathy 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106403	Spg21	implicated_via_orthology	DOID:0060245	Mast syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153272	Trrap	implicated_via_orthology	DOID:0112166	autosomal dominant nonsyndromic deafness 75						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139607	Usp53	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96051	Serpind1	implicated_via_orthology	DOID:0050117	disease by infectious agent						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:0070045	Coffin-Siris syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150016	Spred1	implicated_via_orthology	DOID:0070484	Legius syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040669	Thoc2l	implicated_via_orthology	DOID:0112056	X-linked intellectual disability-short stature-overweight syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0111074	progressive familial heart block type IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933199	Setbp1	implicated_via_orthology	DOID:0070059	autosomal dominant intellectual developmental disorder 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98890	Uba1	implicated_via_orthology	DOID:0080828	VEXAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385332	Uroc1	implicated_via_orthology	DOID:0112180	urocanase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196365	Nus1	implicated_via_orthology	DOID:0080227	autosomal dominant intellectual developmental disorder 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	implicated_via_orthology	DOID:0050463	campomelic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:0110109	atrial heart septal defect 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3783195	Sp110-ps2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328337	Orc1	implicated_via_orthology	DOID:0080512	Meier-Gorlin syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97512	Pcsk2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929481	Slc22a21	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99540	Tal2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919023	Ugt2b1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040688	Slc7a14	implicated_via_orthology	DOID:0110374	retinitis pigmentosa 68						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	implicated_via_orthology	DOID:10811	nasal cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105090	Slc6a5	implicated_via_orthology	DOID:0060698	hyperekplexia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921382	Rnf6	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97549	Pfn1	implicated_via_orthology	DOID:0060209	amyotrophic lateral sclerosis type 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384836	Nepro	implicated_via_orthology	DOID:0080963	anauxetic dysplasia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:0111619	combined D-2- and L-2-hydroxyglutaric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	implicated_via_orthology	DOID:0070466	carpal tunnel syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0050766	choreaacanthocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444417	Sh3tc2	implicated_via_orthology	DOID:0110183	Charcot-Marie-Tooth disease type 4C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104897	Rest	implicated_via_orthology	DOID:0080280	gingival fibromatosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384303	Rp1l1	implicated_via_orthology	DOID:0112145	retinitis pigmentosa 88						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916951	Slc7a6os	implicated_via_orthology	DOID:891	progressive myoclonus epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88283	Serpinh1	implicated_via_orthology	DOID:0110346	osteogenesis imperfecta type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096393	Snai2	implicated_via_orthology	DOID:3263	piebaldism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98512	Ubtf	implicated_via_orthology	DOID:0070474	childhood-onset neurodegeneration with brain atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:11695	portal vein thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859307	Unc93b1	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97272	Myl2	implicated_via_orthology	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:0110826	Usher syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859638	Pqbp1	implicated_via_orthology	DOID:0060179	Renpenning syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095411	Nup214	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9663	aphthous stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647394	Ssxb14	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315213	Nrip1	implicated_via_orthology	DOID:0080205	CAKUT						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313291	Vezf1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:0060075	estrogen-receptor positive breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153588	Ppp1r3a	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344349	Rnf216	implicated_via_orthology	DOID:0111587	Gordon Holmes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915255	Naa10	implicated_via_orthology	DOID:0111799	syndromic microphthalmia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913739	Rpl35	implicated_via_orthology	DOID:0111886	Diamond-Blackfan anemia 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106022	Rpl26	implicated_via_orthology	DOID:0111892	Diamond-Blackfan anemia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	implicated_via_orthology	DOID:0111948	immunodeficiency 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	implicated_via_orthology	DOID:0110408	retinitis pigmentosa 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914517	Uqcc2	implicated_via_orthology	DOID:0080116	mitochondrial complex III deficiency nuclear type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:0112378	muscular dystrophy-dystroglycanopathy type B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	implicated_via_orthology	DOID:0080698	Teebi hypertelorism syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:0110032	autosomal dominant Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	implicated_via_orthology	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0081354	congenital myopathy 22A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923364	Sp110	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3608325	Pdzd7	implicated_via_orthology	DOID:0111635	autosomal recessive nonsyndromic deafness 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921700	Pank2	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442751	Slc22a19	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109282	Speg	implicated_via_orthology	DOID:0111222	centronuclear myopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914831	Tbc1d23	implicated_via_orthology	DOID:0112324	pontocerebellar hypoplasia type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149330	Slc5a5	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446190	Nup188	implicated_via_orthology	DOID:0081272	Sandestig-Stefanova syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98810	Tpm2	implicated_via_orthology	DOID:0111597	distal arthrogryposis type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3607791	Rft1	implicated_via_orthology	DOID:0080566	congenital disorder of glycosylation In						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148050	Nexmif	implicated_via_orthology	DOID:0112044	non-syndromic X-linked intellectual disability 98						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109571	Tulp1	implicated_via_orthology	DOID:0110189	Leber congenital amaurosis 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140260	Pcsk9	implicated_via_orthology	DOID:1390	hypobetalipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921903	Pomk	implicated_via_orthology	DOID:0111235	congenital muscular dystrophy-dystroglycanopathy type A12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	implicated_via_orthology	DOID:2566	corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142454	Usb1	implicated_via_orthology	DOID:0060551	poikiloderma with neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921692	Sgms2	implicated_via_orthology	DOID:0080721	calvarial doughnut lesions with bone fragility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:4511	breast angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926178	Pigt	implicated_via_orthology	DOID:0080140	multiple congenital anomalies-hypotonia-seizures syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:4677	keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920551	Ttc29	implicated_via_orthology	DOID:0111923	spermatogenic failure 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180860	Oas1a	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3615306	Pet100	implicated_via_orthology	DOID:0070498	mitochondrial complex IV deficiency nuclear type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0111554	spondylometaphyseal dysplasia Kozlowski type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919276	Trmu	implicated_via_orthology	DOID:0080716	infantile liver failure syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0080336	mitochondrial DNA depletion syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655711	Rbm28	implicated_via_orthology	DOID:0112244	alopecia, neurologic defects, and endocrinopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109353	Ufd1	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	implicated_via_orthology	DOID:0110285	autosomal recessive limb-girdle muscular dystrophy type 2Q						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353576	Pik3cg	implicated_via_orthology	DOID:0050211	swine influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336878	Taf1	implicated_via_orthology	DOID:0090057	X-linked dystonia-parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:0111490	combined oxidative phosphorylation deficiency 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:0080379	nephrotic syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354175	Txnrd1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922946	Prpf6	implicated_via_orthology	DOID:0110411	retinitis pigmentosa 60						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100881	Prss12	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:0111909	autosomal dominant thrombophilia due to protein C deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:4586	familial meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915549	Vps53	implicated_via_orthology	DOID:0060271	pontocerebellar hypoplasia type 2E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109526	Trpc3	implicated_via_orthology	DOID:0111744	cerebellar ataxia type 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278340	Rpl21	implicated_via_orthology	DOID:0110709	hypotrichosis 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859645	Usp27x	implicated_via_orthology	DOID:0112036	non-syndromic X-linked intellectual disability 105						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0111627	DOORS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	implicated_via_orthology	DOID:0110191	Charcot-Marie-Tooth disease type 4B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441738	Npsr1	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925947	Pus7	implicated_via_orthology	DOID:0081265	intellectual developmental disorder with abnormal behavior, microcephaly, and short stature						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97512	Pcsk2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	implicated_via_orthology	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	implicated_via_orthology	DOID:0080505	Cornelia de Lange syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:3672	rhabdoid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97576	Phka1	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446779	Ssxb10	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109490	Sms	implicated_via_orthology	DOID:0060802	syndromic X-linked intellectual disability Snyder type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891698	Pnkp	implicated_via_orthology	DOID:0080457	microcephaly, seizures, and developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913476	Trappc2	implicated_via_orthology	DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99422	Rapsn	implicated_via_orthology	DOID:0111378	fetal akinesia deformation sequence syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928486	Tdo2	implicated_via_orthology	DOID:0111703	familial hypertryptophanemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:0080109	infantile myofibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914166	Ndufb7	implicated_via_orthology	DOID:0112065	nuclear type mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914082	Rsph3a	implicated_via_orthology	DOID:0110603	primary ciliary dyskinesia 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:1394	urinary schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894806	Mylk	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197010	Sumo1	implicated_via_orthology	DOID:0080403	orofacial cleft 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97548	Pfkm	implicated_via_orthology	DOID:11721	glycogen storage disease VII						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98848	Tshb	implicated_via_orthology	DOID:0070123	congenital nongoitrous hypothyroidism 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97712	Prrx1	implicated_via_orthology	DOID:0060341	agnathia-otocephaly complex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355330	Phgdh	implicated_via_orthology	DOID:0080076	Neu-Laxova syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351628	Rps26	implicated_via_orthology	DOID:0111888	Diamond-Blackfan anemia 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97492	Pax8	implicated_via_orthology	DOID:0070124	congenital nongoitrous hypothyroidism 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:0070082	schizophrenia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913431	Nop10	implicated_via_orthology	DOID:0070015	autosomal recessive dyskeratosis congenita 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:0050657	Bannayan-Riley-Ruvalcaba syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102757	Try4	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97429	Oas1g	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099438	Nsdhl	implicated_via_orthology	DOID:0111822	CHILD syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140279	Tdrd7	implicated_via_orthology	DOID:0110247	cataract 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:0112061	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334433	Pi4kb	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098827	Reep1	implicated_via_orthology	DOID:0111205	autosomal dominant distal hereditary motor neuronopathy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449316	Syne2	implicated_via_orthology	DOID:0070250	autosomal dominant Emery-Dreifuss muscular dystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	implicated_via_orthology	DOID:0110415	retinitis pigmentosa 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105943	Rpl10	implicated_via_orthology	DOID:0080241	syndromic X-linked mental retardation 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153816	Strc	implicated_via_orthology	DOID:0110471	autosomal recessive nonsyndromic deafness 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714359	Srp54c	implicated_via_orthology	DOID:0112135	severe congenital neutropenia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0111552	scapuloperoneal spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:4531	mucoepidermoid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149820	Nans	implicated_via_orthology	DOID:0080576	spondyloepimetaphyseal dysplasia, Genevieve-type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648074	Tmem240	implicated_via_orthology	DOID:0050972	spinocerebellar ataxia type 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:0081139	agammaglobulinemia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913266	Tk2	implicated_via_orthology	DOID:0080120	mitochondrial DNA depletion syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914907	Rabl3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202713	Rhag	implicated_via_orthology	DOID:0050641	Rh deficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316650	Slc37a4	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	implicated_via_orthology	DOID:0060466	gingival fibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:0111313	idiopathic generalized epilepsy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918029	Prdm5	implicated_via_orthology	DOID:0080729	brittle cornea syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442675	Rfx7	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109186	Ncf4	implicated_via_orthology	DOID:0070194	autosomal recessive chronic granulomatous disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916211	Phkg2	implicated_via_orthology	DOID:0111043	glycogen storage disease IXc						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261415	Sgpl1	implicated_via_orthology	DOID:0080265	nephrotic syndrome type 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930923	Slurp1	implicated_via_orthology	DOID:0060862	mal de Meleda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355311	Stag3	implicated_via_orthology	DOID:0112350	spermatogenic failure 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096573	Utp4	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385088	Smc5	implicated_via_orthology	DOID:0080688	mosaic variegated aneuploidy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860055	Panx1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180856	Oas1e	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915384	Upf3b	implicated_via_orthology	DOID:0060821	syndromic X-linked intellectual disability 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:0060867	macrocephaly-autism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681247	Tas2r118	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:0111343	lateral meningocele syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:0080335	mitochondrial DNA depletion syndrome 12b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859158	Pabpn1	implicated_via_orthology	DOID:11719	oculopharyngeal muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714357	Srp54b	implicated_via_orthology	DOID:0112135	severe congenital neutropenia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	implicated_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:0060354	Stormorken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:0080421	developmental and epileptic encephalopathy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917680	Tbce	implicated_via_orthology	DOID:0080722	Kenny-Caffey syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932137	Tnxb	implicated_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652860	Plekhg5	implicated_via_orthology	DOID:0111213	autosomal recessive distal hereditary motor neuronopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:0110112	atrial heart septal defect 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330233	Tcap	implicated_via_orthology	DOID:0110328	hypertrophic cardiomyopathy 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144805	Vipas39	implicated_via_orthology	DOID:0111354	arthrogryposis, renal dysfunction, and cholestasis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97577	Phka2	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915408	Tecr	implicated_via_orthology	DOID:0081188	autosomal recessive intellectual developmental disorder 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	implicated_via_orthology	DOID:0080981	arthrogryposis multiplex congenita-5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920045	Ttc19	implicated_via_orthology	DOID:0060351	mitochondrial complex III deficiency nuclear type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	implicated_via_orthology	DOID:0110338	osteogenesis imperfecta type 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	implicated_via_orthology	DOID:0050818	transcobalamin II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97438	Oprd1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	implicated_via_orthology	DOID:0080623	Heimler syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	implicated_via_orthology	DOID:0112237	lissencephaly 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860283	Ubqln2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354724	Sacs	implicated_via_orthology	DOID:0050946	Charlevoix-Saguenay spastic ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:14453	farmer's lung						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915582	Sdhaf1	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329042	Sgce	implicated_via_orthology	DOID:0090034	myoclonic dystonia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919379	Pex13	implicated_via_orthology	DOID:0080485	peroxisome biogenesis disorder 11A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443219	Tmem260	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889800	Myot	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914514	Ndufb8	implicated_via_orthology	DOID:0112080	nuclear type mitochondrial complex I deficiency 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277134	Per3	implicated_via_orthology	DOID:0110013	advanced sleep phase syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:1192	peripheral nervous system neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103248	Phc1	implicated_via_orthology	DOID:0070287	primary autosomal recessive microcephaly 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894282	Sstr5	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:9240	erythromelalgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917575	Pigw	implicated_via_orthology	DOID:0070432	hyperphosphatasia with impaired intellectual development syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918982	Vps11	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336883	Smad6	implicated_via_orthology	DOID:0060912	craniosynostosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0111240	congenital muscular dystrophy-dystroglycanopathy type A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	implicated_via_orthology	DOID:0080270	autosomal dominant nonsyndromic deafness 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	implicated_via_orthology	DOID:0110249	cataract 11 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934816	Tex15	implicated_via_orthology	DOID:0111920	spermatogenic failure 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915140	Ufm1	implicated_via_orthology	DOID:0080296	hypomyelinating leukodystrophy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:11202	primary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918568	Pmpca	implicated_via_orthology	DOID:0080061	autosomal recessive spinocerebellar ataxia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916948	Slc52a3	implicated_via_orthology	DOID:0080785	Brown-Vialetto-Van Laere syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316659	St3gal3	implicated_via_orthology	DOID:0080414	developmental and epileptic encephalopathy 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	implicated_via_orthology	DOID:2978	carbohydrate metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289288	Slc52a2	implicated_via_orthology	DOID:8454	riboflavin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:0080533	Carney-Stratakis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108173	Prkg2	implicated_via_orthology	DOID:0112295	spondylometaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684894	Nhs	implicated_via_orthology	DOID:0060599	Nance-Horan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923507	Slc38a3	implicated_via_orthology	DOID:0070388	developmental and epileptic encephalopathy 102						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	implicated_via_orthology	DOID:0110552	autosomal dominant nonsyndromic deafness 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914347	Rps10	implicated_via_orthology	DOID:0111884	Diamond-Blackfan anemia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:3491	Turner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0111522	autosomal recessive progressive external ophthalmoplegia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914300	Nkap	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0111589	COACH syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349165	Sdc2	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685847	Pjvk	implicated_via_orthology	DOID:0110511	autosomal recessive nonsyndromic deafness 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349390	Pclo	implicated_via_orthology	DOID:0060272	pontocerebellar hypoplasia type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	implicated_via_orthology	DOID:0112290	spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890505	Plin1	implicated_via_orthology	DOID:0070205	familial partial lipodystrophy type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921932	Wdr35	implicated_via_orthology	DOID:0080804	cranioectodermal dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2665170	P2rx2	implicated_via_orthology	DOID:0110567	autosomal dominant nonsyndromic deafness 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97857	Rarb	implicated_via_orthology	DOID:0111800	syndromic microphthalmia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039785	Syngap1	implicated_via_orthology	DOID:0070035	autosomal dominant intellectual developmental disorder 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927868	Pex14	implicated_via_orthology	DOID:0080487	peroxisome biogenesis disorder 13A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860486	Tdp2	implicated_via_orthology	DOID:0111613	autosomal recessive spinocerebellar ataxia 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0110108	atrial heart septal defect 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933281	Sycp2	implicated_via_orthology	DOID:0070188	spermatogenic failure 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924983	Rnf170	implicated_via_orthology	DOID:0112345	hereditary spastic paraplegia 85						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108176	Prx	implicated_via_orthology	DOID:0050540	Charcot-Marie-Tooth disease type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108415	Pafah1b2	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040695	Palb2	implicated_via_orthology	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0110117	autoimmune lymphoproliferative syndrome type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924467	Rspo4	implicated_via_orthology	DOID:0080082	nonsyndromic congenital nail disorder 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97800	Pthlh	implicated_via_orthology	DOID:0110976	brachydactyly type E2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914838	Rnf41	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913993	Rnf220	implicated_via_orthology	DOID:0070397	hypomyelinating leukodystrophy 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	implicated_via_orthology	DOID:0070225	progressive familial intrahepatic cholestasis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919210	Myh14	implicated_via_orthology	DOID:0110573	autosomal dominant nonsyndromic deafness 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349423	Racgap1	implicated_via_orthology	DOID:1338	congenital dyserythropoietic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385054	Pex6	implicated_via_orthology	DOID:0080624	Heimler syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155865	Rrm2b	implicated_via_orthology	DOID:0080127	mitochondrial DNA depletion syndrome 8a						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914380	Ndufa6	implicated_via_orthology	DOID:0112097	nuclear type mitochondrial complex I deficiency 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346349	Sh3bp2	implicated_via_orthology	DOID:1856	cherubism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924983	Rnf170	implicated_via_orthology	DOID:0111170	autosomal dominant sensory ataxia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919665	Sgo1	implicated_via_orthology	DOID:0060339	chronic atrial and intestinal dysrhythmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684956	Sohlh1	implicated_via_orthology	DOID:0111925	spermatogenic failure 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202713	Rhag	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153816	Strc	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915068	Tmem70	implicated_via_orthology	DOID:0060331	mitochondrial complex V (ATP synthase) deficiency nuclear type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0110433	dilated cardiomyopathy 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	implicated_via_orthology	DOID:0080119	mitochondrial DNA depletion syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97600	Prkch	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098434	Rgs5	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	implicated_via_orthology	DOID:0110005	Leber congenital amaurosis 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335106	Pikfyve	implicated_via_orthology	DOID:0060448	Fleck corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916858	Sec24d	implicated_via_orthology	DOID:0060438	Cole-Carpenter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684944	Myrf	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108056	Nfia	implicated_via_orthology	DOID:0060409	NFIA-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:999	hypereosinophilic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103559	Sox18	implicated_via_orthology	DOID:0111361	hypotrichosis-lymphedema-telangiectasia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915581	Stn1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:14768	Saethre-Chotzen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99557	Pde4b	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	implicated_via_orthology	DOID:0080059	autosomal recessive spinocerebellar ataxia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926334	Ppp2r1a	implicated_via_orthology	DOID:0070066	autosomal dominant intellectual developmental disorder 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346317	Nr2e3	implicated_via_orthology	DOID:0110399	retinitis pigmentosa 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917036	Tprkb	implicated_via_orthology	DOID:0080247	Galloway-Mowat syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:7575	pancreatic intraductal papillary-mucinous neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929215	Vps41	implicated_via_orthology	DOID:0070410	autosomal recessive spinocerebellar ataxia 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153568	Sp7	implicated_via_orthology	DOID:0110348	osteogenesis imperfecta type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138915	Myl9	implicated_via_orthology	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142581	Nsd3	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	implicated_via_orthology	DOID:0110948	Waardenburg syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:0050633	ocular albinism 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3608325	Pdzd7	implicated_via_orthology	DOID:0110838	Usher syndrome type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97514	Pcsk4	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306775	Sucla2	implicated_via_orthology	DOID:0080124	mitochondrial DNA depletion syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924076	Nubpl	implicated_via_orthology	DOID:0112088	nuclear type mitochondrial complex I deficiency 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:3314	angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2158502	Usp48	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919964	Nup37	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915921	Pcyt2	implicated_via_orthology	DOID:0112343	hereditary spastic paraplegia 82						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894698	Sgca	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:0050529	adult spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109279	Nnt	implicated_via_orthology	DOID:0080620	familial glucocorticoid deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443198	Slitrk6	implicated_via_orthology	DOID:0111628	high myopia-sensorineural deafness syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105956	Pde6c	implicated_via_orthology	DOID:0050572	cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99542	Usf1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:0050869	villous adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336213	Mybpc1	implicated_via_orthology	DOID:0111598	distal arthrogryposis type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:3755	antithrombin III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920999	Ttc7	implicated_via_orthology	DOID:14671	multiple intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098658	Stag1	implicated_via_orthology	DOID:0080238	autosomal dominant intellectual developmental disorder 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142075	Nars2	implicated_via_orthology	DOID:0111641	autosomal recessive nonsyndromic deafness 94						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342291	Rlim	implicated_via_orthology	DOID:0112042	Tonne-Kalscheuer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97268	Myl3	implicated_via_orthology	DOID:0110314	hypertrophic cardiomyopathy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106183	Ocln	implicated_via_orthology	DOID:0050656	pseudo-TORCH syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102643	Myh11	implicated_via_orthology	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336172	Tbl1x	implicated_via_orthology	DOID:0111758	Y-linked deafness 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:0050433	fatal familial insomnia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3032636	Ugt1a7c	implicated_via_orthology	DOID:4988	alcoholic pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:0060368	Parkinson's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88283	Serpinh1	implicated_via_orthology	DOID:0111144	preterm premature rupture of the membranes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100882	Phox2b	implicated_via_orthology	DOID:0060731	congenital central hypoventilation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914840	Tctn3	implicated_via_orthology	DOID:0110987	Joubert syndrome 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894697	Rad54l	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349470	Trpc7	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:0111374	selective pituitary thyroid hormone resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98881	Tyrp1	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685233	Ptchd1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:0090136	complex cortical dysplasia with other brain malformations 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685973	Trim71	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913529	Tmem218	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580629	Ugt1a6b	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097692	Opn1mw	implicated_via_orthology	DOID:13909	red-green color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684313	Togaram1	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:9649	congenital nystagmus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645174	Ndufa11b	implicated_via_orthology	DOID:0112094	nuclear type mitochondrial complex I deficiency 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927197	Shoc2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:0080351	CLOVES syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921612	Spag17	implicated_via_orthology	DOID:0112337	spermatogenic failure 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913461	Rpl3l	implicated_via_orthology	DOID:0081160	dilated cardiomyopathy 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3783243	Sp110-ps1	implicated_via_orthology	DOID:0112254	hepatic venoocclusive disease with immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920020	Tmem216	implicated_via_orthology	DOID:0110988	Joubert syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	implicated_via_orthology	DOID:0110955	Waardenburg syndrome type 4C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929473	Rgr	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150308	Plcz1	implicated_via_orthology	DOID:0070174	spermatogenic failure 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	implicated_via_orthology	DOID:0110280	autosomal recessive limb-girdle muscular dystrophy type 2F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97303	Nek1	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97245	Mxi1	implicated_via_orthology	DOID:3512	neurofibrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914542	Pigc	implicated_via_orthology	DOID:0081223	glycosylphosphatidylinositol biosynthesis defect 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98431	Sult1e1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337120	Slc7a7	implicated_via_orthology	DOID:0060439	lysinuric protein intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920918	Ttc21b	implicated_via_orthology	DOID:0110088	asphyxiating thoracic dystrophy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0110532	autosomal recessive nonsyndromic deafness 86						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343103	Ndufa2	implicated_via_orthology	DOID:0112076	nuclear type mitochondrial complex I deficiency 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153470	Scgb3a2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109353	Ufd1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:12678	hypercalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099464	Ssr4	implicated_via_orthology	DOID:0080574	congenital disorder of glycosylation Iy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98460	Syn1	implicated_via_orthology	DOID:0112029	non-syndromic X-linked intellectual disability 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679446	Slitrk1	implicated_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104871	Ppp1cb	implicated_via_orthology	DOID:0080693	Noonan syndrome-like disorder with loose anagen hair 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443588	Pik3r5	implicated_via_orthology	DOID:0060557	ataxia with oculomotor apraxia type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	implicated_via_orthology	DOID:8866	actinic keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913730	Rpl15	implicated_via_orthology	DOID:0111882	Diamond-Blackfan anemia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925542	Orai1	implicated_via_orthology	DOID:0080686	tubular aggregate myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385061	Pcare	implicated_via_orthology	DOID:0110364	retinitis pigmentosa 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98809	Tpm1	implicated_via_orthology	DOID:0110309	hypertrophic cardiomyopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929481	Slc22a21	implicated_via_orthology	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97744	Por	implicated_via_orthology	DOID:0050462	Antley-Bixler syndrome with disordered steroidogenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913382	Prorp	implicated_via_orthology	DOID:0070427	combined oxidative phosphorylation deficiency 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97770	Prodh	implicated_via_orthology	DOID:0080542	hyperprolinemia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144113	Tmem199	implicated_via_orthology	DOID:0070268	congenital disorder of glycosylation type IIp						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137410	Twnk	implicated_via_orthology	DOID:0080126	mitochondrial DNA depletion syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337080	Ncor2	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098610	Psmc3ip	implicated_via_orthology	DOID:0080495	ovarian dysgenesis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:0080815	childhood-onset asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:0110999	Joubert syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915743	Ndufaf4	implicated_via_orthology	DOID:0112077	nuclear type mitochondrial complex I deficiency 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921004	Thap1	implicated_via_orthology	DOID:0090039	torsion dystonia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351500	Nup62	implicated_via_orthology	DOID:4751	striatonigral degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919057	Tars2	implicated_via_orthology	DOID:0111465	combined oxidative phosphorylation deficiency 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919107	Slc17a9	implicated_via_orthology	DOID:3805	porokeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890149	Tpm3	implicated_via_orthology	DOID:0080102	congenital myopathy 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:4992	optic nerve glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441730	Tbl1xr1	implicated_via_orthology	DOID:0081362	Pierpont syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:0080420	developmental and epileptic encephalopathy 62						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289196	Rnf213	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98443	Surf1	implicated_via_orthology	DOID:0070491	mitochondrial complex IV deficiency nuclear type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153072	Trim37	implicated_via_orthology	DOID:0050436	mulibrey nanism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916922	Txndc15	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925850	Pde6h	implicated_via_orthology	DOID:0081025	retinal cone dystrophy 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915467	Prrc2a	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328317	Trex1	implicated_via_orthology	DOID:0111567	retinal vasculopathy with cerebral leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:10930	borderline personality disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894698	Sgca	implicated_via_orthology	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	implicated_via_orthology	DOID:0080379	nephrotic syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443241	Ndufs1	implicated_via_orthology	DOID:0112068	nuclear type mitochondrial complex I deficiency 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306785	Ugdh	implicated_via_orthology	DOID:0112219	developmental and epileptic encephalopathy 84						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181182	Nup155	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	implicated_via_orthology	DOID:0110832	Usher syndrome type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:1062	Fanconi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388481	Ppp2r5d	implicated_via_orthology	DOID:0070065	autosomal dominant intellectual developmental disorder 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648915	Sult2a6	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97930	Rlbp1	implicated_via_orthology	DOID:8499	night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444232	Poglut1	implicated_via_orthology	DOID:0080762	autosomal recessive limb-girdle muscular dystrophy type 2Z						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0110435	dilated cardiomyopathy 1GG						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109258	Nprl3	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104897	Rest	implicated_via_orthology	DOID:0110556	autosomal dominant nonsyndromic deafness 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924007	Trdn	implicated_via_orthology	DOID:0060679	catecholaminergic polymorphic ventricular tachycardia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	implicated_via_orthology	DOID:0060455	Thiel-Behnke corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144865	Tecpr2	implicated_via_orthology	DOID:0110801	hereditary spastic paraplegia 49						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858430	Scarf2	implicated_via_orthology	DOID:0111699	Van den Ende-Gupta syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921325	Syce1	implicated_via_orthology	DOID:0080869	primary ovarian insufficiency 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647985	Rpl10l	implicated_via_orthology	DOID:0112356	spermatogenic failure 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	implicated_via_orthology	DOID:0111019	cone-rod dystrophy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672033	Thsd4	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95909	Slc39a7	implicated_via_orthology	DOID:0081141	agammaglobulinemia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916856	Mtfmt	implicated_via_orthology	DOID:0112090	nuclear type mitochondrial complex I deficiency 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98494	Tbx2	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103021	Recql	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:1558	angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353479	Slc22a4	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918017	Prpf3	implicated_via_orthology	DOID:0110356	retinitis pigmentosa 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:3996	urinary system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685619	Gm773	implicated_via_orthology	DOID:0070176	spermatogenic failure 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667725	Serpina10	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0111645	Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648378	Sult2a5	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261434	Olr1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338015	Sort1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:6498	seborrheic keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893591	Neurog3	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:0050648	atelosteogenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	implicated_via_orthology	DOID:0111731	familial episodic pain syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890816	Vsx1	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136772	Vps16	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096875	Wdfy3	implicated_via_orthology	DOID:0070295	primary autosomal dominant microcephaly 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159344	Vangl1	implicated_via_orthology	DOID:0080700	caudal regression syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151053	Serpinb7	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384851	Slc39a14	implicated_via_orthology	DOID:0080537	hypermanganesemia with dystonia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920963	Rbm20	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685058	Slc30a10	implicated_via_orthology	DOID:0080536	hypermanganesemia with dystonia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891158	Tbx19	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98431	Sult1e1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930252	Srd5a3	implicated_via_orthology	DOID:0080568	congenital disorder of glycosylation Iq						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328359	Pkp1	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321392	Pex7	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	implicated_via_orthology	DOID:0070209	hereditary lymphedema ID						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107807	Uqcrq	implicated_via_orthology	DOID:0080113	mitochondrial complex III deficiency nuclear type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387995	Nek9	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316706	Nfs1	implicated_via_orthology	DOID:0070425	combined oxidative phosphorylation deficiency 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146110	Washc5	implicated_via_orthology	DOID:0060571	Ritscher-Schinzel syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684956	Sohlh1	implicated_via_orthology	DOID:0080497	ovarian dysgenesis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859214	Pmm2	implicated_via_orthology	DOID:5212	congenital disorder of glycosylation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	implicated_via_orthology	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:0110040	Alzheimer's disease 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98443	Surf1	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101877	Tcf12	implicated_via_orthology	DOID:0090070	hypogonadotropic hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109571	Tulp1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651811	Tph2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107877	Prkcsh	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	implicated_via_orthology	DOID:0110943	autosomal recessive osteopetrosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914453	Nde1	implicated_via_orthology	DOID:0112235	lissencephaly 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104574	Ptprj	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107162	Ppp3cc	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	implicated_via_orthology	DOID:0070098	oculocutaneous albinism type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350925	Sec23b	implicated_via_orthology	DOID:0081003	Cowden syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354961	Synj1	implicated_via_orthology	DOID:0060898	Parkinson's disease 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098272	Rnasel	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924197	Ndufaf6	implicated_via_orthology	DOID:0080761	Fanconi renotubular syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354178	Prok2	implicated_via_orthology	DOID:0090077	hypogonadotropic hypogonadism 4 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915677	Slc39a13	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927616	Trps1	implicated_via_orthology	DOID:0080376	trichorhinophalangeal syndrome type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104778	Plcb3	implicated_via_orthology	DOID:0112303	spondylometaphyseal dysplasia with corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276575	Ptdss1	implicated_via_orthology	DOID:0111507	Lenz-Majewski hyperostotic dwarfism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	implicated_via_orthology	DOID:0070168	spermatogenic failure 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:0110312	hypertrophic cardiomyopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:1996	rectum adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893591	Neurog3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:0080633	developmental cardiac valvular defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98477	Tacr2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:0111353	arthrogryposis, renal dysfunction, and cholestasis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3603820	Tctn1	implicated_via_orthology	DOID:0110982	Joubert syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918951	Pnpt1	implicated_via_orthology	DOID:0110521	autosomal recessive nonsyndromic deafness 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97273	Mylpf	implicated_via_orthology	DOID:0112190	distal arthrogryposis type 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102674	Umod	implicated_via_orthology	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109331	Nxn	implicated_via_orthology	DOID:0060254	Robinow syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:0110165	Charcot-Marie-Tooth disease type 2E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201689	Tapbp	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298395	Tspyl1	implicated_via_orthology	DOID:14447	gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923457	Tmem98	implicated_via_orthology	DOID:0080634	nanophthalmos						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99438	Opn1sw	implicated_via_orthology	DOID:11661	blue color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915843	Polrmt	implicated_via_orthology	DOID:0070428	combined oxidative phosphorylation deficiency 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:0111564	hypoplastic or aplastic tibia with polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	implicated_via_orthology	DOID:0081240	peroxisome biogenesis disorder 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2388	renal artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890646	Nek8	implicated_via_orthology	DOID:0111120	nephronophthisis 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0081355	congenital myopathy 22B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918101	Tbc1d8b	implicated_via_orthology	DOID:0070357	nephrotic syndrome type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:0111090	Fanconi anemia complementation group R						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917057	Trim32	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106684	Slc18a1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442995	Rbbp8	implicated_via_orthology	DOID:0070013	Seckel syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684944	Myrf	implicated_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444934	Ppargc1b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095411	Nup214	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335073	Rnaseh1	implicated_via_orthology	DOID:0111515	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894323	Ranbp2	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:1932	Angelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:0050922	gastrointestinal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328317	Trex1	implicated_via_orthology	DOID:0060386	Chilblain lupus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106299	Slx4	implicated_via_orthology	DOID:0111092	Fanconi anemia complementation group P						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355311	Stag3	implicated_via_orthology	DOID:0080865	primary ovarian insufficiency 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385054	Pex6	implicated_via_orthology	DOID:0080479	peroxisome biogenesis disorder 4A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98365	Sox3	implicated_via_orthology	DOID:0111779	X-linked panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333818	Rps7	implicated_via_orthology	DOID:0111881	Diamond-Blackfan anemia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196458	Scarb2	implicated_via_orthology	DOID:0111444	progressive myoclonus epilepsy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	implicated_via_orthology	DOID:11105	fundus albipunctatus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:9007	sudden infant death syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892003	Tcof1	implicated_via_orthology	DOID:2908	Treacher Collins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915541	Mto1	implicated_via_orthology	DOID:0111480	combined oxidative phosphorylation deficiency 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:0090056	dystonia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931787	Scyl1	implicated_via_orthology	DOID:0111155	autosomal recessive spinocerebellar ataxia 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107164	Ppp3ca	implicated_via_orthology	DOID:0080472	developmental and epileptic encephalopathy 91						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917447	Srp68	implicated_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448607	Nyx	implicated_via_orthology	DOID:8499	night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339795	Smc3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97836	Qdpr	implicated_via_orthology	DOID:0081130	BH4-deficient hyperphenylalaninemia C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921382	Rnf6	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924909	Slc25a36	implicated_via_orthology	DOID:0081328	familial hyperinsulinemic hypoglycemia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891916	Plag1	implicated_via_orthology	DOID:14681	Silver-Russell syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916267	Prrt2	implicated_via_orthology	DOID:0090053	episodic kinesigenic dyskinesia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:0060900	Parkinson's disease 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328357	Unc119	implicated_via_orthology	DOID:0050572	cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679336	Satb2	implicated_via_orthology	DOID:0060428	SATB2-associated syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101877	Tcf12	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040695	Palb2	implicated_via_orthology	DOID:0111094	Fanconi anemia complementation group N						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:3529	congenital myopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97614	Plcd1	implicated_via_orthology	DOID:0080081	nonsyndromic congenital nail disorder 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	implicated_via_orthology	DOID:0112019	non-syndromic X-linked intellectual disability 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384919	Rxylt1	implicated_via_orthology	DOID:0111239	congenital muscular dystrophy-dystroglycanopathy type A10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684861	Nlrp1a	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:0050530	intermediate spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918017	Prpf3	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108413	Pde1c	implicated_via_orthology	DOID:0112165	autosomal dominant nonsyndromic deafness 74						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645854	Sult2a4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104513	Nqo2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99782	Nt5e	implicated_via_orthology	DOID:0111582	hereditary arterial and articular multiple calcification syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099835	Skic2	implicated_via_orthology	DOID:0111416	trichohepatoenteric syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:11162	respiratory failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	implicated_via_orthology	DOID:0110277	autosomal recessive limb-girdle muscular dystrophy type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:0080089	tubular aggregate myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:0080610	anterior segment dysgenesis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0060330	Rapp-Hodgkin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336884	Slc22a18	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097692	Opn1mw	implicated_via_orthology	DOID:0050679	blue cone monochromacy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351627	Pdhx	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919299	Tnfrsf13c	implicated_via_orthology	DOID:0081147	common variable immunodeficiency 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928486	Tdo2	implicated_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917057	Trim32	implicated_via_orthology	DOID:0110133	Bardet-Biedl syndrome 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328351	Nts	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321396	Pstpip1	implicated_via_orthology	DOID:0080519	PAPA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444671	Nipal4	implicated_via_orthology	DOID:0060715	autosomal recessive congenital ichthyosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9155	mucocutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106314	Tars1	implicated_via_orthology	DOID:0111870	nonphotosensitive trichothiodystrophy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	implicated_via_orthology	DOID:0111772	46,XY sex reversal 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107550	Sult2a2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684944	Myrf	implicated_via_orthology	DOID:0080634	nanophthalmos						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:0081001	Cowden syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682306	Naf1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97742	Pomc	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443028	Taf2	implicated_via_orthology	DOID:0081205	autosomal recessive intellectual developmental disorder 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891207	Plpbp	implicated_via_orthology	DOID:0080769	early-onset vitamin B6-dependent epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442406	Ust	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	implicated_via_orthology	DOID:0060648	anterior segment dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330305	Trpm1	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338041	Tfg	implicated_via_orthology	DOID:0110809	hereditary spastic paraplegia 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095408	Tuba3b	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921273	Rd3	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97891	Rfc1	implicated_via_orthology	DOID:2366	West Nile fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97822	Nectin2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97491	Pax7	implicated_via_orthology	DOID:0081351	congenital myopathy 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:12558	chronic progressive external ophthalmoplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107486	Pex2	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97578	Phkb	implicated_via_orthology	DOID:0111041	glycogen storage disease IXb						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913302	Sdhc	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346006	Ptpa	implicated_via_orthology	DOID:0070486	Parkinson's disease 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:2736	Hajdu-Cheney syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916952	Ndufaf1	implicated_via_orthology	DOID:0112089	nuclear type mitochondrial complex I deficiency 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441730	Tbl1xr1	implicated_via_orthology	DOID:0070071	autosomal dominant intellectual developmental disorder 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920230	Wdr11	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	implicated_via_orthology	DOID:0110544	autosomal dominant nonsyndromic deafness 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3603204	Piezo1	implicated_via_orthology	DOID:0111576	dehydrated hereditary stomatocytosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922847	Ndufaf2	implicated_via_orthology	DOID:0112075	nuclear type mitochondrial complex I deficiency 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919900	Mtrfr	implicated_via_orthology	DOID:0110807	hereditary spastic paraplegia 55						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3582959	Nlrp1b	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107181	Slc26a3	implicated_via_orthology	DOID:13250	diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	implicated_via_orthology	DOID:0111801	syndromic microphthalmia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	implicated_via_orthology	DOID:0111132	focal segmental glomerulosclerosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98227	Sag	implicated_via_orthology	DOID:8498	hereditary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:0060474	familial erythrocytosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443480	Setx	implicated_via_orthology	DOID:0050755	spinocerebellar ataxia with axonal neuropathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443730	Tnrc6b	implicated_via_orthology	DOID:13560	subserous uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98385	Spta1	implicated_via_orthology	DOID:12971	hereditary spherocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860283	Ubqln2	implicated_via_orthology	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98430	Sult2a1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0110646	long QT syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:12859	choreatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354721	Slc25a13	implicated_via_orthology	DOID:0070341	neonatal-onset type II citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915040	Rab39b	implicated_via_orthology	DOID:0111781	Waisman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178563	Nt5c2	implicated_via_orthology	DOID:0110797	hereditary spastic paraplegia 45						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:0111946	immunodeficiency 31C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	implicated_via_orthology	DOID:0111992	immunodeficiency 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97836	Qdpr	implicated_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345297	Slc35a2	implicated_via_orthology	DOID:0070265	congenital disorder of glycosylation type IIm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321392	Pex7	implicated_via_orthology	DOID:0110851	rhizomelic chondrodysplasia punctata type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917689	Taf15	implicated_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136886	Rtn4r	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345138	Spry2	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98386	Sptan1	implicated_via_orthology	DOID:0080438	developmental and epileptic encephalopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925831	Utp23	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109573	Tep1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:0081079	ectodermal dysplasia and immunodeficiency 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445059	Slc25a21	implicated_via_orthology	DOID:0070449	mitochondrial DNA depletion syndrome 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97829	Pygl	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341840	Six6	implicated_via_orthology	DOID:0080635	optic disc anomalies with retinal and/or macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679262	Rgma	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107558	Sema3a	implicated_via_orthology	DOID:0090080	hypogonadotropic hypogonadism 16 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931028	Recql4	implicated_via_orthology	DOID:0050654	Baller-Gerold syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102643	Myh11	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918951	Pnpt1	implicated_via_orthology	DOID:0111467	combined oxidative phosphorylation deficiency 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	implicated_via_orthology	DOID:0112014	congenital megabladder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0110315	hypertrophic cardiomyopathy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0111118	nephronophthisis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444777	Ncaph	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684988	Pex10	implicated_via_orthology	DOID:0080481	peroxisome biogenesis disorder 6A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97830	Pygm	implicated_via_orthology	DOID:2746	glycogen storage disease V						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:0080109	infantile myofibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891698	Pnkp	implicated_via_orthology	DOID:0081383	ataxia-oculomotor apraxia type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98769	Tlx1	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916737	Ndufaf5	implicated_via_orthology	DOID:0112096	nuclear type mitochondrial complex I deficiency 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919999	Tonsl	implicated_via_orthology	DOID:5684	spondyloepimetaphyseal dysplasia, Sponastrime type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	implicated_via_orthology	DOID:0111287	psoriasis 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0050864	non-arteritic anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:10609	rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918951	Pnpt1	implicated_via_orthology	DOID:0050974	spinocerebellar ataxia type 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:1930	Laurence-Moon syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107370	Stxbp2	implicated_via_orthology	DOID:0110925	familial hemophagocytic lymphohistiocytosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3027894	Rsph4a	implicated_via_orthology	DOID:0110602	primary ciliary dyskinesia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146110	Washc5	implicated_via_orthology	DOID:0110823	hereditary spastic paraplegia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261434	Olr1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97491	Pax7	implicated_via_orthology	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922028	Rrp7a	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:0060866	patterned macular dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344370	Ndufc2	implicated_via_orthology	DOID:0112065	nuclear type mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176887	Tlr8	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	implicated_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917488	Rnf168	implicated_via_orthology	DOID:0090113	RIDDLE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	implicated_via_orthology	DOID:0081366	Paget's disease of bone 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:3261	hyper IgE recurrent infection syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891158	Tbx19	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332247	Slc33a1	implicated_via_orthology	DOID:0110794	hereditary spastic paraplegia 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098808	Pex5	implicated_via_orthology	DOID:0080477	peroxisome biogenesis disorder 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858417	Sec61a1	implicated_via_orthology	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	implicated_via_orthology	DOID:0060601	alpha-2-plasmin inhibitor deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:8029	sporadic breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99833	Rab23	implicated_via_orthology	DOID:0060234	Carpenter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921749	Sost	implicated_via_orthology	DOID:0060251	sclerosteosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932575	Sp6	implicated_via_orthology	DOID:2187	amelogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98359	Sox11	implicated_via_orthology	DOID:0070057	Coffin-Siris syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98295	Shbg	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924894	Steep1	implicated_via_orthology	DOID:0112054	non-syndromic X-linked intellectual disability 107						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929646	Pex3	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929004	Stk4	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152213	Tirap	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	implicated_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277211	Tyrobp	implicated_via_orthology	DOID:0090112	Nasu-Hakola disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146189	Topors	implicated_via_orthology	DOID:0110391	retinitis pigmentosa 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:9834	hyperopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919900	Mtrfr	implicated_via_orthology	DOID:0111487	combined oxidative phosphorylation deficiency 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98927	Vcl	implicated_via_orthology	DOID:0110446	dilated cardiomyopathy 1W						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	implicated_via_orthology	DOID:0060010	Omenn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99666	Syt2	implicated_via_orthology	DOID:0110659	congenital myasthenic syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:3774	chordoid glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891158	Tbx19	implicated_via_orthology	DOID:0080150	adrenocorticotropic hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095733	Pros1	implicated_via_orthology	DOID:0111905	autosomal recessive thrombophilia due to protein S deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384308	Pdk3	implicated_via_orthology	DOID:0110207	Charcot-Marie-Tooth disease X-linked dominant 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101899	Pla2g5	implicated_via_orthology	DOID:0111677	familial benign fleck retina						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0080533	Carney-Stratakis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:0090101	lethal congenital glycogen storage disease of heart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277113	Pacs1	implicated_via_orthology	DOID:0070047	Schuurs-Hoeijmakers Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98387	Sptb	implicated_via_orthology	DOID:12971	hereditary spherocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102556	Tbx4	implicated_via_orthology	DOID:381	arthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923657	Sun5	implicated_via_orthology	DOID:0070184	spermatogenic failure 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138987	Slc4a11	implicated_via_orthology	DOID:0111620	corneal dystrophy-perceptive deafness syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	implicated_via_orthology	DOID:0060902	Norman-Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97897	Rel	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2671932	Tspear	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106013	Slc16a1	implicated_via_orthology	DOID:0070214	familial hyperinsulinemic hypoglycemia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	implicated_via_orthology	DOID:0080954	arthrogryposis multiplex congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97533	Pdha2	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98247	Scn1b	implicated_via_orthology	DOID:0080455	developmental and epileptic encephalopathy 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387188	Slc49a4	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891731	Stub1	implicated_via_orthology	DOID:0111746	cerebellar ataxia type 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917297	Trnt1	implicated_via_orthology	DOID:0080209	sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855692	Nono	implicated_via_orthology	DOID:0060817	syndromic X-linked intellectual disability 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	implicated_via_orthology	DOID:0090017	epidermolysis bullosa simplex with muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913596	Ndufb11b	implicated_via_orthology	DOID:0112098	nuclear type mitochondrial complex I deficiency 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:1214	tympanosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:0070125	congenital nongoitrous hypothyroidism 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917347	Sash1	implicated_via_orthology	DOID:0060304	dyschromatosis universalis hereditaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:14687	diastrophic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913604	Snw1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0080122	Alpers-Huttenlocher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444490	Syt14	implicated_via_orthology	DOID:0080063	autosomal recessive spinocerebellar ataxia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	implicated_via_orthology	DOID:0110310	hypertrophic cardiomyopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441932	Prepl	implicated_via_orthology	DOID:0080587	congenital myasthenic syndrome 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931307	Slc19a3	implicated_via_orthology	DOID:0050659	biotin-responsive basal ganglia disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97770	Prodh	implicated_via_orthology	DOID:0070080	schizophrenia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150019	Spred2	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700014	Sorbs1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442620	Nup133	implicated_via_orthology	DOID:0080393	nephrotic syndrome type 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645873	Sult2a3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:0111537	paroxysmal extreme pain disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385039	Muc20	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:0111387	familial isolated hypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159400	Tmie	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137738	Prcc	implicated_via_orthology	DOID:4465	papillary renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106184	Npm1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921394	Robo4	implicated_via_orthology	DOID:0080977	aortic valve disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97930	Rlbp1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	implicated_via_orthology	DOID:0060650	dicarboxylic aminoaciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	implicated_via_orthology	DOID:0070513	neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0080954	arthrogryposis multiplex congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051532	Unc13a	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924066	Sdccag8	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:2468	psychotic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860488	Proz	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920020	Tmem216	implicated_via_orthology	DOID:0070116	Meckel syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917680	Tbce	implicated_via_orthology	DOID:11199	hypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105976	Myo5a	implicated_via_orthology	DOID:0060832	Griscelli syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138987	Slc4a11	implicated_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921749	Sost	implicated_via_orthology	DOID:0080807	autosomal dominant craniodiaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686271	Opa3	implicated_via_orthology	DOID:0111433	optic atrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:10211	cholelithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104511	Tnfsf4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442058	Nipa1	implicated_via_orthology	DOID:0110811	hereditary spastic paraplegia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645714	Slc22a28	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444401	Snrnp200	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387357	Wac	implicated_via_orthology	DOID:0081126	DeSanto-Shinawi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913358	Ndufa9	implicated_via_orthology	DOID:0112086	nuclear type mitochondrial complex I deficiency 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929470	Tyk2	implicated_via_orthology	DOID:0111989	immunodeficiency 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98812	Tpmt	implicated_via_orthology	DOID:0080172	thiopurine S-methyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444232	Poglut1	implicated_via_orthology	DOID:0060256	Dowling-Degos disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2671987	Shank2	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442111	Ppm1k	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98927	Vcl	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179327	Mvd	implicated_via_orthology	DOID:3805	porokeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102764	Six3	implicated_via_orthology	DOID:0110872	holoprosencephaly 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	implicated_via_orthology	DOID:3614	Kallmann syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340062	Sgk1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920020	Tmem216	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891706	Spen	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105088	Ntn1	implicated_via_orthology	DOID:0111153	congenital mirror movement disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914974	Pop1	implicated_via_orthology	DOID:0080962	anauxetic dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922066	Tpr	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	implicated_via_orthology	DOID:0111330	combined saposin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97937	Rmrp	implicated_via_orthology	DOID:14773	cartilage-hair hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913604	Snw1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351596	Sh2d2a	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:0080549	Noonan syndrome with multiple lentigines 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685159	Pnldc1	implicated_via_orthology	DOID:0112338	spermatogenic failure 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928483	Stx5a	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892968	Tacr3	implicated_via_orthology	DOID:0090071	hypogonadotropic hypogonadism 11 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104807	Pls3	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	implicated_via_orthology	DOID:0110266	cataract 9 multiple types						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914482	Nprl2	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913913	Uba5	implicated_via_orthology	DOID:0111615	autosomal recessive spinocerebellar ataxia 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97272	Myl2	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321152	Ptprt	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:0111103	maturity-onset diabetes of the young type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99459	Nr3c2	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095406	Tuba3a	implicated_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915751	Nsmce2	implicated_via_orthology	DOID:0070008	Seckel syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:218	ascending colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352463	Nr1h2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3783195	Sp110-ps2	implicated_via_orthology	DOID:0112254	hepatic venoocclusive disease with immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888676	Rps27	implicated_via_orthology	DOID:0111880	Diamond-Blackfan anemia 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687325	Pigs	implicated_via_orthology	DOID:0070382	developmental and epileptic encephalopathy 95						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929938	Perp	implicated_via_orthology	DOID:0050467	erythrokeratodermia variabilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917853	Mutyh	implicated_via_orthology	DOID:0080410	familial adenomatous polyposis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913405	Ufc1	implicated_via_orthology	DOID:0070421	neurodevelopmental disorder with spasticity and poor growth						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444341	Phf8	implicated_via_orthology	DOID:0060812	syndromic X-linked intellectual disability Siderius type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97851	Slc20a2	implicated_via_orthology	DOID:0060230	basal ganglia calcification						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	implicated_via_orthology	DOID:0110375	retinitis pigmentosa 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:0081373	disabling pansclerotic morphea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922783	Nme5	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349165	Sdc2	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	implicated_via_orthology	DOID:0081143	agammaglobulinemia 8B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450757	Ush1g	implicated_via_orthology	DOID:0110834	Usher syndrome type 1G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104672	Tfap2b	implicated_via_orthology	DOID:0060563	Char syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916943	Pof1b	implicated_via_orthology	DOID:0080859	primary ovarian insufficiency 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	implicated_via_orthology	DOID:0081365	Paget's disease of bone 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915917	Trpm4	implicated_via_orthology	DOID:0080766	erythrokeratodermia variabilis et progressiva 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704345	Rps27rt	implicated_via_orthology	DOID:0111880	Diamond-Blackfan anemia 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890646	Nek8	implicated_via_orthology	DOID:0060259	renal-hepatic-pancreatic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1584	acute chest syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:2602	chondroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670964	Tent5a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442682	Slc30a8	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347521	Ror2	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443301	Slc35c1	implicated_via_orthology	DOID:0070255	congenital disorder of glycosylation type IIc						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109632	Rax	implicated_via_orthology	DOID:0060842	isolated microphthalmia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98443	Surf1	implicated_via_orthology	DOID:0110187	Charcot-Marie-Tooth disease type 4K						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109571	Tulp1	implicated_via_orthology	DOID:0110381	retinitis pigmentosa 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338882	Pex11b	implicated_via_orthology	DOID:0081274	peroxisome biogenesis disorder 14B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98467	Syp	implicated_via_orthology	DOID:0112035	non-syndromic X-linked intellectual disability 96						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109542	Sycp3	implicated_via_orthology	DOID:0070176	spermatogenic failure 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933754	Nedd4l	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449202	Tpm4	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	implicated_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916380	Vps13b	implicated_via_orthology	DOID:0111590	Cohen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97488	Pax4	implicated_via_orthology	DOID:1837	diabetic ketoacidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309481	Trip12	implicated_via_orthology	DOID:0080234	Clark-Baraitser syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914130	Rsrc1	implicated_via_orthology	DOID:0081231	autosomal recessive intellectual developmental disorder 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102570	Ndp	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384795	Pycr1	implicated_via_orthology	DOID:0070138	autosomal recessive cutis laxa type IIIB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155865	Rrm2b	implicated_via_orthology	DOID:0111518	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333782	Pld3	implicated_via_orthology	DOID:0080288	spinocerebellar ataxia 46						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	implicated_via_orthology	DOID:0112063	X-Linked immunodeficiency 74						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576090	Ugt1a8	implicated_via_orthology	DOID:4988	alcoholic pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159410	Slc34a3	implicated_via_orthology	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101783	Plk4	implicated_via_orthology	DOID:0080106	microcephaly and chorioretinopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0110218	Brugada syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98809	Tpm1	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	implicated_via_orthology	DOID:0060614	ulnar-mammary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97488	Pax4	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97493	Pax9	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0050601	ADULT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343184	Samd9l	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97565	Pgm1	implicated_via_orthology	DOID:0080570	congenital disorder of glycosylation It						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349919	Ndufb11	implicated_via_orthology	DOID:0112098	nuclear type mitochondrial complex I deficiency 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97492	Pax8	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:963	episodic ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109589	Ocrl	implicated_via_orthology	DOID:0050699	Dent disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:0050733	methylmalonic aciduria and homocystinuria type cblG						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	implicated_via_orthology	DOID:0080065	autosomal recessive spinocerebellar ataxia 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103077	Stx3	implicated_via_orthology	DOID:0060774	congenital diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149330	Slc5a5	implicated_via_orthology	DOID:0112185	thyroid dyshormonogenesis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099431	Sptlc1	implicated_via_orthology	DOID:0070152	hereditary sensory and autonomic neuropathy type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	implicated_via_orthology	DOID:0060010	Omenn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924086	Polr3f	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929658	Tbk1	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99461	Piga	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98347	Snrpn	implicated_via_orthology	DOID:11983	Prader-Willi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97253	Myf6	implicated_via_orthology	DOID:422	congenital structural myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042141	Traf7	implicated_via_orthology	DOID:1788	peritoneal mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:3227	tracheal stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97532	Pdha1	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	implicated_via_orthology	DOID:13994	cleidocranial dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443727	Spef2	implicated_via_orthology	DOID:0111917	spermatogenic failure 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933237	Tex11	implicated_via_orthology	DOID:0070185	X-linked spermatogenic failure 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	implicated_via_orthology	DOID:0111513	metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389465	Tbx22	implicated_via_orthology	DOID:0060613	X-linked cleft palate with or without ankyloglossia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98927	Vcl	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919650	Pinx1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916720	Tmem127	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916043	Rab3gap2	implicated_via_orthology	DOID:0110717	Warburg micro syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860267	Set	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:811	lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444518	Samd12	implicated_via_orthology	DOID:0111690	familial adult myoclonic epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916075	Mtmr14	implicated_via_orthology	DOID:0111223	centronuclear myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915160	Rubcn	implicated_via_orthology	DOID:0080057	autosomal recessive spinocerebellar ataxia 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	implicated_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3605624	Slc22a29	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:0070365	nevoid basal cell carcinoma syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:0070016	autosomal dominant dyskeratosis congenita 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0110283	autosomal recessive limb-girdle muscular dystrophy type 2J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681836	Polr3a	implicated_via_orthology	DOID:0060794	hypomyelinating leukodystrophy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645246	Sult2a7	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196365	Nus1	implicated_via_orthology	DOID:0080553	congenital disorder of glycosylation Iaa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913328	Tsen34	implicated_via_orthology	DOID:0060269	pontocerebellar hypoplasia type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	implicated_via_orthology	DOID:0111016	cone-rod dystrophy 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107811	Nptx1	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	implicated_via_orthology	DOID:0060453	Reis-Bucklers corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109351	Slc4a2	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652860	Plekhg5	implicated_via_orthology	DOID:0110198	Charcot-Marie-Tooth disease recessive intermediate C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106624	Myo9b	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	implicated_via_orthology	DOID:0111448	progressive myoclonus epilepsy 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095410	Tuba4a	implicated_via_orthology	DOID:0060355	amyotrophic lateral sclerosis type 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0111538	paramyotonia congenita of Von Eulenburg						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042283	Slc22a27	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:0070119	Meckel syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921626	Myo18b	implicated_via_orthology	DOID:0080592	Klippel-Feil syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921269	Traf3ip1	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345144	Spry4	implicated_via_orthology	DOID:0090079	hypogonadotropic hypogonadism 17 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107735	Myo9a	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104513	Nqo2	implicated_via_orthology	DOID:12987	agranulocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930943	Rrad	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444386	Tmem63c	implicated_via_orthology	DOID:0070456	hereditary spastic paraplegia 87						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151208	Selenon	implicated_via_orthology	DOID:0110633	rigid spine muscular dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0090119	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443730	Tnrc6b	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	implicated_via_orthology	DOID:0060675	catecholaminergic polymorphic ventricular tachycardia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:9563	bronchiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	implicated_via_orthology	DOID:0080278	Joubert syndrome 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203730	Pik3c2g	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923385	Prex2	implicated_via_orthology	DOID:4927	Klatskin's tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385316	Slc22a26	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576092	Ugt1a9	implicated_via_orthology	DOID:4988	alcoholic pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102556	Tbx4	implicated_via_orthology	DOID:0111382	ischiocoxopodopatellar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102469	Nfatc1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:0050456	Buruli ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042141	Traf7	implicated_via_orthology	DOID:746	adenomatoid tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858421	Rfx5	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925224	Rdh12	implicated_via_orthology	DOID:0110330	Leber congenital amaurosis 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914253	Uqcrc2	implicated_via_orthology	DOID:0080114	mitochondrial complex III deficiency nuclear type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143424	Pomgnt2	implicated_via_orthology	DOID:0112382	muscular dystrophy-dystroglycanopathy type C8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442473	Rhbdf2	implicated_via_orthology	DOID:0111506	palmoplantar keratoderma-esophageal carcinoma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385054	Pex6	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347043	Orc4	implicated_via_orthology	DOID:0080513	Meier-Gorlin syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916202	Tlcd3b	implicated_via_orthology	DOID:0050572	cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098827	Reep1	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	implicated_via_orthology	DOID:0111114	nephronophthisis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270843	Pde6d	implicated_via_orthology	DOID:0110991	Joubert syndrome 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:0110875	holoprosencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929473	Rgr	implicated_via_orthology	DOID:0110394	retinitis pigmentosa 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98487	Tat	implicated_via_orthology	DOID:0050725	tyrosinemia type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924221	Sult2a8	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442750	Slc22a30	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923364	Sp110	implicated_via_orthology	DOID:0112254	hepatic venoocclusive disease with immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:8545	malignant hyperthermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685024	Tmem231	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:0060578	Noonan syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095438	Slc2a2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913775	Timm50	implicated_via_orthology	DOID:0070002	3-methylglutaconic aciduria type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197527	Top3a	implicated_via_orthology	DOID:0111524	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685968	Ripply2	implicated_via_orthology	DOID:0112360	spondylocostal dysostosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141950	Syne4	implicated_via_orthology	DOID:0110524	autosomal recessive nonsyndromic deafness 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036251	Pde11a	implicated_via_orthology	DOID:0060280	primary pigmented nodular adrenocortical disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916066	Ppil1	implicated_via_orthology	DOID:0112325	pontocerebellar hypoplasia type 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137698	Ugt1a6a	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195268	Sigmar1	implicated_via_orthology	DOID:0060207	amyotrophic lateral sclerosis type 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106923	Tll1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443219	Tmem260	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98927	Vcl	implicated_via_orthology	DOID:0110321	hypertrophic cardiomyopathy 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	implicated_via_orthology	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:0112066	nuclear type mitochondrial complex I deficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915592	Ndufb10	implicated_via_orthology	DOID:0112139	nuclear type mitochondrial complex I deficiency 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923385	Prex2	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:5408	Paget's disease of bone						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	implicated_via_orthology	DOID:0110830	Usher syndrome type 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890216	Slc6a14	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894407	Tmem165	implicated_via_orthology	DOID:0070263	congenital disorder of glycosylation type IIk						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:12960	acrocephalosyndactylia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098808	Pex5	implicated_via_orthology	DOID:0110854	rhizomelic chondrodysplasia punctata type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155779	Ttbk2	implicated_via_orthology	DOID:0050961	spinocerebellar ataxia type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:0080991	congenital myopathy 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892003	Tcof1	implicated_via_orthology	DOID:0080789	Treacher Collins syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921982	Stx11	implicated_via_orthology	DOID:0110924	familial hemophagocytic lymphohistiocytosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914216	Trit1	implicated_via_orthology	DOID:0111464	combined oxidative phosphorylation deficiency 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97567	Pgr	implicated_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:2739	Gilbert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	implicated_via_orthology	DOID:14365	systemic primary carnitine deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144151	Pnpo	implicated_via_orthology	DOID:0111329	pyridoxamine 5'-phosphate oxidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180203	Tmlhe	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385902	Picalm	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	implicated_via_orthology	DOID:0060730	torsion dystonia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444530	Slc9a7	implicated_via_orthology	DOID:0111844	X-linked intellectual developmental disorder 108						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917125	Ndufa11	implicated_via_orthology	DOID:0112094	nuclear type mitochondrial complex I deficiency 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:14320	generalized anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:2729	dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195268	Sigmar1	implicated_via_orthology	DOID:0111065	autosomal recessive distal hereditary motor neuronopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446190	Nup188	implicated_via_orthology	DOID:11162	respiratory failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353654	Vps26a	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333780	Rps19	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137680	Sfxn4	implicated_via_orthology	DOID:0111484	combined oxidative phosphorylation deficiency 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580642	Ugt1a10	implicated_via_orthology	DOID:4988	alcoholic pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444989	Spg11	implicated_via_orthology	DOID:0110764	hereditary spastic paraplegia 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931835	Trim44	implicated_via_orthology	DOID:12271	aniridia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:0110414	retinitis pigmentosa 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685844	Prdm12	implicated_via_orthology	DOID:0070153	hereditary sensory and autonomic neuropathy type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	implicated_via_orthology	DOID:0112253	combined cellular and humoral immune defects with granulomas						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97386	Ntsr1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920431	Nfatc4	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889844	Sumf1	implicated_via_orthology	DOID:0050441	mucosulfatidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:1148	polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921487	Tubgcp2	implicated_via_orthology	DOID:0081266	pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:0060895	Parkinson's disease 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104856	Rorc	implicated_via_orthology	DOID:0111940	immunodeficiency 42						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913745	Ndufb3	implicated_via_orthology	DOID:0112067	nuclear type mitochondrial complex I deficiency 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98742	Thra	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	implicated_via_orthology	DOID:0110946	autosomal recessive osteopetrosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:11664	nephrosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97750	Ppib	implicated_via_orthology	DOID:0110349	osteogenesis imperfecta type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446244	Setd1a	implicated_via_orthology	DOID:0070471	early-onset epilepsy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	implicated_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:0080333	aortic valve disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	implicated_via_orthology	DOID:0080530	granular corneal dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920180	Ppp2r2b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:1025	tuberculoid leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606571	Stac3	implicated_via_orthology	DOID:0060346	Native American myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0111215	autosomal dominant distal hereditary motor neuronopathy 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:11512	Budd-Chiari syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:0060583	Noonan syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913063	Myoz2	implicated_via_orthology	DOID:0110322	hypertrophic cardiomyopathy 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889411	Tnfrsf13b	implicated_via_orthology	DOID:0081145	common variable immunodeficiency 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97805	Ptpn1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107708	Ss18	implicated_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922184	Odad2	implicated_via_orthology	DOID:0110609	primary ciliary dyskinesia 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894806	Mylk	implicated_via_orthology	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685490	Tmem132e	implicated_via_orthology	DOID:0111634	autosomal recessive nonsyndromic deafness 99						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99660	Pola1	implicated_via_orthology	DOID:0111834	X-linked reticulate pigmentary disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147713	Tmem151a	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:0111739	X-linked deafness 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442751	Slc22a19	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97501	Pck1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858222	Septin9	implicated_via_orthology	DOID:3689	brachial plexus neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930773	Pnkd	implicated_via_orthology	DOID:0090049	paroxysmal nonkinesigenic dyskinesia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1272	telangiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341839	Nod1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	implicated_via_orthology	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:0110922	familial hemophagocytic lymphohistiocytosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:0111944	immunodeficiency 31B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	implicated_via_orthology	DOID:0081352	congenital myopathy 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97305	Neu1	implicated_via_orthology	DOID:0080488	mucolipidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915459	Rnaseh2c	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098583	Stag2	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861606	Tacstd2	implicated_via_orthology	DOID:2566	corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925542	Orai1	implicated_via_orthology	DOID:0111976	immunodeficiency 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	implicated_via_orthology	DOID:0110708	hypotrichosis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12783	migraine without aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925224	Rdh12	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102469	Nfatc1	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890110	Robo2	implicated_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:0110089	asphyxiating thoracic dystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:12558	chronic progressive external ophthalmoplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:4404	occupational dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344375	Prkra	implicated_via_orthology	DOID:0090048	dystonia 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040695	Palb2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441738	Npsr1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196412	Tnpo3	implicated_via_orthology	DOID:0110304	autosomal dominant limb-girdle muscular dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894806	Mylk	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861755	Nsmf	implicated_via_orthology	DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925226	Nuak1	implicated_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:0080055	achondrogenesis type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354373	Sall2	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685563	Pcdh19	implicated_via_orthology	DOID:0060848	developmental and epileptic encephalopathy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:0060230	basal ganglia calcification						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352457	Nr4a3	implicated_via_orthology	DOID:4549	extraskeletal myxoid chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350931	Tcirg1	implicated_via_orthology	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107560	Sema4a	implicated_via_orthology	DOID:0110357	retinitis pigmentosa 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442480	Pigv	implicated_via_orthology	DOID:0070433	hyperphosphatasia with impaired intellectual development syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	implicated_via_orthology	DOID:0070091	schizophrenia 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:10933	obsessive-compulsive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:4404	occupational dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914160	Tmem107	implicated_via_orthology	DOID:0080254	orofaciodigital syndrome XVI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	implicated_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	implicated_via_orthology	DOID:0111008	X-linked cone-rod dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0111385	inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107157	Sin3a	implicated_via_orthology	DOID:0060395	chromosome 15q24 deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	implicated_via_orthology	DOID:0060843	hereditary neuropathy with liability to pressure palsies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915517	Slc25a22	implicated_via_orthology	DOID:0080440	developmental and epileptic encephalopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:0060863	patterned macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97770	Prodh	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684988	Pex10	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444966	Tecrl	implicated_via_orthology	DOID:0060677	catecholaminergic polymorphic ventricular tachycardia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919192	Myof	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101061	Slc18a3	implicated_via_orthology	DOID:0110672	congenital myasthenic syndrome 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:0070145	hereditary sensory and autonomic neuropathy type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:0060009	MHC class I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97724	Pnmt	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0111683	neurofibromatosis-Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97763	Prlr	implicated_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385070	Reep2	implicated_via_orthology	DOID:0110817	hereditary spastic paraplegia 72A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918957	Ubiad1	implicated_via_orthology	DOID:0060456	Schnyder corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921305	Plce1	implicated_via_orthology	DOID:0080382	nephrotic syndrome type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202889	Sema6b	implicated_via_orthology	DOID:891	progressive myoclonus epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107686	Ndufa4	implicated_via_orthology	DOID:0070506	mitochondrial complex IV deficiency nuclear type 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202713	Rhag	implicated_via_orthology	DOID:0111562	overhydrated hereditary stomatocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921273	Rd3	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105068	Rab7	implicated_via_orthology	DOID:0110159	Charcot-Marie-Tooth disease type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	implicated_via_orthology	DOID:0110473	autosomal recessive nonsyndromic deafness 18A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3603756	Primpol	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:10024	migraine with aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914154	Pccb	implicated_via_orthology	DOID:14701	propionic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:11759	hypochromic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107877	Prkcsh	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858225	Tuba8	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649529	Prcd	implicated_via_orthology	DOID:0110405	retinitis pigmentosa 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:0070493	mitochondrial complex IV deficiency nuclear type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102667	Pmp2	implicated_via_orthology	DOID:0111560	Charcot-Marie-Tooth disease type 1G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:0111050	Quebec platelet disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145264	Nhlrc1	implicated_via_orthology	DOID:3534	Lafora disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	implicated_via_orthology	DOID:0060468	Holt-Oram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109577	Taf1b	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4439838	Trac	implicated_via_orthology	DOID:0111977	immunodeficiency 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:4997	Camurati-Engelmann disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97801	Pth1r	implicated_via_orthology	DOID:0111732	Eiken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	implicated_via_orthology	DOID:4586	familial meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104807	Pls3	implicated_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104809	Pls1	implicated_via_orthology	DOID:0112167	autosomal dominant nonsyndromic deafness 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0111340	dominant optic atrophy plus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108114	Slc12a3	implicated_via_orthology	DOID:0050450	Gitelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0060782	EEC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313261	Sptbn2	implicated_via_orthology	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	implicated_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894681	Usp9x	implicated_via_orthology	DOID:0112025	female-restricted syndromic X-linked intellectual disability 99						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	implicated_via_orthology	DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	implicated_via_orthology	DOID:0050792	multiple cutaneous and mucosal venous malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201689	Tapbp	implicated_via_orthology	DOID:0060009	MHC class I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913399	Sptssa	implicated_via_orthology	DOID:0070460	hereditary spastic paraplegia 90B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	implicated_via_orthology	DOID:0070275	hereditary nonpolyposis colorectal cancer type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913399	Sptssa	implicated_via_orthology	DOID:0070459	hereditary spastic paraplegia 90A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	implicated_via_orthology	DOID:0111706	oblique facial clefting 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917192	Rnf113a1	implicated_via_orthology	DOID:0111868	nonphotosensitive trichothiodystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146565	Nsun3	implicated_via_orthology	DOID:0112112	combined oxidative phosphorylation deficiency 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:0070235	Loeys-Dietz syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	implicated_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196261	Trmt10c	implicated_via_orthology	DOID:0111471	combined oxidative phosphorylation deficiency 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095733	Pros1	implicated_via_orthology	DOID:0111900	autosomal dominant thrombophilia due to protein S deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159400	Tmie	implicated_via_orthology	DOID:0110512	autosomal recessive nonsyndromic deafness 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927468	Samhd1	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:0050788	proximal symphalangism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338783	Pts	implicated_via_orthology	DOID:0090106	BH4-deficient hyperphenylalaninemia A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917302	Prpf4	implicated_via_orthology	DOID:0110392	retinitis pigmentosa 70						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97438	Oprd1	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140592	Slc44a1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346021	Slco2a1	implicated_via_orthology	DOID:14283	primary hypertrophic osteoarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97542	Pepd	implicated_via_orthology	DOID:0111540	prolidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143854	Nup107	implicated_via_orthology	DOID:0080385	nephrotic syndrome type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859516	Rps28	implicated_via_orthology	DOID:0111894	Diamond-Blackfan anemia 15 with mandibulofacial dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384936	Spns2	implicated_via_orthology	DOID:0111643	autosomal recessive nonsyndromic deafness 115						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915113	Slc25a11	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682952	Prdm10	implicated_via_orthology	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915722	Tmem126b	implicated_via_orthology	DOID:0112084	nuclear type mitochondrial complex I deficiency 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274789	Taldo1	implicated_via_orthology	DOID:2978	carbohydrate metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919762	Sting1	implicated_via_orthology	DOID:0111457	STING-associated vasculopathy with onset in infancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97856	Rara	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929646	Pex3	implicated_via_orthology	DOID:0080484	peroxisome biogenesis disorder 10A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685024	Tmem231	implicated_via_orthology	DOID:0110989	Joubert syndrome 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914852	Necap1	implicated_via_orthology	DOID:0080443	developmental and epileptic encephalopathy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	implicated_via_orthology	DOID:5768	Nager acrofacial dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446138	Phactr2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:1996	rectum adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923686	Tufm	implicated_via_orthology	DOID:0111494	combined oxidative phosphorylation deficiency 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102790	Rab18	implicated_via_orthology	DOID:0110718	Warburg micro syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155445	Tmprss3	implicated_via_orthology	DOID:0110527	autosomal recessive nonsyndromic deafness 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88034	Prdx3	implicated_via_orthology	DOID:0070413	autosomal recessive spinocerebellar ataxia 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:8704	genital herpes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913302	Sdhc	implicated_via_orthology	DOID:0080533	Carney-Stratakis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921620	Rptor	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98812	Tpmt	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0110827	Usher syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:0080528	bronchiectasis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102567	Nrl	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97744	Por	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:0070234	Loeys-Dietz syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102889	Vcan	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104671	Tfap2a	implicated_via_orthology	DOID:0050691	branchiooculofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894697	Rad54l	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441787	Washc4	implicated_via_orthology	DOID:0081207	autosomal recessive intellectual developmental disorder 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922088	Naa15	implicated_via_orthology	DOID:0080233	autosomal dominant intellectual developmental disorder 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913334	Rmnd1	implicated_via_orthology	DOID:0111481	combined oxidative phosphorylation deficiency 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924393	Trip11	implicated_via_orthology	DOID:0080054	achondrogenesis type IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104754	Sik1	implicated_via_orthology	DOID:0080465	developmental and epileptic encephalopathy 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:218	ascending colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	implicated_via_orthology	DOID:0111381	IVIC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97937	Rmrp	implicated_via_orthology	DOID:0050640	anauxetic dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915513	Pdhb	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107612	Rtn2	implicated_via_orthology	DOID:0110765	hereditary spastic paraplegia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107624	Mvk	implicated_via_orthology	DOID:3805	porokeratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	implicated_via_orthology	DOID:0090029	CINCA Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645174	Ndufa11b	implicated_via_orthology	DOID:2033	communication disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	implicated_via_orthology	DOID:0110148	Charcot-Marie-Tooth disease type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:0080294	Charcot-Marie-Tooth disease dominant intermediate G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:0060000	infective endocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	implicated_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:0060668	anencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099431	Sptlc1	implicated_via_orthology	DOID:0081381	juvenile amyotrophic lateral sclerosis type 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:10024	migraine with aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037150	Slc13a5	implicated_via_orthology	DOID:0080453	developmental and epileptic encephalopathy 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97744	Por	implicated_via_orthology	DOID:0080925	cytochrome P450 oxidoreductase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	implicated_via_orthology	DOID:0110936	nemaline myopathy 5A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107477	Stil	implicated_via_orthology	DOID:0070278	primary autosomal recessive microcephaly 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97577	Phka2	implicated_via_orthology	DOID:0111042	glycogen storage disease IXa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	implicated_via_orthology	DOID:0070149	hereditary sensory and autonomic neuropathy type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930252	Srd5a3	implicated_via_orthology	DOID:0050807	Kahrizi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98306	Sim1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917689	Taf15	implicated_via_orthology	DOID:4549	extraskeletal myxoid chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927555	Slc4a4	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444585	Trappc11	implicated_via_orthology	DOID:0110287	autosomal recessive limb-girdle muscular dystrophy type 2S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:0081007	RNASET2-deficient cystic leukoencephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155445	Tmprss3	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891295	Ube3b	implicated_via_orthology	DOID:0111456	Kaufman oculocerebrofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918339	Septin12	implicated_via_orthology	DOID:0070178	spermatogenic failure 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923206	Srrm2	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98387	Sptb	implicated_via_orthology	DOID:0110917	hereditary spherocytosis type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:0050573	2-hydroxyglutaric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101059	Tnfrsf9	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685891	Odaph	implicated_via_orthology	DOID:0110062	amelogenesis imperfecta hypomaturation type 2A4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915902	Tab2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106403	Spg21	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345183	Tenm3	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98890	Uba1	implicated_via_orthology	DOID:0111827	X-linked spinal muscular atrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916983	Paox	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:11199	hypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:0112240	Leber congenital amaurosis with early-onset deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0111580	Behr syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309526	Rps17	implicated_via_orthology	DOID:0111890	Diamond-Blackfan anemia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98917	Uros	implicated_via_orthology	DOID:13271	cutaneous porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181726	Mtnr1b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202715	Tcf21	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	implicated_via_orthology	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894323	Ranbp2	implicated_via_orthology	DOID:0050905	inflammatory myofibroblastic tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:9245	Alagille syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:4404	occupational dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141599	Tsen2	implicated_via_orthology	DOID:0060268	pontocerebellar hypoplasia type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098272	Rnasel	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98107	Rps14	implicated_via_orthology	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106633	Phox2a	implicated_via_orthology	DOID:0081016	congenital fibrosis of the extraocular muscles 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917923	Prdm16	implicated_via_orthology	DOID:0081157	dilated cardiomyopathy 1LL						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443657	Ttll5	implicated_via_orthology	DOID:0111025	cone-rod dystrophy 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97829	Pygl	implicated_via_orthology	DOID:3650	lactic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918312	Tekt3	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891344	Prg4	implicated_via_orthology	DOID:1787	pericarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:0081017	congenital fibrosis of the extraocular muscles 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289172	Scyl2	implicated_via_orthology	DOID:0080980	arthrogryposis multiplex congenita-4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095411	Nup214	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923515	Tsen54	implicated_via_orthology	DOID:0060274	pontocerebellar hypoplasia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:4586	familial meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890816	Vsx1	implicated_via_orthology	DOID:2566	corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041206	Nlrp2	implicated_via_orthology	DOID:3590	gestational trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933118	Pgam2	implicated_via_orthology	DOID:0080108	myoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	implicated_via_orthology	DOID:14686	Axenfeld-Rieger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670964	Tent5a	implicated_via_orthology	DOID:0111848	osteogenesis imperfecta type 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	implicated_via_orthology	DOID:0110708	hypotrichosis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:0110736	neurodegeneration with brain iron accumulation 2b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:0050649	atransferrinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102764	Six3	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97451	Otx2	implicated_via_orthology	DOID:0111806	syndromic microphthalmia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921372	Tmem43	implicated_via_orthology	DOID:0070252	autosomal dominant Emery-Dreifuss muscular dystrophy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261422	Naga	implicated_via_orthology	DOID:479	angiokeratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109404	Nup98	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096377	Traip	implicated_via_orthology	DOID:0070005	Seckel syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102854	Rpl5	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918529	Slc29a3	implicated_via_orthology	DOID:0111278	histiocytosis-lymphadenopathy plus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98660	Sry	implicated_via_orthology	DOID:14448	46,XY sex reversal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:0111512	metachondromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095733	Pros1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681271	Pigl	implicated_via_orthology	DOID:0112152	CHIME syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153470	Scgb3a2	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387600	Nags	implicated_via_orthology	DOID:0112258	N-acetylglutamate synthase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3012	Li-Fraumeni syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	implicated_via_orthology	DOID:0060468	Holt-Oram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276535	Ncoa3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106598	Myo5b	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	implicated_via_orthology	DOID:0060747	Duane-radial ray syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:9478	postpartum depression						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330223	Papss2	implicated_via_orthology	DOID:0050812	spondyloepimetaphyseal dysplasia, Pakistani type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:3803	Crigler-Najjar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103150	Slc12a1	implicated_via_orthology	DOID:0110142	Bartter disease type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	implicated_via_orthology	DOID:0110119	autoimmune lymphoproliferative syndrome type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443373	Relt	implicated_via_orthology	DOID:0111722	amelogenesis imperfecta type 3C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	implicated_via_orthology	DOID:0081118	benign familial infantile seizures 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352456	Nr4a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353576	Pik3cg	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88278	Serpina6	implicated_via_orthology	DOID:0090030	corticosteroid-binding globulin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107914	Tia1	implicated_via_orthology	DOID:0081380	amyotrophic lateral sclerosis type 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:0111162	epidermal nevus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:0111531	bilateral optic nerve hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98894	Ucp1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:3317	hepatic angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:0111945	immunodeficiency 31A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104673	Ptpn12	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919421	Shq1	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194497	Tgif1	implicated_via_orthology	DOID:0110880	holoprosencephaly 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096380	Psmb10	implicated_via_orthology	DOID:0060919	proteosome-associated autoinflammatory syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	implicated_via_orthology	DOID:0111332	Pitt-Hopkins-like syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676630	Nlrp12	implicated_via_orthology	DOID:0090063	familial cold autoinflammatory syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855692	Nono	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:0081317	multiple synostoses syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446117	Suox	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	implicated_via_orthology	DOID:0050681	Borjeson-Forssman-Lehmann syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201412	Rdh5	implicated_via_orthology	DOID:8499	night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352460	Nr0b1	implicated_via_orthology	DOID:0080156	X-linked adrenal hypoplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306826	Sema7a	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917125	Ndufa11	implicated_via_orthology	DOID:2033	communication disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97499	Pcca	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	implicated_via_orthology	DOID:0110495	autosomal recessive nonsyndromic deafness 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	implicated_via_orthology	DOID:0070489	classic dopamine transporter deficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101834	Tubg1	implicated_via_orthology	DOID:0090138	complex cortical dysplasia with other brain malformations 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	implicated_via_orthology	DOID:0090111	PCWH syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261809	Rad51d	implicated_via_orthology	DOID:5683	hereditary breast ovarian cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	implicated_via_orthology	DOID:0110831	Usher syndrome type 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103291	Rai1	implicated_via_orthology	DOID:0060768	Smith-Magenis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924105	Slc17a5	implicated_via_orthology	DOID:3659	sialuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97740	Polb	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:0090137	complex cortical dysplasia with other brain malformations 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98355	Sos2	implicated_via_orthology	DOID:0060587	Noonan syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202064	Otog	implicated_via_orthology	DOID:0110474	autosomal recessive nonsyndromic deafness 18B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	implicated_via_orthology	DOID:0090013	severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100498	Pitx3	implicated_via_orthology	DOID:0080606	anterior segment dysgenesis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0110682	congenital myasthenic syndrome 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140371	Rusc2	implicated_via_orthology	DOID:0080239	autosomal recessive intellectual developmental disorder 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353656	Slc7a9	implicated_via_orthology	DOID:9266	cystinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138915	Myl9	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891430	Slc36a2	implicated_via_orthology	DOID:0112265	iminoglycinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107363	Stxbp1	implicated_via_orthology	DOID:0050562	West syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135956	Prlhr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096397	Polr1a	implicated_via_orthology	DOID:0060353	acrofacial dysostosis Cincinnati type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916060	Nexn	implicated_via_orthology	DOID:0110326	hypertrophic cardiomyopathy 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	implicated_via_orthology	DOID:0080337	mitochondrial DNA depletion syndrome 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104512	Tnfrsf4	implicated_via_orthology	DOID:0111935	immunodeficiency 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920232	Tmem138	implicated_via_orthology	DOID:0110985	Joubert syndrome 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0111503	Li-Fraumeni syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105943	Rpl10	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:5408	Paget's disease of bone						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:0060326	myelomeningocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144177	Pex12	implicated_via_orthology	DOID:0080478	peroxisome biogenesis disorder 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97724	Pnmt	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:0111115	nephronophthisis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	implicated_via_orthology	DOID:0110248	cataract 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:3204	schwannomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:0111236	congenital muscular dystrophy-dystroglycanopathy type A3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894806	Mylk	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97788	Psph	implicated_via_orthology	DOID:0050724	PSPH deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156687	Slc2a10	implicated_via_orthology	DOID:0050645	arterial tortuosity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933227	Tex14	implicated_via_orthology	DOID:0070181	spermatogenic failure 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0111188	myofibrillar myopathy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	implicated_via_orthology	DOID:0080864	primary ovarian insufficiency 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921358	Parn	implicated_via_orthology	DOID:0070024	autosomal recessive dyskeratosis congenita 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0080123	mitochondrial DNA depletion syndrome 4b						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	implicated_via_orthology	DOID:0110858	polycystic kidney disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313276	Vamp1	implicated_via_orthology	DOID:0050772	spastic ataxia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:5522	basaloid squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098808	Pex5	implicated_via_orthology	DOID:0080622	peroxisome biogenesis disorder 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1926	Gaucher's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442117	Pogz	implicated_via_orthology	DOID:0070067	White-Sutton syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384576	Tti2	implicated_via_orthology	DOID:0081204	autosomal recessive intellectual developmental disorder 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321393	Timeless	implicated_via_orthology	DOID:0050628	advanced sleep phase syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	implicated_via_orthology	DOID:0060744	Pendred Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344372	Rbck1	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104574	Ptprj	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97930	Rlbp1	implicated_via_orthology	DOID:0050683	Bothnia retinal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328317	Trex1	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351333	Thoc5	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922139	Timmdc1	implicated_via_orthology	DOID:0112071	nuclear type mitochondrial complex I deficiency 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	implicated_via_orthology	DOID:0070192	autosomal recessive chronic granulomatous disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443241	Ndufs1	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913299	Rogdi	implicated_via_orthology	DOID:0111668	Kohlschutter-Tonz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679732	Slc9a9	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098604	Rragd	implicated_via_orthology	DOID:0060879	primary hypomagnesemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0060770	dextro-looped transposition of the great arteries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	implicated_via_orthology	DOID:0110826	Usher syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446138	Phactr2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913956	Ndufaf3	implicated_via_orthology	DOID:0112070	nuclear type mitochondrial complex I deficiency 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:4404	occupational dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890948	Supt16	implicated_via_orthology	DOID:0070469	neurodevelopmental disorder with dysmorphic facies and thin corpus callosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:3234	central nervous system lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443366	Nudt15	implicated_via_orthology	DOID:0080172	thiopurine S-methyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106923	Tll1	implicated_via_orthology	DOID:0110111	atrial heart septal defect 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919583	Palld	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914840	Tctn3	implicated_via_orthology	DOID:0060374	orofaciodigital syndrome IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349410	Triobp	implicated_via_orthology	DOID:0110486	autosomal recessive nonsyndromic deafness 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	implicated_via_orthology	DOID:0110981	Joubert syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144467	Wdpcp	implicated_via_orthology	DOID:0111591	congenital heart defects, hamartomas of tongue, and polysyndactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	implicated_via_orthology	DOID:0110130	Bardet-Biedl syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	implicated_via_orthology	DOID:0110329	Leber congenital amaurosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:0050973	spinocerebellar ataxia type 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443377	Unc45b	implicated_via_orthology	DOID:0110259	cataract 43						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106621	Myo1e	implicated_via_orthology	DOID:0111131	focal segmental glomerulosclerosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97801	Pth1r	implicated_via_orthology	DOID:0080020	Jansen's metaphyseal chondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97724	Pnmt	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926483	Nectin1	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	implicated_via_orthology	DOID:0110773	hereditary spastic paraplegia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914797	Slc39a8	implicated_via_orthology	DOID:0070266	congenital disorder of glycosylation type IIn						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	implicated_via_orthology	DOID:0110481	autosomal recessive nonsyndromic deafness 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103559	Sox18	implicated_via_orthology	DOID:0111360	hypotrichosis-lymphedema-telangiectasia-renal defect syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919003	Tmprss6	implicated_via_orthology	DOID:11252	microcytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97303	Nek1	implicated_via_orthology	DOID:0081378	amyotrophic lateral sclerosis type 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349635	Sec23a	implicated_via_orthology	DOID:0070307	craniolenticulosutural dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915677	Slc39a13	implicated_via_orthology	DOID:0080739	Ehlers-Danlos syndrome spondylodysplastic type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	implicated_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927616	Trps1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	implicated_via_orthology	DOID:0050800	cerebral creatine deficiency syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:0080653	urolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	implicated_via_orthology	DOID:0070111	Niemann-Pick disease type A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289155	Trmt1	implicated_via_orthology	DOID:0081229	autosomal recessive intellectual developmental disorder 68						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913664	Ndufa12	implicated_via_orthology	DOID:0112087	nuclear type mitochondrial complex I deficiency 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1350	paranasal sinus benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108173	Prkg2	implicated_via_orthology	DOID:0081238	acromesomelic dysplasia-4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0070482	spinal neurofibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	implicated_via_orthology	DOID:0060444	granular corneal dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444584	Mysm1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891825	Pigb	implicated_via_orthology	DOID:0112216	developmental and epileptic encephalopathy 80						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913302	Sdhc	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338031	Spint2	implicated_via_orthology	DOID:0060781	congenital secretory sodium diarrhea 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891916	Plag1	implicated_via_orthology	DOID:452	pleomorphic adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0110430	dilated cardiomyopathy 1G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	implicated_via_orthology	DOID:0070112	Niemann-Pick disease type B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	implicated_via_orthology	DOID:0110863	congenital stationary night blindness autosomal dominant 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:37	skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98460	Syn1	implicated_via_orthology	DOID:0112122	X-linked epilepsy with variable learning disabilities and behavior disorders						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920328	Pmpcb	implicated_via_orthology	DOID:0070332	multiple mitochondrial dysfunctions syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152345	Taf4b	implicated_via_orthology	DOID:0070182	spermatogenic failure 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97565	Pgm1	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346523	Sgcb	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5621540	Percc1	implicated_via_orthology	DOID:0060774	congenital diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923813	Qrsl1	implicated_via_orthology	DOID:0112117	combined oxidative phosphorylation deficiency 40						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261434	Olr1	implicated_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346317	Nr2e3	implicated_via_orthology	DOID:0090059	enhanced S-cone syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918781	Piezo2	implicated_via_orthology	DOID:0111608	distal arthrogryposis type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:0110459	dilated cardiomyopathy 1FF						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:0111265	Boucher-Neuhauser syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330805	Rab33b	implicated_via_orthology	DOID:0081271	Smith-McCort dysplasia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921387	Nuak2	implicated_via_orthology	DOID:0060668	anencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104803	Siae	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917379	Slc44a4	implicated_via_orthology	DOID:0080268	autosomal dominant nonsyndromic deafness 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:0060009	MHC class I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97283	Ncf1	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106689	Selplg	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104562	Napb	implicated_via_orthology	DOID:0070393	developmental and epileptic encephalopathy 107						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:1681	heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99569	S1pr2	implicated_via_orthology	DOID:0110519	autosomal recessive nonsyndromic deafness 68						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612447	Rbm8a2	implicated_via_orthology	DOID:14699	thrombocytopenia-absent radius syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298388	Umps	implicated_via_orthology	DOID:0050833	orotic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:61	mitral valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915903	Samm50	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930136	Pmfbp1	implicated_via_orthology	DOID:0111922	spermatogenic failure 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914050	Trp53rkb	implicated_via_orthology	DOID:0080246	Galloway-Mowat syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106921	Scn2b	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:1229	paranoid schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913649	Tsfm	implicated_via_orthology	DOID:0111486	combined oxidative phosphorylation deficiency 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3608325	Pdzd7	implicated_via_orthology	DOID:0110839	Usher syndrome type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:2626	choroid plexus papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384871	Slc24a1	implicated_via_orthology	DOID:0110868	congenital stationary night blindness 1D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0090023	split hand-foot malformation 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261835	Vps37a	implicated_via_orthology	DOID:0110805	hereditary spastic paraplegia 53						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351596	Sh2d2a	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104574	Ptprj	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342274	Slc25a15	implicated_via_orthology	DOID:9273	citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155302	Sec63	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0111276	sensory ataxic neuropathy, dysarthria, and ophthalmoparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:0110383	retinitis pigmentosa 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919150	Tmem106b	implicated_via_orthology	DOID:0070405	hypomyelinating leukodystrophy 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151016	Tmc1	implicated_via_orthology	DOID:0110563	autosomal dominant nonsyndromic deafness 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:0112251	Ghosal hematodiaphyseal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:8736	smallpox						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891344	Prg4	implicated_via_orthology	DOID:0090127	camptodactyly-arthropathy-coxa vara-pericarditis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894286	P4ha2	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	implicated_via_orthology	DOID:3783	Coffin-Lowry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917057	Trim32	implicated_via_orthology	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	implicated_via_orthology	DOID:0080445	developmental and epileptic encephalopathy 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385046	Slc26a8	implicated_via_orthology	DOID:0070168	spermatogenic failure 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921353	Nebl	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894697	Rad54l	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97597	Prkcg	implicated_via_orthology	DOID:0050964	spinocerebellar ataxia type 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913521	Tmem126a	implicated_via_orthology	DOID:0111437	optic atrophy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0111514	metatropic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:2300	spondylolysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3033336	Szt2	implicated_via_orthology	DOID:0080413	developmental and epileptic encephalopathy 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346527	Psmb8	implicated_via_orthology	DOID:0050553	proteasome-associated autoinflammatory syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:0112242	congenital symmetric circumferential skin creases 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921293	Pex26	implicated_via_orthology	DOID:0080482	peroxisome biogenesis disorder 7A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195265	Per2	implicated_via_orthology	DOID:0110011	advanced sleep phase syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685351	Sprtn	implicated_via_orthology	DOID:0111264	Ruijs-Aalfs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651811	Tph2	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107363	Stxbp1	implicated_via_orthology	DOID:0080436	developmental and epileptic encephalopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:0080357	mitochondrial complex IV deficiency nuclear type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:4404	occupational dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	implicated_via_orthology	DOID:0060720	autosomal recessive congenital ichthyosis 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195264	Slc3a1	implicated_via_orthology	DOID:9266	cystinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353576	Pik3cg	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915902	Tab2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	implicated_via_orthology	DOID:3210	Pelizaeus-Merzbacher disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	implicated_via_orthology	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655574	Ostm1	implicated_via_orthology	DOID:0110939	autosomal recessive osteopetrosis 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927468	Samhd1	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:0050876	Caroli disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98480	Tal1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915542	Stt3b	implicated_via_orthology	DOID:0080573	congenital disorder of glycosylation Ix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104878	Prkar1a	implicated_via_orthology	DOID:0050471	Carney complex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103581	Musk	implicated_via_orthology	DOID:0110670	congenital myasthenic syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152213	Tirap	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924399	Pacs2	implicated_via_orthology	DOID:0080446	developmental and epileptic encephalopathy 66						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97572	Phb1	implicated_via_orthology	DOID:8029	sporadic breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152419	Stk33	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	implicated_via_orthology	DOID:9406	hypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097692	Opn1mw	implicated_via_orthology	DOID:13910	red color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	implicated_via_orthology	DOID:0110070	arrhythmogenic right ventricular dysplasia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:10016	multiple endocrine neoplasia type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261811	Myo15a	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:0111054	von Willebrand's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144467	Wdpcp	implicated_via_orthology	DOID:0110137	Bardet-Biedl syndrome 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99907	Plod1	implicated_via_orthology	DOID:0080734	Ehlers-Danlos syndrome kyphoscoliotic type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389465	Tbx22	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:0070022	autosomal recessive dyskeratosis congenita 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98247	Scn1b	implicated_via_orthology	DOID:0110222	Brugada syndrome 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:0070046	Coffin-Siris syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929915	Ncoa6	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861755	Nsmf	implicated_via_orthology	DOID:0090085	hypogonadotropic hypogonadism 9 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95453	Smarcad1	implicated_via_orthology	DOID:0080725	BASAN syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343464	Rorb	implicated_via_orthology	DOID:0111316	idiopathic generalized epilepsy 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103079	Pura	implicated_via_orthology	DOID:0070061	autosomal dominant intellectual developmental disorder 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917853	Mutyh	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	implicated_via_orthology	DOID:0060062	familial juvenile hyperuricemic nephropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138365	Tmem237	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0110838	Usher syndrome type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039591	Mtss2	implicated_via_orthology	DOID:0081301	intellectual developmental disorder with ocular anomalies and distinctive facial features						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933247	Usp26	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330819	Osmr	implicated_via_orthology	DOID:0080930	primary localized cutaneous amyloidosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919379	Pex13	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95453	Smarcad1	implicated_via_orthology	DOID:0111357	adermatoglyphia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:3079	childhood astrocytic tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916165	Vars2	implicated_via_orthology	DOID:0111478	combined oxidative phosphorylation deficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	implicated_via_orthology	DOID:0070366	nevoid basal cell carcinoma syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109550	Tnnt3	implicated_via_orthology	DOID:0111601	distal arthrogryposis type 2B2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920026	Sass6	implicated_via_orthology	DOID:0070279	primary autosomal recessive microcephaly 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704336	Rpl10-ps3	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339963	St3gal5	implicated_via_orthology	DOID:0060470	salt and pepper syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149543	Ubap1	implicated_via_orthology	DOID:0112341	hereditary spastic paraplegia 80						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:0112064	immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447362	Slc24a4	implicated_via_orthology	DOID:0110063	amelogenesis imperfecta hypomaturation type 2A5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97495	Pbx1	implicated_via_orthology	DOID:0112359	congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97351	Nkx2-6	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	implicated_via_orthology	DOID:0110068	frontotemporal dementia and/or amyotrophic lateral sclerosis-3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107732	Myo1a	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156538	Pkd1l1	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	implicated_via_orthology	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:0110543	autosomal dominant nonsyndromic deafness 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:0070273	hereditary nonpolyposis colorectal cancer type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915625	Ndufa8	implicated_via_orthology	DOID:0112065	nuclear type mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921372	Tmem43	implicated_via_orthology	DOID:0112373	autosomal dominant auditory neuropathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	implicated_via_orthology	DOID:0110412	retinitis pigmentosa 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384584	Rfwd3	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97749	Ppia	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922656	Ndufs7	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	implicated_via_orthology	DOID:0111336	craniofacial-deafness-hand syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	implicated_via_orthology	DOID:5408	Paget's disease of bone						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921273	Rd3	implicated_via_orthology	DOID:0110080	Leber congenital amaurosis 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101850	Usp45	implicated_via_orthology	DOID:0081169	Leber congenital amaurosis 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:0060651	MYH-9 related disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	implicated_via_orthology	DOID:0110999	Joubert syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914297	Rars1	implicated_via_orthology	DOID:0060791	hypomyelinating leukodystrophy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929096	Thsd1	implicated_via_orthology	DOID:0080975	intracranial berry aneurysm 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:0112103	Sotos syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157980	Vac14	implicated_via_orthology	DOID:4751	striatonigral degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98810	Tpm2	implicated_via_orthology	DOID:0110932	nemaline myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108053	Rit1	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3044321	Tgm6	implicated_via_orthology	DOID:0050982	spinocerebellar ataxia type 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913290	Nfu1	implicated_via_orthology	DOID:0080133	multiple mitochondrial dysfunctions syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:0110790	hereditary spastic paraplegia 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:0111121	nephronophthisis 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102567	Nrl	implicated_via_orthology	DOID:0110397	retinitis pigmentosa 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921086	Slc35b2	implicated_via_orthology	DOID:0070403	hypomyelinating leukodystrophy 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	implicated_via_orthology	DOID:0110324	hypertrophic cardiomyopathy 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107742	Stra6	implicated_via_orthology	DOID:0111807	syndromic microphthalmia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340031	Nfkbil1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924859	Odad3	implicated_via_orthology	DOID:0110624	primary ciliary dyskinesia 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:0080204	renal hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914533	Slc25a19	implicated_via_orthology	DOID:655	inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103039	Stat2	implicated_via_orthology	DOID:0111975	immunodeficiency 44						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384997	Ube2e2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	implicated_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040695	Palb2	implicated_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142989	Ncapd3	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353433	Timm8a1	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913356	Smpx	implicated_via_orthology	DOID:0111735	X-linked deafness 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:13884	sick sinus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137600	Rcc1l	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97372	Npr2	implicated_via_orthology	DOID:0080050	acromesomelic dysplasia, Maroteaux type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196373	Reps1	implicated_via_orthology	DOID:0110734	neurodegeneration with brain iron accumulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:0060668	anencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101876	Tead1	implicated_via_orthology	DOID:0111228	Sveinsson chorioretinal atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107624	Mvk	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921302	Ttc21a	implicated_via_orthology	DOID:0111927	spermatogenic failure 37						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920662	Nme8	implicated_via_orthology	DOID:0110606	primary ciliary dyskinesia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913725	Rps23	implicated_via_orthology	DOID:0070415	brachycephaly, trichomegaly, and developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:0111035	CADASIL 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684938	Prdm6	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	implicated_via_orthology	DOID:12801	mucopolysaccharidosis III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0111078	tibial muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109352	Ung	implicated_via_orthology	DOID:11702	dysgammaglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923515	Tsen54	implicated_via_orthology	DOID:0060273	pontocerebellar hypoplasia type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922656	Ndufs7	implicated_via_orthology	DOID:0112093	nuclear type mitochondrial complex I deficiency 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97351	Nkx2-6	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339639	Ogt	implicated_via_orthology	DOID:0080240	non-syndromic X-linked intellectual disability 106						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105065	Rab24	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	implicated_via_orthology	DOID:0080459	developmental and epileptic encephalopathy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386296	Pars2	implicated_via_orthology	DOID:0112211	developmental and epileptic encephalopathy 75						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446244	Setd1a	implicated_via_orthology	DOID:0070417	neurodevelopmental disorder with speech impairment and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385896	Trappc14	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441856	Sf3b2	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916730	Ttc9	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:4404	occupational dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339656	Pak3	implicated_via_orthology	DOID:0112051	non-syndromic X-linked intellectual disability 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651811	Tph2	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0111001	Joubert syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142075	Nars2	implicated_via_orthology	DOID:0111485	combined oxidative phosphorylation deficiency 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97616	Plcg2	implicated_via_orthology	DOID:0090064	familial cold autoinflammatory syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918294	Trp53rka	implicated_via_orthology	DOID:0080246	Galloway-Mowat syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97857	Rarb	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:0080548	Noonan syndrome with multiple lentigines 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098583	Stag2	implicated_via_orthology	DOID:0111845	Mullegama-Klein-Martinez syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183441	Psat1	implicated_via_orthology	DOID:0080075	Neu-Laxova syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:0110233	cataract 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916856	Mtfmt	implicated_via_orthology	DOID:0111491	combined oxidative phosphorylation deficiency 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858214	Ppm1d	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929996	Trpm7	implicated_via_orthology	DOID:0111246	amyotrophic lateral sclerosis-parkinsonism/dementia complex 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385906	Spg7	implicated_via_orthology	DOID:0110816	hereditary spastic paraplegia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919210	Myh14	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	implicated_via_orthology	DOID:0080219	dystransthyretinemic hyperthyroxinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106264	Trim36	implicated_via_orthology	DOID:0060668	anencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	implicated_via_orthology	DOID:5408	Paget's disease of bone						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147716	Slc16a12	implicated_via_orthology	DOID:0070353	cataract 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:0110432	dilated cardiomyopathy 1NN						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:0060203	amyotrophic lateral sclerosis type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913631	Rnf113a2	implicated_via_orthology	DOID:0111868	nonphotosensitive trichothiodystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913468	Ndufb9	implicated_via_orthology	DOID:0112079	nuclear type mitochondrial complex I deficiency 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446120	Odad1	implicated_via_orthology	DOID:0110625	primary ciliary dyskinesia 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384849	Tnpo2	implicated_via_orthology	DOID:0081262	intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103078	Spr	implicated_via_orthology	DOID:0111168	sepiapterin reductase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140300	Myorg	implicated_via_orthology	DOID:0060230	basal ganglia calcification						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	implicated_via_orthology	DOID:0111548	ring dermoid of cornea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3577015	Otulin	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:11105	fundus albipunctatus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915523	Pomgnt1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103039	Stat2	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98824	Trhr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137410	Twnk	implicated_via_orthology	DOID:0111520	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889800	Myot	implicated_via_orthology	DOID:0080094	myofibrillar myopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102722	Pcnt	implicated_via_orthology	DOID:0060609	microcephalic osteodysplastic primordial dwarfism type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99906	Tie1	implicated_via_orthology	DOID:0050580	hereditary lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261422	Naga	implicated_via_orthology	DOID:2367	neuroaxonal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98813	Tpo	implicated_via_orthology	DOID:0112186	thyroid dyshormonogenesis 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346344	Nr0b2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313275	Nthl1	implicated_via_orthology	DOID:0080411	familial adenomatous polyposis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102896	Sult1a1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144177	Pex12	implicated_via_orthology	DOID:0081241	peroxisome biogenesis disorder 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:0110477	autosomal recessive nonsyndromic deafness 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927197	Shoc2	implicated_via_orthology	DOID:0080692	Noonan syndrome-like disorder with loose anagen hair 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920040	Ssbp1	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916925	Pxdn	implicated_via_orthology	DOID:0080612	anterior segment dysgenesis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316659	St3gal3	implicated_via_orthology	DOID:0081180	autosomal recessive intellectual developmental disorder 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143599	Traf3ip2	implicated_via_orthology	DOID:2058	chronic mucocutaneous candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99261	Ptgds	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109550	Tnnt3	implicated_via_orthology	DOID:0111599	distal arthrogryposis type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0081341	congenital myopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858421	Rfx5	implicated_via_orthology	DOID:5812	MHC class II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	implicated_via_orthology	DOID:0060447	epithelial basement membrane dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2677271	Slc24a5	implicated_via_orthology	DOID:0080614	oculocutaneous albinism type VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96522	Rbpj	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926483	Nectin1	implicated_via_orthology	DOID:0060773	cleft lip-palate-ectodermal dysplasia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330275	Ptgdr2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916867	Pitrm1	implicated_via_orthology	DOID:0070411	autosomal recessive spinocerebellar ataxia 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894681	Usp9x	implicated_via_orthology	DOID:0112026	non-syndromic X-linked intellectual disability 99						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107932	Ndufs6	implicated_via_orthology	DOID:0112073	nuclear type mitochondrial complex I deficiency 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	implicated_via_orthology	DOID:0112157	X-linked atrophic macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137410	Twnk	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0111427	restrictive cardiomyopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:3756	protein C deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927230	Trio	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915228	Tctn2	implicated_via_orthology	DOID:0110993	Joubert syndrome 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:1681	heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103581	Musk	implicated_via_orthology	DOID:0111377	fetal akinesia deformation sequence syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918982	Vps11	implicated_via_orthology	DOID:0060796	hypomyelinating leukodystrophy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354947	Polg2	implicated_via_orthology	DOID:0070447	mitochondrial DNA depletion syndrome 16B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98036	Rpl27	implicated_via_orthology	DOID:0111893	Diamond-Blackfan anemia 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448528	Prdm13	implicated_via_orthology	DOID:0060264	pontocerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108041	Traf3	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:0050547	familial medullary thyroid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442620	Nup133	implicated_via_orthology	DOID:0080694	Galloway-Mowat syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	implicated_via_orthology	DOID:0080349	developmental and epileptic encephalopathy 39						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921381	Sash3	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918103	Vwa3b	implicated_via_orthology	DOID:0111614	autosomal recessive spinocerebellar ataxia 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	implicated_via_orthology	DOID:3495	extrahepatic bile duct adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098267	Ogdh	implicated_via_orthology	DOID:0081326	oxoglutarate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	implicated_via_orthology	DOID:0111028	hemochromatosis type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96522	Rbpj	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917700	Unc13d	implicated_via_orthology	DOID:0110923	familial hemophagocytic lymphohistiocytosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:2218	blood platelet disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	implicated_via_orthology	DOID:0060316	orofaciodigital syndrome I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889583	Sh3kbp1	implicated_via_orthology	DOID:0111999	immunodeficiency 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913676	Ndufaf8	implicated_via_orthology	DOID:0112091	nuclear type mitochondrial complex I deficiency 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98247	Scn1b	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917457	Taco1	implicated_via_orthology	DOID:0070495	mitochondrial complex IV deficiency nuclear type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0110307	hypertrophic cardiomyopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98299	Shmt1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97359	Nodal	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:0081007	RNASET2-deficient cystic leukoencephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648526	Ndufs6b	implicated_via_orthology	DOID:0112073	nuclear type mitochondrial complex I deficiency 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	implicated_via_orthology	DOID:0070169	spermatogenic failure 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:0080954	arthrogryposis multiplex congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97930	Rlbp1	implicated_via_orthology	DOID:11105	fundus albipunctatus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:0050576	Senior-Loken syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923760	Trappc9	implicated_via_orthology	DOID:0081098	autosomal recessive intellectual developmental disorder 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:3507	dermatofibrosarcoma protuberans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336172	Tbl1x	implicated_via_orthology	DOID:0111837	congenital nongoitrous hypothyroidism 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336189	Rs1	implicated_via_orthology	DOID:8465	retinoschisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:0090018	autosomal dominant familial periodic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859214	Pmm2	implicated_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	implicated_via_orthology	DOID:0110961	atypical Gaucher's disease due to saposin c deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330233	Tcap	implicated_via_orthology	DOID:0110281	autosomal recessive limb-girdle muscular dystrophy type 2G						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913129	Rbm8a	implicated_via_orthology	DOID:14699	thrombocytopenia-absent radius syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:0080884	vitamin D-dependent rickets type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924836	Mthfd1l	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104968	Ppox	implicated_via_orthology	DOID:4346	variegate porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	implicated_via_orthology	DOID:0112144	retinitis pigmentosa 87						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933163	Trim2	implicated_via_orthology	DOID:0110161	Charcot-Marie-Tooth disease type 2R						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98227	Sag	implicated_via_orthology	DOID:0110712	Oguchi disease-1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:0050661	vitelliform macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0110308	hypertrophic cardiomyopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920180	Ppp2r2b	implicated_via_orthology	DOID:0050962	spinocerebellar ataxia type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140260	Pcsk9	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97829	Pygl	implicated_via_orthology	DOID:2754	glycogen storage disease VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:11975	coloboma of optic nerve						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:0060692	platelet-type bleeding disorder 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914434	Ndufa13	implicated_via_orthology	DOID:0112095	nuclear type mitochondrial complex I deficiency 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918419	Nbas	implicated_via_orthology	DOID:0080716	infantile liver failure syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:0080390	nephrotic syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0110586	autosomal dominant nonsyndromic deafness 65						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894806	Mylk	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0110453	dilated cardiomyopathy 1EE						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108174	Prkg1	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106054	Psmc1	implicated_via_orthology	DOID:0081324	neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:10966	lipoid nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330305	Trpm1	implicated_via_orthology	DOID:0110867	congenital stationary night blindness 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355330	Phgdh	implicated_via_orthology	DOID:0050722	PHGDH deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888921	P3h1	implicated_via_orthology	DOID:0110336	osteogenesis imperfecta type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328357	Unc119	implicated_via_orthology	DOID:0111987	immunodeficiency 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095405	Ptch2	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99660	Pola1	implicated_via_orthology	DOID:0111840	Van Esch-O'Driscoll syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921932	Wdr35	implicated_via_orthology	DOID:0110090	short-rib thoracic dysplasia 7 with or without polydactyly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891978	Phyh	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919276	Trmu	implicated_via_orthology	DOID:0111734	aminoglycoside-induced deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349482	Nherf1	implicated_via_orthology	DOID:0080078	hypophosphatemic nephrolithiasis/osteoporosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328352	Sh2d1a	implicated_via_orthology	DOID:0060705	X-linked lymphoproliferative syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	implicated_via_orthology	DOID:0111030	hemochromatosis type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	implicated_via_orthology	DOID:0090062	familial cold autoinflammatory syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:12010	anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913496	Osgep	implicated_via_orthology	DOID:0080245	Galloway-Mowat syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352451	Nr2f1	implicated_via_orthology	DOID:0112226	Bosch-Boonstra-Schaaf optic atrophy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	implicated_via_orthology	DOID:0060652	familial erythrocytosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924197	Ndufaf6	implicated_via_orthology	DOID:0112078	nuclear type mitochondrial complex I deficiency 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183703	Nav3	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0110320	hypertrophic cardiomyopathy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149332	Ncr3-ps	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	implicated_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98730	Tgm1	implicated_via_orthology	DOID:0060656	autosomal recessive congenital ichthyosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891247	Otof	implicated_via_orthology	DOID:0110535	autosomal recessive nonsyndromic deafness 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670964	Tent5a	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347023	Txnrd2	implicated_via_orthology	DOID:0080620	familial glucocorticoid deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107172	Ppp3r1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684912	Qrich2	implicated_via_orthology	DOID:0111914	spermatogenic failure 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98660	Sry	implicated_via_orthology	DOID:0111761	46,XX sex reversal 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342274	Slc25a15	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104574	Ptprj	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108053	Rit1	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346029	Slc26a4	implicated_via_orthology	DOID:0110498	autosomal recessive nonsyndromic deafness 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917853	Mutyh	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929915	Ncoa6	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:0070480	schwannomatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:0111383	autosomal dominant keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913826	Uqcrh	implicated_via_orthology	DOID:0111139	mitochondrial complex III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684868	Zfp469	implicated_via_orthology	DOID:14775	brittle cornea syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919241	Ercc8	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277961	Plec	implicated_via_orthology	DOID:0060736	epidermolysis bullosa simplex Ogna type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3032636	Ugt1a7c	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921293	Pex26	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97520	Pcx	implicated_via_orthology	DOID:3651	pyruvate carboxylase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926227	Nup160	implicated_via_orthology	DOID:0080394	nephrotic syndrome type 19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2669254	Nanos1	implicated_via_orthology	DOID:0070171	spermatogenic failure 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99678	Actn3	implicated_via_orthology	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919277	Slc39a4	implicated_via_orthology	DOID:0050605	acrodermatitis enteropathica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137410	Twnk	implicated_via_orthology	DOID:0111520	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:0060369	Parkinson's disease 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97566	Pgm3	implicated_via_orthology	DOID:0111953	immunodeficiency 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330301	Dyrk2	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442557	Frmd5	implicated_via_orthology	DOID:0081275	neurodevelopmental disorder with eye movement abnormalities and ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97311	Nfix	implicated_via_orthology	DOID:0112102	Sotos syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443554	Hook3	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915755	Vps51	implicated_via_orthology	DOID:0112332	pontocerebellar hypoplasia type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353657	Fgd3	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261422	Naga	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914649	Pdlim7	implicated_via_orthology	DOID:0080095	myofibrillar myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101770	Ring1	implicated_via_orthology	DOID:0070416	Luo-Schoch-Yamamoto syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	implicated_via_orthology	DOID:0110956	Waardenburg syndrome type 2E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917834	Pak4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:0080379	nephrotic syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104517	Xrcc5	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:14451	hyperkalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:5076	mixed glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915938	Abhd4	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384987	B4galt7	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95816	Grik3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145317	Brd9	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333865	Rfxank	implicated_via_orthology	DOID:5812	MHC class II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97526	Pde6g	implicated_via_orthology	DOID:0110407	retinitis pigmentosa 57						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101759	Rnf2	implicated_via_orthology	DOID:0070416	Luo-Schoch-Yamamoto syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914434	Ndufa13	implicated_via_orthology	DOID:8161	thyroid gland Hurthle cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917819	Wdr36	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923596	Rars2	implicated_via_orthology	DOID:0060275	pontocerebellar hypoplasia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97394	Oat	implicated_via_orthology	DOID:1415	gyrate atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107861	Tubb2a	implicated_via_orthology	DOID:0090135	complex cortical dysplasia with other brain malformations 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384818	Mtss1	implicated_via_orthology	DOID:0081301	intellectual developmental disorder with ocular anomalies and distinctive facial features						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444797	Xylt2	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:0111441	optic atrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916267	Prrt2	implicated_via_orthology	DOID:0081115	benign familial infantile seizures 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99666	Syt2	implicated_via_orthology	DOID:0110659	congenital myasthenic syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:0090044	dystonia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353423	Zfp292	implicated_via_orthology	DOID:0060307	autosomal dominant intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98266	Sord	implicated_via_orthology	DOID:0081376	sorbitol dehydrogenase deficiency with peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918012	Dclk2	implicated_via_orthology	DOID:4428	dyslexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927345	Xrcc2	implicated_via_orthology	DOID:0080874	primary ovarian insufficiency 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98961	Wnt7a	implicated_via_orthology	DOID:0090067	Fuhrmann syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859778	Hif3a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:0060762	restrictive dermopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444401	Snrnp200	implicated_via_orthology	DOID:0110366	retinitis pigmentosa 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108071	Wnt10a	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914523	Ndufa10	implicated_via_orthology	DOID:0112069	nuclear type mitochondrial complex I deficiency 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341787	Trpv1	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352490	Capn11	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098686	Tmc6	implicated_via_orthology	DOID:13777	epidermodysplasia verruciformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106034	Six4	implicated_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153588	Ppp1r3a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926368	Syt5	implicated_via_orthology	DOID:0110659	congenital myasthenic syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107953	Klc2	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928098	Tspan3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924767	Zfyve26	implicated_via_orthology	DOID:0110768	hereditary spastic paraplegia 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443207	Plekhm1	implicated_via_orthology	DOID:0110945	autosomal recessive osteopetrosis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894687	Xrn2	implicated_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347084	Fgd2	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316650	Slc37a4	implicated_via_orthology	DOID:0081330	glycogen storage disease Ib						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914345	Trak1	implicated_via_orthology	DOID:0112204	developmental and epileptic encephalopathy 68						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0060370	Parkinson's disease 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913500	Taf13	implicated_via_orthology	DOID:0081222	autosomal recessive intellectual developmental disorder 60						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106679	Zic2	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859649	Ctnnal1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109178	Fgf13	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	implicated_via_orthology	DOID:0110928	nemaline myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913277	Crbn	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	implicated_via_orthology	DOID:1068	juvenile glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353652	Tor3a	implicated_via_orthology	DOID:0060730	torsion dystonia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926063	Nckap1l	implicated_via_orthology	DOID:0112015	immunodeficiency 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443034	Mtmr12	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:0080787	proximal symphalangism 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932051	Kat5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923605	Tgds	implicated_via_orthology	DOID:0081122	Catel Manzke syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927489	Pdlim5	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88181	Bmp5	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916538	Rhobtb1	implicated_via_orthology	DOID:0070375	developmental and epileptic encephalopathy 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924408	Coq6	implicated_via_orthology	DOID:0070243	primary coenzyme Q10 deficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:0111904	autosomal recessive thrombophilia due to protein C deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924947	Mmab	implicated_via_orthology	DOID:14749	methylmalonic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138628	Obsl1	implicated_via_orthology	DOID:0060241	3-M syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933126	Cdk5rap3	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894697	Rad54l	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180784	Rac3	implicated_via_orthology	DOID:0080235	autosomal dominant intellectual developmental disorder 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915930	Fitm1	implicated_via_orthology	DOID:0081273	Siddiqi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652820	Setd1b	implicated_via_orthology	DOID:0070417	neurodevelopmental disorder with speech impairment and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106684	Slc18a1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98663	Tef	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106919	Vdac1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:0111517	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:0110584	autosomal dominant nonsyndromic deafness 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924834	Spidr	implicated_via_orthology	DOID:14450	46 XX gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106220	Six5	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927489	Pdlim5	implicated_via_orthology	DOID:0080095	myofibrillar myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924937	Kcnq5	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	implicated_via_orthology	DOID:3852	Peutz-Jeghers syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88401	Vsx2	implicated_via_orthology	DOID:0060839	isolated microphthalmia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143676	Zfp365	implicated_via_orthology	DOID:580	uric acid nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045266	Fan1	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	implicated_via_orthology	DOID:0060706	X-linked lymphoproliferative syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429660	Tbc1d4	implicated_via_orthology	DOID:3138	acanthosis nigricans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343044	Rbmx	implicated_via_orthology	DOID:0060826	syndromic X-linked intellectual disability Shashi type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:0111153	congenital mirror movement disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180854	Rfxap	implicated_via_orthology	DOID:5812	MHC class II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98494	Tbx2	implicated_via_orthology	DOID:0070345	vertebral anomalies and variable endocrine and T-cell dysfunction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107814	Tubb1	implicated_via_orthology	DOID:0090102	autosomal dominant macrothrombocytopenia TUBB1-related						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148924	Clic1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298407	Tspan7	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444889	L3mbtl4	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353609	Zbtb18	implicated_via_orthology	DOID:0070052	autosomal dominant intellectual developmental disorder 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389091	Rps15a	implicated_via_orthology	DOID:0111891	Diamond-Blackfan anemia 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103123	Serpinb6a	implicated_via_orthology	DOID:0110536	autosomal recessive nonsyndromic deafness 91						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915917	Trpm4	implicated_via_orthology	DOID:0111076	progressive familial heart block type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107851	Ndufv1	implicated_via_orthology	DOID:0112082	nuclear type mitochondrial complex I deficiency 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98438	Sts	implicated_via_orthology	DOID:1700	X-linked ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:0080235	autosomal dominant intellectual developmental disorder 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0110182	Charcot-Marie-Tooth disease axonal type 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915902	Tab2	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345153	Pacsin2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890773	Actn4	implicated_via_orthology	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926803	Kcnq4	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	implicated_via_orthology	DOID:0070418	vertebral hypersegmentation and orofacial anomalies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106598	Myo5b	implicated_via_orthology	DOID:0060775	microvillus inclusion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108360	Enah	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333799	Xrcc4	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927345	Xrcc2	implicated_via_orthology	DOID:0112272	spermatogenic failure 50						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095733	Pros1	implicated_via_orthology	DOID:2451	protein S deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444306	Nalcn	implicated_via_orthology	DOID:0081048	congenital limbs-face contractures-hypotonia-developmental delay syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890440	Uchl4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107671	Gpm6a	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109272	Vipr1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682937	Zfp341	implicated_via_orthology	DOID:0080595	hyper IgE recurrent infection syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98953	Wnt1	implicated_via_orthology	DOID:0110347	osteogenesis imperfecta type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919802	Hsdl1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449311	Gemin5	implicated_via_orthology	DOID:0070443	neurodevelopmental disorder with cerebellar atrophy and motor dysfunction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344313	Zeb1	implicated_via_orthology	DOID:0110857	posterior polymorphous corneal dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:4511	breast angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:0080584	autosomal dominant Wolfram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684909	Stox1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:0080598	Kleefstra syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0110184	Charcot-Marie-Tooth disease type 4J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194488	Slc32a1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341850	Rb1cc1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926967	Hsd17b12	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926790	Fzr1	implicated_via_orthology	DOID:0070378	developmental and epileptic encephalopathy 109						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384795	Pycr1	implicated_via_orthology	DOID:0070137	autosomal recessive cutis laxa type IIB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933623	Smarcd1	implicated_via_orthology	DOID:0112372	Coffin-Siris syndrome 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915340	Yif1a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919668	Thoc1	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:0080663	atrial standstill 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931028	Recql4	implicated_via_orthology	DOID:2732	Rothmund-Thomson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159566	Kcnh7	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917723	Rapgef4	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108403	Polr1d	implicated_via_orthology	DOID:0080790	Treacher Collins syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103222	Zbtb16	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197523	Tmprss15	implicated_via_orthology	DOID:0111667	enterokinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106442	Vkorc1	implicated_via_orthology	DOID:0112174	combined deficiency of vitamin K-dependent clotting factors 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923091	Rnf139	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894687	Xrn2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927489	Pdlim5	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354961	Synj1	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929658	Tbk1	implicated_via_orthology	DOID:0110069	frontotemporal dementia and/or amyotrophic lateral sclerosis-4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97801	Pth1r	implicated_via_orthology	DOID:0111341	primary failure of tooth eruption						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201671	Synj2	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913496	Osgep	implicated_via_orthology	DOID:0080245	Galloway-Mowat syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347521	Ror2	implicated_via_orthology	DOID:0110969	brachydactyly type B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108109	Ywhag	implicated_via_orthology	DOID:0080282	developmental and epileptic encephalopathy 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109485	Wnt8b	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	implicated_via_orthology	DOID:12971	hereditary spherocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914513	Zswim6	implicated_via_orthology	DOID:0060342	acromelic frontonasal dysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	implicated_via_orthology	DOID:0112187	thyroid dyshormonogenesis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925213	Hook1	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919785	Aldh1b1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039618	Zbtb24	implicated_via_orthology	DOID:0090009	immunodeficiency-centromeric instability-facial anomalies syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442466	Frmd3	implicated_via_orthology	DOID:0081275	neurodevelopmental disorder with eye movement abnormalities and ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347023	Txnrd2	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98507	Tcf7	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109330	Prop1	implicated_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2451073	Xylt1	implicated_via_orthology	DOID:0060462	Desbuquois dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106054	Psmc1	implicated_via_orthology	DOID:0081324	neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108087	Hars1	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:0080060	autosomal recessive spinocerebellar ataxia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070248	autosomal recessive Emery-Dreifuss muscular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	implicated_via_orthology	DOID:0111592	plasminogen deficiency type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098267	Ogdh	implicated_via_orthology	DOID:0070468	Yoon-Bellen neurodevelopmental syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97499	Pcca	implicated_via_orthology	DOID:14701	propionic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928740	Fads3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444508	Fitm2	implicated_via_orthology	DOID:0081273	Siddiqi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913679	Ufsp2	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385848	Bcas3	implicated_via_orthology	DOID:0070408	Hengel-Maroofian-Schols syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95490	Fbn2	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328317	Trex1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919824	Zc3h14	implicated_via_orthology	DOID:0081217	autosomal recessive intellectual developmental disorder 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98147	Rps24	implicated_via_orthology	DOID:0111887	Diamond-blackfan anemia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918346	Sntg1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94873	Pcbd1	implicated_via_orthology	DOID:0081131	BH4-deficient hyperphenylalaninemia D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330305	Trpm1	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:0070442	paroxysmal nonkinesigenic dyskinesia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913993	Rnf220	implicated_via_orthology	DOID:0070397	hypomyelinating leukodystrophy 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0070247	autosomal dominant Emery-Dreifuss muscular dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95520	Fgf6	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3603821	Zmynd15	implicated_via_orthology	DOID:0070179	spermatogenic failure 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685857	Zfp408	implicated_via_orthology	DOID:0110395	retinitis pigmentosa 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0070247	autosomal dominant Emery-Dreifuss muscular dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0111441	optic atrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181363	Prokr2	implicated_via_orthology	DOID:0090092	hypogonadotropic hypogonadism 3 with or without anosmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388480	Ppp2r5b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	implicated_via_orthology	DOID:0080476	peroxisome biogenesis disorder 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858219	Rcan2	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914160	Tmem107	implicated_via_orthology	DOID:0080253	Meckel syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917665	Stk26	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137706	Actn1	implicated_via_orthology	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036255	Tmtc3	implicated_via_orthology	DOID:0112233	lissencephaly 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	implicated_via_orthology	DOID:0110490	autosomal recessive nonsyndromic deafness 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201406	Slc10a2	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933134	Tusc3	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108071	Wnt10a	implicated_via_orthology	DOID:0111647	Schopf-Schulz-Passarge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108451	Acaca	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3616088	Ogdhl	implicated_via_orthology	DOID:0070468	Yoon-Bellen neurodevelopmental syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915213	Npc2	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933134	Tusc3	implicated_via_orthology	DOID:0081183	autosomal recessive intellectual developmental disorder 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611448	Bin2	implicated_via_orthology	DOID:0111220	centronuclear myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923517	Fads1	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202715	Tcf21	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917232	Spink2	implicated_via_orthology	DOID:0111930	spermatogenic failure 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104665	Soat1	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915127	Naa20	implicated_via_orthology	DOID:0081233	autosomal recessive intellectual developmental disorder 73						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353470	Pdlim4	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914362	Fgf22	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104517	Xrcc5	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687041	Fads2b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924290	Atg16l1	implicated_via_orthology	DOID:0110885	inflammatory bowel disease 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051596	Znhit3	implicated_via_orthology	DOID:0080539	PEHO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353654	Vps26a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136419	Sarm1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107464	Plcb4	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913913	Uba5	implicated_via_orthology	DOID:0111615	autosomal recessive spinocerebellar ataxia 24						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:0111249	uveal coloboma-cleft lip and palate-intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345181	Pacsin1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339639	Ogt	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919055	Nup93	implicated_via_orthology	DOID:0080387	nephrotic syndrome type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98885	Zrsr2-ps1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142292	Mtmr10	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	implicated_via_orthology	DOID:0050548	hereditary sensory neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109192	Actn2	implicated_via_orthology	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913755	Zmynd11	implicated_via_orthology	DOID:0070060	autosomal dominant intellectual developmental disorder 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	implicated_via_orthology	DOID:0080095	myofibrillar myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103574	Amph	implicated_via_orthology	DOID:0111220	centronuclear myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95815	Grik2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641869	Uqcrh-ps1	implicated_via_orthology	DOID:0111139	mitochondrial complex III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891410	Pacsin3	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:2367	neuroaxonal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109272	Vipr1	implicated_via_orthology	DOID:9164	achalasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928761	Slc19a2	implicated_via_orthology	DOID:13382	megaloblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915919	Taok2	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289230	Pxk	implicated_via_orthology	DOID:2835	polycythemia due to hypoxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915237	Ppcs	implicated_via_orthology	DOID:0081159	dilated cardiomyopathy 2C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:14748	Sotos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	implicated_via_orthology	DOID:0060671	cerebral cavernous malformation 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:0112255	homocystinuria-megaloblastic anemia cblE type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159344	Vangl1	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:14452	hypokalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	implicated_via_orthology	DOID:0111770	46,XY sex reversal 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354695	Fbxw7	implicated_via_orthology	DOID:0070420	developmental delay, hypotonia, and impaired language						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933548	Actl6b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96616	Itgb7	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913405	Ufc1	implicated_via_orthology	DOID:0070421	neurodevelopmental disorder with spasticity and poor growth						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102579	Nmt1	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109575	Tecta	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338783	Pts	implicated_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891964	Xrn1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039591	Mtss2	implicated_via_orthology	DOID:0081301	intellectual developmental disorder with ocular anomalies and distinctive facial features						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:0080191	PTEN hamartoma tumor syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914325	Magt1	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:0060574	von Willebrand's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106679	Zic2	implicated_via_orthology	DOID:0110878	holoprosencephaly 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920150	Ndufv2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891247	Otof	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:0110042	Alzheimer's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919541	Sntg2	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929100	Stam2	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859648	Ftsj1	implicated_via_orthology	DOID:0112034	non-syndromic X-linked intellectual disability 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333849	Rasgrp2	implicated_via_orthology	DOID:0111051	platelet-type bleeding disorder 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	implicated_via_orthology	DOID:3529	congenital myopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914490	Taok1	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:0080334	aortic valve disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	implicated_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:13137	Werdnig-Hoffmann disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859648	Ftsj1	implicated_via_orthology	DOID:0112034	non-syndromic X-linked intellectual disability 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98953	Wnt1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685857	Zfp408	implicated_via_orthology	DOID:0111410	exudative vitreoretinopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924504	Yif1b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105090	Slc6a5	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	implicated_via_orthology	DOID:0112013	autosomal dominant mutilating palmoplantar keratoderma with periorificial keratotic plaques						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277977	Ubr1	implicated_via_orthology	DOID:14694	Johanson-Blizzard syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108053	Rit1	implicated_via_orthology	DOID:0060586	Noonan syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180001	Xpnpep2	implicated_via_orthology	DOID:0080941	acquired angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893597	Frg1	implicated_via_orthology	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667778	Serpinb6e	implicated_via_orthology	DOID:0110536	autosomal recessive nonsyndromic deafness 91						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919218	Wdr73	implicated_via_orthology	DOID:0060364	Galloway-Mowat syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107928	Aldh1a2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353450	Aldh1a1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442153	Gak	implicated_via_orthology	DOID:0060891	Parkinson's disease 19A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	implicated_via_orthology	DOID:0070155	hereditary sensory and autonomic neuropathy type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448607	Nyx	implicated_via_orthology	DOID:0110870	congenital stationary night blindness 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181366	Capn8	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914062	Ppcdc	implicated_via_orthology	DOID:0110734	neurodegeneration with brain iron accumulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:0060798	hypomyelinating leukodystrophy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109167	Fgf11	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894688	Serpinb6b	implicated_via_orthology	DOID:0110536	autosomal recessive nonsyndromic deafness 91						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443327	Fa2h	implicated_via_orthology	DOID:0110786	hereditary spastic paraplegia 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106039	Dtna	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351651	Yme1l1	implicated_via_orthology	DOID:0111436	optic atrophy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101772	Snta1	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443101	Trpm3	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	implicated_via_orthology	DOID:9278	hyperargininemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99135	Xpa	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685541	Wdtc1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888984	Tbx21	implicated_via_orthology	DOID:0111579	asthma, nasal polyps, and aspirin intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:0070442	paroxysmal nonkinesigenic dyskinesia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	implicated_via_orthology	DOID:0050891	adrenal cortical adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:0111543	juvenile polyposis-hereditary hemorrhagic telangiectasia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329014	Stam	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916320	Adamts9	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	implicated_via_orthology	DOID:0070238	primary coenzyme Q10 deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388479	Ppp2r5a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891699	Stk25	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96055	Ptpn6	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142227	Lrrk1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109525	Trpc4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353604	Hnf4g	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97932	Xpr1	implicated_via_orthology	DOID:0060230	basal ganglia calcification						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349467	Abcd2	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687041	Fads2b	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921166	Ift57	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685024	Tmem231	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921372	Tmem43	implicated_via_orthology	DOID:0110074	arrhythmogenic right ventricular dysplasia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344338	Tiam2	implicated_via_orthology	DOID:0070444	neurodevelopmental disorder with language delay and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347075	Nbea	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928740	Fads3	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96100	Hivep1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921302	Ttc21a	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	implicated_via_orthology	DOID:0111553	spondyloepiphyseal dysplasia Maroteaux type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:0060916	proteasome-associated autoinflammatory syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	implicated_via_orthology	DOID:0111112	nephronophthisis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916704	Clic3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99603	Smarca2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:0050678	Blau syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98957	Wnt4	implicated_via_orthology	DOID:0111526	Mullerian aplasia and hyperandrogenism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98848	Tshb	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353468	Adamts8	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104576	Lct	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98227	Sag	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298224	Pip5k1c	implicated_via_orthology	DOID:0060653	lethal congenital contracture syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920460	Nup54	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	implicated_via_orthology	DOID:4051	alveolar rhabdomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447762	Yeats2	implicated_via_orthology	DOID:0111693	familial adult myoclonic epilepsy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107335	Bmp8b	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:14452	hypokalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88116	Atp6v0c	implicated_via_orthology	DOID:0070472	early-onset epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858220	Rcan3	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104774	Adra1b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934029	Usp8	implicated_via_orthology	DOID:7004	ACTH-secreting pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352490	Capn11	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921472	Septin14	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	implicated_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894315	Rap1b	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178563	Nt5c2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686271	Opa3	implicated_via_orthology	DOID:0110004	3-methylglutaconic aciduria type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:0060369	Parkinson's disease 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345153	Pacsin2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95810	Gria3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919935	Dnajc6	implicated_via_orthology	DOID:0060891	Parkinson's disease 19A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203732	Slc16a2	implicated_via_orthology	DOID:0050631	Allan-Herndon-Dudley syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143424	Pomgnt2	implicated_via_orthology	DOID:0111231	congenital muscular dystrophy-dystroglycanopathy type A8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98342	Snrpb	implicated_via_orthology	DOID:0111248	cerebrocostomandibular syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929996	Trpm7	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	implicated_via_orthology	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	implicated_via_orthology	DOID:0110581	autosomal dominant nonsyndromic deafness 56						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	implicated_via_orthology	DOID:0111698	proprotein convertase 1/3 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	implicated_via_orthology	DOID:422	congenital structural myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446117	Suox	implicated_via_orthology	DOID:0111270	isolated sulfite oxidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	implicated_via_orthology	DOID:3114	serous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98266	Sord	implicated_via_orthology	DOID:0081376	sorbitol dehydrogenase deficiency with peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203728	Dtnb	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202298	Nmt2	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916704	Clic3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859867	Syt8	implicated_via_orthology	DOID:0110659	congenital myasthenic syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:0110241	cataract 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913382	Prorp	implicated_via_orthology	DOID:0070427	combined oxidative phosphorylation deficiency 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354721	Slc25a13	implicated_via_orthology	DOID:0070342	adult-onset type II citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920334	Pak5	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:0110477	autosomal recessive nonsyndromic deafness 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446244	Setd1a	implicated_via_orthology	DOID:0070417	neurodevelopmental disorder with speech impairment and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687406	Scn4b	implicated_via_orthology	DOID:0110651	long QT syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11963	esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	implicated_via_orthology	DOID:1386	abetalipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	implicated_via_orthology	DOID:0060582	Noonan syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336883	Smad6	implicated_via_orthology	DOID:9827	radioulnar synostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	implicated_via_orthology	DOID:980	choroidal sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	implicated_via_orthology	DOID:12557	Duane retraction syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917206	Ptcd3	implicated_via_orthology	DOID:0112137	combined oxidative phosphorylation deficiency 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	implicated_via_orthology	DOID:0050548	hereditary sensory neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915401	Wls	implicated_via_orthology	DOID:0070473	Zaki syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107246	Tinf2	implicated_via_orthology	DOID:0070018	autosomal dominant dyskeratosis congenita 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384303	Rp1l1	implicated_via_orthology	DOID:0050578	occult macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	implicated_via_orthology	DOID:0070191	autosomal recessive chronic granulomatous disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	implicated_via_orthology	DOID:1926	Gaucher's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917377	Dpf3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:0110149	Charcot-Marie-Tooth disease type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860764	Pde3a	implicated_via_orthology	DOID:0111247	hypertension and brachydactyly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97245	Mxi1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915289	Nmb	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	implicated_via_orthology	DOID:0111252	vestibular schwannomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181366	Capn8	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919602	Zfyve27	implicated_via_orthology	DOID:0110784	hereditary spastic paraplegia 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645398	Fer1l6	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442833	Bbs9	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202384	Ddb1	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88034	Prdx3	implicated_via_orthology	DOID:0070413	autosomal recessive spinocerebellar ataxia 32						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0070117	Meckel syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450877	Tspoap1	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914275	Rpl11	implicated_via_orthology	DOID:0111878	Diamond-Blackfan anemia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915344	Smarcc2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103170	Gfi1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95517	Fgf3	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349482	Nherf1	implicated_via_orthology	DOID:0080078	hypophosphatemic nephrolithiasis/osteoporosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684866	Slfn14	implicated_via_orthology	DOID:0111055	platelet-type bleeding disorder 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338883	Gfpt2	implicated_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140361	Slc35d1	implicated_via_orthology	DOID:0050775	schneckenbecken dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914649	Pdlim7	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933162	Lrba	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99430	Hira	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890564	Rcan1	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932466	Klb	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155456	Bmp2k	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99135	Xpa	implicated_via_orthology	DOID:0110843	xeroderma pigmentosum group A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576090	Ugt1a8	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99523	Prdx1	implicated_via_orthology	DOID:0050715	methylmalonic aciduria and homocystinuria type cblC						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:0110629	Wolfram syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:0060369	Parkinson's disease 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:10632	Wolfram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917951	Nipal1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931627	Fgf16	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890497	Plvap	implicated_via_orthology	DOID:0060774	congenital diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107854	Ess2	implicated_via_orthology	DOID:12583	velocardiofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97485	Pax1	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104517	Xrcc5	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136381	Hadhb	implicated_via_orthology	DOID:0111277	mitochondrial trifunctional protein deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:9296	cleft lip						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	implicated_via_orthology	DOID:0050854	Muckle-Wells syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098687	Aak1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142763	Cyp4v3	implicated_via_orthology	DOID:0050664	Bietti crystalline corneoretinal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138365	Tmem237	implicated_via_orthology	DOID:0110983	Joubert syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446190	Nup188	implicated_via_orthology	DOID:0081272	Sandestig-Stefanova syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109529	Dpf2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87870	Acat1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:0060367	Parkinson's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103150	Slc12a1	implicated_via_orthology	DOID:445	Bartter disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667783	Serpinb6d	implicated_via_orthology	DOID:0110536	autosomal recessive nonsyndromic deafness 91						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344313	Zeb1	implicated_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108061	Wnt10b	implicated_via_orthology	DOID:0090026	split hand-foot malformation 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891731	Stub1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681523	Tnpo1	implicated_via_orthology	DOID:0081262	intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99667	Syt1	implicated_via_orthology	DOID:0110659	congenital myasthenic syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927345	Xrcc2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:0070280	primary autosomal recessive microcephaly 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349919	Ndufb11	implicated_via_orthology	DOID:0111876	linear skin defects with multiple congenital anomalies 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890662	Nherf2	implicated_via_orthology	DOID:0080078	hypophosphatemic nephrolithiasis/osteoporosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681828	Wdr81	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104672	Tfap2b	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103288	Polr1c	implicated_via_orthology	DOID:0060792	hypomyelinating leukodystrophy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107851	Ndufv1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181411	Slc5a2	implicated_via_orthology	DOID:9432	renal glycosuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333871	Hsd17b10	implicated_via_orthology	DOID:0060810	syndromic X-linked intellectual disability type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919055	Nup93	implicated_via_orthology	DOID:0080387	nephrotic syndrome type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:0060368	Parkinson's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:14452	hypokalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444671	Nipal4	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97567	Pgr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0111603	distal arthrogryposis type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96614	Itgb5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:14452	hypokalemic periodic paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891693	Mtmr7	implicated_via_orthology	DOID:14717	centronuclear myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	implicated_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107672	Gpm6b	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138982	Znfx1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927231	Zmym3	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384849	Tnpo2	implicated_via_orthology	DOID:0081262	intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385133	Exosc2	implicated_via_orthology	DOID:0081175	short stature, hearing loss, retinitis pigmentosa, and distinctive facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:4648	familial retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681828	Wdr81	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339949	Adamts4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855701	Zpbp	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:8545	malignant hyperthermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3583957	Wdr72	implicated_via_orthology	DOID:0110061	amelogenesis imperfecta hypomaturation type 2A3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139806	Spart	implicated_via_orthology	DOID:0050886	Troyer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679420	Pak6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347521	Ror2	implicated_via_orthology	DOID:0060764	autosomal recessive Robinow syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98779	Tnnc1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98955	Wnt3	implicated_via_orthology	DOID:0112192	tetraamelia syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922014	Klc4	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	implicated_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920150	Ndufv2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	implicated_via_orthology	DOID:0111083	Fanconi anemia complementation group D2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644133	Zbtb42	implicated_via_orthology	DOID:0060558	lethal congenital contracture syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:2842	Jervell-Lange Nielsen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98881	Tyrp1	implicated_via_orthology	DOID:0070097	oculocutaneous albinism type III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920963	Rbm20	implicated_via_orthology	DOID:0110447	dilated cardiomyopathy 1DD						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:9263	homocystinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:0081154	common variable immunodeficiency 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918041	Hars2	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914481	Tbc1d20	implicated_via_orthology	DOID:0110719	Warburg micro syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	implicated_via_orthology	DOID:0081364	neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333114	Pigq	implicated_via_orthology	DOID:0112213	multiple congenital anomalies-hypotonia-seizures syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352754	Clic4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921968	Snx16	implicated_via_orthology	DOID:2835	polycythemia due to hypoxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889818	Tspan12	implicated_via_orthology	DOID:0111408	exudative vitreoretinopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919027	Ing3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928761	Slc19a2	implicated_via_orthology	DOID:0090117	thiamine-responsive megaloblastic anemia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921275	Nphp3	implicated_via_orthology	DOID:0070121	Meckel syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	implicated_via_orthology	DOID:0111542	familial expansile osteolysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676663	L3mbtl1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915213	Npc2	implicated_via_orthology	DOID:0070114	Niemann-Pick disease type C2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138365	Tmem237	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94866	Dbp	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142227	Lrrk1	implicated_via_orthology	DOID:0060371	Parkinson's disease 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917370	Yars2	implicated_via_orthology	DOID:0111186	myopathy, lactic acidosis, and sideroblastic anemia 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277223	Atxn2	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	implicated_via_orthology	DOID:9258	Waardenburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353605	Tor1b	implicated_via_orthology	DOID:0060730	torsion dystonia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138987	Slc4a11	implicated_via_orthology	DOID:0060649	congenital hereditary endothelial dystrophy of cornea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920393	Wdr37	implicated_via_orthology	DOID:0111675	neurooculocardiogenitourinary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140940	Acacb	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:0060193	amyotrophic lateral sclerosis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101759	Rnf2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109268	Vasp	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277971	Klc3	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859638	Pqbp1	implicated_via_orthology	DOID:0060179	Renpenning syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0070248	autosomal recessive Emery-Dreifuss muscular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387643	B9d2	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88293	Cacna1d	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447813	Serac1	implicated_via_orthology	DOID:0110001	3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183158	Ash1l	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0070248	autosomal recessive Emery-Dreifuss muscular dystrophy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338027	Gdf11	implicated_via_orthology	DOID:0070418	vertebral hypersegmentation and orofacial anomalies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95811	Gria4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98494	Tbx2	implicated_via_orthology	DOID:1681	heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	implicated_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96615	Itgb6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:0050904	salivary gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333883	Lats1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919258	Zfyve19	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:0080235	autosomal dominant intellectual developmental disorder 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140313	Shoc1	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918112	Spata16	implicated_via_orthology	DOID:0070167	spermatogenic failure 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385894	Slc26a1	implicated_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97499	Pcca	implicated_via_orthology	DOID:14701	propionic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919410	Tmem163	implicated_via_orthology	DOID:0070401	hypomyelinating leukodystrophy 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	implicated_via_orthology	DOID:0112253	combined cellular and humoral immune defects with granulomas						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	implicated_via_orthology	DOID:0080450	developmental and epileptic encephalopathy 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103013	Cacna1c	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385007	Stk24	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442463	Irf2bpl	implicated_via_orthology	DOID:0081327	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	implicated_via_orthology	DOID:0060485	Mowat-Wilson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341105	Rp1	implicated_via_orthology	DOID:0110390	retinitis pigmentosa 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97454	Oca2	implicated_via_orthology	DOID:0070096	oculocutaneous albinism type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108092	Bin1	implicated_via_orthology	DOID:0111220	centronuclear myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443231	Wdr19	implicated_via_orthology	DOID:0080806	cranioectodermal dysplasia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891410	Pacsin3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928098	Tspan3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155664	Snx14	implicated_via_orthology	DOID:0080066	autosomal recessive spinocerebellar ataxia 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:0050789	tarsal-carpal coalition syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890496	Elac2	implicated_via_orthology	DOID:0111496	combined oxidative phosphorylation deficiency 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97822	Nectin2	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103569	Xk	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87919	Add2	implicated_via_orthology	DOID:0081361	spastic quadriplegic cerebral palsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387863	Zmynd10	implicated_via_orthology	DOID:0110597	primary ciliary dyskinesia 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920180	Ppp2r2b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194884	Evl	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442058	Nipa1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915267	Mrm2	implicated_via_orthology	DOID:0070448	mitochondrial DNA depletion syndrome 17						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202876	Tcf7l1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:0050438	Frasier syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0111907	thrombophilia due to thrombin defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107978	Klc1	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:2773	contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685145	Oxgr1	implicated_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104779	Prkdc	implicated_via_orthology	DOID:0111961	immunodeficiency 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923517	Fads1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443876	Zbtb11	implicated_via_orthology	DOID:0081230	autosomal recessive intellectual developmental disorder 69						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:0080324	tuberous sclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	implicated_via_orthology	DOID:0110847	xeroderma pigmentosum variant type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576092	Ugt1a9	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	implicated_via_orthology	DOID:6420	pulmonary valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101825	Tango2	implicated_via_orthology	DOID:0081386	TANGO2-related metabolic encephalopathy and arrythmias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	implicated_via_orthology	DOID:0110376	retinitis pigmentosa 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:3764	Denys-Drash syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099809	Fgf10	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97588	Pou1f1	implicated_via_orthology	DOID:9410	panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	implicated_via_orthology	DOID:0110840	Usher syndrome type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107177	Hsd17b3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919686	Tbcd	implicated_via_orthology	DOID:0070423	early onset progressive encephalopathy with brain atrophy and thin corpus callosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345275	Slc11a1	implicated_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194497	Tgif1	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109353	Ufd1	implicated_via_orthology	DOID:12583	velocardiofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330300	Dyrk3	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98885	Zrsr2-ps1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096573	Utp4	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917689	Taf15	implicated_via_orthology	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:3529	congenital myopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679294	Zc4h2	implicated_via_orthology	DOID:0060815	Miles-Carpenter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920933	Atg16l2	implicated_via_orthology	DOID:0110885	inflammatory bowel disease 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352754	Clic4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0060896	Parkinson's disease 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330302	Dyrk1b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196261	Trmt10c	implicated_via_orthology	DOID:0111471	combined oxidative phosphorylation deficiency 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:0050957	spinocerebellar ataxia type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101770	Ring1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106683	Zic1	implicated_via_orthology	DOID:2785	Dandy-Walker syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919192	Myof	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448588	Map3k15	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855691	Map3k6	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333799	Xrcc4	implicated_via_orthology	DOID:4866	salivary gland adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102765	Ptprn	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354947	Polg2	implicated_via_orthology	DOID:0111525	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927345	Xrcc2	implicated_via_orthology	DOID:0111085	Fanconi anemia complementation group U						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0112380	muscular dystrophy-dystroglycanopathy type B2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580642	Ugt1a10	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915548	Ncapd2	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101948	Wnt11	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917285	Rab28	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045342	Zfp711	implicated_via_orthology	DOID:0112046	non-syndromic X-linked intellectual disability 97						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	implicated_via_orthology	DOID:0111766	X-linked VACTERL association						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	implicated_via_orthology	DOID:0110844	xeroderma pigmentosum group C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338073	Cdc45	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924880	Prdm8	implicated_via_orthology	DOID:0111445	progressive myoclonus epilepsy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351335	Atp1a4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107370	Stxbp2	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:0070241	primary coenzyme Q10 deficiency 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108061	Wnt10b	implicated_via_orthology	DOID:0050591	tooth agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444393	Zdhhc9	implicated_via_orthology	DOID:0060824	syndromic X-linked intellectual disability Raymond type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682003	Whrn	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146071	Tubgcp6	implicated_via_orthology	DOID:0080105	microcephaly and chorioretinopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149209	Otoa	implicated_via_orthology	DOID:0110480	autosomal recessive nonsyndromic deafness 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:0110042	Alzheimer's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:13884	sick sinus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921903	Pomk	implicated_via_orthology	DOID:0112381	muscular dystrophy-dystroglycanopathy type C12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914832	Slc25a26	implicated_via_orthology	DOID:0111470	combined oxidative phosphorylation deficiency 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1996	rectum adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917819	Wdr36	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3616088	Ogdhl	implicated_via_orthology	DOID:0070468	Yoon-Bellen neurodevelopmental syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:11963	esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919055	Nup93	implicated_via_orthology	DOID:0080387	nephrotic syndrome type 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:6846	familial melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352748	Dpf1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916997	Zswim7	implicated_via_orthology	DOID:0111910	spermatogenic failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:0112038	non-syndromic X-linked intellectual disability 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923615	Tbx18	implicated_via_orthology	DOID:0080207	CAKUT2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99613	Zap70	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	implicated_via_orthology	DOID:8545	malignant hyperthermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443921	Irf2bp2	implicated_via_orthology	DOID:0081327	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920563	Rpgrip1l	implicated_via_orthology	DOID:0111002	Joubert syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099438	Nsdhl	implicated_via_orthology	DOID:0111898	CK syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106014	Nudc	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99613	Zap70	implicated_via_orthology	DOID:0111943	immunodeficiency 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355274	Uchl3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:0080260	autosomal recessive spinocerebellar ataxia 26						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147627	Yars1	implicated_via_orthology	DOID:0110199	Charcot-Marie-Tooth disease dominant intermediate C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387201	Yrdc	implicated_via_orthology	DOID:0080694	Galloway-Mowat syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659071	Rapgef2	implicated_via_orthology	DOID:0111694	familial adult myoclonic epilepsy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:11589	Riley-Day syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442842	Mtmr9	implicated_via_orthology	DOID:14717	centronuclear myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	implicated_via_orthology	DOID:1882	atrial heart septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298388	Umps	implicated_via_orthology	DOID:0050833	orotic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:0070452	xanthinuria type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441738	Npsr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97512	Pcsk2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929215	Vps41	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889002	Wdr4	implicated_via_orthology	DOID:0080694	Galloway-Mowat syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103306	Tiam1	implicated_via_orthology	DOID:0070444	neurodevelopmental disorder with language delay and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:6270	gastric cardia carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929470	Tyk2	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103287	Zrsr2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277212	Zfp644	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	implicated_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:0060783	ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2451073	Xylt1	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914304	Paics	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	implicated_via_orthology	DOID:0081274	peroxisome biogenesis disorder 14B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:648	kuru						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97394	Oat	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298407	Tspan7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98958	Wnt5a	implicated_via_orthology	DOID:0060766	autosomal dominant Robinow syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660628	Adamts20	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920897	Capn9	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070247	autosomal dominant Emery-Dreifuss muscular dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351471	B9d1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918882	Scn3b	implicated_via_orthology	DOID:0110224	Brugada syndrome 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:0081361	spastic quadriplegic cerebral palsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921941	Tdrd9	implicated_via_orthology	DOID:0111913	spermatogenic failure 30						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153463	Rxfp2	implicated_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334444	Zfpm2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	implicated_via_orthology	DOID:0070093	schizophrenia 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97371	Npr1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:0050650	familial atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145481	Serpinb6c	implicated_via_orthology	DOID:0110536	autosomal recessive nonsyndromic deafness 91						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332635	Mrpl40	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448506	Pi4ka	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	implicated_via_orthology	DOID:0111077	pyruvate kinase deficiency of red cells						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345181	Pacsin1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353424	Timm8b	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926178	Pigt	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109585	Pld1	implicated_via_orthology	DOID:0080633	developmental cardiac valvular defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183747	Fgd4	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655711	Rbm28	implicated_via_orthology	DOID:0112244	alopecia, neurologic defects, and endocrinopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106684	Slc18a1	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679923	Skic3	implicated_via_orthology	DOID:0111415	trichohepatoenteric syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858271	Mtmr1	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353433	Timm8a1	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920897	Capn9	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:0070241	primary coenzyme Q10 deficiency 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333753	Pdcd6ip	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	implicated_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98824	Trhr	implicated_via_orthology	DOID:0111836	congenital nongoitrous hypothyroidism 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102854	Rpl5	implicated_via_orthology	DOID:0111879	Diamond-Blackfan anemia 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3775191	Nlgn4l	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101931	Slc1a2	implicated_via_orthology	DOID:0080442	developmental and epileptic encephalopathy 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	implicated_via_orthology	DOID:9278	hyperargininemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:0111949	immunodeficiency 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107851	Ndufv1	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108114	Slc12a3	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889278	Pdss1	implicated_via_orthology	DOID:0070239	primary coenzyme Q10 deficiency 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97488	Pax4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0060205	frontotemporal dementia and/or amyotrophic lateral sclerosis-6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443207	Plekhm1	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442159	Irf2bp1	implicated_via_orthology	DOID:0081327	neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:0080383	nephrotic syndrome type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0110425	dilated cardiomyopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349473	Ppp2r5e	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:3672	rhabdoid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106034	Six4	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685198	Xirp2	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:12583	velocardiofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:0070369	restrictive dermopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916997	Zswim7	implicated_via_orthology	DOID:14450	46 XX gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859606	Wdr45	implicated_via_orthology	DOID:0110739	neurodegeneration with brain iron accumulation 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106220	Six5	implicated_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913647	Sar1b	implicated_via_orthology	DOID:0060357	chylomicron retention disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041177	Taok3	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106379	Rtcb	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103557	Xpc	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95809	Gria2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924294	Arid2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927347	Smarce1	implicated_via_orthology	DOID:4586	familial meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891217	Zfp423	implicated_via_orthology	DOID:0111122	nephronophthisis 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915268	Cert1	implicated_via_orthology	DOID:0070064	autosomal dominant intellectual developmental disorder 34						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	implicated_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352452	Nr2f2	implicated_via_orthology	DOID:0080943	46,XX sex reversal 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338076	Hivep2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	implicated_via_orthology	DOID:0081152	common variable immunodeficiency 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:0081116	benign familial infantile seizures 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	implicated_via_orthology	DOID:14749	methylmalonic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333799	Xrcc4	implicated_via_orthology	DOID:0050904	salivary gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892977	Slc26a2	implicated_via_orthology	DOID:0070300	multiple epiphyseal dysplasia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3616088	Ogdhl	implicated_via_orthology	DOID:0081326	oxoglutarate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925516	Zfp687	implicated_via_orthology	DOID:0081369	Paget's disease of bone 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919307	Phf10	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914724	Snap29	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098434	Rgs5	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96108	Hlf	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929468	Txn2	implicated_via_orthology	DOID:0111501	combined oxidative phosphorylation deficiency 29						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181664	Hook2	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	implicated_via_orthology	DOID:8545	malignant hyperthermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914649	Pdlim7	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682313	Zfp335	implicated_via_orthology	DOID:0070294	primary autosomal recessive microcephaly 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	implicated_via_orthology	DOID:3529	congenital myopathy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924082	Hyls1	implicated_via_orthology	DOID:0050779	hydrolethalus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97178	Map4	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151070	Ophn1	implicated_via_orthology	DOID:0080311	X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347006	Psma6	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916948	Slc52a3	implicated_via_orthology	DOID:0080632	Fazio-Londe disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351615	Add3	implicated_via_orthology	DOID:0081361	spastic quadriplegic cerebral palsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:1742	drug psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3615492	Timm8a2	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649059	Mymx	implicated_via_orthology	DOID:0080194	Carey-Fineman-Ziter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108061	Wnt10b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913874	Spcs2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920918	Ttc21b	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98472	T	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:0110876	holoprosencephaly 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	implicated_via_orthology	DOID:0060730	torsion dystonia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913725	Rps23	implicated_via_orthology	DOID:0070415	brachycephaly, trichomegaly, and developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098267	Ogdh	implicated_via_orthology	DOID:0081326	oxoglutarate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347520	Ror1	implicated_via_orthology	DOID:0080263	autosomal recessive nonsyndromic deafness 108						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	implicated_via_orthology	DOID:0110949	Waardenburg syndrome type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101772	Snta1	implicated_via_orthology	DOID:9007	sudden infant death syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384837	Slc66a1	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893591	Neurog3	implicated_via_orthology	DOID:0060779	congenital malabsorptive diarrhea 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	implicated_via_orthology	DOID:0050726	tyrosinemia type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675603	Trpm6	implicated_via_orthology	DOID:0060883	intestinal hypomagnesemia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:0070094	oculocutaneous albinism type IA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387643	B9d2	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933199	Setbp1	implicated_via_orthology	DOID:0070509	Schinzel Giedion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98282	Spi1	implicated_via_orthology	DOID:0081142	agammaglobulinemia 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684729	Unc79	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913293	Atp5f1d	implicated_via_orthology	DOID:0070463	mitochondrial complex V (ATP synthase) deficiency nuclear type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445001	Rab3gap1	implicated_via_orthology	DOID:0110716	Warburg micro syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1862037	Slc12a5	implicated_via_orthology	DOID:0111315	idiopathic generalized epilepsy 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922901	Psmg2	implicated_via_orthology	DOID:0060915	proteosome-associated autoinflammatory syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448530	Vps13d	implicated_via_orthology	DOID:0111611	autosomal recessive spinocerebellar ataxia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:0080598	Kleefstra syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107418	Ptprn2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353425	Opn4	implicated_via_orthology	DOID:0110372	retinitis pigmentosa 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183549	Lctl	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	implicated_via_orthology	DOID:758	situs inversus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446242	Atxn2l	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917566	Ndufab1	implicated_via_orthology	DOID:0110734	neurodegeneration with brain iron accumulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135625	Glrx	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099431	Sptlc1	implicated_via_orthology	DOID:0070152	hereditary sensory and autonomic neuropathy type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109183	Fgf12	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:12549	hepatitis A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	implicated_via_orthology	DOID:0081385	ataxia-telangiectasia-like disorder-2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928894	Rpl35a	implicated_via_orthology	DOID:0111883	Diamond-Blackfan anemia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:6271	gastric cardia adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	implicated_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342284	Slc34a2	implicated_via_orthology	DOID:12117	pulmonary alveolar microlithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445217	Xpnpep3	implicated_via_orthology	DOID:0111117	nephronophthisis-like nephropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330861	Dclk1	implicated_via_orthology	DOID:4428	dyslexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448528	Prdm13	implicated_via_orthology	DOID:0070439	North Carolina macular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447362	Slc24a4	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931749	Pum1	implicated_via_orthology	DOID:0111743	cerebellar ataxia type 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143628	L3mbtl3	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103287	Zrsr2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385286	Pgap2	implicated_via_orthology	DOID:0070435	hyperphosphatasia with impaired intellectual development syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135272	Vangl2	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2451073	Xylt1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98809	Tpm1	implicated_via_orthology	DOID:0110457	dilated cardiomyopathy 1Y						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861606	Tacstd2	implicated_via_orthology	DOID:0060449	gelatinous drop-like corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108074	Sptlc2	implicated_via_orthology	DOID:0070157	hereditary sensory and autonomic neuropathy type 1C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913679	Ufsp2	implicated_via_orthology	DOID:0111367	Beukes hip dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	implicated_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	implicated_via_orthology	DOID:3996	urinary system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142763	Cyp4v3	implicated_via_orthology	DOID:0050664	Bietti crystalline corneoretinal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:0080235	autosomal dominant intellectual developmental disorder 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:0070293	primary autosomal recessive microcephaly 2 with or without cortical malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347344	Gla	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95758	Slc2a4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	implicated_via_orthology	DOID:2810	middle lobe syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444461	Pgap3	implicated_via_orthology	DOID:0070436	hyperphosphatasia with impaired intellectual development syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385297	Tpcn2	implicated_via_orthology	DOID:10123	pigmentation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107681	Rps29	implicated_via_orthology	DOID:0111889	Diamond-Blackfan anemia 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106683	Zic1	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384909	Micu1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353496	Slc25a5	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914446	Ube2t	implicated_via_orthology	DOID:0111081	Fanconi anemia complementation group T						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107227	Gtf2h5	implicated_via_orthology	DOID:0111866	trichothiodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890816	Vsx1	implicated_via_orthology	DOID:0110855	posterior polymorphous corneal dystrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98254	Scp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918605	Col24a1	implicated_via_orthology	DOID:37	skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921812	Fer1l4	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97501	Pck1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103020	Syn2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913266	Tk2	implicated_via_orthology	DOID:0111523	autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913596	Ndufb11b	implicated_via_orthology	DOID:0111876	linear skin defects with multiple congenital anomalies 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352463	Nr1h2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95519	Fgf5	implicated_via_orthology	DOID:0080425	developmental and epileptic encephalopathy 47						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443187	Terb1	implicated_via_orthology	DOID:0112355	spermatogenic failure 60						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443631	Pou6f2	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:0080508	Cornelia de Lange syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914690	Mtpap	implicated_via_orthology	DOID:0050943	spastic ataxia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145637	Mtmr6	implicated_via_orthology	DOID:14717	centronuclear myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917680	Tbce	implicated_via_orthology	DOID:0060348	hypoparathyroidism-retardation-dysmorphism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:8505	dermatitis herpetiformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99960	Ewsr1	implicated_via_orthology	DOID:0060198	amyotrophic lateral sclerosis type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338024	Mapk11	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	implicated_via_orthology	DOID:0050833	orotic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928370	Rhog	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681865	Zfat	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:0090041	torsion dystonia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	implicated_via_orthology	DOID:0081364	neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0070379	developmental and epileptic encephalopathy 6B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:0080504	Parkinson's disease 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045253	Scube3	implicated_via_orthology	DOID:0112358	short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106920	Tmpo	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445102	Dhx33	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98961	Wnt7a	implicated_via_orthology	DOID:0112181	Schinzel type phocomelia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	implicated_via_orthology	DOID:0110372	retinitis pigmentosa 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105124	Stt3a	implicated_via_orthology	DOID:0080572	congenital disorder of glycosylation Iw						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	implicated_via_orthology	DOID:0070019	autosomal recessive dyskeratosis congenita 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917912	Clic5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913918	Nipa2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652817	Mtmr11	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:0081129	mandibuloacral dysplasia type B lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:2978	carbohydrate metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913869	Atat1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:11633	thyroid hormone resistance syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931749	Pum1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102537	Nat3	implicated_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922403	Lemd1	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102570	Ndp	implicated_via_orthology	DOID:0111413	X-linked exudative vitreoretinopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196293	Tubgcp4	implicated_via_orthology	DOID:0080107	microcephaly and chorioretinopathy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921585	Xrcc3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97279	Nat1	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891731	Stub1	implicated_via_orthology	DOID:0080029	autosomal recessive spinocerebellar ataxia 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146607	Clic6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106589	Hivep3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920974	Mcee	implicated_via_orthology	DOID:14749	methylmalonic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344037	Rpgr	implicated_via_orthology	DOID:0110414	retinitis pigmentosa 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916966	Trip13	implicated_via_orthology	DOID:0080689	mosaic variegated aneuploidy syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652875	Wnk3	implicated_via_orthology	DOID:0060805	Prieto syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338759	Sec22b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	implicated_via_orthology	DOID:0050947	hereditary hypophosphatemic rickets with hypercalciuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686934	Zfhx2	implicated_via_orthology	DOID:0081075	Marsili syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931751	Pum2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:12271	aniridia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346341	Rnf13	implicated_via_orthology	DOID:0112209	developmental and epileptic encephalopathy 73						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925947	Pus7	implicated_via_orthology	DOID:0081265	intellectual developmental disorder with abnormal behavior, microcephaly, and short stature						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0080719	congenital myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3522699	Trpa1	implicated_via_orthology	DOID:0111729	familial episodic pain syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924066	Sdccag8	implicated_via_orthology	DOID:0110138	Bardet-Biedl syndrome 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387600	Nags	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97801	Pth1r	implicated_via_orthology	DOID:0060387	chondrodysplasia Blomstrand type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261834	Wnt2b	implicated_via_orthology	DOID:0060774	congenital diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154263	Bicra	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261428	Chchd2	implicated_via_orthology	DOID:0080504	Parkinson's disease 22						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446084	Wnt9a	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:0080452	developmental and epileptic encephalopathy 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889002	Wdr4	implicated_via_orthology	DOID:0081051	microcephaly, growth deficiency, seizures, and brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103569	Xk	implicated_via_orthology	DOID:0112107	McLeod syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	implicated_via_orthology	DOID:0112344	hereditary spastic paraplegia 79B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917205	Fars2	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180557	Rhobtb2	implicated_via_orthology	DOID:0070375	developmental and epileptic encephalopathy 64						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	implicated_via_orthology	DOID:13382	megaloblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108071	Wnt10a	implicated_via_orthology	DOID:2121	ectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891965	Vps45	implicated_via_orthology	DOID:0112132	severe congenital neutropenia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3616091	Fer1l5	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261422	Naga	implicated_via_orthology	DOID:0112318	Schindler disease type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141255	Zfp513	implicated_via_orthology	DOID:0110362	retinitis pigmentosa 58						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:0110629	Wolfram syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107363	Stxbp1	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915344	Smarcc2	implicated_via_orthology	DOID:0112367	Coffin-Siris syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861453	Actl6a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98812	Tpmt	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97243	Mx1	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914495	Peli1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921821	Kcnk16	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347084	Fgd2	implicated_via_orthology	DOID:0110192	Charcot-Marie-Tooth disease type 4H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444136	Mars2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	implicated_via_orthology	DOID:9280	carbamoyl phosphate synthetase I deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:0050883	infantile cerebellar-retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154405	Map4k3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329026	Clcnka	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151114	Dgcr8	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355274	Uchl3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860275	Cts8	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890498	Mcoln1	implicated_via_orthology	DOID:0080490	mucolipidosis type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0060173	Timothy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385331	Stard13	implicated_via_orthology	DOID:14447	gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0050557	congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353604	Hnf4g	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	implicated_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107168	Aurkb	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580376	Lemd3	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913316	Gng11	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183703	Nav3	implicated_via_orthology	DOID:0070338	cerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:0050530	intermediate spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039623	Thada	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336213	Mybpc1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893584	Gngt2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347359	Homer3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913125	Pias1	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106213	Chrna6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298230	Cnot7	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442402	Cnot1	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2674366	Rims4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298234	Kcnk4	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346074	Fxr2	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914147	Naa16	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684058	Tbpl2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329045	Tulp3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145950	Scrib	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346882	Map4k1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97252	Myf5	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88047	Aplp2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916992	Tm2d2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353596	Tor2a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3613677	Shank1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96964	Mep1b	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670976	Fez1	implicated_via_orthology	DOID:0111723	Jacobsen Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88393	Chd1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109526	Trpc3	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146616	Eaf2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194503	Atp2a3	implicated_via_orthology	DOID:0050692	Brody myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349470	Trpc7	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686151	Kif28	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921570	Wdr33	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861376	Slc15a1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103300	Rbl1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88294	Cacna1s	implicated_via_orthology	DOID:0060173	Timothy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347354	Homer2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104750	Nrcam	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261820	Cand1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109620	Arvcf	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917278	Dop1b	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142581	Nsd3	implicated_via_orthology	DOID:0112103	Sotos syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442486	Slc25a40	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915841	Mocos	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444912	Mbnl3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890440	Uchl4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107891	Nop2	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099431	Sptlc1	implicated_via_orthology	DOID:0070162	hereditary sensory and autonomic neuropathy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99533	Mef2d	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919246	Fthl17a	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918974	Aox3	implicated_via_orthology	DOID:0060236	xanthinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346883	Map4k2	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	implicated_via_orthology	DOID:0060352	Kleefstra syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924197	Ndufaf6	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106184	Npm1	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921355	Gga2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098268	Kif5b	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:0080508	Cornelia de Lange syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98329	Sstr3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384892	Rhot2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922654	Arhgap36	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443195	Orai2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344394	Lamc3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675856	Fez2	implicated_via_orthology	DOID:0111723	Jacobsen Syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3845785	Jmjd7	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860040	Trim3	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103575	Skp1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0112374	muscular dystrophy-dystroglycanopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918041	Hars2	implicated_via_orthology	DOID:2491	sensory peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385045	Lemd2	implicated_via_orthology	DOID:0110243	cataract 46 juvenile-onset						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138584	Gigyf2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97844	Rab3d	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920497	Mrgbp	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105058	Atp2a1	implicated_via_orthology	DOID:0050692	Brody myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914094	Ormdl2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443731	Mat2a	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855690	Snrpa	implicated_via_orthology	DOID:2994	germ cell cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915930	Fitm1	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96660	Kcna3	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:0081356	spinal muscular atrophy, Jokela type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441841	Cdc42bpa	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918552	Arhgap26	implicated_via_orthology	DOID:0080311	X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860276	Ubqln1	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97253	Myf6	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352451	Nr2f1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096372	Ybx2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388820	Sgcz	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107432	Drp2	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924001	Chd9	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140435	Calr4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916409	Rhebl1	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105926	Rab5a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918770	Grap	implicated_via_orthology	DOID:0111642	autosomal recessive nonsyndromic deafness 114						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153589	Acap3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109528	Trpc1	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:0050669	spastic cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916366	Ubr4	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346052	Apc2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933623	Smarcd1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99532	Mef2a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	implicated_via_orthology	DOID:2717	Bloom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096341	E2f2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919508	Kcnk10	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916320	Adamts9	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913853	Gemin2	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914953	Kirrel3	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276124	Ep400	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918993	Coasy	implicated_via_orthology	DOID:0110740	neurodegeneration with brain iron accumulation 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914545	Rab3c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103016	Ppp1ca	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892995	Dnajc5	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196396	Dpagt1	implicated_via_orthology	DOID:0080562	congenital disorder of glycosylation Ij						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195966	Ctnnd2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:0060486	Perry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181669	Ormdl1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861380	Sphk2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685119	Eif4e1b	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681862	Obscn	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924193	Psapl1	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107184	Cct7	implicated_via_orthology	DOID:2491	sensory peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685177	Megf10	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347004	Mapkbp1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102705	Gng2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135601	Slc1a4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919912	Dis3	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142581	Nsd3	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387863	Zmynd10	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441730	Tbl1xr1	implicated_via_orthology	DOID:0050155	sensory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925542	Orai1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96176	Hoxa4	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99666	Syt2	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177268	Ppp1r3b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97844	Rab3d	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97450	Otx1	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329027	Gk2	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919358	Ddhd2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037820	Kcna10	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336173	Prkaa2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104685	Twist2	implicated_via_orthology	DOID:14768	Saethre-Chotzen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920432	Pear1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679630	Tfap2e	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353563	Snai3	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923831	Wipi2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98368	Sox6	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684313	Togaram1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:0111194	autosomal dominant adult-onset proximal spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915252	Sdhaf4	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443113	Jph4	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104753	Nfasc	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330828	Cdk5r2	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:0060178	familial hemiplegic migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927230	Trio	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105068	Rab7	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916863	Pofut2	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96086	Hhex	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105085	Rbl2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156052	Slc17a6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333752	Hdac6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99425	Rab11b	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:0110403	retinitis pigmentosa 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101772	Snta1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934943	Amn	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932915	Ndel1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149839	Hycc1	implicated_via_orthology	DOID:0060793	hypomyelinating leukodystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105372	Sstr4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922542	Prkd3	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109164	Gng5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107418	Ptprn2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107486	Pex2	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914490	Taok1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87886	Chrna2	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353652	Tor3a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98542	Tcp10b	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:1062	Fanconi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894810	Uty	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894282	Sstr5	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353496	Slc25a5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917452	Ctsll3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915769	Eml1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913472	Serpinb1a	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97245	Mxi1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201386	Nrdc	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104671	Tfap2a	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261428	Chchd2	implicated_via_orthology	DOID:0060214	frontotemporal dementia and/or amyotrophic lateral sclerosis-2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109550	Tnnt3	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036273	Kcnt2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98357	Sox1	implicated_via_orthology	DOID:0111779	X-linked panhypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685011	Dchs1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96840	Ltk	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682300	BC051665	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922570	Etnk1	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99458	Mef2c	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154405	Map4k3	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101781	Sntb1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926803	Kcnq4	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	implicated_via_orthology	DOID:0080093	myofibrillar myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388820	Sgcz	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99603	Smarca2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0050557	congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309489	Cask	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860283	Ubqln2	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354961	Synj1	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921677	Eaf1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353651	Gnl3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109163	Gng8	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685089	Npc1l1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:0080324	tuberous sclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:0080096	myofibrillar myopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351502	Nup50	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96663	Kcna6	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152971	Rims1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:0050547	familial medullary thyroid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442555	Dis3l2	implicated_via_orthology	DOID:0060476	Perlman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145597	Mbnl2	implicated_via_orthology	DOID:450	myotonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183549	Lctl	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915342	Ncbp2	implicated_via_orthology	DOID:0060419	chromosome 3q29 microdeletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915094	Rab32	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914523	Ndufa10	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925764	Arhgap10	implicated_via_orthology	DOID:0080311	X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201671	Synj2	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442117	Pogz	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443111	Abcc4	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913576	Dnajc5b	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444672	Madd	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88341	Cd53	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98367	Sox5	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347009	Psma5	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917158	Rab3b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926048	Eml4	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353657	Fgd3	implicated_via_orthology	DOID:6683	X-linked Aarskog syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918215	Psd3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861600	Tulp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347084	Fgd2	implicated_via_orthology	DOID:6683	X-linked Aarskog syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355329	Mink1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096393	Snai2	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330307	Dmrt2	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446166	Marveld2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330302	Dyrk1b	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921507	Tspan17	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916510	Ing2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108177	Dhx9	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0070202	familial partial lipodystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338034	Phf2	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108110	Sparcl1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681835	Nlgn2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385079	Ndufs8	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917680	Tbce	implicated_via_orthology	DOID:0060348	hypoparathyroidism-retardation-dysmorphism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448556	Stard8	implicated_via_orthology	DOID:14447	gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925868	Acap2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107423	Numb	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194882	Irs3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96178	Hoxa6	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932544	Ndst3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96659	Kcna2	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101931	Slc1a2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646958	Rplp1rt	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99458	Mef2c	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106594	Gk	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928740	Fads3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347345	Homer1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103265	Frk	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925503	Map4k5	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141917	Prkd2	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109377	Ell	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445001	Rab3gap1	implicated_via_orthology	DOID:0060237	Warburg micro syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159344	Vangl1	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923206	Srrm2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685325	Hspb6	implicated_via_orthology	DOID:0080093	myofibrillar myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329033	Agxt	implicated_via_orthology	DOID:0111670	primary hyperoxaluria type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915344	Smarcc2	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933180	Fthl17e	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922656	Ndufs7	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:0060214	frontotemporal dementia and/or amyotrophic lateral sclerosis-2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645690	Gng14	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101771	Sntb2	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891341	Lpin2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	implicated_via_orthology	DOID:0111208	obsolete distal hereditary motor neuronopathy type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346093	Psmc4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918794	Arhgap42	implicated_via_orthology	DOID:0080311	X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580376	Lemd3	implicated_via_orthology	DOID:0110243	cataract 46 juvenile-onset						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104689	Cct4	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101898	Pou2f1	implicated_via_orthology	DOID:2914	immune system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045291	Ubqln3	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890496	Elac2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99667	Syt1	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96605	Itga6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888677	Gigyf1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442334	Kirrel2	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889364	Akirin2	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328359	Pkp1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652875	Wnk3	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045256	Fat4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97815	Ptprs	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105074	Slc9a4	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919030	Isyna1	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353657	Fgd3	implicated_via_orthology	DOID:0110192	Charcot-Marie-Tooth disease type 4H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444912	Mbnl3	implicated_via_orthology	DOID:450	myotonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96208	Hoxd4	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321392	Pex7	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606576	Cdnf	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041177	Taok3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353604	Hnf4g	implicated_via_orthology	DOID:1062	Fanconi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387006	Gipc3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107186	Cct2	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104750	Nrcam	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919307	Phf10	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87879	Aco1	implicated_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888498	Gabrq	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916412	Sec31a	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444087	Slc1a7	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917143	Coa7	implicated_via_orthology	DOID:0070465	spinocerebellar ataxia with axonal neuropathy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95620	Gabrb2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919824	Zc3h14	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444508	Fitm2	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194882	Irs3	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98368	Sox6	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:14320	generalized anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932545	Ndst4	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0050766	choreaacanthocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914243	Smarcd3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103013	Cacna1c	implicated_via_orthology	DOID:0060173	Timothy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105073	Tnni1	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108519	Meis3	implicated_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136940	Pias4	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96661	Kcna4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141070	Ccz1	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915344	Smarcc2	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276574	Nsd2	implicated_via_orthology	DOID:0112103	Sotos syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329027	Gk2	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99435	Arf6	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97440	Oprl1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385045	Lemd2	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685187	Sec31b	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107184	Cct7	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:0111619	combined D-2- and L-2-hydroxyglutaric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098615	Kank3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97555	Pgk1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927144	Sav1	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153063	Parvb	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921241	Atl1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95590	Ftl2-ps	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889619	Cts6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913325	Chchd3	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95485	Fasn	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97843	Rab3a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930618	Krit1	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928268	Ireb2	implicated_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3043381	Kank4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97770	Prodh	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353589	Cbx8	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336175	Kcnk5	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99917	Slc1a3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195276	Bloc1s1	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918615	Pdss2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098266	Chl1	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109359	Nek2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929492	Atl2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102703	Gng4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352448	Pkd2l1	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95619	Gabrb1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196288	Eif6	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652845	Cdc42bpg	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349481	Ing1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443331	Rims3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096349	Ptprq	implicated_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914953	Kirrel3	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098754	Psmc3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99603	Smarca2	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917656	Vps26b	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925875	Acsbg3	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108074	Sptlc2	implicated_via_orthology	DOID:0070162	hereditary sensory and autonomic neuropathy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915237	Ppcs	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88431	Cnbp	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103265	Frk	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109571	Tulp1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109525	Trpc4	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894702	Numbl	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917979	Nos1ap	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354947	Polg2	implicated_via_orthology	DOID:0111525	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:0112103	Sotos syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137668	Zfhx4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685228	Gm382	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921831	Sbf2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891342	Lpin3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106684	Slc18a1	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922088	Naa15	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915192	Atp5mc2	implicated_via_orthology	DOID:0111143	mitochondrial complex V (ATP synthase) deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913775	Timm50	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351511	Psmd7	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915237	Ppcs	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99780	Kdm5d	implicated_via_orthology	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891915	Foxo4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109366	Kcnk2	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354373	Sall2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444036	Srcap	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3713070	Fthl17d	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929913	Bcl11b	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95594	Fut4	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096566	Pias2	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4938017	Gm17190	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109339	Eya3	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316649	Sphk1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0080096	myofibrillar myopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917689	Taf15	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915202	Tomm20	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98361	Sox13	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109341	Eya2	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330302	Dyrk1b	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96921	Max	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928379	Get3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388270	Acap1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890621	Donson	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103150	Slc12a1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102844	Mybpc3	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95822	Grin2c	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915021	Arpc5	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:0060236	xanthinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	implicated_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443881	Rasal2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104515	Bmp8a	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103040	Rsu1	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923805	Mmaa	implicated_via_orthology	DOID:14749	methylmalonic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330828	Cdk5r2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97451	Otx2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109353	Ufd1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449316	Syne2	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384583	Zfp280d	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353654	Vps26a	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891496	Jph2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891833	Pfkp	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919379	Pex13	implicated_via_orthology	DOID:0080485	peroxisome biogenesis disorder 11A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336170	Mybpc2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109490	Sms	implicated_via_orthology	DOID:0060802	syndromic X-linked intellectual disability Snyder type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934943	Amn	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314882	Hipk3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341265	Camk2d	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336169	Gng10	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183683	Nav1	implicated_via_orthology	DOID:0070338	cerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933623	Smarcd1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926135	Coro7	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104991	Mxd4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920978	Psd	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338046	Mrps33	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444306	Nalcn	implicated_via_orthology	DOID:0081048	congenital limbs-face contractures-hypotonia-developmental delay syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97438	Oprd1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918957	Ubiad1	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915300	Akirin1	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889818	Tspan12	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109550	Tnnt3	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919683	Rab38	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95805	Grb2	implicated_via_orthology	DOID:0111642	autosomal recessive nonsyndromic deafness 114						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926078	Rhot1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919884	Tdrkh	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150309	Dscaml1	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915938	Abhd4	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:0110317	hypertrophic cardiomyopathy 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180784	Rac3	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914338	Cand2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145597	Mbnl2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107185	Cct5	implicated_via_orthology	DOID:2491	sensory peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894313	Rab6a	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096361	Jpt1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135608	Pard3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444678	Sptlc3	implicated_via_orthology	DOID:0070162	hereditary sensory and autonomic neuropathy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108447	Anp32a	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99914	Lamc1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98179	Rras	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270850	Slc6a2	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105938	Rab5b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096331	Slc1a6	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588271	Degs1l	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95823	Grin2d	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918843	Llgl2	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104805	Snrpb2	implicated_via_orthology	DOID:2994	germ cell cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389091	Rps15a	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151156	Stim2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:0050524	maturity-onset diabetes of the young						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276558	Slc13a2	implicated_via_orthology	DOID:0111668	Kohlschutter-Tonz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109258	Nprl3	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890500	Mcoln3	implicated_via_orthology	DOID:0080490	mucolipidosis type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137385	Ctsq	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858229	Ppp1r3c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919301	Pard3b	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444049	P4ha3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917171	Hnrnpa3	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105306	Rab5c	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915192	Atp5mc2	implicated_via_orthology	DOID:0070445	early-onset dystonia and/or spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039785	Syngap1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449316	Syne2	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335092	Casp14	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:0111627	DOORS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096340	E2f3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916806	Bod1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108411	Prkag1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3617850	Pnpla1	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913658	Aptx	implicated_via_orthology	DOID:0050754	ataxia with oculomotor apraxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107370	Stxbp2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261428	Chchd2	implicated_via_orthology	DOID:0081356	spinal muscular atrophy, Jokela type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921821	Kcnk16	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87912	Acvr2b	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150152	Ubqln4	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108114	Slc12a3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921821	Kcnk16	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917171	Hnrnpa3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0050766	choreaacanthocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347004	Mapkbp1	implicated_via_orthology	DOID:0070293	primary autosomal recessive microcephaly 2 with or without cortical malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:2960	photosensitive trichothiodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933163	Trim2	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914280	Fancl	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929093	Prodh2	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448567	Chd2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353605	Tor1b	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927099	Rplp1	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	implicated_via_orthology	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445415	Pknox2	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442035	Atp5mc3	implicated_via_orthology	DOID:0070445	early-onset dystonia and/or spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88474	Cox5a	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858231	Pkd2l2	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102806	Acvr2a	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108403	Polr1d	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441841	Cdc42bpa	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146207	Gga1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96604	Itga5	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442368	Tmcc1	implicated_via_orthology	DOID:0050667	alcohol-related neurodevelopmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354949	Dlc1	implicated_via_orthology	DOID:14447	gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261864	Wipi1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140844	Nsun5	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928277	Afg3l1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343094	Kat2b	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338068	Pdpk1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:0050692	Brody myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105922	Rpl13	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99832	Sec13	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102682	Llgl1	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681835	Nlgn2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388820	Sgcz	implicated_via_orthology	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098784	Hycc2	implicated_via_orthology	DOID:0060793	hypomyelinating leukodystrophy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588203	Gabrr3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148802	Sec16b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96605	Itga6	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098604	Rragd	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96963	Mep1a	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915344	Smarcc2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685627	Kcnk18	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036255	Tmtc3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3642940	Fthl17b	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336175	Kcnk5	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98953	Wnt1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037820	Kcna10	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183747	Fgd4	implicated_via_orthology	DOID:6683	X-linked Aarskog syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926224	Rbfox1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384159	Gga3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99677	Adcy1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921748	Gorasp1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891495	Jph1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914072	Fbxo25	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037150	Slc13a5	implicated_via_orthology	DOID:0111668	Kohlschutter-Tonz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926943	Atp12a	implicated_via_orthology	DOID:0060178	familial hemiplegic migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353652	Tor3a	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104717	Meis1	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925542	Orai1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858260	Gosr1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96663	Kcna6	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4938017	Gm17190	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913126	Pias3	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924145	Bicd2	implicated_via_orthology	DOID:0070349	spinal muscular atrophy with lower extremity predominant 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354159	E2f6	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922994	Svip	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149021	Unc13c	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	implicated_via_orthology	DOID:12803	Sly syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919122	Aox4	implicated_via_orthology	DOID:0060236	xanthinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105085	Rbl2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336175	Kcnk5	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105941	Mpp1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921821	Kcnk16	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645359	Cc2d2b	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919912	Dis3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107283	Rab6b	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342278	Unc13b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99532	Mef2a	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103305	Alk	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927136	Arl6	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108389	Kif4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:0111194	autosomal dominant adult-onset proximal spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685229	4921511C20Rik	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353468	Adamts8	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387597	Gabrp	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443498	Togaram2	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350917	Rps3	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143854	Nup107	implicated_via_orthology	DOID:0080498	ovarian dysgenesis 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891915	Foxo4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136459	Cdc42bpb	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915919	Taok2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:0060201	amyotrophic lateral sclerosis type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98541	Tcp10a	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88259	Camk2g	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:0070293	primary autosomal recessive microcephaly 2 with or without cortical malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353496	Slc25a5	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261415	Sgpl1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154238	Plxnb1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142973	Lars2	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5825566	Mef2bl	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858751	Rragc	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97812	Ptprd	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917309	Degs2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933621	Smarcd2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353568	Tor1a	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104526	Mef2b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097682	Rps5	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261415	Sgpl1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:0050575	D-2-hydroxyglutaric aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346525	Sgcd	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:0060178	familial hemiplegic migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448492	Kdm6b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104853	Hes1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351628	Rps26	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154240	Plxnb3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329013	Cct6b	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676586	Foxo6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923373	Gpsm2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3529596	Aox2	implicated_via_orthology	DOID:0060236	xanthinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929004	Stk4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045263	Dnajc5g	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101760	Bicd1	implicated_via_orthology	DOID:0070349	spinal muscular atrophy with lower extremity predominant 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445363	Serpinb1c	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918742	Bbs7	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103265	Frk	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920897	Capn9	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330859	Fut9	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343101	Kat2a	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930643	Clcnkb	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916375	Cnot8	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179432	Mycbp2	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891990	Gykl1	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858202	Rab11a	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98328	Sstr2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261428	Chchd2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920455	C9orf72	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861723	Ctsr	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151070	Ophn1	implicated_via_orthology	DOID:0080311	X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106014	Nudc	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101759	Rnf2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926252	Gipc1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99458	Mef2c	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928487	Stk3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101877	Tcf12	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88293	Cacna1d	implicated_via_orthology	DOID:0060173	Timothy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107335	Bmp8b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336172	Tbl1x	implicated_via_orthology	DOID:0050155	sensory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107949	Rhob	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106213	Chrna6	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107653	Atp5mc1	implicated_via_orthology	DOID:0111143	mitochondrial complex V (ATP synthase) deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106217	Cacna1e	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98361	Sox13	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353596	Tor2a	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139793	Cept1	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443388	Kdm7a	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443241	Ndufs1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104649	Cox6a2	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914453	Nde1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276545	Nsd1	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915181	Serpini2	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920897	Capn9	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99780	Kdm5d	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108174	Prkg1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914545	Rab3c	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101877	Tcf12	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104778	Plcb3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339639	Ogt	implicated_via_orthology	DOID:0080240	non-syndromic X-linked intellectual disability 106						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97316	Nfya	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385112	Ndufs2	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891384	Mov10l1	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137379	Med15	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927152	Syne1	implicated_via_orthology	DOID:11726	Emery-Dreifuss muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445114	Pisd	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045323	Trim67	implicated_via_orthology	DOID:0080697	Opitz GBBB syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0070202	familial partial lipodystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914878	Anp32b	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385325	Pnpla7	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684927	Cenpj	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104695	Scnn1g	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921445	Elp3	implicated_via_orthology	DOID:11589	Riley-Day syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926368	Syt5	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685627	Kcnk18	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346524	Sgcg	implicated_via_orthology	DOID:0110436	dilated cardiomyopathy 1L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309489	Cask	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925732	Nup50l	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353604	Hnf4g	implicated_via_orthology	DOID:0050524	maturity-onset diabetes of the young						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913348	Chchd6	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3642941	Fthl17f	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135755	Cox4i2	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196365	Nus1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104631	Utrn	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96660	Kcna3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352452	Nr2f2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096362	Nrxn2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385175	Msto1	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:14768	Saethre-Chotzen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	implicated_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098624	Hes2	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	implicated_via_orthology	DOID:1064	cystinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923022	Pnpla5	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651573	Tub	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890496	Elac2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289294	Dop1a	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891497	Jph3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0050557	congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147707	Kank1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384568	Kank2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104672	Tfap2b	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891396	Kirrel1	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139422	Duox1	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107733	Dctn2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99533	Mef2d	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915743	Ndufaf4	implicated_via_orthology	DOID:0112077	nuclear type mitochondrial complex I deficiency 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106340	Rcor1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0060202	amyotrophic lateral sclerosis type 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:0112374	muscular dystrophy-dystroglycanopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95626	Gabrr2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103099	Cox6a1	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333745	Snapin	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106354	Vps25	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97532	Pdha1	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	implicated_via_orthology	DOID:0060178	familial hemiplegic migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441920	Rcor3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685385	Kalrn	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102806	Acvr2a	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144805	Vipas39	implicated_via_orthology	DOID:0050763	ARC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652875	Wnk3	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685008	Hipk4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153466	Tfap2d	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385325	Pnpla7	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922857	Wnk2	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894653	Npm3	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154239	Plxnb2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387176	Tmem18	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97491	Pax7	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442900	Tmcc3	implicated_via_orthology	DOID:0050667	alcohol-related neurodevelopmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346883	Map4k2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919412	Dhx36	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931144	Parva	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3525200	Anp32-ps	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105064	Slc9a3	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891340	Lpin1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916125	Tmcc2	implicated_via_orthology	DOID:0050667	alcohol-related neurodevelopmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921442	Arpc5l	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051532	Unc13a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135593	Hadha	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914365	Rpl14	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	implicated_via_orthology	DOID:0110192	Charcot-Marie-Tooth disease type 4H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	implicated_via_orthology	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96908	Mxd1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924408	Coq6	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352453	Nr2f6	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109281	Pkp4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445361	Serpinb1b	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	implicated_via_orthology	DOID:0080093	myofibrillar myopathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384841	Chpt1	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096372	Ybx2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913913	Uba5	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926803	Kcnq4	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97547	Pfkl	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914884	Ftmt	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107464	Plcb4	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196281	Dscam	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97487	Pax3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194506	Serpini1	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276574	Nsd2	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347076	Rpl27a	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925230	Sbf1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921252	Psd2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102565	Pou2f3	implicated_via_orthology	DOID:2914	immune system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98330	Snai1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99533	Mef2d	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:0050340	opportunistic bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136459	Cdc42bpb	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888742	Extl1	implicated_via_orthology	DOID:206	hereditary multiple exostoses						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102695	Ptprf	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925503	Map4k5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685574	Dnai2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918639	Chd6	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932139	Oga	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98327	Sstr1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099442	Atxn3	implicated_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87891	Chrnb2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096867	Etv5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913290	Nfu1	implicated_via_orthology	DOID:0080133	multiple mitochondrial dysfunctions syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270850	Slc6a2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96055	Ptpn6	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443195	Orai2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105075	Slc9a2	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858943	Arl6ip1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384781	Tspan10	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339639	Ogt	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:0050430	multiple endocrine neoplasia type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109339	Eya3	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920566	Calr3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926884	Huwe1	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352490	Capn11	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444128	Rasal3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88046	Aplp1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99780	Kdm5d	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96664	Kcna7	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660628	Adamts20	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917745	Atp6ap2	implicated_via_orthology	DOID:5212	congenital disorder of glycosylation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:0050669	spastic cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97276	Myog	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104872	Ppp1cc	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:0110403	retinitis pigmentosa 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104860	Fxr1	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196325	Tspan14	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	implicated_via_orthology	DOID:450	myotonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914724	Snap29	implicated_via_orthology	DOID:0060337	CEDNIK syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920393	Wdr37	implicated_via_orthology	DOID:0111675	neurooculocardiogenitourinary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353605	Tor1b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98367	Sox5	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98353	Son	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	implicated_via_orthology	DOID:0060194	amyotrophic lateral sclerosis type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915089	Gpsm1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201686	Ctbp2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97295	Casp2	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98543	Tcp10c	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097695	Ezh1	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891343	Prkag3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:9263	homocystinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098266	Chl1	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	implicated_via_orthology	DOID:896	metal metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3512628	Cbx6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88475	Cox5b	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88035	Aox1	implicated_via_orthology	DOID:0060236	xanthinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337104	Eya4	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859867	Syt8	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336171	Gng12	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97275	Myod1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101897	Pou2f2	implicated_via_orthology	DOID:2914	immune system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096393	Snai2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923760	Trappc9	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932466	Klb	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98299	Shmt1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385656	Acsbg1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109533	Abcb7	implicated_via_orthology	DOID:0050554	X-linked sideroblastic anemia with ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927343	Rps6kb2	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104526	Mef2b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333883	Lats1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107465	Plcb2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328314	Matn4	implicated_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97347	Nkx2-2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913956	Ndufaf3	implicated_via_orthology	DOID:0112070	nuclear type mitochondrial complex I deficiency 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95625	Gabrr1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88181	Bmp5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96664	Kcna7	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920951	Megf11	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155959	Lnx2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102965	Scn7a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782541	Gng5c	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87912	Acvr2b	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442313	Lrrc1	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107692	Fut7	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039586	Orai3	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685627	Kcnk18	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196332	Arhgap6	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928487	Stk3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917158	Rab3b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137354	Trim9	implicated_via_orthology	DOID:0080697	Opitz GBBB syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919488	Tbc1d5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99423	Etv4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444341	Phf8	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342286	Flii	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136381	Hadhb	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5825566	Mef2bl	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3573933	Serpinb3a	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97843	Rab3a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194882	Irs3	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098266	Chl1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914103	Pnpla2	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924937	Kcnq5	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102854	Rpl5	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448557	Gnl3l	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891396	Kirrel1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685542	Slc9a5	implicated_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928096	Tspan5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339949	Adamts4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3705221	Fthl17c	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278335	Lnx1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95403	Stom	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921392	Lonp1	implicated_via_orthology	DOID:0111274	CODAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88257	Camk2b	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927229	Ctsm	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096875	Wdfy3	implicated_via_orthology	DOID:0070295	primary autosomal dominant microcephaly 18						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442334	Kirrel2	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95588	Fth1	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922258	4930486L24Rik	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:0060393	chromosome 15q11.2 deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919819	Bbs5	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104750	Nrcam	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933134	Tusc3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102765	Ptprn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889209	Gipc2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:92356	Csde1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336175	Kcnk5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353425	Opn4	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0080122	Alpers-Huttenlocher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87886	Chrna2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929501	Arl6ip5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316649	Sphk1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685336	Ubqlnl	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152972	Rims2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136381	Hadhb	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97563	Pgk2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0080096	myofibrillar myopathy 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149021	Unc13c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88449	Col15a1	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101763	Cfl2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136419	Sarm1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105061	Clcn2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913721	Anp32e	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039586	Orai3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349467	Abcd2	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444401	Snrnp200	implicated_via_orthology	DOID:0110366	retinitis pigmentosa 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88417	Clcn1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925860	Uvrag	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	implicated_via_orthology	DOID:14320	generalized anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104649	Cox6a2	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96602	Itga3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0111596	distal arthrogryposis type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108087	Hars1	implicated_via_orthology	DOID:2491	sensory peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201685	Ctbp1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104576	Lct	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346882	Map4k1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104696	Scnn1b	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107653	Atp5mc1	implicated_via_orthology	DOID:0070445	early-onset dystonia and/or spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	implicated_via_orthology	DOID:0060352	Kleefstra syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95787	Gng7	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95305	Eif4e	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685024	Tmem231	implicated_via_orthology	DOID:4501	orofaciodigital syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914453	Nde1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196386	Slc25a39	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109524	Trpc5	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447532	Als2cl	implicated_via_orthology	DOID:0060194	amyotrophic lateral sclerosis type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:11720	distal myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3775191	Nlgn4l	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96659	Kcna2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152695	Col4a6	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109341	Eya2	implicated_via_orthology	DOID:14702	branchiootorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95622	Gabrd	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104987	Mxd3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384210	Nphp4	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445415	Pknox2	implicated_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352490	Capn11	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152889	Dner	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99960	Ewsr1	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891990	Gykl1	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346330	Banf1	implicated_via_orthology	DOID:0081334	Nestor-Guillermo progeria syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:2106	myotonia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051532	Unc13a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932915	Ndel1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97602	Prkcz	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261425	Drosha	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195985	Cbx4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321119	Aurkc	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104717	Meis1	implicated_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95589	Ftl1	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918673	Epg5	implicated_via_orthology	DOID:0060356	Vici syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97040	Ndst2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99879	Prkd1	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919390	Cep89	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914172	Rras2	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859607	Praf2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444804	Bod1l	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88017	Mat1a	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183691	Nav2	implicated_via_orthology	DOID:0070338	cerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:0060413	chromosome 22q11.2 deletion syndrome, distal						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097711	Degs1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450915	Sec23ip	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929270	Dstn	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101770	Ring1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913862	Ormdl3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685263	Dchs2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442035	Atp5mc3	implicated_via_orthology	DOID:0111143	mitochondrial complex V (ATP synthase) deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858494	Bok	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919455	Eml2	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97178	Map4	implicated_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915062	Ubxn4	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914243	Smarcd3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107851	Ndufv1	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142227	Lrrk1	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103300	Rbl1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97178	Map4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99532	Mef2a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915938	Abhd4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3652039	Rad21l	implicated_via_orthology	DOID:0080508	Cornelia de Lange syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104753	Nfasc	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922857	Wnk2	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	implicated_via_orthology	DOID:3852	Peutz-Jeghers syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99256	Hdlbp	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924937	Kcnq5	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97912	Rheb	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298204	Ppt1	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351315	Eloa	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96661	Kcna4	implicated_via_orthology	DOID:0050989	episodic ataxia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135272	Vangl2	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98810	Tpm2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890811	Npm2	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314873	Hipk1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676586	Foxo6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915529	Mcoln2	implicated_via_orthology	DOID:0080490	mucolipidosis type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096389	Nrxn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095405	Ptch2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135962	Gorasp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102704	Gng3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924627	Kcnt1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151929	Cts3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921496	Gale	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105100	Ctnnd1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	implicated_via_orthology	DOID:206	hereditary multiple exostoses						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107363	Stxbp1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103099	Cox6a1	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96602	Itga3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:0050763	ARC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387612	Eml3	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920211	Slc17a7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	implicated_via_orthology	DOID:6683	X-linked Aarskog syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342278	Unc13b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927343	Rps6kb2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890457	Slc15a2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106594	Gk	implicated_via_orthology	DOID:0060363	glycerol kinase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88113	Atp4a	implicated_via_orthology	DOID:0060178	familial hemiplegic migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685089	Npc1l1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922314	Zcchc13	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183747	Fgd4	implicated_via_orthology	DOID:0110192	Charcot-Marie-Tooth disease type 4H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329034	Ccne2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686934	Zfhx2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859026	Cnot4	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914325	Magt1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916625	Btbd9	implicated_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919425	Mfsd8	implicated_via_orthology	DOID:0110722	neuronal ceroid lipofuscinosis 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919819	Bbs5	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2674093	Psd4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334458	Pex19	implicated_via_orthology	DOID:0080486	peroxisome biogenesis disorder 12A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0070202	familial partial lipodystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181366	Capn8	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861380	Sphk2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95621	Gabrb3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664670	Pkd1l3	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933621	Smarcd2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916161	Pygo2	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914482	Nprl2	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108029	Scn10a	implicated_via_orthology	DOID:0111294	generalized epilepsy with febrile seizures plus 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:0060809	syndromic X-linked intellectual disability Claes-Jensen type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98809	Tpm1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914981	Fbxo32	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106028	Rhoc	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0110454	dilated cardiomyopathy 1S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96185	Hoxb4	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923517	Fads1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095405	Ptch2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106368	Rbfox3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914935	Dnaaf4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97054	Mov10	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:2907	Goldenhar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916264	Tnik	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	implicated_via_orthology	DOID:2729	dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919390	Cep89	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384909	Micu1	implicated_via_orthology	DOID:0111335	myopathy with extrapyramidal signs						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914832	Slc25a26	implicated_via_orthology	DOID:0111470	combined oxidative phosphorylation deficiency 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96654	Kcna1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107943	Cct6a	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385079	Ndufs8	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97533	Pdha2	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652845	Cdc42bpg	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351335	Atp1a4	implicated_via_orthology	DOID:0060178	familial hemiplegic migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154244	Plxnd1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2671987	Shank2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929913	Bcl11b	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349426	Ctsj	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99254	Etv1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891989	Npbwr1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314872	Hipk2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0111269	autosomal dominant hyaline body myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:0050778	Meckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860765	Extl3	implicated_via_orthology	DOID:206	hereditary multiple exostoses						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109165	Gngt1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106032	Tfap2c	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351511	Psmd7	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141101	Depdc5	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096377	Traip	implicated_via_orthology	DOID:0070005	Seckel syndrome 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277989	Shmt2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101780	Serpine2	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181366	Capn8	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139207	Sec16a	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929004	Stk4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96195	Hoxc4	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924270	Atl3	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919385	Pygo1	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97548	Pfkm	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	implicated_via_orthology	DOID:4479	pseudohypoaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3775191	Nlgn4l	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107854	Ess2	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341299	Dnm3	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179288	Rttn	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	implicated_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108519	Meis3	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859854	Rcor2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443883	Aldh4a1	implicated_via_orthology	DOID:0080543	hyperprolinemia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443760	Etnk2	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687041	Fads2b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137410	Twnk	implicated_via_orthology	DOID:0111518	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351471	B9d1	implicated_via_orthology	DOID:12712	nephronophthisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0111605	distal arthrogryposis type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588199	Cntnap3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649894	Idi1-ps1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3057108	Lhfpl4	implicated_via_orthology	DOID:0110518	autosomal recessive nonsyndromic deafness 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107157	Sin3a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890357	Igf2bp1	implicated_via_orthology	DOID:0060158	acquired metabolic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98791	Top2b	implicated_via_orthology	DOID:2115	B cell deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913997	Capza1b	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860276	Ubqln1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921268	Als2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:0080391	nephrotic syndrome type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99423	Etv4	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150152	Ubqln4	implicated_via_orthology	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108087	Hars1	implicated_via_orthology	DOID:0110842	Usher syndrome type 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096389	Nrxn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441950	Adgrl3	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	implicated_via_orthology	DOID:0050951	hereditary ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932557	Letm1	implicated_via_orthology	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99780	Kdm5d	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138968	Clp1	implicated_via_orthology	DOID:0060279	pontocerebellar hypoplasia type 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051372	Usp17ld	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782485	Gm4305	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101781	Sntb1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135601	Slc1a4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104860	Fxr1	implicated_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0111190	distal myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353425	Opn4	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88113	Atp4a	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101877	Tcf12	implicated_via_orthology	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926943	Atp12a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106217	Cacna1e	implicated_via_orthology	DOID:0111181	familial hemiplegic migraine 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098827	Reep1	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098808	Pex5	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096584	Psmd2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197517	Limk2	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893578	Scarb1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588271	Degs1l	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201671	Synj2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353437	Scd3	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	implicated_via_orthology	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890358	Igf2bp2	implicated_via_orthology	DOID:0060158	acquired metabolic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96764	Ldhc	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346527	Psmb8	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929264	Sae1	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95542	Fkbp2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106613	Dvl2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443225	Gatad2b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351660	Csnk1e	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108029	Scn10a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352490	Capn11	implicated_via_orthology	DOID:0110821	hereditary spastic paraplegia 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97533	Pdha2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446089	Flnb	implicated_via_orthology	DOID:0111190	distal myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109353	Ufd1	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	implicated_via_orthology	DOID:0050884	triosephosphate isomerase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88046	Aplp1	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344351	Dlg2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444121	Tanc2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	implicated_via_orthology	DOID:2115	B cell deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045256	Fat4	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106221	Capza3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341857	Mad1l1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916672	Pex5l	implicated_via_orthology	DOID:0080477	peroxisome biogenesis disorder 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99435	Arf6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107185	Cct5	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101763	Cfl2	implicated_via_orthology	DOID:0110934	nemaline myopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913565	Senp7	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918788	Fbxo9	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918041	Hars2	implicated_via_orthology	DOID:0110842	Usher syndrome type 3B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045256	Fat4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928947	Scamp4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106028	Rhoc	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105047	Psmc5	implicated_via_orthology	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917176	Dnah17	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5591876	Cdc5lrt1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98511	Tfe3	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103010	Epb41l1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443696	Emc1	implicated_via_orthology	DOID:0081276	cerebellar atrophy, visual impairment, and psychomotor retardation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:0110721	neuronal ceroid lipofuscinosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916409	Rhebl1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261415	Sgpl1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:0050539	Charcot-Marie-Tooth disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277223	Atxn2	implicated_via_orthology	DOID:0050955	spinocerebellar ataxia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136171	Aff4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0111580	Behr syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913750	Slc30a7	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918843	Llgl2	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105374	Npy4r	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051498	Usp17lb	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	implicated_via_orthology	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341044	Alyref	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860374	Mad2l1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444232	Poglut1	implicated_via_orthology	DOID:0110274	autosomal recessive limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97897	Rel	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343094	Kat2b	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051498	Usp17lb	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109550	Tnnt3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442463	Irf2bpl	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341898	Nmur1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3664583	Cntnap5b	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97178	Map4	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353592	Hacd1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051372	Usp17ld	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099431	Sptlc1	implicated_via_orthology	DOID:0050548	hereditary sensory neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145950	Scrib	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917410	Vps36	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316714	Cox7a1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859214	Pmm2	implicated_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	implicated_via_orthology	DOID:0050585	congenital generalized lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354713	Acsl4	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444979	Letm2	implicated_via_orthology	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95822	Grin2c	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679255	Ssh2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339970	Rtn3	implicated_via_orthology	DOID:0110765	hereditary spastic paraplegia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442313	Lrrc1	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330302	Dyrk1b	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104557	Rps6ka3	implicated_via_orthology	DOID:3783	Coffin-Lowry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:422	congenital structural myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858313	Uba2	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922394	Pdzd2	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351511	Psmd7	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139806	Spart	implicated_via_orthology	DOID:0050886	Troyer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87920	Plin2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:10016	multiple endocrine neoplasia type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782483	Gm4303	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106040	Cyp51	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346022	Mab21l2	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195272	Eda	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349406	Ddx3y	implicated_via_orthology	DOID:0050457	Sertoli cell-only syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443397	Trib1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923515	Tsen54	implicated_via_orthology	DOID:0060273	pontocerebellar hypoplasia type 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915270	Coa8	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150309	Dscaml1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0050539	Charcot-Marie-Tooth disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97178	Map4	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:0070042	Coffin-Siris syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890505	Plin1	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98443	Surf1	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917810	Wars2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106927	Aff3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0080125	mitochondrial DNA depletion syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289252	Ppp2r2d	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664902	Mark1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915164	Coq9	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919586	Iars2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104724	Fdxr	implicated_via_orthology	DOID:2742	auditory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139714	Adgrl2	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355333	Nckap1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102944	Ube2b	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442313	Lrrc1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679260	Crb2	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918639	Chd6	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309465	Slc12a4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915835	Rtn4	implicated_via_orthology	DOID:0110765	hereditary spastic paraplegia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153089	Mrps2	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106589	Hivep3	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:0070113	Niemann-Pick disease type C1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443456	Tbc1d24	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:896	metal metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914103	Pnpla2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:0060900	Parkinson's disease 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107157	Sin3a	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645984	Skor2	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584508	Kcnh5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338890	Cacna2d3	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105306	Rab5c	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446237	Vps33b	implicated_via_orthology	DOID:0050763	ARC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105938	Rab5b	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858219	Rcan2	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97805	Ptpn1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681828	Wdr81	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96100	Hivep1	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915240	Mpc1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109296	Sqle	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109446	Doc2a	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178798	Vps54	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443301	Slc35c1	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920907	Fbrsl1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:0050524	maturity-onset diabetes of the young						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:0070046	Coffin-Siris syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914838	Rnf41	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159566	Kcnh7	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159566	Kcnh7	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889583	Sh3kbp1	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921437	Katnb1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97357	Mycn	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918238	4931428L18Rik	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045291	Ubqln3	implicated_via_orthology	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037150	Slc13a5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915302	Rps13	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353424	Timm8b	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919379	Pex13	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108174	Prkg1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102500	mt-Nd2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98907	Uox	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858210	Stx7	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145597	Mbnl2	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443473	Skor1	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346831	Esrra	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859993	Smad9	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107335	Bmp8b	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933623	Smarcd1	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96055	Ptpn6	implicated_via_orthology	DOID:0060578	Noonan syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95776	Gnaq	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444912	Mbnl3	implicated_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105068	Rab7	implicated_via_orthology	DOID:0050539	Charcot-Marie-Tooth disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104684	Eps8	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88930	Reep3	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353425	Opn4	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107495	Myl7	implicated_via_orthology	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97348	Nkx2-3	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97912	Rheb	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924001	Chd9	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914345	Trak1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915566	Apoo	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88065	Araf	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914218	Plin5	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916043	Rab3gap2	implicated_via_orthology	DOID:0060237	Warburg micro syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446242	Atxn2l	implicated_via_orthology	DOID:0050955	spinocerebellar ataxia type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154239	Plxnb2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104783	Atxn1	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387176	Tmem18	implicated_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915240	Mpc1	implicated_via_orthology	DOID:0080363	mitochondrial pyruvate carrier deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97040	Ndst2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:0110735	neurodegeneration with brain iron accumulation 2a						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	implicated_via_orthology	DOID:0050593	primary congenital glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917297	Trnt1	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385025	Alg12	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345146	Grk1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95769	Gna14	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342273	Gsto1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347056	Esrrg	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384159	Gga3	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343135	Ndufs4	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861438	Gcm2	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646013	Cntnap5c	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349480	Scamp1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919594	Usp36	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917689	Taf15	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183158	Ash1l	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442153	Gak	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:8712	neurofibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194490	Diaph1	implicated_via_orthology	DOID:0060690	autosomal dominant auditory neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0111181	familial hemiplegic migraine 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346074	Fxr2	implicated_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:0110640	congenital muscular dystrophy due to LMNA mutation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914285	Dnajb4	implicated_via_orthology	DOID:0081353	congenital myopathy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890564	Rcan1	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:0060038	specific developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932544	Ndst3	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88108	Atp1b1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921372	Tmem43	implicated_via_orthology	DOID:0110074	arrhythmogenic right ventricular dysplasia 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107697	Usp17le	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104659	Dll1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96522	Rbpj	implicated_via_orthology	DOID:0060227	Adams-Oliver syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106912	Adgre1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925144	Prickle2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914272	Acad9	implicated_via_orthology	DOID:0112072	nuclear type mitochondrial complex I deficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914155	Plin3	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338001	Gdap2	implicated_via_orthology	DOID:0111616	autosomal recessive spinocerebellar ataxia 27						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3617850	Pnpla1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105073	Tnni1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0111385	inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443760	Etnk2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102952	Dgka	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328787	Smad5	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104753	Nfasc	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916165	Vars2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:0060578	Noonan syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345283	Slc25a1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917162	Nup43	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139916	Med12l	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194503	Atp2a3	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914960	Polr2g	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925927	Rnf20	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341907	Fjx1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934852	Acox2	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100819	Aff1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384936	Spns2	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96799	Mycl	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913612	Exosc3	implicated_via_orthology	DOID:0060266	pontocerebellar hypoplasia type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704336	Rpl10-ps3	implicated_via_orthology	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	implicated_via_orthology	DOID:0110171	Charcot-Marie-Tooth disease axonal type 2S						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346346	Scamp3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352448	Pkd2l1	implicated_via_orthology	DOID:0110859	polycystic kidney disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649020	Gm5698	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98541	Tcp10a	implicated_via_orthology	DOID:0070290	primary autosomal recessive microcephaly 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137513	Slc24a3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927144	Sav1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935129	Smarca5	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890500	Mcoln3	implicated_via_orthology	DOID:3343	glycoproteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355272	Csnk1d	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202063	Rps3a1	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924001	Chd9	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:0080840	optic atrophy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387176	Tmem18	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98240	Scd2	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97050	Mdh2	implicated_via_orthology	DOID:0080433	developmental and epileptic encephalopathy 51						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:0060160	childhood spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918007	Hacd2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104517	Xrcc5	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333752	Hdac6	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105943	Rpl10	implicated_via_orthology	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97273	Mylpf	implicated_via_orthology	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914430	Yipf5	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670962	Hk3	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097711	Degs1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915089	Gpsm1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919799	Reep4	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	implicated_via_orthology	DOID:13374	fibrodysplasia ossificans progressiva						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443241	Ndufs1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920908	Spns1	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913878	Thg1l	implicated_via_orthology	DOID:0050950	autosomal recessive cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95766	Gna11	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098268	Kif5b	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442632	Cacna2d4	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858220	Rcan3	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351335	Atp1a4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96086	Hhex	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107252	Nsun2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922088	Naa15	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109528	Trpc1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97770	Prodh	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924050	Usp42	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782482	Gm4302	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933947	Rtn1	implicated_via_orthology	DOID:0110765	hereditary spastic paraplegia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0060370	Parkinson's disease 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859214	Pmm2	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98542	Tcp10b	implicated_via_orthology	DOID:0070290	primary autosomal recessive microcephaly 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916948	Slc52a3	implicated_via_orthology	DOID:0050694	Brown-Vialetto-Van Laere syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891917	Ywhab	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105926	Rab5a	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104968	Ppox	implicated_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647146	Cdc5lrt7	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098808	Pex5	implicated_via_orthology	DOID:0080477	peroxisome biogenesis disorder 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109609	Faah	implicated_via_orthology	DOID:0060367	Parkinson's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97548	Pfkm	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858259	Tomm40	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	implicated_via_orthology	DOID:1969	cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107624	Mvk	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860283	Ubqln2	implicated_via_orthology	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	implicated_via_orthology	DOID:0080506	Cornelia de Lange syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104631	Utrn	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88116	Atp6v0c	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3664583	Cntnap5b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338829	Pex16	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99846	Gdi1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196281	Dscam	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889583	Sh3kbp1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349635	Sec23a	implicated_via_orthology	DOID:0070307	craniolenticulosutural dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194513	Psmb5	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100499	Vps4b	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107698	Usp17lc	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98388	Sptbn1	implicated_via_orthology	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183572	Cntnap4	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922831	Yipf7	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927125	Dmrtb1	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920045	Ttc19	implicated_via_orthology	DOID:0060351	mitochondrial complex III deficiency nuclear type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924045	Tbc1d9b	implicated_via_orthology	DOID:0070357	nephrotic syndrome type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929461	Adgrl1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342290	Rps6ka2	implicated_via_orthology	DOID:3783	Coffin-Lowry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143854	Nup107	implicated_via_orthology	DOID:14450	46 XX gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:0111218	Friedreich ataxia 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339970	Rtn3	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104515	Bmp8a	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:0080391	nephrotic syndrome type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333868	Tnnt1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96522	Rbpj	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385262	Kmt5c	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0060205	frontotemporal dementia and/or amyotrophic lateral sclerosis-6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87920	Plin2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3694797	Atxn1l	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:0060762	restrictive dermopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684972	Fhdc1	implicated_via_orthology	DOID:0110205	Charcot-Marie-Tooth disease dominant intermediate E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920036	Tdp1	implicated_via_orthology	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388711	Abca16	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913144	Alyref2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3029632	Med13	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346333	Mrps12	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928277	Afg3l1	implicated_via_orthology	DOID:0080840	optic atrophy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152214	Pip4k2c	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146207	Gga1	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444087	Slc1a7	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914953	Kirrel3	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88449	Col15a1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	implicated_via_orthology	DOID:0080111	mitochondrial complex III deficiency nuclear type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685336	Ubqlnl	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99917	Slc1a3	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339795	Smc3	implicated_via_orthology	DOID:0080507	Cornelia de Lange syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385070	Reep2	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355326	Preb	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935127	Smarca1	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919214	Atad3a	implicated_via_orthology	DOID:440	neuromuscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347056	Esrrg	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913663	Psmd6	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353433	Timm8a1	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:0110640	congenital muscular dystrophy due to LMNA mutation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670962	Hk3	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346051	Dut	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98250	Scn4a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353604	Hnf4g	implicated_via_orthology	DOID:0111099	maturity-onset diabetes of the young type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107321	Cux2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104853	Hes1	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914688	Rfk	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917745	Atp6ap2	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95790	Gnrhr	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685013	Cog7	implicated_via_orthology	DOID:0070257	congenital disorder of glycosylation type IIe						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647985	Rpl10l	implicated_via_orthology	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:0112050	non-syndromic X-linked intellectual disability 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347075	Nbea	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	implicated_via_orthology	DOID:0111099	maturity-onset diabetes of the young type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860283	Ubqln2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921809	Elovl7	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914672	Dhdds	implicated_via_orthology	DOID:0110352	retinitis pigmentosa 59						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183441	Psat1	implicated_via_orthology	DOID:0080075	Neu-Laxova syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:0070044	Coffin-Siris syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102682	Llgl1	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683486	Rere	implicated_via_orthology	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88107	Atp1a3	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261856	Ankle2	implicated_via_orthology	DOID:0070289	primary autosomal recessive microcephaly 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933621	Smarcd2	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196224	Cdk8	implicated_via_orthology	DOID:0112221	developmental and epileptic encephalopathy 87						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347004	Mapkbp1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098266	Chl1	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918843	Llgl2	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105060	Dgkg	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914321	Rps6ka6	implicated_via_orthology	DOID:3783	Coffin-Lowry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99147	Yes1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88046	Aplp1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036260	Htra4	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107788	Atp1b3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927225	Tbc1d8	implicated_via_orthology	DOID:0070357	nephrotic syndrome type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313261	Sptbn2	implicated_via_orthology	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103197	Mcm5	implicated_via_orthology	DOID:0060306	Meier-Gorlin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104860	Fxr1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106354	Vps25	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858271	Mtmr1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891457	Polh	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888999	Angptl4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107891	Nop2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922579	Atf7ip2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354692	Lsm4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109525	Trpc4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434648	Gm21293	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107949	Rhob	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151156	Stim2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:0080409	familial adenomatous polyposis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920234	Ciz1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685336	Ubqlnl	implicated_via_orthology	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107365	Ube2i	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104884	Psmb1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107162	Ppp3cc	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87867	Acadm	implicated_via_orthology	DOID:0080153	medium chain acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102944	Ube2b	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	implicated_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97831	Ppa1	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:7319	axonal neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914243	Smarcd3	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045291	Ubqln3	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109525	Trpc4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860040	Trim3	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183446	Agap3	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105386	Dbt	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97772	Prox1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95728	Gli2	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97547	Pfkl	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	implicated_via_orthology	DOID:12802	mucopolysaccharidosis I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893597	Frg1	implicated_via_orthology	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920924	Wdr75	implicated_via_orthology	DOID:0111169	subcortical band heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919214	Atad3a	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181366	Capn8	implicated_via_orthology	DOID:0110821	hereditary spastic paraplegia 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104632	Ube2h	implicated_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931027	Stx12	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135593	Hadha	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339710	Myh2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104752	Nfkbib	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95742	Glo1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106919	Vdac1	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098268	Kif5b	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860276	Ubqln1	implicated_via_orthology	DOID:0060206	amyotrophic lateral sclerosis type 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098592	Alg3	implicated_via_orthology	DOID:5212	congenital disorder of glycosylation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914290	Ddx17	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107158	Sin3b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782524	Gm4340	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346831	Esrra	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927868	Pex14	implicated_via_orthology	DOID:0080487	peroxisome biogenesis disorder 13A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926803	Kcnq4	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932545	Ndst4	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444315	Idi2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333773	Mab21l1	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97912	Rheb	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98362	Sox14	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316714	Cox7a1	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96763	Ldhb	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196365	Nus1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108100	Dvl3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105073	Tnni1	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915941	Kansl1l	implicated_via_orthology	DOID:0050880	Koolen de Vries syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443331	Rims3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447532	Als2cl	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107876	Uqcrc1	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106222	Capza2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918952	Cdc5l	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920672	Prox2	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107464	Plcb4	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107329	Mrpl50	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96759	Ldha	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917205	Fars2	implicated_via_orthology	DOID:0110822	hereditary spastic paraplegia 77						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385325	Pnpla7	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443154	Cnot6l	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97591	Pkm	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915367	Apool	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915382	Lhfpl5	implicated_via_orthology	DOID:0110518	autosomal recessive nonsyndromic deafness 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329034	Ccne2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97846	Rac2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932545	Ndst4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917976	Angptl6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384774	Alg1	implicated_via_orthology	DOID:5212	congenital disorder of glycosylation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337080	Ncor2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927222	Diaph3	implicated_via_orthology	DOID:0060690	autosomal dominant auditory neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643524	Cdc5lrt5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289279	Dnah9	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858959	Elovl1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330281	Cd2ap	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684927	Cenpj	implicated_via_orthology	DOID:0070290	primary autosomal recessive microcephaly 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913576	Dnajc5b	implicated_via_orthology	DOID:0110720	neuronal ceroid lipofuscinosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860454	Phc2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145950	Scrib	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441890	Gpr21	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87866	Acadl	implicated_via_orthology	DOID:0112072	nuclear type mitochondrial complex I deficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88113	Atp4a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891963	Ywhaq	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930018	Dnajb5	implicated_via_orthology	DOID:0081353	congenital myopathy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442313	Lrrc1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179276	Rhbdl3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353425	Opn4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102965	Scn7a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922570	Etnk1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109161	Grk5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685402	Espnl	implicated_via_orthology	DOID:0110494	autosomal recessive nonsyndromic deafness 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:1932	Angelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102959	Ube2a	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685541	Wdtc1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270129	Dnaja1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919650	Pinx1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146350	Scaf4	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606484	Kdm4d	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329033	Agxt	implicated_via_orthology	DOID:2977	primary hyperoxaluria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860276	Ubqln1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929864	Myg1	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644216	Cdc5lrt10	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351617	Abca3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2686240	Ssh1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920908	Spns1	implicated_via_orthology	DOID:1927	sphingolipidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926063	Nckap1l	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138261	Smap1	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:0060581	Noonan syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0050951	hereditary ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351335	Atp1a4	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918639	Chd6	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151156	Stim2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97178	Map4	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:0070045	Coffin-Siris syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384567	Cbr4	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:0111190	distal myopathy 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298224	Pip5k1c	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145950	Scrib	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101805	Gys1	implicated_via_orthology	DOID:3534	Lafora disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156052	Slc17a6	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442474	Dgkb	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103270	Tfeb	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154240	Plxnb3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95823	Grin2d	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107697	Usp17le	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387863	Zmynd10	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929004	Stk4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102682	Llgl1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180784	Rac3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099438	Nsdhl	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861438	Gcm2	implicated_via_orthology	DOID:11199	hypoparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345675	Trib3	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97532	Pdha1	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99254	Etv1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098590	Npy6r	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915336	Zdhhc15	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917649	Wwtr1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683546	Ssh3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915529	Mcoln2	implicated_via_orthology	DOID:3343	glycoproteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:7319	axonal neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	implicated_via_orthology	DOID:0111181	familial hemiplegic migraine 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95401	Epb41	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102965	Scn7a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913838	Cmpk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109524	Trpc5	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196259	Tnfsf12	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647143	Cdc5lrt8	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202294	Aff2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924909	Slc25a36	implicated_via_orthology	DOID:0081328	familial hyperinsulinemic hypoglycemia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859635	Prickle3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914110	Tanc1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858201	Cntnap1	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344338	Tiam2	implicated_via_orthology	DOID:0070354	cataract 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925976	Scaper	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351651	Yme1l1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146830	Ldhal6b	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107672	Gpm6b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145597	Mbnl2	implicated_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106227	Capza1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103248	Phc1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859310	Asah2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107930	Pip5k1b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100526	Nr2e1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101766	Ryk	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442159	Irf2bp1	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3587728	Acsbg2	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2677270	Pdzd8	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917030	Smap2	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107699	Usp17la	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103008	Epb41l3	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347094	Parg	implicated_via_orthology	DOID:0070352	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102682	Llgl1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917706	Mpc2	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443239	Snx33	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351651	Yme1l1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919202	Riox1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106911	Hccs	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342283	Slc12a7	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88181	Bmp5	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150152	Ubqln4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195276	Bloc1s1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94890	Dhfr	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888986	Dlg3	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921355	Gga2	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933163	Trim2	implicated_via_orthology	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934234	Pip4k2b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98147	Rps24	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385325	Pnpla7	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99960	Ewsr1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97597	Prkcg	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109528	Trpc1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144164	Tbc1d10a	implicated_via_orthology	DOID:3369	Ewing sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88065	Araf	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926943	Atp12a	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332635	Mrpl40	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918639	Chd6	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108559	Macf1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183158	Ash1l	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917806	Slc25a33	implicated_via_orthology	DOID:0081328	familial hyperinsulinemic hypoglycemia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330281	Cd2ap	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103009	Epb41l2	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924270	Atl3	implicated_via_orthology	DOID:0110791	hereditary spastic paraplegia 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385096	Pprc1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135960	Slc12a6	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929470	Tyk2	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106054	Psmc1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914302	Ndc80	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98494	Tbx2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444413	Sdk1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341865	Mark3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928137	Mrps22	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655562	Adgrl4	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108029	Scn10a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107671	Gpm6a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97788	Psph	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343102	Robo3	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91842	D1Pas1	implicated_via_orthology	DOID:0050457	Sertoli cell-only syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144023	Fbxw11	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929646	Pex3	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276558	Slc13a2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444552	Actbl2	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922985	Pank1	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105047	Psmc5	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:0110859	polycystic kidney disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343161	Snf8	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103306	Tiam1	implicated_via_orthology	DOID:0070354	cataract 48						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104659	Dll1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107163	Ppp3cb	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387357	Wac	implicated_via_orthology	DOID:0081126	DeSanto-Shinawi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918560	Tbc1d9	implicated_via_orthology	DOID:0070357	nephrotic syndrome type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385656	Acsbg1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915941	Kansl1l	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927204	Gosr2	implicated_via_orthology	DOID:891	progressive myoclonus epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926212	Med12	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918614	Jmjd1c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109484	Ywhaz	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106295	Tomm70a	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103575	Skp1	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934950	Csnk1a1	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915183	Hcfc2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782481	Gm4301	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102959	Ube2a	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353418	Pmm1	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385254	Gys2	implicated_via_orthology	DOID:3534	Lafora disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98543	Tcp10c	implicated_via_orthology	DOID:0070290	primary autosomal recessive microcephaly 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104883	Psma3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332242	Mycs	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858201	Cntnap1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384892	Rhot2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:0080325	tuberous sclerosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929004	Stk4	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104627	Dst	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670997	Scd4	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920955	Mark4	implicated_via_orthology	DOID:0070356	visual impairment and progressive phthisis bulbi						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333883	Lats1	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107321	Cux2	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261856	Ankle2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925976	Scaper	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142048	Rnf40	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933162	Lrba	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154244	Plxnd1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444557	Kmt5b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921487	Tubgcp2	implicated_via_orthology	DOID:0081266	pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109524	Trpc5	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	implicated_via_orthology	DOID:2717	Bloom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102944	Ube2b	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644213	Cdc5lrt9	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921373	Foxp4	implicated_via_orthology	DOID:0060038	specific developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915464	Gsto2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347078	Grk6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919935	Dnajc6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913276	Ngly1	implicated_via_orthology	DOID:0060728	NGLY1-deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448520	Pip5kl1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918101	Tbc1d8b	implicated_via_orthology	DOID:0070357	nephrotic syndrome type 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921152	Psmb11	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858943	Arl6ip1	implicated_via_orthology	DOID:0110812	hereditary spastic paraplegia 61						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892995	Dnajc5	implicated_via_orthology	DOID:0110720	neuronal ceroid lipofuscinosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442334	Kirrel2	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104510	Myo7a	implicated_via_orthology	DOID:2742	auditory system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096331	Slc1a6	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102682	Llgl1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94941	Dvl1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102788	Rph3a	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97806	Ptpn2	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388709	Abca15	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643623	Cntnap5a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97602	Prkcz	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919228	Ppp2r2a	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920672	Prox2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384585	Gatad2a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106217	Cacna1e	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929492	Atl2	implicated_via_orthology	DOID:0110791	hereditary spastic paraplegia 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924197	Ndufaf6	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384910	Hkdc1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927347	Smarce1	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924150	Ssbp4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924050	Usp42	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924767	Zfyve26	implicated_via_orthology	DOID:0110768	hereditary spastic paraplegia 15						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444430	Pomt2	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933947	Rtn1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	implicated_via_orthology	DOID:3672	rhabdoid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888986	Dlg3	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354961	Synj1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643515	Myh15	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338829	Pex16	implicated_via_orthology	DOID:0080483	peroxisome biogenesis disorder 8A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097686	H3f3a	implicated_via_orthology	DOID:0080684	diffuse midline glioma, H3 K27M-mutant						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102959	Ube2a	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913633	Iscu	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653690	Agap1	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105085	Rbl2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338002	Gdap1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104750	Nrcam	implicated_via_orthology	DOID:0060246	MASA syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3608413	Rhbdl2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914218	Plin5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915237	Ppcs	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913866	Snx9	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104558	Rps6ka1	implicated_via_orthology	DOID:3783	Coffin-Lowry syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346518	Scamp2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104572	Limk1	implicated_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346863	Mapk10	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	implicated_via_orthology	DOID:0050884	triosephosphate isomerase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152695	Col4a6	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344351	Dlg2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105941	Mpp1	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916231	Snrpa1	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441890	Gpr21	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915221	Tppp3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923373	Gpsm2	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105058	Atp2a1	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349717	Ncor1	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921496	Gale	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920180	Ppp2r2b	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098727	Trappc1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894407	Tmem165	implicated_via_orthology	DOID:0050571	congenital disorder of glycosylation type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97860	Rasa1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924827	Spns3	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343101	Kat2a	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:0110640	congenital muscular dystrophy due to LMNA mutation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3615492	Timm8a2	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929270	Dstn	implicated_via_orthology	DOID:0110934	nemaline myopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97860	Rasa1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97772	Prox1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858965	Atf7ip	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195276	Bloc1s1	implicated_via_orthology	DOID:896	metal metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88169	Blk	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917309	Degs2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351639	Mrpl15	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298206	Pip4k2a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890410	Acss2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289288	Slc52a2	implicated_via_orthology	DOID:0050694	Brown-Vialetto-Van Laere syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99638	Mark2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99603	Smarca2	implicated_via_orthology	DOID:0070046	Coffin-Siris syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:3620	central nervous system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926250	Doc2g	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926078	Rhot1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891705	Myl10	implicated_via_orthology	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915084	Idh3a	implicated_via_orthology	DOID:439	neuromuscular junction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916637	Dnajb13	implicated_via_orthology	DOID:0081353	congenital myopathy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152972	Rims2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782487	Gm4307	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95527	Fgr	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145021	Trib2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924134	Cyfip2	implicated_via_orthology	DOID:0060393	chromosome 15q11.2 deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929260	Mtch2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338076	Hivep2	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588199	Cntnap3	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704398	Idi2l	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109295	Sall3	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	implicated_via_orthology	DOID:0110792	hereditary spastic paraplegia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:0070042	Coffin-Siris syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685089	Npc1l1	implicated_via_orthology	DOID:14504	Niemann-Pick disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2664902	Mark1	implicated_via_orthology	DOID:0070356	visual impairment and progressive phthisis bulbi						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915181	Serpini2	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0112374	muscular dystrophy-dystroglycanopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97599	Prkce	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916952	Ndufaf1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138828	Eps8l2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104724	Fdxr	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:1926	Gaucher's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444847	Ncoa7	implicated_via_orthology	DOID:0070339	cerebellar hyplasia/atrophy, epilepsy, and global developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:854	collagen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334458	Pex19	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914675	Eps8l1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315195	Emg1	implicated_via_orthology	DOID:0050684	Bowen-Conradi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927638	Dnaja4	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098270	Jag2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914155	Plin3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858500	Diaph2	implicated_via_orthology	DOID:0060690	autosomal dominant auditory neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99923	Kcnma1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144529	Cnot6	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:14320	generalized anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921330	Nmnat3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351477	Cars1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98342	Snrpb	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104708	Cct3	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917685	Inf2	implicated_via_orthology	DOID:0110205	Charcot-Marie-Tooth disease dominant intermediate E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202300	Kcnu1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142227	Lrrk1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194882	Irs3	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103064	Ddx3x	implicated_via_orthology	DOID:0050457	Sertoli cell-only syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99780	Kdm5d	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	implicated_via_orthology	DOID:0050539	Charcot-Marie-Tooth disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860040	Trim3	implicated_via_orthology	DOID:0110282	autosomal recessive limb-girdle muscular dystrophy type 2H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444155	Nmnat2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	implicated_via_orthology	DOID:1064	cystinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277989	Shmt2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922485	Exd2	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782493	Gm4312	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933163	Trim2	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646013	Cntnap5c	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890498	Mcoln1	implicated_via_orthology	DOID:3343	glycoproteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670178	Med13l	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931874	Dnajb1	implicated_via_orthology	DOID:0081353	congenital myopathy 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918843	Llgl2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045263	Dnajc5g	implicated_via_orthology	DOID:0110720	neuronal ceroid lipofuscinosis 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442579	Frmd6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916672	Pex5l	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103305	Alk	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441765	Nmur2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107698	Usp17lc	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0060581	Noonan syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154049	Smc1b	implicated_via_orthology	DOID:0080506	Cornelia de Lange syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929261	Mtch1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152971	Rims1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384936	Spns2	implicated_via_orthology	DOID:1927	sphingolipidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916409	Rhebl1	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930787	Insm2	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97594	Prkacb	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096331	Slc1a6	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141101	Depdc5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144151	Pnpo	implicated_via_orthology	DOID:0111329	pyridoxamine 5'-phosphate oxidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104725	Atn1	implicated_via_orthology	DOID:0060162	dentatorubral-pallidoluysian atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95801	Grk4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914147	Naa16	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913288	Sdhaf3	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0111559	Charcot-Marie-Tooth disease type 2EE						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346074	Fxr2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96796	Lmnb2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98299	Shmt1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101768	H3f3b	implicated_via_orthology	DOID:0080684	diffuse midline glioma, H3 K27M-mutant						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928477	Cnpy2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931256	Cubn	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098757	Coa3	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:0080390	nephrotic syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858231	Pkd2l2	implicated_via_orthology	DOID:0110859	polycystic kidney disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109452	Smad1	implicated_via_orthology	DOID:0050787	juvenile polyposis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107612	Rtn2	implicated_via_orthology	DOID:0110765	hereditary spastic paraplegia 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914176	Trmt6	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926368	Syt5	implicated_via_orthology	DOID:439	neuromuscular junction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442264	Idi1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931882	Dnaja2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651811	Tph2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202066	Sec61g	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0060581	Noonan syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346333	Mrps12	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88109	Atp1b2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179326	Oxr1	implicated_via_orthology	DOID:0070339	cerebellar hyplasia/atrophy, epilepsy, and global developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925076	Lhfpl3	implicated_via_orthology	DOID:0110518	autosomal recessive nonsyndromic deafness 67						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920211	Slc17a7	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929988	Klf15	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037150	Slc13a5	implicated_via_orthology	DOID:0050667	alcohol-related neurodevelopmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99845	Gdi2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915884	Tm2d3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136343	Crb1	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98239	Scd1	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915600	Mul1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589112	Tomm40l	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352448	Pkd2l1	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0080336	mitochondrial DNA depletion syndrome 14						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443921	Irf2bp2	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147627	Yars1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932544	Ndst3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97783	Psap	implicated_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96840	Ltk	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107929	Pip5k1a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919725	Ssbp3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096867	Etv5	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925808	Htra3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98347	Snrpn	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:0060038	specific developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928738	Slc25a20	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924193	Psapl1	implicated_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103300	Rbl1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928897	Piwil1	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:896	metal metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3625331	Abca17	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88449	Col15a1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	implicated_via_orthology	DOID:0111459	classic galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137642	Snx18	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923969	Kansl1	implicated_via_orthology	DOID:0050880	Koolen de Vries syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346832	Esrrb	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	implicated_via_orthology	DOID:0060393	chromosome 15q11.2 deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277186	Atg5	implicated_via_orthology	DOID:0050951	hereditary ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	implicated_via_orthology	DOID:0070025	X-linked dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99667	Syt1	implicated_via_orthology	DOID:439	neuromuscular junction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338871	Btrc	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928487	Stk3	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105047	Psmc5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924937	Kcnq5	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353425	Opn4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860283	Ubqln2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681835	Nlgn2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890574	Sptbn4	implicated_via_orthology	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96196	Hoxc5	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107486	Pex2	implicated_via_orthology	DOID:0080480	peroxisome biogenesis disorder 5A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:90675	Vars1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890359	Igf2bp3	implicated_via_orthology	DOID:0060158	acquired metabolic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2674366	Rims4	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388708	Abca14	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354723	Pnpla6	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890505	Plin1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925584	Cdk19	implicated_via_orthology	DOID:0112221	developmental and epileptic encephalopathy 87						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915140	Ufm1	implicated_via_orthology	DOID:0050950	autosomal recessive cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344351	Dlg2	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151071	C1galt1	implicated_via_orthology	DOID:0060050	autoimmune disease of blood						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105070	Tnni2	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914220	Ssbp2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924827	Spns3	implicated_via_orthology	DOID:1927	sphingolipidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353627	Angptl3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914040	Grtp1	implicated_via_orthology	DOID:3369	Ewing sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861099	Ubr2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105942	Hcfc1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97272	Myl2	implicated_via_orthology	DOID:0110316	hypertrophic cardiomyopathy 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	implicated_via_orthology	DOID:0110821	hereditary spastic paraplegia 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181434	Phc3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384583	Zfp280d	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385163	Gdap1l1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858210	Stx7	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914703	Slc25a46	implicated_via_orthology	DOID:0080068	Charcot-Marie-Tooth disease type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183572	Cntnap4	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96052	Hck	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927070	Dusp10	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	implicated_via_orthology	DOID:0110934	nemaline myopathy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679787	Nploc4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135601	Slc1a4	implicated_via_orthology	DOID:0050994	episodic ataxia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444552	Actbl2	implicated_via_orthology	DOID:10486	intestinal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346052	Apc2	implicated_via_orthology	DOID:0080409	familial adenomatous polyposis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925875	Acsbg3	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920328	Pmpcb	implicated_via_orthology	DOID:0060892	late onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107699	Usp17la	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386723	Glis1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102965	Scn7a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	implicated_via_orthology	DOID:0110174	Charcot-Marie-Tooth disease axonal type 2L						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930252	Srd5a3	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88047	Aplp2	implicated_via_orthology	DOID:0080348	Alzheimer's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684988	Pex10	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920198	Tppp	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914218	Plin5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108029	Scn10a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336181	Kcnq3	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931027	Stx12	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3607791	Rft1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88114	Atp4b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87919	Add2	implicated_via_orthology	DOID:1969	cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888986	Dlg3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346832	Esrrb	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891833	Pfkp	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858231	Pkd2l2	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921241	Atl1	implicated_via_orthology	DOID:0110791	hereditary spastic paraplegia 3A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	implicated_via_orthology	DOID:1933	Rubinstein-Taybi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88449	Col15a1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922026	Ppa2	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97040	Ndst2	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927339	Pals1	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923215	Zdhhc20	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933388	Bicc1	implicated_via_orthology	DOID:2975	cystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94891	Dhh	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924001	Chd9	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350341	Sgsh	implicated_via_orthology	DOID:0111395	mucopolysaccharidosis type IIIA						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915022	Chd8	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106054	Psmc1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95811	Gria4	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097163	Pold2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341865	Mark3	implicated_via_orthology	DOID:0070356	visual impairment and progressive phthisis bulbi						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316649	Sphk1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916794	Wdr5b	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891342	Lpin3	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88568	Cux1	implicated_via_orthology	DOID:2531	hematologic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918843	Llgl2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096875	Wdfy3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	implicated_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931787	Scyl1	implicated_via_orthology	DOID:0111155	autosomal recessive spinocerebellar ataxia 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449470	Dmrt3	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923596	Rars2	implicated_via_orthology	DOID:0060275	pontocerebellar hypoplasia type 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289282	Zfp622	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106922	Vdac3	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442660	Ppp2r2c	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891396	Kirrel1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917297	Trnt1	implicated_via_orthology	DOID:0080209	sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684950	Becn2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330812	Acox1	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685336	Ubqlnl	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045291	Ubqln3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098260	Kif1c	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345149	Scn11a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339967	Myh13	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861380	Sphk2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88065	Araf	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353418	Pmm1	implicated_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890520	Vps4a	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915071	Atp1b4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915835	Rtn4	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918025	Zmynd8	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95809	Gria2	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107164	Ppp3ca	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098268	Kif5b	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891340	Lpin1	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442117	Pogz	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927343	Rps6kb2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88568	Cux1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387464	Pank3	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388271	Mylip	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	implicated_via_orthology	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	implicated_via_orthology	DOID:0050338	primary bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354373	Sall2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859638	Pqbp1	implicated_via_orthology	DOID:0060179	Renpenning syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444136	Mars2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351615	Add3	implicated_via_orthology	DOID:1969	cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107158	Sin3b	implicated_via_orthology	DOID:0060037	developmental disorder of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344351	Dlg2	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442402	Cnot1	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346333	Mrps12	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350925	Sec23b	implicated_via_orthology	DOID:0070307	craniolenticulosutural dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97351	Nkx2-6	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309489	Cask	implicated_via_orthology	DOID:0060309	syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99917	Slc1a3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338069	Itsn1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914047	Cntnap2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347005	Psma1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:0060170	generalized epilepsy with febrile seizures plus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150152	Ubqln4	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106217	Cacna1e	implicated_via_orthology	DOID:0050951	hereditary ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913941	Gapvd1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98387	Sptb	implicated_via_orthology	DOID:0050882	spinocerebellar ataxia type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858202	Rab11a	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447362	Slc24a4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109284	Psen2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104631	Utrn	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99638	Mark2	implicated_via_orthology	DOID:0070356	visual impairment and progressive phthisis bulbi						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919276	Trmu	implicated_via_orthology	DOID:310	MERRF syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443241	Ndufs1	implicated_via_orthology	DOID:0112068	nuclear type mitochondrial complex I deficiency 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96795	Lmnb1	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101772	Snta1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444289	Glis3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105073	Tnni1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339709	Myh3	implicated_via_orthology	DOID:0111602	distal arthrogryposis type 2B3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098826	Coq4	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333883	Lats1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384910	Hkdc1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919824	Zc3h14	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5591961	Cdc5lrt4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920955	Mark4	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106100	Etfdh	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929285	Orc6	implicated_via_orthology	DOID:0080514	Meier-Gorlin syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99919	Vcp	implicated_via_orthology	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354713	Acsl4	implicated_via_orthology	DOID:0112050	non-syndromic X-linked intellectual disability 63						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309526	Rps17	implicated_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341721	Kcnh1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915240	Mpc1	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1862037	Slc12a5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444087	Slc1a7	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88047	Aplp2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333760	Tfec	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096362	Nrxn2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104719	Ndst1	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106915	Vdac2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276558	Slc13a2	implicated_via_orthology	DOID:0050667	alcohol-related neurodevelopmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923452	Zdhhc2	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101780	Serpine2	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338049	Itsn2	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333883	Lats1	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444912	Mbnl3	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347043	Orc4	implicated_via_orthology	DOID:0080513	Meier-Gorlin syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913498	Alg5	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100497	Doc2b	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923969	Kansl1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341722	Kcnh2	implicated_via_orthology	DOID:10273	heart conduction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	implicated_via_orthology	DOID:0110821	hereditary spastic paraplegia 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154238	Plxnb1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914703	Slc25a46	implicated_via_orthology	DOID:870	neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88116	Atp6v0c	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859867	Syt8	implicated_via_orthology	DOID:439	neuromuscular junction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339711	Myh1	implicated_via_orthology	DOID:0080326	familial hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277977	Ubr1	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891341	Lpin2	implicated_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647148	Cdc5lrt6	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309503	Kcnq2	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97600	Prkch	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101771	Sntb2	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913833	Exosc1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443847	Sdk2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	implicated_via_orthology	DOID:0110821	hereditary spastic paraplegia 76						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104648	Fbrs	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919847	Auts2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928487	Stk3	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860299	Dnah10	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923022	Pnpla5	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918077	Trak2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684923	Tppp2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104614	Cox6c	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925212	Scaf8	implicated_via_orthology	DOID:225	syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107612	Rtn2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346037	Insrr	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:0070044	Coffin-Siris syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890110	Robo2	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88456	Col4a5	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155884	Wdr5	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97623	Plp1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137022	Tm2d1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928948	Scamp5	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643623	Cntnap5a	implicated_via_orthology	DOID:0060308	autosomal recessive intellectual developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95810	Gria3	implicated_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148705	Foxp2	implicated_via_orthology	DOID:0060038	specific developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99460	Notch3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888986	Dlg3	implicated_via_orthology	DOID:0060072	benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861630	Espn	implicated_via_orthology	DOID:0110494	autosomal recessive nonsyndromic deafness 36						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99425	Rab11b	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99666	Syt2	implicated_via_orthology	DOID:439	neuromuscular junction disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	implicated_via_orthology	DOID:0110408	retinitis pigmentosa 11						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336173	Prkaa2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385906	Spg7	implicated_via_orthology	DOID:0110816	hereditary spastic paraplegia 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:0081112	Baraitser-Winter syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859183	Smarcal1	implicated_via_orthology	DOID:0060490	Schimke immuno-osseous dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654070	Sox21	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580016	Agap2	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919594	Usp36	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679260	Crb2	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147627	Yars1	implicated_via_orthology	DOID:870	neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108087	Hars1	implicated_via_orthology	DOID:0110162	Charcot-Marie-Tooth disease, axonal type 2W						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98443	Surf1	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143057	Pif1	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913440	Acer3	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915582	Sdhaf1	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103286	Atp6v0a1	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107760	Chka	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913496	Osgep	implicated_via_orthology	DOID:0060879	primary hypomagnesemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914147	Naa16	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88579	Cyct	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914216	Trit1	implicated_via_orthology	DOID:0111464	combined oxidative phosphorylation deficiency 35						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144164	Tbc1d10a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107804	Tuba1b	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096573	Utp4	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920210	Top1mt	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99461	Piga	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143886	Dot1l	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914081	Cab39l	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384838	Prpsap2	implicated_via_orthology	DOID:0050647	Arts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913612	Exosc3	implicated_via_orthology	DOID:0060266	pontocerebellar hypoplasia type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	implicated_via_orthology	DOID:0110965	brachydactyly type A2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919772	Atxn7l2	implicated_via_orthology	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685089	Npc1l1	implicated_via_orthology	DOID:0070113	Niemann-Pick disease type C1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0060896	Parkinson's disease 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141969	Efl1	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108039	Dbil5	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104855	Atp6v0a2	implicated_via_orthology	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3034635	Eif1ad2	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352500	Tpk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:12705	Friedreich ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153480	Atp6v0a4	implicated_via_orthology	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97566	Pgm3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2677836	Dolk	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	implicated_via_orthology	DOID:0080506	Cornelia de Lange syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443220	Slc4a5	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095406	Tuba3a	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95298	Eif1a	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925055	Esco1	implicated_via_orthology	DOID:5325	Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915013	Prpsap1	implicated_via_orthology	DOID:0050647	Arts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103249	Calm3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915267	Mrm2	implicated_via_orthology	DOID:3687	MELAS syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647985	Rpl10l	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108411	Prkag1	implicated_via_orthology	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923935	Eif4g3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109618	Atp6v1b2	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:2960	photosensitive trichothiodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095406	Tuba3a	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107207	Coq7	implicated_via_orthology	DOID:0070245	primary coenzyme Q10 deficiency 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350925	Sec23b	implicated_via_orthology	DOID:5325	Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:0111442	optic atrophy 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150302	Ddhd1	implicated_via_orthology	DOID:0110806	hereditary spastic paraplegia 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88015	Ampd1	implicated_via_orthology	DOID:0060264	pontocerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100856	Mras	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891825	Pigb	implicated_via_orthology	DOID:10112	sleeping sickness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704336	Rpl10-ps3	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:0111272	occipital horn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154049	Smc1b	implicated_via_orthology	DOID:0080506	Cornelia de Lange syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109555	Psmc2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648085	Eif1ad15	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95778	Gnat1	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714359	Srp54c	implicated_via_orthology	DOID:0112135	severe congenital neutropenia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858271	Mtmr1	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98179	Rras	implicated_via_orthology	DOID:0050469	Costello syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:0060480	left ventricular noncompaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101947	Hnrnpd	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353432	Timm13	implicated_via_orthology	DOID:0050757	deafness-dystonia-optic neuronopathy syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105943	Rpl10	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924408	Coq6	implicated_via_orthology	DOID:3204	schwannomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095410	Tuba4a	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353498	Slc25a3	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913633	Iscu	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:10155	intestinal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99135	Xpa	implicated_via_orthology	DOID:0110843	xeroderma pigmentosum group A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104872	Ppp1cc	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647101	Eif1ad18	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920421	Trmt10a	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104808	Lcp1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098746	Ankzf1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098592	Alg3	implicated_via_orthology	DOID:0080556	congenital disorder of glycosylation Id						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197010	Sumo1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890467	Vps35	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914454	Eif2s2	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:0112182	mismatch repair cancer syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919379	Pex13	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106040	Cyp51	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915142	Coa6	implicated_via_orthology	DOID:0050713	COX deficiency, infantile mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330808	Hsd17b7	implicated_via_orthology	DOID:1701	steroid inherited metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107814	Tubb1	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109350	Slc4a3	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450125	Atp10d	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913300	Trappc2b	implicated_via_orthology	DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341299	Dnm3	implicated_via_orthology	DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918982	Vps11	implicated_via_orthology	DOID:0060796	hypomyelinating leukodystrophy 12						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	implicated_via_orthology	DOID:0070347	encephalopathy due to defective mitochondrial and peroxisomal fission 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180699	Mtmr4	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:10939	antisocial personality disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349635	Sec23a	implicated_via_orthology	DOID:5325	Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0111441	optic atrophy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353497	Slc25a10	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98791	Top2b	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:9263	homocystinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859648	Ftsj1	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916165	Vars2	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97548	Pfkm	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928745	Slc4a8	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103286	Atp6v0a1	implicated_via_orthology	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102779	Fen1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105943	Rpl10	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353451	Aldh3a1	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914247	Psmd12	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891693	Mtmr7	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918000	Kdsr	implicated_via_orthology	DOID:0080250	erythrokeratodermia variabilis et progressiva 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858429	Cdc34b	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443822	Pigz	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:90675	Vars1	implicated_via_orthology	DOID:0111478	combined oxidative phosphorylation deficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97555	Pgk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349431	Eif2s3x	implicated_via_orthology	DOID:0060801	MEHMO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629896	Mir665	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330294	Hnrnpab	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104571	Clcn4	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0111611	autosomal recessive spinocerebellar ataxia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443480	Setx	implicated_via_orthology	DOID:0050755	spinocerebellar ataxia with axonal neuropathy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914378	Ube2g1	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104571	Clcn4	implicated_via_orthology	DOID:0050699	Dent disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105037	Ddx5	implicated_via_orthology	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915237	Ppcs	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2158650	Idh3b	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:12253	testicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347353	Atp2b3	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858225	Tuba8	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913699	Pam16	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95871	Guk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355326	Preb	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3044182	Cox6b2	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96960	Rab8a	implicated_via_orthology	DOID:0060247	Smith-McCort dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927232	Rab13	implicated_via_orthology	DOID:0111167	Dyggve-Melchior-Clausen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443760	Etnk2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:1891	optic nerve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780242	Eif1ad17	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384838	Prpsap2	implicated_via_orthology	DOID:0050566	X-linked nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932557	Letm1	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891207	Plpbp	implicated_via_orthology	DOID:0080769	early-onset vitamin B6-dependent epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349467	Abcd2	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913833	Exosc1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914040	Grtp1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180699	Mtmr4	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095408	Tuba3b	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448567	Chd2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105066	Rab10	implicated_via_orthology	DOID:0060247	Smith-McCort dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346093	Psmc4	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353496	Slc25a5	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97518	Cdk18	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676903	Mir27b	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140726	Guf1	implicated_via_orthology	DOID:0050562	West syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138994	Pomt1	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858225	Tuba8	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916326	Triap1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103250	Calm2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0080125	mitochondrial DNA depletion syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0050766	choreaacanthocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928744	Vapb	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2158813	Sumo2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0111590	Cohen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3833940	Naa12	implicated_via_orthology	DOID:0050781	Ogden syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443030	Flad1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102581	Rdh11	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922985	Pank1	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914939	Aldh3b1	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384802	Eif2b1	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103285	Atp6v1b1	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:0050569	Seckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142610	Snx25	implicated_via_orthology	DOID:0080066	autosomal recessive spinocerebellar ataxia 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681839	Aars2	implicated_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704359	Pam16l	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0060896	Parkinson's disease 23						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	implicated_via_orthology	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	implicated_via_orthology	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97517	Cdk17	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:0110164	Charcot-Marie-Tooth disease type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920583	Slc25a31	implicated_via_orthology	DOID:0111517	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141314	Naa11	implicated_via_orthology	DOID:0050781	Ogden syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:1441	autosomal dominant cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341299	Dnm3	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914172	Rras2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914040	Grtp1	implicated_via_orthology	DOID:3369	Ewing sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444552	Actbl2	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:90675	Vars1	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97547	Pfkl	implicated_via_orthology	DOID:2747	glycogen storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354713	Acsl4	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926790	Fzr1	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891341	Lpin2	implicated_via_orthology	DOID:0080108	myoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858225	Tuba8	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107814	Tubb1	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442496	Gatb	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916165	Vars2	implicated_via_orthology	DOID:0111478	combined oxidative phosphorylation deficiency 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914544	Elp1	implicated_via_orthology	DOID:11589	Riley-Day syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143585	Fig4	implicated_via_orthology	DOID:0110184	Charcot-Marie-Tooth disease type 4J						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444233	Ythdf2	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922066	Tpr	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:4159	skin cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915142	Coa6	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182585	Med17	implicated_via_orthology	DOID:0111262	infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661416	Snx13	implicated_via_orthology	DOID:0080066	autosomal recessive spinocerebellar ataxia 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355326	Preb	implicated_via_orthology	DOID:0050577	cranioectodermal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355299	Hnrnpdl	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95775	Gnao1	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918305	Nemf	implicated_via_orthology	DOID:440	neuromuscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:5750	endometrial serous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106341	Atp5po	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:1781	thyroid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97741	Pold1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099463	Idh3g	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914062	Ppcdc	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202301	Itch	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921435	Gbe1	implicated_via_orthology	DOID:2750	glycogen storage disease IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	implicated_via_orthology	DOID:12995	conduct disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:0111517	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107861	Tubb2a	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109351	Slc4a2	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107861	Tubb2a	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138987	Slc4a11	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916221	Tamm41	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142973	Lars2	implicated_via_orthology	DOID:0050857	Perrault syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103016	Ppp1ca	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098727	Trappc1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179381	Prpf8	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196437	Hltf	implicated_via_orthology	DOID:3119	gastrointestinal system cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922066	Tpr	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704336	Rpl10-ps3	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350931	Tcirg1	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914414	Lipt2	implicated_via_orthology	DOID:9268	glycine encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919558	Brf1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104809	Pls1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919027	Ing3	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144208	Tubg2	implicated_via_orthology	DOID:0090138	complex cortical dysplasia with other brain malformations 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:8712	neurofibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894407	Tmem165	implicated_via_orthology	DOID:0070263	congenital disorder of glycosylation type IIk						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913878	Thg1l	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928277	Afg3l1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914062	Ppcdc	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914172	Rras2	implicated_via_orthology	DOID:0050469	Costello syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444486	Tars3	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183447	Ugp2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921552	Mtmr3	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915201	Tubb6	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584458	Atxn7l1	implicated_via_orthology	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893586	Snu13	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095410	Tuba4a	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891808	Tollip	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095410	Tuba4a	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387464	Pank3	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919238	Esco2	implicated_via_orthology	DOID:5325	Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107876	Uqcrc1	implicated_via_orthology	DOID:0070332	multiple mitochondrial dysfunctions syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108411	Prkag1	implicated_via_orthology	DOID:0090101	lethal congenital glycogen storage disease of heart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681836	Polr3a	implicated_via_orthology	DOID:0060786	hypomyelinating leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99954	Ighmbp2	implicated_via_orthology	DOID:0111064	autosomal recessive distal hereditary motor neuronopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916115	Arv1	implicated_via_orthology	DOID:0080417	developmental and epileptic encephalopathy 38						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97824	Pvt1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145118	Eif2b2	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107861	Tubb2a	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5439387	Eif1ad13	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97297	Nedd4	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350925	Sec23b	implicated_via_orthology	DOID:0111401	congenital dyserythropoietic anemia type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858233	Nphp1	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99603	Smarca2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443760	Etnk2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916867	Pitrm1	implicated_via_orthology	DOID:9277	primary cerebellar degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333783	Ccs	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142973	Lars2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345633	Mars1	implicated_via_orthology	DOID:0110173	Charcot-Marie-Tooth disease axonal type 2U						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150150	Slc4a10	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927555	Slc4a4	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145637	Mtmr6	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916867	Pitrm1	implicated_via_orthology	DOID:0050951	hereditary ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780204	Eif1ad14	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196365	Nus1	implicated_via_orthology	DOID:5212	congenital disorder of glycosylation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922780	Lyrm7	implicated_via_orthology	DOID:3650	lactic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:4852	pleomorphic xanthoastrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145637	Mtmr6	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:0111272	occipital horn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914676	Coq8a	implicated_via_orthology	DOID:0080391	nephrotic syndrome type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914216	Trit1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333783	Ccs	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96250	Hsp90aa1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107487	Pxmp2	implicated_via_orthology	DOID:0080121	mitochondrial DNA depletion syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107814	Tubb1	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328368	Cdk9	implicated_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096344	Ampd3	implicated_via_orthology	DOID:0060264	pontocerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922780	Lyrm7	implicated_via_orthology	DOID:0111139	mitochondrial complex III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0050557	congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328362	Blm	implicated_via_orthology	DOID:2717	Bloom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588217	Usp51	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97394	Oat	implicated_via_orthology	DOID:1415	gyrate atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349430	Eif2s3y	implicated_via_orthology	DOID:0060801	MEHMO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915201	Tubb6	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932040	Sil1	implicated_via_orthology	DOID:0080195	Marinesco-Sjogren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109533	Abcb7	implicated_via_orthology	DOID:0050554	X-linked sideroblastic anemia with ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107861	Tubb2a	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045301	Ankk1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918041	Hars2	implicated_via_orthology	DOID:0110162	Charcot-Marie-Tooth disease, axonal type 2W						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107365	Ube2i	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444979	Letm2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:90675	Vars1	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925495	Acbd7	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107460	Cox6b1	implicated_via_orthology	DOID:890	mitochondrial encephalomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180139	Edem1	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444966	Tecrl	implicated_via_orthology	DOID:0050889	non-syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450915	Sec23ip	implicated_via_orthology	DOID:0110806	hereditary spastic paraplegia 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923558	Rab1b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	implicated_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0080908	Cockayne syndrome B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913833	Exosc1	implicated_via_orthology	DOID:0112331	pontocerebellar hypoplasia type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917822	Ipo5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:0111273	NARP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349430	Eif2s3y	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915255	Naa10	implicated_via_orthology	DOID:0050781	Ogden syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934754	Kars1	implicated_via_orthology	DOID:0110534	autosomal recessive nonsyndromic deafness 89						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919027	Ing3	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349431	Eif2s3x	implicated_via_orthology	DOID:9406	hypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	implicated_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:12678	hypercalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	implicated_via_orthology	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095410	Tuba4a	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915938	Abhd4	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916167	Hint2	implicated_via_orthology	DOID:0050526	Gamstorp-Wohlfart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347014	Psmb3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925224	Rdh12	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928894	Rpl35a	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105047	Psmc5	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147627	Yars1	implicated_via_orthology	DOID:070355	multisystem proteinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095409	Tuba1c	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442982	Rab8b	implicated_via_orthology	DOID:0111167	Dyggve-Melchior-Clausen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105491	Cdipt	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780185	Eif1ad3	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930018	Dnajb5	implicated_via_orthology	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916867	Pitrm1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343262	Timm44	implicated_via_orthology	DOID:8161	thyroid gland Hurthle cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442510	Dars2	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3583944	Cdk15	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928277	Afg3l1	implicated_via_orthology	DOID:0050977	spinocerebellar ataxia type 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932557	Letm1	implicated_via_orthology	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920402	Rdh14	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914147	Naa16	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920382	Slc25a16	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588268	Gnat3	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922570	Etnk1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107804	Tuba1b	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:2717	Bloom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920036	Tdp1	implicated_via_orthology	DOID:0090115	spinocerebellar ataxia with axonal neuropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926083	Gins3	implicated_via_orthology	DOID:0060306	Meier-Gorlin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107450	Dld	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858429	Cdc34b	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97842	Rab1a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88393	Chd1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109292	Rad50	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931874	Dnajb1	implicated_via_orthology	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779631	Eif1ad16	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:1540	parathyroid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:0070113	Niemann-Pick disease type C1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88016	Ampd2	implicated_via_orthology	DOID:0060264	pontocerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924753	Alg9	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106362	Sco1	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196356	Iqsec1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917431	Ythdf1	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914378	Ube2g1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931237	Wwox	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353496	Slc25a5	implicated_via_orthology	DOID:0111517	autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107760	Chka	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107186	Cct2	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354713	Acsl4	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0111590	Cohen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3607791	Rft1	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919358	Ddhd2	implicated_via_orthology	DOID:0110779	hereditary spastic paraplegia 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95305	Eif4e	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915201	Tubb6	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445217	Xpnpep3	implicated_via_orthology	DOID:0111117	nephronophthisis-like nephropathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350931	Tcirg1	implicated_via_orthology	DOID:0110942	autosomal recessive osteopetrosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88431	Cnbp	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:0111223	centronuclear myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353561	Vapa	implicated_via_orthology	DOID:0050752	amyotrophic lateral sclerosis type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922088	Naa15	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450915	Sec23ip	implicated_via_orthology	DOID:0110779	hereditary spastic paraplegia 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384774	Alg1	implicated_via_orthology	DOID:0080563	congenital disorder of glycosylation Ik						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351613	Txnl4a	implicated_via_orthology	DOID:0050781	Ogden syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384782	Slc25a38	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917171	Hnrnpa3	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913300	Trappc2b	implicated_via_orthology	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104772	Cdk2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:0112202	developmental and epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584510	Wdfy4	implicated_via_orthology	DOID:2935	Chediak-Higashi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:0050977	spinocerebellar ataxia type 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444401	Snrnp200	implicated_via_orthology	DOID:0110366	retinitis pigmentosa 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444031	Alg6	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095409	Tuba1c	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353497	Slc25a10	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107949	Rhob	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443883	Aldh4a1	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915084	Idh3a	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:0060893	juvenile-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:0090101	lethal congenital glycogen storage disease of heart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98917	Uros	implicated_via_orthology	DOID:13270	erythropoietic protoporphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341299	Dnm3	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644018	Eif1ad10	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328313	Chkb	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444552	Actbl2	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88111	Atp2b4	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891340	Lpin1	implicated_via_orthology	DOID:0080108	myoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107438	Cab39	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920583	Slc25a31	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:1540	parathyroid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920328	Pmpcb	implicated_via_orthology	DOID:0070332	multiple mitochondrial dysfunctions syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095406	Tuba3a	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202882	Rhd	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917156	Slc25a32	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349430	Eif2s3y	implicated_via_orthology	DOID:9406	hypopituitarism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104724	Fdxr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095408	Tuba3b	implicated_via_orthology	DOID:0112232	lissencephaly 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354721	Slc25a13	implicated_via_orthology	DOID:9273	citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916165	Vars2	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	implicated_via_orthology	DOID:4006	bladder urothelial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341299	Dnm3	implicated_via_orthology	DOID:11252	microcytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681836	Polr3a	implicated_via_orthology	DOID:0060794	hypomyelinating leukodystrophy 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109585	Pld1	implicated_via_orthology	DOID:0080633	developmental cardiac valvular defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:13934	facial paralysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353452	Aldh3a2	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889002	Wdr4	implicated_via_orthology	DOID:0050569	Seckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442842	Mtmr9	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103064	Ddx3x	implicated_via_orthology	DOID:3869	childhood medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180561	Atpaf2	implicated_via_orthology	DOID:0050768	mitochondrial complex V (ATP synthase) deficiency nuclear type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349427	Exo1	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141959	Alg8	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385054	Pex6	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349406	Ddx3y	implicated_via_orthology	DOID:3869	childhood medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714357	Srp54b	implicated_via_orthology	DOID:0112135	severe congenital neutropenia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922780	Lyrm7	implicated_via_orthology	DOID:0080117	mitochondrial complex III deficiency nuclear type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095408	Tuba3b	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196288	Eif6	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104807	Pls3	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643794	Eif1ad8	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858271	Mtmr1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107912	Ssrp1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920428	Wasl	implicated_via_orthology	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914144	Wwp2	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444207	Vps13c	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277977	Ubr1	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:11252	microcytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142174	4933405O20Rik	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	implicated_via_orthology	DOID:0070238	primary coenzyme Q10 deficiency 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0080121	mitochondrial DNA depletion syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917633	Cox10	implicated_via_orthology	DOID:3762	cytochrome-c oxidase deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0110175	Charcot-Marie-Tooth disease axonal type 2O						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917655	Calml3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915408	Tecr	implicated_via_orthology	DOID:0050889	non-syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99927	mt-Atp6	implicated_via_orthology	DOID:0111755	Leber hereditary optic neuropathy and dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704336	Rpl10-ps3	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102657	Cdc34	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925947	Pus7	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915472	Tubb4b	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349216	Abcd3	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917665	Stk26	implicated_via_orthology	DOID:863	nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914677	Rps20	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923813	Qrsl1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104724	Fdxr	implicated_via_orthology	DOID:5723	optic atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890496	Elac2	implicated_via_orthology	DOID:0111753	infantile hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:3650	lactic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95773	Gnai3	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443764	Iqcb1	implicated_via_orthology	DOID:0110414	retinitis pigmentosa 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921496	Gale	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915337	Dcakd	implicated_via_orthology	DOID:0110740	neurodegeneration with brain iron accumulation 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919912	Dis3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:0080463	developmental and epileptic encephalopathy 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780191	Eif1ad4	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915013	Prpsap1	implicated_via_orthology	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913288	Sdhaf3	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106028	Rhoc	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685748	Mrs2	implicated_via_orthology	DOID:0050476	Barth syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:11252	microcytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109404	Nup98	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144157	Usp22	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098604	Rragd	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202713	Rhag	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891829	Rbx1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922675	Tti1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333804	Vbp1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916637	Dnajb13	implicated_via_orthology	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914071	Bcs1l	implicated_via_orthology	DOID:0080111	mitochondrial complex III deficiency nuclear type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384774	Alg1	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915201	Tubb6	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914721	Gpatch1	implicated_via_orthology	DOID:0111446	progressive myoclonus epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891343	Prkag3	implicated_via_orthology	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915549	Vps53	implicated_via_orthology	DOID:0060271	pontocerebellar hypoplasia type 2E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336153	Prkag2	implicated_via_orthology	DOID:384	Wolff-Parkinson-White syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915142	Coa6	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342274	Slc25a15	implicated_via_orthology	DOID:0050720	ornithine translocase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354721	Slc25a13	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918632	Pex1	implicated_via_orthology	DOID:0080377	peroxisomal biogenesis disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:0050699	Dent disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103555	Clcn3	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096881	Eef1a1	implicated_via_orthology	DOID:0080463	developmental and epileptic encephalopathy 33						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858225	Tuba8	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858963	Gnpnat1	implicated_via_orthology	DOID:0080753	keratosis follicularis spinulosa decalvans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107813	Tubb3	implicated_via_orthology	DOID:0112227	tubulinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	implicated_via_orthology	DOID:0110999	Joubert syndrome 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:0111273	NARP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443732	Dna2	implicated_via_orthology	DOID:0070009	Seckel syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890496	Elac2	implicated_via_orthology	DOID:0060536	mitochondrial complex I deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385133	Exosc2	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919358	Ddhd2	implicated_via_orthology	DOID:0110806	hereditary spastic paraplegia 54						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:0060893	juvenile-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	implicated_via_orthology	DOID:4137	common bile duct disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	implicated_via_orthology	DOID:0050427	xeroderma pigmentosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95852	Gss	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3044182	Cox6b2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913288	Sdhaf3	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87880	Aco2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444401	Snrnp200	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921552	Mtmr3	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0111557	Charcot-Marie-Tooth disease type 2A2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917678	Polr3b	implicated_via_orthology	DOID:0060786	hypomyelinating leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892877	Pld2	implicated_via_orthology	DOID:0080633	developmental cardiac valvular defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	implicated_via_orthology	DOID:2962	Cockayne syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442982	Rab8b	implicated_via_orthology	DOID:0060247	Smith-McCort dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0060537	mitochondrial complex II deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095409	Tuba1c	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349441	Mecr	implicated_via_orthology	DOID:0111756	Leber hereditary optic neuropathy with demyelinating disease of CNS						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891379	Bhmt2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97533	Pdha2	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444552	Actbl2	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309481	Trip12	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	implicated_via_orthology	DOID:0111216	autosomal recessive centronuclear myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922088	Naa15	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333783	Ccs	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	implicated_via_orthology	DOID:0111557	Charcot-Marie-Tooth disease type 2A2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917585	Reep6	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913476	Trappc2	implicated_via_orthology	DOID:0080362	X-linked spondyloepiphyseal dysplasia tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107624	Mvk	implicated_via_orthology	DOID:0050452	mevalonic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685119	Eif4e1b	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104653	Atp2b1	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:11252	microcytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98791	Top2b	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915542	Stt3b	implicated_via_orthology	DOID:0080572	congenital disorder of glycosylation Iw						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891693	Mtmr7	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107448	Lyst	implicated_via_orthology	DOID:2935	Chediak-Higashi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918993	Coasy	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100856	Mras	implicated_via_orthology	DOID:0050469	Costello syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109207	Eif4g2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683212	Ranbp6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107861	Tubb2a	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914865	Ube2r2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913476	Trappc2	implicated_via_orthology	DOID:14789	spondyloepiphyseal dysplasia congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648257	Eif1ad7	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858751	Rragc	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890508	Zmpste24	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647985	Rpl10l	implicated_via_orthology	DOID:0060807	syndromic X-linked intellectual disability Najm type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91842	D1Pas1	implicated_via_orthology	DOID:3869	childhood medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107185	Cct5	implicated_via_orthology	DOID:0110132	Bardet-Biedl syndrome 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349635	Sec23a	implicated_via_orthology	DOID:0111401	congenital dyserythropoietic anemia type II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:2351	iron metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927204	Gosr2	implicated_via_orthology	DOID:0111449	progressive myoclonus epilepsy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442842	Mtmr9	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924408	Coq6	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321133	Hint1	implicated_via_orthology	DOID:0050526	Gamstorp-Wohlfart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3078	anaplastic astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921496	Gale	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106314	Tars1	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028576	Dhx37	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913440	Acer3	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918590	Riok1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782201	Eif1ad6	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349431	Eif2s3x	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194921	Ttk	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103555	Clcn3	implicated_via_orthology	DOID:0050699	Dent disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917701	Dhrs13	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095409	Tuba1c	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922570	Etnk1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858963	Gnpnat1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914290	Ddx17	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927379	Rhbg	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:0111139	mitochondrial complex III deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:0070270	hereditary nonpolyposis colorectal cancer type 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107814	Tubb1	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:12558	chronic progressive external ophthalmoplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338073	Cdc45	implicated_via_orthology	DOID:0060306	Meier-Gorlin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333783	Ccs	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894835	Rbbp6	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3051596	Znhit3	implicated_via_orthology	DOID:0080539	PEHO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920924	Wdr75	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918850	Ythdf3	implicated_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351613	Txnl4a	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107848	Tubb4a	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107812	Tubb5	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330809	Atp10a	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103285	Atp6v1b1	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442306	Fancm	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434734	Gm21379	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:0111340	dominant optic atrophy plus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096881	Eef1a1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270152	Reep5	implicated_via_orthology	DOID:0110782	hereditary spastic paraplegia 31						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0110155	Charcot-Marie-Tooth disease type 2A2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98037	Rpl30	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	implicated_via_orthology	DOID:5015	fibrolamellar carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98788	Top1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933754	Nedd4l	implicated_via_orthology	DOID:0050477	Liddle syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181510	Dhrsx	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914672	Dhdds	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3645211	Lipt1	implicated_via_orthology	DOID:3652	Leigh disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341299	Dnm3	implicated_via_orthology	DOID:0111223	centronuclear myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629896	Mir665	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	implicated_via_orthology	DOID:0070351	spinal muscular atrophy with lower extremity predominant 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107487	Pxmp2	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444068	Atp13a5	implicated_via_orthology	DOID:0060556	Kufor-Rakeb syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332236	Cds2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926211	Trappc4	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894318	Cdk14	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95299	Eif2s1	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914903	4930544G11Rik	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:0111755	Leber hereditary optic neuropathy and dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096875	Wdfy3	implicated_via_orthology	DOID:2935	Chediak-Higashi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336201	Sumo3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914175	Sdhd	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105047	Psmc5	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919027	Ing3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384784	Eif4g1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105037	Ddx5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329021	Msh5	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934754	Kars1	implicated_via_orthology	DOID:0050987	hypomyelinating leukoencephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915383	Gcsh	implicated_via_orthology	DOID:9268	glycine encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3818630	Sco2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913485	Eif1ax	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384560	Aars1	implicated_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921376	Syvn1	implicated_via_orthology	DOID:13372	alpha 1-antitrypsin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	implicated_via_orthology	DOID:0111223	centronuclear myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277186	Atg5	implicated_via_orthology	DOID:0080259	autosomal recessive spinocerebellar ataxia 25						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349467	Abcd2	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095406	Tuba3a	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346333	Mrps12	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	implicated_via_orthology	DOID:0050939	uterine corpus endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913833	Exosc1	implicated_via_orthology	DOID:11343	scleral disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891342	Lpin3	implicated_via_orthology	DOID:0080108	myoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443384	Slc4a9	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921662	Gle1	implicated_via_orthology	DOID:0060559	lethal congenital contracture syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095408	Tuba3b	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:2861	congenital nonspherocytic hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:13317	hyperinsulinemic hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889008	Atp2c1	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346087	Srp54a	implicated_via_orthology	DOID:0112135	severe congenital neutropenia 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0111611	autosomal recessive spinocerebellar ataxia 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:0060893	juvenile-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780224	Eif1ad11	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	implicated_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442688	Atp10b	implicated_via_orthology	DOID:0070221	progressive familial intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96960	Rab8a	implicated_via_orthology	DOID:0111167	Dyggve-Melchior-Clausen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914290	Ddx17	implicated_via_orthology	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916931	Cdk3	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354721	Slc25a13	implicated_via_orthology	DOID:4137	common bile duct disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920960	Tubb2b	implicated_via_orthology	DOID:0060260	ptosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921846	Cds1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150302	Ddhd1	implicated_via_orthology	DOID:0110779	hereditary spastic paraplegia 28						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384838	Prpsap2	implicated_via_orthology	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915201	Tubb6	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351613	Txnl4a	implicated_via_orthology	DOID:0080695	Burn-McKeown syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647985	Rpl10l	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104855	Atp6v0a2	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928898	Usp14	implicated_via_orthology	DOID:649	prion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444552	Actbl2	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105066	Rab10	implicated_via_orthology	DOID:0111167	Dyggve-Melchior-Clausen disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385133	Exosc2	implicated_via_orthology	DOID:0081175	short stature, hearing loss, retinitis pigmentosa, and distinctive facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925947	Pus7	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345633	Mars1	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147627	Yars1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920924	Wdr75	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88579	Cyct	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923607	Trmt5	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916847	Afg3l2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102657	Cdc34	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915541	Mto1	implicated_via_orthology	DOID:0050563	nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891343	Prkag3	implicated_via_orthology	DOID:0090101	lethal congenital glycogen storage disease of heart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:0060480	left ventricular noncompaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183441	Psat1	implicated_via_orthology	DOID:0050723	PSAT deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98179	Rras	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3809095	Atp6-ps	implicated_via_orthology	DOID:1781	thyroid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196391	Pole	implicated_via_orthology	DOID:10021	duodenum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913496	Osgep	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	implicated_via_orthology	DOID:9273	citrullinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919057	Tars2	implicated_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95771	Gnai1	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039623	Thada	implicated_via_orthology	DOID:0050776	non-syndromic X-linked intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915339	Arpc4	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444304	Vps13a	implicated_via_orthology	DOID:0050766	choreaacanthocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929721	Rrs1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855697	Atp5f1e	implicated_via_orthology	DOID:0060332	mitochondrial complex V (ATP synthase) deficiency nuclear type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861099	Ubr2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108403	Polr1d	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924956	Abcb5	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927232	Rab13	implicated_via_orthology	DOID:0060247	Smith-McCort dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098643	Coq5	implicated_via_orthology	DOID:0050730	coenzyme Q10 deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915434	Denr	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923380	Las1l	implicated_via_orthology	DOID:0060814	Wilson-Turner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919019	Bbs10	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916297	Atp2c2	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147613	Aldh3b2	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445114	Pisd	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107814	Tubb1	implicated_via_orthology	DOID:0090132	complex cortical dysplasia with other brain malformations 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104589	Actg2	implicated_via_orthology	DOID:13832	patent ductus arteriosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096881	Eef1a1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859645	Usp27x	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105124	Stt3a	implicated_via_orthology	DOID:0080572	congenital disorder of glycosylation Iw						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922314	Zcchc13	implicated_via_orthology	DOID:0050759	myotonic dystrophy type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94865	Dbi	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101789	Lig1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:8712	neurofibromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920121	Pfn4	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107487	Pxmp2	implicated_via_orthology	DOID:0080125	mitochondrial DNA depletion syndrome 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924408	Coq6	implicated_via_orthology	DOID:0070243	primary coenzyme Q10 deficiency 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919558	Brf1	implicated_via_orthology	DOID:0080898	cerebellofaciodental syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915013	Prpsap1	implicated_via_orthology	DOID:0050566	X-linked nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96247	Hsp90ab1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179277	Atxn7	implicated_via_orthology	DOID:0050958	spinocerebellar ataxia type 7						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104871	Ppp1cb	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916974	Rnaseh2a	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349431	Eif2s3x	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108403	Polr1d	implicated_via_orthology	DOID:0080790	Treacher Collins syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143057	Pif1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105368	Atp2b2	implicated_via_orthology	DOID:0050429	Hailey-Hailey disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443878	Slc4a7	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:0050729	Chanarin-Dorfman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105943	Rpl10	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153480	Atp6v0a4	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924366	Mtmr2	implicated_via_orthology	DOID:0111225	centronuclear myopathy X-linked						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109547	Dnm2	implicated_via_orthology	DOID:0111223	centronuclear myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95530	Fh1	implicated_via_orthology	DOID:5138	leiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914285	Dnajb4	implicated_via_orthology	DOID:0110305	autosomal dominant limb-girdle muscular dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932051	Kat5	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099835	Skic2	implicated_via_orthology	DOID:0111416	trichohepatoenteric syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0080122	Alpers-Huttenlocher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444979	Letm2	implicated_via_orthology	DOID:0050460	Wolf-Hirschhorn syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	implicated_via_orthology	DOID:0080918	polymicrogyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349430	Eif2s3y	implicated_via_orthology	DOID:10579	leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107804	Tuba1b	implicated_via_orthology	DOID:0050453	lissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647569	Eif1ad12	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685387	Atp13a3	implicated_via_orthology	DOID:0060893	juvenile-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921734	Rbm31y	implicated_via_orthology	DOID:0110306	autosomal dominant limb-girdle muscular dystrophy type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	implicated_via_orthology	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	implicated_via_orthology	DOID:13099	Moyamoya disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387466	Pank4	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924456	Atp13a4	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101834	Tubg1	implicated_via_orthology	DOID:0090138	complex cortical dysplasia with other brain malformations 4						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107460	Cox6b1	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87906	Actg1	implicated_via_orthology	DOID:0110550	autosomal dominant nonsyndromic deafness 20						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353497	Slc25a10	implicated_via_orthology	DOID:0070329	mitochondrial DNA depletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	implicated_via_orthology	DOID:3829	pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97563	Pgk2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434674	Eif1ad19	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914865	Ube2r2	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918732	Rdh13	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924139	Coq8b	implicated_via_orthology	DOID:0080391	nephrotic syndrome type 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88251	Calm1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888517	Rhcg	implicated_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95780	Gnaz	implicated_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107804	Tuba1b	implicated_via_orthology	DOID:0112234	microlissencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920708	Aldh3b3	implicated_via_orthology	DOID:14501	Sjogren-Larsson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931881	Dnajb12	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137907	Slc25a2	implicated_via_orthology	DOID:0050720	ornithine translocase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97532	Pdha1	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276574	Nsd2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109618	Atp6v1b2	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916115	Arv1	implicated_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347043	Orc4	implicated_via_orthology	DOID:0060306	Meier-Gorlin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88174	Bmi1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99515	Syk	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98229	Apcs	implicated_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920501	Setd7	implicated_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87934	Adra2a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88067	Arc	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:0111862	congenital bilateral absence of vas deferens						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:693	dental enamel hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98477	Tacr2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97795	Ptger3	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919558	Brf1	implicated_via_orthology	DOID:0050871	fibroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	implicated_via_orthology	DOID:3324	mood disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:0080006	bone development disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	implicated_via_orthology	DOID:5804	discrete subaortic stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	implicated_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	implicated_via_orthology	DOID:0050454	periventricular nodular heterotopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97438	Oprd1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915050	Dgat2	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94919	Dpp4	implicated_via_orthology	DOID:0080642	Middle East respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:13812	adhesions of uterus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100509	Kcnk3	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277179	Pde9a	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	implicated_via_orthology	DOID:801	hemarthrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104772	Cdk2	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928323	Nisch	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108042	Ccna1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87929	Adh5	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102499	mt-Nd3	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98474	Tac1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0080908	Cockayne syndrome B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922954	Ces1h	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347344	Gla	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:13252	mesenteric vascular occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206591	Bik	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:11994	atrophy of testis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103064	Ddx3x	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88396	Chrm1	implicated_via_orthology	DOID:0050214	Lambert-Eaton myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98907	Uox	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206591	Bik	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0111128	focal segmental glomerulosclerosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87935	Adra2b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108212	Ripk1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333791	Artn	implicated_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148800	Aipl1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95299	Eif2s1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88335	Cd4	implicated_via_orthology	DOID:10303	sialadenitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96918	Mas1	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95789	Gnrh1	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314842	Kcnj16	implicated_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921593	Crtc2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	implicated_via_orthology	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346542	Bace1	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97267	Myl4	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108442	Cpeb1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927073	Slc29a1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341787	Trpv1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101789	Lig1	implicated_via_orthology	DOID:7725	epilepsy with generalized tonic-clonic seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913102	Cldn13	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138151	Kmo	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104772	Cdk2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385054	Pex6	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349717	Ncor1	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298392	Bscl2	implicated_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344410	Ubd	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183450	Uts2r	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0050152	aspiration pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103579	Madcam1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108029	Scn10a	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	implicated_via_orthology	DOID:9220	central sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95432	Ces1e	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:11049	meconium aspiration syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779470	Ces1b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99502	Ltbp2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3522699	Trpa1	implicated_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99495	Brd2	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338056	Klf5	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88335	Cd4	implicated_via_orthology	DOID:813	septic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098222	Resp18	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97440	Oprl1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	implicated_via_orthology	DOID:628	combined T cell and B cell immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96606	Itgal	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	implicated_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104689	Cct4	implicated_via_orthology	DOID:0050548	hereditary sensory neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104853	Hes1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	implicated_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351602	Dguok	implicated_via_orthology	DOID:0080121	mitochondrial DNA depletion syndrome 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99257	Eif3e	implicated_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:2475	chronic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:7614	meninges sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352454	Nr4a1	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338803	Aire	implicated_via_orthology	DOID:14040	autoimmune polyendocrine syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445094	Plekha7	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151139	Il22b	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:1556	arthus reaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151886	Ngb	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:12986	leukostasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:10966	lipoid nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97849	Rag2	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	implicated_via_orthology	DOID:0080354	Phelan-McDermid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429637	Adamts16	implicated_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96912	Mag	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354184	Nox4	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270840	Ehf	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195268	Sigmar1	implicated_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580016	Agap2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446632	Ago2	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:13100	intracranial vasospasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95415	Erg	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341787	Trpv1	implicated_via_orthology	DOID:2548	reflex epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915050	Dgat2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313314	Cldn4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097680	C3ar1	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91842	D1Pas1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99916	Lamb2	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:790	ocular hypotension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355307	Il22	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:3356	localized osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88222	Tspo	implicated_via_orthology	DOID:14502	cholesterol ester storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:0050562	West syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339759	Csf2rb	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149481	Cygb	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352452	Nr2f2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142687	Ces1f	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87930	Adk	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	implicated_via_orthology	DOID:431	myofascial pain syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861457	Dynll1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859169	Azin1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105091	E2f5	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861457	Dynll1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352508	Stau2	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347344	Gla	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88350	Cdc25c	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:3345	xanthomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106212	Chrnb3	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99555	Pde4d	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429637	Adamts16	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:0050934	ovarian clear cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:2537	inflammatory and toxic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349164	Sdc4	implicated_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	implicated_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95818	Grik5	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346833	Nr5a1	implicated_via_orthology	DOID:14447	gonadal dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:0080884	vitamin D-dependent rickets type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679262	Rgma	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94919	Dpp4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355307	Il22	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109147	Oxtr	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151139	Il22b	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	implicated_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2671987	Shank2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	implicated_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314842	Kcnj16	implicated_via_orthology	DOID:4500	hypokalemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:1697	ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97532	Pdha1	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309998	Marco	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347244	Axl	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648919	Ces1a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	implicated_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101910	F2rl1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:0080886	vitamin D-dependent rickets type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913102	Cldn13	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181726	Mtnr1b	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929666	Sorcs1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	implicated_via_orthology	DOID:1064	cystinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	implicated_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:169	neuroendocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95420	Ces1c	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3522699	Trpa1	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95774	Gnal	implicated_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	implicated_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149481	Cygb	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927664	Sirt2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94917	Dpep1	implicated_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97488	Pax4	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97848	Rag1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429637	Adamts16	implicated_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:3721	plasmacytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:2384	Wernicke encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99458	Mef2c	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	implicated_via_orthology	DOID:2773	contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351331	Chaf1a	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:0050200	Korean hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313314	Cldn4	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	implicated_via_orthology	DOID:594	panic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333825	Dgat1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104772	Cdk2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:0050890	synucleinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	implicated_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104650	Cnr2	implicated_via_orthology	DOID:848	arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447992	Trim63	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107777	Atp5pf	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:3234	central nervous system lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	implicated_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97793	Ptger1	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103298	Apobec1	implicated_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88053	Apoc1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	implicated_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98496	Tbxa2r	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919238	Esco2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88067	Arc	implicated_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099800	Nfkb2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924294	Arid2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353576	Pik3cg	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891999	Adarb1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861691	Lgi1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	implicated_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924294	Arid2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148202	Ces1d	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:13250	diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444110	Sgms1	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88396	Chrm1	implicated_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932575	Sp6	implicated_via_orthology	DOID:2187	amelogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97795	Ptger3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:0050437	Danon disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861691	Lgi1	implicated_via_orthology	DOID:7725	epilepsy with generalized tonic-clonic seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102849	Klkb1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103579	Madcam1	implicated_via_orthology	DOID:3044	food allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932286	Egln1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329040	Dkk1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88378	Ces1g	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102463	Nfatc2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919641	Cdkn3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109408	Reg3a	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96918	Mas1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97453	Oxt	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	implicated_via_orthology	DOID:1062	Fanconi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154244	Plxnd1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	implicated_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921346	Hvcn1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206591	Bik	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99473	Arrb1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	implicated_via_orthology	DOID:3803	Crigler-Najjar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	implicated_via_orthology	DOID:365	bladder disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891999	Adarb1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:9513	plasma cell leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346036	Pin1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98474	Tac1	implicated_via_orthology	DOID:9220	central sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	implicated_via_orthology	DOID:8616	Peyronie's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347094	Parg	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88174	Bmi1	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:5434	scrapie						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:12308	Dubin-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108024	Rgn	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104779	Prkdc	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:4543	retrograde amnesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97525	Pde6b	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445094	Plekha7	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88322	Cd22	implicated_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:9775	diastolic heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649546	Pin1rt1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:0080821	exercise-induced bronchoconstriction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153182	Kcnn2	implicated_via_orthology	DOID:4990	essential tremor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:4677	keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104853	Hes1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98477	Tacr2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	implicated_via_orthology	DOID:0060013	X-linked severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96223	Hr	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443902	Nell1	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98296	Shc1	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102499	mt-Nd3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710243	Myh7b	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105098	Ube3a	implicated_via_orthology	DOID:1932	Angelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87934	Adra2a	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:0070272	hereditary nonpolyposis colorectal cancer type 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351339	Grm2	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384902	Rnpep	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183450	Uts2r	implicated_via_orthology	DOID:12932	endomyocardial fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	implicated_via_orthology	DOID:12450	pancytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352454	Nr4a1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913276	Ngly1	implicated_via_orthology	DOID:0060728	NGLY1-deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:1206	Rett syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	implicated_via_orthology	DOID:0050726	tyrosinemia type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:1063	interstitial nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351331	Chaf1a	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651499	Pde5a	implicated_via_orthology	DOID:4762	vasculogenic impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339760	Csf2rb2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	implicated_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88141	Bcr	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098222	Resp18	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:8536	herpes zoster						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109175	Dab2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202394	Cblif	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351615	Add3	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3522699	Trpa1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277179	Pde9a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289263	Ccdc39	implicated_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	implicated_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88190	Braf	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332226	Soat2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927126	Slc5a7	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676817	Mir132	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:8465	retinoschisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96561	Il7	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88047	Aplp2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96949	Mdk	implicated_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87931	Cfd	implicated_via_orthology	DOID:1556	arthus reaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	implicated_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338758	Adnp	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183450	Uts2r	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923650	Pbp2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338068	Pdpk1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104662	Pml	implicated_via_orthology	DOID:4159	skin cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:1063	interstitial nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107657	Ifnb1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3642232	Nps	implicated_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96274	Htr1b	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108429	Lpar1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921392	Lonp1	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95514	Fes	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922090	Manf	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344408	Pebp1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	implicated_via_orthology	DOID:8683	myeloid sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316649	Sphk1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97621	Plk1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	implicated_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108111	Slc22a1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88244	S100a8	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98824	Trhr	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:11516	hypertensive heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916833	Tnfsf13	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	implicated_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104816	Hnrnpl	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88114	Atp4b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104662	Pml	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104815	Ier2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:10605	short bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330294	Hnrnpab	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:6195	conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102688	H2ax	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104854	Zfp91	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:10914	amnestic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	implicated_via_orthology	DOID:12932	endomyocardial fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106199	Vegfb	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916823	Hilpda	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98239	Scd1	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919200	Nanog	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:4306	radiculopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309472	Ltb4r1	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97243	Mx1	implicated_via_orthology	DOID:4492	avian influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98282	Spi1	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:13250	diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:4990	essential tremor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101947	Hnrnpd	implicated_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103267	Eif4ebp1	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921305	Plce1	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334203	Kcnmb1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920318	Fut11	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100882	Phox2b	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98181	Rrm2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106594	Gk	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921406	Acot12	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913293	Atp5f1d	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927244	Ralb	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	implicated_via_orthology	DOID:4906	small intestine adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278342	Lect2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106919	Vdac1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338758	Adnp	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96922	Mb	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442524	Heatr1	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97742	Pomc	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443514	Wdhd1	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105107	P2ry2	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97576	Phka1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316648	Ahnak	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333871	Hsd17b10	implicated_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:0050742	nicotine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:8456	choline deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:12098	trigeminal neuralgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914981	Fbxo32	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96396	Id1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:1003	pelvic inflammatory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916487	Gtpbp4	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103021	Recql	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922984	Mff	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341157	Sox30	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151053	Serpinb7	implicated_via_orthology	DOID:0050831	familial encephalopathy with neuroserpin inclusion bodies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276535	Ncoa3	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106067	Smc2	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106921	Scn2b	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:13593	eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:12679	nephrocalcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	implicated_via_orthology	DOID:8534	gastroesophageal reflux disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	implicated_via_orthology	DOID:2044	drug-induced hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:13100	intracranial vasospasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88233	C6	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:7305	astroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96912	Mag	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924222	Snhg20	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109366	Kcnk2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95791	Got1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913604	Snw1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924825	Kmt2e	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:0040085	bacterial sepsis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684079	Ffar1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104650	Cnr2	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107785	Mesp1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108466	Ralbp1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346882	Map4k1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97602	Prkcz	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676902	Mir27a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97050	Mdh2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619328	Mir302d	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109292	Rad50	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95791	Got1	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13088	periventricular leukomalacia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	implicated_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105094	Adcyap1	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915304	Serpina12	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915304	Serpina12	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	implicated_via_orthology	DOID:5637	pancreatic adenosquamous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197515	Irx1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:8411	kidney angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97453	Oxt	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98214	Rxra	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333112	Ran	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270126	Ulk1	implicated_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96437	Igfbp2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676875	Mir200b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:0111252	vestibular schwannomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	implicated_via_orthology	DOID:5426	primary ovarian insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159605	Acot2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	implicated_via_orthology	DOID:0080821	exercise-induced bronchoconstriction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345146	Grk1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108409	Rgs4	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145895	Slc38a1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339968	Cth	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99532	Mef2a	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148742	Cldn16	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	implicated_via_orthology	DOID:4079	heart valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:2797	idiopathic interstitial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:1919	Lesch-Nyhan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676812	Mir127	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96382	Iapp	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97385	Ntrk3	implicated_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97749	Ppia	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104576	Lct	implicated_via_orthology	DOID:13250	diarrhea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:8683	myeloid sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	implicated_via_orthology	DOID:8456	choline deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860476	Nmu	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:9965	toxoplasmosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88523	Crygc	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108093	Bid	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97614	Plcd1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:0110663	congenital myasthenic syndrome 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	implicated_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99445	Mtpn	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100509	Kcnk3	implicated_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97614	Plcd1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:2548	reflex epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:3355	fibrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107657	Ifnb1	implicated_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98257	Msr1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278342	Lect2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	implicated_via_orthology	DOID:3950	adrenal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916823	Hilpda	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102778	Six2	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676859	Mir195a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443388	Kdm7a	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96391	Ica1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619391	Mir381	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095403	Sf1	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98823	Trh	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	implicated_via_orthology	DOID:0081082	acute myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108470	St6gal1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333112	Ran	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:3247	rhabdomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103021	Recql	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:12143	neurogenic bladder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:12577	urethral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328365	Aanat	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386323	Acmsd	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	implicated_via_orthology	DOID:3721	plasmacytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385891	Zc3h12a	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97769	Prnp	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107157	Sin3a	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	implicated_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	implicated_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103039	Stat2	implicated_via_orthology	DOID:0060478	Zika fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108053	Rit1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:7843	female breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928323	Nisch	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354736	Kdm2a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	implicated_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	implicated_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445126	Tut4	implicated_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96755	Lcat	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105051	Ksr1	implicated_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:4552	large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	implicated_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	implicated_via_orthology	DOID:76	stomach disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098772	Pik3r2	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	implicated_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107414	Tnfsf10	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042141	Traf7	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98266	Sord	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339795	Smc3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	implicated_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	implicated_via_orthology	DOID:5151	plexiform neurofibroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104814	Ier3	implicated_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	implicated_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347078	Grk6	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:4906	small intestine adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261758	Suz12	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:0050642	hypochromic microcytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096879	Fxn	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927468	Samhd1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107438	Cab39	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:8566	herpes simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102765	Ptprn	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109452	Smad1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97385	Ntrk3	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861735	Tmeff2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196250	Klrk1	implicated_via_orthology	DOID:4231	histiocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928268	Ireb2	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629886	Mir497	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676818	Mir133a-1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97267	Myl4	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	implicated_via_orthology	DOID:2326	gastroenteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87919	Add2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99495	Brd2	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	implicated_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13452	scleritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915522	Lingo1	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97050	Mdh2	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	implicated_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104854	Zfp91	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:9427	hypertensive encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	implicated_via_orthology	DOID:2518	orchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:640	encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88297	Cck	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	implicated_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	implicated_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102683	Grb7	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102688	H2ax	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	implicated_via_orthology	DOID:76	stomach disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442401	Ppp1r9a	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920180	Ppp2r2b	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:5176	renal Wilms' tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97549	Pfn1	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101761	Hmga2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855693	Nap1l1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:3410	carotid artery thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338947	S100a9	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	implicated_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619332	Mir320	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914625	Qprt	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:4492	avian influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:3612	retinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914211	Neat1	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99571	Glp1r	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95937	H2-Q8	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098275	Gse1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:8455	pyridoxine deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97352	Nkx3-1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97749	Ppia	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105958	Cox8b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:8455	pyridoxine deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100886	Prom1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917979	Nos1ap	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98325	Smpd1	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096345	Gckr	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95814	Grik1	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619363	Mir34a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97275	Myod1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914404	Mtdh	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700010	Sh3gl1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:649	prion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87879	Aco1	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107949	Rhob	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:1798	pancreatic endocrine carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	implicated_via_orthology	DOID:4492	avian influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:0060597	atypical chronic myeloid leukemia, BCR-ABL1 negative						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329016	Sel1l	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	implicated_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	implicated_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102768	Mfge8	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	implicated_via_orthology	DOID:0050458	juvenile myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	implicated_via_orthology	DOID:438	autoimmune disease of the nervous system						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:12010	anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87879	Aco1	implicated_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:8029	sporadic breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339468	S100a10	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101802	F2r	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096385	Bcan	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107801	Atp5f1b	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108008	Nutf2-ps1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:3500	gallbladder adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:13208	background diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:686	liver carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	implicated_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:0080158	herpes simplex virus keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	implicated_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99486	Clcn5	implicated_via_orthology	DOID:447	renal tubular transport disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:0080743	transverse myelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676881	Mir206	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347244	Axl	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:8743	erythema infectiosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:8472	localized scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:11450	allergic cutaneous vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449816	Cyp2j7	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	implicated_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	implicated_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95286	Eed	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99700	Cenpc1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	implicated_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97050	Mdh2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619421	Mir484	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859169	Azin1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333802	Hs3st2	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921392	Lonp1	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:0050459	hyperphosphatemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102688	H2ax	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:11249	vitamin K deficiency bleeding						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108091	Bcar1	implicated_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	implicated_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	implicated_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:1891	optic nerve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333802	Hs3st2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	implicated_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921769	Cyp2j9	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152453	Gsk3a	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	implicated_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644668	Prlh	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619443	Mir9-3	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:0080832	mild cognitive impairment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916885	Dapk1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109448	Cfc1	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919027	Ing3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	implicated_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96837	Ltf	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676825	Mir140	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105380	Mcm2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918708	Bcor	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:3594	choriocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99402	Adora2a	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87995	Aldob	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:4371	Schnitzler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135738	Abo	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138169	Cfhr1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98159	Rps6	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106295	Tomm70a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	implicated_via_orthology	DOID:0050214	Lambert-Eaton myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95674	Gcg	implicated_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342287	Klf4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892968	Tacr3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104650	Cnr2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109483	Rnf103	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88096	Atf4	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96829	Lrpap1	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921330	Nmnat3	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181411	Slc5a2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88077	Arsa	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649546	Pin1rt1	implicated_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88116	Atp6v0c	implicated_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105094	Adcyap1	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97501	Pck1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914555	Gpx7	implicated_via_orthology	DOID:7941	Barrett's adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	implicated_via_orthology	DOID:13768	opisthorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717097	Cyp2j12	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202394	Cblif	implicated_via_orthology	DOID:13381	pernicious anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88375	Cenpa	implicated_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684762	Lzts1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97512	Pcsk2	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915192	Atp5mc2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915301	Nutf2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107657	Ifnb1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88374	Cel	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449816	Cyp2j7	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	implicated_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107657	Ifnb1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	implicated_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101910	F2rl1	implicated_via_orthology	DOID:0060496	respiratory allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100508	Kcnj8	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891917	Ywhab	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1556	arthus reaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:4531	mucoepidermoid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:8337	appendicitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343142	Arpc1b	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108445	Ciita	implicated_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	implicated_via_orthology	DOID:8515	Cor pulmonale						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105064	Slc9a3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629927	Mir615	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932288	Egln3	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97435	Mog	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:0110278	autosomal recessive limb-girdle muscular dystrophy type 2D						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:8472	localized scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	implicated_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916788	Antxr1	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449817	Cyp2j8	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:3798	pleural empyema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96382	Iapp	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:0060496	respiratory allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140224	Cyp2j11	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924809	Agl	implicated_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	implicated_via_orthology	DOID:2044	drug-induced hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103107	F10	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88235	C7	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0080158	herpes simplex virus keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97830	Pygm	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96070	Hbegf	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	implicated_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:5050	Ehrlich tumor carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353451	Aldh3a1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448558	Fancb	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95728	Gli2	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915192	Atp5mc2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333802	Hs3st2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926471	Fancg	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919164	Antxr2	implicated_via_orthology	DOID:7427	anthrax disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98658	Cripto	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97435	Mog	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:7941	Barrett's adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140224	Cyp2j11	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	implicated_via_orthology	DOID:2352	hemochromatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99700	Cenpc1	implicated_via_orthology	DOID:0060218	CREST syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930134	Ern1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	implicated_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88114	Atp4b	implicated_via_orthology	DOID:0040090	autoimmune gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	implicated_via_orthology	DOID:5015	fibrolamellar carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	implicated_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298209	Hcn4	implicated_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146430	Cblb	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	implicated_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96949	Mdk	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	implicated_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927664	Sirt2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	implicated_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95514	Fes	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443671	Dlec1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:11249	vitamin K deficiency bleeding						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932286	Egln1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443065	Agps	implicated_via_orthology	DOID:2580	rhizomelic chondrodysplasia punctata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88114	Atp4b	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:12259	hemophilia B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333783	Ccs	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140224	Cyp2j11	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676905	Mir29b-1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717097	Cyp2j12	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341803	Lipg	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3689889	Fancf	implicated_via_orthology	DOID:4943	adenocarcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	implicated_via_orthology	DOID:14499	Fabry disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349444	Haao	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101910	F2rl1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	implicated_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	implicated_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96837	Ltf	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11573	listeriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717097	Cyp2j12	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108093	Bid	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	implicated_via_orthology	DOID:0060075	estrogen-receptor positive breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88174	Bmi1	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889272	Cadm1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	implicated_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098776	Lbp	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	implicated_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1556	arthus reaction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:9938	dacryocystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:3491	Turner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	implicated_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	implicated_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:13252	mesenteric vascular occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98957	Wnt4	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385197	Cyp2j13	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	implicated_via_orthology	DOID:26	pancreas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385197	Cyp2j13	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195256	Pla2g4a	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104755	Kcnj5	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99253	Etv2	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:0060218	CREST syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	implicated_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	implicated_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270149	Cyp2j5	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2389490	B3gat2	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097717	Ankrd1	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	implicated_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106915	Vdac2	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108092	Bin1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	implicated_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104744	Kcnj2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	implicated_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351615	Add3	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	implicated_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859314	Barhl2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99571	Glp1r	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270854	Gck	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:4371	Schnitzler syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109292	Rad50	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143886	Dot1l	implicated_via_orthology	DOID:9953	acute biphenotypic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97435	Mog	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	implicated_via_orthology	DOID:3594	choriocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108429	Lpar1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	implicated_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153093	Cspg4	implicated_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:8472	localized scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	implicated_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:11249	vitamin K deficiency bleeding						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101849	Rack1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	implicated_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	implicated_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:12987	agranulocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650907	Rps6-ps4	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663233	Muc6	implicated_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106915	Vdac2	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95805	Grb2	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95299	Eif2s1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	implicated_via_orthology	DOID:8557	oropharynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917138	Cyp2c66	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104816	Hnrnpl	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921769	Cyp2j9	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918929	Atp5pd	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:77	gastrointestinal system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	implicated_via_orthology	DOID:4552	large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921769	Cyp2j9	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103008	Epb41l3	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:12678	hypercalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270149	Cyp2j5	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96837	Ltf	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330841	Bcl2l10	implicated_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107474	Cd38	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101863	Aldoc	implicated_via_orthology	DOID:438	autoimmune disease of the nervous system						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:8927	learning disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	implicated_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891925	Hnrnph1	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88376	Cenpb	implicated_via_orthology	DOID:2952	inner ear disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88376	Cenpb	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351331	Chaf1a	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:5050	Ehrlich tumor carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449817	Cyp2j8	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	implicated_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915963	Ifitm1	implicated_via_orthology	DOID:3500	gallbladder adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	implicated_via_orthology	DOID:5627	adenosquamous gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96949	Mdk	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	implicated_via_orthology	DOID:2755	Mycobacterium avium complex disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103298	Apobec1	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	implicated_via_orthology	DOID:8029	sporadic breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919553	Cyp2c65	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	implicated_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96915	Maoa	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097717	Ankrd1	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105061	Clcn2	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329034	Ccne2	implicated_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333802	Hs3st2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3689889	Fancf	implicated_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346036	Pin1	implicated_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861379	Klk4	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	implicated_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928480	Acp3	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	implicated_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	implicated_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	implicated_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932287	Egln2	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	implicated_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	implicated_via_orthology	DOID:11801	protein-energy malnutrition						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915963	Ifitm1	implicated_via_orthology	DOID:5627	adenosquamous gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	implicated_via_orthology	DOID:1222	cartilage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:9810	polyarteritis nodosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	implicated_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914751	Ccdc50	implicated_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95791	Got1	implicated_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927555	Slc4a4	implicated_via_orthology	DOID:12387	nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:8505	dermatitis herpetiformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385197	Cyp2j13	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914186	Asph	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97807	Ptpn5	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:178	vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99612	Epha3	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	implicated_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	implicated_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:4492	avian influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	implicated_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	implicated_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	implicated_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	implicated_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928375	Arpc3	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	implicated_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195985	Cbx4	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108451	Acaca	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	implicated_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330294	Hnrnpab	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:285	hairy cell leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	implicated_via_orthology	DOID:3355	fibrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914555	Gpx7	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097717	Ankrd1	implicated_via_orthology	DOID:422	congenital structural myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97801	Pth1r	implicated_via_orthology	DOID:12678	hypercalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	implicated_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096863	Entpd2	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	implicated_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105049	P2ry1	implicated_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449816	Cyp2j7	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:3911	progeria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88174	Bmi1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343051	Actl7a	implicated_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95660	Gas6	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96441	Igfbp6	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676888	Mir212	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96391	Ica1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95393	Eno1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	implicated_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	implicated_via_orthology	DOID:12531	von Willebrand's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	implicated_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330841	Bcl2l10	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88114	Atp4b	implicated_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	implicated_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99846	Gdi1	implicated_via_orthology	DOID:2468	psychotic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	implicated_via_orthology	DOID:0050782	Zollinger-Ellison syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449817	Cyp2j8	implicated_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341803	Lipg	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	implicated_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648653	Eno1b	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	implicated_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	implicated_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87881	Acp1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96247	Hsp90ab1	implicated_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333800	Il18bp	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341272	Col14a1	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	implicated_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	implicated_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95514	Fes	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	implicated_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140940	Acacb	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333800	Il18bp	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96916	Maob	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	implicated_via_orthology	DOID:1508	candidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	implicated_via_orthology	DOID:0080188	chronic myelomonocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	implicated_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95805	Grb2	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270149	Cyp2j5	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107657	Ifnb1	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106183	Ocln	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:3012	Li-Fraumeni syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106199	Vegfb	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921727	4933427D14Rik	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685177	Megf10	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859270	Exoc7	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922028	Rrp7a	implicated_via_orthology	DOID:0070297	primary microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102563	Dct	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443626	Vps18	implicated_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920912	Apol7c	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779453	Prps1l3	implicated_via_orthology	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3583950	Apol7b	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	implicated_via_orthology	DOID:0050463	campomelic dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891978	Phyh	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921700	Pank2	implicated_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098238	Kif6	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927551	Osbpl1a	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914582	Snrpd3	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306784	Cited2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100508	Kcnj8	implicated_via_orthology	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106022	Rpl26	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918000	Kdsr	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	implicated_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915509	Ift80	implicated_via_orthology	DOID:0050592	asphyxiating thoracic dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922869	Fastkd2	implicated_via_orthology	DOID:0060286	combined oxidative phosphorylation deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135272	Vangl2	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442479	Elfn1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336170	Mybpc2	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444912	Mbnl3	implicated_via_orthology	DOID:450	myotonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345150	Cdc6	implicated_via_orthology	DOID:0060306	Meier-Gorlin syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3610364	Rbm24	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780112	Cyp4f37	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107418	Ptprn2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104884	Psmb1	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	implicated_via_orthology	DOID:10632	Wolfram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98742	Thra	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919570	Kifbp	implicated_via_orthology	DOID:0060481	Goldberg-Shprintzen syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	implicated_via_orthology	DOID:0070343	CSF1R-related brain malformation and osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:0060186	chemical colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98342	Snrpb	implicated_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929628	Rsad2	implicated_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923120	Tcam1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102965	Scn7a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98003	Rpl18	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152819	B3galt6	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	biomarker_via_orthology	DOID:0050890	synucleinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0110827	Usher syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920347	Dact2	implicated_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	implicated_via_orthology	DOID:0050644	arterial calcification of infancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103006	Epb41l5	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	implicated_via_orthology	DOID:7442	monoclonal gammopathy of uncertain significance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182543	Grhl2	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142124	AU018091	implicated_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	implicated_via_orthology	DOID:14686	Axenfeld-Rieger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97273	Mylpf	implicated_via_orthology	DOID:0111597	distal arthrogryposis type 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915526	Toe1	implicated_via_orthology	DOID:0060264	pontocerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97775	Prps1	implicated_via_orthology	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99459	Nr3c2	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141101	Depdc5	implicated_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194899	Inpp5k	implicated_via_orthology	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916218	Cdan1	implicated_via_orthology	DOID:0111396	congenital dyserythropoietic anemia type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153040	Slc45a2	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98107	Rps14	implicated_via_orthology	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684063	Asxl1	implicated_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704456	Apol7e	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107163	Ppp3cb	implicated_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202302	Pms1	implicated_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915146	Ccdc80	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923294	Ncapg2	implicated_via_orthology	DOID:0050737	autosomal recessive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914287	Pmf1	implicated_via_orthology	DOID:4007	bladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917609	Gtpbp3	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917351	Cyp4f16	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	implicated_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	implicated_via_orthology	DOID:0111160	camptodactyly-tall stature-scoliosis-hearing loss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:3247	rhabdomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108025	Prkar2a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918084	Spag9	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932386	Ift122	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141135	Hscb	implicated_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913647	Sar1b	implicated_via_orthology	DOID:0060357	chylomicron retention disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102539	Tbx6	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106030	Gucy2d	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098567	Astn1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	implicated_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:2450	central retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039785	Syngap1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918000	Kdsr	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	implicated_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104687	Col4a4	implicated_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921341	Npl	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139422	Duox1	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98359	Sox11	implicated_via_orthology	DOID:1925	Coffin-Siris syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	implicated_via_orthology	DOID:450	myotonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340034	Sema3e	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385311	Dlat	implicated_via_orthology	DOID:3650	lactic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103288	Polr1c	implicated_via_orthology	DOID:2908	Treacher Collins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	implicated_via_orthology	DOID:1923	disorder of sexual development						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097711	Degs1	implicated_via_orthology	DOID:0060786	hypomyelinating leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88329	Cd34	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917302	Prpf4	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	implicated_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135267	Bbs2	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142454	Usb1	implicated_via_orthology	DOID:0060551	poikiloderma with neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919680	B4gat1	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329037	Strap	implicated_via_orthology	DOID:4552	large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176159	Cyp26b1	implicated_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203732	Slc16a2	implicated_via_orthology	DOID:0050631	Allan-Herndon-Dudley syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	implicated_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860493	Arhgef7	implicated_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106100	Etfdh	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97876	Rbp1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95623	Gabrg2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:12583	velocardiofacial syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	implicated_via_orthology	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88253	Car8	implicated_via_orthology	DOID:0050997	cerebellar ataxia, mental retardation and dysequlibrium syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98331	Snap25	implicated_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98310	Ski	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347469	Foxl1	implicated_via_orthology	DOID:12185	otosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	implicated_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109489	Snrpc	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101833	Elk1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97138	Mpv17	implicated_via_orthology	DOID:0070329	mitochondrial DNA depletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96394	Icam2	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138281	Lbr	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913484	Msmo1	implicated_via_orthology	DOID:2581	chondrodysplasia punctata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858305	Pgrmc1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333883	Lats1	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95495	Ms4a2	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	implicated_via_orthology	DOID:2975	cystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	implicated_via_orthology	DOID:3049	Churg-Strauss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351634	Abcc6	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	implicated_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449311	Gemin5	implicated_via_orthology	DOID:0050753	cerebellar ataxia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	implicated_via_orthology	DOID:9834	hyperopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	implicated_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	implicated_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443590	Ddx11	implicated_via_orthology	DOID:0060535	Warsaw breakage syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333780	Rps19	implicated_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1107	esophageal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923824	Mfsd2a	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109489	Snrpc	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924859	Odad3	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98813	Tpo	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	implicated_via_orthology	DOID:0090118	congenital amegakaryocytic thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109257	Smn1	implicated_via_orthology	DOID:12377	spinal muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:971	tendinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:9667	placental abruption						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2660628	Adamts20	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335093	Ppp2r3d	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388124	Clrn1	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97239	Mmut	implicated_via_orthology	DOID:14749	methylmalonic acidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	implicated_via_orthology	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97473	Pah	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95747	Glra1	implicated_via_orthology	DOID:0060695	hyperekplexia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	implicated_via_orthology	DOID:9258	Waardenburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	implicated_via_orthology	DOID:0080097	myofibrillar myopathy 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98247	Scn1b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148811	Npnt	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	implicated_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109350	Slc4a3	implicated_via_orthology	DOID:0050793	short QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145645	Exoc5	implicated_via_orthology	DOID:0080332	bicuspid aortic valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924983	Rnf170	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442796	Smyd4	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109277	Pik3r3	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97359	Nodal	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915396	Arl13b	implicated_via_orthology	DOID:0111003	Joubert syndrome 8						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	implicated_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336194	Tpp1	implicated_via_orthology	DOID:0110726	neuronal ceroid lipofuscinosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914275	Rpl11	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	implicated_via_orthology	DOID:0081007	RNASET2-deficient cystic leukoencephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:8506	bullous pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580376	Lemd3	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:0110838	Usher syndrome type 2A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109626	Tafazzin	implicated_via_orthology	DOID:0050476	Barth syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890564	Rcan1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684944	Myrf	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	implicated_via_orthology	DOID:0050437	Danon disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	implicated_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891428	Pcdh15	implicated_via_orthology	DOID:0110832	Usher syndrome type 1F						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349428	Foxl2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142124	AU018091	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917297	Trnt1	implicated_via_orthology	DOID:0080209	sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349635	Sec23a	implicated_via_orthology	DOID:0070307	craniolenticulosutural dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915266	Cavin4	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442543	Vash1	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860137	Gp9	implicated_via_orthology	DOID:2217	Bernard-Soulier syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	implicated_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919338	Ush1c	implicated_via_orthology	DOID:0050439	Usher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107595	Sp4	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107821	Has2	biomarker_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354736	Kdm2a	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336213	Mybpc1	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926142	Crispld2	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443939	Cenpt	implicated_via_orthology	DOID:0050569	Seckel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913921	Ccnh	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341157	Sox30	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99569	S1pr2	implicated_via_orthology	DOID:305	carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109589	Ocrl	implicated_via_orthology	DOID:1056	oculocerebrorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:8741	seborrheic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108050	Ext2	implicated_via_orthology	DOID:206	hereditary multiple exostoses						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105371	Spock1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176375	Ucn2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861735	Tmeff2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	implicated_via_orthology	DOID:0060186	chemical colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98849	Tshr	implicated_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344385	Med24	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:3798	pleural empyema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98216	Rxrg	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99673	Adcy5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101834	Tubg1	implicated_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:0080390	nephrotic syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338820	Bmp10	implicated_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384831	Cc2d1a	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921437	Katnb1	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148202	Ces1d	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:178	vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98002	Rpl12	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332226	Soat2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108186	Aldh7a1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	implicated_via_orthology	DOID:1206	Rett syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97857	Rarb	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101913	Chml	implicated_via_orthology	DOID:9821	choroideremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108520	Fzd4	implicated_via_orthology	DOID:0050535	exudative vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347058	Hsf4	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919847	Auts2	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:5744	ovary serous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921642	Specc1l	implicated_via_orthology	DOID:0050567	orofacial cleft						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328318	Atp6v0e	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335098	Lig4	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176159	Cyp26b1	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107363	Stxbp1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:0080883	vitamin D-dependent rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918711	Ptk7	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95791	Got1	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87968	Ahcy	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106036	Lrrn3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107730	Hoxb13	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930705	Stx1b	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99150	Yy1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922672	Mettl5	implicated_via_orthology	DOID:0080765	autosomal recessive intellectual developmental disorder 72						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346087	Srp54a	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892979	Chm	implicated_via_orthology	DOID:9821	choroideremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:0050644	arterial calcification of infancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347048	Clcn7	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643902	Gnptab	implicated_via_orthology	DOID:0080070	mucolipidosis II alpha/beta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108543	Tfpi2	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2674311	Sspo	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105058	Atp2a1	implicated_via_orthology	DOID:0050692	Brody myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932134	Rpgrip1	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	implicated_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	implicated_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	implicated_via_orthology	DOID:0081007	RNASET2-deficient cystic leukoencephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:7725	epilepsy with generalized tonic-clonic seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920347	Dact2	implicated_via_orthology	DOID:4897	bile duct carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333763	Epn1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	implicated_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445019	Pik3c3	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349482	Nherf1	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107595	Sp4	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107465	Plcb2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	implicated_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107172	Ppp3r1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344385	Med24	implicated_via_orthology	DOID:870	neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924487	Cc2d2a	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1289196	Rnf213	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101783	Plk4	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87989	Alas1	biomarker_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859214	Pmm2	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923696	Wdr62	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88176	Bmp1	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:0110339	osteogenesis imperfecta type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913666	Ndufa7	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98037	Rpl30	implicated_via_orthology	DOID:8566	herpes simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891978	Phyh	implicated_via_orthology	DOID:906	peroxisomal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98923	Vav1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930016	Shank3	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	implicated_via_orthology	DOID:0070222	progressive familial intrahepatic cholestasis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914287	Pmf1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916320	Adamts9	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923510	Ttc8	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102695	Ptprf	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:2451	protein S deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	implicated_via_orthology	DOID:10881	hand, foot and mouth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194993	Dsc3	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88293	Cacna1d	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714359	Srp54c	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177763	Hps1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143311	Bbs4	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153272	Trrap	implicated_via_orthology	DOID:0050564	autosomal dominant nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107414	Tnfsf10	implicated_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140940	Acacb	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	implicated_via_orthology	DOID:0060186	chemical colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890498	Mcoln1	implicated_via_orthology	DOID:0080490	mucolipidosis type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339984	Pak2	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096381	Bmal1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917431	Ythdf1	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:13399	color blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99894	Hnrnpk	implicated_via_orthology	DOID:10300	Raynaud disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351615	Add3	implicated_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	implicated_via_orthology	DOID:0060348	hypoparathyroidism-retardation-dysmorphism syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328361	Bard1	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98812	Tpmt	implicated_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	implicated_via_orthology	DOID:0050167	autoimmune polyendocrine syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336884	Slc22a18	implicated_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	implicated_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103220	Meox1	implicated_via_orthology	DOID:10426	Klippel-Feil syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925482	Trappc6b	implicated_via_orthology	DOID:0050888	syndromic intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95791	Got1	implicated_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932872	Ctns	implicated_via_orthology	DOID:1064	cystinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338833	Dio2	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443805	Bnc2	implicated_via_orthology	DOID:5200	urinary tract obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97857	Rarb	implicated_via_orthology	DOID:7596	asbestos-related lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109489	Snrpc	implicated_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3026965	Mcu	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914724	Snap29	implicated_via_orthology	DOID:0060337	CEDNIK syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109173	Dsc1	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107537	Cln3	implicated_via_orthology	DOID:0110731	neuronal ceroid lipofuscinosis 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	implicated_via_orthology	DOID:0080883	vitamin D-dependent rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355315	Tmod3	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927197	Shoc2	implicated_via_orthology	DOID:0080691	Noonan syndrome-like disorder with loose anagen hair						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354756	Crim1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913808	Lars1	implicated_via_orthology	DOID:0080717	infantile liver failure syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333780	Rps19	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98658	Cripto	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	implicated_via_orthology	DOID:11633	thyroid hormone resistance syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685726	Pitpnm3	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	implicated_via_orthology	DOID:0080883	vitamin D-dependent rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915581	Stn1	implicated_via_orthology	DOID:1272	telangiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385205	Ipo13	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144151	Pnpo	implicated_via_orthology	DOID:0111329	pyridoxamine 5'-phosphate oxidase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	implicated_via_orthology	DOID:13366	Stiff-Person syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917685	Inf2	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135625	Glrx	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	implicated_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151054	Cnnm2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	implicated_via_orthology	DOID:1907	malignant fibrous histiocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8717	decubitus ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3610364	Rbm24	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	implicated_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	implicated_via_orthology	DOID:2843	long QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96070	Hbegf	implicated_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913389	Mymk	implicated_via_orthology	DOID:0080194	Carey-Fineman-Ziter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109355	Stx1a	implicated_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108449	Adcyap1r1	implicated_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	implicated_via_orthology	DOID:11830	myopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	implicated_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100882	Phox2b	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101061	Slc18a3	biomarker_via_orthology	DOID:365	bladder disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330238	Dpm2	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	implicated_via_orthology	DOID:0060473	Kabuki syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921357	Cep55	implicated_via_orthology	DOID:0080327	multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	implicated_via_orthology	DOID:3193	peripheral nerve sheath neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919070	Dync2i2	implicated_via_orthology	DOID:0080074	neural tube defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	implicated_via_orthology	DOID:0060473	Kabuki syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140367	Fbxl4	implicated_via_orthology	DOID:0080131	mitochondrial DNA depletion syndrome 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100521	Slc7a3	implicated_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101780	Serpine2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	implicated_via_orthology	DOID:2101	vulva squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	implicated_via_orthology	DOID:0060484	EAST syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933209	Tm6sf1	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861380	Sphk2	implicated_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	implicated_via_orthology	DOID:14686	Axenfeld-Rieger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858751	Rragc	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915520	Dnaaf1	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920982	Muc16	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	implicated_via_orthology	DOID:0050558	Ullrich congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151054	Cnnm2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195276	Bloc1s1	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105956	Pde6c	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913311	Dynlt2b	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606001	Apol9a	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915509	Ift80	implicated_via_orthology	DOID:0110086	asphyxiating thoracic dystrophy 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	implicated_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98368	Sox6	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329037	Strap	implicated_via_orthology	DOID:3168	squamous cell neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096359	Cyp26a1	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337120	Slc7a7	implicated_via_orthology	DOID:0060439	lysinuric protein intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	implicated_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914291	Oxct1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385957	Mfrp	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:0060474	familial erythrocytosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97577	Phka2	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104968	Ppox	implicated_via_orthology	DOID:4346	variegate porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194899	Inpp5k	implicated_via_orthology	DOID:0080197	congenital muscular dystrophy with cataracts and intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107440	Cep131	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606571	Stac3	implicated_via_orthology	DOID:0060346	Native American myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155302	Sec63	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914864	Atp6v1h	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	implicated_via_orthology	DOID:0050793	short QT syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95862	Gstm4	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329037	Strap	implicated_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	implicated_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	implicated_via_orthology	DOID:0050773	paraganglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	implicated_via_orthology	DOID:0060058	lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	implicated_via_orthology	DOID:66	muscle tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97896	Reg2	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679294	Zc4h2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:1035	aggressive NK-cell leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99928	Jak3	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151156	Stim2	implicated_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	implicated_via_orthology	DOID:0060186	chemical colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921703	Cfap53	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646230	Clrn2	implicated_via_orthology	DOID:0050565	autosomal recessive nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141101	Depdc5	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684139	Kcnh6	implicated_via_orthology	DOID:0110645	long QT syndrome 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442832	Osbpl2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576497	Greb1l	implicated_via_orthology	DOID:14766	renal agenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444169	Lmod3	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	implicated_via_orthology	DOID:0070309	absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449057	Gars1	implicated_via_orthology	DOID:0050539	Charcot-Marie-Tooth disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923097	Crppa	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915509	Ift80	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330239	Dpm1	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352494	Hspb7	implicated_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	implicated_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921662	Gle1	implicated_via_orthology	DOID:0060559	lethal congenital contracture syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98277	Epha4	biomarker_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	implicated_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	implicated_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915520	Dnaaf1	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	implicated_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	implicated_via_orthology	DOID:0060569	hypertrichotic osteochondrodysplasia Cantu type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95689	Gdf6	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	implicated_via_orthology	DOID:0050572	cone-rod dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927165	Mettl3	implicated_via_orthology	DOID:5223	infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384795	Pycr1	implicated_via_orthology	DOID:0070137	autosomal recessive cutis laxa type IIB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914365	Rpl14	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107876	Uqcrc1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	implicated_via_orthology	DOID:0080883	vitamin D-dependent rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3607720	Dnaaf6	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329037	Strap	implicated_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891700	Ncstn	implicated_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446294	Megf8	implicated_via_orthology	DOID:0060234	Carpenter syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918084	Spag9	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	implicated_via_orthology	DOID:0111030	hemochromatosis type 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922022	Atp13a2	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102765	Ptprn	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104574	Ptprj	implicated_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:8689	anorexia nervosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108014	Polr1b	implicated_via_orthology	DOID:2908	Treacher Collins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098283	Per1	implicated_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106598	Myo5b	implicated_via_orthology	DOID:0060775	microvillus inclusion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918943	Colec11	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384831	Cc2d1a	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	implicated_via_orthology	DOID:0080883	vitamin D-dependent rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341155	Gldc	implicated_via_orthology	DOID:9268	glycine encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921357	Cep55	implicated_via_orthology	DOID:4626	hydranencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653690	Agap1	implicated_via_orthology	DOID:1969	cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	implicated_via_orthology	DOID:0080092	myofibrillar myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858222	Septin9	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335082	Invs	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101834	Tubg1	implicated_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444748	Chd7	implicated_via_orthology	DOID:0050834	CHARGE syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	implicated_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98506	Tcf4	implicated_via_orthology	DOID:0060488	Pitt-Hopkins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682064	Ift172	implicated_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	implicated_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:12986	leukostasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919148	Apol9b	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714357	Srp54b	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107164	Ppp3ca	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139422	Duox1	implicated_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95779	Gnat2	implicated_via_orthology	DOID:13911	achromatopsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:0110042	Alzheimer's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97742	Pomc	implicated_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202302	Pms1	implicated_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105491	Cdipt	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920347	Dact2	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	implicated_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98341	Snrnp70	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	implicated_via_orthology	DOID:0050563	nonsyndromic deafness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384987	B4galt7	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	implicated_via_orthology	DOID:9835	refractive error						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	implicated_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97914	Rho	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338833	Dio2	implicated_via_orthology	DOID:4194	glucose metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	implicated_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104884	Psmb1	implicated_via_orthology	DOID:1059	intellectual disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891207	Plpbp	implicated_via_orthology	DOID:0080769	early-onset vitamin B6-dependent epilepsy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:0080196	mandibulofacial dysostosis, Guion-Almeida type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921605	Smchd1	implicated_via_orthology	DOID:9574	choanal atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443893	Ccdc40	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349217	Abcd4	implicated_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298230	Cnot7	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	biomarker_via_orthology	DOID:3073	brain glioblastoma multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95621	Gabrb3	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386403	Csmd3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039618	Zbtb24	implicated_via_orthology	DOID:0090007	immunodeficiency-centromeric instability-facial anomalies syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714359	Srp54c	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916238	Prpf31	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179729	Vwa1	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444921	Apol8	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588194	Prdm14	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914152	Mtap	implicated_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922706	Prps1l1	implicated_via_orthology	DOID:0110210	Charcot-Marie-Tooth disease X-linked recessive 5						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102854	Rpl5	implicated_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	implicated_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100521	Slc7a3	implicated_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349482	Nherf1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341292	Ush2a	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098754	Psmc3	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929996	Trpm7	implicated_via_orthology	DOID:0050824	sinoatrial node disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	implicated_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346319	Hax1	implicated_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	implicated_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920543	Ccdc103	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107704	Abcg1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	implicated_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919189	Apol6	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443731	Mat2a	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98366	Sox4	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98358	Sox10	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920939	Bloc1s2	implicated_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104685	Twist2	implicated_via_orthology	DOID:0060550	ablepharon macrostomia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385205	Ipo13	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858896	Spast	implicated_via_orthology	DOID:2476	hereditary spastic paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095405	Ptch2	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685857	Zfp408	implicated_via_orthology	DOID:0050535	exudative vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384298	Sbno1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448607	Nyx	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	implicated_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:0060573	von Willebrand's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97895	Reg1	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261856	Ankle2	implicated_via_orthology	DOID:0070289	primary autosomal recessive microcephaly 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	implicated_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916231	Snrpa1	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:0111902	thrombophilia due to activated protein C resistance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921958	Dnaaf6rt	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101780	Serpine2	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136772	Vps16	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107486	Pex2	implicated_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178103	Arhgdia	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104805	Snrpb2	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333819	Tekt1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922783	Nme5	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684950	Becn2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	implicated_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442062	Sh3pxd2b	implicated_via_orthology	DOID:0111789	Frank-Ter Haar syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	implicated_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148811	Npnt	implicated_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	implicated_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914831	Tbc1d23	implicated_via_orthology	DOID:0060264	pontocerebellar hypoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448607	Nyx	implicated_via_orthology	DOID:0110870	congenital stationary night blindness 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109355	Stx1a	implicated_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923928	Tmem67	implicated_via_orthology	DOID:1088	meningocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342276	Mfap4	implicated_via_orthology	DOID:0060768	Smith-Magenis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329037	Strap	implicated_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:612	primary immunodeficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	implicated_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920455	C9orf72	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96785	Lhx2	implicated_via_orthology	DOID:9650	pathologic nystagmus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	implicated_via_orthology	DOID:1172	hyperlipoproteinemia type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3781032	Kcnj13	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97524	Pde6a	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915760	Ints1	implicated_via_orthology	DOID:0070346	neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927468	Samhd1	implicated_via_orthology	DOID:0050629	Aicardi-Goutieres syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861727	Dkc1	implicated_via_orthology	DOID:2729	dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	implicated_via_orthology	DOID:14118	familial lipoprotein lipase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923011	Apol7a	implicated_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913961	Sbds	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930153	Popdc3	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	implicated_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096397	Polr1a	implicated_via_orthology	DOID:0060353	acrofacial dysostosis Cincinnati type						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	implicated_via_orthology	DOID:8549	chronic ulcer of skin						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	implicated_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	implicated_via_orthology	DOID:1926	Gaucher's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298209	Hcn4	implicated_via_orthology	DOID:13884	sick sinus syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343050	Tnfrsf17	implicated_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919276	Trmu	implicated_via_orthology	DOID:2952	inner ear disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97603	Pkd1	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443588	Pik3r5	implicated_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097712	Npc1	implicated_via_orthology	DOID:0070113	Niemann-Pick disease type C1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142454	Usb1	implicated_via_orthology	DOID:0060550	ablepharon macrostomia syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339795	Smc3	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924859	Odad3	implicated_via_orthology	DOID:9562	primary ciliary dyskinesia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96785	Lhx2	implicated_via_orthology	DOID:9649	congenital nystagmus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925927	Rnf20	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	implicated_via_orthology	DOID:0090116	spondylocarpotarsal synostosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106092	Etfa	implicated_via_orthology	DOID:0060358	multiple acyl-CoA dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921456	Sipa1l3	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	implicated_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97292	Neb	implicated_via_orthology	DOID:3191	nemaline myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180307	Hps5	implicated_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201787	Socs2	implicated_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144151	Pnpo	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142808	Cog4	implicated_via_orthology	DOID:0111673	Saul-Wilson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277989	Shmt2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	implicated_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643647	Ahcyl	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201673	Shox2	implicated_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913431	Nop10	implicated_via_orthology	DOID:2729	dyskeratosis congenita						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95557	Flnc	implicated_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	implicated_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932040	Sil1	implicated_via_orthology	DOID:0080195	Marinesco-Sjogren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107477	Stil	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196457	Atp5if1	implicated_via_orthology	DOID:1432	blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347007	Plod2	implicated_via_orthology	DOID:0060231	Bruck syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855690	Snrpa	implicated_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100508	Kcnj8	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97075	Mpi	implicated_via_orthology	DOID:0050570	congenital disorder of glycosylation type I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9637	stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:14503	neuronal ceroid lipofuscinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99676	Adcy2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:162	cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333825	Dgat1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914713	Poc5	implicated_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714357	Srp54b	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	implicated_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102643	Myh11	implicated_via_orthology	DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	implicated_via_orthology	DOID:5230	hepatoerythropoietic porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	implicated_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443157	Mib1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	implicated_via_orthology	DOID:0040085	bacterial sepsis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343050	Tnfrsf17	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138584	Gigyf2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384919	Rxylt1	implicated_via_orthology	DOID:0050560	Walker-Warburg syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87885	Chrna1	implicated_via_orthology	DOID:3635	congenital myasthenic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351500	Nup62	implicated_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108403	Polr1d	implicated_via_orthology	DOID:2908	Treacher Collins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277953	Rp2	implicated_via_orthology	DOID:0110415	retinitis pigmentosa 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88474	Cox5a	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337065	Ap4s1	implicated_via_orthology	DOID:0110804	hereditary spastic paraplegia 52						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103221	Dsc2	implicated_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351605	Rpl3	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347469	Foxl1	implicated_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:2217	Bernard-Soulier syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:0060500	drug allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97742	Pomc	implicated_via_orthology	DOID:11613	hyperandrogenism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105059	Was	implicated_via_orthology	DOID:9169	Wiskott-Aldrich syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	implicated_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917379	Slc44a4	implicated_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108186	Aldh7a1	implicated_via_orthology	DOID:0080768	pyridoxine-dependent epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	implicated_via_orthology	DOID:0110636	congenital merosin-deficient muscular dystrophy 1A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	implicated_via_orthology	DOID:11151	cholecystolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860488	Proz	implicated_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96074	Hexb	implicated_via_orthology	DOID:3211	lysosomal storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447586	Fkrp	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	implicated_via_orthology	DOID:0050459	hyperphosphatemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933210	Tm6sf2	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143558	Chchd10	implicated_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919238	Esco2	implicated_via_orthology	DOID:5325	Roberts syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442184	Flcn	implicated_via_orthology	DOID:0050676	Birt-Hogg-Dube syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923442	Abhd12	implicated_via_orthology	DOID:0080181	PHARC syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	implicated_via_orthology	DOID:0050632	oculocutaneous albinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	implicated_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891836	Mkks	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	implicated_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	implicated_via_orthology	DOID:9651	systolic heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860299	Dnah10	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98249	Scn3a	implicated_via_orthology	DOID:0080422	Dravet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278344	Nipsnap1	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915760	Ints1	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	implicated_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338765	Fhl4	implicated_via_orthology	DOID:423	myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104621	Alx1	implicated_via_orthology	DOID:0081047	frontonasal dysplasia 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098754	Psmc3	implicated_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	implicated_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	implicated_via_orthology	DOID:14320	generalized anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919192	Myof	implicated_via_orthology	DOID:11724	limb-girdle muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102541	Tbx5	implicated_via_orthology	DOID:0060468	Holt-Oram syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	implicated_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915562	Gstm7	implicated_via_orthology	DOID:0050451	Brugada syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	implicated_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3482	plague						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385328	Dnai4	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892032	Frzb	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	implicated_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915520	Dnaaf1	implicated_via_orthology	DOID:5557	testicular germ cell cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107742	Stra6	implicated_via_orthology	DOID:0111807	syndromic microphthalmia 9						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	implicated_via_orthology	DOID:0080883	vitamin D-dependent rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313286	Eif2b3	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	implicated_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:12531	von Willebrand's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442620	Nup133	implicated_via_orthology	DOID:0060364	Galloway-Mowat syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	implicated_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	implicated_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107750	Dync1i2	implicated_via_orthology	DOID:0070296	primary autosomal recessive microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201787	Socs2	implicated_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107730	Hoxb13	implicated_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	implicated_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194497	Tgif1	implicated_via_orthology	DOID:4621	holoprosencephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105922	Rpl13	implicated_via_orthology	DOID:0080027	spondyloepimetaphyseal dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351655	Shroom3	implicated_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298378	Dhcr7	implicated_via_orthology	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98345	Snrpd2	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679420	Pak6	implicated_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	implicated_via_orthology	DOID:12347	osteogenesis imperfecta						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344385	Med24	implicated_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	implicated_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913612	Exosc3	implicated_via_orthology	DOID:0060266	pontocerebellar hypoplasia type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684313	Togaram1	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	implicated_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	implicated_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104652	Capzb	implicated_via_orthology	DOID:674	cleft palate						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2673002	Arhgef17	implicated_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387863	Zmynd10	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	implicated_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385311	Dlat	implicated_via_orthology	DOID:3649	pyruvate decarboxylase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384303	Rp1l1	implicated_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	implicated_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919782	Sap130	implicated_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	implicated_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88176	Bmp1	implicated_via_orthology	DOID:0110342	osteogenesis imperfecta type 13						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	implicated_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	implicated_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349385	Dysf	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	implicated_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442252	Lrp4	implicated_via_orthology	DOID:0080006	bone development disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155302	Sec63	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	implicated_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442479	Elfn1	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914311	Dzip1	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930618	Krit1	implicated_via_orthology	DOID:0080491	cerebral cavernous malformation 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97857	Rarb	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894810	Uty	implicated_via_orthology	DOID:0060473	Kabuki syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916703	Prss56	implicated_via_orthology	DOID:9835	refractive error						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891037	Mtrr	implicated_via_orthology	DOID:0050545	visceral heterotaxy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	implicated_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927753	Inpp5e	implicated_via_orthology	DOID:0050777	Joubert syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104757	Ephb4	implicated_via_orthology	DOID:75	lymphatic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	implicated_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444585	Trappc11	implicated_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95593	Fuca1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3584243	Mks1	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95609	Gaa	implicated_via_orthology	DOID:2752	glycogen storage disease II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	implicated_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859993	Smad9	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443409	Gpr179	implicated_via_orthology	DOID:0110869	congenital stationary night blindness 1E						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448567	Chd2	implicated_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150656	Man2a2	implicated_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	implicated_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96417	Ids	implicated_via_orthology	DOID:12799	mucopolysaccharidosis II						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	implicated_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918711	Ptk7	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099452	Mtm1	implicated_via_orthology	DOID:14717	centronuclear myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2674311	Sspo	implicated_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202717	Psen1	implicated_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	implicated_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	implicated_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102809	Sars1	implicated_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107363	Stxbp1	implicated_via_orthology	DOID:0050709	early infantile epileptic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	implicated_via_orthology	DOID:1172	hyperlipoproteinemia type IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202296	Sorl1	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202302	Pms1	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442092	Wnk1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98248	Scn2a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442543	Vash1	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	implicated_via_orthology	DOID:0111459	classic galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	implicated_via_orthology	DOID:0050539	Charcot-Marie-Tooth disease type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917609	Gtpbp3	implicated_via_orthology	DOID:700	mitochondrial metabolism disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918019	Nolc1	implicated_via_orthology	DOID:2908	Treacher Collins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:6196	reactive arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97385	Ntrk3	implicated_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98341	Snrnp70	implicated_via_orthology	DOID:150	disease of mental health						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927139	Sv2a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923714	Knl1	implicated_via_orthology	DOID:0070297	primary microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104650	Cnr2	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384917	Cep290	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	implicated_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644133	Zbtb42	implicated_via_orthology	DOID:0050646	distal arthrogryposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444631	Bltp1	implicated_via_orthology	DOID:0111555	Alkuraya-Kucinskas syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914797	Slc39a8	implicated_via_orthology	DOID:0060250	idiopathic scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96080	Mst1	implicated_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354756	Crim1	implicated_via_orthology	DOID:10629	microphthalmia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891112	Gmds	implicated_via_orthology	DOID:0070255	congenital disorder of glycosylation type IIc						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384924	Ccm2	implicated_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	implicated_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	implicated_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915520	Dnaaf1	implicated_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918673	Epg5	implicated_via_orthology	DOID:0060356	Vici syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96743	Lamb1	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105386	Dbt	implicated_via_orthology	DOID:9269	maple syrup urine disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195266	Tnfaip6	implicated_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	implicated_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700010	Sh3gl1	implicated_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934606	Alms1	implicated_via_orthology	DOID:0050473	Alstrom syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98246	Scn1a	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	implicated_via_orthology	DOID:0050588	muscular dystrophy-dystroglycanopathy type B1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	implicated_via_orthology	DOID:2908	Treacher Collins syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349215	Abcd1	implicated_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	implicated_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	biomarker_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107427	Elavl4	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104779	Prkdc	implicated_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	implicated_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87978	Ak2	implicated_via_orthology	DOID:0060020	reticular dysgenesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346022	Mab21l2	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	implicated_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106676	Zic3	implicated_via_orthology	DOID:0060856	right atrial isomerism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	implicated_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098824	Odf2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277956	Pycr2	implicated_via_orthology	DOID:0070137	autosomal recessive cutis laxa type IIB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	implicated_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916193	Pink1	implicated_via_orthology	DOID:0060894	early-onset Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588271	Degs1l	implicated_via_orthology	DOID:0060786	hypomyelinating leukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	implicated_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	implicated_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446176	Eif2b5	implicated_via_orthology	DOID:0060868	leukoencephalopathy with vanishing white matter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	implicated_via_orthology	DOID:5940	malignant peripheral nerve sheath tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928386	Rassf1	implicated_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	implicated_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	implicated_via_orthology	DOID:7725	epilepsy with generalized tonic-clonic seizures						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95638	Galt	implicated_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676921	Focad	implicated_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	implicated_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	implicated_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	implicated_via_orthology	DOID:0080887	vitamin D-dependent rickets type 1B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277215	Bbs1	implicated_via_orthology	DOID:1935	Bardet-Biedl syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	implicated_via_orthology	DOID:0050663	Bethlem myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923032	Lca5	implicated_via_orthology	DOID:14791	Leber congenital amaurosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	implicated_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	implicated_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685870	Pdp1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859639	Cacna1f	implicated_via_orthology	DOID:0050534	congenital stationary night blindness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107877	Prkcsh	implicated_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:2236	congenital afibrinogenemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	implicated_via_orthology	DOID:1838	Menkes disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445160	Kcnh8	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	implicated_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	implicated_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346013	Bves	implicated_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	implicated_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	implicated_via_orthology	DOID:657	adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145597	Mbnl2	implicated_via_orthology	DOID:450	myotonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107418	Ptprn2	implicated_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	implicated_via_orthology	DOID:14069	cerebral malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95852	Gss	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	implicated_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	implicated_via_orthology	DOID:1107	esophageal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	implicated_via_orthology	DOID:0080325	tuberous sclerosis 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	implicated_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	implicated_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	implicated_via_orthology	DOID:0080715	developmental and epileptic encephalopathy 82						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88248	Calb1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927197	Shoc2	implicated_via_orthology	DOID:0080690	RASopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88474	Cox5a	implicated_via_orthology	DOID:0060340	ciliopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	implicated_via_orthology	DOID:77	gastrointestinal system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	implicated_via_orthology	DOID:5688	Werner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108571	Fzd5	implicated_via_orthology	DOID:12270	coloboma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	implicated_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	implicated_via_orthology	DOID:484	vascular hemostatic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	implicated_via_orthology	DOID:3030	mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:0060186	chemical colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915050	Dgat2	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	implicated_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98310	Ski	implicated_via_orthology	DOID:2340	craniosynostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	implicated_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	implicated_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	implicated_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919847	Auts2	implicated_via_orthology	DOID:10907	microcephaly						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	implicated_via_orthology	DOID:583	hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	implicated_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	implicated_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	implicated_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	implicated_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	implicated_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099447	Golgb1	implicated_via_orthology	DOID:0111063	hyperphosphatemic familial tumoral calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104816	Hnrnpl	implicated_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	implicated_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346087	Srp54a	implicated_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	implicated_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	implicated_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890613	Pes1	implicated_via_orthology	DOID:0060479	Shwachman-Diamond syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101931	Slc1a2	implicated_via_orthology	DOID:0080442	developmental and epileptic encephalopathy 41						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	implicated_via_orthology	DOID:0110030	alpha thalassemia-X-linked intellectual disability syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	implicated_via_orthology	DOID:11198	DiGeorge syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88459	Col6a1	implicated_via_orthology	DOID:0050557	congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104688	Col4a3	implicated_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919399	Strada	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107636	Scn9a	implicated_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315204	Slc40a1	implicated_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	implicated_via_orthology	DOID:0050854	Muckle-Wells syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	implicated_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	implicated_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	implicated_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	implicated_via_orthology	DOID:10881	hand, foot and mouth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	implicated_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95674	Gcg	implicated_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913976	Nipbl	implicated_via_orthology	DOID:11725	Cornelia de Lange syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88034	Prdx3	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	biomarker_via_orthology	DOID:4674	androgen insensitivity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316660	Cacng2	biomarker_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261433	Endog	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920211	Slc17a7	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:885	fascioliasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	biomarker_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443582	Abat	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354161	Sirt6	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88067	Arc	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96234	Hsd3b2	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354184	Nox4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104872	Ppp1cc	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334203	Kcnmb1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:1742	drug psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336883	Smad6	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	biomarker_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97171	Mt1	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8717	decubitus ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298210	Hcn2	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611747	Cyp4a12b	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96070	Hbegf	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135637	Park7	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316649	Sphk1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890216	Slc6a14	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96250	Hsp90aa1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106040	Cyp51	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:1002	endometritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159682	Havcr2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:10113	trypanosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861731	Ccl28	biomarker_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98956	Wnt3a	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:365	bladder disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917233	Sis	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95757	Slc2a3	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:520	aortic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:77	gastrointestinal system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109175	Dab2	biomarker_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109484	Ywhaz	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103013	Cacna1c	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337040	Nr1i2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97379	Slc10a1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891427	Fgf23	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107760	Chka	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:12030	panuveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914342	Gatm	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:12577	urethral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98180	Rrm1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891917	Ywhab	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2680765	Hcrtr2	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97856	Rara	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:76	stomach disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87997	Alox15	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100509	Kcnk3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106368	Rbfox3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096385	Bcan	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:4306	radiculopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109452	Smad1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98474	Tac1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88548	Csnk2b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	biomarker_via_orthology	DOID:3125	multiple endocrine neoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351891	Slco1a1	biomarker_via_orthology	DOID:12308	Dubin-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927248	Kcnj1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97602	Prkcz	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321398	F11r	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353427	Eif2ak4	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88111	Atp2b4	biomarker_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88285	Cbs	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:0050152	aspiration pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88215	Btg1	biomarker_via_orthology	DOID:11801	protein-energy malnutrition						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3032636	Ugt1a7c	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87997	Alox15	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96836	Lta4h	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339949	Adamts4	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96916	Maob	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349473	Ppp2r5e	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98214	Rxra	biomarker_via_orthology	DOID:12935	alcoholic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:10966	lipoid nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109598	Hsd3b6	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351901	Trpm2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102965	Scn7a	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915816	Caly	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98239	Scd1	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96570	Inhba	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927072	Ppp1r15a	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109514	Cstb	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102499	mt-Nd3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99150	Yy1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96570	Inhba	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309998	Marco	biomarker_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135625	Glrx	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106921	Scn2b	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87934	Adra2a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892968	Tacr3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100818	Crcp	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924148	B3gat1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444155	Nmnat2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101780	Serpine2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95758	Slc2a4	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96235	Hsd3b3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98239	Scd1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338850	Mthfd2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313314	Cldn4	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339984	Pak2	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:1742	drug psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276523	Ncoa1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108442	Cpeb1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:7997	thyrotoxicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341296	Tlr6	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:0050152	aspiration pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	biomarker_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700009	Sh3gl2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97475	Pam	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102759	Prss2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918910	Rarres2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101061	Slc18a3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	biomarker_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927126	Slc5a7	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097680	C3ar1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261437	Atp5f1c	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442784	Slco4c1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109207	Eif4g2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:11801	protein-energy malnutrition						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98282	Spi1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347094	Parg	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88543	Csnk2a1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95818	Grik5	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99959	Tgfbi	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334263	Neurl1a	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336205	Fkbp1b	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95697	Gfap	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444854	Amigo3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102849	Klkb1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106212	Chrnb3	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919959	C1qtnf6	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96603	Itga4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333825	Dgat1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109484	Ywhaz	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446117	Suox	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	biomarker_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88497	Crhbp	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858179	Nucb2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106091	Cyp7a1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9446	cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:14679	VACTERL association						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101759	Rnf2	biomarker_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448715	Cxcr1	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99558	Pde4a	biomarker_via_orthology	DOID:11077	brucellosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926952	Cyb5a	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	biomarker_via_orthology	DOID:2562	suppurative periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:4762	vasculogenic impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98923	Vav1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	biomarker_via_orthology	DOID:14692	Smith-Lemli-Opitz syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105094	Adcyap1	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	biomarker_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104652	Capzb	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135958	Scap	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:2518	orchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96787	Lif	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:11044	gastroschisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321151	Ptpru	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107163	Ppp3cb	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103224	Fdx1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99667	Syt1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97567	Pgr	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107587	Irf9	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139369	Rtel1	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894698	Sgca	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261758	Suz12	biomarker_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932052	Chia1	biomarker_via_orthology	DOID:12053	cryptococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97614	Plcd1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108047	Bag1	biomarker_via_orthology	DOID:12528	lesion of sciatic nerve						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917351	Cyp4f16	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105368	Atp2b2	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	biomarker_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97895	Reg1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99571	Glp1r	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102797	Acsl1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915842	Syf2	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87929	Adh5	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:13767	clonorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	biomarker_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349482	Nherf1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101784	Nes	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041197	Serpina7	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041197	Serpina7	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103202	Adsl	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96247	Hsp90ab1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99261	Ptgds	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:14550	root resorption						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891247	Otof	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97895	Reg1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351896	Slco1a4	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88224	C1qb	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	biomarker_via_orthology	DOID:0050336	hypophosphatemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351339	Grm2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:2615	papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316652	Prmt2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101863	Aldoc	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888517	Rhcg	biomarker_via_orthology	DOID:4500	hypokalemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9402	epididymitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180699	Mtmr4	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917745	Atp6ap2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	biomarker_via_orthology	DOID:4762	vasculogenic impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107414	Tnfsf10	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927669	Cyp4f14	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104560	Nsf	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102501	mt-Cytb	biomarker_via_orthology	DOID:7997	thyrotoxicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88612	Cyp4a12a	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350929	Asns	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99500	Ephx2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339713	Myh4	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195256	Pla2g4a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98326	Sst	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:8456	choline deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:9427	hypertensive encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88047	Aplp2	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344313	Zeb1	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98958	Wnt5a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96269	Ranbp1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:1969	cerebral palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333784	Hdac5	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334203	Kcnmb1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	biomarker_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97795	Ptger3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96918	Mas1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933966	Mcam	biomarker_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88321	Ms4a1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87905	Actc1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96062	Hdc	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098239	Kif7	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108451	Acaca	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919643	Faim2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921932	Wdr35	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097680	C3ar1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270839	Cacybp	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99480	Cebpa	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:1188	mononeuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351645	Prmt5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	biomarker_via_orthology	DOID:3877	functional colonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102889	Vcan	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102759	Prss2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99673	Adcy5	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107498	Ltc4s	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681835	Nlgn2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101939	Hmgcs2	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:2518	orchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103197	Mcm5	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109249	Adamts1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99261	Ptgds	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87870	Acat1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	biomarker_via_orthology	DOID:971	tendinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97836	Qdpr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96759	Ldha	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:5463	cochlear disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153093	Cspg4	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98904	Uck1	biomarker_via_orthology	DOID:573	nerve compression syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109151	Ltbp1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107976	Slc8a3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107801	Atp5f1b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	biomarker_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	biomarker_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861457	Dynll1	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98796	Tph1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:12010	anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346325	Gadd45g	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:607	paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684983	Ndufb6	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151886	Ngb	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338016	Bex3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347007	Plod2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:9286	priapism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96570	Inhba	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	biomarker_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9402	epididymitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860764	Pde3a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105372	Sstr4	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196389	Polg	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915599	Ndufs3	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201402	Ccr8	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178051	Cacna1i	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99558	Pde4a	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:10690	mastitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098271	Rgs2	biomarker_via_orthology	DOID:365	bladder disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333812	Mbd3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:12577	urethral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919020	Ap2b1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448526	Gmps	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109553	Ctsc	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109249	Adamts1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101759	Syt4	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	biomarker_via_orthology	DOID:13268	porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96247	Hsp90ab1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:12897	submandibular gland disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97594	Prkacb	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:2388	renal artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155808	Pkhd1	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333777	Aqp3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685628	Card9	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149481	Cygb	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346542	Bace1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98159	Rps6	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:10113	trypanosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934765	Gpnmb	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444210	Nr1d1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:0050665	fetal alcohol syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87979	Ak4	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102967	Mtnr1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933966	Mcam	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95639	Gap43	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109598	Hsd3b6	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108451	Acaca	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102805	Entpd1	biomarker_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96648	Jund	biomarker_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107437	Capn3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888517	Rhcg	biomarker_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:14484	sporotrichosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105057	Cdh5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:10605	short bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352463	Nr1h2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176375	Ucn2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:13812	adhesions of uterus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3780112	Cyp4f37	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338044	Cyp8b1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96217	Hprt1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338016	Bex3	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96396	Id1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97509	Pcp4	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96440	Igfbp5	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98117	Rps15	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445289	Plac8	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298366	Atf1	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97515	Pcsk5	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261433	Endog	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109553	Ctsc	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:4692	endophthalmitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:9965	toxoplasmosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860139	Gabbr1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109297	Slpi	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87978	Ak2	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98239	Scd1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97276	Myog	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306782	Dio3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:4556	lung large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97795	Ptger3	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104615	Cnr1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924058	Rpl18a	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106091	Cyp7a1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94941	Dvl1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87941	Grk3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353576	Pik3cg	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891496	Jph2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891291	Kcnk6	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928745	Slc4a8	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108111	Slc22a1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	biomarker_via_orthology	DOID:607	paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:11801	protein-energy malnutrition						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108554	Dab1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147790	Fermt3	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:5022	aflatoxins-related hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183439	Mcfd2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98747	Thy1	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105115	Ctf1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97143	Marcksl1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109366	Kcnk2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352456	Nr4a2	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2797	idiopathic interstitial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684864	Pfas	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	biomarker_via_orthology	DOID:0060475	myoclonic-atonic epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096337	Ephb1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97591	Pkm	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109433	Oaz1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109297	Slpi	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:0060189	ileitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650907	Rps6-ps4	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96235	Hsd3b3	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97169	Msx2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96829	Lrpap1	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109279	Nnt	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918910	Rarres2	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261434	Olr1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194503	Atp2a3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96234	Hsd3b2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88451	Col18a1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385262	Kmt5c	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106368	Rbfox3	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2152453	Gsk3a	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932286	Egln1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88594	Cyp27a1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:11382	corneal neovascularization						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933825	Jam3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349717	Ncor1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926943	Atp12a	biomarker_via_orthology	DOID:4500	hypokalemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298398	Mcm7	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97523	Pde1b	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915202	Tomm20	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925571	Ankrd23	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:12574	posterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101784	Nes	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88024	Ank1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	biomarker_via_orthology	DOID:3125	multiple endocrine neoplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097716	Arx	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87995	Aldob	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101833	Elk1	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:12215	oligohydramnios						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:11613	hyperandrogenism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894687	Xrn2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87989	Alas1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917979	Nos1ap	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443111	Abcc4	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145895	Slc38a1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928761	Slc19a2	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859169	Azin1	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891915	Foxo4	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270844	Cideb	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101784	Nes	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917979	Nos1ap	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101910	F2rl1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653833	Nlrp3	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102469	Nfatc1	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108078	Sfrp2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99252	Egr4	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:6088	acute stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:12308	Dubin-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332226	Soat2	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927184	Nrgn	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349763	Dpysl2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107427	Elavl4	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:12932	endomyocardial fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932052	Chia1	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344418	Cib1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97772	Prox1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108564	Meis2	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87997	Alox15	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179435	Nlgn1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109351	Slc4a2	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333791	Artn	biomarker_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109545	Gpr182	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96777	Lgals1	biomarker_via_orthology	DOID:707	B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101784	Nes	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98970	Xbp1	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:971	tendinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109366	Kcnk2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344395	Chd3	biomarker_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328355	Wfs1	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932288	Egln3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096863	Entpd2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102503	mt-Co2	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95809	Gria2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195256	Pla2g4a	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103190	Muc13	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:10113	trypanosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97569	Abcb4	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915289	Nmb	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102760	Star	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338947	S100a9	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:2518	orchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354168	Ttpa	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932051	Kat5	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914166	Ndufb7	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:12577	urethral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:14183	alcoholic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670972	Frem1	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913335	Eif3f	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96777	Lgals1	biomarker_via_orthology	DOID:10966	lipoid nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103250	Calm2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195256	Pla2g4a	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098434	Rgs5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107823	Ctsk	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914930	Sdhb	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:9455	lipid storage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928268	Ireb2	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920590	Nptxr	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347098	Slc27a1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97631	Pmp22	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889272	Cadm1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97350	Nkx2-5	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96702	Krt5	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913208	Carm1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108409	Rgs4	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717148	Cyp4a32	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97795	Ptger3	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928268	Ireb2	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88038	Fabp4	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859546	Syt10	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328351	Nts	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919161	Bdh1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:374	nutrition disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96269	Ranbp1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:57	aortic valve insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107823	Ctsk	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103249	Calm3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:403	mouth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95613	Gabra1	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099818	Pkd2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346344	Nr0b2	biomarker_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108093	Bid	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99517	Hspa1b	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	biomarker_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:11049	meconium aspiration syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104650	Cnr2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96912	Mag	biomarker_via_orthology	DOID:573	nerve compression syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88038	Fabp4	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:11044	gastroschisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:11996	spermatic cord torsion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347098	Slc27a1	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328364	Fmod	biomarker_via_orthology	DOID:971	tendinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	biomarker_via_orthology	DOID:11836	clubfoot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663979	Galp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88236	C8b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101802	F2r	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:2235	prothrombin deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860764	Pde3a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914780	Uqcrb	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306778	Map1b	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:4306	radiculopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95728	Gli2	biomarker_via_orthology	DOID:0080171	esophageal atresia/tracheoesophageal fistula						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028580	Cyp4a31	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098271	Rgs2	biomarker_via_orthology	DOID:724	female stress incontinence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934754	Kars1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102805	Entpd1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96916	Maob	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350328	Ofd1	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892877	Pld2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:2518	orchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97601	Prkcq	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344410	Ubd	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387203	Ppat	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106673	Adra1d	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891340	Lpin1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108054	Rit2	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98419	Sri	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87977	Ak1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931882	Dnaja2	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:10533	viral pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95415	Erg	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109151	Ltbp1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099809	Fgf10	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:3071	gliosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354734	Rgs3	biomarker_via_orthology	DOID:365	bladder disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108111	Slc22a1	biomarker_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109297	Slpi	biomarker_via_orthology	DOID:4692	endophthalmitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443041	Plekhs1	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:9974	drug dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:14550	root resorption						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	biomarker_via_orthology	DOID:13711	dental fluorosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446632	Ago2	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341872	Tjp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98474	Tac1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925906	Brd8	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	biomarker_via_orthology	DOID:12387	nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717145	Cyp4a30b	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:2297	leptospirosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:9281	phenylketonuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:14026	folic acid deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932286	Egln1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8717	decubitus ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107801	Atp5f1b	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:12932	endomyocardial fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139279	Hrh3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917097	Wnk4	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98477	Tacr2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	biomarker_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96437	Igfbp2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104596	Procr	biomarker_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109482	Cacna1a	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:1063	interstitial nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:10966	lipoid nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95623	Gabrg2	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338859	P2rx4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98874	Txn1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109538	Cort	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892013	Agrp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96748	Lamp2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:5463	cochlear disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861731	Ccl28	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:0080108	myoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97347	Nkx2-2	biomarker_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321151	Ptpru	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931307	Slc19a3	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183450	Uts2r	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:2297	leptospirosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:10690	mastitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681835	Nlgn2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109147	Oxtr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108173	Prkg2	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108069	Ccna2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95791	Got1	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858256	Naip7	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:0090131	complex cortical dysplasia with other brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096550	Cyp4a14	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196378	Habp2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914434	Ndufa13	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104579	Il12rb1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888517	Rhcg	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96648	Jund	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2673307	Mafa	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344345	Smc1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	biomarker_via_orthology	DOID:0050890	synucleinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321398	F11r	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194497	Tgif1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102791	Prph2	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3028580	Cyp4a31	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104770	Ephb3	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351659	Abcg5	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96009	Hadh	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717148	Cyp4a32	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:7166	thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929915	Ncoa6	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346344	Nr0b2	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4692	endophthalmitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101765	Cdk5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96173	Hoxa13	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347098	Slc27a1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109380	Il10rb	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	biomarker_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:2772	irritant dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88589	Cyp1a2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138151	Kmo	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653863	Gpbar1	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104596	Procr	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918910	Rarres2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183450	Uts2r	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87930	Adk	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340062	Sgk1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88392	Chat	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344408	Pebp1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96918	Mas1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9286	priapism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347098	Slc27a1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919711	Prcp	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99445	Mtpn	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96602	Itga3	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87870	Acat1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153060	Gjc2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914853	Dusp6	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354734	Rgs3	biomarker_via_orthology	DOID:12528	lesion of sciatic nerve						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201403	Gfra3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96828	Lrp1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097161	Bak1	biomarker_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107816	Pfkfb1	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351659	Abcg5	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142048	Rnf40	biomarker_via_orthology	DOID:12387	nephrogenic diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107821	Has2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109599	Has3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888513	Fzd2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97622	Pln	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150380	Srd5a2	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95498	Fcgr1	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97836	Qdpr	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894292	Mtr	biomarker_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107976	Slc8a3	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108449	Adcyap1r1	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298220	Naip5	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107427	Elavl4	biomarker_via_orthology	DOID:8927	learning disability						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98296	Shc1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88495	Crem	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104638	Tff3	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105381	Rpsa	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107571	Cav2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109366	Kcnk2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96777	Lgals1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:403	mouth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	biomarker_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261433	Endog	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339977	Agtrap	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88067	Arc	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:8549	chronic ulcer of skin						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105064	Slc9a3	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	biomarker_via_orthology	DOID:8456	choline deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109162	Gpam	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98476	Tac2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135593	Hadha	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354184	Nox4	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928268	Ireb2	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95773	Gnai3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103298	Apobec1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336883	Smad6	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182474	Irak4	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2518	orchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:9446	cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333784	Hdac5	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352630	Abcc9	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107414	Tnfsf10	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443111	Abcc4	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107932	Ndufs6	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298226	Naip2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679262	Rgma	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926562	Gucy1a1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195256	Pla2g4a	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88096	Atf4	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:5733	salpingitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891915	Foxo4	biomarker_via_orthology	DOID:607	paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276112	Cldn5	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99439	Btc	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98330	Snai1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098684	Eif2a	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309469	Casq2	biomarker_via_orthology	DOID:1929	supravalvular aortic stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916969	Cad	biomarker_via_orthology	DOID:3247	rhabdomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88096	Atf4	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:5113	nutritional deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109172	Dspp	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103149	Uchl1	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97440	Oprl1	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108409	Rgs4	biomarker_via_orthology	DOID:365	bladder disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107824	Ccr4	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95664	Gata4	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:971	tendinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:13711	dental fluorosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349451	Corin	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107733	Dctn2	biomarker_via_orthology	DOID:0050890	synucleinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96919	Ascl1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337040	Nr1i2	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141980	Scaf1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347098	Slc27a1	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99458	Mef2c	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:4692	endophthalmitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334417	Grpel1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858317	Timm23	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102700	Itga7	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916289	Insig1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341800	Hey1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98438	Sts	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913296	Ndufb5	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:11996	spermatic cord torsion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88598	Cyp2b10	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108511	Mobp	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098733	Slc46a1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	biomarker_via_orthology	DOID:12800	mucopolysaccharidosis VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913066	Sh3rf1	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151886	Ngb	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96570	Inhba	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88248	Calb1	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103298	Apobec1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:11121	pulpitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889272	Cadm1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298398	Mcm7	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036230	Slc27a6	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932288	Egln3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385297	Tpcn2	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108409	Rgs4	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97816	Ptprz1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298223	Naip1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107996	Slc8a2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95757	Slc2a3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95292	Egfbp2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298210	Hcn2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:12932	endomyocardial fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109162	Gpam	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88611	Cyp4a10	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98894	Ucp1	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151886	Ngb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096385	Bcan	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95296	Egr2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442401	Ppp1r9a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104876	Hes5	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88251	Calm1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104653	Atp2b1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	biomarker_via_orthology	DOID:5463	cochlear disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88067	Arc	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99400	Atp7a	biomarker_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915851	Qars1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95719	Gjb1	biomarker_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99879	Prkd1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:10113	trypanosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860055	Panx1	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107592	Hmgcs1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107489	Phex	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	biomarker_via_orthology	DOID:0060564	spinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96918	Mas1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97495	Pbx1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97724	Pnmt	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107821	Has2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97249	Myb	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107172	Ppp3r1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354175	Txnrd1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99912	Lama2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336205	Fkbp1b	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:4556	lung large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927664	Sirt2	biomarker_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95720	Gjb2	biomarker_via_orthology	DOID:12577	urethral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107474	Cd38	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298222	Naip6	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384561	Nae1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101839	Rpl28	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88497	Crhbp	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341847	Hhip	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919133	Coq2	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646098	Cbr1b	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914514	Ndufb8	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103177	Mpz	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333777	Aqp3	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87995	Aldob	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99782	Nt5e	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103221	Dsc2	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106215	Aqp5	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:1742	drug psychosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2661081	Acvr1c	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306784	Cited2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96949	Mdk	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926944	Calcrl	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913208	Carm1	biomarker_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104778	Plcb3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96274	Htr1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98797	Tpi1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098271	Rgs2	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097668	Upp1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87995	Aldob	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927664	Sirt2	biomarker_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95772	Gnai2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109585	Pld1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107689	Kif3a	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352750	Cabp1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341878	Ehd1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447992	Trim63	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96602	Itga3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345146	Grk1	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444672	Madd	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95305	Eif4e	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:8440	ileus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96918	Mas1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106188	Gstt2	biomarker_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:26	pancreas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921588	Slc6a19	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96437	Igfbp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351330	Cartpt	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914291	Oxct1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142523	Crtc1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332235	Nrf1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107913	Tial1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351896	Slco1a4	biomarker_via_orthology	DOID:12308	Dubin-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927224	Yeats4	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	biomarker_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:0080171	esophageal atresia/tracheoesophageal fistula						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156052	Slc17a6	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:8440	ileus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889549	Txnip	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913125	Pias1	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105381	Rpsa	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98728	Tgfbr1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106590	Has1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107757	Gfer	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098776	Lbp	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99555	Pde4d	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87941	Grk3	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889679	Slco1c1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101947	Hnrnpd	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97171	Mt1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96571	Inhbb	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:13711	dental fluorosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201387	Nlk	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352480	Igfbp7	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95395	Eno3	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343262	Timm44	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:2450	central retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	biomarker_via_orthology	DOID:5022	aflatoxins-related hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859993	Smad9	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109280	Nudt1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102716	Cryba4	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	biomarker_via_orthology	DOID:686	liver carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107996	Slc8a2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107824	Ccr4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97314	Nefm	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:11121	pulpitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859287	Dnmt3l	biomarker_via_orthology	DOID:8456	choline deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95634	Gad2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99682	Tmbim6	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:14183	alcoholic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444110	Sgms1	biomarker_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:654	overnutrition						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2451073	Xylt1	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446632	Ago2	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859778	Hif3a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:11823	hepatorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151796	Pnpla3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330806	Arg2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97599	Prkce	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354161	Sirt6	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88284	Cbr1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920590	Nptxr	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88611	Cyp4a10	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179733	Mpst	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201402	Ccr8	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:14221	abdominal obesity-metabolic syndrome 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97567	Pgr	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96298	Hyal1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98823	Trh	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:10554	meningoencephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648653	Eno1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:1340	pure red-cell aplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98747	Thy1	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95479	Fabp1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	biomarker_via_orthology	DOID:12388	neurohypophyseal diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88244	S100a8	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442409	Dpp10	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95808	Gria1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332659	Bnip3l	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95630	Slc6a11	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98326	Sst	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181667	Bbc3	biomarker_via_orthology	DOID:3669	intermittent claudication						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655562	Adgrl4	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:13767	clonorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87871	Acat2	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99698	Clock	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349717	Ncor1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:13088	periventricular leukomalacia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:0050562	West syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098271	Rgs2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97502	Pcmt1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915050	Dgat2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890472	Il19	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917936	Dusp16	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444934	Ppargc1b	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611747	Cyp4a12b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351896	Slco1a4	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107846	Prmt1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107801	Atp5f1b	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	biomarker_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923517	Fads1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444210	Nr1d1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:12215	oligohydramnios						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:1340	pure red-cell aplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101772	Snta1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88061	Aprt	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99538	Acsm3	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151053	Serpinb7	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3071	gliosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98438	Sts	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653863	Gpbar1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97379	Slc10a1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:1002	endometritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:0060611	abdominal obesity-metabolic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88589	Cyp1a2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:1255	trichostrongyloidiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109249	Adamts1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926157	Atf6	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88559	Ctrb1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96756	Lck	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9402	epididymitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919224	Prmt3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96281	Htr2c	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104729	Akap1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103219	Meox2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106687	Pon2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195256	Pla2g4a	biomarker_via_orthology	DOID:2615	papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914853	Dusp6	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99841	Htr7	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87934	Adra2a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:0090109	autosomal dominant hypocalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:0050152	aspiration pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2178103	Arhgdia	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:0050876	Caroli disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95299	Eif2s1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:1002	endometritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:14183	alcoholic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107570	Cav3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891978	Phyh	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96759	Ldha	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339468	S100a10	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98715	Ift88	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039629	Slc17a8	biomarker_via_orthology	DOID:9784	trichinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341830	Eif2ak3	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109161	Grk5	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97297	Nedd4	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140940	Acacb	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098776	Lbp	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927636	Rplp0	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201378	Anxa3	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098772	Pik3r2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94860	Ppp1r1b	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:11119	Gilles de la Tourette syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346330	Banf1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:4500	hypokalemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344416	Ash2l	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104580	Rapgef1	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95688	Gdf5	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891427	Fgf23	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109277	Pik3r3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277211	Tyrobp	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915010	Slc38a2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339760	Csf2rb2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88108	Atp1b1	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107931	Sqstm1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95619	Gabrb1	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109182	Acat3	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103221	Dsc2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:3146	lipid metabolism disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913208	Carm1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339759	Csf2rb	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104593	Xcl1	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103071	Rangap1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151886	Ngb	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98326	Sst	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330808	Hsd17b7	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103070	H2-Ab1	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915835	Rtn4	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:3227	tracheal stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306776	Map1a	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351338	Grm1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88612	Cyp4a12a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332243	Ugcg	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95710	Ghrhr	biomarker_via_orthology	DOID:535	sleep disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	biomarker_via_orthology	DOID:0080333	aortic valve disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97379	Slc10a1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108384	Btg2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	biomarker_via_orthology	DOID:2856	euthyroid sick syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924161	Brd1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918929	Atp5pd	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:0090109	autosomal dominant hypocalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444210	Nr1d1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146921	Cyp4f15	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354171	Ebi3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105100	Ctnnd1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927655	Ggcx	biomarker_via_orthology	DOID:0080653	urolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97816	Ptprz1	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580629	Ugt1a6b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95541	Fkbp1a	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87917	Adcy6	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95393	Eno1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99698	Clock	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333811	Mbd1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109249	Adamts1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350929	Asns	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108482	Hrh2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858494	Bok	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933154	Slc26a5	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332659	Bnip3l	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:12935	alcoholic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	biomarker_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87931	Cfd	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:12932	endomyocardial fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:13100	intracranial vasospasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102774	Aimp1	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:10112	sleeping sickness						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2180756	Mchr1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270844	Cideb	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:8432	polycythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270850	Slc6a2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321159	Ppp2ca	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88071	Arnt	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315202	Slit3	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913293	Atp5f1d	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102504	mt-Co1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96009	Hadh	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:607	paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109207	Eif4g2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88475	Cox5b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338016	Bex3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196287	Dffb	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109452	Smad1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95872	Gusb	biomarker_via_orthology	DOID:12798	mucopolysaccharidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106183	Ocln	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109161	Grk5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387203	Ppat	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298211	Hcn3	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	biomarker_via_orthology	DOID:3602	toxic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105064	Slc9a3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104773	Adra1a	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96247	Hsp90ab1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387581	Ppp1r9b	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	biomarker_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329044	Cldn3	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:2548	reflex epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96670	Kcnc4	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096880	Phlda1	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	biomarker_via_orthology	DOID:1063	interstitial nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351619	Abcb11	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96907	Marcks	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104576	Lct	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	biomarker_via_orthology	DOID:1799	islet cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107760	Chka	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195271	Aqp8	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97275	Myod1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107438	Cab39	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355331	Olig2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102462	Slc9a1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312922	Casp12	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101931	Slc1a2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95588	Fth1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338071	Ikbkb	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104629	Penk	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442926	Mettl14	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107801	Atp5f1b	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338044	Cyp8b1	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354161	Sirt6	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106066	Ptafr	biomarker_via_orthology	DOID:6195	conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:8437	intestinal obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97284	Ncf2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	biomarker_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87947	Adss1	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0080176	meningococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97373	Npr3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102501	mt-Cytb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333776	Ahrr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333811	Mbd1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923517	Fads1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98970	Xbp1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103182	Slc19a1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916401	Lzic	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384902	Rnpep	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109452	Smad1	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:0080178	mucositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:0050868	hepatocellular adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88516	Cryab	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102501	mt-Cytb	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99441	Ckmt1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109155	Kcnab1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98898	Ugt1a1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88346	Cd8a	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109553	Ctsc	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95697	Gfap	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341847	Hhip	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109249	Adamts1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441906	Ghsr	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109366	Kcnk2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95774	Gnal	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181667	Bbc3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444210	Nr1d1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913704	Nmnat1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97501	Pck1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106091	Cyp7a1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345143	Pde10a	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104580	Rapgef1	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929481	Slc22a21	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346344	Nr0b2	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	biomarker_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:431	myofascial pain syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933623	Smarcd1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	biomarker_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107588	Gjb6	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109175	Dab2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98497	Tbxas1	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:8549	chronic ulcer of skin						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195269	Slc22a12	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99844	Gem	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102503	mt-Co2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:4377	egg allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915021	Arpc5	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100508	Kcnj8	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109297	Slpi	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:1002	endometritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195462	Gfra2	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95588	Fth1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97453	Oxt	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890473	Il20	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:11573	listeriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109162	Gpam	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109201	Nat2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106653	Epcam	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333812	Mbd3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:2297	leptospirosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109452	Smad1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890110	Robo2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261433	Endog	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96928	Mc2r	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860604	Gucy1b1	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298210	Hcn2	biomarker_via_orthology	DOID:2723	dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155888	Il25	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101783	Plk4	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098776	Lbp	biomarker_via_orthology	DOID:13603	obstructive jaundice						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97629	Pmch	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	biomarker_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88515	Cryaa	biomarker_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1335072	Slc22a2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8437	intestinal obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	biomarker_via_orthology	DOID:14219	renal tubular acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:520	aortic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97807	Ptpn5	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109340	Pitx2	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88105	Atp1a1	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88295	Cacna2d1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97816	Ptprz1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098282	C9	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914720	Abcg8	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104638	Tff3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306778	Map1b	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:251	alcohol-induced mental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97440	Oprl1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926144	Aacs	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106639	Mthfr	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98878	Tyms	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321398	F11r	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106091	Cyp7a1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107587	Irf9	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102759	Prss2	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915391	Gpt2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101863	Aldoc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95715	Gja4	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:5154	borna disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:10605	short bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95794	Lrp2	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105058	Atp2a1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338044	Cyp8b1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109132	Snap91	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88121	Avp	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95284	Edn2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679262	Rgma	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679262	Rgma	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2668347	C8a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:2920	membranoproliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923507	Slc38a3	biomarker_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:0050152	aspiration pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915050	Dgat2	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919508	Kcnk10	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108111	Slc22a1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87977	Ak1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444609	Nlgn3	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923507	Slc38a3	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98467	Syp	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670976	Fez1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88025	Ank2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931221	Hdac9	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332659	Bnip3l	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107285	Ctsh	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96238	Hsf1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98214	Rxra	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:649	prion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347347	Slc27a4	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96690	Krt16	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:5742	pancreatic acinar cell adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87948	Adss2	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196334	Hyal2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105925	Cdo1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:14525	Reye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101791	Isl1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096550	Cyp4a14	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107171	Ppp3r2	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106199	Vegfb	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105089	Hsd17b4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:585	nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:0050859	hemorrhagic cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344313	Zeb1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351891	Slco1a1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105308	Pnoc	biomarker_via_orthology	DOID:0050696	fetal alcohol spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339949	Adamts4	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88529	Cs	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	biomarker_via_orthology	DOID:0050758	metabolic acidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:649	prion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:5295	intestinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109528	Trpc1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:12215	oligohydramnios						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914317	Romo1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928485	Mlycd	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892877	Pld2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917171	Hnrnpa3	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:0090109	autosomal dominant hypocalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97495	Pbx1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96561	Il7	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88223	C1qa	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:12577	urethral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:0050200	Korean hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:0050328	congenital hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:2972	renal artery obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923517	Fads1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:8440	ileus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:12215	oligohydramnios						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147834	Slc6a8	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924143	Cers2	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137698	Ugt1a6a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352454	Nr4a1	biomarker_via_orthology	DOID:4783	mesangial proliferative glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107438	Cab39	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932576	Akap12	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920249	Insig2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338946	Acvrl1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	biomarker_via_orthology	DOID:11716	prediabetes syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349763	Dpysl2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917747	Arhgap17	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441738	Npsr1	biomarker_via_orthology	DOID:2560	morphine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922637	Sirt4	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889273	Fxyd1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102805	Entpd1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	biomarker_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	biomarker_via_orthology	DOID:12935	alcoholic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102805	Entpd1	biomarker_via_orthology	DOID:1852	intrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157018	Nphs2	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050152	aspiration pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098271	Rgs2	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915348	Rchy1	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109267	Gzmb	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107498	Ltc4s	biomarker_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	biomarker_via_orthology	DOID:12098	trigeminal neuralgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:14679	VACTERL association						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107914	Tia1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:9870	galactosemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95564	Fmr1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922857	Wnk2	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:1222	cartilage disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:0060249	scoliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12800	mucopolysaccharidosis VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88497	Crhbp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88452	Col2a1	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929064	Chst12	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096391	Nrxn1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87867	Acadm	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96159	Hmgcr	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315197	Hk2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106341	Atp5po	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:885	fascioliasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97601	Prkcq	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107376	Msi1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:6132	bronchitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88106	Atp1a2	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87977	Ak1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97604	Pklr	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858179	Nucb2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96274	Htr1b	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447992	Trim63	biomarker_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890662	Nherf2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338824	Rgs9	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:574	peripheral nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2234	focal epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927184	Nrgn	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914588	Rffl	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88508	Crk	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107376	Msi1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135548	Il24	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106210	Dmbt1	biomarker_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102774	Aimp1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333784	Hdac5	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270849	Rps6kb1	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919082	Csl	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88067	Arc	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102469	Nfatc1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97295	Casp2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346542	Bace1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914853	Dusp6	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916034	Prickle1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98181	Rrm2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108409	Rgs4	biomarker_via_orthology	DOID:12528	lesion of sciatic nerve						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88468	Col1a2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:1002	endometritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	biomarker_via_orthology	DOID:3877	functional colonic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442543	Vash1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97275	Myod1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:4692	endophthalmitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261434	Olr1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:10376	amblyopia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109297	Slpi	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858745	Icos	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923959	Arpc2	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88235	C7	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923688	Rftn1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99457	Mc4r	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:12176	goiter						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:607	paraplegia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:12935	alcoholic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98923	Vav1	biomarker_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88110	Atp2a2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340024	Aldh1l1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95489	Fbn1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:9588	encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108409	Rgs4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95792	Got2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97511	Pcsk1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107777	Atp5pf	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106915	Vdac2	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861457	Dynll1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99907	Plod1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97168	Msx1	biomarker_via_orthology	DOID:11383	cryptorchidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:0081292	traumatic brain injury						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893578	Scarb1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	biomarker_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:10124	corneal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351659	Abcg5	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104853	Hes1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:0080000	muscular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920211	Slc17a7	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105115	Ctf1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:12215	oligohydramnios						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109351	Slc4a2	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:13619	extrahepatic cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88293	Cacna1d	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:571	median neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346307	Nr1i3	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98296	Shc1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:11044	gastroschisis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648919	Ces1a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313314	Cldn4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:893	Wilson disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88224	C1qb	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105043	Ahr	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88053	Apoc1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:3159	photosensitivity disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859288	Barhl1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916603	Creb3l4	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352456	Nr4a2	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137336	Baiap2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11823	hepatorenal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106295	Tomm70a	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105057	Cdh5	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919238	Esco2	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:5241	hemangioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	biomarker_via_orthology	DOID:0080092	myofibrillar myopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927072	Ppp1r15a	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99146	Ybx1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88399	Chrm4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87929	Adh5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8440	ileus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:4531	mucoepidermoid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9065	leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932682	Cxcl16	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150380	Srd5a2	biomarker_via_orthology	DOID:12700	hyperprolactinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13801	pharyngoconjunctival fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314881	Chaf1b	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88453	Col3a1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924018	Alpi	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:0080521	lung non-squamous non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346316	Ccl19	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88053	Apoc1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328361	Bard1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88445	Col10a1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891387	Ccl19-ps1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924587	Akr1c21	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107674	Cd1d1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9201	lichen planus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:4930	nasal cavity adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3717097	Cyp2j12	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103169	Scn8a	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88113	Atp4a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87902	Acta1	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:4468	clear cell adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580016	Agap2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915115	Rgs10	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:767	muscular atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107571	Cav2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314881	Chaf1b	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:0050853	chronic venous insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:10887	lepromatous leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97816	Ptprz1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88224	C1qb	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:0050639	primary cutaneous amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347095	Adgre5	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107571	Cav2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95432	Ces1e	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88378	Ces1g	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96836	Lta4h	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859216	Avpr1a	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97816	Ptprz1	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:3305	teratocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88235	C7	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97810	Ptprc	biomarker_via_orthology	DOID:8466	retinal degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913585	Atp6v1c1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103157	Dnase1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88582	Cyp11a1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446107	Pde2a	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:5463	cochlear disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108384	Btg2	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919297	Ddx42	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99701	Cdc25b	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:10690	mastitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13276	Mycoplasma pneumoniae pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106203	Skil	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894312	Crhr2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096383	Fgf15	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87977	Ak1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109484	Ywhaz	biomarker_via_orthology	DOID:1825	childhood absence epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648919	Ces1a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927169	B4galt5	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890410	Acss2	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97724	Pnmt	biomarker_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097680	C3ar1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88350	Cdc25c	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88296	Cacna1b	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341265	Camk2d	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344407	Zeb2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140224	Cyp2j11	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:3114	serous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88568	Cux1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104564	Cdkn1c	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930079	Fads2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142687	Ces1f	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103267	Eif4ebp1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88123	Avpr2	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:823	periapical periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:288	endometriosis of uterus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108069	Ccna2	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922954	Ces1h	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931256	Cubn	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:10772	thrombotic thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926945	Trpv4	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95482	Fah	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:363	uterine cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87931	Cfd	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344405	Agr2	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107675	Cd1d2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88373	Cebpb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:636	central pontine myelinolysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449817	Cyp2j8	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:4617	periapical granuloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928842	Cacna1h	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347008	Plod3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:1564	fungal infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:0060322	mastoiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88586	Cyp17a1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	biomarker_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96274	Htr1b	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	biomarker_via_orthology	DOID:0111715	Schaaf-Yang syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88518	Cryba1	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103011	Ccr7	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915917	Trpm4	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96787	Lif	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:0050169	cutaneous lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	biomarker_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914280	Fancl	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:8717	decubitus ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913585	Atp6v1c1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:0090109	autosomal dominant hypocalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	biomarker_via_orthology	DOID:657	adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321390	Enpp2	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94862	Slc6a3	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913102	Cldn13	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88332	Cd3e	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346342	Clca1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201374	Anxa8	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97171	Mt1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101833	Elk1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643681	Bhmt1b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913363	Apoa5	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927753	Inpp5e	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913440	Acer3	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:9507	ethmoid sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:11624	penile benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:9849	Meniere's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270149	Cyp2j5	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:2734	keratosis follicularis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919238	Esco2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102688	H2ax	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95537	Ccn2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442925	Atad5	biomarker_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858964	Actr1a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96892	Lyn	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149481	Cygb	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	biomarker_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321398	F11r	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	biomarker_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107796	Akr7a5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102845	Bdkrb2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913293	Atp5f1d	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:10887	lepromatous leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95639	Gap43	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:12549	hepatitis A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103147	Dync1h1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:9201	lichen planus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2158492	Ahsp	biomarker_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	biomarker_via_orthology	DOID:12800	mucopolysaccharidosis VI						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4439832	Carmn	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913440	Acer3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:2615	papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:13533	osteopetrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87984	Akp3	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339972	Bhmt	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88141	Bcr	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88537	Csk	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88587	Cyp19a1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352629	Abcc8	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108442	Cpeb1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:8506	bullous pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859314	Barhl2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:2972	renal artery obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:631	fibromyalgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347353	Atp2b3	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107285	Ctsh	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	biomarker_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314881	Chaf1b	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316649	Sphk1	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385197	Cyp2j13	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:5845	anterolateral myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103297	Atp7b	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	biomarker_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444926	Ckap4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:4138	bile duct disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99473	Arrb1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107745	Dctn1	biomarker_via_orthology	DOID:0050890	synucleinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101878	Ccl8	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:3713	ovary adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88378	Ces1g	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194504	Kcnj10	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88215	Btg1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779470	Ces1b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:631	fibromyalgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	biomarker_via_orthology	DOID:3500	gallbladder adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:7698	non-functioning pancreatic endocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096865	Aqp2	biomarker_via_orthology	DOID:1837	diabetic ketoacidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102956	Cdk7	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137586	Dtnbp1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107501	Kcnj11	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88350	Cdc25c	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336166	Cflar	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95284	Edn2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139135	Anapc2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915021	Arpc5	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859288	Barhl1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347078	Grk6	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88031	Anxa7	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343142	Arpc1b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	biomarker_via_orthology	DOID:0080941	acquired angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:4166	syphilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88361	Cdx2	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:12510	retinal ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434459	Ccl19-ps6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142687	Ces1f	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108091	Bcar1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95401	Epb41	biomarker_via_orthology	DOID:2373	hereditary elliptocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:0060001	withdrawal disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88454	Col4a1	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345284	Slc34a1	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:10787	premature menopause						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88537	Csk	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918910	Rarres2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859637	Nphs1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892013	Agrp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9478	postpartum depression						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	biomarker_via_orthology	DOID:0060040	pervasive developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88568	Cux1	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:1564	fungal infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:0060319	cardiac arrest						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344380	Chd4	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109344	Eya1	biomarker_via_orthology	DOID:699	mitochondrial myopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:0080941	acquired angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108554	Dab1	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:0050851	glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860203	Cxcl11	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141291	Bud31	biomarker_via_orthology	DOID:1395	schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	biomarker_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353427	Eif2ak4	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96688	Krt14	biomarker_via_orthology	DOID:7134	esophagus small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:0050933	ovarian serous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97572	Phb1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:10533	viral pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	biomarker_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921256	Dnm1l	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106341	Atp5po	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927999	Mlxipl	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88224	C1qb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314647	Aqp7	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:8252	chronic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96205	Hoxd13	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923959	Arpc2	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98874	Txn1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95405	Ephx1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3693096	Ccl19-ps5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148202	Ces1d	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449816	Cyp2j7	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104774	Adra1b	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:0080122	Alpers-Huttenlocher syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2388804	Brms1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95432	Ces1e	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95691	Mstn	biomarker_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933403	Erap1	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:6705	gastric body carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87911	Acvr1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924587	Akr1c21	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097161	Bak1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	biomarker_via_orthology	DOID:2256	osteochondrodysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3512628	Cbx6	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:631	fibromyalgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99701	Cdc25b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:8506	bullous pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88251	Calm1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:6271	gastric cardia adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97592	Prkaca	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102503	mt-Co2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860835	Ak3	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098282	C9	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101802	F2r	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921769	Cyp2j9	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102806	Acvr2a	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109562	Ackr3	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270148	Cyp2j6	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930704	Bhlhe41	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87918	Add1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94927	Drd5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96925	Mbp	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88562	Ctsd	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88005	Amelx	biomarker_via_orthology	DOID:0090109	autosomal dominant hypocalcemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:10533	viral pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	biomarker_via_orthology	DOID:0080144	childhood acute lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:0111536	Buschke-Ollendorff syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148202	Ces1d	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352493	Bag3	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914342	Gatm	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338938	Bmpr1a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922954	Ces1h	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95485	Fasn	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88384	F9	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94900	Dlk1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860835	Ak3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108028	Atr	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109548	Adam10	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097161	Bak1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:853	polymyalgia rheumatica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95304	Eif4b	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96836	Lta4h	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:12375	bronchopneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:13948	bladder neck obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99495	Brd2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2140885	Napepld	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:2741	bilirubin metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:6195	conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:13208	background diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919439	Bag6	biomarker_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098271	Rgs2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107177	Hsd17b3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921494	Atg7	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94876	Ddc	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5000466	Anpep	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891391	Ccl19-ps3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98923	Vav1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913963	Actr2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99701	Cdc25b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108024	Rgn	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102496	mt-Nd5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102695	Ptprf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107825	Adam8	biomarker_via_orthology	DOID:9498	pulmonary eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926471	Fancg	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333784	Hdac5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88269	Car2	biomarker_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:0080159	Cryptococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916603	Creb3l4	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136171	Aff4	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107231	Dlg1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343051	Actl7a	biomarker_via_orthology	DOID:4006	bladder urothelial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:1564	fungal infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919161	Bdh1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109185	Ccn3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87941	Grk3	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109615	Mia	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108009	Alppl2	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919519	Cda	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96670	Kcnc4	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349763	Dpysl2	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045421	Ank	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:0080522	thyroid gland anaplastic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:900	hepatopulmonary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98277	Epha4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685104	Akap5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:670	amphetamine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95420	Ces1c	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:13976	peptic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	biomarker_via_orthology	DOID:303	substance-related disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:4251	conjunctival disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99918	Mecp2	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859167	Cacng4	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	biomarker_via_orthology	DOID:11121	pulpitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181667	Bbc3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339639	Ogt	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	biomarker_via_orthology	DOID:14755	argininosuccinic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346542	Bace1	biomarker_via_orthology	DOID:2491	sensory peripheral neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:14095	boutonneuse fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353449	Eif2ak2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340034	Sema3e	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353589	Cbx8	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891389	Ccl27b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:8741	seborrheic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	biomarker_via_orthology	DOID:1540	parathyroid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87930	Adk	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:3951	acute myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109533	Abcb7	biomarker_via_orthology	DOID:8955	sideroblastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:0080322	polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892013	Agrp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343459	Ccl27a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88031	Anxa7	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107427	Elavl4	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916788	Antxr1	biomarker_via_orthology	DOID:0060081	triple-receptor negative breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922715	Dynlrb2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708691	Ccl19-ps4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:14654	prostatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:0080599	Coronavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099440	Suv39h1	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675303	Tnfrsf14	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88375	Cenpa	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:178	vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927070	Dusp10	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270863	Prep	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104518	Cntn2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106653	Epcam	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153093	Cspg4	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779470	Ces1b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:13254	diverticulitis of colon						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94900	Dlk1	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109611	Dsp	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339949	Adamts4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94864	Dbh	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3713752	Ccl27al	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:8161	thyroid gland Hurthle cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891915	Foxo4	biomarker_via_orthology	DOID:251	alcohol-induced mental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277186	Atg5	biomarker_via_orthology	DOID:326	ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101833	Elk1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861457	Dynll1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:13133	HELLP syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927555	Slc4a4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913612	Exosc3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096337	Ephb1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913128	Bet1l	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:10316	pneumoconiosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	biomarker_via_orthology	DOID:0060745	Doyne honeycomb retinal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:0050452	mevalonic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88473	Cox4i1	biomarker_via_orthology	DOID:11801	protein-energy malnutrition						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330841	Bcl2l10	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95420	Ces1c	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:4780	anti-basement membrane glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:288	endometriosis of uterus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930134	Ern1	biomarker_via_orthology	DOID:8557	oropharynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:93830	Adipor2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139135	Anapc2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913293	Atp5f1d	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	biomarker_via_orthology	DOID:4556	lung large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88609	Cyp3a11	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	biomarker_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106212	Chrnb3	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:13955	uterus interstitial leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139135	Anapc2	biomarker_via_orthology	DOID:1405	primary angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:3713	ovary adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88604	Cyp2d12	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88390	Cga	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	biomarker_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101916	Fabp7	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107760	Chka	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916788	Antxr1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385848	Bcas3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:1564	fungal infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341098	Chil4	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88053	Apoc1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2475	chronic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346316	Ccl19	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:4468	clear cell adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104772	Cdk2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88263	Capn1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915816	Caly	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	biomarker_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:0060284	paroxysmal nocturnal hemoglobinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:0080390	nephrotic syndrome type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109608	Fap	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921455	Acsl3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:8691	mycosis fungoides						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109372	Cbx5	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88350	Cdc25c	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107438	Cab39	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917976	Angptl6	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106671	Cdh16	biomarker_via_orthology	DOID:1781	thyroid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:11963	esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923529	Cyp2d26	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344405	Agr2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:6088	acute stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99701	Cdc25b	biomarker_via_orthology	DOID:2101	vulva squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109383	Casp7	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:11512	Budd-Chiari syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146430	Cblb	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916978	Card11	biomarker_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:1350	paranasal sinus benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346342	Clca1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101790	Fabp5	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:2722	acrodermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:1390	hypobetalipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88498	Crhr1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107824	Ccr4	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88390	Cga	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:2797	idiopathic interstitial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095734	Ccng2	biomarker_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139135	Anapc2	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101764	Cdk5r1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88458	Col5a2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:0111144	preterm premature rupture of the membranes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88071	Arnt	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346316	Ccl19	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	biomarker_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447658	Disc1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:9463	otitis externa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444812	Camkk2	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648919	Ces1a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107714	Dnah8	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328368	Cdk9	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108442	Cpeb1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:0050175	tick-borne encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88602	Cyp2d10	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914853	Dusp6	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107714	Dnah8	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330841	Bcl2l10	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923959	Arpc2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924294	Arid2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:0060750	familial temporal lobe epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107674	Cd1d1	biomarker_via_orthology	DOID:1394	urinary schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107796	Akr7a5	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:2738	pseudoxanthoma elasticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917336	Cysltr2	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343142	Arpc1b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103582	Ercc5	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	biomarker_via_orthology	DOID:3388	periodontal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097158	Calu	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:11100	Q fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098802	Cdk12	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	biomarker_via_orthology	DOID:0050671	female breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101864	Dag1	biomarker_via_orthology	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924018	Alpi	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	biomarker_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	biomarker_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139135	Anapc2	biomarker_via_orthology	DOID:5386	lung adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	biomarker_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:0050120	hemophagocytic lymphohistiocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104728	Caml	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99529	Cd63	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106221	Capza3	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333777	Aqp3	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	biomarker_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:5199	ureteral obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333791	Artn	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:5241	hemangioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88346	Cd8a	biomarker_via_orthology	DOID:0050185	erythema multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:13139	crescentic glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:3410	carotid artery thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913102	Cldn13	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:3073	brain glioblastoma multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95414	Ercc3	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99701	Cdc25b	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	biomarker_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105303	Cxcr2	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:6195	conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:2452	thrombophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109447	Ctcf	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	biomarker_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109247	Ddit3	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88262	Cap1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108384	Btg2	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107675	Cd1d2	biomarker_via_orthology	DOID:1394	urinary schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103198	Cdc25a	biomarker_via_orthology	DOID:2101	vulva squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109608	Fap	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88329	Cd34	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277959	Dlg4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	biomarker_via_orthology	DOID:2228	thrombocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894663	Ext1	biomarker_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	biomarker_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109372	Cbx5	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096317	Eef1a2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106190	Bcl11a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:640	encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891391	Ccl19-ps3	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333111	Amd2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107168	Aurkb	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107824	Ccr4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:2297	leptospirosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88031	Anxa7	biomarker_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3779470	Ces1b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:10603	glucose intolerance						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3693096	Ccl19-ps5	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913945	Aspn	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88293	Cacna1d	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3045315	Bpi	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860440	Bace2	biomarker_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928953	Ccl24	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889575	Adar	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88590	Cyp1b1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0080821	exercise-induced bronchoconstriction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644226	Eif4a3l1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88390	Cga	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	biomarker_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	biomarker_via_orthology	DOID:1498	cholera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88026	Ank3	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108384	Btg2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101878	Ccl8	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88259	Camk2g	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096359	Cyp26a1	biomarker_via_orthology	DOID:7941	Barrett's adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646594	Eif4a3l2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:0080941	acquired angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202394	Cblif	biomarker_via_orthology	DOID:10808	gastric ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384790	Fanci	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102708	Efnb1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:0050909	extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925571	Ankrd23	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916524	Ctdspl	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385022	Cyp2d34	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	biomarker_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97295	Casp2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347010	Avpr1b	biomarker_via_orthology	DOID:7004	ACTH-secreting pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:646	viral encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095407	Bmpr2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88256	Camk2a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102676	Abcc1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87853	a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	biomarker_via_orthology	DOID:7596	asbestos-related lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95432	Ces1e	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105062	Amhr2	biomarker_via_orthology	DOID:4441	dysgerminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:5015	fibrolamellar carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916788	Antxr1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:6827	pancreatic solid pseudopapillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891387	Ccl19-ps1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351597	Atp5mg	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103008	Epb41l3	biomarker_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:1206	Rett syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:5744	ovary serous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:10887	lepromatous leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:4617	periapical granuloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:9810	polyarteritis nodosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:1390	hypobetalipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:3965	Merkel cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88378	Ces1g	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107285	Ctsh	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106099	Cyp3a16	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:0050185	erythema multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096340	E2f3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88346	Cd8a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:2755	Mycobacterium avium complex disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929955	Akr1a1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:11429	endometriosis of pelvic peritoneum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99474	Arrb2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3693096	Ccl19-ps5	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:4531	mucoepidermoid carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88335	Cd4	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104653	Atp2b1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:0050782	Zollinger-Ellison syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917336	Cysltr2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347050	Aldh1a7	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88350	Cdc25c	biomarker_via_orthology	DOID:2101	vulva squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332623	Dok2	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109168	Fat1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88548	Csnk2b	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88111	Atp2b4	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933403	Erap1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88606	Cyp2d9	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859288	Barhl1	biomarker_via_orthology	DOID:0060081	triple-receptor negative breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096340	E2f3	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87990	Alas2	biomarker_via_orthology	DOID:3890	acute intermittent porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926129	Arid1b	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109384	Atf3	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144423	Arhgap44	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99607	Abca1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858964	Actr1a	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:14089	root caries						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449818	Cyp3a44	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88574	Cybb	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3511177	Calm5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107824	Ccr4	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343098	Aif1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104518	Cntn2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913208	Carm1	biomarker_via_orthology	DOID:0060075	estrogen-receptor positive breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:540	strabismus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88053	Apoc1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177632	Cys1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:895149	Acadvl	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104757	Ephb4	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:0080177	hepatic veno-occlusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105115	Ctf1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3714859	Cyp3a41b	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923959	Arpc2	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87892	Chrnb4	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95485	Fasn	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88374	Cel	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931464	Calm4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105062	Amhr2	biomarker_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096335	Adam17	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101932	Cpe	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94885	Des	biomarker_via_orthology	DOID:988	mitral valve prolapse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913393	Eef1e1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860203	Cxcl11	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353450	Aldh1a1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314881	Chaf1b	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343142	Arpc1b	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142687	Ces1f	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449119	A2m	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:5162	arteriolosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036280	Duox2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88603	Cyp2d11	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:1390	hypobetalipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:0050486	exanthem						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98258	Ccl1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929474	Cyp2d22	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915368	Atg101	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88115	Atp5f1a	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:10533	viral pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:0080750	erythema nodosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:0060750	familial temporal lobe epilepsy 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88489	Cr2	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99484	Chuk	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87939	Adrb3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708691	Ccl19-ps4	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858451	Cyp3a41a	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107825	Adam8	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346330	Banf1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:6498	seborrheic keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916788	Antxr1	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:9428	intracranial hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108384	Btg2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859388	Dll4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321398	F11r	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095734	Ccng2	biomarker_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914789	Dock6	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102805	Entpd1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94893	Cyb5r3	biomarker_via_orthology	DOID:0060076	estrogen-receptor negative breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345964	Coro1c	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:1911	endodermal sinus tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:11555	Fuchs' endothelial dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330841	Bcl2l10	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861731	Ccl28	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106248	Eif5a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:2725	capillary hemangioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:1928	Williams-Beuren syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:10824	malignant hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	biomarker_via_orthology	DOID:0080641	tongue carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99851	Cbfb	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109324	Fadd	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682303	Chil6	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928480	Acp3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932052	Chia1	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351644	Abcc5	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313314	Cldn4	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:10211	cholelithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88064	Ar	biomarker_via_orthology	DOID:10892	hypospadias						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88610	Cyp3a13	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88348	Cd9	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914789	Dock6	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	biomarker_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88250	Cald1	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:6171	uterine carcinosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108009	Alppl2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100495	Atp5pb	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913963	Actr2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:13767	clonorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88346	Cd8a	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580016	Agap2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88070	Arg1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344392	Capn10	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347353	Atp2b3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923731	Eif4a3	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201607	Blzf1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314647	Aqp7	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096359	Cyp26a1	biomarker_via_orthology	DOID:8866	actinic keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921367	Actr3	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:10772	thrombotic thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891352	Psg20	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107168	Aurkb	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:9282	ocular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434459	Ccl19-ps6	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:13580	cholestasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88385	Cfh	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860440	Bace2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:4247	coronary restenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99830	Cmpk2	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104653	Atp2b1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:169	neuroendocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654144	Ercc6l	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915021	Arpc5	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344405	Agr2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036258	Chd5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708691	Ccl19-ps4	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	biomarker_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206586	Bap1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:10300	Raynaud disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924294	Arid2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99480	Cebpa	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346831	Esrra	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860203	Cxcl11	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101802	F2r	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:9498	pulmonary eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859920	Ebag9	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148202	Ces1d	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100494	Ercc6	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105037	Ddx5	biomarker_via_orthology	DOID:3151	skin squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095734	Ccng2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88594	Cyp27a1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443472	Atf7	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676458	Birc7	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684986	Asap3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:8534	gastroesophageal reflux disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103238	Cyp2c29	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919004	Cyp2d40	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306819	Cyp2c38	biomarker_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676649	Chil5	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646434	Cfhr4	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144423	Arhgap44	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306818	Cyp2c39	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107569	Epx	biomarker_via_orthology	DOID:9415	allergic asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261423	Casp8	biomarker_via_orthology	DOID:417	autoimmune disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922954	Ces1h	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88255	Anxa6	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:12783	migraine without aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102797	Acsl1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109337	Brca2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442892	Clptm1l	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916885	Dapk1	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:1800	neuroendocrine carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88543	Csnk2a1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655562	Adgrl4	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88289	Cbx2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	biomarker_via_orthology	DOID:0050211	swine influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87938	Adrb2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:11729	Lyme disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95420	Ces1c	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:9597	Krukenberg carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646788	Atg5lrt	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88065	Araf	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316658	Cyba	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87983	Alpl	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:5759	sebaceous gland neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87859	Abl1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196466	Dsg2	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:0050169	cutaneous lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915368	Atg101	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88059	App	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:1996	rectum adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88004	Amd1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891391	Ccl19-ps3	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107508	Ereg	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891374	Brdt	biomarker_via_orthology	DOID:14227	azoospermia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136878	B3galt5	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:543	dystonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932288	Egln3	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103157	Dnase1	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096863	Entpd2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448558	Fancb	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098802	Cdk12	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346321	Adamts5	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104617	Ccr1l1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:705	Leber hereditary optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:1799	islet cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146430	Cblb	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147497	Cyp2c50	biomarker_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306806	Cyp2c37	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87937	Adrb1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448715	Cxcr1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928375	Arpc3	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932376	Cacng8	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:8683	myeloid sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3689889	Fancf	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929955	Akr1a1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919598	Aif1l	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:1407	anterior uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88264	Capn2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:13767	clonorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:0050083	Keshan disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195458	Abce1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914634	Bag4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096385	Bcan	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913393	Eef1e1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353589	Cbx8	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88111	Atp2b4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88068	Areg	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097158	Calu	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88351	Cdk1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103202	Adsl	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355321	Chek2	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891837	Cpb2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95408	Epor	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:2972	renal artery obstruction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330860	Chil3	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891387	Ccl19-ps1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:0050185	erythema multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108042	Ccna1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:1350	paranasal sinus benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099442	Atxn3	biomarker_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87984	Akp3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:13576	twin-to-twin transfusion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:3371	chondrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913843	Diablo	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95415	Erg	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105923	Ednra	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891716	Emcn	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104618	Ccr1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105091	E2f5	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88031	Anxa7	biomarker_via_orthology	DOID:4159	skin cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108515	Cbx3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434459	Ccl19-ps6	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98659	Dntt	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87904	Actb	biomarker_via_orthology	DOID:10881	hand, foot and mouth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448480	Fancd2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343459	Ccl27a	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:3178	skin papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333889	Bub1b	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95388	Emx2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107777	Atp5pf	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330860	Chil3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88373	Cebpb	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888993	Api5	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343459	Ccl27a	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914063	Bcl2l14	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95299	Eif2s1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:10457	Legionnaires' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676897	Mir23a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95304	Eif4b	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330299	Dyrk1a	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108047	Bag1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:5138	leiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87999	Alox5	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94890	Dhfr	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:3304	germinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914829	Cpeb4	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612791	Kir3dl2	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3710514	Ccl21f	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99578	Drd1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1003	pelvic inflammatory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107384	Dnm1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647143	Cdc5lrt8	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928953	Ccl24	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:1063	interstitial nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105368	Atp2b2	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:813	septic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104757	Ephb4	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347010	Avpr1b	biomarker_via_orthology	DOID:3829	pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94909	Dmd	biomarker_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88031	Anxa7	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385656	Acsbg1	biomarker_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88383	F8	biomarker_via_orthology	DOID:0060574	von Willebrand's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88084	Asl	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676649	Chil5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157948	Cd209e	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101357	Ece1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108047	Bag1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88373	Cebpb	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	biomarker_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107675	Cd1d2	biomarker_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:14095	boutonneuse fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101833	Elk1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:12804	mucopolysaccharidosis IV						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107700	Casp4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88437	Cnp	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619423	Mir486	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:6255	growth hormone secreting pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196274	Cdca8	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159682	Havcr2	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:13812	adhesions of uterus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096337	Ephb1	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157947	Cd209d	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3037818	Cxcl3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914829	Cpeb4	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97545	Cfp	biomarker_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106091	Cyp7a1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88335	Cd4	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88568	Cux1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99529	Cd63	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:9201	lichen planus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	biomarker_via_orthology	DOID:0060040	pervasive developmental disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104816	Hnrnpl	biomarker_via_orthology	DOID:0050457	Sertoli cell-only syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88090	Ass1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:1214	tympanosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:0080301	atypical hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	biomarker_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336166	Cflar	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:9123	eczema herpeticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676816	Mir130a	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923959	Arpc2	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136171	Aff4	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349183	Ccl21a	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88467	Col1a1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:668	myositis ossificans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107189	Ahsg	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87870	Acat1	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:4617	periapical granuloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103011	Ccr7	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891389	Ccl27b	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88031	Anxa7	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894678	Aurka	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:12683	vestibular neuronitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:8476	Whipple disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87888	Chrna4	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888996	Cd59b	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891427	Fgf23	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96941	Cma1	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647148	Cdc5lrt6	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95284	Edn2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354163	Ercc4	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107823	Ctsk	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352447	Abcc2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351331	Chaf1a	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88315	Ccnd3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88613	Ccn1	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:112	esophageal varix						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443910	Bcorl1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919595	Amer1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107569	Epx	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918952	Cdc5l	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87909	Acta2	biomarker_via_orthology	DOID:4977	lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88455	Col4a2	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930088	Clcf1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919158	Cldn23	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933736	Adgrb1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928953	Ccl24	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676907	Mir30a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195458	Abce1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104737	Cdkn2b	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:7910	maxillary sinus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108448	Angpt1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314647	Aqp7	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88174	Bmi1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:636	central pontine myelinolysis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676458	Birc7	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444008	Bptf	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442306	Fancm	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270862	Axin2	biomarker_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676897	Mir23a	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858304	Ctps1	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915368	Atg101	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:0050175	tick-borne encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99481	F11	biomarker_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	biomarker_via_orthology	DOID:0050750	splenic marginal zone lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:4607	biliary tract cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94872	Dcn	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	biomarker_via_orthology	DOID:0050891	adrenal cortical adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339751	Csf3	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340894	Adam2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101757	Cfl1	biomarker_via_orthology	DOID:11457	brain compression						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88216	Btk	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891379	Bhmt2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102720	Ednrb	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106209	Hells	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306779	Ccl22	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:3049	Churg-Strauss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96031	Hc	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	biomarker_via_orthology	DOID:4159	skin cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3713752	Ccl27al	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934950	Csnk1a1	biomarker_via_orthology	DOID:3429	inclusion body myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097153	Cx3cl1	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87941	Grk3	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270839	Cacybp	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107285	Ctsh	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95617	Gabra5	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94919	Dpp4	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109562	Ackr3	biomarker_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3611575	Cfhr2	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:13166	allergic bronchopulmonary aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345147	Akt3	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148922	Ehmt2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96853	Alad	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916415	Cd209b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88274	Ctnna1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930704	Bhlhe41	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105369	Cbx1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88458	Col5a2	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914318	Dynlrb1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338944	Acvr1b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096878	Defb1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0050120	hemophagocytic lymphohistiocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098802	Cdk12	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2449771	Cyp2r1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206591	Bik	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:5015	fibrolamellar carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343094	Kat2b	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108391	Kif1a	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87889	Chrna5	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928896	Arpc1a	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95284	Edn2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101941	E2f1	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:13276	Mycoplasma pneumoniae pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918111	Akr1cl	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145420	Akr1c18	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336880	Eftud2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109384	Atf3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8536	herpes zoster						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:0080379	nephrotic syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102890	Ccng1	biomarker_via_orthology	DOID:11934	head and neck cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444008	Bptf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107825	Adam8	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:1891	optic nerve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99479	Cckbr	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197015	Daxx	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891389	Ccl27b	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109177	Cd59a	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098273	Amacr	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919641	Cdkn3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:8469	influenza						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99600	Aldh2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096863	Entpd2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1754	mitral valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	biomarker_via_orthology	DOID:11520	benign hypertensive renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95476	Fabp3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2655562	Adgrl4	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88248	Calb1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919924	Adipor1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888520	Brd4	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352449	Cxcl9	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:11656	cicatricial pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157942	Cd209a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88494	Creb1	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105937	Cfi	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676824	Mir139	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107341	Ctss	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95288	Eef2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109326	Bnip3	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104850	Cd55	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442722	Cadm2	biomarker_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107730	Hoxb13	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87878	Apoc4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2177178	Dicer1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94926	Drd4	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306797	Aoc3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107824	Ccr4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96544	Casp1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	biomarker_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:0050855	renal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443035	Brinp3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097161	Bak1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108047	Bag1	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926952	Cyb5a	biomarker_via_orthology	DOID:9637	stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261819	Dnmt3b	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109185	Ccn3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151253	Calca	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88038	Fabp4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339753	Csf1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88496	Crh	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105988	Adam28	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:8717	decubitus ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88382	F5	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109608	Fap	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88054	Apoc2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:8515	Cor pulmonale						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96608	Itgav	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333791	Artn	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:8566	herpes simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349415	Cops5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103064	Ddx3x	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314653	Afdn	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:4325	Ebola hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105097	Efnb2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91842	D1Pas1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99551	Cdh13	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913509	Camk2n1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88246	Anxa2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928380	B4galt6	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276116	Ep300	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	biomarker_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108052	Bcl2l2	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145995	Amigo2	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349766	Brd7	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109349	Atf2	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88039	Apc	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682303	Chil6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:11162	respiratory failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351660	Csnk1e	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95479	Fabp1	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109328	Bnip1	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108186	Aldh7a1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341098	Chil4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99779	Chrna7	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88397	Chrm2	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5591961	Cdc5lrt4	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:13254	diverticulitis of colon						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107387	Aqp4	biomarker_via_orthology	DOID:3275	thymoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	biomarker_via_orthology	DOID:9123	eczema herpeticum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342279	Aicda	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314647	Aqp7	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3711256	Ccl21e	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88056	Apod	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88388	Cftr	biomarker_via_orthology	DOID:5733	salpingitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:8515	Cor pulmonale						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88564	Ctsl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105057	Cdh5	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924933	Ehmt1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915385	Eif3h	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917258	Ace2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5753381	Apoc2l	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97370	Enpp1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88568	Cux1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107674	Cd1d1	biomarker_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97295	Casp2	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99701	Cdc25b	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97568	Abcb1b	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95295	Egr1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913208	Carm1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355272	Csnk1d	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97007	Mmp10	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94924	Drd2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105368	Atp2b2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931838	Dbn1	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94925	Drd3	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:74	hematopoietic system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333882	Adam15	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88583	Cyp11b1	biomarker_via_orthology	DOID:0050891	adrenal cortical adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95394	Eno2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88316	Ccne1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096340	E2f3	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88139	Bcl2l1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88248	Calb1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915339	Arpc4	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87951	Afp	biomarker_via_orthology	DOID:1911	endodermal sinus tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103202	Adsl	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:12134	factor VIII deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340094	Cxcl2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351612	Defb3	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99611	Ephb2	biomarker_via_orthology	DOID:1561	cognitive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87997	Alox15	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916812	Cdk13	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88398	Chrm3	biomarker_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339752	Csf2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:3179	inverted papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:1687	neovascular glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:0050486	exanthem						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203290	Cd46	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889272	Cadm1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619129	Mir224	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345277	Ddr2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88058	Apoh	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13564	aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99401	Adora1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95480	Fancc	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927667	Defb4	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336166	Cflar	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95317	Eln	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644213	Cdc5lrt9	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99473	Arrb1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88057	Apoe	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890472	Il19	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2654206	Defb8	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99439	Btc	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349419	Aifm1	biomarker_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104537	Brca1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:11561	hypertensive retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88476	Cp	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352750	Cabp1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108360	Enah	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143261	A4gnt	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:0050771	pheochromocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88051	Apoa4	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88002	Ambp	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139667	Dpyd	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353624	Apln	biomarker_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107765	Apbb1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652397	Kir3dl1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341813	Adam33	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87966	Agtr2	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99430	Hira	biomarker_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104659	Dll1	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106211	Cdc42	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097680	C3ar1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915192	Atp5mc2	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859314	Barhl2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333815	Cx3cr1	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103226	Cox7c	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3713752	Ccl27al	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1312921	Casp6	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157945	Cd209c	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88252	Calr	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101773	Cd86	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88607	Cyp2e1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88556	Ctla4	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103064	Ddx3x	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88174	Bmi1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	biomarker_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97570	Abcb1a	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685556	Adamts13	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104651	Cd82	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:9279	hyperhomocysteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99845	Gdi2	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916851	Dab2ip	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136853	Fam20c	biomarker_via_orthology	DOID:0050445	X-linked dominant hypophosphatemic rickets						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933153	Defb5	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441808	Cdc14b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88055	Apoc3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:94912	Dnmt1	biomarker_via_orthology	DOID:4926	bronchiolo-alveolar adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88127	B2m	biomarker_via_orthology	DOID:8622	measles						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151104	Akr1c20	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914184	Dsn1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096340	E2f3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87876	Ache	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88269	Car2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0080038	pycnodysostosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109169	Epas1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647146	Cdc5lrt7	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88022	Ang	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:811	lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:0060449	gelatinous drop-like corneal dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306796	Apaf1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95411	Erbb3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098280	Crebbp	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921379	Dmgdh	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	biomarker_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88561	Ctsb	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87887	Chrna3	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384876	Cdc73	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103170	Gfi1	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87963	Agt	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88208	Bsg	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107438	Cab39	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87912	Acvr2b	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88588	Cyp1a1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88593	Cyp24a1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88050	Apoa2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179200	Defb7	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277171	Dcx	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108359	Alx4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891209	Efemp2	biomarker_via_orthology	DOID:3376	bone osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933427	Akr1c6	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104686	Crkl	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103556	Cxcl12	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1334448	Aspm	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934582	Cxcr6	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:646	viral encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195261	Eef2k	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106008	Anxa5	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202890	Angpt2	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87971	Ahi1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87998	Alox12	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88297	Cck	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104849	Cd55b	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95455	Ets1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99216	Ddr1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88177	Bmp2	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107191	Bmpr1b	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88289	Cbx2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88336	Cd40	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101833	Elk1	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932052	Chia1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339758	Csf1r	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96431	Cd79b	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:1564	fungal infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914342	Gatm	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339998	Efemp1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201374	Anxa8	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096385	Bcan	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:11446	sciatic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:14261	fragile X syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88461	Col6a3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104771	Erbb4	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99602	Acan	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	biomarker_via_orthology	DOID:0050891	adrenal cortical adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108224	Ccl12	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105975	Cfb	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195261	Eef2k	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106096	Loxl1	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88381	F3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146616	Eaf2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3643524	Cdc5lrt5	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933185	Ctps2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:8295	scabies						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	biomarker_via_orthology	DOID:0050590	severe congenital neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:91842	D1Pas1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351624	Abcg3	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96564	Il9r	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88049	Apoa1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329031	Ccl20	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88578	Cycs	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88155	Bglap3	biomarker_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3648694	Ccnb1-ps	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107505	Alox5ap	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333797	Ccr6	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88138	Bcl2	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145458	Akr1c14	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101790	Fabp5	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103201	Aqp1	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96819	Anxa1	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88357	Cdk4	biomarker_via_orthology	DOID:1799	islet cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105100	Ctnnd1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103067	Atrx	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:0050864	non-arteritic anterior ischemic optic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108068	Cxcl1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2679229	Elane	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103302	Bmp7	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151044	Defb6	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:2030	anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107208	Hoxa11os	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934950	Csnk1a1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104556	Cdkn1a	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277162	Cdk6	biomarker_via_orthology	DOID:7698	non-functioning pancreatic endocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5591876	Cdc5lrt1	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88314	Ccnd2	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528599	Ang5	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261827	Dnmt3a	biomarker_via_orthology	DOID:288	endometriosis of uterus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88439	Cntf	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88302	Ccnb1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443910	Bcorl1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109325	F7	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95283	Edn1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88144	Bdkrb1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314653	Afdn	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103221	Dsc2	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109563	Cxcr4	biomarker_via_orthology	DOID:3753	Hermansky-Pudlak syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102519	Cst3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176159	Cyp26b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:12895	keratoconjunctivitis sicca						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351351	Casr	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:4006	bladder urothelial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3525201	Mdc1	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197009	Birc2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96396	Id1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3589281	Ccl26	biomarker_via_orthology	DOID:4031	eosinophilic gastroenteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88261	Canx	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105120	Dusp1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352467	Esr1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098274	Cyp27b1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861377	Fgf21	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107739	Casp3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103576	Ccl11	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276109	Cldn1	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277207	Cxcr3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314647	Aqp7	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88182	Bmp6	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890410	Acss2	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891999	Adarb1	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88313	Ccnd1	biomarker_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:809	cocaine abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88276	Ctnnb1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915260	Bambi	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88232	C5ar1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351331	Chaf1a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104565	Cdkn1b	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340899	Chi3l1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923658	Abcc3	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103157	Dnase1	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913393	Eef1e1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261437	Atp5f1c	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107182	Ccr5	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98260	Ccl3	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098236	Cast	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914719	Abhd5	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891828	Becn1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107187	Bcl6	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100495	Atp5pb	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103163	Azgp1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101878	Ccl8	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443564	Ambra1	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95479	Fabp1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107899	Cd36	biomarker_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87874	Ace	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106341	Atp5po	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3505689	Cdsn	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105376	Adam9	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916800	Bst2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197007	Birc3	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921395	F13a1	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99478	Cckar	biomarker_via_orthology	DOID:10211	cholelithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891012	F12	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932682	Cxcl16	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203517	Birc5	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447188	Car9	biomarker_via_orthology	DOID:3883	Lynch syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098296	Cpt1a	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107940	Ezh2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891996	Cps1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894278	Bche	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88470	Comt	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99255	Fasl	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:3362	coronary aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893592	Ager	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88318	Cd14	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87916	Ada	biomarker_via_orthology	DOID:8618	oral cavity cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99538	Acsm3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349182	Ccl21b	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913616	Ergic3	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096327	Axin1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676859	Mir195a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914184	Dsn1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196439	Cbx7	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88042	Apex1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99702	Bax	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88584	Cyp11b2	biomarker_via_orthology	DOID:0050891	adrenal cortical adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2672966	Defb37	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88052	Apob	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88512	Crp	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95290	Egf	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914179	Asf1b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644216	Cdc5lrt10	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87964	Agtr1a	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102709	Cav1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329039	Ccl17	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88342	Cd68	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347061	Abcg2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434896	Ccl21d	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104984	Ang2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95407	Epo	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338801	Cyfip1	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096868	Cxcl5	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442524	Heatr1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106185	Ccr2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88327	Cd28	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88279	Cbl	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87965	Agtr1b	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914829	Cpeb4	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88271	Cat	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859314	Barhl2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347090	Anxa10	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277950	Casp9	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104738	Cdkn2a	biomarker_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87991	Alb	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88226	C2	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:11695	portal vein thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88180	Bmp4	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195458	Abce1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196625	Fzd1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87986	Akt1	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2656551	Ang4	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103250	Calm2	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88156	Bglap	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88145	Bdnf	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95412	Ercc1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096330	Bad	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88394	Chga	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109392	Esr2	biomarker_via_orthology	DOID:657	adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88158	Bgn	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106675	Adipoq	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201793	Ang3	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341902	Ccr9	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930704	Bhlhe41	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107202	Atm	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98262	Ccl5	biomarker_via_orthology	DOID:0080546	non-alcoholic fatty liver						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:11077	brucellosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95392	Eng	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95294	Egfr	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442836	Brip1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98259	Ccl2	biomarker_via_orthology	DOID:811	lipodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195985	Cbx4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3528602	Ang6	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88354	Cdh1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98261	Ccl4	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354386	Lats2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135946	Cd163	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95413	Ercc2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88006	Amh	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	biomarker_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88338	Cd44	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676905	Mir29b-1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88380	F2	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352450	Cxcl10	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353494	Akr1b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106664	Cd93	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1935147	Arid1a	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88423	Clu	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95484	Fas	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107795	Hnrnpc	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88157	Bglap2	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88227	C3	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104616	Ccr3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108058	Adm	biomarker_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926446	Cd274	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99512	Ccl7	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339755	Csf3r	biomarker_via_orthology	DOID:2226	myeloproliferative neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104874	Akt2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101775	Cd80	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88337	Cd40lg	biomarker_via_orthology	DOID:0050169	cutaneous lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314881	Chaf1b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95410	Erbb2	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926218	Cysltr1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336166	Cflar	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	biomarker_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923709	Car12	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352745	Fscn1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96765	Ldlr	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96250	Hsp90aa1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	biomarker_via_orthology	DOID:2129	atypical teratoid rhabdoid tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	biomarker_via_orthology	DOID:0001816	angiosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	biomarker_via_orthology	DOID:9810	polyarteritis nodosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858195	Hnrnpu	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95683	Gdf1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96705	Krt8	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676809	Mir125a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619329	Mir30e	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347476	Foxa2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3525201	Mdc1	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107177	Hsd17b3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147707	Kank1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0080933	immunoglobulin light chain amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95582	Fshb	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	biomarker_via_orthology	DOID:916	liver benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619120	Mir106a	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920318	Fut11	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619440	Mir96	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347487	Foxm1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098644	Mfhas1	biomarker_via_orthology	DOID:4415	fibrous histiocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3606484	Kdm4d	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917329	Golm1	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102849	Klkb1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:37	skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96440	Igfbp5	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618737	Mir181c	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9563	bronchiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96235	Hsd3b3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96558	Il5ra	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:4033	bacterial gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676907	Mir30a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97513	Furin	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782634	Hsd3b9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98817	Hsp90b1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924285	Kdm8	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95818	Grik5	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2673307	Mafa	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196250	Klrk1	biomarker_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:0050920	tonsil squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676851	Mir187	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:255	hemangioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914718	Mmd	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109255	Gzmd	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96628	Jak1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:285	hairy cell leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313297	Gpr37	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:9182	pemphigus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	biomarker_via_orthology	DOID:4897	bile duct carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328364	Fmod	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926465	Hnrnpm	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917329	Golm1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298387	Fhl1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:9362	status asthmaticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:11162	respiratory failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195267	Ilk	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:12206	dengue hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914286	Mrpl45	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342771	Klf1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:3078	anaplastic astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102683	Grb7	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676812	Mir127	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309517	Itm2b	biomarker_via_orthology	DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926465	Hnrnpm	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619129	Mir224	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95776	Gnaq	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619431	Mir542	biomarker_via_orthology	DOID:7305	astroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95526	Fgg	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:0050782	Zollinger-Ellison syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96418	Idua	biomarker_via_orthology	DOID:12802	mucopolysaccharidosis I						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96022	Hbb-b2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676835	Mir150	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151139	Il22b	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676663	L3mbtl1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105077	Hsd17b1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101939	Hmgcs2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8506	bullous pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933966	Mcam	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347481	Foxc2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888513	Fzd2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1094	attention deficit hyperactivity disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:903	gastrointestinal lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109161	Grk5	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:3087	gingivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1313297	Gpr37	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346345	Map2k5	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:3491	Turner syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109256	Gzmc	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619382	Mir377	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:2468	psychotic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105052	Il13ra1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:10457	Legionnaires' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:2997	Sertoli-Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97007	Mmp10	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341721	Kcnh1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:1884	viral hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629927	Mir615	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	biomarker_via_orthology	DOID:680	tauopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107668	Ifna1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341803	Lipg	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96561	Il7	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:2280	hidradenitis suppurativa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:0060161	Kennedy's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:1673	pneumothorax						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:8649	tongue cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	biomarker_via_orthology	DOID:13208	background diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3826586	Hotair	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1687	neovascular glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96250	Hsp90aa1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105383	Il18r1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:13189	gout						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8881	rosacea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352745	Fscn1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	biomarker_via_orthology	DOID:8970	subacute sclerosing panencephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96067	Htt	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618735	Mir181b-1	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	biomarker_via_orthology	DOID:3594	choriocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341800	Hey1	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95683	Gdf1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	biomarker_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	biomarker_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1123	spondyloarthropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336881	Mok	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96949	Mdk	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107973	Igfals	biomarker_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:6713	cerebrovascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914631	Med4	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619412	Mir451a	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:9810	polyarteritis nodosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:0060672	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96188	Hoxb7	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676809	Mir125a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933966	Mcam	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104645	Hsd3b5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619441	Mir98	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448492	Kdm6b	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861377	Fgf21	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676883	Mir208a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346870	Map2k6	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:11077	brucellosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202398	Kera	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107662	Ifna6	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676856	Mir192	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:118	pericardial effusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619363	Mir34a	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676908	Mir30b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347487	Foxm1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:9498	pulmonary eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619365	Mir34c	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	biomarker_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675494	Gzmn	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676891	Mir215	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355307	Il22	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928482	Mbnl1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96550	Il2rb	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147790	Fermt3	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:1289	neurodegenerative disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619129	Mir224	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434255	Gapdh-ps15	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:9733	renal tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619363	Mir34a	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:0080933	immunoglobulin light chain amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96837	Ltf	biomarker_via_orthology	DOID:13689	prostate calculus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:589	congenital hemolytic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676897	Mir23a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619420	Mir483	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1475	lymphangioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619376	Mir375	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108570	Fzd7	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107661	Ifna7	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96437	Igfbp2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914342	Gatm	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:13450	coccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104644	Il15ra	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:0080933	immunoglobulin light chain amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3179	inverted papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3615275	Klk13	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:2055	post-traumatic stress disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109320	Mmp15	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:6812	childhood pilocytic astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0080552	congenital disorder of glycosylation Ia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333752	Hdac6	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342542	Ikzf3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:0111151	Prinzmetal angina						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100512	Mre11a	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676795	Mirlet7c-1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108083	Kcnq1	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107973	Igfals	biomarker_via_orthology	DOID:0060870	isolated growth hormone deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109267	Gzmb	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:631	fibromyalgia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:10887	lepromatous leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:9790	toxocariasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107420	Irak1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347466	Foxc1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:3049	Churg-Strauss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109334	Irs2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	biomarker_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106609	Gpx2	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	biomarker_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0050827	rheumatic heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	biomarker_via_orthology	DOID:0070004	myeloid neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195267	Ilk	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109161	Grk5	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:9741	biliary tract disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:5389	oxyphilic adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0080333	aortic valve disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353635	Lmcd1	biomarker_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100842	Gfra1	biomarker_via_orthology	DOID:3049	Churg-Strauss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	biomarker_via_orthology	DOID:8584	Burkitt lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:0080933	immunoglobulin light chain amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:8986	narcolepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99894	Hnrnpk	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:369	olfactory neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446977	Kif18a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914152	Mtap	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95697	Gfap	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:0111363	Heinz body anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332240	Heph	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96704	Krt7	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619063	Mir107	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96820	Lpl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355307	Il22	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676903	Mir27b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4079	heart valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354737	Kdm2b	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9498	pulmonary eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96016	Hba-a2	biomarker_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:5031	adult pineal parenchymal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96570	Inhba	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:13148	acute cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:8632	Kaposi's sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098221	Gamt	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:1697	ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676890	Mir214	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95675	Gch1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	biomarker_via_orthology	DOID:1911	endodermal sinus tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676904	Mir29a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:9159	gas gangrene						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95663	Gata3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917329	Golm1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346047	Gdf15	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919539	Malat1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915864	Letmd1	biomarker_via_orthology	DOID:363	uterine cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346867	Map2k2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917565	Hdac8	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346863	Mapk10	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3711284	Hsd3b8	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338074	Ikbkg	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107587	Irf9	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619065	Mir17	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104813	Jarid2	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:0070227	intrahepatic cholestasis of pregnancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96570	Inhba	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333813	Mbd2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96561	Il7	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105051	Ksr1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	biomarker_via_orthology	DOID:3603	mucinous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105383	Il18r1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:9065	leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104990	Gclc	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916790	Klk10	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:4441	dysgerminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	biomarker_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96558	Il5ra	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443308	Mcph1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9563	bronchiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96188	Hoxb7	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1197019	Kcns1	biomarker_via_orthology	DOID:9428	intracranial hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924825	Kmt2e	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:8472	localized scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107785	Mesp1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676835	Mir150	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106188	Gstt2	biomarker_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915864	Letmd1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107730	Hoxb13	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95654	Gart	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105383	Il18r1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619399	Mir411	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921054	Kif2c	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95494	Fcer1a	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676875	Mir200b	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96395	Irf8	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:9521	Laron syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619064	Mir10a	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676907	Mir30a	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:13481	thanatophoric dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96558	Il5ra	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8564	lip cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:4085	trophoblastic neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:1996	rectum adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105052	Il13ra1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:1781	thyroid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	biomarker_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95593	Fuca1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:12704	ataxia telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474852	Hbb-bs	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95698	Gfpt1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102503	mt-Co2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:1024	leprosy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:8536	herpes zoster						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:0111079	birdshot chorioretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:9778	irritable bowel syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	biomarker_via_orthology	DOID:3596	placental site trophoblastic tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354737	Kdm2b	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96673	Kcne1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96610	Itgb1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3718458	Mir193b	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99915	Lamb3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96437	Igfbp2	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:4031	eosinophilic gastroenteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619376	Mir375	biomarker_via_orthology	DOID:4033	bacterial gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916823	Hilpda	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109253	Gzmg	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917770	Glipr2	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	biomarker_via_orthology	DOID:8970	subacute sclerosing panencephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:9521	Laron syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355318	Il27ra	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328364	Fmod	biomarker_via_orthology	DOID:3087	gingivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:987	alopecia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1580	diffuse scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446977	Kif18a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619324	Mir301	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:0080375	gastroesophageal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96558	Il5ra	biomarker_via_orthology	DOID:350	mastocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:2942	bronchiolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96790	Lipe	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96551	Il2rg	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343094	Kat2b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179507	Fktn	biomarker_via_orthology	DOID:0050559	Fukuyama congenital muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104717	Meis1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:3044	food allergy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:12337	varicocele						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676875	Mir200b	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96236	Hsd3b4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109266	Gzma	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619358	Mir342	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333800	Il18bp	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95593	Fuca1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95583	Fshr	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333854	Gab2	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338056	Klf5	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	biomarker_via_orthology	DOID:8488	polyhydramnios						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619332	Mir320	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95823	Grin2d	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629945	Mir146b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155888	Il25	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96025	Hbb-bh2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87941	Grk3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109210	Ifna11	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107516	Gata6	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3525201	Mdc1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106609	Gpx2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196356	Iqsec1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	biomarker_via_orthology	DOID:11263	chlamydia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922762	Gpx6	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109191	Hfe	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	biomarker_via_orthology	DOID:0111947	immunodeficiency 21						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:4905	pancreatic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104815	Ier2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8481	rheumatic myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:12732	intermediate uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:4033	bacterial gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95498	Fcgr1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619439	Mir93	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104744	Kcnj2	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8691	mycosis fungoides						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:363	uterine cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109442	Itga8	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96234	Hsd3b2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619063	Mir107	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:5593	gastric papillary adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:1498	cholera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95716	Gja5	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96021	Hbb-b1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:1532	pleural disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676818	Mir133a-1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108426	Kif1b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107934	Mdm4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:12895	keratoconjunctivitis sicca						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618746	Mir1a-2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96837	Ltf	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107663	Ifna5	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629896	Mir665	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96599	Itga1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107664	Ifna4	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96437	Igfbp2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914113	Lztr1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107795	Hnrnpc	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641425	Ifna14	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927140	Git1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343094	Kat2b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96704	Krt7	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888992	Msln	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95753	Glud1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:1993	rectum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915864	Letmd1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:6595	gastric tubular adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102683	Grb7	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891340	Lpin1	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676324	Ifna12	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2667155	Ifna13	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96670	Kcnc4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107659	Ifna9	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:0060901	lymphoplasmacytic lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96550	Il2rb	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3718542	Mir493	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96561	Il7	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347078	Grk6	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95665	Gba1	biomarker_via_orthology	DOID:0050474	Netherton syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95560	Flt3l	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135593	Hadha	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96624	Itpr3	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96770	Lef1	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444886	Miat	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676818	Mir133a-1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96611	Itgb2	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151136	Lrp1b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109598	Hsd3b6	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109254	Gzmf	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676836	Mir151	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861379	Klk4	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676829	Mir144	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333752	Hdac6	biomarker_via_orthology	DOID:0050770	polycystic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346871	Map2k7	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99501	Fgb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2670976	Fez1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5474850	Hbb-bt	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	biomarker_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:5213	chronic inflammatory demyelinating polyradiculoneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109536	Itih4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96783	Lhcgr	biomarker_via_orthology	DOID:3114	serous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96912	Mag	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277979	Itgb2l	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:1657	ventricular septal defect						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385001	Fermt2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:962	neurofibroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333784	Hdac5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619332	Mir320	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136980	Kdm5a	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195267	Ilk	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:11030	corneal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:5453	pulmonary venoocclusive disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99894	Hnrnpk	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95915	H2-M3	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9362	status asthmaticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:12842	Guillain-Barre syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155888	Il25	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:3611	acute retinal necrosis syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153181	Hnmt	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:10590	mild pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097683	Ifnab	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618720	Mir133b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:750	peptic ulcer disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104815	Ier2	biomarker_via_orthology	DOID:0070323	childhood acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:3049	Churg-Strauss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95797	Gpi1	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	biomarker_via_orthology	DOID:2797	idiopathic interstitial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341884	Hey2	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	biomarker_via_orthology	DOID:1761	Melkersson-Rosenthal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913633	Iscu	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676848	Mir184	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:0080546	non-alcoholic fatty liver						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354692	Lsm4	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096392	Hcn1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151139	Il22b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107689	Kif3a	biomarker_via_orthology	DOID:10325	silicosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96837	Ltf	biomarker_via_orthology	DOID:65	connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442786	Mfsd4a	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:1037	lymphoid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676896	Mir22	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:5679	retinal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:0050873	follicular lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0111563	Sturge-Weber syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343101	Kat2a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95632	Gad1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344412	Ldb3	biomarker_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915391	Gpt2	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0080743	transverse myelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96015	Hba-a1	biomarker_via_orthology	DOID:1099	alpha thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349444	Haao	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342540	Ikzf1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101771	Kl	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:2527	nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684762	Lzts1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	biomarker_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96648	Jund	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649260	Ifna16	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107666	Ifna2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333784	Hdac5	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649418	Ifna15	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104554	Mitf	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342542	Ikzf3	biomarker_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:10456	tonsillitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:8463	corneal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109265	Gzme	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	biomarker_via_orthology	DOID:3304	germinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:8481	rheumatic myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346347	Mapk7	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:4250	conjunctivochalasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619363	Mir34a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922855	Kdm5b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95619	Gabrb1	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96995	Kmt2a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96108	Hlf	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:5016	hepatocellular clear cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4644	epidermolysis bullosa simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96704	Krt7	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95708	Ghr	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	biomarker_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:3382	liposarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196256	Kdm1a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:12351	alcoholic hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	biomarker_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182799	Kat7	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	biomarker_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619440	Mir96	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:0060180	colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96103	Hk1	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95835	Hspa5	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96235	Hsd3b3	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2662992	Mgat4a	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:11266	Hantavirus hemorrhagic fever with renal syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676856	Mir192	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196250	Klrk1	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2652894	Mapk15	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104815	Ier2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95752	Gls	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915864	Letmd1	biomarker_via_orthology	DOID:4451	renal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3711284	Hsd3b8	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619396	Mir409	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0070344	ocular tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:3179	inverted papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102503	mt-Co2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96794	Lmna	biomarker_via_orthology	DOID:0080334	aortic valve disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:0060691	platelet-type bleeding disorder 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346865	Mapk14	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:1107	esophageal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676888	Mir212	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:14256	adult-onset Still's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:319	spinal cord disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:10322	berylliosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	biomarker_via_orthology	DOID:1725	peritoneum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619063	Mir107	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:1724	duodenal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:0050744	anaplastic large cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346868	Map2k3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102469	Nfatc1	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619064	Mir10a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676897	Mir23a	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95640	Gapdh	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99913	Lamc2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104579	Il12rb1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179523	Fcgr4	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95602	Fyn	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202306	Hcrt	biomarker_via_orthology	DOID:11983	Prader-Willi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95942	H2-T10	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341800	Hey1	biomarker_via_orthology	DOID:5241	hemangioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097705	Kng1	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:14176	selective IgG deficiency disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96600	Itga2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921164	Irak3	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676896	Mir22	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145261	Kdm1b	biomarker_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98848	Tshb	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343961	Msh6	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107973	Igfals	biomarker_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933825	Jam3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:11832	visual epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676908	Mir30b	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:104	bacterial infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99502	Ltbp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109521	Htr2a	biomarker_via_orthology	DOID:0080546	non-alcoholic fatty liver						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346859	Mapk3	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96188	Hoxb7	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:3829	pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102850	Klk1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349428	Foxl2	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619364	Mir34b	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96817	Lox	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676897	Mir23a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676875	Mir200b	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276524	H2-M10.3	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96396	Id1	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434255	Gapdh-ps15	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676875	Mir200b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96273	Htr1a	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:0050169	cutaneous lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97322	Klk1b3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102694	Ptprm	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:1227	neutropenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309466	Gstm5	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:646	viral encephalitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106609	Gpx2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176887	Tlr8	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96742	Lalba	biomarker_via_orthology	DOID:2326	gastroenteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:853	polymyalgia rheumatica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96782	Lhb	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387123	Lnpep	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109128	Hnf4a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	biomarker_via_orthology	DOID:0060060	non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918490	Osbpl7	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333752	Hdac6	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:2297	leptospirosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102683	Grb7	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347473	Foxd3	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:3965	Merkel cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:10247	pleurisy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927899	Mmp19	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96441	Igfbp6	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892019	Klk1b1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	biomarker_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619421	Mir484	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95637	Gal	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676821	Mir136	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858179	Nucb2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95915	H2-M3	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676898	Mir23b	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861379	Klk4	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342771	Klf1	biomarker_via_orthology	DOID:1339	Diamond-Blackfan anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914767	Norad	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109320	Mmp15	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916790	Klk10	biomarker_via_orthology	DOID:363	uterine cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97824	Pvt1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619060	Mir106b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892023	Klk1b11	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104645	Hsd3b5	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891982	Klk1b16	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:13208	background diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96787	Lif	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892020	Klk1b5	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95520	Fgf6	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105383	Il18r1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95820	Grin2a	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354736	Kdm2a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1924	hypogonadism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96382	Iapp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109347	Lum	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:11476	osteoporosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861377	Fgf21	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:11656	cicatricial pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96441	Igfbp6	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676875	Mir200b	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676890	Mir214	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:224	transient cerebral ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:77	gastrointestinal system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:1697	ichthyosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629597	Mir488	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676835	Mir150	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104853	Hes1	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1067	open-angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102683	Grb7	biomarker_via_orthology	DOID:1107	esophageal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97175	Map2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96233	Hsd3b1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109598	Hsd3b6	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:4250	conjunctivochalasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:627	severe combined immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:9663	aphthous stomatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:8566	herpes simplex						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109267	Gzmb	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915023	Kat8	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99418	Itpr2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102858	Fosl2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:0050904	salivary gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:9008	psoriatic arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:1205	allergic disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663985	Kiss1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101947	Hnrnpd	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346877	Map3k7	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96250	Hsp90aa1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:11506	suppurative otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100860	Frs2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336200	Hpca	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676865	Mir199b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316726	Fga	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892014	Sfrp1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676905	Mir29b-1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96976	Mgp	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:8649	tongue cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95729	Gli3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:934	viral infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892022	Klk1b21	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101787	mt-Nd1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109323	Htr2b	biomarker_via_orthology	DOID:0080546	non-alcoholic fatty liver						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96560	Il6st	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097705	Kng1	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:4250	conjunctivochalasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859179	Irf3	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915661	Map1lc3a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316731	Stc2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:11263	chlamydia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676811	Mir126a	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915023	Kat8	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109265	Gzme	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:1790	malignant mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676833	Mir148a	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629896	Mir665	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:9409	diabetes insipidus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:0111563	Sturge-Weber syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107655	Ifngr1	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:3565	meningioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96648	Jund	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181693	Il23r	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106038	Lrrn1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105979	G6pdx	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95901	H2-Eb1	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8549	chronic ulcer of skin						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96615	Itgb6	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342287	Klf4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352745	Fscn1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333871	Hsd17b10	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676817	Mir132	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891981	Klk1b26	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96590	Irf1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97172	Mt2	biomarker_via_orthology	DOID:2468	psychotic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:4226	endometrial stromal sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619066	Mir221	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676896	Mir22	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96545	Il1r1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102498	mt-Nd4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333800	Il18bp	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890472	Il19	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96778	Lgals3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96250	Hsp90aa1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102779	Fen1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892021	Klk1b24	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96563	Il9	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333871	Hsd17b10	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104815	Ier2	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916790	Klk10	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446210	Kdm4a	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892018	Klk1b8	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96416	Ido1	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:0080539	PEHO syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:9498	pulmonary eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298398	Mcm7	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95561	Flt4	biomarker_via_orthology	DOID:1475	lymphangioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618750	Mir200c	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96247	Hsp90ab1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:9563	bronchiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95556	Flna	biomarker_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96382	Iapp	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99533	Mef2d	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:4959	epidermolysis bullosa dystrophica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3718458	Mir193b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890475	Il21r	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96623	Itpr1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:0080652	calcium oxalate nephrolithiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0111563	Sturge-Weber syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924104	Gper1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97076	Mpl	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95588	Fth1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343094	Kat2b	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3525201	Mdc1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95616	Gabra4	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333800	Il18bp	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107490	Pdcd4	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96533	Ihh	biomarker_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:4325	Ebola hemorrhagic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2683854	Klhl41	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95607	G6pc1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98763	Tk1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104993	Lepr	biomarker_via_orthology	DOID:5016	hepatocellular clear cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676888	Mir212	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888513	Fzd2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097166	Tcl1	biomarker_via_orthology	DOID:5603	T-cell acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2665139	Rerg	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:10952	nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891835	Hdac7	biomarker_via_orthology	DOID:986	alopecia areata						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:4465	papillary renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109526	Trpc3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:4079	heart valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105384	Hspa8	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	biomarker_via_orthology	DOID:13271	cutaneous porphyria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921373	Foxp4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	biomarker_via_orthology	DOID:3113	papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923356	Kdm3b	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336161	Klrc1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104756	Itga9	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676825	Mir140	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619332	Mir320	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347078	Grk6	biomarker_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:8568	infectious mononucleosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676904	Mir29a	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96413	Idh1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278315	Lrp5	biomarker_via_orthology	DOID:4079	heart valve disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102688	H2ax	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97007	Mmp10	biomarker_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182799	Kat7	biomarker_via_orthology	DOID:4674	androgen insensitivity syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104820	Hnrnpa1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:5577	gastrinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96662	Kcna5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95757	Slc2a3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915391	Gpt2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95524	Fgfr3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675494	Gzmn	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861379	Klk4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891835	Hdac7	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109254	Gzmf	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103170	Gfi1	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109267	Gzmb	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676859	Mir195a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914664	Mfn1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	biomarker_via_orthology	DOID:4471	chromophobe renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676904	Mir29a	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341884	Hey2	biomarker_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676857	Mir193a	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95293	Klk1b9	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619355	Mir340	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890473	Il20	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104816	Hnrnpl	biomarker_via_orthology	DOID:1319	brain cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676824	Mir139	biomarker_via_orthology	DOID:3073	brain glioblastoma multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:7736	retinal telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351345	Grm8	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:401	multidrug-resistant tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:87940	Grk2	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96549	Il2ra	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:11265	trachoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276570	H2-M9	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146636	Hrg	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149728	Impa2	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109256	Gzmc	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915383	Gcsh	biomarker_via_orthology	DOID:9252	amino acid metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104566	Fgd1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95728	Gli2	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97137	Mpo	biomarker_via_orthology	DOID:9362	status asthmaticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96412	Ide	biomarker_via_orthology	DOID:0050850	diabetic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352745	Fscn1	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618716	Mir130b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107973	Igfals	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109253	Gzmg	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270855	Il16	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96234	Hsd3b2	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:9620	vesicoureteral reflux						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629917	Mir19b-1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336200	Hpca	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346858	Mapk1	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:4166	syphilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619064	Mir10a	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96546	Il1r2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450574	Ifnl3	biomarker_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0070227	intrahepatic cholestasis of pregnancy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676904	Mir29a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:13767	clonorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:2938	Epstein-Barr virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928676	Htra2	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3027157	Kng2	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97621	Plk1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276527	H2-M10.4	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95802	Gpt	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105304	Il6ra	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355307	Il22	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	biomarker_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202395	Mmp8	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333744	Gp1ba	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914981	Fbxo32	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:4358944	Mir432	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:13276	Mycoplasma pneumoniae pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96245	Hspa9	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346862	Mapk9	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138151	Kmo	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924384	Hnrnpa0	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913975	Lrrk2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:409	liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921394	Robo4	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95522	Fgfr1	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107504	Gip	biomarker_via_orthology	DOID:11465	autonomic nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95931	H2-Q2	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:2797	idiopathic interstitial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341721	Kcnh1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98874	Txn1	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105052	Il13ra1	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333800	Il18bp	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:4250	conjunctivochalasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:1387	hypolipoproteinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194891	Gpc1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98257	Msr1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109564	Kif5a	biomarker_via_orthology	DOID:7596	asbestos-related lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96240	Hspb1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:10128	venous insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97005	Mmp12	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629661	Mir592	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338947	S100a9	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96564	Il9r	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:3454	brain infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3027157	Kng2	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96236	Hsd3b4	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350924	Irf5	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196250	Klrk1	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96787	Lif	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95574	Fos	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109565	Kmt2b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:1824	status epilepticus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96242	Hspd1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95727	Gli1	biomarker_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352753	Gipr	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:350	mastocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95589	Ftl1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97173	Mt3	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96977	Mgmt	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106026	Gstm3	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96539	Il12a	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95678	Gda	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96575	Insr	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104720	Hsd11b2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:3827	congenital diaphragmatic hernia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916823	Hilpda	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107973	Igfals	biomarker_via_orthology	DOID:8689	anorexia nervosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196250	Klrk1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919539	Malat1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2682319	Kmt2d	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384409	Il27	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101816	Msh2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96612	Itgb3	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860604	Gucy1b1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890473	Il20	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618734	Mir148b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101938	Mlh1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:0060061	primary cutaneous T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619118	Mir222	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924825	Kmt2e	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109255	Gzmd	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95895	H2-Aa	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782634	Hsd3b9	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96601	Itga2b	biomarker_via_orthology	DOID:0060691	platelet-type bleeding disorder 16						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:4606	bile duct cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95851	Gsn	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96924	Mbl2	biomarker_via_orthology	DOID:12375	bronchopneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096873	Irf4	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96441	Igfbp6	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103014	Il15	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384588	Neil3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96646	Jun	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930008	Ghrl	biomarker_via_orthology	DOID:11983	Prader-Willi syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618746	Mir1a-2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0080746	Sweet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:8553	pyoderma gangrenosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618737	Mir181c	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202886	Meg3	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676860	Mir196a-1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:4250	conjunctivochalasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676907	Mir30a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629888	Mir423	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0080334	aortic valve disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676839	Mir154	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95523	Fgfr2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:3033	colon signet ring adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890081	Foxo3	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:11678	onchocerciasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342771	Klf1	biomarker_via_orthology	DOID:0090016	chromosome 5q deletion syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619404	Mir433	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347093	Fto	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914211	Neat1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342292	Hspa4	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:9446	cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2687364	H2-M10.6	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95933	H2-Q4	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653863	Gpbar1	biomarker_via_orthology	DOID:0110861	autosomal recessive polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676844	Mir18	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96224	Hras	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444959	Kmt2c	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:11111	hydronephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109265	Gzme	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99781	Kdm5c	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104903	Gpc3	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916782	Hopx	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:0014667	disease of metabolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196294	Fubp1	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2385078	Gstp3	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:4866	salivary gland adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:3963	thyroid gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95661	Gata1	biomarker_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102683	Grb7	biomarker_via_orthology	DOID:0050922	gastrointestinal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97180	Mapt	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3708786	Gapdhrt2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342540	Ikzf1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3647279	Ifnl2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95832	Grn	biomarker_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95860	Gstm1	biomarker_via_orthology	DOID:299	adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277954	Il13ra2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619266	Mir25	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:10983	Alport syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101769	Mcl1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:13328	diabetic cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95805	Grb2	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98504	Hnf1a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:4250	conjunctivochalasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676828	Mir143	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96572	Ins1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:8536	herpes zoster						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338009	Irs4	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98427	Il1rl1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676896	Mir22	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2653863	Gpbar1	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924825	Kmt2e	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95959	H2-T3	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619363	Mir34a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:10241	thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95928	H2-Q1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107430	Gdnf	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	biomarker_via_orthology	DOID:13375	temporal arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95864	Gstp2	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892032	Frzb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104887	Gpx1	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0080746	Sweet syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:13413	hepatic encephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95575	Fosb	biomarker_via_orthology	DOID:9973	substance dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:4029	gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96677	Kit	biomarker_via_orthology	DOID:6171	uterine carcinosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:8997	polycythemia vera						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159682	Havcr2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346876	Map3k5	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448492	Kdm6b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098275	Gse1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96540	Il12b	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107179	Fosl1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341155	Gldc	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1309467	Gstm6	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106918	Hif1a	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95739	Glul	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098269	Kif5c	biomarker_via_orthology	DOID:0110042	Alzheimer's disease 3						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95913	H2-M1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96573	Ins2	biomarker_via_orthology	DOID:1920	hyperuricemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95935	H2-Q6	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676860	Mir196a-1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105367	Il4ra	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99913	Lamc2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1278342	Lect2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95707	Gh	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629656	Mir671	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102849	Klkb1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298398	Mcm7	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:824	periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95521	Fgf7	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95706	Ggt1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353633	Fus	biomarker_via_orthology	DOID:1115	sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3718454	Mir18b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:1394	urinary schistosomiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782011	Gapdhrt	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95494	Fcer1a	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96922	Mb	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96433	Igf1r	biomarker_via_orthology	DOID:5577	gastrinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619370	Mir363	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109255	Gzmd	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676905	Mir29b-1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95929	H2-Q10	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96112	Hmbs	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:12662	paracoccidioidomycosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:8553	pyoderma gangrenosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8472	localized scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95713	Gja1	biomarker_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95662	Gata2	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277957	Kcnn4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347472	Foxa1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:4251	conjunctival disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96556	Il4	biomarker_via_orthology	DOID:0050634	alopecia universalis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96435	Igf2r	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442355	Kdm4b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95902	H2-Eb2	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109256	Gzmc	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96607	Itgam	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5434102	Ftl1-ps2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95590	Ftl2-ps	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890077	Foxo1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1316736	Men1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889810	Gp6	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913687	Fis1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277947	Fhit	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619064	Mir10a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96257	Hspg2	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:3904	bronchus carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276578	Gfi1b	biomarker_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924104	Gper1	biomarker_via_orthology	DOID:14320	generalized anxiety disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:0080158	herpes simplex virus keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619330	Mir31	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107730	Hoxb13	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676827	Mir142	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99604	Fgf8	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915864	Letmd1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96216	Lipc	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343166	Klk6	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914004	Foxp1	biomarker_via_orthology	DOID:0090131	complex cortical dysplasia with other brain malformations						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676837	Mir152	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921164	Irak3	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95936	H2-Q7	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917329	Golm1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104819	Hnrnpa2b1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346861	Mapk8	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676817	Mir132	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:0080784	urinary tract infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96569	Inha	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914059	Krt20	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105102	Gpx3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108520	Fzd4	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96441	Igfbp6	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858732	Keap1	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96922	Mb	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106035	Mki67	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676637	H2-M11	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:5327	retinal detachment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346878	Map3k8	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:1858	McCune Albright syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109254	Gzmf	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:9271	ornithine carbamoyltransferase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95865	Gstp1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95558	Flt1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675494	Gzmn	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108085	Hpgd	biomarker_via_orthology	DOID:6255	growth hormone secreting pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96562	Il7r	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:8704	genital herpes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:331	central nervous system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95861	Gstm2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96547	Il1rn	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104797	Lta	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676805	Mir122	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:1586	rheumatic fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:10017	multiple endocrine neoplasia type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276525	H2-M10.2	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346866	Map2k1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96113	Hmgb1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346872	Map3k1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95499	Fcgr2b	biomarker_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95956	H2-T22	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104767	Gpx4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:5477161	Mir155hg	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2136381	Hadhb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96543	Il1b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2148793	Kiss1r	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894659	Hbp1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95833	Grp	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95819	Grin1	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96211	Hp	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3039605	Timd6	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892032	Frzb	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	biomarker_via_orthology	DOID:3369	Ewing sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097691	Hdac2	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96668	Kcnc2	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095419	Kdm6a	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3718458	Mir193b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96552	Il3	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676881	Mir206	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924825	Kmt2e	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619129	Mir224	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159680	Havcr1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96163	Hmox1	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96432	Igf1	biomarker_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933847	Mmp1b	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96542	Il1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96629	Jak2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676812	Mir127	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932051	Kat5	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97009	Mmp2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95559	Flt3	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95915	H2-M3	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619363	Mir34a	biomarker_via_orthology	DOID:11294	arteriovenous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891980	Klk1b27	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95717	Gja6	biomarker_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3615275	Klk13	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109253	Gzmg	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95709	Ghrh	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107656	Ifng	biomarker_via_orthology	DOID:9065	leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95904	H2-K1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96952	Mdm2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95669	Gc	biomarker_via_orthology	DOID:12205	dengue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619348	Mir335	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98847	Kdm3a	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929076	Htra1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103189	Mmp7	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890226	Fxyd6	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:865	vasculitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:2508	Takayasu's arteritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107364	Il17a	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96721	L1cam	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917329	Golm1	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95896	H2-D1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629651	Mir491	biomarker_via_orthology	DOID:8649	tongue cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3619426	Mir494	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96692	Krt18	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108086	Hdac1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349394	Map4k4	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96414	Idh2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96434	Igf2	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782108	Gstp-ps	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676830	Mir145a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99454	Irs1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95525	Fgfr4	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96650	Jup	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105977	G6pd2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104663	Lep	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2151139	Il22b	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96392	Icam1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346869	Map2k4	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95777	Gnas	biomarker_via_orthology	DOID:0080222	pseudohypoparathyroidism type IB						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891925	Hnrnph1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924054	Kdm4c	biomarker_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96436	Igfbp1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861437	Gsk3b	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95291	Klk1b22	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276522	H2-M10.1	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342541	Ikzf2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442230	Mfn2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276526	H2-M10.5	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676872	Mir20a	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3629886	Mir497	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95912	H2-L	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106609	Gpx2	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3618741	Mir196b	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676831	Mir146	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96283	Htr5a	biomarker_via_orthology	DOID:9428	intracranial hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95566	Fn1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340026	Mmp13	biomarker_via_orthology	DOID:1245	vulva cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97010	Mmp3	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890474	Il21	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2159681	Timd2	biomarker_via_orthology	DOID:12556	acute kidney tubular necrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95593	Fuca1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:0080207	CAKUT2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95513	Fech	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96683	Kdr	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98735	Th	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95790	Gnrhr	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107379	Gstt1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96541	Il13	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95515	Fgf1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96438	Igfbp3	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96660	Kcna3	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913633	Iscu	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96557	Il5	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676856	Mir192	biomarker_via_orthology	DOID:13768	opisthorchiasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96757	Lcn2	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3036234	Hdac4	biomarker_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676890	Mir214	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	biomarker_via_orthology	DOID:686	liver carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330294	Hnrnpab	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147134	Fbxo11	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:13922	eosinophilic esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924007	Trdn	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96680	Kras	biomarker_via_orthology	DOID:6726	fibrillary astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96648	Jund	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95900	H2-Ea	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96548	Il2	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96244	Hspa1a	biomarker_via_orthology	DOID:9651	systolic heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95914	H2-M2	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103562	Hsd11b1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95804	Gsr	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676840	Mir155	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95917	H2-M5	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891436	Foxp3	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95500	Fcgr3	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96079	Hgf	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95821	Grin2b	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97004	Mme	biomarker_via_orthology	DOID:9246	cerebral amyloid angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685113	Macc1	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684360	Mir223	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676886	Mir210	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095416	Jag1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97320	Klk1b4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343091	Hdac3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:0110276	autosomal recessive limb-girdle muscular dystrophy type 2B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102688	H2ax	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107936	Il18	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97011	Mmp9	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96982	Mif	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104723	Fgf9	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101900	Mmp14	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650838	Timd5	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96537	Il10	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924375	Il33	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933846	Mmp1a	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95516	Fgf2	biomarker_via_orthology	DOID:9810	polyarteritis nodosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96647	Junb	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859086	Irx5	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96559	Il6	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95636	Galc	biomarker_via_orthology	DOID:13276	Mycoplasma pneumoniae pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96969	Met	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:2006	preretinal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99829	Runx2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109297	Slpi	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8717	decubitus ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890615	Panx2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107876	Uqcrc1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97385	Ntrk3	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	biomarker_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:1798	pancreatic endocrine carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88244	S100a8	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927259	Trpv6	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917128	Snrpf	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:1459	hypothyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103021	Recql	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351645	Prmt5	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387581	Ppp1r9b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	biomarker_via_orthology	DOID:1911	endodermal sinus tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109338	Rap1gap	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101783	Plk4	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351630	Sergef	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	biomarker_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97596	Prkcb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855696	Tslp	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:3672	rhabdoid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108212	Ripk1	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107365	Ube2i	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202879	Tcf7l2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95994	Selenos	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351641	Naglu	biomarker_via_orthology	DOID:12801	mucopolysaccharidosis III						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1588	thrombocytopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98460	Syn1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142572	Mtus1	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:3702	cervical adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:8534	gastroesophageal reflux disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914291	Oxct1	biomarker_via_orthology	DOID:2978	carbohydrate metabolic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276523	Ncoa1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:768	retinoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97386	Ntsr1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203729	Pik3c2a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	biomarker_via_orthology	DOID:10608	celiac disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98287	Srsf5	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923650	Pbp2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104562	Napb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	biomarker_via_orthology	DOID:4441	dysgerminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920145	Setd5	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:12549	hepatitis A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347007	Plod2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:0060322	mastoiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349165	Sdc2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109579	Serpinb5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98474	Tac1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:3672	rhabdoid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336212	Ncr1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329012	Slc22a5	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:0111582	hereditary arterial and articular multiple calcification syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104528	S100g	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918089	P2ry12	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97795	Ptger3	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913974	Tab3	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:0080379	nephrotic syndrome type 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150380	Srd5a2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98216	Rxrg	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145955	Prkaa1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916457	Srsf11	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95994	Selenos	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102756	Try5	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:9498	pulmonary eosinophilia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338031	Spint2	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103581	Musk	biomarker_via_orthology	DOID:437	myasthenia gravis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109292	Rad50	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:2797	idiopathic interstitial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341839	Nod1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	biomarker_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98484	Tap2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109524	Trpc5	biomarker_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102851	Pdx1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336212	Ncr1	biomarker_via_orthology	DOID:0060704	lymphoproliferative syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109277	Pik3r3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:10595	Charcot-Marie-Tooth disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106028	Rhoc	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913974	Tab3	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:0080827	human cytomegalovirus infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921559	Osbp2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3782198	Tmed10-ps	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386711	Txnrd3	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:8929	atrophic gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201787	Socs2	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933159	Rnf114	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	biomarker_via_orthology	DOID:8541	Sezary's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444341	Phf8	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276523	Ncoa1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:0070355	overactive bladder syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929600	Pmepa1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144114	Tug1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:0081294	neuronal intranuclear inclusion disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:13515	tuberous sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102758	Prss3	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:11263	chlamydia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855696	Tslp	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107163	Ppp3cb	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104896	Srsf9	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:2224	essential thrombocythemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97486	Pax2	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892014	Sfrp1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179725	Ovca2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:1591	renovascular hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97502	Pcmt1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:12241	beta thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2651811	Tph2	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:7736	retinal telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101058	Tnfsf9	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104562	Napb	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107164	Ppp3ca	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:1826	epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920180	Ppp2r2b	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153470	Scgb3a2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918910	Rarres2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95757	Slc2a3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:3049	Churg-Strauss syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102757	Try4	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930943	Rrad	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202864	Myoc	biomarker_via_orthology	DOID:1070	primary open angle glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:3713	ovary adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96739	Stmn1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337080	Ncor2	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098772	Pik3r2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3641889	Prss3l	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98848	Tshb	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:12918	thromboangiitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8536	herpes zoster						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3087	gingivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858303	Srrm1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929481	Slc22a21	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98330	Snai1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106581	Tsg101	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101857	Usp15	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:700010	Sh3gl1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340062	Sgk1	biomarker_via_orthology	DOID:3603	mucinous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142572	Mtus1	biomarker_via_orthology	DOID:4866	salivary gland adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350932	Ncoa4	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153470	Scgb3a2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:0080827	human cytomegalovirus infection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913745	Ndufb3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98251	Scn5a	biomarker_via_orthology	DOID:0050431	arrhythmogenic right ventricular cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:4606	bile duct cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920982	Muc16	biomarker_via_orthology	DOID:9368	keratoconjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99260	Prkci	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:9146	visceral leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2675303	Tnfrsf14	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:3672	rhabdoid cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109408	Reg3a	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684864	Pfas	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106926	Mttp	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:853	polymyalgia rheumatica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98387	Sptb	biomarker_via_orthology	DOID:12971	hereditary spherocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98467	Syp	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:5593	gastric papillary adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97385	Ntrk3	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97447	Osbp	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429764	Trpv5	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98742	Thra	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:3798	pleural empyema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102778	Six2	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97440	Oprl1	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:3178	skin papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108072	Traf6	biomarker_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109520	Pafah1b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99511	Ptpn11	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921382	Rnf6	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:0050157	cryptogenic organizing pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894288	Selenop	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1194921	Ttk	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109523	Trpc6	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1925226	Nuak1	biomarker_via_orthology	DOID:13223	uterine fibroid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347355	Slc7a11	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351872	Slco2b1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	biomarker_via_orthology	DOID:10772	thrombotic thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347347	Slc27a4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101058	Tnfsf9	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	biomarker_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:3458	breast adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:4677	keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101924	Slc12a2	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:10320	asbestosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97509	Pcp4	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	biomarker_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339712	Myh8	biomarker_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:9810	polyarteritis nodosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926224	Rbfox1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098772	Pik3r2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:6595	gastric tubular adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0081312	T-cell non-Hodgkin lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915831	Tmed10	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277179	Pde9a	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99682	Tmbim6	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104511	Tnfsf4	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3644625	Uba52-ps	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88192	Smarca4	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:13514	venous tributary occlusion of retina						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	biomarker_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859650	Ramp2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95758	Slc2a4	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9884	muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97352	Nkx3-1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108395	Vnn1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:0112313	brain small vessel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351320	Trp53bp1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915309	Tm9sf2	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12297	Vogt-Koyanagi-Harada disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927126	Slc5a7	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341157	Sox30	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103294	Prg2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:3495	extrahepatic bile duct adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107557	Sema3c	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:0060643	primary sclerosing cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921394	Robo4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2145895	Slc38a1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104805	Snrpb2	biomarker_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0111253	neurofibromatosis 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107996	Slc8a2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97723	Pnliprp1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:1073	renal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270156	Septin4	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:0050157	cryptogenic organizing pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109573	Tep1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	biomarker_via_orthology	DOID:10908	hydrocephalus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444210	Nr1d1	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108024	Rgn	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890577	Srsf4	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99682	Tmbim6	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104671	Tfap2a	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147616	Otub1	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12306	vitiligo						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926424	Nelfcd	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442211	Prrg4	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101783	Plk4	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050475	Weill-Marchesani syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:0050746	mantle cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155600	Myh7	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202880	Traf4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:0080016	spina bifida						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:799	varicose veins						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1337080	Ncor2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98874	Txn1	biomarker_via_orthology	DOID:820	myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914302	Ndc80	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:3493	signet ring cell adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98299	Shmt1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:0080159	Cryptococcal meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	biomarker_via_orthology	DOID:2862	glucosephosphate dehydrogenase deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923810	Prss8	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:0080899	lung pleomorphic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98342	Snrpb	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353576	Pik3cg	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2179715	Plaat3	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:678	progressive supranuclear palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684864	Pfas	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98935	Vldlr	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704271	Ptges3-ps	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859993	Smad9	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:3905	lung carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9651	systolic heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97613	Plcb1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:0050731	vitamin B12 deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:4202	brain stem glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95757	Slc2a3	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	biomarker_via_orthology	DOID:6419	tetralogy of Fallot						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142572	Mtus1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:6039	uveal melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101782	Scnn1a	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:3121	gallbladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98366	Sox4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859152	Pla2g6	biomarker_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98812	Tpmt	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97502	Pcmt1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8506	bullous pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3179	inverted papilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98874	Txn1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97549	Pfn1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914603	Rab31	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109338	Rap1gap	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:9220	central sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:6255	growth hormone secreting pituitary adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:1168	familial hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:8691	mycosis fungoides						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107543	Sox17	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	biomarker_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97509	Pcp4	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3646222	Prss1l	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:12148	alveolar echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107163	Ppp3cb	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923810	Prss8	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929600	Pmepa1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:6364	migraine						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:9206	Barrett's esophagus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344414	Sra1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97760	Prkar2b	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:9253	gastrointestinal stromal tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:3073	brain glioblastoma multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12895	keratoconjunctivitis sicca						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:0111144	preterm premature rupture of the membranes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339708	Neurod1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919583	Palld	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103294	Prg2	biomarker_via_orthology	DOID:1725	peritoneum cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:13068	renal osteodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101783	Plk4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	biomarker_via_orthology	DOID:4159	skin cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3687012	Try10	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:639	acute disseminated encephalomyelitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916703	Prss56	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343262	Timm44	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88244	S100a8	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927243	Rala	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:12554	hemolytic-uremic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95834	Pdia3	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:0050904	salivary gland carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:83	cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97572	Phb1	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:3308	embryonal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:1687	neovascular glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929282	Ptges3	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919247	Smg9	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:4762	vasculogenic impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446138	Phactr2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:2006	preretinal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:8869	neuromyelitis optica						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:9719	neovascular inflammatory vitreoretinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	biomarker_via_orthology	DOID:11624	penile benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98763	Tk1	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894675	Tnfrsf18	biomarker_via_orthology	DOID:321	tropical spastic paraparesis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101884	Ppard	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914528	Pagr1a	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107717	Myh9	biomarker_via_orthology	DOID:0060651	MYH-9 related disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1860292	Ramp3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101759	Rnf2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201691	Rnf4	biomarker_via_orthology	DOID:1932	Angelman syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929282	Ptges3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:10460	nasopharyngitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041197	Serpina7	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:936	brain disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109338	Rap1gap	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894288	Selenop	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340062	Sgk1	biomarker_via_orthology	DOID:2999	granulosa cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923385	Prex2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:4166	syphilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154952	Ripk3	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855692	Nono	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9563	bronchiectasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97749	Ppia	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276574	Nsd2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095438	Slc2a2	biomarker_via_orthology	DOID:5577	gastrinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:4074	pancreatic adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387581	Ppp1r9b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108466	Ralbp1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102759	Prss2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:2451	protein S deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	biomarker_via_orthology	DOID:0050425	restless legs syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344408	Pebp1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:1287	cardiovascular system disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107173	Serpinf2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920982	Muc16	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:1107	esophageal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2676278	Muc19	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176375	Ucn2	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97496	Pbx3	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:4195	hyperglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:3594	choriocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:2559	opiate dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142572	Mtus1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:657	adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0050185	erythema multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347075	Nbea	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97363	Notch1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858171	Tlr5	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929600	Pmepa1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98285	Srsf3	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932915	Ndel1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:3314	angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2447992	Trim63	biomarker_via_orthology	DOID:14557	primary pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98839	Prss1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931744	Uck2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927184	Nrgn	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:3594	choriocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919907	Selenoh	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181407	Trpv3	biomarker_via_orthology	DOID:8881	rosacea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	biomarker_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916686	Mtfp1	biomarker_via_orthology	DOID:0060369	Parkinson's disease 6						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	biomarker_via_orthology	DOID:2156	ovarian germ cell cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277179	Pde9a	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:0080207	CAKUT2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:0112313	brain small vessel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109604	Plk3	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:9952	acute lymphoblastic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156378	Rnf39	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:13891	bird fancier's lung						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:0080771	beta-thalassemia major						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	biomarker_via_orthology	DOID:0050153	pulmonary aspergilloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109338	Rap1gap	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103294	Prg2	biomarker_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97742	Pomc	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:2216	factor V deficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:0050853	chronic venous insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340062	Sgk1	biomarker_via_orthology	DOID:3114	serous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107162	Ppp3cc	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96055	Ptpn6	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353431	Pcsk1n	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107949	Rhob	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107164	Ppp3ca	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:14018	alcoholic liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:8867	molluscum contagiosum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684864	Pfas	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:9513	plasma cell leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104637	Tgfbr3	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97897	Rel	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:891	progressive myoclonus epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107170	Ptpn22	biomarker_via_orthology	DOID:1040	chronic lymphocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108470	St6gal1	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442401	Ppp1r9a	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107365	Ube2i	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97475	Pam	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:8866	actinic keratosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97301	Nedd8	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104662	Pml	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351625	Nbn	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:1996	rectum adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920982	Muc16	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:9669	senile cataract						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3649356	Uba52rt	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:0040089	autoimmune optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387629	Tardbp	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:11713	diabetic angiopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:8725	vascular dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8463	corneal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098693	Tet1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353431	Pcsk1n	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346834	Nr5a2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:13550	angle-closure glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	biomarker_via_orthology	DOID:9446	cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0050589	inflammatory bowel disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104662	Pml	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351872	Slco2b1	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350932	Ncoa4	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98344	Snrpd1	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341295	Tlr1	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:0060669	cerebral cavernous malformation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97806	Ptpn2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95627	Slc6a1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349717	Ncor1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104311	Ptger4	biomarker_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:3840	craniopharyngioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:0060573	von Willebrand's disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:0050811	congenital adrenal hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588263	Muc3a	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:341	peripheral vascular disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95757	Slc2a3	biomarker_via_orthology	DOID:3138	acanthosis nigricans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:13544	low tension glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97598	Prkcd	biomarker_via_orthology	DOID:10762	portal hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923385	Prex2	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:11339	pneumocystosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	biomarker_via_orthology	DOID:1574	alcohol use disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97902	Ret	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:2913	acute pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:4896	bile duct adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97359	Nodal	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1917834	Pak4	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	biomarker_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:9368	keratoconjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108016	Rad21	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2659021	Phactr1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:893598	Sh2b3	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2181726	Mtnr1b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894288	Selenop	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97816	Ptprz1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98507	Tcf7	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:1074	kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914302	Ndc80	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1555	urticaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:13809	familial combined hyperlipidemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97301	Nedd8	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:8337	appendicitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:1679	cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	biomarker_via_orthology	DOID:1884	viral hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442543	Vash1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2386711	Txnrd3	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345279	Slc11a2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:3457	invasive lobular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98887	Uba52	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2183102	Sardh	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	biomarker_via_orthology	DOID:2917	cryoglobulinemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104785	Myo6	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336884	Slc22a18	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:3702	cervical adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704271	Ptges3-ps	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88244	S100a8	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920145	Setd5	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103187	Nqo1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:14323	Marfan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98287	Srsf5	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11656	cicatricial pemphigoid						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:0111535	progressive osseous heteroplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342005	Mthfd1	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:1247	blood coagulation disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930125	Pdcd1lg2	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2684909	Stox1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:576	proteinuria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88095	Serpinc1	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2448536	Pdap1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0060688	arteriovenous malformations of the brain						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336884	Slc22a18	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892877	Pld2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:0050700	cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277152	Parl	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920982	Muc16	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341870	Stk11	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894675	Tnfrsf18	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927470	Spag5	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98366	Sox4	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0050847	sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:11963	esophagitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:4033	bacterial gastritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98475	Tacr1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:5016	hepatocellular clear cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8515	Cor pulmonale						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298226	Naip2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	biomarker_via_orthology	DOID:0050073	invasive aspergillosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104859	Selenbp2	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101058	Tnfsf9	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98759	Tjp1	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:3113	papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97807	Ptpn5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663233	Muc6	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101931	Slc1a2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99261	Ptgds	biomarker_via_orthology	DOID:11664	nephrosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97566	Pgm3	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108082	Npy5r	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2755	Mycobacterium avium complex disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913604	Snw1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099446	Synpo	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:263	kidney cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108037	Vegfd	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915246	Srsf6	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	biomarker_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97890	Rad51	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109393	Slc4a1	biomarker_via_orthology	DOID:2373	hereditary elliptocytosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918898	Optn	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109486	Prdx2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:4977	lymphedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:3030	mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:11723	Duchenne muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:10772	thrombotic thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3040696	Prex1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97478	Reg3b	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2157785	Peg10	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:0080001	bone disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915261	Snrpg	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923385	Prex2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103289	Relb	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:3702	cervical adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:2316	brain ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444777	Ncaph	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99445	Mtpn	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:13949	interstitial cystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98180	Rrm1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2685936	Plpp4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914152	Mtap	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918573	Rassf8	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:10976	membranous glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923810	Prss8	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:14453	farmer's lung						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914514	Ndufb8	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104512	Tnfrsf4	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104740	Ppara	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:3627	aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:3304	germinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298223	Naip1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3032636	Ugt1a7c	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	biomarker_via_orthology	DOID:8481	rheumatic myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855693	Nap1l1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050452	mevalonic aciduria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050426	Stevens-Johnson syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109280	Nudt1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:0080822	aspirin-induced respiratory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98483	Tap1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104631	Utrn	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429764	Trpv5	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341090	Tnfrsf10b	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336884	Slc22a18	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2138327	Phlpp1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:0080797	nasal type extranodal NK/T-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97808	Ptpra	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97364	Notch2	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926232	Srsf7	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98510	Tcf3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384590	Ndrg4	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927259	Trpv6	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704482	Nutf2-ps2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:9743	diabetic neuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101061	Slc18a3	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88184	Bmyc	biomarker_via_orthology	DOID:0110858	polycystic kidney disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:0080799	sinonasal undifferentiated carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:8649	tongue cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:8923	skin melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97856	Rara	biomarker_via_orthology	DOID:3324	mood disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:8622	measles						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099443	Nnmt	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98295	Shbg	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	biomarker_via_orthology	DOID:0050745	diffuse large B-cell lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:676	juvenile rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109338	Rap1gap	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:10584	retinitis pigmentosa						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914652	Txndc8	biomarker_via_orthology	DOID:12336	male infertility						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351645	Prmt5	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104642	Pla2g2a	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934664	Rpph1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104662	Pml	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106067	Smc2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13636	Fanconi anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:0060081	triple-receptor negative breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:0080832	mild cognitive impairment						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	biomarker_via_orthology	DOID:4556	lung large cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97374	Npy	biomarker_via_orthology	DOID:1307	dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:14256	adult-onset Still's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:6543	acne						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928394	Mtor	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:9065	leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:0050610	oral cavity carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913150	Trem2	biomarker_via_orthology	DOID:4166	syphilis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1203524	Smarcc1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276535	Ncoa3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:106	pleural tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858256	Naip7	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:6193	epithelioid sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108008	Nutf2-ps1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0110429	dilated cardiomyopathy 1H						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576090	Ugt1a8	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97896	Reg2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:5394	prolactinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13276	Mycoplasma pneumoniae pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109354	Ucp2	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109132	Snap91	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:0050852	limb ischemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2141503	Pot1a	biomarker_via_orthology	DOID:1949	cholecystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384561	Nae1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97244	Mx2	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97597	Prkcg	biomarker_via_orthology	DOID:3525	middle cerebral artery infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:8805	intermediate coronary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:10487	Hirschsprung's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321159	Ppp2ca	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3650419	Snrpert	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98894	Ucp1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926080	Slc25a12	biomarker_via_orthology	DOID:0060041	autism spectrum disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914514	Ndufb8	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97281	Ncam1	biomarker_via_orthology	DOID:0050933	ovarian serous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923385	Prex2	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919448	Mtrex	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104288	Pms2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927555	Slc4a4	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104596	Procr	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195266	Tnfaip6	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107606	Srebf1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97495	Pbx1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106202	Spink1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:0080909	castration-resistant prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:11335	sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	biomarker_via_orthology	DOID:8567	Hodgkin's lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95755	Slc2a1	biomarker_via_orthology	DOID:255	hemangioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103062	Stat4	biomarker_via_orthology	DOID:869	cholesteatoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915902	Tab2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104638	Tff3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:615	leukopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:8463	corneal ulcer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108037	Vegfd	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:3030	mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:0060036	intrinsic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1931139	Ppp1r14a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:3314	angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:10126	keratoconus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108388	Sephs2	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1270156	Septin4	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107414	Tnfsf10	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97249	Myb	biomarker_via_orthology	DOID:0050523	adult T-cell leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:8677	perinatal necrotizing enterocolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:3702	cervical adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103035	Stat5b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921319	Serpina3a	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2139360	Sall4	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3576092	Ugt1a9	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	biomarker_via_orthology	DOID:5241	hemangioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916686	Mtfp1	biomarker_via_orthology	DOID:769	neuroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:0060322	mastoiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107365	Ube2i	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915301	Nutf2	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:1875	impotence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98346	Snrpe	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099443	Nnmt	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107742	Stra6	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97771	Proc	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:5614	eye disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:12140	Chagas disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:4914	esophagus adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98181	Rrm2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:4449	macular retinal edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:1577	limited scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:3492	mixed connective tissue disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98371	Sox9	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:13141	uveitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106686	Pon3	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3042	allergic contact dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103098	Pdpn	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108388	Sephs2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:8472	localized scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:1184	nephrotic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:614	lymphopenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050881	inclusion body myopathy with Paget disease of bone and frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:1389	polyneuropathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153568	Sp7	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916906	Pir	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97895	Reg1	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041197	Serpina7	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915445	Rnaset2a	biomarker_via_orthology	DOID:5410	pulmonary neuroendocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96055	Ptpn6	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:13025	retinopathy of prematurity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103181	Sod3	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103293	Ptpn13	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097156	Ptgis	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97550	Pfn2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341157	Sox30	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97243	Mx1	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98880	Tyr	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98341	Snrnp70	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1347008	Plod3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108420	Nfe2l2	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:9368	keratoconjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:1495	cystic echinococcosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:557	kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855693	Nap1l1	biomarker_via_orthology	DOID:11240	appendiceal neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:4677	keratitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3042141	Traf7	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:0080191	PTEN hamartoma tumor syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108037	Vegfd	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888984	Tbx21	biomarker_via_orthology	DOID:12365	malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:9477	pulmonary embolism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2143151	Rpp25	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3512	neurofibrosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890577	Srsf4	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98330	Snai1	biomarker_via_orthology	DOID:9655	oral mucosa leukoplakia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109408	Reg3a	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:12466	secondary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102643	Myh11	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96083	Nrg1	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:3490	Noonan syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97896	Reg2	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:14067	Plasmodium falciparum malaria						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	biomarker_via_orthology	DOID:686	liver carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149332	Ncr3-ps	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142572	Mtus1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:0050741	alcohol dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1274781	Robo1	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338033	Spint1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102848	Serpina3c	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105083	Slc1a1	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919035	Pdgfd	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3580642	Ugt1a10	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:12120	pulmonary alveolar proteinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97551	Prf1	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99684	Ryr3	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104662	Pml	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97895	Reg1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:9470	bacterial meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97847	Raf1	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:7693	abdominal aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:559	acute pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103039	Stat2	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102695	Ptprf	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:10223	dermatomyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:0050804	glioblastoma proneural subtype						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350932	Ncoa4	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107742	Stra6	biomarker_via_orthology	DOID:13641	exfoliation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109124	Vegfc	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107476	Stim1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446229	Tet3	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:11088	asphyxia neonatorum						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336212	Ncr1	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98001	Rpe65	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:643	progressive multifocal leukoencephalopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104597	Tnnt2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354956	Tfr2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	biomarker_via_orthology	DOID:2349	arteriosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	biomarker_via_orthology	DOID:2237	hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97312	Nfkb1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:3310	atopic dermatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:12177	common variable immunodeficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98729	Tgfbr2	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:9408	acute myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98214	Rxra	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:11506	suppurative otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:633	myositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182843	Serpina3j	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:5485	synovial sarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355328	Nasp	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97490	Pax6	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98743	Thrb	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102967	Mtnr1a	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109486	Prdx2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176887	Tlr8	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:12132	granulomatosis with polyangiitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102548	Tsc2	biomarker_via_orthology	DOID:3314	angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:11123	Henoch-Schoenlein purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915902	Tab2	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:12143	neurogenic bladder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104908	Ptk2b	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918084	Spag9	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915599	Ndufs3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:13359	Ehlers-Danlos syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105046	Serpina3g	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:2957	pulmonary tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:11984	hypertrophic cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97621	Plk1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98285	Srsf3	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298222	Naip6	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97897	Rel	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2441741	Rapgef3	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96269	Ranbp1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338068	Pdpk1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13088	periventricular leukomalacia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	biomarker_via_orthology	DOID:1003	pelvic inflammatory disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:2987	familial mediterranean fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919722	Slc16a10	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104741	Nfkbia	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1858214	Ppm1d	biomarker_via_orthology	DOID:0060071	pre-malignant neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:8283	peritonitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101838	Tbp	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:13129	severe pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109272	Vipr1	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97255	Myh6	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918177	Setd2	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98279	Sell	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98763	Tk1	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:11624	penile benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918248	Phf6	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444112	Sox2ot	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:11202	primary hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351663	Skp2	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:1884	viral hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442408	Syne3	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98932	Vim	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2154952	Ripk3	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106684	Slc18a1	biomarker_via_orthology	DOID:14175	von Hippel-Lindau disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926375	Rassf5	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103223	Vhl	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97572	Phb1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8505	dermatitis herpetiformis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:4676	uremia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97621	Plk1	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107585	Srebf2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182835	Serpina3b	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108037	Vegfd	biomarker_via_orthology	DOID:7575	pancreatic intraductal papillary-mucinous neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:11247	disseminated intravascular coagulation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:9643	babesiosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103063	Stat1	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:0080202	adenoid cystic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277977	Ubr1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345643	Sufu	biomarker_via_orthology	DOID:3073	brain glioblastoma multiforme						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:3314	angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97376	Nras	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:7998	hyperthyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:5052	melioidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97572	Phb1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98664	Tek	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97895	Reg1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101922	Tnc	biomarker_via_orthology	DOID:13100	intracranial vasospasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97614	Plcd1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97799	Pth	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106206	Nrp1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101931	Slc1a2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891831	Sfn	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109272	Vipr1	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	biomarker_via_orthology	DOID:11722	myotonic dystrophy type 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	biomarker_via_orthology	DOID:264	hemangiopericytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:9351	diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915902	Tab2	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109517	Sftpc	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:4001	ovarian carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:3069	malignant astrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336883	Smad6	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107164	Ppp3ca	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:3742	bladder squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109338	Rap1gap	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:0050433	fatal familial insomnia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918910	Rarres2	biomarker_via_orthology	DOID:10825	essential hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1195266	Tnfaip6	biomarker_via_orthology	DOID:4251	conjunctival disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:0050424	familial adenomatous polyposis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:9007	sudden infant death syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384590	Ndrg4	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98278	Sele	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341157	Sox30	biomarker_via_orthology	DOID:3907	lung squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98864	Ttn	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384310	Rbm10	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915045	Rnls	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349162	Sdc1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106658	Srf	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2146901	Trip10	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98493	Tbx1	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919583	Palld	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913604	Snw1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97531	Pdgfrb	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:3114	serous cystadenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106013	Slc16a1	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182841	Serpina3i	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:2006	preretinal fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97749	Ppia	biomarker_via_orthology	DOID:1474	aggressive periodontitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855692	Nono	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:7305	astroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928894	Rpl35a	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1891706	Spen	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:0110858	polycystic kidney disease 1						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98874	Txn1	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	biomarker_via_orthology	DOID:1949	cholecystitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:1909	melanoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:11166	Human papillomavirus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919762	Sting1	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588194	Prdm14	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:11132	prostatic hypertrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98378	Serpina3m	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97448	Otc	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3041197	Serpina7	biomarker_via_orthology	DOID:1837	diabetic ketoacidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:13810	familial hypercholesterolemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101884	Ppard	biomarker_via_orthology	DOID:4607	biliary tract cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97747	Pparg	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104327	Nog	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176375	Ucn2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0060903	thrombosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:0060318	acute promyelocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:446	primary hyperaldosteronism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1196377	Tnfaip3	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:0060322	mastoiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2147616	Otub1	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97503	Pcna	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:10588	adrenoleukodystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2387581	Ppp1r9b	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921430	Muc5b	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153470	Scgb3a2	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:2018	hyperinsulinism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:12449	aplastic anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:0050784	primary progressive multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97356	Nme2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894323	Ranbp2	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:8692	myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106295	Tomm70a	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2155445	Tmprss3	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:9120	amyloidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:0050912	colon adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:0060574	von Willebrand's disease 2						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:11981	morbid obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:0050697	chorioamnionitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:1440	Machado-Joseph disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105045	Serpina3n	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2182838	Serpina3f	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343085	Spop	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314891	Tnfrsf11a	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104641	Ptx3	biomarker_via_orthology	DOID:14115	toxic shock syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321159	Ppp2ca	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351327	Pla2g7	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:13378	Kawasaki disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353422	Spdef	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:289	endometriosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98296	Shc1	biomarker_via_orthology	DOID:9452	steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:4248	coronary stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:7188	autoimmune thyroiditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339639	Ogt	biomarker_via_orthology	DOID:1712	aortic valve stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106016	Tra2b	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3891	placental insufficiency						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:10923	sickle cell anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99655	Prdm1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106919	Vdac1	biomarker_via_orthology	DOID:0080855	Parkinsonism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2137495	Myocd	biomarker_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149961	Pawr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98181	Rrm2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1098211	Pik3cd	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918040	Ubr5	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98940	Vtn	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2142572	Mtus1	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98488	Slc6a6	biomarker_via_orthology	DOID:4752	multiple system atrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98865	Ttr	biomarker_via_orthology	DOID:0050860	colorectal adenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0111046	platelet-type bleeding disorder 10						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1930005	Trem1	biomarker_via_orthology	DOID:874	bacterial pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932339	Sf3b1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109604	Plk3	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914302	Ndc80	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920212	Tymp	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:2998	testicular cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1349164	Sdc4	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927593	Ptges	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99261	Ptgds	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339975	Pak1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890577	Srsf4	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:231	motor neuron disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923206	Srrm2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:5425	ovarian hyperstimulation syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107976	Slc8a3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:9255	frontotemporal dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108051	Smad2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1928396	Pdcd10	biomarker_via_orthology	DOID:2870	endometrial adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1916457	Srsf11	biomarker_via_orthology	DOID:0050908	myelodysplastic syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:2366	West Nile fever						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2149332	Ncr3-ps	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98284	Srsf2	biomarker_via_orthology	DOID:5410	pulmonary neuroendocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98790	Top2a	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663233	Muc6	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:552	pneumonia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3588263	Muc3a	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98495	Tbx3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1202709	Tert	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1339364	Muc2	biomarker_via_orthology	DOID:3030	mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97804	Ptn	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915452	Ndufa5	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104963	Npy1r	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88283	Serpinh1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106028	Rhoc	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96285	Slc6a4	biomarker_via_orthology	DOID:7475	diverticulitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98869	Tuba1a	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:0060224	atrial fibrillation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1329042	Sgce	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1861735	Tmeff2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:3265	chronic granulomatous disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2445126	Tut4	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109125	Timp4	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855690	Snrpa	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920982	Muc16	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:850	lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:1727	retinal vein occlusion						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2442609	Rnf43	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97309	Nefh	biomarker_via_orthology	DOID:1210	optic neuritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2135607	Sirt1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2150380	Srd5a2	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1099787	Ucp3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	biomarker_via_orthology	DOID:14735	hereditary angioedema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108418	Npy2r	biomarker_via_orthology	DOID:0050830	peripheral artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888711	Pf4	biomarker_via_orthology	DOID:2988	antiphospholipid syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1919907	Selenoh	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98181	Rrm2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338864	Stau1	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105305	Slc1a5	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:9471	meningitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109518	Sftpa1	biomarker_via_orthology	DOID:841	extrinsic allergic alveolitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:10964	cholesteatoma of middle ear						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97896	Reg2	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1855692	Nono	biomarker_via_orthology	DOID:0080685	aortic dissection						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1343103	Ndufa2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98916	Urod	biomarker_via_orthology	DOID:3132	porphyria cutanea tarda						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:10966	lipoid nephrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927578	Smpd3	biomarker_via_orthology	DOID:9675	pulmonary emphysema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890149	Tpm3	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:10230	aortic atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97762	Prl	biomarker_via_orthology	DOID:9993	hypoglycemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920145	Setd5	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:0060108	brain glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:892014	Sfrp1	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:0050625	biliary tract benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:0080365	endometrial hyperplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1920086	Pot1b	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2429397	Nod2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3702087	Rnaset2b	biomarker_via_orthology	DOID:5410	pulmonary neuroendocrine tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:2378	relapsing-remitting multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103034	Stat6	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:1883	hepatitis C						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1921393	Opa1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97369	Nppc	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:2841	asthma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923998	Pbrm1	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98783	Tnni3	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276535	Ncoa3	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2663233	Muc6	biomarker_via_orthology	DOID:3030	mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201674	Smad3	biomarker_via_orthology	DOID:3744	cervical squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:5773	oral submucous fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97249	Myb	biomarker_via_orthology	DOID:0080630	B-lymphoblastic leukemia/lymphoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109516	Sftpb	biomarker_via_orthology	DOID:12716	newborn respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:3021	acute kidney failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98400	Srd5a1	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98397	Src	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3070	high grade glioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922656	Ndufs7	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:8161	thyroid gland Hurthle cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933973	Rbfox2	biomarker_via_orthology	DOID:9955	hypoplastic left heart syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97528	Pdgfb	biomarker_via_orthology	DOID:13208	background diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:11396	pulmonary edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338881	St14	biomarker_via_orthology	DOID:4441	dysgerminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98377	Serpina3k	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:11049	meconium aspiration syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98534	Tcn2	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	biomarker_via_orthology	DOID:3526	cerebral infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101949	Rad52	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:0050872	large cell neuroendocrine carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1859821	Prdx5	biomarker_via_orthology	DOID:10459	common cold						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98217	S100b	biomarker_via_orthology	DOID:12783	migraine without aura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97323	Ngfr	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:13608	biliary atresia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97321	Ngf	biomarker_via_orthology	DOID:10003	sensorineural hearing loss						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1927665	Sirt3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107810	Tfam	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914434	Ndufa13	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:10241	thalassemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:11168	anogenital venereal wart						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102672	Runx3	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97515	Pcsk5	biomarker_via_orthology	DOID:234	colon adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:3082	interstitial lung disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201791	Socs3	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:3347	osteosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99694	Rasgrf1	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102780	Six1	biomarker_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98373	Sparc	biomarker_via_orthology	DOID:182	calcinosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100089	Tnfsf11	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:11612	polycystic ovary syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103151	Pltp	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1328366	Smarcb1	biomarker_via_orthology	DOID:0050861	colorectal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109634	Terf1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109580	Sf3b4	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102809	Sars1	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1096342	Rhoa	biomarker_via_orthology	DOID:2377	multiple sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:2921	glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:88135	Tff1	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2444386	Tmem63c	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:13241	Behcet's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:11204	allergic conjunctivitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0080998	acute necrotizing pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:0081267	graft-versus-host disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336212	Ncr1	biomarker_via_orthology	DOID:635	acquired immunodeficiency syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1101061	Slc18a3	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	biomarker_via_orthology	DOID:4948	gallbladder carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894696	Serping1	biomarker_via_orthology	DOID:898	autosomal dominant polycystic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97527	Pdgfa	biomarker_via_orthology	DOID:2526	prostate adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109587	Tnfrsf11b	biomarker_via_orthology	DOID:3407	carotid artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99659	Ryr1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1934229	Setdb1	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:2043	hepatitis B						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929600	Pmepa1	biomarker_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915051	Pllp	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:4481	allergic rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1355296	Prkn	biomarker_via_orthology	DOID:12217	Lewy body dementia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929865	Nampt	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352464	Nr1h4	biomarker_via_orthology	DOID:0080547	metabolic dysfunction-associated steatohepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96825	Selenbp1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891968	Serpina1d	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891970	Serpina1b	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97874	Rb1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891967	Serpina1e	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891971	Serpina1a	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:891969	Serpina1c	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107956	Slc8a1	biomarker_via_orthology	DOID:6432	pulmonary hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97384	Ntrk2	biomarker_via_orthology	DOID:5419	schizophrenia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98724	Tgfa	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346526	Psmb9	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:1470	major depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:1596	depressive disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103076	Vdr	biomarker_via_orthology	DOID:0080208	metabolic dysfunction-associated steatotic liver disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276533	Ncoa2	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97798	Ptgs2	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97621	Plk1	biomarker_via_orthology	DOID:10286	prostate carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298220	Naip5	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109634	Terf1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1206581	Pik3ca	biomarker_via_orthology	DOID:5041	esophageal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1342774	Ppargc1a	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914380	Ndufa6	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3495	extrahepatic bile duct adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106919	Vdac1	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:2596	larynx cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:4897	bile duct carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98254	Scp2	biomarker_via_orthology	DOID:905	Zellweger syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97306	Nf1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929183	Tsc1	biomarker_via_orthology	DOID:4852	pleomorphic xanthoastrocytoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:7474	malignant pleural mesothelioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:8544	chronic fatigue syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97250	Myc	biomarker_via_orthology	DOID:13543	hyperparathyroidism						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97621	Plk1	biomarker_via_orthology	DOID:2152	ovary epithelial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330275	Ptgdr2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1097693	Ogg1	biomarker_via_orthology	DOID:3314	angiomyolipoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103172	Zfp354a	biomarker_via_orthology	DOID:4440	seminoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	biomarker_via_orthology	DOID:1380	endometrial cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:1520	colon carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98297	Shh	biomarker_via_orthology	DOID:1312	focal segmental glomerulosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98733	Tg	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1922019	Pik3cb	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:0080899	lung pleomorphic carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:9111	cutaneous leishmaniasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913789	Xpo5	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98366	Sox4	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2156367	Tlr3	biomarker_via_orthology	DOID:10873	Kuhnt-Junius degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:2986	IgA glomerulonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:3192	neurilemmoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:14004	thoracic aortic aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95824	Nr3c1	biomarker_via_orthology	DOID:0080162	lupus nephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:10754	otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261834	Wnt2b	biomarker_via_orthology	DOID:3307	teratoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:332	amyotrophic lateral sclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103172	Zfp354a	biomarker_via_orthology	DOID:8719	in situ carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:8778	Crohn's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926007	Rictor	biomarker_via_orthology	DOID:5409	lung small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98962	Wnt7b	biomarker_via_orthology	DOID:1618	breast fibroadenoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1915116	Wfdc1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314884	Tnfrsf1a	biomarker_via_orthology	DOID:0050848	obstructive sleep apnea						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346329	Uts2	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:3312	bipolar disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:12361	Graves' disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0050866	oral squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:2394	ovarian cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:526	human immunodeficiency virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1261834	Wnt2b	biomarker_via_orthology	DOID:1911	endodermal sinus tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109495	Nfil3	biomarker_via_orthology	DOID:2945	severe acute respiratory syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98389	Spp1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2450016	Nox1	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:4989	pancreatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:106677	Slc18a2	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97898	Ren1	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98962	Wnt7b	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:5520	head and neck squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107157	Sin3a	biomarker_via_orthology	DOID:12858	Huntington's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108075	Smo	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	biomarker_via_orthology	DOID:8991	cervix uteri carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:0050127	sinusitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:0050902	medulloblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109635	Wrn	biomarker_via_orthology	DOID:397	restrictive cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101893	Pou5f1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446084	Wnt9a	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104528	S100g	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99180	Zfp36	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:8924	autoimmune thrombocytopenic purpura						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330275	Ptgdr2	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103295	Pon1	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97612	Plaur	biomarker_via_orthology	DOID:11729	Lyme disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97749	Ppia	biomarker_via_orthology	DOID:12506	Bell's palsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97567	Pgr	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1918882	Scn3b	biomarker_via_orthology	DOID:4724	brain edema						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98958	Wnt5a	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99852	Runx1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98752	Timp1	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1913755	Zmynd11	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:8947	diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1890577	Srsf4	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:102722	Pcnt	biomarker_via_orthology	DOID:14250	Down syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:3213	demyelinating disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2446084	Wnt9a	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98961	Wnt7a	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888496	Tbx20	biomarker_via_orthology	DOID:1682	congenital heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:114	heart disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:9261	nasopharynx carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3612191	Nlrc5	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298397	Sncg	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894293	Smad4	biomarker_via_orthology	DOID:4928	intrahepatic cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107471	Notch4	biomarker_via_orthology	DOID:7148	rheumatoid arthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889585	Sall1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98919	Scgb1a1	biomarker_via_orthology	DOID:2799	bronchiolitis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1330810	Trp63	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98354	Sos1	biomarker_via_orthology	DOID:4362	cervical cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95606	Xrcc6	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153470	Scgb3a2	biomarker_via_orthology	DOID:4483	rhinitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109528	Trpc1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276523	Ncoa1	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98753	Timp2	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1321159	Ppp2ca	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:10591	pre-eclampsia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1338947	S100a9	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1932389	Tlr9	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333778	Spa17	biomarker_via_orthology	DOID:3965	Merkel cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12236	primary biliary cholangitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:4929	tubular adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095438	Slc2a2	biomarker_via_orthology	DOID:3892	insulinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:37	skin disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98959	Wnt5b	biomarker_via_orthology	DOID:127	leiomyoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:3030	mucinous adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:4971	myelofibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1354910	Socs1	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:8761	acute megakaryocytic leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888506	Retn	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97899	Ren2	biomarker_via_orthology	DOID:9970	obesity						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98364	Sox2	biomarker_via_orthology	DOID:0050865	tongue squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2176882	Tlr7	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97595	Prkca	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98954	Wnt2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98280	Selp	biomarker_via_orthology	DOID:5844	myocardial infarction						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1341157	Sox30	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1889011	Sncb	biomarker_via_orthology	DOID:3981	pantothenate kinase-associated neurodegeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:7031	glottis squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98941	Vwf	biomarker_via_orthology	DOID:10941	intracranial aneurysm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97535	Pdyn	biomarker_via_orthology	DOID:9976	heroin dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105095	Pgf	biomarker_via_orthology	DOID:11400	pyelonephritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:105373	Ptch1	biomarker_via_orthology	DOID:2512	nevoid basal cell carcinoma syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97439	Oprk1	biomarker_via_orthology	DOID:11206	opioid abuse						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1332638	Wiz	biomarker_via_orthology	DOID:1936	atherosclerosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1314883	Tnfrsf1b	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103036	Stat5a	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929282	Ptges3	biomarker_via_orthology	DOID:3181	oligodendroglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99603	Smarca2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98822	Tfrc	biomarker_via_orthology	DOID:2671	transitional cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:8398	osteoarthritis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107371	Rtkn	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:4682	extrahepatic bile duct carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:2048	autoimmune hepatitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:2696	Leydig cell tumor						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:3328	temporal lobe epilepsy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97537	Pecam1	biomarker_via_orthology	DOID:12849	autistic disorder						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	biomarker_via_orthology	DOID:0050685	small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344408	Pebp1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95481	Ptk2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97797	Ptgs1	biomarker_via_orthology	DOID:2893	cervix carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1306805	Tff2	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:783	end stage renal disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97479	Pappa	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:2355	anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:0080199	colorectal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1277151	Snca	biomarker_via_orthology	DOID:11870	Pick's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97383	Ntrk1	biomarker_via_orthology	DOID:13406	pulmonary sarcoidosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:399	tuberculosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1353495	Slc25a4	biomarker_via_orthology	DOID:11727	facioscapulohumeral muscular dystrophy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97583	Pik3r1	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98726	Tgfb2	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97367	Nppa	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:1270	hereditary hemorrhagic telangiectasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98351	Sod1	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2443298	Tet2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97380	Ntf3	biomarker_via_orthology	DOID:3083	chronic obstructive pulmonary disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153530	Hamp2	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103038	Stat3	biomarker_via_orthology	DOID:0050156	idiopathic pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1333805	Srsf10	biomarker_via_orthology	DOID:4448	macular degeneration						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98352	Sod2	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108005	Myd88	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1346060	Tlr2	biomarker_via_orthology	DOID:8893	psoriasis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98283	Srsf1	biomarker_via_orthology	DOID:8552	chronic myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:14566	disease of cellular proliferation						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923650	Pbp2	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108109	Ywhag	biomarker_via_orthology	DOID:11949	Creutzfeldt-Jakob disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2681862	Obscn	biomarker_via_orthology	DOID:12930	dilated cardiomyopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:5517	stomach carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108080	Serpinf1	biomarker_via_orthology	DOID:9744	type 1 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914195	Sdha	biomarker_via_orthology	DOID:14330	Parkinson's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109583	Pten	biomarker_via_orthology	DOID:0050933	ovarian serous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97879	Rbp4	biomarker_via_orthology	DOID:13207	proliferative diabetic retinopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1350932	Ncoa4	biomarker_via_orthology	DOID:10283	prostate cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98725	Tgfb1	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109515	Sftpd	biomarker_via_orthology	DOID:9074	systemic lupus erythematosus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97620	Plg	biomarker_via_orthology	DOID:10159	osteonecrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:12894	Sjogren's syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1924882	Pramel13	biomarker_via_orthology	DOID:9119	acute myeloid leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:10140	dry eye syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97615	Plcg1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97361	Nos2	biomarker_via_orthology	DOID:3393	coronary artery disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98834	Trp53	biomarker_via_orthology	DOID:0002116	pterygium						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:687	hepatoblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1201787	Socs2	biomarker_via_orthology	DOID:0060074	ductal carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98973	Xdh	biomarker_via_orthology	DOID:9538	multiple myeloma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1095418	Tfpi	biomarker_via_orthology	DOID:1240	leukemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1352462	Nr1h3	biomarker_via_orthology	DOID:13001	carotid stenosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:418	systemic scleroderma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98962	Wnt7b	biomarker_via_orthology	DOID:11054	urinary bladder cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1914227	Nuf2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:11650	bronchopulmonary dysplasia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97307	Nf2	biomarker_via_orthology	DOID:12689	acoustic neuroma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98926	Vcam1	biomarker_via_orthology	DOID:8481	rheumatic myocarditis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1923688	Rftn1	biomarker_via_orthology	DOID:1686	glaucoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104879	Pdcd1	biomarker_via_orthology	DOID:1273	respiratory syncytial virus infectious disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98727	Tgfb3	biomarker_via_orthology	DOID:219	colon cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104517	Xrcc5	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96955	Slc3a2	biomarker_via_orthology	DOID:3910	lung adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97530	Pdgfra	biomarker_via_orthology	DOID:3459	breast carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95606	Xrcc6	biomarker_via_orthology	DOID:1749	squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97231	Muc1	biomarker_via_orthology	DOID:11394	adult respiratory distress syndrome						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97441	Oprm1	biomarker_via_orthology	DOID:9975	cocaine dependence						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	biomarker_via_orthology	DOID:1324	lung cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109585	Pld1	biomarker_via_orthology	DOID:3498	pancreatic ductal adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	biomarker_via_orthology	DOID:3007	breast ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99137	Xrcc1	biomarker_via_orthology	DOID:3571	liver cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97313	Nefl	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101948	Wnt11	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98736	Thbd	biomarker_via_orthology	DOID:7147	ankylosing spondylitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97362	Nos3	biomarker_via_orthology	DOID:3319	lymphangioleiomyomatosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:12549	hepatitis A						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98287	Srsf5	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98737	Thbs1	biomarker_via_orthology	DOID:4947	cholangiocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1340806	Parp1	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1351899	Slco1b2	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104798	Tnf	biomarker_via_orthology	DOID:0080600	COVID-19						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97610	Plat	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1926321	Postn	biomarker_via_orthology	DOID:90	degenerative disc disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1344332	Wif1	biomarker_via_orthology	DOID:3008	invasive ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98957	Wnt4	biomarker_via_orthology	DOID:2871	endometrial carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:1485	cystic fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1888712	Ppbp	biomarker_via_orthology	DOID:4467	clear cell renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1298205	Slc7a5	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97355	Nme1	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97809	Ptprb	biomarker_via_orthology	DOID:3068	glioblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:9352	type 2 diabetes mellitus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:3704271	Ptges3-ps	biomarker_via_orthology	DOID:3181	oligodendroglioma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:894687	Xrn2	biomarker_via_orthology	DOID:1967	leiomyosarcoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97368	Nppb	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99685	Ryr2	biomarker_via_orthology	DOID:11714	gestational diabetes						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98872	Twist1	biomarker_via_orthology	DOID:3770	pulmonary fibrosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98933	Vip	biomarker_via_orthology	DOID:8577	ulcerative colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:3717	gastric adenocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1100518	Smad7	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:101875	Thpo	biomarker_via_orthology	DOID:5160	arteriosclerosis obliterans						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:3748	esophagus squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:95758	Slc2a4	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104697	Muc5ac	biomarker_via_orthology	DOID:3587	pancreatic ductal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98821	Trf	biomarker_via_orthology	DOID:10763	hypertension						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	biomarker_via_orthology	DOID:0050933	ovarian serous carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1929600	Pmepa1	biomarker_via_orthology	DOID:1612	breast cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:99948	Zfhx3	biomarker_via_orthology	DOID:3908	lung non-small cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2144013	Xpo1	biomarker_via_orthology	DOID:1793	pancreatic cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1276123	Ucn	biomarker_via_orthology	DOID:6000	congestive heart failure						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:104517	Xrcc5	biomarker_via_orthology	DOID:2513	basal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2153525	Muc4	biomarker_via_orthology	DOID:4608	common bile duct neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:96824	Tlr4	biomarker_via_orthology	DOID:11506	suppurative otitis media						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1336991	Trp73	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	biomarker_via_orthology	DOID:784	chronic kidney disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97360	Nos1	biomarker_via_orthology	DOID:10652	Alzheimer's disease						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97608	Serpine1	biomarker_via_orthology	DOID:0081120	Graves ophthalmopathy						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1315205	Slit2	biomarker_via_orthology	DOID:0080745	polymyositis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:107572	Xiap	biomarker_via_orthology	DOID:4450	renal cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:109484	Ywhaz	biomarker_via_orthology	DOID:684	hepatocellular carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103262	Yap1	biomarker_via_orthology	DOID:9256	colorectal cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97845	Rac1	biomarker_via_orthology	DOID:10534	stomach cancer						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:2384933	Wrap53	biomarker_via_orthology	DOID:1984	rectal benign neoplasm						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98968	Wt1	biomarker_via_orthology	DOID:2154	nephroblastoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103022	Reln	biomarker_via_orthology	DOID:5082	liver cirrhosis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1345282	Slc30a4	biomarker_via_orthology	DOID:8634	prostate carcinoma in situ						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108212	Ripk1	biomarker_via_orthology	DOID:9201	lichen planus						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103290	Rela	biomarker_via_orthology	DOID:2876	laryngeal squamous cell carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:103178	Vegfa	biomarker_via_orthology	DOID:0060181	ischemic colitis						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:97611	Plau	biomarker_via_orthology	DOID:3969	thyroid gland papillary carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:1933533	Hamp	biomarker_via_orthology	DOID:11758	iron deficiency anemia						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:108072	Traf6	biomarker_via_orthology	DOID:2600	laryngeal carcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance
NCBITaxon:10090	Mus musculus	gene	MGI:98754	Timp3	biomarker_via_orthology	DOID:3594	choriocarcinoma						ECO:0000501	evidence used in automatic assertion	MGI:6194238	20240226	Alliance